Foraging areas of black‐browed and grey‐headed albatrosses breeding on Macquarie Island in relation to marine protected areas

• 1. Although marine protected areas (MPAs) are often established to protect threatened top‐order predators, there is a paucity of data that can be used to evaluate their efficacy in achieving this purpose.
• 2. We assessed the effectiveness of a network of MPAs around Macquarie Island in the Southern Ocean by examining the foraging areas of breeding black‐browed Thalassarche melanophrys and grey‐headed albatrosses T. chrysostoma.
• 3. During late incubation and brood periods over 90% of time spent foraging by black‐browed albatrosses was contained within MPAs, principally the Economic Exclusion Zone (EEZ) around Macquarie Island. In contrast, grey‐headed albatrosses spent only 34% of their time foraging in MPAs.
• 4. Black‐browed and grey‐headed albatrosses spent 30% and 15% of their respective foraging times in the Marine Park around Macquarie Island.
• 5. Both black‐browed and grey‐headed albatrosses foraged in Antarctic waters under the jurisdiction of the Convention for the Conservation of Antarctic Marine Living Resources (CCAMLR), accounting for 5% and 12% of the total foraging times respectively.
• 6. The spatial extent of MPAs around Macquarie Island appear to adequately cover much of the foraging distribution of breeding black‐browed albatrosses from Macquarie Island.
• 7. Breeding grey‐headed albatrosses spend significantly more time in waters outside the spatial extent of the surrounding MPAs and are at higher risk from fisheries activities and other threats.
• 8. Further information on the foraging movements both of albatrosses outside the breeding season and of juvenile albatrosses is required to more fully assess the efficacy of MPAs in protecting foraging habitats of these species.

Copyright © 2005 John Wiley & Sons, Ltd.     

Foraging ecology and interactions with fisheries of wandering albatrosses (Diomedea exulans) breeding at South Georgia

Knowledge about the areas used by the foraging wandering albatross, Diomedea exulans, its prey and overlap with longline fisheries is important information not only for the conservation of this species but also for furthering our understanding of the ecology of its prey. We attached satellite‐tracking devices and activity recorders to wandering albatrosses between May and July of 1999 and 2000 (years of differing food availability around South Georgia) in order to assess inter‐annual variation in the main foraging areas, association with oceanographic features (i.e. fronts, bathymetry), diet and interactions with fisheries. The overall foraging patterns of the tracked birds were similar in 1999 and 2000, ranging between southern Brazil (28°S) and the Antarctic Peninsula (63°S) and between the waters off Tristan da Cunha (19°W) and the Patagonian Shelf and oceanic waters south of Cape Horn (68°W) in the South Atlantic. In 1999, wandering albatrosses spent most time in sub‐Antarctic oceanic waters, their trip durations were significantly longer and they fed on fish and cephalopods (53 and 42% by mass, respectively). In contrast, in 2000, they spent more time in Antarctic waters, foraging trips were shorter and the diet was predominantly fish (84% by mass). Wandering albatrosses were associated with the sub‐Antarctic Front (SAF; both years), Subtropical Front (STF; in 1999) and the Tropical Front (TF; in 2000) suggesting that this species exploits prey concentrated at oceanic fronts. Fisheries discards also seemed to provide a very good source of food. Several fish species that are targeted (e.g. Patagonian toothfish, Dissostichus eleginoides) or are available as offal/discards from commercial fisheries (e.g. the macrourids, Antimora rostrata and Macrourus holotrachys) were mainly associated with the South Georgia shelf and the Patagonian Shelf, respectively. Wandering albatross foraging areas overlapped with longline fisheries in three different regions: around South Georgia, at the Patagonian Shelf and in oceanic waters north of 40°S. Females commuted more frequently to the Patagonian Shelf and to oceanic areas where longline fisheries were operating. Males, on the other hand, spent more time on the shelf/shelf slope of South Georgia where they were more at risk from the local Patagonian toothfish fishery, particularly in 2000. These results emphasize that inter‐annual variation in foraging preferences could lead to increased incidental mortality of this vulnerable species. Potential evidence for this is provided by a satellite‐tracked wandering albatross (male; 1.8‐day trip), whose diet contained a Patagonian toothfish head and a longline hook, and who spent extensive time in the water (44% of the time wet; 0.3 days of the trip) where a Patagonian toothfish longline fishing vessel was operating.     

Bycatch susceptibility in pelagic longline fisheries: are albatrosses affected by the diving behaviour of medium‐sized petrels?

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The year-round distribution and habitat preferences of Campbell albatross (Thalassarche impavida)

1. The use of miniaturized electronic tracking devices has illuminated our understanding of seabird distributions and habitat use, and how anthropogenic threats interact with seabirds in both space and time. To determine the year-round distribution of adult Campbell albatross (Thalassarche impavida), a single-island endemic, breeding only at Campbell Island in New Zealand's subantarctic, a total of 68 year-long location data sets were acquired from light-based geolocation data-logging tags deployed on breeding birds in 2009 and 2010.
2. During the incubation and chick-guard phases of the breeding season, birds used cool (<10°C) waters over the Campbell Plateau, but also ranged over deeper, shelf-break and oceanic waters (4,000–5,500 m) beyond the Plateau. Later in the breeding season, during post-guard chick-rearing, Campbell albatrosses exploited generally deep waters (4,000–5,000 m) beyond the Campbell Plateau.
3. During the non-breeding period, adults tended to move northwards into warmer (approximately 15°C) waters and occupied areas beyond western Australia in the west to offshore from Chile in the east. Overall, about 30% of adults spent some of their non-breeding period in the central and eastern Pacific Ocean, substantially expanding the previously reported range for this species.
4. One bird, that failed in its breeding attempt in October 2009, departed Campbell Island and circumnavigated the southern oceans before being recaptured back at Campbell Island in October 2010. This is the first example of an annually-breeding albatross species completing a circumnavigation between breeding attempts.
5. Overlap with fishing effort, using data from the Global Fishing Watch database, was assessed on a monthly and seasonal basis. Generally, levels of overlap between Campbell albatross and fishing effort were relatively low during the breeding season but were approximately 60% higher during the non-breeding period, underlining the need for international initiatives to safeguard this species.

     

Genetic population structure of black‐browed and Campbell albatrosses,and implications for assigning provenance of birds killed in fisheries

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Identifying the origins of fishing gear ingested by seabirds: a novel multivariate approach

• 1. The global decline of albatrosses (Diomedidae: Procellariiformes) is thought to have occurred largely as a direct result of fishery‐related mortality. Albatrosses and other large petrels interact with fisheries in several ways, including scavenging used bait and discarded offal, which may contain hooks.
• 2. Hooks that are ingested by breeding birds are often fed to chicks which subsequently regurgitate them shortly before fledging.
• 3. In this study a series of mathematical (cladistic, cluster and principal components) analyses are applied to a sample of 241 items of fishing gear (hook, snood and hook/snood unit) collected from seabird nest sites on Bird Island, South Georgia, and 44 reference gear items provided by four South Atlantic regional fisheries.
• 4. The five separate analyses failed to assign most gear to a particular fishery or to identify any consistent annual trends. The homogeneous nature of the material, which was largely derived from the same manufacturers, meant that gear origin could not be determined. This suggests that hooks found at seabird colonies in this, and potentially other regions, will be of limited use in identifying offending fisheries, unless operators are obliged to deploy gear with unique marks in the future.
• 5. Nevertheless, it is suggested that this approach should work effectively where birds interact with a range of fisheries targeting different species using variable gear. This study therefore represents an innovative approach to the characterization of lost fishing gear with potentially widespread application. Copyright © 2010 John Wiley & Sons, Ltd.

     

Sea turtle strandings reveal high anthropogenic mortality in Italian waters

• 1. Spatio‐temporal distribution and anthropogenic mortality factors were investigated in loggerhead turtles (Caretta caretta) found stranded or floating in the waters around Italy. A total of 5938 records for the period 1980–2008 were analysed concerning loggerhead turtles measuring from 3.8 to 97 cm curved carapace length (mean: 48.3 cm).
• 2. Results highlighted the following conservation issues: (i) in the study area, anthropogenic mortality is higher than natural mortality; (ii) interaction with fisheries is by far the most important anthropogenic mortality factor; (iii) longlines are an important mortality factor in the southern areas; (iv) trawlers are the cause of high numbers of dead strandings in the north Adriatic; (v) entanglement in ghost‐gear or in other anthropogenic debris affects high numbers of turtles; and (vi) boat strikes are an important source of mortality in most areas but mostly in the warm seasons.
• 3. Results also indicate that: (vii) the north Adriatic is the area with the highest turtle density; and (viii) the south Adriatic and to a lesser extent the surrounding areas of the north Adriatic and the Ionian, are important developmental areas for loggerhead turtles in the first years of life.
• 4. Italy is in the centre of the Mediterranean Sea and borders major foraging areas for the loggerhead turtles in the region, and these results confirm previous concerns about the level of anthropogenic mortality in Italian waters. Copyright © 2010 John Wiley & Sons, Ltd.

     

Improved line weighting reduces seabird bycatch without affecting fish catch in the Brazilian pelagic longline fishery

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Identifying mangrove areas for fisheries enhancement; population assessment in a patchy habitat

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167 individuals versus millions of hooks: bycatch mitigation in longline fisheries underlies conservation of Amsterdam albatrosses

1. Industrial fisheries represent one of the most serious threats worldwide to seabird conservation. Death of birds in fishing operations (i.e. bycatch) has especially adverse effects on populations of albatrosses, which have extremely low fecundity. 2. The single population worldwide of Amsterdam albatross (Diomedea amsterdamensis) comprises only 167 individuals and risks considerable decline over the mid‐term from additional mortality levels potentially induced by fisheries. The priority actions listed in the current conservation plan for this species included characterizing the longline fisheries operating within its range, dynamically analysing the overlap between albatrosses and these fisheries, and providing fisheries management authorities with potential impact estimates of longline fisheries on the Amsterdam albatross. 3. During all life‐cycle stages and year quarters the birds overlapped extensively with fishing effort in the southern Indian and Atlantic oceans. Fishing effort, and consequently overlap score (calculated as the product of fishing effort and time spent by the birds in a spatial unit) was highest in July–September (45% of the hooks annually deployed). Just three fleets (Taiwanese, Japanese and Spanish) contributed to >98% of the overlap scores for each stage (72% from the Taiwanese fleet alone, on average). Daily overlap scores were higher for the non‐breeding versus the breeding stages (3‐fold factor on average). 4. Based on previous bycatch rates for other albatross species, this study estimated that longline fisheries currently have the potential to remove ~2–16 individuals (i.e. ~5%) each year from the total Amsterdam albatross population, depending on whether bycatch mitigation measures were or were not systematically employed during the fishing operations. 5. Recent bycatch mitigation measures may be instrumental in the conservation of the Amsterdam albatross. This study suggests three further key recommendations: (1) to focus conservation efforts on the austral winter; (2) to require all operating vessels to report ring recoveries; and (3) to allocate special regulation of fishing operations in the areas of peak bycatch risk for the Amsterdam albatrosses. Copyright © 2015 John Wiley & Sons, Ltd.     

Seabird interactions and by‐catch in the anchovy pelagic trawl fishery operating in northern Argentina

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Assessing the effectiveness of conservation management decisions: likely effects of new protection measures for Hector's dolphin (Cephalorhynchus hectori)

• 1. Fisheries bycatch affects many species of marine mammals, seabirds, turtles and other marine animals.
• 2. New Zealand's endemic Hector's dolphins overlap with gillnet and trawl fisheries throughout their geographic range. The species is listed as Endangered by the IUCN. In addition, the North Island subspecies has been listed as Critically Endangered.
• 3. Estimates of catch rates in commercial gillnets from an observer programme (there are no quantitative estimates of bycatch by amateur gillnetters or in trawl fisheries) were used in a simple population viability analysis to predict the impact of this fishery under three scenarios: Option (A) status‐quo management, (B) new regulations announced by the Minister of Fisheries in 2008 and (C) total protection.
• 4. Uncertainty in estimates of population size and growth rate, number of dolphins caught and other model inputs are explicitly included in the analysis. Sensitivity analyses are carried out to examine the effect of variation in catch rate and the extent to which fishing effort is removed from protected areas but displaced to unprotected areas.
• 5. These methods are applicable to many other situations in which animals are removed from populations, whether deliberately (e.g. fishing) or not (e.g. bycatch).
• 6. The current Hector's dolphin population is clearly depleted, at an estimated 27% of the 1970 population. Population projections to 2050 under Options A and B predict that the total population is likely to continue declining. In the case of Option B this is driven mainly by continuing bycatch due to the much weaker protection measures on the South Island west coast.
• 7. Without fishing mortality (Option C) all populations are projected to increase, with the total population approximately doubling by 2050 and reaching half of its 1970 population size in just under 40 years. Copyright © 2009 John Wiley & Sons, Ltd.

     

Incidental capture of leatherback sea turtles in fixed fishing gear off Atlantic Canada

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Characterization of seabird bycatch in eastern Canadian waters, 1998–2011, assessed from onboard fisheries observer data

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Vulnerabilities and fisheries impacts: the uncertain future of manta and devil rays

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Linking the biology and ecology of key herbivorous unicornfish to fisheries management in the Pacific

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High mortality of adult female Magellanic penguins by gillnet fisheries in southern Brazil

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Breaking the ice: the introduction of biofouling organisms to Antarctica on vessel hulls

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Migrations and harvest rates of Arctic charr (Salvelinus alpinus) in a marine protected area

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Changes in northern Tanzania coral reefs during a period of increased fisheries management and climatic disturbance

• 1. Surveys of coral reefs in northern Tanzania were conducted in 2004/5 with the aim of comparing them over an～8‐year period during a time of increased efforts at fisheries management and the 1998 El Niño Southern Oscillation (ENSO) and Indian Ocean Dipole (IOD) coral mortality event that caused 45% mortality in northern Tanzania and much of the Indian Ocean.
• 2. Changes associated with both management, its absence, and the ENSO were found but changes were generally small and ecological measures indicated stability or improvements over this period, particularly when compared with reports from much of the northern Indian Ocean.
• 3. Fisheries management in two areas increased the biomass of fish and benthic communities. A small fisheries closure (0.3 km²) displayed little change in the coral community but ecological conditions declined as measured by sea urchins and fish abundances. This change may be associated with its small size because similar changes were not measured in the large closure (28 km²).
• 4. The few sites without any increased management were still degraded and one site had experienced a population explosion of a pest sea urchin, Echinometra mathaei.
• 5. The lack of significant changes across this disturbance indicates that these reefs are moderately resilient to climate change and, therefore, a high priority for future conservation actions.

Copyright © 2009 John Wiley & Sons, Ltd.