Use of foster parents in species conservation may cause conflicting objectives: hybridization between Lesser White-fronted Goose Anser erythropus and Barnacle Goose Branta leucopsis

Following the use of Barnacle Geese Branta leucopsis as foster parents in a conservation program for the endangered Lesser White-fronted Goose Anser erythropus in Sweden 1981–1999, mixed breeding pairs of the two species were established in the wild. We find indications that this was related to shared moulting habits of the two species in the Bothnian Sea during late 1990s. Starting in 2003, five mixed pairs produced at least 49 free-flying hybrid offspring until 2013, when the last breeding was confirmed. Reported numbers of hybrids did not increase in parallel to the production of young hybrids over time. After 2013, the number of hybrids started to decrease in Sweden and the Netherlands. Lower numbers of hybrids than expected can partly be explained by management actions taken, but may also be associated with low survival due to genetic outbreeding. Mixed pairs and their offspring entirely adopted the migratory habits of Barnacle Geese, overlapping very little with sites used by Lesser White-fronted Geese. We find no evidence that the hybrids ever posed a serious threat to Lesser White-fronted Geese breeding in Fennoscandia.

Circadian and Seasonal Patterns of Body Temperature in Arctic Migratory and Temperate Non-migratory Geese

Arctic migration presents unique challenges to circadian physiology. In addition to the metabolic cost of maintaining a relatively high body temperature (Tb) above ambient temperature, migratory birds are also exposed to rapidly changing light conditions as they transition between light-dark cycles and a 24-hour polar day. A previous study suggested that Arctic-migratory barnacle geese (Branta leucopsis) may utilise adaptive heterothermy (i.e., a controlled decrease in core Tb) during and around the autumn migratory period in order to minimise the metabolic cost of migration, but the impact of seasonally changing daylight conditions on other parameters of the circadian profile of Tb in these geese remained obscure. Here, we provide a detailed comparative analysis on the circadian rhythm of Tb and its seasonal development in free-living barnacle geese from three study populations that differ in their migratory behaviour and in the environments they occupy. We recorded abdominal Tb in non-migratory geese from a temperate breeding colony in Netherlands and in migratory geese from a colony in the Russian low Arctic, and analysed these data together with previously published Tb data on geese from a migratory colony in the high Arctic of Svalbard. We found that the circadian Tb profile in the barnacle goose was well aligned with the daily and seasonally changing daylight conditions. In the migratory populations, a fast re-entrainment of the rhythm and its phase was observed when zeitgeber conditions changed during migratory movements. The circadian rhythmicity of Tb was lost once the geese encountered permanent daylight at their northern staging and breeding sites. Circadian Tb rhythmicity was re-established when the period of permanent daylight ended, at rates corresponding to rates of seasonal changes in daylength in the high and low Arctic. Although our data corroborated findings of a decrease in daily mean Tb before autumn migration in both migratory populations in this study, the pre-migratory decrease in Tb was less drastic than previously reported. Moreover, in contrast to previous study, the decrease in Tb stopped at the onset of migration. Overall, our data reveal no evidence that heterothermy in the barnacle goose is functionally linked to migration.

Plasmids conferring resistance to extended-spectrum beta-lactamases including a rare IncN+IncR multireplicon carrying blaCTX-M-1 in Escherichia coli recovered from migrating barnacle geese (Branta leucopsis)

Background: Increasing antimicrobial resistance (AMR) is a global threat and wild migratory birds may act as mediators of resistant bacteria across country borders. Our objective was to study extended-spectrum beta-lactamase (ESBL) and plasmid-encoded AmpC (pAmpC) producing Escherichia coli in barnacle geese using whole genome sequencing (WGS) and to identify plasmids harboring bla genes. Methods: Barnacle geese feces (n=200) were collected during fall 2017 and spring 2018 from an urban area in Helsinki, Finland. ESBL/AmpC-producing E. coli were recovered from nine samples (4.5%) and isolates were subjected to WGS on both short- and long-read sequencers, enabling hybrid assembly and determination of the genomic location of bla genes. Results: A rare multireplicon IncN+IncR was recovered from one isolate carrying blaCTX-M-1 in addition to aadA2b, lnu(F), and qnrS1. Moreover, rarely detected IncY plasmids in two isolates were found to harbor multiple resistance genes in addition to the human-associated blaCTX-M-15. Poultry-associated blaCMY-2 was identified from the widely distributed IncI1 and IncK plasmids from four different isolates. One isolate harbored an IncI1 plasmid with blaCTX-M-1 and flor. A chromosomal point mutation in the AmpC promoter was identified in one of the isolates. WGS analysis showed isolates carried multiple resistance and virulence genes and harbored multiple different plasmid replicons in addition to bla-carrying plasmids. Conclusions: Our findings suggest that wild migratory birds serve as a limited source of ESBL/AmpC-producing E. coli and may act as disseminators of the epidemic plasmid types IncI1 and IncK but also rarely detected plasmid types carrying multidrug resistance. Human and livestock-associated ESBL enzyme types were recovered from samples, suggesting a potential for interspecies transmission. WGS offers a thorough method for studying AMR from different sources and should be implemented more widely in the future for AMR surveillance and detection. Understanding plasmid epidemiology is vital for efforts to mitigate global AMR spread.

Microbial responses to herbivory-induced vegetation changes in a high-Arctic peatland

Herbivory by barnacle geese (Branta leucopsis) alters the vegetation cover and reduces ecosystem productivity in high-Arctic peatlands, limiting the carbon sink strength of these ecosystems. Here we investigate how herbivory-induced vegetation changes affect the activities of peat soil microbiota using metagenomics, metatranscriptomics and targeted metabolomics in a comparison of fenced exclosures and nearby grazed sites. Our results show that a different vegetation with a high proportion of vascular plants developed due to reduced herbivory, resulting in a larger and more diverse input of polysaccharides to the soil at exclosed study sites. This coincided with higher sugar and amino acid concentrations in the soil at this site as well as the establishment of a more abundant and active microbiota, including saprotrophic fungi with broad substrate ranges, like Helotiales (Ascomycota) and Agaricales (Basidiomycota). A detailed description of fungal transcriptional profiles revealed higher gene expression for cellulose, hemicellulose, pectin, lignin and chitin degradation at herbivory-exclosed sites. Furthermore, we observed an increase in the number of genes and transcripts for predatory eukaryotes such as Entomobryomorpha (Arthropoda). We conclude that in the absence of herbivory, the development of a vascular vegetation alters the soil polysaccharide composition and supports larger and more active populations of fungi and predatory eukaryotes.

Seasonal variation in sleep homeostasis in migratory geese: a rebound of NREM sleep following sleep deprivation in summer but not in winter

Sleep is a behavioral and physiological state that is thought to serve important functions. Many animals go through phases in the annual cycle where sleep time might be limited, for example, during the migration and breeding phases. This leads to the question whether there are seasonal changes in sleep homeostasis. Using electroencephalogram (EEG) data loggers, we measured sleep in summer and winter in 13 barnacle geese (Branta leucopsis) under semi-natural conditions. During both seasons, we examined the homeostatic regulation of sleep by depriving the birds of sleep for 4 and 8 h after sunset. In winter, barnacle geese showed a clear diurnal rhythm in sleep and wakefulness. In summer, this rhythm was less pronounced, with sleep being spread out over the 24-h cycle. On average, the geese slept 1.5 h less per day in summer compared with winter. In both seasons, the amount of NREM sleep was additionally affected by the lunar cycle, with 2 h NREM sleep less during full moon compared to new moon. During summer, the geese responded to 4 and 8 h of sleep deprivation with a compensatory increase in NREM sleep time. In winter, this homeostatic response was absent. Overall, sleep deprivation only resulted in minor changes in the spectral composition of the sleep EEG. In conclusion, barnacle geese display season-dependent homeostatic regulation of sleep. These results demonstrate that sleep homeostasis is not a rigid phenomenon and suggest that some species may tolerate sleep loss under certain conditions or during certain periods of the year.

Pre-winter fattening and fat loss during wing moult: the annual cycle of fat deposition in captive barnacle geese (branta leucopsis)

Many different physiological changes have been observed in wild waterfowl during the flightless stage of wing moult, including a loss of body mass. Previously we established that captive barnacle geese (Branta leucopsis) underwent this characteristic decrease in body mass during their wing moult, even though they had unlimited and unrestricted access to food. In the present study we aimed to determine if this body mass loss during moult comprised mainly a reduction in fat stores, and to ascertain if the captive geese undergo pre-migratory and pre-winter fattening over a similar temporal scale to their wild conspecifics. The non-destructive technique of deuterium oxide isotope dilution was employed to provide repeated measurements of estimated fat deposition from a captive flock of fourteen barnacle geese. Birds were injected with deuterium oxide at 7 distinct intervals for one annual cycle. During the flightless period of the moult, body fat decreased by approximately 40% from the pre-moult value. During late-September and early October, body fat reached its highest point in the annual cycle, both as an absolute value and as a percentage of total body mass. We propose that while the energetic cost of wing moult is not the ultimate cause of fat loss in moulting barnacle geese, the approximate 212 g of fat catabolised during moult would provide sufficient energy to cover the cost of the replacement of the flight feathers, estimated to be 6384 kJ, over an approximate 42 day period. We conclude that the previously recorded increase in metabolism during moult in the geese, led to the use of endogenous fat reserves because the birds reduced rather than increased their food intake rates owing to the increased risk of predation when flightless. We also conclude that captive barnacle geese do undergo pre-winter and pre-migratory fattening, providing further evidence of the innate nature of these fat deposition cycles.

Mechanics Of Flight Feathers: Effects Of Captivity?

ABSTRACTFeathers act as aerodynamic cantilevers, and to withstand the prolonged cyclical loading that occurs during flight, feathers must be stiff, lightweight and strong. We experimentally tested the differences in feather structure, primarily stiffness and size, between (a) wild and captive Barnacle Geese Branta leucopsis, and (b) primary feathers dropped during the annual flight feather moult, and those feathers freshly regrown during the moult process. We found that, despite having undergone a 5,000km round-trip migration, flight feathers dropped during moult in the wild geese were stiffer than those measured in the captive geese, both for those dropped during moult and those re-grown. We propose that this may be related to diet or stress in the captive geese.