PROPAGULE DISPERSAL DISTANCE AND THE SIZE AND SPACING OF MARINE RESERVES

By A. Shanks, B. Grantham, M. Carr. 2003

975 citations recorded by the source corpus.

Subfields: Ecology, Global and Planetary Change, Oceanography

View Paper: https://www.semanticscholar.org/paper/ebcb0a6af6b9cc11c09d71dc879b521dfc8f5b9a

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Citations in the corpus

Lagrangian descriptions of marine larval dispersion (2003, neutral): “1), although exceptions do exist (Shanks et al. 2003).”
Guiding ecological principles for marine spatial planning (2010, neutral): “of kilometers [118–120].”
Behavior constrains the dispersal of long-lived spiny lobster larvae (2011, result): “These new findings refute the conventional wisdom that PLD is a good predictor of dispersal and indicate that the population dynamics of many species are probably more ‘closed’ than previously believed (Shanks et al. 2003).”
Population ecology of the invasive kelp Undaria pinnatifida in California: environmental and biological controls on demography (2004, background): “Demography may be more variable among locations (Shanks et al. 2003), but in many cases this variation is at least partially predictable from local environmental and ecological factors.”
Beyond corals and fish: the effects of climate change on noncoral benthic invertebrates of tropical reefs (2008, background): “…not be directly lethal to larvae of thermally tolerant species, they may accelerate growth rates and reduce time spent in the water column (Ettinger-Epstein et al., 2007), thereby limiting or redu- cing gene flow between otherwise connected populations (Shanks et al., 2003; O’Connor et al., 2007).”
SPORE SUPPLY AND HABITAT AVAILABILITY AS SOURCES OF RECRUITMENT LIMITATION IN THE GIANT KELP MACROCYSTIS PYRIFERA (PHAEOPHYCEAE) 1 (2004, background): “…kelp populations in the absence of a local spore source presents an apparent paradox given the common perception that effective spore dispersal in kelps is limited to a few meters of the parent plant (Dayton 1985, Schiel and Foster 1986, Santelices 1990, Murray and Bray 1993, Shanks et al. 2003).”
Endemism and dispersal: comparative phylogeography of three surgeonfishes across the Hawaiian Archipelago (2009, background): “Hence, the Wnding of subtle population subdivisions in C. strigosus and more pronounced subdivisions in the other Hawaiian endemic reef Wshes is notable because the endemics exhibit greater genetic partitioning over a small geographic range than their widespread counterparts, indicating lower disper”
Nonindigenous biota on artificial structures: could habitat creation facilitate biological invasions? (2007, background): “Despite being fast occupiers of space and producing large numbers of recruits, many fouling organisms such as bryozoans and colonial ascidians have a restricted invasive potential due to their limited natural dispersal (Keough and ChernoV 1987; Todd 1998; Shanks et al. 2003 ).”
Can protected areas contribute to poverty reduction? Opportunities and limitations. (2004, background): “The importance for local fisheries of marine protected areas and no-fishing zones, particularly those which incorporate fish spawning and nursery habitats such as estuaries, coral reefs and mangroves, is now well documented (e.g., Wells and Hildesley 1999; Ward et al. 2001; Roberts et al. 2001; Shan”
CONFOUNDING EFFECTS OF THE EXPORT OF PRODUCTION AND THE DISPLACEMENT OF FISHING EFFORT FROM MARINE RESERVES (2004, background): “For most species of fish and invertebrates this may be a reasonable starting assumption (e.g., see Kinlan and Gaines 2003, Shanks et al. 2003) given the size distribution of existing marine reserves (Halpern 2003).”
Non-indigenous marine and estuarine species in The Netherlands. (2005, positive): “This is immediately clear for planktonic and nektonic organisms (Shanks et al., 2003).”