Observations on the external locations of harpoon wounds were made on 127 minke whales Balaenoptera acutorostrata taken during Japanese commercial whaling operations in the 1978/79 Antarctic season. The numbers of wounds per whale did not vary between catcher boats, the average being 1.2. Although the cranio-thoracic region seemed to be the target of choice (bearing 60.5% of all wounds examined), the proportion of wounds in this region varied significantly between catcher boats, ranging from 43.6 to 75.7 per cent. It is suggested that this variation arose because to hit the cranio-thoracic region, the first section of the whale to surface, requires considerable skill on the part of the gunner.

Approximately 1500 Minke whales are killed annually under permit from the International Whaling Commission (IWC). This hunt supports a modest industry in Norway and in Japan; however, the welfare of whales during hunting and killing is such a cause of concern that in 1980 the IWC formed a sub-group entitled ‘Working Group on Whale Killing Methods and Associated Welfare Issues’ devoted to discussing the issue. This commentary suggests that, when using the Norwegian penthrite grenade-tipped harpoon (‘Whalegrenade-99‘), it is necessary to hit a relatively well-defined target area in order to effect an immediately immobile, and presumed unconscious state in the Minke whale.

Relatively little is known about the distribution and diversity of marine mammals around offshore anthropogenic structures. We present results obtained from incidental sightings of marine mammals around oil and gas installations located 200 km off the Danish coast. A total of 131 sightings corresponding to about 288 animals were reported between May 2013 and May 2016. A total of seven marine mammal species were identified, five cetaceans: harbour porpoise (Phocoena phocoena), minke whale (Balaenoptera acutorostrata), white-beaked dolphin (Lagenorhynchus albirostris), killer whale (Orcinus orca), pilot whales (Globicephala spp.) and two species of pinnipeds: harbour (Phoca vitulina) and grey seals (Halichoerus grypus). The most sighted species were harbour porpoise (41%) and minke whale (31%). Relative counts and biodiversity of marine mammals observed around installations corresponded well with the expected distribution in the central North Sea. Several taxon-specific correlations were identified between number of sightings and environmental parameters (depth and latitude) or installation characteristics (installation aerial footprint). Furthermore, 85% of sightings were made during spring and summer and it is unclear whether the pattern observed reflected a natural seasonal occurrence of marine mammals in the area or an effect of reduced effort during autumn and winter. Despite the potential caveats, results obtained during this programme provide an insight into the relationship between marine mammals and oil and gas offshore installations in the North Sea.

The waters off north-west Scotland are known to provide important habitat for the harbour porpoise (Phocoena phocoena) and the minke whale (Balaenoptera acutorostrata). Between October 2008 and April 2011, systematic land-based surveys were carried out to assess the seasonal occurrence, group size and group behaviours of both species in a study area located off Melvaig, near Gairloch. Data were collected on 47 separate days, with a total of 4543 minutes of survey effort (in sea states ≤3) recorded during the spring months and 8204 minutes of effort during the autumn. A total of 189 sightings of marine fauna were recorded, comprising 126 cetacean sightings, 50 seal sightings and 13 sightings of basking sharks (Cetorhinus maximus). Six species of cetacean were identified, with most sightings comprising harbour porpoise (N = 72) or minke whale (N = 38). Harbour porpoise abundance was higher in autumn than in spring and there was a variation between years in numbers of minke whales sighted. In porpoises, sea state and cloud cover both influenced sightings and increasing sea state influenced survey area. Foraging behaviour was exhibited in 13% of harbour porpoise sightings and 34% of minke whale sightings. Results demonstrate a regular occurrence of harbour porpoises and minke whales in nearshore waters off Gairloch. Densities are comparable to boat surveys in the region and so support the use of land-based watches as a potential longer-term monitoring method for these species in coastal waters. Given the regular use of this area by these two European Protected Species, as well as the occurrence of a range of human activities potentially affecting them in the region, it may be appropriate to consider protecting this area for their conservation.

Interspecies microinsemination assay was applied to examine the ability of minke whale haploid spermatogenic cells to induce Ca2+ oscillations and oocyte activation. Populations of round spermatids (RS), early-stage elongating spermatids (e-ES), late-stage elongating spermatids (1-ES) and testicular spermatozoa (TS) were cryopreserved in the presence of 7.5% glycerol on board ship in the Antarctic Ocean. Repetitive increases of intracellular Ca2+ concentration occurred in 0, 65, 81 and 96% of BDF1 mouse oocytes injected with the postthaw RS, e-ES, 1-ES and TS, respectively. A normal pattern of the Ca2+ oscillations was observed in 26–47% of the responding oocytes. Most oocytes that exhibited Ca2+ oscillations, regardless of the oscillation pattern, resumed meiosis (83–94%). These results indicate that whale spermatogenic cells acquire SOAF activity, which is closely related to their Ca2+ oscillation-inducing ability at the relatively early stage of spermiogenesis.

Using an interspecies microinsemination assay with bovine oocytes, it was examined whether centrosomes of Antarctic minke whale spermatozoa function as the microtubule-organizing centre (MTOC). Bull and rat spermatozoa were used as positive and negative controls, respectively. Vitrified-warmed bovine mature oocytes were subjected to immunostaining against α-tubulin 4–6 h after intracytoplasmic injection (ICSI) of 5 mM dithiothreitol-treated spermatozoa. Aster formation occurred from whale spermatozoa (33%) and bull spermatozoa (33%), but very little from rat spermatozoa (3%). Activation treatment for the microinseminated oocytes with 7% ethanol + 2 mM 6-dimethylaminopurine resulted in a similar proportion of oocytes forming a whale sperm aster (35% vs 27% in the non-treated group; 4 h after ICSI) but a significantly larger aster (ratio of aster diameter to oocyte diameter, 0.57 vs 0.30 in the non-treated group). These results indicate that the centrosome introduced into bovine oocytes by whale spermatozoa contributes to the MTOC and that assembly of the microtubule network is promoted by oocyte activation.

Simultaneous, but contrary, decadal-scale changes in population trajectories of two penguin species in the western Pacific and Ross Sea sectors of the Southern Ocean, during the early/mid-1970s and again during 1988–89, correspond to changes in weather and sea ice patterns. These in turn are related to shifts in the semi-annual and Antarctic oscillations. Populations of the two ecologically dissimilar penguin species - Adélie Pygoscelis adeliae and emperor Aptenodytes forsteri - have been tallied annually since the 1950s making these the longest biological datasets for the Antarctic. Both species are obligates of sea ice and, therefore, allowing for the demographic lags inherent in the response of long-lived species to habitat or environmental variation, the proximate mechanisms responsible for the shifts involved changes in coastal wind strength and air and sea temperatures, which in turn affected the seasonal formation and decay of sea ice and polynyas. The latter probably affected such rates as the proportion of adults breeding and ultimately the reproductive output of populations in ways consistent with the two species' opposing sea ice needs. Corresponding patterns for the mid-1970s shift were reflected also in ice-obligate Weddell seal Leptonychotes weddelli populations and the structure of shallow-water sponge communities in the Ross Sea. The 1988–89 shift, by which time many more datasets had become available, was reflected among several ice-frequenting vertebrate species from all Southern Ocean sectors. Therefore, the patterns most clearly identified in the Pacific Sector were apparently spread throughout the high latitudes of the Southern Ocean.

Germinal-vesicle-stage oocytes enclosed with compact cumulus cell layers (COCs) were recovered from adult or prepubertal minke whale ovaries, and were vitrified in a solution containing 15% ethylene glycol, 15% DMSO and 0.5 M sucrose using either a Cryotop or an open-pulled straw (OPS) as the cryodevice. The post-warm COCs with normal morphology were cultured for 40 h in a 390 mosmol in vitro maturation medium, and oocytes extruding the first polar body were considered to be matured. The proportion of morphologically normal COCs after vitrification and warming was higher when the COCs were cryopreserved by Cryotop (adult origin, 88.4%; prepubertal origin, 80.8%) compared with the OPS (adult origin, 67.7%; prepubertal origin, 64.2%). The oocyte maturation rate was higher in the adult/Cryotop group (29.1%) compared with those of the prepubertal/Cryotop group (14.4%), the adult/OPS group (14.3%) and the prepubertal/OPS group (10.6%). These results indicate that the Cryotop is a better device than the OPS for vitrification of immature oocytes from adult minke whales.

The present study aimed to determine the relationship among changes in the number of preantral follicles and concentrations of follicle-stimulating hormone (FSH), luteinizing hormone (LH), progesterone (P4), androstenedione (A) and estradiol-17β (E2) in the fetal heart, umbilical cord and maternal blood. Primordial follicles had already appeared in a 20 cm fetus and primary follicles were observed in a 50 cm fetus. In a 70 cm fetus, the number of primordial and primary follicles increased rapidly and secondary follicles were present. The concentrations of LH and FSH did not change between 20 cm and 160 cm in fetal length. When the fetal length became >70 cm, serum levels in the fetus, umbilical cord and mothers, and E2 levels in umbilical cord increased synchronously (p<0.05). These results showed increases in the number of preantral follicles in the Antarctic minke whale fetal ovary along with fetal growth during the early gestation period. These findings suggest that the change in preantral follicles was associated with changes in the concentration of steroids in early gestation periods. The changes in steroid concentrations in the fetal and umbilical cord blood and the increased number of preantral follicles were coincident at around 70 cm in fetal length, whereas the growth and differentiation of primordial and primary follicles appeared to be independent of FSH and LH.

The consumption of Antarctic krill (Euphausia superba) by an “average-sized” (male 6994 kg; female 8249 kg), sexually mature Minke whale (Balaenoptera acutorostrata) was estimated, from stomach capacity, ingestion rate and respiratory allometry methods. Estimates obtained from the stomach capacity and respiratory allometry methods differed by 17%–23%. An “average-sized” male Minke whale consumes 37.2 t of krill during a 90-day stay, and an “average-sized” female Minke whale consumes 56.2 t of krill during a 120-day stay, in Antarctic waters during the austral summer. It is estimated that the Minke whale population in the Antarctic (60°S and higher) consumes 35.5 × 106 t of krill annually.

As part of the multi-disciplinary project, Antarctic Marine Ecosystem Research at the Ice Edge Zone (AMERIEZ), habitat selection by marine mammals was investigated within the marginal ice zone in relation to measured ice variables and other environmental factors. Data were collected on three cruises to the southern Scotia and northern Weddell seas during spring 1983, autumn 1986, and winter 1988. During winter, Antarctic fur seals were significantly associated with drift, pancake, brash ice, icebergs, and areas of uneven floe distribution, all characteristic of the marginal ice zone. Fur seals were seen in open water close to the ice edge during autumn, but during spring, as the pack ice began to retreat rapidly, animals were seen more often away from the ice. Minke whales were also associated with pancake and new ice but were seen further into the pack ice during both winter and autumn. The largest groups of minke whales during winter were observed with a large krill swarm in new ice. Crabeater seal was exclusively a species of the deep pack ice during all seasons and was associated with ice cover of 7–8 oktas and evenly distributed ice floes.

Little is known about the characteristics of fertilisation events in minke whales. Cryopreserved minke whale oocytes and spermatozoa do not fertilise in a standard IVF. This study was conducted to investigate the pronucleus formation ability of cryopreserved minke whale oocytes and their subsequent development following intracytoplasmic sperm injection (ICSI). In experiment 1, frozen-thawed minke whale immature oocytes were cultured for in vitro maturation (IVM) in a maturation medium (TCM199) supplemented with either porcine follicle stimulating hormone (pFSH)/estradiol-17β(E2) or pregnant mare's serum gonadotropin (PMSG)/human chorionic gonadotropin (hCG). After 120 h of IVM, oocyte survival was examined before ICSI, and showed no significant difference in morphological normality (24-36%) between the two IVM media. Two-cell embryos (two oocytes from 21 sperm-injected oocytes) were obtained when the maturation medium was supplemented with pFSH/E2 or PMSG/hCG. In experiment 2, cryopreserved maturing oocytes were investigated for the effects of repeat-culture (2 h or 24 h) on survival before ICSI. Pronuclear formation and development were examined for the effects of sperm pretreatment with dithiothreitol (DTT) and oocyte activation with ethanol at ICSI. A frequency of 49-69% of frozen-thawed maturing oocytes was used for ICSI. Although oocyte activation did not produce a significant difference in survival, pronucleus formation and embryonic development, 2- and 4-cell cleaved oocytes were observed after injection of sperm pretreated with DTT.

This study was conducted to investigate the possibility of using bovine oocytes for a heterologous fertility test by intracytoplasmic sperm injection (ICSI) and to compare the pronuclear formation of ram, bull and minke whale spermatozoa after injection into bovine oocytes. Bovine oocytes were cultured in vitro for 24 h and those with a polar body were selected for ICSI. Frozen-thawed semen from the three species were treated with 5 mM dithiothreitol for 1 h and spermatozoa were killed by storing them in a -20 °C refrigerator before use. ICSI was performed using a Piezo system. Three experiments were designed. In experiment 1, a higher (p < 0.05) male pronuclear formation rate was found in the oocytes injected with ram (52.6%) or bull (53.4%) spermatozoa than with minke whale spermatozoa (39.1%). In experiment 2, sperm head decondensation was detected at 2 h after ICSI in the oocytes injected with a spermatozoon of each species. Male pronuclei were first observed at 4 h in the oocytes injected with ram or bull spermatozoa and at 6 h in oocytes injected with minke whale spermatozoa. The mean diameters of male pronuclei derived from both whale and bull spermatozoa were larger than those from ram spermatozoa (30.4 μm and 28.3 μm vs 22.4 μm, p < 0.005). The mean diameter of female pronuclei in the oocytes injected with whale spermatozoa was also larger than with ram spermatozoa (29.3 μm vs 24.7 μm, p < 0.05). The development of male and female pronuclei was synchronous. In experiment 3, ethanol-activated oocytes injected with a spermatozoon from any of the three species achieved significantly higher (p < 0.05-0.001) cleavage rates than control oocytes. Blastocyst formation was only observed when bull spermatozoa were used. The results of this study indicate that dead foreign spermatozoa can participate in fertilisation activities in bovine oocytes after ICSI.

Minke whales (Balaenopteva acutorostruta) have developed a compartmentalized stomach system, which includes a non-glandular forestomach containing high concentrations of indigenous bacteria. The forestomach contents serve as microbial substrate, and samples were collected from fiveadult minke whales eating capelin (Mallotus villosus) and crustaceans (Thysanoessa sp.). Chemical analysis of the forestomach contents revealed that they consisted of crude protein (650 (SD 58) g/kg DM), lipid (330 (SD77) g/kg DM) and water-soluble carbohydrates (53.3 (SD 7·3) g/kg DM). The contribution of energy from volatile fatty acids (VFA), produced by forestomach bacterial fermentation, to the total energy budget was estimated. The forestomach concentration ofVFA ranged from 13·2 to 68·5 mmol/l, and the pH was 5·83 (SD 0·41). VFA pool size ranged from 72·8 to 638·1 mmol and represented from 0·169 to 2·107 kJ/kg live weight (W)0·75 Maximal recorded forestomach VFA production rate was 1694 mmol/h in one capelin-eating minke whalewith 42·6 litres of forestomach fluid. Energy from VFA produced by forestomach fermentation represented 6–107 kJ/kg w0·75 per d, which accounts for only 0·9–16·9% of the average daily energy expenditure of minke whales. This study suggests that the bacterial fermentation in the minke whale forestomach varies, depending on the volume and the quality of substrate available, inlinencing fermentation rates and concentration of VFA. Due to the small relative size of the forestomach, the contribution of VFA to the daily energy requirement in minke whales would be of less importance than in ruminants even when assuming the same production rate of VFA as in a ruminant.

Mammals are known to utilize wax esters with an efficiency of less than 50%. The purpose of the present study was to examine whether or not minke whales (Balaenoptera acutorostrata), which at times may eat considerable amounts of wax-ester-rich krill, represent an exception to this general pattern. Samples of fresh undigested forestomach, as well as colon, contents were obtained from minke whales (n 5) that had been feeding on krill (Thysanoessa inermis) for some time. The samples were analysed for dry mass, energy density, lipid content and the major lipid classes, including wax esters. The concentrations of wax esters were compared with previous estimates of dry-matter disappearance of the same type of prey using an in vitro technique, to calculate the dry-matter digestibility of wax esters (DMDwax). Wax esters contributed 21% of the energy and 47% of total lipids in the krill diet. The energy density of gut contents decreased by 50% after their passage from forestomach to the end of the colon. The DMDwax was 94·1 (SD 2·8)% (n 5). This high DMDwax and the occurrence of fatty alcohols, one of the products of wax-ester hydrolysis, in faeces show that minke whales are very efficient digesters of wax esters and absorb most of the energy-rich products of this process.

Apparent digestible efficiency (% DE) was studied by use of dietary Mn as an inert marker, in minke whales (Balaenoptera acutorostrata) and crabeater seals (Lobodon carcinophagus) which had been eating krill. Median % DE in minke whales (n 5) eating krill of the genus Thysanoessa sp. (energy density (ED) 23·8 kJ/g) was 93 (range 87–93). Median % DE in crabeater seals (n 6) eating krill of the species Euphausia superba (ED 20·8 kJ/g) was 84 (range 79–85), which is significantly lower than the % DE of krill in minke whales (P = 0·008). Since the chemical composition in E. superba and in Thysanoessa sp. is similar, it is suggested that the complex multi-stomached system of minke whales, which contains both chitinase (EC 3.2.1.14)-producing as well as several other types of bacteria, is superior to the single-stomached system of crabeater seals with regard to krill digestion. It is worth noting, however, that the % DE of krill in the crabeater seal is still very high.