scholarly journals Demersal fish fauna of the continental slope off Nova Scotia, Canada, based on exploratory bottom trawl surveys in 1994�95

2012 ◽  
Vol 44 ◽  
pp. 41-60 ◽  
Author(s):  
R G Halliday ◽  
L V Guelpen ◽  
D E Themelis
1988 ◽  
Vol 66 (9) ◽  
pp. 1952-1960 ◽  
Author(s):  
Douglas F. Markle ◽  
Michael J. Dadswell ◽  
Ralph G. Halliday

Four 200-m depth strata were sampled for fish and decapod crustaceans on the upper continental slope (400–1200 m) off Nova Scotia. There was more-or-less continuous replacement of fish fauna with depth. Numerically dominant fishes in the upper two strata (< 800 m) were Sebastes spp., Phycis chesteri, and Glyptocephalus cynoglossus. Predominant fishes in the lower two strata (> 800 m) were Centroscyllium fabricii, Synaphobranchus kaupii, and Coryphaenoides rupestris. Nezumia bairdii was relatively abundant throughout the depth range sampled. The ichthyofauna of the upper slope was similar to that off the Middle Atlantic States and off Newfoundland at comparable depths, but qualitative differences existed in losses of some and additions of other species. Dominant decapod crustaceans in the shallowest stratum (200–400 m) were Pontophilus norvegicus, Plesiopenaeus edwardsianus, and Panalus propinquus. This stratum appeared to be a transition zone between shelf and slope decapod faunas. More species occurred and at higher densities in the deeper strata; predominant were Acanthephyra spp., Pasiphaea tarda, Metacrangon jacqueti, and Sabinea hystrix. The decapod fauna off Nova Scotia is similar to that of the mid-Atlantic Bight but less diverse.


2005 ◽  
Vol 62 (8) ◽  
pp. 1597-1602 ◽  
Author(s):  
Toshihide Hamazaki ◽  
Lowell Fair ◽  
Leslie Watson ◽  
Elisabeth Brennan

Abstract This study retrospectively examined evidence of ocean climate regime shift effects on epifauna and demersal fish of Norton Sound, Alaska, northeast Bering Sea, based on triennial bottom-trawl surveys from 1976 to 2002. Throughout the period, benthic fauna was dominated by sea stars (48–78%), followed by cods (5–19%), flatfish (5–15%), sculpins (1.5–7%), and crabs (2–6%). From 1976 to 2002, the cpue index of total species increased exponentially (4.5% y−1) by threefold with some declines in 1991 and 1999. The increase was also observed in sea stars (5.1% y−1), flatfish (6.1% y−1), and crabs (2.5% y−1). However, trends of cods and sculpins were mixed. Regression analysis showed the cpue index of total species to be positively correlated with survey years and bottom-water temperature. However, bottom-water temperature, when considered by itself, was not significant. Results suggest that regime shifts caused biomass increases of Norton Sound epifauna and demersal fish.


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.


2011 ◽  
Vol 110 (1) ◽  
pp. 198-206 ◽  
Author(s):  
Stan Kotwicki ◽  
Michael H. Martin ◽  
Edward A. Laman
Keyword(s):  

2007 ◽  
Vol 27 (3) ◽  
pp. 735-749 ◽  
Author(s):  
Jason D. Stockwell ◽  
Daniel L. Yule ◽  
Thomas R. Hrabik ◽  
Jean V. Adams ◽  
Owen T. Gorman ◽  
...  

Parasitology ◽  
1998 ◽  
Vol 116 (1) ◽  
pp. 73-83 ◽  
Author(s):  
D. J. MARCOGLIESE ◽  
D. K. CONE

Species richness and diversity of macroparasite assemblages were compared among American eels (Anguilla rostrata) from Nova Scotia, European eels (A. anguilla) from the United Kingdom (Kennedy, Bush & Aho, 1986; Esch et al. 1988; Kennedy, 1990, 1993), and Australian eels (A. reinhardtii) from Queensland (Kennedy, 1995). Community richness and diversity of the macroparasite fauna of American and European eels did not differ significantly for total parasite component communities, intestinal parasite component communities, and intestinal parasite infracommunities. The similarities in richness and diversity between the parasite communities of American and European eels are not surprising given the common, recent origin of these sister species. However, differences in species composition were noted between Nova Scotia and the UK. Both species of eels were infected by a nearly identical suite of specialists, but differences occurred in the species number and composition of generalist parasites. In addition, generalist species were rarely dominant in Nova Scotia, but commonly so in the UK. These differences can be attributed to the differences in the freshwater fish fauna and their parasites that occur between Nova Scotia and the UK. American and European eels are derived from a common ancestor and, whereas they have carried with them a common suite of specialist parasites during their brief period of independence, they acquired different suites of generalists apparently from their respective continental faunas after they diverged. In contrast, parasite communities of American and European eels were significantly less diverse and speciose than those of Australian eels regardless of scale (total component community, intestinal component community, intestinal infracommunity). These results support the notion that parasite communities have had more time to evolve and/or that tropical conditions have promoted parasite speciation in Australian eels.


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