Empirical models for predicting the excretion of nutrients (N and P) by aquatic metazoans: taxonomic differences in rates and element ratios

1. We developed empirical models for predicting the release of nutrients [nitrogen (N) and phosphorus (P)] by aquatic metazoans (zooplankton, mussels, benthic macroinvertebrates and fish). 2. The number of species represented in each model ranged from 9 to 74 (n = 40 – 1122), organism dry mass from 1 × 10^?5 to 8 × 10⁴ mg and water temperature from ?1.8 to 32 °C for all models. Organisms were from marine and freshwater (both lotic and lentic) environments. 3. Rates and ratios of nutrient excretion were modelled and intra‐ and intertaxon differences in excretion were examined. Rates of N and P excretion were not significantly different between marine and freshwater species within the same taxon (e.g. zooplankton). However, rates of excretion (as a function of organism dry mass and water temperature) were significantly different among different orders of zooplankton, mussels and fish. However, excretion of N was similar among different orders of benthic macroinvertebrates. 4. Detritivorous fish excreted both N and P at rates greater than all other taxa; whereas mussels excreted N and P generally at rates less than other taxa. There were no significant differences in the rate of N and P excretion between zooplankton and fish (i.e. the allometry of N and P excretion was similar between zooplankton and fish). 5. Molar N : P ratios of nutrients excreted increased with increasing organism dry mass for each group of metazoans, except for zooplankton and detritivorous fish (where N : P ratios declined with increasing organism dry mass). Molar N : P ratios in the excretions of aquatic metazoans were generally below the Redfield ratio of 16:1. 6. We examined the influence of variable abundance of zooplankton, benthic macroinvertebrates and fish on assemblage excretion rates. Rates of N and P excretion were calculated by applying our models to metazoan biomass and abundance data over seven consecutive years in two oligotrophic lakes. Rates of N and P excretion (g ha^?1 day^?1) increased linearly with increasing assemblage biomass (kg ha^?1). However, rates of N and P excretion were significantly and negatively correlated with the relative abundance of fish and positively correlated with the relative abundance of zooplankton.     

A metabolic theory of ecology applied to temperature and mass dependence of N and P excretion by common carp

Our study used a metabolic theory of ecology (MTE) to explore scaling of metabolic rates by body size and temperature, and to predict nutrient excretion by common carp (Cyprinus carpio). At high biomasses, common carp have negative impacts on water quality, and one mechanism is excretion of the nutrients N and P. We measured whole-body and mass-specific excretion rates during summer and winter for fish of different sizes (wet mass range 28–1,196 g) to produce an allometric scaling model capable of predicting excretion at different temperatures. We found positive relationships between both dissolved and total nutrient concentrations and fish wet mass in summer and winter, with greater excretion rates in summer (mean water temperature 24.2°C) than in winter (mean water temperature 9.2°C). Mass-specific excretion rates decreased with increasing fish size, consistent with the MTE, and the temperature-adjusted model explained more variation for N excretion than for P. The proportion of dissolved nutrients (NH₄ and PO₄) to total nutrients increased with increasing fish size. The significance of these models is that they can be used to predict population-based nutrient excretion by common carp when thermal history, fish density and size distribution in a water body are known.     

Organismal stoichiometry at the temporal scale: Seasonal variability shapes interspecific differences in fish

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Ecological responses to simulated benthic-derived nutrient subsidies mediated by omnivorous fish

1. Fish can play an important role in coupling benthic and pelagic habitats by consuming benthic prey and providing essential nutrients to algae in dissolved form. However, little is known about the factors affecting the magnitude of this nutrient subsidy. 2. Using laboratory and mesocosm experiments we evaluated how varying ingestion rates of bluegill sunfish (Lepomis macrochirus) affects fish excretion rates of both nitrogen (N) and phosphorus (P). During the 10‐week mesocosm experiment, we also evaluated how varying ingestion rates may affect plankton community dynamics, and nutrient flux between pelagic and benthic habitats. Lastly, bioenergetic/mass balance models were used to examine the nutrient stoichiometry of fish body composition and excretion products. 3. Under laboratory conditions, both N and P excretion rates increased with increased ingestion of benthic prey surrogates (earthworms). This effect was more pronounced for N than P. Furthermore, under the more realistic conditions of the mesocosm experiment ingestion rate had no significant effect on P excretion rate. 4. Increased fish ingestion rate in the mesocosm experiment increased total algal biomass and the flux of nutrients from the water column to sediments. Effects of variable ingestion were much stronger on periphyton biomass and algal sedimentation rates than on phytoplankton or zooplankton biomass or composition. 5. Fish body nutrient composition was greatly affected by ingestion rate. N content increased and P content decreased with ingestion rate. As a result, the N : P ratio of fish bodies also increased with ingestion rate. The N : P ratio of nutrients excreted by fish also increased with ingestion rate, counter to predictions of stoichiometric theory, which predicts that excreted N : P ratio is negatively correlated to body N : P. However, this finding can be explained by relaxing the assumption of constant nutrient assimilation rates, and our mass balance data suggest that assimilation rates vary indeed with ingestion rate. 6. Our study provides experimental evidence that translocation of benthic‐derived nutrients by fish can affect the flux of nutrients among habitats, while also suggesting that stoichiometry models need to better incorporate how variable ingestion rates affect nutrient assimilation and excretion rates.     

Biotic and abiotic controls on the ecosystem significance of consumer excretion in two contrasting tropical streams

1. Excretion of nitrogen (N) and phosphorus (P) is a direct and potentially important role for aquatic consumers in nutrient cycling that has recently garnered increased attention. The ecosystem‐level significance of excreted nutrients depends on a suite of abiotic and biotic factors, however, and few studies have coupled measurements of excretion with consideration of its likely importance for whole‐system nutrient fluxes. 2. We measured rates and ratios of N and P excretion by shrimps (Xiphocaris elongata and Atya spp.) in two tropical streams that differed strongly in shrimp biomass because a waterfall excluded predatory fish from one site. We also made measurements of shrimp and basal resource carbon (C), N and P content and estimated shrimp densities and ecosystem‐level N and P excretion and uptake. Finally, we used a 3‐year record of discharge and NH₄‐N concentration in the high‐biomass stream to estimate temporal variation in the distance required for excretion to turn over the ambient NH₄‐N pool. 3. Per cent C, N, and P body content of Xiphocaris was significantly higher than that of Atya. Only per cent P body content showed significant negative relationships with body mass. C:N of Atya increased significantly with body mass and was higher than that of Xiphocaris. N : P of Xiphocaris was significantly higher than that of Atya. 4. Excretion rates ranged from 0.16–3.80 μmol NH₄‐N shrimp^?1 h^?1, 0.23–5.76 μmol total dissolved nitrogen (TDN) shrimp^?1 h^?1 and 0.002–0.186 μmol total dissolved phosphorus (TDP) shrimp^?1 h^?1. Body size was generally a strong predictor of excretion rates in both taxa, differing between Xiphocaris and Atya for TDP but not NH₄‐N and TDN. Excretion rates showed statistically significant but weak relationships with body content stoichiometry. 5. Large between‐stream differences in shrimp biomass drove differences in total excretion by the two shrimp communities (22.3 versus 0.20 μmol NH₄‐N m^?2 h^?1, 37.5 versus 0.26 μmol TDN m^?2 h^?1 and 1.1 versus 0.015 μmol TDP m^?2 h^?1), equivalent to 21% and 0.5% of NH₄‐N uptake and 5% and <0.1% of P uptake measured in the high‐ and low‐biomass stream, respectively. Distances required for excretion to turn over the ambient NH₄‐N pool varied more than a hundredfold over the 3‐year record in the high‐shrimp stream, driven by variability in discharge and NH₄‐N concentration. 6. Our results underscore the importance of both biotic and abiotic factors in controlling consumer excretion and its significance for nutrient cycling in aquatic ecosystems. Differences in community‐level excretion rates were related to spatial patterns in shrimp biomass dictated by geomorphology and the presence of predators. Abiotic factors also had important effects through temporal patterns in discharge and nutrient concentrations. Future excretion studies that focus on nutrient cycling should consider both biotic and abiotic factors in assessing the significance of consumer excretion in aquatic ecosystems.     

Stoichiometry of nutrient excretion by fish: interspecific variation in a hypereutrophic lake

This study investigates how nutrient cycling rates and ratios vary among fish species, with a particular focus on comparing an ecologically dominant detritivore (gizzard shad) to other fishes in a productive lake. We also examined how nutrient cycling rates are mediated by body size (as predicted by allometry theory), and how variation in nutrient cycling is related to body and food nutrient contents (according to predictions of ecological stoichiometry). As predicted by allometry, per capita nitrogen and phosphorus excretion rates increased and mass-specific excretion rates decreased, with increasing mass. Body phosphorus content was correlated with body mass only in one species, bluegill. Contrary to stoichiometric predictions, there was no relationship between body P and mass-normalized P excretion rate, or between body N:P and excreted N:P, when all individuals of all species were considered.
However, at the species level, we observed some support for a body nutrient content effect on excretion as predicted by stoichiometry theory. For example, gizzard shad had lower body P (high body N:P) and also excreted P at higher rates (lower N:P) than bluegill, which had high body P (lower body N:P). We applied the Sterner (1990) homeostatic stoichiometry model to the two most common species in the study – gizzard shad and bluegill and found that food N:P had a greater effect than consumer body N:P on excreted N:P. This indicates that, in terms of variation among these species, nutrient excretion may be more of a function of food nutrient content than the nutrient content of the consumer. These results suggest that stoichiometry can provide a framework for variation among species in nutrient cycling and for evaluating the ecosystem consequences of biodiversity loss.     

Stoichiometry of benthic invertebrate nutrient recycling: interspecific variation and the role of body mass

Ecological stoichiometry (ES) and allometry offer frameworks for predicting how nutrient recycling varies within and among animal species. Despite the importance of benthic-derived nutrients in most aquatic systems, predictions based on ES and allometry have been poorly tested among benthic invertebrate consumers. Here, we show that the rates and ratios at which three freshwater benthic invertebrate species (a crustacean, an insect, and a polychaeta) recycled nitrogen (N) and phosphorus (P) can be partially predicted by ES and allometry depending on whether data are analyzed intra- or interspecifically. Mass-specific N and P excretion rates were negatively correlated with invertebrate body size both among and within taxa, supporting allometric predictions. However, mass-specific N and P excretion rates were positively and negatively correlated to invertebrate body N and P, respectively, but only when data were analyzed intraspecifically. As a corollary, the mass-specific N:P excretion ratio was positively related to body N:P ratio. Such a contrasting pattern on excretion-mediated N and P recycling suggests that stoichiometric constraints regarding consumer-resource imbalances for the three species utilized in this study may be stronger for P than for N. Our results indicate that the variation in nutrient recycling, which is mediated by taxonomic constraints on stoichiometry and allometry, may substantially help us to understand the importance of benthic detritivorous species to the functioning of aquatic ecosystems.     

Length‐weight relationship and condition factor of 11 fish species of the Igarapé Fortaleza basin,a tributary from the Amazon River system in eastern Amazon (Brazil)

The present study investigated the length‐weight relationship (LWR) and allometric condition factor for 11 freshwater fish species of the Igarapé Fortaleza basin (00°02037.5″N; 51°06019.2″W), a tributary from the Amazon River system in the State of Amapá, northern Brazil. The fish were collected in the period from 2012 to 2014 using gillnets with different mesh sizes (10–40 mm between opposite knots). LWR parameters were estimated had angular coefficient (b) varying from 2.055 to 3.158. The allometric condition factor presented interspecific variation. These data complement the efforts to understand the biology of these Amazonian fish species.     

Impact of the removal of gizzard shad (Dorosoma cepedianum) on nutrient cycles in Lake Apopka,Florida

1. The St. Johns River Water Management District removed over 5.4 million kg of gizzard shad (Dorosoma cepedianum) from Lake Apopka, FL during 1993–2005, as a means of reducing lake phosphorus and phytoplankton concentrations and improving water clarity. Other steps included reduction of external nutrient inputs and operation of a treatment wetland. We measured nutrient excretion by Lake Apopka gizzard shad to quantify the nutrient effect of this biomanipulation. 2. Both N and P excretion were significantly affected by fish body mass and temperature. Larger fish had lower mass‐specific rates of excretion than smaller fish. 3. High water temperature increased P excretion to a much greater extent than N, resulting in a low N : P of nutrient excretion in midsummer. The N : P of excretion was lower than has been observed in other systems, probably because of higher water temperature. 4. Removal of gizzard shad >200 g prevented the annual release of 45 800 kg N year^?1 (3.46 kg N ha^?1 year^?1) and 7700 kg P year^?1 (0.62 kg P ha^?1 year^?1) on average. The actual impact on the P cycle varied substantially from year to year (range 7900–78 800 kg N year^?1; 1200–14 800 kg P year^?1), primarily because of fluctuations in the catch. 5. On an annual basis, the P directly removed in fish tissues was similar to that removed by the treatment wetland. The P excretion prevented by the removal of fish was approximately 20% of the reduction in external P loading achieved during 1993–2005. 6. In the short term, most of the P demand of planktonic primary producers is met through recycling of P, which greatly exceeds external P loading. Depending on population biomass, phosphorus excretion by the resident gizzard shad population was similar in magnitude to the P release by diffusive flux from the sediments.     

Marine nutrient contributions to freshwater apex predators

Recent investigations into the nutrient cycling of coastal ecosystems have suggested that migratory or anadromous fish could be important vectors of marine nutrients. Anadromous fish have assimilated marine nutrients that would contribute to the nutrient budgets of freshwater systems by excretion, gamete release, or the decay of post-reproductive carcasses. However, the extent to which freshwater predators utilize marine material is not well understood. In systems where anadromous fish temporarily constitute a major portion of the fish community, they may contribute substantially to the diet of piscivorous fish and other predators. Here we show the contribution of anadromous blueback herring, shad, and alewife (Alosa) to diets of large, non-indigenous piscivorous catfish (Ictalurus furcatus) using δ³⁴S and δ¹³C. The spawning anadromous Alosa, captured in tidal freshwater, had enriched δ³⁴S and δ¹³C values compared to resident, native freshwater species. As a result of consuming the anadromous Alosa, the I. furcatus isotope signature shifted towards the marine signal. The isotope analysis revealed that anadromous fish contribute substantially to the diet of most captured I. furcatus. The percentage of anadromous Alosa carbon and sulfur that was incorporated into I. furcatus (≥38 cm total length) ranged from 0 to 84% and 10 to 69%, and had means (±SD) of 42 (±24) and 43 (±16)%, respectively. Although the δ¹⁵N signal of marine-derived biomass is enriched by approximately 3‰ relative to terrestrial or freshwater biomass, it was not as useful as δ³⁴S and δ¹³C for nutrient source owing to trophic fractionation. This study demonstrates that anadromous fish may be a significant source of nutrients to tidal freshwater apex predators. Received: 19 March 1999 / Accepted: 26 October 1999     

Quantification of allochthonous nutrient input into freshwater bodies by herbivorous waterbirds

1. Waterbirds are considered to import large quantities of nutrients to freshwater bodies but quantification of these loadings remains problematic. We developed two general models to calculate such allochthonous nutrient inputs considering food intake, foraging behaviour and digestive performance of waterbirds feeding in terrestrial habitats: an intake model (IM), mainly based on an allometric relationship for energy requirements and a dropping model (DM), based on allometric relationships for defaecation. 2. Reviewed data of nitrogen (N) and phosphorus (P) content of herbivorous food varied according to diet type (foliage, seeds and roots), season and fertilization. For model parameterization average foliage diet contained 38.20 mg N g^?1 and 3.21 mg P g^?1 (dry weight), whereas mean faeces composition was 45.02 mg N g^?1 and 6.18 mg P g^?1. 3. Daily allochthonous nutrient input increased with body mass ranging from 0.29 g N and 0.03 g P in teals Anas crecca to 5.69 g N and 0.57 g P in mute swans Cygnus olor. Results from IM differed from those of DM from ducks to swans by 63–108% for N and by ?4 to 23% for P. Model uncertainty was lowest for the IM and mainly caused by variation in estimates of food retention time (RT). In DM food RT and dropping mass determined model uncertainty in similar extent. 4. Exemplarily applying the models to Dutch wetlands resulted in mean annual contribution of herbivorous waterbirds to allochthonous nutrient loading of 382.8 ± 167.1 tonnes N a^?1and 34.7 ± 2.3 tonnes P a^?1, respectively, which corresponds to annual surface‐water loadings of 1.07 kg N ha^?1 and 0.10 kg P ha^?1. 5. There was a distinct seasonal pattern with peak loadings in January, when bird abundances were highest. Lowest inputs were in August, when bird abundance and nutrient content in food was low and birds foraged less in terrestrial habitats. Three‐quarters of all nutrient input was contributed by greater white‐fronted goose Anser albifrons, greylag goose Anser anser, wigeon Anas penelope and barnacle goose Branta leucopsis alone. 6. We provide general, easy to use calculation methods for the estimation of allochthonous nutrient inputs by waterbirds, which are applicable to a range of waterbird species, a variety of potential diets and feeding behaviours, and across spatial scales. Such tools may greatly assist in the planning and execution of management actions for wetland nutrient budgets.     

Importance of Terrestrial Arthropods as Subsidies in Lowland Neotropical Rain Forest Stream Ecosystems

The importance of terrestrial arthropods has been documented in temperate stream ecosystems, but little is known about the magnitude of these inputs in tropical streams. Terrestrial arthropods falling from the canopy of tropical forests may be an important subsidy to tropical stream food webs and could also represent an important flux of nitrogen (N) and phosphorus (P) in nutrient‐poor headwater streams. We quantified input rates of terrestrial insects in eight streams draining lowland tropical wet forest in Costa Rica. In two focal headwater streams, we also measured capture efficiency by the fish assemblage and quantified terrestrially derived N‐ and P‐excretion relative to stream nutrient uptake rates. Average input rates of terrestrial insects ranged from 5 to 41 mg dry mass/m²/d, exceeding previous measurements of aquatic invertebrate secondary production in these study streams, and were relatively consistent year‐round, in contrast to values reported in temperate streams. Terrestrial insects accounted for half of the diet of the dominant fish species, Priapicthys annectens. Although terrestrially derived fish excretion was found to be a small flux relative to measured nutrient uptake rates in the focal streams, the efficient capture and processing of terrestrial arthropods by fish made these nutrients available to the local stream ecosystem. This aquatic‐terrestrial linkage is likely being decoupled by deforestation in many tropical regions, with largely unknown but potentially important ecological consequences.     

Fish as sources and sinks of nutrients in lakes

1. The release of total phosphorus (TP) and nitrogen (N in ammonium) was measured for the five most abundant fish species (>85% of biomass) in Mouse and Ranger Lakes, two biomanipulated, oligotrophic lakes in Ontario. 2. The specific release rate of both nutrients was significantly related to fish mass; log₁₀ TP release rate (μg h^?1) = 0.793 (±0.109) [log₁₀ wet mass (g)] + 0.7817 (±0.145), and log₁₀ N release rate (μg h^?1) = 0.6946 (±0.079) [log₁₀wet mass (g)] + 1.7481 (±0.108). 3. When fish nutrient release was standardized for abundance (all populations, 1993–95) and epilimnetic volume, fish were estimated to contribute 0.083 (±0.061) μg TP L^?1 day^?1, and 0.41 (±0.17) μg N L^?1 day^?1 in Mouse L., and 0.062 (±0.020) μg TP L^?1 day^?1 and 0.31 (±0.08) μg N L^?1 day^?1 in Ranger L. 4. In comparison, concurrent rates of total planktonic P regeneration were 1.02 (±0.45) μg L^?1 day^?1 (Mouse L.) and 0.85 (±0.19) μg L^?1 day^?1 (Ranger L.). Fish represented 8% of planktonic P release in Mouse L. and 7% in Ranger L. 5. Fish dry mass had mean elemental body compositions of 39.3% carbon, 10.9% nitrogen, and 4.0% phosphorus (all fish combined), with a mean molar C : N : P ratio of 27 : 6 : 1. This comprised about 55% and 23% of the total epilimnetic particulate P and N respectively. 6. Turnover times of P and N in fish were approximately 103 and 48 days respectively. In comparison, planktonic turnover times of particulate P in Mouse and Ranger Lakes were 4.3 and 4.4 days respectively. Given their high P content and low turnover rates, fish appear to be important P sinks in lakes.     

Nutrient recycling by two phosphorus-rich grazing catfish: the potential for phosphorus-limitation of fish growth

In ecosystems where excretion by fish is a major flux of nutrients, the nitrogen (N) to phosphorus (P) ratio released by fish can be important in shaping patterns of algal biomass, community composition, primary production, and nutrient limitation. Demand for N and P as well as energy influences N/P excretion ratios and has broad implications in ecosystems where nutrient recycling by fishes is substantial. Bioenergetics and stoichiometric models predict that natural fish populations are generally energy-limited and therefore N/P recycling by fishes is relatively invariant. Yet, the potential for P limitation of growth has not been examined in herbivorous fishes, which are common in many aquatic habitats. We examined N/P excretion ratios and P demand in two P-rich herbivorous catfishes of the family Loricariidae, Ancistrus triradiatus (hereafter Ancistrus) and Chaetostoma milesi (hereafter Chaetostoma). Both fishes are common grazers in the Andean piedmont region of Venezuela where we conducted this study. Mass balance (MB) models indicate that these fishes have a high P demand. In fact, our Ancistrus’ P MB model predicted negative P excretion rates, indicating that Ancistrus did not consume enough P to meet its P demand for growth. Direct measurement of excretion rates showed positive, but very low P excretion rates and high N/P excretion ratios for both taxa. To obtain measured P excretion rates of Ancistrus from the MB model, gross growth efficiency must be reduced by 90%. Our results suggest that growth rates of both of these herbivorous and P-rich fish are likely P-limited. If P limitation of growth is common among herbivorous fish populations, herbivorous fishes recycle likely at high N/P ratios and act to diminish the quality of their food.     

The importance of nutrient supply by fish excretion and watershed streams to a eutrophic lake varies with temporal scale over 19 years

Animals transform and translocate nutrients at ecologically relevant rates, contributing to eutrophication in aquatic ecosystems by mobilizing otherwise unavailable nutrients. Yet we know little about how animal-mediated nutrient cycling compares with external abiotic nutrient sources over long periods (years–decades) and at multiple timescales. To address this, we conducted a 19-year study in a eutrophic reservoir examining nitrogen (N) and phosphorus (P) inputs from watershed streams versus excretion by an abundant fish (gizzard shad, Dorosoma cepedianum) at weekly, monthly and seasonal timescales. Over the entire time period, watershed N and P loading was 33- and 3-fold greater than fish N and P excretion, respectively. However, fish N excretion exceeded watershed nutrient loading in 36% of weeks and 43% of months, and fish P excretion in 68% of weeks and 58% of months during the growing season. Fish excretion had lower temporal variability in both supply rate and N:P ratio than watershed loading. Fish excretion also supplied nutrients at a much lower molar N:P ratio than the watershed (mean of daily N:P supply ratios were 15 and 723, respectively). In eutrophic lakes with high fish biomass, fish excretion can strongly influence algal biomass and community composition. Eutrophication management efforts should consider removal of benthivorous fish, like gizzard shad, in addition to other watershed management practices to improve water quality. Future climate change will modulate the interplay between fish- and watershed-mediated nutrient dynamics by altering the geographic distribution of detritivorous fish and the frequency and severity of storm and drought events.     

Influence of intra‐ and interspecific variation in predator–prey body size ratios on trophic interaction strengths

1. Predation is a pervasive force that structures food webs and directly influences ecosystem functioning. The relative body sizes of predators and prey may be an important determinant of interaction strengths. However, studies quantifying the combined influence of intra‐ and interspecific variation in predator–prey body size ratios are lacking.
2. We use a comparative functional response approach to examine interaction strengths between three size classes of invasive bluegill and largemouth bass toward three scaled size classes of their tilapia prey. We then quantify the influence of intra‐ and interspecific predator–prey body mass ratios on the scaling of attack rates and handling times.
3. Type II functional responses were displayed by both predators across all predator and prey size classes. Largemouth bass consumed more than bluegill at small and intermediate predator size classes, while large predators of both species were more similar. Small prey were most vulnerable overall; however, differential attack rates among prey were emergent across predator sizes. For both bluegill and largemouth bass, small predators exhibited higher attack rates toward small and intermediate prey sizes, while larger predators exhibited greater attack rates toward large prey. Conversely, handling times increased with prey size, with small bluegill exhibiting particularly low feeding rates toward medium–large prey types. Attack rates for both predators peaked unimodally at intermediate predator–prey body mass ratios, while handling times generally shortened across increasing body mass ratios.
4. We thus demonstrate effects of body size ratios on predator–prey interaction strengths between key fish species, with attack rates and handling times dependent on the relative sizes of predator–prey participants.
5. Considerations for intra‐ and interspecific body size ratio effects are critical for predicting the strengths of interactions within ecosystems and may drive differential ecological impacts among invasive species as size ratios shift.

     

Stoichiometry of nutrient recycling by vertebrates in a tropical stream: linking species identity and ecosystem processes

Ecological stoichiometry offers a framework for predicting how animal species vary in recycling nutrients, thus providing a mechanism for how animal species identity mediates ecosystem processes. Here we show that variation in the rates and ratios at which 28 vertebrate species (fish, amphibians) recycled nitrogen (N) and phosphorus (P) in a tropical stream supports stoichiometry theory. Mass-specific P excretion rate varied 10-fold among taxa and was negatively related to animal body P content. In addition, the N : P ratio excreted was negatively related to body N : P. Body mass (negatively related to excretion rates) explained additional variance in these excretion parameters. Body P content and P excretion varied much more among taxonomic families than among species within families, suggesting that familial composition may strongly influence ecosystem-wide nutrient cycling. Interspecific variation in nutrient recycling, mediated by phylogenetic constraints on stoichiometry and allometry, illustrates a strong linkage between species identity and ecosystem function.     

Detritivory and the stoichiometry of nutrient cycling by a dominant fish species in lakes of varying productivity

Little is known about the stoichiometry of nutrient cycling by detritivores. Therefore, we explored stoichiometric relationships in an omnivorous/detritivorous fish (gizzard shad, Dorosoma cepedianum) in three lakes that differed in productivity. Gizzard shad can feed on plankton and sediment detritus, but in all three lakes adult gizzard shad derived >98% of carbon (C) and phosphorus (P), and >90% of nitrogen (N) from sediment detritus, and the remainder from zooplankton.
Gizzard shad selectively consumed detritus with higher C, N and P concentrations than ambient lake sediments. Selective detritivory (i.e. the nutrient content of consumed detritus divided by the nutrient content of ambient detritus) was most pronounced in the lake with the lowest detrital nutrient concentrations. N and P cycling rates per fish were also consistently higher in this lake, in agreement with the prediction of stoichiometry theory that excretion rates should increase with food nutrient content. Among-lake differences in nutrient cycling rates were unrelated to inter-lake variation in fish body nutrient contents, which was minimal. The N:P ratio excreted was near Redfield (∼14:1) in all three lakes.
Stoichiometric analyses showed that the C:N and C:P ratios of sediment detritus were much higher (∼2.8×) than ratios of gizzard shad bodies, revealing substantial N and P imbalances between consumers and their food source. Gizzard shad alleviate N imbalance by selectively feeding on high N detritus (low C:N, high N:P), and apparently alleviate P imbalance by excreting nutrients at a higher N:P than that of their food or their bodies. Thus, this detritivore apparently regulates nutrient acquisition and allocation via both pre-absorption processes (selective feeding) and post-absorptive processes (differential N and P excretion).     

Factors influencing nitrogen and phosphorus excretion rates of fish in a shallow lake

Summary 1. Fish excretion can be an important source of nutrients in aquatic ecosystems. Nitrogen (N) and phosphorus (P) excretion rates are influenced by many factors, including fish diet, fish growth rate and fish size. However, the relative influence of these and other factors on community‐level excretion rates of fish is unknown. 2. We used bioenergetics modeling to estimate excretion rates of eight fish species in a shallow, Minnesota (U.S.A.) lake over four months in both 2004 and 2005. Excretion rates of each species were summed for community‐level N and P excretion rates, as well as the N : P ratio of excretion. We then used a model‐selection approach to assess ability of independent variables to predict excretion rates, and to identify the most parsimonious model for predicting N : P excretion ratios and P and N excretion rates at the community scale. Predictive models were comprised of the independent variables water temperature and average fish density, fish size, fish growth rate, nutrient content of fish and nutrient content of fish diets at the community scale. 3. Fish density and nutrient content of fish diets (either N or P) were the most parsimonious models for predicting both N and P excretion rates, and explained 96% and 92% of the variance in N and P excretion, respectively. Moreover, fish density and nutrient models had 1400‐fold more support for predicting N and 21‐fold more support for predicting P excretion relative to models based on fish density only. Water temperature, fish size, fish growth rates and nutrient content of fish showed little influence on excretion rates, and none of our independent variables showed a strong relationship with N : P ratios of excretion. 4. Past work has focused on the importance of fish density as a driver of fish excretion rates on a volumetric basis. However, our results indicate that volumetric excretion rates at the community scale will also change substantially in response to changes in relative abundance of fish prey or shifts in relative dominance of planktivores, benthivores, or piscivores. Changes in community‐scale excretion rates will have subsequent influences on algal abundance, water clarity, and other ecosystem characteristics.     

Ontogeny, diet shifts, and nutrient stoichiometry in fish

Most stoichiometric models do not consider the importance of ontogenetic changes in body nutrient composition and excretion rates. We quantified ontogenetic variation in stoichiometry and diet in gizzard shad, Dorosoma cepedianum , an omnivorous fish with a pronounced ontogenetic diet shift; and zebrafish, Danio rerio, grown in the lab with a constant diet. In both species, body stoichiometry varied considerably along the life cycle. Larval gizzard shad and zebrafish had higher molar C:P and N:P ratios than larger fish. Variation in body nutrient ratios was driven mainly by body P, which increased with size. Gizzard shad body calcium content was highly correlated with P content, indicating that ontogenetic P variation is associated with bone formation. Similar trends in body stoichiometry of zebrafish, grown under constant diet in the laboratory, suggest that ontogeny (e.g. bone formation) and not diet shift is the main factor affecting fish body stoichiometry in larval and juvenile stages. The N:P ratio of nutrient excretion also varied ontogenetically in gizzard shad, but the decline from larvae to juveniles appears to be largely associated with variation in the N:P of alternative food resources (zooplankton vs detritus) rather than by fish body N:P. Furthermore, the N:P ratio of larval gizzard shad excretion appears to be driven more by the N:P ratio at which individuals allocate nutrients to growth, more so than static body N:P, further illustrating the need to consider ontogenetic variation. Our results thus show that fish exhibit considerable ontogenetic variation in body stoichiometry, driven by an inherent increase in the relative allocation of P to bones, whereas ontogenetic variation in excretion N:P ratio of gizzard shad is driven more by variation in food N:P than by body N:P.