A retrospective analysis of mortality in captive Magellanic penguins (Spheniscus magellanicus) in the United States, 2008–2018

Mortality data for Magellanic penguins (Spheniscus magellanicus) housed in zoos and aquariums in the United States has not previously been published. Necropsy and histopathology records were examined for Magellanic penguins housed at 12 Association of Zoos and Aquariums institutions from 2008 through 2018. If birds lived through the first year, the mean longevity was found to be 18.9 years of age (standard deviation: 7.9). Prefledge chicks and geriatric penguins experienced the highest mortality rates. Aspergillosis was a major cause of death in this species. There was no significant difference in mortality between males and females. Based on these data, recommendations for the husbandry and veterinary care of captive Magellanic penguins can be made.     

Flipper bands do not affect foraging‐trip duration of Magellanic Penguins

ABSTRACT Flipper bands are used to mark penguins because leg bands can injure their legs. However, concerns remain over the possible effects of flipper bands on penguins. We examined the effects of stainless‐steel flipper bands on the duration of foraging trips by Magellanic Penguins (Spheniscus magellanicus) at Punta Tombo, Argentina, using an automated detection system. We predicted that, if bands were costly and increased drag, flipper‐banded penguins would make longer foraging trips than those with small or no external markings. We tagged 121 penguins with radio‐frequency identification (RFID) tags and an additional external mark. We placed either a stainless‐steel band on the left flipper (N= 62) or a 2×10‐mm small‐animal ear tag in the outside web of the left foot (N= 59). We measured foraging‐trip durations (N= 376 trips) for 68 adult penguins with chicks from 15 December 2007 to 28 February 2008. Contrary to predictions, trip duration was similar for banded and web‐tagged penguins (P= 0.22) and for males and females (P= 0.52), with no interaction between tag type and sex (P= 0.52). No penguins marked in the 2007 breeding season and recaptured between 30 September and 30 November 2008 (N= 113) lost flipper bands or web tags, but three RFID tags failed between March and September 2008. Properly designed and applied flipper bands were a reliable marking method for Magellanic Penguins, had a lower failure rate than RFIDs, and did not affect foraging‐trip duration.     

Vision of the Humboldt penguin (Spheniscus humboldti) in air and water

Refractive states measured by retinoscopy and photorefraction indicate that the eyes of the Humboldt penguin, Spheniscus humboldti, are approximately emmetropic in air and water. Extensive myopia in air, as predicted by earlier authors and by a recent anatomical study, is non-existent. Photorefractive measurements of the refractive state, in water, of the Humboldt penguin indicate that it can accommodate sufficiently to make up the loss of the refractive power of the cornea. The cornea of the Humboldt penguin is flattened relative to the overall size of the eye. In all these respects (corneal flattening, and accommodation in air and water) the eyes of Humboldt penguins are like those of gentoo, (Pygoscelis papua), rockhopper (Eudyptes crestatus), Magellanic (Spheniscus magellanicus), and king penguins (Aptenodytes patagonica).     

Effects of double bands on Magellanic Penguins

ABSTRACT Banding penguins is controversial because bands can alter the survival, reproduction, and behavior of marked individuals. The effects of bands are not consistent among band types and, although stainless steel is thought to be better than other materials, tests of the long‐term impact of bands on tag‐loss rates and the reproduction and survival of individuals are needed. We tested three types of external tags on Magellanic Penguins (Spheniscus magellanicus) to measure band effects and tag‐loss rates. In 1993, we double‐tagged 300 penguins with aluminum flipper bands, stainless‐steel flipper bands, or small (2 mm × 10 mm) metal tags attached to foot webbing. We searched for double‐tagged birds for 13 of 15 yrs (1994–2008). Aluminum bands deformed, caused feather wear, injured and killed some penguins, and were lost more often than stainless‐steel bands or web tags. During the first 2 yrs of our study, at least nine penguins lost one aluminum band (N= 71 penguins resighted), but no penguins lost a stainless‐steel band (N= 84) or a web tag (N= 88). During the next 13 yrs, five penguins lost one of their two web tags (N= 89), but none lost a stainless‐steel band (N= 84). Females laid eggs of similar size before they carried a band and in the year following tagging (P= 0.09). The type of tags a female carried did not significantly change egg size (P > 0.22). During the first breeding season after tagging, penguins with aluminum bands had lower reproductive success than penguins with stainless‐steel bands or web‐tags (P= 0.04). The annual survival of females with two stainless‐steel bands was lower (0.79) than that of males with two stainless‐steel bands or males and females with two web‐tags (0.87). Aluminum bands injured Magellanic Penguins, were lost at high rates, and should not be used. Double stainless‐steel bands had no apparent effects on adult male Magellanic Penguins, but reduced survival rates of adult females. A single stainless‐steel band would likely have less impact than two bands, and our results suggest that the impact of a single band would be difficult to measure.     

An ARMS-based technique for sex determination of red panda (Ailurus fulgens)

Molecular sexing is a key component in the investigation of wild populations. In this study, we developed a fast, accurate and reliable amplification refractory mutation system (ARMS) technique for sex determination of red panda based on the exon 4 of the ZFX/ZFY gene. The amplicons were distinguished simply by agarose gel electrophoresis, exhibiting one fragment in females (X: 300 bp) and two in males (X: 300 bp, Y: 166 bp). Robustness of this ARMS system was confirmed by testing both 43 captive red pandas using DNA samples with known-sex and 10 wild red pandas using faecal DNA samples with unknown sex.     

New morphological data on the acanthocephalan <Emphasis Type="Italic">Hypoechinorhynchus magellanicus</Emphasis> Szidat, 1950 (Palaeacanthocephala: Arhythmacanthidae)

Hypoechinorhynchus magellanicus Szidat, 1950 (Acanthocephala: Arhythmacanthidae) is redescribed based on specimens collected from a sub-Antarctic notothenioid fish, Champsocephalus esox (Günther). The host was caught in the Beagle Channel (Magellanic sub-region). H. magellanicus has a trunk with an antero-dorsal curvature, a spherical proboscis, spines on the anterior region of the trunk, narrow lemnisci which are considerably longer than the proboscis receptacle, six cement glands and a single vaginal sphincter. The proboscis is armed with 40 hooks, including 15 large hooks with roots and 25 rootless basal spines. The large hooks are arranged in 10 alternate rows of one and two hooks. Each single large hook is followed by two spines, and pairs of large hooks are followed by single spines. Ten single spines are also present at the base of the proboscis between the rows. The eggs have polar prolongations of the middle envelope.     

Sex Identification of Four Penguin Species Using Locus‐Specific PCR

Traditional methods for sex identification are not applicable to sexually monomorphic species, leading to difficulties in the management of their breeding programs. To identify sex in sexually monomorphic birds, molecular methods have been established. Two established primer pairs (2550F/2718R and p8/p2) amplify the CHD1 gene region from both the Z and W chromosomes. Here, we evaluated the use of these primers for sex identification in four sexually monomorphic penguin species: king penguins (Aptenodytes patagonicus), rockhopper penguins (Eudyptes chrysocome), gentoo penguins (Pygoscelis papua), and Magellanic penguins (Spheniscus magellanicus). For all species except rockhopper penguins, primer pair 2550F/2718R resulted in two distinct CHD1Z and CHD1W PCR bands, allowing for sex identification. For rockhopper penguins, only primer pair p8/p2 yielded different CHD1Z and CHD1W bands, which were faint and similar in size making them difficult to distinguish. As a result, we designed a new primer pair (PL/PR) that efficiently determined the gender of individuals from all four penguin species. Sequencing of the PCR products confirmed that they were from the CHD1 gene region. Primer pair PL/PR can be evaluated for use in sexing other penguin species, which will be crucial for the management of new penguin breeding programs. Zoo Biol 32:257–261, 2013. © 2012 Wiley Periodicals, Inc.     

Magellanic penguin telomeres do not shorten with age with increased reproductive effort,investment, and basal corticosterone

All species should invest in systems that enhance longevity; however, a fundamental adult life‐history trade‐off exists between the metabolic resources allocated to maintenance and those allocated to reproduction. Long‐lived species will invest more in reproduction than in somatic maintenance as they age. We investigated this trade‐off by analyzing correlations among telomere length, reproductive effort and output, and basal corticosterone in Magellanic penguins (Spheniscus magellanicus). Telomeres shorten with age in most species studied to date, and may affect adult survival. High basal corticosterone is indicative of stressful conditions. Corticosterone, and stress, has been linked to telomere shortening in other species. Magellanic penguins are a particularly good model organism for this question as they are an unusually long‐lived species, exceeding their mass‐adjusted predicted lifespan by 26%. Contrary to our hypothesis, we found adults aged 5 years to over 24 years of age had similar telomere lengths. Telomeres of adults did not shorten over a 3‐year period, regardless of the age of the individual. Neither telomere length, nor the rate at which the telomeres changed over these 3 years, correlated with breeding frequency or investment. Older females also produced larger volume clutches until approximately 15 years old and larger eggs produced heavier fledglings. Furthermore, reproductive success (chicks fledged/eggs laid) is maintained as females aged. Basal corticosterone, however, was not correlated with telomere length in adults and suggests that low basal corticosterone may play a role in the telomere maintenance we observed. Basal corticosterone also declined during the breeding season and was positively correlated with the age of adult penguins. This higher basal corticosterone in older individuals, and consistent reproductive success, supports the prediction that Magellanic penguins invest more in reproduction as they age. Our results demonstrate that telomere maintenance may be a component of longevity even with increased reproductive effort, investment, and basal corticosterone.     

Differences of the porcine amelogenin X and Y chromosome genes (AMELX and AMELY) and their application for sex determination in pigs

Molecular sexing in wild and domestic animals has becoming an important issue in several fields including reproduction. X and Y chromosome-specific sequence differences of the amelogenin genes (AMELX and AMELY) have been described in different mammalian species and used for sex determination. We studied the possibility to use sequence variability between the porcine AMELX and AMELY genes for sex determination in pigs. Sequence analysis of about 400 bp of intron 3 of the porcine amelogenin genes showed the presence of a 9-10 bp deletion in AMELY gene compared to AMELX sequences. Moreover, one single nucleotide polymorphism (SNP) was detected for the AMELY sequence. Four other SNPs and 1 bp insertion differentiated three AMELX haplotypes indicating an unexpected quite high nucleotide diversity for a chromosome X region. Two sex determination assays targeting the 9-10 bp difference between AMELX and AMELY were developed. Assessment of the accuracy of the amelogenin assays to correctly sex individuals was tested on 329 pigs belonging to different breeds/lines. All analysed animals were correctly sexed with the new designed amelogenin tests. No amplification was obtained in human, cattle, goat, sheep, and horse genomic DNA. These assays can be used for sex diagnosis of small amounts of genomic DNA (20 pg) obtained from different sources including embryo biopsies, hair, meat, and other biological specimens. Thus, apart from the application in the reproduction field, these tests can be useful in several other sectors including forensics, archaeozoology, meat production, and processing as well as for quality control in sample identification.     

Magellanic Penguin eggshell pores: does number matter?

Most penguin species lay two eggs 3–4 days apart that hatch 1–2 days apart. Hypotheses to explain the shorter incubation period for the second egg include differences in porosity of the eggshells. Eggs with more or larger pores and/or thinner shells have higher gas exchange rates and faster embryonic development. We used eggshells from hatchling Magellanic Penguins Spheniscus magellanicus to test whether eggshell thickness and pore density affect incubation period. We expected: (i) second eggs to have thinner shells and/or more pores than first eggs; (ii) eggs to have thinner shells and/or more pores if they were laid by older females, later in the season, or in burrow nests (more humid than open nests under bushes). We found no support for these hypotheses. Egg pores and shell thickness were not related to incubation period. Eggs from the same clutch were similar in eggshell thickness and pore density. Female age, laying date and nest type were poor predictors of eggshell thickness and pore density. Egg pores, we conclude, have little explanatory power for differences in incubation time of eggs in Magellanic Penguins, and suggest that synchronous onset of incubation matters.     

Satellite tracking of the winter migration of Magellanic Penguins Spheniscus magellanicus breeding in the Falkland Islands

Magellanic penguin populations in the Falkland Islands may have decreased over the past decade. The post-breeding migration may be the period in which the birds are most vulnerable. To investigate this we equipped ten Magellanic Penguins after their moult at Seal Bay (51̀38'S, 58̀03'W), East Falkland, with satellite transmitters. The movements of the penguins were tracked for between 15 and 99 days until transmission ceased. All birds initially migrated to the northwest. However, four birds entered Argentinean coastal waters, then headed northeast following the coastline, The other penguins remained offshore, but also changed to a northeasterly course. Two birds migrated beyond 36̀S with a maximum distance to the colony of more than 1800 km, while the minimum distance travelled was up to 2700 km. Initially, the birds migrated quickly but their speed was reduced and became more variable as time progressed. A high concentration of positional fixes, associated with low travelling speeds, indicated at least four different areas where birds were assumed to forage efficiently. The relevance of these areas is discussed with respect to the diet of Magellanic Penguins and possible interactions with human activities.     

How Much Is Too Much? Assessment of Prey Consumption by Magellanic Penguins in Patagonian Colonies

Penguins are major consumers in the southern oceans although quantification of this has been problematic. One suggestion proposes the use of points of inflection in diving profiles (‘wiggles’) for this, a method that has been validated for the estimation of prey consumption by Magellanic penguins (Spheniscus magellanicus) by Simeone and Wilson (2003). Following them, we used wiggles from 31 depth logger-equipped Magellanic penguins foraging from four Patagonian colonies; Punta Norte (PN), Bahía Bustamente (BB), Puerto Deseado (PD) and Puerto San Julián (PSJ), all located in Argentina between 42–49° S, to estimate the prey captured and calculate the catch per unit time (CPUT) for birds foraging during the early chick-rearing period. Numbers of prey caught and CPUT were significantly different between colonies. Birds from PD caught the highest number of prey per foraging trip, with CPUT values of 68±19 prey per hour underwater (almost two times greater than for the three remaining colonies). We modeled consumption from these data and calculate that the world Magellanic penguin population consumes about 2 million tons of prey per year. Possible errors in this calculation are discussed. Despite this, the analysis of wiggles seems a powerful and simple tool to begin to quantify prey consumption by Magellanic penguins, allowing comparison between different breeding sites. The total number of wiggles and/or CPUT do not reflect, by themselves, the availability of food for each colony, as the number of prey consumed by foraging trip is strongly associated with the energy content and wet mass of each colony-specific ‘prey type’. Individuals consuming more profitable prey could be optimizing the time spent underwater, thereby optimizing the energy expenditure associated with the dives.     

Winning and losing: causes for variability in outcome of fights in male Magellanic penguins (Spheniscus magellanicus)

Game theory models predict that fighting ability should be moreimportant in contest outcome when the payoffs of winning arehigh for both contestants, and ownership should be more importantwhen payoffs are low. Male Magellanic penguins (Spheniscusmagellanicus) provide an opportunity to test these predictionsin a natural setting because payoffs of winning are higher for penguins fighting before egg laying and lower for penguinsfighting after egg laying, allowing the prediction of differencesin who should win and lose. We watched an area of approximately2000 Magellanic penguin nests from 1992 to 1996 at Punta Tombobreeding colony, Argentina; we quantified fighting behavior,banded contestants, measured their body size (here used as anindex of fighting ability), determined ownership status whenpossible, and monitored their reproductive success. We determinedthat male Magellanic penguins fought for nests and mates. Astheory predicts, before egg laying, body size difference wasmore important than ownership as a predictor of contest outcome and fight duration. After egg laying, owners won fights, andsize did not predict who won or how long they fought. Our comparisonsof nest ownership, nest quality, and chicks fledged by winnersand losers suggested that our predictions on the change inbenefits of winning before and after egg laying were correct.We conclude that game theory models are useful in predictingwho won or lost fights in male Magellanic penguins and thatultimate benefits of winning fights are related to fitness.     

Liver and plasma retinol (vitamin A) in wild, and liver retinol in captive penguins (Spheniscidae)

In rockhopper penguins ( Eudyptes crestatus ), liver concentrations of retinol (vitamin A) were significantly higher in post-moult than in pre-moult birds. In Magellanic penguins ( Spheniscus magelianicus ), plasma concentrations of retinol were significantly higher in post-moult than in pre-moult birds; liver retinol concentrations were also higher, but not significantly so.
The pre- and post-moult Magellanics had higher liver and lower plasma retinol concentrations than the pre- and post-moult rockhoppers.
Captive blackfooted (jackass) ( Spheniscus demersus ), king ( Aptenodytes patagonica ) and Humboldt ( Spheniscus humboldti ) penguins had liver vitamin A stores significantly lower than those of the free-living rockhopper, Magellanic, gentoo ( Pygoscelis papua ), emperor ( Aptenodytes forsteri ), chinstraps ( Pygoscelis antarctica ) and Adélie ( Pygoscelis adeliae ) penguins.     

Plasmodium relictum as a cause of avian malaria in wild-caught magellanic penguins (Spheniscus magellanicus)

Avian malaria (Plasmodium relictum) caused significant mortality in wild-caught Magellanic penguins (Spheniscus magellanicus) in 1986 at the Blank Park Zoo in Des Moines, Iowa (USA). In early winter, wild birds were captured off the southern coast of Chile and flown to Detroit, Michigan for a 38 day quarantine. After quarantine, 18 birds were dispersed to Lansing, Michigan, six to a facility in Maine, and 46 to Des Moines, Iowa. Upon arrival in Des Moines, several penguins became weak and inactive, had to be force-fed, and died after 2 days. Gross lesions at postmortem included splenomegaly, hepatomegaly, and pulmonary edema. Histopathological examination revealed numerous intraendothelial schizonts in spleen, lung, liver, heart and kidney. Schizonts were generally 16 to 28 micron by 11 to 16 micron and contained merozoites of two distinct sized (macromerozoites, nuclei 1.0 micron; micromerozoites, nuclei 0.5 micron). Based on the morphology of the abundant exoerythrocytic forms, a tentative diagnosis of avian malaria (Plasmodium sp.) was made. Subsequent transmission electron microscopic examination of schizonts in formalized tissue revealed merozoites with tear-shaped rhoptries. Antimalarial therapy was initiated early but deaths continued for 5 mo. Mortality, which eventually totaled 83%, occurred in three distinct waves, each separated by a hiatus of approximately 1 mo. Despite examinations of repeated blood smears, intraerythrocytic Plasmodium relictum was not detected until late in the outbreak. Diagnosis was based on morphologic characteristics including schizonts with eight to 12 merozoites/segmenter and round gametocytes that displaced and turned the infected erythrocyte nucleus. In addition to malaria, penguins showed evidence of aspergillosis, bacterial enteritis (Escherichia coli; Proteus sp.; and Edwardsiella sp.), and helminthiasis (Contracaecum sp. and Tetrabothrius sp.). Based on gross and histological lesions, disease prevalence in this group of penguins was malaria 58%, aspergillosis 61%, enteritis 60%, helminthiasis 26%. Epidemiologic investigation including group transport history, disease prevalence in co-quarantined birds not sent to Des Moines and climatological data implicated Des Moines as the likely site for initial exposure, although information is not conclusive. Stress and concurrent disease certainly contributed to the severe mortality in this group of penguins infected with P. relictum.     

Foraging behaviour of Magellanic Penguins during the early chick‐rearing period at Isla de los Estados,Argentina

Studies of the at‐sea distribution and trophic ecology of penguins are essential to understand their role in the broader marine food web. Magellanic Penguins Spheniscus magellanicus have a wide distribution and their foraging behaviour varies across breeding sites and between sexes, among others. In this study, we characterized the at‐sea areas, the diving strategies and the relative trophic level of Magellanic Penguins breeding at Isla de los Estados, Argentina, during the early chick‐rearing period. In addition, we quantified the interannual, sexual and individual variability in those parameters during three breeding seasons (2011–2013) using devices recording position and dive depth, and obtained blood samples for stable isotope analysis. During the early chick‐rearing period, Magellanic Penguins showed small differences between the sexes in their foraging behaviour and large overlap in the at‐sea areas used, suggesting no intraspecific variation between sexes. Although there was interannual variability in the foraging behaviour and the trophic level of the penguins, most of the studied nests managed successfully to raise both chicks during the first stage of the breeding cycle (guard stage). The foraging ecology of Magellanic Penguins from this colony was comparable with results of past studies at other breeding colonies. This study contributes to the identification of important at‐sea areas for Magellanic Penguins at the southern edge of their distribution and also to the identification of possible threats in the study area such as interaction with fisheries.     

A multiplex PCR assay for molecular sexing of the naked mole-rat (Heterocephalus glaber)

For molecular sexing of the naked mole-rat (Heterocephalus glaber), we designed a PCR primer set to amplify part of the Y-linked DBY gene. When this primer set was applied to the samples of known sex with the 16S rRNA gene (16S rDNA) primers as control, PCR products were successfully obtained as two DNA bands in males, a male-specific 163 bp DBY band and a 446 bp band of 16S rDNA shared with females, whereas females showed only the common band. This result shows that this multiplex PCR assay is useful for sex identification of H. glaber.     

Geographic morphological variation of Gentoo penguin (Pygoscelis papua) and sex identification: using morphometric characters and molecular markers

Gentoo penguins Pygoscelis papua have sexual dimorphism, which females have smaller morphological measurements than males. P. papua also shows a geographic morphological variation, decreasing in size toward southern latitudes. Therefore, morphological measurements may vary in space and overlap in the distribution of traits between females and males, which could lead to sex misidentification. A total of 300 blood samples and eight measurements and weight were obtained for Gentoo penguins from three localities in the South Shetland Islands and the Antarctic Peninsula. The molecular sex was identified for all individuals using two primer pairs (P2/P8 and PL/PR). We obtained higher success amplification for P2/P8 compared to PL/PR. We used 172 adults to create a morphological discriminant function using the backward stepwise method. We established a discriminant function for sex identification of each locality due to significant morphological differences found between sexes and between the three studied localities for adult Gentoo penguins. Using these functions, the percentages of individuals correctly assigned was 93.87 % in Ardley Island, 88.09 % in Bernardo O’Higgins, and 83.95 % in Gabriel Gonzalez Videla. The most southern locality studied was the most morphologically divergent from the others and with low divergence between sexes. Moreover, we also established a general function for the Gentoo penguin, which can be used to identify the sex of penguins from a broad number of localities. Therefore, molecular and biometric are useful techniques for sexing Gentoo penguins.     

Contrasting patterns of selection between MHC I and II across populations of Humboldt and Magellanic penguins

The evolutionary and adaptive potential of populations or species facing an emerging infectious disease depends on their genetic diversity in genes, such as the major histocompatibility complex (MHC). In birds, MHC class I deals predominantly with intracellular infections (e.g., viruses) and MHC class II with extracellular infections (e.g., bacteria). Therefore, patterns of MHC I and II diversity may differ between species and across populations of species depending on the relative effect of local and global environmental selective pressures, genetic drift, and gene flow. We hypothesize that high gene flow among populations of Humboldt and Magellanic penguins limits local adaptation in MHC I and MHC II, and signatures of selection differ between markers, locations, and species. We evaluated the MHC I and II diversity using 454 next‐generation sequencing of 100 Humboldt and 75 Magellanic penguins from seven different breeding colonies. Higher genetic diversity was observed in MHC I than MHC II for both species, explained by more than one MHC I loci identified. Large population sizes, high gene flow, and/or similar selection pressures maintain diversity but limit local adaptation in MHC I. A pattern of isolation by distance was observed for MHC II for Humboldt penguin suggesting local adaptation, mainly on the northernmost studied locality. Furthermore, trans‐species alleles were found due to a recent speciation for the genus or convergent evolution. High MHC I and MHC II gene diversity described is extremely advantageous for the long‐term survival of the species.