SPOTLIGHT 4 New England and Corner Rise Seamounts

SPOTLIGHT 4 New England and Corner Rise Seamounts

or collective redistirbution of any portion of this article by photocopy machine, reposting, or other means is permitted only with the approval of The approval Oceanography portionthe ofwith any articlepermitted only photocopy by is of machine, reposting, this means or collective or other redistirbution This article has This been published in MOUNTAINS IN THE Sea SPOTLIGHT 4 New England and Corner Rise Seamounts Oceanography By Timothy M. Shank , Volume 23, Number 1, a quarterly journal of The 23, NumberOceanography 1, a quarterly , Volume One of the longest seamount tracks in with ~ 75 morphotypes unique to the for understanding the changes in North the Atlantic Ocean was formed by the Corner Rise and ~ 60 unique to the Atlantic open-ocean circulation through Great Meteor or New England hotspot. New England Seamounts (Cho, 2008). time and the impact these changes have This more than 3000-km-long hotspot Interestingly, a variety of invertebrates on population connectivity. For example, track formed both the New England and are revealing differing levels of specificity corals in the northern North Atlantic Corner Rise seamounts, with a pause to their host corals, ranging from “facul- prospered during past interglacial in volcanism 83 million years ago as tative” to “obligate” (see Shank, 2010). periods and in particular throughout evidenced by the morphological gap For example, the galatheid Uroptychus the past 11,000 years, yet apparently between chains (Figure 1). The New has been observed only on the antipatha- disappeared during glacial times England and Corner Rise seamounts rian Parantipathes sp., and the ophiuroid (above 50°N). In contrast, corals in the S each have more than 35 and 50 major Ophiocreas oedipus only on the coral temperate North Atlantic were sustained ociety. peaks, respectively, with summit reliefs Metallogorgia melanotrichos (Figure 2). during glacial times. © 2010 by The 2010 by Oceanography from 400 m to more than 5000 m. Under Paleoclimate studies, using water All of the studies noted above highly diverse oceanographic settings, mass chemical properties (such as postdate intense fishing practices in these seamounts harbor complex coral uranium and thorium) recorded in the 1970s and 1980s, which caused ecosystems comprised of host corals the fossil skeletons of the solitary coral extensive seafloor damage due to trawl and sponges as well as many associate Desmophylum dianthus, have revealed fishing (Figure 3; Waller et al., 2007). S species (Shank et al., 2006; Mosher and that changes in coral population density Reports indicate that ~ 20,000 tons reproduction, systemmatic Republication, article use for research. and this copy in teaching to granted rights All reserved. is ociety. Permission Watling, 2009) that are now the focus coincide with times of large-scale ocean of fish (175 species, predominantly S of intense ecological and evolutionary circulation changes in the deep North Alfonsino) were removed from the ociety. studies. More than 270 morphospecies Atlantic (e.g., Robinson et al., 2007). Corner Rise seamounts from 1976–1996 S end all correspondence to: [email protected] or Th e [email protected] Oceanography to: correspondence all end have been observed within this region, Corals thus provide excellent records (Vinnichenko, 1997). However, in a precautionary management measure, 13 fishable seamounts, including 25 peaks shallower than 2000 m on the New England and Corner Rise seamounts (Figure 1), were closed to demersal fishing gear beginning January 1, 2007. This closure is sched- uled to be lifted on December 31, 2010. Future knowledge of the connectivity of deep-water corals and their associ- S ates will provide fundamental insights PO Box 1931, Rockville,ociety, MD 20849-1931, into coral habitat dependence and “co-connectivity,” and can be used to inform and guide effective management and protection of diverse and valuable Figure 1. Map of the North Atlantic locating the New England and Corner Rise seamounts. Yellow boxes cold-water resources in our deep ocean. indicate regions protected by North Atlantic Fisheries Organization closings due in large part to damage from bottom-trawling fisheries activities. Timothy M. Shank ([email protected]) is Associate Scientist, Biology Department, Woods Hole Oceanographic Institution, Woods Hole, MA, USA. US A. 104 Oceanography Vol.23, No.1 A B C D E Figure 2. Characteristic features of the New England and Corner Rise seamounts. Habitat-forming coral ecosystems support diverse invertebrate associations on the New England and Corner Rise seamounts, including (a) ophiuroids, shrimp, hydroids, and galatheid crabs associated with the scleractinian Enallopsammia on Lyman Seamount (1450 m), (b) chyrostylid crabs on the antipatharian Plumapathes on Kükenthal Seamount (915m), (c) Ophiocreas oedipus ophiuroid wrapped around the coral Metallogorgia melan- otrichos, (d) spiraling Iridogorgia corals along with Metalogorgia corals and sponges living on an outcrop on the Corner Rise Seamounts, and (e) a soft coral community of Paramuricea sp., Calyptrophora sp., and Chrysogorgia sp. from Corner Seamount (1220 m). A B Figure 3. Fisheries damage on the Corner Rise Seamounts. Habitat destruction from years of fisheries activities, now evident by the criss- crossing trails of gear marks on the Kükenthal peak on Corner Seamount (725 m), and (b) large scar marks on the edge of the summit of Kükenthal peak caused by trawling gear impact with the seafloor. ReferenceS depth distributions in the Northwest Atlantic Vinnichenko, V.I. 1997. Russian investigations Cho, W. 2008. Faunal Biogeography, Community for the last 225,000 years. Bulletin of Marine and deep water fishery on the Corner Rising Structure, and Genetic Connectivity of North Science 81(3):371–391. Seamount in Subarea 6. North Atlantic Atlantic Seamounts. PhD Dissertation MIT/ Shank, T.M. 2010. Seamounts: Deep-ocean labo- Fisheries Organization Scientific Council WHOI Joint Program, 181 pp. ratories of faunal connectivity, evolution, and Studies 30:41–49. Mosher, C.V., and L. Watling. 2009. Partners for endemism. Oceanography 23(1):108–122. Waller, R., L. Watling, P. Auster, and T.M. Shank. life: A brittle star and its octocoral host. Marine Shank, T.M., W. Cho, R. Waller, and S.C. France. 2007. Fisheries impacts on the Corner Ecology Progress Series 397:81–88. 2006. Stepping stones across the Atlantic: Rise Seamounts. Journal of the Marine Robinson, L.F., J.F. Adkins, D.S. Scheirer, Co-evolution and dispersal of deep-water corals Biological Association of the United D.P. Fernandez, A. Gagnon, and R.G. Waller. and their associates on NW Atlantic seamounts. Kingdom 87:1,075–1,076. 2007. Deep-sea scleractinian coral age and Eos, Transactions, American Geophysical Union 87(52):V13A-0655. Oceanography March 2010 105.

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