1,397 research outputs found

    Habitat connectivity in coastal environments: patterns and movements of Caribbean coral reef fishes with emphasis on Bluestriped Grunt, Haemulon sciurus

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    Habitat connectivity within tropical marine seascapes may be greatly dependent on the movement of large organisms, particularly fishes. Using visual and trap sampling within two small bays in Virgin Islands National Park/Biosphere Reserve, St. John, U.S. Virgin Islands, we documented that large coral reef fishes, particularly large adult grunts, which shelter by day on coral reefs and make nocturnal feeding migrations into seagrass beds, accounted for the greatest biomass and abundance of fishes sampled in seagrass habitat. Using passive tags and sonic telemetry, we documented the nocturnal migration patterns of large adult grunts (bluestriped grunts, Haemulon sciurus), which are similar to the well-documented migration patterns of juvenile grunts. Large grunts showed high site fidelity to nocturnal foraging sites in seagrass beds. Sonictagged grunts demonstrated little movement in their diurnal shelter sites in the boulder-coral zone, with most individuals making nocturnal migrations into the adjacent seagrass bed. These results provide evidence for strong linkage among adjacent habitats at a small spatial scale and emphasize the importance of inclusion of a diversity of habitats in Marine Protected Areas

    Biodiversity and Ecosystem Health of the Aldabra Group, Southern Seychelles: Scientific Report to the Government of Seychelles.

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    National Geographic's Pristine Seas project, in collaboration with the government of the Seychelles, the Island Conservation Society (ICS), the Seychelles Islands Foundation (SIF), and the Waitt Foundation, conducted an expedition to explore the poorly known marine environment around these islands. The goals were to assess the biodiversity of the nearshore marine environment and to survey the largely unknown deep sea realm. The data collected contribute to the marine spatial planning of the Seychelles, in particular the creation of large marine reserves

    Tumour ADC measurements in rectal cancer: effect of ROI methods on ADC values and interobserver variability

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    OBJECTIVES: To assess the influence of region of interest (ROI) size and positioning on tumour ADC measurements and interobserver variability in patients with locally advanced rectal cancer (LARC). METHODS: Forty-six LARC patients were retrospectively included. Patients underwent MRI including DWI (b0,500,1000) before and 6-8 weeks after chemoradiation (CRT). Two readers measured mean tumour ADCs (pre- and post-CRT) according to three ROI protocols: whole-volume, single-slice or small solid samples. The three protocols were compared for differences in ADC, SD and interobserver variability (measured as the intraclass correlation coefficient; ICC). RESULTS: ICC for the whole-volume ROIs was excellent (0.91) pre-CRT versus good (0.66) post-CRT. ICCs were 0.53 and 0.42 for the single-slice ROIs versus 0.60 and 0.65 for the sample ROIs. Pre-CRT ADCs for the sample ROIs were significantly lower than for the whole-volume or single-slice ROIs. Post-CRT there were no significant differences between the whole-volume ROIs and the single-slice or sample ROIs, respectively. The SDs for the whole-volume and single-slice ROIs were significantly larger than for the sample ROIs. CONCLUSIONS: ROI size and positioning have a considerable influence on tumour ADC values and interobserver variability. Interobserver variability is worse after CRT. ADCs obtained from the whole tumour volume provide the most reproducible results. Key Points • ROI size and positioning influence tumour ADC measurements in rectal cancer • ROI size and positioning influence interobserver variability of tumour ADC measurements • ADC measurements of the whole tumour volume provide the most reproducible results • Tumour ADC measurements are more reproducible before, rather than after, chemoradiation treatment • Variations caused by ROI size and positioning should be taken into account when using ADC as a biomarker for tumour response
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