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Kyne & Simpfendorfer.. - Shark Specialist Group

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SEGREGATION, MOVEMENT AND MIGRATION PATTERNS OF DEEPWATER<br />

CHONDRICHTHYANS<br />

Deepwater chondrichthyans are often segregated bathymetrically by size, sex or maturity<br />

stage. Segregation has been demonstrated by changes in the catch composition with depth,<br />

including for such species as the New Zealand lanternshark Etmopterus baxteri, the black<br />

dogfish Centroscyllium fabricii, the great lanternshark E. princeps, the roughskin dogfish<br />

Centroscymnus owstoni, the Portuguese dogfish C. coelolepis and the spotted ratfish<br />

Hydrolagus colliei (Yano and Tanaka 1988, Wetherbee 1996, Jakobsdóttir 2001, Didier and<br />

Rosenberger 2002). Several studies have noted a lack of gravid females, and it has been<br />

suggested that these may make movements into, or occur in, deeper water (possibly<br />

occupying nursery areas) or that they may be bathypelagic (and thus less susceptible to<br />

capture in benthic fishing gear) (Yano and Tanaka 1988, Wetherbee 1996, Jakobsdóttir 2001).<br />

Nursery areas have not been identified for deepwater shark species.<br />

The short and long-term (including seasonal) movement and migration patterns of deepwater<br />

chondrichthyans are poorly-known. The problems associated with tagging animals caught<br />

from depth and ensuring their survival once returned to the water, along with logistical<br />

constraints, has limited the tagging and tracking of deepwater species. As such tracking<br />

studies of 'deepwater' species has largely been restricted to species which also regularly occur<br />

in the epipelagic zone, at or close to the surface, such as the basking shark Cetorhinus<br />

maximus (discussed briefly under that species' account in the main body of this Section),<br />

sleeper sharks (Somniosus microcephalus and S. pacificus) and the bigeye thresher shark<br />

(Alopias superciliosus). Preliminary tracking of deeper water species has been trialled on the<br />

bluntnose sixgill shark Hexanchus griseus (Carey and Clark 1995), the needle dogfish<br />

Centrophorus acus (Yano and Tanaka 1986) and the Portuguese dogfish Centroscymnus<br />

coelolepis (Bagley et al. 1994).<br />

A number of deepwater squaloid sharks, particularly small pelagic species in the family<br />

Dalatiidae, are vertical migrators. These sharks undertake daily migrations from deep water<br />

towards to the surface at night, returning to depth during the day. Daily vertical movements<br />

may be in excess of 3000m (Compagno in prep. a) and these appear to be linked to the diel<br />

migrations of their prey. Hulbert et al. (2006) showed that diel vertical migrations in S.<br />

pacificus occurred only 25% of the time (i.e. 177 out of 726 days) and as such movement<br />

patterns are more complex than daily repeated vertical movements. <strong>Shark</strong>s were seen to also<br />

undertake 'systematic vertical oscillations' ('methodical ascents and descents with little pause<br />

in transition') and 'irregular vertical movements' ('small-amplitude movements with random<br />

frequency') with the most time spent at depths of 150-450m (Hulbert et al. 2006).<br />

Diel vertical migration also occurs in the bignose shark Carcharhinus altimus. Anderson and<br />

Stevens (1996) reviewed catch records of the poorly-known species determining that the<br />

sharks occupy epibenthic waters at depths of 90–500m during the day, moving either into<br />

shallower water or upwards into the epipelagic zone at night. Telemetry studies employing<br />

acoustic tags (short-term) and pop-up satellite archival tags (long-term) of another vertical<br />

migrator, A. superciliosus, has revealed consistent diel movement patterns with the species<br />

occurring at depth during the day (generally 200–500m, but with dives to 732m) and moving<br />

up in the water column to occupy depths of 10–130m by night (Nakano et al. 2003, Weng and<br />

Block 2004).<br />

Bagley et al. (1994) used acoustic transmitters imbedded in baits employed at 1517–1650m to<br />

briefly track three C. coelolepis, the deepest tracked chondrichthyans. All sharks moved<br />

outside the range of the recording equipment (500m) within 6 hours of bait deployment and<br />

Bagley et al. (1994) suggested that this indicated no site fidelity. A single C. acus acoustically<br />

tracked for nearly 21 hours in Japan generally swam parallel to the 500m depth contour,<br />

mostly remaining close to the seafloor although making some vertical movements to between<br />

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