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  • 1. Adam, B.
    et al.
    Klawonn, I.
    Svedén, J.
    Bergkvist, J.
    Nahar, N.
    Walve, J.
    Littmann, S.
    Whitehouse, Martin J.
    Swedish Museum of Natural History, Department of Geology.
    Lavik, G.
    Kuypers, M.M.M.
    Ploug, H.
    N2-fixation, ammonium release, and N-transfer to the microbial and classical food web within a plankton community.2016In: The ISME Journal, ISSN 1751-7362, E-ISSN 1751-7370, Vol. 19, p. 450-459Article in journal (Refereed)
    Abstract [en]

    We investigated the role of N2-fixation by the colony-forming cyanobacterium, Aphanizomenon spp., for the plankton community and N-budget of the N-limited Baltic Sea during summer by using stable isotope tracers combined with novel secondary ion mass spectrometry, conventional mass spectrometry and nutrient analysis. When incubated with 15N2, Aphanizomenon spp. showed a strong 15N-enrichment implying substantial 15N2-fixation. Intriguingly, Aphanizomenon did not assimilate tracers of 15NH4+ from the surrounding water. These findings are in line with model calculations that confirmed a negligible N-source by diffusion-limited NH4+ fluxes to Aphanizomenon colonies at low bulk concentrations (<250 nm) as compared with N2-fixation within colonies. No N2-fixation was detected in autotrophic microorganisms <5 μm, which relied on NH4+ uptake from the surrounding water. Aphanizomenon released about 50% of its newly fixed N2 as NH4+. However, NH4+ did not accumulate in the water but was transferred to heterotrophic and autotrophic microorganisms as well as to diatoms (Chaetoceros sp.) and copepods with a turnover time of ~5 h. We provide direct quantitative evidence that colony-forming Aphanizomenon releases about half of its recently fixed N2 as NH4+, which is transferred to the prokaryotic and eukaryotic plankton forming the basis of the food web in the plankton community. Transfer of newly fixed nitrogen to diatoms and copepods furthermore implies a fast export to shallow sediments via fast-sinking fecal pellets and aggregates. Hence, N2-fixing colony-forming cyanobacteria can have profound impact on ecosystem productivity and biogeochemical processes at shorter time scales (hours to days) than previously thought.

  • 2.
    Ahmed, Mohammed
    et al.
    Swedish Museum of Natural History, Department of Zoology.
    Boström, Sven
    Swedish Museum of Natural History, Department of Zoology.
    Holovachov, Oleksandr
    Swedish Museum of Natural History, Department of Zoology.
    Rik rundmaskfauna i Store Mosse nationalpark hittades med DNA-metastreckkodning2023In: Fauna och flora : populär tidskrift för biologi, ISSN 0014-8903, Vol. 118, no 2, article id 24-33Article in journal (Other (popular science, discussion, etc.))
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  • 3.
    Ahmed, Mohammed
    et al.
    Swedish Museum of Natural History, Department of Zoology.
    Slos, Dieter
    Holovachov, Oleksandr
    Swedish Museum of Natural History, Department of Zoology.
    Assessing the diversity of nematodes in the Store Mosse National Park (Sweden) using metabarcoding2024In: Metabarcoding and Metagenomics, E-ISSN 2534-9708, Vol. 8, p. 1-8Article in journal (Refereed)
  • 4.
    Ahola, Markus
    Swedish Museum of Natural History, Department of Environmental research and monitoring.
    Climate Change in the Baltic Sea2021 Fact Sheet: Baltic Sea Environment Proceedings n°180. HELCOM/Baltic Earth 20212021Report (Other academic)
  • 5. Alerstam, Thomas
    et al.
    Rosén, Mikael
    Bäckman, Johan
    Ericson, Per G P
    Swedish Museum of Natural History, Research Division.
    Hellgren, Olof
    Flight speeds among bird species: allometric and phylogenetic effects.2007In: PLoS biology, ISSN 1544-9173, E-ISSN 1545-7885, Vol. 5, no 8, p. e197-Article in journal (Refereed)
    Abstract [en]

    Flight speed is expected to increase with mass and wing loading among flying animals and aircraft for fundamental aerodynamic reasons. Assuming geometrical and dynamical similarity, cruising flight speed is predicted to vary as (body mass)(1/6) and (wing loading)(1/2) among bird species. To test these scaling rules and the general importance of mass and wing loading for bird flight speeds, we used tracking radar to measure flapping flight speeds of individuals or flocks of migrating birds visually identified to species as well as their altitude and winds at the altitudes where the birds were flying. Equivalent airspeeds (airspeeds corrected to sea level air density, Ue) of 138 species, ranging 0.01-10 kg in mass, were analysed in relation to biometry and phylogeny. Scaling exponents in relation to mass and wing loading were significantly smaller than predicted (about 0.12 and 0.32, respectively, with similar results for analyses based on species and independent phylogenetic contrasts). These low scaling exponents may be the result of evolutionary restrictions on bird flight-speed range, counteracting too slow flight speeds among species with low wing loading and too fast speeds among species with high wing loading. This compression of speed range is partly attained through geometric differences, with aspect ratio showing a positive relationship with body mass and wing loading, but additional factors are required to fully explain the small scaling exponent of Ue in relation to wing loading. Furthermore, mass and wing loading accounted for only a limited proportion of the variation in Ue. Phylogeny was a powerful factor, in combination with wing loading, to account for the variation in Ue. These results demonstrate that functional flight adaptations and constraints associated with different evolutionary lineages have an important influence on cruising flapping flight speed that goes beyond the general aerodynamic scaling effects of mass and wing loading.

  • 6. Alvarez, Belinda
    et al.
    Frings, Patrick J
    Swedish Museum of Natural History, Department of Geology.
    Clymans, Wim
    Fontorbe, Guillaume
    Conley, Daniel
    Assessing the Potential of Sponges (Porifera) as Indicators of Ocean Dissolved Si Concentrations2017In: Frontiers in Marine Science, E-ISSN 2296-7745, Vol. 4, no 373Article in journal (Refereed)
    Abstract [en]

    We explore the distribution of sponges along dissolved silica (dSi) concentration gradients to test whether sponge assemblages are related to dSi and to assess the validity of fossil sponges as a palaeoecological tool for inferring dSi concentrations of the past oceans. We extracted sponge records from the publically available Global Biodiversity Information Facility (GBIF) database and linked these records with ocean physiochemical data to evaluate if there is any correspondence between dSi concentrations of the waters sponges inhabit and their distribution. Over 320,000 records of Porifera were available, of which 62,360 met strict quality control criteria. Our analyses was limited to the taxonomic levels of family, order and class. Because dSi concentration is correlated with depth in the modern ocean, we also explored sponge taxa distributions as a function of depth. We observe that while some sponge taxa appear to have dSi preferences (e.g., class Hexactinellida occurs mostly at high dSi), the overall distribution of sponge orders and families along dSi gradients is not sufficiently differentiated to unambiguously relate dSi concentrations to sponge taxa assemblages. We also observe that sponge taxa tend to be similarly distributed along a depth gradient. In other words, both dSi and/or another variable that depth is a surrogate for, may play a role in controlling sponge spatial distribution and the challenge is to distinguish between the two. We conclude that inferences about palaeo-dSi concentrations drawn from the abundance of sponges in the stratigraphic records must be treated cautiously as these animals are adapted to a great range of dSi conditions and likely other underlying variables that are related to depth. Our analysis provides a quantification of the dSi ranges of common sponge taxa, expands on previous knowledge related to their bathymetry preferences and suggest that sponge taxa assemblages are not related to particular dSi conditions. 

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  • 7.
    Arcalís-Planas, Anna
    et al.
    Department of Biology, Universitat de Barcelona.
    Sveegaard, Signe
    Department of Bioscience, Aarhus University.
    Karlsson, Olle
    Swedish Museum of Natural History, Department of.
    Harding, Karin C.
    Department of Biological and Environmental Sciences, University of Gothenburg.
    Wåhlin, Anna
    Department of Earth Sciences, University of Gothenburg.
    Härkönen, Tero
    Swedish Museum of Natural History, Department of.
    Teilmann, Jonas
    Department of Bioscience, Aarhus University.
    Limited use of sea ice by the Ross seal (Ommatophoca rossii), in Amundsen Sea, Antarctica, using telemetry and remote sensing data2015In: Polar Biology, ISSN 0722-4060, E-ISSN 1432-2056Article in journal (Refereed)
  • 8.
    Arribas, Paula
    et al.
    Island Ecology and Evolution Research Group Instituto de Productos Naturales y Agrobiología (IPNA‐CSIC) San Cristóbal de la Laguna Spain.
    Andújar, Carmelo
    Island Ecology and Evolution Research Group Instituto de Productos Naturales y Agrobiología (IPNA‐CSIC) San Cristóbal de la Laguna Spain.
    Bidartondo, Martin I.
    Department of Life Sciences Imperial College London London UK;Comparative Plant and Fungal Biology Royal Botanic Gardens London UK.
    Bohmann, Kristine
    Section for Evolutionary Genomics, Faculty of Health and Medical Sciences, Globe Institute University of Copenhagen Copenhagen Denmark.
    Coissac, Éric
    Université Grenoble Alpes, CNRS, Université Savoie Mont Blanc LECA, Laboratoire d’Ecologie Alpine Grenoble France.
    Creer, Simon
    School of Natural Sciences Bangor University Gwynedd UK.
    deWaard, Jeremy R.
    Centre for Biodiversity Genomics University of Guelph Guelph Canada;School of Environmental Sciences University of Guelph Guelph Canada.
    Elbrecht, Vasco
    Centre for Biodiversity Monitoring (ZBM) Zoological Research Museum Alexander Koenig Bonn Germany.
    Ficetola, Gentile F.
    Université Grenoble Alpes, CNRS, Université Savoie Mont Blanc LECA, Laboratoire d’Ecologie Alpine Grenoble France;Department of Environmental Sciences and Policy University of Milano Milano Italy.
    Goberna, Marta
    Department of Environment and Agronomy INIA Madrid Spain.
    Kennedy, Susan
    Biodiversity and Biocomplexity Unit Okinawa Institute of Science and Technology Graduate University Onna‐son Japan;Department of Biogeography Trier University Trier Germany.
    Krehenwinkel, Henrik
    Department of Biogeography Trier University Trier Germany.
    Leese, Florian
    Aquatic Ecosystem Research, Faculty of Biology University of Duisburg‐Essen Essen Germany;Centre for Water and Environmental Research (ZWU) Essen University of Duisburg‐Essen Essen Germany.
    Novotny, Vojtech
    Biology Centre, Institute of Entomology Czech Academy of Sciences Ceske Budejovice Czech Republic;Faculty of Science University of South Bohemia Ceske Budejovice Czech Republic.
    Ronquist, Fredrik
    Swedish Museum of Natural History, Department of Bioinformatics and Genetics.
    Yu, Douglas W.
    State Key Laboratory of Genetic Resources and Evolution Kunming Institute of Zoology, Chinese Academy of Sciences Kunming China;Center for Excellence in Animal Evolution and Genetics Chinese Academy of Sciences Kunming China;School of Biological Sciences University of East Anglia Norwich UK.
    Zinger, Lucie
    Institut de Biologie de l’ENS (IBENS), Département de biologie, École normale supérieure, CNRS, INSERM Université PSL Paris France.
    Creedy, Thomas J.
    Department of Life Sciences Natural History Museum London UK.
    Meramveliotakis, Emmanouil
    Department of Biological Sciences University of Cyprus Nicosia Cyprus.
    Noguerales, Víctor
    Department of Biological Sciences University of Cyprus Nicosia Cyprus.
    Overcast, Isaac
    Institut de Biologie de l’ENS (IBENS), Département de biologie, École normale supérieure, CNRS, INSERM Université PSL Paris France;Division of Vertebrate Zoology American Museum of Natural History New York USA.
    Morlon, Hélène
    Institut de Biologie de l’ENS (IBENS), Département de biologie, École normale supérieure, CNRS, INSERM Université PSL Paris France.
    Vogler, Alfried P.
    Department of Life Sciences Imperial College London London UK;Department of Life Sciences Natural History Museum London UK.
    Papadopoulou, Anna
    Department of Biological Sciences University of Cyprus Nicosia Cyprus.
    Emerson, Brent C.
    Island Ecology and Evolution Research Group Instituto de Productos Naturales y Agrobiología (IPNA‐CSIC) San Cristóbal de la Laguna Spain.
    Connecting high‐throughput biodiversity inventories: Opportunities for a site‐based genomic framework for global integration and synthesis2021In: Molecular Ecology, ISSN 0962-1083, E-ISSN 1365-294X, Vol. 30, no 5, p. 1120-1135Article in journal (Refereed)
  • 9. Authier, Matthieu
    et al.
    Brasseur, Sophie
    Carlén, Ida
    Carlström, Julia
    Swedish Museum of Natural History, Department of Environmental research and monitoring.
    Evans, Peter
    Fernández, Ruth
    Galatius, Anders
    Gilles, Anita
    Hammond, Philip
    Kaminska, Katarzyna
    Kavanagh, Ailbhe
    Kingston, Allen
    Königson, Sara
    Koschinski, Sven
    Larsen, Finn
    Macleod, Kelly
    Mugerza, Estanis
    Müller, Miriam
    Ojaveer, Henn
    Papaioannou, Eva
    Peltier, Hélène
    Pierce, Graham
    Pusch, Christian
    Ridoux, Vincent
    Santos, Begona
    Sigurðsson, Guðjón
    Tachoires, Stéphanie
    Vinther, Morten
    Woźniczka, Adam
    Königson, Sara (Editor)
    MacLeod, Kelly (Editor)
    Workshop on fisheries Emergency Measures to minimize BYCatch of short-beaked common dolphins in the Bay of Biscay and harbour porpoise in the Baltic Sea (WKEMBYC)2020Report (Other academic)
  • 10.
    Barboutis, Christos
    et al.
    Antikythira Bird Observatory, Hellenic Ornithological Society/BirdLife Greece, 52 Ag. Konstantinou Str., GR-10437 Athens, Greece;Department of Biological Applications and Technology, University of Ioannina, GR-45110 Ioanrnina, Greece.
    Bounas, Anastasios
    Department of Biological Applications and Technology, University of Ioannina, GR-45110 Ioanrnina, Greece.
    Navarrete, Elisabeth
    Antikythira Bird Observatory, Hellenic Ornithological Society/BirdLife Greece, 52 Ag. Konstantinou Str., GR-10437 Athens, Greece.
    Fransson, Thord
    Swedish Museum of Natural History, Department of Environmental research and monitoring.
    Stopover Ecology of the European Turtle Dove (Streptopelia turtur), a Threatened Migratory Bird Species, after the Crossing of an Extended Ecological Barrier2023In: Birds, ISSN 2673-6004, Vol. 4, no 2, p. 202-212Article in journal (Refereed)
  • 11.
    Barboutis, Christos
    et al.
    Natural History Museum of Crete, University of Crete, Iraklion, Greece.
    Henshaw, Ian
    Department of Zoology, Stockholm University.
    Kullberg, Cecilia
    Department of Zoology, Stockholm University.
    Nikolopoulou, Stamatina
    Institute of Marine Biology and Genetics, Hellenic Centre for Marine Research, Iraklion, Crete,.
    Fransson, Thord
    Swedish Museum of Natural History, Department of.
    Fuelling in front of the barrier — are there age based behavioral differences in Garden Warblers Sylvia borin?2014In: PeerJ, ISSN 2167-8359Article in journal (Refereed)
    Abstract [en]

    Garden Warblers Sylvia borin were studied during autumn stopover in Crete before

    crossing the barrier of theMediterranean Sea and the Sahara Desert. Birds followed

    with transmitters show extensive stopover periods, which were longer in first-year

    birds, 16 days, compared with adult birds, 14 days. The distribution of body masses

    frombirds trapped in fig trees were used to estimate the departure body mass and the

    results found indicate that both age categories on average depart with a fuel load close

    to 100% of lean body mass. The movement of transmitter birds shows di

    fferences between

    first-year and adult birds. Adult birds move further away from the release site

    and many also left the study area. Several were found settled outside the study area,

    up to 17 km away, indicating that they regularly make longer stopover movements. It

    is suggested that this might be a result of that they return to a place where they stayed

    during an earlier migration. It was shown that stopover site fidelity exists and nine

    garden warblers were recaptured in the area during a following autumn. The results

    found highlights the importance of stopover areas close to the SaharaDesert.

  • 12. Barboutis, Christos
    et al.
    Larsson, Leo
    Steinholtz, Åsa
    Fransson, Thord
    Swedish Museum of Natural History, Department of Environmental research and monitoring.
    From Mediterranean to Scandinavia – timing and body mass condition in four long distance migrants2015In: Ornis Svecica, ISSN 1102-6812, E-ISSN 2003-2633, Vol. 25, p. 51-58Article in journal (Refereed)
    Abstract [en]

    In spring, long-distance migrants are considered to adopta time-minimizing strategy to promote early arrival atbreeding sites. The phenology of spring migration wasexamined and compared between two insular stopoversites in Greece and Sweden for Icterine Warbler, WoodWarbler, Spotted Flycatcher and Collared Flycatcher. All  of them migrate due north which means that some proportion of birds that pass through Greece are headingto Scandinavia. The Collared Flycatcher had the earliestand the Icterine Warbler the latest arrival time. Thedifferences in median dates between Greece and Swedenwere 3–4 weeks and the passages in Sweden weregenerally more condensed in time. The average overallspeed estimates were very similar and varied between129 and 137 km/d. In most of the species higher speedestimates were associated with years when birds arrivedlate in Greece. After crossing continental Europe birdsarrive at the Swedish study site with significantly higherbody masses compared to when they arrive in Greece andthis might indicate a preparation for arriving at breedinggrounds with some overload.

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  • 13.
    Barboutis, Christos
    et al.
    Department of Biological Applications and Technology , University of Ioannina , Ioannina , GR-45110 , Greece;Antikythira Bird Observatory, Hellenic Ornithological Society/BirdLife Greece , Themistokleous 80 , Athens , GR-10681 , Greece.
    Navarrete, Elisabeth
    Antikythira Bird Observatory, Hellenic Ornithological Society/BirdLife Greece , Themistokleous 80 , Athens , GR-10681 , Greece.
    Karris, Georgios
    Lab of Environmental Physics, Energy and Environmental Biology, Department of Environment, Faculty of Environment , Ionian University , Panagoula, GR-29100, Zakynthos , Greece.
    Xirouchakis, Stavros
    Natural History Museum of Crete , University of Crete, University Campus (Knossos) , GR-71409 Heraklion, Crete , Greece.
    Fransson, Thord
    Swedish Museum of Natural History, Department of Environmental research and monitoring. Department of Environmental Research and Monitoring , Swedish Museum of Natural History , , Stockholm , Sweden.
    Bounas, Anastasios
    Department of Biological Applications and Technology , University of Ioannina , Ioannina , , Greece.
    Arriving depleted after crossing of the Mediterranean: obligatory stopover patterns underline the importance of Mediterranean islands for migrating birds2022In: Animal Migration, E-ISSN 2084-8838, Vol. 9, no 1, p. 27-36Article in journal (Refereed)
  • 14.
    Bennike, Ole
    et al.
    Geological Survey of Denmark and Greenland Øster Voldgade 10 DK‐1350 Copenhagen K Denmark.
    Colgan, William
    Geological Survey of Denmark and Greenland Øster Voldgade 10 DK‐1350 Copenhagen K Denmark.
    Hedenäs, Lars
    Swedish Museum of Natural History, Department of Botany.
    Heiri, Oliver
    Department of Environmental Sciences University of Basel Klingelbergsstrasse 27 4056 Basel Switzerland.
    Lemdahl, Geoffrey
    Linnaeus University SE‐391 82 Kalmar Sweden.
    Wiberg‐Larsen, Peter
    Institute for Ecoscience, Aarhus University Vejlsøvej 25 DK‐8600 Silkeborg Denmark.
    Ribeiro, Sofia
    Geological Survey of Denmark and Greenland Øster Voldgade 10 DK‐1350 Copenhagen K Denmark.
    Pronzato, Roberto
    Dipartimento per lo Studio del Territorio dell’Ambiente e della Vita (DiSTAV) Università degli Studi di Genova Corso Europa 26 16132 Genova Italy.
    Manconi, Renata
    Dipartimento di Medicina Veterinaria Università di Sassari Via Vienna 2 07100 Sassari Italy.
    Bjørk, Anders A.
    Department of Geosciences and Natural Resource Management University of Copenhagen Øster Voldgade 10 DK‐1350 Copenhagen K Denmark.
    An Early Pleistocene interglacial deposit at Pingorsuit, North‐West Greenland2022In: Boreas, ISSN 0300-9483, E-ISSN 1502-3885Article in journal (Refereed)
  • 15. Bennike, Ole
    et al.
    Hedenäs, Lars
    Swedish Museum of Natural History, Department of Botany.
    Lemdahl, Geoffrey
    Wiberg-Larsen, Peter
    A multiproxy macrofossil record of Eemian palaeoenvironments from Klaksvík, the Faroe Islands2018In: Boreas, ISSN 0300-9483, E-ISSN 1502-3885, Vol. 47, p. 106-113Article in journal (Refereed)
  • 16. Bergamini, Ariel
    et al.
    Studer, Lisa
    Valentini, Maya
    Jacot, Katja
    Bisang, Irene
    Swedish Museum of Natural History, Department of Botany.
    Profitieren Moose von Biodiversitätsförderflächen im Landwirtschaftsgebiet?2017In: NL-Inside, Vol. 1//17, p. 17-20Article in journal (Other (popular science, discussion, etc.))
  • 17.
    Bisang, Irene
    et al.
    Swedish Museum of Natural History, Department of Botany.
    Bergamini, Ariel
    Agricultural intensification, sustainable farming and the fate of arable bryophytes in Switzerland2021In: The Changing Status of Arable Habitats in Europe / [ed] Hurford C., Wilson P., Storkey J., Cham, Switzerland: Springer, 2021, p. 139-156Chapter in book (Refereed)
    Abstract [en]

    Land-use changes including agricultural intensification are major drivers of biodiversity loss. As other countries, Switzerland introduced agri-environment schemes (AES) to counteract declining agro-biodiversity. Among numerous bryophytes of the agricultural landscape, arable bryophytes have adapted to recurrent tillage. They are short-lived above-ground, while their diaspores may build up a persistent diaspore bank in the soil. We monitored the field hornwort and the Carolina hornwort, characteristic species of the Central European arable bryophyte flora over a period of almost three decades, and studied effects of Biodiversity Promoting Areas (BPAS), a key element of Swiss AES, on arable bryophyte diversity. Hornwort occurrences strongly declined, and stubble-fields left unprocessed until late autumn, the favourite habitat of arable specialist bryophytes, nearly disappeared from 1991 to 2018. The loss of suitable habitats follows from decreased cereal cultivation and direct post-harvest management. Different BPA-fallows, designed to promote birds, flowering plants, or ecosystem services, harboured arable bryophyte specialists, but their richness decreased with fallow age. Diaspore banks contained arable bryophyte specialists not occurring above-ground and may serve as a reservoir during unsuitable cultivation. Targeted modifications of current AES, aiming to maintain habitats favourable for arable bryophytes, are necessary to safeguard the typical arable bryophytes in the Swiss arable landscape.

  • 18.
    Bisang, Irene
    et al.
    Swedish Museum of Natural History, Department of Botany.
    Bergamini, Ariel
    Fördern die Massnahmen des Ökologischen Leistungsnachweises die Ackermoose im Schweizer Mittelland?2022In: N L Inside, Vol. 1/22, p. 20-24Article in journal (Refereed)
    Abstract [de]

    Ähnlich wie die Wildkräuter in Äckern sind auch die typischen, hochspezialisieren Ackermoose stark gefährdet und im Rückgang begriffen. Biodiversitätsförderflächen könnten dazu beitragen, ihren Rückgang zu stoppen. Entscheidend für den Erhalt der Ackermoose im Schweizer Kulturland ist jedoch, dass genügend und sorgfältig ausgewählte Getreidestoppelfelder nicht vor Ende Oktober gepflügt oder anderweitig bearbeitet werden. 

  • 19.
    Bisang, Irene
    et al.
    Swedish Museum of Natural History, Department of Botany.
    Ehrlén, Johan
    Hedenäs, Lars
    Swedish Museum of Natural History, Department of Botany.
    Life history characteristics and historical factors are important to explain regional variation in reproductive traits and genetic diversity in perennial mossesIn: Annals of Botany, ISSN 0305-7364, E-ISSN 1095-8290Article in journal (Refereed)
    Abstract [en]

    Background and aims Plants have evolved an unrivalled diversity of reproductive strategies, including variation in the degree of sexual versus clonal reproduction. This variation has important effects on the dynamics and genetic structure of populations. We examined the association between large-scale variation in reproductive patterns and intraspecific genetic diversity in two moss species where sex is manifested in the dominant haploid generation and sex expression is irregular. We predicted that in regions with more frequent realised sexual reproduction, populations should display less skewed sex ratios, more often express sex, and have higher genetic diversity than in regions with largely clonal reproduction.

    Methods We assessed reproductive status and phenotypic sex in the dioicous long-lived Drepanocladus trifarius and D. turgescens, in 248 and 438 samples across two regions in Scandinavia with frequent or rare, respectively, realised sexual reproduction. In subsets of the samples, we analysed genetic diversity using nuclear and plastid sequence information and identified sex with a sex-specific molecular marker in non-reproductive samples.

    Key results Contrary to our predictions, sex ratios did not differ between regions, genetic diversity did not differ in D. trifarius and was higher in the region with rare sexual reproduction in D. turgescens. Supporting our predictions, relatively more samples expressed sex in D. trifarius in the region with frequent sexual reproduction. Overall, samples were mostly female. Degree of sex expression and genetic diversity differed between sexes.

    Conclusions Sex expression levels, regional sex ratios and genetic diversity were not directly associated with regional frequency of realised sexual reproduction, and relationships and variation patterns differed between species. We conclude that a combination of species-specific life histories such as longevity, overall degree of successful sexual reproduction and recruitment, and historic factors, are important to explain this variation. Our data on haploid-dominated plants significantly complement plant reproductive biology.

  • 20.
    Bisang, Irene
    et al.
    Swedish Museum of Natural History, Department of Botany.
    Ehrlén, Johan
    Korpelainen, Helena
    University of Helsinki.
    Hedenäs, Lars
    Swedish Museum of Natural History, Department of Botany.
    No evidence of sexual niche partitioning in a dioecious moss with raresexual reproduction2015In: Annals of Botany, ISSN 0305-7364, E-ISSN 1095-8290Article in journal (Refereed)
    Abstract [en]

    Background and Aims. Roughly half of the species of bryophytes have separate sexes (dioecious) and half are hermaphroditic (monoecious). This variation has major consequences for the ecology and evolution of the different species. In some sexually reproducing dioecious bryophytes, sex ratio has been shown to vary with environmental conditions. This study focuses on the dioecious wetland moss Drepanocladus trifarius, which rarely produces sexual branches or sporophytes and lacks apparent secondary sex characteristics, and examines whether genetic sexes exhibit different habitat preferences, i.e. whether sexual niche partitioning occurs.

    Methods. A total of 277 shoots of D. trifarius were randomly sampled at 214 locations and 12 environmental factors were quantified at each site. Sex was assigned to the individual shoots collected in the natural environments, regardless of their reproductive status, using a specifically designed molecular marker associated with female sex.

    Key Results. Male and female shoots did not differ in shoot biomass, the sexes were randomly distributed with respect to each other, and environmental conditions at male and female sampling locations did not differ. Collectively, this demonstrates a lack of sexual niche segregation. Adult genetic sex ratio was female-biased, with 28 females for every male individual.

    Conclusions. The results show that although the sexes of D. trifarius did not differ with regard to annual growth, spatial distribution or habitat requirements, the genetic sex ratio as nevertheless significantly female-biased. This supports the notion that factors other than sex-related differences in reproductive costs and sexual dimorphism can also drive the evolution of biased sex ratios in plants

  • 21.
    Bisang, Irene
    et al.
    Swedish Museum of Natural History, Department of Botany.
    Ehrlén, Johan
    Persson, Christin
    Hedenäs, Lars
    Swedish Museum of Natural History, Department of Botany.
    Family affiliation, sexratio and sporophyte frequency in unisexual mosses2014In: Botanical journal of the Linnean Society, ISSN 0024-4074, E-ISSN 1095-8339, Vol. 174, p. 163-172Article in journal (Refereed)
    Abstract [en]

    Patterns of sex expression and sex ratios are key features of the life histories of organisms. Bryophytes are the only haploid-dominant land plants. In contrast with seed plants, more than half of bryophyte species are dioecious, with rare sexual expression and sporophyte formation and a commonly female-biased sex ratio. We asked whether variation in sex expression, sex ratio and sporophyte frequency in ten dioecious pleurocarpous wetland mosses of two different families was best explained by assuming that character states  evolved: (1) in ancestors within the respective families or (2) at the species level as a response to recent habitat conditions. Lasso regression shrinkage identified relationships between family membership and sex ratio and sporophyte frequency, whereas environmental conditions were not correlated with any investigated reproductive trait. Sex ratio and sporophyte frequency were correlated with each other. Our results suggest that ancestry is more important than the current environment in explaining reproductive patterns at and above the species level in the studied wetland mosses, and that mechanisms controlling sex ratio and sporophyte frequency are phylogenetically conserved. Obviously, ancestry should be considered in the study of reproductive character state variation in plants.

  • 22.
    BISANG, IRENE
    et al.
    Swedish Museum of Natural History, Department of Botany.
    HEDENÄS, LARS
    Swedish Museum of Natural History, Department of Botany.
    Agricultural management, bedrock, and vulnerability of sexual reproduction to climate change affect the occurrence of a European near-endemic moss2022In: Bryophyte Diversity and Evolution, ISSN 2381-9677, Vol. 45, no 1, p. 176-187Article in journal (Refereed)
    Abstract [en]

    We investigated whether the European near-endemic moss Drepanocladus lycopodioides has declined in its core distributionarea in the southern Baltic Sea region and explored potential explanations for this. First, we re-visited sites with documentedrecords from 1854 to 1957 in the Stockholm archipelago and nearby mainland in southern Sweden. Second, we comparedthe numbers and distributions of Swedish occurrences, their habitats, and substrates up to 1950 (289 herbarium records),and from 1951 onwards (347) using different map layers. Third, we explored whether inter-annual variation in reproductiveperformance was related to moisture conditions at five sites on an island in the Stockholm archipelago during nine years. Weestimated moisture conditions based on precipitation data and dry days during the time when fertilization occurs in the yearprior to sporophyte maturation. Drepanocladus lycopodioides has strongly decreased in intensively managed agriculturallandscapes but remains frequent in natural or semi-natural habitats on limestone. Sporophyte development varied betweenyears and depended on the weather condition during the fertilization period. Climate forecasts for the study area predict longerdry spells during late spring to late summer, which coincides with the timing of sexual branch initiation and fertilization inthe species. We expect that sporophyte production will likely decrease in the future, which will affect the species’ abilities tore-colonize spots where it vanishes during years with poor growth conditions.

  • 23.
    Bisang, Irene
    et al.
    Swedish Museum of Natural History, Department of Botany.
    Lienhard, Luc
    Bergamini, Ariel
    Entwicklung von Ackermoospopulationen und ihren Lebensräumen im Schweizer Mittelland während 28 Jahren von 1991 bis 2018: Schlussbericht2019Report (Other academic)
    Abstract [de]

    Die Vorkommen von Hornmoosen in den

    Äckern des Mittellandes haben seit den frühen 1990er Jahren stark abgenommen (Abb. 2). Die Feldbewirtschaftung, insbesondere das frühe Pflügen und die Bearbeitung von Stoppelfeldern im Herbst, erklären wesentlich die Abnahme der Hornmoose. Damit verschwinden die bevorzugten Standorte für Hornmoose und andere Ackermoos-Spezialisten. Die Einführung des ÖLN, unter anderem wegen der Bodenschutzauflage, die seit 2015 eine Einsaat zeitig nach der Ernte verlangt, hatte also keinen positiven Einfluss auf die Hornmoosvorkommen. Eine hohe Luftfeuchtigkeit im Sommer fördert andererseits die Hornmoosentwicklung, aber dieser Witterungseffekt ist deutlich geringer als der Bewirtschaftungseffekt.

  • 24.
    Bisang, Irene
    et al.
    Swedish Museum of Natural History, Department of Botany.
    Lienhard, Luc
    Bergamini, Ariel
    Immer weniger Ackermoose im Schweizer Mittelland2021Other (Other (popular science, discussion, etc.))
    Abstract [de]

    Ähnlich wie die Wildkräuter in Äckern sind auch die typischen, hoch-spezialisieren Ackermoose gefährdet und im Rückgang begriffen. Im Schweizer Mittelland sind ihre bevorzugten Lebensräume, bis in den Spätherbst unbearbeitete Getreidestoppelfelder, fast vollständig verschwunden. Biodiversitätsförderflächen (BFF) können dazu beitragen, ihren Rückgang zu stoppen, allerdings nur so lange nicht die dichte Vegetationsbedeckung und Streuauflagen in den älteren BFF die Ackermoose verdrängen. Entscheidend für den Erhalt der Ackermoose im Schweizer Kulturland ist deshalb die Förderung von kurzlebigen BFF und vor allem von Getreidestoppelfeldern, in denen die Bearbeitungszeitpunkte sorgfältig angepasst sind.

  • 25.
    Bisang, Irene
    et al.
    Swedish Museum of Natural History, Department of Botany.
    Lienhard, Luc
    Bergamini, Ariel
    The fate of arable bryophytes in the Swiss Plateau: Agricultural intensification, sustainable farming, agro-biodiversity promotion and three decades of monitoring hornworts: Ackermoose im Schweizer Mittelland: Landwirtschaftliche Intensivierung, ökologischer Leistungsnachweis, Biodiversitätsförderung und drei Jahrzehnte Monitoring2022Other (Other academic)
    Abstract [en]

    We asked how arable management and the introduction of AES-measures affect the specialised bryophyte flora of arable land, whether these specialist species do occur in existing BPAs, and how weather conditions affect the development of arable bryophyte populations. 

    We  propose tailored amendments of certain directives of the Swiss Agri-environmental Schemes (AES) to safeguard the characteristic arable specialist bryophytes in the Swiss arable landscape. 

  • 26.
    Bisang, Irene
    et al.
    Swedish Museum of Natural History, Department of Botany.
    Lienhard, Luc
    Bergamini, Ariel
    Three decades of field surveys reveal a decline of arable bryophytes in the Swiss lowlands despite agri-environment schemes2021In: Agriculture, Ecosystems & Environment. Applied Soil Ecology, ISSN 0929-1393, E-ISSN 1873-0272, Vol. 313Article in journal (Refereed)
    Abstract [en]

    Agricultural intensification represents one of the major drivers for the dramatic loss of biodiversity worldwide. To halt the decline of farmland biodiversity, Switzerland adopted agri-environment schemes (AES) in 1998. Here, we monitored the occurrence, abundance and habitats of two species of arable bryophyte specialists, the Field hornwort (Anthoceros agrestis) and the Carolina hornwort (Phaeoceros carolinianus), in 28 crop fields in the intensively cultivated Swiss Plateau from 1991–2018, to investigate the effects of arable management, AES directives, and weather conditions on their performance. The target species are characteristic of the specialized short-lived arable bryophyte flora of Central Europe that depend on bare substrate in low-intensively cultivated and regularly ploughed fields. Trends in their occurrence thus reflect in many respects the status of the arable bryophytes in cultivated fields. Hornwort occurrence significantly declined between 1991 and 2018. A strong decrease in stubble fields that remain unmanaged after harvest, the favourite habitat for many arable specialists in the study area, largely accounted for the decline. Stubble fields nearly disappeared in the study area because of a gradual reduction in the cultivation area of cereals and the increasing practice of immediate post-harvest tillage. The latter is common in intensive arable farming and was accentuated by AES directives amended in 2005. Hornwort occurrences were positively affected by high air humidity during summer, but weather effects were subordinate to management effects. We propose tailored amendments of AES regulations, that aremented at selected sites, to maintain the characteristic arable specialist bryophytes in the Swiss Plateau: crop rotation with adequate proportions of cereals that are regularly ploughed but not before the end of October, no post-harvest processing of stubble fields, and optimization of the existing instrument ‘Biodiversity Promoting Areas’, e.g., short-term fallows in crop fields. Late-autumn or overwintering stubbles and short-term fallows will benefit many other organisms that depend on extensively managed open habitats, for example arableflowers, farmland breeding birds and specialized arthropods

  • 27.
    Bisang, Irene
    et al.
    Swedish Museum of Natural History, Department of Botany.
    Schnyder, Norbert
    Bergamini, Ariel
    Are agri-environment schemes beneficial to arable specialist bryophytes in Switzerland?2021In: Field Bryology, ISSN 1747-8200, Vol. 125, p. 50-59Article in journal (Other academic)
    Abstract [en]

    Implications of long-term monitoring of arable bryophytes for the conservation of these species in Switzerland

  • 28. Blicharska, Malgorzata
    et al.
    Andersson, Johan
    Bergsten, Johannes
    Swedish Museum of Natural History, Department of Zoology.
    Bjelke, Ulf
    Swedish Biodiversity Centre.
    Hilding-Rydevik, Tuija
    Johansson, Frank
    Uppsala University.
    Effects of management intensity, function and vegetation on the biodiversity in urban ponds2016In: Urban Forestry & Urban Greening, ISSN 1618-8667, E-ISSN 1610-8167, Vol. 20, p. 103-112Article in journal (Refereed)
    Abstract [en]

    Ponds are important elements of green areas in cities that help counteract the negative consequences of urbanization, by providing important habitats for biodiversity in cities and being essential nodes in the overall landscape-scale habitat network. However, there is relatively little knowledge about the impacts of pond management intensity, function and environmental variables on urban pond biodiversity. In this study we addressed this gap by investigating which factors were correlated with the level of biodiversity in urban ponds, indicated by species richness of aquatic insects, in Stockholm, Sweden. Our study did not confirm any direct link between the perceived intensity of management or function of ponds and overall biodiversity. However, it seems that management can influence particular groups of species indirectly, since we found that Trichoptera richness (Caddisflies) was highest at intermediate management intensity. We suggest that this is caused by management of vegetation, as the amount of floating and emergent vegetation was significantly correlated with both the overall species richness and the richness of Trichoptera (Caddisflies). This relationship was non-linear, since ponds with an intermediate coverage of vegetation had the highest richness. Interestingly, the amount of vegetation in the pond was significantly affected by pond function and pond management. The overall species richness and richness of Trichoptera were also positively correlated with pond size. Since we found that the pattern of relations between species richness and environmental variables differed between the insect groups we suggest that it will be difficult to provide overall design and management recommendations for ponds in urban green areas. Therefore, it is recommended that to provide high aquatic diversity of species in urban areas one should aim at promoting high diversity of different types of ponds with differing management and environmental factors that shape them.

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  • 29. Blicharska, Malgorzata
    et al.
    Andersson, Johan
    Bergsten, Johannes
    Swedish Museum of Natural History, Department of Zoology.
    Bjelke, Ulf
    Hilding-Rydevik, Tuija
    Thomsson, Michaela
    Östh, John
    Johansson, Frank
    Uppsala University.
    Is there a relationship between socio-economic factors and biodiversity in urban ponds? A study in the city of Stockholm2017In: Urban Ecosystems, ISSN 1083-8155, E-ISSN 1573-1642, p. 1-12Article in journal (Refereed)
    Abstract [en]

    Urban small water bodies, such as ponds, are essential elements of human socio-economic landscapes. Ponds also provide important habitats for species that would otherwise not survive in the urban environment. Knowledge on the biodiversity of urban ponds and the relationship between their ecological value and factors linked to urbanization and socio-economic status is crucial for decisions on where and how to establish and manage ponds in cities to deliver maximum biodiversity benefits. Our study investigates if the pattern of urban-pond biodiversity can be related to different socio-economic factors, such as level of wealth, education or percentage of buildings of different types. Because of lack of previous studies investigating that, our study is of exploratory character and many different variables are used.We found that the biodiversity of aquatic insects was significantly negatively associated with urbanisation variables such as amount of buildings and number of residents living around ponds. This relationship did not differ depending on the spatial scale of our investigation. In contrast, we did not find a significant relationship with variables representing socio-economic status, such as education level and wealth of people. This latter result suggests that the socio-economic status of residents does not lead to any particular effect in terms of the management and function of ponds that would affect biodiversity. However, there is a need for a finer-scale investigation of the different potential mechanism in which residents in areas with differing socio-economic status could indirectly influence ponds.

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  • 30. Boscaro, Vittorio
    et al.
    Holt, Corey C.
    Van Steenkiste, Niels W. L.
    Herranz, M
    Irwin, Nicholas A. T.
    Àlvarez-Campos, Patricia
    Grzelak, Katarzyna
    Holovachov, Oleksandr
    Swedish Museum of Natural History, Department of Zoology.
    Kerbl, A.
    Mathur, V.
    Okamoto, N.
    Piercey, Rebecca S.
    Worsaae, Katrine
    Leander, Brian S.
    Keeling, Patrick J.
    Microbiomes of microscopic marine invertebrates do not reveal signatures of phylosymbiosis2022In: Nature Microbiology, E-ISSN 2058-5276, Vol. 7, no 6, p. 810-819Article in journal (Refereed)
    Abstract [en]

    Animals and microorganisms often establish close ecological relationships. However, much of our knowledge about animal microbiomes comes from two deeply studied groups: vertebrates and arthropods. To understand interactions on a broader scale of diversity, we characterized the bacterial microbiomes of close to 1,000 microscopic marine invertebrates from 21 phyla, spanning most of the remaining tree of metazoans. Samples were collected from five temperate and tropical locations covering three marine habitats (sediment, water column and intertidal macroalgae) and bacterial microbiomes were characterized using 16S ribosomal RNA gene sequencing. Our data show that, despite their size, these animals harbour bacterial communities that differ from those in the surrounding environment. Distantly related but coexisting invertebrates tend to share many of the same bacteria, suggesting that guilds of microorganisms preferentially associated with animals, but not tied to any specific host lineage, are the main drivers of the ecological relationship. Host identity is a minor factor shaping these microbiomes, which do not show the same correlation with host phylogeny, or ‘phylosymbiosis’, observed in many large animals. Hence, the current debate on the varying strength of phylosymbiosis within selected lineages should be reframed to account for the possibility that such a pattern might be the exception rather than the rule.

  • 31.
    Bosco, Laura
    et al.
    The Helsinki Lab of Ornithology, Finnish Museum of Natural History University of Helsinki Helsinki Finland.
    Otterbeck, Andreas
    The Helsinki Lab of Ornithology, Finnish Museum of Natural History University of Helsinki Helsinki Finland.
    Fransson, Thord
    Swedish Museum of Natural History, Department of Environmental research and monitoring. Department of Environmental Research and Monitoring Swedish Museum of Natural History Stockholm Sweden.
    Lindén, Andreas
    Natural Resources Institute Finland (Luke) Helsinki Finland.
    Piha, Markus
    Natural Resources Institute Finland (Luke) Helsinki Finland.
    Lehikoinen, Aleksi
    The Helsinki Lab of Ornithology, Finnish Museum of Natural History University of Helsinki Helsinki Finland.
    Increasing winter temperatures explain body size decrease in wintering bird populations of Northern Europe—But response patterns vary along the spatioclimatic gradient2023In: Global Ecology and Biogeography, ISSN 1466-822X, E-ISSN 1466-8238, ISSN 1466-822X, Vol. 32, no 12, p. 2100-2110Article in journal (Refereed)
  • 32.
    Brault, EK
    et al.
    University of California Santa Cruz.
    Koch, Paul L
    University of California Santa Cruz.
    Costa, Daniel P.
    University of California Santa Cruz.
    McCarthy, Matthew D.
    University of California Santa Cruz.
    Hückstädt, Luis A
    University of California Santa Cruz.
    T. Goetz, Kimberly T
    National Institute of Water and Atmospheric Research, Wellington, New Zealand.
    McMahon, Kelton W.
    University of Rhode Island.
    Goebel, Michael E.
    Southwest Fisheries Science Center, La Jolla, USA.
    Karlsson, Olle
    Swedish Museum of Natural History, Department of Environmental research and monitoring.
    Teilmann, Jonas
    Aarhus University.
    Harkonen, Tero
    Swedish Museum of Natural History, Department of Environmental research and monitoring.
    Harding, Karin
    University of Gothenburg.
    Trophic position and foraging ecology of Ross,Weddell, and crabeater seals revealed bycompound-specific isotope analysis2019In: Marine Ecology Progress Series, ISSN 0171-8630, E-ISSN 1616-1599, Vol. 611Article in journal (Refereed)
  • 33.
    Brinkmann, I.
    et al.
    Department of Geology Lund University Lund Sweden.
    Ni, S.
    Department of Geology Lund University Lund Sweden; Centre for Environmental and Climate Research Lund University Lund Sweden.
    Schweizer, M.
    UMR 6112 LPG‐BIAF Université d'Angers Université de Nantes CNRS Angers France.
    Oldham, V. E.
    Woods Hole Oceanographic Institution Woods Hole MA USA;Now at University of Rhode Island Kingston RI USA.
    Quintana Krupinski, N. B.
    Department of Geology Lund University Lund Sweden; Now at Department of Earth and Environment WSP Sweden Malmö Sweden.
    Medjoubi, K.
    Nanoscopium Synchrotron SOLEIL Saint‐Aubin Gif‐sur‐Yvette Cedex France.
    Somogyi, A.
    Nanoscopium Synchrotron SOLEIL Saint‐Aubin Gif‐sur‐Yvette Cedex France.
    Whitehouse, Martin J.
    Swedish Museum of Natural History, Department of Geology.
    Hansel, C. M.
    Woods Hole Oceanographic Institution Woods Hole MA USA.
    Barras, C.
    UMR 6112 LPG‐BIAF Université d'Angers Université de Nantes CNRS Angers France.
    Bernhard, J. M.
    Woods Hole Oceanographic Institution Woods Hole MA USA.
    Filipsson, H. L.
    Department of Geology Lund University Lund Sweden.
    Foraminiferal Mn/Ca as Bottom‐Water Hypoxia Proxy: An Assessment of Nonionella stella in the Santa Barbara Basin, USA2021In: Paleoceanography and Paleoclimatology, ISSN 2572-4517, E-ISSN 2572-4525, Vol. 36, no 11Article in journal (Refereed)
  • 34.
    Britt-Marie, Bäcklin
    et al.
    Swedish Museum of Natural History, Department of Environmental research and monitoring.
    Sara, Persson
    Swedish Museum of Natural History, Department of Environmental research and monitoring.
    Suzanne, Faxneld
    Swedish Museum of Natural History, Department of Environmental research and monitoring.
    Frank, Rigét F.
    Anna, Roos M.
    Swedish Museum of Natural History, Department of Environmental research and monitoring. phD, Curator.
    Temporal and Geographical Variation of Intestinal Ulcers in Grey Seals (Halichoerus grypus) and Environmental Contaminants in Baltic Biota during Four Decades2021In: Animals, E-ISSN 2076-2615, Vol. 11, no 10, p. 2968-2968Article in journal (Refereed)
  • 35.
    Brodin, Yngve
    et al.
    Swedish Museum of Natural History, Department of Zoology.
    Hellberg, Jörgen
    Smaller, lighter coloured and less hairy Procladius (Diptera, Chironomidae) in warmer climate2023In: Biologia, ISSN 0006-3088, E-ISSN 1336-9563, Vol. 78, no 8, p. 2091-2098Article in journal (Refereed)
  • 36.
    Broman, Elias
    et al.
    Stockholm University.
    Bonaglia, Stefano
    Stockholm University.
    Holovachov, Oleksandr
    Swedish Museum of Natural History, Department of Zoology.
    Marzocchi, Ugo
    Aarhus University.
    Hall, Per O.J.
    University of Gothenburg.
    Nascimento, Francisco J.A.
    Stockholm University.
    Uncovering diversity and metabolic spectrum of animals in dead zone sediments2020In: Communications Biology, E-ISSN 2399-3642, Vol. 3, p. 1-12, article id 106Article in journal (Refereed)
    Abstract [en]

    Ocean deoxygenation driven by global warming and eutrophication is a primary concern for marine life. Resistant animals may be present in dead zone sediments, however there is lack of information on their diversity and metabolism. Here we combined geochemistry, microscopy, and RNA-seq for estimating taxonomy and functionality of micrometazoans along an oxygen gradient in the largest dead zone in the world. Nematodes are metabolically active at oxygen concentrations below 1.8μmolL−1, and their diversity and community structure are different between low oxygen areas. This is likely due to toxic hydrogen sulfide and its potential to be oxidized by oxygen or nitrate. Zooplankton resting stages dominate the metazoan community, and these populations possibly use cytochrome c oxidase as an oxygen sensor to exit dormancy. Our study sheds light on mechanisms of animal adaptation to extreme environments. These biological resources can be essential for recolonization of dead zones when oxygen conditions improve.

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  • 37.
    Bury, SJ
    et al.
    National Institute of Water & Atmospheric Research (NIWA), Hataitai, Wellington 6021, New Zealand.
    Peters, KJ
    Marine Vertebrate Ecology Lab, Environmental Futures, School of Earth, Atmospheric and Life Sciences, University of Wollongong, Wollongong, NSW 2522, Australia;Cetacean Ecology Research Group, College of Sciences, Massey University, Auckland 0632, New Zealand;Evolutionary Genetics Group, Department of Anthropology, University of Zurich, 8057 Zurich, Switzerland.
    Sabadel, AJM
    National Institute of Water & Atmospheric Research (NIWA), Hataitai, Wellington 6021, New Zealand;Department of Zoology, University of Otago, Dunedin 9016, New Zealand;Department of Environmental Science, Auckland University of Technology, Auckland 1010, New Zealand.
    St John Glew, K
    Ocean and Earth Sciences, University of Southampton Waterfront Campus, Southampton SO14 3ZH, UK.
    Trueman, C
    Ocean and Earth Sciences, University of Southampton Waterfront Campus, Southampton SO14 3ZH, UK.
    Wunder, MB
    Department of Integrative Biology, Denver, CO 80204, USA.
    Cobain, MRD
    Department of Biological and Environmental Science, University of Jyväskylä, 40014 Jyväskylä yliopisto, Finland.
    Schmitt, N
    Australian Antarctic Division, Department of Agriculture, Water and the Environment, Kingston, TAS 7050, Australia;Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario L8S 4K1, Canada.
    Donnelly, D
    Australian Antarctic Division, Department of Agriculture, Water and the Environment, Kingston, TAS 7050, Australia;Killer Whales Australia, 17 Eric Crescent, Mornington, VIC 3931, Australia.
    Magozzi, S
    Department of Integrated Marine Ecology, Stazione Zoologica Anton Dohrn, Fano Marine Centre, 61032 Fano (PU), Italy.
    Owen, K
    Swedish Museum of Natural History, Department of Population Analysis and Monitoring. Department of Environmental Research and Monitoring, Swedish Museum of Natural History, Stockholm 104 05, Sweden.
    Brown, JCS
    National Institute of Water & Atmospheric Research (NIWA), Hataitai, Wellington 6021, New Zealand;Bloomsbury Environmental Isotope Facility, Department of Earth Sciences, University College London, London WC1E 6BT, UK.
    Escobar-Flores, P
    National Institute of Water & Atmospheric Research (NIWA), Hataitai, Wellington 6021, New Zealand.
    Constantine, R
    School of Biological Sciences, University of Auckland, Auckland 1010, New Zealand.
    O’Driscoll, RL
    National Institute of Water & Atmospheric Research (NIWA), Hataitai, Wellington 6021, New Zealand.
    Double, M
    Australian Antarctic Division, Department of Agriculture, Water and the Environment, Kingston, TAS 7050, Australia.
    Gales, N
    Australian Antarctic Division, Department of Agriculture, Water and the Environment, Kingston, TAS 7050, Australia;30 Power Road, North Bruny, TAS 7150, Australia.
    Childerhouse, S
    Cawthron Institute, Nelson 7010, New Zealand;Environmental Law Initiative, Epworth House, Te Aro, Wellington 6011, New Zealand.
    Pinkerton, MH
    National Institute of Water & Atmospheric Research (NIWA), Hataitai, Wellington 6021, New Zealand.
    Southern Ocean humpback whale trophic ecology. I. Combining multiple stable isotope methods elucidates diet, trophic position and foraging areas2024In: Marine Ecology Progress Series, ISSN 0171-8630, E-ISSN 1616-1599, Vol. 734, p. 123-155Article in journal (Refereed)
  • 38. Büdel, B.
    et al.
    Colesie, C.
    Green, T.G.A.
    Grube, Martin
    Lázaro Suau, R.
    Loewen-Schneider, K.
    Maier, S.
    Peer, T.
    Pintado, A.
    Raggio, J.
    Ruprecht, U.
    Sancho, L. G.
    Schroeter, B.
    Türk, R.
    Weber, B.
    Wedin, Mats
    Swedish Museum of Natural History, Department of Botany.
    Westberg, Martin
    Swedish Museum of Natural History, Department of Botany.
    Williams, L.
    Zheng, L.
    Improved appreciation of the functioning and importance of biological soil crusts in Europe – the Soil Crust International project (SCIN)2014In: Biodiversity and Conservation, ISSN 0960-3115, E-ISSN 1572-9710, Vol. 23, p. 1639-1658Article in journal (Refereed)
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  • 39. Callaghan, D. A.
    et al.
    Aleffi, M.
    Bisang, Irene
    Swedish Museum of Natural History, Department of Botany.
    Blockeel, T.
    Collarte, F.
    Dragićeviće, S.
    Draper, I.
    Erdağ, A.
    Erzberger, P.
    Garcia, C.
    Garilleti, R.
    Huggonot, V.
    Lara, F.
    Natcheva, R.
    Németh, C.
    Papp, B.
    Sabovljević, M.
    Sérgio, C.
    Sim-Sim, M.
    Vanderpoorten, A.
    Geographic range and population size of the habitat specialist Codonoblepharon forsteri in a changing climate2022In: Journal of Bryology, ISSN 0373-6687, E-ISSN 1743-2820, Vol. 44, no 1, p. 35-40Article in journal (Refereed)
    Abstract [en]

    Introduction: Codonoblepharon forsteri is a rare epiphytic moss characteristically associated with water-filled holes in trees. This study aims to review its range and population and assess effects of climate change.

    Methods: An inventory of sites from where C. forsteri has been recorded was compiled. Extent of Occurrence (EOO) and Area of Occupancy (AOO) were calculated. Population size was estimated, using an occupied tree as an ‘individual-equivalent’ of the moss. Climatic conditions of its current distribution were characterised, and an ensemble model of its distribution generated. The latter was projected onto present and future climatic layers.

    Results: C. forsteri has been recorded from 205 sites in 18 countries, in Europe, N Africa and SW Asia. It has been undergoing an overall decline. Most sites have few occupied trees, and a world population of 1000–10,000 individual-equivalents is estimated. Model projections suggest the species will experience a range increase of +0.27–0.78 by 2050 and +0.34–0.97 by 2070, especially in the NW, in particular across France and the UK. Range loss is predicted to be -0.16–0.23 in 2050 and -0.18–0.32 in 2070, affecting the driest areas of the current range around the Mediterranean, especially in N Africa.

    Conclusions: C. forsteri has a relatively large EOO but a relatively small AOO, likely the product of its habitat specialism. A major reason for recent declines appears to be widespread abandonment of traditional ‘pollarding’ of trees. The potential climatic range of the species will shift significantly northwards over the next few decades

  • 40. Canelo, Tara
    et al.
    Marquina, Daniel
    Chozas, Sergio
    Bergsten, Johannes
    Swedish Museum of Natural History, Department of Zoology.
    Gaytán, Álvaro
    Pérez-Izquierdo, Carlos
    Bonal, Raúl
    Effects of livestock on arthropod biodiversity in Iberian holm oak savannas revealed by metabarcoding2024In: Journal of Environmental Management, ISSN 0301-4797, E-ISSN 1095-8630, Vol. 365, p. 121619-121619, article id 121619Article in journal (Refereed)
    Abstract [en]

    Increasing food production while avoiding negative impacts on biodiversity constitutes one of the main challenges of our time. Traditional silvopastoral systems like Iberian oak savannas (“dehesas”) set an example, where free-range livestock has been reared for centuries while preserving a high natural value. Nevertheless, factors decreasing productivity need to be addressed, one being acorn losses provoked by pest insects. An increased and focalized grazing by livestock on infested acorns would kill the larvae inside and decrease pest numbers, but increased livestock densities could have undesired side effects on ground arthropod communities as a whole. We designed an experimental setup including areas under trees with livestock exclosures of different ages (short-term: 1-year exclusion, long-term: 10-year exclusion), along with controls (continuous grazing), using DNA metabarcoding (mitochondrial markers COI and 16S) to rapidly assess arthropod communities’ composition. Livestock removal quickly increased grass cover and arthropod taxonomic richness and diversity, which was already higher in short-term (1-year exclosures) than beneath the canopies of control trees. Interestingly, arthropod diversity was not highest at long-term exclosures (≥10 years), although their community composition was the most distinct. Also, regardless of treatment, we found that functional diversity strongly correlated with the vegetation structure, being higher at trees beneath which there was higher grass cover and taller herbs. Overall, the taxonomic diversity peak at short term exclosures would support the intermediate disturbance hypothesis, which relates it with the higher microhabitat heterogeneity at moderately disturbed areas. Thus, we propose a rotatory livestock management in dehesas: plots with increased grazing should co-exist with temporal short-term exclosures. Ideally, a few long-term excluded areas should be also kept for the singularity of their arthropod communities. This strategy would make possible the combination of biological pest control and arthropod conservation in Iberian dehesas.

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  • 41.
    Carlström, Julia
    et al.
    Swedish Museum of Natural History, Department of Population Analysis and Monitoring.
    Eriksson, Pia
    Swedish Museum of Natural History, Department of Population Analysis and Monitoring.
    Owen, Kylie
    Swedish Museum of Natural History, Department of Population Analysis and Monitoring.
    Sköld, Martin
    Swedish Museum of Natural History, Department of Bird Ringing and Palynology.
    Optimisation of static passive acoustic monitoring of harbour porpoises in the Kattegat Sea2024Report (Other academic)
    Abstract [en]

    Long-term monitoring of species is necessary for estimating trends in abundance and distribution, andassessing impacts of human activities and conservation actions. As the monitoring needs often exceedavailable resources, optimisation of monitoring effort is important. As part of the Swedish nationalmonitoring programme of harbour porpoises, echolocation activity has been measured at 14 stationslocated in five Natura 2000 sites in the Kattegat Sea over four years (2019–2023). We aimed to evaluatewhether monitoring effort could be reduced while still providing the power to detect a 30% decline overthree generations (equivalent to an annual decline of 1.6%) with 80% power and 20% significance, i.e.similar to OSPAR’s threshold for abundance of cetacean assessment units. Stations were divided intofour groups (3–5 stations/group) based on their spatial distribution and the level and variation in the ratioof the weekly buzz-positive minutes (BPM) to detection-positive minutes (DPM). The BPM metrics wereassumed to indicate differences in habitat use. For each station, daily DPM was modelled as a functionof the Julian day and year to create annual indices. For each group, the trend of the annual indices andassociated power was calculated using a log-linear model over the four years. Finally, the power todetect a trend over time using 1–3 stations per group was estimated, assuming three levels of variance.The variance levels chosen were similar to the lowest, mean and highest variance observed for the 14stations over the four monitoring years. For all four groups of stations, a significant trend was estimatedto be detected within 12 years. The power analysis showed that decreasing the number of stations withina group from 3 to 2 delays the time to reach 80% power by approximately 1 year, while decreasing it from2 to 1 delays it by approximately 2 years. Alternating stations within a group has negligible impact on thepower. Depending on the assumed level of variance, a significant trend could be detected using 2 stationsper group within 6 (σ=0.05), 12 (σ=0.15), or 18 years (σ=0.30). The results indicate that monitoring effortcan be moved to other areas, while still providing sufficient power to allow declines in detections to bedetected within 12 years. Further, they demonstrate that clear objectives and evaluation of the effortneeded are crucial for optimisation among areas, populations or species when resources are limited.

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  • 42. Carlén, Ida
    et al.
    Thomas, Len
    Carlström, Julia
    Swedish Museum of Natural History, Department of Environmental research and monitoring.
    Amundin, Mats
    Teilmann, Jonas
    Tregenza, Nick
    Tougaard, Jakob
    Koblitz, Jens C
    Sveegaard, Signe
    Wennerberg, Daniel
    Loisa, Olli
    Dähne, Michael
    Brundiers, Katharina
    Kosecka, Monika
    Kyhn, Line A
    Tiberi Ljungqvist, Cinthia
    Pawliczka, Iwona
    Koza, Radomil
    Arciszewski, Bartlomiej
    Galatius, Anders
    Jabbusch, Martin
    Laaksonlaita, Jussi
    Niemi, Jussi
    Lyytinen, Sami
    Gallus, Anja
    Benke, Harald
    Blankett, Penina
    Skóra, Krzysztof E
    Acevedo-Gutiérrez, Alejandro
    Basin-scale distribution of harbour porpoises in the Baltic Sea provides basisfor effective conservation actions2018In: Biological Conservation, ISSN 0006-3207, E-ISSN 1873-2917, Vol. 226, p. 42-53Article in journal (Refereed)
  • 43.
    Carroll, Daire
    et al.
    Department of Biology and Environmental Sciences University of Gothenburg Gothenburg Sweden;Gothenburg Global Biodiversity Centre Gothenburg Sweden.
    Ahola, Markus P.
    Swedish Museum of Natural History, Department of Population Analysis and Monitoring.
    Carlsson, Anja M.
    Swedish Museum of Natural History, Department of Population Analysis and Monitoring.
    Sköld, Martin
    Swedish Museum of Natural History, Department of Population Analysis and Monitoring.
    Harding, Karin C.
    Department of Biology and Environmental Sciences University of Gothenburg Gothenburg Sweden.
    120‐years of ecological monitoring data shows that the risk of overhunting is increased by environmental degradation for an isolated marine mammal population: The Baltic grey seal2024In: Journal of Animal Ecology, ISSN 0021-8790, E-ISSN 1365-2656, Vol. 93, no 5, p. 525-539Article in journal (Refereed)
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  • 44. Chapman, Abbie S.A.
    et al.
    Stöhr, Sabine
    Swedish Museum of Natural History, Department of Zoology.
    Bates, Amanda E.
    sFDvent: A global trait database for deep‐sea hydrothermal‐vent fauna2019In: Global Ecology and Biogeography, ISSN 1466-822X, E-ISSN 1466-8238, Vol. 28, no 11, p. 1538-1551Article in journal (Refereed)
  • 45. Collart, Flavien
    et al.
    Hedenäs, Lars
    Swedish Museum of Natural History, Department of Botany.
    Broennimann, Olivier
    Guisan, Antoine
    Vanderpoorten, Alain
    Intraspecific differentiation: Implications for niche and distribution modelling2021In: Journal of Biogeography, ISSN 0305-0270, E-ISSN 1365-2699, Vol. 48, p. 415-426Article in journal (Refereed)
  • 46. Dalerum, F.
    et al.
    Freire, S.
    Angerbjorn, A.
    Lecomte, N.
    Lindgren, A.
    Meijer, T.
    Pecnerova, P.
    Dalen, L.
    Swedish Museum of Natural History, Department of Bioinformatics and Genetics.
    Exploring the diet of arctic wolves (Canis lupus arctos) at their northern range limit2018In: Canadian Journal of Zoology, ISSN 0008-4301, E-ISSN 1480-3283, Vol. 96, no 3, p. 277-281Article in journal (Refereed)
  • 47. Dalerum, Fredrik
    et al.
    Hellström, Peter
    Swedish Museum of Natural History, Department of Environmental research and monitoring.
    Miranda, Maria
    Nyström, Jesper
    Ekenstedt, Johan
    Angerbjörn, Anders
    Network topology of stable isotope interactions in a sub-arctic raptor guild2016In: Oecologia, ISSN 0029-8549, E-ISSN 1432-1939, Vol. 182, no 2, p. 511-518Article in journal (Refereed)
    Abstract [en]

    Predation is an ecologically important process, and intra-guild interactions may substantially influence the ecological effects of predator species. Despite a rapid expansion in the use of mathematical graph theory to describe trophic relations, network approaches have rarely been used to study interactions within predator assemblages. Assemblages of diurnal raptors are subject to substantial intra- and interspecific competition. Here we used the novel approach of applying analyzes based on network topology to species-specific data on the stable isotopes 13C and 15N in feathers to evaluate patterns of relative resource utilization within a guild of diurnal raptors in northern Sweden. Our guild consisted of the golden eagle (Aquila chrysaetos), the gyrfalcon (Falco rusticolus), the peregrine falcon (Falco peregrinus) and the rough-legged buzzard (Buteo lagopus). We found a modular trophic interaction structure within the guild, but the interactions were less nested than expected by chance. These results suggest low redundancy and hence a strong ecological importance of individual species. Our data also suggested that species were less connected through intra-guild interactions than expected by chance. We interpret our results as a convergence on specific isotope niches, and that body size and different hunting behaviour may mediate competition within these niches. We finally highlight that generalist predators could be ecologically important by linking specialist predator species with disparate dietary niches.

  • 48. Dias, Arildo S.
    et al.
    Santos, Karin
    Swedish Museum of Natural History, Department of Botany.
    Maës dos Santos, Flavio Antonio
    Martins, Fernando R.
    How liana loads alter tree allometry intropical forests2016In: Plant Ecology, ISSN 1385-0237, E-ISSN 1573-5052Article in journal (Refereed)
    Abstract [en]

    Intense competition with lianas (woodclimbers) can limit tree growth, reproduction, andsurvival. However, the negative effects of liana loadson tree allometry have not yet been addressed. Weinvestigated the hypothesis that liana loading on treecrown alters tree’s allometry, expressed throughslenderness (height–diameter ratio). The relationshipbetween trunk slenderness and percentage of treecrown covered by lianas was investigated for 12 treespecies from 10 fragments of the SemideciduousSeasonal Forest in Southeastern Brazil. We also testedwhether the relationship between slenderness andwood density differ between trees without lianas andtrees heavily infested. Liana loads significantly alteredtree allometry by decreasing slenderness, even whenlianas covered less than 25% of tree crown. Heavywoodspecies decreased their trunk slenderness in agreater ratio than light-wood species. Our findingsindicate that liana infestation shifts tree allometry, andthese effects are stronger on heavy-wood tree species.

  • 49. Diogo, Ivan Jefferson Sampaio
    et al.
    Santos, Karin
    Swedish Museum of Natural History, Department of Botany.
    Effects of topography and climate on Neotropical mountain forests structure in the semiarid region2020In: Applied Vegetation Science, ISSN 1402-2001, E-ISSN 1654-109XArticle in journal (Refereed)
    Abstract [en]

    QuestionWe aimed to analyze how the topography, temperature and rainfall influence the floristic distribution in three different topographic areas and their surrounding vegetation. We addressed three main questions: (i) How is the distribution of species among the topographic areas? (ii) Which abiotic variable is driving this distribution? and (iii) What is the difference among the mountain forests and between mountain forests and the Caatinga vegetation?LocationThe Maranguape mountain forest were divided into three topographic categories: windward (600–800 m, WMA), leeward (600–800 m, LMA) and top (above 800 m, TMA). We also considered another six areas of mountain forests and four Caatinga areas in Ceará State.MethodsWe calculated different structural parameters and the floristic diversity of each category. A Principal Correspondence Analysis was performed to analyze the indirect ordination of forest sites by species abundance. A Canonical Correspondence Analysis was conducted to evaluate which variables were driving species distribution. We used non‐metric multidimensional scaling distance and the average linkage method to investigate the similarity among mountain forests and Caatinga.ResultsA total of 1,536 individuals belonging to 144 tree species distributed in 44 families and 93 genera were recorded. Myrtaceae, Fabaceae and Rubiaceae were the most species‐rich families. Myrcia splendens had the highest importance value followed by Guapira nitida and Mollinedia ovata. The leeward slope showed the highest richness and diversity index, whereas the windward showed the highest density and the top showed the highest basal area. The ordination indicated a greater similarity between TMA and WMA than LMA.ConclusionOur results suggest that temperature, precipitation and slope angle are the abiotic factors driving species distribution in Maranguape. Those mountains are heavily anthropized and continuously explored, therefore these outcomes will be useful for conservation and restoration purposes in the poorly known semiarid region of Northeast Brazil.

  • 50.
    dos Santos, Wagner Luiz
    et al.
    Department of Plant Biology, University of Campinas , Rua Monteiro Lobato 255 , Barão Geraldo, Campinas, São Paulo , Brazil.
    Pôrto, Kátia Cavalcanti
    Department of Botany, Federal University of Pernambuco , Avenida Moraes Rego , s/n, University City, Recife, Pernambuco , Brazil.
    Bordin, Juçara
    State University of Rio Grande do Sul , Machado de Assis, 1456, RS 95520-000 , Brasil.
    Pinheiro, Fábio
    Department of Plant Biology, University of Campinas , Rua Monteiro Lobato 255 , Barão Geraldo, Campinas, São Paulo , Brazil.
    Bisang, Irene
    Swedish Museum of Natural History, Department of Botany.
    The spatial arrangement of sexes is related to reproductive allocation in mosses: a comparative study of reproductive allocation in three different monoicous sexual systems2023In: Annals of Botany, ISSN 0305-7364, E-ISSN 1095-8290, Vol. 131, no 5, p. 885-896Article in journal (Refereed)
    Abstract [en]

    Background and AimsWe examined the relationship between reproductive allocation and vegetative growth in three monoicous sexual systems of bryophytes. The sexual systems show a gradient of increasing distance between the sexes, from gonioautoicous to cladautoicous to rhizautoicous. Here, we investigated the following two hypotheses: (1) reproductive allocation differs between sexes and sexual systems, and male reproductive allocation increases with increasing distance between male and female gametangia; and (2) reproductive allocation is negatively related to vegetative growth.MethodsWe sampled the three sexual systems, represented by three moss species of the genus Fissidens in the Atlantic Forest of Southeastern Brazil. Ramets were washed in the laboratory; the reproductive structures were detached from the vegetative ramets and sorted regarding sex and individual, dried at 70 °C for 72 h, and weighed in an ultramicrobalance. We calculated the mean reproductive and vegetative mass and reproductive allocation and used generalized linear models to test our predictions.Key ResultsReproductive allocation differed between species and sexes. It was higher in the rhizautoicous than in the cladautoicous and gonioautoicous species. Mean reproductive allocation was greater in males than in females of the rhizautoicous species, greater in females than males of the cladautoicous species, and did not differ between the sexes in the gonioautoicous species. Estimates of reproductive and vegetative mass were positively related in females of the rhizautoicous species. Vegetative mass was not related to reproductive allocation in the gonioautoicous species, but negatively related to reproductive allocation in the male and female branchlets of the cladautoicous species and in the female ramets of the rhizautoicous species.ConclusionsThe reproductive allocation patterns differ between the rhizautoicous species and the ‘truly’ monoicous species, with shorter intersexual distances, which implies that our hypotheses were supported only in part. We suggest that the hypotheses should be reformulated and tested further by comparing ‘truly’ monoicous species with dioicous species and by including other genera.

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