Pandanipora fragilis—a new deep-water cyclostome bryozoan from the subequatorial Mid-Atlantic Ridge, Atlantic Ocean, and a review of Pandanipora worldwide

Zootaxa ◽  
2020 ◽  
Vol 4895 (4) ◽  
pp. 594-600
Author(s):  
ANDREI V. GRISCHENKO ◽  
DENNIS P. GORDON ◽  
VIACHESLAV P. MELNIK

A new cyclostome bryozoan, Pandanipora fragilis n. sp., is described from 3453 m depth on the subequatorial Mid-Atlantic Ridge. It differs from the type species, P. helix Grischenko, Gordon & Melnik, 2018, by a combination of colonial and zooidal characters. These include regular branching of a uniserial stem along the entire colony length; a straight or just slightly elevated and gently curved distal autozooidal peristomial component, forming a sharp angle with the frontal wall of the next zooid; the pattern of zooidal budding, achieved via development of a partition from the floor of the parent zooid in its distal quarter to third, leaving the proximal portion of daughter zooids not overlapping, so that preceding and subsequent zooids are not appressed along their proximal segments; props are uniformly straight and filiform, with their diameter much smaller than in P. helix; the exceptionally rare presence of slit-like pseudopores, restricted to props; and wedge-shaped crystallites on the internal surface of developing zooids, with irregular, ragged edges. The discovery of P. fragilis suggests that Pandanipora is most likely a relict element of a more-widespread ancient distribution that existed in tropical and boreal zones of both the Atlantic and Pacific Oceans prior to formation of the Isthmus of Panama in the Pliocene. 

1993 ◽  
Vol 71 (5) ◽  
pp. 997-1002 ◽  
Author(s):  
Dale R. Calder

Bougainvillia aberrans n.sp. is described from Bermuda in the western North Atlantic Ocean. Specimens were collected at a depth of 150 fathoms (274 m) from the polypropylene buoy line of a crab trap. The hydroid colony of B. aberrans is erect, with a polysiphonic hydrocaulus, a smooth to somewhat wrinkled perisarc, hydranths having a maximum of about 16 tentacles, and medusa buds arising only from hydranth pedicels. Medusae liberated in the laboratory from these hydroids differ from all other known species of the genus in having a long, spindle-shaped manubrium, lacking oral tentacles, having marginal tentacles reduced to mere stubs, and being very short-lived (surviving for a few hours at most). Gonads develop in medusa buds while they are still attached to the hydroids, and gametes are shed either prior to liberation of the medusae or shortly thereafter. The eggs are surrounded by an envelope bearing nematocysts (heterotrichous microbasic euryteles). The cnidome of both hydroid and medusa stages consists of desmonemes and heterotrichous microbasic euryteles. The diagnosis of the genus Bougainvillia is modified to accommodate this new deep-water species.


2010 ◽  
Vol 68 (2) ◽  
pp. 319-332 ◽  
Author(s):  
F. J. Murillo ◽  
P. Durán Muñoz ◽  
A. Altuna ◽  
A. Serrano

Abstract Murillo, F. J., Durán Muñoz, P., Altuna, A., and Serrano, A. 2011. Distribution of deep-water corals of the Flemish Cap, Flemish Pass, and the Grand Banks of Newfoundland (Northwest Atlantic Ocean): interaction with fishing activities. – ICES Journal of Marine Science, 68: 319–332. The distribution of deep-water corals of the Flemish Cap, Flemish Pass, and the Grand Banks of Newfoundland is described based on bycatch from Spanish/EU bottom trawl groundfish surveys between 40 and 1500 m depth. In all, 37 taxa of deep-water corals were identified in the study area: 21 alcyonaceans (including the gorgonians), 11 pennatulaceans, 2 solitary scleractinians, and 3 antipatharians. The greatest diversity of coral species was on the Flemish Cap. Corals were most abundant along the continental slope, between 600 and 1300 m depth. Soft corals (alcyonaceans), sea fans (gorgonians), and black corals (antipatharians) were most common on bedrock or gravel, whereas sea pens (pennatulaceans) and cup corals (solitary scleractinians) were found primarily on mud. The biomass of deep-water corals in the bycatches was highest in previously lightly trawled or untrawled areas, and generally low in the regularly fished grounds. The information derived from bottom-trawl bycatch records is not sufficient to map vulnerable marine ecosystems (VMEs) accurately, but pending more detailed habitat mapping, it provides a valuable indication of the presence/absence of VMEs that can be used to propose the candidate areas for bottom fishery closures or other conservation measures.


2012 ◽  
Vol 81 (3) ◽  
pp. 1133-1137 ◽  
Author(s):  
R. P. Vieira ◽  
B. Christiansen ◽  
S. Christiansen ◽  
J. M. S. Gonçalves

2018 ◽  
Vol 61 (2) ◽  
pp. 103-110 ◽  
Author(s):  
Carlos Sangil ◽  
Laura Martín-García ◽  
Julio Afonso-Carrillo ◽  
Jacinto Barquín ◽  
Marta Sansón

AbstractExtensive offshore meadows ofHalimeda incrassataare documented for the first time in sandy bottoms of La Palma, Canary Islands.Halimeda incrassataforms dense sublittoral assemblages between 20 and 55 m, but isolated populations occur down to 65 m depth. This species currently spreads over an area of 9.14 ha. Population coverage varies with depth, with the highest values at 35–40 m and an average cover of 62.34%. The calcified segments ofH. incrassataact as a stable substratum in these soft bottoms for the growth of other macroalgae, such as the rhodophytesLophocladia trichocladosandCottoniella filamentosa. Specimens reach lengths of up to 10 cm, shorter than individuals from the Caribbean. Although it is difficult to ascertain whether this species is a recent introduction, there is evidence of a correlation between the increase in population coverage and recent ocean warming, constituting another example of the tropicalization of the marine flora of this region.


<em>Abstract</em>.—The biology and fisheries of macrourid species in the NE Atlantic are reviewed. Of about 30 species that occur within that area, the roundnose grenadier <em>Coryphaenoides rupestris </em>is one of the main target species of deep-water fisheries. Roughhead grenadier <em>Macrourus berglax </em>is a minor bycatch of other deep-water fisheries and an occasional target of some small fisheries. Other macrourid species are not commercially exploited because they are too small and/or in too deep waters, but some are also taken as accidental bycatch. There are three main fisheries for roundnose grenadier: north and west of the British Isles, Skagerrak, and Mid-Atlantic Ridge. The Skagerrak fishery is mainly for fish meal while the others are for human consumption. Due to data availability, a range of assessment methods has been trialled primarily for stocks to the north and west of the British Isles. Although uncertain, these assessments provide evidence that the stock has been severely depleted. Fisheries were largely unregulated until the early 2000s, but following repeated International Council for the Exploration of the Sea (ICES) advice, total allowable catches were introduced in 2003 together with effort and capacity regulations. Roundnose grenadier is the most studied species. It lives more than 50 years, compared to 30 years or more for roughhead grenadier. The limited knowledge of other species suggests a contrasting picture of maximum age ranging from 10 to 40 years. Taking into account the limited biological knowledge for these species, the pros and cons of the current management regime are discussed.


2019 ◽  
Vol 28 (6) ◽  
pp. 723-734 ◽  
Author(s):  
Régis Santos ◽  
Mário Pinho ◽  
Octávio Melo ◽  
João Gonçalves ◽  
Ana Leocádio ◽  
...  

Zootaxa ◽  
2012 ◽  
Vol 3393 (1) ◽  
pp. 27 ◽  
Author(s):  
TOMOYUKI KOMAI ◽  
SHINJI TSUCHIDA

A poorly known deep-water axiid shrimp, Eiconaxius acutifrons Bate, 1888, the type species of the genus, is redescribedon the basis of the two type specimens (lectotype and paralectotype, designated herein) from the Banda Sea, Indonesia,and three recently collected specimens from the Myojin Knoll, Izu Islands, Japan. Diagnostic characters of this speciesare reassessed, and the comparison with closely allied congeneric species is made. Previous records referred to E.acutifrons are reviewed. It has been confirmed that none of the subsequent records under the name represent the true E.acutifrons. We found that Eiconaxius albatrossae Kensley, 1996 and E. faxoni Sakai, 2011 were based on the same seriesof material from the eastern Pacific, referred to E. acutifrons by Faxon (1895), but the Sakai’s (2011) taxon name is unavailable because of the lack of an explicit type fixation.


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