Fróðskaparrit - 01.01.1987, Side 82

Fróðskaparrit - 01.01.1987, Side 82
86 SPAWNING OF ATLANTIC HALIBUT tween 10 and 900 m (Table 1). The hauls la- sted between 45 and 130 minutes and filte- red between 2100 and 5600 m3 sea water at the sampling depths. 5 halibut eggs were captured. South of 61°30’N, 2 eggs were found at 800 m depth. In the northern area, 1 and 2 halibut eggs were found at 50 and 100 m depth respectively. The latter gives the largest egg concentration observed at any depth with 0.48 eggs per 1000 m3 filte- red sea water. The average diameter of the halibut eggs was 3.22 ± 0.12 mm. Unfortu- nately, all halibut eggs were dead and cyto- lized after capture, such that their develop- mental stages could not be determined. Additional to the halibut eggs, 3 small eggs (two with diameter less than 2.0 mm, and one with diameter 2.7 mm, species unknown) and 20 larger eggs with average diameter 3.60 ± 0.08 mm, segmented yolk, and a single yellow oil globule(average diameter 0.97 ± 0.12 mm), were captured during the surveys. Discussion Apparently, some differentiation exists in the distribution of halibut with respect to age/size during winter in the investigated area. Most of the fish in deep water were mature, while in shallower strata small, immature fish were more abundant. This is consistent with observations made in the Nova Scotia/New Foundland area in North America (McCracken 1958). Furthermore, the almost complete absence of immature fish below 700 m depth, which from the ap- pearance of fish with running gonads and pelagic eggs in the water column clearly should be considered a spawning area for the species, is consistent with observations from spawning areas on the coast of Nor- way (Devold 1938, Mathisen & Olsen 1968, Haug & Tjemsland 1986). The occur- rence in February of some mature fish with running gonads at depths above 700 m, indicate that some spawning must also take place at these depths. The apparent sexual difference in age distribution in the deeper strata, with a large proportion of males being younger, must be attributable to the lower size and age at which the males attain sexual matu- rity (Jákupsstovu & Haug 1987), and, thus, recruit to the spawning stock. Based on data from the coast of North Norway, Olsen (1969) suggested that old fish which had spawned in previous years arrived on the spawning grounds earlier than first time spawners. The present size compostion data give no evidence for such conclusions i the Faroe area. Our hydrographical observations of ex- tremely cold bottom water in the north- most part of the protected area are consi- stent with the fact that this is a part of the Faroe Bank Channel which runs north- westwards between the Faroe Plateau and the Faroe Bank and is the deepest channel through in the Greenland-Scotland ridge. Trough this channel is a continuous over- flow of cold water masses from the Norwe- gian Sea to the North Eastern Atlantic; this cold subsurface current then follows the western flank of the Iceland-Faroe ridge, westwards along the deep parts of the southern Icelandic slope before it turns southwards to the southwest of Iceland (Hansen 1985). There also is some evi- dence for another branch of this flow descending westwards along the northern slope of the Faroe Bank (Hansen loc. cit.),
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