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Escaping paradise: larval export from Hawaii in an Indo-Pacific reef fish, the yellow tang Zebrasoma flavescens

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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/mpev.1998.0542openalex-snapshot

Phylogenetic Relations among Percid Fishes as Inferred from Mitochondrial CytochromebDNA Sequence Data

inferredcites →https://doi.org/10.1007/bf00004879openalex-snapshot

Patterns of recruitment and spawning in Hawaiian reef fishes

inferredcites →https://doi.org/10.1007/s00227-003-1224-3openalex-snapshot

High genetic diversities and complex genetic structure in an Indo-Pacific tropical reef fish (Chlorurus sordidus): evidence of an unstable evolutionary past?

inferredcites →https://doi.org/10.1007/s00227-005-0001-xopenalex-snapshot

Critical swimming speeds of late-stage coral reef fish larvae: variation within species, among species and between locations

inferredcites →https://doi.org/10.1007/s00227-008-1119-4openalex-snapshot

Endemism and dispersal: comparative phylogeography of three surgeonfishes across the Hawaiian Archipelago

inferredcites →https://doi.org/10.1007/s00338-006-0118-5openalex-snapshot

Colonization of the Hawaiian Archipelago via Johnston Atoll: a characterization of oceanographic transport corridors for pelagic larvae using computer simulation

inferredcites →https://doi.org/10.1007/s10872-009-0030-zopenalex-snapshot

Observations of the North Equatorial Current, Mindanao Current, and Kuroshio current system during the 2006/07 El Niño and 2007/08 La Niña

inferredcites →https://doi.org/10.1016/0169-5347(87)90016-4openalex-snapshot

Ecology, biogeography and evolution of corals in Hawaii

inferredcites →https://doi.org/10.1016/0169-5347(87)90017-6openalex-snapshot

Endemism and evolution in Hawaiian marine invertebrates

inferredcites →https://doi.org/10.1016/0169-5347(87)90018-8openalex-snapshot

Mid-ocean isolation and the evolution of Hawaiian reef fishes

inferredcites →https://doi.org/10.1016/0169-5347(96)10049-5openalex-snapshot

Microsatellites, from molecules to populations and back

inferredcites →https://doi.org/10.1016/j.biocon.2008.12.029openalex-snapshot

Impacts of a Hawaiian marine protected area network on the abundance and fishery sustainability of the yellow tang, Zebrasoma flavescens

inferredcites →https://doi.org/10.1016/j.dsr2.2008.01.008openalex-snapshot

Eddy activity in the lee of the Hawaiian Islands

inferredcites →https://doi.org/10.1016/s0377-8398(03)00062-8openalex-snapshot

Spatial and temporal variability of surface water in the Kuroshio source region, Pacific Ocean, over the past 21,000 years: evidence from planktonic foraminifera

inferredcites →https://doi.org/10.1017/cbo9780511626920.004openalex-snapshot

How to use MIGRATE or why are Markov chain Monte Carlo programs difficult to use?

inferredcites →https://doi.org/10.1023/a:1015213626922openalex-snapshot

Is F ST obsolete?

inferredcites →https://doi.org/10.1029/2001jc001225openalex-snapshot

Seasonal variation and instability nature of the North Pacific Subtropical Countercurrent and the Hawaiian Lee Countercurrent

inferredcites →https://doi.org/10.1029/jc088ic12p07507openalex-snapshot

The near‐surface circulation of the North Pacific using satellite tracked drifting buoys

inferredcites →https://doi.org/10.1046/j.1365-294x.2000.01020.xopenalex-snapshot

TCS: a computer program to estimate gene genealogies

inferredcites →https://doi.org/10.1046/j.1365-294x.2001.01190.xopenalex-snapshot

Detection of reduction in population size using data from microsatellite loci

inferredcites →https://doi.org/10.1046/j.1365-294x.2002.01650.xopenalex-snapshot

A simulated annealing approach to define the genetic structure of populations

inferredcites →https://doi.org/10.1046/j.1469-1809.2005.00162.xopenalex-snapshot

The Effect of Genetic Drift in a Young Genetically Isolated Population

inferredcites →https://doi.org/10.1046/j.1523-1739.1996.10061500.xopenalex-snapshot

Relationship of Genetic Variation to Population Size in Wildlife

inferredcites →https://doi.org/10.1073/pnas.0611164104openalex-snapshot

Integration within the Felsenstein equation for improved Markov chain Monte Carlo methods in population genetics

inferredcites →https://doi.org/10.1073/pnas.081068098openalex-snapshot

Maximum likelihood estimation of a migration matrix and effective population sizes in n subpopulations by using a coalescent approach

inferredcites →https://doi.org/10.1093/bioinformatics/btg359openalex-snapshot

DnaSP, DNA polymorphism analyses by the coalescent and other methods

inferredcites →https://doi.org/10.1093/genetics/111.3.675openalex-snapshot

POPULATION BOTTLENECKS AND NONEQUILIBRIUM MODELS IN POPULATION GENETICS. II. NUMBER OF ALLELES IN A SMALL POPULATION THAT WAS FORMED BY A RECENT BOTTLENECK

inferredcites →https://doi.org/10.1093/genetics/133.3.693openalex-snapshot

Statistical tests of neutrality of mutations.

inferredcites →https://doi.org/10.1093/genetics/144.4.2001openalex-snapshot

Description and Power Analysis of Two Tests for Detecting Recent Population Bottlenecks From Allele Frequency Data

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/164.4.1567openalex-snapshot

Inference of Population Structure Using Multilocus Genotype Data: Linked Loci and Correlated Allele Frequencies

inferredcites →https://doi.org/10.1093/jhered/89.5.415openalex-snapshot

Shallow population histories in deep evolutionary lineages of marine fishes: insights from sardines and anchovies and lessons for conservation

inferredcites →https://doi.org/10.1093/jhered/90.4.502openalex-snapshot

Computer note. BOTTLENECK: a computer program for detecting recent reductions in the effective size using allele frequency data

inferredcites →https://doi.org/10.1093/jhered/esq036openalex-snapshot

Phylogeography of Two Moray Eels Indicates High Dispersal Throughout the Indo-Pacific

inferredcites →https://doi.org/10.1093/molbev/msj079openalex-snapshot

Accuracy of Coalescent Likelihood Estimates: Do We Need More Sites, More Sequences, or More Loci?

inferredcites →https://doi.org/10.1093/nar/gkf436openalex-snapshot

MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025612openalex-snapshot

Numerous transposed sequences of mitochondrial cytochrome oxidase I-II in aphids of the genus Sitobion (Hemiptera: Aphididae)

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040727openalex-snapshot

Population growth makes waves in the distribution of pairwise genetic differences.

inferredcites →https://doi.org/10.1093/plankt/10.6.1209openalex-snapshot

Larval fishes and zooplankton in a cyclonic eddy in Hawaiian waters

inferredcites →https://doi.org/10.1093/sysbio/30.3.309openalex-snapshot

Taxonomic Congruence in the Leptopodomorpha Re-examined

inferredcites →https://doi.org/10.1098/rspb.2009.2214openalex-snapshot

Ocean currents help explain population genetic structure

inferredcites →https://doi.org/10.1111/j.0014-3820.2005.tb01814.xopenalex-snapshot

A STANDARDIZED GENETIC DIFFERENTIATION MEASURE

inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01874.xopenalex-snapshot

USING THE AMOVA FRAMEWORK TO ESTIMATE A STANDARDIZED GENETIC DIFFERENTIATION MEASURE

inferredcites →https://doi.org/10.1111/j.1365-2699.2010.02358.xopenalex-snapshot

Origins, ages and population histories: comparative phylogeography of endemic Hawaiian butterflyfishes (genus Chaetodon)

inferredcites →https://doi.org/10.1111/j.1365-294x.1992.tb00152.xopenalex-snapshot

Unusual mitochondrial DNA polymorphism in two local populations of blue tit Parus caeruleus

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.2010.04521.xopenalex-snapshot

Rolling stones and stable homes: social structure, habitat diversity and population genetics of the Hawaiian spinner dolphin (Stenella longirostris)

inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04658.xopenalex-snapshot

Taking the chaos out of genetic patchiness: seascape genetics reveals ecological and oceanographic drivers of genetic patterns in three temperate reef species

inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04836.xopenalex-snapshot

Isolation by distance across the Hawaiian Archipelago in the reef‐building coral Porites lobata

inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04942.xopenalex-snapshot

The West Pacific diversity hotspot as a source or sink for new species? Population genetic insights from the Indo-Pacific parrotfish Scarus rubroviolaceus

inferredcites →https://doi.org/10.1111/j.1461-0248.2006.00889.xopenalex-snapshot

Microsatellites for ecologists: a practical guide to using and evaluating microsatellite markers

inferredcites →https://doi.org/10.1111/j.1471-8286.2004.00684.xopenalex-snapshot

micro ‐ checker : software for identifying and correcting genotyping errors in microsatellite data

inferredcites →https://doi.org/10.1111/j.1523-1739.2003.00379.xopenalex-snapshot

Effects of Aquarium Collectors on Coral Reef Fishes in Kona, Hawaii

inferredcites →https://doi.org/10.1111/j.1558-5646.1993.tb01215.xopenalex-snapshot

ISOLATION BY DISTANCE IN EQUILIBRIUM AND NON-EQUILIBRIUM POPULATIONS

inferredcites →https://doi.org/10.1111/j.1558-5646.1995.tb04456.xopenalex-snapshot

AN EXACT TEST FOR POPULATION DIFFERENTIATION

inferredcites →https://doi.org/10.1111/j.1558-5646.1999.tb03769.xopenalex-snapshot

COINCIDENT BIOGEOGRAPHIC PATTERNS: INDO-WEST PACIFIC OCEAN

inferredcites →https://doi.org/10.1111/j.1755-0998.2008.02354.xopenalex-snapshot

Isolation and characterization of 23 microsatellite loci in the yellow tang, Zebrasoma flavescens (Pisces: Acanthuridae)

inferredcites →https://doi.org/10.1111/j.1755-0998.2009.02591.xopenalex-snapshot

Inferring weak population structure with the assistance of sample group information

inferredcites →https://doi.org/10.1139/z91-013openalex-snapshot

Preservation of avian blood and tissue samples for DNA analyses

inferredcites →https://doi.org/10.1146/annurev.ecolsys.38.091206.095815openalex-snapshot

The Great American Schism: Divergence of Marine Organisms After the Rise of the Central American Isthmus

inferredcites →https://doi.org/10.1146/annurev.marine.010908.163757openalex-snapshot

Larval Dispersal and Marine Population Connectivity

inferredcites →https://doi.org/10.1155/2011/460173openalex-snapshot

Defining Boundaries for Ecosystem-Based Management: A Multispecies Case Study of Marine Connectivity across the Hawaiian Archipelago

inferredcites →https://doi.org/10.1155/2011/518516openalex-snapshot

Not All Larvae Stay Close to Home: Insights into Marine Population Connectivity with a Focus on the Brown Surgeonfish (Acanthurus nigrofuscus)

inferredcites →https://doi.org/10.1155/2011/765353openalex-snapshot

Genetic Analyses and Simulations of Larval Dispersal Reveal Distinct Populations and Directional Connectivity across the Range of the Hawaiian Grouper (Epinephelus quernus)

inferredcites →https://doi.org/10.1155/2011/783030openalex-snapshot

Gateways to Hawai‘i: Genetic Population Structure of the Tropical Sea CucumberHolothuria atra

inferredcites →https://doi.org/10.1155/2011/839134openalex-snapshot

Phylogeography of the Pacific Blueline Surgeonfish, Acanthurus nigroris , Reveals High Genetic Connectivity and a Cryptic Endemic Species in the Hawaiian Archipelago

inferredcites →https://doi.org/10.1155/2011/934269openalex-snapshot

Widespread Dispersal of the Crown-of-Thorns Sea Star, Acanthaster planci , across the Hawaiian Archipelago and Johnston Atoll

inferredcites →https://doi.org/10.1175/1520-0485(1992)022<1062:ivitma>2.0.co;2openalex-snapshot

Interannual Variability in the Mid- and Low-Latitude Western North Pacific

inferredcites →https://doi.org/10.1175/1520-0485(2000)030<0003:igcait>2.0.co;2openalex-snapshot

Interannual Geostrophic Current Anomalies in the Near-Equatorial Western Pacific

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/10.1186/1471-2148-8-157openalex-snapshot

Comparative phylogeography of Atlantic reef fishes indicates both origin and accumulation of diversity in the Caribbean

inferredcites →https://doi.org/10.1353/psc.2004.0024openalex-snapshot

Evaluating Effectiveness of a Marine Protected Area Network in West Hawai'i to Increase Productivity of an Aquarium Fishery

inferredcites →https://doi.org/10.1371/journal.pone.0015715openalex-snapshot

Larval Connectivity in an Effective Network of Marine Protected Areas

inferredcites →https://doi.org/10.1534/genetics.105.049080openalex-snapshot

Fast and Accurate Estimation of the Population-Scaled Mutation Rate, θ, From Microsatellite Genotype Data

inferredcites →https://doi.org/10.1534/genetics.107.078931openalex-snapshot

Estimation of the Population Scaled Mutation Rate From Microsatellite Data

inferredcites →https://doi.org/10.1554/0014-3820(2001)055[1029:pottar]2.0.co;2openalex-snapshot

PHYLOGEOGRAPHY OF THE TRUMPETFISHES (AULOSTOMUS): RING SPECIES COMPLEX ON A GLOBAL SCALE

inferredcites →https://doi.org/10.1890/02-0254openalex-snapshot

INDO-PACIFIC BIODIVERSITY OF CORAL REEFS: DEVIATIONS FROM A MID-DOMAIN MODEL

inferredcites →https://doi.org/10.1890/1051-0761(2000)010[1792:soeffa]2.0.co;2openalex-snapshot

SPILLOVER OF EXPLOITABLE FISHES FROM A MARINE PARK AND ITS EFFECT ON THE ADJACENT FISHERY

inferredcites →https://doi.org/10.2307/2413252openalex-snapshot

Taxonomic Congruence in the Leptopodomorpha Re-Examined

inferredcites →https://doi.org/10.2307/2845572openalex-snapshot

The Vortex Model of Coral Reef Biogeography

inferredcites →https://doi.org/10.3354/meps08114openalex-snapshot

Habitat- and sex-specific life history patterns of yellow tang Zebrasoma flavescens in Hawaii, USA

inferredcites →https://doi.org/10.3354/meps224103openalex-snapshot

Settlement of the gregarious tube worm Hydroides dianthus (Polychaeta: Serpulidae). I. Gregarious and nongregarious settlement

inferredcites →https://doi.org/10.3354/meps285223openalex-snapshot

Swimming speeds of larval coral reef fishes: impacts on self-recruitment and dispersal

inferredcites →https://doi.org/10.3354/meps334245openalex-snapshot

High genetic connectivity across the Indian and Pacific Oceans in the reef fish Myripristis berndti (Holocentridae)

inferredcites →https://doi.org/10.4135/9781412961288.n455openalex-snapshot

Teoria Statistica Delle Classi e Calcolo Delle Probabilità

inferredcites →https://doi.org/10.7312/nei-92038openalex-snapshot

Molecular Evolutionary Genetics

What points at this work

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

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Junior synonymy of Mulloides armatus and intraspecific comparisons of the yellowstripe goatfish Mulloidichthys flavolineatus (Mullidae) using a comprehensive alpha-taxonomy approach

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Genomic islands of divergence in the Yellow Tang and the Brushtail Tang Surgeonfishes

inferred← citeshttps://doi.org/10.1002/ece3.4566openalex-snapshot

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inferred← citeshttps://doi.org/10.1007/s00227-012-1878-9openalex-snapshot

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inferred← citeshttps://doi.org/10.1007/s00227-018-3395-yopenalex-snapshot

Comparative phylogeography of widespread and endemic damselfishes in the Hawaiian Archipelago

inferred← citeshttps://doi.org/10.1007/s00338-022-02257-4openalex-snapshot

Genomic assessment of an endemic Hawaiian surgeonfish, Acanthurus triostegus sandvicensis, reveals high levels of connectivity and fine-scale population structure

inferred← citeshttps://doi.org/10.1007/s00360-025-01627-yopenalex-snapshot

Aerobic scope and temperature preference in yellow tang (Zebrasoma flavescens) at current and elevated sea temperatures

inferred← citeshttps://doi.org/10.1007/s10641-017-0697-8openalex-snapshot

Assemblage-level effects of the introduced peacock hind (Cephalopholis argus) on Hawaiian reef fishes

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Genetic connectivity in a herbivorous coral reef fish (Acanthurus leucosternon Bennet, 1833) in the Eastern African region

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New microsatellite DNA markers to resolve population structure of the convict surgeonfish, Acanthurus triostegus, and cross-species amplifications on thirteen other Acanthuridae

inferred← citeshttps://doi.org/10.1016/b978-0-08-100853-9.00053-1openalex-snapshot

The Hawaiian Archipelago

inferred← citeshttps://doi.org/10.1016/b978-0-12-409548-9.11947-5openalex-snapshot

Island Biogeography of Marine Shallow-Water Organisms

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Species range evolution of the rocky intertidal leaf oyster Isognomon nucleus (Lamarck, 1819) in the Indo-Pacific

inferred← citeshttps://doi.org/10.1016/j.jembe.2020.151325openalex-snapshot

Population genetics of the banded coral shrimp, Stenopus hispidus ( ), in the Indonesian archipelago

inferred← citeshttps://doi.org/10.1016/j.tree.2013.01.018openalex-snapshot

The origins of tropical marine biodiversity

inferred← citeshttps://doi.org/10.1016/j.ympev.2011.11.007openalex-snapshot

The role of peripheral endemism in species diversification: Evidence from the coral reef fish genus Anampses (Family: Labridae)

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The Three Domains of Conservation Genetics: Case Histories from Hawaiian Waters

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Common misconceptions in molecular ecology: echoes of the modern synthesis

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CONCORDANCE BETWEEN GENETIC AND SPECIES DIVERSITY IN CORAL REEF FISHES ACROSS THE PACIFIC OCEAN BIODIVERSITY GRADIENT

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Origins and relationships of endemic Hawaiian sabre‐toothed blennies in the genus Plagiotremus (Blennioidei: Blenniidae)

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Defining Boundaries for Ecosystem-Based Management: A Multispecies Case Study of Marine Connectivity across the Hawaiian Archipelago

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Artificial Culture Technology of Zebrasoma flavescens (Yellow Tang)

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Larval Connectivity in an Effective Network of Marine Protected Areas

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inferred← citeshttps://doi.org/10.1371/journal.pone.0081847openalex-snapshot

Global Biogeography of Reef Fishes: A Hierarchical Quantitative Delineation of Regions

inferred← citeshttps://doi.org/10.1371/journal.pone.0167626openalex-snapshot

Modeled Population Connectivity across the Hawaiian Archipelago

inferred← citeshttps://doi.org/10.14203/oseana.2021.vol.46no.1.101openalex-snapshot

SPESIASI DAN BIOGEOGRAFI IKAN DI KAWASAN SEGITIGA TERUMBU KARANG

inferred← citeshttps://doi.org/10.1674/0003-0031-178.2.260openalex-snapshot

Phylogeographic Characterization of Genetic Variation in the Biological Control Agent Milfoil Weevil (Euhrychiopsis lecontei) throughout North America

inferred← citeshttps://doi.org/10.21425/f5fbg57427openalex-snapshot

The Habitat Persistence Hypothesis: a new perspective on the distribution of coral-reef organisms

inferred← citeshttps://doi.org/10.2305/iucn.ch.2017.pag.26.enopenalex-snapshot

Large-Scale Marine Protected Areas: guidelines for design and management

inferred← citeshttps://doi.org/10.25268/bimc.invemar.2017.46.2.728openalex-snapshot

Variación espacio temporal del ensamble de larvas de peces coralinos en isla Gorgona, Pacífico colombiano

inferred← citeshttps://doi.org/10.2983/035.032.0116openalex-snapshot

Assessment of Self-Recruitment in a Pink Abalone (Haliotis corrugata) Aggregation by Parentage Analyses

inferred← citeshttps://doi.org/10.5343/bms.2012.1107openalex-snapshot

The scope of published population genetic data for Indo-Pacific marine fauna and future research opportunities in the region

inferred← citeshttps://doi.org/10.5343/bms.2013.1007openalex-snapshot

Phylogeography unplugged: comparative surveys in the genomic era

inferred← citeshttps://doi.org/10.5343/bms.2013.1053openalex-snapshot

High levels of mesophotic reef fish endemism in the Northwestern Hawaiian Islands

inferred← citeshttps://doi.org/10.70675/0f12a13fz7e1az4402z99a7z9c8028bf13fdopenalex-snapshot

Diversité et évolution des algues vertes Udoteaceae et Rhipiliaceae (Bryopsidales, Chlorophyta)

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