Abstract:SynopsisSubmersible dives were made on a site in the Gulf of Mexico 160km southeast of Galveston, Texas in September 1984. Both yellowedge, Epinephelus flavolimbatus, and snowy grouper, E. niveatus, were observed utilizing shelter around rock ridge habitats. The yellowedge grouper also sought shelter within three types of burrows cut into soft sediment. Many of these burrows were significant excavations consisting of large trenches 7-8 m long, 2-3 m wide, and l-l.5 m deep. Burrows were found in depths from 265… Show more
“…Burrows are home to a number of fishes and are found in a wide continuum of aquatic habitats from fresh to marine waters of varying substrates (Atkinson and Taylor 1991) and from air-exposed tidal zones (Clayton 1993;Ishimatsu et al 1998Ishimatsu et al , 2007Itani and Uchino 2003) to deep-sea environments (Jones et al 1989). Fish burrows provide many benefits, including protection from predators and environmental extremes, feeding grounds, and spawning and egg incubation chambers (Silverberg et al 1987;Atkinson and Taylor 1991;Takegaki and Nakazono 2000).…”
Odontamblyopus lacepedii inhabits burrows in mudflats and breathes air at the surface opening. Investigations of the intertidal burrows using resin casting demonstrated a highly branched burrow system. The burrows are composed primarily of branching patterns of interconnected tunnels and shafts that communicate into two to seven surface openings. Bulbous chambers (i.e., dilated portions of the burrow) at branching sections of the tunnels or shafts are common features of the burrow. The presence of these chambers accords the fish adequate space to maneuver inside the burrow, and thus constant access to the surface. The combination of all burrow characteristics and previously reported variability in air breathing patterns are ostensibly of selective value for aerial predator avoidance during air breathing in O. lacepedii.
“…Burrows are home to a number of fishes and are found in a wide continuum of aquatic habitats from fresh to marine waters of varying substrates (Atkinson and Taylor 1991) and from air-exposed tidal zones (Clayton 1993;Ishimatsu et al 1998Ishimatsu et al , 2007Itani and Uchino 2003) to deep-sea environments (Jones et al 1989). Fish burrows provide many benefits, including protection from predators and environmental extremes, feeding grounds, and spawning and egg incubation chambers (Silverberg et al 1987;Atkinson and Taylor 1991;Takegaki and Nakazono 2000).…”
Odontamblyopus lacepedii inhabits burrows in mudflats and breathes air at the surface opening. Investigations of the intertidal burrows using resin casting demonstrated a highly branched burrow system. The burrows are composed primarily of branching patterns of interconnected tunnels and shafts that communicate into two to seven surface openings. Bulbous chambers (i.e., dilated portions of the burrow) at branching sections of the tunnels or shafts are common features of the burrow. The presence of these chambers accords the fish adequate space to maneuver inside the burrow, and thus constant access to the surface. The combination of all burrow characteristics and previously reported variability in air breathing patterns are ostensibly of selective value for aerial predator avoidance during air breathing in O. lacepedii.
“…Habitat engineers in other ecosystems and fisheries are not limited to herbivores that influence the dynamics of algae and hard substrata, however. Golden tilefish ( Lopholatilus chamaeleonticeps , Malacanthidae), for example, importantly contribute to multiple bottom longline fisheries of the Northwest Atlantic and Gulf of Mexico; their extensive burrows in soft sediments add critical habitat dimensionality that supports diverse communities of benthic organisms (Grimes, Able, & Jones, ; Jones, Gutherz, Nelson, & Matlock, ). In some regions, burrow associates include other important fishery targets like the yellowedge grouper ( Hyporthodus flavolimbatus , Epinephelidae) (Matlock et al, ).…”
Surprisingly little published information exists on the pros and cons of managing extracted resources that are pooled as compound taxa such as species complexes. Current fisheries management includes many species complexes; in Hawaii, this includes two taxa of species pooled at subfamily and higher levels. These include seven species of parrotfishes (Scarinae, Labridae) and a seven‐species ‘bottomfish’ complex (the ‘Deep‐7’: comprising six species of snappers [Etelinae, Lutjanidae] and a single species of grouper [Epinephelidae]). Recent research on key vital rates (growth, reproduction) for major species in both taxa indicates that these complexes consist of species with disparate life histories. Species in the parrotfish taxon exhibit fast to very fast growth and short to moderate longevities, whilst Deep‐7 bottomfishes exhibit moderate to very slow growth and long to very long lifespans. These data clearly indicate that, although pooling species is a tempting default option in data‐poor situations, it is at best a necessary evil to be avoided when sufficient data on the demographics of component species become available. Pooling species is especially problematic when the ecosystem effects of extracting functionally dominant species should be an important management consideration in addition to that of species demographics. Assessments that recognize and quantify the ecosystem importance of habitat engineers and other ecological dominants could substantively improve management of species complexes. Ultimately, complexes of resource species need to be evaluated and managed based on many, sometimes conflicting and sometimes reinforcing, but always careful considerations such as those contrasted herein between the parrotfishes and bottomfishes of Hawaii.
“…Δ 14 C measurements from yellowedge grouper (Epinephelus flavolimbatus, Cook et al 2009) and barrelfish (Hyperoglyphe perciformis, Filer and Sedberry 2008) provided an offset context of Δ 14 C values, relative to the regional time-specific Δ 14 C references from the Northwestern Atlantic (Loess -NWA otolith, Campana et al 2008) and the Gulf of Mexico (Loess -GOM coral, Andrews et al 2013a), and a basis for exploring the possible reasons for the anomalous Δ 14 C values measured for golden tilefish (Harris 2005). Loess curves are a smoothed function to provide a visual representation of the trends provided by the original data series burrows (Jones et al 1989). Even though juvenile yellowedge grouper can recruit to shallower depths (25-125 m; Cook et al 2009), reduced Δ 14 C levels in otoliths of this species indicate it may typically recruit to greater depths with a prompt migration to even greater depths (Andrews et al 2013a).…”
There is a growing concern over the lack of life history information for many deepwater fisheries species, including golden tilefish, Lopholatilus chamaeleonticeps. Fundamental life history characteristics, like age and growth, are required for effective, agestructured stock assessments and management decisions. A previous effort to validate golden tilefish age estimates using bomb radiocarbon dating was inconclusive, which led to an application of lead-radium dating in the current study. Lead-radium dating uses the radioactive disequilibrium of lead-210 ( 210 Pb) and radium-226 ( 226 Ra) in otoliths as an independent estimate of age. Ages were also estimated using traditional age estimates by counting growth zones in thin otolith sections and lead-radium dating was used to test these estimates. Radiometric ages (corrected for time since capture) were similar to age estimates from growth zone counts for two of the female age groups and the two oldest age groups of unknown sex, which confirmed an annual growth zone deposition. However, radiometric ages did not agree with age estimates from growth zone counts for males. The difference may be attributed to geographical variations in radium levels, growth rates and growth zone formation by gender or gender transition. Male sagittal otoliths revealed inconsistent growth zone patterns in thin sections, which may have contributed to underageing. Golden tilefish longevity was confirmed to 26 years.
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