Integrating spatial data and shorebird nesting locations to predict the potential future impact of global warming on coastal habitats: A case study on Farasan Islands,Saudi Arabia

One of the expected effects of the global warming is changing coastal habitats by accelerating the rate of sea level rise. Coastal habitats support large number of marine and wetland species including shorebirds (plovers, sandpipers and allies). In this study, we investigate how coastal habitats may be impacted by sea level rise in the Farasan Islands, Kingdom of Saudi Arabia. We use Kentish plover Charadrius alexandrinus – a common coastal breeding shorebird – as an ecological model species to predict the influence of sea level rise. We found that any rise of sea level is likely to inundate 11% of Kentish plover nests. In addition, 5% of the coastal areas of Farasan Islands, which support 26% of Kentish plover nests, will be flooded, if sea level rises by one metre. Our results are constrained by the availability of data on both elevation and bird populations. Therefore, we recommend follow-up studies to model the impacts of sea level rise using different elevation scenarios, and the establishment of a monitoring programme for breeding shorebirds and seabirds in Farasan Islands to assess the impact of climate change on their populations.     

Extensive Use of Intertidal Habitat by Shorebirds Outside Protected Nesting Areas

Conservation of shorebirds throughout their breeding and migratory ranges has become a priority as shorebird populations decline globally. Along the North Atlantic Coast, management efforts have particularly focused on preserving nesting habitat for piping plovers (Charadrius melodus), which are protected under the Endangered Species Act. It is unclear whether these conservation measures suffice to protect foraging habitat for piping plovers and other shorebirds on stopover during migration along the Atlantic Flyway. To evaluate the extent to which conservation of piping plover nesting areas extends to all habitats used by plovers, and to determine whether these protections also benefited non-breeding migratory shorebirds in the region, we conducted weekly shorebird surveys, recording the number and locations of piping plovers and other species, during northward and southward migration on Fire Island and Westhampton Island, New York, USA, from 2014–2016. We used canonical correspondence analysis (CCA) to assess the degree of spatiotemporal overlap between breeding plovers, foraging plovers, and other migratory shorebirds that temporarily stage at the site. The spatiotemporal distribution of migratory shorebirds matched more closely with piping plovers seen during foraging than piping plovers observed tending nests and engaging in other breeding activities. Migratory shorebirds and foraging piping plovers were more abundant and frequent in wet intertidal zones outside of fenced-off nesting areas, which were not protected under current management regimes. Therefore, additional protection of piping plover foraging habitat could benefit plovers and migratory shorebirds that use similar feeding grounds during stopover on northward and southward migration. © 2020 The Wildlife Society.     

Climate as a driver of phenological change in southern seabirds

Seabirds are one of the most threatened groups of birds globally and, overall, their conservation status is deteriorating rapidly. Southern hemisphere countries are over-represented in the number of species of conservation concern yet long-term phenological data on seabirds in the southern hemisphere is limited. A better understanding of the implications of changes in the marine and terrestrial environments to seabird species is required in order to improve their management and conservation status. Here we conducted a meta-analysis of the phenological drivers and trends among southern hemisphere seabirds. Overall there was a general trend towards later phenological events over time (34 % of all data series, N?=?47; 67 % of all significant trends), though this varied by taxa and location. The strongest trends towards later events were for seabirds breeding in Australia, the Laridae (gulls, noddies, terns) and migratory southern polar seabirds. In contrast, earlier phenologies were more often observed for the Spheniscidae (penguins) and for other seabirds breeding in the Antarctic and subantarctic. Phenological changes were most often associated with changes in oceanographic conditions, with sea-ice playing an important role for more southerly species. For some species in some locations, such as the Little Penguin Eudyptula minor in south-eastern Australia, warmer oceans projected under various climate change scenarios are expected to correspond to increased seabird productivity, manifested through earlier breeding, heavier chicks, an increased chance of double brooding, at least in the short-term.     

Predicting Vulnerabilities of North American Shorebirds to Climate Change

Despite an increase in conservation efforts for shorebirds, there are widespread declines of many species of North American shorebirds. We wanted to know whether these declines would be exacerbated by climate change, and whether relatively secure species might become at–risk species. Virtually all of the shorebird species breeding in the USA and Canada are migratory, which means climate change could affect extinction risk via changes on the breeding, wintering, and/or migratory refueling grounds, and that ecological synchronicities could be disrupted at multiple sites. To predict the effects of climate change on shorebird extinction risks, we created a categorical risk model complementary to that used by Partners–in–Flight and the U.S. Shorebird Conservation Plan. The model is based on anticipated changes in breeding, migration, and wintering habitat, degree of dependence on ecological synchronicities, migration distance, and degree of specialization on breeding, migration, or wintering habitat. We evaluated 49 species, and for 3 species we evaluated 2 distinct populations each, and found that 47 (90%) taxa are predicted to experience an increase in risk of extinction. No species was reclassified into a lower–risk category, although 6 species had at least one risk factor decrease in association with climate change. The number of species that changed risk categories in our assessment is sensitive to how much of an effect of climate change is required to cause the shift, but even at its least sensitive, 20 species were at the highest risk category for extinction. Based on our results it appears that shorebirds are likely to be highly vulnerable to climate change. Finally, we discuss both how our approach can be integrated with existing risk assessments and potential future directions for predicting change in extinction risk due to climate change.     

SHOREBIRD HABITAT USE AND NEST-SITE SELECTION IN THE PLAYA LAKES REGION

Abstract: Wetlands in the Playa Lakes Region (PLR) provide important habitats for wintering waterfowl, cranes, and both migrant and breeding shorebirds. Playa Lakes Region wetlands experience naturally fluctuating hydroperiods but are exposed to anthropogenic stresses, which are exacerbated during summer and may influence PLR wetland occupancy and selection by breeding shorebirds. We examined wetland-scale habitat use and nest-site selection of the 4 dominant shorebirds (American avocets [Recurvirostra americana], black-necked stilts [Himantopus mexicanus], killdeer [Charadrius vociferus], snowy plovers [C. alexandrinus]) nesting in playas, saline lakes, and in both created and riparian wetlands in the PLR of Texas, USA. All 4 species nested in saline lakes. Only avocets and killdeer nested in playas, and snowy plovers nested in riparian wetlands. No nests were found in created wetlands. Wetland habitat changed (P < 0.001) during the breeding season, while water habitats generally decreased. Used (i.e., shorebirds found nesting) wetlands had more (P < 0.05) mudflats than non-used (i.e., shorebirds not found nesting) wetlands, which had more (P < 0.05) dry habitats. Used and non-used wetlands had similar (P > 0.05) amounts of water habitats. Nests were located close to vegetation on bare dry ground and dry ground with vegetation. Because water is ephemeral in PLR wetlands, shorebirds must select—in a somewhat predictive manner upon arrival—wetlands with suitable nest-site and brood-rearing habitat. Although surface water is necessary for nesting, its presence is not adequate for delineating suitable PLR wetland habitat for breeding shorebirds. Our findings that created wetlands cannot compensate for regional wetland losses in habitat or function highlights the need for conservation of natural PLR wetlands     

Using miniaturized radiotelemetry to discover the breeding grounds of the endangered New Zealand Storm Petrel Fregetta maoriana

Identification of breeding sites remains a critical step in species conservation, particularly in procellariiform seabirds whose threat status is of global concern. We designed and conducted an integrative radiotelemetry approach to uncover the breeding grounds of the critically endangered New Zealand Storm Petrel Fregetta maoriana (NZSP), a species considered extinct before its rediscovery in 2003. Solar‐powered automated radio receivers and hand‐held telemetry were used to detect the presence of birds on three island groups in the Hauraki Gulf near Auckland, New Zealand. At least 11 NZSP captured and radiotagged at sea were detected at night near Te Hauturu‐o‐Toi/Little Barrier Island with the detection of an incubating bird leading to the discovery of the first known breeding site for this species. In total, four NZSP breeding burrows were detected under mature forest canopy and three adult NZSP and two NZSP chicks were ringed. Telemetry data indicated NZSP showed strong moonlight avoidance behaviour over the breeding site, had incubation shifts of approximately 5 days and had a breeding season extending from February to June/July, a different season from other Procellariiformes in the region. Radiotelemetry, in combination with rigorously collected field data on species distribution, offers a valuable technique for locating breeding grounds of procellariiform seabirds and gaining insights into breeding biology while minimizing disturbance to sensitive species or damage to fragile habitat. Our study suggests an avenue for other breeding ground searches in one of the most threatened avian Orders, and highlights the general need for information on the location of breeding sites and understanding the breeding biology in data‐deficient birds.     

Gill Memorial Medal Address Holding the mirror up to nature

Since the early 1980s, there have been large decreases in numbers breeding in South Africa of three seabirds that compete with fisheries for food: African Penguin Spheniscus demersus, Cape Cormorant Phalacrocorax capensis and Bank Cormorant P. neglectus. By contrast, two other species that compete with fisheries but which have a larger foraging range when breeding or are nomadic between breeding localities, Cape Gannet Morus capensis and the nominate race of Swift Tern Thalasseus bergii bergii, have increased. Five seabirds that do not compete with fisheries for prey have maintained stable populations or increased. The decreases in the three species have led to deterioration in the overall conservation status of South Africa's seabirds, of which 10 of 15 species (67%) are presently classified as Threatened or Near-threatened, including six of the seven species that are endemic to the Benguela ecosystem off western southern Africa.     

THE BREEDING SEABIRDS OF TROMELIN ISLAND (WESTERN INDIAN OCEAN): POPULATION SIZES,TRENDS AND BREEDING PHENOLOGY

Le Corre, M. 1996. The breeding seabirds of Tromelin Island (western Indian Ocean): population sizes, trends and breeding phenology. Ostrich 67: 155–159.

Formerly six or eight species of seabirds bred on Tromelin Island, but currently only two species do so: The Redfooted Booby Sula sula and the Masked Booby S. dactylatra. The last two species which became locally extinct, the Lesser Frigatebird Fregata ariel and the Greater Frigatebird F. minor, probably stopped breeding on the island as a consequence of human disturbance to breeding colonies. The populations of the two species of booby have opposing trends since 1954. The Masked Booby's population increased from 60 pairs in 1954 to 200–250 pairs in 1996 while the Red-footed Booby's population decreased from 500 pairs in 1968 to 130–180 pairs in 1996. The impacts of human settlement, introduced brown rats Rattus norvegicus, local extinction of the Greater Frigatebird and other factors are discussed to explain these changes in population sizes. New data are provided on the breeding phenology of the two species of booby. Finally, the importance of this island for the conservation of seabirds in the western Indian Ocean is discussed.     

Do the high energy lifestyles of shorebirds result in high maximal metabolic rates? Basal and maximal metabolic rates in least and pectoral sandpipers during migration

Shorebirds have high resting and field metabolic rates relative to many other bird groups, and this is posited to be related to their high‐energy lifestyle. Maximum metabolic outputs for cold or exercise are also often high for bird groups with energetically demanding lifestyles. Moreover, shorebirds demonstrate flexible basal and maximal metabolic rates, which vary with changing energy demands throughout the annual cycle. Consequently, shorebirds might be expected to have high maximum metabolic rates, especially during migration periods. We captured least Calidris minutilla and pectoral C. melanotos sandpipers during spring and fall migration in southeastern South Dakota and measured maximal exercise metabolic rate (MMR; least sandpipers only), summit metabolic rate (M_sum, maximal cold‐induced metabolic rate) and basal metabolic rate (BMR, minimum maintenance metabolic rate) with open‐circuit respirometry. BMR for both least and pectoral sandpipers exceeded allometric predictions by 3–14%, similar to other shorebirds, but M_sum and MMR for both species were either similar to or lower than allometric predictions, suggesting that the elevated BMR in shorebirds does not extend to maximal metabolic capacities. Old World shorebirds show the highest BMR during the annual cycle on the Arctic breeding grounds. Similarly, least sandpiper BMR during migration was lower than on the Arctic breeding grounds, but this was not the case for pectoral sandpipers, so our data only partially support the idea of similar seasonal patterns of BMR variation in New World and Old World shorebirds. We found no correlations of BMR with either M_sum or MMR for either raw or mass‐independent data, suggesting that basal and maximum aerobic metabolic rates are modulated independently in these species.     

Populations and trends of Canadian Arctic seabirds

Canada’s eastern Arctic (Nunavut and Arctic Quebec—Nunavik, N of 60°) supports large numbers of seabirds in summer. Seabird breeding habitat in this region includes steep, rocky coasts and low-lying coasts backed by lowland sedge-meadow tundra. The former areas support colonial cliff- and scree-nesting seabirds, such as murres and fulmars; the latter inland or coastal seabirds, such as terns, gulls and jaegers. The region supports some 4 million breeding seabirds, of which the most numerous are thick-billed murres (Uria lomvia; 75%), black guillemots (Cepphus grylle; 9%), northern fulmars (Fulmarus glacialis; 8%) and black-legged kittiwakes (Rissa tridactyla; 6%). The majority of Arctic seabirds breed in a small number of very large colonies (>10,000 birds), but there are also substantial numbers of non-colonial or small-colony breeding populations that are scattered more widely (e.g. terns, guillemots). Population trends among Canadian Arctic seabirds over the past few decades have been variable, with no strongly negative trends except for the rare ivory gull (Pagophila eburnea): this contrasts with nearby Greenland, where several species have shown steep declines. Although current seabird trends raise only small cause for concern, climate amelioration may enable increased development activities in the north, potentially posing threats to some seabirds on their breeding grounds.     

Stress in seabirds: causes, consequences and diagnostic value

We describe a range of anthropogenic stressors thatimpact seabirds, review the effects of these stressorson individuals and populations and discuss the roleand value of seabirds as monitors of marine ecosystemhealth. Stressors described are restricted to thosewhich affect seabirds directly or indirectly throughthe marine environment; we have not dealt withterrestrially based stressors such as introducedmammalian predators or loss of habitat, which canpotentially affect seabirds whilst breeding. Wediscuss three broad categories of stress in seabirds.Marine pollutants (including biologicallynon-essential heavy metals, oil, organic pesticidesand polychlorinated biphenyls (PCBs), and plastics),industrial fisheries (further divided into the effectsof depletion of prey stocks and direct mortality), andclimate change. Additionally we highlight the role ofseabirds as monitors of marine ecosystem health,taking the example of long-term mercury contaminationas a case study. We conclude that seabirds are exposedto an increasing array of potential stressors, andthat the impact of a particular source of stress onseabirds varies markedly between species in relationto foraging and breeding ecology. The most seriousthreat to seabirds is direct mortality of adultsresulting from industrial and commercial fishingactivities. In some cases this is a significant threatto individual populations or even entire species.     

Community composition, seasonal dynamics and interspecific correlation of waterbirds in the Qiantangjiang River estuary and Hangzhou Bay

Waterbird surveys were conducted regularly in the Qiantangjiang River estuary and Hangzhou Bay from July 2007 to November 2011. A total of 128 species (nine orders and 18 families) were recorded, including 119 migrants which accounted for 93% of the total species; eleven species were listed as National Protected Species. Inter-specific correlation analysis for 13 shorebird populations and nine duck populations recorded over time found that 21 pairs of shorebirds and 23 pairs of ducks were correlated. By looking at seasonal dynamics and migration patterns we were able to divide the migration process into six stages: (1) late July to late September was the migration peak of shorebirds, which were dominated by Limosa limosa, Calidris ruficollis and Charadrius mongolus. (2) Early October to mid-December was the migration peak of wintering migrants of shorebirds and ducks, which were the first two large groups in our study areas. (3) Late December to mid-February was the wintering period of migration waterbirds. (4) Late February to late March was the peak migration of ducks and the winter migrants of shorebirds dominated by Calidris alpina. (5) Early April to mid-May was the migration peak of passage migrants such as, Calidris ruficollis, Calidris acuminate and Limosa limosa but the population size of shorebird winter migrants dominated by Calidris alpine was still larger than the former. (6) Late May to mid-July was the breeding season of all egrets, summer migrants of gulls and several species of shorebirds. Our surveys show that interaction among species is possibly an important determinant of community composition of shorebirds and wintering ducks during the migration season. It may be the geographical position and community composition of migrant shorebirds across Hangzhou Bay that mean during the northward migration there are far more shorebirds than during the southward migration.     

Patterns and determinants of shorebird species richness in the circumpolar Arctic

Aim The intention with this study was first to investigate and describe the broad‐scale geographical patterns of species richness of breeding shorebirds (Charadriiformes; families: Charadriidae, Scolopacidae and Haematopodidae) throughout the arctic tundra biome. Secondly, after compensating for the positive relationship between net primary productivity (NPP) and species richness, the relative importance of additional ecological and historical variables for species richness was investigated. The main variables considered are NPP, length of snow‐ and ice‐free season, accessibility of regions depending on migratory flyway systems, tundra area at Pleistocene (120 and 20–18 ka bp ) and Holocene (8 ka bp ) times, and tundra area at present. Methods Information on shorebird species breeding distributions was compiled from distribution atlases and species accounts. The breeding distributions of shorebirds with ranges partly or completely in the Arctic (a total of 50 species) were mapped in ArcView 3.2 to create a raster grid layer of shorebird species richness at a 1° latitude × longitude resolution. The total and mean species richness value was calculated per each 10° of longitude sector of the Arctic. The relationships between species richness and the different climatic and environmental variables were analysed on the basis of this sector‐wise division of the arctic tundra. The influence of each variable on species richness was investigated using univariate and multivariate analyses (multivariate linear regression and general linear model). Results We found that patterns of breeding shorebird species richness in the Arctic tundra biome are to a large degree determined by the NPP, the length of the snow‐ or ice‐free season, the diversity of migratory flyways, as well as the historical extent of tundra habitat area during the maximum cooling of the last glacial period. Essentially, two main regions are distinguishable in the circumpolar Arctic regarding shorebird community richness. These are a species‐rich Beringia‐centred region and a species‐poor Atlantic‐centred region. Main conclusions The underlying explanations to these major trends may primarily be attributed to factors that operate at present through accessibility of areas from contemporary migration flyways, as well as processes that operated in the past during and after the last glacial cycle. The most prominent influence on the shorebird diversity was found for NPP in combination with the diversity of migratory flyways. These flyways provide the links between breeding and wintering resources, often separated by huge distances, and the geographical and ecological conditions associated with the shorebirds’ migration seem to be of particular importance for their breeding diversity in different sectors of circumpolar tundra.     

Disease‐limited distributions? Contrasts in the prevalence of avian malaria in shorebird species using marine and freshwater habitats

Migratory shorebirds show strong dichotomies in habitat choice during both the breeding and nonbreeding season. Whereas High Arctic breeding species are restricted to coastal marine and saline habitats during the nonbreeding season, more southerly breeding species tend to use freshwater habitats away from coasts. It has been proposed that this co-variation in habitat use is a consequence of a single axis of adaptation to pathogens and parasites, which are hypothesized to be relatively scarce in High Arctic, marine, and saline habitats and relatively common at lower latitudes and in freshwater habitats. Here we examine this contrast by comparing the prevalence of avian malaria infections in shorebirds occupying different habitats. We used a PCR-based assay on 1319 individuals from 31 shorebird species sampled in the Arctic, in temperate Europe and in inland and marine habitats in West Africa. Infections mainly occurred in tropical wetlands, with the shorebirds in freshwater inland habitats having significantly higher prevalence of malaria than birds in marine coastal habitats. Infections were not found in birds migrating through Europe even though conspecifics did show infections in tropical Africa. Adults should resist infection better than juveniles, but showed higher malaria prevalence, suggesting that infection probability increases with cumulative exposure. We argue that exposure to vectors is the main factor explaining the habitat-related differences in malaria prevalence.     

Predictive Modelling to Identify Near-Shore,Fine-Scale Seabird Distributions during the Breeding Season

During the breeding season seabirds are constrained to coastal areas and are restricted in their movements, spending much of their time in near-shore waters either loafing or foraging. However, in using these areas they may be threatened by anthropogenic activities such as fishing, watersports and coastal developments including marine renewable energy installations. Although many studies describe large scale interactions between seabirds and the environment, the drivers behind near-shore, fine-scale distributions are not well understood. For example, Alderney is an important breeding ground for many species of seabird and has a diversity of human uses of the marine environment, thus providing an ideal location to investigate the near-shore fine-scale interactions between seabirds and the environment. We used vantage point observations of seabird distribution, collected during the 2013 breeding season in order to identify and quantify some of the environmental variables affecting the near-shore, fine-scale distribution of seabirds in Alderney’s coastal waters. We validate the models with observation data collected in 2014 and show that water depth, distance to the intertidal zone, and distance to the nearest seabird nest are key predictors in the distribution of Alderney’s seabirds. AUC values for each species suggest that these models perform well, although the model for shags performed better than those for auks and gulls. While further unexplained underlying localised variation in the environmental conditions will undoubtedly effect the fine-scale distribution of seabirds in near-shore waters we demonstrate the potential of this approach in marine planning and decision making.     

Lack of sperm production and sperm storage by arctic-nesting shorebirds during spring migration

Birds nesting at high latitudes may copulate during migration to arrive on the nesting grounds ready to breed. We surveyed 12 species of shorebirds during spring migration to determine whether (1) males produced abundant sperm and (2) females harboured functional sperm storage tubules (SSTs). Sperm production by males on migration was rare. Only four of seven species (9.8% of 41 males) of long-distance migrants harboured sperm, whereas all four species (100% of eight males) of short-distance migrants held sperm. In females, no long-distance migrants held sperm in their SSTs ( n  = 28 females) and SSTs were small compared to long-distance migrants collected on their breeding grounds. Our results indicate that shorebirds nesting at high latitudes were generally not reproductively active during migration and that any sexual behaviour on migration is unlikely to lead directly to fertilizations.     

Diverging phenological responses of Arctic seabirds to an earlier spring

The timing of annual events such as reproduction is a critical component of how free‐living organisms respond to ongoing climate change. This may be especially true in the Arctic, which is disproportionally impacted by climate warming. Here, we show that Arctic seabirds responded to climate change by moving the start of their reproduction earlier, coincident with an advancing onset of spring and that their response is phylogenetically and spatially structured. The phylogenetic signal is likely driven by seabird foraging behavior. Surface‐feeding species advanced their reproduction in the last 35 years while diving species showed remarkably stable breeding timing. The earlier reproduction for Arctic surface‐feeding birds was significant in the Pacific only, where spring advancement was most pronounced. In both the Atlantic and Pacific, seabirds with a long breeding season showed a greater response to the advancement of spring than seabirds with a short breeding season. Our results emphasize that spatial variation, phylogeny, and life history are important considerations in seabird phenological response to climate change and highlight the key role played by the species’ foraging behavior.     

Status of breeding seabirds on the Northern Islands of the Red Sea,Saudi Arabia

We undertook breeding surveys between 2010 and 2011 to assess the status of breeding birds on 16 islands in the northern Saudi Arabia. Sixteen bird species were found breeding at three different seasons; i.e. winter (Osprey), spring (Caspian and Saunder’s Terns), and summer (Lesser Crested, White-cheeked, Bridled Terns). It is postulated that food availability is an important factor influencing the breeding of seabirds in the northern Saudi Arabian Red Sea. Several species laid eggs earlier in northern parts of the Red Sea than in southern parts. The predicted increases in temperatures (T_a) could have a negative effect on species survival in the future, especially on those whose nests that are in the open. Finally, disturbance, predation and egg collection were probably the main immediate threats affecting the breeding seabird species in the northern Red Sea.     

Borrelia garinii and Francisella tularensis subsp. holarctica detected in migratory shorebirds in Portugal

Migratory shorebirds use, among many, the East Atlantic Flyway that links breeding areas as north as Tundra habitats to aquatic wintering grounds in West Africa. As a consequence, they are potentially important in the spread of global zoonotic diseases transmitted by ticks, such as Lyme borreliosis and tularemia—two diseases previously detected in Portugal. In this study, we looked at the infection status of seven populations of shorebirds during their migration, breeding, or wintering in the Portuguese wetlands to access if they carry these pathogens and to discuss their potential risk in the Portuguese wetlands. A total of 212 migratory shorebirds captured in the Tagus and Sado estuaries; key staging and wintering sites in this flyway and important breeding areas for some species were analyzed for the presence of Borrelia burgdorferi sensu lato and Francisella tularensis. In the present study, B. garinii was identified in seven (3%) specimens (five black-tailed godwits Limosa limosa, one common redshank Tringa totanus, and one little stint Calidris minuta), whereas F. tularensis subsp. holarctica was identified in one (0.4%) little stint. To our knowledge, this is the first evidence that shorebirds that migrate through or winter in Portugal transport these pathogens, potentially contributing for their introduction along the flyway, including the Mediterranean region.     

Status,trends, and patterns of covariation of breeding seabirds at St Lazaria Island,Southeast Alaska, 1994–2006

Aim We examined patterns of covariation among piscivorous and planktivorous seabirds breeding at St Lazaria Island in order to evaluate their responses to interannual changes in sea surface temperature, a variable that affects marine food webs. In addition, we evaluated seabird population trends for responses to decadal‐scale changes in the marine ecosystem. Location St Lazaria Island, Sitka Sound, Alaska. Methods Established seabird monitoring protocols for the Alaska Maritime National Wildlife Refuge were followed in estimating population trends, the timing of nesting events and the reproductive success of eight species of seabirds between 1994 and 2006. Results  Population increases were noted for storm‐petrels (Oceanodroma furcata and O. leucorhoa), rhinoceros auklets (Cerorhinca monocerata) and glaucous‐winged gulls (Larus glaucescens). We found no population trend for pelagic cormorants (Phalacrocorax pelagicus), but it appeared that populations of common (Uria aalge) and thick‐billed (U. lomvia) murres and of tufted puffins (Fratercula cirrhata) declined. We detected no linear trends in either breeding chronology or reproductive success over the study period for any seabird. All species of piscivorous seabirds apparently responded similarly to environmental cues as there was a positive covariation among species in the timing of nesting. Piscivores tended to nest earlier, and most species had higher rates of reproductive success in years with relatively warm spring sea temperatures. In contrast, planktivorous Leach’s storm‐petrels (O. leucorhoa) tended to nest earlier when spring and summer sea temperatures were relatively cool. Clearly, seabirds at St Lazaria were responding to interannual changes in sea temperatures near the breeding colony, probably as a result of effects on the food webs. Main conclusions Every seabird species we monitored at St Lazaria exhibited significant population trends between 1994 and 2006. For most species there appeared to be a relationship between both the timing of nesting and reproductive rates and spring or summer sea surface temperatures. Responses at both decadal (populations) and interannual (timing and reproductive success) scales make seabirds useful candidates for helping to monitor change in the marine environment.