Notes: Internal stomach melanism was observed in two scalloped ribbonfish Zu cristatus from the Ligurian Sea. The phenomenon may help prevent advertizing the presence of this species after consumption of bioluminescent prey.

Notes: Six postlarval and an adult bathydraconid were collected in Terra Nova Bay, Ross Sea, during January-February 1988 and February 1998, respectively. The adult was identified as Acanthodraco dewitti Skóra, 1995 (type locality South Shetland Islands), a species not recorded in the Ross Sea. The postlarvae may be those of A. dewitti. The morphology and pigmentation patterns of the postlarvae are described and compared with those of other bathydraconids.

Notes: The differences among blennioid assemblages (families Blenniidae and Tripterygiidae) on different habitats were assessed at two localities of the Ligurian Sea, namely Arenzano and Riva Trigoso. The assemblage composition and species relative density were evaluated visually on four different habitats of diverse wave exposure and substratum orientation (macro-habitat characteristics): two vertical intertidal and subtidal habitats (exposed and sheltered rockwalls) and two horizontal subtidal habitats (semi-exposed flat rock and boulders and pebbles). Each habitat was also characterized in relation to micro-habitat features, such as substratum complexity, heterogeneity and amount of algae cover. Patterns of differences among habitats in assemblage variables and fish density, and the influences of macro- and micro-habitat features on these patterns were studied at small (within localities) and large (across localities) spatial scales. Higher values of species richness (S), diversity 〈inlineGraphic alt="inline image" href="urn:x-wiley:00221112:JFB684:JFB_684_mu1" location="equation/JFB_684_mu1.gif"/〉 and evenness (J) were generally associated with vertical habitats, as a result of a positive correlation with substratum orientation. The presence of an intertidal zone in the rockwall habitats may partially explain the observed differences in assemblage variables between vertical and horizontal habitats. The strength of relationships between S, 〈inlineGraphic alt="inline image" href="urn:x-wiley:00221112:JFB684:JFB_684_mu2" location="equation/JFB_684_mu2.gif"/〉 and J and the other investigated habitat variables (exposure, complexity, heterogeneity and algae cover) varied greatly depending on spatial scale. All these relationships were positive, except for complexity. Significant variation in the assemblage total density among habitats was recorded only at Arenzano, where a larger number of fishes were counted on rockwalls rather than on the horizontal habitats. The positive effect of orientation on fish total density was strictly dependent on spatial scale. Fish total density showed a negative correlation with complexity and a positive correlation with heterogeneity, both relationships being unaffected by spatial scale. The unexpected relationship with complexity was probably due to the fact that, in the most complex habitat (i.e. boulder and pebbles), the potential positive effect of high complexity on fish density might be overcome by the negative influence of other environmental features, such as horizontal orientation and low wave exposure. Complexity and heterogeneity thus seemed good predictors of fish total density, but their role needs to be carefully interpreted. The most marked differences in species composition and relative density were found between rockwalls and the other habitats, mostly due to an unbalanced distribution of some stenoecious species. Variations in species relative density were related to different combinations of both macro- and micro-habitat features, and these relationships usually changed depending on spatial scale.

Notes: Summary The age composition of Chionodraco hamatus samples caught by fixed nets in Terra Nova Bay during the Austral summer 1987/88 was determined by examination of thin otolith sections. Individual ages were estimated by counting the number of annuli seen in the sections, since we postulated that annuli were laid down yearly. Fish were estimated to be 5–10 years old. Although our “apparent ages” were not confirmed by other independent estimates, our data seem to compare well with the values reported for other Antarctic fishes. Females in our samples were on average larger than males of the same age and grow somewhat faster, at least over much of the sampled size range.

Notes: Abstract Forty-three and 49 specimens of the Antarctic fish Trematomus newnesi were collected in the coastal waters of Terra Nova Bay, Ross Sea, during December 1994 and February 1998, respectively. The dietary composition of the two fish samples was determined by means of stomach content analysis and then compared. In general, as reported in most of the previous studies, planktivory appeared to be the main feeding habit of T. newnesi. However, the different environmental conditions occurring in the study area in the two periods investigated, such as the degree of the sea-ice coverage and the related amount of light available below the ice, influenced the food composition of T. newnesi. In December 1994, the whole area investigated was covered by a thick layer of sea ice and the diet of T. newnesi consisted of few prey taxa. Some species that characterize the so-called “cryopelagic habitat”, such as the euphausiid Euphausia crystallorophias and the copepod Metridia gerlachei, were by far the most important prey, followed by amphipods and the pteropod Limacina helicina. Conversely, the ostracod Alacia belgicae and larval stages of fish (Pleuragramma antarcticum) were consumed occasionally. In late summer (February 1998), the lack of sea-ice coverage and changes in the associated fauna influenced the feeding habit of T. newnesi. In this period the food spectrum appeared to be more diverse, revealing an active feeding search in the water column. The bulk of food was composed of several prey groups, such as E. crystallorophias, hyperiid amphipods (Hyperiella dilatata), copepods, L. helicina and several species of fish larvae. Present data provide evidence of a marked feeding plasticity of T. newnesi, in response to diverse environmental conditions that characterize the High-Antarctic Zone.

Notes: Abstract  A study of feeding ecology in Trematomus hansoni Boulenger 1902 and Trematomus loennbergii Regan 1913 was carried out from samples collected in the austral summer 1990–1991 off Terra Nova Bay, Ross Sea. T. hansoni was caught between 35 and 566 m and T loennbergii between 311 and 543 m. Stomach contents analysis shows that T. loennbergii relies on a wider range of prey than T. hansoni. Fish and decapods are the main food resources of T. loennbergii, which feeds also on epifaunal and tube-dwelling polychaetes. T. hansoni mostly relies on fish resources that are made up of juvenile stages of fish and eggs. Despite the common area occupied by the two species, the interspecific competition is mostly mitigated due either to taking different prey or to taking different amounts of the same prey.

Notes: Abstract Age and growth of the nototheniid fishTrematomus bernacchii Boulenger 1902 were estimated by reading the sagittal otoliths of 457 adult specimens caught off Terra Nova Bay (Ross Sea) in the austral summer 1990–1991. Annuli in ground and polished otoliths were examined using a dissecting microscope under reflected light. The Von Bertalanffy growth equation was Lt=273.5 [1 − e−0.109(t+2.10)] for males (n=122) and Lt=422.2 [1 − e−0.055(t+1.92)] for females (n=211) where L is total length in millimetres. Maximum estimated age was 21 years for females and 16 years for males. This is in agreement with the hypothesis that considers slow growth and old age as a typical feature of Antarctic fishes.

Notes: Abstract  Age and growth of the nototheniid fish Trematomus bernacchii Boulenger 1902 were estimated by reading the sagittal otoliths of 457 adult specimens caught off Terra Nova Bay (Ross Sea) in the austral summer 1990–1991. Annuli in ground and polished otoliths were examined using a dissecting microscope under reflected light. The Von Bertalanffy growth equation was Lt=273.5 [1−e-0.109(t+2.10)] for males (n=122) and Lt=422.2 [1−e-0.055(t+1.92)] for females (n=211) where L is total length in millimetres. Maximum estimated age was 21 years for females and 16 years for males. This is in agreement with the hypothesis that considers slow growth and old age as a typical feature of Antarctic fishes.