Movements of Fishes Within and Among Fringing Coral Reefs in Barbados

By Matthew R. Chapman, D. Kramer. Environmental Biology of Fishes, 2004

232 citations recorded by the source corpus.

Subfields: Ecology, Global and Planetary Change, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/b7ea94d6a0722f9b729cf3cc3f2a9d82cfab6b70

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In Nature and Landscape Conservation

Citations in the corpus

Patterns and prediction of population recovery in marine reserves (2000, background): “For many reef species, movements are closely related to habitat, and natural boundaries, such as large areas of sand adjacent to a reef reserve, may limit movement (Chapman and Kramer, 2000).”
An age-based demographic analysis of the Caribbean stoplight parrotfish Sparisoma viride (2003, methodology): “At Barbados counts were made in 2 habitats: (1) at 2 to 5 m on the high relief coral matrix habitats usually with a shoreward zone of dead A. palmata (Chapman & Kramer 2000), and (2) on offshore, gorgonian-dominated bank reefs at 12 to 15 m depth.”
Home range and habitat utilization of adult California sheephead, Semicossyphus pulcher (Labridae), in a temperate no-take marine reserve (2005, unknown): “Labrids, being reef/structure-associated ﬁsh, are generally thought to exhibit high site attachment and have relatively small home ranges (e.g. Barrett 1995; Bradbury et al. 1995; Chapman and Kramer 2000).”
Reef fish and habitat relationships in a Caribbean seascape: the importance of reef context (2007, background): “For example, several tagging studies revealed transit distances of 100–400 m for adult haemulids (H. plumieri, Tulevech and Recksiek 1994; H. sciurus, Beets et al. 2003) and lutjanids (L. apodus, Chapman and Kramer 2000 ).”
Connectivity, sustainability, and yield: bridging the gap between conventional fisheries management and marine protected areas (2009, background): “In addition, habitat structure can affect movement by acting as physical or behavioral barriers (Chapman and Kramer 2000).”
Social status determines behaviour and habitat usage in a temperate parrotfish: implications for marine reserve design (2008, background): “Strong site attachment of parrotfishes has been previously hypothesized based on indirect evidence from a few tag-recapture studies for several tropical parrotfish species in coral reefs of Kenya (Kaunda-Arara & Rose 2004) and the Caribbean (Ogden & Buckman 1973, Chapman & Kramer 2000).”
Phase shifts and the role of herbivory in the resilience of coral reefs (2007, background): “The size of MPAs is likely to be an important factor determining their role in the promotion of resilience, although the numerical abundance and biomass of herbivorous fishes has been shown to be enhanced even in very small MPAs (Halpern 2003), probably reflecting the strong site attachment of many ”
Mangroves enhance the biomass of coral reef fish communities in the Caribbean (2004, background): “As migrations from the nearest mangrove resource, across 10–25 km of open ocean with depths exceeding 2,000 m, are likely to be insignificant for demersal reef specie”
Movement patterns, home range size and habitat utilization of the bluespine unicornfish, Naso unicornis (Acanthuridae) in a Hawaiian marine reserve (2005, unknown): “For example, in order to reduce the probability of fish home ranges extending into unprotected areas, reserve boundaries could be placed along natural borders between discrete areas of habitat rather than dividing regions of contiguous habitat (Barrett 1995, Chapman & Kramer 2000).”
Diel movements of fishes linked to benthic seascape structure in a Caribbean coral reef ecosystem (2011, background): “Many common species of fish connect multiple patch types through routine daily foraging movements, ontogenetic shifts, and seasonal and spawning migrations (Parrish 1989, Chapman & Kramer 2000, Pittman & McAlpine 2003).”
The relationship of reef fish densities to the proximity of mangrove and seagrass nurseries (2004, background): “Studies have shown that fishes are able to migrate along reefs over distances ranging from hundreds of metres to several kilometres (Tulevech and Recksiek, 1994; Kanashiro, 1998; Mazeroll and Montgomery, 1998; Zeller, 1998; Chapman and Kramer, 2000).”