Procyonid (Procyonidae) Care Manual
Procyonid (Procyonidae) Care Manual
Procyonid (Procyonidae) Care Manual
(Procyonidae)
CARE MANUAL
CREATED BY THE
AZA Small Carnivore Taxon Advisory Group
IN ASSOCIATION WITH THE
AZA Animal Welfare Committee
Procyonid (Procyonidae) Care Manual
Reviewers:
Sue Booth-Binczik, Ph.D., Dallas Zoo
Denise Bressler, Logan & Abby‟s Fund
Kristofer Helgen, Smithsonian Institution
Kim Schilling, Animals for Awareness
Mindy Stinner, Conservators‟ Center, Inc.
Debbie Thompson, Little Rock Zoo
Rhonda Votino
Debborah Colbert Ph.D., AZA, Vice President of Animal Conservation
Paul Boyle Ph.D., AZA, Senior Vice President of Conservation and Education
Disclaimer: This manual presents a compilation of knowledge provided by recognized animal experts
based on the current science, practice, and technology of animal management. The manual assembles
basic requirements, best practices, and animal care recommendations to maximize capacity for
excellence in animal care and welfare. The manual should be considered a work in progress, since
practices continue to evolve through advances in scientific knowledge. The use of information within this
manual should be in accordance with all local, state, and federal laws and regulations concerning the
care of animals. While some government laws and regulations may be referenced in this manual, these
are not all-inclusive nor is this manual intended to serve as an evaluation tool for those agencies. The
recommendations included are not meant to be exclusive management approaches, diets, medical
treatments, or procedures, and may require adaptation to meet the specific needs of individual animals
and particular circumstances in each institution. Commercial entities and media identified are not
necessarily endorsed by AZA. The statements presented throughout the body of the manual do not
represent AZA standards of care unless specifically identified as such in clearly marked sidebar boxes.
Table of Contents
Introduction ............................................................................................................................................... 5
Taxonomic Classification ...................................................................................................................... 5
Genus, Species, and Status ................................................................................................................. 5
General Information ............................................................................................................................... 5
Chapter 1. Ambient Environment ........................................................................................................ 9
1.1 Temperature and Humidity ............................................................................................................ 9
1.2 Light ................................................................................................................................................... 9
1.3 Water and Air Quality.................................................................................................................... 10
1.4 Sound and Vibration ..................................................................................................................... 10
Chapter 2. Habitat Design and Containment .................................................................................. 11
2.1 Space and Complexity.................................................................................................................. 11
2.2 Safety and Containment ............................................................................................................... 14
Chapter 3. Transport ............................................................................................................................. 17
3.1 Preparations ................................................................................................................................... 17
3.2 Protocols ......................................................................................................................................... 17
Chapter 4. Social Environment........................................................................................................... 19
4.1 Group Structure and Size ............................................................................................................ 19
4.2 Influence of Other Species and Conspecifics ........................................................................... 20
4.3 Introductions and Reintroductions .............................................................................................. 21
Chapter 5. Nutrition ............................................................................................................................... 23
5.1 Nutritional Requirements.............................................................................................................. 23
5.2 Diets ................................................................................................................................................ 26
5.3 Nutritional Evaluations .................................................................................................................. 31
Chapter 6. Veterinary Care .................................................................................................................. 33
6.1 Veterinary Services ....................................................................................................................... 33
6.2 Identification Methods ................................................................................................................... 35
6.3 Transfer Examination and Diagnostic Testing Recommendations........................................ 35
6.4 Quarantine ...................................................................................................................................... 35
6.5 Preventive Medicine...................................................................................................................... 37
6.6 Capture, Restraint, and Immobilization ...................................................................................... 41
6.7 Management of Diseases, Disorders, Injuries and/or Isolation.............................................. 42
Chapter 7. Reproduction ...................................................................................................................... 47
7.1 Reproductive Physiology and Behavior ..................................................................................... 47
7.2 Assisted Reproductive Technology ............................................................................................ 49
7.3 Pregnancy and Parturition ........................................................................................................... 49
7.4 Birthing Facilities ........................................................................................................................... 51
7.5 Assisted Rearing ........................................................................................................................... 51
7.6 Contraception................................................................................................................................. 55
Chapter 8. Behavior Management ..................................................................................................... 57
8.1 Animal Training .............................................................................................................................. 57
8.2 Environmental Enrichment ........................................................................................................... 58
8.3 Staff and Animal Interactions ...................................................................................................... 61
8.4 Staff Skills and Training................................................................................................................ 62
Chapter 9. Program Animals ............................................................................................................... 64
9.1 Program Animal Policy ................................................................................................................. 64
Introduction
Preamble
Association of Zoos & Aquariums (AZA) accredited institutions are required to comply with all relevant
local, state, and federal wildlife laws and regulations in addition to all AZA accreditation standards.
AZA accreditation standards, relevant to the topics discussed in this manual, are highlighted in boxes
such as this throughout the document (Appendix A).
AZA accreditation standards are continuously being raised or added. Staff from AZA-accredited
institutions are required to know and comply with all AZA accreditation standards, including those most
recently listed on the AZA website (www.aza.org) which might not be included in this manual.
Taxonomic Classification
Table 1: Taxonomic classification for Procyonidae
Classification Taxonomy Additional information
Kingdom Animalia
Phylum Chordata
Class Mammalia
Order Carnivora
Suborder Caniformia
Family Procyonidae
Subfamily Potosinae Kinkajou & olingo
Procyoninae Raccoon, coati, cacomistle, ringtail
General Information
The information contained within this Animal Care Manual (ACM) provides a compilation of animal
care and management knowledge that has been gained from recognized species experts, including AZA
Taxon Advisory Groups (TAGs), Species Survival Plan® Programs (SSPs), biologists, veterinarians,
nutritionists, reproduction physiologists, behaviorists and researchers. They are based on the most
current science, practices, and technologies used in animal care and management and are valuable
resources that enhance animal welfare by providing information about the basic requirements needed
and best practices known for caring for ex situ procyonid populations. This ACM is considered a living
document that is updated as new information becomes available and at a minimum of every five years.
Information presented is intended solely for the education and training of zoo and aquarium personnel
at AZA-accredited institutions. Recommendations included in the ACM are not exclusive management
approaches, diets, medical treatments, or procedures, and may require adaptation to meet the specific
needs of individual animals and particular circumstances in each institution. Statements presented
throughout the body of the manuals do not represent specific AZA accreditation standards of care unless
specifically identified as such in clearly marked sidebar boxes. AZA-accredited institutions which care for
procyonids must comply with all relevant local, state, and federal wildlife laws and regulations; AZA
accreditation standards that are more stringent than these laws and regulations must be met (AZA
Accreditation Standard 1.1.1).
hind foot posture to descend from trees headfirst. The table (Table 3) below gives generalized information
on each species.
Table 3: Morphological and ecological information on procyonid species
Social
Head-Body System
Arboreal/ Carnivore/ Noct/Diurn/
Species Length (S-solitary,
Terrestrial Omnivore Crepuscular
(centimeters) P-pair, G-
group)
Olingo 35-48cm S, P A O N
Ringtail 30.5-42cm S, P A/T C/O N
C.A. cacomistle 30-47cm S, P A O N
White-nosed coati 41-67cm G* B O D
Brown-nosed coati 49-54cm G* B O D
Island coati 74.4-78.5cm G* B O D
Mountain coati 36-39cm G* A,B O D
Kinkajou 45-75cm S, P A O N
Crab-eating raccoon 54-65cm S, G(females) B, W O N
Raccoon S,
45-65cm B, W O N
G(females)
Social System codes indicate how they have been kept in zoos, where available, or what is known of their social system in the wild.
An * is used to indicate species in which the males are primarily solitary. Arboreal/Terrestrial indicates where they spend most of
their time. Species listed as both are those that are considered terrestrial but are known to climb well. A „W‟ has been given to
species that swim well, or appear to enjoy water features in their exhibits. Carnivore/Omnivore – species are listed as carnivorous if
they predominantly eat animal protein however, they may eat some vegetation as well. An Omnivorous listing was given to those
that are known to eat vegetative matter regularly. They are given a C/O if they lean more towards carnivorous habits but are known
to regularly eat fruit, etc. Nocturnal (N), Diurnal (D), or Crepuscular (C) codes indicate their typical, peak activity periods (Nowak
1999; Rodriguez-Bolanos et al. 2000; Reed-Smith et al. 2003).
The AZA Small Carnivore TAG has designated four species of Procyonidae to be managed under the
AZA Taxon Advisory Group (2009 SCTAG Regional Collection Plan). These are the ringtail (Bassariscus
astutus), white-nosed coati (Nasua narica), kinkajou (Potos flavus) and common raccoon (Procyon lotor).
The brown-nosed coati (Nasua nasua) and Central American cacomistle (B. sumichrasti) previously
managed are currently recommended for Phase Out. The following guidelines are designed specifically
with these species in mind; however some individuals of other Procyonidae species are housed in AZA
institutions and may be used as related-species examples.
Conservation Status: The following table (Table 4) provides information on the conservation status of
procyonid species, based on CITES and IUCN lists.
It is preferable that all species be kept in situations that account for the typical seasonal light changes
that would be found in their native range (Roberts 1997). According to Poglayen-Neuwall (1995), it is
important that artificial light is added year round to indoor exhibits, particularly for the ringtail in which light
is a key factor in stimulating breeding.
Increasing winter photoperiod plays an important role in initiating reproduction for seasonally breeding
procyonids (raccoon, ringtail, and cacomistle) (Poglayen-Neuwall 1995; Roberts 1997).
1.3 Water and Air Quality
AZA-accredited institutions must have a regular program of
AZA Accreditation Standard
monitoring water quality for collections of aquatic animals and a
written record must document long-term water quality results and (1.5.9) The institution must have a regular
chemical additions (AZA Accreditation Standard 1.5.9). program of monitoring water quality for
collections of fish, pinnipeds, cetaceans,
Monitoring selected water quality parameters provides and other aquatic animals. A written
confirmation of the correct operation of filtration and disinfection record must be maintained to document
of the water supply available for the collection. Additionally, high long-term water quality results and
quality water enhances animal health programs instituted for chemical additions.
aquatic collections.
Air Quality: The number of air changes per hour needed to maintain desired temperature ranges indoors
will vary according to the volume of the enclosure. Standardized rates of change for various human-
occupied enclosures suggest that pet shops require a rate of air exchange, on non-recirculated air equal
to 1 cubic foot of air per minute per square foot of floor space in order to keep odors down to a level
acceptable by the public. Depending on size, cubbing dens may well need higher rates of air exchange in
order to maintain air quality (Anon 1981).
Water Quality: No standards have been set for non- or semi-aquatic species. Chemical residues,
bacterial counts, mineral levels, and salts should be kept as low as possible. Fecal material and food
remnants should be removed daily. The pH tolerance for procyonids is not known, but is not likely to be
vitally important for these species. Turbidity, except for isolated areas, should be kept to a minimum to
encourage use of water features.
1.4 Sound and Vibration
Consideration should be given to controlling sounds and vibrations that can be heard by procyonids in
the care of AZA-accredited zoos and aquariums. Many procyonids anecdotally show sensitivity to loud
noises, particularly during parturition and early kit rearing. Every effort should be made to reduce loud or
unusual noises and minimize continuous vibrations during these sensitive periods. Little is known about
sound or vibration sensitivity in these species and should be investigated in the future.
2 2
Roberts 1997 8 m /86 ft
40.6 cm 2 2
Ringtail Formula IIIb 7.4 m /80 ft
(16 in) 2 2
Formula IVb 16.4 m /177 ft
2 2
Roberts 1997 8 m /86 ft
45.7 cm 2 2
Cacomistle Formula IIIb 8.4 m /90 ft
(18 in) 2 2
Formula IVb 21 m /225 ft
2 2
Standley 1992 (group exhibit) 70 m /753.5ft
2 2
66 cm Roberts 1997 16 m /172 ft
White-nosed coati 2 2
(26 in) Formula IIb 12.1 m /130 ft
2 2
Formula IIIb 43.6 m /469 ft
* Provide an extra 25% for each additional animal
The formulas used to determine appropriate enclosure sizes are based on three factors: 1) species
average head and body length; 2) typical home range size, daily travel distances, and activity level; and
3) professional experience with these species to date. The recommendations were then sent out for
review by the AZA SCTAG Institutional Representatives and responses were incorporated. The exhibit
size formulas below are based on HBL (head and body length) and are given in inches:
Formula I – (HBL/12 x X) (with a large home range/daily travel distance). Seven to eight feet
2
vertical space should be allowed for more arboreal species. For highly terrestrial social species,
go up one size group.
2 2
o Small animals: 10-15 inches – (HBL/12 x 6) = # feet
2 2
o Medium animals: 15-30 inches – (HBL/12 x 10) = # feet
2 2
o Large animals: over 30 inches – (HBL/12 x 12) = # feet
Formula II – (HBL/12 x X) x given dimension for depth (with a small home range/daily travel
distance). Seven to eight feet vertical space should be allowed for more arboreal species. For
highly terrestrial social species go up one size group.
2
o Small animals: 10-15 inches – (HBL x 6)/12 x 3 feet = # feet
2
o Medium animals: 15-30 inches – (HBL x 10)/12 x 6 feet = # feet
2
o Large animals: over 30 inches – (HBL x 12)/12 x 10 feet = # feet
Formula III – A minimum of 8-10 feet vertical useable space and Formula II floor space.
Formula IV – A minimum of 8-10 feet vertical useable space and Formula I floor space.
2 2
Previous authors have suggested a minimum of 8 m (86 ft ) floor area and 2.5 m (8.2 ft) enclosure
height for 1-2 kinkajou, olingo, ringtail, or cacomistle; this space should be provided with climbing
apparatuses and nest boxes (see below for species specific information and current recommendations).
Cacomistle and ringtail: Ringtail and cacomistle engage in ricocheting, chimney stemming, and power
leaping locomotion (Trapp 1972). As these colorful descriptions imply, such species may require special
containment measures. Therefore, the AZA SCTAG suggests that these species be housed in completely
contained exhibits (i.e., roofed) with 3.05-3.66 m (10-12 ft) of useable vertical space. The current AZA
2 2 2
SCTAG recommendations call for a minimum exhibit size of 16.4 m (177 ft ) for two ringtails and 21 m
2
(225 ft ) for two cacomistles (AZA Small Carnivore TAG unpublished recommendation 2005). Water
moats can be used for ringtail and cacomistle (Roberts 1997). Studying ringtail in Texas, Ackerson and
2
Harveson (2006) determined a mean summer home range size of 0.28 +/- 0.163 km and mean winter
2
home range size of 0.63 +/- 0.219 km ; 80.6% of dens found were located on slopes between 30-60°.
Coati and raccoon: Roberts (1997) states that the larger size and greater terrestriality of the raccoons and
2 2
coatis dictate a floor area of at least 16 m (172 ft ) for one to two animals. Due to their tendency to spend
a fair amount of time in the trees, the AZA SCTAG recommends an enclosure height of at least 3.66 m
(12 ft) of useable space (AZA Small Carnivore TAG recommendation 2005). Standley (1992) suggested
2 2
larger group enclosures offering an example of a 70 m (753.5 ft ) moated exhibit. The AZA SCTAG is
2 2
recommending a minimum exhibit floor space of at least 43.6 m (469 ft ) for two animals with an increase
of 25% for each additional animal (AZA Small Carnivore TAG recommendation 2005). Outdoor, moated
enclosures are ideal for raccoons and coatis as long as the perimeters are secured to prevent escape
through climbing, jumping, or digging. Any enclosures with scalable walls (e.g., wire mesh or roughly
textured surfaces) should be completely contained to prevent escape (Roberts 1997). Exhibits should
have escape-proof substrates, hard surfaces, or a subsoil barrier of some kind (Standley 1992). Water
moats can be used for coatis (Roberts 1997).
Hass (2002) quantified home-range size and overlap among white-nosed coati matriarchal troops and
2
solitary males during a 4 year study in southeastern Arizona. “Home ranges of coatis averaged 13.57 km
2
± 1.72 SE for troops (n=9) and 6.11 ± 1.42 km for solitary males (n=7; kernel-density estimator).” She
also documented an overlap of male home-ranges of ~61%, home-ranges of troops overlapped ~ 80%,
and home ranges of males overlapped those of troops ~67% (Hass 2002 abstract).
2 2
Kinkajou: Roberts (1997) recommended 16 m (172 ft ) exhibit space for one to two animals. The AZA
SCTAG agrees with this recommendation. This species should be provided with at least 3.05-3.66 m (10-
12 ft) of useable, complex vertical space.
Enclosure Design: For management purposes, all procyonids should be considered partly arboreal and
be provided with ample climbing apparatuses as well as arboreal and terrestrial nesting/sleeping areas.
Enclosure furnishings should enable animals to execute a full range of normal locomotor functions and
provide visual isolation from the public and conspecifics. Logs and shrubs on enclosure floors, branches
and hollows of various diameters set at different heights and angles in the upper reaches of the enclosure
are ideal for most species. Rope hawsers suspended throughout the enclosure and sandboxes and
mulch piles for digging are enriching additions to enclosures (Roberts 1997). The placement of ropes
should be done with care to ensure there are no loops that an animal can become caught in, or entangle
itself in (coatis have been known to become entangled in loops of ropes) (D. Bressler, personal
communication).
The intimate association between locomotory and feeding behaviors in procyonids should be kept in
mind when designing enclosure furniture. For example, kinkajous with their prehensile tails and highly
flexible axial and appendicular skeletons are well suited for arboreal food acquisition (e.g., terminal
branch feeding) - their movements more closely resemble those of cebids than other carnivores.
Enclosure furniture and feeding stations should be designed and located accordingly.
Coatis and raccoons find most of their food on the ground, and their limb morphologies and
locomotory behaviors reflect this. Coatis are excellent diggers and probers and are viewed by many zoo
and aquarium caregivers as having fine digital control equal to that of raccoons (K.Schilling, personal
experience; D.Bressler, personal communication). Shilling (personal communication) reports coati are
capable of turning round door knobs to open doors. Associated anatomical adaptations may also limit
arboreal locomotion and preclude terminal branch feeding as seen in kinkajous. Raccoons have semi-
digitigrade forelimbs, the locomotory postures, and fine digit control, but lack the convergent grip of
kinkajous precluding locomotion on narrow supports (such as those traversed by kinkajous). Enclosure
design should reflect these specific differences in each species‟ locomotory, social, and feeding biology
(Roberts 1997).
As with all species, exhibit “furniture” should be changed periodically (at least twice a year), but not all
at the same time. These changes can include repositioning features (e.g., moving deadfall) or bringing in
new items. If nesting/sleeping/hiding areas are altered, at least one should be left the same, and scents
should not be removed from those that are moved (Reed-Smith et al. 2003).
Animals housed indoors should be protected as much as possible from disturbance by the visiting
public. Noise from environmental systems should be kept at a low level and parturient females should be
housed away from loud noises and high traffic areas. Animals should always be provided with an area in
their exhibit where they can retreat and feel safe when disturbed by loud noise, bright lights, or any other
sudden disturbance.
Water features: Some of the procyonid species may benefit from a small pool or stream located in their
exhibits. Misters and waterfalls also provide opportunities for the animals to cool off and explore other
dimensions of their surroundings. All water features should be constructed in such a way to allow for easy
cleaning. Space dedicated to pools/streams, etc. should be deducted from the usable floor-space
calculations (Carnio 1996). Water features should have a variety of shallow depths, particularly for
raccoon and coati that may benefit from an ability to explore shallows for enrichment items.
Ringtail: In the wild, ringtails are seldom found more than 0.8 km (0.5 mi) from water, preferring
habitats that include dense riparian growth, chaparral, and rocky hillsides (Trapp 1972).
Substrates and bedding: Natural substrates are recommended for all of the procyonid species (AZA Small
Carnivore TAG recommendation 2005). Recommended surfaces include: dry sphagnum moss, hay, soil,
sod, pine needles, leaves, pebbles, sand, wood shavings, wood wool, straw, small sticks, river rock,
pebbles, or something similar. Bedding materials of all types can be used as long as caution is exercised
that the animals do not 1) eat it, 2) chew it up, and 3) show an allergic reaction to it. Some wood shavings
(e.g., conifers, some pine or fir) contain residues that can strip the water proofing/oils from their coats,
and/or may cause sneezing. Cedar contains aromatic phenols, which are irritating to the skin and
respiratory system. Several studies indicated that close, chronic contact with cedar shavings contributed
to infant mortality (Burkhart & Robinson 1978), respiratory disease (Ayars et al. 1989), and liver damage
(Vesell 1967) in rodents. Caution also should be exercised if using bedding such as towels because some
individuals will eat the fabric (D. Bressler, personal communication; K. Schilling, personal experience).
Species-appropriate Behaviors: Forest species such as the kinkajou and olingo should be provided
with good vertical and ground cover to mimic their natural forest habitat. More terrestrial species such as
the coatis and raccoons should be provided with some vertical space, ground cover, and open areas
(Roberts 1997). Arboreal species should be provided with extensive branching to allow for movement
from one part of the exhibit to another without having to descend to the ground. These arboreal pathways
should be of varying sizes and stability. Branches, vines, etc. should all be secured against falling, but not
all should be fixed in place. Instead, some should be allowed to sway with the animal‟s weight (Roberts
1997).
All of the procyonid species will benefit from complex, well-furnished exhibits. Exhibits should include
natural substrates such as soil, sand, river rock, and leaf litter. These can be placed on artificial surfaces
making it easier to change them when they become soiled. Placement on artificial surfaces also will
provide added security against escape due to the tendency of some of these species (e.g., coatis) to dig.
Exhibits also should be provided with non-toxic (pre-approved by the veterinarian and horticultural staff)
vegetation (trees, bushes, and grass), hollow logs, climbing ropes (caution should be used with ropes as
animals can become entangled in them), deadfall, rock piles, streams, pools, etc. All of the procyonids,
particularly the coatis (Standley 1992), may benefit from decomposing logs that provide an opportunity for
them to engage in natural foraging behaviors.
Nest boxes, feeding stations, waterers, and covered
sleeping/hiding spots should be located in the trees
(e.g., kinkajou, olingo; see photo at right by A. Moresco)
or on the ground and elevated (e.g., raccoon) as
appropriate for their species-typical behavioral pattern
(i.e., arboreal or terrestrial) (M. Dulaney, personal
communication). Nest box choices for raccoons and
coatis should be placed terrestrially and arboreally. At
least one sheltered resting area per animal should be
provided with at least one location large enough to allow
all animals to sleep together if they choose.
Coati: Coatis should be provided with complex climbing
structures offering secured, swaying limbs and trunks
large enough (able to hold their weight) for them to
exhibit their ability to climb down headfirst. They also
should be offered heated nest boxes or kept inside at temperatures of 4.4°C (40°F) or below because
their tails suffer quickly from frostbite. A coati group should be provided multiple nest boxes or sleeping
areas.
Ringtail: At least two nest boxes should be provided for singletons or pairs, more for a family group.
Ringtails are known to use one box as a latrine and the other as a den. If they are not provided with
enough boxes to accommodate this behavior they frequently use their den box for urination and
defecation causing unhealthy conditions (D. Bressler, personal communication).
Enclosure Cleaning: Because many of the procyonid species are known to mark their environments with
urine or other scents (e.g., ringtail, cacomistle, coati, and kinkajou) (IUCN 1995), furnishings in an exhibit
should not all be cleaned at the same time. Instead, they should be cleaned as needed on a rotating
basis. Fecal material and leftover food should be removed daily with the associated substrate cleaned or
removed (Partridge 1992).
Ringtail: In the wild, ringtails mark their territory by urinating on rocks and branches (Grizmek 1972;
Poglayen-Neuwall 1973). Latrine areas with accumulations of feces also have been found (Mead & Van
Devender 1981; Thompson 2003).
2.2 Safety and Containment AZA Accreditation Standard
Procyonids housed in free-ranging environments should be (11.3.3) Special attention must be given
carefully selected, monitored and treated humanely so that the to free-ranging animals so that no undue
safety of these animals and persons viewing them is ensured threat is posed to the animal collection,
free-ranging animals, or the visiting
(AZA Accreditation Standard 11.3.3). public. Animals maintained where they
Procyonid exhibits and holding areas in all AZA-accredited will be in contact with the visiting public
institutions must be secured to prevent unintentional animal must be carefully selected, monitored,
egress (AZA Accreditation Standard 11.3.1). Exhibit design and treated humanely at all times.
should be considered carefully to ensure that all areas are secure
and particular attention should be given to shift doors, gates, AZA Accreditation Standard
keeper access doors, locking mechanisms and exhibit barrier (11.3.1) All animal exhibits and holding
dimensions and construction. areas must be secured to prevent
Exhibits in which the visiting public may have contact with unintentional animal egress.
procyonids must have a guardrail/barrier that separates the two AZA Accreditation Standard
(AZA Accreditation Standard 11.3.6).
All emergency safety procedures must be clearly written, (11.3.6) Guardrails/barriers must be
constructed in all areas where the visiting
provided to appropriate staff and volunteers, and readily available public could have contact with other than
for reference in the event of an actual emergency (AZA handleable animals.
Accreditation Standard 11.2.3).
Coati: The AZA SCTAG recommends containment walls for open-top exhibits are at least 2-2.44 m (6.6-8
ft) high with an inward facing overhang, of non-climbable material, at least 31-61 cm (1-2 ft) (AZA Small
Carnivore TAG recommendation 2005). While water moats (3 m/10 ft wide at one facility) are used
successfully, this species swims well and there should still be a low barrier with a 61 cm (2 ft) inward-
facing overhang around water moats.
In open exhibits, trees, bushes, and other exhibit furniture should be placed away from the perimeter
so they cannot be used as a means of escape. Coatis have been reported jumping across a distance of
(~1.22 m (4 ft) landing on a surface roughly 15.25 cm (6 in) higher than the surface they started from (K.
Kimble, personal experience). Outdoor exhibits should have security entrances with a secondary catch
area for animals that sneak through the door. Security doors should be provided with snap hooks or
padlocks because coatis and raccoons are capable of manipulating common gate latches and opening
them (K. Schilling, personal experience).
Animals housed indoors should be maintained in exhibits that have been checked to insure there are
no escape holes. Smaller coatis (adults and juveniles) are capable of squeezing through openings as
small as 7.6 cm (3 in) (K. Schilling, personal experience).
Raccoon: This species has been maintained in open-air exhibits contained by smooth concrete walls
1.12-1.8 m (3.8-5.6 ft) high, with an 46 cm (18 in) inward overhang topped with a 31 cm (12 in) electrified
fence on the top of the containment wall (A. Dosch, personal communication). Ideally this species should
be kept in enclosed exhibits to prevent escape and ingress by wild raccoons.
Ringtail: This species should be kept in completely contained exhibits as they have been reported
capable of ascending or descending steep or vertical surfaces. One animal was observed walking upside
down sloth-like on a 0.5 cm (0.2 in) cord strung between two supports, and another walking upside down
along a board in the ceiling of its exhibit (Trapp 1972). The ringtail is capable of rotating its hind foot 180°,
allowing them to climb downward like a tree squirrel (Trapp 1972).
Chapter 3. Transport
3.1 Preparations
Animal transportation must be conducted in a manner that
adheres to all laws, is safe, and minimizes risk to the animal(s), AZA Accreditation Standard
employees, and general public (AZA Accreditation Standard (1.5.11) Animal transportation must be
1.5.11). Safe animal transport requires the use of appropriate conducted in a manner that is safe, well-
planned and coordinated, and minimizes
conveyance and equipment that is in good working order.
risk to the animal(s), employees, and
The equipment should provide for the adequate containment, general public. All applicable local, state,
life support, comfort, temperature control, food/water, and safety and federal laws must be adhered to.
of the animal(s).
Safe transport also requires the assignment of an adequate number of appropriately trained
personnel (by institution or contractor) who are equipped and prepared to handle contingencies and/or
emergencies that may occur in the course of transport. Planning and coordination for animal transport
requires good communication among all affected parties, plans for a variety of emergencies and
contingencies that may arise, and timely execution of the transport. At no time should the animal(s) or
people be subjected to unnecessary risk or danger.
When transporting procyonids there should always be at least two people present; if animals have
been anesthetized the veterinarian should always be present. Staff involved in transports should
understand their duties and have a clear idea of the institution‟s policies regarding transports. The AZA
SCTAG has no specific recommendations regarding staff roles in transports, but does recommend
procedures and policies be clearly defined and understood in advance by all participating staff.
AZA SCTAG Recommendations: All possible relevant regulatory agencies should always be checked
for shipping, health, and permit requirements before transporting animals (USF&W, State, CITES, etc.).
The International Air Transport Association (IATA) publishes specific guidelines for transport containers
used for animal shipments. These guidelines are available from the Publication Assistant, IATA, 2000
Peel Street, Montreal, Quebec, Canada, H3A 2R4 (Ott Joslin & Collins 1999). An alternate address for
IATA is: International Air Transport Association, 800 Place Victoria, P.O. Box 113, Montreal, Quebec,
Canada, H4Z 1M1. The Live Animals Regulations document is available in print or CD ROM format and
can be ordered from [email protected].
Transport Container: In general, the following crate design guidelines are true for all species and
required by IATA (IATA 2009): 1) “Crates must be able to withstand external damage from other freight
and any internal damage caused by the animal.” 2) “Crate doors must not come open accidentally, but,
must be securely fastened.” 3) “All shipping crates must allow for adequate ventilation.” 4) “Ventilation
apertures must be small enough to prevent the escape of the animal and small enough that the animal
cannot get any part of its body through the opening.” 5) “Crates must be large enough to allow the animal
to stand up and turn around” (IATA 2009).
Coatis & Raccoons: Crates used for coatis and raccoons should be additionally secured where the top
meets the bottom (when using two-piece air-kennel type crates). This will prevent the animal from using
force to physically separate the crate (K.Schilling, personal communication; D.Bressler, personal
communication).
3.2 Protocols
Transport protocols should be well defined and clear to all animal care staff. All materials required for
a successful transport should be gathered in advance. The SCTAG recommends maintaining a transport
protocol book for every species.
Procyonids should always be shipped individually. Pregnant or lactating females should not be
shipped. The only exception to this would be the shipment of very young littermates that may fare better
when shipped in pairs or groups (D.Bressler, personal communication).
Food and Water: While generally not required, or advised, “…the crate must allow for feeding and
watering of the animal if needed” (IATA 2009). “The food and water ports should be clearly marked on the
outside of the crate. Food/water dishes must be securely attached for shipping (IATA 2009) or animals
may remove them.” On long flights, provisions should be made for feeding in transit (this may necessitate
shipping food with the animal).
In general, the Procyonid species should be fine for 24 hours without food and water. However, if long
layovers or temperatures over 21.1°C (70ºF) will be encountered, the need for provision of water should
be considered (Roberts 1997). Water-heavy fruits, such as apples (or oranges for coatis) (Valenzuela
1998), are good sources of hydration during transportation and should be placed in the crate for all
shipments of long duration (K.Schilling, personal experience).
Shipments requiring more than 24 hours should be accompanied with food and watering instructions.
In these cases it may be necessary to make arrangements with a zoological facility close to one of the
layover points.
Bedding and Substrate: The crate bottom should be leak-proof and bedded with some form of
absorbent material. Some air carriers prohibit certain bedding materials, therefore in the case of air
shipments the selected carrier should be consulted first for any specific restrictions.
Temperature, Light, and Sound: USFW and IATA regulations for shipments to the United States
indicate that temperatures in the holding area, cargo, or terminal should be at least 12.8 ºC (55 ºF) and no
higher than 26.7 ºC (80 ºF). Also, if ambient temperatures are higher than 23.9 ºC (75 ºF), ancillary
ventilation should be provided (Ott Joslin & Collins 1999).
For shipments within the United States, the AWA requires that ambient temperatures in the holding
area should not be less than 7.2 ºC (45 ºF) or more than 29.5 ºC (85 ºF) for more than four consecutive
hours. Animals being transported between holding areas to the aircraft should not be exposed to ambient
temperatures higher than 29.5 ºC (85 ºF) or colder than 7.2 ºC (45 ºF) for more than 45 minutes (Ott
Joslin & Collins 1999). These guidelines are suitable for the procyonid species, but whenever possible
shipments should be planned to avoid temperatures at either extreme, particularly at the high end for the
raccoon species and the low end for the more tropical olingo, kinkajou, or cacomistle.
Mesh doors or side windows (as in air kennels) should be covered with a breathable, opaque material
to allow for ventilation and privacy for the animal (Ott Joslin & Collins 1999), as well as preventing
unauthorized personnel from making physical contact with the crated animal.
All openings should be covered with 1.27 cm (0.5 in) wire mesh. This should then be covered with air-
permeable material that will help provide a sense of security for animals being shipped. All pieces of the
crate should then be secured with wire or cable ties to prevent escapes during transit. Polite requests to
the airline staff to place live animals in locations where loud noises are at a minimum during layovers and
away from any other live animal shipments in the cargo hold are advised.
Animal Monitoring: Most small carnivores will not require anesthesia for crating. In the event that
anesthesia is required, the animal should be fully recovered (standing and stable) prior to shipping.
Ideally, an inhalant or reversible anesthetic should be used in these cases.
Transport periods greater than 24 hours in length should be accompanied with food and water
instructions specific to the species. In these cases, it may be necessary to make arrangements with a
zoological facility close to the lay-over points prior to shipping for food and water provisions. A contact
number for the closest zoological facility should be provided, and after 24 hours (or less in some cases)
the animals should be checked on by trained professionals from this facility; if needed, water and food
should be provided. There is no definitive information available at this time as to whether there should be
a maximum duration of transport for procyonids.
Post-transport Release: Shipping crates should be placed directly into the quarantine space and the
animals allowed to exit on their own volition and at their own pace. It is recommended that all animals be
weighed at this time. The crate and animal can be weighed first and the crate weighed again after the
animal has exited.
breeding. While males also can be choosey, they will usually accept the female paired with them
(Poglayen-Neuwall 1995). Although it is rare, male ringtails have been known to be overly aggressive
during introductions to females or during breeding season. A few of these cases have resulted in the
death of the female. The larger the enclosure, the less likely this is to occur. Keepers should monitor all
interactions and be aware of unusually aggressive behavior (K. Schilling, personal experience). However,
in general, adults may live together amicably in the same enclosure and even sleep peacefully together in
the same nest box regardless of sex or season. Males apparently provide no direct parental care to
infants.
Young from the previous litter can be kept with an adult pair until the onset of the next breeding cycle
at which time they should be removed to eliminate the possibility of fighting and other interferences with
reproduction.
Ringtails and cacomistles can be housed as heterosexual pairs or as one male/two female (1.2) trios
(Partridge 1992). In the case of pairs, they can be introduced at any time during the year. Trios should all
be introduced into the exhibit at the same time (Partridge 1992). Keepers should observe all interactions
between new pairs/trios and monitor closely an unusually aggressive behavior.
Kinkajou: The social organizations of olingos and kinkajous are less well known. In the wild, kinkajous
have been observed in aggregations around clumped resources, although solitary individuals are most
commonly seen. In zoos and aquariums, kinkajous are socially tolerant although clear dominance
hierarchies develop among individuals. Care should be taken to avoid overcrowding enclosures because
overt aggression is not readily apparent. Kinkajous do well as pairs or trios. Introducing a second female
to a pair can be done at any time with little to no tension between the individuals. Each animal should
have separate sleeping quarters available should they choose to sleep alone (K. Schilling, personal
communication; D. Bressler, personal communication).The following is a summary of a behavioral study
conducted by Kays and Gittleman (2001):
“The social organization of the kinkajou Potos flavus is described from 380 hours of observations
on habituated, free-ranging animals. Individuals were most often alone while feeding at night, yet
they regularly interacted in stable social groups. Four social groups were observed, each
consisting of a single adult female, two adult males, one sub-adult and one juvenile. At least one
breeding female was solitary and did not reside within a group. Social groups were consolidated
primarily at denning sites and large fruiting trees by group feeding, allogrooming and scent
marking. However, kinkajous were most often observed solitarily, as social feeding only occurred
in 19.6 of total feeding bouts (mainly among males) and individuals rarely travelled together.
Although the composition of social groups was polyandrous, males also copulated with non-group
females which suggests a promiscuous mating system. Female-biased dispersal and patterns of
male association seem to be patrilineal and based on resource defense.”
4.2 Influence of Other Species and Conspecifics
Mixed-species Enclosures: Before any mixed exhibits are
considered, the potential for inter-species aggression or
disease transmission should be evaluated. Species
appropriate sleeping platforms/nest boxes/rest areas, shade,
feeding stations, watering spots, and visual barriers should be
provided for each species within a mixed exhibit. These
comfort and sustenance areas should be available to all
individuals of every species housed in an exhibit.
Elevated areas such as dead/live trees, platforms, mock
barns/buildings, etc. should be provided for the more arboreal
species (raccoons, kinkajous). Ground surfaces of varied
heights, vegetation, rock piles, deadfall, etc. should be
provided as hiding places and visual barriers for the more
terrestrial species. Measures should be taken to prevent
Photo credit: S. Carter
woodchucks or other burrowing species from burrowing too deeply.
Coati: Neutered coatis have been successfully maintained in an enclosure with neutered raccoons, and
one old coati was housed with a pair of striped skunks (K. Schilling, personal experience). These animals
were introduced as adults. Institution A successfully housed an adult male coati with an adult male
capybara (S. Carter, personal communication).
At one AZA-accredited institution, coatis were exhibited with spectacled bear, while another institution
exhibited them with squirrel monkeys. In the latter combination, the squirrel monkeys were reported as
being prone to showing aggression towards coati young, even stealing and killing them at times.
Raccoon: Raccoons, striped skunks, and North American woodchucks have been housed together
successfully with very little aggressive interaction. It is important that appropriate shelter and denning
facilities be provided for each species, and that feeding/watering stations are established to minimize
aggression over food (G. Granat, unpublished information, 2003).
Raccoons also have been housed with coatis (see above) and silver, red, and arctic fox (K. Schilling,
personal experience). In the latter instances, there may be some aggression at feeding time, which
should be anticipated and prevented by offering multiple feeding locations. In the past, ex situ populations
of raccoons and fox have shown an inclination to share den boxes, especially in cold climates, even when
multiple denning locations were provided (K. Schilling, personal experience).
4.3 Introductions and Reintroductions
Managed care for and reproduction of procyonids housed in AZA-accredited institutions are dynamic
processes. Procyonids born in or moved between and within institutions require introduction and
sometimes reintroductions to other animals. It is important that all introductions are conducted in a
manner that is safe for all animals and humans involved.
Since the potential for harm, or even fatalities, are always a possibility during the introduction of new
animals, introductions should proceed slowly. The use of howdy doors, scent, visual and tactile
acclimation are all useful tools when introducing new animals. The use of training techniques in the
management of the procyonid species has not been explored as thoroughly as in some of the other
mammal and avian species. However, there is no reason to assume these techniques would not be
useful in some situations. Andrews (2001) stresses three components (1-3) for a successful introduction,
to which we add three more (4-6):
1. Adequate space.
2. Know your animals.
3. Staff preparedness.
4. Familiarize the animals with their new space and allow them ample time to mark it with their
scent.
5. Take the next step in the introduction process based on the animals‟ behavior not a preset
timetable.
6. If possible, introduce new animals in neutral environments.
Space: Ideally, the exhibit and holding space should be designed so that each animal can be individually
rotated through all areas without physical contact with a conspecific. Initial contact should be through a
small mesh fabric (wire), providing visual, olfactory, and auditory contact, but not physical contact. If the
approach of shared space is not possible, howdy cages or alternating between cages with only a small
see-through partition is recommended. If one animal is noticeably more timid than the other, we
recommend that this timid animal‟s cage be used for the physical introduction, thereby allowing it the
advantage of being in familiar territory.
Sometimes it is helpful during physical introductions to temporarily “confuse” the olfactory senses of
these species to minimize aggression. A drop or two of a non-toxic scent such as perfume or vanilla can
be placed, or sprayed, on all animals involved in the introduction; this may be successful in thwarting
aggression and replacing it with curiosity. Animals that are busy, or preoccupied, with the discovery of
interesting (non-threatening) scents have less time for aggression. Becoming familiar with each other
during this scent exploration is an inevitable by-product. However, this procedure does not guarantee
successful cohabitation. If anything, it may be used when other efforts have failed. (K. Schilling, personal
experience)
Knowing Your Animals: The decision to move from visual contact to physical contact should be made
carefully. Things to consider during the initial physical introduction include making sure that each animal
is fully aware of the other‟s presence. It is also recommended that no matter how compatible a pair may
seem in the first meetings, the animals should be separated at night until they have consistently exhibited
positive behavior in full-day encounters and appear totally at ease with each other and their surroundings
(AZA Small Carnivore TAG recommendation 2005). When introducing a new animal to a group it may be
advisable to perform introductions with the least dominant animal first.
Staff Preparedness: Andrews (2001) recommends that during an introduction, staff should prepare for
the worst-case scenario, planning strategies ahead of time. Planning should include knowing the
availability of the veterinarian, location of transport carriers, and exact plan of action with intervention or
distraction roles clearly defined (K. Schilling, personal experience).
Familiarize Animals With Their Space: New animals should be allowed to become familiar with the
exhibit and holding areas before introductions are attempted.
Take the Cues From the Animals: Know your animals and let them dictate when the next step should
take place. Some animals will take longer to acclimate to new surroundings and cohorts than others.
Coati: Coati can be difficult to introduce; some introductions proceed quickly and smoothly, others may
require staff patience and extended periods of olfactory and visual introductions only. Animals should be
“howdied” (placed in adjoining areas where they can see and smell but not touch each other) until they
begin to show signs of affiliative behaviors (e.g. sleeping next to one another, etc.). Some institutions
report difficulties with female-female introductions; in these cases moving slowly through the introduction
steps, insuring both animals were familiar with the environment, and that the introduction did not occur in
space considered home by the dominant (or older animal) facilitated the introduction. In cases of
apparently incompatible animals introductions may succeed if conducted slowly or they may not succeed;
however, all introductions should be observed closely and stopped if it appears the animals are becoming
too aggressive (growling, lunging, biting at or striking at the other animal).
Chapter 5. Nutrition
5.1 Nutritional Requirements
A formal nutrition program is recommended to meet the
behavioral and nutritional needs of all procyonids (AZA AZA Accreditation Standard
Accreditation Standard 2.6.2). Diets should be developed using (2.6.2) A formal nutrition program is
the recommendations of nutritionists, the Nutrition Advisory recommended to meet the behavioral and
Group‟s feeding guidelines nutritional needs of all species and
specimens within the collection.
(www.nagonline.net/feeding_guidelines.htm), and veterinarians,
as well as AZA Taxon Advisory Groups and Species Survival
Plan® Programs. Diet formulation criteria should address the animal‟s nutritional needs, feeding ecology,
as well as individual and natural histories to ensure that species-specific feeding patterns and behaviors
are stimulated.
As a group, procyonids exhibit diverse natural feeding strategies and foraging behaviors. Although
classified as carnivores, most procyonids are omnivorous, but the range of foods eaten and the means of
procurement differ considerably among genera. Raccoons forage for invertebrates, small vertebrates, and
fruits along bodies of water (Poglayen-Neuwall 1990; Nowak 1999). Ringtails and cacomistles feed
primarily on small vertebrates, insects, and fruit (Poglayen-Neuwall 1990; Nowak 1999). Kinkajous are
largely arboreal, mainly frugivorous, and have been observed to consume fruit pulp and seeds, flowers,
honey, young leaves and buds, and small invertebrates and vertebrates (Ford & Hoffman 1988;
Poglayen-Neuwall 1990; Denver 2003). Coatis forage for invertebrates, small vertebrates, and fruits on
the forest floor and in trees (Poglayen-Neuwall 1990; Nowak 1999).
Digestive System Morphology and Physiology: Morphological and
behavioral adaptations for foraging are diverse across procyonids. Kinkajous
have a long, protrusable tongue, presumably for obtaining food from crevices,
and prehensile tails which permit terminal branch feeding. Raccoons have
highly prehensile forepaws, which they use to search for, manipulate, and
capture prey that cannot be readily seen underwater. In general, the stomach
of procyonids is simple (note figure to left, raccoon gastrointestinal tract; Steven
and Hume 1995) and the distal segment of the stomach is marked only by a
sudden change in mucosa. The intestine of the raccoon is longer than that of
the dog or cat (2.7 times body length), and the hindgut is shorter, with neither a
cecum nor a distinct ileocolonic valve (Stevens and Hume 1995). No grossly
visible specialization for frugivory has been noted in kinkajous Steven and Hume 1995
(Wright and Edwards 2009).
Energy Requirements: Available information suggests that energy requirements are closely related to
body mass, food habits, climate, and activity level, but these factors are all interrelated and some exert
more influence than others. Work done by Muñoz-Garcia and Williams (2005) on the basal metabolic rate
(BMR) of 58 Carnivora species indicated, after controlling for body mass, a strong correlation between
home range size (used as a proxy for level of activity), diet, and BMR (Table 6). Based upon this work,
Muñoz-Garcia and Williams (2005) concluded that “…species that eat meat have larger home ranges and
higher BMR than species that eat vegetable matter.”
Procyonids have lower than predicted metabolic rates as compared to the Kleiber curve, suggesting
that relative energy requirements are lower than those of felids, canids, and mustelids of comparable size
(McNab 1989). This has been attributed in part to reduced muscle mass of some of the arboreally
adapted species in the group. Basal metabolic rates are not species constant and will be higher (as much
as twice) for growing individuals compared to adults (Robbins 1993). See Table 6 for the Basal Metabolic
Rate for selected procyonid species. Paradoxically, despite a depressed metabolic rate, some species
(e.g., kinkajou, ringtail, and cacomistle) have limited ability to dissipate heat and may become
hyperthermic at even moderately high ambient temperatures (>33 °C/91 °F). Observations of kinkajous
indicate that they need approximately 50 kcals/d less than an equivalently sized mammal along the
mouse-elephant (placental mammal) body curve because its BMR is 30-34% lower (Wright and Edwards
2009). Thus, a diet formulated for kinkajous based on a metabolic rate formula for other similarly sized
mammals can provide too much food and increase risk for obesity.
Table 6: Basal Metabolic Rate (BMR) of selected procyonid species (from: Muñoz-Garcia & Williams 2005, citing
original sources)
2
BMR Diet (%) Home range (km )
Species Body Mass (g)
(kJ/d) (meat/invert/veg) (females only)
Nasua nasua 3,850 ± 212 486.02 ± 38 2/58/41 Not listed
Nasua narica 3,630 ± 548 573.25 ± 77 Not listed Not listed
Bassariscus astutus 860.7 185.5 Not listed 1.85
B. sumichrasti 1,287.3 ± 133 305.24 ± 25 Not listed Not listed
Potos flavus 2,688 447.71 0/21/78 0.2
Procyon lotor 4,847 742.23 0/73.5/26.5 1.22
P. cancrivorus 1,160 221.75 13.5/20.5/65.5 Not listed
Nutrient Requirements: Although we know many of the items consumed by procyonids, the nutrient
content of these items has not been completely characterized. Beyond this, diversity within the family‟s
feeding ecology precludes species or even genera-specific target nutrient levels. In the case of
procyonids, target nutrient levels are based on those of well-studied omnivores. Ranges are provided to
best describe the needs across a variety of genera, with the high ends of each range for growing and
lactating animals. In most cases, they reflect the highest values reported. Based on the emphasis of
foraging strategy of the genus or species in question, a range of target nutrient values has been provided
for more omnivorous individuals (see Table 7). These ranges are provided in comparison to straight dog
(NRC 1974; AAFCO 1999), Arctic fox (NRC 1982) and Mink (NRC, 1982). As additional information
becomes available, these ranges should be adjusted to reflect new knowledge.
Table 7. Target nutrient ranges for baseline species (dry matter basis).
1
Nutrient More Omnivorous
Kinkajou (potos flavus), Ringtail (bassariscus astutus), Coati
(nasua narica), Raccoon (procyon lotor)
1a
Protein (%) 17.5-26.0
Fat (%) 5-8.5
Linoleic Acid (%) 1.0-1.3
Vitamin A (IU/g) 0.5-5.9
Vitamin D (IU/g) 0.5-0.55
Vitamin E (mg/kg) 27-50
Thiamin (mg/kg) 1.0-2.25
Riboflavin (mg/kg) 1.6-10.5
Pantothenic acid (mg/kg) 7.4-15.0
Niacin (mg/kg) 11.4-20.0
Pyridoxine (mg/kg) 1.0-1.8
Folacin (mg/kg) 0.18-0.5
Biotin (mg/kg) 0.1-0.12
Vitamin B12 (mg/kg) 0.022-0.035
1b
Calcium (%) 0.3-1.2
1b
Phosphorus (%) 0.3-1.0
Potassium (%) 0.4-0.6
Sodium (%) 0.04-0.3
Magnesium (%) 0.04-0.06
Iron (mg/kg) 30-90
Zinc (mg/kg) 50-120
Copper (mg/kg) 6.0-12.4
Iodine (mg/kg) 0.9-1.54
Selenium (mg/kg) 0.1-0.35
1
Dog NRC (2006), Dog AAFCO (1999) (All numbers are based on requirement set for maintenance); Mink NRC (1982);
Fox NRC (1982) (for mink and fox NRC protein is range of growth and maintenance, vitamins are for growth, and minerals for
growth and maintenance).
1a
Authors of this chapter are not comfortable recommending a 10% protein for maintenance as the Dog NRC 2006 suggests.
1b
Authors of this chapter would caution feeding diets with 0.3% calcium and/or phosphorus as the Dog NRC 2006 suggests.
Several factors affect nutrient requirements. These factors include: age, physiological state, health
status, environment, activity, and group dynamics. The target nutrient values in these standard
recommendations encompass the needs for maintenance of adults and reproducing animals (gestation
and lactation), as well as the needs of growing animals. The sample diets included in section 5.2 have
supported all life stages.
Seasonal changes in nutritional requirements: Development of individual standard and predictable
feeding behavior patterns based on seasons can serve as effective diet management tools.
Coatis: Male coatis appear particularly prone to weight gain in the fall; while this gain may be temporary,
due to their tendency to have a reduced appetite during the winter months, care should be taken to make
sure they do not become too obese during this period; weight gained in the fall is often naturally dropped
in the spring (Standley 1992).
Raccoons: Raccoons may lose as much as 30-50% of their peak autumn body weight during the winter
dormant period. Thus, the normal weight dynamic patterns of raccoons over parts of their range may be
considerably more variable than those for subtropical or tropical species or other procyonid genera
(Roberts 1997). Raccoons are somewhat unusual among the procyonids in that they undergo variable
periods of dormancy during the winter over much of their range (from central United States to Canada).
Interestingly, it is the appearance of a permanent snow cover, rather than low temperatures per se, which
appears to initiate the onset of dormancy in free-ranging raccoons. This suggests that the (lack of)
availability of resources may play a role in triggering this phenomenon. Dormancy should not be confused
with hibernation or torpor, as dormant raccoons are easily aroused. However, activity and food
consumption drop dramatically during exposure to prolonged low temperatures, and animals rely on
accumulated fat stores to meet energy requirements.
5.2 Diets
The formulation, preparation, and delivery of all diets must
be of a quality and quantity suitable to meet the animal‟s AZA Accreditation Standard
nutritional, psychological and behavioral needs (AZA (2.6.3) Animal diets must be of a quality
Accreditation Standard 2.6.3). Food should be purchased from and quantity suitable for each animal‟s
reliable, sustainable and well-managed sources. The nutritional nutritional and psychological needs. Diet
formulations and records of analysis of
analysis of the food should be regularly tested and recorded. appropriate feed items should be
Food preparation must be performed in accordance with all maintained and may be examined by the
relevant federal, state, or local regulations (AZA Accreditation Visiting Committee. Animal food,
Standard 2.6.1). Meat processed on site must be processed especially seafood products, should be
purchased from reliable sources that are
following all USDA standards. sustainable and/or well managed.
If browse plants are used within the animal‟s diet or for
enrichment, all plants must be identified and assessed for safety. AZA Accreditation Standard
The responsibility for approval of plants and oversight of the
(2.6.1) Animal food preparations must
program should be assigned to at least one qualified individual meet all local, state/provincial, and federal
(AZA Accreditation Standard 2.6.4). The program should identify regulations.
if the plants have been treated with any chemicals or near any
point sources of pollution and if the plants are safe for the AZA Accreditation Standard
species. If animals have access to plants in and around their (2.6.4) The institution should assign at
exhibits, there should be a staff member responsible for ensuring least one person to oversee appropriate
that toxic plants are not available. browse material for the collection.
Sample Diets: There is a wide range of diets that can be appropriate for procyonids. As omnivores, diets
that contain a variety of food items and food groups appear most appropriate, with emphasis added
toward the vertebrate and invertebrate portions of the diet for more carnivorous members of the group
(raccoon, coati, ringtail and cacomistle) and fruits for the more frugivorous members (kinkajou). It should
be noted that the nutrient content of all items consumed (whole prey, nutritionally complete foods,
produce, etc) should be known and included in the nutrient analysis of the diet. This will help to develop
and maintain a diet which meets both the nutritional needs of the species and also avoid incidence of
metabolic problems (metabolic bone disease, obesity, anorexia, etc).
In this case, sample diets are provided as examples only. The goal is to provide a diet that meets
target nutrient values and is readily consumed. Ideally, a palatable nutritionally complete food item should
be used as the base of the diet, to which vertebrate and invertebrate prey, and produce may be added as
appropriate based on feeding strategy. Offering hard food items (bones, biscuits, etc) will encourage
natural tooth abrasion and promote dental health. Although the North American raccoon is not managed
within the AZA SCTAG, two diets are provided for additional reference in Table 8.
Table 8. Sample diets from AZA institutions of procyonid species as fed daily*
1
Species Common Name Institution Food Item grams/day % in diet
Potos flavus Kinkajou Institution B Seasonal fruit – used apple 115 43.00
Insectivore- Reliable Protein Prod 60 22.43
ZuPreem Feline canned 60 22.43
2
Nectar Mix 30 11.22
Purina Labdiet 5045 High Protein 2 0.75
Crickets 0.4 0.15
Mealworms 0.07 0.03
Total 267.47 100
Institution C Mazuri Omnivore Biscuit 86 33.34
Vegetable – used carrot 86 33.33
Fruit – used apple 86 33.33
Total 258 100
Institution D Corn on the cob 50 13.24
Apple 50 13.24
Hill‟s Science Canine Light dry 50 13.24
Hill‟s Science Original Adult dry 50 13.24
IAMS Adult Chicken Entrée can 28 7.41
Mazuri Browse Biscuit 12 3.18
Night crawlers (4g Sun) 0.57 0.15
Cantaloupe (50 g T/Th) 14.2 3.78
Kiwi (50 g W) 7.1 1.89
Papaya (50 g Th) 7.1 1.89
Mealworms (0.1 g W) 0.01 0.004
Grapes 50 13.24
Banana (40 g M,W,F) 17.1 4.54
Fig (40 g M,Th,F) 17.1 4.54
Egg, hard-boiled (40 g M,T,W,F) 22.8 6.05
DAK primate Gel (10g Sun) 1.4 0.38
Total 377.7 100
Bassariscus astutus Ringtail/Cacomistle Institution B Nebraska Special Beef Feline 35 22.22
Chicks (30 g M,W,F) 12.8 8.16
Mouse (30 g Su,T,Th,Sa) 17.1 10.88
Fruit – used apple 35 22.22
Insectivore– Reliable Protein Prod 35 22.22
Egg, Hard-boiled 22.5 14.29
Total 157.4 100
Institution E Natural Balance Carnivore 5% 24 37.33
Premium Edge Chicken/Rice Dog 11.1 17.33
Egg, hard-boiled 3.4 5.33
Fruit used apple 7.7 12.0
Vegetable used carrot 7.7 12.0
Mealworms 1.7 2.67
Crickets 0.57 0.89
Mouse (56 g Th- only mouse fed) 8 12.44
Total 64.17 100
3
Institution C Fruit Mix 55 53.40
Natural Balance Carnivore 10% 29 28.16
ZuPreem Feline Canned 10 9.71
Mouse 9 8.74
Total 103 100
Nasua narica Coati (white nosed) Institution B Fruit used apple 120 23.83
Vegetable used carrot 120 23.83
Nebraska Special Beef Feline 120 23.83
ZuPreem Feline can 60 11.91
Purina Labdiet 5045 high protein 60 11.91
Egg, hard-boiled 19.3 3.83
Cooked Roast Beef 4.3 0.85
Total 503.6 100
Institution E Natural Balance Carnivore 5% 43 20.84
1
Species Common Name Institution Food Item grams/day % in diet
Nasua narica Coati (white nosed) Institution E Premium Edge Chicken/Rice Dog 60 29.09
Lake Smelt 4.3 2.08
Mealworms 8 3.88
Crickets 8 3.88
Egg, hard-boiled 28 13.57
Apple 28 13.57
Banana 27 13.09
Total 206.3 100
Institution C (brown
Mazuri Omnivore 103 41.56
nosed)
Egg, hard-boiled 33 13.32
Banana 10.8 4.38
Apple 20.0 8.07
Grapes 6.4 2.59
Orange 17.0 6.86
Sweet potato cooked 9.3 3.75
Mealworms 8.1 3.29
Crickets 10.8 4.38
Mice 29.2 11.8
Total 247.8 100
Procyon lotor Raccoon Institution D Hill‟s Science Original Adult dry 85.0 63.33
Grapes 16.0 11.92
Carrots 9.7 7.24
Cantaloupe 0.85 0.64
Apple 0.85 0.64
Banana 0.43 0.32
Super worms 0.85 0.64
Cricket (3/4”) 0.21 0.16
Sweet Potato 6.0 4.47
Apple Juice Concentrate 14.3 10.64
Total 134.2 100
Institution F Apple 8 4.15
Grape 9 4.66
Carrot 16.5 8.55
Sweet Potato 16.5 8.55
4
Leafy Mix 27 13.99
Sports Mix Dog Food dry 58 30.05
Purina Labdiet 5038 Monkey 58 30.05
Total 193 100
1
Reliable Protein Products, Phoenix, AZ 85050; Zupreem, Shawnee, KS 66214; PMI Nutrition International, Grays Summit, MO 63039; Hill‟s
Pet Nutrition, Inc. Topeka, KS 66603; P&G Pet Care (IAMS), Cincinnati, OH 45220; Central Nebraska Packing, Inc. North Platte, NE 69103;
Natural Balance Pet Foods, Inc. Pacoima, CA 91331; Premium Edge Brand® Meta, MO 65058; Midwestern Pet Foods, Inc. Evansville, IN
47725.
2
Nectar mix from Omaha contains 9% raw egg, 5% Roudybush nectar 3 powder, 2% dry rice baby cereal, 4% honey, and 80% water.
3
Fruit mix from Institution C is a combination of 16.26% apple, 27.49% banana, 6.71% grape, 3.47% orange, 6.35% papaya, 11.73% pear,
4.27% white potato, 13.63% sweet potato, 6.76% carrot, and 3.33% hard-boiled egg; Vegetable mix is a combination of 11.15% apple, 6.15%
carrots, 8.92% pear, 1.44% collard greens, 6.34% green beans, 3.70% kale, 13.74% romaine, 10.94% pear, 9.87% white potato, 5.21%
spinach, and 22.54% sweet potato.
4
Institution F Leafy Mix is 45% iceberg lettuce, 11% kale, 22% spinach, and 22% celery shredded.
* The AZA SCTAG does not specifically endorse the use of any mentioned products.
The following table (Table 9) provides a comparison of the sample diets listed in Table 8 to target
nutrient levels identified in section 5.1.
1
Table 9. Nutrient content of sample diets (dry matter basis)
Institution B Institution C Institution D
Kinkajou Kinkajou Kinkajou More Omnivorous
Nutrient
Protein (%) 28.2 21.9 21.3 17.5-26.0
Fat (%) 16.7 6.7 10.5 5-8.5
2
Vitamin A (IU/g) 9.2 92 6.2 0.5-5.9
Vitamin D (IU/g) 0.45 3.1 0.27 0.5-0.55
Vitamin E (mg/kg) 56.9 70 183 27-50
Thiamin (mg/kg) 7.3 14.0 1.7 1.0-2.25
Riboflavin (mg/kg) 8.0 6.3 2.3 1.6-10.5
Pantothenic acid (mg/kg) 18.7 19.0 8.6 7.4-15.0
Niacin (mg/kg) 52.6 78.9 11.9 11.4-20.0
Pyridoxine (mg/kg) 3.4 9.7 2.9 1.0-1.8
Folacin (mg/kg) 0.95 2.3 1.2 0.18-0.5
Biotin (mg/kg) 0.26 0.16 0.03 0.1-0.12
Vitamin B12 (mg/kg) 0.03 0.04 0.01 0.022-0.035
Calcium (%) 0.38 2.0 0.54 0.3-1.2
Phosphorus (%) 0.31 1.4 0.46 0.3-1.0
Potassium (%) 0.36 1.1 0.72 0.4-0.6
Sodium (%) 0.12 0.30 0.21 0.04-0.3
Magnesium (%) 0.03 0.20 0.10 0.04-0.06
Iron (mg/kg) 118 481 36 30-90
Zinc (mg/kg) 66 157 15.3 50-120
Copper (mg/kg) 5.4 13.4 3.5 6.0-12.4
Iodine (mg/kg) 0.77 1.2 0.18 0.9-1.54
Selenium (mg/kg) 0.02 0.45 0.07 0.1-0.35
Institution B Institution E Institution C
Ringtail Ringtail Ringtail More Omnivorous
Nutrient
Protein (%) 38.4 40.8 33.2 17.5-26.0
Fat (%) 21.8 18.4 19.7 5-8.5
Vitamin A (IU/g) 9.0 95.6 61.9 0.5-5.9
Vitamin D (IU/g) 1.3 0.55 0.72 0.5-0.55
Vitamin E (mg/kg) 195 261 174 27-50
Thiamin (mg/kg) 29.9 5.2 8.1 1.0-2.25
Riboflavin (mg/kg) 9.2 8.9 12.0 1.6-10.5
Pantothenic acid (mg/kg) 13.9 21.3 24.6 7.4-15.0
Niacin (mg/kg) 35.2 96.4 84.2 11.4-20.0
Pyridoxine (mg/kg) 5.9 6.4 10.2 1.0-1.8
Folacin (mg/kg) 1.4 0.22 11.8 0.18-0.5
Biotin (mg/kg) 0.15 0.57 0.81 0.1-0.12
Vitamin B12 (mg/kg) 0.09 0.05 0.06 0.022-0.035
Calcium (%) 1.1 0.97 1.1 0.3-1.2
Phosphorus (%) 0.89 0.68 0.54 0.3-1.0
Potassium (%) 0.50 0.40 0.65 0.4-0.6
Sodium (%) 0.28 0.26 0.49 0.04-0.3
Magnesium (%) 0.07 0.19 0.18 0.04-0.06
Iron (mg/kg) 164 82.4 109 30-90
Zinc (mg/kg) 74.6 121 120 50-120
Copper (mg/kg) 10.5 9.2 11.8 6.0-12.4
Iodine (mg/kg) 0.69 0.40 0.68 0.9-1.54
Selenium (mg/kg) 0.29 0.43 0.12 0.1-0.35
Institution B Institution E Institution C
Coati Coati Coati (brown-nosed) More Omnivorous
Nutrient
Protein (%) 31.9 33.8 29.8 17.5-26.0
Fat (%) 20.2 17.6 13.4 5-8.5
2 2
Vitamin A (IU/g) 229 4.4 28.7 0.5-5.9
Provision of Food and Water: Heavy water bowls made from metal, or a sturdy, non-chewable plastic
can be used for water and food. Small pools with running water may also be used as watering points. All
food and water containers should be cleaned and disinfected daily. Water containers used for ringtails
and coatis should be heated in winter, otherwise their body temperatures may drop too low as they drink
ice cold water. Ice-cold water also may prevent them from drinking an adequate amount of water
(D.Bressler, personal communication). Water should always be available, but it is particularly important
for ringtails if they are not provided with enough fruit (from which they naturally obtain water) in their diet
(Reed-Smith et al. 2003).
In general, only foods that can easily be contaminated by dirt (e.g., moist foods or fruit) should be
placed in containers, the rest should be scattered or hidden for the animals to find (K. Schilling, personal
experience). This portion of the daily diet should be reserved for use as enrichment during the course of
the exhibit day. Dry foods, or foods that can be left whole, should be scattered or hidden around the
exhibit. Fruit can be placed on branches or skewered onto heavy bolts placed in branches. This will
promote activity and provide the animals an opportunity to engage in natural foraging behaviors. The
provision of decomposing logs that can be torn apart, or logs with holes for hiding insects, larvae, fruit,
etc. also will encourage foraging behaviors.
Procyonids eat a wide variety of foods. Procyonids should be provided with food at least twice a day,
preferably three, and it is recommended that the diet be provided in ways that promote species-
appropriate foraging and feeding behaviors (e.g., hidden, scattered, hung, etc.), where appropriate. Given
that coatis can spend 95% of their active time foraging in the wild (Kaufmann 1962), it is important that
the frequency of food delivery, and the means of presenting the food to these animals, be closely based
on the natural history of the species in order to promote species-appropriate foraging, and prevent the
development of abnormal behaviors.
Ringtail and cacomistle: The AZA SCTAG recommends that a well-balanced diet includes a variety of
items as noted in previous sections and that animals‟ weight and physical condition should be checked
regularly. Carbohydrate consumption (including fruit and vegetable forms) should be monitored,
particularly the amounts offered males, as ringtails and cacomistles are prone to obesity (D. Bressler,
personal communication).
Coati: Coatis benefit from a scattered feeding approach, allowing them to exercise their natural foraging
approach to feeding. All items can be scattered or hidden as long as keepers monitor that all individuals
are feeding, and leftover food is cleaned up daily.
Kinkajou: The unfortunate title "honey bear" for kinkajou has often led to the erroneous assumption that
this species requires honey or other sweets in its diet. Overindulgence in sweets can have disastrous
dietary and medical consequences and should be avoided (Roberts 1997).
Species-appropriate Foraging and Feeding: Most procyonids are nocturnal or crepuscular, meaning
active at or between dusk and dawn; the notable exception is the coati, which forages during the day
(Denver 2003). While it is not possible to mimic the same diet (or environment) for ex situ populations of
animals as their free-ranging conspecifics would utilize, it is recommended that the diet is offered during
the period of the day when the animals would typically be expected to actively forage (AZA Small
Carnivore TAG recommendation 2005). This will not only discourage pest species, but will encourage
typical foraging behavior. Easily soiled food such as meat products should be offered in containers that
are cleaned and sanitized after each use.
Procyonids have been observed to consume anything from soft fruits and berries to acorns and
crayfish, and most have well developed canines and a strong dentition. Many are highly dexterous or
have relatively well developed prehensile abilities, thus altering diet item size or form and scattering part
of the diet can contribute to stimulating natural foraging behaviors, encourage problem solving, and in
general provide variety in daily activity patterns.
Feeding soft foods only (such as canned dog food, cottage cheese, etc.) will promote dental tartar,
which, if left untreated, can lead to gingivitis and eventual loss of teeth (Roberts 1997). However, soft
foods should not be completely ruled out as occasional enriching treats (K.Schilling, personal
experience).
5.3 Nutritional Evaluations
Group dynamics often play a role in the nutrient content of the diet consumed by individuals in the
group. When housed in groups, procyonids should be observed to insure the subordinate animals
consume the correct proportions of diet ingredients. Often increasing the number of feeding times per
day, placing the food in several locations, distracting some of the animals to allow others adequate
access to food, or separating animals when possible are necessary in a group of procyonids.
Diets should be formulated taking into account an animal‟s size, activity level, age, and over-all
health. Target weights should be set for each animal and diets formulated to maintain that weight.
Procyonids have been noted to become obese from overfeeding, lack of exercise, or a combination of the
two. “Goal weights” for individuals should be established (ideally, general, and seasonal), and body
weight checked frequently, so that diet adjustments can be made in a timely fashion to avoid over or
under-condition.
Ringtails and cacomistles have been noted to easily gain weight in zoos and aquariums. This can be
managed by regularly monitoring their weight and adjusting diets as needed.
Health Status: Increased or decreased requirements for illness, thermoregulation, or activity can be met
by offering diets ad libitum and monitoring body weight and condition over time. In general, diets should
be offered so that a small amount of food is remaining at the end of the feeding period; however this
should be managed on an individual basis to avoid obesity.
Analysis of weight fluctuations can be a valuable tool for managing individuals and populations.
Weight changes can reflect nutritional problems (obesity and under-conditioning), illness (cancer, organ
failure, etc.), other medical conditions (intestinal blockage, etc.), changes in reproductive condition (e.g.,
pregnancy or weight loss during lactation), and hormonally or environmentally induced changes in
metabolism (e.g., prior to dormancy and the onset of the breeding season). Correlating weight changes
with key life history parameters will enable animals to be managed much more effectively and efficiently.
administered, differential diagnosis, assessment, and future plans for treatment. A computerized medical
record system, which can help track problems and can be easily transmitted from one institution to the
next, is extremely beneficial. The AZA SCTAG encourages the use of ZIMS (Zoological Information
Management System) when it becomes available to replace MedARKS (International Species Information
System, 12101 Johnny Cake Ridge Road, Apple Valley, MN 55124, U.S.A.) as a universal medical record
program. Many institutions use MedARKS, making it easy to transfer information between them. The
medical record should include the following information:
Medical history
Identification (current ARKS record, transponder numbers, tattoos, etc.)
Clinical notes (including exam findings, diagnoses, vaccination history, etc.)
Parasitology
Anesthesia
Clinical pathology
Treatments (current medications, recent treatments, etc.)
Pathology
Reproductive status (contracepted, cycle details or abnormalities, etc.)
Nutritional information (nutritional deficiencies, supplements, allergies, etc.)
Behavioral/social group notes (social traumas, aggression, training for medical procedures, etc.)
Any pertinent group history should be included as well, especially if there is a history of infectious
disease within the group or exhibit.
As small carnivores are prone to dental disease, a thorough history of dental problems and,
preferably, a dental chart noting extractions, root canals, problems, etc. is recommended.
Necropsy: All small carnivores that die should receive a thorough necropsy in a timely manner. This will
help establish cause of death, provide valuable insight into the health of the collection, and help protect
the other animals in the social grouping by delineating any immediate concerns. The following protocol is
adapted from the AAZV „Small Carnivore Medical Management Guidelines‟ (Manharth & Shellebarger
2003) (see Appendix G and Appendix M):
1. Blood: serum banking
2. Radiographs post-mortem (if possible)
3. External exam, including weight and description of condition of body
4. Internal exam
a. A detailed written report should be completed.
b. Cultures should be submitted, if indicated
c. Photo documentation, if possible
d. Submission of a representative sample of all lesions AND routine tissues:
- Skin, muscle, sciatic nerve, bone (femur), tongue, salivary gland, eye, brain, pituitary,
trachea, thyroid, parathyroid, thymus, esophagus, lymph nodes (thoracic and abdominal),
lung, bronchus, heart, aorta, liver, gall bladder, diaphragm, spleen, pancreas, stomach,
duodenum, jejunum, ileum, ileocolic jxn, colon, adrenal, kidneys, bladder, ureter, urethra,
reproductive organs
- It is recommended that a pathologist familiar with non-traditional species be used for
histopathology.
- Reproductive organs should be submitted to: Dr. Linda Munson, VM -Pathology
Microbiology & Immunology, 4206 Vet Med 3A, One Shields Ave
Davis, CA 95616, as a standing request. Tissues should be fixed in 10% formalin and
accompanied by a submission form. More detailed submission instructions and the
submission form are available at:
www.stlzoo.org/animals/scienceresearch/contraceptioncenter/.
- Frozen set of tissues should be stored: heart, liver, kidney, brain, serum, lesions
- Any stones (uroliths, renoliths, etc.) should be submitted for analysis to: Minnesota
Urolith Center, Dept. of Small Animal Clinical Sciences, College of Veterinary Medicine,
University of Minnesota, 1352 Boyd Avenue, St. Paul, MN 55108
A complete report, including histopathology and test results, should be submitted to the veterinary
advisor on an annual basis.
After it has been decided by authorized staff that euthanasia is indicated, these species can be
anesthetized (see anesthesia section). Once the animal is adequately anesthetized, an injection of
pentobarbital can be given intravenously or intraperitoneally. NOTE that pentobarbital is a controlled
substance and DEA regulations for its use should be followed. Heart should be auscultated to ensure the
animal has died prior to disposing of the animal according to institutional guidelines. For more detailed
information on alternative methods and on euthanasia guidelines please refer to the AVMA guidelines on
euthanasia, a copy can be found at: www.avma.org/issues/animal_welfare/euthanasia.pdf.
AZA SCTAG Recommendations: Foot baths should be used in all quarantine situations; gloves and
masks should be used around sick animals or animals that came in from the wild (e.g. raccoons, rehab
ringtail, etc.).
The importance of a preventive medical program for zoo animals cannot be emphasized enough.
Animals entering a collection should undergo quarantine in an isolated facility designed to allow handling
of the animals and proper cleaning and sanitizing of the enclosures. The shipping crate should be
cleaned and disinfected before it leaves the quarantine area, and the crate‟s contents disposed of
appropriately. Quarantine facilities require barriers against ingress of potential vectors and vermin.
Animals in quarantine should be cared for by separate keepers who are skilled at recognizing signs of
stress and disease and who will carefully monitor feed intake and fecal characteristics. Since diets
change between institutions it is recommended that the sending institutions diet be obtained in advance
of the animal‟s arrival. This enables the receiving institution to provide a familiar diet to the animal upon
arrival and for the first week of quarantine. The sending institution may want to send some of the regular
diet with the animal.
After the first week of quarantine, if the animal is doing well, the new diet should slowly be introduced.
If this is done at a rate of approximately 25% of new diet exchanged for old per week, the animal should
be converted to the new diet by the end of quarantine, and should avoid any problems associated with
dietary change.
AZA Accreditation Standards and Related Policies
See Appendix A for specific animal care and management recommendations for small carnivore
quarantine, which are included in the AZA Accreditation Standards and Related Policies (AZA 2008).
During quarantine, animals should receive appropriate vaccinations and diagnostic testing (see
section 6.2). They should be examined for ecto- and endoparasites and treated appropriately. Depending
on what has been done at the shipping institution, before release from quarantine the animal should
receive physical and laboratory examinations, including hematology, serum biochemistry, urinalysis, and
radiographs. Serum should be frozen (banked) for future reference and possible epidemiologic studies.
All procedures and results should be recorded and become the start of the animal‟s record.
A minimum of three consecutive negative fecals (fresh direct and float or sedimentation), each one
week apart, should be obtained before clearing from quarantine. Appropriate treatment for any parasites
should be administered while in quarantine and three negative fecals should be obtained post-treatment.
Cultures and special stains should be repeated during this time if there has been a history of
infectious disease in this animal or its previous group. In the event of an infectious bacterial intestinal
disease (e.g., salmonellosis), it is recommended that repeated cultures be submitted (three per week) in
order to identify or document the condition.
6.5 Preventive Medicine
AZA-accredited institutions should have an extensive
veterinary program that must emphasize disease prevention (AZA AZA Accreditation Standard
Accreditation Standard 2.4.1). The American Association of Zoo (2.4.1) The veterinary care program must
Veterinarians (AAZV) has developed an outline of an effective emphasize disease prevention.
preventative veterinary medicine program that should be
implemented to ensure proactive veterinary care for all animals
(www.aazv.org/associations/6442/files/zoo_aquarium_vet_med_g AZA Accreditation Standard
uidelines.pdf).
(11.1.2) Training and procedures must be
As stated in Chapter 6.4, AZA institutions must have zoonotic in place regarding zoonotic diseases.
disease prevention procedures and training protocols established
to minimize the risk of transferable diseases (AZA Accreditation
Standard 11.1.2) with all animals. Keepers should be designated to care for only healthy resident
animals, however if they need to care for both quarantined and resident animals of the same class, they
should care for the resident animals before caring for the quarantined animals. Care should be taken to
ensure that these keepers are “decontaminated” before caring for
the healthy resident animals again. Equipment used to feed, care AZA Accreditation Standard
for, and enrich the healthy resident animals should only be used (1.5.5) For animals used in offsite
with those animals. programs and for educational purposes,
the institution must have adequate
Procyonids that are taken off zoo/aquarium grounds for any
protocols in place to protect the rest of the
purpose have the potential to be exposed to infectious agents that collection from exposure to infectious
could spread to the rest of the institution‟s healthy population. agents.
AZA-accredited institutions must have adequate protocols in
AZA Accreditation Standard
place to avoid this (AZA Accreditation Standard 1.5.5).
Also stated in Chapter 6.4, a tuberculin testing and (11.1.3) A tuberculin testing and
surveillance program must be established for animal care staff, as surveillance program must be established
for appropriate staff in order to ensure the
appropriate, to protect the health of both staff and animals (AZA health of both the employees and the
Accreditation Standard 11.1.3). Depending on the disease and animal collection.
history of the animals, testing protocols for procyonids may vary
from an initial quarantine test, to annual repetitions of diagnostic tests as determined by the veterinarian.
To prevent specific disease transmission, vaccinations should be updated as appropriate for the species.
Vaccinations: Preventive medicine should be tailored to the risk of exposure, which varies by location
and with management practices. The veterinary staff should set up a preventive protocol that is
appropriate for the risk of exposure at each institution. Vaccination schedules should be viewed in light of
the real risk of animals contracting these diseases and the consequences of clinical disease, keeping in
mind that overly aggressive vaccination schedules may not be innocuous. Titers are useful if the assay
that measures them has been validated for the species in particular. However, in many (most) zoo
species it is not known for certain what constitutes a protective titer. That is, even if we know the test
actually reflects the titers, what do they mean in terms of protection? In order to assess the latter point it
is recommended that, if possible, institutions still gather titer information for use at a later date. Specifics
on red pandas are addressed in a separate document. For more information also see the Guidelines for
zoo and aquarium veterinary medical programs and veterinary hospitals available as a PDF at
www.aazv.org/Webaddit.pdf.
Specifics regarding type/lot of vaccine and site of injection should be recorded in the animal‟s record.
Many of the following recommendations have been taken from the AAZV website and this can be
checked for regular updates (Manharth & Shellebarger 2003).
Rabies: Rabies is recommended for all carnivores. Only a killed rabies vaccine product should be used.
Imrab 3 (Merial Ltd., 3239 Satellite Blvd., Duluth, GA 30096) has been used extensively in small
carnivores without apparent adverse effects. Dose: 1ml, i.m.. Frequency: once at 16 weeks of age, then
annually thereafter. Animals experiencing an adverse reaction to a vaccine should be administered an
antihistamine (e.g., diphenhydramine hydrochloride, 0.5-2mg/kg intravenously or intramuscularly) or for
severe reactions, epinephrine (20µg/kg intravenously, intramuscularly, subcutaneously, or intra-
tracheally), and supportive care (Fernandez-Moran 2003). PUREVAX Feline Rabies (Merial Ltd., 3239
Satellite Blvd., Duluth, GA 30096) is a live canarypox vectored, nonadjuvanted recombinant rabies
vaccine that is currently being used at some institutions for small carnivores. (1ml; i.m.). The frequency of
vaccination should be once at age 8 weeks or older, then annually. This has been used without adverse
effects in binturongs (A.Moresco, personal communication). Though it is recommended, use of rabies
vaccines in these species will be extra-label and will not be considered protective in the event of a bite.
Canine distemper: Procyonids are susceptible to canine distemper (raccoon, coati, and kinkajou). All
collection animals should be vaccinated against canine distemper. However, the safety and efficacy of
modified live canine distemper vaccinations in exotic species of carnivores has been problematic. In fact,
some exotic carnivores‟ canine distemper can be induced by administering live or modified live vaccines
(Carpenter et al. 1976; Pearson 1977). Therefore, it is recommended to NOT use live and modified live
vaccines in procyonids (Blomqvist & Rudbäck 2001). Vaccination may be indicated for other diseases
depending, as mentioned above, on the risk. Unfortunately, killed virus vaccines, with or without
adjuvants, have failed to induce persistent high titers in any species.
®
Recently, a recombinant canarypox-vectored canine distemper virus vaccine (Purevax Ferret
Distemper vaccine by Merial, Ltd., Inc. Athens, Georgia) has been found safe and efficacious in
herpestids (meerkats: Coke et al. 2005). Animals should be vaccinated annually (Roberts 1997;
Fernandez-Moran 2003). Use 1ml i.m. (Coke et al. 2005). Vaccinate previously vaccinated adults yearly,
unvaccinated adults twice 3-4 weeks apart, then annually and juveniles: three vaccinations, every three to
four weeks from 8-16 weeks of age (e.g., 8, 12 and 16 weeks).
The USDA-approved Fervac-D (United Vaccines, Inc., Madison, Wisconsin 53744, USA) has induced
disease in red pandas and anaphylaxis in some mustelids (notably ferrets) and viverrids (R.Montali,
unpublished data). The use of multivalent vaccines containing CDV, such as Galaxy-6-MPH-L (Solvay), is
discouraged, because of possible immunosuppression and clinical disease brought about by other MLV
components. Data on maternal antibody interference with vaccination of raccoons and ferrets suggest
that a final CDV vaccine should be administered at 18–20 weeks of age in raccoons (reviewed in Deem et
al. 2000). Vaccination schedules may require modification during canine distemper epidemics, or periods
of increased risk of exposure.
Feline Panleukopenia: AAZV‟s Infectious Disease Notebook notes that some small carnivores are
susceptible to feline panleukopenia and should be vaccinated and many small carnivores have been
vaccinated with a combination product in the past. However, a number of veterinary advisors do not
suggest vaccination in their recommendations, including red pandas and black-footed ferrets. Veterinary
advisor recommendations should be followed primarily.
Feline panleukopenia has been reported in raccoons and coatis (Bittle 1981). Vaccination with a
killed product is recommended. A killed panleukopenia vaccine is available by utilizing the panleukopenia
fraction of a multivalent feline vaccine. FPV-1 Feline Panleukopenia Vaccine (Biocor Animal Health Inc.,
th
2720 North 84 Street, Omaha, NE 68134) is a new non-adjuvanted, killed vaccine. The frequency of
vaccination should be at least two vaccines three weeks apart at/after 12 weeks of age. If started before
12 weeks, give a third vaccine, then vaccinate annually. This vaccine has been shown to be safe in
pregnant domestic cats.
th
Parvovirus: Parvocine (Biocor Animal Health Inc., 2720 North 84 Street, Omaha, NE 68134) is a killed
univalent parvovirus vaccine. Dose: 1ml. Route: IM. Frequency: same as listed above for canine
distemper.
Other vaccinations: In some areas where canine leptospirosis and canine hepatitis are a problem,
vaccination may be considered (Carnio 1996). Leptospirosis has been reported in raccoons (Shotts
1981). If canine leptospirosis vaccination is deemed necessary, vaccinate annually with multivalent
bacterin (Joslin et al. 1998).
Table 10: Vaccinations for raccoon, coati, and kinkajou (Castro & Heuschele 1992)
Vaccine Vaccine type Frequency
Canine distemper Killed/modified live* Annual
Feline panleukopenia Killed/modified live Annual
Canine adenovirus – 2 Killed/modified live Annual
Leptospira Bacterin-CI Killed/modified live Annual
Rabies Killed Annual
* Vaccine should not be of ferret origin, avian origin is preferred.
Coatis should be vaccinated for the first time at 6, 9, and 12 weeks of age, or until they have received
a series of three vaccinations three weeks apart, and vaccinated for rabies at 16 weeks.
6 weeks – DHPP (Canine distemper/Parvo) They should not be vaccinated for Lepto or Corona*.
9 weeks – DHPP
12 weeks - DHP
16 weeks – Imrab rabies
* Durmune Max 5™ without Lepto, made by Fort Dodge, has been used successfully in the coati (K.Schilling, personal experience).
Physical Examinations: It is recommended that all animals have regular routine physical examinations.
Young healthy animals can be examined biannually, while clinically healthy but geriatric animals or those
with shorter lifespan may be examined more frequently, at the discretion of the attending veterinarian.
Additionally any animal that has clinical signs of disease should be evaluated by the attending
veterinarian and if indicated, the animal is anesthetized to obtain diagnostic samples and physiologic
parameters. It is ideal to train animals to be able to obtain samples (e.g., blood) and receive vaccinations
without anesthesia or darting in order to be able to monitor animals more closely without the need of
anesthesia. During the physical examination the following is recommended (see Appendix G for
additional recommendations for procyonid physical examinations). The need for each test may vary
depending on the geographic location, species, and tests performed at the sending institution.
Transponders and/or tattoos should be checked and reapplied if they are not readable.
Baseline physiological parameters, such as weight and body condition scoring, body temperature,
heart rate, and respiratory rate, and hydration status should be obtained and recorded.
Oral exam: including dental chart documentation. Any problems should be noted and addressed if
possible. Dental cleaning and polishing should be completed if necessary.
Ophthalmologic exam; Ear exam: appropriate diagnostics should be completed if there is any
indication of problems. Cleaning and treatment should be done if necessary.
Chest and abdominal auscultation and palpation.
Assessment of genitalia. Care should be taken to record any changes in the external genitalia,
such as vulvar swelling or discharge, testicular enlargement, and mammary gland changes.
Contraceptive implants should also be checked to make sure they are in place and not causing
any local irritation.
Skin, feet and nails.
Anesthesia monitoring sheet.
Radiographs should be taken and compared to previous ones if possible.
Hematology and serum biochemistry profile should be performed. For animals that are housed
outside in heartworm endemic areas, this can include monitoring for heartworm infection by
performing a heartworm ELISA antigen test (will not detect all male infections nor infections with
less than three female nematodes). If infection is suspected, POSITIVELY identify the microfilaria
as pathogenic before instituting treatment. Treatment is not benign and mortality has been
associated with melarsomine dihydrochloride administration to North American river otters and a
red panda (Neiffer et al. 2002).
Serum should be banked whenever possible.
In some cases urine can be collected from the cage before anesthesia and a urinalysis
performed. If any abnormalities are detected, urine should be collected by cystocentesis for a
complete urinalysis (may need to include culture and sensitivity).
Regular fecal examination should be performed to check for internal parasites. The frequency
may vary depending on environmental conditions and personnel but should be performed at least
annually. Anthelmintics should be administered as needed necessary. Fecal testing should
include both a direct smear examination as well as a fecal flotation, and if possible, sedimentation
techniques. Baermann fecal examination techniques help identify certain parasites such as
lungworms that are otherwise difficult to detect.
Vaccines should be administered as needed.
Reports of disease issues, adverse drug reactions, etc. should be reported to the veterinary
advisor or AZA TAG on an annual basis, in addition to submission of necropsy reports.
NOTE in ovariohysterectomy cases, and necropsies of intact animals, it is strongly
recommended that the reproductive tissues be submitted for histopathological examination
(even if it is grossly normal) as many diseases may be subclinical and may not affect the
individual animal but may have an impact on the reproductive potential of the species.
Perhaps the best way to monitor condition, short of a complete physical examination, is through daily
visual inspections combined with the keeper‟s knowledge of each individual‟s typical behavior.
Parasite Control: It is recommended to diagnose first and treat appropriately. Parasites such as ear
mites, fleas, ticks, etc., can be detected during routine physical examination (Petrini 1998). Small
carnivores are susceptible to the same parasites as the domestic carnivores, and antiparasite drugs
applied to other carnivores (e.g., Piperazine, Telmin, Furacin, Caricide, Yomesan, etc.) have generally
proven successful for procyonids as well (Roberts 1997). Species housed out of doors should be routinely
administered heartworm preventative in areas where this parasite is endemic (Denver 2003). Fecal
examinations should be performed at least annually, but may be more frequent depending on the risk of
exposure. The following are recommendations for parasite testing and treatment:
Internal Annual/ semiannual fecal examination (direct smear, fecal flotation, and
sedimentation or Baermann). De-worming should be done as determined by the
results of regular fecal exams. As a screening test, samples from the same cage
can be pooled. If results are positive, it is possible to perform a separate fecal
examination on each animal in order to determine who is positive. However, it is
very likely that all animals in the enclosure will need to be treated.
Quarantine fecal examination: 3 negative results of 1/week fecal direct smear and
flotation.
Coati: Butorphanol, using a small cat dosage of 0.4mg/kg SQ, has been used successfully as analgesia
for coati (S.Grant, personal communication). Ketamine/Rompun (3:1 ratio) at a dose of 3mg/kg IM is a
successful anesthesia for coatis (S.Grant, personal communication). Booth-Binczik (2001) effectively
used Telazol at a dosage of 6-10mg/kg for hundreds of coati immobilizations in the wild, with no muscular
rigidity or respiratory depression seen.
More extensive details on adequate anesthesia protocols can be found in Kollias and Abu-Madi, 2007.
6.7 Management of Diseases, Disorders, Injuries and/or Isolation
AZA-accredited institutions should have an extensive
veterinary program that manages animal diseases, disorders, or AZA Accreditation Standard
injuries and has the ability to isolate these animals in a hospital (2.4.2) Keepers should be trained to
setting for treatment if necessary. Staff should be trained for recognize abnormal behavior and clinical
meeting the animal‟s dietary, husbandry, and enrichment needs, symptoms of illness and have knowledge
as well as in restraint techniques, and recognizing behavioral of the diets, husbandry (including
enrichment items and strategies), and
indicators animals may display when their health becomes restraint procedures required for the
compromised (AZA Accreditation Standard 2.4.2). Protocols animals under their care. However,
should be established for reporting these observations to the keepers should not evaluate illnesses nor
veterinary department. Hospital facilities should have x-ray prescribe treatment.
equipment or access to x-ray services (AZA Accreditation
Standard 2.3.2), contain appropriate equipment and supplies on AZA Accreditation Standard
hand for treatment of diseases, disorders or injuries, and have (2.3.2) Hospital facilities should have x-
staff available that are trained to address health issues, manage ray equipment or have access to x-ray
short and long term medical treatments and control for zoonotic services.
disease transmission.
AZA-accredited institutions must have a clear process for
identifying and addressing animal welfare concerns within the AZA Accreditation Standard
institution (AZA Accreditation Standard 1.5.8) and should have (1.5.8) The institution must develop a
an established Institutional Animal Welfare Committee. This clear process for identifying and
process should identify the protocols needed for animal care addressing animal welfare concerns
staff members to communicate animal welfare questions or within the institution.
concerns to their supervisors, their Institutional Animal Welfare
Committee or if necessary, the AZA Animal Welfare Committee. Protocols should be in place to document
the training of staff about animal welfare issues, identification of any animal welfare issues, coordination
and implementation of appropriate responses to these issues, evaluation (and adjustment of these
responses if necessary) of the outcome of these responses, and the dissemination of the knowledge
gained from these issues.
As care givers for the animals residing in our zoos and aquariums, it is vital that we provide the best
care possible for them until the time their health deteriorates to a point where euthanasia is the most
humane treatment, or the animal dies on its own. Necropsies should be conducted on deceased
procyonids to determine their cause of death and the subsequent
disposal of the body must be done in accordance with any local, AZA Accreditation Standard
state, or federal laws (AZA Accreditation Standard 2.5.1). (2.5.1) Deceased animals should be
Necropsies should include a detailed external and internal gross necropsied to determine the cause of
death. Disposal after necropsy must be
morphological examination and representative tissue samples
done in accordance with local/federal
form the body organs should be submitted for histopathological laws.
examination.
Diseases that are out of the ordinary or if multiple cases of a certain disease occur, as well as
cases of reproductive diseases and contraception problems should also be reported to the veterinary
advisor.
AZA SCTAG Recommendations: The following table (Table 12) provides a list of diseases and
associated clinical signs observed/reported in procyonids; it is not intended as a comprehensive table.
For proper treatment and management the reader is referred to more extensive medicine texts. The last
column lists the procyonid species in which the disease has been reported; other species may also be
susceptible.
Table 12: Diseases that affect procyonids (created by A.Moresco 2003).
Disease Clinical description
Rabies
Transmission Contact of infected saliva with mucosal surface or open wound.
Clinical signs Considered in any animal with outdoor access with neurologic signs.
Diagnosis Can only be diagnosed definitively post mortem. Histopath on brain.
Susceptible species All mammals are susceptible.
Canine Distemper
Transmission Aerosol exposure or direct contact with conjunctiva, nasal exudates, urine, or
feces. Vaccine (modified live) induced transmission has been reported in red
panda.
Clinical signs Anorexia, vomiting, diarrhea, weight loss, hyperemia of face & ears,
hyperkeratosis of nasal planum & footpads, oculonasal discharge, neurologic
signs.
Diagnosis Immunofluorescent antibody test or PCR of conjunctival swab. Histopath exam
of affected tissue. May be found with other concurrent diseases.
Susceptible species Many, including Red panda (Bush et al. 1976; Bush & Roberts 1977; Qin et al.
2007)and raccoon (Wojcinski & Barker 1986; Hamir et al. 1998; Lemberger et al.
2005); MLV vaccine induced in kinkajou and red panda (Bush et al. 1976;
Kazacos et al. 1981).
Parvovirus
Transmission Direct contact
Clinical signs Diarrhea, gastroenteritis.
Diagnosis IFA test on feces. PCR (Elia et al. 2007).
Susceptible species Raccoon (Martin & Zeidner 1992), red panda (Qin et al. 2007).
Feline panleukopenia
Transmission Direct contact with infected animals or via fomite transmission of excreta, in
utero from infected mother.
Clinical signs Vomiting, diarrhea, lethargy, fever, depression, eventually dehydration,
leucopenia, abortion. Can be fatal, especially in younger animals.
Diagnosis Quantitative PCR on blood; Antigen detection in feces.
Susceptible species Raccoon, Coati (Barker & Parrish 2001; Denver 2003).
Toxoplasmosis
Transmission Exposure to sporulated oocysts, ingestion of intermediate host or ingestion of
uncooked infected meat.
Clinical signs Anorexia, lethargy, fever, lymphadenitis, spenomegaly, corneal edema,
myocarditis, hepatitis, pneumonitis, neurologic signs.
Diagnosis Serology, PCR.
Susceptible species All species (Denver 2003), but frequently reported in wild raccoons (Lindsay et
al. 2001).
Neospora
Transmission Ingestion of infected tissues or feces.
Clinical signs Exposure in wild raccoons is minimal, but has been reported. Can occur as a
co-infection with other disease.
Diagnosis Serology, PCR.
Susceptible species Raccoons (Lindsay et al. 2001; Lemberger et al. 2005)
GI parasites
Transmission Similar to domestic dogs and cats, often fecal-oral route.
Clinical signs Similar to domestic dogs and cats. Baylisascaris procyonis (roundworm of
raccoons) is zoonotic, causing cerebral nematodiasis in other species.
Diagnosis Fecal exam (float, sedimentation, direct).
Susceptible species All species.
Lungworm
Transmission Depending on the species of lungworm involved, transmission can be direct, by
ingestion of L1 from feces or sputum of infected animals, or indirect by ingestion
of the intermediate host.
Clinical signs Can present as coughing, dyspnea, hyperpnea, nasal discharge, or neurological
signs.
Diagnosis First stage infective larva in fecal exam.
Susceptible species Red pandas usually without clinical disease (Montali et al. 1984).
Heartworm
Transmission Bite from infected mosquito.
Clinical signs Respiratory and cardiac signs. Not all microfilaria infections develop into clinical
disease. Often no clinical signs are seen.
Diagnosis Antigen detection in blood (ELISA), microfilaria in blood (Knott‟s test/ blood
smear), necropsy findings.
Sarcoptic mange
Transmission Exposure to infected animals.
Clinical signs Scabs around head and neck, tail, feet.
Diagnosis Finding the mites in skin scrapings or biopsy.
Susceptible species Many
Fleas
Transmission Can transfer from other animals, although tend to prefer specific host.
Clinical signs Signs may vary from asymptomatic to fleabite allergy. Pruritus, inflammation, or
anemia can also occur, especially in young or sick animals with heavy
infestation.
Diagnosis Finding fleas or flea dirt in the coat.
Susceptible species Many
Ticks
Transmission Similar to transmission in other mammals
Clinical signs Itching. May transmit other diseases.
Diagnosis Finding ticks on animals. Others in group may be affected.
Susceptible species Many
Non-infectious disease
Dental disease
Risk factor ---
Clinical Signs Decreased appetite, weight loss.
Diagnosis Physical exam, radiographs.
Species reported Red pandas are prone to it (Denver 2003).
Hyperthyroidism
Risk factor ---
Clinical Signs ---
Diagnosis Physical exam, serum chemistry.
Species reported Raccoon (Denver 2003).
Hepatic disease
Risk factor Diet change.
Clinical Signs Increased ATL.
Diagnosis Blood chemistry, biopsy.
Species reported Red panda (Montali et al. 1989).
Uterine neoplasia
Risk factor Possibly MGA implants.
Clinical Signs Purulent vaginal discharge
Diagnosis Physical exam, histopathology.
Species reported Coati (Chittick et al. 2001)
Useful Veterinary References: (This list is not exhaustive, but a sampling of medical references not
cited.)
Fournier, P., Fournier-Chambrillon, C., Vie, J.C. (1998). Immobilization of wild kinkajous (Potos flavus)
with medetomidine-ketamine and reversal by atipamezole. Journal of Zoo and Wildlife Medicine
29(2):190-194.
Hanson, W.L., Boggs, D.F., Kay, J.M., Hofmeister, S.E., Okada, O., Wagner, Jr. W.W. (2000). Pulmonary
vascular response of the coati to chronic hypoxia. Journal of Applied Physiology 88(3): 981-986.
Chapter 7. Reproduction
7.1 Reproductive Physiology and Behavior
It is important to have a comprehensive understanding of the reproductive physiology and behaviors
of the animals in our care. This knowledge facilitates all aspects of reproduction, artificial insemination,
birthing, rearing, and even contraception efforts that AZA-accredited zoos and aquariums strive to
achieve.
Procyonids have relatively small litters (usually 1-4 young per litter and most often 2-3) of altricial
young that remain nest bound for at least 45 days. The temperate species (raccoon and ringtail) tend to
be seasonal breeders and the approximate timing of parturition can be predicted with some confidence.
(Ringtails‟ estrus lasts one to two days, generally occurring in April or May.) The tropically distributed
species (e.g., kinkajou, olingo, and some raccoon species) are not seasonal, and should be monitored
much more closely for evidence of pending parturition.
Table 13: Selected Procyonidae reproduction/development parameters (from: Denver 2003; Reed-Smith et al. 2003,
Appendix K)
Brown/white
Raccoon Kinkajou Ringtail Cacomistle
Parameter** nosed coati
(Procyon lotor) (Potos flavus) (B. astutus) (B. sumichrasti)
(Nasua)
Breeding season Mid-Dec to Feb-Apr in Nonseasonal Feb-May Year-round, peaks
early August Panama; in late winter
Non-seasonal in
zoos
Estrous freq. Typically 1-3 times per Polyestrous Monestrous ---
monestrous year
Estrus duration 9 days 10 days Estrus lasts 4- 24-36 hours 24 hour
6 days every conception period
60 days or so
Courtship Elaborate Lek-like mating Non-ritualized. Increased, Submissive
movement system localized urine chirps, crouches,
patterns depositing and and “coy” behavior
scattering of
feces
Copulation May last as 23-60 minutes, Several times Several times Several times per
long as an repeatedly over over several per hour for a hour for a few
hour the course of 10 days few minutes minutes at a time
days
Gestation (days) 60-75 70-77 112-118 51-54 63-64
No. of offspring 1-7, usually 3- 2-7,usually 3-5 1, rarely 2 1-5, usually 2-4 1-5
4
Birth weight (g) 60-75 100-180 150-200 28 Ave. 28
First solid food ~7-8 weeks 8-10 weeks 7-8 weeks ~4 weeks ~4 weeks
Sexual maturity* Females at 9- ~2 years for Males at 1½ ~9-10 months Some say ~10
10 months; males & females years and months, others 1.9
males at ~2 females at 2¼ years
years years.
* Capable of breeding but may not be successful until older
** Poglayen-Neuwall 1995; Gompper & Decker 1998; Stanley et al. 1999; Haas & Roback 2000; B.Snyder, unpublished information.
It has been speculated that ringtail and cacomistle (Bassariscus spp.) may mate permanently or
semi-permanently in the wild but there is no evidence of direct male parental care, and females even
endeavor to keep males away from the nest containing infants. Most female procyonids reproduce in their
second year and males become sexually mature somewhat later; all have reproductive life spans in
excess of 10 years. Females may be seasonally polyestrous (although some, like Bassariscus, are
monestrous) and adult females not reproducing in the spring may cycle again within four months with the
result that a second birthing season may occur unusually late in the year. While breeding is seasonal in
many species in the wild, this appears to be a resource-based effect, with reproductive seasons tending
to decay and even disappear in zoos or aquariums. Increasing winter photoperiod plays an important role
in initiating reproduction for seasonal breeders. Some of the procyonids do show marked behavioral
differences seasonally. Typically these changes are observed during the breeding season or when a
female is in estrus, for example when male coatis join the female troop during breeding season. Also,
typically solitary animals, such as the raccoon, olingo, ringtail, and cacomistle, may spend more time with
an exhibit mate (Roberts 1997). Hormonal tracking of a male or female‟s reproductive status is possible
using fecal or urine hormonal metabolite testing. If this is required, the AZA SCTAG Chair should be
contacted for the current Reproductive Advisor‟s name and contact information.
Gestations tend to scale with body size and most range between 60 days (ringtail and cacomistle)
and 72-77 days (coati). A gestation of 113-117 days is on record for the kinkajou (B.Snyder, unpublished
information, 2003). The onset of the breeding season is marked by increased activity and agonism,
especially among males; mating itself is prolonged and vigorous. This is especially the case for raccoons
where males have a very long, re-curved baculum, which presumably has evolved as a result of inter-
sexual competition among males. Most species are solitary and females should be isolated from all
conspecifics during the birth and rearing period. While coatis are gregarious during the non-breeding
period, females leave the band to give birth and typically do not rejoin the group until some weeks after
parturition. Therefore, provision should be made to isolate expectant females in this species as well
(Roberts 1997).
In ringtail and cacomistle females there is a clear swelling of the vulva 7-10 days before peak estrus;
females of these species are receptive only for about 24 hours (Partridge 1992). Successful breeding in
the ringtail often can be marked by observing the female whose vulva has sealed shut with a layer of
dried vaginal fluid covering it. This is normal and no attempts should be made to clear this up unless there
is evidence of another underlying condition that mandates intervention.
Coati: Female coatis should be housed as a group, neutered/young males can be housed with the
females, but the breeding male should be introduced only when a female shows signs of estrus. Groups
of females with young are the typical social structure of the coati species. Male coatis should be
introduced to females once they begin to show behavioral signs of estrus. It is suggested that the
breeding pair be introduced to one another in a neutral space, or one familiar to the female. Off-exhibit
holding areas are ideal for this if they are large enough (V.Walkosak, unpublished information 2003). The
male and female should also be introduced to one another away from the group; if excessive aggression
occurs the pair should be separated and reintroduced several hours to a day later (V.Walkosak,
unpublished information 2003). Due to the generally solitary nature of coati males, provisions should be
made to allow for isolation of males if required (Standley 1992). Typically males only join female groups
for mating. Outside of the breeding season the females and juveniles drive the males away. In zoos and
aquariums, females are particularly intolerant of males following parturition (Standley 1992).
Male coatis can remain apart from female groups except during the breeding season, but coatis have
a flexible social organization, and in some locations males associate with female groups at all times of
year (Booth-Binczik 2001; Hirsch 2007). When female groups are very large, male coatis exhibit lek-like
mating behaviors (Booth-Binczik et al. 2004, personal communication); during the breeding season males
display to attract females. Such displays include fighting with other males, which frequently results in
serious injury and, occasionally death of the opponent.
Young males should be removed from coati groups before they reach sexual maturity at about two
years of age (Campbell 2001). Neutered males can be maintained in all-female groups (V.Walkosak,
unpublished information 2003).
Ringtail and cacomistle: Typically, male ringtails and cacomistles play no role in the rearing of young
(Partridge 1992). Some experts believe the female will allow the male to rejoin the family group when the
young are roughly three weeks of age (Poglayen-Neuwall & Toweill 1988). Others believe the young are
still vulnerable to infanticide at that age and that the male should not be reintroduced until much later
(K.Schilling, personal experience).
Ringtail and cacomistle females housed in trios should be separated from the other female as they
are likely to interfere with one another‟s litters resulting in infanticide (Partridge 1992). Pregnant females
also will become hostile to the male, who should also be removed. Sometimes this expected aggression
does not occur, usually when pairs are housed together. In these cases, the male may be driven from the
communal nest box, and so alternate sleeping boxes should be provided for him shortly before parturition
(Partridge 1992).
The rate of cannibalism is extremely high in ex situ populations of ringtails (K.Schilling, personal
experience). Females should feel safe and secure when raising a litter. Removal of the male is highly
advisable to prevent one or both of the ringtails from cannibalizing the kits (K.Schilling, personal
experience).
Kinkajou: Kinkajou trios can be left together at all times during breeding. Some trios may be kept together
through parturition with one female even helping care for the other‟s young. In other cases the pregnant
female may need to be moved to other quarters. Close monitoring by keepers will determine the
appropriate course of action for a particular trio (Kays & Gittleman 2001). See Appendix K for more
detailed information.
Facilities for Reproduction: Proper nest and maternal management is essential if successful
reproduction is a primary goal of ex situ population maintenance. Prior to parturition, females will locate a
suitable nest site and will prepare it by adding nest material. Straw, hay, grasses, leaves, twigs, and
sticks will be used if available. Some procyonids routinely move infants during the nest bound phase of
development so alternative nest areas should be provided to accommodate for this behavior. While some
species (e.g., raccoon) are fairly adaptable to zoos and aquariums and will rear young in almost any nest
area provided, other species (e.g., ringtail and cacomistle) are much less flexible, and care should be
taken to provide appropriate and secure nest areas. Often, the provision of a number of nest areas prior
to birth allowing the expectant mother to choose an acceptable one is all that is necessary (Roberts
1997).
Pregnant females should be provided with a nest box located away from the group (coatis) or male
(kinkajou, ringtail, cacomistle, and olingo). If the exhibit is large enough to allow a parturient female to
isolate herself, it is acceptable to leave her with the group. This size may vary from female to female, in
general it should be interpreted as large enough to allow the female complete separation from the sounds
and smells of conspecifics. Typically, a parturient female should be moved to a quiet, secure location,
which she has previously been familiarized with (Campbell 2001; Reed-Smith et al. 2003). See Section
7.3 for additional species-specific information.
7.2 Assisted Reproductive Technology
The practical use of artificial insemination (AI) with animals was developed during the early 1900s to
replicate desirable livestock characteristics to more progeny. Over the last decade or so, AZA-accredited
zoos and aquariums have begun using AI processes more often with many of the animals residing in their
care. AZA Studbooks are designed to help manage animal populations by providing detailed genetic and
demographic analyses to promote genetic diversity with breeding pair decisions within and between our
institutions. While these decisions are based upon sound biological reasoning, the efforts needed to
ensure that transports and introductions are done properly to facilitate breeding between the animals are
often quite complex, exhaustive, and expensive, and conception is not guaranteed.
AI has become an increasingly popular technology that is being used to meet the needs identified in
the AZA Studbooks without having to re-locate animals. Males are trained to voluntarily produce semen
samples and females are being trained for voluntary insemination and pregnancy monitoring procedures
such as blood and urine hormone measurements and ultrasound evaluations. Techniques used to
preserve and freeze semen have been achieved with a variety, but not all, taxa and should be
investigated further.
AI is not a technique currently used in procyonids.
7.3 Pregnancy and Parturition
It is extremely important to understand the physiological and behavioral changes that occur
throughout a procyonid‟s pregnancy.
Coati: In the wild, female coatis will leave the band to give birth, and will not rejoin it until the young are
roughly six weeks of age (Standley 1992). Parturient females should be separated from the group or
other exhibit mates; females are known to vigorously defend their nests, which could lead to animal injury
or neglect of the young (Standley 1992).
Female coatis left with the group to give birth have exhibited aggression towards the male (Campbell
2001), and if there is insufficient cage space „kidnapping‟ of the young among the mothers has been
reported (Grzimek 1990). Walkosak (unpublished information 2003) states the separation of a parturient
female coati into an adjacent suite, which includes nest box, climbing structures, food, water, etc. has
been key to the successful rearing of young; this should be an area the female is familiar with. Some
managers recommend the male should be removed from the females after breeding season and not held
within scent/visual range when the female gives birth. Booth-Binczik (personal communication) offers this
observation from the wild: “…females interact amicably with males throughout pregnancy and nesting -
they just don't allow them to actually go to the nest. They generally don't allow other females to go to the
nest either…females sharing a nest was observed on a couple of occasions.” It may not be necessary to
remove the male from scent/visual range, something that should be evaluated in each situation, and
closely bonded females pregnant simultaneously may be able to be left together in some situations.
Management choices should be evaluated based on physical size/layout of the exhibit and individual
animals involved (Booth-Binczik, personal communication).
Female coatis should be provided with their own nest box that should be approximately 61 cm x 46
cm x 61 cm (2 ft long x 1.5 ft wide x 2 ft high) (Standley 1992; Campbell 2001), as well as an alternate
nesting site where she can move her young if she becomes nervous (Standley 1992; V. Walkosak,
unpublished information 2003). Female coatis should be separated from the group just prior to giving birth
(V. Walkosak, unpublished information 2003). The female should be left alone without human
interference, unless required, or the mother can become too stressed (Haas & Roback 2000).
The well-bedded nest boxes should be provided in quiet, private areas easily accessed by the keeper
staff, once the female has settled down, for cleaning and monitoring of young development.
Kinkajou: Kinkajou pairs can be left together for parturition but should be monitored for aggression or
excessive interference by the male with the young (B. Snyder, unpublished information 2003). Some trios
can be left together but should be closely monitored, especially the first time one of the females gives
birth (Kays & Gittleman 2001). See Appendix K for more detailed information.
Ringtail and Cacomistle: There is a high rate of cannibalism of ringtail babies in ex situ populations,
often as the result of improper husbandry. This is a highly sensitive species that should be given ample
time (several weeks) to become accustomed to new surroundings before giving birth. Schilling
recommends isolating female ringtails in familiar surroundings and that unfamiliar/loud noises should be
kept to a minimum (K. Schilling, personal experience). Females should be given quiet and privacy as well
as nest box choices. Females of both species should be separated from exhibit mates. Primiparous
ringtail females should be monitored to ensure they are caring for their young and have not abandoned or
eaten them. Poglayen-Neuwall (1980b) reports for the ringtail:
“The annual breeding season extends from Feb. into May, with the majority of matings taking
place in April. The female is receptive during a 24 hour period only, which coincides with the peak
of the estrous swelling of her vulva. If conception has occurred, vulval swelling commences again
a few days after the termination of the estrous cycle and shows another peak at the time of
parturition. Recurring vulval swelling is an indication of pregnancy in addition to mammary
development and increased abdominal girth. The gestation period in this species varies from 51
days and 8 hours to 53 days and 14 hours, and parturition may last from 85-126 min. This is the
shortest gestation period among Procyonidae. No post-partum estrus with copulations was
observed even after the loss of neonate young.”
In another article (original articles in German, this information is taken from English summaries),
Poglayen-Neuwall, I. (1980a) states:
“Young ringtails frequently ingest saliva from the mother's mouth during the nutritional weaning
stage, when the mother's mammary glands begin to dry up. Spontaneously, or more often after
prodding by the young, the mother facilitates the saliva licking by opening her mouth and bending
her head toward the young. When the young are essentially weaned, fully mobile and capable of
following the mother on extended foraging excursions, the mother will deny the young access to
her mouth and the interest of the young in this source of fluid will wane rapidly. This behavior may
contribute to the survival of young ringtails under conditions of aridity and excessive heat by
minimizing the danger of dehydration.”
See Table 13 for estrus, courtship, copulation, gestation, and kit development information.
7.4 Birthing Facilities
As parturition approaches, animal care staff should ensure that the mother is comfortable in the area
where the birth will take place, and that this area is “baby-proofed.” See below for summary information
about birthing facilities, however Section 7.1 and 7.3 also should be consulted for management
considerations.
Coati: Female coatis should be provided with their own nest box that should be approximately 61cm x
46cm x 61cm (2 ft long x 1.5 ft wide x 2 ft high) (Standley 1992, Campbell 2001), as well as an alternate
nesting site where she can move her young if she becomes nervous (Standley 1992; V.Walkosak,
unpublished information 2003). Female coatis should be separated from the group just prior to giving birth
(V.Walkosak, unpublished information 2003). The female should be left alone without human interference,
unless required, or the mother can become too stressed (Haas & Roback 2000).
The well-bedded nest boxes should be provided in quiet, private areas easily accessed by the keeper
staff, once the female has settled down, for cleaning and monitoring of young development.
Kinkajou: No information is available on recommended nest box size for this species. The female should
be provided with at least two nest box choices; boxes should be large enough for her to turn around in
and to accommodate the presence of young. Boxes should be provided with dry nesting material.
Females should not be disturbed immediately after parturition unless trouble is suspected. Normal
routines should be maintained but noise kept to a minimum.
Ringtail and Cacomistle: There is a high rate of cannibalism of ringtail babies in ex situ populations,
often as the result of improper husbandry. This is a highly sensitive species that should be given ample
time (several weeks) to become accustomed to new surroundings before giving birth. Schilling
recommends isolating female ringtails in familiar surroundings and that unfamiliar/loud noises should be
kept to a minimum (K. Schilling, personal experience). Females should be given quiet and privacy as well
as nest box choices. Females of both species should be separated from exhibit mates. Primiparous
ringtail females should be monitored to ensure they are caring for their young and have not abandoned or
eaten them.
7.5 Assisted Rearing
Although mothers may successfully give birth, there are times when they are not able to properly care
for their offspring, both in the wild and in ex situ populations. Fortunately, animal care staff in AZA-
accredited institutions are able to assist with the rearing of these offspring if necessary.
Hand-rearing: Hand rearing may be necessary for a variety of reasons – rejection by the parents, ill
health of the mother, or weakness of the offspring. Careful consideration should be given as hand rearing
requires a great deal of time and commitment (Muir 2003).
Before the decision to hand rear is made, the potential for undesirable behavioral problems in a hand-
reared adult should be carefully weighed (aggression towards humans, inappropriate species-specific
behavior, etc.), and plans made to minimize deleterious effects on the development of natural behaviors
as far as possible. This may require extensive time commitment on the part of staff, plans for fostering,
relocation of the young, exposure to species-specific sounds, etc. Once the decision has been made and
the young have been abandoned by the mother, or are consistently getting weaker/losing weight, it is best
to remove the infants as soon as possible.
If young have been abandoned by their mother it is best to remove them to prevent infanticide. If the
offspring are being cared for but receiving no milk they will be restless, possibly calling continuously, or
conversely they may be hypothermic and scattered around the enclosure. Another indicator of trouble
would be the female moving around the exhibit continuously while carrying the young; this could mean
she is not comfortable with the denning provided, or there is something wrong with her or the young (Muir
2003).
If it is necessary to remove offspring because of an exceptionally large litter, it is best to remove two
of the largest infants. The temptation is often to take the smallest, but they stand the best chance if raised
by their mother. Hand-rearing of singletons is more likely to lead to severe imprinting than if they have a
conspecific to play with (Muir 2003).
Physical care: Incubators are the best source of warmth; heat lamps are too intense and can be
dehydrating or cause serious burns. Hot water bottles can be used in a pinch and hypothermic babies can
be warmed slowly by placing them next to your body (Muir 2003). Most babies will feel more secure if
wrapped in layers of towels; this also aids in keeping them warm (Muir 2003). Ringtails and cacomistles
should be placed in an incubator with a floor temperature of ~38ºC (100ºF) (Partridge 1992).
Feeding Protocols: Young mammals require a specific number of kcal/day for optimum development
and growth. If the formula being offered is nutritionally dense, fewer feedings will be necessary than with
formulas that are more dilute or low in fat or protein. Following is a method for calculating the volume of
food to be offered daily, the volume that should be offered at each feeding and the number of feedings
per day (adapted from Grant 2004).
The Basal Metabolic Rate (BMR) or Basal Energy Requirement (BER) is the amount of energy (kcal)
an animal needs for basic metabolic function at rest in a thermoneutral zone. In other words, the amount
of calories it needs to stay alive, without having to use energy to maintain normal body temperatures. The
0.75
formula to determine the BER/BMR is: 70 x body wt (in kg.) (Kleiber 1947). For a 30g infant the BER
0.75 0.75
would be: 70 x 0.03 = 5.0 kcal/day. For a 90g infant the BER would be: 70 x 0.09 = 11.5 kcal/day.
For this formula, 0.75 is an exponent that is multiplied by the body weight to put mammals of different
sizes on the same playing field when assessing metabolism. As body weight increases, metabolism
decreases, so a larger animal will not have the same caloric requirement as a much smaller animal (e.g.,
mice consume a much higher percentage of their body weight than an elephant does). In order to
complete the calculations, you will need a scientific calculator that does exponents other than squares.
Follow steps 1-3 below to calculate the BER. Add step 4 if you want to calculate the Maintenance Energy
Requirement. Table 14 provides some pre-calculated MER values.
1. Key in the body weight (in kg) into the calculator
y
2. Press the exponent key (on Texas Instrument calculators the button is marked by the symbol x
representing x with the exponent y) and type in 0.75
3. Press the equals sign, and then multiply that by 70 to get the BER.
4. To calculate the MER, multiply this value by the MER factor (i.e., 2, 3 or 4) to get the kcal
required for that particular animal. .
Once the BER is established, the Maintenance Energy Requirement (MER) can be calculated. This
measurement determines the amount of calories the animal needs to function in a normal capacity at its
life stage. For adults in a maintenance life stage, the BER is multiplied by 2. For infants that have a higher
metabolism and are developing and growing, the BER is multiplied by 3 or 4 (Evans 1987), depending on
the species and other factors.
The stomach capacity for most placental mammals is 5-7% of the total body weight (Meehan 1994).
Convert the body weight into grams to find the stomach volume in ml/cc. To calculate the stomach
capacity in ounces, convert body weight into grams (30g ~ 1oz). It is important that units are the same for
body weight and stomach volume. The stomach capacity is the amount of formula an infant can
comfortably consume at one feeding. Offering much more than this value may lead to overfilling, stomach
distension and bloat. It also prevents complete emptying of the stomach before the next feeding and
promotes the overgrowth of potentially pathogenic bacteria, diarrhea, and enteritis (Evans 1987).
The following calculations will determine the total volume and kcal to feed/day, as well as the amount
of formula for each feeding and the total number of feedings daily (see Table 14 for sample calculated
kcal/day and stomach capacity for various body weights).
0.75
1. Calculate Maintenance Energy Requirement (MER): 70 x body wt (kg) x 3 or 4.
2. Determine stomach capacity (amount that can be fed at each meal): Body weight (in grams or
ounces) x 0.05.
3. Divide MER (number of calories required per day) by the number of kcal/ml in the formula to
determine the volume to be consumed per day. This value can be converted into ounces, by
dividing it by 30.
4. Divide ml of formula per day by volume to be consumed at each meal (stomach capacity). This
gives the number of meals to be offered per day.
5. Divide 24 hours by the number of feedings/day to find the time interval between feedings.
Table 14: Chart for determining kcal/day and stomach capacity for various body weights (Grant 2004)
Weight MER (kcal/day) MER (kcal/day) Stomach capacity
0.75 0.75
(grams) [70 x bw (kg) x 3] [70 x bw (kg) x 4] (ml/feeding)
5.0 3.95 5.25 0.25
6.0 4.5 6.0 0.30
7.0 5.1 6.8 0.35
8.0 5.6 7.5 0.40
9.0 6.1 8.2 0.45
10.0 6.6 8.9 0.50
11.0 7.1 9.5 0.55
12.0 7.6 10.2 0.60
13.0 8.1 10.8 0.65
14.0 8.5 11.4 0.70
15.0 9.0 12.0 0.75
16.0 9.4 12.6 0.80
17.0 9.9 13.2 0.85
18.0 10.3 13.8 0.90
19.0 10.7 14.3 0.95
20.0 11.2 14.9 1.0
25.0 13.2 17.6 1.25
30.0 15.1 20.2 1.50
35.0 17.0 22.7 1.75
40.0 18.8 25.0 2.0
45.0 20.5 27.4 2.25
50.0 22.2 29.6 2.5
55.0 23.9 31.8 2.75
60.0 25.5 33.9 3.0
65.0 27.0 36.0 3.25
70.0 28.6 38.1 3.5
75.0 30.1 40.1 3.75
80.0 31.6 42.1 4.0
85.0 33.1 44.0 4.25
90.0 34.5 46.0 4.5
95.0 35.9 47.9 4.75
100 37.3 49.8 5.0
125 44.1 58.9 6.25
150 50.6 67.5 7.5
175 56.8 75.8 8.75
200 62.8 83.7 10.0
250 74.2 --- 12.5
300 85.1 --- 15.0
350 95.6 --- 17.5
400 105.6 --- 20.0
Initially the animal should receive only an electrolyte solution for the first 2-3 feedings, depending on
how compromised it is. This is to rehydrate the animal and clear the stomach of the maternal milk. Then
the artificial formula is started at a diluted concentration, generally at a 1:4 ratio (mixed formula: water) for
another two to three feedings. It generally takes 48-72 hours to get the animal on full-strength formula by
gradually offering higher concentrations. Depending on the species, three to four feedings of each
concentration level (1:3, 1:2, 1:1, full-strength) are recommended to allow for adaptation and to minimize
the onset of digestive problems, particularly diarrhea. During the initial phase, weight loss is to be
expected but the animal should quickly begin to maintain weight and then start gaining as the formula
concentration increases. It‟s important that the infants not be given full strength formula too soon (in less
than 48 hours after pulling for hand-rearing) because the likelihood of diarrhea occurring is extremely
high. Diarrhea is of particular concern with neonates less than one week of age because they have very
little or no immunity to infections.
The stomach capacity of most eutherian mammals is 5% body weight (bw). This is the volume of
formula that should be offered at each feeding (Grant 2004). The total volume offered per day will depend
on how nutrient dense the formula is. The optimal amount would be the number of kcal calculated from
the infant‟s body weight (see Table 14).
As a general rule, animals should not have an overnight break between feedings that are longer than
twice the time period between daytime feedings (equivalent to missing one feeding). For example, if you
are feeding every three hours during the day, they can go six hours at night without food. When they are
eating every four hours, they can go eight hours at night. It is not advisable to go more than eight hours
between feedings with species that typically nurse throughout the day when mother-raised. Intervals
between feeding also will depend on how healthy or strong the infants are. Very weak neonates will
probably need feedings every few hours even through the night; typically this is necessary for only a few
days to a week.
Feed only if the infant is hungry and suckling vigorously. Weak infants may be hypothermic,
dehydrated and/or hypoglycemic. It is recommended to not offer anything by mouth until the body
temperature is within the normal range for its age. Offer oral electrolytes if it will suckle, or give
subcutaneously if it is weak or dehydrated. Offer 2.5-5% dextrose to raise glucose level, if necessary.
Babies will not die from being slightly underfed, but overfeeding may result in gastrointestinal disease that
is potentially fatal. Young animals will be hungry at some feedings, less at others, but this is quite normal
(Muir 2003).
It is important to keep in mind that neonates are obligate nose breathers and incapable of breathing
through their mouths and nursing at the same time. For this reason, respiratory infections can be life
threatening because they may interfere with breathing and make nursing difficult or impossible (Meier
1985). Aspirated formula is frequently a contributing factor to neonatal respiratory infections; to avoid this
be sure to select the appropriate nipple. The nipple‟s hole should suit the neonate‟s sucking reflex. Also, if
a nipple is too stiff, the pup may tire and refuse to nurse.
Hold the pup in the correct nursing position; ventrally or sternally recumbent (tummy down, not on its
back), with the head up. Place the hand holding the bottle in such a way that it provides a surface for the
pup to push against with its front feet. If milk comes through their nose the nipple hole may be too large or
the pup may be trying to eat too quickly.
If an animal aspirates fluids the recommended protocol is to hold the infant with head and chest lower
than the hind end. A rubber bulb syringe should be used to suck out as much fluid from the nostrils and
the back of the throat as possible. If aspiration is suspected, or if fluid is heard in the lungs, contact the
veterinarian immediately; do not administer drugs without the veterinarian‟s involvement. Monitor body
temperature closely for the occurrence of a fever and a decline in the animal‟s appetite and general
attitude. Depending on the condition and age of the animal, diagnostic procedures may include
radiographs, CBC, chemistry. It is possible to start a course of antibiotics while results from the blood
work are pending, and the attending veterinarian can prescribe an appropriate antibiotic course.
Digestive upset is a common issue with hand-reared neonates, and may be associated with several
factors (Meier 1985): a) inappropriate milk formula, b) feeding frequency, c) overfilling the stomach, d)
rapid changes in the diet, and e) improper storage of formula (spoilage). Unused formula requires
refrigeration, and is safe to use for 24-36 hours after preparation and refrigeration. Refer to the label
guidelines of the formula manufacturer. When digestive upset, characterized by diarrhea, bloating,
inappetance, and/or extreme fuzziness occurs, it is recommended that one factor is analyzed and/or
changed at a time. Lactose intolerance also should be considered, particularly for the coati (D.Bressler,
personal communication).
® ® ® ®
Ringtail and cacomistle: The formula of choice is Esbilac (Pet Ag manufacture KMR , Esbilac , Multi-
® ®
Milk and the Zoologic Milk Matrix line; contact details: 261 Keyes Ave., Hampshire, IL. 60140, 1-800-
323-0877/ 1-800-323-6878 www.petag.com), which should be offered 9 times per day for the first 14
days. Total intake per day should be about 6ml per 24 hours for this period. On days 15-30, 18ml should
be offered, daily, in 7 feedings (Partridge 1992). Total food amounts should be based on the infant‟s
®
weight. KMR should not be used for ringtail; they appear to respond initially but then can go downhill
quickly, often dying.
Kittens should be stimulated to urinate and defecate for the first three weeks. Solid food should be
introduced into the diet on approximately day 35 at which time the Esbilac can be increased up to ~43ml
per day and the number of feedings reduced to five. By day 60, Esbilac should be reduced to one feeding
of ~30ml and can be eliminated entirely by day 80. The amount of solids offered should be gradually
increased to ~140grams by day 90. Artificial heating can be discontinued when the kittens are about five
weeks of age as long as the ambient temperature stays between 24-30ºC (75-86ºF) (Partridge 1992).
® ® ®
Raccoons: The formula of choice for these species is KMR or Milk Matrix 42/25 (Pet Ag ). Mix one part
powder to two parts water by volume for either product after first ensuring that the kit is well hydrated. The
kit should be offered 3:1 rehydrating solution to formula, then half and half before being fed 100%
®
formula. The weaning diet should be comprised of soaked puppy chow, Gerber high-protein baby cereal,
and KMR powder with enough water to make up an oatmeal-like consistency. Kits with their eyes still
closed may need to be tube feed (DeGhetto et al. 2002).
®
Coati: The formula of choice is Esbilac /water mixed at a 1:2 ratio. Day one pups should start with a
hydrating formula solution, progressing gradually over several days to a 1:1 formula/water mix then to
straight formula. Formula should be kept at 35-37.8°C (95-100°F) or the baby coati will refuse it. All
nipples should be the same size, color, and texture or they might refuse the bottle. Pups should be fed
every 2 hours until two weeks of age, and every 3 hours until three weeks of age; at this stage rice cereal
should be added to the formula (just enough to thicken it). At 3 weeks, the pups should be fed every 4
hours with a mixture of 1 part formula, 2 parts water, 1 part cereal, 1 part baby peaches (jarred) until five
weeks of age. At five weeks of age, pups can go 6 hours overnight without feeding them (D. Bressler,
®
personal communication). Since coatis are lactose intolerant, Lactaid pills should now be added to
mixture (2 crushed pills for every 12 scoops of formula) (D. Bressler, personal communication).
Final weaning should not occur before 16 weeks of age (weaning age in the wild). However, weaning
may begin at 8 weeks of age with the addition of foods, such as mashed bananas, soaked puppy food,
dry puppy food, and scrambled eggs. At this time, the pup should be offered formula in a bottle 4 times a
day. Pups should be stimulated to urinate until they are three to four weeks of age. The amount of
formula offered should be based on the pups age and weight (see Table 14) (D. Bressler, personal
communication).
7.6 Contraception
Many procyonids cared for in AZA-accredited institutions breed so successfully that contraception
techniques are implemented to ensure that the population remains at a healthy size.
In addition to reversible contraception, reproduction can be prevented by separating the sexes or by
permanent sterilization. In general, reversible contraception is preferable because it allows natural social
groups to be maintained while managing the genetic health of the population. Permanent sterilization may
be considered for individuals that are genetically well-represented or for whom reproduction would pose
health risks. The contraceptive methods most suitable for procyonids are outlined below. More details on
products, application, and ordering information can be found on the AZA Wildlife Contraception Center
(WCC) webpage: www.stlzoo.org/contraception.
The progestin-based melengestrol acetate (MGA) implant, previously the most widely used
contraceptive in zoos, has been associated with uterine and mammary pathology in felids and suspected
in other carnivore species (Harrentstein et al 1996, Munson et al 2002, Munson 2006). Other progestins
® ®
(e.g., Depo-Provera , Ovaban ) are likely to have the same deleterious effects (e.g., Chittick et al. 2001;
Munson et al. 2002). For carnivores, the AZA Wildlife Contraception Center now recommends GnRH
® ®
agonists, e.g., Suprelorin (deslorelin) implants or Lupron Depot (leuprolide acetate) as safer
alternatives. Although it appears safe and effective, dosages and duration of efficacy have not been
systematically evaluated for all species. GnRH agonists can be used in either females or males, and side
effects are generally those associated with gonadectomy, especially weight gain, which should be
®
managed through diet. Suprelorin was developed for domestic dogs, but has been tested in very few
procyonids (e.g., coati).
®
Gonadotropin Releasing Hormone (GnRH) Agonists: GnRH agonists (Suprelorin implants, or Lupron
®
Depot ) achieve contraception by reversibly suppressing the reproductive endocrine system and
preventing production of pituitary (FSH and LH) and gonadal hormones (estradiol and progesterone in
females and testosterone in males) (Munson et al. 2001). The observed effects are similar to those
following either ovariectomy in females or castration in males, but are reversible. GnRH agonists first
stimulate the reproductive system, which can result in estrus and ovulation in females or temporary
enhancement of testosterone and semen production in males. Then, down-regulation follows the initial
stimulation. The stimulatory phase can be prevented in females by daily Ovaban administration for one
week before and one week after implant placement (Wright et al. 2001).
GnRH agonists should not be used during pregnancy, since they may cause spontaneous abortion or
prevent mammary development necessary for lactation. They may prevent initiation of lactation by
inhibiting progesterone secretion, but effects on established lactation are less likely. New data from
domestic cats have shown no effect on subsequent reproduction when treatment began before puberty;
no research in prepubertal procyonids has been conducted (Bertschinger et al. 2001).
A drawback of these products is that time of reversal cannot be controlled. Neither the implant
® ®
(Suprelorin ) nor the depot vehicle (Lupron ) can be removed to shorten the duration of efficacy to time
reversals. The most widely used formulations are designed to be effective either 6 or 12 months, but
those are for the most part minimum durations, which can be longer in some individuals.
Although GnRH agonists can also be an effective contraceptive in males, they are more commonly
used in females, because monitoring efficacy by suppression of estrous behavior or cyclic gonadal
steroids in feces is usually easier than ensuring continued absence of sperm in males, since most
®
institutions cannot perform regular semen collections. Suprelorin has been tested primarily in domestic
®
dogs, whereas Lupron Depot has been used primarily in humans, but should be as effective as
®
Suprelorin , since the GnRH molecule is identical in all mammalian species.
If used in males, disappearance of sperm from the ejaculate following down-regulation of testosterone
may take an additional 6 weeks, as with vasectomy. It should be easier to suppress the onset of
spermatogenesis in seasonally breeding species, but that process begins at least 2 months before the
first typical appearance of sperm. Thus, treatment should be initiated at least 2 months before the
anticipated onset of breeding.
® ®
Progestins: If progestins (Melengestrol acetate (MGA) implants, Depo-Provera injections, Ovaban
pills) have to be used, they should be administered for no more than 2 years, and then discontinued to
allow for a pregnancy. Discontinuing progestin contraception and allowing non-pregnant cycles does not
substitute for a pregnancy. Use of progestins for more than a total of 4 years is not recommended. MGA
implants last at least 2 years, and clearance of the hormone from the system occurs rapidly after implant
removal. Progestins are considered safe to use during lactation.
Vaccines: The porcine zona pellucida (PZP) vaccine has not been tested in procyonids but may cause
permanent sterility in many carnivore species after only one or two treatments. This method is not
recommended.
Ovariectomy or Ovariohysterectomy: Removal of ovaries is a safe and effective method to prevent
reproduction for animals that are eligible for permanent sterilization. In general, ovariectomy is sufficient
in young females, whereas, removal of the uterus as well as ovaries is preferable in older females, due to
the increased likelihood of uterine pathology with age.
Coati: In consultation with the AZA Small Carnivore TAG, ovariohistorectomies may be performed at ~6
months of age and are performed as other spay procedures on mammals: 2-0 PDS or Maxon is
recommended for ligating the pedicles and muscle layer; SQ and intra-dermal sutures are very important.
The skin can be closed with a small amount of surgical glue (e.g., Nexaband) (S. Grant, personal
communication).
Vasectomy: Vasectomy of males will not prevent potential adverse effects to females that can result from
prolonged, cyclic exposure to the endogenous progesterone associated with the pseudo-pregnancy that
follows ovulation. This method is not recommended for procyonids.
are inappropriate unless serious injury of keeper or animal is imminent (e.g., serious fight). Many of the
procyonids respond to profound aversive stimuli with fear and/or aggression. It is best to maintain all
keeper/animal interactions positive and pleasant. Assessing the animal‟s motivation (why should it “want”
to come in? Why does it “want” to stay outside?) is a useful exercise when training problems occur.
Patience and planning are keys to success (Wooster 1998). See Appendix H for examples of commonly
trained behaviors (AAZK Animal Training Committee). The following table (Table 16) provides
descriptions of behavioral cues and criteria for trained behaviors used with procyonids.
Table 16: Sample trained behaviors, cues, and reinforcement criteria*
Species Behavior Verbal cue** Visual cue** Criteria for reinforcement
Coati Stationing Station ----- Standing in assigned spot
Coati Target on Target Tennis ball on a stick Standing with nose on target
item
Coati Scale Scale Point to scale Standing calmly on scale
Kinkajou Go into crate Crate Point to crate Animal enters and allows door
to be closed
Kinkajou Collar with Collar Show collar Animal has collar & leash put
leash on while staying calm
Raccoon Target Target Target stick presented Stands with nose on target
Raccoon Up Up Arm extended with hand Stands on hind feet while front
flat against mesh of cage feet rest on wire mesh
Raccoon Follow Follow Right index finger points Animal follows trainer
at animal
Raccoon Crate in Crate Right index finger points Animal enters crate and waits
at animal & then at crate
Raccoon Crate out Out Right index finger points Animal leaves crate
at animal & then away
from crate
Raccoon Scale Scale Animal is targeted to scale Animal stands calmly on scale
Raccoon Paw present Touch Touch apparatus is moved Animal holds bar until bridged
to front of cage
* Information from: B.Stark, Institution H; A.Varsik, Institution I; C.Shultz, Institution J; A.Dosch, Institution K; J.Gramieri, Institution L
** Verbal and visual cues may differ between facilities; the above table is intended to illustrate examples of cues used successfully.
Animal Management and Exhibit Design: In general, procyonid species can be trained in protected-
contact (i.e., keeper and animal should be separated by a mesh barrier) or free contact situations; these
decisions should be made by the institution‟s management staff, taking the species and individual animal
into consideration. It is advised that all facilities have holding areas in order to shift animals into/out of
their primary enclosure. Husbandry training may occur anywhere the individual animal seems to feel
comfortable and where the keeper can safely access them through a mesh screen. Care should be given
not to encroach upon the animal‟s flight distance. Managers and caretakers should decide if food rewards
can be hand fed through/under mesh screen or if a meat stick should be used to deliver the food.
8.2 Environmental Enrichment
Environmental enrichment, also called behavioral enrichment, refers to the practice of providing a
variety of stimuli to the animal‟s environment, or changing the environment itself to increase physical
activity, stimulate cognition, and promote natural behaviors. Stimuli, including natural and artificial objects,
scents, and sounds are presented in a safe way for the animals to interact with. Some suggestions
include providing food in a variety of ways (i.e., frozen in ice or in a manner that requires an animal to
solve simple puzzles to obtain it), using the presence or scent/sounds of other animals of the same or
different species, and incorporating an animal training (husbandry or behavioral research) regime in the
daily schedule.
It is recommended that an enrichment program be based on current information in biology, and
should include the following elements: goal-setting, planning and approval process, implementation,
documentation/record-keeping, evaluation, and subsequent program refinement. Environmental
13. Can the manner of enrichment presentation (i.e., one item or items placed in a small area)
promote aggression or harmful competition?
14. Has browse been determined to be non-toxic?
15. Do the animals show signs of allergies to new items (food, browse, substrates, etc.)?
16. Does the enrichment cause abnormally high stress levels?
17. Does the enrichment cause stimulation at a high level for extended periods of time that do not
allow the animal natural down time in the species' normal repertoire (e.g., constant activity for
public enjoyment when the animal would normally be inactive in its native habitat)?
AAZK Enrichment Committee, Enrichment Caution List
Dietary Enrichment
- Food enrichment, if uncontrolled, can lead to obesity and tooth decay; deviation from the normal diet
can cause nutritional problems. Keepers can consult with the nutritionist or commissary staff to
determine the best method of introducing novel food items.
- New food items introduced without analysis may cause colic, rumenitis or metabolic acidosis in
ungulates.
- Food items can spoil and cause animal illness if left in the exhibit for extended periods of time.
Enrichment food items should be removed within a reasonable amount of time to prevent spoilage.
- Animals can have adverse reactions to toxic plants and chemicals. Keepers should be able to
correctly discern between toxic and browse plants, ensure that browse is free of fertilizers and
herbicides, and wash plants to remove free ranging bird and animal feces and debris.
- Foraging or social feedings may give rise to aggression and possible injuries within the animal
population.
- Competition for enrichment items may lead to social displacement of subordinate animals. These
concerns can be minimized by providing enough enrichment to occupy all of the animals within the
population.
- Carcass feedings for omnivores and carnivores may be hazardous if the source of the carcass is not
determined and appropriate precautions taken. Diseased animals, chemically euthanized animals or
those with an unknown cause of death are not appropriate for an enrichment program. Freezing the
carcasses of animals that are determined to be safe to feed to exhibit animals can help minimize the
risk of parasitism and disease. Providing enough carcasses in group feedings can minimize
competition and aggression within an exhibit.
- Carefully introducing a group of animals to the idea of social feedings can be done by moving carcass
pieces closer together at each feeding until the animals are sharing one carcass. This can allow
social carnivores to exhibit normal dominance posturing while minimizing the possibility of
aggression. During live feedings, prey animals may fight back. Care should be taken to ensure such
prey can only inflict superficial wounds on zoo animals.
- Cage furniture may interrupt flight paths or entangle horns and hooves if poorly placed. Careful
planning can prevent this.
- If unsecured, some items may fall on an animal or be used as a weapon and cause injuries.
- If position is not thoughtfully considered, limbs and apparatus may provide avenues for escape or
may block access into exhibit safety zones, leaving subordinate animals feeling trapped and
vulnerable.
- Animals that crib or chew wood should be provided with non-toxic limbs and untreated wood furniture.
- Water features should be tailored to the inhabitants to prevent drowning and ensure that animals
such as box turtles can right themselves if they flip over on their backs.
- Animals can be injured in filtration systems if water intake areas are not protected.
- Substrates should provide adequate traction and not cause an intestinal impaction if ingested.
- Caution should be exercised when ropes, cables, or chains are used to hang or secure articles to
prevent animals from becoming entangled. Generally, the shortest length possible is recommended.
Chain can be covered with a sheath such as PVC pipe; swivels can be used to connect the chain to
the enrichment item to minimize kinking.
Olfactory Enrichment
- Scents from different animals or species can lead to aggression if there is an assertion of dominant
animals or subordinate animals attempting to use enrichment to advance their status in the hierarchy.
- Animal feces used for olfactory enrichment should be determined to be parasite free through fecal
testing and as with other animal by-products such as feathers, sheds, wool and hair, come from only
healthy animals. Many of these items can be autoclaved for sterilization.
- Perfumes can be overwhelming to some animals (and keepers) and are therefore best used in open,
ventilated areas.
- Some spices may be too strong or toxic to some animals.
Auditory Enrichment
- When provided with audio enrichment, animals may be less threatened by deflected sounds rather
than those directed at the animals.
- Some animals may have adverse reactions to recordings of predator calls and should be closely
observed when this type of enrichment is provided.
- Providing the animals with an option for escape or the means to mobilize for confrontation when
predator calls are played can lessen the stress of this type of enrichment and allow the animals to
investigate the sounds and their environment over a period of time.
Manipulable Enrichment
- Individual parts or enrichment devices may be swallowed resulting in choking or asphyxiation.
- If ingested, indigestible enrichment items may cause a gut impaction or linear obstruction.
- Broken items may have sharp edges that can cut an animal. Only items that are appropriate for the
species should be provided. For example, some devices will hold up to the play of a fox but not a wolf
- When building or designing enrichment items from wood, it may be wise to use dovetail cuts and glue
rather than screws and nails. Rounded corners and sanded edges can prevent the animals from
getting splinters.
- Many paints and other chemicals are toxic if eaten. When providing enrichment involving paint or
other chemicals, only non-toxic items should be used.
- If used, destructible items such as cardboard boxes and paper bags should be free of staples, tape,
wax, strings or plastic liners.
Factors that should be considered when determining how often behavioral or environmental
enrichment is offered include the species and individual(s) involved as well as the physical characteristics
of the exhibit. Large, complex exhibits may offer ample opportunities for animals to exercise natural
behaviors with infrequent enrichment (2-3 times weekly). Other exhibits or individuals may require more
frequent enrichment (daily or multiple times per day). Husbandry staff should monitor all individuals in an
exhibit and structure an enrichment schedule for the needs of those animals, providing them opportunities
several times a day to interact positively with their environment. Enrichment should never be offered on a
regular schedule, instead times, items, and delivery methods should be rotated so there is always an
element of novelty associated with each item or activity.
Many of the procyonid species have acute olfactory senses, enrichment designed to stimulate these
senses and encourage foraging should be well-received and stimulate species-appropriate behaviors
(Campbell 2001). Additionally, some species are very tactile oriented (e.g., raccoons and coatis), and will
benefit from rotating new and unusual tactile stimuli. This is particularly useful for education animals
generally housed in smaller enclosures. All enrichment items should be approved by an institution‟s
management team, including the veterinarian and horticulturist.
More information on enrichment initiatives, resources, and references can be found in the following
appendices: Appendix I (enrichment and training resources), Appendix J (sample enrichment ideas and
techniques).
8.3 Staff and Animal Interactions
Animal training and environmental enrichment protocols and techniques should be based on
interactions that promote safety for all involved. See Section 8.1 for exhibit design tips to facilitate exhibit
design.
Animal management staff should be encouraged to form a trusting relationship with the animals in
their care. This, however, does not mean one in which the animals are made pets. All animals should be
treated with respect; keeper staff should learn the behavioral profiles of each individual animal and
structure their working routines to maximize the animal‟s comfort. Behavioral management in the form of
training for husbandry procedures, both routine and non-routine, is encouraged. Interactions with
procyonid species while the public is present should be primarily for educational purposes; interactions
with procyonid species for medical emergency or routine husbandry purposes while the public is present
should be limited. If these activities have to be carried out while the public is present, it is suggested that
an interpreter be present to explain what is happening and why.
Each zoo should have written standard operating guidelines that address the safety of both the
animal and the keeper. Keepers should avoid entering the enclosure with the animals present if possible.
Where this is not possible, the animals should be given time to get to know the standard husbandry
routine and be allowed to separate themselves from the keepers (Roberts 1997).
Keepers should take care to keep outside the flight distance of the individuals involved. This will
minimize stress to the animal and the keeper (Roberts 1997). Coatis and kinkajous can become very
accustomed to people; sudden movements and excessive interaction with the animals should be avoided.
Coati and Raccoons: Keepers should wear protective gear on their hands when working with raccoons
that have not been treated for parasites. Both coatis and raccoons show a propensity towards “object
claiming”. Keepers who have direct contact with these species should keep this in mind. The wearing of
jewelry while working with these animals should be restricted. Even animals that are not acclimated to
direct human contact will behave with great curiosity and approach to get a better view of items such as
watches, earrings, bracelets, and necklaces. Additionally, curious animals also may vehemently search
keepers‟ pockets, so care should be taken to keep pocket contents to a minimum. Bolder animals will
make daring attempts to remove or claim such items.
Both raccoons and coatis can behave very aggressively when defending an object they have claimed
as their own. This does not apply only to items claimed off of humans, but also objects within their
enclosures. Both coatis and raccoons will demonstrate overt aggression when they feel their prize is
being threatened. Their claims may be on a particular stick in the enclosure, an edible treat, or a toy
placed there for enrichment. In general, if the animal is presently preoccupied with an object, greater
caution should be exercised around the animal to prevent defensive attacks on the keeper (K.Schilling,
personal experience).
Maintaining eye contact, not turning your back, and keeping your head above the coatis and raccoons
whenever possible will help the keeper staff hold a dominant position to the animals (D.Bressler, personal
experience; K. Schilling, personal experience). Some coatis and raccoons display aggression as the
result of certain sounds. The same sounds may induce playful behaviors in other individuals. Keepers
should be aware of this and familiarize themselves with individual animals that demonstrate such
behavior and the triggers that may solicit it. Some of the typical sounds that elicit these responses
include: jingling keys, squeaky toys, or bells (K.S chilling, personal experience).
8.4 Staff Skills and Training
Staff members should be trained in all areas of animal behavior management. Funding should be
provided for AZA continuing education courses, related meetings, conference participation, and other
professional opportunities. A reference library appropriate to the size and complexity of the institution
should be available to all staff and volunteers to provide them with accurate information on the behavioral
needs of the animals with which they work.
The following technical skills and competencies are recommended for all animal care staff working
with small carnivores.
Keepers and managers should have an in-depth understanding of the species natural history and
the individual‟s history.
Keepers and managers should have an in-depth understanding of the individual animal‟s
behaviors, an understanding of the function of those behaviors, and the ability to describe those
behaviors orally and in writing.
Keepers should be able to recognize signs of illness and injury in the procyonid species they are
working with and to communicate those signs orally or in writing to managers and veterinarians.
Keepers should be able to accurately assess the appropriate level of cleanliness and safety of the
animal‟s exhibit, holding area, and food-prep area.
Keepers should have the skills to safely capture or restrain the procyonid species in question.
Keepers should have some understanding of the species natural diet and foraging style.
Keepers and managers should have an understanding of enrichment concepts and have a
commitment to consistently enhance the environments of the species in their care.
Keepers should understand the concepts of animal learning and training, be able to use a variety
of techniques (e.g., habituation, operant conditioning) to train the animals under their care, and to
create a training plan (identifying training steps, cues, and criteria). See www.animaltraining.org
for additional details.
Managers should understand the concepts of animal learning and training, be able to coach
keepers in all aspects of training, review their training plans, look for consistency among keepers
in their training techniques, and help their teams prioritize training, enrichment, and other
husbandry goals.
such an appendage. Its diet consists essentially of fruit supplemented by insects (Bisbal 1987). Charles-
Dominique et al. (1981) states that kinkajous play an important role in dispersing the seeds of some plant
species. Their social behavior has been little studied. Apart from observations of females with their young,
kinkajous are normally seen singly, although several may feed together in fruiting trees (Ewer 1973).
They have been observed with olingos, and the two species can be confused by some observers. As this
is a highly arboreal species, even though we have no evidence that it is becoming threatened, it must be
presumed that its numbers decrease with extensive human disturbance (Glatston 1994).”
Threats include extensive human disturbance, deforestation, and the pet trade (Glatston 1994, IUCN
Red List 2009)
Ringtail: “Of the two species (cacomistle and ringtail), the ringtail has been studied in some detail (Trapp
1972; 1978). This species is known to be nocturnal and solitary in its habits. It inhabits a variety of
habitats including rocky or cliff areas, areas of dense riparian or evergreen forest, scrub, and desert. It is
restricted to altitudes of less than 2,800 m. Its diet consists of small vertebrates, fruits, and insects. Much
of the food is succulent and ringtails are able to produce highly concentrated urine (Richards 1976), and
so can live in fairly arid habitats (Kaufmann 1982). The cacomistle is much less well-known than the
ringtail but the information available indicates that it inhabits wetter forests than the ringtail and that it is
highly arboreal and nocturnal. It is solitary outside of the breeding season (Poglayen-Neuwall & Toweill
1988). It forages alone and emits a high-pitched long call which apparently serves as a spacing function
(Coates-Estrada & Estrada 1986). However, it is not yet certain whether its behavior and ecology are
similar to those of the ringtail. Threats to the ringtail include automobiles and trappers. Threats to the
cacomistle include habitat disturbance, deforestation, and fragmentation of populations (Glatston 1994).”
Raccoon: There is dispute over how many species of raccoon should be recognized. The common
raccoon and crab-eating raccoon have the widest distribution while all other raccoon species, or
subspecies, are confined to islands. Some confusion arises from what is thought to be the relatively
recent arrival of the island raccoons due to rafting or human introduction. The IUCN Red List recognizes
only one of the island raccoons as a separate species, the Cozumel or pygmy raccoon (P. pygmaeus),
which is listed as Critically Endangered with a decreasing population. The common raccoon should be
used to educate the visiting public about raccoons, their natural history, and the threats to the pygmy
raccoon and other island raccoons.
“The crab-eating raccoon is naturally rare in some areas of its range and it does not seem as
adaptable to human activity as the common raccoon, although it is probably stable throughout
South America where viable areas exist. Threats to this species include overhunting for pelts, use
for target practice, the pet trade, and, in some areas, habitat destruction (being a rain forest
species). Little is known of any of the island forms of raccoon in regards to distribution or natural
history. However, they have probably never been very numerous, given the small size of their
island ranges and the undoubted negative influence of tourism. Their habitats are probably
diminishing and one form, the Barbados raccoon P. gloverallenis, is probably extinct. The last
sighting occurred in the early 1960s. The status of the rest is indeterminate at present (Glatston
1994).”
The IUCN Procyonid and Ailurid Action Plan (Glatston 1994) has this to say about the cultural
significance of the procyonid species:
There does not appear to be any appreciable folklore associated with any species, although it is
possible that there may be some references to these species in the folklore of current
Amerindians or in those of past cultures such as the Toltecs, Aztecs, Incas, or Mayas. For
example, the coati is thought to have been a fertility symbol for the Maya and was also used as a
pet and a source of food (possibly eaten only by the women) (Hamblin 1984). Indeed, Bixler
(unpublished) speculates that the Cozumel coati may have been brought to that island by the
Maya, as Cozumel was an important center for the worship of Ix Chel, the goddess of fertility.
Other indications of the interest that some procyonid species may have held for the indigenous
people of the Americas are to be found in their local names. The name cacomistle is derived from
the Mexican Nathuatl Indian word, “Tlacomiztli”, meaning “half mountain lion”; coati is derived
from the name “Kuat-I” used by the indigenous Guarani Indians, while raccoon comes from the
word “Aroughcoune,” used by the Algonquin Indians of Virginia to mean “he scratches with his
hands.” Further information regarding what, if anything, these animals meant to the tribes
concerned is unknown. On the subject of names, the cacomistle (or ringtail) has also been known
as the “miner‟s cat,” a name earned because ringtails were placed in frontier mines to control
rodents as they were supposed to be better mousers than cats (Poglayen-Neuwall & Toweill
1988; Whitaker 1988). Otherwise, cultural interest in procyonids only involves their use as
companion animals or as sport. Some procyonid species, notably coatis and kinkajous, are kept
as pets in various countries throughout Central and South America today. Some species, again
notably the kinkajou and coati, are also hunted for their meat by the indigenous peoples of
Mexico and Central America. However, this kind of hunting activity is strictly limited.
9.3 Program Evaluation
AZA-accredited institutions which have an Institutional Program Animal Plan are required to evaluate
the efficacy of the plan routinely (see Appendix E for recommendations). Education and conservation
messaging content retention, animal health and well-being, guest responses, policy effectiveness, and
accountability and ramifications of policy violations should be assessed and revised as needed. The AZA
SCTAG has no specific recommendations regarding program evaluation format.
Acknowledgements
The AZA SCTAG would like to thank the numerous people who contributed their knowledge and
experience to the creation of this document; for a complete list please see Appendix L. Special thanks go
to Dr. Joseph Barber, original facilitator for the AZA Animal Care Manuals for his editing, patience, help,
and encouragement.
References
AAFCO (Association of American Feed Control Officials) 1999. Nutrient Guidelines for Dogs. Pet Food
Regulations. AAFCO, Inc., Atlanta.
Ackerson, B.K., Harveson, L.A. (2006). Characteristics of a ringtail (Bassariscus astutus) population in
Trans Pecos, Texas. Texas Journal of Science 58(2):169-184.
Andrews, P. (2001). Introducing adult males and females. In: Mellen J, Wildt D. (eds.), Husbandry manual
for small felids. Lake Buena Vista, FL: Disney‟s Animal Kingdom. (available on Felid TAG web
site: www.csew.com/felidtag/)
Anon. (1981). Outdoor Air Requirements for Ventilation (ASHRAE Standard 62-1981) 3.1 Commercial
Facilities (Offices, Stores, Shops, Hotels, Sports Facilities, etc.). American Society of Heating,
Refrigeration, Air Conditioning Engineers: 74-85.
AWR (Animal Welfare Regulations) 2005. Animal Welfare Act, 7 U.S.C. Animal Welfare Regulations, 9
CFR Chapter 1, Subchapter A, Parts 1-4.
Ayars, G.H., Altman L.C., Frazier C.E., Chi E.Y. (1989). The toxicity of constituents of cedar and pine
woods to pulmonary epithelium. Journal of Allergy and Clinical Immunology 83: 610-618.
AZA (Association of Zoos and Aquariums) 2008. Accreditation Standards and Related policies.
Association of Zoos and Aquariums, Silver Spring, MD.
AZA SCTAG 2008. Otter Care Manual. Association of Zoos and Aquariums, Silver Spring, MD. p.119.
Barker, I.K., Parrish C.R. (2001). Parvovirus infections. In: Williams ES, Barker IK (eds.), Infectious
Diseases of Wild Mammals, 3rd Ed., Iowa State University Press, Ames, IA. pp.131-146.
Barja, I. (2006). Faecal marking behaviour in ringtails (Bassariscus astutus) during the non-breeding
period: spatial characteristics of latrines and single faeces. Chemoecology 16(4):219-222.
Bertschinger, H.J., Asa, C.S., Calle, P.P., Long, J.A., Bauman, K., DeMatteo, K., Jochle, W., Trigg, T.E.,
Human A. (2001). Control of reproduction and sex related behaviour in exotic wild carnivores with
the GnRH analogue deslorelin: preliminary observations. Journal of Reproduction and Fertility,
Supplement 57: 275-283.
Bisbal, F.L. (1987). The carnivores of Venezuela: their distribution and the ways they have been affected
by human activities. Unpublished PhD Thesis, Univ. of Florida
Bitgood, S., Patterson, D., Benefield, A. (1986). Understanding your visitors: ten factors that influence
visitor behavior. Annual Proceedings of the American Association of Zoological Parks and
Aquariums, 726-743.
Bitgood, S., Patterson, D., Benefield, A. (1988). Exhibit design and visitor behavior. Environment and
Behavior 20(4): 474-491.
Bittle, J.L.(1981) Feline panleukopenia. In: Davis JW, Karstad LH, Trainer DO. (eds), Infectious Diseases
of Wild Mammals, 2nd ed. Ames, IA; Iowa State University Press: pp.97-101.
Blomqvist, L., Rudbäck, E. (2001). Management & Medical Care. In: Management of Captive Wolverines,
Gulo gulo, in Europe: Studbook, & Guidelines o Husbandry, Vol. 2. EAZA, Swedish Zoo
Association and The Nordic Ark Foundation.
Booth-Binczik, S.D. (2001). Ecology of coati social behavior in Tikal National Park, Guatemala. Ph.D.
dissertation, University of Florida, Gainesville, FL.
Booth-Binczik, S., Binczik, G.A., Labisky, R.F. (2004). Lek-like mating in white nose coati (Nasua narica)
Socio-ecological correlates of intra-specific variability in mating systems. Journal Zoological
Society (London)262: 179-185.
Burkhart, C.A, Robinson, J.L. (1978). High rat pup mortality attributed to the use of cedar wood shavings
as bedding. Laboratory Animals 12: 221-222.
Bush, M., Roberts, M. (1977). Distemper in captive red pandas. International Zoo Yearbook 17: 194-196.
Bush, M., Montali, R.J., Brownstein O., James E., Appel MJG. 1976. Vaccine-induced canine distemper in
a lesser panda. Journal of the American Veterinary Medical Association 169: 959-960.
Campbell, H. (2001). Brown-nosed Coati (Nasua nasua) & White-nosed Coati (Nasua narica) North
American Regional Studbook, 1st Edition. Detroit Zoological Institute, Detroit, MI.
Carnio, J. (1996). Minimum Husbandry Guidelines for Mammals: Viverrids and Mongooses. Metropolitan
Toronto Zoo, AZA Mammal Standards Task Force 1996.
Carpenter, J.W., Appel, M.J., Erickson, R.C., Novilla, M.N. (1976). Fatal vaccine-induced canine
distemper virus infection in black-footed ferrets. Journal of the American Veterinary Medical
Association 169: 961-964.
Castro, A.E., Heuschele, W.P. (1992). Veterinary Diagnostic Virology: A Practioner’s Guide. Mosby Year
Book, Inc., St. Louis and Baltimore, U.S.A.
Charles-Dominique, P., Atramentowicz M., Charles-Dominique M., Gerard H., Hladik A., Hladik C.M.,
Prevost M.F. (1981). Les mammiferes frugivores aboricoles noctunes d‟une foret gutanaise:
Interrelations plantes-animaux. Revue d’Ecologie: La Terre et la Vie 35:341-435.
Chittick, E., Rotstein, D., Brown, T., Wolfe, B. (2001). Pyometra and uterine adenocarcinoma in a
melengestrol acetate-implanted captive coati (Nasua nasua). Journal of Zoo and Wildlife
Medicine 32: 245-251.
Churchman, D. (1985). How and what do recreational visitors learn at zoos? Annual Proceedings of the
American Association of Zoological Parks and Aquariums, 160-167.
Coke, R.L., Backues, K.A., Hoover, J.P., Saliki, J.T., Ritchey, J.W., West, G.D. (2005). Serologic
responses after vaccination of fennec foxes (Vulpes zerda) and meerkats (Suricata suricatta) with
a live, canarypox-vectored canine distemper virus vaccine. Journal of Zoo and Wildlife Medicine
36: 326-330.
Conway, W. (1995). Wild and zoo animal interactive management and habitat conservation. Biodiversity
and Conservation 4: 573-594.
Corbet, G.B., Hill, J.E. (1991). A World List of Mammalian Species. Oxford University Press, Natural
History Museum Publications, Oxford, England.
Davison, V.M., McMahon, L., Skinner, T.L., Horton, C.M., Parks, B.J. (1993). Animals as actors: take 2.
Annual Proceedings of the American Association of Zoological Parks and Aquariums, 150-155.
Deem, S.L., Spelman, L.H., Yates, R.A., Montali, R.J. (2000). Canine distemper in terrestrial carnivores: a
review. Journal of Zoo and Wildlife Medicine 31: 441-451.
DeGhetto, D., Papageorgiou, S., Convy, J. (2002). Raccoons. Chapter 25, In: Gage LJ (ed.), Hand-
Rearing Wild and Domestic Animals. Iowa State Press, Ames, Iowa. pp.191-202.
Denver, M. 2003. Procyonidae and Viverridae. In: Fowler ME, Miller RE. (eds.), Zoo and Wild Animal
Medicine, 5th Ed., Saunders, St. Louis, Missouri. pp.516-523.
Elia, G., Cavalli, A., Desario, C., Lorusso, E., Lucente, M.S., Decaro, N., Martella, V., Buonavoglia, C.
(2007).Detection of infectious canine parvovirus type 2 by mRNA real-time RT-PCR. Journal of
Virological Methods 146: 202-208.
Evans, R.H. (1987). Rearing orphaned wild mammals. In: Vet Clinics of North America 17(3). W.B.
Saunders, Philadelphia, PA. pp.754-784.
Ewer, R.E. (1973). The Carnivores. Wiedenfeld & Nicolson, London
Fernandez-Moran, J. (2003). Mustelidae. In: Zoo and Wild Animal Medicine 5th Edition. M. Fowler & R.
Miller Editors. Saunders, St. Louis, Missouri. Pp 501-515.
Ford, L., Hoffmann, R. (1988). Potos flavus. American Society of Mammalogists Species Sheets # 321.
pp.1-9.
Glatston, A.R. (1994). The Red Panda, Olingos, Coatis, Raccoons, and their Relatives: Status Survey
and Conservation Action Plan for Procyonids and Ailurids. IUCN/SSC Mustelid, Viverrid, and
Procyonid Specialist Group. IUCN, Gland, Switzerland. ISBN 2-8317-0046-9
Gompper, M.E. (1994). The importance of ecology, behavior, and genetics in the maintenance of coati
(Nasua narica) social structure. Ph.D. dissertation, University of Tennessee, Knoxville, TN.
Gompper, M. (1995). Nasua narica. American Society of Mammalogists Species Sheets #487. pp.1-10.
Gompper, M., Decker, D. (1998). Nasua nasua. American Society of Mammalogists Species Sheets #
580. pp.1-9.
Grant, K. (2004). Erethizon dorsatum. AZA Porcupine Husbandry Manual.
www.glenoakzoo.org/Rodent%20TAG.htm.
Grzimek, B. (1972). Grzimek’s Animal Life Encyclopedia. New York, NY. Van Nostrand Reinhold
Company. pp.90-95.
Grzimek, B. (1990). Grzimek’s Encyclopedia of Mammals. Vol. 3. McGraw-Hill Publishers, New York,
New York. pp.461-464.
Haas, C.C. (2002). Home-range dynamics of white-nosed coatis in southeastern Arizona. Journal of
Mammalogy 83(4):943-946.
Haas, C., Roback, J. (2000). Copulatory Behavior of the White Nosed Coatis. Western Naturalist 45(3).
Hamir, A.N., Summers, B.A., Rupprecht, C.E. (1998). Concurrent rabies and canine distemper
encephalitis in a raccoon (Procyon lotor). Journal of Veterinary Diagnostic Investigation 10: 194-
196.
Hamir, A.N., Hanlon, C.A., Niezgoda, M., Rupprecht, C.E. (2001). The prevalence of interstitial nephritis
and leptospirosis in 283 raccoons (Procyon lotor) from 5 different sites in the United States. The
Canadian Veterinary Journal. 42: 869-871.
Harrenstien, L.A., Munson, L., Group, U.S. (1996). Seal And American Zoo And Aquarium Association
Mammary Cancer Study Mammary cancer in captive wild felids and risk factors for its
development: A retrospective study of the clinical behavior of 31 cases Journal of Zoo and
Wildlife Medicine 27 (4): 468-476.
Hirsch, B.T. (2007). Within-group spatial position in ring-tailed coatis (Nasua nasua); balancing predation,
feeding success, and social competition. Ph.D. dissertation, Stony Brook University, Stony Brook,
NY.
IATA (International Air Transport Association) 2009. IATA Live Animal Requirements, 36th edition.
International Air Transport Association, Montreal-Geneva (ISBN978-92-9229-058-0). Pp.345-346.
IUCN. 1995. The world conservation unit. Raccoons and Their Relatives: 8317-0051-5.
IUCN Red List of Threatened Species. 2009. Version 2009.1, www.iucnredlist.org/search. Downloaded
June 9, 2009.
Johnston, R.J. (1998). Exogenous factors and visitor behavior: a regression analysis of exhibit viewing
time. Environment and Behavior 30(3): 322-347.
Joslin, J.O., Amand, W., Cook, R., Hinshaw, K., McBain, J., Oosterhuis, J. (1998). Guidelines for Zoo and
Aquarium Veterinary Medical Programs and Veterinary Hospitals (www.aazv.org/Webaddit.pdf).
Kaufmann, J.H. (1962). Ecology and social behavior of the coati, Nasua narica on Barro Colorado Island
Panama. University of California Publications in Zoology 60: 95-222.
Kays, R.W, Gittleman, J.L. (2001). The Social Organization of the Kinkajou Potos flavus (Procyonidae).
Journal of Zoology 253: 491-504.
Kazacos, K.R., Thacker, H.L., Shivaprasad, H.L., Burger, P.P. (1981). Vaccination-induced distemper in
kinkajous. Journal of the American Veterinary Medical Association 179: 1166-1169.
Kearns, K.S, Pollock, C., Ramsay, E.C. (1999). Dermatophytosis in red pandas (Ailurus fulgens fulgens):
a review of 14 cases. Journal of Zoo and Wildlife Medicine 30: 561-562.
Kiku, M., Byeong-Kirl, B., Chae-Woong, L. (2003). Eurasian otter (Lutra lutra), a definitive host for
Dirofilaria immitis. Journal of Zoo and Wildlife Medicine 34: 200-201.
Kleiber, M. (1947). Body size and metabolic rate. Physiological Review 27: 511-541.
Kollias,, G. V. and N. Abu-Madi. (2007). Procyonids and mustelids. In: West, G., D. Heard, and N.
Caulkett (eds.). Zoo Animal and Wildlife Anesthesia and Immobilization, 1st Ed., Blackwell
Publishing, Ames, IA. Pp. 417 - 428.
Langan, J., Bemis, D., Harbo, S., Pollock, C., Schumacher, J. (2000). Tyzzer's disease in a red panda
(Ailurus fulgens). Journal of Zoo and Wildlife Medicine 31: 558-562.
Larsen, R.S., Loomis, M.R., Kelly, B.T., Sladky, K.K., Stoskopf, M.K., Horne, W.A. (2002).
Cardiorespiratory effects of medetomidine-butorphanol, medetomidine-butorphanol-diazepam,
and medetomidine-butorphanol-ketamine in captive red wolves (Canis rufus). Journal of Zoo and
Wildlife Medicine 33(2):101-7.
Legrand-Defretin, V., Munday, H. (1993). Feeding Dogs and Cats for Life. In: Burger IH. (ed.), The
Waltham Book of Companion Animal Nutrition. Pergamon Press, New York, NY, pp.57-68.
Lemberger, K.Y., Gndim, .L.F.P., Pessier, A.P., McAllister, M.M., Kinsel, M.J. (2005). Neospora caninum
infection in a free-ranging raccoon (Procyon lotor) with concurrent canine distemper virus
infection. Journal of Parasitology 91: 960-961.
Lindsay, D.S., Spencer, J.A., Rupprecht, C.E., Blagburn, B.L. (2001). Prevalence of agglutinating
antibodies to Neospora caninum in raccoons, Procyon lotor. Journal of Parasitology 87: 1197-
1198.
MacMillen, O. (1994). Zoomobile effectiveness: sixth graders learning vertebrate classification. Annual
Proceedings of the American Association of Zoological Parks and Aquariums, 181-183.
Manharth, A., Shellebarger, W. (2003). Small Carnivore Medical Management Guidelines.
(aazv.org/displaycommon.cfm?an=1&subarticlenbr=272)
Maran, T., Robinson, P. (1996). European Mink, Mustela lutreola, Captive Breeding and Husbandry
Protocol. Tallinn Zoological Gardens, Estonia.
Martin, H.D., Zeidner, N.S. (1992). Concommittant cryptosporidia, coronavirus, and parvovirus infection in
a raccoon (Procyon lotor). Journal of Wildlife Diseases 28: 113-115.
McNab, B.K. (1989). Basal Rate of Metabolism, Body Size, and Food Habits in the Order Carnivora. In:
Gittleman, J.L. (ed.), Carnivore Behavior, Ecology, and Evolution. Vol 1, pp.335-354.
Mead, J.L., Van Devender, T.R. (1981). Late Holocene Diet of Bassariscus astutus in the Grand Canyon,
Arizona. Journal of Mammalogy 62: 439-442.
Meehan, T. (1994). Hand-rearing Felids. In: AZA Infant Diet Notebook. American Zoo and Aquarium
Assoc. Silver Springs, MD.
Meier, J.E. (1985). Hand Rearing Techniques for Neonatal Exotic Animals. In: Meehan T, Allen ME.
(eds.), Proceedings of the Fourth and Fifth Dr. Scholl Conferences on the Nutrition of Captive
Wild Animals. Dec. 7 & 8, 1984; Dec. 13 & 14, 1985 Lincoln Park Zoological Gardens, Chicago,
IL. Pp.36-48.
Montali, R.J., Roberts, M., Freeman, R.A., Bush, M. (1984). Pathology survey of the red panda (Ailurus
fulgens). In: Ryder OA, Byrd ML. (eds.), One Medicine, Springer-Verlag, Berlin. Pp.128-140.
Montali, R.J., Wallace, R., Phillips, L.G. Jr., Bush, M., Roberts, M., Crissey, S.D., Warnell, K.J., Oftedal,
O.T., Edwards, M., Rabin, L. (1989). Hepatopathy and hypercholesterolemia in red pandas
associated with a diet change. In: Glatston AJ. (ed.), Red Panda Biology. SPB Academic
Publishing, The Hague, The Netherlands. Pp.31-40.
Moore, D. (1997). Zoo Standards for Keeping Mustelids in Captivity. Central Park Zoo, New York. Pp.1-6.
Morgan, J.M., Hodgkinson, M. (1999). The motivation and social orientation of visitors attending a
contemporary zoological park. Environment and Behavior 31(2): 227-239.
Muir, S. (2003). Hand-rearing guidelines for small carnivores. Shaldon Wildlife Trust, UK.
Muñoz-Garcia, A., Williams, J.B. (2005). Basal Metabolic Rate in carnivores is associated with diet after
controlling for phylogeny. Physiological & Biochemical Zoology. 78(6): 1039-1056.
Munson, L. (2006). Contraception in felids. Theriogenology 66: 126-34.
Munson, L., Bauman, J.E., Asa, C.S., Jochle, W., Trigg, T.E. (2001). Efficacy of the GnRH analogue
deslorelin for suppression of oestrus cycle in cats. Journal of Reproduction and Fertility,
Supplement 57: 269-273.
Munson, L., Gardner, A., Mason, R.J., Chassy, L.M., Seal, U.S. (2002). Endometrial hyperplasia and
mineralization in zoo felids treated with melengestrol acetate contraceptives. Veterinary
Pathology 39(4): 419-27.
Nava-Vargas, V., Tejero-Diez, J.D., Chavez-Tapia, C.B. (1999). Food habits of the ringtail Bassariscus
astutus (Carnivora: Procyonidae) in a xerophitic bush in Hidalgo, Mexico. Anales del Instituto de
Biologia Universidad nacional Autonoma de Mexico Serie Zoologia 70(1):51-63.
Neiffer, D.L., Klein, E.C., Calle, P.P., Terrell, S.P., Walker, R.L., Todd, D., Vice, C.C., Marks, S.K. (2002).
Mortality associated with melarsomine dihydrochloride administration in two North American river
otters (Lontra canadensis) and a red panda (Ailurus fulgens fulgens). Journal of Zoo & Wildlife
Medicine 33(3): 242-248.
Nowak, R. (1999). Walker’s Mammals of the World, 6th Ed., Vol 1. The Johns Hopkins University Press,
Baltimore, MD. pp.1097-1104.
NRC (National Research Council) 2006. Nutrient Requirements of Dogs. National Academy Press,
Washington, DC.
NRC (National Research Council) 1982. Nutrient Requirements of Mink and Fox. National Academy
Press, Washington, DC.
Ott Joslin, J., Collins, D. (1999). Chapter 5: Designing an Ideal Animal Shipment. In: Fowler M, Miller R.
(eds.), Zoo and Wild Animal Medicine, current therapy 4. W.B. Saunders Co., Philadelphia and
London. Pp.17-26.
Partridge, J. (1992). Husbandry notes on the maintenance of cacomistles and ringtails. In: Management
Guidelines for Bears and Raccoons. J. Partridge editor. Association of British Wild Animal
Keepers (ABWAK), Bristol, England. Pp.149-151.
Pearson, G.L. (1977). Vaccine-induced canine distemper virus in black-footed ferrets. Journal of the
American Veterinary Medical Association 170: 103, 106, 109.
Petrini, K. (1998). Health Care Section. In: Asian small-clawed Otter Husbandry Manual. Asian small-
clawed Otter SSP, Columbus Zoological Park
Poglayen-Neuwall, I. (1973). Preliminary notes on maintenance and behaviour of the Central American
cacomistle, Bassariscus sumichrasti at Louisville Zoo. International Zoo Yearbook, 13: 207-11.
Poglayen-Neuwall, I. (1980a). Gestation period and parturition of the ringtail Bassariscus astutus.
Zeitschrift fuer Saeugetierkunde 45(2):73-81.
Poglayen-Neuwall, I. (1980b). Saliva licking a possible adaptation enhancing the survival of young
ringtails, Bassariscus astutus. Zoologische Beitraege 26(2):319-328.
Poglayen-Neuwall, I. (1990). Procyonids. In: Grzimek B. (ed.), Encyclopedia of Mammals. Vol 3, pp.450-
468.
Poglayen-Neuwall, I. (1995). Observation on ethology of the Central American cacomistle, Bassariscus
sumichrasti. Ecology Zoological Garten N.F. 65: 11-49.
Poglayen-Neuwall, I., Toweill, D.E. (1988). Bassariscus astutus. Mammalian Species Account Number
327, pp.8.
Poglayen-Neuwall, I., Shively, J.N. (1991). Testicular cycles of the ringtail Bassariscus astutus (Carnivora:
Procyonidae). Zeitschrift fuer Saeugetierkunde 56(2):72-80.
Povey, K.D. (2002). Close encounters: the benefits of using education program animals. Annual
Proceedings of the Association of Zoos and Aquariums.
Povey, K.D., Rios, J. (2002). Using interpretive animals to deliver affective messages in zoos. Journal of
Interpretation Research 7: 19-28.
Qin, Q., Wei, F., Li, M., Dubovi, E., Loeffler, I.K. (2007). Serosurvey of infectious disease agents of
carnivores in captive red pandas (Ailurus fulgens) in China. Journal of Zoo and Wildlife Medicine
38: 42-50.
Reed-Smith, J., Wagner, D., Riger, P., Bernier, D. (2003). AAZK Biological Information on Selected
Mammal Species CD, American Association of Zoo Keepers (AAZK) Topeka, KA.
Robbins, C. (1993). Wildlife Feeding and Nutrition. Academic Press, Inc. New York, NY.
Roberts, M. (1997). General Husbandry Requirements for Procyonidae. AZA Minimum Husbandry
Standards.
Rodriguez-Bolanos, A., Cadena, A., Sanchez, P. (2000). Trophic characteristics in social groups of the
mountain coati, Nasuella olivacea (Carnivora: Procyonidae). Small Carnivore Conservation 23,
October 2000:1-6.
Samudio, R., Kays, R., Cuarón, A.D., Pino, J.L., Helgen, K. (2008). Nasua narica. In: IUCN 2009. IUCN
Red List of Threatened Species. Version 2009.1. www.iucnredlist.org. Downloaded on
26 August 2009.
Sasai, H., Kato, K., Sasaki, T., Koyama, S., Kotani, T., Fukata, T. (2000). Echocardiographic diagnosis of
dirofilariasis in a ferret. Journal of Small Animal Practice 41: 172-174.
Sherwood, K.P., Rallis, S.F., Stone, J. (1989). Effects of live animals vs. preserved specimens on student
learning. Zoo Biology 8: 99-104.
Shotts, E.B. (1981). Leptospirosis. In: Davis JW, Karstad LH, Trainer DO. (eds), Infectious Diseases of
Wild Animals, 2nd ed. Ames, IA; Iowa State University Press: pp.323-331.
Snyder, D.E., Hamir, A.N., Nettles, V.G., Rupprecht, C.E. (1989a). Dirofilaria immitis in a river otter (Lutra
canadensis) from Louisiana. Journal of Wildlife Diseases 25: 629.
Snyder, D.E., Hamir, A.N., Hanlon, C.A., Rupprecht, C.E. (1989b). Dirofilaria immitis in a raccoon
(Procyon lotor). Journal of Wildlife Diseases 25: 130-131.
Standley, S. (1992). The ring tailed coati. In: Partridge J. (ed.), Management Guidelines for Bears and
Raccoons. ABWAK, Bristol, England. Pp.143-148.
Stanley, D., Fritzell, G., Fritzell, E. (1999). Behavior aspects of the raccoon mating system: determinant of
consortship success. Animal Behavior 7: 593-601.
Stephens, C.E., Hume, I.D. (1995). Comparative Physiology of the Vertebrate Digestive System. 2nd Ed.
Cambridge University Press. New York, NY.
Telford, S.R., Forrester, D.J. (1991). Hemoparasites of raccoons (Procyon lotor) in Florida. Journal of
Wildlife Diseases 27: 486-490.
Thompson, D. (2003). North American Regional Studbook Ringtail/Cacomistle, 1st Edition March 2003.
Little Rock Zoo, Little Rock, AR. ([email protected]).
Trapp, G.R. (1972). Some anatomical and behavioral adaptations of ringtails, Bassariscus astutus.
Journal of Mammalogy 53: 549-57.
Trapp, G.R. (1978). Comparative behavioural ecology of the ringtail and the Gray Fox in Southwest Utah.
Carnivore, 1. Pp. 3-31.
USDA 2003. USDA Guidelines for the care and use of laboratory animals.
www.nap.edu/readingroom/books/labrats/chaps.html
Valenzuela, D. (1998). Natural history of the white nose coati, Nasua nasua in the tropical dry forests of
Western Mexico. Revista Mexicana de Mastoxoologia, 3: 26-44.
Vesell, E.S. (1967). Induction of drug-metabolizing enzymes in liver microsomes of mice and rats by
softwood bedding. Science 157: 1057-1058.
Wilson, D.E., Reeder, D.M. (1992). Mammal Species of the World, A Taxonomic and Geographic
Reference, 2nd Edition. Smithsonian Institution Press, Washington D.C.
Wojcinski, Z.W., Barker, I.K. (1986). Tyzzer's disease as a complication of canine distemper in a raccoon
(Procyon lotor). Journal of Wildlife Diseases 22: 55-59.
Wolf, R.L., Tymitz, B.L. (1981). Studying visitor perceptions of zoo environments: a naturalistic view. In:
Olney PJS. (Ed.), International Zoo Yearbook. Dorchester: The Zoological Society of London.
pp.49-53.
Wooster, D. (1998). Role of the Keeper in Management of Small Cats. In: Mellen J, Wildt D. (eds.),
Husbandry Manual for Small Felids. AZA & Disney Wild Animal Kingdom. Chapter 10.
Wright, K. and M. Edwards. 2009. Considerations for Kinkajou Captive Diets. The Veterinary Clinics of
North America Exotic Animal Practice 12: 171-185.
Wright, P.J., Verstegen, J.P., Onclin, K., Jochle, W., Armour, A.F., Martin, G.B., Trigg, T.E. (2001).
Suppression of the oestrous responses of bitches to the GnRH analogue deslorelin by progestin.
Journal of Reproduction and Fertility, Supplement 57: 263-268.
Yerke, R., Burns, A. (1991). Measuring the impact of animal shows on visitor attitudes. Annual
Proceedings of the American Association of Zoological Parks and Aquariums, 532-534.
Yerke, R., Burns, A. (1993). Evaluation of the educational effectiveness of an animal show outreach
program for schools. Annual Proceedings of the American Association of Zoological Parks and
Aquariums, 366-368.
Personal Communications and Unpublished Sources:
Booth-Binczik, S. Dallas Zoo, [email protected]
Moresco, A. U.C. Davis. AZA SCTAG Vet Advisor. [email protected].
Bressler, D.: Logan & Abby‟s Fund (coati rescue organization). [email protected].
Carter, S: Curator of Mammals, Detroit Zoological Park.
Chapman, J.: Educator and Enrichment Co. Co-Chair, Caldwell Zoo. [email protected]
Dosch, A.: Cosley Zoo, Sr. Keeper. [email protected].
Dulaney, M: Cincinnati Zoo & Botanical Garden, Cincinnati, OH 45220.
Granat, G.: Brookfield Zoo, Brookfield, IL. Unpublished information, 2003.
Grant, S.: Veterinary specialist dealing with coatimundi.
Kimble, K.: Santa Barbara Zoo. [email protected].
Kirkendall, L. Sacramento Zoo, [email protected]
Montali, R.: Smithsonian Institute, National Zoo.
Schilling, K.: 2005. Animals for Awareness. [email protected]
Snyder B.: John Ball Zoo, Grand Rapids, Michigan. Unpublished information, 2003.
Walkosak, V.: Arizona Sonora Desert Museum. Unpublished information, 2003.
Useful References:
Ford L, Hoffmann RS. 1988. Potos flavus. Mammalian Species, 321, pp.9.
Fowler ME. 1986. Restraint. In: Fowler ME. (ed.), Zoo and Wild Animal Medicine. W.B. Saunders and
Co., Philadelphia. Pp.37-50.
Kaufmann JH. 1982. Raccoons and allies. In: Chapman A, Feldhamer GA. (eds.), Wild Mammals of North
America, Journal The Johns Hopkins University Press, Baltimore. . pp.567-585.
McClearn D. 1992. Locomotion, posture, and feeding behavior of kinkajous, coatis and raccoons. Journal
of Mammalogy, 73: 245-261.
Mehren KG. 1986. Procyonidae. In: Fowler ME. (ed.), Zoo and Wild Animal Medicine. W.B. Saunders and
Co., Philadelphia. pp.816-820.
Wozencraft WC. 1989. The phylogeny of the recent Carnivora. In: Gittleman J. (ed.), Carnivore Behavior,
Ecology and Evolution. Cornell University Press. pp.495-535.
safety procedures or the physical facility must be prepared and maintained for five years from the
date of the incident.
Chapter 3
(1.5.11) Animal transportation must be conducted in a manner that is safe, well-planned and coordinated,
and minimizes risk to the animal(s), employees, and general public. All applicable local, state, and
federal laws must be adhered to.
Chapter 5
(2.6.2) A formal nutrition program is recommended to meet the behavioral and nutritional needs of all
species and specimens within the collection.
(2.6.3) Animal diets must be of a quality and quantity suitable for each animal‟s nutritional and
psychological needs. Diet formulations and records of analysis of appropriate feed items should be
maintained and may be examined by the Visiting Committee. Animal food, especially seafood
products, should be purchased from reliable sources that are sustainable and/or well managed.
(2.6.1) Animal food preparations must meet all local, state/provincial, and federal regulations.
(2.6.4) The institution should assign at least one person to oversee appropriate browse material for the
collection.
Chapter 6
(2.1.1) A full-time staff veterinarian is recommended. However, the Commission realizes that in some
cases such is not practical. In those cases, a consulting/part-time veterinarian must be under contract
to make at least twice monthly inspections of the animal collection and respond as soon as possible
to any emergencies. The Commission also recognizes that certain collections, because of their size
and/or nature, may require different considerations in veterinary care.
(2.1.2) So that indications of disease, injury, or stress may be dealt with promptly, veterinary coverage
must be available to the animal collection 24 hours a day, 7 days a week.
(2.2.1) Written, formal procedures must be available to the animal care staff for the use of animal drugs
for veterinary purposes and appropriate security of the drugs must be provided.
(1.4.6) A staff member must be designated as being responsible for the institution's animal record-
keeping system. That person must be charged with establishing and maintaining the institution's
animal records, as well as with keeping all animal care staff members apprised of relevant laws and
regulations regarding the institution's animal collection.
(1.4.7) Animal records must be kept current, and data must be logged daily.
(1.4.5) At least one set of the institution‟s historical animal records must be stored and protected. Those
records should include permits, titles, declaration forms, and other pertinent information.
(1.4.4) Animal records, whether in electronic or paper form, including health records, must be duplicated
and stored in a separate location.
(1.4.3) Animals must be identifiable, whenever practical, and have corresponding ID numbers. For
animals maintained in colonies or other animals not considered readily identifiable, the institution
must provide a statement explaining how record keeping is maintained.
(1.4.1) An animal inventory must be compiled at least once a year and include data regarding acquisitions
and dispositions in the animal collection.
(1.4.2) All species owned by the institution must be listed on the inventory, including those animals on
loan to and from the institution. In both cases, notations should be made on the inventory.
(2.7.1) The institution must have holding facilities or procedures for the quarantine of newly arrived
animals and isolation facilities or procedures for the treatment of sick/injured animals.
(2.7.3) Quarantine, hospital, and isolation areas should be in compliance with standards or guidelines
adopted by the AZA.
(2.7.2) Written, formal procedures for quarantine must be available and familiar to all staff working with
quarantined animals.
(11.1.2) Training and procedures must be in place regarding zoonotic diseases.
(11.1.3) A tuberculin testing and surveillance program must be established for appropriate staff in order to
ensure the health of both the employees and the animal collection.
(2.5.1) Deceased animals should be necropsied to determine the cause of death. Disposal after necropsy
must be done in accordance with local/federal laws.
(2.4.1) The veterinary care program must emphasize disease prevention.
(1.5.5) For animals used in offsite programs and for educational purposes, the institution must have
adequate protocols in place to protect the rest of the collection from exposure to infectious agents.
(2.3.1) Capture equipment must be in good working order and available to authorized, trained personnel
at all times.
(2.4.2) Keepers should be trained to recognize abnormal behavior and clinical symptoms of illness and
have knowledge of the diets, husbandry (including enrichment items and strategies), and restraint
procedures required for the animals under their care. However, keepers should not evaluate illnesses
nor prescribe treatment.
(2.3.2) Hospital facilities should have x-ray equipment or have access to x-ray services.
(1.5.8) The institution must develop a clear process for identifying and addressing animal welfare
concerns within the institution.
Chapter 8
(1.6.1) The institution must have a formal written enrichment program that promotes species-appropriate
behavioral opportunities.
(1.6.2) The institution must have a specific staff member(s) or committee assigned for enrichment
program oversight, implementation, training, and interdepartmental coordination of enrichment efforts.
Chapter 9
(5.3) A written policy on the use of live animals in programs should be on file. Animals in education
programs must be maintained and cared for by trained staff, and housing conditions must meet
standards set for the remainder of the animal collection, including species-appropriate shelter,
exercise, social and environmental enrichment, access to veterinary care, nutrition, etc. Since some
of these requirements can be met outside of the primary enclosure, for example, enclosures may be
reduced in size provided that the animal‟s physical and psychological needs are being met.
(1.5.3) If animal demonstrations are a part of the institution‟s programs, an education and conservation
message must be an integral component.
Chapter 10
(5.3) Institutions should maximize the generation of scientific knowledge gained from the animal
collection. This might be achieved by participating in AZA TAG/SSP sponsored research when
applicable, conducting original research projects, affiliating with local universities, and/or employing
staff with scientific credentials.
(5.2) Institutions must have a written policy that outlines the type of research that it conducts, methods,
staff involvement, evaluations, animals to be involved, and guidelines for publication of findings.
(5.1) Research activities must be under the direction of a person qualified to make informed decisions
regarding research.
IV(a). General Acquisitions: Animals are to be acquisitioned into an AZA member institution‟s collection if
the following conditions are met:
1. Acquisitions must meet the requirements of all applicable local, state, federal and international
regulations and laws.
2. The Director or Chief Executive Officer of the institution is charged with the final authority and
responsibility for the monitoring and implementation of all acquisitions.
3. Acquisitions must be consistent with the mission of the institution, as reflected in its Institutional
Collection Plan, by addressing its exhibition/education, conservation, and/or scientific goals.
4. Animals that are acquired for the collection, permanently or temporarily, must be listed on
institutional records. All records should follow the Standards for Data Entry and Maintenance of
®
North American Zoo and Aquarium Animal Records Databases .
5. Animals may be acquired temporarily for reasons such as, holding for governmental agencies,
rescue and/or rehabilitation, or special exhibits. Animals should only be accepted if they will not
jeopardize the health, care or maintenance of the animals in the permanent collection or the
animal being acquired.
6. The institution must have the necessary resources to support and provide for the professional
care and management of a species, so that the physical and social needs of both specimen and
species are met.
7. Attempts by members to circumvent AZA conservation programs in the acquisition of SSP
animals are detrimental to the Association and its conservation programs. Such action may be
detrimental to the species involved and is a violation of the Association's Code of Professional
Ethics. All AZA members must work through the SSP program in efforts to acquire SSP species
and adhere to the AZA Full Participation policy.
8. Animals are only to be acquired from sources that are known to operate legally and conduct their
business in a manner that reflects and/or supports the spirit and intent of the AZA Code of
Professional Ethics as well as this policy. Any convictions of state, federal, or international wildlife
laws should be reviewed, as well as any previous dealings with other AZA-accredited institutions.
9. When acquiring specimens managed by an AZA PMP, institutions should consult with the AZA
PMP manager.
10. Institutions should consult AZA Wildlife Conservation and Management Committee (WCMC)-
approved Regional Collection Plans (RCPs) when making acquisition decisions.
IV(b). Acquisitions from the Wild: The maintenance of wild animal populations for education and wildlife
conservation purposes is a unique responsibility of AZA member zoos and aquariums. To accomplish
these goals, it may be necessary to acquire wild-caught specimens. Before acquiring animals from the
wild, institutions are encouraged to examine sources including other AZA institutions or regional
zoological associations.
When acquiring animals from the wild, careful consideration must be taken to evaluate the long-term
impacts on the wild population. Any capture of free-ranging animals should be done in accordance with all
local, state, federal, and international wildlife laws and regulations and not be detrimental to the long-term
viability of the species or the wild or captive population(s). In crisis situations, when the survival of a
population is at risk, rescue decisions are to be made on a case-by-case basis.
V(a). Disposition Requirements – living animals: Successful conservation and animal management efforts
rely on the cooperation of many entities, both within and outside of AZA. While preference is given to
placing animals within AZA member institutions, it is important to foster a cooperative culture among
those who share the primary mission of AZA-accredited facilities. The AZA draws a strong distinction
between the mission, stated or otherwise, of non-AZA member organizations and the mission of
professionally managed zoological parks and aquariums accredited by the AZA.
An accredited AZA member balances public display, recreation, and entertainment with demonstrated
efforts in education, conservation, and science. While some non-AZA member organizations may meet
minimum daily standards of animal care for wildlife, the AZA recognizes that this, by itself, is insufficient to
warrant either AZA membership or participation in AZA's cooperative animal management programs.
When an animal is sent to a non-member of AZA, it is imperative that the member be confident that the
animal will be cared for properly.
Animals may only be disposed of from an AZA member institution's collection if the following
conditions are met:
1. Dispositions must meet the requirements of all applicable local, state, federal and international
regulations and laws.
2. The Director or Chief Executive Officer of the institution is charged with the final authority and
responsibility for the monitoring and implementation of all dispositions.
3. Any disposition must abide by the Mandatory Standards and General Advisories of the AZA Code
of Professional Ethics. Specifically, "a member shall make every effort to assure that all animals
in his/her collection and under his/her care are disposed of in a manner which meets the current
disposition standards of the Association and do not find their way into the hands of those not
qualified to care for them properly."
4. Non-domesticated animals shall not be disposed of at animal auctions. Additionally, animals shall
not be disposed of to any organization or individual that may use or sell the animal at an animal
auction. In transactions with AZA non-members, the recipient must ensure in writing that neither
the animal nor its offspring will be disposed of at a wild animal auction or to an individual or
organization that allows the hunting of the animal.
5. Animals shall not be disposed of to organizations or individuals that allow the hunting of these
animals or their offspring. This does not apply to individuals or organizations which allow the
hunting of only free-ranging game species (indigenous to North America) and established long-
introduced species such as, but not limited to, white-tailed deer, quail, rabbit, waterfowl, boar,
ring-necked pheasant, chukar, partridge, and trout. AZA distinguishes hunting/fishing for sport
from culling for sustainable population management and wildlife conservation purposes.
6. Attempts by members to circumvent AZA conservation programs in the disposition of SSP
animals are detrimental to the Association and its conservation programs. Such action may be
detrimental to the species involved and is a violation of the Association's Code of Professional
Ethics. All AZA members must work through the SSP program in efforts to deacquisition SSP
species and adhere to the AZA Full Participation policy.
7. Domesticated animals are to be disposed of in a manner consistent with acceptable farm
practices and subject to all relevant laws and regulations.
8. Live specimens may be released within native ranges, subject to all relevant laws and
regulations. Releases may be a part of a recovery program and any release must be compatible
with the AZA Guidelines for Reintroduction of Animals Born or Held in Captivity, dated June 3,
1992.
9. Detailed disposition records of all living or dead specimens must be maintained. Where
applicable, proper animal identification techniques should be utilized.
10. It is the obligation of every loaning institution to monitor, at least annually, the conditions of any
loaned specimens and the ability of the recipient to provide proper care. If the conditions and care
of animals are in violation of the loan agreement, it is the obligation of the loaning institution to
recall the animal. Furthermore, an institution's loaning policy must not be in conflict with this A/D
Policy.
11. If live specimens are euthanized, it must be done in accordance with the established policy of the
institution and the Report of the American Veterinary Medical Association Panel on Euthanasia
(Journal of the American Veterinary Medical Association 218 (5): 669-696, 2001).
12. In dispositions to non-AZA members, the non-AZA member's mission (stated or implied) must not
be in conflict with the mission of AZA, or with this A/D Policy.
13. In dispositions to non-AZA member facilities that are open to the public, the non-AZA member
must balance public display, recreation, and entertainment with demonstrated efforts in
conservation, education, and science.
14. In dispositions to non-AZA members, the AZA members must be convinced that the recipient has
the expertise, records management practices, financial stability, facilities, and resources required
to properly care for and maintain the animals and their offspring. It is recommended that this
documentation be kept in the permanent record of the animals at the AZA member institution.
15. If living animals are sent to a non-AZA member research institution, the institution must be
registered under the Animal Welfare Act by the U.S. Department of Agriculture Animal and Plant
Health Inspection Service. For international transactions, the receiving facility should be
registered by that country's equivalent body with enforcement over animal welfare.
16. No animal disposition should occur if it would create a health or safety risk (to the animal or
humans) or have a negative impact on the conservation of the species.
17. Inherently dangerous wild animals or invasive species should not be dispositioned to the pet
trade or those unqualified to care for them.
18. Under no circumstances should any primates be dispositioned to a private individual or to the pet
trade.
19. Fish and aquatic invertebrate species that meet ANY of the following are inappropriate to be
disposed of to private individuals or the pet trade:
a. species that grow too large to be housed in a 72-inch long, 180 gallon aquarium (the largest
tank commonly sold in retail stores)
b. species that require extraordinary life support equipment to maintain an appropriate captive
environment (e.g., cold water fish and invertebrates)
c. species deemed invasive (e.g., snakeheads)
d. species capable of inflicting a serious bite or venomous sting (e.g., piranha, lion fish, blue-
ringed octopus)
e. species of wildlife conservation concern
20. When dispositioning specimens managed by an AZA PMP, institutions should consult with the
AZA PMP manager.
21. Institutions should consult WCMC-approved RCPs when making disposition decisions.
V(b). Disposition Requirements – dead specimens: Dead specimens (including animal parts and
samples) are only to be disposed of from an AZA member institution's collection if the following conditions
are met:
1. Dispositions of dead specimens must meet the requirements of all applicable local, state, federal
and international regulations and laws.
2. Maximum utilization is to be made of the remains, which could include use in educational
programs or exhibits.
3. Consideration is given to scientific projects that provide data for species management and/or
conservation.
4. Records (including ownership information) are to be kept on all dispositions, including animal
body parts, when possible.
5. SSP and TAG necropsy protocols are to be accommodated insofar as possible.
VI. Transaction Forms: AZA member institutions will develop transaction forms to record animal
acquisitions and dispositions. These forms will require the potential recipient or provider to adhere to the
AZA Code of Professional Ethics, the AZA Acquisition/Disposition Policy, and all relevant AZA and
member policies, procedures and guidelines. In addition, transaction forms must insist on compliance with
the applicable laws and regulations of local, state, federal and international authorities.
Required:
1. direct and floatation fecals
2. vaccinate as appropriate
Strongly Recommended:
1. CBC/sera profile
2. urinalysis
3. appropriate serology (FIP, FeLV, FIV)
4. heartworm testing in appropriate species
essential to ensuring effective care, welfare, and management. Some of these requirements can be met
outside of the primary exhibit enclosure while the animal is involved in a program or is being transported.
For example, free-flight birds may receive appropriate exercise during regular programs, reducing the
need for additional exercise. However, the institution must ensure that in such cases, the animals
participate in programs on a basis sufficient to meet these needs or provide for their needs in their home
enclosures; upon return to the facility the animal should be returned to its species-appropriate housing as
described above.
Knowledge Acquisition
Improving our visitors' knowledge and understanding regarding wildlife and wildlife conservation is a
fundamental goal for many zoo educators using program animals. A growing body of evidence supports
the validity of using program animals to enhance delivery of these cognitive messages as well.
MacMillen (1994) found that the use of live animals in a zoomobile outreach program significantly
enhanced cognitive learning in a vertebrate classification unit for sixth grade students.
Sherwood and his colleagues (1989) compared the use of live horseshoe crabs and sea stars to the
use of dried specimens in an aquarium education program and demonstrated that students made the
greatest cognitive gains when exposed to programs utilizing the live animals.
Povey and Rios (2002) noted that in response to an open-ended survey question (“Before I saw this
animal, I never realized that . . . ”), visitors watching a presentation utilizing a program animal
provided 69% cognitive responses (i.e., something they learned) versus 9% made by visitors viewing
the same animal in its exhibit (who primarily responded with observations).
Povey (2002) recorded a marked difference in learning between visitors observing animals on exhibit
versus being handled during informal presentations. Visitors to demonstrations utilizing a raven and
radiated tortoises were able to answer questions correctly at a rate as much as eleven times higher
than visitors to the exhibits.
Enhanced Environmental Attitudes
Program animals have been clearly demonstrated to increase affective learning and attitudinal change.
Studies by Yerke and Burns (1991) and Davison and her colleagues (1993) evaluated the effect live
animal shows had on visitor attitudes. Both found their shows successfully influenced attitudes about
conservation and stewardship.
Yerke and Burns (1993) also evaluated a live bird outreach program presented to Oregon fifth-
graders and recorded a significant increase in students' environmental attitudes after the
presentations.
Sherwood and his colleagues (1989) found that students who handled live invertebrates in an
education program demonstrated both short and long-term attitudinal changes as compared to those
who only had exposure to dried specimens.
Povey and Rios (2002) examined the role program animals play in helping visitors develop positive
feelings about the care and well-being of zoo animals.
As observed by Wolf and Tymitz (1981), zoo visitors are deeply concerned with the welfare of zoo
animals and desire evidence that they receive personalized care.
Conclusion
Creating positive impressions of aquarium and zoo animals, and wildlife in general, is crucial to the
fundamental mission of zoological institutions. Although additional research will help us delve further into
this area, the existing research supports the conclusion that program animals are an important tool for
conveying both cognitive and affective messages regarding animals and the need to conserve wildlife and
wild places.
Acknowledgements
The primary contributors to this paper were Karen Povey and Keith Winsten with valuable comments
provided from members of both the Conservation Education Committee and the Children's Zoo Interest
Group.
References
Bitgood, S., Patterson, D., & Benefield, A. (1986). Understanding your visitors: ten factors that influence
visitor behavior. Annual Proceedings of the American Association of Zoological Parks and Aquariums,
726-743.
Bitgood, S., Patterson, D., & Benefield, A. (1988). Exhibit design and visitor behavior. Environment and
Behavior, 20 (4), 474-491.
Churchman, D. (1985). How and what do recreational visitors learn at zoos? Annual Proceedings of the
American Association of Zoological Parks and Aquariums, 160-167.
Davison, V.M., McMahon, L., Skinner, T.L., Horton, C.M., & Parks, B.J. (1993). Animals as actors: take 2.
Annual Proceedings of the American Association of Zoological Parks and Aquariums, 150-155.
Johnston, R.J. (1998). Exogenous factors and visitor behavior: a regression analysis of exhibit viewing
time. Environment and Behavior, 30 (3), 322-347.
MacMillen, Ollie. (1994). Zoomobile effectiveness: sixth graders learning vertebrate classification. Annual
Proceedings of the American Association of Zoological Parks and Aquariums, 181-183.
Morgan, J.M. & Hodgkinson, M. (1999). The motivation and social orientation of visitors attending a
contemporary zoological park. Environment and Behavior, 31 (2), 227-239.
Povey, K.D. (2002). Close encounters: the benefits of using education program animals. Annual
Proceedings of the Association of Zoos and Aquariums, in press.
Povey, K.D. & Rios, J. (2002). Using interpretive animals to deliver affective messages in zoos. Journal of
Interpretation Research, in press.
Sherwood, K. P., Rallis, S. F. & Stone, J. (1989). Effects of live animals vs. preserved specimens on
student learning. Zoo Biology 8: 99-104.
Wolf, R.L. & Tymitz, B.L. (1981). Studying visitor perceptions of zoo environments: a naturalistic view. In
Olney, P.J.S. (Ed.), International Zoo Yearbook (pp.49-53). Dorchester: The Zoological Society of
London.
Yerke, R. & Burns, A. (1991). Measuring the impact of animal shows on visitor attitudes. Annual
Proceedings of the American Association of Zoological Parks and Aquariums, 532-534.
Yerke, R. & Burns, A. (1993). Evaluation of the educational effectiveness of an animal show outreach
program for schools. Annual Proceedings of the American Association of Zoological Parks and
Aquariums, 366-368.
Rationale
Membership in AZA requires that an institution meet the AZA Accreditation Standards collectively
developed by our professional colleagues. Standards guide all aspects of an institution's operations;
however, the accreditation commission has asserted that ensuring that member institutions demonstrate
the highest standards of animal care is a top priority. Another fundamental AZA criterion for membership
is that education be affirmed as core to an institution's mission. All accredited public institutions are
expected to develop a written education plan and to regularly evaluate program effectiveness.
The inclusion of animals (native, exotic and domestic) in educational presentations, when done correctly,
is a powerful tool. CEC's Program Animal Position Statement describes the research underpinning the
appropriate use of program animals as an important and powerful educational tool that provides a variety
of benefits to zoo and aquarium educators seeking to convey cognitive and affective messages about
conservation and wildlife.
Ongoing research, such as AZA's Multi-Institutional Research Project (MIRP) and research conducted by
individual AZA institutions will help zoo educators to determine whether the use of program animals
conveys intended and/or conflicting messages and to modify and improve programs accordingly and to
ensure that all program animals have the best possible welfare.
When utilizing program animals our responsibility is to meet both our high standards of animal care and
our educational goals. Additionally, as animal management professionals, we must critically address both
the species' conservation needs and the welfare of the individual animal. Because "wild creatures differ
endlessly," in their forms, needs, behavior, limitations and abilities (Conway, 1995), AZA, through its
Animal Welfare Committee, has recently given the responsibility to develop taxon- and species-specific
animal welfare standards and guidelines to the Taxon Advisory Groups (TAG) and Species Survival
Plan® Program (SSP). Experts within each TAG or SSP, along with their education advisors, are charged
with assessing all aspects of the taxons' and/or species‟ biological and social needs and developing
Animal Care Manuals (ACMs) that include specifications concerning their use as program animals.
However, even the most exacting standards cannot address the individual choices faced by each AZA
institution. Therefore, each institution is required to develop a program animal policy that articulates and
evaluates program benefits. The following recommendations are offered to assist each institution in
formulating its own Institutional Program Animal Policy, which incorporates the AZA Program Animal
Policy and addresses the following matters.
The Policy Development Process
Within each institution, key stakeholders should be included in the development of that institution's policy,
including, but not limited to representatives from:
the Education Department
the Animal Husbandry Department
the Veterinary and Animal Health Department
the Conservation & Science Department
the Behavioral Husbandry Department
any animal show staff (if in a separate department)
departments that frequently request special program animal situations (e.g., special events,
development, marketing, zoo or aquarium society, administration)
Additionally, staff from all levels of the organization should be involved in this development (e.g., curators,
keepers, education managers, interpreters, volunteer coordinators).
To develop a comprehensive Program Animal Policy, we recommend that the following components be
included:
I. Philosophy
In general, the position of the AZA is that the use of animals in up close and personal settings, including
animal contact, can be extremely positive and powerful, as long as:
1. The use and setting is appropriate.
2. Animal and human welfare is considered at all times.
3. The animal is used in a respectful, safe manner and in a manner that does not misrepresent or
degrade the animal.
4. A meaningful conservation message is an integral component. Read the AZA Board-approved
Conservation Messages.
5. Suitable species and individual specimens are used.
Institutional program animal policies should include a philosophical statement addressing the above, and
should relate the use of program animals to the institution's overall mission statement.
II. Appropriate Settings
The Program Animal Policy should include a listing of all settings both on and off site, where program
animal use is permitted. This will clearly vary among institutions. Each institution's policy should include a
comprehensive list of settings specific to that institution. Some institutions may have separate policies for
each setting; others may address the various settings within the same policy. Examples of settings
include:
I. On-site programming
A. Informal and non-registrants:
1. On-grounds programming with animals being brought out (demonstrations,
lectures, parties, special events, and media)
2. Children's zoos and contact yards
3. Behind-the-scenes open houses
4. Shows
5. Touch pools
B. Formal (registration involved) and controlled settings
1. School group programs
2. Summer Camps
3. Overnights
4. Birthday Parties
5. Animal rides
6. Public animal feeding programs
II. Offsite and Outreach
1. PR events (TV, radio)
2. Fundraising events
3. Field programs involving the public
4. School visits
5. Library visits
6. Nursing Home visits (therapy)
7. Hospital visits
8. Senior Centers
9. Civic Group events
In some cases, policies will differ from setting to setting (e.g., on-site and off-site use with media). These
settings should be addressed separately, and should reflect specific animal health issues, assessment of
distress in these situations, limitations, and restrictions.
X. Staff Training
Thorough training for all handling staff (keepers, educators, and volunteers, and docents) is clearly
critical. Staff training is such a large issue that many institutions may have separate training protocols and
procedures. Specific training protocols can be included in the Institutional Program Animal Policy or
reference can be made that a separate training protocol exists.
It is recommended that the training section of the policy address:
1. Personnel authorized to handle and present animals.
2. Handling protocol during quarantine.
3. The process for training, qualifying and assessing handlers including who is authorized to train
handlers.
4. The frequency of required re-training sessions for handlers.
5. Personnel authorized to train animals and training protocols.
6. The process for addressing substandard performance and noncompliance with established
procedures.
7. Medical testing and vaccinations required for handlers (e.g., TB testing, tetanus shots, rabies
vaccinations, routine fecal cultures, physical exams, etc.).
8. Training content (e.g., taxonomically specific protocols, natural history, relevant conservation
education messages, presentation techniques, interpretive techniques, etc.).
9. Protocols to reduce disease transmission (e.g., zoonotic disease transmission, proper hygiene
and hand washing requirements, as noted in AZA's Animal Contact Policy).
10. Procedures for reporting injuries to the animals, handling personnel or public.
11. Visitor management (e.g., ensuring visitors interact appropriately with animals, do not eat or drink
around the animal, etc.).
XI. Review of Institutional Policies
All policies should be reviewed regularly. Accountability and ramifications of policy violations should be
addressed as well (e.g., retraining, revocation of handling privileges, etc.). Institutional policies should
address how frequently the Program Animal Policy will be reviewed and revised, and how accountability
will be maintained.
XII. TAG and SSP Recommendations
Following development of taxon-specific recommendations from each TAG and SSP, the institution policy
should include a statement regarding compliance with these recommendations. If the institution chooses
not to follow these specific recommendations, a brief statement providing rationale is recommended.
Pyridoxine (B-6): Pyridoxine also known as B-6 is a water-soluble vitamin, which aids the body in the
synthesis of antibodies by the immune system. It also plays a role in the formation of red blood cells and
helps to promote healthy nerve functions. Pyridoxine is required to produce the chemical activity
necessary for protein digestion.
Choline: Choline is an essential nutrient, which contributes to the function of nerve cells. It is a
component (helps to form phosphatidylcholine, the primary phospholipid of cell membranes) of the
phospholipid lecithin (found in cells throughout the body) and is critical to normal membrane structure and
formation. It also functions as a “methyl donor”, but this role can be completely replaced by excess
amounts of the amino acid methionine in the diet.
Folacin (Folate, Folic Acid, B-9, Pteroylglutamic Acid): Folacin, or folate, is a water-soluble vitamin, which
assists the body in the formation of red blood cells. It also plays a major role in the formation of genetic
material (synthesis of DNA, the hereditary and functioning blueprint of all cells)within all living cells.
Folacin functions as a coenzyme, which is important at the cellular and subcellular levels in
decarboxylation, oxidation-reduction, transamination, deamination, phosphorylation, and isomerization
reactions. Working in conjunction with Vitamin C and B-12, Folacin assists in digestion and protein
utilization and synthesis. This vitamin may be used to increase appetite and stimulate healthy digestive
acids.
Vitamin B-12: Vitamin B-12 is a water-soluble vitamin, which functions as a coenzyme in single carbon
and carbohydrate metabolism. In addition to playing a role in metabolism, B-12 assists in the formation of
red blood cells and aids in the maintenance of the central nervous system.
Pantothenic Acid: Pantothenic acid is a water-soluble vitamin and part of the B vitamin complex. It is
needed to break down and use (metabolize) food. Pantothenic acid also is needed for the synthesis of
both hormones and cholesterol.
Calcium: The mineral calcium (in association with phosphorus) is a major component of the body and is
largely associated with skeletal formation. It is important in blood clotting, nerve function, acid-base
balance, enzyme activation, muscle contraction, and eggshell, tooth, and bone formation and
maintenance. It is one of the most important minerals required for growth, maintenance, and reproduction
of vertebrates.
Phosphorus: In addition to acting as a major component of the body and being largely associated with
skeletal and tooth formation (in conjunction with calcium), phosphorus is involved in almost every aspect
of metabolism (energy metabolism, muscle contractions, nerve function, metabolite transport, nucleic acid
structure, and carbohydrate, fat, and amino acid metabolism). Phosphorus is needed to produce ATP,
which is a molecule the body uses to store energy. Working with the B vitamins, this mineral also assists
the kidneys in proper functioning and helps to maintain regularity in heartbeat.
Magnesium: Magnesium is a mineral, which serves several important metabolic functions. It plays a role
in the production and transport of energy. It also is important for the contraction and relaxation of
muscles. Magnesium is involved in the synthesis of protein, and it assists in the functioning of certain
enzymes in the body.
Potassium: Potassium is a mineral that is involved in both electrical and cellular functions in the body. (In
the body it is classified as an electrolyte.) It has various roles in metabolism and body functions.
Potassium assists in the regulation of the acid-base balance and water balance in blood and the body
tissues. It also assists in protein synthesis from amino acids and in carbohydrate metabolism. Potassium
is necessary for the building of muscle and for normal body growth, as well as proper functioning of nerve
cells, in the brain and throughout the body.
Sodium (salt): Sodium is an element, which the body uses to regulate blood pressure and blood volume.
Sodium also is critical for the functioning of muscles and nerves.
Iron: Iron is a trace element and is the main component of hemoglobin (oxygen carrier in the blood),
myoglobin in muscles (oxygen carrier with a higher affinity for oxygen than hemoglobin), and many
proteins and enzymes within the body. It also functions in immune defenses against infection.
Zinc: Zinc also is a trace element that is second only to iron in terms of concentration within the body.
Zinc plays an important role in the proper functioning of the immune system in the body. It is required for
the enzyme activities necessary for cell division, cell growth, and wound healing. It plays a role in the
acuity of the senses of smell and taste. Zinc also is involved in the metabolism of carbohydrates. Zinc is
essential for synthesis of DNA, RNA, and proteins, and it is a component or cofactor of many enzyme
systems.
Manganese: Manganese is essential for carbohydrate and lipid metabolism, for synthesis of one of the
precursors to cartilage formation, and for proper bone formation. Manganese plays a key role in the
growth and maintenance of tissues and cartilage, specifically proper bone development. It particularly
aids in development at the ends of bones where new bone formation takes place. This therefore helps to
reduce the risk of osteoporosis. Manganese also helps to produce certain hormones, metabolizes fat, and
is part of superoxide dismutase (SOD) an antioxidant. Studies on humans have shown that manganese
also may lower the frequency of epileptic seizures and enhance immune functioning.
Copper: Copper is an essential trace mineral present in all body tissues. Copper, along with iron, helps in
the formation of red blood cells. It also helps in keeping the blood vessels, bones, and nervous and
immune systems healthy.
Selenium: Selenium is an essential trace element. It is an integral part of enzymes, which are critical for
the control of the numerous chemical reactions involved in brain and body functions. Selenium has a
variety of functions. The main one is its role as an antioxidant in the enzyme selenium-glutathione-
peroxidase. This enzyme neutralizes hydrogen peroxide, which is produced by some cell processes and
would otherwise damage cell membranes. Selenium also seems to stimulate antibody formation in
response to vaccines. It also may provide protection from the toxic effects of heavy metals and other
substances. Selenium may assist in the synthesis of protein, in growth and development. In humans,
selenium has been shown to improve the production of sperm and sperm motility.
Iodine: Iodine is a trace mineral and an essential nutrient. Iodine is essential for the normal metabolism of
cells. It is a necessary nutrient for the production of thyroid hormones and normal thyroid function.
12. Any pertinent group history should be included as well, especially if there is a history of infectious
disease within the group or exhibit.
13. As small carnivores are prone to dental disease, a thorough history of dental problems and,
preferably, a dental chart noting extractions, root canals, problems, etc. is recommended.
Identification: All individuals should be permanently identified prior to shipment. Transponder chips are
recommended as a primary method, tattooing may be done in addition (males should be tattooed on the
inner right thigh and females on the inner left). Two main brands of transponders are used and
recommended: 1) Trovan (InfoPet Inc., 415 W. Travelers Trial, Burnsville, MN 55337-2548); and 2)
AVID (Avid, 3179 Hamner Ave., Norco, CA 91760). Chip type and implantation site may be specifically
recommended based on the species (e.g., bridge of nose for otters) or even sex (e.g., AVID behind right
ear for male black-footed ferrets), otherwise the general standard of over the back between the scapulae
to the left of the midline should be applied.
Genetic materials banking: Prior to shipping, it is recommended that genetic materials be banked. This
may provide positive identification should there ever be any question regarding an animal‟s identity (e.g.
transponder loss or breakage). In addition, the materials may serve as a future resource for research.
Methods are detailed at the end of this Appendix.
Examination: Ideally, the pre-shipment examination should occur at least two weeks prior to shipment.
This enables the animal to fully recover from anesthesia and respond to any vaccinations or treatments
given. There is also time for test results to be forwarded to the receiving institution. With most small
carnivores, crating does not require the use of an anesthetic, so this guideline should be not be a
hardship with appropriate planning. A complete pre-shipment examination should include the following,
and results should be documented in the record (photo documentation of specific problems may be
valuable):
1. Physical exam
a. Body weight and body condition scoring (assessment scaled 1-5 or 1-10)
b. Heart rate, respiratory rate, body temperature, hydration status
c. Oral exam: including dental chart documentation. Any problems should be noted and
addressed if possible. Dental cleaning and polishing should be completed if necessary.
d. Ophthalmologic exam
e. Ear exam: appropriate diagnostics should be completed if there is any indication of problems.
Cleaning and treatment should be done if necessary.
f. Auscultation
g. Abdominal palpation
h. Assessment of genitalia, including rectal palpation in both sexes if of a size to permit safely
i. Skin/coat assessment: any problems should be worked up with appropriate diagnostics.
j. Feet/nails
univalent parvovirus vaccine. A 1ml (IM) dose should be given at the same frequency listed
for canine distemper
3. Leptospirosis
a. If leptospirosis has been diagnosed or is endemic in the area, a killed bacterin could be used,
though most of these are currently in combination vaccines.
4. Rabies
a. Only a killed rabies vaccine product should be used. Though it is recommended, use of
rabies vaccines in these species will be extra-label and will not be considered protective in
the event of a bite.
b. Imrab3 (Merial Ltd., 3239 Satellite Blvd., Duluth, GA 30096) is a killed rabies vaccine that
has been used extensively in small carnivores without apparent adverse effects. A 1ml (IM)
dose should be given once at 16 weeks of age, and then annually.
c. PUREVAX Feline Rabies (Merial Ltd., 3239 Satellite Blvd., Duluth, GA 30096) is a live
canarypox vectored, nonadjuvanted recombinant rabies vaccine that is currently being used
at some institutions for small carnivores. A 1ml (IM) dose should be given once at 8 weeks
(or older), and then annually.
5. Feline Panleukopenia
a. AAZV‟s Infectious Disease Notebook notes that some small carnivores are susceptible to
feline panleukopenia and should be vaccinated and many small carnivores have been
vaccinated with a combination product in the past. However, a number of veterinary advisors
do not recommend vaccination for red pandas and black-footed ferrets. Veterinary advisor
recommendations should be followed primarily.
b. If there is significant risk of exposure to feline panleukopenia (e.g., feral cat population),
vaccination should be considered.
c. FPV-1 Feline Panleukopenia Vaccine (Biocor Animal Health Inc., 2720 North 84 Street,
th
Omaha, NE 68134) is a new non-adjuvanted, killed vaccine. This vaccine has been shown to
be safe in pregnant domestic cats A 1ml (SQ) dose should be given at the following
frequency:
- At least two vaccines three weeks apart at/after 12 weeks of age. If started before 12
weeks, give a third vaccine – then annually.
6. Titer Evaluations
a. Distemper, parvovirus, and leptospiral titers can be evaluated by submitting serum to: Cornell
Diagnostic Laboratory, College of Veterinary Medicine, Cornell University, Upper Tower
Road, Ithaca, NY 14851-0786, Ph: 607-253-3900
Transport: With the wide variety of species included within “small carnivore”, only general
recommendations will be provided.
1. Crates should be designed so that the animal can assume normal postures, including turning
around. IATA recommendations should be followed. Crates should be of impervious materials as
many small carnivores are diggers or chewers and this will allow for proper disinfection as well.
Some small carnivores are considered “injurious species” (e.g., meerkats) and are required to be
double crated for shipment.
2. Animals should be crated individually to avoid aggression.
3. Animals should only be shipped when the weather is appropriate at all points along the shipping
route. Unplanned delays and errors should be considered as possibilities and risky shipments
(e.g., too hot at site of layover) should be rescheduled. This may be true even for counter-to-
counter shipments.
4. Appropriate temperature ranges will vary by species, but a “safe” window would be between 10-
21°C (50-75°F) for most small carnivores.
5. Methods of providing visual access and water to the animal should be addressed. The crate
should otherwise be secure from tampering.
6. Most small carnivores will not require anesthesia for crating. In the event that anesthesia is
required, the animal should be fully recovered (standing and stable) prior to shipping. Ideally, an
inhalant or reversible anesthetic should be used in these cases.
Quarantine: Quarantine is the next step in assuring the health of the new arrival and the protection of the
animals already in the collection. General quarantine guidelines have been outlined by AAZV and AZA. It
is critical that protocols be developed and followed.
1. Length – minimum of 30 days for small carnivores
2. Examination
a. Visual exam should be performed upon arrival, preferably at uncrating. A body weight can
easily be obtained at this time as well (in the crate).
b. Ideally, a physical exam should be completed during the third week of the quarantine. This
allows the animal to adjust to the environment and dietary changes and allows test results to
come back before the end of quarantine.
- Physical exam, verification of ID, sample collection, and radiographs should be completed
as detailed for pre-shipment.
- Repeating this work will provide a baseline for the animal at the new institution (especially
for radiographs), allow any problems to be rechecked, and potentially reveal new
problems that may have developed during the stress of shipment and quarantine.
- Vaccinations should have been given during pre-shipment if needed, but, if not, should be
given during quarantine before exposure to a new environment.
3. Fecals
a. A minimum of three (3) consecutive negative fecals (fresh direct and float or sedimentation),
each one week apart, should be obtained before clearing from quarantine.
b. Appropriate treatment for any parasites should be administered while in quarantine and three
negative fecals should be obtained post-treatment.
c. Cultures and special stains should be repeated during this time if there has been a history of
infectious disease in this animal or its previous group. In the event of an infectious bacterial
intestinal disease (e.g., salmonellosis), it is recommended that repeated cultures be
submitted (three per week) in order to identify or document the condition.
4. Nutrition
a. Most diets are not going to be identical from one institution to the next. It is recommended
that the sending institutions diet be obtained in advance of the animal‟s arrival. This enables
the receiving institution to provide a familiar diet to the animal upon arrival and for the first
week of quarantine. The sending institution may want to send some of the regular diet with
the animal.
b. After the first week of quarantine, if the animal is doing well, the new diet should slowly be
introduced. If this is done at a rate of approximately 25% of new diet exchanged for old per
week, the animal should be converted to the new diet by the end of quarantine and should
avoid any problems associated with dietary change.
Preventive Health: In order to appropriately ensure the health of small carnivores, it is recommended that
a physical examination take place on a routine basis. The following is recommended for a routine exam:
1. Physical exam: as detailed in pre-shipment
2. Verification of identification
3. Sample collection
a. Blood
- CBC/chem. panel
- HW antigen
- Serum banking
- Research requests
- Viral titers: as there is little information about vaccine titer levels in many of these species, it
is suggested that titers be run opportunistically and documented as to time from
vaccination(s), route, vaccine product and titer level. See above for information on
obtaining titers.
b. Urine: as detailed in pre-shipment
c. Fecals: should be submitted at a minimum of annually; twice annually is recommended
d. Genetic materials should only need to be collected once if preserved properly.
4. Radiographs: chest and abdomen minimally (this is especially important for monitoring renal
calculi in otters)
5. Vaccination: as detailed above
Miscellaneous: Ideally, weights should be recorded monthly (accomplished with the aid of training). In
areas where the animal is housed outside and heartworm is endemic, ivermectin at 0.006mg/kg orally
once a month may be used for prevention. This dose has been used safely and effectively in a number of
small carnivores. Reports of disease issues, adverse drug reactions, etc. should be reported to the
veterinary advisor or TAG on an annual basis, in addition to submission of necropsy reports.
Necropsy: All small carnivores that die should receive a thorough necropsy in a timely manner. This will
help establish cause of death, provide valuable insight into the health of the collection, and help protect
the other animals in the social grouping by delineating any immediate concerns. A complete report,
including histopath and test results, should be submitted to the veterinary advisor on an annual basis.
1. Blood: serum banking
2. Radiographs post-mortem
3. External exam, including weight and description of condition of body
4. Internal exam
a. A detailed written report should be completed.
b. Cultures should be submitted, if indicated
c. Photo documentation, if possible
d. Submission of a representative sample of all lesions AND routine tissues:
- Skin, muscle, sciatic nerve, bone (femur), tongue, salivary gland, eye, brain, pituitary,
trachea, thyroid, parathyroid, thymus, esophagus, lymph nodes (thoracic and
abdominal), lung, bronchus, heart, aorta, liver, gall bladder, diaphragm, spleen,
pancreas, stomach, duodenum, jejunum, ileum, ileocolic jxn, colon, adrenal, kidneys,
bladder, ureter, urethra, reproductive organs
- It is recommended that a pathologist familiar with non-traditional species be used for
histopathology.
- Reproductive organs should be submitted to: Dr. Linda Munson, Dept. of VM-PM1,
Haring Hall, School of Veterinary Medicine, University of California, Davis, CA 95616
as a standing request.
e. Frozen set of tissues: heart, liver, kidney, brain, serum, lesions
f. Any stones (uroliths, renoliths, etc.) should be submitted for analysis to: Minnesota
Urolith Center, Dept. of Small Animal Clinical Sciences, College of Veterinary Medicine,
University of Minnesota, 1352 Boyd Avenue, St. Paul, MN 55108
Methods for Banking Genetic Materials: Avoid contamination of genetic samples; wear gloves, clean
equipment, etc. The protocols are listed in preferential order:
1. Whole Blood
A. Minimum required volume: 0.05ml (1 drop)
B. Lysis buffer (all ingredients may be obtained from Sigma)
0.1 M Tris-HCl (pH 8.0) (bring to pH with HCl)
0.1 M EDTA (pH 8.0) (bring to pH with NaOH)
0.1 M NaCl
2% (w/v) SDS (sodium dodecyl sulfate)
C. Protocol
- Draw blood; if anti-coagulant is needed, heparin is preferable, but EDTA is acceptable
- Mix 1:1 with buffer (a little more buffer is acceptable) in cryovial
- Label with Animal, ID#, Date, Institution, Sample type (e.g. whole blood with heparin in lysis
buffer)
- Freeze at -57°C (-70°F)
2. Tissue Biopsies (skin with dermis or muscle)
A. Minimum required volume: at least this “” big. Maximum required volume: piece(s) should be
3
no larger than 0.4 cm , section if necessary
B. Place in cryovial
C. Label with Animal, ID#, Date, Institution, Sample type
D. Freeze immediately at -57°C (-70°F)
3. Hair
A. Minimum required amount: 1 follicle; 10-20 preferred. Follicles must be attached.
B. Place follicle ends in a cryovial; with sterile scissors cut follicles into vial. Always use gloves
when handling the hairs.
C. Label with Animal, ID#, Date, Institution, Sample type
D. Freeze immediately at -57°C (-70°F)
The following list of behaviors was derived using data from a 2003 survey conducted by the American
Association of Zoo Keepers Animal Training Committee (AAZK, ATC). The goal of the survey was to
census the existence and depth of training programs for species in AZA facilities. For each species
trained, each respondent was asked to list trained behaviors, types of reinforcement and conditioned
reinforcers used. Additional information about facility design, training tools, and general comments was
also requested. The ATC hopes that this data will aid in the design of training programs for the Mustelid,
Procyonid, and Viverrid taxa. Where appropriate, these commonly trained behaviors can greatly enhance
the husbandry of species in this group. Not every behavior will work for every animal. The
appropriateness of a behavioral goal for an individual will depend on management policy and building
design of the facility, as well as the needs and disposition of the animal. For questions or comments
about this list or the Trained Behaviors Survey, please contact the AAZK Animal Training Committee at
www.aazk.org.
Survey results pertaining to the list of behaviors: 219 AZA facilities were surveyed. There were 71
respondents. 31 of these train species within the Procyonid taxonomic group. Because many similarities
were found within taxonomic groups, commonly trained behaviors were compiled to serve as a reference
for animal training programs. Of the 31 respondents that train within this group, the percentage that trains
each behavior is listed next to the behavior.
Raccoons % Used Red pandas % Used Ringtails % Used
Paws/feet 25% Belly 33% Target 67%
Separations 50% Paws/feet 67% Stethoscope 33%
Station 50% Sides (torso) 33% Station 67%
Target 75% Shift 83% Belly 33%
Oral meds 25% Station 67% Paws/feet 67%
Squeeze/crate 75% Squeeze/crate 83% Sides (torso) 33%
Climb 50% Scale 83% Station 67%
Carry object 25% Come down 17% Scale 67%
Stand up 50% Target 83% Injection 33%
Nail trim 25% Tactile desensitization 67% Climb 67%
Belly 25% Vaginal swab 17% Shift 33%
Shifting 75% Ultrasound 17%
Hand injection 17%
Oral meds 50%
Ears 17%
Coati % Used Kinkajou % Used
Belly 40% Oral meds 33%
Paws/feet 20% Blood collection 33%
Separations 40% Squeeze/crate 67%
Shift 80% Injection 33%
Station 60% Ophthalmoscope 33%
Squeeze/crate 100% Otoscope 33%
Coati % Used Kinkajou % Used
Scale 60% Stethoscope 33%
Climb 20% Climb 33%
Leash on/off 33%
A to B 33%
Sevenich MacPhee M, Mellen J. 2000a. Framework for planning, documenting, and evaluating
enrichment programs (and the Director‟s, Curator‟s, and Keeper‟s roles in the Process). Proceedings
of the AZA Annual Meeting. Wheeling. WV:AZA.
Sevenich MacPhee M, Mellen J. 2000b. Training and enrichment models for avian exhibits. Proceedings
of the AZA Annual Meeting. Wheeling. WV:AZA.
Sheng S. 1992. The ultimate enriched environment. In: Proceedings of the AAZPA Annual Meeting.
Wheeling. WV:AAZPA. pp 124-27.
Shepherdson D. 1992. Environmental enrichment: an overview. In: Proceedings of the AAZPA Annual
Meeting. Wheeling. WV:AAZPA. pp 100-3.
Shepherdson D. 1997. The animal‟s perspective: Developing strategies for successful enrichment. In:
Proceedings of the AAZPA Annual Meeting. Wheeling. WV:AAZPA. pp 486-89.
Shepherdson D. Tracing the path of environmental enrichment in zoos. In: Shepherdson, D, Mellen, J,
Hutchins, M, editors. Second nature: Environmental enrichment for captive animals. Washington, DC:
Smithsonian Institution Press; 1998. p. 1-14.
Shepherdson D, Carlstead K. 2000. When did you last forget to feed your tiger? Proceedings of the AZA
Annual Meeting. Wheeling. WV:AZA.
Shepherdson D, Mellen J. 1993. Environmental enrichment: Carrying forth the message. In: Proceedings
of the AAZPA Annual Meeting. Wheeling. WV:AAZPA. pp 216-18.
Shields J. 1995. Behavioral enrichment for the rest of the zoo. In: Proceedings of the AAZPA Annual
Meeting. Wheeling. WV:AAZPA. pp 456-57.
Smith C. 1993. An inexpensive simulated thundershower for small enclosures. AAZK Forum: 20(9):322-
23.
Stern S. 1994. Whose life is really being enriched here anyway? Shape of enrichment 3(3).
Widner K. 1994. Initiation of the zoo-wide enrichment program at the Knoxville Zoo. In: Proceedings of
the AAZPA Annual Meeting. Wheeling. WV:AAZPA. pp 51-2.
Williams L. 1996. Ethological considerations for designing behavioral enrichment. Lab Animal. pp 29-33.
Whorley KE, Hare VJ. 1995. An overview of the 1995 Environmental Enrichment Conference. The Shape
of Enrichment. Vol. 4, No. 4, November.
There are also many enrichment resources available on-line and in print, including:
"Enrichment Options" – A regular column featuring brief descriptions of ideas published monthly in the
Animal Keepers' Forum. Published by the American Association of Zoo Keepers, Inc. AAZK
Administrative Office, Susan Chan, Editor. 3601 S.W. 29th Street, Suite 133 Topeka, KS 66614.
Phone: (785) 273-9149, Fax: (785) 273-1980. Email: [email protected]. Website:
www.aazk.org
"The Shape of Enrichment" Newsletter – A newsletter devoted entirely to enrichment of captive wild
animals. Published by The Shape of Enrichment, Inc., V. Hare & K. Worley, (eds.). 1650 Minden
Drive, San Diego, CA 92111. Phone: (619) 270-4273. Fax: (619) 279-4208. E-mail:
[email protected]. Website: www.enrichment.org
The American Association of Zoo Keepers Enrichment Committee www.aazk.org
Disney Animal Kingdom - www.animalenrichment.org
AAZK Enrichment Notebook 3rd ed. 2004 ISBN1-929672-11-X,
www.aazk.org/2004enrichnotebookcd.php.
Fort Worth Zoo‟s Enrichment Online: www.enrichmentonline.org/browse/index.asp
Training
Baker A. 1991. Training as a management tool: Creating the climate and maintaining the momentum. In:
AAZPA Annual Conference Proceedings. Wheeling, W.Va.: American Association of Zoological Parks
and Aquariums. p. 563-568.
Blasko D, Doyle C, Laule G, Lehnhardt J. 1996. Training terms list. Principles of Elephant Management
School. St. Louis: American Zoo and Aquarium Association, Schools for Zoo and Aquarium
Personnel.
Bloomsmith M, Laule G, Thurston R, Alford P. 1992. Using training to moderate chimpanzee aggression.
In: AAZPA Regional Conference Proceedings. Wheeling, W.Va.: American Association of Zoological
Parks and Aquariums. p. 719-722.
Coe J. 1992. Animal training and facility design – a collaborative approach. In: AAZPA/CAZPA Regional
Conference Proceedings. Wheeling, W.Va.: American Association of Zoological Parks and
Aquariums. p. 411-414.
Coe J. 1992. Animal training and facility design – a collaborative approach. In: AAZPA/CAZPA Regional
Conference Proceedings. Wheeling, W.Va.: American Association of Zoological Parks and
Aquariums. p. 411-414.
Dewsbury D. 1978. Comparative animal behavior. New York: McGraw-Hill.
Grandin T. 1995. Thinking in pictures. New York: Vintage book. 222 p.
Hediger H. 1950. Wild animals in captivity. London: Butterworths. 207 p.
Hediger H. 1969. Man and animal in the zoo. London: Routledge and Kegon Paul. 303 p.
Kazdin A. 1994. Behavior modification in applied settings. Pacific Grove CA: Brooks/Cole Publishing
Company. 508 p.
Kleiman D, Allen M, Thompson K, Lumpkin S, editors. 1996. Wild mammals in captivity: Principles and
techniques.
Laule G. 1992. Addressing psychological well-being: Training as enrichment. In: AAZPA/CAZPA Annual
Conference Proceedings. Wheeling, W.Va.: American Association of Zoological Parks and
Aquariums. p. 415-422.
Laule G. 1995. The role of behavioral management in enhancing exhibit design and use. In: AZA
Regional Conference Proceedings. Wheeling, W.Va.: American Association of Zoological Parks and
Aquariums. p. 83-88.
Lyons J. 1991. Lyons on horses: John Lyons‟ proven conditioned-response training program. New York:
Doubleday. 228p.
Mellen J, Ellis S. 1996. Animal learning and husbandry training. In: Kleiman D, Allen M, Thompson K,
Lumpkin S, editors. Wild mammals in captivity: Principles and techniques. Chicago: The University of
Chicago Press. p. 88-99.
Mellen J, Sevenich MacPhee M. (2001). Philosophy of environmental enrichment: Past, present, and
future. Zoo Biology 20: 211-226.
Pryor K. 1984. Don‟t shoot the dog! Simon & Schuster: New York.
Pryor K. 1995. On behavior. North Bend: Sunshine Books, Inc.
Ramirez K. 1999. Animal training: Successful animal management through positive reinforcement.
Chicago: Ken Ramirez and The Shedd Aquarium. 578 p.
Reichard T, Shellabarger W, Laule G. 1992. Training for husbandry and medical purposes. In: AAZPA
Annual Conference Proceedings. Wheeling, W.Va.: American Association of Zoological Parks and
Aquariums. p. 396-402.
Reynolds G. 1975. A primer of operant conditioning. Palo Alto: Scott, Foresman and Co.
Sevenich MacPhee M, Mellen J. 2000. Framework for planning, documenting, and evaluating enrichment
programs (and the director‟s, curator‟s, and keeper‟s roles in the process). In: AAZPA Annual
Conference Proceedings. Wheeling, W.Va.: American Association of Zoological Parks and
Aquariums.
Shepherdson DJ. 1998. Tracing the path of environmental enrichment in zoos. In: Shepherdson DJ,
Mellen JD, Hutchins, M, editors. Second nature: Environmental enrichment for captive animals.
Washington, DC: Smithsonian Institution Press. p. 1-12.
Shepherdson D, Carlstead K. 2000. When did you last forget to feed your tiger? In: AAZPA Annual
Conference Proceedings. Wheeling, W.Va.: American Association of Zoological Parks and
Aquariums.
Stevens B, Groff A, Joseph S, Mellen J, Ogden J, Plasse R. 2000. Evolving a new species of animal care
professional: Combining AZA expertise with Disney leadership. In: AAZPA Annual Conference
Proceedings. Wheeling, W.Va.: American Association of Zoological Parks and Aquariums.
Wilkes G. 1994. A behavior sampler. North Bend: Sunshine Books, Inc.
COATIS/RACCOONS
CACOMISTLE/RINGTAIL
Behavioral/social
Visual access to contra specifics (DAF animals)
Visual access to decoys & stuffed toys
Window walker
Information taken from: Institution N, Institution O‟s Enrichment Online*, Institution K
Following parturition, efforts should be made to keep the environment quiet and stable for at least two
weeks, allowing the female to bond with the offspring. Females will aggressively defend the nest if they
feel threatened, so only staff familiar to the kinkajou should work in the area if possible. Husbandry efforts
should be kept to a minimum while maintaining good sanitation. This should continue until the female is
comfortable and relaxed around staff. If the male is present in the enclosure, he will have no active part in
rearing the offspring, but also will defend the nest if the female is threatened.
Kinkajou Young: The newborn kinkajou is altricial and should begin to nurse within a few hours of birth.
Typical birth weights range between 150 and 180 grams. It is not unusual to see the newborn lying away
from the mother in the same nest box for extended periods, especially in hot weather. It will lie next to or
on top of the dam and nurse frequently throughout the day and night and will sometimes favor one teat
over the other. If the diet of the female has not yet been increased, it must be increased to maintain
lactation and provide proper nutrition for the infant. The diet increase should range between 35 and 40%
of the female‟s maintenance diet; all dietary items should be increased equally. If the female loses an
infant, she typically will have an estrus cycle within a few days.
Young kinkajous‟ eyes begin opening at about 1 week of age. Weight should increase steadily
reaching ~200 – 270g at 1 week, 600 – 800g at 6 weeks, and 1.3 – 1.7kg at 6 months when they are
roughly 75% adult size. The young become independently mobile at about 5 to 6 weeks and will begin
showing an interest in solid food being eaten by their mother around 8 weeks of age. At about 10 to 12
weeks of age they will begin to consume solid foods taken from their mother and are typically weaned by
14 to 16 weeks. A young kinkajou will continue nursing as long as the mother allows, even after they have
begun consuming the majority of their calories from solid foods. Food amounts offered should be
increased to accommodate weanlings.
I. Historical Data (Attach additional sheets as needed & attach pertinent medical
records.)
Species: _________________
Stud Book# ISIS#
Age/Birth date: Sex Weight: Acquisition: (Circle)
(Circle) Kg
(Circle) Actual or Estimated M F (Circle) Actual or Captive Born or
Estimated
Wild Captured
Date & Time of Death post mortem interval __________hrs
Site/Enclosure_________________________________________
1. Was animal euthanized? (Circle) Y or N If so, what method? _____________________________
3. Member of Group? (Circle) Y or N Number in Group # Sick # Dead ______
4. Vaccinations:
_____________________________________________________________________________
Additional History: (Signs, stress factors, previous disease, treatments, pertinent feed or feed additives, time period animal was on
premises, clinical lab results).
4. Respiratory System (pharynx, larynx, nasal passages, trachea, bronchi, lungs, hilar lymph
nodes).
6. Cardiovascular System (pericardium, heart: valves & chambers, aorta, large vessels
7. Digestive System (Mouth, teeth, esophagus, stomach, intestines, liver, pancreas, mesenteric
lymph nodes). Neonates: is milk present in the stomach?).
10. Endocrine System (thyroids, parathyroids, adrenals, pituitary, pineal gland-if found
11. Nervous System (brain, meninges/dura mater, spinal cord, peripheral nerves