BIOLOGY OF THE BANK CORMORANT,PART 3: FORAGING BEHAVIOUR

Cooper, J. 1985. Biology of the Bank Cormorant, Part 3: Foraging behaviour. Ostrich 56: 86–95.

The Bank Cormorant Phalacrocorax neglectus, endemic to southern Africa, is primarily a solitary inshore forager. Bank Cormorants forage Primarily on the bottom among kelp beds but also may forage over shingle or coarse sand substrates or in midwater. Breeding birds forage up to 9 km from their colony. Little is known of foraging depth but birds may dive as deep as 28 m. Mean dive duration was 44,9 s and ratio of dives to surface rests was 2,18. In most cases prey is swallowed under water, presumably to avoid kleptoparasitism. Bank Cormorants foraged during daylight hours from before sunrise to after sunset. Birds did not forage in exceptionally rough seas. Mean female foraging bout duration (84,3 min) was significantly longer than that of males (68,4 min) in breeding individuals. Breeding males undertook significantly more foraging bouts (3,47 boutdday) than did females (3,02 bouts/day). No significant differences were found between the sexes when total time spent foraging/day by breeding birds was compared. It is not clear why males foraged more often, but for shorter periods, than did females, but the differences may be related to sexual dimorphism, males being larger than females.     

Population changes in sympatric Great and Long-tailed Cormorants (Phalacrocorax carbo and P. africanus): the effects of niche overlap or environmental change?

Between January 1993 and January 1995, the number of Great Cormorants (Phalacrocorax carbo) using Lake Naivasha, Kenya (00° 45 S, 36° 20 E) for foraging and resting increased 56%, while the number of sympatric Long-tailed Cormorants (Phalacrocorax africanus) decreased 64%. In 1995 and 1996, we documented habitat changes and conducted monthly population and resource-use surveys of the two species in an attempt to discover the most likely reasons for these changes. The increase in Great Cormorants was probably the result of immigration from nearby Lake Nakuru due to extreme water level reductions there. Lake Naivasha also experienced falling water levels and transparency during this period, but these changes were not as severe and are not considered likely reasons for the decline in Long-tailed Cormorant numbers. Despite some probable dietary overlap, the two species were well separated in terms of foraging locations, foraging methods, resting habitats and breeding timing. The decline in Long-tailed Cormorant numbers may be connected with increased disturbance by fishermen along the lake littoral, this species' primary feeding location.     

THE PROBLEM OF NOMENCLATURE

Whitfield, A. K. &; Blaber, S. J. M. 1978. Feeding ecology of piscivorous birds at Lake St Lucia, Part 3: Swimming birds. Ostrich 50:10-20. The diets, foraging periodicities and feeding behaviour of the Reed Cormorant Phalacrocorax africanus, Whitebreasted Cormorant Phalacrocorax carbo and White Pelican Pelecanus onocrotalus were studied at Lake St Lucia, Natal, South Africa, during 1975 and 1976. The Reed Cormorant fishes in shallow water within 100 m of the shore and mainly caught Sarotherodon mossambicus and Solea bleekeri, while the Whitebreasted Cormorant caught Mugilidae, Rhabdosargus sarba and Thryssa vitrirostris in deeper water. The diet of the White Pelican followed three distinct phases: a pre-incubation phase when the birds followed and preyed heavily on migrating Mugil cephalus shoals; an incubation and post-incubation phase when the adults flew a round trip of 200 km to the north to obtain freshwater fish, mainly cichlids, from the Pongolo pans where fishes were concentrated and densities high; and a post-fledgling phase when both adults and juveniles fed on a variety of marine species of fish in Lake St Lucia for about a month before dispersing to other areas. The feeding and breeding of Reed Cormorants and White-breasted Cormorants is discussed in relation to wind speeds, water turbidity and flooding of backwaters. The diet and long-range foraging behaviour of White Pelicans at St Lucia are compared with data from other African lakes. The breeding season of White Pelicans at St Lucia is related to availability of fish and inaccessibility of the breeding site to predators. The latter is determined by lake levels.     

Habitat use and spatial fidelity of male South American sea lions during the nonbreeding period

Conditions experienced during the nonbreeding period have profound long‐term effects on individual fitness and survival. Therefore, knowledge of habitat use during the nonbreeding period can provide insights into processes that regulate populations. At the Falkland Islands, the habitat use of South American sea lions (Otaria flavescens) during the nonbreeding period is of particular interest because the population is yet to recover from a catastrophic decline between the mid‐1930s and 1965, and nonbreeding movements are poorly understood. Here, we assessed the habitat use of adult male (n = 13) and juvenile male (n = 6) South American sea lions at the Falkland Islands using satellite tags and stable isotope analysis of vibrissae. Male South American sea lions behaved like central place foragers. Foraging trips were restricted to the Patagonian Shelf and were typically short in distance and duration (127 ± 66 km and 4.1 ± 2.0 days, respectively). Individual male foraging trips were also typically characterized by a high degree of foraging site fidelity. However, the isotopic niche of adult males was smaller than juvenile males, which suggested that adult males were more consistent in their use of foraging habitats and prey over time. Our findings differ from male South American sea lions in Chile and Argentina, which undertake extended movements during the nonbreeding period. Hence, throughout their breeding range, male South American sea lions have diverse movement patterns during the nonbreeding period that intuitively reflects differences in the predictability or accessibility of preferred prey. Our findings challenge the long‐standing notion that South American sea lions undertake a winter migration away from the Falkland Islands. Therefore, impediments to South American sea lion population recovery likely originate locally and conservation measures at a national level are likely to be effective in addressing the decline and the failure of the population to recover.     

Diving pattern and performance in relation to foraging ecology in the gentoo penguin, Pygoscelis papua

We present data on diving pattern and performance (dive depth, duration, frequency and organization during the foraging trip) in gentoo penguins Pygoscelis papua , obtained using time-depth recorders ( n = 9 birds, 99 foraging trips). These data are used to estimate various parameters of foraging activity, e.g. foraging range, prey capture rates, and are compared in relation to breeding chronology. Foraging trip duration was 6 h and 10 h, and trip frequency 1.0/day and 0.96/day, during the brooding and creche periods, respectively. Birds spent on average 52%of each foraging trip diving. Dive depth and duration were highly bimodal: shallow dives (< 21 m) averaged 4 m and 0.23 min, and deep dives (> 30 m) 80 m and 2.5 min, respectively. Birds spent on average 71%and 25%of total diving time in deep and shallow dives, respectively. For deep dives, dive duration exceeded the subsequent surface interval, but shallow dives were followed by surface intervals 2–3 times dive duration. We suggest that most shallow dives are searching/exploratory dives and most deep dives are feeding dives. Deep dives showed clear diel patterns averaging 40 m at dawn and dusk and 80–90 m at midday. Estimated foraging ranges were 2.3 km and 4.1 km during the brood and creche period, respectively. Foraging trip duration increased by 4 h between the brood and creche periods but total time spent in deep dives (i.e. time spent feeding) was the same (3 h). Of 99 foraging trips, 56%consisted of only one dive bout and 44%of 2–4 bouts delimited by extended surface intervals > 10 min. We suggest that this pattern of diving activity reflects variation in spatial distribution of prey rather than the effect of physiological constraints on diving ability.     

Movements and home ranges of monk seals in the main Hawaiian Islands

Hawaiian monk seals (Neomonachus schauinslandi) began recolonizing the main Hawaiian Islands (MHI) roughly 20 yr ago. The species’ abundance is still declining, but the subpopulation in the MHI is increasing by 6.5% per year. This difference may be due to differences in prey availability or habitat quality between the northwest (NWHI) and main Hawaiian Islands, which could be reflected in the movements and behavior of the seals. For example, foraging trip durations may be shorter in areas with higher forage quality. From 2007 to 2014 we deployed GPS phone tags on the islands of Molokai (n = 7), Kauai (n = 6), and Oahu (n = 6) to study movements and dive behavior. Foraging trips typically lasted 0.57 d (IQR: 0.34–0.83) and seals traveled 18 km (IQR: 10.2–30.5) per trip. Seals began benthic dives shortly after entering the water, with most dives to depths of 12–32 m. The median 95% and 50% kernel density isopleths for seals in the MHI were 149.2 km² and 23.2 km², respectively. The duration and distance of foraging trips in the MHI were shorter than that observed in other studies from the NWHI, suggesting that foraging habitat is currently better in the MHI.     

Foraging behaviour of Razorbills Alca torda during chick-rearing at the largest colony in the Baltic Sea

Capsule: Foraging behaviour in the Razorbill Alca torda during breeding was similar to that found elsewhere, aside from dive shape.

Aims: To investigate the foraging behaviour of Razorbills during the breeding season at the largest colony in the central Baltic Sea.

Methods: A combination of global positioning system (GPS) and time-depth recorder (TDR) devices were used on Razorbills breeding on the island of Stora Karlsö, Baltic Sea, during the chick-rearing period.

Results: Five GPS tracks and nine TDR logs were retrieved from 12 Razorbills, and 7399 dives were analysed. Razorbills foraged south and southwest of the colony. Maximum and mean (±sd) foraging range from the colony was 72.7?km and 13.1?±?13.5?km, respectively. Mean dive depth (15.3?±?2.4?m) and duration (53.1?±?8.5?s) were similar to those of a more southern Baltic Sea Razorbill colony. Dive depth had a bimodal distribution, with 70% of dives deeper than 10?m and 30% shallower than 10?m. There was a clear diel foraging pattern with 89% of dives occurring during daytime and a higher proportion of shallow dives at night. Unexpectedly, dives were primarily U-shaped. The Razorbills spent 31% of their overall time activity budget flying or diving.

Conclusion: Aside from dive shape, foraging behaviour was consistent with that reported at other colonies of Razorbills. Inconsistency in dive shape may be due to a bimodal foraging strategy, local prey behaviour or competition with the Common Guillemot Uria aalge.     

Diving behaviour, dive cycles and aerobic dive limit in the platypus Ornithorhynchus anatinus

We investigated the diving behaviour, the time allocation of the dive cycle and the behavioural aerobic dive limit (ADL) of platypuses (Ornithorhynchus anatinus) living at a sub-alpine Tasmanian lake. Individual platypuses were equipped with combined data logger-transmitter packages measuring dive depth. Mean dive duration was 31.3 s with 72% of all dives lasting between 18 and 40 s. Mean surface duration was 10.1 s. Mean dive depth was 1.28 m with a maximum of 8.77 m. Platypuses performed up to 1600 dives per foraging trip with a mean of 75 dives per hour. ADL was estimated by consideration of post-dive surface intervals vs. dive durations. Only 15% of all dives were found to exceed the estimated ADL of 40 s, indicating mainly aerobic diving in the species. Foraging platypuses followed a model of optimised recovery time, the optimal breathing theory. Total bottom duration or total foraging duration per day is proposed as a useful indicator of foraging efficiency and hence habitat quality in the species.     

Diving in shallow water: the foraging ecology of darters (Aves: Anhingidae)

Diving birds have to overcome buoyancy, especially when diving in shallow water. Darters and anhingas (Anhingidae) are specialist shallow-water divers, with adaptations for reducing their buoyancy. Compared to closely-related cormorants (Phalacrocoracidae), darters have fully wettable plumage, smaller air sacs and denser bones. A previous study of darter diving behaviour reported no relationship between dive duration and water depth, contrary to optimal dive models. In this study I provide more extensive observations of African darters Anhinga melanogaster rufa diving in water<5 m deep at two sites. Dive duration increases with water depth at both sites, but the relationship is weak. Dives were longer than dives by cormorants in water of similar depth (max 108 s in water 2.5 m deep), with dives of up to 68 s observed in water<0.5 m deep. Initial dives in a bout were shorter than expected, possibly because their plumage was not fully saturated. Dive efficiency (dive:rest ratio) was 5–6, greater than cormorants (2.7±0.4 for 18 species) and other families of diving birds (average 0.2–4.3). Post-dive recovery periods increased with dive duration, but only slowly, resulting in a strong increase in efficiency with dive duration. All dives are likely to fall within the theoretical anaerobic dive limit. Foraging bouts were short (17.8±4.3 min) compared to cormorants, with birds spending 80±5% of time underwater. Darters take advantage of their low buoyancy to forage efficiently in shallow water, and their slow, stealthy dives are qualitatively different from those of other diving birds. However, they are forced to limit the duration of foraging bouts by increased thermoregulatory costs associated with wettable plumage.     

SUCCESSFUL USE OF A TRANSLOCATION PROGRAM TO INVESTIGATE DIVING BEHAVIOR IN A MALE AUSTRALIAN FUR SEAL, ARCTOCEPHALUS PUSILLUS DORIFERUS

This study reports some of the first foraging behavior data collected for male fur seals. A nonbreeding male Australian fur seal, Arctocephalus pusillus doriferus , captured at a commercial salmon farm in southern Tasmania, Australia, was relocated 450 km from the site of capture. The animal was equipped with a geolocating time-depth recorder that recorded diving behavior and approximate location for the 14.4 d that it took the seal to travel down the east coast of Tasmania and be recaptured at the salmon farm. During its time at sea, the seal spent most of its time over the relatively shallow shelf waters. It spent 30% of its time ashore on a number of different haul-out sites. The deepest dive was 102 m and the maximum duration was 6.8 min. "Foraging" type dives made up 31.2% of the time at sea and had a median duration of 2.5 min and a median depth of 14 m. The seal performed these dives more commonly during the latter part of its time at sea, while it was on the east coast. Unlike other fur seal species studied to date, there was no evidence of a diurnal foraging pattern; it made dives at all times of the day and night.     

Migration and wintering sites of Pelagic Cormorants determined by satellite telemetry

ABSTRACT Factors affecting winter survival may be key determinants of status and population trends of seabirds, but connections between breeding sites and wintering areas of most populations are poorly known. Pelagic Cormorants (Phalacrocorax pelagicus; N= 6) surgically implanted with satellite transmitters migrated from a breeding colony on Middleton Island, northern Gulf of Alaska, to wintering sites in southeast Alaska and northern British Columbia. Winter locations averaged 920 km (range = 600–1190 km) from the breeding site. Migration flights in fall and spring lasted ≤5 d in four instances. After reaching wintering areas, cormorants settled in narrowly circumscribed inshore locations (～10‐km radius) and remained there throughout the nonbreeding period (September– March). Two juveniles tagged at the breeding colony as fledglings remained at their wintering sites for the duration of the tracking interval (14 and 22 mo, respectively). Most cormorants used multiple sites within their winter ranges for roosting and foraging. Band recoveries show that Pelagic Cormorants in southern British Columbia and Washington disperse locally in winter, rather than migrating like the cormorants in our study. Radio‐tagging and monitoring cormorants and other seabirds from known breeding sites are vital for understanding migratory connectivity and improving conservation strategies for local populations.     

The diving behavior of blue and fin whales: is dive duration shorter than expected based on oxygen stores?

Many diving seabirds and marine mammals have been found to regularly exceed their theoretical aerobic dive limit (TADL). No animals have been found to dive for durations that are consistently shorter than their TADL. We attached time-depth recorders to 7 blue whales and 15 fin whales (family Balaenopteridae). The diving behavior of both species was similar, and we distinguished between foraging and traveling dives. Foraging dives in both species were deeper, longer in duration and distinguished by a series of vertical excursions where lunge feeding presumably occurred. Foraging blue whales lunged 2.4 (+/-1.13) times per dive, with a maximum of six times and average vertical excursion of 30.2 (+/-10.04) m. Foraging fin whales lunged 1.7 (+/-0.88) times per dive, with a maximum of eight times and average vertical excursion of 21.2 (+/-4.35) m. The maximum rate of ascent of lunges was higher than the maximum rate of descent in both species, indicating that feeding lunges occurred on ascent. Foraging dives were deeper and longer than non-feeding dives in both species. On average, blue whales dived to 140.0 (+/-46.01) m and 7.8 (+/-1.89) min when foraging, and 67.6 (+/-51.46) m and 4.9 (+/-2.53) min when not foraging. Fin whales dived to 97.9 (+/-32.59) m and 6.3 (+/-1.53) min when foraging and to 59.3 (+/-29.67) m and 4.2 (+/-1.67) min when not foraging. The longest dives recorded for both species, 14.7 min for blue whales and 16.9 min for fin whales, were considerably shorter than the TADL of 31.2 and 28.6 min, respectively. An allometric comparison of seven families diving to an average depth of 80-150 m showed a significant relationship between body mass and dive duration once Balaenopteridae whales, with a mean dive duration of 6.8 min, were excluded from the analysis. Thus, the short dive durations of blue whales and fin whales cannot be explained by the shallow distribution of their prey. We propose instead that short duration diving in large whales results from either: (1) dispersal behavior of prey; or (2) a high energetic cost of foraging.     

Foraging behavior of lactating northern fur seals (<Emphasis Type="Italic">Callorhinus ursinus</Emphasis>) in the Commander Islands,Russia

We characterized the foraging behavior and habitat associations of lactating female northern fur seals (Callorhinus ursinus) from two of four rookeries comprising the stable population on the Commander Islands (CI). The CI females included in the study were from Severo-Zapadnoe rookery (SZR in 2008 and 2009) and Servernoe rookery (SR in 2009) which are 16 km apart on the northern tip of Bering Island (BI). We used satellite-linked tags and time–depth recorders to track the animals at sea and record dive behavior. For SZR females, the average foraging trip duration, mean dive depth, and maximum travel distance for both years were 3.4 ± 1.42 days, 16 ± 9.8 m, and 85 ± 59.6 km, respectively. The same measures for SR females were 4.4 ± 1.90 days, 20 ± 9.7 m, and 159 ± 70.8 km, respectively. The mean duration of foraging trips, mean number of bouts per trip and trip duration, mean direction of foraging trips, and size of foraging areas were significantly different between females from SR and SZR. Foraging trips of females from neither rookery were associated with high chl-a concentration. Overall, females on the CI appeared to expend less time and energy during foraging trips than females on the Pribilof Islands, and this may explain why the latter population is declining while the CI population is stable.     

Seasonal and annual variation in the diving behaviour of Hutton's shearwater (Puffinus huttoni)

ABSTRACT

With the development and implementation of tracking technology, we are now able to monitor the foraging behaviour of seabirds while at sea. Time-Depth Recorders (TDRs) were fitted to Hutton's shearwaters (Puffinus huttoni), an endangered endemic New Zealand species, to measure how diving behaviour varies over the breeding cycle. Hutton's shearwaters (～350?g) dive up to 339 times per day (average 68.8) at depths to 35?m (average 5.6?m), and for periods up to 60?s (average 19.2?s). Incubating birds dived deeper than birds feeding chicks, and a significant difference in diving depth and dive duration were detected at different times of the day. Neither dive frequency nor dive duration differed significantly between years, but there was some annual variation in dive depths. The temporal variation we observed in the diving behaviour of Hutton's shearwaters suggests they are likely to exploit different types of pelagic prey at different stages in their breeding cycle. With on-going changes in the marine environment, monitoring changes in feeding behaviour using TDRs may provide a way to assess environmental change and improve the conservation of this species.     

The relationship between sea surface temperature and population change of Great Cormorants Phalacrocorax carbo breeding near Disko Bay,Greenland

Arctic seas have warmed and sea ice has retreated. This has resulted in range contraction and population declines in some species, but it could potentially be a boon for others. Great Cormorants Phalacrocorax carbo have a partially wettable plumage and seem poorly suited to foraging in Arctic waters. We show that rates of population change of Cormorant colonies around Disko Bay, Greenland, are positively correlated with sea surface temperature, suggesting that they may benefit from a warming Arctic. However, although Cormorant populations may increase in response to Arctic warming, the extent of expansion of their winter range may ultimately be limited by other factors, such as sensory constraints on foraging behaviour during long Arctic nights.     

Foraging ecology of Gentoo Penguins Pygoscelis papua at Macquarie Island during the period of chick care

The diet, diving behaviour, swimming velocity and foraging range of Gentoo Penguins Pygoscelis papua were studied at Macquarie Island during the breeding season in the 1993–1994 austral summer. Gentoo Penguins are considered to be inshore feeders, and at Macquarie Island the diet and estimated foraging ranges supported this. The diet consisted of 91.6% fish and 8.3% squid, by mass. The dominant prey taxa were the fish Gymnoscopelus sp. and Paranotothenia magellanica. A mixture of pelagic and benthic prey was consumed, with a greater proportion of benthic species occurring later in the season. The penguins exhibited a strong diurnal pattern in their diving behaviour. Deep diving (≥30 m) began near sunrise (03.00 h) and finished close to sunset (21.00 h). Diving at night was less common and very shallow (<10 m). Early in the breeding season, dive profiles indicated that birds were probably following vertically migrating pelagic prey through the water column and were foraging in waters over 100 m deep. Later in the season, more uniform, shallower depths were used, suggesting an increase in benthic foraging activity. These changes in dive pattern and depth were consistent with the habitat preferences of prey species found in the diet. Gentoo Penguins swam at 1.04 m per s and had a maximum potential foraging range of about 26 km for single-day trips. They tended to forage within 14 km of the colony, with a mean range of 5.4 km. This range encompassed the deep ocean habitat to the west and east of the island and a shallow area to the north.     

Satellite tracking of Bulwer's Petrels Bulweria bulwerii in the Canary Islands

Capsule?The breeding foraging and post-breeding dispersal movements of five satellite-tagged Bulwer's Petrels from the Canary Islands were recorded. Foraging trips lasted 5.6 days in average (n?=?3), while the mean distance covered was 1261 km, and foraging areas were located over the continental slope and the adjacent pelagic waters, around 1200–2000 m depth and up to 350 km from the colony. After the chick-rearing period, birds dispersed southwestwards to the tropical waters of the central Atlantic.     

Body temperature and insulation in diving Great Cormorants and European Shags

1. Cormorants are typically considered as wettable diving birds with high thermoregulatory costs and are presumed to exert substantial predatory pressure on fish stocks.
2. The stomach temperatures of seven Great Cormorants and three European Shags were recorded during a total of 108 foraging trips undertaken near the Chausey Islands breeding colony (France).
3. Both species kept a constant body temperature during the dive series which lasted up to 158 min and were conducted in 12°C water. Consequently, assuming that heat loss to the water is equal to heat production in diving Great Cormorants, the minimal insulating plumage air volume was calculated to be 0·371 × 10^–3 m³ (corresponding to a 1·62-mm air layer) in males and 0·347 × 10^–3 m³ (corresponding to a 1·90-mm air layer) in females.
4. Furthermore, it is shown that plumage air volume and dive depth are the major factors influencing heat flux to the water and that the energetics of diving Great Cormorants may also vary substantially according to fat layer thickness, water temperature and body temperature. Swim speed plays only a minor role.
5. Considering these results, it is postulated that Great Cormorants may have optimized plumage air volume so as to minimize both mechanical costs (upthrust) and thermoregulatory costs of swimming in cold, shallow water.
6. Finally, body temperature patterns recorded in different cormorant species while diving are compared.     

Longline Fisheries and Foraging Distribution of Flesh-Footed Shearwaters in Eastern Australia

ABSTRACT Incidental seabird mortality associated with bycatch during longline commercial fishing is a conservation concern. An initial step to estimating likelihood of seabird bycatch and conceiving conservation strategies is determining amount of overlap between foraging birds and commercial fishing effort, identifying oceanographic features associated with foraging birds, and quantifying dive characteristics. We tracked 24 adult flesh-footed shearwaters (Puffinus carneipes) breeding on Lord Howe Island located east of Australia during incubation and early and late chick-rearing periods from 6 January to 17 April 2005. At-sea foraging distribution of flesh-footed shearwaters was primarily confined within the jurisdictional Australian Fishing Zone. Foraging was strongly associated with sea-surface temperature >24°C. Spatial and temporal overlap of longline fishing with foraging shearwaters varied throughout the breeding season, but was greatest (63% overlap) during early chick-rearing. Mean maximum distance reached from the breeding colony during a foraging event was 804 km (SD = 280) from Lord Howe Island. Foraging behavior was strongly diurnal, with 91% of dives occurring during daylight, and most dives (77%) were <5 m. Given that longline fishing and flesh-footed shearwaters overlap substantially, the Australian Fisheries Management Authority should consider implementing additional regulations to further reduce bycatch. Conservation strategies such as setting longlines at nights may reduce flesh-footed shearwater bycatch.     

BIOLOGY OF THE BANK CORMORANT,PART 1: DISTRIBUTION,POPULATION SIZE,MOVEMENTS AND CONSERVATION

Cooper, J. 1981. Biology of the Bank Cormorant, Part 1: Distribution, population size, movements and conservation. Ostrich 52: 208–215.

The Bank Cormorant Phalacrocorax neglectus is a marine species, endemic to southern Africa. Its non-breeding range extends from Walvis Bay to Cape Agulhas. Breeding range extends from Hollamsbird Island to Quoin Rock. Its distribution is broadly similar to that of kelp beds Ecklonia maxima. A total of 44 breeding localities supports approximately 18 000 adult birds; 12 800 (71%) occur on two islands (Ichaboe and Mercury) north of large kelp beds. Adult Bank Cormorants are resident but juveniles may disperse several hundred kilometres. The species is not considered to be seriously at risk to disturbance at most breeding localities. However, modern expansion of fishing activities may affect the very large populations of Ichaboe and Mercury Islands.