Course Reader Week 4
Course Reader Week 4
MOOC
Aquaponics - the circular food production system
Course reader
Week 4 – Hydroponics Part 1
4.1.2 SUBSTRATES................................................................................................................................................... 2
4.1.2.1 Light expanded clay aggregate (LECA) ............................................................................................... 3
4.1.2.2 Volcanic gravel (tuff) .......................................................................................................................... 3
4.1.2.3 Limestone gravel ................................................................................................................................ 3
4.1.2.4 Vermiculite ......................................................................................................................................... 3
4.1.2.5 Perlite ................................................................................................................................................. 3
4.1.2.6 Pumice ................................................................................................................................................ 3
4.1.2.7 Rock wool ........................................................................................................................................... 4
4.1.2.8 Coconut fibre (or coir) ......................................................................................................................... 4
4.1.4 REFERENCES................................................................................................................................................. 10
4.2.4 REFERENCES................................................................................................................................................. 17
4.3 NUTRIENT SUPPLY .................................................................................................................................... 18
4.3.1 PLANT REQUIREMENTS ................................................................................................................................... 18
4.3.1.1 Essential nutrient elements .............................................................................................................. 18
4.3.1.2 Nutrient availability and pH ............................................................................................................. 21
4.3.1.3 Nutritional disorders in plants .......................................................................................................... 22
4.3.4 REFERENCES................................................................................................................................................. 31
4.1 Hydroponic Systems
Table 1: Classification of soil-independent plant cultivation systems (Adapted after Maucieri et al, 2019)
Aeroponic
4.1.2 Substrates
Depending on the hydroponic system, a different substrate is more or less suitable. The substrate may
be organic, inorganic, or synthetic (Table 1). It needs to have an adequate surface area while remaining
permeable for water and air, thus allowing bacterial growth, water flow, and root respiration. It must
be non-toxic, have a neutral pH, and be resistant to mould growth. It must also not be so lightweight
that it floats. Water retention, aeration and pH balance are all aspects that vary depending on the
substrate. Water is retained on the surface of the particles and within the pore space, so water
retention is determined by particle size, shape, and porosity (Table 2). The smaller the particles, the
greater the surface area and pore space, and hence the greater the water retention. Irregularly shaped
particles have a lager surface area and hence higher water retention than smooth, round particles.
Porous materials can store water; therefore, water retention is high. While the substrate must be
capable of good water retention, it must also be capable of good drainage. Therefore, too fine
materials must be avoided in order to prevent excessive water retention and lack of oxygen (Resh
2013, Maucieri et al. 2019).
Substrates can be classified as either granular or fibrous. Granular substrates include light expanded
clay aggregate, gravel, vermiculite, perlite, and pumice. Fibrous substrates include rock wool and
coconut fibre. Water is mainly held in the micropore space of a substrate, while rapid drainage and air
entry is facilitated by the macropores (Drzal et al. 1999). An adequate combination of large and small
pores is therefore essential (Raviv et al. 2002). Granular substrates have high macroporosity (air
availability) but comparatively low microporosity (water availability), while fibrous substrates have
high microporosity but comparatively low macroporosity (Maucieri et al., 2019).
4.1.2.4 Vermiculite
Vermiculite is a micaceous mineral which expands when heated above 1000 ⁰C. The water turns to
steam, forming small, porous, sponge-like kernels. Vermiculite is very light in weight and can absorb
large quantities of water. Chemically, it is a hydrated magnesium-aluminium-iron silicate. It is neutral
in reaction with good buffering properties, and has a relatively high cation exchange capacity and thus
can hold nutrients in reserve and later release them. It also contains some magnesium and potassium,
which is available to plants (Resh 2013).
4.1.2.5 Perlite
Perlite is a siliceous material of volcanic origin, mined from lava flows. It is heated to 760 ⁰C, which
turns the small amount of water into steam, thereby expanding the particles to small, sponge-like
kernels. Perlite is very lightweight and will hold three to four times its weight of water. It is essentially
neutral, with a pH of 6.0–8.0, but with no buffering capacity; unlike vermiculite, it has no cation
exchange capacity and contains no minor nutrients. It should not to be used on its own, but rather
mixed with another substrate in order to improve drainage and aeration (Resh 2013).
4.1.2.6 Pumice
Pumice, like perlite, is a siliceous material of volcanic origin and has essentially the same properties.
However, it is the crude ore after crushing and screening, without any heating process, and therefore
it is heavier and does not absorb water as readily, since it has not been hydrated (Resh 2013).
Non-recirculating system:
In industrial cultivation, there are often non-recovery systems in use to achieve optimal yield. The
plants are always supplied with fresh and equal adjusted nutrient solution. Nothing is circulated, e.g.
to avoid the spread of pathogens. However, this process consumes much more water and more
nutrients get lost.
Recirculating system:
The nutrient solution is collected and returned to the plants via a pump. By this, resource consumption
is much lower. However, a recirculating system is harder to control and if something happens such as
pest or pathogen infestation, is harder to deal with it.
As for the role of the design of the hydroponic component on the overall performance and water
consumption of aquaponic systems, a literature review by Maucieri et al. 2018 found that NFT is less
efficient than media bed or DWC hydroponics, although the results were not unequivocal. The
hydroponic component directly influences water quality, which is essential for fish rearing, and is also
one of the main sources of water loss by plant evapotranspiration. The design of the hydroponic
Figure 1: Tomato transplants growing in a media bed container system with drip irrigation and LECA substrate
(source: https://commons.wikimedia.org/wiki/Category:Hydroponics#/media/File:Hydroponic_Farming.jpg)
There are different techniques for delivering nutrient-enriched water to media beds. It can be simply
trickled from drippers attached to pipes uniformly distributed on the medium (Figure 1). Alternatively,
a method called flood-and-drain (or ebb-and-flow) causes the media beds to be periodically flooded
with water which then drains back to a reservoir. The alternation between flooding and draining
ensures that the plants have fresh nutrients and adequate air (and thus oxygen) flow in the root zone.
It also ensures that enough moisture is in the media bed at all times so the bacteria can thrive in their
optimal conditions. The nature of a flood-and-drain media bed creates three separate zones which are
differentiated by their water and oxygen content (Somerville et al. 2014b):
Figure 4: Sloping NFT channels. The NFT channel is 12.5 m long and was fed with water from the adjacent fish
tank. No nutrients were supplemented. One can observe the increasing nutrient limitation along the channel.
Figure 5: Basil and other plants growing in the DWC system in the CDC South Aquaponics greenhouse in Brooks,
Alberta (source: https://commons.wikimedia.org/wiki/File:CDC_South_Aquaponics_Raft_Tank_1_2010-07.jpg)
In aeroponics, the plants are grown and nourished by suspending their root structures in air and
regularly spraying them with a nutrient solution. There are two main types of aeroponics: (i) high
pressure and (ii) low pressure, the main difference being the droplet size of the mist used in each case.
Low-pressure aeroponics uses low-pressure, high-flow pumps, whereas high-pressure aeroponics uses
high-pressure (around 120 PSI), low-flow pumps to atomize water and create water droplets of 50
4.1.4 References
Drzal, M.S., Keith Cassel, D. & Fonteno, W.C. 1999. Pore fraction analysis: A new tool for substrate
testing. Acta Horticulturae 481, 43-54.
Lee, S. & Lee, J. 2015. Beneficial bacteria and fungi in hydroponic systems: Types and characteristics of
food production methods. Scientia Horticulturae 195, 206-215.
Li, Q., Li, X., Tang, B. & Gu, M. 2018. Growth responses and root characteristics of lettuce grown in
aeroponics, hydroponics, and substrate culture. Horticulturae 4 (4), 35.
Maucieri, C., Nicoletto, C., Junge, R., Schmautz, Z., Sambo, P. & Borin, M. 2018. Hydroponic systems
and water management in aquaponics: A review. Italian Journal of Agronomy 13: 1012.
Maucieri, C., Nicoletto, C., van Os, E., Anseeuw, D., Van Havermaet., and Junge, R. (2019) Hydroponic
Technologies. In: Aquaponics Food Production Systems: Combined Aquaculture and Hydroponic
Production Technologies for the Future. Goddek, S., Joyce, A., Kotzen, B., Burnell G.M. (Eds.). pp. 77-
110. Springer Nature Switzerland AG. ISBN 978-3-030-15942-9.
NASA 1991. Technical Reports Server (NTRS). ntrs.nasa.gov. Retrieved 2020-12-19.
Raviv, M., Wallach, R., Silber, A. & Bar-Tal, A. 2002. Substrates and their analysis. In Passam, H. & Savvas,
D. (eds.) Hydroponic Production of Vegetables and Ornamentals. Embryo Publications, Athens, pp. 25-
105.
Resh, H.M. 2013. Hydroponic Food Production: A Definitive Guidebook for the Advanced Home
Gardener and the Commercial Hydroponic Grower (7th edition). Newconcept Press, Mahwah, SA.
Somerville et al. 2014b. Design of aquaponics units. In Somerville, C., Cohen, M., Pantanella, E.,
Stankus, A. & Lovatelli, A. Small-Scale Aquaponic Food Production – Integrated Fish and Plant Farming.
FAO Fisheries and Aquaculture Technical Paper No. 589. Food and Agriculture Organization of the
United Nations, Rome, pp. 35-74.
Somerville et al. 2015a. Additional topics on aquaponics. In Somerville, C., Cohen, M., Pantanella, E.,
Stankus, A. & Lovatelli, A. Small-Scale Aquaponic Food Production – Integrated Fish and Plant Farming.
FAO Fisheries and Aquaculture Technical Paper No. 589. Food and Agriculture Organization of the
United Nations, Rome, pp. 141-155.
Somerville et al. 2014c. Plants in aquaponics. In Somerville, C., Cohen, M., Pantanella, E., Stankus, A. &
Lovatelli, A. Small-Scale Aquaponic Food Production – Integrated Fish and Plant Farming. FAO Fisheries
and Aquaculture Technical Paper No. 589. Food and Agriculture Organization of the United Nations,
Rome, pp. 83-102.
Figure 6 illustrates the basic anatomy of a plant. The hypocotyl is the portion of the stem which at its
base links with the root. At the other end of the stem is the terminal bud, or apical bud, which is the
growing point. The stem is normally divided into nodes and internodes. The nodes hold one or more
leaves, which are attached to the stem by petioles, as well as buds which can grow into branches with
leaves or flowers. The internodes distance one node from another. The stem and its branches allow
leaves to be arranged to maximize exposure to sunlight, and flowers to be arranged to best attract
pollinators. Branching arises from the activity of apical and axillary buds. Apical dominance occurs
when the shoot apex inhibits the growth of lateral buds so that the plant may grow vertically. The
shoots, which bear the leaves, flowers, and fruit, grow towards a light source. The leaves usually
contain pigments and are the sites of photosynthesis. The leaves also contain stomata, pores through
which water exits and through which gas exchange occurs (carbon dioxide in and oxygen out).
4.2.2.1 Photosynthesis
All green plants generate their own food using photosynthesis. Photosynthesis is the process by which
plants are able to use light to produce energy and carbohydrates through the fixation of CO2:
6 𝐶𝑂2 + 6 𝐻2 𝑂 → 𝐶6 𝐻12 𝑂6 + 6 𝑂2
Chloroplasts are cell organelles that contain chlorophyll, a pigment that uses energy from sunlight to
create high-energy sugar molecules such as glucose. Once created, the sugar molecules are
transported throughout the plant where they are used for all the physiological processes such as
growth, reproduction, and metabolism. Photosynthesis requires light, carbon dioxide, and water.
4.2.2.2 Respiration
The process of respiration in plants involves using the sugars produced during photosynthesis plus
oxygen to produce energy for plant growth:
While photosynthesis takes place in the green parts only, respiration occurs in all parts of the plant.
Plants obtain oxygen from the air through the stomata, and respiration takes place in the mitochondria
of the cell in the presence of oxygen. Plant respiration occurs 24 hours per day, but night respiration
is more evident since the photosynthesis process ceases. During the night, it is very important that the
temperature is cooler than during the day because this reduces the rate of respiration, and thus allows
plants to accumulate glucose and synthesise other substances from it that are needed for their growth.
High night temperatures cause high respiration rates, which can result in flower damage and poor
plant growth.
4.2.2.4 Transpiration
Transpiration is the loss of water from a plant in the form of water vapour. This water is replaced by
additional absorption of water through the roots, leading to a continuous column of water inside the
plant. The process of transpiration provides the plant with evaporative cooling, nutrients, carbon
dioxide entry, and water. When a plant is transpiring, its stomata are open, allowing gas exchange
between the atmosphere and the leaf: water vapour can leave the leaf, and carbon dioxide (CO2) can
enter. Temperature greatly influences transpiration rate. As air temperature increases, the water
holding capacity of that air increases sharply. Warmer air will therefore increase the driving force for
transpiration, while cooler air will decrease it (Sterling 2004).
4.2.2.5 Phototropism
Phototropism is a directional response of plants to grow towards (positive), or in some cases away
from (negative), a source of light (Liscum et al. 2014). Shoots, or above-ground parts of plants,
generally display positive phototropism. This response helps the green parts of the plant to get closer
to a source of light energy, which is then used for photosynthesis. Roots, on the other hand, will tend
to grow away from light. The hormone controlling phototropism is auxin. Its principal function is to
stimulate increase in cell length, especially near stem and root tips. In stems illuminated from above,
cells undergo equal rates of elongation, resulting in vertical growth. But when lit from one side, stems
change direction because auxin accumulates in the shaded side, causing the cells there to grow faster
than those toward the light. Phototropism can therefore cause plants to grow tall and thin as they
stretch and bend to find an adequate light source.
4.2.2.6 Photoperiodism
Photoperiodism is the regulation of physiology or development in response to day length, which allows
some plant species to flower – switch to reproductive mode – only at certain times of the year. Plants
generally fall into three photoperiod categories: long-day plants, short-day plants, and day-neutral
plants. The photoperiodism can also affect the growth of roots and stems, and the loss of leaves
(abscission) during different seasons. Long-day plants generally flower during the summer months
when nights are short. Examples of long-day plants are cabbages, lettuces, onions and spinach. On the
4.2.3.1 Light
Light transmission, of the appropriate quantity and quality, is crucial for optimal photosynthesis,
growth, and yield. The sun produces photons with a wide range of wavelengths (Figure 8): UVC 100-
280 nanometres (nm), UVB 280-315 nm, UVA 315-400 nm, visible or photosynthetically active
radiation (PAR) 400-700 nm, far-red 700-800 nm, and infrared 800-4000 nm. Within the visible range
of the spectrum the wavebands can be further divided into colours: blue 400-500 nm, green 500-600
nm, and red 600-700 nm.
Chlorophyll a is the most common photosynthetic pigment and absorbs blue, red and violet
wavelengths in the visible spectrum. It participates mainly in oxygenic photosynthesis in which oxygen
is the main by-product of the process. Chlorophyll b primarily absorbs blue light and is used to
complement the absorption spectrum of chlorophyll a by extending the range of light wavelengths a
Plant light responses have evolved to help plants acclimatise to a wide variety of light conditions. All
plants respond differently to high and low light conditions, but some species are adapted to perform
optimally under full sun, while others prefer more shade. In darkness, plants respire and produce CO2.
As the light intensity increases, the photosynthetic rate also increases, and at a certain light intensity
(the light compensation point), the rate of respiration is equal to the rate of photosynthesis (no net
uptake or loss of CO2). In addition to light intensity, the colour of light also influences the rate of
photosynthesis. Plants are able to use wavelengths between 400 nm and 700 nm for photosynthesis.
This waveband is called photosynthetically active radiation (PAR) (Davis 2015).
The amount of light available for plants is highly variable across the globe and through the seasons.
For example, at low solar elevations the light must pass through a larger volume of atmosphere before
it reaches the earth’s surface, which causes changes in the spectrum, as the atmosphere filters
proportionately more of the shorter wavelength of light, so it filters more UV than blue, and more blue
than green or red. Changes in spectral composition with season and location influence plant light
responses (Davis 2015).
The ideal water temperature range for most vegetables is 14-22 ⁰C, though the optimal growing
temperatures varies between different plant species. Generally, it is the water temperature that has
the greatest effect on the plants, rather than the air temperature. The bacteria and other micro-
organisms that inhabit aquaponic systems also have a preferred temperature range. For example, the
nitrification bacteria prefer an average temperature of approximately 20 ⁰C (Somerville et al. 2014c).
The availability of many nutrients depends on the pH of the water. In general, the tolerance range for
most plants is pH 5.5-7.5. If the pH goes outside of this range, plants experience nutrient lockout, which
means that although the nutrients are present in the water, the plants are unable to use them. This is
especially true for iron, calcium and magnesium. However, there is evidence that nutrient lockout is
less common in mature aquaponic systems than in hydroponics, because aquaponics is an entire
ecosystem, while hydroponics is a semi-sterile undertaking. Consequently, in aquaponic systems there
are biological interactions occurring between the plant roots, bacteria and fungi that may allow
nutrient uptake even at higher levels than pH 7.5. However, the best course of action is to attempt to
maintain slightly acidic pH (6–7), but understand that higher pH (7–8) may also function (Somerville et
al. 2014c).
Davis, P. 2015. Lighting: The Principles. Agriculture and Horticulture Development Board Technical
Guide.
Dramm, 2014. Dissolved Oxygen in the Greenhouse. White Paper.
Körner, O., & Challa, H. (2003). Process-based humidity control regime for greenhouse crops.
Computers and electronics in agriculture, 39(3), 173-192.
Liscum, E., Askinosie, S. K., Leuchtman, D. L., Morrow, J., Willenburg, K. T., & Coats, D. R. (2014).
Phototropism: growing towards an understanding of plant movement. The Plant Cell, 26(1), 38-55.
Mortensen, L. M. 1987. CO2 enrichment in greenhouses. Crop responses. Scientia Horticulturae, 33(1-
2), 1-25.)
Mortensen, L. M. (1986). Effect of relative humidity on growth and flowering of some greenhouse
plants. Scientia horticulturae, 29(4), 301-307
Rauscher, F. 2017. Improving the Flavor of Crops with Photoperiodism. Maximum Yield magazine.
Somerville et al. 2014c. Plants in aquaponics. In Somerville, C., Cohen, M., Pantanella, E., Stankus, A. &
Lovatelli, A. Small-Scale Aquaponic Food Production – Integrated Fish and Plant Farming. FAO Fisheries
and Aquaculture Technical Paper No. 589. Food and Agriculture Organization of the United Nations,
Rome, pp. 83-102.
Sterling, T. M. (2004) Transpiration – Water Movement through Plants’
Willits, D. H., & Peet, M. M. 1989. Predicting yield responses to different greenhouse CO2 enrichment
schemes: cucumbers and tomatoes. Agricultural and Forest Meteorology, 44(3), 275–293.
Plants normally obtain their water and mineral needs from the soil. In soilless cultivation they need to
be supplied with water and minerals. In aquaponics, the situation is complicated by the fact, that the
system water contains a highly complex mixture of organic and inorganic compounds originating from
fish waste and fish feed. There are two major categories of nutrients: macronutrients and
micronutrients (Figure 10). Both types are essential, but in differing amounts. Much larger quantities
of the six macronutrients are needed compared with the micronutrients, which are only needed in
trace amounts (Jones & Olson-Rutz 2016).
Figure 10: Classification of essential elements (nutrients) that are needed for the plant growth
Macronutrients are divided into three groups. The terms 'primary' and 'secondary' refer to the
quantity, and not to the importance of a nutrient. A lack of a secondary nutrient is just as detrimental
to plant growth as a deficiency of any one of the three primary nutrients, or a deficiency of
micronutrients. A basic understanding of the function of each nutrient is important in order to
appreciate how they affect plant growth (Table 3). A good orientation of how much of particular
nutrient is required gives the elemental composition of plant material (Figure 11). If nutrient
deficiencies occur, it is important to be able to identify which element is lacking in the system and
adjust it accordingly by adding supplemental fertilizer or increasing.
Oxygen O is a component of many organic and inorganic compounds in plants. Only a few organic
(O) compounds, such as carotene, do not contain O. It can be acquired in many forms: O 2 and
CO2, H2O, NO3-, H2PO4- and SO42−. It is also involved in anion exchange between roots and
the external medium. Plants produce O2 during photosynthesis but then require O 2 to
undergo aerobic respiration and break down this glucose to produce ATP.
Nitrogen N is part of a large number of organic compounds, including amino acids, proteins,
(N) coenzymes, nucleic acids, and chlorophyll. It is essential for photosynthesis, cell growth,
and metabolic processes. Usually, dissolved N is in the form of nitrate, but plants can
utilize moderate quantities of ammonia and even free amino acids.
Phosphorus P is part of the phospholipid backbone of nucleic acids (such as DNA, deoxyribonucleic
(P) acid), and adenosine triphosphate (ATP, the molecule that stores energy in the cells), and
is contained in certain coenzymes. It is essential for photosynthesis, as well as the
formation of oils and sugars, and encourages germination and root development in
seedlings. As young tissues require more energy, it is particularly important for juveniles.
Potassium K acts as a coenzyme or activator for many enzymes. Protein synthesis requires high
(K) potassium levels. It is used for cell signalling via controlled ion flow through membranes. K
also controls the opening of the stomata, and is involved in the development of flowers
and fruit. It is also involved in the production and transportation of sugars, water uptake,
disease resistance, and the ripening of fruits. K does not form a stable structural part of
any molecules inside plant cells.
Calcium Ca is found in cell walls as calcium pectate, which cements together primary walls of
(Ca) adjacent cells. It is involved in strengthening stems, and contributes to root development.
Required to maintain membrane integrity and is part of the enzyme α-amylase. It
precipitates as crystals of calcium oxalate in vacuoles. Sometimes interferes with the
ability of magnesium to activate enzymes.
Magnesium Mg is an essential part of the chlorophyll molecule. Without Mg, chlorophyll cannot
(Mg) capture the solar energy needed for photosynthesis. Mg is also required for activation of
many enzymes needed for growth. It is essential to maintain ribosome structure, thus
contributing to protein synthesis.
Sulphur S is incorporated into several organic compounds including amino acids (methionine and
(S) cysteine) and proteins (like photosynthetic enzymes). Coenzyme A and the vitamins
thiamine and biotin also contain S.
Boron B is one of the less understood nutrients. It is used with Ca in cell wall synthesis and is
(B) essential for cell division. B increases the rate of transport of sugars from mature plant
leaves to actively growing regions (growing point, roots, root nodules in legumes) and also
to developing fruits. B requirements are much higher for reproductive growth as it helps
with pollination, and fruit and seed development. Other functions include N metabolism,
formation of certain proteins, regulation of hormone levels and transportation of K to
stomata (which helps regulate internal water balance).
Copper Cu activates some enzymes which are involved in lignin synthesis and it is essential in
(Cu) several enzyme systems. It is also required in photosynthesis, plant respiration, and assists
in plant metabolism of carbohydrates and proteins. Cu also serves to intensify flavour and
colour in vegetables, and colour in flowers.
Iron Fe is required for the synthesis of chlorophyll and some other pigments and is an essential
(Fe) part of ferredoxins. Ferredoxins are small proteins containing Fe and S atoms that act as
electron carriers in photosynthesis and respiration. Fe is also part of the nitrate reductase
and activates certain other enzymes.
Manganese Mn activates one or more enzymes in fatty acid synthesis, the enzymes responsible for
(Mn) DNA and RNA formation, and the enzymes involved in respiration. It participates directly in
the photosynthetic production of O2 from H2O and is involved in chloroplast formation,
nitrogen assimilation and synthesis of some enzymes. It plays role in pollen germination,
pollen tube growth, root cell elongation, and resistance to root pathogens.
Molybdenum Mo acts as an electron carrier in the conversion of nitrate to ammonium before it is used
(Mo) to synthesize amino acids within the plant. It is essential for nitrogen fixation. Within the
plant, Mo is used in conversion of inorganic phosphorus into organic forms.
Nickel Ni is the metal cofactor of urease-enzymes: without it they are inactive (Polacco et al.
(Ni) 2013). Ureases are present in bacteria, fungi, algae, and plants - but they are absent from
fish and other animals. Urease enzymes are responsible for the catabolic detoxification of
urea, potentially phytotoxic waste excreted by the fish.
Zinc Zn activates a series of enzymes that are responsible for the synthesis of certain proteins,
(Zn) including some important enzymes like alcohol dehydrogenase, lactic acid dehydrogenase
etc. It is used in the formation of chlorophyll and some carbohydrates, conversion of
starches to sugars and its presence in plant tissue helps the plant to withstand cold
temperatures. Zn is required for the formation of auxins, which are hormones which help
with growth regulation and stem elongation.
Table 4: Absorbed nutrient forms and approximate concentrations in dry plant tissue
(adapted from Jones & Olson-Rutz 2016)
Element Form absorbed Concentration range in dry plant
tissue (%)
Nitrogen (N) NO3- (nitrate) / NH4+ (ammonium) 1–5
- 2-
Phosphorus (P) H2PO4 , HPO4 (phosphate) 0.1 – 0.5
Potassium (K) K+ 0.5 – 0.8
Calcium (Ca) Ca2+ 0.2 – 1.0
Magnesium (Mg) Mg2+ 0.1 – 0.4
Sulphur (S) SO42- (sulfate) 0.1 – 0.4
Boron (B) H3BO3 (boric acid) / H2BO3- (borate) 0.0006 – 0.006
-
Chlorine (Cl) Cl (chloride) 0.1 – 1.0
Copper (Cu) Cu2+ 0.0005 – 0.002
Iron (Fe) Fe2+, Fe3+ 0.005 – 0.025
Manganese (Mn) Mn2+ 0.002 – 0.02
Molybdenum (Mo) MoO42- (molybdate) 0.000005 – 0.00002
Nickel (Ni) Ni2+ 0.00001 – 0.0001
2+
Zinc (Zn) Zn 0.0025 – 0.015
The pH of the solution determines the availability of the various elements to the plant (Figure 12). The
pH value is a measure of acidity. A solution is acidic if the pH is less than 7, neutral if the pH is at 7, and
alkaline if the pH is above 7. Since pH is a logarithmic function, a one-unit change in pH means a 10-
fold change in H+ concentration. Therefore, any small change in pH can have a large effect on the ion
availability to plants. Most plants prefer a pH between 5.5 and 6.5 for optimum nutrient uptake.
Figure 12: The effect of pH on the availability of plant nutrients (source: Roques et al. 2013)
One aspect of the diagnosis is the distinction between mobile (Mg, P, K, Zn, N) and immobile elements
(Ca, Fe, S, B, Cu, Mn). All nutrients move relatively easily from the root to the growing portion of the
plant through the xylem. However, mobile elements can also be repositioned from older leaves to the
actively growing region of the plant (younger leaves), when the deficiency occurs. As a result, the
deficiency symptoms first appear on the older leaves. Conversely, immobile elements, once
incorporated into the various structures, cannot be disassembled from these structures and re-
transported through the plant. Deficiency symptoms first appear on the upper young leaves of the
plant. Other aspects of diagnosis and their terminology are summarized in Table 5. Descriptions of
deficiency and toxicity symptoms for essential elements are presented in Table 6.
Table 5: Terminology used for the description of symptoms of nutritional disorders (adapted from Resh 2013)
Term Description
Generalized Symptoms spread over entire plant or leaf
Localized Symptoms limited to one area of plant or leaf
Drying Necrosis—scorched, dry, papery appearance
Marginal Chlorosis or necrosis—on margins of leaves; usually spreads inward as symptom
progresses
Interveinal chlorosis Chlorosis (yellowing) between veins of leaves
Mottling Irregular blotchy pattern of indistinct light (chlorosis) and dark areas; often
associated with virus diseases
Spots Discoloured area with distinct boundaries adjacent to normal tissue
Colour of leaf Often a particular coloration occurs on the lower surface of the leaves, for
undersides example, phosphorus deficiency—purple coloration of leaf undersides
Cupping Leaf margins or tips may cup or bend upward or downward
Checkered (reticulate) Pattern of small veins of leaves remaining green while interveinal tissue
yellows— manganese deficiency
Brittle tissue Leaves, petioles, stems may lack flexibility, break off easily when touched—
calcium or boron deficiency
Soft tissue Leaves very soft, easily damaged—nitrogen excess
Dieback Leaves or growing point dies rapidly and dries out—boron or calcium
deficiencies
Stunting Plant shorter than normal
Spindly Growth of stem and leaf petioles very thin and succulent
Nutrients enter an aquaponic system via added water and fish feed (Schmautz et al. 2016). In terms of
elemental composition, fish feed contains about 7.5 % nitrogen, 1.3% phosphorus and 46% carbon
(Schmautz, unpublished data). In terms of organic compounds, fish feed contains proteins (fishmeal or
plant based), fats (fish oil, plant oils) and carbohydrates (Boyd 2015). Herbivorous fish (like carp) and
omnivorous fish (like tilapia) need only about 25% protein in their feed, compared to carnivorous fish
which require around 55% protein (Boyd 2015). Both fishmeal and soya are unsustainable (for different
reasons), so there is intense research towards finding suitable fishmeal replacements and plant-based
diets (Boyd 2015; Davidson et al. 2013; Tacon & Metian 2008).
If the feeding ratios are calculated correctly, all the feeds added to the system are eaten, and only
whatever is not used for growth and metabolism is excreted (Figure 13). The proportion of excreted
nutrients also depends on the quality and digestibility of the diet (Buzby & Lin 2014). The digestibility
of the fish feed, the size of the faeces, and the settling ratio are all very important for the system
operation (Yavuzcan Yildiz et al. 2017). Therefore, the nutrient composition of aquaponic system
water, resulting from the quality of the added water, the added fish feeds, and the entire metabolic
reactions in the system, is extremely complex and does not always match the plant requirements.
However, the fish health and welfare should be of central concern, and fish feed should be chosen to
fit the fish species at each development stage according to their needs. The availability of nutrients
that can be assimilated by plants has to be regulated in a second step.
Figure 13: Environmental flow of nitrogen and phosphorus (in %) for (a) Nile Tilapia cage production (after
Montanhini Neto & Ostrensky 2015); (b) RAS production (data from Strauch et al. 2018). 'Unexplained'
denotes the fraction of N and P that could not be attributed to any category
The data in Table 7 show that most plant nutrients, but especially P and Fe, were at significantly lower
concentrations in the investigated aquaponic system as compared with the standard hydroponic
Unfortunately, interpretation of these data is very difficult. The reason is that very recently in plant
nutrition the nearly two-century-old 'Liebig's law' (plant growth is controlled by the scarcest resource)
has been superseded by complicated mathematical models that take the interactions between the
individual nutrient elements, compounds, and ions into account (Baxter 2015). These methods do not
allow a simple evaluation of the effects of changes in nutrient levels in a hydroponic or aquaponic
system. Also, we must bear in mind that a perfect formulation of nutritional requirements for a
particular crop does not exist. The nutritional requirements vary with variety, life cycle stage, day
length, and weather conditions (Bittszansky et al. 2016; Resh 2013; Sonneveld & Voogt 2009).
Very generally, for good plant growth in hydroponics, nitrogen concentration should stay above 165
mg/l N, phosphorus above 50 mg/l, and potassium above 210 mg/l (Resh 2013). In aquaponics, such
high concentrations are difficult to achieve for several relevant elements because of three reasons:
1. The higher the concentrations in the water, the higher is the loss of nutrients through water
exchange or sludge. However, even in closed system, a certain level of water exchange is
required, in order to compensate for evapotranspiration losses and to reduce accumulation of
unwanted components.
2. With the elevated concentration of nutrients in the water, components like salt or toxins
accumulate in the system as well.
3. Phosphorus reacts with calcium if this is present in higher concentrations and precipitates as
calcium phosphate.
Plants growing in the hydroponic unit of an aquaponic system have specific requirements which
depend on the plant variety and the growth stage (Resh 2013). Nutrients can be supplemented either
via the system water (Schmautz et al. 2016) or via foliar application (Roosta & Hamidpour 2011).
Table 7: Comparison of concentrations of nutrients in standard hydroponic solution and in water from a closed
aquaponic system (Schmautz, unpublished data)
Concentration [mg/l]
Aquaponics Hydroponics
(Schmautz, (optimized for Concentration ratio
unpublished) lettuce, Resh 2013) (hydroponic/aquaponic)
Macronutrients
N (as NO3-) 147 165 1.1
N (as NH4+) 2.8 15 5.4
3-
P (as PO4 ) 5.1 50 10
K (as K+) 84 210 2.5
Mg (as Mg2+) 18 45 2.5
Ca (as Ca2+) 180 190 1.1
S (as SO42-) 21 65 3.1
Micronutrients
Fe (as Fe2+) 0.2 4 20
Zn (Zn2+) 0.2 0.1 0.5
B (as B[OH4]-) 0.1 0.5 5
Mn (as Mn2+) 1.4 0.5 0.4
Cu (as Cu2+) 0.1 0.1 1
2-
Mo (as MoO4 ) 0.002 0.05 25
Potassium (K) is not necessary for fish which leads to a low potassium composition of the fish feed and
to even lower levels of potassium available for the plants (Seawright et al. 1998). To supply potassium,
KOH pH buffer is often used, as the pH often decreases in aquaponics due to nitrification (Graber &
Junge 2009). This has the added benefit of raising the potassium levels, although it can be toxic to fish.
The LC50 value of acute fish toxicity was reported to be in the order of 80 mg/l. In aquaponic systems
planted with tomato, potassium accumulated mainly in the fruits (Schmautz et al. 2016).
Iron (Fe) is also often a limiting factor in aquaponics, therefore it can be added as a preventive measure
before the deficiencies become apparent. High concentrations of iron will not harm an aquaponic
system, although it may give a slight red colour to the water. In order to ensure easy uptake by plants,
iron has to be added as chelated iron, otherwise known as sequestered iron. There are different types
of iron chelates: Fe-EDTA, Fe-IDHA, Fe-DTPA, Fe-EDDHA and Fe-HBED. Iron can be added into the
system water (for example 2 mg L−1 once every two weeks) or sprayed directly on the leaves (foliar
application) of 0.5 g L−1) (Roosta & Hamidpour 2011).
The main source of calcium (Ca), magnesium (Mg), and sulphur (S) is tap water, which facilitates the
absorption by the plants as the nutrients are already available (Delaide et al. 2017). Nevertheless, these
elements are often at low levels in aquaponic systems (Graber & Junge 2009; Seawright et al. 1998,
Schmautz, unpublished data). Especially Ca is often a limiting factor in aquaponics, as it can only be
transported through active xylem transpiration. When conditions are too humid, calcium can be
available but locked out because the plants are not transpiring. Increasing air flow with vents or fans
can prevent this problem. Otherwise, calcium carbonate (CaCO3) or calcium hydroxide (Ca(OH)2) ought
to be supplemented.
Zinc (Zn) is used as part of the galvanisation process of some metal parts, which may be used in
construction of AP (fish tanks, bolts etc.), and it is found in fish waste. While zinc deficiencies are rare,
zinc toxicity can pose a problem in aquaponics, because while plants can tolerate an excess, fish
cannot. Levels of zinc should be kept between 0.03 - 0.05 mg/l. Most fish will be stressed at 0.1 to 1
mg/l, and will start dying at 4-8 mg/l. The best way to keep zinc levels within harmless range is to avoid
galvanised equipment (Storey 2018). Nevertheless, in some systems zinc deficiencies might occur. Zinc
deficiency can be alleviated by foliar application of chelated zinc (Treadwell et al. 2010).
The question thus arises whether it is necessary and effective to add nutrients to aquaponic systems
(Nozzi et al. 2018). Provided that the system is stocked with enough fish, and the pH is within correct
level it is usually not necessary to add nutrients for plants with a short cropping cycle which do not
produce fruits (e.g. leafy greens; Nozzi et al. 2018). In contrast, fruiting vegetables (e.g. tomatoes,
aubergines) require nutrient supplementation. The amount of required mineral fertilizers can be
calculating by using the HydroBuddy software (Fernandez 2016). In addition to our experience in
supplementing mineral nutrients, in the future commercially available organic hydroponic fertilizers
should be tested in order to define which ones do not harm fish. The treatment of the fish sludge in a
In most countries help will be available from government agencies to keep aquaponic farmers in line
with the law, and they should therefore seek comprehensive information from the competent
authorities concerning their particular situation.
The next level in terms of complexity and cost are tests using chemical reagents and a colour chart.
Here the sample is put into a small test tube and drops of reagents are added according to the
instructions. A reaction occurs and the colour of the solution in the test tube is compared to the colour
chart that comes with the kit. A more precise and advanced version of these tests measures the colour
with spectrophotometers.
Spectrometry is a method of quantitative analysis that utilises the absorbance of light. Usually a water
sample is filtered to remove suspended solids and a reagent specific to the desired test is added. This
is then placed inside a spectrophotometer for analysis. The reading given by the spectrophotometer
can then be related to known standard curves for that particular chemical parameter to give a
concentration. Some manufacturers also provide test kits for a quicker analysis, without the need to
use calibration curves, and these are available for a wide range of water quality parameters.
The most advanced and expensive approach to monitoring involves using probes and electronic
meters. The probes are connected to a digital electronic meter and submerged in the water.
Continuous online monitors can also be installed inside the fish tank, with a probe constantly in contact
with the water (Klinger-Bowen et al. 2011).
The chosen monitoring approach is usually associated with the size of the aquaponic system and the
level of productivity. Professional commercial systems usually employ continuous online monitors for
temperature, dissolved oxygen (DO), water level and electrical conductivity. On the other hand, hobby
backyard systems often rely on the simplest and cheapest approaches, such as test strips, or even just
visual inspections of water turbidity, oxygenation in biofilter, plant and fish health.
The goal is to maintain a healthy ecosystem with all parameters at levels that satisfy the requirements
for fish, vegetables, and bacteria simultaneously. There are occasions when the water quality will need
to be actively manipulated in order to meet these criteria and keep the system functioning properly.
Sampling/ monitoring
PHYSICAL PARAMETERS CHEMICAL PARAMETERS BIOLOGICAL PARAMETERS
details
Electrical Water
Time of Dissolved Ammonia Phosphate
conductivity temperature pH Nitrate [mg/L] Nitrite [mg/L] Appearance & Appearance of
Date sampling oxygen [mg/L] [mg/L] [mg/L] Mass of fish [g]
[μS/cm] [°C] behaviour of fish plants
(h:min)
SS1 SS2 SS3 SS1 SS2 SS3 SS1 SS2 SS3 SS1 SS2 SS3 SS1 SS2 SS3 SS1 SS2 SS3 SS1 SS2 SS3 SS1 SS2 SS3
Figure 14: An example of monitoring data log table. SS in the table stands for 'sample site'