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Le Port, A., Lavery, S., and Montgomery, J. C. 2012. Conservation of coastal stingrays: seasonal abundance and population structure of the short-tailed stingray Dasyatis brevicaudata at a Marine Protected Area. – ICES Journal of Marine Science, 69: .Elasmobranch (shark, ray, and skate) populations around the world are in decline, and effective conservation measures are urgently needed. Marine Protected Areas (MPA) placed in locations important for key life-history stages may form part of an effective conservation strategy. In this context, we examined the seasonal abundance and population structure of the short-tailed stingray (Dasyatis brevicaudata) at an offshore MPA in northeastern New Zealand, and the reported use of this location as a mating ground. Diver surveys were conducted from 2004 to 2007 at the Poor Knights Islands Marine Reserve (PKIMR). During this time, we observed: (i) a substantial increase in adult and subadult numbers, particularly females during the suggested breeding season, and a corresponding increase in females bearing fresh mating scars; and (ii) large numbers of smaller (probably immature) D. brevicaudata individuals of both sexes from spring to autumn. These results suggest that the PKIMR acts as both a mating aggregation location and a nursery for this species. We suggest that for coastal stingrays such as D. brevicaudata, small MPAs may be effective at protecting key life-history stages, but that as movements outside of reserve boundaries also occur, additional management tools may also be necessary. [ABSTRACT FROM PUBLISHER]

The top predators in coastal marine ecosystems, such as whales, dolphins, seabirds, and large predatory fishes (including sharks), may compete with each other to exploit food aggregations. Finding these patchy food sources and being first to a food patch could provide a significant competitive advantage. Our hypothesis is that food patches have specific sound signatures that marine predators could detect and that acoustic sources and animal sensory capabilities may contribute to competition dynamics. Preliminary analysis shows that diving gannets have a distinct spectral signature between 80 and 200 Hz, which falls within the hearing sensitivity of large pelagic fishes. Therefore, we suggest that diving birds may contribute to the sound signatures of food aggregations, linking competition dynamics both above and below the water surface.

This study investigated the movement patterns of yellow moray eels Gymnothorax prasinus using acoustic telemetry. Gymnothorax prasinus were found to use multiple sites within a localized area or home range., (© 2011 The Authors. Journal of Fish Biology © 2011 The Fisheries Society of the British Isles.)

Genetic variability among Leptospira borgpetersenii serovar hardjo type hardjo-bovis isolates representing several geographical regions was determined by restriction endonuclease analysis. Five previously unidentified EcoRI digestion patterns and one previously unidentified HhaI digestion pattern were seen with the various isolates. The copy number and genomic distribution of an L. borgpetersenii insertion sequence (IS1533) was determined. Hardjo-bovis isolate 033 (the type strain for hardjo-bovis) contained 40 well dispersed copies of IS1533. IS1533 probes were used to compare hardjo-bovis isolates by DNA blot hybridization analysis. Use of these probes showed the presence of additional genetic heterogeneity among hardjo-bovis isolates, which restriction endonuclease analysis did not show. Pulsed-field gel electrophoretic analysis of DNAs from several isolates suggested that some polymorphisms arose by genomic rearrangements. All hardjo-bovis isolates were categorized into 14 distinct groups on the basis of common hybridization and endonuclease digestion patterns. Most of these groups were isolated from distinct geographical regions, suggesting that several different clonal populations of hardjo-bovis exist.

Adaptation of sleep and circadian rhythms was examined in three temperate zone dwellers arriving in Antarctica during summer. Rectal temperature, wrist activity, and heart rate were monitored continuously, sleep timing and quality noted on awakening, and mood and fatigue rated every 2 h while awake. Sleep was poorer in 2/3 subjects in Antarctica, where all subjects reported more difficulty rising. Sleep occurred at the same clock times in New Zealand and Antarctica, however, the rhythms of temperature, activity, and heart rate underwent a delay of about 2 h. The subject with the most Antarctic experience had the least difficulty adapting to sleeping during constant daylight. The subject with the most delayed circadian rhythms had the most difficulty. The delay in the circadian system with respect to sleep and clock time is hypothesized to be due to differences in zeitgeber strength and/or zeitgeber exposure between Antarctica and New Zealand.