6 resultados para M seamount

em Aquatic Commons


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Davidson Seamount is one of the largest seamounts in U.S. waters and the first to be characterized as a “seamount.” In 2002 and 2006, the Monterey Bay National Marine Sanctuary (MBNMS) led two multi-institutional expeditions to characterize the geology and natural history of Davidson Seamount. Results from these expeditions to Davidson Seamount are adding to the scientific knowledge of seamounts, including the discovery of new species. In November 2008, the MBNMS boundary was expanded to include the Davidson Seamount. In addition, a management plan for Davidson Seamount was created to develop resource protection, education, and research strategies for the area. The purpose of this taxonomic guide is to create an inventory of benthic and mid-water organisms observed at the Davidson Seamount to provide a baseline taxonomic characterization. At least 237 taxa were observed and are presented in this guide; including 15 new or undescribed species (8 sponges, 3 corals, 1 ctenophore, 1 nudibranch, 1 polychaete, 1 tunicate) recently or currently being described by taxonomic experts. This is the first taxonomic guide to Davidson Seamount, and is intended to be revised in the future as we learn more about the seamount and the organisms that live there. (PDF has 145 pages.)

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Pelagic fishes are not evenly dispersed in the oceans, but aggregate at distinct locations in this vast and open environment. Nomadic species such as mackerels, tunas, and sharks form assemblages at seamounts (Klimley and Butler, 1988; Fontenau, 1991). Fishermen have recognized this behavior and have placed moorings with surface buoys in deep waters to provide artificial landmarks, around which fish concentrate and are more easily captured. These fish aggregating devices (termed FADs) are common in the tropical oceans (see review, Holland, 1996). In a sense, it may only be the larger size that separates a seamount from a man-made FAD.

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The data from two years' monitoring of the Tongan seamount fishery were analyzed the two main export species are Pristipomoides filamentosus and Etelis coruscans. K.R. Allen's model was used to obtain estimates of catchability and recruitment and of a surplus production of 737 kg per nautical mile (nm) of 200 m contour. This compared reasonably well to total landings. Using this estimate, the annual surplus production for Tonga's 294 nm of 200 m contour is 217 t. The level of fishing mortality was found to be 0.3/year.

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Sablefish, Anoplopoma fimbria, were tagged and released on Gulf of Alaska seamounts during 1999–2002 to determine the extent, if any, of emigration from the seamounts back to the continental slope and of movement between seamounts. Seventeen sablefish from Gulf of Alaska seamounts have been recovered on the continental slope since tagging began, verifying that seamount to slope migration occurs. Forty-two sablefish were recovered on the same seamounts where they were tagged, and none have been recaptured on seamounts other than the ones where they were released. Sablefish populations on Gulf of Alaska seamounts are made up of individuals mostly older than 5 years and are maledominant, with sex ratios varying from 4:1 up to 10:1 males to females. Males are smaller than females, but the average age of males is greater than that of females, and males have a greater range of age (4–64 yr) than females (4–48 yr). Otoliths of seamount fish frequently have an area of highly compressed annuli, known as the transition zone, where growth has suddenly and greatly slowed or even stopped. Because transition zones can be present in both younger and older seamount fish and are rare in slope fish, formation of otolith transition zones may be related to travel to the seamounts. The route sablefish use to reach the seamounts is so far unknown. One possibility is that fish enter the eastward-flowing North Pacific Current off the Aleutian Islands or western Gulf of Alaska and travel more or less passively on the current until encountering a seamount. The route from seamount back to slope would likely be the northwardflowing Alaska Current. These routes are discussed in light of tag recovery locations of slope- and seamount-tagged fish.

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The fishery for deepwater precious corals in the Hawaiian Islands has experienced an on-and-off history for almost 40 years. In spite of this, research, driven primarily by the precious coral jewelry industry, remains active. In this paper, the results of deepwater surveys in 2000 and 2001 are reported. In summary, a new bed on the summit of Cross Seamount is described and revised estimates of MSY’s for pink coral, Corallium secundum; red coral, Corallium regale; and gold coral, Ger ardia sp., in the two known beds off Makapuu, Oahu, and Keahole Point, Hawaii, in the main Hawaiian Islands, are presented. The population dynamics of each species is described, as well as their ecological limits on Hawaii’s deep reefs, island shelves, and seamounts. The local supply of precious coral in the main Hawaiian Islands is sufficient to support the local industry, but cost/ benefits of selective harvest requirements and weather constraints limit profitability of the fish

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Tag release and recapture data of bigeye (Thunnus obesus) and yellowfin tuna (T. albacares) from the Hawaii Tuna Tagging Project (HTTP) were analyzed with a bulk transfer model incorporating size-specific attrition to infer population dynamics and transfer rates between various fishery components. For both species, the transfer rate estimates from the offshore handline fishery areas to the longline fishery area were higher than the estimates of transfer from those same areas into the inshore fishery areas. Natural and fishing mortality rates were estimated over three size classes: yellowfin 20–45, 46–55, and ≥56 cm and bigeye 29–55, 56–70, and ≥71 cm. For both species, the estimates of natural mortality were highest in the smallest size class. For bigeye tuna, the estimates decreased with increasing size and for yellowfin tuna there was a slight increase in the largest size class. In the Cross Seamount fishery, the fishing mortality rate of bigeye tuna was similar for all three size classes and represented roughly 12% of the gross attrition rate (includes fishing and natural mortality and emigration rates). For yellowfin tuna, fishing mortality ranged between 7% and 30%, the highest being in the medium size class. For both species, the overall attrition rate from the entire fishery area was nearly the same. However, in the specific case of the Cross Seamount fishery, the attrition rate for yellowfin tuna was roughly twice that for bigeye. This result indicates that bigeye tuna are more resident at the Seamount than yellowfin tuna, and larger bigeye tunas tend to reside longer than smaller individuals. This may result in larger fish being more vulnerable to capture in the Seamount fishery. The relatively low level of exchange between the Sea-mount and the inshore and longline fisheries suggests that the fishing activity at the Seamount need not be of great management concern for either species. However, given that the current exploitation rates are considered moderate (10–30%), and that Seamount aggregations of yellowfin and bigeye tuna are highly vulnerable to low-cost gear types, it is recommended that further increases in fishing effort for these species be monitored at Cross Seamount.