2022
DOI: 10.1007/s10641-021-01207-3
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Discovery of a putative scalloped hammerhead shark Sphyrna lewini (Carcharhiniformes: Sphyrnidae) nursery site at the Galapagos Islands, Eastern Tropical Pacific

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Cited by 6 publications
(2 citation statements)
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“…The functions of such aggregation behaviors have been hypothesized to include reproduction (Klimley, 1987;Chaikin et al, 2020;Sims et al, 2022), feeding (De-la-Parra-Venegas et al, 2011), energy conservation, (Klimley and Nelson, 1984;Economakis and Lobel, 1998;Hight and Lowe, 2007), refuge from predators (Heupel et al, 2007;McAllister et al, 2017) and social learning (Sih et al, 2009;Brown and Laland, 2011). The formation of these aggregations can be seasonal and is often linked to environmental factors and life history stages (Rohner et al, 2013;Kajiura and Tellman, 2016), food abundance (Clua et al, 2013;Hacohen-Domenéet al, 2015), critical habitats (Oh et al, 2017;Chiriboga-Paredes et al, 2022) and reproduction (Heupel and Simpfendorfer, 2005;Reyier et al, 2008). The seasonality of these aggregation events, along with the large number of individuals at specific areas (i.e., coastal areas, productive systems) can also increase the likelihood and intensity of exposure to anthropogenic threats such as targeted fishing (Litvinov, 2006;Croll et al, 2016), bycatch (Watson et al, 2009;Hall and Roman, 2013), habitat degradation (Cattano et al, 2021), irresponsible tourism (Venables et al, 2016;Zemah-Shamir et al, 2019), boat strikes (Lester et al, 2020;Allen et al, 2021;Womersley et al, 2022) or climate change (particularly if mismatches in the timing of migration, reproduction or foraging interactions occur).…”
Section: Introductionmentioning
confidence: 99%
“…The functions of such aggregation behaviors have been hypothesized to include reproduction (Klimley, 1987;Chaikin et al, 2020;Sims et al, 2022), feeding (De-la-Parra-Venegas et al, 2011), energy conservation, (Klimley and Nelson, 1984;Economakis and Lobel, 1998;Hight and Lowe, 2007), refuge from predators (Heupel et al, 2007;McAllister et al, 2017) and social learning (Sih et al, 2009;Brown and Laland, 2011). The formation of these aggregations can be seasonal and is often linked to environmental factors and life history stages (Rohner et al, 2013;Kajiura and Tellman, 2016), food abundance (Clua et al, 2013;Hacohen-Domenéet al, 2015), critical habitats (Oh et al, 2017;Chiriboga-Paredes et al, 2022) and reproduction (Heupel and Simpfendorfer, 2005;Reyier et al, 2008). The seasonality of these aggregation events, along with the large number of individuals at specific areas (i.e., coastal areas, productive systems) can also increase the likelihood and intensity of exposure to anthropogenic threats such as targeted fishing (Litvinov, 2006;Croll et al, 2016), bycatch (Watson et al, 2009;Hall and Roman, 2013), habitat degradation (Cattano et al, 2021), irresponsible tourism (Venables et al, 2016;Zemah-Shamir et al, 2019), boat strikes (Lester et al, 2020;Allen et al, 2021;Womersley et al, 2022) or climate change (particularly if mismatches in the timing of migration, reproduction or foraging interactions occur).…”
Section: Introductionmentioning
confidence: 99%
“…Larger‐bodied coastal sharks are hypothesized to use shallow, nearshore waters as nursery habitats in many contexts (Knip et al , 2010). Yet testing this hypothesis has been difficult given the inherent obstacles of studying wide‐ranging, highly mobile juveniles that are often found in physically and/or geographically inaccessible areas ( e.g ., Chiriboga‐Paredes et al , 2022; Garla et al , 2006; Llerena et al , 2015; Weideli et al , 2019). Indeed, while nursery areas have been defined for some populations, the criteria proposed to identify shark nurseries (Heupel et al , 2007) have yet to be rigorously tested for most coastal sharks in part due to inaccessibility and data limitations, hindering conservation and management efforts (Heupel et al , 2019).…”
Section: Introductionmentioning
confidence: 99%