The Amundsen Sea Polynya International Research Expedition (ASPIRE)

In search of an explanation for some of the greenest waters ever seen in coastal Antarctica and their possible link to some of the fastest melting glaciers and declining summer sea ice, the Amundsen Sea Polynya International Research Expedition (ASPIRE) challenged the capabilities of the US Antarctic Program and RVIB Nathaniel B. Palmer during Austral summer 2010–2011. We were well rewarded by both an extraordinary research platform and a truly remarkable oceanic setting. Here we provide further insights into the key questions that motivated our sampling approach during ASPIRE and present some preliminary findings, while highlighting the value of the Palmer for accomplishing complex, multifaceted oceanographic research in such a challenging environment

Environmental compensation for biodiversity and ecosystem services: A flexible framework that addresses human wellbeing

Environmental compensation should address negative impacts from human activities on nature, including loss of biodiversity and ecosystem services. However, successful compensation, achieving no net loss, requires broad quantitative information on different types of losses and gains. We find that the scope of compensatory schemes varies in what is considered compensable, which makes it challenging to apply a conceptual approach consistently across schemes with different needs. We propose a flexible yet structured framework for determining which values should be compensated and how. Our framework focuses specifically on habitat deterioration and is illustrated with a case study involving loss of eelgrass habitat. The framework helps identify compensation needs and selects among suitable compensation options, merging science-based information with normative issues and local concerns. By integrating the ecosystem services cascade model, it encompasses aspects from biodiversity structure to human wellbeing. The framework prefers in-kind compensation because this targets the structure level and thus meets compensation needs in all subsequent levels of the cascade model; further, it is more likely to capture non-instrumental values (i.e. in nature) and reduce exposure to uncertainty. We highlight the importance of spatial aspects of ecosystem functions, services and their subsequent impacts on wellbeing. Although our selection hierarchy assumes a "similar and nearby" principle for habitat restoration (preference for in-kind/on-site), this criterion is not universal. We underscore the hierarchy's implicit normative assumptions and suggest that apparent disagreement about who should benefit may be traced to an unresolved conflict between egalitarianism and utilitarianism

Transporting ideas between marine and social sciences: experiences from interdisciplinary research programs.

The oceans comprise 70% of the surface area of our planet, contain some of the world’s richest natural resources and are one of the most significant drivers of global climate patterns. As the marine environment continues to increase in importance as both an essential resource reservoir and facilitator of global change, it is apparent that to find long-term sustainable solutions for our use of the sea and its resources and thus to engage in a sustainable blue economy, an integrated interdisciplinary approach is needed. As a result, interdisciplinary working is proliferating. We report here our experiences of forming interdisciplinary teams (marine ecologists, ecophysiologists, social scientists, environmental economists and environmental law specialists) to answer questions pertaining to the effects of anthropogenic-driven global change on the sustainability of resource use from the marine environment, and thus to transport ideas outwards from disciplinary confines. We use a framework derived from the literature on interdisciplinarity to enable us to explore processes of knowledge integration in two ongoing research projects, based on analyses of the purpose, form and degree of knowledge integration within each project. These teams were initially focused around a graduate program, explicitly designed for interdisciplinary training across the natural and social sciences, at the Gothenburg Centre for Marine Research at the University of Gothenburg, thus allowing us to reflect on our own experiences within the context of other multi-national, interdisciplinary graduate training and associated research programs

Are Cuckoos Maximizing Egg Mimicry by Selecting Host Individuals with Better Matching Egg Phenotypes?

Background: Avian brood parasites and their hosts are involved in complex offence-defense coevolutionary arms races. The most common pair of reciprocal adaptations in these systems is egg discrimination by hosts and egg mimicry by parasites. As mimicry improves, more advanced host adaptations evolve such as decreased intra- and increased interclutch variation in egg appearance to facilitate detection of parasitic eggs. As interclutch variation increases, parasites able to choose hosts matching best their own egg phenotype should be selected, but this requires that parasites know their own egg phenotype and select host nests correspondingly. Methodology/Principal Findings: We compared egg mimicry of common cuckoo Cuculus canorus eggs in naturally parasitized marsh warbler Acrocephalus palustris nests and their nearest unparasitized conspecific neighbors having similar laying dates and nest-site characteristics. Modeling of avian vision and image analyses revealed no evidence that cuckoos parasitize nests where their eggs better match the host eggs. Cuckoo eggs were as good mimics, in terms of background and spot color, background luminance, spotting pattern and egg size, of host eggs in the nests actually exploited as those in the neighboring unparasitized nests. Conclusions/Significance: We reviewed the evidence for brood parasites selecting better-matching host egg phenotypes from several relevant studies and argue that such selection probably cannot exist in host-parasite systems where hos

Egg rejection in blackbirds Turdus merula: a by-product of conspecific parasitism or successful resistance against interspecific brood parasites?

Traditional theory assumes that egg recognition and rejection abilities arise as a response against interspecific brood parasitism (IBP). However, rejection also appears in some species that are currently not exploited by interspecific parasites, such as Turdus thrushes. Recent evidences suggest that rejection abilities evolved in these species as a response to conspecific brood parasitism (CBP). To test these two alternative hypotheses, we performed an experimental study by parasitizing nests of the common blackbird (Turdus merula) with conspecifics or heterospecific eggs under different risk of parasitism (presence of interspecific or conspecific parasites near the nest). Common blackbird is a potential host of the common cuckoo (Cuculus canorus) but suffers low levels of CBP too. Results: We found that blackbirds were able to recognize and eject heterospecific eggs at high rates whereas most of conspecifics eggs were not recognized and, therefore, accepted. Ejection rates of conspecific eggs did not exceed 13 %, even in situations of high risk of CBP (blackbird female placed near the nest), which contradict the main prediction derived from the CBP hypothesis. Conversely, ejection rates of experimental eggs simulating IBP were much higher (80–100 %). Furthermore, female blackbirds were more aggressive towards cuckoos than towards blackbird dummies. Conclusions: Our results considered together support the IBP hypothesis, indicating that recognition and rejection of parasitic eggs in blackbirds have probably evolved due to previous cuckoo parasitism. The current absence of IBP in blackbirds may be due to the highly efficient rejection abilities in this species. Thus, these abilities have been retained in absence of brood parasitism as a consequence of the low costs involved for blackbirds, resulting in a successful resistance against interspecific brood parasitism.Financial support has been provided by the Consejería Economía, Innovación, Ciencia y Empleo. Junta de Andalucia (research project CVI-6653)

Uncovering Dangerous Cheats: How Do Avian Hosts Recognize Adult Brood Parasites?

BACKGROUND: Co-evolutionary struggles between dangerous enemies (e.g., brood parasites) and their victims (hosts) lead to the emergence of sophisticated adaptations and counter-adaptations. Salient host tricks to reduce parasitism costs include, as front line defence, adult enemy discrimination. In contrast to the well studied egg stage, investigations addressing the specific cues for adult enemy recognition are rare. Previous studies have suggested barred underparts and yellow eyes may provide cues for the recognition of cuckoos Cuculus canorus by their hosts; however, no study to date has examined the role of the two cues simultaneously under a consistent experimental paradigm. METHODOLOGY/PRINCIPAL FINDINGS: We modify and extend previous work using a novel experimental approach--custom-made dummies with various combinations of hypothesized recognition cues. The salient recognition cue turned out to be the yellow eye. Barred underparts, the only trait examined previously, had a statistically significant but small effect on host aggression highlighting the importance of effect size vs. statistical significance. CONCLUSION: Relative importance of eye vs. underpart phenotypes may reflect ecological context of host-parasite interaction: yellow eyes are conspicuous from the typical direction of host arrival (from above), whereas barred underparts are poorly visible (being visually blocked by the upper part of the cuckoo's body). This visual constraint may reduce usefulness of barred underparts as a reliable recognition cue under a typical situation near host nests. We propose a novel hypothesis that recognition cues for enemy detection can vary in a context-dependent manner (e.g., depending on whether the enemy is approached from below or from above). Further we suggest a particular cue can trigger fear reactions (escape) in some hosts/populations whereas the same cue can trigger aggression (attack) in other hosts/populations depending on presence/absence of dangerous enemies that are phenotypically similar to brood parasites and costs and benefits associated with particular host responses

Kompensation för miljöpåverkan vid kustexploatering – dagens tillämpning av ekologisk kompensation och särskild fiskeavgift samt möjlig vidareutveckling

Kustekosystemen är mycket viktiga för både biologisk mångfald och ekosystemtjänster, men påverkas samtidigt negativt av ett kontinuerligt ökat nyttjande av kustzonen för boende och olika verksamheter. Ekologisk kompensation är ett förvaltningsverktyg som syftar till att gottgöra oundviklig skada på naturmiljöer, exempelvis arter, naturtyper, ekosystemfunktioner och upplevelsevärden, i samband med mänsklig verksamhet. Verktyget har dock hittills använts i mycket begränsad omfattning i grunda kustmiljöer.Inom projektet ECOCOA, finansierat av Naturvårdsverket, har vi fokuserat på att utvärdera förutsättningarna för ökad användning av ekologisk kompensation i kustområden, som ett av flera verktyg som kan stöda miljövården. Projektets slutrapport (Bergström m.fl. 2021) ger en övergripande bild av samtliga resultat, medan vi i föreliggande rapport ger en fördjupning av de mer konkreta problem som kan uppstå vid handläggning av miljöärenden i förvaltningen, och möjliga lösningar på kort och lång sikt. Rapporten riktar sig i första hand till handläggare som vill utveckla tillämpningen av ekologisk kompensation vid vattenverksamhetsärenden, till tekniska råd vid markoch miljödomstolar, samt miljökonsulter och andra som kan behöva insyn i hur ekologisk kompensation kan användas och vidareutvecklas inom svensk kustmiljöförvaltning. I rapporten återger vi hur man hanterar ekologisk kompensation i svenska kustområden idag, till exempel hur handläggare arbetar med att mäta skada och bedöma omfattningen av kompensationsbehov. Vi beskriver även problematiken med småskaliga anmälningspliktiga ärenden, där den sammanlagda påverkan från många små exploateringar ger upphov till betydande förluster av biologisk mångfald och ekosystemtjänster. Slutligen beskriver vi hur den så kallade särskilda fiskeavgiften, som syftar till att tillvarata fiskeintresset i samband med vattenverksamhetsfrågor, tillämpas idag, samt analyserar hur beräkningsgrunderna skulle kunna utvecklas för att stärka användningen av ekologisk kompensationen som verktyg. Vår sammanställning och utvärdering utgår från ett generellt ramverk som utvecklats inom ECOCOA för att skatta skada och identifiera kompensationsbehov. Ramverket baseras på en kaskadmodell, som visar kopplingar mellan ekosystemets struktur, funktion, ekosystemtjänster och nyttigheter för människor. Modellen kan användas för att synliggöra hur verksamheter påverkar arter och livsmiljöer och vilka kostnader och förluster detta medför. Ramverket kan även användas för att bedöma i vilken omfattning en föreslagen åtgärd faktiskt kompenserar för de förluster som verksamheten innebär.Här följer en kort sammanfattning av resultaten som presenteras i rapporten: • En enkätundersökning riktad till aktörer inom kustförvaltningen visar att ekologisk kompensation i praktiken tillämpas mycket sällan inom kustmiljöförvaltningen idag, och att det finns ett stort behov av att ta fram riktlinjer för dess tillämpning, som stöd till handläggare, konsulter, domstolar och andra aktörer. På en mer generell nivå omfattar detta även ett behov av att förbättra kunskapen om restaureringsmetoder samt att ta fram metoder för värdering av skador på naturvärden. Det finns även ett behov av resurser för Sammanfattning 6 handläggare i form av tid och stöd för att tillämpa ekologisk kompensation i kustförvaltningen. • En utvärdering av befintliga domslut för ett antal tillståndspliktiga (dvs. storskaliga) vattenverksamhetsärenden visar att biologisk mångfald och ekosystemtjänster mycket sällan beaktas på ett sätt som är i linje med Sveriges åtaganden inom till exempel konventionen för biologisk mångfald och EU:s biodiversitetstrategi, där en bärande princip är att ingen nettoförlust ska ske. Det finns ett förbättringsutrymme som borde kunna mötas direkt genom en ökad kunskapsdelning mellan aktörer, och en förbättrad praxis gällande tillämpning av ekologisk kompensation. Samtidigt uppstår flera mer komplexa frågor som berör till exempel behovet av en gemensam fysisk planering och identifiering av lämpliga kompensationsåtgärder, där ett kunskapsbyggande behövs. • Småskalig kustexploatering, exempelvis bryggbyggen och små muddringar, är en särskilt utmanande fråga. Enskilda små ingrepp är anmälningspliktiga (dvs. sällan tillståndspliktiga), och trots att det vid handläggningen av dessa ärenden ställs krav på miljöhänsyn kan det ofta inte bedömas som skäligt att kräva att exploatören själv utför ekologisk kompensation. Den sammanlagda påverkan av dessa många små ingrepp är dock betydande, och det är angeläget att utforma ett system där även småskalig vattenverksamhet kompenserar för sina miljökostnader. Vi undersöker hur ett system för ekologisk kompensation som även omfattar småskalig exploatering skulle kunna se ut, i relation till konceptet habitatbanker eller kompensationspooler, där exploatören kan bidra ekonomiskt till habitatrestaureringar i stället för att själv utföra dem. • Den särskilda fiskeavgiften syftar till att kompensera för skador från vattenverksamheter på fisket och skulle kunna betraktas som ett förvaltningsverktyg för kompensation av en viss typ av förlust. I rapporten utvärderar vi hur det rådande fiskeavgiftssystemet fungerar och utforskar hur det kan fungera ur ett kompensationsperspektiv, samt ger förslag på hur beräkningsmodellen kan utvecklas.Sammantaget finns det ett stort behov av att utveckla ekologisk kompensation som ett av de verktyg som kan bidra till att motverka den allt snabbare förlusten av biologisk mångfald och ekosystemfunktioner. Parallellt behövs ytterligare åtgärder för att stärka skyddet av de känsligaste livsmiljöerna i kustzonen, eftersom bevarande av fungerande livsmiljöer är att föredra som ett mer kostnadseffektivt verktyg än restaurering av störda miljöer

Coevolution in Action: Disruptive Selection on Egg Colour in an Avian Brood Parasite and Its Host

Trait polymorphism can evolve as a consequence of frequency-dependent selection. Coevolutionary interactions between hosts and parasites may lead to selection on both to evolve extreme phenotypes deviating from the norm, through disruptive selection.Here, we show through detailed field studies and experimental procedures that the ashy-throated parrotbill (Paradoxornis alphonsianus) and its avian brood parasite, the common cuckoo (Cuculus canorus), have both evolved egg polymorphism manifested in discrete immaculate white, pale blue, and blue egg phenotypes within a single population. In this host-parasite system the most common egg colours were white and blue, with no significant difference in parasitism rates between hosts laying eggs of either colour. Furthermore, selection on parasites for countering the evolution of host egg types appears to be strong, since ashy-throated parrotbills have evolved rejection abilities for even partially mimetic eggs.The parrotbill-cuckoo system constitutes a clear outcome of disruptive selection on both host and parasite egg phenotypes driven by coevolution, due to the cost of parasitism in the host and by host defences in the parasite. The present study is to our knowledge the first to report the influence of disruptive selection on evolution of discrete phenotypes in both parasite and host traits in an avian brood parasitism system

No barrier to emergence of bathyal king crabs on the Antarctic shelf

Cold-water conditions have excluded durophagous (skeleton-breaking) predators from the Antarctic seafloor for millions of years. Rapidly warming seas off the western Antarctic Peninsula could now facilitate their return to the continental shelf, with profound consequences for the endemic fauna. Among the likely first arrivals are king crabs (Lithodidae), which were discovered recently on the adjacent continental slope. During the austral summer of 2010‒2011, we used underwater imagery to survey a slope-dwelling population of the lithodid Paralomis birsteini off Marguerite Bay, western Antarctic Peninsula for environmental or trophic impediments to shoreward expansion. The population density averaged ∼4.5 individuals × 1,000 m(−2) within a depth range of 1,100‒1,500 m (overall observed depth range 841–2,266 m). Images of juveniles, discarded molts, and precopulatory behavior, as well as gravid females in a trapping study, suggested a reproductively viable population on the slope. At the time of the survey, there was no thermal barrier to prevent the lithodids from expanding upward and emerging on the outer shelf (400- to 550-m depth); however, near-surface temperatures remained too cold for them to survive in inner-shelf and coastal environments (<200 m). Ambient salinity, composition of the substrate, and the depth distribution of potential predators likewise indicated no barriers to expansion of lithodids onto the outer shelf. Primary food resources for lithodids—echinoderms and mollusks—were abundant on the upper slope (550–800 m) and outer shelf. As sea temperatures continue to rise, lithodids will likely play an increasingly important role in the trophic structure of subtidal communities closer to shore

Outcomes of Brood Parasite–Host Interactions Mediated by Egg Matching: Common Cuckoos Cuculus canorus versus Fringilla Finches

Antagonistic species often interact via matching of phenotypes, and interactions between brood parasitic common cuckoos (Cuculus canorus) and their hosts constitute classic examples. The outcome of a parasitic event is often determined by the match between host and cuckoo eggs, giving rise to potentially strong associations between fitness and egg phenotype. Yet, empirical efforts aiming to document and understand the resulting evolutionary outcomes are in short supply.We used avian color space models to analyze patterns of egg color variation within and between the cuckoo and two closely related hosts, the nomadic brambling (Fringilla montifringilla) and the site fidelic chaffinch (F. coelebs). We found that there is pronounced opportunity for disruptive selection on brambling egg coloration. The corresponding cuckoo host race has evolved egg colors that maximize fitness in both sympatric and allopatric brambling populations. By contrast, the chaffinch has a more bimodal egg color distribution consistent with the evolutionary direction predicted for the brambling. Whereas the brambling and its cuckoo host race show little geographical variation in their egg color distributions, the chaffinch's distribution becomes increasingly dissimilar to the brambling's distribution towards the core area of the brambling cuckoo host race.High rates of brambling gene flow is likely to cool down coevolutionary hot spots by cancelling out the selection imposed by a patchily distributed cuckoo host race, thereby promoting a matching equilibrium. By contrast, the site fidelic chaffinch is more likely to respond to selection from adapting cuckoos, resulting in a markedly more bimodal egg color distribution. The geographic variation in the chaffinch's egg color distribution could reflect a historical gradient in parasitism pressure. Finally, marked cuckoo egg polymorphisms are unlikely to evolve in these systems unless the hosts evolve even more exquisite egg recognition capabilities than currently possessed