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Reduced genetic diversity and increased reproductive isolation follow population-level loss of larval dispersal in a marine gastropod
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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/scdb.2000.0194openalex-snapshot
Phylogenetic analyses of mode of larval development
inferredcites →https://doi.org/10.1007/s002270050055openalex-snapshot
Effects of contrasting modes of larval development on the genetic structures of populations of three species of prosobranch gastropods
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Invertebrate Species with Nonpelagic Larvae Have Elevated Levels of Nonsynonymous Substitutions and Reduced Nucleotide Diversities
inferredcites →https://doi.org/10.1007/s10682-012-9555-5openalex-snapshot
Methodological issues and advances in biological meta-analysis
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STRUCTURE HARVESTER: a website and program for visualizing STRUCTURE output and implementing the Evanno method
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Mitochondrial DNA phylogeny and rates of larval evolution in Macrophiothrix brittlestars
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The genetic structure of intertidal populations of two species of nudibranch molluscs with planktotrophic and pelagic lecithotrophic larval stages: are pelagic larvae “for” dispersal?
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Does parental divergence predict reproductive compatibility?
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Invasion and the evolution of speed in toads
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Detection of reduction in population size using data from microsatellite loci
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The effects of mode of development on phylogeography and population structure of North Atlantic Crepidula (Gastropoda: Calyptraeidae)
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Regulatory punctuated equilibrium and convergence in the evolution of developmental pathways in direct‐developing sea urchins
inferredcites →https://doi.org/10.1073/pnas.96.18.10272openalex-snapshot
Developmental shifts and species selection in gastropods
inferredcites →https://doi.org/10.1080/01650526909360411openalex-snapshot
Euthyneure Meeresschnecken Brasiliens (2)
inferredcites →https://doi.org/10.1080/10635150490468675openalex-snapshot
A Phylogenetic Mixture Model for Detecting Pattern-Heterogeneity in Gene Sequence or Character-State Data
inferredcites →https://doi.org/10.1080/10635150490522629openalex-snapshot
Frequentist Properties of Bayesian Posterior Probabilities of Phylogenetic Trees Under Simple and Complex Substitution Models
inferredcites →https://doi.org/10.1086/bblv216n2p188openalex-snapshot
Evidence for Costs of Mating and Self-Fertilization in a Simultaneous Hermaphrodite With Hypodermic Insemination, the OpisthobranchAlderia willowi
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Pre-Settlement Behavior in Larval Bryozoans: The Roles of Larval Age and Size
inferredcites →https://doi.org/10.1086/bblv216n3p355openalex-snapshot
Not My “Type”: Larval Dispersal Dimorphisms and Bet-Hedging in Opisthobranch Life Histories
inferredcites →https://doi.org/10.1093/bioinformatics/btl446openalex-snapshot
RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
inferredcites →https://doi.org/10.1093/bioinformatics/bts199openalex-snapshot
Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data
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Statistical method for testing the neutral mutation hypothesis by DNA polymorphism.
inferredcites →https://doi.org/10.1093/genetics/147.2.915openalex-snapshot
Statistical Tests of Neutrality of Mutations Against Population Growth, Hitchhiking and Background Selection
inferredcites →https://doi.org/10.1093/genetics/155.2.945openalex-snapshot
Inference of Population Structure Using Multilocus Genotype Data
inferredcites →https://doi.org/10.1093/icb/30.1.197openalex-snapshot
Why Life Histories Evolve Differently in the Sea
inferredcites →https://doi.org/10.1093/icb/icq068openalex-snapshot
It's About Time: Divergence, Demography, and the Evolution of Developmental Modes in Marine Invertebrates
inferredcites →https://doi.org/10.1093/icb/ics055openalex-snapshot
Asymmetric Dispersal Can Maintain Larval Polymorphism: A Model Motivated by Streblospio benedicti
inferredcites →https://doi.org/10.1093/icb/ics059openalex-snapshot
Seasonal Polyphenism in Larval Type: Rearing Environment Influences the Development Mode Expressed by Adults in the Sea Slug Alderia willowi
inferredcites →https://doi.org/10.1093/icb/ics065openalex-snapshot
Nontraditional Life-History Choices: What Can "Intermediates" Tell Us about Evolutionary Transitions between Modes of Invertebrate Development?
inferredcites →https://doi.org/10.1093/icb/ics077openalex-snapshot
Poecilogony and Population Genetic Structure in Elysia pusilla (Heterobranchia: Sacoglossa), and Reproductive Data for Five Sacoglossans that Express Dimorphisms in Larval Development
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Bayesian Coalescent Inference of Past Population Dynamics from Molecular Sequences
inferredcites →https://doi.org/10.1093/molbev/mss075openalex-snapshot
Bayesian Phylogenetics with BEAUti and the BEAST 1.7
inferredcites →https://doi.org/10.1093/mollus/68.2.101openalex-snapshot
COMPARISON OF BIOCHEMICAL COMPOSITION AND DEVELOPMENTAL MODE IN TWO POPULATIONS OF COSTASIELLA [OPISTHOBRANCHIA: ASCOGLOSSA (= SACOGLOSSA)]
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A review of taxonomy and phylogenetic relationships in the genusCostasiella(Heterobranchia: Sacoglossa), with a description of a new species
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An Empirical Test of Bootstrapping as a Method for Assessing Confidence in Phylogenetic Analysis
inferredcites →https://doi.org/10.1093/sysbio/syv046openalex-snapshot
Species Selection Favors Dispersive Life Histories in Sea Slugs, but Higher Per-Offspring Investment Drives Shifts to Short-Lived Larvae
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Shallow gene pools in the high intertidal: extreme loss of genetic diversity in viviparous sea stars ( Parvulastra )
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A candidate locus for variation in dispersal rate in a butterfly metapopulation
inferredcites →https://doi.org/10.1098/rspb.2008.0216openalex-snapshot
Global patterns in marine dispersal estimates: the influence of geography, taxonomic category and life history
inferredcites →https://doi.org/10.1098/rspb.2012.1343openalex-snapshot
Extraordinarily rapid life-history divergence between Cryptasterina sea star species
inferredcites →https://doi.org/10.1109/gce.2010.5676129openalex-snapshot
Creating the CIPRES Science Gateway for inference of large phylogenetic trees
inferredcites →https://doi.org/10.1111/1365-2745.12405openalex-snapshot
Dispersal mode mediates the effect of patch size and patch connectivity on metacommunity diversity
inferredcites →https://doi.org/10.1111/bij.12006openalex-snapshot
Very fine-scale population genetic structure of sympatric asterinid sea stars with benthic and pelagic larvae: influence of mating system and dispersal potential
inferredcites →https://doi.org/10.1111/ede.12128openalex-snapshot
Gene‐based polymorphisms reveal limited genomic divergence in a species with a heritable life‐history dimorphism
inferredcites →https://doi.org/10.1111/eva.12154openalex-snapshot
Joint effects of population size and isolation on genetic erosion in fragmented populations: finding fragmentation thresholds for management
inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb01290.xopenalex-snapshot
DIVERGENT EVOLUTION OF DISPERSAL IN A HETEROGENEOUS LANDSCAPE
inferredcites →https://doi.org/10.1111/j.0014-3820.2004.tb01729.xopenalex-snapshot
PHYLOGENETIC EFFECTS, THE LOSS OF COMPLEX CHARACTERS, AND THE EVOLUTION OF DEVELOPMENT IN CALYPTRAEID GASTROPODS
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01866.xopenalex-snapshot
EVOLUTION OF POECILOGONY FROM PLANKTOTROPHY: CRYPTIC SPECIATION, PHYLOGEOGRAPHY, AND LARVAL DEVELOPMENT IN THE GASTROPOD GENUS ALDERIA
inferredcites →https://doi.org/10.1111/j.1095-8312.1991.tb00553.xopenalex-snapshot
Dispersal and connectivity in metapopulations
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02553.xopenalex-snapshot
Detecting the number of clusters of individuals using the software structure : a simulation study
inferredcites →https://doi.org/10.1111/j.1365-294x.2007.03385.xopenalex-snapshot
Contrasting phylogeography in three endemic Hawaiian limpets (Cellana spp.) with similar life histories
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.03787.xopenalex-snapshot
A restoration genetics guide for coral reef conservation
inferredcites →https://doi.org/10.1111/j.1365-294x.2009.04127.xopenalex-snapshot
Does life history predict past and current connectivity for rocky intertidal invertebrates across a marine biogeographic barrier?
inferredcites →https://doi.org/10.1111/j.1365-294x.2009.04169.xopenalex-snapshot
Spatial and temporal population genetic structure of four northeastern Pacific littorinid gastropods: the effect of mode of larval development on variation at one mitochondrial and two nuclear DNA markers
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04854.xopenalex-snapshot
Divergence genetics analysis reveals historical population genetic processes leading to contrasting phylogeographic patterns in co‐distributed species
inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05609.xopenalex-snapshot
Theoretical limits to the correlation between pelagic larval duration and population genetic structure
inferredcites →https://doi.org/10.1111/j.1461-0248.2012.01794.xopenalex-snapshot
Body size and dispersal mode as key traits determining metacommunity structure of aquatic organisms
inferredcites →https://doi.org/10.1111/j.1471-8286.2007.01884.xopenalex-snapshot
msatcommander : detection of microsatellite repeat arrays and automated, locus‐specific primer design
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PATTERNS OF SPECIATION IN DROSOPHILA
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THE GENETIC INTERPRETATION OF INBREEDING DEPRESSION AND OUTBREEDING DEPRESSION
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POPULATION GENETIC CONSEQUENCES OF DEVELOPMENTAL EVOLUTION IN SEA URCHINS (GENUS HELIOCIDARIS )
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GENETIC EVIDENCE FOR LONG TERM PERSISTENCE OF MARINE INVERTEBRATE POPULATIONS IN AN EPHEMERAL ENVIRONMENT
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HETEROSIS AND OUTBREEDING DEPRESSION IN INTERPOPULATION CROSSES SPANNING A WIDE RANGE OF DIVERGENCE
inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00305.xopenalex-snapshot
INTERPOPULATION HYBRID BREAKDOWN MAPS TO THE MITOCHONDRIAL GENOME
inferredcites →https://doi.org/10.1111/j.1558-5646.2010.01143.xopenalex-snapshot
ASYMMETRIC PATCH SIZE DISTRIBUTION LEADS TO DISRUPTIVE SELECTION ON DISPERSAL
inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01705.xopenalex-snapshot
TESTING THE INFLUENCE OF FAMILY STRUCTURE AND OUTBREEDING DEPRESSION ON HETEROZYGOSITY-FITNESS CORRELATIONS IN SMALL POPULATIONS
inferredcites →https://doi.org/10.1111/j.1600-0706.2013.00706.xopenalex-snapshot
Where am I and why? Synthesizing range biology and the eco‐evolutionary dynamics of dispersal
inferredcites →https://doi.org/10.1111/j.1749-6632.2009.04919.xopenalex-snapshot
The Genetics and Ecology of Reinforcement
inferredcites →https://doi.org/10.1111/j.1755-0998.2010.02847.xopenalex-snapshot
Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows
inferredcites →https://doi.org/10.1111/j.1755-0998.2011.02988.xopenalex-snapshot
Skyline‐plot methods for estimating demographic history from nucleotide sequences
inferredcites →https://doi.org/10.1111/mec.12040openalex-snapshot
Consequences of a poecilogonous life history for genetic structure in coastal populations of the polychaete S treblospio benedicti
inferredcites →https://doi.org/10.1111/mec.13031openalex-snapshot
Evolutionary history of a dispersal‐associated locus across sympatric and allopatric divergent populations of a wing‐polymorphic beetle across A tlantic E urope
inferredcites →https://doi.org/10.1126/science.287.5454.857openalex-snapshot
Connectivity of Marine Populations: Open or Closed?
inferredcites →https://doi.org/10.1146/annurev-ecolsys-102710-145004openalex-snapshot
The Biogeography of Marine Invertebrate Life Histories
inferredcites →https://doi.org/10.1146/annurev.ecolsys.38.091206.095611openalex-snapshot
How Does It Feel to Be Like a Rolling Stone? Ten Questions About Dispersal Evolution
inferredcites →https://doi.org/10.1146/annurev.es.16.110185.002011openalex-snapshot
Feeding and Nonfeeding Larval Development and Life-History Evolution in Marine Invertebrates
inferredcites →https://doi.org/10.1177/117693430500100003openalex-snapshot
Arlequin (version 3.0): An integrated software package for population genetics data analysis
inferredcites →https://doi.org/10.1186/s40462-015-0045-6openalex-snapshot
Identifying the key biophysical drivers, connectivity outcomes, and metapopulation consequences of larval dispersal in the sea
inferredcites →https://doi.org/10.1371/journal.pone.0008594openalex-snapshot
Genetic Structure Among 50 Species of the Northeastern Pacific Rocky Intertidal Community
inferredcites →https://doi.org/10.1371/journal.pone.0062992openalex-snapshot
The Confounding Effect of Population Structure on Bayesian Skyline Plot Inferences of Demographic History
inferredcites →https://doi.org/10.1534/genetics.108.092718openalex-snapshot
The Different Sources of Variation in Inbreeding Depression, Heterosis and Outbreeding Depression in a Metapopulation of Physa acuta
inferredcites →https://doi.org/10.1890/13-0871.1openalex-snapshot
Dispersal potential and population genetic structure in the marine intertidal of the eastern North Pacific
inferredcites →https://doi.org/10.1890/13-0970.1openalex-snapshot
Circulation constrains the evolution of larval development modes and life histories in the coastal ocean
inferredcites →https://doi.org/10.2307/1938632openalex-snapshot
Implications of Alternative Reproductive Modes for Seasonality and Demography in an Estuarine Polychaete
inferredcites →https://doi.org/10.2307/2409938openalex-snapshot
Population Genetic Consequences of Developmental Evolution in Sea Urchins (Genus heliocidaris)
inferredcites →https://doi.org/10.2307/2640438openalex-snapshot
Heterosis and Outbreeding Depression in Interpopulation Crosses Spanning a Wide Range of Divergence
inferredcites →https://doi.org/10.2307/2992540openalex-snapshot
An Empirical Test of Bootstrapping as a Method for Assessing Confidence in Phylogenetic Analysis
inferredcites →https://doi.org/10.3354/meps08287openalex-snapshot
Population genetics, larval dispersal, and connectivity in marine systems
inferredcites →https://doi.org/10.3354/meps09238openalex-snapshot
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inferredcites →https://doi.org/10.3354/meps177269openalex-snapshot
On the advantages and disadvantages of larval stages in benthic marine invertebrate life cycles
inferredcites →https://doi.org/10.4003/006.032.0208openalex-snapshot
Molecular Data Reveal an Undescribed Cryptic Species ofCostasiellaPruvot-Fol, 1951 (Euthyneura: Sacoglossa: Limapontidae) in the Bahamas
inferredcites →https://doi.org/10.5281/zenodo.15145663openalex-snapshot
Table 1 in A new Gammarus species from Xinjiang Uygur Autonomous Region (China) with a key to Xinjiang freshwater gammarids (Crustacea, Amphipoda, Gammaridae)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4148.1.1zenodo-depositor-declared
Molecular and morphological systematics of Elysia Risso, 1818 (Heterobranchia: Sacoglossa) from the Caribbean region
inferred← citeshttps://doi.org/10.5852/ejt.2020.665zenodo-depositor-declared
Unraveling one of the ‘Big Five’: update of the taxonomy of Triphoridae (Gastropoda, Triphoroidea) from Brazil
inferred← citeshttps://doi.org/10.1002/eap.1978openalex-snapshot
Considerations for maximizing the adaptive potential of restored coral populations in the western Atlantic
inferred← citeshttps://doi.org/10.1002/ece3.11014openalex-snapshot
Validating a molecular clock for nudibranchs—No fossils to the rescue
inferred← citeshttps://doi.org/10.1002/ece3.73677openalex-snapshot
Will the Mediterranean Sea Be a Cul‐de‐Sac for Marine Gastropods Under Climate Change?
inferred← citeshttps://doi.org/10.1002/ece3.8136openalex-snapshot
Plasticity and artificial selection for developmental mode in a poecilogonous sea slug
inferred← citeshttps://doi.org/10.1007/s10646-023-02725-9openalex-snapshot
Contamination acts as a genotype-dependent barrier to gene flow, causing genetic erosion and fine-grained population subdivision in Mussels from the Strait of Istanbul
inferred← citeshttps://doi.org/10.1007/s12526-017-0812-2openalex-snapshot
Integrative systematics of Placida cremoniana (Trinchese, 1892) (Gastropoda, Heterobranchia, Sacoglossa) reveals multiple pseudocryptic species
inferred← citeshttps://doi.org/10.1007/s12526-019-01027-wopenalex-snapshot
Stargazing under the sea: molecular and morphological data reveal a constellation of species in the Berthella stellata (Risso, 1826) species complex (Mollusca, Heterobranchia, Pleurobranchidae)
inferred← citeshttps://doi.org/10.1016/j.marenvres.2017.04.001openalex-snapshot
Do larval types affect genetic connectivity at sea? Testing hypothesis in two sibling marine gastropods with contrasting larval development
inferred← citeshttps://doi.org/10.1016/j.rsma.2018.09.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ympev.2018.02.027openalex-snapshot
A biting commentary: Integrating tooth characters with molecular data doubles known species diversity in a lineage of sea slugs that consume “killer algae”
inferred← citeshttps://doi.org/10.1016/j.ympev.2022.107523openalex-snapshot
Ecological speciation by sympatric host shifts in a clade of herbivorous sea slugs, with introgression and localized mitochondrial capture between species
inferred← citeshttps://doi.org/10.1071/is19039openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/biolinnean/blaf111openalex-snapshot
Integrating host use and dispersal ability with species delimitation to unravel a cryptic radiation of photosynthetic sea slugs
inferred← citeshttps://doi.org/10.1093/mollus/eyz032openalex-snapshot
High genetic connectivity in a gastropod with long-lived planktonic larvae
inferred← citeshttps://doi.org/10.1093/oso/9780198786962.003.0004openalex-snapshot
Evolutionary Transitions in Mode of Development
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlad111openalex-snapshot
A cryptic radiation of Caribbean sea slugs revealed by integrative analysis: Cyerce ‘antillensis’ (Sacoglossa: Caliphyllidae) is six distinct species
inferred← citeshttps://doi.org/10.1093/zoolinnean/zly050openalex-snapshot
Systematics of Polybranchia Pease, 1860 (Mollusca: Gastropoda: Sacoglossa) based on molecular and morphological data
inferred← citeshttps://doi.org/10.1101/2022.09.30.510344openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/1365-2656.70049openalex-snapshot
Metapopulation‐level analyses reveal positive fitness consequences of immigration in a small bird
inferred← citeshttps://doi.org/10.1111/brv.13183openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/jeb.13735openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/maec.12639openalex-snapshot
Are populations of economically important bonefish and queen conch 'open' or 'closed' in the northern caribbean basin?
inferred← citeshttps://doi.org/10.1111/mec.16143openalex-snapshot
Balanced polymorphism fuels rapid selection in an invasive crab despite high gene flow and low genetic diversity
inferred← citeshttps://doi.org/10.2108/zs240028openalex-snapshot
Comparison of Genetic Structures Among Sympatric, Red-Listed Salt-Marsh Snails in Mainland Japan (Gastropoda: Ellobiidae)
inferred← citeshttps://doi.org/10.26686/wgtn.17019374openalex-snapshot
Crawling to connectivity? The direct-developing journey of the spotted whelk (Cominella maculosa)
inferred← citeshttps://doi.org/10.3390/d16010040openalex-snapshot
The Dancing Marsenia: The First Record of a Swimming Velutinid Mollusc
inferred← citeshttps://doi.org/10.3390/genes13122221openalex-snapshot
Salmonidae Genome: Features, Evolutionary and Phylogenetic Characteristics
inferred← citeshttps://doi.org/10.3800/pbr.17.66openalex-snapshot
Population differentiation of the endangered salt-marsh snail Ellobium chinense in Japan (Gastropoda: Ellobiidae)
inferred← citeshttps://doi.org/10.4003/006.042.0107openalex-snapshot
A Mimic's Mimic: Redescription of Elysia corinneae (Ev. Marcus, 1973), One of Three Halimeda-Eating Elysia (Gastropoda: Heterobranchia) Misclassified as Bosellia Due to Fused Parapodia
inferred← citeshttps://doi.org/10.70675/48563200z3aa3z4a88zad8bza48188b574b3openalex-snapshot
Histoire évolutive et influence de la sélection sur la diversité génétique des annélides polychètes d’environnements extrêmes
inferred← citeshttps://doi.org/10.7287/peerj.2410v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Extremely low genetic variability within and among locations of the greenfish holothurian Stichopus chloronotus Brandt, 1835 in Okinawa, Japan (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.2410v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Extremely low genetic variability within and among locations of the greenfish holothurian Stichopus chloronotus Brandt, 1835 in Okinawa, Japan (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.2410v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Extremely low genetic variability within and among locations of the greenfish holothurian Stichopus chloronotus Brandt, 1835 in Okinawa, Japan (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.2410v0.1/reviews/4openalex-snapshot
Peer Review #4 of "Extremely low genetic variability within and among locations of the greenfish holothurian Stichopus chloronotus Brandt, 1835 in Okinawa, Japan (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.2410openalex-snapshot
Extremely low genetic variability within and among locations of the greenfish holothurian Stichopus chloronotus Brandt, 1835 in Okinawa, Japan
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