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The Timing of Copepod Diapause as an Evolutionarily Stable Strategy

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Evolution of Insect Migration and Diapause

inferredcites →https://doi.org/10.1007/978-1-4615-6941-1_12openalex-snapshot

Escape in Space and Time — Concluding Remarks

inferredcites →https://doi.org/10.1007/978-1-4684-7862-4_22openalex-snapshot

Evolution and the Theory of Games

inferredcites →https://doi.org/10.1007/978-3-642-93067-6_14openalex-snapshot

Evolution and the Theory of Games

inferredcites →https://doi.org/10.1007/bf00346713openalex-snapshot

Oscillations in the reproductive condition of Diaptomus leptopus (Copepoda: Calanoida) and their relation to rates of egg-clutch production

inferredcites →https://doi.org/10.1007/bf00379086openalex-snapshot

Population differences in the timing of diapause: adaptation in a spatially heterogeneous environment

inferredcites →https://doi.org/10.1007/bf00540137openalex-snapshot

Delayed germination and dispersal in desert annuals: Escape in space and time

inferredcites →https://doi.org/10.1016/0022-5193(67)90050-1openalex-snapshot

Optimizing reproduction in a randomly varying environment when a correlation may exist between the conditions at the time a choice has to be made and the subsequent outcome

inferredcites →https://doi.org/10.1016/0040-5809(80)90044-1openalex-snapshot

Optimal switching to diapause in relation to the onset of winter

inferredcites →https://doi.org/10.1016/0040-5809(84)90028-5openalex-snapshot

Dispersal strategies in patchy environments

inferredcites →https://doi.org/10.1016/b978-0-120-84380-0.x5001-7openalex-snapshot

Insect Photoperiodism

inferredcites →https://doi.org/10.1016/s0031-9422(00)86489-4openalex-snapshot

The control of growth and differentiation in plants

inferredcites →https://doi.org/10.1080/03680770.1974.11896398openalex-snapshot

Reynolds number, diapause, and predatory copepods

inferredcites →https://doi.org/10.1080/03680770.1983.11897852openalex-snapshot

Bet-hedging and environmentally cued diapause strategies of diaptomid copepods

inferredcites →https://doi.org/10.1086/282672openalex-snapshot

A Theoretical Model for the Optimal Timing of Diapause

inferredcites →https://doi.org/10.1086/282887openalex-snapshot

Demographic Strategy of Vertical Migration by a Marine Copepod

inferredcites →https://doi.org/10.1093/besa/25.2.169openalex-snapshot

Evolution of Insect Migration and Diapause

inferredcites →https://doi.org/10.1093/biomet/33.3.183openalex-snapshot

ON THE USE OF MATRICES IN CERTAIN POPULATION MATHEMATICS

inferredcites →https://doi.org/10.1139/f80-204openalex-snapshot

Subitaneous and Resting Eggs of Copepods: Relative Rates of Clutch Production by Diaptomus leptopus

inferredcites →https://doi.org/10.1139/f81-168openalex-snapshot

Prey Location Volume of a Planktivorous Fish: A New Measure of Prey Vulnerability

inferredcites →https://doi.org/10.1163/156854078x00178openalex-snapshot

The Effect of Temperature On the Development of Diapausing and Subitaneous Eggs in Several Freshwater Copepods

inferredcites →https://doi.org/10.2307/1541095openalex-snapshot

PHOTOPERIODIC CONTROL OF DIAPAUSE IN THE MARINE CALANOID COPEPODLABIDOCERA AESTIVA

inferredcites →https://doi.org/10.2307/1936308openalex-snapshot

Selective Predation of Ephippal Daphnia and the Resistance of Ephippal Eggs to Digestion

inferredcites →https://doi.org/10.2307/1943511openalex-snapshot

Population Dynamics in Daphnia obtusa Kurz

inferredcites →https://doi.org/10.2307/1948560openalex-snapshot

The Passive Dispersal of Small Aquatic Organisms and Their Colonization of Isolated Bodies of Water

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Insect Population Ecology: An Analytical Approach.

inferredcites →https://doi.org/10.2307/2332297openalex-snapshot

On the Use of Matrices in Certain Population Mathematics

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Population Biology of Plants.

inferredcites →https://doi.org/10.2307/3556openalex-snapshot

Insect Population Ecology: an Analytical Approach

inferredcites →https://doi.org/10.2307/3808208openalex-snapshot

Hibernation and Torpor in Mammals and Birds

inferredcites →https://doi.org/10.4319/lo.1974.19.4.0636openalex-snapshot

The use of field data to derive population statistics of multivoltine copepods1

inferredcites →https://doi.org/10.4319/lo.1980.25.4.0742openalex-snapshot

On the diel variation of copepod pigmentation

inferredcites →https://doi.org/10.4319/lo.1983.28.5.0935openalex-snapshot

The causes and consequences of sex‐specific mortality in a freshwater copepod1

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Copepod eggs survive a decade in the sediments of the Baltic Sea

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Role of parthenogenetic natality and emergence from diapausing eggs in the dynamics of some rotifer populations

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inferred← citeshttps://doi.org/10.1111/j.1365-2427.2009.02287.xopenalex-snapshot

Invasion, genetic variation and species identity of the calanoid copepod Sinodiaptomus valkanovi

inferred← citeshttps://doi.org/10.1111/j.1365-2427.2009.02389.xopenalex-snapshot

Predation cues do not affect the induction and termination of diapause in small‐bodied cladocerans

inferred← citeshttps://doi.org/10.1111/j.1365-2745.2011.01899.xopenalex-snapshot

Variable offspring size as an adaptation to environmental heterogeneity in a clonal plant species: integrating experimental and modelling approaches

inferred← citeshttps://doi.org/10.1111/j.1420-9101.2009.01825.xopenalex-snapshot

Spatially heterogeneous stochasticity and the adaptive diversification of dormancy

inferred← citeshttps://doi.org/10.1111/j.1420-9101.2011.02403.xopenalex-snapshot

The impact of intraspecific variation in a fish predator on the evolution of phenotypic plasticity and investment in sex in Daphnia ambigua

inferred← citeshttps://doi.org/10.1111/j.1439-0469.1986.tb00636.xopenalex-snapshot

The effect of diapause on the genetic structure of Daphnia magna populations

inferred← citeshttps://doi.org/10.1111/j.1461-0248.2005.00812.xopenalex-snapshot

Rapid evolution and the convergence of ecological and evolutionary time

inferred← citeshttps://doi.org/10.1111/j.1558-5646.1986.tb00518.xopenalex-snapshot

EFFECTS OF PARENTAL PHOTOPERIOD REGIME ON PROGENY DEVELOPMENT TIME IN DROSOPHILA SIMULANS

inferred← citeshttps://doi.org/10.1111/j.1558-5646.1988.tb04194.xopenalex-snapshot

EFFECTS OF PARENTAL PHOTOPERIOD ON DEVELOPMENT TIME AND DENSITY SENSITIVITY OF PROGENY IN DROSOPHILA MELANOGASTER

inferred← citeshttps://doi.org/10.1111/j.1558-5646.1990.tb05250.xopenalex-snapshot

FLUCTUATING SELECTION AND RESPONSE IN A POPULATION OF FRESHWATER COPEPODS

inferred← citeshttps://doi.org/10.1111/j.1558-5646.1999.tb05337.xopenalex-snapshot

THE ROLES OF FLUCTUATING SELECTION AND LONG-TERM DIAPAUSE IN MICROEVOLUTION OF DIAPAUSE TIMING IN A FRESHWATER COPEPOD

inferred← citeshttps://doi.org/10.1111/j.1570-8703.2006.00471.xopenalex-snapshot

Effects of host‐plant species on diapause induction of the Kanzawa spider mite, Tetranychus kanzawai

inferred← citeshttps://doi.org/10.1111/jbi.13414openalex-snapshot

Copepod diapause and the biogeography of the marine lipidscape

inferred← citeshttps://doi.org/10.1111/jeb.12474openalex-snapshot

Why wait? Three mechanisms selecting for environment‐dependent developmental delays

inferred← citeshttps://doi.org/10.1127/1863-9135/2012/0251openalex-snapshot

To rest in hydration: hatching phenology of resting eggs of Heterocypris incongruens (Crustacea: Ostracoda)

inferred← citeshttps://doi.org/10.1152/ajpregu.00250.2015openalex-snapshot

Mechanisms of animal diapause: recent developments from nematodes, crustaceans, insects, and fish

inferred← citeshttps://doi.org/10.1163/1937240x-00002488openalex-snapshot

Collecting and processing living, non-marine ostracods

inferred← citeshttps://doi.org/10.1371/journal.pone.0175927openalex-snapshot

How long to rest in unpredictably changing habitats?

inferred← citeshttps://doi.org/10.15298/invertzool.21.3.08openalex-snapshot

The impact of temperature on hatching rates of diapause eggs and subsequent development in a tropical freshwater copepod, Mongolodiaptomus malaindosinensis (Copepoda: Calanoida)

inferred← citeshttps://doi.org/10.1590/s1679-87592014064706203openalex-snapshot

Influence of Experimental Thermal Shifts and Overcrowding on Fecundity in Wild Females of Acartia Tonsa of the Bahía Blanca Estuary

inferred← citeshttps://doi.org/10.1890/0012-9658(1997)078[0442:aemods]2.0.co;2openalex-snapshot

AN EMPIRICAL MODEL OF DIAPAUSE STRATEGIES OF THE CRICKETALLONEMOBIUS SOCIUS

inferred← citeshttps://doi.org/10.1890/0012-9658(2002)083[0370:ffaail]2.0.co;2openalex-snapshot

FLASH FLOODS AND AQUATIC INSECT LIFE-HISTORY EVOLUTION: EVALUATION OF MULTIPLE MODELS

inferred← citeshttps://doi.org/10.1890/03-0804openalex-snapshot

TIMING OF DISTURBANCE AND COEXISTENCE IN A SPECIES-RICH RUDERAL PLANT COMMUNITY

inferred← citeshttps://doi.org/10.1890/06-1495openalex-snapshot

BET HEDGING IN A GUILD OF DESERT ANNUALS

inferred← citeshttps://doi.org/10.1890/09-0366.1openalex-snapshot

Eco‐evolutionary dynamics: fluctuations in population growth rate reduce effective population size in chinook salmon

inferred← citeshttps://doi.org/10.22541/au.170670618.82786328/v1openalex-snapshot

Trade-offs in dormancy phenology in endotherms and ectotherms

inferred← citeshttps://doi.org/10.2307/1352298openalex-snapshot

Modelling the Ecological Constraints on Growth and Movement of Juvenile American Shad (Alosa sapidissima) in the Hudson River Estuary

inferred← citeshttps://doi.org/10.2307/1467247openalex-snapshot

Responses of a Freshwater Shrimp to Chemical and Tactile Stimuli from a Large Decapod Predator

inferred← citeshttps://doi.org/10.2307/1467433openalex-snapshot

Habitat Duration and Community Structure in Temporary Ponds

inferred← citeshttps://doi.org/10.2307/1541912openalex-snapshot

PARTIAL PHOTOPERIODIC CONTROL OF DIAPAUSE IN THREE POPULATIONS OF THE FRESHWATER COPEPODDIAPTOMUS SANGUINEUS

inferred← citeshttps://doi.org/10.2307/1542185openalex-snapshot

Are Temperature and Photoperiod Necessary Cues for Encystment in the Marine Benthic Harpacticoid Copepod Heteropsyllus nunni Coull?

inferred← citeshttps://doi.org/10.2307/1542200openalex-snapshot

The Interaction of Photoperiod and Temperature in Diapause Timing: A Copepod Example

inferred← citeshttps://doi.org/10.2307/1938151openalex-snapshot

The Joint Evolution of Diapause and Insecticide Resistance: A Test of an Optimality Model

inferred← citeshttps://doi.org/10.2307/1938197openalex-snapshot

The Seed Bank of a Freshwater Crustacean: Copepodology for the Plant Ecologist

inferred← citeshttps://doi.org/10.2307/1938634openalex-snapshot

A Field Test for the Cues of Disapause in a Freshwater Copepod

inferred← citeshttps://doi.org/10.2307/1940482openalex-snapshot

Bet Hedging and the Diapause Strategies of the Cricket Allonemobius Fasciatus

inferred← citeshttps://doi.org/10.2307/2265740openalex-snapshot

Phenotypic Variation in a Zooplankton Egg Bank

inferred← citeshttps://doi.org/10.2307/2409018openalex-snapshot

Effects of Parental Photoperiod on Development Time and Density Sensitivity of Progeny in Drosophila melanogaster

inferred← citeshttps://doi.org/10.2307/2426855openalex-snapshot

Evidence for Diapause in the Freshwater Copepod Skistodiaptomus pallidus

inferred← citeshttps://doi.org/10.3354/meps028121openalex-snapshot

Factors controlling seasonal succession of the copepods Acartia hudsonica and A. tonsa in Narragansett Bay, Rhode Island: temperature and resting egg production

inferred← citeshttps://doi.org/10.3354/meps077307openalex-snapshot

Viability of subitaneous copepod eggs following fish predation on egg-carrying calanoids

inferred← citeshttps://doi.org/10.3354/meps09342openalex-snapshot

Calanus finmarchicus diapause initiation: new view from traditional life history-based model

inferred← citeshttps://doi.org/10.3389/fmars.2025.1624922openalex-snapshot

Efficacies of cooking and depuration for reducing current-use pesticide residues in wild-caught giant mud crabs (Scylla serrata)

inferred← citeshttps://doi.org/10.4081/jlimnol.2004.s1.26openalex-snapshot

Diapause in Calanoid Copepods: within-clutch hatching patterns

inferred← citeshttps://doi.org/10.4319/lo.1985.30.1.0167openalex-snapshot

Factors regulating the reproductive phenology of Onychodiaptomus birgei (Copepoda: Calanoida)1

inferred← citeshttps://doi.org/10.4319/lo.1988.33.4_part_2.0931openalex-snapshot

Ecological principles affecting community structure and secondary production by zooplankton in marine and freshwater environments

inferred← citeshttps://doi.org/10.4319/lo.2004.49.4_part_2.1333openalex-snapshot

To sink or swim: Variable diapause strategies among Daphnia species

inferred← citeshttps://doi.org/10.4319/lo.2004.49.4_part_2.1341openalex-snapshot

Rotifers from diapausing, fertilized eggs: Unique features and emergence

inferred← citeshttps://doi.org/10.4319/lo.2005.50.3.0923openalex-snapshot

Subitaneous eggs of freshwater copepods pass through fish guts: Survival, hatchability, and potential ecological implications

inferred← citeshttps://doi.org/10.64898/2026.05.06.723256openalex-snapshot

Adaptation to Environmental Variability Shapes Dormancy in Daphnia

inferred← citeshttps://doi.org/10.70675/9f3bca07zc7dfz4fc3za10ez867b8b2ff14bopenalex-snapshot

Evolutionary causes and consequences of hibernation phenology : evolutionary approaches to changes in phenology in the context of global changes

inferred← citeshttps://doi.org/10.7554/elife.89644openalex-snapshot

Evolutionary trade-offs in dormancy phenology

inferred← citeshttps://doi.org/10.7554/elife.89644.1openalex-snapshot

Trade-offs in dormancy phenology in endotherms and ectotherms

inferred← citeshttps://doi.org/10.7554/elife.89644.2openalex-snapshot

Evolutionary trade-offs in dormancy phenology

inferred← citeshttps://doi.org/10.7554/elife.89644.3openalex-snapshot

Evolutionary trade-offs in dormancy phenology

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