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Body size, sexual size dimorphism, and Rensch's rule in adult hydropsychid caddisflies (Trichoptera: Hydropsychidae)

https://doi.org/10.1139/z03-194
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What this work says

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

inferredcites →https://doi.org/10.1006/jhev.1998.0281openalex-snapshot
Statistics of sexual size dimorphism
inferredcites →https://doi.org/10.1007/bf00333717openalex-snapshot
Body size and fecundity in the waterstrider Aquarius remigis: a test of Darwin's fecundity advantage hypothesis
inferredcites →https://doi.org/10.1007/bf00379291openalex-snapshot
Particle size, resource concentration, and the distribution of net-spinning caddisflies
inferredcites →https://doi.org/10.1007/bf01237728openalex-snapshot
Growth and foraging consequences of facultative paedomorphosis in the tiger salamander,Ambystoma tigrinum nebulosum
inferredcites →https://doi.org/10.1038/360156a0openalex-snapshot
Sexual dimorphism and distorted sex ratios in spiders
inferredcites →https://doi.org/10.1046/j.1365-2427.2003.00997.xopenalex-snapshot
Caddisfly life histories along permanence gradients in high‐altitude wetlands in Colorado (U.S.A.)
inferredcites →https://doi.org/10.1073/pnas.94.18.9740openalex-snapshot
Character displacement in some Cnemidophorus lizards revisited: A phylogenetic analysis
inferredcites →https://doi.org/10.1080/08927014.1999.9522841openalex-snapshot
The effect of male size, age, and mating behavior on sexual selection in the seed beetleCallosobruchus maculatus
inferredcites →https://doi.org/10.1086/284325openalex-snapshot
Phylogenies and the Comparative Method
inferredcites →https://doi.org/10.1086/284779openalex-snapshot
Sexual Size Dimorphism in Relation to Fecundity in Some Swedish Satyrid Butterflies
inferredcites →https://doi.org/10.1086/284935openalex-snapshot
A Comparative Method
inferredcites →https://doi.org/10.1086/285082openalex-snapshot
Factors Influencing Sexual Size Dimorphism in Temperate Waterstriders
inferredcites →https://doi.org/10.1086/285663openalex-snapshot
Sexual Selection and the Evolution of Allometry for Sexual Size Dimorphism in the Water Strider, Aquarius remigis
inferredcites →https://doi.org/10.1086/285901openalex-snapshot
Ecological Causes of Adaptive Radiation
inferredcites →https://doi.org/10.1086/286004openalex-snapshot
A Comparative Analysis of Allometry for Sexual Size Dimorphism: Assessing Rensch's Rule
inferredcites →https://doi.org/10.1086/303406openalex-snapshot
Rensch’s Rule Crosses the Line: Convergent Allometry of Sexual Size Dimorphism in Hummingbirds and Flower Mites
inferredcites →https://doi.org/10.1086/338512openalex-snapshot
Character Displacement in Giant Rhinoceros Beetles
inferredcites →https://doi.org/10.1086/393620openalex-snapshot
The Evolution of Body Size: What Keeps Organisms Small?
inferredcites →https://doi.org/10.1093/aesa/85.1.34openalex-snapshot
Body Size Asymmetries in Predatory Interactions among Robber Flies (Diptera: Asilidae)
inferredcites →https://doi.org/10.1093/aesa/90.5.705openalex-snapshot
Larvae of the North American Caddisfly Genera (Trichoptera), 2nd ed.
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb01341.xopenalex-snapshot
POPULATION VARIATION IN SEXUAL SELECTION AND ITS EFFECT ON SIZE ALLOMETRY IN TWO DUNG FLY SPECIES WITH CONTRASTING SEXUAL SIZE DIMORPHISM
inferredcites →https://doi.org/10.1111/j.1558-5646.1995.tb02313.xopenalex-snapshot
SELECTION ON FECUNDITY AND VARIATION IN THE DEGREE OF SEXUAL SIZE DIMORPHISM AMONG SPIDER SPECIES (CLASS ARANEAE)
inferredcites →https://doi.org/10.1139/cjz-77-10-1637openalex-snapshot
Ecology of two large, net-spinning caddisfly species in a mountain stream: distribution, abundance, and metabolic response to a thermal gradient
inferredcites →https://doi.org/10.1139/f80-017openalex-snapshot
The River Continuum Concept
inferredcites →https://doi.org/10.1139/f92-030openalex-snapshot
Season and Body Size Influence Movement of Hydropsychid Caddisfly Larvae (Trichoptera: Hydropsychidae)
inferredcites →https://doi.org/10.1139/z04-063openalex-snapshot
Proximate mechanisms that contribute to female-biased sexual size dimorphism in an anguid lizard
inferredcites →https://doi.org/10.1139/z79-121openalex-snapshot
Life history patterns of some species of Hydropsyche (Trichoptera: Hydropsychidae) in southern Ontario
inferredcites →https://doi.org/10.1146/annurev.ecolsys.27.1.111openalex-snapshot
EVOLUTIONARY SIGNIFICANCE OF RESOURCE POLYMORPHISMS IN FISHES, AMPHIBIANS, AND BIRDS
inferredcites →https://doi.org/10.1146/annurev.ecolsys.28.1.659openalex-snapshot
Allometry for Sexual Size Dimorphism: Pattern and Process in the Coevolution of Body Size in Males and Females
inferredcites →https://doi.org/10.1146/annurev.en.24.010179.001153openalex-snapshot
Ecological Diversity in Trichoptera
inferredcites →https://doi.org/10.1146/annurev.ento.43.1.63openalex-snapshot
Plasticity in Life-History Traits
inferredcites →https://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
inferredcites →https://doi.org/10.21900/j.inhs.v23.199openalex-snapshot
The Caddis Flies, or Trichoptera, of Illinois
inferredcites →https://doi.org/10.2307/1467330openalex-snapshot
Phylogeny of Pupation in Trichoptera, with Proposals on the Origin and Higher Classification of the Order
inferredcites →https://doi.org/10.2307/1467812openalex-snapshot
Phylogenetic Relationships among Subfamily Groups in the Hydropsychidae (Trichoptera) with Diagnoses of the Smicrideinae, New Status, and the Hydropsychinae
inferredcites →https://doi.org/10.2307/1468385openalex-snapshot
Life History and Production of a Semi-Terrestrial Limnephilid Caddisfly in an Intermittent Platte River Wetland
inferredcites →https://doi.org/10.2307/1938234openalex-snapshot
Some Relationships between Systematics and Trophic Ecology in Nearctic Aquatic Insects, with Special Reference to Trichoptera
inferredcites →https://doi.org/10.2307/1940688openalex-snapshot
Niche Overlap and the Potential for Competition and Intraguild Predation Between Size‐Structured Populations
inferredcites →https://doi.org/10.2307/2265635openalex-snapshot
Adaptation to Predators in a New Community: Swimming Performance and Predator Avoidance in Damselflies
inferredcites →https://doi.org/10.2307/3493930openalex-snapshot
Larvae of the North American Caddisfly Genera (Trichoptera)
inferredcites →https://doi.org/10.2307/3544943openalex-snapshot
Intraspecific Variation in Body Size and Fecundity in Insects: A General Relationship
inferredcites →https://doi.org/10.2307/3545503openalex-snapshot
Lake Outlets and the Distribution of Filter Feeders: An Assessment of Hypotheses
inferredcites →https://doi.org/10.2307/3547015openalex-snapshot
Evolution of Net-Spinning Caddisflies: A Hypothetical Mechanism for the Reproductive Isolation of Conspecific Competitors
inferredcites →https://doi.org/10.2307/3565338openalex-snapshot
Abdomen Size, Body Size and the Reproductive Effort of Insects
inferredcites →https://doi.org/10.2307/3565785openalex-snapshot
Prey Size and Predation as Factors Governing the Distribution of Lotic Polycentropodid Caddisfly Larvae
inferredcites →https://doi.org/10.2307/5403openalex-snapshot
The Evolution of Life-histories
inferredcites →https://doi.org/10.5860/choice.189072openalex-snapshot
The Evolution of insect mating systems
inferredcites →https://doi.org/10.5860/choice.45-3789openalex-snapshot
An Introduction to the aquatic insects of North America

What points at this work

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

inferred← citeshttps://doi.org/10.1093/zoolinnean/zlae003zenodo-depositor-declared
Miocene caddisflies from Australia: iron-rich sediments preserve internal organs, tracheoles, and corneal nanocoating of larvae and pupae
inferred← citeshttps://doi.org/10.1002/mmnz.200700003openalex-snapshot
Estimating body size in apoid wasps: the significance of linear variables in a morphologically diverse taxon (Hymenoptera, Apoidea)
inferred← citeshttps://doi.org/10.1002/rra.1274openalex-snapshot
Linking the hydraulic world of individual organisms to ecological processes: Putting ecology into ecohydraulics
inferred← citeshttps://doi.org/10.1007/s10682-008-9242-8openalex-snapshot
A test of Rensch’s rule in dwarf chameleons (Bradypodion spp.), a group with female-biased sexual size dimorphism
inferred← citeshttps://doi.org/10.1007/s13744-014-0196-yopenalex-snapshot
Allometry for Sexual Size Dimorphism in Stoneflies Defies the Rensch’s Rule
inferred← citeshttps://doi.org/10.1016/j.ecoinf.2008.08.001openalex-snapshot
Using neural networks to detect patterns in inter-specific data: An example from net-spinning caddisflies (Trichoptera: Annulipalpia)
inferred← citeshttps://doi.org/10.1086/510597openalex-snapshot
Proximate Causes of Rensch’s Rule: Does Sexual Size Dimorphism in Arthropods Result from Sex Differences in Development Time?
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.001.0001openalex-snapshot
Sex, Size and Gender Roles
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.002.0003openalex-snapshot
Copyright Page
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.002.0006openalex-snapshot
Contributors
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0001openalex-snapshot
Introduction: the enigma of sexual size dimorphism
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0002openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0003openalex-snapshot
Sexual size dimorphism in mammals
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0004openalex-snapshot
Sexual size dimorphism in birds
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0005openalex-snapshot
The evolution of sexual size dimorphism in reptiles
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0006openalex-snapshot
Sexual size dimorphism in amphibians: an overview
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0007openalex-snapshot
Rensch's rule in insects: patterns among and within species
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0008openalex-snapshot
Sexual size dimorphism in spiders: patterns and processes
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0009openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0010openalex-snapshot
Variation in selection, phenotypic plasticity, and the ecology of sexual size dimorphism in two seed-feeding beetles
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0011openalex-snapshot
Sexual dimorphism in the water strider,Aquarius remigis: a case study of adaptation in response to sexually antagonistic selection
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0012openalex-snapshot
Case studies of the differential-equilibrium hypothesis of sexual size dimorphism in two dung fly species
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0013openalex-snapshot
The genetic integration of sexually dimorphic traits in the dioecious plant,Silene latifolia
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0014openalex-snapshot
Dimorphism in the hartebeest
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0015openalex-snapshot
Sexual size dimorphism and offspring vulnerability in birds
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0016openalex-snapshot
Variation in sexual size dimorphism within a widespread lizard species
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0017openalex-snapshot
Phylogenetic analysis of sexual dimorphism in eye-lid geckos (Eublepharidae): the effects of male combat, courtship behavior, egg size, and body size
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0018openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0019openalex-snapshot
Sex differences: genetic, physiological, and ecological mechanisms
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0020openalex-snapshot
The genetic architecture of sexual dimorphism: the potential roles of genomic imprinting and condition-dependence
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0021openalex-snapshot
Irreconcilable differences: when sexual dimorphism fails to resolve sexual conflict
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0022openalex-snapshot
Development of sexual size dimorphism in lizards: testosterone as a bipotential growth regulator
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.003.0023openalex-snapshot
Sexual differences in insect development time in relation to sexual size dimorphism
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199208784.005.0001openalex-snapshot
Supplementary Tables
inferred← citeshttps://doi.org/10.1093/evolut/qpad172openalex-snapshot
Rensch’s rule: linking intraspecific to evolutionary allometry
inferred← citeshttps://doi.org/10.1111/1744-7917.12272openalex-snapshot
Lack of support for Rensch's rule in an intraspecific test using red flour beetle (Tribolium castaneum) populations
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2006.tb01838.xopenalex-snapshot
WHEN RENSCH MEETS BERGMANN: DOES SEXUAL SIZE DIMORPHISM CHANGE SYSTEMATICALLY WITH LATITUDE?
inferred← citeshttps://doi.org/10.1111/j.1365-2699.2009.02263.xopenalex-snapshot
The effect of environmental diversification on species diversification in New Caledonian caddisflies (Insecta: Trichoptera: Hydropsychidae)
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2006.01092.xopenalex-snapshot
Selection on body size and sexual size dimorphism differs between host species in a seed-feeding beetle
inferred← citeshttps://doi.org/10.1139/cjz-2018-0063openalex-snapshot
Testing Rensch’s rule in Acanthoscelides macrophthalmus, a seed-feeding beetle infesting Leucaena leucocephala plants
inferred← citeshttps://doi.org/10.1139/z04-063openalex-snapshot
Proximate mechanisms that contribute to female-biased sexual size dimorphism in an anguid lizard
inferred← citeshttps://doi.org/10.12976/jib/2013.1.12openalex-snapshot
Rensch's rule is not verified in melanopline grasshoppers (Acrididae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0000897openalex-snapshot
Only Half Right: Species with Female-Biased Sexual Size Dimorphism Consistently Break Rensch's Rule
inferred← citeshttps://doi.org/10.1554/06-110.1openalex-snapshot
WHEN RENSCH MEETS BERGMANN: DOES SEXUAL SIZE DIMORPHISM CHANGE SYSTEMATICALLY WITH LATITUDE?
inferred← citeshttps://doi.org/10.22271/j.ento.2018.v6.i1b.03openalex-snapshot
Allometry for sexual dimorphism in millipedes (Diplopoda)
inferred← citeshttps://doi.org/10.22271/j.ento.2018.v6.i1i.03openalex-snapshot
Sexual dimorphism in pill millipedes (Diplopoda)
inferred← citeshttps://doi.org/10.22271/j.ento.2018.v6.i1v.07openalex-snapshot
Sexual size dimorphism and the rejection of Rensch’s rule in Diplopoda (Arthropoda)
inferred← citeshttps://doi.org/10.22271/j.ento.2018.v6.i3.9.09openalex-snapshot
Trigoniulid size dimorphism breaks Rensch
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