Deep-Sea Faunal Zonation of Benthos along Beaufort-Bermuda Transect in the North-western Atlantic

Author(s):  
Robert Y. George ◽  
Robert J. Menzies

SynopsisIn this paper the subject of faunal zonation in the ocean floor from the intertidal, and over the continental shelf, slope and rise and to the abyssal plain is examined on the basis of faunal change at the generic and species level. The region investigated over a period of five years aboard R/V Eastward is a Beaufort-Bermuda transect, approximately 75 kilometres wide and 500 kilometres long and bounded between 32° and 36°N latitude and 64° and 79°W longitude. A new method, involving numerical indices reflecting changes in the composition of taxa, endemism and diversity between adjacent depth levels, was developed for defining faunal boundaries. Isotherms and isobaths utilised by earlier authors for characterising deep-sea boundary on a global scale do not coincide with natural faunal boundaries. This study analyses the vertical distribution of 128 species of isopod crustaceans and 28 species of large epibenthic invertebrates. The zonation patterns seem to correspond with correlations in environmental conditions such as currents, topography and sediments.We suggest four major vertical faunal provinces, characterised at the generic level, namely (1) the Intertidal Faunal Province; (2) the Shelf Faunal Province; (3) the Archibenthal Zone of Transition; and (4) the Abyssal Faunal Province and internal zones within these characterised at the species level. The main aspects of interest include the presence of a narrow ‘meso abyssal zone’ with a species maximum, the demonstration of the true transitional nature of the Archibenthal Zone in biotic and abiotic factors and the characteristic low-biomass Red Clay environment showing definite faunal isolation from the continental margin.

Zootaxa ◽  
2013 ◽  
Vol 3613 (3) ◽  
pp. 281-288 ◽  
Author(s):  
MARIA ALEKSANDRA BITNER ◽  
VJACHESLAV P. MELNIK ◽  
OLGA N. ZEZINA

New Recent very small but sexually mature brachiopods have been found at abyssal depths (4580–4850 m) in the Clarion- Clipperton Zone of the Pacific Ocean. They are characterized by simple (under-developed, juvenile) morphological fea-tures, which are interpreted here as paedomorphic, indicating the importance of heterochrony in the evolution of deep-sea brachiopods. We have described these brachiopods as representing two new genera and species, i.e. Oceanithyris juveni-formis Bitner & Zezina (Family ?Dyscoliidae) and Simpliciforma profunda Bitner & Zezina (Superfamily Gwynioidea).


2012 ◽  
Vol 92 (5) ◽  
pp. 1083-1088 ◽  
Author(s):  
I.A. Cardoso ◽  
C.H.J.M. Fransen

The hippolytid genusLeontocarisincludes eight species, all restricted to the deep sea (240–2182 m). Associations with deep sea coralline habitats were reported and are herein confirmed. Three Australian species were recorded at seamounts as were the specimens herein identified asL. smarensissp. nov. These specimens were sampled at the South Mid-Atlantic Ridge (SMAR) by the Mar Eco project during 12 bottom trawls using a Sigsbee trawl. The SMAR is a seamount chain that rises from 4000 m depth, with mountains of 100–200 km wide and 14,000 km length.Leontocaris smarensissp. nov. shows closest affinity toL. larfrom the north-western Atlantic andL. yarramundi, from Australia and New Zealand. It differs fromL. larmainly in: (1) the scaphocerite distolateral tooth reaching the distal margin of the blade while clearly falling short in the latter species; and (2) the mandibular palp possessing three distal setae while setae are absent inL. lar. The new species differs fromL. yarramundiin the number and disposition of dorsal teeth on rostrum and in the absence of an acute posterolateral spine on abdominal somites 4 and 5.


Author(s):  
J.T.P. Copley ◽  
H.C. Flint ◽  
T.J. Ferrero ◽  
C.L. Van Dover

The ecology and biogeography of meiofauna at deep-sea hydrothermal vents have historically received less attention than those of mega- and macrofauna. This study examines the composition of major meiofaunal taxa in beds of the mussel Bathymodiolus thermophilus at hydrothermal vents on the northern and southern East Pacific Rise (EPR) and presents the first comparison of species assemblages of the dominant taxon, the nematodes, among sites spanning 27 degrees of latitude. Meiofaunal samples were collected by submersible from three mussel beds at 9°N on the EPR and four mussel beds between 17 and 18°S in 1999. Estimated ages of the mussel beds at the time of sampling range from 4 to >20 years, enabling investigation of the influence of mussel bed age on meiofaunal assemblages. Overall, the meiofauna of the mussel beds was dominated by nematodes, with copepods constituting the second most abundant meiofaunal group. There was variation in the ratio of nematodes to copepods between sites, however, with copepods more abundant than nematodes in the youngest mussel beds. Apart from polychaete larvae, other meiofaunal groups were generally present at very low abundance (<1%) in the samples and restricted in diversity to gastropod larvae, acari, foraminifera, ostracoda and turbellaria. Seventeen nematode species from 14 genera and 11 families were found in the samples, with no evidence of endemicity to hydrothermal vents at the generic level. Four genera present were not previously recorded at hydrothermal vents. Nematode species richness, species:genus ratios and abundances were low compared with other deep-sea habitats, though the ecological relevance of comparisons with soft-sediment benthos is discussed. Nematode assemblages exhibited high dominance by a few species, with one species of Thalassomonhystera most abundant at five of the seven vent sites. Multivariate analysis of nematode assemblages reveals similarities among sites that do not match geographical proximity. The youngest mussel beds were most similar to each other and exhibited lower species richness than other sites, consistent with colonization of mussel bed habitat by nematodes over time. Similarity in the composition of nematode assemblages among sites separated by ~3000 km indicates that they lie within a single biogeographic province, consistent with that proposed for mussel bed macrofauna. At a generic level, samples exhibited some overlap with nematode assemblages at vents elsewhere on the EPR, on the Mid Atlantic Ridge and in the North Fiji Basin.


Zootaxa ◽  
2017 ◽  
Vol 4347 (1) ◽  
pp. 1 ◽  
Author(s):  
ÁLVARO L. PEÑA CANTERO ◽  
TAMMY HORTON

The deep-sea benthic hydroid fauna remains poorly known, in part because of less frequent sampling than the shelf fauna, in part owing to the immense study area, and partly also because available samples have been little studied by experts. In order to correct this, deep-sea benthic hydroid material from the modern Discovery Collections has been studied. Samples come from localities in the North-East Atlantic including the Porcupine Seabight, Porcupine Abyssal Plain, Rockall Trough, Rockall Bank, and the Mid-Atlantic Ridge. Sixteen species belonging to 12 families and 16 genera were found. Leptothecata are clearly dominant, being represented by 14 species; the remaining species belong to Anthoathecata. Lafoeidae and Tiarannidae are the most diverse families with three species each; the remaining families being represented by a single species. The low species diversity is remarkable at the generic level, with each genus being represented by a single species. Hydroid occurrence is low: twelve species were found in ≤ 9% of stations; Amphinema biscayana has the highest occurrence (27% of stations). Fifteen species were recorded in the Porcupine Seabight, two in the Rockall Trough, one at Rockall Bank, one on the Porcupine Abyssal Plain, and two at the Mid-Atlantic Ridge. The known bathymetric range for a third of the species is extended; the increase is particularly noteworthy in Amphinema biscayana, Acryptolaria crassicaulis, Clytia gigantea and Schizotricha profunda. Two distinct bathymetric groups are recognized: strictly deep-sea inhabitants and eurybathic species. Most species are globally distributed, some are widely distributed in the Atlantic, and others are limited to the North Atlantic or the Northeast Atlantic. 


Lowstands of sea level produce significant unconformities, both on the continental shelves as subaerial unconformities and on the ocean basin slopes and floors by submarine erosion and shifts in depositions patterns. This report utilizes seismic data from the eastern Atlantic off Africa and the western Atlantic off the Blake Escarpment to illustrate the recognition and dating of deep sea unconformities. Twenty-eight major and minor deep sea unconformities are identified on these seismic data and tentatively dated by means of well control and a chart showing global relative changes of sea level. The major unconformities identified are basal Sinemurian, basal Callovian, basal Valanginian, basal middle Aptian, basal middle Cenomanian, basal Thanetian, basal upper Ypresian, basal middle Chattian, basal Burdigalian, basal middle Tortonian, and basal Messinian. Unconformity identification and correlation on seismic data from the deep sea is useful for building a stratigraphic framework for palaeoenvironmental studies and correlating deep-sea stratigraphy with the stratigraphy of continental shelves and interior basins.


2007 ◽  
pp. 13-22 ◽  
Author(s):  
T. K. Yurkovskaya

I have focused only on some features of structure in the taiga vegetation cover. In conclusion I would like to tell some words about the causes of complicated space structure of the taiga and tundra vegetation cover. The causes of latitudinal differentiation are climatic undoubtedly, but heterogeneity of vegetation cover within the limits of tundra and taiga subzones is accounted for different factors. In tundra abiogenic factors prevail, first of all the permafrost processes. That is the reason why tundra vegetation cover is so sensible to any disturbances and so hard regenerates after various transformations. In taiga the space structure is mostly the result of self-regulation and self- restoration of biota. The abiotic factors, certainly, play significant role, but they recede to the second plan. So we showed that in the north and middle taiga the structure of vegetation cover, during the Holocene up to present time, is determined in many respects by the increasing role of mires. Suffice it to look at the map of distribution of mires in order to estimate their role in vegetation cover of the easteuropean taiga (Yurkovskaya, 1980). So, the increase of mire area on the Russian Plain in m2/year per 1000 ha varies between 200 and 700, the average increas is ca 300—400 m2/year (Elina et all., 2000). The mires favour peniplenization and unite the separate areas of forest communities into the whole by means of forming the buffer paludificated territories (various hydrophilous variants of forest communities). But if mires, at all their stability, after destroying practically don't restore, the forests even after continuous cuttings restore their structure and composition through the series of successional stages unless an ecotope is damaged completely. Hence the space structure of taiga is the result, first of all, self development and self regulation of its vegetation cover. But, as it is known, at present time the process of destruction of natural biota has gone too far that the question arises not only about supporting its state and structure but also about the survival of the mankind itself. In this regard the vegetation map of Europe is the invaluable basis, which gives the starting point for all conservational, ecological and economical measures. But it is important to learn reading and using the map. And this is one of our actual goals.


Phytotaxa ◽  
2019 ◽  
Vol 415 (4) ◽  
pp. 233-239
Author(s):  
MARION A. WOLF ◽  
ALESSANDRO BUOSI ◽  
ABDUL-SALAM F. JUHMANI ◽  
ADRIANO SFRISO

Centroceras Kützing is a small red algal genus with 18 currently accepted species (Guiry & Guiry 2019), characterized by simple filamentous thalli with erect axes arising from a prostrate system and di-trichotomous branching (Hommersand 1963). The characters used to distinguish species are primarily cortical filament morphology: shape and number of the acropetal cortical cells, shape of gland cells, and shape of spines (Won et al. 2009). The generitype C. clavulatum (C. Agardh) Montagne has been viewed for a long time as a highly variable and cosmopolitan species (Hommersand 1963). Molecular and detailed morphological analyses brought Barros-Barreto et al. (2006) to report that C. clavulatum may consist of a species complex and Won et al. (2009) confirmed this hypothesis identifying eight taxonomic entities phylogenetically segregated from genuine C. clavulatum. Seven of these entities were assigned to the following species: C. gasparrinii (Meneghini) Kützing, C. hommersandii Won, T.O. Cho & Fredericq, C. hyalacanthum Kützing, C. micracanthum Kützing, C. natalensis Won, T.O. Cho & Fredericq, C. rodmanii Won, T.O. Cho & Fredericq, and C. tetrachotomum Won, T.O. Cho & Fredericq, (Won et al. 2009). Centroceras gasparrinii, C. hyalacanthum, and C. micracanthum are three western Atlantic species listed as synonyms of C. clavulatum since the middle of the 19th century and resurrected from the ‘C. clavulatum complex’ by Won et al. (2009). In particular, two of these taxa were described from specimens of the Mediterranean Sea: C. gasparrinii (as Ceramium gasparrinii Meneghini, type locality Palermo, Italy) and C. micracanthum (reported with the synonym Centroceras leptacanthum Kützing, type locality Genoa, Italy). Therefore, the numerous Mediterranean records of C. clavulatum (e.g., Gómez Garreta et al. 2001; Verlaque 2001; Sfriso & Curiel 2007; Taşkýn et al. 2013) most probably belong to one of these two species and have to be re-examined for a correct identification and to understand the spatial distribution of the different taxa (Tsiamis et al. 2010). For this reason, in the last years in Greece (Tsiamis et al. 2010), Spain (Gallardo et al. 2016) and Morocco (Hassoun et al. 2018) accurate sampling and morphological analyses of specimens previously identified as C. clavulatum were conducted to determine their correct taxonomic identities. In all cases the recognized species was C. gasparrinii, which can be distinguished morphologically from the other ones previously known as C. clavulatum by the presence of ovoid gland cells and ovoid terminal acropetal cortical cells (Won et al. 2009). As reported by Tsiamis et al. (2010), Greek samples differed from those described by Won et al. (2009), in the smaller number of periaxial cells (10–12 against 13–19).


2017 ◽  
Vol 98 (7) ◽  
pp. 1619-1644 ◽  
Author(s):  
Alexandre Dias Pimenta ◽  
Bruno Garcia Andrade ◽  
Ricardo Silva Absalão

A taxonomic revision of the Nystiellidae from Brazil, including samples from the Rio Grande Rise, South Atlantic, was performed based on shell morphology. Five genera and 17 species were recognized. For the richest genus,Eccliseogyra, the three species previously recorded from Brazil were revised:E. brasiliensisandE. maracatu, previously known only from their respective type series, were re-examined. Newly available material ofE. maracatuexpanded the known geographic range of this species to off south-east Brazil.Eccliseogyra nitidais now recorded from north-eastern to south-eastern Brazil, as well as from the Rio Grande Rise. Three species ofEccliseogyraare newly recorded from the South Atlantic:E. monnioti, previously known from the north-eastern Atlantic, occurs off eastern Brazil and on the Rio Grande Rise; its protoconch is described for the first time, confirming its family allocation.Eccliseogyra pyrrhiasoccurs off eastern Brazil and on the Rio Grande Rise, andE. folinioff eastern Brazil. The genusIphitusis newly recorded from the South Atlantic.Iphitus robertsiwas found off northern Brazil, although the shells show some differences from the type material, with less-pronounced spiral keels. Additional new finds showed thatIphitus cancellatusranges from eastern Brazil to the Rio Grande Rise, and Iphitusnotiossp. nov. is restricted to the Rio Grande Rise.Narrimania, previously recorded from Brazil based on dubious records, is confirmed, including the only two living species described for the genus:N. azelotes, previously only known from the type locality in Florida, andN. concinna, previously known from the Mediterranean. A third species,Narrimania raquelaesp. nov. is described from eastern Brazil, diagnosed by its numerous and thinner cancellate sculpture. To the three species ofOpaliopsispreviously known from Brazil, a fourth species,O. arnaldoisp. nov., is added from eastern Brazil, and diagnosed by its very thin spiral sculpture, absence of a varix, and thinner microscopic parallel axial striae.Papuliscala nordestina, originally described from north-east Brazil, is recorded off eastern Brazil and synonymized withP. elongata, a species previously known only from the North Atlantic.


1997 ◽  
Vol 75 (2) ◽  
pp. 308-316 ◽  
Author(s):  
Marcel Le Pennec ◽  
Peter G. Beninger

To enhance our understanding of the reproductive biology of deep-sea hydrothermal vent mytilids, the histology of the male gonad and the ultrastructure of its gametes were studied in Bathymodiolus thermophilus, B. puteoserpentis, and B. elongatus. Specimens of B. thermophilus were collected at the 13°N site on the East Pacific ridge, while B. puteoserpentis were sampled from the Snake Pit site of the mid-Atlantic ridge and B. elongatus were obtained from the North Fiji Basin. Gonad histology conformed to the typical bivalve profile; the differences in the proportions of acinal and interacinal tissue, as well as differences in acinal fullness in B. puteoserpentis, indicate that gametogenesis is discontinuous in these deep-sea mytilids. Evidence of protandric hermaphroditism was observed in B. elongatus, which exhibited acini containing both maturing and residual male gametes and immature oocytes. The ultrastructural characteristics of the male gametes conform to those described for littoral bivalve species, and the spermatozoon is of the primitive type. No species-specific differences in spermatozoon ultrastructure were discerned. No evidence of bacterial inclusions was found in either the gametes or the associated gonad cells in any of the species examined. The male gametes are thus probably not vectors for the endosymbiotic bacteria that characterize the nutritional biology of the adults in this genus.


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