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Seascape genetics at its finest: dispersal patchiness within a well-connected population

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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/ece3.208openalex-snapshot
Persistence of self‐recruitment and patterns of larval connectivity in a marine protected area network
inferredcites →https://doi.org/10.1002/ecy.2480openalex-snapshot
The formation of marine kin structure: effects of dispersal, larval cohesion, and variable reproductive success
inferredcites →https://doi.org/10.1007/bf00394818openalex-snapshot
Differences between the reproductive biologies of Tripterygion tripteronotus and T. delaisi (Pisces, Perciformes, Tripterygiidae): the adaptive significance of an alternative mating strategy and a red instead of a yellow nuptial colour
inferredcites →https://doi.org/10.1007/bf00397680openalex-snapshot
Chaotic genetic patchiness in an intertidal limpet, Siphonaria sp.
inferredcites →https://doi.org/10.1007/s00227-006-0513-zopenalex-snapshot
High self-recruitment levels in a Mediterranean littoral fish population revealed by microsatellite markers
inferredcites →https://doi.org/10.1007/s002270000535openalex-snapshot
Planktonic larval duration and settlement marks on the otoliths of Mediterranean littoral fishes
inferredcites →https://doi.org/10.1007/s002270050522openalex-snapshot
Microstructure of settlement-marks in the otoliths of tropical reef fishes
inferredcites →https://doi.org/10.1007/s00338-008-0461-9openalex-snapshot
Climate change and coral reef connectivity
inferredcites →https://doi.org/10.1007/s00338-009-0469-9openalex-snapshot
Larval retention and connectivity among populations of corals and reef fishes: history, advances and challenges
inferredcites →https://doi.org/10.1016/j.cub.2012.04.008openalex-snapshot
Larval Export from Marine Reserves and the Recruitment Benefit for Fish and Fisheries
inferredcites →https://doi.org/10.1016/j.ecss.2004.11.018openalex-snapshot
Environmental influences on temporal patterns of settlement in two littoral labrid fishes in the Mediterranean Sea
inferredcites →https://doi.org/10.1016/j.jembe.2003.09.001openalex-snapshot
Temperature influences swimming speed, growth and larval duration in coral reef fish larvae
inferredcites →https://doi.org/10.1016/s0169-5347(02)02584-3openalex-snapshot
Are populations of coral reef fish open or closed?
inferredcites →https://doi.org/10.1038/s41559-017-0148openalex-snapshot
Larval fish dispersal in a coral-reef seascape
inferredcites →https://doi.org/10.1038/srep23705openalex-snapshot
Looking for hotspots of marine metacommunity connectivity: a methodological framework
inferredcites →https://doi.org/10.1046/j.1471-8286.2002.00305.xopenalex-snapshot
spag e d i: a versatile computer program to analyse spatial genetic structure at the individual or population levels
inferredcites →https://doi.org/10.1073/pnas.0603422104openalex-snapshot
Temperature control of larval dispersal and the implications for marine ecology, evolution, and conservation
inferredcites →https://doi.org/10.1073/pnas.0606777104openalex-snapshot
Smelling home can prevent dispersal of reef fish larvae
inferredcites →https://doi.org/10.1073/pnas.0806804106openalex-snapshot
The influence of oceanographic fronts and early-life-history traits on connectivity among littoral fish species
inferredcites →https://doi.org/10.1073/pnas.0808007106openalex-snapshot
Larval dispersal connects fish populations in a network of marine protected areas
inferredcites →https://doi.org/10.1093/bioinformatics/bts460openalex-snapshot
GenAlEx 6.5: genetic analysis in Excel. Population genetic software for teaching and research—an update
inferredcites →https://doi.org/10.1093/cz/zow094openalex-snapshot
Current hypotheses to explain genetic chaos under the sea
inferredcites →https://doi.org/10.1093/icb/ics101openalex-snapshot
Reproductive Output and Duration of the Pelagic Larval Stage Determine Seascape-Wide Connectivity of Marine Populations
inferredcites →https://doi.org/10.1098/rsbl.2013.0454openalex-snapshot
Kinship and the evolution of social behaviours in the sea
inferredcites →https://doi.org/10.1098/rspb.2001.1751openalex-snapshot
The influence of parental relatedness on reproductive success
inferredcites →https://doi.org/10.1098/rspb.2002.2128openalex-snapshot
The structure of reef fish metapopulations: modelling larval dispersal and retention patterns
inferredcites →https://doi.org/10.1098/rspb.2009.2214openalex-snapshot
Ocean currents help explain population genetic structure
inferredcites →https://doi.org/10.1098/rspb.2010.2780openalex-snapshot
Connectivity dominates larval replenishment in a coastal reef fish metapopulation
inferredcites →https://doi.org/10.1098/rspb.2014.0556openalex-snapshot
Kinship analyses identify fish dispersal events on a temperate coastline
inferredcites →https://doi.org/10.1111/1755-0998.12155openalex-snapshot
SNP development from RNA ‐seq data in a nonmodel fish: how many individuals are needed for accurate allele frequency prediction?
inferredcites →https://doi.org/10.1111/gcb.13159openalex-snapshot
Climate change and larval transport in the ocean: fractional effects from physical and physiological factors
inferredcites →https://doi.org/10.1111/gcb.13347openalex-snapshot
Larval connectivity across temperature gradients and its potential effect on heat tolerance in coral populations
inferredcites →https://doi.org/10.1111/gcb.13915openalex-snapshot
Complex effect of projected sea temperature and wind change on flatfish dispersal
inferredcites →https://doi.org/10.1111/j.1365-294x.2006.03003.xopenalex-snapshot
Population structure within and between subspecies of the Mediterranean triplefin fish Tripterygion delaisi revealed by highly polymorphic microsatellite loci
inferredcites →https://doi.org/10.1111/j.1365-294x.2011.05176.xopenalex-snapshot
From global to local genetic structuring in the red gorgonian Paramuricea clavata: the interplay between oceanographic conditions and limited larval dispersal
inferredcites →https://doi.org/10.1111/j.1365-294x.2011.05355.xopenalex-snapshot
Matching genetics with oceanography: directional gene flow in a Mediterranean fish species
inferredcites →https://doi.org/10.1111/j.1439-0310.1978.tb00253.xopenalex-snapshot
The Behaviour of the Mediterranean Tripterygion Species (Pisces, Blennioidei)
inferredcites →https://doi.org/10.1111/j.1461-0248.2010.01562.xopenalex-snapshot
Reserve design for uncertain responses of coral reefs to climate change
inferredcites →https://doi.org/10.1111/j.1558-5646.1989.tb04226.xopenalex-snapshot
ESTIMATING RELATEDNESS USING GENETIC MARKERS
inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01826.xopenalex-snapshot
GENETIC DRIFT AND COLLECTIVE DISPERSAL CAN RESULT IN CHAOTIC GENETIC PATCHINESS
inferredcites →https://doi.org/10.1111/jfb.13143openalex-snapshot
Tiny estimates of the Ne/N ratio in marine fishes: Are they real?
inferredcites →https://doi.org/10.1111/mec.12274openalex-snapshot
Self‐recruitment in a C aribbean reef fish: a method for approximating dispersal kernels accounting for seascape
inferredcites →https://doi.org/10.1111/mec.12341openalex-snapshot
Combined analyses of kinship and FST suggest potential drivers of chaotic genetic patchiness in high gene‐flow populations
inferredcites →https://doi.org/10.1111/mec.12824openalex-snapshot
Spatial and temporal patterns of larval dispersal in a coral‐reef fish metapopulation: evidence of variable reproductive success
inferredcites →https://doi.org/10.1146/annurev.marine.010908.163757openalex-snapshot
Larval Dispersal and Marine Population Connectivity
inferredcites →https://doi.org/10.1186/1471-2164-15-167openalex-snapshot
Transcriptome analyses and differential gene expression in a non-model fish species with alternative mating tactics
inferredcites →https://doi.org/10.1371/journal.pone.0042672openalex-snapshot
Evidence for Cohesive Dispersal in the Sea
inferredcites →https://doi.org/10.1371/journal.pone.0151984openalex-snapshot
Expectation-Maximization Binary Clustering for Behavioural Annotation
inferredcites →https://doi.org/10.1371/journal.pone.0153381openalex-snapshot
Kin-Aggregations Explain Chaotic Genetic Patchiness, a Commonly Observed Genetic Pattern, in a Marine Fish
inferredcites →https://doi.org/10.1371/journal.pone.0176419openalex-snapshot
Impact of life history traits on gene flow: A multispecies systematic review across oceanographic barriers in the Mediterranean Sea
inferredcites →https://doi.org/10.1890/0012-9658(2006)87[3082:csakae]2.0.co;2openalex-snapshot
CURRENT SHIFTS AND KIN AGGREGATION EXPLAIN GENETIC PATCHINESS IN FISH RECRUITS
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.3354/meps09238openalex-snapshot
Marine connectivity: a new look at pelagic larval duration and genetic metrics of dispersal
inferredcites →https://doi.org/10.3354/meps10819openalex-snapshot
Local genetic patchiness but no regional differences between Indo-West Pacific populations of the dogtooth tuna Gymnosarda unicolor
inferredcites →https://doi.org/10.3354/meps12792openalex-snapshot
Limited dispersal explains the spatial distribution of siblings in a reef fish population
inferredcites →https://doi.org/10.3354/meps327257openalex-snapshot
Relationship between pelagic larval duration and geographic distribution of Mediterranean littoral fishes
inferredcites →https://doi.org/10.3389/fmars.2015.00056openalex-snapshot
Footprints of climate change on Mediterranean Sea biota

What points at this work

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

inferred← citeshttps://doi.org/10.1111/jfb.14656openalex-snapshot
Drivers for genetic structure at different geographic scales for Pacific red snapper ( Lutjanus peru ) and yellow snapper ( Lutjanus argentiventris ) in the tropical eastern Pacific
inferred← citeshttps://doi.org/10.3390/w16213084openalex-snapshot
Larval Transport Pathways for Lutjanus peru and Lutjanus argentiventris in the Northwestern Mexico and Tropical Eastern Pacific
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