Larval Dispersal and Marine Population Connectivity

ISOLATION BY DISTANCE

Wright, S. (1943) · Genetics · doi:10.1093/genetics/28.2.114 · Cited by 5,620

ISOLATION BY DISTANCE IN EQUILIBRIUM AND NON-EQUILIBRIUM POPULATIONS

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Spatial patterns of seed dispersal, their determinants and consequences for recruitment

Nathan, R., & Muller‐Landau, H. C. (2000) · Trends in Ecology & Evolution · doi:10.1016/s0169-5347(00)01874-7 · Cited by 2,076

Scaling of connectivity in marine populations

Cowen, R. K., Paris, C. B., & Srinivasan, A. (2006) · Science · doi:10.1126/science.1122039 · Cited by 1,354

RECRUITMENT AND THE LOCAL DYNAMICS OF OPEN MARINE POPULATIONS

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Distinguishing Migration From Isolation: A Markov Chain Monte Carlo Approach

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Climate change and marine plankton

Hays, G. C., Richardson, A. J., & Robinson, C. (2005) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2005.03.004 · Cited by 1,311

Recruitment Dynamics in Complex Life Cycles

Roughgarden, J., Gaines, S. D., & Possingham, H. P. (1988) · Science · doi:10.1126/science.11538249 · Cited by 1,206

POPULATION GENETICS, DEMOGRAPHIC CONNECTIVITY, AND THE DESIGN OF MARINE RESERVES

Palumbi, S. R. (2003) · Ecological Applications · doi:10.1890/1051-0761(2003)013[0146:pgdcat]2.0.co;2 · Cited by 1,192

Connectivity of Marine Populations: Open or Closed?

Cowen, R. K., Lwiza, K. M. M., Sponaugle, S., Paris, C. B., & Olson, D. B. (2000) · Science · doi:10.1126/science.287.5454.857 · Cited by 1,171

A molecular phylogeny of the spiny lobster Panulirus homarus highlights a separately evolving lineage from the Southwest Indian Ocean

Singh, S. P., Groeneveld, J. C., Al-Marzouqi, A. A., & Willows‐Munro, S. (2017) · PeerJ · doi:10.7717/peerj.3356 · Cited by 25

The interaction between suction feeding performance and prey escape response determines feeding success in larval fish

Sommerfeld, N., & Holzman, R. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.204834 · Cited by 26

Combining seascape connectivity with cumulative impact assessment in support of ecosystem‐based marine spatial planning

Jonsson, P. R., Hammar, L., Wåhlström, I., Pålsson, J., Hume, D., Almroth‐Rosell, E., & Mattsson, M. (2020) · Journal of Applied Ecology · doi:10.1111/1365-2664.13813 · Cited by 25

Temporal characteristics of plankton indicators in coastal waters: High-frequency data from PlanktonScope

Bi, H., Song, J., Zhao, J., Liu, H., Cheng, X., Wang, L., Cai, Z., Benfield, M. C., Otto, S. A., Goberville, É., et al. (2022) · Journal of Sea Research · doi:10.1016/j.seares.2022.102283 · Cited by 25

Progress and Direction in the Use of Stable Isotopes to Understand Complex Coral Reef Ecosystems: A Review

Skinner, C., Cobain, M. R. D., Zhu, Y., Wyatt, A. S. J., & Polunin, N. V. C. (2022) · CRC Press eBooks · doi:10.1201/9781003288602-8 · Cited by 27

Limited connectivity and a phylogeographic break characterize populations of the pink anemonefish, A mphiprion perideraion, in the I ndo‐ M alay A rchipelago: inferences from a mitochondrial and microsatellite loci

Dohna, T. A., Timm, J., Hamid, L., & Kochzius, M. (2015) · Ecology and Evolution · doi:10.1002/ece3.1455 · Cited by 25

Physical and behavioural influences on larval fish retention: contrasting patterns in two Antarctic fishes

Young, E. F., Rock, J., Meredith, M. P., Belchier, M., Murphy, E., & Carvalho, G. (2012) · Marine Ecology Progress Series · doi:10.3354/meps09908 · Cited by 25

Influence of seasonal and latitudinal temperature variation on early life-history traits of a coral reef fish

Takahashi, M., McCormick, M. I., Munday, P. L., & Jones, G. P. (2012) · Marine and Freshwater Research · doi:10.1071/mf11278 · Cited by 25

Active positioning of vent larvae at a mid-ocean ridge

Mullineaux, L. S., McGillicuddy, D. J., Mills, S. W., Kosnyrev, V., Thurnherr, A. M., Ledwell, J. R., & Lavelle, J. W. (2013) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2013.03.032 · Cited by 25

Subtidal macroalgal richness, diversity and turnover, at multiple spatial scales, along the southwestern Australian coastline

Smale, D. A., Kendrick, G. A., & Wernberg, T. (2010) · Estuarine Coastal and Shelf Science · doi:10.1016/j.ecss.2010.10.022 · Cited by 25

Genetic diversity, population structure, and demographic history of exploited sea urchin populations (Tripneustes gratilla) in the Philippines

Casilagan, I. L. N., Juinio‐Meñez, M. A., & Crandall, E. D. (2013) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2013.09.012 · Cited by 28

Population divergences despite long pelagic larval stages: lessons from crocodile icefishes ( C hannichthyidae)

Damerau, M., Matschiner, M., Salzburger, W., & Hanel, R. (2013) · Molecular Ecology · doi:10.1111/mec.12612 · Cited by 25

Modeling connectivity of walleye pollock in the Gulf of Alaska: Are there any linkages to the Bering Sea and Aleutian Islands?

Parada, C., Hinckley, S. L., Horne, J. K., Mazur, M. M., Hermann, A. J., & Curchister, E. (2015) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2015.12.010 · Cited by 25

The relative effect of behaviour in larval dispersal in a low energy embayment

Daigle, R., Chassé, J., & Meta×as, A. (2016) · Progress In Oceanography · doi:10.1016/j.pocean.2016.04.001 · Cited by 25

Seascape attributes, at different spatial scales, determine settlement and post-settlement of juvenile fish

Cuadros, A., Moranta, J., Cardona, L., Thiriet, P., Pastor, J., Arroyo, N. L., & Cheminée, A. (2016) · Estuarine Coastal and Shelf Science · doi:10.1016/j.ecss.2016.12.014 · Cited by 29

Evidence for interannual variation in genetic structure of Dungeness crab (Cancer magister) along the California Current System

Jackson, T. M., Roegner, G. C., & O’Malley, K. G. (2017) · Molecular Ecology · doi:10.1111/mec.14443 · Cited by 25

Integrating population genomics and biophysical models towards evolutionary-based fisheries management

Baltazar‐Soares, M., Hinrichsen, H., & Eizaguirre, C. (2017) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsx244 · Cited by 25

DNA barcoding reveals clear delineation between spawning sites for neritic versus oceanic fishes in the Gulf of Mexico

Burrows, M., Browning, J. S., Breitbart, M., Murawski, S. A., & Peebles, E. B. (2018) · Fisheries Oceanography · doi:10.1111/fog.12404 · Cited by 26

A multidisciplinary analytical framework to delineate spawning areas and quantify larval dispersal in coastal fish

Legrand, T., FRANCO, A. D., Ser‐Giacomi, E., Calò, A., & Rossi, V. (2019) · Marine Environmental Research · doi:10.1016/j.marenvres.2019.104761 · Cited by 25

Effects of sediment resuspension on the larval stage of the model sponge Carteriospongia foliascens

Wahab, M. A. A., Maldonado, M., Luter, H. M., Jones, R. J., & Ricardo, G. F. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.133837 · Cited by 25

Larval assemblages over the abyssal plain in the Pacific are highly diverse and spatially patchy

Kersten, O., Vetter, E. W., Jungbluth, M. J., Smith, C. R., & Goetze, E. (2019) · PeerJ · doi:10.7717/peerj.7691 · Cited by 25

A Molecular Approach to Explore the Background Benthic Fauna Around a Hydrothermal Vent and Their Larvae: Implications for Future Mining of Deep-Sea SMS Deposits

Klunder, L., de Stigter, H., Lavaleye, M., van Bleijswijk, J. D. L., van der Veer, H. W., Reichart, G., & Duineveld, G. (2020) · Frontiers in Marine Science · doi:10.3389/fmars.2020.00134 · Cited by 25

Applied connectivity modelling at local to regional scale: The potential for sea lice transmission between Scottish finfish aquaculture management areas

Rabe, B., Gallego, A., Wolf, J., Murray, R. O., Stuiver, C., Price, D., & Johnson, H. (2020) · Estuarine Coastal and Shelf Science · doi:10.1016/j.ecss.2020.106716 · Cited by 25

Comparison of population‐genetic structuring in congeneric kelp‐ versus rock‐associated snails: a test of a dispersal‐by‐rafting hypothesis

Nikula, R., Spencer, H. G., & Waters, J. M. (2011) · Ecology and Evolution · doi:10.1002/ece3.16 · Cited by 25

The ontogeny of larval swimming behavior in the crab Hemigrapsus sanguineus: Implications for larval transport

Cohen, J. H., Hanson, C. K., Dittel, A. I., Miller, D. C., & Tilburg, C. E. (2014) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2014.10.003 · Cited by 25

Temporal variability in the environmental and geographic predictors of spatial-recruitment in nearshore rockfishes

Markel, R. W., Lotterhos, K. E., & Robinson, C. (2017) · Marine Ecology Progress Series · doi:10.3354/meps12120 · Cited by 25

Potential connectivity between marine protected areas in the Mesoamerican Reef for two species of virtual fish larvae: Lutjanus analis and Epinephelus striatus

Martínez, S., Carrillo, L., & Marinone, S. G. (2019) · Ecological Indicators · doi:10.1016/j.ecolind.2019.02.027 · Cited by 24

Hidden similarities in the dynamics of a weakly synchronous marine metapopulation

Rogers, T. L., & Munch, S. B. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1910964117 · Cited by 24

Gene flow in the Antarctic bivalve Aequiyoldia eightsii (Jay, 1839) suggests a role for the Antarctic Peninsula Coastal Current in larval dispersal

Muñoz-Ramírez, C. P., Barnes, D. K. A., Cárdenas, L., Meredith, M. P., Morley, S. A., Roman-Gonzalez, A., Sands, C. J., Scourse, J. D., & Brante, A. (2020) · Royal Society Open Science · doi:10.1098/rsos.200603 · Cited by 24

Incorporating abiotic controls on animal movements in metacommunities

McLeod, A. M., & Leroux, S. (2021) · Ecology · doi:10.1002/ecy.3365 · Cited by 24

Genomic survey of edible cockle (Cerastoderma edule) in the Northeast Atlantic: A baseline for sustainable management of its wild resources

Vera, M., Maroso, F., Wilmes, S. B., Hermida, M., Blanco, A., Fernández, C., Groves, E. A., Malham, S. K., Bouza, C., Robins, P., et al. (2021) · Evolutionary Applications · doi:10.1111/eva.13340 · Cited by 24

Zooplankton Abundance Reflects Oxygen Concentration and Dissolved Organic Matter in a Seasonally Hypoxic Estuary

Weinstock, J. B., Vargas, L., & Collin, R. (2022) · Journal of Marine Science and Engineering · doi:10.3390/jmse10030427 · Cited by 26

Behaviour influences larval dispersal in shelf sea gyres: Nephrops norvegicus in the Irish Sea

Phelps, J. J. C., Polton, J. A., Souza, A. J., & Robinson, L. (2014) · Marine Ecology Progress Series · doi:10.3354/meps11040 · Cited by 24

Effects of habitat fragmentation on the genetic structure and connectivity of the black-lipped pearl oyster Pinctada margaritifera populations in French Polynesia

Lemer, S., & Planes, S. (2014) · Marine Biology · doi:10.1007/s00227-014-2484-9 · Cited by 24

Plankton community structure and connectivity in the Kimberley-Browse region of NW Australia

McKinnon, A. D., Duggan, S., Holliday, D., & Brinkman, R. (2014) · Estuarine Coastal and Shelf Science · doi:10.1016/j.ecss.2014.11.006 · Cited by 24

Modeled connectivity of Acropora millepora populations from reefs of the Spratly Islands and the greater South China Sea

Dorman, J. G., Castruccio, F. S., Curchitser, E., Kleypas, J. A., & Powell, T. M. (2015) · Coral Reefs · doi:10.1007/s00338-015-1354-3 · Cited by 24

Patterns and scales of connectivity: temporal stability and variation within a marine metapopulation

Corre, N. L., Johnson, L. E., Smith, G. K., & Guichard, F. (2015) · Ecology · doi:10.1890/14-2126.1 · Cited by 24

Anisotropic larval connectivity and metapopulation structure driven by directional oceanic currents in a marine fish targeted by small-scale fisheries

Munguía‐Vega, A., Marinone, S. G., Paz‐García, D. A., Girón‐Nava, A., Plomozo-Lugo, T., González-Cuéllar, O. T., Weaver, A. H., García‐Rodríguez, F. J., & Reyes‐Bonilla, H. (2017) · Marine Biology · doi:10.1007/s00227-017-3267-x · Cited by 24

A decision tree that can address connectivity in the design of Marine Protected Area Networks (MPAn)

Smith, J., & Meta×as, A. (2017) · Marine Policy · doi:10.1016/j.marpol.2017.11.034 · Cited by 24

Paradigm shifts in community ecology: Open versus closed units, challenges and limits of connectivity studies

Giangrande, A., Gambi, M. C., & Gravina, M. F. (2017) · Marine Ecology · doi:10.1111/maec.12480 · Cited by 24

The proportion of flatfish recruitment in the North Sea potentially affected by offshore windfarms

Barbut, L., Vastenhoud, B. M. J., Vigin, L., Degraer, S., VOLCKAERT, F. A. M., & Lacroix, G. (2019) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsz050 · Cited by 24

Ocean currents and the population genetic signature of fish migrations

Krueck, N. C., Treml, E. A., Innes, D. J., & Ovenden, J. R. (2020) · Ecology · doi:10.1002/ecy.2967 · Cited by 24

Larval connectivity of northern shrimp (Pandalus borealis) in the Northwest Atlantic

Corre, N. L., Pepin, P., Burmeister, A., Walkusz, W., Skanes, K. R., Wang, Z., Brickman, D., & Snelgrove, P. V. R. (2020) · Canadian Journal of Fisheries and Aquatic Sciences · doi:10.1139/cjfas-2019-0454 · Cited by 24

Agent-based modeling and genetics reveal the Limfjorden, Denmark, as a well-connected system for mussel larvae

Pastor, A., Larsen, J., Hansen, F. T., Simon, A., Bierne, N., & Maar, M. (2020) · Marine Ecology Progress Series · doi:10.3354/meps13559 · Cited by 24

Developmental series of gene expression clarifies maternal mRNA provisioning and maternal-to-zygotic transition in a reef-building coral

Chille, E. E., Strand, E., Neder, M., Schmidt, V., Sherman, M., Mass, T., & Putnam, H. M. (2021) · BMC Genomics · doi:10.1186/s12864-021-08114-y · Cited by 24

Evidence of stable genetic structure across a remote island archipelago through self‐recruitment in a widely dispersed coral reef fish

Priest, M. A., Halford, A. R., & McIlwain, J. L. (2012) · Ecology and Evolution · doi:10.1002/ece3.260 · Cited by 23

The influence of environmental characteristics on fish larvae spatial patterns related to a marine protected area: The Medes islands (NW Mediterranean)

López‐Sanz, À., Stelzenmüller, V., Maynou, F., & Sabatés, A. (2011) · Estuarine Coastal and Shelf Science · doi:10.1016/j.ecss.2011.02.006 · Cited by 23

Uncovering the relative influences of space and environment in shaping the biogeographic patterns of mangrove mollusk diversity

Chen, G., Wang, W., Liu, Y., Zhang, Y., Ma, W., Xin, K., & Wang, M. (2019) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsz204 · Cited by 23

They Came From the Pacific: How Changing Arctic Currents Could Contribute to an Ecological Regime Shift in the Atlantic Ocean

Kelly, S., Popova, E. E., Aksenov, Y., Marsh, R., & Yool, A. (2020) · Earth s Future · doi:10.1029/2019ef001394 · Cited by 23

Permeability of coastal biogeographic barriers to marine larval dispersal on the east and west coasts of North America

Krumhansl, K. A., Gentleman, W. C., Lee, K., Ramey, P. A., Goodwin, J., Wang, Z., Lowen, B., Lyons, D. A., Therriault, T. W., & DiBacco, C. (2023) · Global Ecology and Biogeography · doi:10.1111/geb.13654 · Cited by 23

Complex metacommunity structure for benthic invertebrates in a low‐diversity coastal system

Valanko, S., Heino, J., Westerbom, M., Viitasalo, M., & Norkko, A. M. (2015) · Ecology and Evolution · doi:10.1002/ece3.1767 · Cited by 23

Putative involvement of adrenergic receptors in regulation of mussel (Perna canaliculus) larval settlement

Young, T., Alfaro, A. C., Sánchez-Lazo, C., & Robertson, J. (2015) · Marine Biology Research · doi:10.1080/17451000.2014.979833 · Cited by 23

Connectivity and larval dispersal along the Oregon coast estimated by numerical simulations

Kim, S., & Barth, J. A. (2011) · Journal of Geophysical Research Atmospheres · doi:10.1029/2010jc006741 · Cited by 23

Conservation of passively dispersed organisms in the context of habitat degradation and destruction

Teller, B. J., Miller, A. D., & Shea, K. (2014) · Journal of Applied Ecology · doi:10.1111/1365-2664.12379 · Cited by 23

Fish larval transport in a macro-tidal regime: Gulf of Kachchh, west coast of India

George, G., VETHAMONY, P., Sudheesh, K., & Babu, M. T. (2011) · Fisheries Research · doi:10.1016/j.fishres.2011.04.002 · Cited by 23

Larval behavior and settlement dynamics of a ubiquitous Caribbean octocoral and its implications for dispersal

Coelho, M., & Lasker, H. R. (2016) · Marine Ecology Progress Series · doi:10.3354/meps11941 · Cited by 23

Considering reefscape configuration and composition in biophysical models advance seascape genetics

Wynsberge, S. V., Andréfouët, S., Gaertner‐Mazouni, N., Tiavouane, J., Grulois, D., Lefèvre, J., Pinsky, M. L., & Fauvelot, C. (2017) · PLoS ONE · doi:10.1371/journal.pone.0178239 · Cited by 23

Differences in larval growth of Pacific bluefin tuna (Thunnus orientalis) between two spawning areas, and an evaluation of the growth-dependent mortality hypothesis

Ishihara, T., Watai, M., Ohshimo, S., & Abe, O. (2019) · Environmental Biology of Fishes · doi:10.1007/s10641-019-00855-w · Cited by 24

Setting priorities for conservation at the interface between ocean circulation, connectivity, and population dynamics

Boschetti, F., Babcock, R. C., Doropoulos, C., Thomson, D. P., Feng, M., Slawinski, D., Berry, O., & Vanderklift, M. A. (2019) · Ecological Applications · doi:10.1002/eap.2011 · Cited by 23

Filling gaps: closing the life cycle of the endangered Mediterranean limpet Patella ferruginea Gmelin, 1791 (Gastropoda, Patellidae)

Guallart, J., Peña, J. B., Pérez-Larruscain, J., Luque, Á. A., & Templado, J. (2020) · Mediterranean Marine Science · doi:10.12681/mms.22508 · Cited by 23

Comparative phylogeography to test for predictions of marine larval dispersal in three amphidromous shrimps

Fujita, J., Zenimoto, K., Iguchi, A., Kai, Y., Ueno, M., & Yamashita, Y. (2016) · Marine Ecology Progress Series · doi:10.3354/meps11911 · Cited by 23

Genetic evidence supports larval retention in the Western Caribbean for an invertebrate with high dispersal capability (Ophiothrix suensonii: Echinodermata, Ophiuroidea)

Richards, V. P., DeBiasse, M. B., & Shivji, M. S. (2014) · Coral Reefs · doi:10.1007/s00338-014-1237-z · Cited by 22

Using species distribution models to assess the long‐term impacts of changing oceanographic conditions on abalone density in south east Australia

Young, M. A., Treml, E. A., Beher, J., Fredle, M., Gorfine, H. K., Miller, A. D., Swearer, S. E., & Ierodiaconou, D. A. (2020) · Ecography · doi:10.1111/ecog.05181 · Cited by 23

A Water Mass Classification Approach to Tracking Variability in the East Australian Current

Phillips, L. R., Carroll, G., Jonsen, I. D., Harcourt, R. G., & Roughan, M. (2020) · Frontiers in Marine Science · doi:10.3389/fmars.2020.00365 · Cited by 22

Individual variation in marine larval‐fish swimming speed and the emergence of dispersal kernels

Burgess, S. C., Bode, M., Leis, J. M., & Mason, L. B. (2022) · Oikos · doi:10.1111/oik.08896 · Cited by 22

Crabs Go With the Flow: Declining Conductivity and Cooler Temperatures Trigger Spawning Migrations for Female Giant Mud Crabs (Scylla serrata) in Subtropical Estuaries

Hewitt, D. E., Niella, Y. V., Johnson, D. D., Suthers, I. M., & Taylor, M. D. (2022) · Estuaries and Coasts · doi:10.1007/s12237-022-01061-1 · Cited by 22

Identifying barriers to gene flow and hierarchical conservation units from seascape genomics: a modelling framework applied to a marine predator

Boussarie, G., Momigliano, P., Robbins, W. D., Bonnin, L., Cornu, J., Fauvelot, C., Kiszka, J. J., Manel, S., Mouillot, D., & Vigliola, L. (2022) · Ecography · doi:10.1111/ecog.06158 · Cited by 25

Metal contamination and heat stress impair swimming behavior and acetylcholinesterase activity in embryo-larval stages of the Mediterranean mussel, Mytilus galloprovincialis

Boukadida, K., Bannı, M., Romero‐Ramirez, A., Clérandeau, C., Gourvès, P.-Y., & Cachot, J. (2022) · Marine Environmental Research · doi:10.1016/j.marenvres.2022.105677 · Cited by 22

One Antarctic slug to confuse them all: the underestimated diversity of Doris kerguelenensis

Maroni, P. J., Baker, B. J., Moran, A. L., Woods, H. A., Àvila, C., Johnstone, G. J., Stark, J. S., Kocot, K. M., Lockhart, S. J., Saucède, T., et al. (2022) · Invertebrate Systematics · doi:10.1071/is21073 · Cited by 22

Combined biophysical and genetic modelling approaches reveal new insights into population connectivity of New Zealand green-lipped mussels

Quigley, C. N., Roughan, M., Chaput, R., JEFFS, A. G., & Gardner, J. P. A. (2022) · Frontiers in Marine Science · doi:10.3389/fmars.2022.971209 · Cited by 22

Subtle genetic structure reveals restricted connectivity among populations of a coral reef fish inhabiting remote atolls

Underwood, J. N., Travers, M. J., & Gilmour, J. (2012) · Ecology and Evolution · doi:10.1002/ece3.80 · Cited by 22

Four-dimensional connectivity modelling with application to Australia's north and northwest marine environments

Kool, J., & Nichol, S. (2014) · Environmental Modelling & Software · doi:10.1016/j.envsoft.2014.11.022 · Cited by 23

Modelling the potential transport of tropical fish larvae in the Leeuwin Current

Pearce, A., Slawinski, D., Feng, M., Hutchins, B., & Fearns, P. R. C. S. (2011) · Continental Shelf Research · doi:10.1016/j.csr.2011.10.006 · Cited by 22

Searching for common threads in threadfins: phylogeography of Australian polynemids in space and time

Horne, J. B., Momigliano, P., Welch, D., Newman, S. J., & van Herwerden, L. (2011) · Marine Ecology Progress Series · doi:10.3354/meps09557 · Cited by 22

Observations of Migrant Exchange and Mixing in a Coral Reef Fish Metapopulation Link Scales of Marine Population Connectivity

Horne, J. B., van Herwerden, L., Abellana, S. L., & McIlwain, J. L. (2013) · Journal of Heredity · doi:10.1093/jhered/est021 · Cited by 22

Stock-specific advection of larval walleye (Sander vitreus) in western Lake Erie: Implications for larval growth, mixing, and stock discrimination

Fraker, M. E., Anderson, E. J., May, C. J., Chen, K., Davis, J. J., DeVanna, K. M., DuFour, M. R., Marschall, E. A., Mayer, C. M., Miner, J. G., et al. (2015) · Journal of Great Lakes Research · doi:10.1016/j.jglr.2015.04.008 · Cited by 23

Disentangling the genetic and morphological structure ofPatella candeicomplex in Macaronesia ( NE Atlantic)

Faria, J., Martins, G. M., Pita, A., Ribeiro, P. A., Hawkins, S. J., Presa, P., & Neto, A. I. (2017) · Ecology and Evolution · doi:10.1002/ece3.3121 · Cited by 22

Settlement Patterns of Corals and other Benthos on Reefs with Divergent Environments and Disturbances Histories around the Northeastern Arabian Peninsula

Bento, R. C., Feary, D. A., Hoey, A. S., & Burt, J. A. (2017) · Frontiers in Marine Science · doi:10.3389/fmars.2017.00305 · Cited by 22

Population genetic structure of Patagonian toothfish ( Dissostichus eleginoides ) in the Southeast Pacific and Southwest Atlantic Ocean

Canales‐Aguirre, C. B., Ferrada-Fuentes, S., Galleguillos, R., Oyarzún, F. X., & Hernández, C. E. (2018) · PeerJ · doi:10.7717/peerj.4173 · Cited by 22

Seeds in motion: Genetic assignment and hydrodynamic models demonstrate concordant patterns of seagrass dispersal

Sinclair, E. A., Ruiz‐Montoya, L., Krauss, S. L., Anthony, J. M., Hovey, R. K., Lowe, R. J., & Kendrick, G. A. (2018) · Molecular Ecology · doi:10.1111/mec.14939 · Cited by 22

Reverse engineering field-derived vertical distribution profiles to infer larval swimming behaviors

James, M. K., Polton, J. A., Brereton, A., Howell, K. L., Nimmo-Smith, A., & Knights, A. M. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1900238116 · Cited by 23

Blue crab larval dispersal highlights population connectivity and implications for fishery management

Criales, M. M., Chérubin, L. M., Gandy, R., Garavelli, L., Ghannami, M. A., & Crowley, C. (2019) · Marine Ecology Progress Series · doi:10.3354/meps13049 · Cited by 22

A process‐based model supports an association between dispersal and the prevalence of species traits in tropical reef fish assemblages

Donati, G., Parravicini, V., Leprieur, F., Hagen, O., Gaboriau, T., Heine, C., Kulbicki, M., Rolland, J., Salamin, N., Albouy, C. P., et al. (2019) · Ecography · doi:10.1111/ecog.04537 · Cited by 22

Northward shift of a biogeographical barrier on China’s coast

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Large-scale biogeographic patterns are reflected in the genetic structure of a broadcast spawning stony coral

van der Ven, R. M., Ratsimbazafy, H. A., & Kochzius, M. (2022) · Coral Reefs · doi:10.1007/s00338-022-02220-3 · Cited by 23

Simulating larval dispersal processes for abalone using a coupled particle-tracking and hydrodynamic model: implications for refugium design

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Impact of hydrographic parameters and seasonal variation in sediment fluxes on coral status at Chumbe and Bawe reefs, Zanzibar, Tanzania

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Modeling Fish Egg Production and Spatial Distribution from Acoustic Data: A Step Forward into the Analysis of Recruitment

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Metapopulation structure of a semi-anadromous fish in a dynamic environment

Feyrer, F. V., Hobbs, J. A., Acuña, S., Mahardja, B., Grimaldo, L. F., Baerwald, M. R., Johnson, R. C., & Teh, S. J. (2015) · Canadian Journal of Fisheries and Aquatic Sciences · doi:10.1139/cjfas-2014-0433 · Cited by 23

Stretched to the limit; can a short pelagic larval duration connect adult populations of an I ndo‐ P acific diadromous fish ( K uhlia rupestris)?

Feutry, P., Vergnes, A., Broderick, D., Lambourdière, J., Keith, P., & Ovenden, J. R. (2013) · Molecular Ecology · doi:10.1111/mec.12192 · Cited by 22

Shifts in the composition and distribution of Pacific Arctic larval fish assemblages in response to rapid ecosystem change

Axler, K. E., Goldstein, E. D., Nielsen, J. M., Deary, A. L., & Duffy‐Anderson, J. T. (2023) · Global Change Biology · doi:10.1111/gcb.16721 · Cited by 23

Large‐scale changes in macrobenthic biodiversity driven by mangrove afforestation

Chen, G., Gu, X., Capinha, C., Lee, S. Y., Cui, B., Yang, F., Lin, Y.-F. F., Jia, M., Wang, M., & Wang, W. (2023) · Journal of Applied Ecology · doi:10.1111/1365-2664.14462 · Cited by 21

Considering biotic interactions exacerbates the predicted impacts of climate change on coral‐dwelling species

Zhang, Z., Ma, S., Bede‐Fazekas, Á., Mammola, S., Qu, M., Zhou, J., Feng, E. Y., Qin, G., & Lin, Q. (2023) · Journal of Biogeography · doi:10.1111/jbi.14789 · Cited by 21

Life history matters: comparisons of population structuring in sympatric octopus species that differ in the presence of a pelagic larval stage

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Population Connectivity Shifts at High Frequency within an Open-Coast Marine Protected Area Network

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Does otolith chemistry indicate the natal habitat of Newfoundland capelin Mallotus villosus?

Davoren, G. K., Woloschiniwsky, C. S. A., Halden, N. M., & Wang, F. (2015) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2014.10.025 · Cited by 21

Subtle Population Genetic Structure in Yelloweye Rockfish (Sebastes ruberrimus) Is Consistent with a Major Oceanographic Division in British Columbia, Canada

Siegle, M. R., Taylor, E. B., Miller, K. M., Withler, R. E., & Yamanaka, K. L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071083 · Cited by 21

Larval ecology of the fluted giant clam, Tridacna squamosa, and its potential effects on dispersal models

Neo, M. L., Vicentuan, K., Teo, S. L., Erftemeijer, P. L. A., & Todd, P. A. (2015) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2015.04.012 · Cited by 21

Elemental fingerprints of southern calamary (Sepioteuthis australis) reveal local recruitment sources and allow assessment of the importance of closed areas

Pecl, G. T., Tracey, S., Danyushevsky, L. V., Wotherspoon, S. J., & Moltschaniwskyj, N. A. (2011) · Canadian Journal of Fisheries and Aquatic Sciences · doi:10.1139/f2011-059 · Cited by 21

Can the source–sink hypothesis explain macrofaunal abundance patterns in the abyss? A modelling test

Mincks, S. L., Smith, C. R., & Thurnherr, A. M. (2015) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2015.0193 · Cited by 21

Workshop held to discuss population connectivity in marine systems

Cowen, R. K., Thorrold, S. R., Pineda, J., & Gawarkiewicz, G. G. (2003) · Eos · doi:10.1029/2003eo130004 · Cited by 2

Reproductive Output and Duration of the Pelagic Larval Stage Determine Seascape-Wide Connectivity of Marine Populations

Treml, E. A., Roberts, J. J., Chao, Y., Halpin, P. N., Possingham, H. P., & Riginos, C. (2012) · Integrative and Comparative Biology · doi:10.1093/icb/ics101 · Cited by 266

Paradigm shifts in community ecology: Open versus closed units, challenges and limits of connectivity studies

Giangrande, A., Gambi, M. C., & Gravina, M. F. (2017) · Marine Ecology · doi:10.1111/maec.12480 · Cited by 24

Scaling of connectivity in marine populations

Cowen, R. K., Paris, C. B., & Srinivasan, A. (2006) · Science · doi:10.1126/science.1122039 · Cited by 1,354

Recent progress in understanding larval dispersal: new directions and digressions

Levin, L. A. (2006) · Integrative and Comparative Biology · doi:10.1093/icb/icj024 · Cited by 779