SEASONAL DISTRIBUTION OF STELLER'S SEA LIONS AT ROOKERIES AND HAUL-OUT SITES IN ALASKA

The Steller's sea lion population has declined by 60%-70% over much of Alaska since the late 1970s. Overlap in species composition and sizes of fishes consumed by sea lions and harvested by commercial fisheries, particularly during winter, has led to examination of potential interaction between commercial fisheries and Steller's sea lions. Abundance and distribution data for Steller's sea lions in Alaska were derived from aerial surveys conducted during the breeding season, mid-June to early July 1992, 1994, and 1996. To study winter distribution of sea lions, we conducted aerial surveys during March 1993, November-December 1994, and March 1999. We counted about one-half as many sea lions during winter surveys compared to the breeding-season surveys. Numbers of sea lions at rookery sites dropped off considerably during winter, whereas numbers at haul-out sites did not. We found little evidence of large-scale, seasonal movement, at least for the western stock of sea lions. Rather, differences between summer and winter distribution were primarily a function of sea lions dispersing to local haul-out sites during the winter. Terrestrial sites, both rookeries and haul-outs, clearly are important to Steller's sea lions during the entire year. Individual sites may be occupied year-round or only during particular times of year.     

Daily and seasonal variation in the haul-out behavior of the South American sea lion

In the South American sea lion (Otaria flavescens), daily fluctuations in abundance have been analyzed based on sequential counts of the number of animals hauled-out. However, no studies have analyzed haul-out activity in relation to an annual cycle or according to different age/sex classes. The objective of this study was to determine the daily and seasonal haul-out patterns of each age/sex class of South American sea lions as a function of the time of the day. A total of 222 days were analyzed in a breeding colony of Chile, from May 2008 to December 2010. During the non-breeding season (March to December) males, females, and juveniles showed a unimodal pattern, in which few sea lions are hauled-out in the morning and maximum numbers are found in the rookery during the early afternoon (1330–1630). In contrast, during the breeding season (austral summer) the proportion of individuals hauled-out shifted from a unimodal to a bimodal pattern, especially in the case of juveniles. Our results indicate that there are fine scale differences in haul-out behavior among age/sex classes, as well as larger scale seasonal differences in the proportion of sea lions ashore. These differences appear to be related to reproductive activities, food availability and thermoregulatory requirements. These patterns of seasonal variability of South American sea lion haul-out should be taken into consideration when planning surveys to estimate population abundance.     

HAUL-OUT ACTIVITY OF RINGED SEALS (PHOCA HISPIDA) DETERMINED FROM SATELLITE TELEMETRY

The haul-out activity of 15 ringed seals ( Phoca hispida ) equipped with satellite-linked radio transmitters was studied in NW Greenland ( ca. 73°-78°N). Between 19 June 1997 and 30 June 1999, telemetry data on haulout activity were obtained by the "Land-Sea-Reporter" (LSR), "Time-at-Depth" (TAD), and "Timelines" (TIM) systems housed within the satellite transmitters. The haul-out activity (% of total time hauled out) reported by the TIM system, which is specifically designed for collecting haul-out data, was about 1.4 times higher than that inferred from the LSR, but only about 0.7 of that inferred from TAD data. The TIM were used to describe haul-out activity. A total of 1,011 d with TIM were obtained (64.5% of a total of 1,568 "seal-days" monitored) representing data from nearly an entire annual cycle. No differences were found in percentage of time hauled out per month among various age categories. At all seasons the haul-out time showed considerable individual variation. There were no trends in percentage of time hauled out per month during late summer, fall, and winter (August-February). During the High Arctic winter darkness (November-January) the percentage of haul-out per month ranged between 3.9% in an adult (SD = 2.44, range: 1.1%-5.7%, n = 3 mo) and 15.7% in a subadult (SD = 1.95, range: 13.7%-17.6%, n = 3 mo). From late March there was a significant increase in haul-out time. Between 1 and 30 June, when aerial surveys of basking ringed seals usually are conducted, the haul-out time (% per day) increased from about 25% to about 57%. No tendencies in diel haul-out activity were revealed.     

Linking seasonal distribution patterns with prey availability in a central-place forager, the Steller sea lion

Aim We used a novel approach to infer foraging areas of a central‐place forager, the Steller sea lion (Eumetopias jubatus), by assessing changes in the temporal and spatial distribution patterns of sea lions at terrestrial sites. Specifically, our objectives were (1) to classify seasonal distribution patterns of Steller sea lions and (2) to determine to what extent the seasonal distribution of Steller sea lions is explained by seasonal concentrations of prey. Location Southeast Alaska, USA. Methods Steller sea lions of all age classes were counted monthly (2001–04) by aerial surveys at 28 terrestrial sites. Hierarchical cluster analysis and principal components analysis were used to classify seasonal distribution patterns of Steller sea lions at these terrestrial sites. We estimated the proportion of sea lions in the study area that were associated with each seasonal distribution pattern. Results Multivariate ordination techniques revealed four distinct seasonal distributional patterns. During December, 55% of the sea lions in the study area were found at Type 1 sites, located near over‐wintering herring aggregations. During May, 56% of sea lions were found at Type 2 sites, near aggregations of spring‐spawning forage fish. In July, 78% of sea lions were found at Type 3 sites, near summer migratory corridors of salmon. During September, 44% of sea lions were found at Type 4 sites, near autumn migratory corridors of salmon. Main conclusions Seasonal attendance patterns of sea lions were commonly associated with the seasonal availability of prey species near terrestrial sites and reflected seasonal foraging patterns of Steller sea lions in Southeast Alaska. A reasonable annual foraging strategy for Steller sea lions is to forage on herring (Clupea pallasii) aggregations in winter, spawning aggregations of forage fish in spring, salmon (Oncorhynchus spp.) in summer and autumn, and pollock (Theragra chalcogramma) and Pacific hake (Merluccius productus) throughout the year. The seasonal use of haulouts by sea lions and ultimately haulout‐specific foraging patterns of Steller sea lions depend in part upon seasonally available prey species in each region.     

The influence of precocious sexual maturation on survival to adulthood of river stocked Baltic salmon, Salmo salar, smolts

During three consequtive years, 1975–1977, Individually tagged Baltic salmon Salmo salar smolts of sexually immature male and female fish (n = 35027, mean size: 15.2 cm) and precocious males (n = 6518, mean size: 14.2 cm) were released into Umeälven (Ume river), northern Sweden. Rate of survival (% captured adults) based on 3714 recoveries was significantly higher (p < 0.01) for smolts from immature fish (10.2%) than those from smolts of early maturing males, i.e. precocious males (2.2%). corresponding to an average yield of 474 and 85 kg per KHX) smolts released, respectively. Gain in survival was on average 2.5% and 1.4% per cm increase in smolt size for immature smolts and smolts from precocious males, respectively. The poor survival among smolts of precocious males is suggested to he related to an interaction between sexual maturation and smolting linked to incompletely resorbed gonads leading to a non migratory behaviour. These non migratory males are then suggested to suffer heavily by predation in the river.
The two smolt categories had a similar growth pattern in sea. Smolts from precocious males did not mature early in sea indicating no relation to grisling, i.e. sexually maturing fish returning after first winter in sea. Adult weight of fish returning the fourth summer after release was related to smolt size (P < 0.05). Our Response Surface Model (RSA) predicted that large smolts (19.0 cm) had a higher specific growth rate over their life-span compared to small smolts (<15.0 cm), 0.86% d⁻¹ and 0.46% d⁻¹, respectively. Large smolts (19.0 cm) attained a size of 3.0 kg during their second winter in sea about six months earlier than small smolts (13.0 cm). The paper discusses alternative release strategies that can be employed if the ultimate goal of salmon stocking is maximizing yield.     

高原鼠兔(Ochotona curzoniae)冬季自然死亡率

以耳标观察法。1985年4-7月共捕标了样地内高原鼠兔(Ochotona curzoniae)幼鼠114只。到入冬前,死亡率为50.88%。第2胎出生的鼠死亡率明显地高于第1胎的死亡率。冬季死亡率呈现波动,入冬及开春时死亡率较高。鼠兔种群进入繁殖前期死亡率趋于零。初春样区存活标志鼠6只,经夏秋冬3季总计死亡率达94.74%。如按入冬时实有标志鼠计算,冬季死亡率为91.04%。     

Changes in glucocorticoids, IGF-I and thyroid hormones as indicators of nutritional stress and subsequent refeeding in Steller sea lions (Eumetopias jubatus)

Physiological responses to changes in energy balance are tightly regulated by the endocrine system through glucocorticoids, IGF-I and thyroid hormones. Changes in these hormones were studied in eight captive female Steller sea lions that experienced changes in food intake, body mass, body composition, and blood metabolites during summer and winter. During a period of energy restriction, one group of sea lions was fed reduced amounts of Pacific herring and another was fed an isocaloric diet of walleye pollock, after which both groups returned to their pre-experimental diets of herring. Cortisol was negatively and IGF-I was positively associated with changes in body mass during periods of energy restriction (mass loss associated with increase in cortisol and decrease in IGF-I) and refeeding (body mass maintenance associated with stable hormone concentrations in summer and compensatory growth linked to decrease in cortisol and increase in IGF-I in winter). Cortisol and IGF-I were also correlated with changes in lipid and lean mass, respectively. Consequently, these two hormones likely make adequate biomarkers for nutritional stress in sea lions, and when combined provide indication of the energetic strategy (lipid vs lean mass catabolism) animals adopt to cope with changes in nutrient intake. Unlike type of diet fed to the sea lions, age of the animals also impacted hormonal responses, with younger animals showing more intense hormonal changes to nutritional stress. Thyroid hormones, however, were not linked to any physiological changes observed in this study.     

STELLER SEA LION BODY CONDITION INDICES

We evaluated various measurements of mass, morphology, and blubber thickness as indices of fatness for Steller sea lions by correlation with the percentage of total body mass comprised by the sculp (%SCULP). We concluded LMD-index was the best index evaluated because it had a relatively high r ² (0.58), had a linear relationship with %SCULP, and the intercept term was not different from O. We suggest the development of a LMD-index for otariids would likely reduce the unexplained variation in the index. We developed a multiple regression model ( r ²= 0.745, P < 0.001) for predicting %SCULP with LMD-index and functions of sex, age, and season as predictor variables. Steller sea lions < 5 yr of age had higher %SCULP values than those ≥ 5 yr. %SCULP declined with age for sea lions < 5 yr. Both younger and older males were fatter during the winter/spring period than during summer/ fall. Females of both age classes had similar %SCULP values throughout the year. Steller sea lions are relatively lean pinnipeds; estimates of blubber and total body lipids ranged from 5% to 17% of total body mass.     

The role of Steller sea lions in a large population decline of harbor seals

We provide the first direct evidence that Steller sea lions will prey on harbor seals. Direct observations of predation on marine mammals at sea are rare, but when observed rates of predation are extrapolated, predation mortality may be found to be significant. From 1992 to 2002, harbor seals in Glacier Bay declined steeply, from 6,200 to 2,500 (∼65%). After documenting that Steller sea lions were preying on seals in Glacier Bay, we investigated increased predation by sea lions as a potential explanation for the large decline. In five independent data sets spanning 21–25 yr and including 14,308 d of observations, 13 predation events were recorded. We conducted a fine-scale analysis for an intensively studied haul-out (Spider Island) and a broader analysis of all of Glacier Bay. At Spider Island, estimated predation by sea lions increased and could account for the entirety of annual pup production in 5 of 8 yr since 1995. The predation rate, however, was not proportional to the number of predators. Predation by Steller sea lions is a new source of mortality that contributed to the seal declines; however, life history modeling indicates that it is unlikely that sea lion predation is the sole factor responsible for the large declines.     

QUANTIFICATION OF TERRESTRIAL HAUL-OUT AND ROOKERY CHARACTERISTICS OF STELLER SEA LIONS

Steller sea lions ( Eumetopias jubatus ) are known to have occupied the same terrestrial haul-out and rookery sites across the North Pacific Rim for centuries, but it is not known why they choose and stay at these locations, or what defines their preferred habitat. Classifying and comparing the shoreline type of haul-outs and rookeries against sites not used by Steller sea lions showed that they preferentially locate their haul-outs and rookeries on exposed rocky shorelines and wave-cut platforms. However, no preference was found for selecting rookeries on sheltered shore types. Shoreline types used less frequently by sea lions included fine-to-medium-grained sand beaches, mixed sand and gravel beaches, gravel beaches, and sheltered rocky shores. Quantifying the shoreline types used by sea lions confirms anecdotal reports of habitat preferences and may prove useful in identifying and protecting sea lion terrestrial habitat, or in forecasting how climate change might affect the distribution of sea lions.     

DEVELOPMENT OF DISPERSAL, MOVEMENT PATTERNS, AND HAUL-OUT USE BY PUP AND JUVENILE STELLER SEA LIONS (EUMETOPIAS JUBATUS) IN ALASKA

Population declines of Steller sea lions ( Eumetopias juhatus ) in western Alaska (west of 144°W) may be a result of reduced juvenile survival. We used satellite telemetry to study the at-sea distribution and movement patterns of pup (1.6–11.9 mo) and juvenile (12.0–35.1 mo) Steller sea lions. We studied trip distance, duration, and interhaul-out movements of sea lions in relation to age, sex, and month of year in the decreasing western population (WP; Prince William Sound, Kodiak, Aleutian Islands, Alaska) and the increasing eastern population (EP; Southeast Alaska). We deployed 103 satellite transmitters (29 WP; 74 EP) on sea lions between 1998 and 2001. Round trip distance and duration increased with age, trip distance was greater in the WP than the EP, trip duration was greater for females than males, and haul-out use was clustered. Changes in round trip distance and duration occurred from April to June for all age classes studied indicating that the annual timing of weaning may be less variable than the age of weaning. Overall, 90% of round trips were ≤ 15 km from haul-outs and 84% were <20 h, indicating nearshore areas adjacent to haulouts are critical to the developing juvenile.     

Variation in behavioral responses of the South American sea lion to tourism disturbance: Implications for tourism management

Due to the highly predictable patterns of occupancy on land, pinnipeds are one of the main marine resources observed by tourists, which, in turn, could strongly perturb their behavior. We analyzed the behavioral responses of the South American sea lion (Otaria byronia) to the presence of tourists and its variation according to temporal (2012 vs. 2013 austral summer months), spatial (breeding vs. nonbreeding sites of the colony), and age/sex class (adult males vs. subadult males vs. females) factors, and determined the relationship between the degree of responses by sea lions and the distance of the vessel to the colony, visitation time, and tourist behavior. We recorded 1,232 boat visits during 2012 and 2013. Subadult males were the age/sex class most affected in the breeding site, followed by adult females at the nonbreeding site. More disturbing conduct by tourists, longer visitation time, and vessels closer to the colony caused greater responses by sea lions. The established minimum distance from the colony is not enforced, generating an adverse response by sea lions. We recommend the development of management plans with the local coastal communities to decrease the impact of ecotourism on the species and enhance the sustainability of this industry.     

Distribution, pup production and mortality of New Zealand sea lion

Surveys were undertaken at Campbell Island / Motu Ihupuku during January and February 2008, to determine the distribution and pup production of New Zealand sea lions (NZ sea lion; Phocarctos hookeri). In addition, necropsies were performed at the main breeding site of Davis Point to determine the principal causes of early mortality for NZ sea lion pups. In total, 397 pups were tagged and 186 untagged pups were found dead, giving a minimum pup production of 583 pups and a one month of age mortality estimate of 40%. This represents a higher pup production than previous estimates from Campbell Island (although survey techniques are not comparable), and equates to 21% of the total pup production for NZ sea lions in the 2007/08 season. Early pup mortality was high (40%) at Campbell Island, with trauma, starvation, and drowning in rock pools and peat mires the major causes of death. Pups were concentrated in two colonial breeding sites: Davis Point on the north shore of Perseverance Harbour (76%) and a newly recorded breeding site (Paradise Point) on the southern shore of Perseverance Harbour (21%). Non-colonial breeding or single pups occurred around the southern parts of the island from sea level to 400 m; however, these only contributed 3% of the known pup production.     

Seasonal variation in the prevalence and intensity of canine Gnathostoma spinigerum infection in northeastern Thailand.

Gnathostoma spinigerum was found in gastric nodules in 4.1% of 2940 dogs surveyed in northeastern Thailand. The prevalence and worm burden of G. spinigerum exhibited a seasonal fluctuation. The parasites were more abundant in the rainy season and the early winter (August-December) than in the summer (April-March). Most parasites were sexually mature between August and December while immature worms were observed during March and April. The distribution of gnathostomes within the sampled dogs was highly dispersed and few animals were found to harbour more than five worms.     

THE POPULATION DYNAMICS OF NORTHERN SEA LIONS, 1975-1985

Abstract: Populations of northern sea lions ( Eumetopias jubatus ) in the vicinity of Marmot Island, Alaska declined during 1975–1985 at about 5% per year (Merrick et al. 1987). The cause of this decline is not known. A life table for the northern sea lion was calculated assuming that life spans follow a Weibull distribution. Samples of northern sea lions taken in the vicinity of Marmot Island, Alaska during 1975–1978 and 1985–1986 indicate that the average age of females older than 3 yr increased about 1.55 yr (SD = 0.35 yr) while the population was declining at about 5% per year. Fecundity rates decreased by 10% over the same period, but the decrease was not statistically significant (Calkins and Goodwin 1988). Possible causes of the population decline and the change in age structure were examined by writing the Leslie matrix population equation in terms of changes in juvenile and adult survival rates and fecundity, and examining the short–term behavior of the trajectories of the average age of adult females, total number of females, and total number of pups with respect to those changes in the vital parameters. From the observed rate of declines of adults and the changes in average age of adult females and fecundity, estimates of the changes in adult and juvenile survival were calculated; estimates of the standard deviations of these changes were estimated via a bootstrap procedure. One purpose of this exercise is to aid in setting priorities for research for determining the cause of the decline. An explanation for the observed declines in numbers of adult sea lions consistent with the observed fecundity rates, a rate of decrease of 5% in the number of adults, and the corresponding increase in average age (of females age 3 yr and older) was a 10%–20% decrease in the survival of juveniles (age 0-3 yr) coupled with an insignificant change in adult survival (0.03%, SD = 1%).     

South American sea lions in Peru have a lek‐like mating system

Five years of behavioral observations revealed significant effects of high air temperatures and breeding site topography on the mating system of South American sea lions in Peru. Unlike most polygynous mammals that defend females or fixed territories, male sea lions in Peru maintained positions along the shoreline where females passed each day to thermoregulate, and where most copulations occurred. Sex ratios (1 male per 17 females) and male mating success were extremely skewed (14% of males achieved 50% of the copulations, and 25% of them did not copulate at all). The mass daily movements of females toward the water and cool substrate of the shoreline, along with a highly skewed sex ratio, accentuated the difficulty for males to monopolize and restrict female movements. Females moved freely and chose their mates, unlike in temperate regions of their range where male South American sea lions control groups of females or access to tide pools. Our observations indicate that the South American sea lion in Peru has a lek‐like breeding system. This is a rare alternative to the common male strategies of defending females and resources, and is likely an evolutionary product of their highly skewed sex ratio, protracted breeding season, and the extreme subtropical climate where they breed.     

INCIDENTAL MORTALITY OF NORTHERN SEA LIONS IN SHELIKOF STRAIT, ALASKA

The incidental catch of northern sea lions ( Eumetopias jubatus ) in the walleye pollock ( Theragra chalcogramma ) joint-venture fishery in Shelikof Strait, Alaska, was studied during 1982–1984 to assess the nature and magnitude of the catch. Data were obtained by placing U.S. observers on foreign processing vessels. Dead sea lions recovered from trawl nets were counted, sexed and measured, teeth were removed for age determination by dental laminae; and stomach contents were analyzed. Although the fishery has continued to expand both in number of boats and estimated total catch (74,136 metric tons [t] in 1982 to 171,539 t in 1984), the estimated incidental catch of northern sea lions has declined (ranging from 958 to 1,436 in 1982, 216 to 324 in 1983 and 237 to 355 in 1984). Of the sea lions processed, 73 percent were caught between 2000 and 0500 h, probably during net retrieval. Most caught sea lions were females ranging in age from 1–25 yr with a mean age of 6.43 yr; 79 percent of the females were sexually mature and probably part of the reproducing population. Males had a mean age of 4.8 yr and only 12 percent were old enough to obtain and defend territories. Analysis of stomach contents showed that the sea lions consumed pollock the same size as that taken by the commercial fishery. The impact of the incidental catch on the Gulf of Alaska sea lion population is unknown.     

Impact of changing diet regimes on Steller sea lion body condition

A leading theory for the cause of the decline of Steller sea lions is nutritional stress, which led to chronic high juvenile mortality and possibly episodic adult mortality. Nutritional stress may have resulted from either poor quality or low abundance of prey. The objective of this study was to determine whether we could predict shifts in body condition (i.e., body mass or body fat content) over different seasons associated with a change in diet (i.e., toward lower quality prey). Captive Steller sea lions (n= 3) were fed three different diet regimes, where Diet 1 approximated the diet in the Kodiak area in the 1970s prior to the documented decline in that area, Diet 2 approximated the species composition in the Kodiak area after the decline had begun, and Diet 3 approximated the diet in southeast Alaska where the Steller sea lion population has been increasing for over 25 yr. All the animals used in this study were still growing and gained mass regardless of diet. Body fat (%) varied between 13% and 28%, but was not consistently high or low for any diet regime or season. Mean intake (in kg) of Diet 2 was significantly greater for all sea lions during all seasons. All animals did, however, tend to gain less body mass on Diets 2 and 3, as well as during the breeding and postbreeding seasons. They also tended to gain more mass during the winter and on Diet 1, though these differences were not statistically significant. Thus, changing seasonal physiology of Steller sea lions appears to have more impact on body condition than quality of prey, provided sufficient quantity of prey is available. Steller sea lions are opportunistic predators and are evidently able to thrive on a variety of prey. Our results indicate that Steller sea lions are capable of compensating for prey of low quality.     

The reproductive ecology and abundance of Symptevygia bonapavtii endemic to the south-west Atlantic

Logistical ogives gave an estimated L _T50 value (i.e. the total length at which 50% individuals are sexually mature) of 635 mm for female and 650 mm for male Sympterygia bonapartii . Mature individuals of both sexes had significantly larger livers than immature ones and females had a significantly heavier liver than males. Clasper elongation was the first step in male maturation, followed by clasper calcification and the development of alar thorns. In mature females, the right ovary was larger than the left, which was apparently due to differences in stroma tissue. Gonadosomatic index and diameter of ovarian follicles of mature females peaked in late spring and was at a minimum from late summer and through the winter. Juvenile S. bonapartii were more abundant near estuarine areas during winter, and adults appeared in estuaries by late spring and summer. Females carrying egg-cases were found near the shore in late spring and egg-cases were found in benthic samples only in shallow waters suggesting that S. bonapartii deposits egg-cases in shallow waters during late spring-summer and that nursery areas are in outer estuarine zones. In the southern part (38°–42° S) of the study area S. bonapartii showed a strong movement to shallow waters in late spring and summer, spreading over the entire coastal area in winter. These movements are discussed in relation to water temperature and trophic interactions.     

Body mass and composition responses to short-term low energy intake are seasonally dependent in Steller sea lions (Eumetopias jubatus)

Steller sea lions (Eumetopias jubatus) were fed restricted iso-caloric amounts of Pacific herring (Clupea pallasi) or walleye pollock (Theragra chalcogramma) for 8–9 days, four times over the course of a year to investigate effects of season and prey composition on sea lion physiology. At these levels, the sea lions lost body mass at a significantly higher rate during winter (1.6 ± 0.14 kg day⁻¹), and at a lower rate during summer (1.2 ± 0.32 kg day⁻¹). Decreases in body fat mass and standard metabolic rates during the trials were similar throughout the seasons and for both diet types. The majority of the body mass that was lost when eating pollock derived from decreases in lipid mass, while a greater proportion of the mass lost when eating herring derived from decreases in lean tissue, except in the summer when the pattern was reversed. Metabolic depression was not observed during all trials despite the constant loss of body mass. Our study supports the hypothesis that restricted energy intake may be more critical to Steller sea lions in the winter months, and that the type of prey consumed (e.g., herring or pollock) may have seasonally specific effects on body mass and composition.