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Sexual dimorphism in Apfelbeckia insculpta (L. Koch, 1867) (Myriapoda: Diplopoda: Callipodida)
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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/ece3.466openalex-snapshot
Divergence in genital morphology may contribute to mechanical reproductive isolation in a millipede
inferredcites →https://doi.org/10.1002/jez.583openalex-snapshot
An experimental test of body volume constraint on female reproductive output
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/bf01237760openalex-snapshot
Time and energy constraints and the evolution of sexual size dimorphism ? to eat or to mate?
inferredcites →https://doi.org/10.1007/s00442-011-1934-zopenalex-snapshot
Size correction in biology: how reliable are approaches based on (common) principal component analysis?
inferredcites →https://doi.org/10.1016/j.zool.2008.05.001openalex-snapshot
Sexual dimorphism in bill morphology and feeding ecology in Cory's shearwater (Calonectris diomedea)
inferredcites →https://doi.org/10.1016/s0031-4056(24)00180-xopenalex-snapshot
The reproductive biology and post-embryonic development of Streptogonopus phipsoni (Diplopoda : Polydesmoidea)
inferredcites →https://doi.org/10.1017/s0952836903003820openalex-snapshot
Sexual dimorphism of body size and shell shape in European tortoises
inferredcites →https://doi.org/10.1017/s0952836903004321openalex-snapshot
Body size plasticity and local variation of relative head and body size sexual dimorphism in garter snakes ( Thamnophis sirtalis )
inferredcites →https://doi.org/10.1023/a:1007736214299openalex-snapshot
Copulatory Sequences and Sexual Struggles in Millipedes
inferredcites →https://doi.org/10.1046/j.1365-2311.2002.00428.xopenalex-snapshot
Sexual size dimorphism in the two spot ladybird beetle Adalia bipunctata : developmental mechanism and its consequences for mating
inferredcites →https://doi.org/10.1071/zo10011openalex-snapshot
Copulation, mating system and sexual dimorphism in an Australian millipede, Cladethosoma clarum
inferredcites →https://doi.org/10.1071/zo9860837openalex-snapshot
Recognition of Mates in the Portuguese Millipede, Ommatoiulus-Moreletii
inferredcites →https://doi.org/10.1073/pnas.0404503101openalex-snapshot
Sexual selection explains Rensch's rule of size dimorphism in shorebirds
inferredcites →https://doi.org/10.1080/00222933.2011.651636openalex-snapshot
How many species are there ofPachyiulus? A contribution to the taxonomy of Europe's largest millipedes (Diplopoda: Julida: Julidae)
inferredcites →https://doi.org/10.1086/444600openalex-snapshot
Allometry for Sexual Size Dimorphism: Testing Two Hypotheses for Rensch’s Rule in the Water Strider Aquarius remigis
inferredcites →https://doi.org/10.1086/520118openalex-snapshot
Geographic Variation in Body Size and Sexual Size Dimorphism of a Seed‐Feeding Beetle
inferredcites →https://doi.org/10.1086/587075openalex-snapshot
Complex Copulatory Behavior and the Proximate Effect of Genital and Body Size Differences on Mechanical Reproductive Isolation in the Millipede Genus Parafontaria
inferredcites →https://doi.org/10.1093/acprof:oso/9780199208784.003.0003openalex-snapshot
Sexual size dimorphism in mammals
inferredcites →https://doi.org/10.1093/acprof:oso/9780199208784.003.0004openalex-snapshot
Sexual size dimorphism in birds
inferredcites →https://doi.org/10.1093/acprof:oso/9780199208784.003.0008openalex-snapshot
Sexual size dimorphism in spiders: patterns and processes
inferredcites →https://doi.org/10.1093/acprof:oso/9780199208784.003.0016openalex-snapshot
Variation in sexual size dimorphism within a widespread lizard species
inferredcites →https://doi.org/10.1093/mollus/66.4.489openalex-snapshot
SEXUAL DIMORPHISM OF NUCELLA LAPILLUS (GASTROPODA: MURICIDAE) IN NORTH WALES, UK
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00719.xopenalex-snapshot
EXPERIMENTAL EVIDENCE FOR THE ADAPTIVE EVOLUTION OF GROWTH RATE IN THE GARTER SNAKE THAMNOPHIS ELEGANS
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00722.xopenalex-snapshot
THE EVOLUTION OF SEXUAL DIMORPHISM IN THE HOUSE FINCH. I. POPULATION DIVERGENCE IN MORPHOLOGICAL COVARIANCE STRUCTURE
inferredcites →https://doi.org/10.1111/j.0030-1299.2005.13609.xopenalex-snapshot
Sexual size dimorphism within species increases with body size in insects
inferredcites →https://doi.org/10.1111/j.1096-3642.1973.tb00790.xopenalex-snapshot
The evolution of arthropodan locomotory mechanisms
inferredcites →https://doi.org/10.1111/j.1365-2311.2011.01279.xopenalex-snapshot
Female‐biased size dimorphism in a diapausing caddisfly, Mesophylax aspersus : effect of fecundity and natural and sexual selection
inferredcites →https://doi.org/10.1111/j.1439-0310.2005.01147.xopenalex-snapshot
Behavioral Causes and Consequences of Sexual Size Dimorphism
inferredcites →https://doi.org/10.1111/j.1469-7998.1978.tb03366.xopenalex-snapshot
The post‐embryonic development and life history of the millipede, Ommatoiulus moreletii (Diplopoda: Iulidae), introduced in south‐eastern Australia
inferredcites →https://doi.org/10.1111/j.1558-5646.1989.tb04220.xopenalex-snapshot
ANALYZING TABLES OF STATISTICAL TESTS
inferredcites →https://doi.org/10.1111/j.1600-0706.2008.17327.xopenalex-snapshot
Geographic variation in body size, sexual size dimorphism and fitness components of a seed beetle: local adaptation versus phenotypic plasticity
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/10.1146/annurev-ento-112408-085500openalex-snapshot
Sex Differences in Phenotypic Plasticity Affect Variation in Sexual Size Dimorphism in Insects: From Physiology to Evolution
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.ento.45.1.341openalex-snapshot
Evolutionary Ecology of Progeny Size in Arthropods
inferredcites →https://doi.org/10.1146/annurev.ento.52.111805.090210openalex-snapshot
Current Status of the Myriapod Class Diplopoda (Millipedes): Taxonomic Diversity and Phylogeny
inferredcites →https://doi.org/10.1163/156853993x00498openalex-snapshot
Mating Tactics in the Tropical Millipede Alloporus Uncinatus (Diplopoda: Spirostreptidae)
inferredcites →https://doi.org/10.1163/9789004188273_017openalex-snapshot
Diplopoda — taxonomic overview
inferredcites →https://doi.org/10.11646/zootaxa.1706.1.1openalex-snapshot
An annotated world catalogue of the millipede order Callipodida (Arthropoda: Diplopoda)
inferredcites →https://doi.org/10.13140/rg.2.2.35963.05924openalex-snapshot
Sexual size dimorphism in Neurergus kaiseri (Caudata: Salamandridae) in south-western Zagros Mountains, Iran
inferredcites →https://doi.org/10.1371/journal.pone.0000897openalex-snapshot
Only Half Right: Species with Female-Biased Sexual Size Dimorphism Consistently Break Rensch's Rule
inferredcites →https://doi.org/10.1371/journal.pone.0014603openalex-snapshot
Intersexual Trophic Niche Partitioning in an Ant-Eating Spider (Araneae: Zodariidae)
inferredcites →https://doi.org/10.1537/ase1887.22.495openalex-snapshot
The descent of man and selection in relation to sex
inferredcites →https://doi.org/10.1665/1082-6467-17.2.265openalex-snapshot
Population and environmental effects on the size-fecundity relationship in a common grasshopper across an aridity gradient
inferredcites →https://doi.org/10.2298/abs150802128iopenalex-snapshot
Anamorphic development of Apfelbeckia insculpta (L. Koch, 1867) (Diplopoda: Callipodida: Schizopetalidae)
inferredcites →https://doi.org/10.2307/1446982openalex-snapshot
Sexual Size Dimorphism in Snakes Revisited
inferredcites →https://doi.org/10.2307/2527939openalex-snapshot
193. Note: The Multivariate Generalization of the Allometry Equation
inferredcites →https://doi.org/10.2307/30119668openalex-snapshot
Complex Copulatory Behavior and the Proximate Effect of Genital and Body Size Differences on Mechanical Reproductive Isolation in the Millipede Genus Parafontaria
inferredcites →https://doi.org/10.2307/3473067openalex-snapshot
Allometry for Sexual Size Dimorphism: Testing Two Hypotheses for Rensch's Rule in the Water Strider Aquarius remigis
inferredcites →https://doi.org/10.2307/3544943openalex-snapshot
Intraspecific Variation in Body Size and Fecundity in Insects: A General Relationship
inferredcites →https://doi.org/10.3897/zookeys.483.9150openalex-snapshot
A new millipede of the family Ammodesmidae found in central Africa (Diplopoda, Polydesmida)
inferredcites →https://doi.org/10.5772/55154openalex-snapshot
The Evolution of Sexual Dimorphism: Understanding Mechanisms of Sexual Shape Differences
inferredcites →https://doi.org/10.5962/bhl.title.2112openalex-snapshot
The descent of man, and selection in relation to sex
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3906/zoo-1701-28zenodo-depositor-declared
Mating behaviour and its relationship with morphological features in the millipede Pachyiulus hungaricus (Karsch, 1881) (Myriapoda, Diplopoda, Julida)
inferred← citeshttps://doi.org/10.1093/aesa/saac010openalex-snapshot
Thermal tolerance in the millipedeEuryurus leachiiGray (Polydesmida: Euryuridae)
inferred← citeshttps://doi.org/10.1098/rsbl.2022.0211openalex-snapshot
Beyond facial width-to-height ratios: bizygomatic width is highly sexually dimorphic when adjusting for allometry
inferred← citeshttps://doi.org/10.1111/azo.70011openalex-snapshot
Morphological Variability in Two Populations of Millipede Glomeris hexasticha Brandt, 1833 (Diplopoda: Glomerida: Glomeridae): Traditional and Geometric Morphometric Approaches
inferred← citeshttps://doi.org/10.1163/15707563-20191113openalex-snapshot
Sexual dimorphism in some morphological traits of three European millipedes (Diplopoda, Julida, Julidae)
inferred← citeshttps://doi.org/10.1163/18759866-08703001openalex-snapshot
Sexual behaviour and morphological variation in the millipede Megaphyllum bosniense (Verhoeff, 1897)
inferred← citeshttps://doi.org/10.1163/18759866-bja10033openalex-snapshot
Morphology and mating behaviour in the millipede Megaphyllum unilineatum (C.L. Koch, 1838) (Myriapoda, Diplopoda, Julida) under laboratory conditions
inferred← citeshttps://doi.org/10.17352/gjz.000010openalex-snapshot
Centrobolus silvanus dimorphism based on tergite width
inferred← citeshttps://doi.org/10.22271/j.ento.2016.v4.i6g.08openalex-snapshot
The relative sexual size dimorphism of Centrobolus inscriptus compared to 18 congenerics
inferred← citeshttps://doi.org/10.22271/j.ento.2016.v4.i6g.1381openalex-snapshot
The relative sexual size dimorphism of Centrobolus inscriptus compared to 18 congenerics
inferred← citeshttps://doi.org/10.22271/j.ento.2017.v5.i2u.04openalex-snapshot
Relative sexual size dimorphism in Centrobolus digrammus (Pocock) compared to 18 congenerics
inferred← citeshttps://doi.org/10.22271/j.ento.2017.v5.i3b.01openalex-snapshot
Relative sexual size dimorphism in Centrobolus fulgidus (Lawrence) compared to 18 congenerics
inferred← citeshttps://doi.org/10.22271/j.ento.2017.v5.i3c.07openalex-snapshot
Relative sexual size dimorphism Centrobolus ruber (Attems) compared to 18 congenerics
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.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
inferred← citeshttps://doi.org/10.22271/j.ento.2018.v6.i6.3.05openalex-snapshot
Centrobolus sagatinus sexual size dimorphism based on differences in horizontal tergite widths
inferred← citeshttps://doi.org/10.22271/j.ento.2019.v7.i3m.5267openalex-snapshot
Non-significant intersexual differences in millipede mass
inferred← citeshttps://doi.org/10.3897/zookeys.1149.99651openalex-snapshot
A new species of Paracortina from a Vietnamese cave, with remarkable secondary sexual characters in males (Callipodida, Paracortinidae)
inferred← citeshttps://doi.org/10.3897/zookeys.930.48285openalex-snapshot
Sexual size and shape dimorphism in Brachydesmus troglobius Daday, 1889 (Diplopoda, Polydesmida)
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