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Energy Reserve Lipids of Zooplanktonic Crustaceans from an Oligotrophic Saline Lake In Relation to Food Resources and Temperature
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/iroh.19780630303openalex-snapshot
The Saline Lakes of Saskatchewan III. Chemical Characterization
inferredcites →https://doi.org/10.1002/iroh.19860710603openalex-snapshot
A Study of Benthic Communities in Some Saline Lakes in Saskatchewan and Alberta, Canada
inferredcites →https://doi.org/10.1002/jez.1402560207openalex-snapshot
Fatty acid synthesis and accumulation rates in daphniids
inferredcites →https://doi.org/10.1007/978-94-009-0603-7_16openalex-snapshot
Distribution and abundance of littoral benthic fauna in Canadian prairie saline lakes
inferredcites →https://doi.org/10.1007/978-94-009-3095-7_6openalex-snapshot
Aquatic macrophytes in saline lakes of the Canadian prairies
inferredcites →https://doi.org/10.1007/978-94-017-0918-7_28openalex-snapshot
Salinity tolerance and morphology of the osmoregulation organs in Cladocera with special reference to Cladocera from the Aral sea
inferredcites →https://doi.org/10.1007/bf00026269openalex-snapshot
Aquatic macrophytes in saline lakes of the Canadian prairies
inferredcites →https://doi.org/10.1007/bf00026949openalex-snapshot
Distribution and abundance of littoral benthic fauna in Canadian prairie saline lakes
inferredcites →https://doi.org/10.1007/bf00028407openalex-snapshot
Salinity tolerance and morphology of the osmoregulation organs in Cladocera with special reference to Cladocera from the Aral sea
inferredcites →https://doi.org/10.1007/bf00347591openalex-snapshot
The filtration apparatus of Cladocera: Filter mesh-sizes and their implications on food selectivity
inferredcites →https://doi.org/10.1016/s0021-9258(18)64849-5openalex-snapshot
A SIMPLE METHOD FOR THE ISOLATION AND PURIFICATION OF TOTAL LIPIDES FROM ANIMAL TISSUES
inferredcites →https://doi.org/10.1080/03680770.1989.11898770openalex-snapshot
Seasonal trends in planktonic lipid content and lipid class
inferredcites →https://doi.org/10.1093/plankt/11.6.1201openalex-snapshot
Lipids in Acanthodiaptomus denticomis during starvation and fed on three different algae
inferredcites →https://doi.org/10.1093/plankt/14.10.1449openalex-snapshot
Lipid-ovary indices in food-limited Daphnia
inferredcites →https://doi.org/10.1111/j.0022-3646.1981.00374.xopenalex-snapshot
PHYTOPLANKTON LIPIDS: INTERSPECIFIC DIFFERENCES AND EFFECTS OF NITRATE, SILICATE AND LIGHT-DARK CYCLES1
inferredcites →https://doi.org/10.1111/j.1529-8817.1981.tb00865.xopenalex-snapshot
PHYTOPLANKTON LIPIDS: INTERSPECIFIC DIFFERENCES AND EFFECTS OF NITRATE, SILICATE AND LIGHT‐DARK CYCLES1
inferredcites →https://doi.org/10.1139/f87-078openalex-snapshot
Factors Influencing the Distribution of Phytoplankton in 97 Headwater Lakes in Insular Newfoundland
inferredcites →https://doi.org/10.1139/f92-250openalex-snapshot
Light, Nutrients, and Water Temperature as Determinants of Phytoplankton Production in Two Saline, Prairie Lakes with High Sulphate Concentrations
inferredcites →https://doi.org/10.1139/z52-036openalex-snapshot
THE ENTOMOSTRACA OF SOUTHERN SASKATCHEWAN
inferredcites →https://doi.org/10.1139/z70-212openalex-snapshot
Predator–prey relationships and predation rates for crustacean zooplankters from some lakes in western Canada
inferredcites →https://doi.org/10.2307/1940440openalex-snapshot
Omnivory and Food Chain Length in Zooplankton Food Webs
inferredcites →https://doi.org/10.2307/2260522openalex-snapshot
The Ecology of Freshwater Phytoplankton.
inferredcites →https://doi.org/10.4319/lo.1979.24.1.0015openalex-snapshot
The adaptive significance of color polymorphism in two species of Diaptomus (Copepoda)1
inferredcites →https://doi.org/10.4319/lo.1984.29.4.0731openalex-snapshot
Night synthesis of protein by algae1
inferredcites →https://doi.org/10.4319/lo.1985.30.5.1099openalex-snapshot
Micromethod for lipids in aquatic invertebrates1
inferredcites →https://doi.org/10.4319/lo.1989.34.1.0213openalex-snapshot
[Methyl‐3H]thymidine macromolecular incorporation and lipid labeling: Their significance to DNA labeling during measurements of aquatic bacterial growth rate
inferredcites →https://doi.org/10.4319/lo.1992.37.1.0208openalex-snapshot
Trophic cascade and biomanipulation: Interface of research and management‐A reply to the comment by DeMelo et al
inferredcites →https://doi.org/10.4319/lo.1992.37.2.0413openalex-snapshot
Lipids and life‐cycle strategy of a hypolimnetic copepod in Lake Michigan
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/neobiota.93.121346zenodo-depositor-declared
Functional responses correspond to stable isotope-based trophic positions among four invasive Ponto-Caspian mysid species (Crustacea, Mysida)
inferred← citeshttps://doi.org/10.1007/978-1-4612-0547-0_12openalex-snapshot
Comparison of Lipids in Marine and Freshwater Organisms
inferred← citeshttps://doi.org/10.1007/978-1-4612-0547-0_5openalex-snapshot
Lipids in Freshwater Zooplankton:Selected Ecological and Physiological Aspects
inferred← citeshttps://doi.org/10.1007/978-94-011-4928-0_16openalex-snapshot
Ecophysiology of Lipids in Pelagic Crustacean Zooplankton Communities
inferred← citeshttps://doi.org/10.1007/bf00122171openalex-snapshot
Spatial and temporal variability in lipid dynamics of common amphipods: assessing the potential for uptake of lipophilic contaminants
inferred← citeshttps://doi.org/10.1007/s00343-021-0351-3openalex-snapshot
Factors affecting lipid and fatty acid composition of Calanus sinicus in the Yellow Sea and the East China Sea in spring
inferred← citeshttps://doi.org/10.1007/s11745-005-1421-1openalex-snapshot
Daphnia magna can tolerate short‐term starvation without major changes in lipid metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-12-822701-5.00020-3openalex-snapshot
Ecology and Functioning of Zooplankton Communities
inferred← citeshttps://doi.org/10.1016/j.envpol.2018.08.067openalex-snapshot
Protein and lipid growth rates regulate bioaccumulation of PCBs and Hg in Bighead Carp (Hypophthalmichthys nobilis) and Silver Carp (Hypophthalmichthys molitrix) from the Three Gorges Reservoir, China
inferred← citeshttps://doi.org/10.1016/s0380-1330(97)70892-xopenalex-snapshot
Lipid Concentration and Size Variation of Bythotrephes (Cladocera: Cercopagidae) from Lakes Erie, Huron, and Michigan
inferred← citeshttps://doi.org/10.1023/a:1002933706785openalex-snapshot
Bacterial lipolytic activity in a hypertrophic dead arm of the river Danube in Vienna
inferred← citeshttps://doi.org/10.1023/a:1009911811188openalex-snapshot
Photosynthate production in laboratory cultures (UV conditioned and unconditioned) of Cryptomonas erosa under simulated doses of UV radiation
inferred← citeshttps://doi.org/10.1080/03680770.1998.11901593openalex-snapshot
Size-dependent UVR sensitivity in Redberry Lake phytoplankton communities
inferred← citeshttps://doi.org/10.1080/10236240802506805openalex-snapshot
Diel vertical distribution of freshwater calanoid copepods in a shallow lake: its variability in males with and without an oil sac
inferred← citeshttps://doi.org/10.1093/plankt/20.8.1581openalex-snapshot
Limnocalanus macrurus (Copepoda: Calanoida) retains a marine arctic lipid and life cycle strategy in Lake Michigan
inferred← citeshttps://doi.org/10.1093/plankt/22.7.1277openalex-snapshot
Effects of chronic, low levels of UV radiation on carbon allocation in Cryptomonas erosa and competition between C.erosa and bacteria in continuous cultures
inferred← citeshttps://doi.org/10.1093/plankt/fbu111openalex-snapshot
Physiological condition and differential feeding behaviour in the cryptic species complex Eurytemora affinis in the St Lawrence estuary
inferred← citeshttps://doi.org/10.1111/j.1365-2427.2005.01336.xopenalex-snapshot
Temporal variation in body composition (C : N) helps explain seasonal patterns of zooplankton δ13C
inferred← citeshttps://doi.org/10.1139/cjfas-2014-0209openalex-snapshot
Nutrient excretion by crustacean zooplankton in the deep chlorophyll layer of Lake Superior
inferred← citeshttps://doi.org/10.1139/cjfas-53-5-1048openalex-snapshot
Algal productivity, algal biomass, and zooplankton biomass in a phosphorus-rich, saline lake: deviations from regression model predictions
inferred← citeshttps://doi.org/10.1139/cjfas-54-2-320openalex-snapshot
Impacts of a herbicide and fertilizers on the microbial community of a saline prairie lake
inferred← citeshttps://doi.org/10.1139/f08-135openalex-snapshot
Comparison of three microquantity techniques for measuring total lipids in fish
inferred← citeshttps://doi.org/10.1139/f92-250openalex-snapshot
Light, Nutrients, and Water Temperature as Determinants of Phytoplankton Production in Two Saline, Prairie Lakes with High Sulphate Concentrations
inferred← citeshttps://doi.org/10.1890/1051-0761(1997)007[1024:fyrolb]2.0.co;2openalex-snapshot
FIRST-YEAR RECRUITMENT OF LARGEMOUTH BASS: THE INTERDEPENDENCY OF EARLY LIFE STAGES
inferred← citeshttps://doi.org/10.3354/meps13578openalex-snapshot
Lipid allocation in late-stage barnacle larvae from subtropical and temperate waters
inferred← citeshttps://doi.org/10.3390/hydrobiology4020013openalex-snapshot
The Diversity and Biochemical Composition of Zooplankton as a Potential Indicator of Dietary Requirements for Pikeperch Larvae (Sander lucioperca)
inferred← citeshttps://doi.org/10.4319/lo.2000.45.4.0763openalex-snapshot
Changes in composition and reactivity of allochthonous DOM in a prairie saline lake
inferred← citeshttps://doi.org/10.4319/lo.2003.48.5.1977openalex-snapshot
Compositional and interlake variability of zooplankton affect baseline stable isotope signatures
inferred← citeshttps://doi.org/10.4319/lo.2007.52.5.2135openalex-snapshot
A standard protocol for stable isotope analysis of zooplankton in aquatic food web research using mass balance correction models
inferred← citeshttps://doi.org/10.4319/lo.2014.59.3.0947openalex-snapshot
Famine and feast in a common freshwater calanoid: Effects of diet and temperature on fatty acid dynamics of Eudiaptomus gracilis
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