Movement Patterns, Habitat Utilization, Home Range Size and Site Fidelity of Whitesaddle Goatfish, Parupeneus Porphyreus, In a Marine Reserve

By C. Meyer, K. Holland, B. Wetherbee, Christopher G. Lowe. Environmental Biology of Fishes, 2000

177 citations recorded by the source corpus.

Subfields: Ecology, Global and Planetary Change, Oceanography

View Paper: https://www.semanticscholar.org/paper/7d63708dac56881ad0fea2c583d7fac15bf14b3f

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Citations in the corpus

Connectivity, sustainability, and yield: bridging the gap between conventional fisheries management and marine protected areas (2009, background): “Parupeneus porphyreus 19,201 Meyer et al. (2000) Plectropomus leopardus 10,458 Kramer and Chapman (1999) a”
Behavior of yellowfin (Thunnus albacares) and bigeye (T. obesus) tuna in a network of fish aggregating devices (FADs) (2007, methodology): “We inserted tags in the peritoneal cavity using standard fish tag implantation techniques (e.g., Meyer and Holland 2000; Schaefer and Fuller 2002).”
Differential movement patterns and site fidelity among trophic groups of reef fishes in a Hawaiian marine protected area (2010, background): “Short-term active tracking of coral reef fishes at MPA sites has shown that a wide variety of targeted coral reef fishes are site-attached to well-defined home ranges and have predictable daily movement patterns (Holland et al. 1993, 1996; Meyer et al. 2000; Meyer 2003; Meyer and Holland 2005).”
Movement patterns, home range size and habitat utilization of the bluespine unicornfish, Naso unicornis (Acanthuridae) in a Hawaiian marine reserve (2005, unknown): “Similar ontogenetic habitat shifts are thought to occur in other surgeonfishes (HarmelinVivien 1984, Lawson et al. 1999) and are a possible mechanism of long-term dispersal from marine reserves to fished areas (e.g., Meyer et al. 2000).”
Multi-scale patterns of habitat use in a highly mobile reef fish, the white trevally Pseudocaranx dentex, and their implications for marine reserve design (2009, background): “…short-term HRs of many other reef fishes, which have been typically shown to be only a few tens or hundreds of meters in length and 1 to 10 ha in size (e.g. Holland et al. 1996, Samoilys 1997, Lowry & Suthers 1998, Meyer et al. 2000, Meyer & Holland 2005, Lowe et al. 2003, Afonso et al. 2008a).”
Social status determines behaviour and habitat usage in a temperate parrotfish: implications for marine reserve design (2008, background): “…of magnitude larger than those found in most previous telemetry studies of HR of other (non-parrotfish) demersal reef fishes from both temperate and tropical environments (Samoilys 1997, Lowry & Suthers 1998, Meyer et al. 2000, Lowe et al. 2003, Meyer & Holland 2005, but see Topping et al. 2005).”
Residence and movement patterns of cownose rays Rhinoptera bonasus within a south‐west Florida estuary (2007, background): “The advent of passive acoustic monitoring technology has allowed the movements of multiple animals to be continuously tracked over extended time frames (Klimley et al., 1988; Meyer et al., 2000; Heupel & Hueter, 2001; Voegeli et al., 2001; Heupel et al., 2004) permitting predictions regarding long”
Density-dependent spillover from a marine reserve: long-term evidence (2005, background): “Fish may emigrate from a reserve during daily or seasonal movements within their home ranges (Holland et al. 1996, Zeller and Russ 1998, Meyer et al. 2000, Eristhee and Oxenford 2001, Tremain et al. 2004).”
Passive acoustic telemetry reveals highly variable home range and movement patterns among unicornfish within a marine reserve (2011, background): “…daily crepuscular movement between habitats, with the magnitude of movement varying (metres–kilometres) relative to species and body size (e.g., Holland et al. 1993, 1996; Zeller 1997; Meyer and Holland 2005; Meyer and Honebrink 2005; Meyer et al. 2000, 2007a,b, 2010; Claisse et al. 2011).”
Gradients of abundance of fish across no‐take marine reserve boundaries: evidence from Philippine coral reefs (2006, background): “It is unlikely that spillover from the reserve increased stock abundance throughout the whole fishing area at Balicasag island, simply because reef fishes have limited movement potential, usually on the scale of hundreds of metres (Zeller and Russ, 1998; Chapman and Kramer, 2000; Meyer et al., 2000)”
Seasonal, diel, and tidal movements of green jobfish (Aprion virescens, Lutjanidae) at remote Hawaiian atolls: implications for marine protected area design (2007, methodology): “We aim to address these questions in future studies by using active tracking to obtain more complete, higher resolution information on the short-term movements of uku, and by increasing the number of receivers deployed around individual atolls to obtain a more complete, longterm picture of uku movem”
Limited movement in blue rockfish Sebastes mystinus: internal structure of home range (2006, background): “Among the few studies examining movement within home ranges, disproportionately high use of particular areas within the home range (core areas) has commonly been detected (e.g. Holland et al. 1993, 1996, Meyer et al. 2000, Eristhee & Oxenford 2001, Lowe et al. 2003, Parsons et al. 2003).”
Movement patterns, home range, and habitat utilization of adult kelp bass Paralabrax clathratus in a temperate no-take marine reserve (2003, background): “One of the most effective ways to determine home range size, diel activity patterns, site fidelity, and habitat preferences of fish species is through the use of acoustic telemetry (Holland et al. 1996, Zeller 1999, Meyer et al. 2000).”