TL;DR: Deep-water, ahermatypic coral mounds are present at water depths of 1,000-1,300 m on the lower slope of Little Bahama Bank.
Abstract: Deep-water, ahermatypic coral mounds are present at water depths of 1,000-1,300 m on the lower slope north of Little Bahama Bank. The mounds are patchily distributed over a minimum area of 2,500 km2 and typically display 5-40 m of relief above the surrounding sea bottom. A diverse benthic community exists on these apparently unlithified mounds, including l 1 genera and 16 species of ahermatypic coral (Bathypsammia, Caryophyllia, Deltocyathus, Desmophyllum, Enallopsammia, Javania, Madrepora, Polymyces, Solenosmilia, Stephanocyathus, and a previously undescribed genus), alcyonaceans, gorgonians, antipatharians, hydroids, ophiuroids, crinoids, barnacles, galatheid crabs, polychaetes, gastropods, bivalves, and sponges. Conspicuously absent from the coral fauna are Lop elia and Dendrophyllia, common deep-water corals in other parts of the Atlantic. Radiocarbon dates on fresh coral and gorgonian fragments of 940 ± 40 and 860 ± 50 years indicate the mounds are at least in part Recent and are probably actively forming today. Bored and stained corals date at around 22 10314C years B. P., which establishes a minimum age for these mounds. We speculate that the mounds develop on sea-floor perturbations in areas where strong bottom currents provide needed oxygen and nutrients to the fauna. The mounds may have undergone multi-stage evolution from colony to thicket to coppice to bank. This evolution may be accomplished through the in situ contribution of skeletal material along with the baffling and trapping of fine-grained carbonate sediment winnowed from adjacent areas by bottom currents. If found in the rock record, the coral mounds north of Little Bahama Bank would probably be considered bioherms. Geologists should thus be aware that scleractinian bioherms are not uniquely shallow-water in origin. The distinction between ancient deep- and shallow-water coral buildups involves using multiple recognition criteria, including: 1) presence or absence of algae; 2) diversity of corals; 3) coral morphology and microstructure; 4) abundance of planktonic/benthonic components; 5) microborings; 6) surrounding litho- and biofacies; 7) stable isotopes of carbon and oxygen; and 8) trace element geochemistry, particularly Sr and U concentrations. The distinction between deep- and shallow-water bioherms is crucial to regional paleoenvironmental and stratigraphic interpretations.
TL;DR: Corals are common by-catch in bottom longline fisheries around the Azores and so conservation measures may be required.
Abstract: The impact of bottom trawling on cold-water corals (CWC) has been thoroughly studied and shown to be long-lasting; however the effects of bottom longlining on CWC ecosystems have received little attention. The present paper identifies the principal CWC species landed by bottom longlining in Faial (Azores) from 150 to 600 m depth. Data were obtained from a survey of 297 landings during four months coupled with 1 6 interviews with fishermen. A distinction was made among corals brought on deck directly entangled in the fishing gear (primary by-catch) from corals brought up associated with other larger CWC species or rocks (secondary by-catch). Forty-five (15.2%) of 297 fishing trips surveyed landed coral specimens. The survey recorded 39 different CWC taxa in the by-catch, belonging to five different orders (Scleractinia, Alcyonacea, Antipatharia, Zoanthidea and Anthoathecata). Secondary by-catch included a larger number of species but the total number of corals was in the same order of magnitude for both groups. The taxa most frequently encountered were Leiopathes spp., Errina dabneyi and Dendrophyllia sp. CWC taxa in the by-catch were mostly medium size (10― 6 0 cm), 3-dimensional and branched colonies. Local ecological knowledge of fishermen confirmed that the corals recorded were representative of their past experience and also revealed a general agreement that there has been a decrease of CWC by-catch on traditional fishing grounds. Corals are common by-catch in bottom longline fisheries around the Azores and so conservation measures may be required.
Abstract: The dendrophylliid Dendrophyllia sp. of Palawan contains the indole alkaloids 2′-demethylaplysinopsin (4) and 2′-demethyl-3′-N-methylaplysinopsin (6) and their 6-bromo analogues in H (Z/E) ratio larger than 95:5; these mixtures undergo facile photoisomerization to give mixtures richer in the (E) stereoisomer which undergo thermal isomerization to give back the original mixtures.
TL;DR: The prevailing environmental conditions of the deep Red Sea may require distinct functional adaptations, and the data suggest that bacterial communities may contribute to coral functioning in this challenging environment.
Abstract: Microbes associated with deep-sea corals remain poorly studied. The lack of symbiotic algae suggests that associated microbes may play a fundamental role in maintaining a viable coral host via acquisition and recycling of nutrients. Here we employed 16 S rRNA gene sequencing to study bacterial communities of three deep-sea scleractinian corals from the Red Sea, Dendrophyllia sp., Eguchipsammia fistula, and Rhizotrochus typus. We found diverse, species-specific microbiomes, distinct from the surrounding seawater. Microbiomes were comprised of few abundant bacteria, which constituted the majority of sequences (up to 58% depending on the coral species). In addition, we found a high diversity of rare bacteria (taxa at 90% of all bacteria). Interestingly, we identified anaerobic bacteria, potentially providing metabolic functions at low oxygen conditions, as well as bacteria harboring the potential to degrade crude oil components. Considering the presence of oil and gas fields in the Red Sea, these bacteria may unlock this carbon source for the coral host. In conclusion, the prevailing environmental conditions of the deep Red Sea (>20 °C, <2 mg oxygen L−1) may require distinct functional adaptations, and our data suggest that bacterial communities may contribute to coral functioning in this challenging environment.
TL;DR: In this article, a comparison of the fossil coral assemblages with the recent fauna was made, and the authors concluded that the middle Eocene Crescent formation had a tropical environment similar to that now at 20? latitude on the Pacific Coast, and that the upper Oligocene Blakeley formation had tropical or subtropical affinities.
Abstract: Thirty-three new and four old species of corals and one hydrocoralline are considered. The new species are: Turbinolia quaylei, T. weaveri, Trochocyathus townsendensis, Stephanocyathus holcombensis, Stephanocyathus? sp., Caryophyllia blakeleyensis, C. woodmanensis, C. wynoocheensis, Paracyathus sp. A, P? sp. B, Discotrochus sp., Platycyathus? sp., Flabellum hertleini, Coenocyathus? hannibali, Archohelia weaveri, Sclerhelia? sp., Madracis stewarti, M. crescentensis, Astrangia clarki, Eusmilia bainbridgensis, Colpophyllia reagani, Leptophyllastrea vaughani, Siderastrea washingtonensis, Siderastrea? sp., agaricid sp., Balanophyllia washingtonensis, B. fulleri, Dendrophyllia cowlitzensis, Tubastrea nomlandi, eupsammid sp., Montipora schencki, Astreopora duwamishensis, A. sanjuanensis, and Stylaster milleri. Balanophyllia teglandae Durham is proposed as a new name for B. blakeleyensis Quayle in Tegland (nomen nudum). By a comparison of the fossil coral assemblages with the recent fauna, it is concluded that the middle Eocene Crescent formation had a tropical environment similar to that now at 20? latitude on the Pacific Coast; that the upper Eocene had tropical or subtropical affinities; that the lower Oligocene shale on the Willapa river near Holcomb was deposited in depths of 250 or more meters in a subtropical climate; that the lower Oligocene Quimper sandstone was deposited under subtropical conditions similar to those in the Gulf of California 18? farther south than the fossil occurrence; that the upper Oligocene Blakeley formation had a like habitat although possibly slightly deeper water. Two new formations of lower Oligocene age, separated by an unconformity, are described. The lower is the Townsend shale, apparently the equivalent of the Keasey formation of Oregon; the upper is the Quimper sandstone, correlating with the type Gries Ranch beds and overlapping older rocks of several ages. D URING the course of faunal investigation in the Oligocene and, locally, the underlying Eocene strata of Washington, the writer has collected numerous species of corals. As only three species have been noted previously from these strata, and as important climatic inferences can be made from them, the corals are here described in a separate paper.1 Dr. John W. Wells, of Ohio State University, has kindly examined most of the material here described and has given valuable suggestions as to generic assignments, for which the author makes grateful acknowledgement. As the writer, while working on these faunas, has had occasion to note the occurrence of scattered corals throughout the Tertiary of California, it appears probable that investigation will show the presence of a considerable variety of corals not hitherto noted on the Pacific Coast, and that the 1 Assistance in the preparation of this manuscript was furnished by the personnel of the Works Projects Administration, Official Project No. 65-1-08-62, Unit A-1. 84 faunas of Washington are not unique in this respect. Thirty-four new and four old species are considered. They were found in formations ranging in age from early middle Eocene (Capay) to late Oligocene. Fragmentary material from several localities indicates that numerous species are yet to be collected and described. Of the species referred to, 22 are colonial and 16 are solitary forms. All of the coral localities except 7162, A-78, A-1810 (=C.A.S. 912), and N.P. 51, occur between 47?30' and 49? north latitude, 18? to 20? farther north than most corals are found living on the Pacific Coast. The excepted localities are all north of 46?30' latitude. The ecology of the recent corals, in certain aspects as least, is better known than that of many marine organisms. Vaughan (1940, pp. 458-464) has recently reviewed the available data and given references. Many genera are limited both thermally and bathymetrically in their recent distribution. Although some of the genera ranging throughout the Tertiary may have had a This content downloaded from 207.46.13.178 on Wed, 15 Jun 2016 06:43:22 UTC All use subject to http://about.jstor.org/terms CORAL FAUNAS OF WASHINGTON different distribution in the past than in the recent faunas, it seems that the average environment of the fossil assemblage should approximate that of like recent assemblages. Upon this basis, the coral assemblages from the different localities have been compared with similar modern faunas, and the probable past environment postulated. The results of these comparisons are as follows: