David Aurioles-Gamboa

Isolation by distance among California sea lion populations in Mexico: redefining management stocks

Understanding the spatial structure of a population is critical for effective assessment and management. However, direct observation of spatial dynamics is generally difficult, particularly for marine mammals. California sea lions (Zalophus californianus) are polygynous pinnipeds distributed along the Pacific coast of North America. The species’ range has been subdivided into three management stocks based on differences in mitochondrial DNA, but to date no studies have considered nuclear genetic variation, and thus we lack a comprehensive understanding of gene flow patterns among sea lion colonies. In light of recent population declines in the Gulf of California, Mexico, it is important to understand spatial structure to determine if declining sea lion colonies are genetically isolated from others. To define population subdivision and identify sex biases in gene flow, we analysed a 355‐bp sequence of the mitochondrial DNA control region and 10 polymorphic microsatellite loci from 355 tissue samples collected from six colonies distributed along Mexican waters. Using a novel approach to estimate sex biases in gene flow, we found that male sea lions disperse on average 6.75 times more frequently than females. Analyses of population subdivision strongly suggest a pattern of isolation by distance among colonies and challenge current stock definitions. Based on these results, we propose an alternative classification that identifies three Mexican management units: Upper Gulf of California, Southern Baja Peninsula, and Upper Pacific Coast of Baja. This revised classification should be considered in future assessment and management of California sea lion populations in Mexican waters.

Survival Rates of the California Sea Lion, Zalophus californianus, in Mexico

Abstract California sea lions (Zalophus californianus) in the Gulf of California have declined by 20% over the past 2 decades. The lack of data on life-history parameters for this species has limited the development of demographic models to assess the status of this population. We estimated age- and sex-specific annual survival probabilities for California sea lions using resighting data on 5 pup cohorts from 1981 to 2006. We modeled apparent survival and resighting probability using age-class, sex, and time as potential explanatory variables. Apparent survival rates varied for different age- and sex-classes. Only survival of pups varied by year (from 0.556 to 0.998). Survival was the same for immature males and females (0.90), but differed by sex for young (males = 0.90, females = 0.97) and old (males = 0.75, females = 0.91) adults. Resighting probabilities varied by time, age-class, and sex. Resighting probabilities were higher for females than for males, and lowest for juveniles. The survival estimates presented here provide practical insight into understanding age- and sex-specific survival rates for California sea lions.

Prepartum and postpartum trophic segregation between sympatrically breeding female Arctocephalus australis and Otaria flavescens

Abstract In Uruguay, the South American fur seal population (Arctocephalus australis) is increasing, whereas the South American sea lion (Otaria flavescens) population is declining. Previous research using fecal analysis suggested a high degree of trophic overlap between these species. In this study we used stable isotope analysis to assess whether trophic overlap occurs between female fur seals and sea lions during the breeding season. We measured &dgr;15N and &dgr;13C values in serum and skin from pups of both species (n  =  47) to reflect pre- and postpartum maternal feeding habits, respectively. Our results suggested a lack of trophic overlap between lactating females; both serum and skin samples from sea lion pups had significantly greater &dgr;13C and &dgr;15N values than samples from fur seal pups, suggesting that lactating sea lions forage near shore, whereas lactating fur seals forage offshore. The pre- to postpartum diet shift in fur seals would be mainly caused by a reduction in the diversity of the exploited trophic levels, whereas in sea lions the shift could be related to a decrease in the diversity of foraging areas used. The observed trophic segregation between these sympatric otariids is probably driven by their synchronous breeding and similar maternal strategies.

Evidence of Leptospira interrogans infection in California sea lion pups from the Gulf of California.

Forty-two urine and 96 blood and serum samples were obtained from California sea lion (Zalophus californianus) pups from the Gulf of California during the 2000 reproductive season. Antibody prevalence to 13 serovars of Leptospira interrogans was determined by microagglutination tests (MAT); presence of pathogenic leptospires was detected by polymerase chain reaction (PCR). Samples with antibody titers ≥1:25 or 115 bp fragments on ethidium bromide-stained 1.5% agarose gels were considered positive. Antibody prevalence was 54% overall with highest prevalence against serovar cynopteri (50% of all positive reactions). Highest antibody titers (1:50) were detected against serovars cynopteri and pomona. Polymerase chain reaction products were observed in two of 42 urine samples, six of 96 blood samples, and one of 96 serum samples. Presence of PCR products in blood and serum was demonstrated in pups that were seronegative. Kruskall-Wallis tests and corresponding post hoc Tukey tests (α=0.05) showed that prevalence of leptospirosis was significantly different among all rookeries. The high seroprevalence (54%), low antibody titers (maximum 1:50), absence of pups showing clinical signs indicative of the disease, and lack of recent reports of increased mortality of sea lions in the Gulf of California are suggestive of the presence of enzootic host-adapted serovars. Crowding in rookeries as well as the presence of bats and rodents on some of the islands may explain infection by L. interrogans (sensu lato) and some of the differences in seroprevalence among reproductive rookeries.

Polychlorinated Biphenyls and Polybrominated Diphenyl Ethers in Galapagos Sea Lions (Zalophus wollebaeki)

Concentrations of polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), polychlorinated dibenzo-p-dioxins (PCDDs), and polychlorinated dibenzofurans (PCDFs) were measured in muscle-blubber biopsy samples from 21 Galapagos sea lion (Zalophus wollebaeki) pups that were live captured in the Galapagos Islands (Ecuador) using gas chromatography/high-resolution mass spectrometry. Only traces of PBDEs were detected in one male pup, whereas PCDDs and PCDFs were not detected in any sample. The total concentration of PCBs (ΣPCB) in the pups averaged 104 μg/kg lipid (range, 49-384 μg/kg). No statistically significant differences in ΣPCB were observed among the four study sites in the Galapagos Islands. Concentrations of PCB congeners in Galapagos sea lion pups were dominated by low-molecular-weight congeners. These results suggest that global transport is the main source for PCBs in Galapagos sea lions. The ΣPCB levels were below immunotoxic and endocrine-disruption thresholds in pinnipeds, suggesting a limited risk of adverse health effects. The present study indicates that Galapagos sea lions can serve as a useful sentinel of pollutants with a long-range transport capacity and that Galapagos Islands are not exempt from the threats of global pollutants despite its remote locale.

Stable Isotope Differences between Sea Lions (Zalophus) from the Gulf of California and Galápagos Islands

Abstract Spatial or temporal isotopic variation, or both, in primary producers must be controlled for when investigating the foraging and trophic ecology of top consumers using isotopic data. Populations of the sister species Zalophus californianus and Z. wollebaeki are separated by approximately 3,350 km in the eastern tropical Pacific Ocean, which prevents contact and mixing between the 2 populations. To explore differences in trophic ecology between these species, as well as the impact of differences in baseline food-web isotope values between the 2 regions, we compared conventional dietary data derived from analyses of scat contents to isotopic values of hair collected from pups at 13 rookeries in the Gulf of California (Z. californianus) and 11 rookeries on the Galápagos Islands (Z. wollebaeki). Mean ± 1 SD δ13C and δ15N values were −15.9‰ ± 0.5‰ and 21.8 ± 0.7‰ in the Gulf of California, whereas for the Galápagos they were −14.5‰ ± 0.5‰ and 13.1‰ ± 0.5‰. Examination of scat data suggested overlap in 6 of the 10 most common prey consumed by sea lions. Trophic level (TL) derived from scat analysis was positively related with δ15N values for the Gulf of California rookeries, but estimates of TL for each region were similar (4.4 for Galápagos and 4.1 for Gulf of California), suggesting that foraging behavior makes a limited contribution to the large difference in δ15N value between the 2 populations. Particulate organic matter δ15N values near the Galápagos Islands are ∼5.3‰ lower than values in the Gulf of California, suggesting that the baseline food-web values account for approximately two-thirds of the observed difference in pup hair δ15N values. This study may provide clues to better understand isotopic values of marine top predators migrating across the eastern Pacific Ocean.

A NONINVASIVE DEMOGRAPHIC ASSESSMENT OF SEA LIONS BASED ON STAGE-SPECIFIC ABUNDANCES

A pressing need exists to develop new approaches for obtaining information on demographic rates without causing further threats to imperiled animal populations. In this paper, we illustrate and apply a data-fitting technique based on quadratic programming that uses stage-specific abundance data to estimate demographic rates and asymptotic population growth rates (lambda). We used data from seven breeding colonies of California sea lions (Zalophus californianus) in the Gulf of California, Mexico. Estimates of lambda were similar to those from previous studies relying on a diffusion approximation using trends in total abundance. On average, predicted abundances were within 24% of the observed value for the inverse estimation method and within 29% of the observed value for the diffusion approximation. Our results suggest that three of the seven populations are declining (lambda < 1), but as many as six may be at risk. Elasticity and sensitivity analyses suggest that population management in most sites should focus on the protection of adults, whose survival generally contributes the most to lambda. The quadratic programming approach is a promising noninvasive technique for estimating demographic rates and assessing the viability of populations of imperiled species.

Estimating Sustainable Bycatch Rates for California Sea Lion Populations in the Gulf of California

Commercial and subsistence fisheries pressure is increasing in the Gulf of California, Mexico. One consequence often associated with high levels of fishing pressure is an increase in bycatch of marine mammals and birds. Fisheries bycatch has contributed to declines in several pinniped species and may be affecting the California sea lion (Zalophus californianus) population in the Gulf of California. We used data on fisheries and sea lion entanglement in gill nets to estimate current fishing pressure and fishing rates under which viable sea lion populations could be sustained at 11 breeding sites in the Gulf of California. We used 3 models to estimate sustainable bycatch rates: a simple population-growth model, a demographic model, and an estimate of the potential biological removal. All models were based on life history and census data collected for sea lions in the Gulf of California. We estimated the current level of fishing pressure and the acceptable level of fishing required to maintain viable sea lion populations as the number of fishing days (1 fisher/boat setting and retrieving 1 days worth of nets) per year. Estimates of current fishing pressure ranged from 101 (0-405) fishing days around the Los Machos breeding site to 1887 (842-3140) around the Los Islotes rookery. To maintain viable sea lion populations at each site, the current level of fishing permissible could be augmented at some sites and should be reduced at other sites. For example, the area around San Esteban could support up to 1428 (935-2337) additional fishing days, whereas fishing around Lobos should be reduced by at least 165 days (107-268). Our results provide conservation practitioners with site-specific guidelines for maintaining sustainable sea lion populations and provide a method to estimate fishing pressure and sustainable bycatch rates that could be used for other marine mammals and birds.

Relation of dental wear to the concentrations of essential minerals in teeth of the California Sea lion Zalophus californianus californianus

Tooth wear in marine mammals has been attributed to age, feeding habits, behavior, and contaminants. Advanced tooth wear in some California sea lions, including some of very young age (<5 yr), in the Gulf of California, suggests that there are variations in chemical composition of tooth parts, wherein the concentrations of certain trace minerals might be anomalous, making them more susceptible to erosion. The concentrations of the essential minerals Ca, P, K, Na, Fe, Mg, and Zn in the dentition of Zalophus c. californianus are documented for the first time and are compared for sea lion teeth with different degrees of wear. Canine teeth and molars from 45 skulls collected at 15 localities since 1978 were digested in perchloric acid and analyzed using atomic adsorption spectrometry, the results being expressed in milligrams per 100 g. An index of tooth wear (Id) was established, involving the average wear on the teeth and the age of the organism. No significant difference was detected in the variables, but there was one between ages (p=0.02). A higher degree of wear was observed up to 7 yr of age than from this age onward. Mineral concentrations did not explain the excessive wear observed (correlation, p>0.09; ANOVA, p>0.15); however, the Ca concentration of the teeth was inversely proportional to the age of the animal (sexes combined, p=0.026) and particularly significant for the females (r2=0.112, r=−0.335, p=0.039). Females could be more prone to decalcification because of their annual bone investment in their offspring. Animals of both sexes were susceptible to tooth wear as their age increased, but the higher frequency of animals between 4 and 7 yr suggests an impact on survival at early stages probably linked to deficient feeding and chronic malnutrition.

The Use of Surrogate Data in Demographic Population Viability Analysis: A Case Study of California Sea Lions

Reliable data necessary to parameterize population models are seldom available for imperiled species. As an alternative, data from populations of the same species or from ecologically similar species have been used to construct models. In this study, we evaluated the use of demographic data collected at one California sea lion colony (Los Islotes) to predict the population dynamics of the same species from two other colonies (San Jorge and Granito) in the Gulf of California, Mexico, for which demographic data are lacking. To do so, we developed a stochastic demographic age-structured matrix model and conducted a population viability analysis for each colony. For the Los Islotes colony we used site-specific pup, juvenile, and adult survival probabilities, as well as birth rates for older females. For the other colonies, we used site-specific pup and juvenile survival probabilities, but used surrogate data from Los Islotes for adult survival probabilities and birth rates. We assessed these models by comparing simulated retrospective population trajectories to observed population trends based on count data. The projected population trajectories approximated the observed trends when surrogate data were used for one colony but failed to match for a second colony. Our results indicate that species-specific and even region-specific surrogate data may lead to erroneous conservation decisions. These results highlight the importance of using population-specific demographic data in assessing extinction risk. When vital rates are not available and immediate management actions must be taken, in particular for imperiled species, we recommend the use of surrogate data only when the populations appear to have similar population trends.