The influence of autotrophic and heterotrophic foods on the demography of Daphnia longispina under starved, semi-natural and enriched conditions

We tested the influence of different types of food on the fitnessof Daphnia longispina during a period of poor resources by comparingthe growth and reproduction of individuals fed on differentdiets. When Daphnia were under starvation conditions, both dissolvedorganic carbon and metabolic products enhanced bacterial growth,and the cladoceran produced 15 neonates and survived for the55 days of experiment. In the natural water, the edible foodconsisted essentially of bacteria and heterotrophic flagellates,which enabled the cladoceran to grow and reproduce. In waterenriched with Cryptomonas (an alga) or Chilomonas (a heterotrophicflagellate), the daphnid growth rates increased considerablyfrom generation to generation, but later in the time courseof the experiment with Chilomonas than with Cryptomonas. Thisalga enhanced the phosphorus:carbon ratio. The primiparous daphnidsfed with Cryptomonas were smaller than those fed with the heterotrophicflagellate and enrichment with the heterotrophic flagellatealso enhanced reproduction. In Lake Tazenat, when the algalbiomass was insufficient to support the Daphnia life cycle,the heterotrophic organisms were an essential food source. Whenfeeding essentially on bacteria, Daphnia has the capacity togrow and reproduce at very low food concentrations, and thisis important in determining its fitness under competitive conditions.     

The effects of Daphnia on nutrient stoichiometry and filamentous cyanobacteria: a mesocosm experiment in a eutrophic lake

1. Stoichiometric theory predicts that the nitrogen : phosphorus (N : P) ratio of recycled nutrients should increase when P‐rich zooplankton such as Daphnia become dominant. We used an enclosure study to test the hypothesis that an increased biomass of Daphnia will increase the relative availability of N versus P sufficiently to decrease the abundance of filamentous cyanobacteria. The experiment was conducted in artificially enriched Lake 227 (L227) in the Experimental Lakes Area (ELA), north‐western Ontario, Canada. Previous studies in L227 have shown that the dominance of filamentous, N‐fixing cyanobacteria is strongly affected by changes in the relative loading rates of N and P. 2. We used a 2 × 2 factorial design with the addition or absence of D. pulicaria and high or low relative loading rates of N and P (+NH₄, –NH₄) in small enclosures as treatment variables. If Daphnia can strongly affect filamentous cyanobacteria by altering N and P availability, these impacts should be greatest with low external N : P loading rates. The phytoplankton community of L227 was predominantly composed of filamentous Aphanizomenon spp. at the start of the experiment. 3. Daphnia strongly reduced filamentous cyanobacterial density in all enclosures to which they were added. The addition of NH₄ had only a small impact on algal community composition. Hence, we conclude that Daphnia did not cause reductions in cyanobacteria by altering the N : P ratio of available nutrients. 4. Despite the lack of evidence that Daphnia affected filamentous cyanobacteria by altering the relative availability of N and P, we found changes in nutrient cycling consistent with other aspects of stoichiometric theory. In the presence of Daphnia, total P in the water column decreased because of an increase in P sedimentation. In contrast to P, a decrease in suspended particulate N was offset by an increase in dissolved N (especially NH₄). Hence, dissolved and total N : P ratios in the water column increased with Daphnia as a result of differences in the fate of suspended particulate N versus P. There was minimal accumulation and storage of P in Daphnia biomass in the enclosures. 5. Our experiment demonstrated that Daphnia can strongly limit filamentous cyanobacterial abundance and affect the biogeochemical cycling of nutrients. In our study, changes in nutrient cycling were apparently insufficient to cause the changes in phytoplankton community composition that we observed. Daphnia therefore limited filamentous cyanobacteria by other mechanisms.     

Elemental composition (C:N:P) and growth rates of bacteria and Rhodomonas grazed by Daphnia

The elemental composition and growth rate of Rhodomonas andheterotrophic bacteria were studied in batch cultures in thepresence and absence of Daphnia and at two different levelsof phosphorus limitation. The elemental content of single cellswas measured with X-ray microanalysis. Simultaneously, dilutionexperiments were performed in order to estimate grazing losses,growth rates and dominant nutrient sources for bacteria andRhodomonas. The phosphorus:carbon (P:C) ratios of the bacteriawere generally higher in the experiment with the stronger Plimitation of the system. High P:C ratios were taken as an indicationthat bacteria were carbon limited. The presence of Daphnia resultedin a further increase in bacterial P:C ratios and increasedspecific growth rates. Thus, grazing increased the availabilityboth of inorganic nutrients and organic substrates, stimulatingthe growth of the bacteria. P:C ratios of Rhodomonas decreasedwith increasing P limitation of the system. Only at strong Plimitation did the presence of Daphnia result in increased P:Cratios of Rhodomonas compared with the control without daphnids.This study shows that the elemental content and growth rateof heterotrophic bacteria and Rhodomonas are influenced by grazingand nutrient regeneration by daphnids. The response is dynamicand depends on the level of nutrient limitation of the system. Present address: Department of Microbiology, University of BergenJahnebakken 5, NO-5020 Bergen, Norway     

Estimation of phosphorus metabolic rates of Daphnia galeata using a three-compartment model

A compartment model to estimate the different phosphorus metabolicrates in Daphnia galeata is presented. The model has three compartments:gut, metabolic pool and structural pool. Existing two-compartmentmodels used for carbon and phosphorus turnover in Daphnia donot allow estimation of ingestion and egestion rates. We extendedexisting two-compartment models with one more compartment, thegut, which allowed us to estimate both the ingestion and theegestion rates. Parameters of the model are estimated from asingle experiment of feeding unlabelled Daphnia with ³²P-labelledScenedesmus obliquus. Separate experiments with juvenile andadult daphnids were carried out in order to compare their metabolisms.This model permits a reliable estimation of the different metabolicrates of Daphrna in a single experiment and discriminates clearlybetween animals of different sizes.     

Response of phytoplankton and bacteria to nutrients and zooplankton: a mesocosm experiment

Although both nutrient inputs and zooplankton grazing are importantto phytoplankton and bacteria in lakes, controversy surroundsthe relative importance of grazing pressure for these two groupsof organisms. For phytoplankton, the controversy revolves aroundwhether zooplankton grazers, especially large cladocerans likeDaphnia, can effectively reduce phytoplankton populations regardlessof nutrient conditions. For bacteria, little is known aboutthe balance between possible direct and indirect effects ofboth nutrients and zooplankton grazing. However, there is evidencethat bacteria may affect phytoplankton responses to nutrientsor zooplankton grazing through direct or apparent competition.We performed a mesocosm experiment to evaluate the relativeimportance of the effects of nutrients and zooplankton grazingfor phytoplankton and bacteria, and to determine whether bacteriamediate phytoplankton responses to these factors. The factorialdesign crossed two zooplankton treatments (unsieved and sieved)with four nutrient treatments (0, 0.5, 1.0 and 2.0 µgphosphorus (P) l^–1 day^–1 together with nitrogen(N) at a N:P ratio of 20:1 by weight). Weekly sieving with 300µm mesh reduced the average size of crustacean zooplanktonin the mesocosms, decreased the numbers and biomass of Daphnia,and increased the biomass of adult copepods. Nutrient enrichmentcaused significant increases in phytoplankton chlorophyll a(4–5x), bacterial abundance and production (1.3x and 1.6x,respectively), Daphnia (3x) and total zooplankton biomass (2x).Although both total phytoplankton chlorophyll a and chlorophylla in the <35 µm size fraction were significantly lowerin unsieved mesocosms than in sieved mesocosms, sieving hadno significant effect on bacterial abundance or production.There was no statistical interaction between nutrient and zooplanktontreatments for total phytoplankton biomass or bacterial abundance,although there were marginally significant interactions forphytoplankton biomass <35 µm and bacterial production.Our results do not support the hypothesis that large cladoceransbecome less effective grazers with enrichment; rather, the differencebetween phytoplankton biomass in sieved versus unsieved zooplanktontreatments increased across the gradient of nutrient additions.Furthermore, there was no evidence that bacteria buffered phytoplanktonresponses to enrichment by either sequestering P or affectingthe growth of zooplankton.     

Contrasting ‘Top-Down’ Effects of Crustacean Zooplankton Grazing on Bacteria and Phytoflagellates

The combined effects of grazing and nutrient regeneration by Daphnia and Eudiaptomus on the growth of Rhodomonas and heterotrophic bacteria was assessed experimentally. The responses of Rhodomonas and bacteria to the grazers were measured as net specific growth rate over the entire experimental periods, as well as production and specific production at the end of the experiments. Both zooplankton species had a negative effect on Rhodomonas net specific growth rate due to grazing and a positive effect on specific primary production due to nutrient regeneration. Daphnia had no effect on bacterial net specific growth rate, bacterial production or specific bacterial production in one of two experiments. In the other experiment, however, both bacterial growth rate and production decreased as a result of grazing. Furthermore, Daphnia had a negative effect on specific bacterial production, but Eudiaptomus had a positive effect on all bacterial parameters due to nutrient regeneration, probably of phosphorus. Positive effects of copepods on bacterial growth has previously been attributed to trophic cascades via protozoa. However, the present experiments show that regeneration of nutrients, especially phosphorus, may account for a large part of the stimulation of bacterial growth.     

Demography of a natural population of Daphnia retrocurva in a lake with low food quality

The hypothesis was tested that Daphnia exhibit low populationrecruitment in a lake with phosphorus (P)-deficient food, whereDaphnia populations failed to increase in response to greatlylowered minnow density. Egg ratio analysis was performed onDaphnia retrocurva from L110 of the Experimental Lakes Area,Ontario, in 1994. L110 has high food abundance (seston carbon(C) 100 µM C), but the seston is P deficient (C:P atomic- 600). Chrysophytes dominated the algal community. The fishcommunity in this lake was manipulated in 1993 and 1994 by theaddition of northern pike, Esox lucius. Zooplanktivorous minnowswere greatly reduced after the piscivore addition, but the expectedincrease in abundance of the Daphnia to this altered predationregime was not observed, If food quality constrains the responseof the Daphnia to changed predation, there should be low recruitment in the relatively sparse Daphnia population in this lake.Birth rates estimated by standard egg ratio analysis were <0.1day^–1 for most of the sample period. In comparison toannual averages from the literature, recruitment in L110 wasmoderately, but not dramatically, low. Daphnia exhibited pronounced‘normal’ vertical migration (up at night, down duringthe day) all year, and a strongly declining size at first reproductionthrough the season. Population density and birth rates seemedto show much less short-term change than previously observedin other lakes. Although the demo graphic predictions for foodquality constraints seemed clear, in situ demography unfortunatelyneither supported nor strongly rejected the overall hypothesisof food quality limitation in this lake with very high C:P ratios.Possibly, direct demographic effects of low food quality willbe difficult to observe in nature.     

Effects of rotifers and ciliates on the growth and survival of Daphnia

Daphnia can suppress ciliates and rotifers through predationand interference competition, but it is not known whether thisproduces any direct benefit to Daphnia. We conducted survivorshipand cohort lifetable experiments to determine whether Daphniacan utilize ciliates and rotifers as food. Three species ofoligotrich ciliates (Halteria grandinella, Strobilidium gyransand Strobilidiumvelox) and one rotifer (Keratella cochlearis)were used. Lifetable experiments were conducted with a basallevel of algae (Cryptomonas sp.), plus either ciliates or rotifers,while survivorship experiments had only the rotifers or ciliates.Densities of 30 H.grandinella ml^–1, 50 S.gyrans ml^–1and 15 S.velox ml^–1 enhanced Daphnia pulex's populationgrowth rate 35–50% over controls with only algae. TenS.gyrans ml^–1 did not produce a significant change inDaphnia's growth rate. Densities of 100 and 300 K.cochlearis^–1 increased Daphnia population growth rates by II and10%, respectively. Both 10 and 50 S.gyrans ml^–1 enhancedDaphnia's survivorship compared to starved controls, but neither100 nor 300 K.cochlearis l^–1 enhanced its survivorship.The amount of enhancement of Daphnia growth rates by rotifersand ciliates is roughly proportional to the death rates imposedby Daphnia. The death rate imposed by Daphnia on rotifers isa function of both algal density and Daphnia size. Per unitbiomass, neither ciliates nor Keratella appear to be as nutritiousfor Daphnia as is Cryptomonas.     

In situ filtration responses of Daphnia galeata to changes in food quality

In the stoichiometric study of phyto–zooplankton interactions,a controversy exists about how Daphnia species regulate theirfeeding rate when submitted to low-quality food (i.e. high dietarycarbon:phosphorus [C:P] ratio). In this study, we gathered dataover 3 years on in situ clearance rates of a Daphnia galeatapopulation, by conducting grazing experiments from April 1998to October 2000 in the Esch-sur-Sûre reservoir (Grand-Duchyof Luxembourg). Observed clearance rates (2.5–13.5 mLindividual^–1 day^–1, mean 7.0 mL individual^–1day^–1) were correlated with population and environmentalvariables. Mean body size of Daphnia individuals was the bestpredictor of clearance rate (r² = 0.639), followed by watertemperature (r² = 0.262) and P concentration in the seston (r²     

Field evidence for stoichiometric relationships between zooplankton and N and P availability in a shallow calcareous lake

1. According to stoichiometric theory, zooplankters have a species‐specific elemental composition. Daphniids have a relatively high phosphorus concentration in their tissues and copepods high nitrogen. Daphniids should, therefore, be more sensitive to phosphorus limitation and copepods more sensitive to nitrogen. A 2‐year study of a shallow marl lake in the west of Ireland investigated whether population fluctuations of the two dominant taxa, Daphnia spp. and the calanoid Eudiaptomus gracilis, were associated with the availability of phosphorus and nitrogen. 2. In accordance with stoichiometric predictions, Daphnia and Eudiaptomus reproduction had contrasting relationships with dietary phosphorus and nitrogen availability. Egg production by Daphnia was negatively associated with the ratio of dissolved inorganic nitrogen (DIN) : total phosphorus (TP) and the ratio of light to TP which was used as an indirect index for seston carbon (C) : phosphorus (P). Conversely calanoid egg production had a positive relationship with the DIN : TP ratio and was unrelated to the estimated C : P (light : TP) ratio. 3. Daphnia biomass was not, however, correlated with phosphorus availability, and neither was calanoid biomass correlated with nitrogen. The high ratio of DIN : TP when Daphnia dominated the zooplankton biomass and the low ratio when calanoids dominated, is consistent with Daphnia acting as a sink for phosphorus and calanoids as a sink for nitrogen and suggests consumer‐driven nutrient recycling.     

Effects of Daphnia longispina on rotifer populations in a natural environment: relative importance of food limitation and interference competition

To test the relative importance of exploitative and interferencecompetition from Daphnia limiting rotifer populations in Bermejalesreservoir, birth rates of rotifers, food abundance, zooplanktonbiomass and size distribution of Daphnia were analysed fromhigh frequency sampling at two depths. A depletion in food abundanceby Daphnia feeding should be reflected in the birth rates ofrotifers susceptible to exploitative competition, while interferenceshould produce direct negative relationships between the numberof individuals of the interacting species. Results show thatsignificant relationships between food (chlorophyll-a) and birthrates of rotifers are found when the ratio chlorophyll-a/herbivorouszooplankton biomass is used as a measure of food availability.In our study, Anuraeopsis fissa was only affected through exploitativecompetition by Daphnia, while only Synchaeta oblonga showedevidence of being suppressed through interference competitionby this cladoceran.     

Does interference competition from Daphnia affect populations of Keratella cochlearis in Loch Leven, Scotland?

A very marked inverse relationship between Daphnia hyalina var.lacustris Sars and Keratella cochlearis (Gosse) population densitieswas observed in Loch Leven, Scotland, UK between 1978 and 1982.The natural death rates of the rotifer population were far lowerthan would have been expected in response to interference competitionfrom Daphnia. Keratella birth rates fell, along with chlorophylla concentrations, when Daphnia filtration rates were high. Theresults indicate that, when Daphnia were abundant, direct competitionfor food was the most likely factor suppressing Keratella populationgrowth.     

Daphnia dominance and zooplankton community structure in fishless ponds

Predation by fish has commonly been viewed as a primary driverof spatial and seasonal variation in Daphnia dominance and thesize structure of zooplankton communities. Yet, previous researchsuggests that large Daphnia do not always dominate in the absenceof predation. As alternatives to the planktivory model, numerousmechanisms have been put forth, including the effect of resourcecompetition and its interaction with resource quantity and qualityand abiotic factors (e.g. temperature). Here results are presentedof a field survey of 18 fishless, permanent ponds in southwestMichigan in which spatiotemporal variation in Daphnia pulexabundance and several potential determinants of this variationare explored. Results revealed a large amount of variation inD. pulex incidence and relative biomass, with some ponds exhibitingseasonal losses, some having few or no Daphnia, and some beingdominated by D. pulex for the entire sample period. Redundancyanalysis of zooplankton composition and pond environmental variables(biotic and abiotic) showed no relationship between D. pulexbiomass and measures of Chaoborus abundance, algal resourceproduction, or algal resource quality (including seston C:N:P).Instead, pH and temperature (both of which covaried) showedthe strongest relationship with D. pulex biomass.     

Zooplankton community grazing in a hypertrophic lake (Hartbeespoort Dam, South Africa)

Seasonal abundance as total biomass and specific densities ofthe main herbivorous zooplankton (>60 µm) in hypertrophicHartbeespoort Dam from 1981 to 1983 are described. After springzooplankton biomass maxima each year there followed a mid-summerdecline in the Daphnia population and a shift to a smaller bodiedcladoceran community dominated by Ceriodaphnia concomitant witha change from largely edible phytoplankton species to abundantcolonial Microcystis. In situ community grazing rates were measuredthroughout 1983 using a ¹⁴C-labelled unicellular alga. Integratedcommunity grazing rates measured in the aerobic water columnwere highest in December (260.2%/day) when Daphnia was abundantand the edible component of the phytoplankton was diminishing.Lowest integrated community grazing rates occurred in January–February(19.8–35.3%/day) and July (28.3%/day) when the phytoplanktonwas composed almost entirely of Microcysris, and Ceriodaphniadominated the zooplankton community whilst food availabilitywas low. Feeding in Ceriodaphnia was not hindered by abundantlarge Microcysris colonies; total biomass specific grazing ratewas high when Ceriodaphnia dominated and low when Daphnia dominatedthe zoo-plankton community. Results indicate that in hypertrophicconditions it is unlikely that large filter-feeders such asDaphnia are able to retard or limit the development of Cyanophyceaeblooms by high grazing pressure.     

Keeping Daphnia out of the surface film with cetyl alcohol

Some Daphnia species are difficult to culture due to a tendencyto become trapped in the surface film. A low level of cetylalcohol (1.26 0.12 mg) was shown to be highly effective inreducing the surface film entrapment of a Daphnia species typicallysusceptible to such a problem (D.rosea). In a species that doesnot exhibit surface film problems (D.pulicaria), a low levelof cetyl alcohol had no effect, indicating that this substanceis not toxic to Daphnia in low quantities. However, a high level(10.6 1.0 mg) of cetyl alcohol was shown to decrease the survivalof both species and reproduction of the susceptible species.     

Fish predators, food availability and diel vertical migration in Daphnia

Diel vertical migration of zooplankton is a highly variableand complex behaviour which apparently cannot be explained byany single factor. We determined the relative importance offish predation, food availability and water depth in shapingthe migratory behaviour of Daphnia. A modified 2x2x2 factorialexperiment provided two levels of fish density (present/absent),food availability (ambient/high) and depth (4–10 m); shallowtreatments with fish were excluded. Triplicate 1.2 m diameterenclosures for each of the six treatments were held in an 18unit array in Peter Lake, Gogebic Co., MI, USA. Repeated measuresANOVA identified significant trends in daphnid density, migrationand fitness (determined by lipid-ovary-egg index, LOE) as wellas in chlorophyll a content of the water column for part ofa 4-week experiment in July 1988. In deep enclosures with fish,Daphnia performed significantly more intense migrations thanin fishless enclosures, save those in fishless ambient-foodenclosures. Daphnia in deep fishless enclosures without abundantfood at depth performed significantly reduced migrations. DaphnidLOE index was significantly influenced only by food content.Our results were consistent with the predator-avoidance hypothesisas well as with observations of greatest migrations where largevertical differences in food abundance exist. They support ahierarchical view of vertical migration, with presence of fishthe primary factor, and food availability the secondary factor.     

Consumer-dependent responses of lake ecosystems to nutrient loading

The nutrient loading concept proposes that algal biomass, waterclarity and the processes of lake eutrophication are a functionof nutrient loading. We hypothesized that grazers play an importantrole in determining the impacts of nutrient loading on algalbiomass and water clarity, and the overall eutrophication process.To test how the contrasting grazer communities modify the fateof nutrients, we added nutrients (nitrate and phosphate) ata known loading rate to four large enclosures, but in two ofthe four enclosures large cladoceran grazers (Daphnia >1mm mean length) were allowed to develop by removing the planktivorousfish. In the remaining two enclosures, the development of largeDaphnia was prevented by adding planktivorous fish. The concentrationsof epilimnetic total phosphorus (TP) increased at a similarrate in all four enclosures. However, the daily accumulationof added phosphate into the participate or planktonic forms,especially into plankton <20 µm, was three times fasterwhen large Daphnia were absent than when large Daphnia wereabundant. In the enclosures with large Daphnia, added phosphatewas accumulated in the dissolved pool instead. At a constantnutrient loading, algal biomass (chlorophyll a) increased fourtimes faster in the enclosures without large Daphnia than inthose with large Daphnia. Similarly, Secchi depth declined from3.5 to <1 m when Daphnia were absent, but did not declinewhen Daphnia were common. Our results demonstrate that the samenutrient loading and the resultant increase in epilimnetic TPdo not produce the same trophic conditions, as indicated byalgal biomass and water clarity, if the grazers of the majorassimilators of nutrients (the fraction of plankton edible toDaphnia) are different. We suggest that stratified lake ecosystemshaving functionally dominant large grazer communities may beless prone to eutrophication than those lacking large grazers.Consistent with the nutrient loading concept, epilimnetic concentrationsof phosphorus increase proportionately with increased loadingof phosphorus, but the trophic conditions of ecosystems indicatedby algal biomass and water clarity do not follow the same patternsunder contrasting conditions of grazer communities. We suggestthat models predicting algal biomass from loading rates shouldaccount for the role of grazers.     

Multiple predator defence strategies in Daphnia pulex and their relation to native habitat

Daphnia may respond with an array of anti-predator defences(behavioural, morphological and life history) to a chemicalcue (kairomone) exuded by its predators: fish and Chaoborus.Given the wide array of potential responses, it is an interestingquestion whether anti-predator defences are coupled or independentof each other. Since anti-predator responses are costly andeven possessing the genetic information to respond to a certainpredator might involve a cost, clones may only react to predatorsthey co-occur with in nature. In this study, we provide evidencefor an uncoupling of responses by Daphnia pulex in several anti-predatordefences against Chaoborus. We were unable to detect a correlationbetween behavioural (migration), morphological (neck-spine induction)and life history [growth rate, neonate size and size at firstreproduction (SFR)] responses. Furthermore, anti-predator responsesdid not always comply with what is commonly believed. We foundthat Daphnia clones can migrate up or down when exposed to fishor Chaoborus kairomone and that population growth rate, neonatesize and SFR can increase or decrease in response to Chaoboruskairomone. We also show patterns in anti-predator defences thatseem to relate to the habitat from which clones were derived.Daphnia clones that were collected in habitats with Chaoborusas the dominant predator tended to react strongly to Chaoboruskairomone by migrating upward and producing neck-spines. Themigration behaviour against fish kairomone in these clones wasoften an unexpected upward migration. The Daphnia clone thatco-existed with fish predators showed a downward migration inthe presence of fish as well as Chaoborus kairomone. Clonesthat had occurred with either both or no predators had mixedresponses. We sometimes found an upward migration in combinationwith smaller body size as a response to Chaoborus kairomone.This may be interpreted as a behavioural defence against Chaoborusand a life-history defence against fish. Daphnia seem not toexhibit defence behaviour against predators they do not co-occurwith. It might be costly for Daphnia to maintain genetic informationto respond to these predators and protect that information fromgenetic drift.     

Carbon, nitrogen and phosphorus status in Daphnia at varying food conditions

The planktonic crustacean Daphnia magna was fed varying quantitiesor quality (C:N:P ratio) of phytoplankton in a flow-throughchemostat culture. Size-specific dry weight (DW) and egg productionvaried with a factor of >3, mainly governed by food quantity.A maximum was reached at 4 mg C/l. Mean C/DW was 43.96 ±4.43% and insignificant variations were recorded between thegroups of fed animals, but a decrease to 38.09 was found instarved animals. Mean N/DW was 8.18 ± 1.02% with smallvariation between the treatments, and again with the lowestvalue in starved individuals. The mean P/DW of 1.38 ±0.3% of DW, was largely unaffected by food quantity or the absoluteand relative supply of paniculate P in the food. The resultsindicate a rather constant element/DW ratio in Daphnia withinnormal ranges of food supply. This has strong implications forbiomass determinations, and is in particular important whenmodelling elemental turnover and release from Daphnia.     

Midsummer decline of a Daphnia population attributed in part to cyanobacterial capsule production

A midsummer decline in a Daphnia population has been documentedin Lake Winnebago, Wisconsin, USA, similar to that which typicallyoccurs in other freshwater lakes throughout the world. We investigatedthe role of two products of the cyanobacterium Microcystis aeruginosa(microcystin and polysaccharide capsular matrix) in contributingto this population decrease by utilizing laboratory and lakestudies. Feeding on either the microcystin-producing, minimallyencapsulated M. aeruginosa strain PCC 7820 or the highly encapsulated,non-microcystin-producing strain C3-40, resulted in decreasedsurvival when compared with animals fed chlorophytes. The survivorshipof Daphnia fed C3-40 cells washed to remove the capsule increasedby 30% over that seen in animals fed encapsulated C3-40. Feedingpurified microcystin or capsule alone decreased Daphnia survivalto a greater degree than did starvation. Physiological studiesconducted while Daphnia were exposed to these food sources showedthat ingestion of capsular material resulted in increased post-abdominalclaw movements and decreased mandibular movements. Concurrently,elevated respiration rates were measured in Daphnia, implyingthat capsule increased the energy expended by these animalsthrough increased attempts to reject the material and decreasedfood intake. Lake studies reflected the results of the laboratoryexperiments. The midsummer decline of the Daphnia populationoccurs as the Microcystis biovolume increases and both microcystinand capsular matrix levels rise. While both cyanobacterial productsmay contribute to the midsummer decline in Daphnia pulicaria,laboratory studies suggest that encapsulation may play the greaterrole.