28 results on '"Sabatini FM"'
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2. sPlotOpen – An environmentally balanced, open‐access, global dataset of vegetation plots
- Author
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Ben Sparrow, V. B. Martynenko, Jonathan Lenoir, Eszter Ruprecht, Idoia Biurrun, Luzmila Arroyo, Borja Jiménez-Alfaro, Aníbal Pauchard, Roberto Venanzoni, Stephan M. Hennekens, Mohamed Z. Hatim, Cyrus Samimi, Arkadiusz Nowak, Gerhard E. Overbeck, Petr Sklenář, Renata Ćušterevska, Valentin Golub, Eduardo Vélez-Martin, Gwendolyn Peyre, Inger Greve Alsos, Ioannis Tsiripidis, Tarek Hattab, Andrey Yu. Korolyuk, Jutta Kapfer, Jörg Ewald, Donald M. Waller, Ute Jandt, Tetiana Dziuba, Marco Schmidt, Alvaro G. Gutiérrez, Thomas Wohlgemuth, Adrian Indreica, Zygmunt Kącki, Jürgen Dengler, Željko Škvorc, Dirk Nikolaus Karger, Panayotis Dimopoulos, Viktor Onyshchenko, Hanhuai Shan, John Janssen, Hua Feng Wang, Holger Kreft, Jérôme Munzinger, Brian J. Enquist, Frederic Lens, Wannes Hubau, Birgit Jedrzejek, Alexander Christian Vibrans, Miguel D. Mahecha, Emmanuel Garbolino, Sophie Gachet, Abel Monteagudo Mendoza, Josep Peñuelas, Melisa A. Giorgis, Svetlana Aćić, Débora Vanessa Lingner, Victor V. Chepinoga, Richard Field, Ladislav Mucina, Michele De Sanctis, Mohamed A. El-Sheikh, Isabelle Aubin, Hamid Gholizadeh, Fahmida Sultana, Fabio Attorre, Valerijus Rašomavičius, Cindy Q. Tang, Tomáš Černý, Gonzalo Rivas-Torres, Donald A. Walker, Alicia Teresa Rosario Acosta, Timothy J. Killeen, Francesco Maria Sabatini, Susan K. Wiser, Urban Šilc, Andraž Čarni, Florian Jansen, Valério D. Pillar, Jonas V. Müller, Aaron Pérez-Haase, Els De Bie, Antonio Galán-de-Mera, Zhiyao Tang, Anne D. Bjorkman, Sylvia Haider, Kiril Vassilev, Risto Virtanen, Henrik von Wehrden, Hjalmar S. Kühl, Manfred Finckh, Zvjezdana Stančić, Pavel Shirokikh, Elizabeth Kearsley, Petr Petřík, Yves Bergeron, Iva Apostolova, Emiliano Agrillo, Jozef Šibík, Norbert Jürgens, Marta Gaia Sperandii, Anna Kuzemko, Jens-Christian Svenning, Timothy J. S. Whitfeld, Michael Kessler, Bruno Hérault, John-Arvid Grytnes, Laura Casella, Tomáš Peterka, Miguel Alvarez, Tsipe Aavik, Gregory Richard Guerin, André Luis de Gasper, Corrado Marcenò, Luis Cayuela, Brody Sandel, Cyrille Violle, Jens Kattge, Guillermo Hinojos Mendoza, Anke Jentsch, Arindam Banerjee, Jesper Erenskjold Moeslund, Mohammed Abu Sayed Arfin Khan, Patrice de Ruffray, Milan Chytrý, S. M. Yamalov, Tatiana Lysenko, Meelis Pärtel, Viktoria Bondareva, Helge Bruelheide, John S. Rodwell, Jiri Dolezal, Oliver L. Phillips, Rasmus Revermann, Larisa Khanina, Erwin Bergmeier, Robert K. Peet, Jörg Brunet, Solvita Rūsiņa, Oliver Purschke, Gianmaria Bonari, Jürgen Homeier, Martin Zobel, János Csiky, Marijn Bauters, Jalil Noroozi, Karsten Wesche, Kim André Vanselow, Norbert Hölzel, Flavia Landucci, Farideh Fazayeli, Wolfgang Willner, Viktoria Wagner, Alireza Naqinezhad, Aurora Levesley, Vadim Prokhorov, Hongyan Liu, Ali Kavgaci, Rodolfo Vásquez Martínez, Franziska Schrodt, Attila Lengyel, Elise A. Arnst, Sabatini F.M., Lenoir J., Hattab T., Arnst E.A., Chytry M., Dengler J., De Ruffray P., Hennekens S.M., Jandt U., Jansen F., Jimenez-Alfaro B., Kattge J., Levesley A., Pillar V.D., Purschke O., Sandel B., Sultana F., Aavik T., Acic S., Acosta A.T.R., Agrillo E., Alvarez M., Apostolova I., Arfin Khan M.A.S., Arroyo L., Attorre F., Aubin I., Banerjee A., Bauters M., Bergeron Y., Bergmeier E., Biurrun I., Bjorkman A.D., Bonari G., Bondareva V., Brunet J., Carni A., Casella L., Cayuela L., Cerny T., Chepinoga V., Csiky J., Custerevska R., De Bie E., de Gasper A.L., De Sanctis M., Dimopoulos P., Dolezal J., Dziuba T., El-Sheikh M.A.E.-R.M., Enquist B., Ewald J., Fazayeli F., Field R., Finckh M., Gachet S., Galan-de-Mera A., Garbolino E., Gholizadeh H., Giorgis M., Golub V., Alsos I.G., Grytnes J.-A., Guerin G.R., Gutierrez A.G., Haider S., Hatim M.Z., Herault B., Hinojos Mendoza G., Holzel N., Homeier J., Hubau W., Indreica A., Janssen J.A.M., Jedrzejek B., Jentsch A., Jurgens N., Kacki Z., Kapfer J., Karger D.N., Kavgaci A., Kearsley E., Kessler M., Khanina L., Killeen T., Korolyuk A., Kreft H., Kuhl H.S., Kuzemko A., Landucci F., Lengyel A., Lens F., Lingner D.V., Liu H., Lysenko T., Mahecha M.D., Marceno C., Martynenko V., Moeslund J.E., Monteagudo Mendoza A., Mucina L., Muller J.V., Munzinger J., Naqinezhad A., Noroozi J., Nowak A., Onyshchenko V., Overbeck G.E., Partel M., Pauchard A., Peet R.K., Penuelas J., Perez-Haase A., Peterka T., Petrik P., Peyre G., Phillips O.L., Prokhorov V., Rasomavicius V., Revermann R., Rivas-Torres G., Rodwell J.S., Ruprecht E., Rusina S., Samimi C., Schmidt M., Schrodt F., Shan H., Shirokikh P., Sibik J., Silc U., Sklenar P., Skvorc Z., Sparrow B., Sperandii M.G., Stancic Z., Svenning J.-C., Tang Z., Tang C.Q., Tsiripidis I., Vanselow K.A., Vasquez Martinez R., Vassilev K., Velez-Martin E., Venanzoni R., Vibrans A.C., Violle C., Virtanen R., von Wehrden H., Wagner V., Walker D.A., Waller D.M., Wang H.-F., Wesche K., Whitfeld T.J.S., Willner W., Wiser S.K., Wohlgemuth T., Yamalov S., Zobel M., Bruelheide H., Sabatini, Fm, Lenoir, J, Hattab, T, Arnst, Ea, Chytry, M, Dengler, J, De Ruffray, P, Hennekens, Sm, Jandt, U, Jansen, F, Jimenez-Alfaro, B, Kattge, J, Levesley, A, Pillar, Vd, Purschke, O, Sandel, B, Sultana, F, Aavik, T, Acic, S, Acosta, Atr, Agrillo, E, Alvarez, M, Apostolova, I, Khan, Masa, Arroyo, L, Attorre, F, Aubin, I, Banerjee, A, Bauters, M, Bergeron, Y, Bergmeier, E, Biurrun, I, Bjorkman, Ad, Bonari, G, Bondareva, V, Brunet, J, Carni, A, Casella, L, Cayuela, L, Cerny, T, Chepinoga, V, Csiky, J, Custerevska, R, De Bie, E, de Gasper, Al, De Sanctis, M, Dimopoulos, P, Dolezal, J, Dziuba, T, El-Sheikh, Mam, Enquist, B, Ewald, J, Fazayeli, F, Field, R, Finckh, M, Gachet, S, Galan-de-Mera, A, Garbolino, E, Gholizadeh, H, Giorgis, M, Golub, V, Alsos, Ig, Grytnes, Ja, Guerin, Gr, Gutierrez, Ag, Haider, S, Hatim, Mz, Herault, B, Mendoza, Gh, Holzel, N, Homeier, J, Hubau, W, Indreica, A, Janssen, Jam, Jedrzejek, B, Jentsch, A, Jurgens, N, Kacki, Z, Kapfer, J, Karger, Dn, Kavgaci, A, Kearsley, E, Kessler, M, Khanina, L, Killeen, T, Korolyuk, A, Kreft, H, Kuhl, H, Kuzemko, A, Landucci, F, Lengyel, A, Lens, F, Lingner, Dv, Liu, Hy, Lysenko, T, Mahecha, Md, Marceno, C, Martynenko, V, Moeslund, Je, Mendoza, Am, Mucina, L, Muller, Jv, Munzinger, Jm, Naqinezhad, A, Noroozi, J, Nowak, A, Onyshchenko, V, Overbeck, Ge, Partel, M, Pauchard, A, Peet, Rk, Penuelas, J, Perez-Haase, A, Peterka, T, Petrik, P, Peyre, G, Phillips, Ol, Prokhorov, V, Rasomavicius, V, Revermann, R, Rivas-Torres, G, Rodwell, J, Ruprecht, E, Rusina, S, Samimi, C, Schmidt, M, Schrodt, F, Shan, Hh, Shirokikh, P, Sibik, J, Silc, U, Sklenar, P, Skvorc, Z, Sparrow, B, Sperandii, Mg, Stancic, Z, Svenning, Jc, Tang, Zy, Tang, Cq, Tsiripidis, I, Vanselow, Ka, Martinez, Rv, Vassilev, K, Velez-Martin, E, Venanzoni, R, Vibrans, Ac, Violle, C, Virtanen, R, von Wehrden, H, Wagner, V, Walker, Da, Waller, Dm, Wang, Hf, Wesche, K, Whitfeld, Tj, Willner, W, Wiser, Sk, Wohlgemuth, T, Yamalov, S, Zobel, M, Bruelheide, H, Ecologie et Dynamique des Systèmes Anthropisés - UMR CNRS 7058 (EDYSAN), Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS), MARine Biodiversity Exploitation and Conservation (UMR MARBEC), Institut de Recherche pour le Développement (IRD)-Institut Français de Recherche pour l'Exploitation de la Mer (IFREMER)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), Institut méditerranéen de biodiversité et d'écologie marine et continentale (IMBE), Avignon Université (AU)-Aix Marseille Université (AMU)-Institut de recherche pour le développement [IRD] : UMR237-Centre National de la Recherche Scientifique (CNRS), Centre de recherche sur les Risques et les Crises (CRC), Mines Paris - PSL (École nationale supérieure des mines de Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL), Botanique et Modélisation de l'Architecture des Plantes et des Végétations (UMR AMAP), Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD [France-Sud])-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Centre d’Ecologie Fonctionnelle et Evolutive (CEFE), Université Paul-Valéry - Montpellier 3 (UPVM)-École Pratique des Hautes Études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD [France-Sud])-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Institut Agro - Montpellier SupAgro, Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro), ANR-07-BDIV-0006,BIONEOCAL,L'endémisme en Nouvelle-Calédonie : étude phylogénétique et populationnelle des son émergence.(2007), ANR-07-BDIV-0008,INC,Incendies et biodiversité de écosystèmes en Nouvelle-Calédonie.(2007), ANR-07-BDIV-0010,ULTRABIO,Biodiversité et stratégies adaptatives végétales et microbiennes des écosystèmes ultramafiques en Nouvelle-Calédonie.(2007), European Project: 610028,EC:FP7:ERC,ERC-2013-SyG,IMBALANCE-P(2014), European Project: 291585,EC:FP7:ERC,ERC-2011-ADG_20110209,T-FORCES(2012), Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM)-Institut Français de Recherche pour l'Exploitation de la Mer (IFREMER)-Institut de Recherche pour le Développement (IRD), MINES ParisTech - École nationale supérieure des mines de Paris, Université Paul-Valéry - Montpellier 3 (UPVM)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-École pratique des hautes études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD [France-Sud])-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), and Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)
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0106 biological sciences ,Biome ,Bos- en Landschapsecologie ,Biodiversity ,DIVERSITY ,FOREST VEGETATION ,01 natural sciences ,purl.org/becyt/ford/1 [https] ,Abundance (ecology) ,big data ,Vegetation type ,PHYTOSOCIOLOGICAL DATABASE ,parcelle ,Forest and Landscape Ecology ,functional traits ,vascular plants ,biodiversity ,biogeography ,database ,macroecology ,vegetation plots ,Macroecology ,[SDV.EE]Life Sciences [q-bio]/Ecology, environment ,Global and Planetary Change ,Ecology ,vascular plant ,Vegetation ,F70 - Taxonomie végétale et phytogéographie ,PE&RC ,Vegetation plot ,Geography ,580: Pflanzen (Botanik) ,Ecosystems Research ,Diffusion de l'information ,Plantenecologie en Natuurbeheer ,Vegetatie, Bos- en Landschapsecologie ,Biodiversité ,ARCHIVE ,Communauté végétale ,Evolution ,[SDE.MCG]Environmental Sciences/Global Changes ,Biogéographie ,GRASSLAND VEGETATION ,Plant Ecology and Nature Conservation ,[SDV.BID]Life Sciences [q-bio]/Biodiversity ,010603 evolutionary biology ,Behavior and Systematics ,Couverture végétale ,577: Ökologie ,PLANT ,purl.org/becyt/ford/1.6 [https] ,functional trait ,Biology ,Ecology, Evolution, Behavior and Systematics ,Vegetatie ,010604 marine biology & hydrobiology ,Impact sur l'environnement ,DRY GRASSLANDS ,Plant community ,15. Life on land ,Végétation ,WETLAND VEGETATION ,Earth and Environmental Sciences ,UNIVERSITY ,Physical geography ,Vegetation, Forest and Landscape Ecology ,[SDE.BE]Environmental Sciences/Biodiversity and Ecology ,données ouvertes - Abstract
Datos disponibles en https://github.com/fmsabatini/sPlotOpen_Code, EU H2020 project BACI, Grant No. 640176 (...), Sabatini, F.M., Lenoir, J., Hattab, T., Arnst, E.A., Chytrý, M., Dengler, J., De Ruffray, P., Hennekens, S.M., Jandt, U., Jansen, F., Jiménez-Alfaro, B., Kattge, J., Levesley, A., Pillar, V.D., Purschke, O., Sandel, B., Sultana, F., Aavik, T., Aćić, S., Acosta, A.T.R., Agrillo, E., Alvarez, M., Apostolova, I., Arfin Khan, M.A.S., Arroyo, L., Attorre, F., Aubin, I., Banerjee, A., Bauters, M., Bergeron, Y., Bergmeier, E., Biurrun, I., Bjorkman, A.D., Bonari, G., Bondareva, V., Brunet, J., Čarni, A., Casella, L., Cayuela, L., Černý, T., Chepinoga, V., Csiky, J., Ćušterevska, R., De Bie, E., de Gasper, A.L., De Sanctis, M., Dimopoulos, P., Dolezal, J., Dziuba, T., El-Sheikh, M.A.E.-R.M., Enquist, B., Ewald, J., Fazayeli, F., Field, R., Finckh, M., Gachet, S., Galán-de-Mera, A., Garbolino, E., Gholizadeh, H., Giorgis, M., Golub, V., Alsos, I.G., Grytnes, J.-A., Guerin, G.R., Gutiérrez, A.G., Haider, S., Hatim, M.Z., Hérault, B., Hinojos Mendoza, G., Hölzel, N., Homeier, J., Hubau, W., Indreica, A., Janssen, J.A.M., Jedrzejek, B., Jentsch, A., Jürgens, N., Kącki, Z., Kapfer, J., Karger, D.N., Kavgacı, A., Kearsley, E., Kessler, M., Khanina, L., Killeen, T., Korolyuk, A., Kreft, H., Kühl, H.S., Kuzemko, A., Landucci, F., Lengyel, A., Lens, F., Lingner, D.V., Liu, H., Lysenko, T., Mahecha, M.D., Marcenò, C., Martynenko, V., Moeslund, J.E., Monteagudo Mendoza, A., Mucina, L., Müller, J.V., Munzinger, J., Naqinezhad, A., Noroozi, J., Nowak, A., Onyshchenko, V., Overbeck, G.E., Pärtel, M., Pauchard, A., Peet, R.K., Peñuelas, J., Pérez-Haase, A., Peterka, T., Petřík, P., Peyre, G., Phillips, O.L., Prokhorov, V., Rašomavičius, V., Revermann, R., Rivas-Torres, G., Rodwell, J.S., Ruprecht, E., Rūsiņa, S., Samimi, C., Schmidt, M., Schrodt, F., Shan, H., Shirokikh, P., Šibík, J., Šilc, U., Sklenář, P., Škvorc, Ž., Sparrow, B., Sperandii, M.G., Stančić, Z., Svenning, J.-C., Tang, Z., Tang, C.Q., Tsiripidis, I., Vanselow, K.A., Vásquez Martínez, R., Vassilev, K., Vélez-Martin, E., Venanzoni, R., Vibrans, A.C., Violle, C., Virtanen, R., von Wehrden, H., Wagner, V., Walker, D.A., Waller, D.M., Wang, H.-F., Wesche, K., Whitfeld, T.J.S., Willner, W., Wiser, S.K., Wohlgemuth, T., Yamalov, S., Zobel, M., Bruelheide, H.
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- 2021
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3. Global decoupling of functional and phylogenetic diversity in plant communities.
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Hähn GJA, Damasceno G, Alvarez-Davila E, Aubin I, Bauters M, Bergmeier E, Biurrun I, Bjorkman AD, Bonari G, Botta-Dukát Z, Campos JA, Čarni A, Chytrý M, Ćušterevska R, de Gasper AL, De Sanctis M, Dengler J, Dolezal J, El-Sheikh MA, Finckh M, Galán-de-Mera A, Garbolino E, Gholizadeh H, Golub V, Haider S, Hatim MZ, Hérault B, Homeier J, Jandt U, Jansen F, Jentsch A, Kattge J, Kessler M, Khanina L, Kreft H, Küzmič F, Lenoir J, Moeslund JE, Mucina L, Naqinezhad A, Noroozi J, Pérez-Haase A, Phillips OL, Pillar VD, Rivas-Torres G, Ruprecht E, Sandel B, Schmidt M, Schmiedel U, Schnitzer S, Schrodt F, Šilc U, Sparrow B, Sporbert M, Stančić Z, Strohbach B, Svenning JC, Tang CQ, Tang Z, Vibrans AC, Violle C, Waller D, Wana D, Wang HF, Whitfeld T, Zizka G, Sabatini FM, and Bruelheide H
- Abstract
Plant communities are composed of species that differ both in functional traits and evolutionary histories. As species' functional traits partly result from their individual evolutionary history, we expect the functional diversity of communities to increase with increasing phylogenetic diversity. This expectation has only been tested at local scales and generally for specific growth forms or specific habitat types, for example, grasslands. Here we compare standardized effect sizes for functional and phylogenetic diversity among 1,781,836 vegetation plots using the global sPlot database. In contrast to expectations, we find functional diversity and phylogenetic diversity to be only weakly and negatively correlated, implying a decoupling between these two facets of diversity. While phylogenetic diversity is higher in forests and reflects recent climatic conditions (1981 to 2010), functional diversity tends to reflect recent and past climatic conditions (21,000 years ago). The independent nature of functional and phylogenetic diversity makes it crucial to consider both aspects of diversity when analysing ecosystem functioning and prioritizing conservation efforts., Competing Interests: Competing interests: The authors declare no competing interests., (© 2024. The Author(s), under exclusive licence to Springer Nature Limited.)
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- 2024
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4. Systematic Review of Gender and Sex Terminology Use in Arthroplasty Research: There Is Room for Improvement.
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Bellamy JL, Goodrich ER, Sabatini FM, Mounce SD, Ovadia SA, Kolin DA, Odum SM, Cohen-Rosenblum A, and Landy DC
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- Humans, Male, Female, Gender Identity, Transgender Persons, Biomedical Research, Terminology as Topic, Arthroplasty statistics & numerical data
- Abstract
Background: There is increasing appreciation of the distinction between gender and sex as well as the importance of accurately reporting these constructs. Given recent attention regarding transgender and gender nonconforming (TGNC) and intersex identities, it is more necessary than ever to understand how to describe these identities in research. This study sought to investigate the use of gender- and sex-based terminology in arthroplasty research., Methods: The 5 leading orthopaedic journals publishing arthroplasty research were reviewed to identify the first twenty primary clinical research articles on an arthroplasty topic published after January 1, 2022. Use of gender- or sex-based terminology, whether use was discriminate, and whether stratification or adjustment based on gender or sex was performed, were recorded., Results: There were 98 of 100 articles that measured a construct of gender or sex. Of these, 15 articles used gender-based terminology, 45 used sex-based terminology, and 38 used a combination of gender- and sex-based terminology. Of the 38 articles using a combination of terminology, none did so discriminately. All articles presented gender and sex as binary variables, and 2 attempted to explicitly define how gender or sex were defined. Of the 98 articles, 31 used these variables for statistical adjustments, though only 6 reported stratified results., Conclusions: Arthroplasty articles infrequently describe how gender or sex was measured, and frequently use this terminology interchangeably. Additionally, these articles rarely offer more than 2 options for capturing variation in sex and gender. Future research should be more precise in the treatment of these variables to improve the quality of results and ensure findings are patient-centered and inclusive., (Copyright © 2024 Elsevier Inc. All rights reserved.)
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- 2024
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5. A multitaxonomic assessment of Natura 2000 effectiveness across European biogeographic regions.
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Ricci L, Di Musciano M, Sabatini FM, Chiarucci A, Zannini P, Gatti RC, Beierkuhnlein C, Walentowitz A, Lawrence A, Frattaroli AR, and Hoffmann S
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- Europe, Animals, European Union, Birds physiology, Biodiversity, Conservation of Natural Resources methods
- Abstract
The Natura 2000 (N2K) protected area (PA) network is a crucial tool to limit biodiversity loss in Europe. Despite covering 18% of the European Union's (EU) land area, its effectiveness at conserving biodiversity across taxa and biogeographic regions remains uncertain. Testing this effectiveness is, however, difficult because it requires considering the nonrandom location of PAs, and many possible confounding factors. We used propensity score matching and accounted for the confounding effects of biogeographic regions, terrain ruggedness, and land cover to assess the effectiveness of N2K PAs on the distribution of 1769 species of conservation priority in the EU's Birds and Habitats Directives, including mammals, birds, amphibians, reptiles, arthropods, fishes, mollusks, and vascular and nonvascular plants. We compared alpha, beta, and gamma diversity between matched selections of protected and unprotected areas across EU's biogeographic regions with generalized linear models, generalized mixed models, and nonparametric tests for paired samples, respectively, for each taxonomic group and for the entire set of species. PAs in N2K hosted significantly more priority species than unprotected land, but this difference was not consistent across biogeographic regions or taxa. Total alpha diversity and alpha diversity of amphibians, arthropods, birds, mammals, and vascular plants were significantly higher inside PAs than outside, except in the Boreal biogeographical region. Beta diversity was in general significantly higher inside N2K PAs than outside. Similarly, gamma diversity had the highest values inside PAs, with some exceptions in Boreal and Atlantic regions. The planned expansion of the N2K network, as dictated by the European Biodiversity Strategy for 2030, should therefore target areas in the southern part of the Boreal region where species diversity of amphibians, arthropods, birds, mammals, and vascular plants is high and species are currently underrepresented in N2K., (© 2024 The Authors. Conservation Biology published by Wiley Periodicals LLC on behalf of Society for Conservation Biology.)
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- 2024
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6. Randomized Controlled Trial of Irrigation-Coupled Bipolar Electrocautery Versus Tourniquet in Total Knee Arthroplasty.
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Landy DC, Mounce SD, Sabatini FM, Chapek JA, Conley CE, and Duncan ST
- Abstract
Background: Recovery from total knee arthroplasty remains arduous for some patients, prompting interest in perioperative management. While tourniquet use is not associated with longer-term outcomes, its effect on quadriceps strength in the immediate postoperative window is unknown., Methods: A single-center, double-blind, randomized controlled trial of 66 patients undergoing primary total knee arthroplasty from 2019 to 2022 was performed to compare the use of an irrigation-coupled bipolar device (ICBD) and no tourniquet (ICBD group, N = 34) to tourniquet use with no ICBD (tourniquet group, N = 32). Groups were similar with respect to age, sex, and obesity. The primary outcome was quadriceps strength at 2 weeks, measured using a handheld dynamometer and standardized to the contralateral side. Knee Injury and Osteoarthritis Outcome Score for Joint Replacement was measured with the difference from baseline serving as a secondary outcome. Comparisons were performed using the Student's t-test., Results: Only 28 patients, 14 in each group, had primary outcome data. At 2-weeks, quadriceps strength was higher in the ICBD group compared to the tourniquet group (83% vs 70%), though not statistically significant ( P = .16). There was no difference between the ICBD and tourniquet groups in Knee Injury and Osteoarthritis Outcome Score for Joint Replacement changed at 2-weeks (13 vs 10, P = .37) or 6-weeks (16 vs 17, P = .76)., Conclusions: Tourniquet use was associated with a small but not statistically significant difference in quadriceps strength at 2 weeks that may justify further study given the loss of power here. There can be limitations to conducting randomized controlled trials that are important for early-career investigators to consider and that were magnified due to COVID-related restrictions in the present study, which we discuss., Level of Evidence: Level II., (© 2024 The Authors.)
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- 2024
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7. Rooting depth and xylem vulnerability are independent woody plant traits jointly selected by aridity, seasonality, and water table depth.
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Laughlin DC, Siefert A, Fleri JR, Tumber-Dávila SJ, Hammond WM, Sabatini FM, Damasceno G, Aubin I, Field R, Hatim MZ, Jansen S, Lenoir J, Lens F, McCarthy JK, Niinemets Ü, Phillips OL, Attorre F, Bergeron Y, Bruun HH, Byun C, Ćušterevska R, Dengler J, De Sanctis M, Dolezal J, Jiménez-Alfaro B, Hérault B, Homeier J, Kattge J, Meir P, Mencuccini M, Noroozi J, Nowak A, Peñuelas J, Schmidt M, Škvorc Ž, Sultana F, Ugarte RM, and Bruelheide H
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- Water physiology, Wood physiology, Xylem physiology, Plants, Plant Leaves physiology, Droughts, Groundwater, Embolism
- Abstract
Evolutionary radiations of woody taxa within arid environments were made possible by multiple trait innovations including deep roots and embolism-resistant xylem, but little is known about how these traits have coevolved across the phylogeny of woody plants or how they jointly influence the distribution of species. We synthesized global trait and vegetation plot datasets to examine how rooting depth and xylem vulnerability across 188 woody plant species interact with aridity, precipitation seasonality, and water table depth to influence species occurrence probabilities across all biomes. Xylem resistance to embolism and rooting depth are independent woody plant traits that do not exhibit an interspecific trade-off. Resistant xylem and deep roots increase occurrence probabilities in arid, seasonal climates over deep water tables. Resistant xylem and shallow roots increase occurrence probabilities in arid, nonseasonal climates over deep water tables. Vulnerable xylem and deep roots increase occurrence probabilities in arid, nonseasonal climates over shallow water tables. Lastly, vulnerable xylem and shallow roots increase occurrence probabilities in humid climates. Each combination of trait values optimizes occurrence probabilities in unique environmental conditions. Responses of deeply rooted vegetation may be buffered if evaporative demand changes faster than water table depth under climate change., (© 2023 The Authors. New Phytologist © 2023 New Phytologist Foundation.)
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- 2023
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8. Incidence of Rapidly Progressive Osteoarthritis Following Intra-articular Hip Corticosteroid Injection: A Systematic Review and Meta-Analysis.
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Sabatini FM, Cohen-Rosenblum A, Eason TB, Hannon CP, Mounce SD, Krueger CA, Gwathmey FW, Duncan ST, and Landy DC
- Abstract
Background: The American Academy of Orthopedic Surgery recommends intra-articular corticosteroid injections (CSIs) for managing hip osteoarthritis (OA) based on short-term, prospective studies. Recent retrospective studies have raised concerns that CSIs may lead to rapidly progressive OA (RPOA). We sought to systematically review the literature of CSIs for hip OA to estimate the incidence of RPOA., Methods: MEDLINE, Embase, and Cochrane Library were searched to identify original research of hip OA patients receiving CSIs. Overall, 27 articles involving 5831 patients published from 1988 to 2022 were included. Study design, patient characteristics, CSI details, follow-up, and cases of RPOA were recorded. Studies were classified by their ability to detect RPOA based on follow-up. Random effects meta-analysis was used to calculate the incidence of RPOA for studies able to detect RPOA., Results: The meta-analytic estimate of RPOA incidence was 6% (95% confidence interval, 3%-9%) based on 10 articles classified as able to detect RPOA. RPOA definitions varied from progression of OA within 6 months to the presence of destructive changes. These studies were subject to bias from excluding patients with missing post-CSI radiographs. The remaining 17 articles were classified as unable to detect RPOA, including all of the studies cited in the American Academy of Orthopedic Surgery recommendation., Conclusions: The incidence of RPOA after CSIs remains unknown due to variation in definitions and follow-up. While RPOA following CSIs may be 6%, many cases are not severe, and this may reflect selection bias. Further research is needed to understand whether clinically significant RPOA is incident enough to limit CSI use., (© 2023 The Authors.)
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- 2023
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9. The importance of trait selection in ecology.
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Weigelt A, Mommer L, Andraczek K, Iversen CM, Bergmann J, Bruelheide H, Freschet GT, Guerrero-Ramírez NR, Kattge J, Kuyper TW, Laughlin DC, Meier IC, van der Plas F, Poorter H, Roumet C, van Ruijven J, Sabatini FM, Semchenko M, Sweeney CJ, Valverde-Barrantes OJ, York LM, and McCormack ML
- Subjects
- Ecology
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- 2023
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10. Protect old-growth forests in Europe now.
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Mikolāš M, Piovesan G, Ahlström A, Donato DC, Gloor R, Hofmeister J, Keeton WS, Muys B, Sabatini FM, Svoboda M, and Kuemmerle T
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- Europe, Forests, Trees, Conservation of Natural Resources
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- 2023
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11. A quixotic view of spatial bias in modelling the distribution of species and their diversity.
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Rocchini D, Tordoni E, Marchetto E, Marcantonio M, Barbosa AM, Bazzichetto M, Beierkuhnlein C, Castelnuovo E, Gatti RC, Chiarucci A, Chieffallo L, Da Re D, Di Musciano M, Foody GM, Gabor L, Garzon-Lopez CX, Guisan A, Hattab T, Hortal J, Kunin WE, Jordán F, Lenoir J, Mirri S, Moudrý V, Naimi B, Nowosad J, Sabatini FM, Schweiger AH, Šímová P, Tessarolo G, Zannini P, and Malavasi M
- Abstract
Ecological processes are often spatially and temporally structured, potentially leading to autocorrelation either in environmental variables or species distribution data. Because of that, spatially-biased in-situ samples or predictors might affect the outcomes of ecological models used to infer the geographic distribution of species and diversity. There is a vast heterogeneity of methods and approaches to assess and measure spatial bias; this paper aims at addressing the spatial component of data-driven biases in species distribution modelling, and to propose potential solutions to explicitly test and account for them. Our major goal is not to propose methods to remove spatial bias from the modelling procedure, which would be impossible without proper knowledge of all the processes generating it, but rather to propose alternatives to explore and handle it. In particular, we propose and describe three main strategies that may provide a fair account of spatial bias, namely: (i) how to represent spatial bias; (ii) how to simulate null models based on virtual species for testing biogeographical and species distribution hypotheses; and (iii) how to make use of spatial bias - in particular related to sampling effort - as a leverage instead of a hindrance in species distribution modelling. We link these strategies with good practice in accounting for spatial bias in species distribution modelling., (© 2023. The Author(s).)
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- 2023
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12. Climate-trait relationships exhibit strong habitat specificity in plant communities across Europe.
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Kambach S, Sabatini FM, Attorre F, Biurrun I, Boenisch G, Bonari G, Čarni A, Carranza ML, Chiarucci A, Chytrý M, Dengler J, Garbolino E, Golub V, Güler B, Jandt U, Jansen J, Jašková A, Jiménez-Alfaro B, Karger DN, Kattge J, Knollová I, Midolo G, Moeslund JE, Pielech R, Rašomavičius V, Rūsiņa S, Šibík J, Stančić Z, Stanisci A, Svenning JC, Yamalov S, Zimmermann NE, and Bruelheide H
- Subjects
- Europe, Seeds, Ecosystem, Plants
- Abstract
Ecological theory predicts close relationships between macroclimate and functional traits. Yet, global climatic gradients correlate only weakly with the trait composition of local plant communities, suggesting that important factors have been ignored. Here, we investigate the consistency of climate-trait relationships for plant communities in European habitats. Assuming that local factors are better accounted for in more narrowly defined habitats, we assigned > 300,000 vegetation plots to hierarchically classified habitats and modelled the effects of climate on the community-weighted means of four key functional traits using generalized additive models. We found that the predictive power of climate increased from broadly to narrowly defined habitats for specific leaf area and root length, but not for plant height and seed mass. Although macroclimate generally predicted the distribution of all traits, its effects varied, with habitat-specificity increasing toward more narrowly defined habitats. We conclude that macroclimate is an important determinant of terrestrial plant communities, but future predictions of climatic effects must consider how habitats are defined., (© 2023. The Author(s).)
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- 2023
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13. Additional Distal Femoral Resection Minimally Improves Terminal Knee Extension: A Systematic Review and Meta-Regression Challenging the Dogma.
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Hardy WR, Landy DC, Chalmers BP, Sabatini FM, and Duncan ST
- Abstract
Background: Additional distal femoral resection is a common technique to address a flexion contracture during primary total knee arthroplasty (TKA) but can lead to midflexion instability and patella baja. Prior reports regarding the magnitude of knee extension obtained with additional femoral resection have varied. This study sought to systematically review research describing the effect of femoral resection on knee extension and to perform meta-regression to estimate this relationship., Methods: A systematic review was conducted using MEDLINE, PubMed, and Cochrane databases by combining the terms ("flexion contracture" OR "flexion deformity") AND ("knee arthroplasty" OR "knee replacement") to identify 481 abstracts. In total, 7 articles reporting change in knee extension after additional femoral resection or augmentation across 184 knees were included. The mean value for knee extension, its standard deviation, and the number of knees tested were recorded for each level. Meta-regression was performed using weighted mixed-effects linear regression., Results: Meta-regression estimated that each 1mm resected from the joint line produced a 2.5° gain of extension (95% confidence interval, 1.7 to 3.2). Sensitivity analyses excluding outlying observations estimated each 1mm resected from the joint line produced a 2.0° gain of extension (95% confidence interval, 1.9 to 2.2)., Conclusions: Each millimeter of additional femoral resection is likely to produce only a 2° improvement in knee extension. Thus, an additional resection of 2 mm is likely to improve knee extension by less than 5°. Alternative techniques, including posterior capsular release and posterior osteophyte resection, should be considered in correcting a flexion contracture during TKA., (© 2022 The Authors.)
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- 2023
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14. Hemoglobinopathy is Associated With Total Hip Arthroplasty Indication Even Beyond Sickle Cell Anemia.
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Rakutt MJ, Bracey DN, Cohen-Rosenblum A, Sculco PK, Sabatini FM, Jacobs CA, Duncan ST, and Landy DC
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Background: The extent to which hemoglobinopathies other than sickle anemia (HbSS) are associated with hip osteonecrosis is unknown. Sickle cell trait (HbS), hemoglobin SC (HbSC), and sickle/β-thalassemia (HbSβTh) may also predispose to osteonecrosis of the femoral head (ONFH). We sought to compare the distributions of indications for a total hip arthroplasty (THA) in patients with and without specific hemoglobinopathies., Methods: PearlDiver, an administrative claims database, was used to identify 384,401 patients aged 18 years or older undergoing a THA not for fracture from 2010 to 2020, with patients grouped by diagnosis code (HbSS N = 210, HbSC N = 196, HbSβTh N = 129, HbS N = 356). β-Thalassemia minor (N = 142) acted as a negative control, and patients without hemoglobinopathy as a comparison group (N = 383,368). The proportion of patients with ONFH was compared to patients without it by hemoglobinopathy groups using chi-squared tests before and after matching on age, sex, Elixhauser Comorbidity Index, and tobacco use., Results: The proportion of patients with ONFH as the indication for THA was higher among those with HbSS (59%, P < .001), HbSC (80%, P < .001), HbSβTh (77%, P < .001), and HbS (19%, P < .001) but not with β-thalassemia minor (9%, P = .6) than the proportion of patients without hemoglobinopathy (8%). After matching, the proportion of patients with ONFH remained higher among those with HbSS (59% vs 21%, P < .001), HbSC (80% vs 34%, P < .001), HbSβTh (77% vs 26%, P < .001), and HbS (19% vs 12%, P < .001)., Conclusions: Hemoglobinopathies beyond sickle cell anemia were strongly associated with having osteonecrosis as the indication for THA. Further research is needed to confirm whether this modifies THA outcomes., (© 2022 The Authors.)
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- 2022
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15. Citizen science plant observations encode global trait patterns.
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Wolf S, Mahecha MD, Sabatini FM, Wirth C, Bruelheide H, Kattge J, Moreno Martínez Á, Mora K, and Kattenborn T
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- Plants, Citizen Science
- Abstract
Global maps of plant functional traits are essential for studying the dynamics of the terrestrial biosphere, yet the spatial distribution of trait measurements remains sparse. With the increasing popularity of species identification apps, citizen scientists contribute to growing vegetation data collections. The question emerges whether such opportunistic citizen science data can help map plant functional traits globally. Here we show that we can map global trait patterns by complementing vascular plant observations from the global citizen science project iNaturalist with measurements from the plant trait database TRY. We evaluate these maps using sPlotOpen, a global collection of vegetation plot data. Our results show high correlations between the iNaturalist- and sPlotOpen-based maps of up to 0.69 (r) and higher correlations than to previously published trait maps. As citizen science data collections continue to grow, we can expect them to play a significant role in further improving maps of plant functional traits., (© 2022. The Author(s), under exclusive licence to Springer Nature Limited.)
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- 2022
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16. More losses than gains during one century of plant biodiversity change in Germany.
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Jandt U, Bruelheide H, Jansen F, Bonn A, Grescho V, Klenke RA, Sabatini FM, Bernhardt-Römermann M, Blüml V, Dengler J, Diekmann M, Doerfler I, Döring U, Dullinger S, Haider S, Heinken T, Horchler P, Kuhn G, Lindner M, Metze K, Müller N, Naaf T, Peppler-Lisbach C, Poschlod P, Roscher C, Rosenthal G, Rumpf SB, Schmidt W, Schrautzer J, Schwabe A, Schwartze P, Sperle T, Stanik N, Storm C, Voigt W, Wegener U, Wesche K, Wittig B, and Wulf M
- Subjects
- Germany, Species Specificity, Time Factors, Datasets as Topic, Biodiversity, Plants classification
- Abstract
Long-term analyses of biodiversity data highlight a 'biodiversity conservation paradox': biological communities show substantial species turnover over the past century
1,2 , but changes in species richness are marginal1,3-5 . Most studies, however, have focused only on the incidence of species, and have not considered changes in local abundance. Here we asked whether analysing changes in the cover of plant species could reveal previously unrecognized patterns of biodiversity change and provide insights into the underlying mechanisms. We compiled and analysed a dataset of 7,738 permanent and semi-permanent vegetation plots from Germany that were surveyed between 2 and 54 times from 1927 to 2020, in total comprising 1,794 species of vascular plants. We found that decrements in cover, averaged across all species and plots, occurred more often than increments; that the number of species that decreased in cover was higher than the number of species that increased; and that decrements were more equally distributed among losers than were gains among winners. Null model simulations confirmed that these trends do not emerge by chance, but are the consequence of species-specific negative effects of environmental changes. In the long run, these trends might result in substantial losses of species at both local and regional scales. Summarizing the changes by decade shows that the inequality in the mean change in species cover of losers and winners diverged as early as the 1960s. We conclude that changes in species cover in communities represent an important but understudied dimension of biodiversity change that should more routinely be considered in time-series analyses., (© 2022. The Author(s), under exclusive licence to Springer Nature Limited.)- Published
- 2022
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17. Global patterns of vascular plant alpha diversity.
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Sabatini FM, Jiménez-Alfaro B, Jandt U, Chytrý M, Field R, Kessler M, Lenoir J, Schrodt F, Wiser SK, Arfin Khan MAS, Attorre F, Cayuela L, De Sanctis M, Dengler J, Haider S, Hatim MZ, Indreica A, Jansen F, Pauchard A, Peet RK, Petřík P, Pillar VD, Sandel B, Schmidt M, Tang Z, van Bodegom P, Vassilev K, Violle C, Alvarez-Davila E, Davidar P, Dolezal J, Hérault B, Galán-de-Mera A, Jiménez J, Kambach S, Kepfer-Rojas S, Kreft H, Lezama F, Linares-Palomino R, Monteagudo Mendoza A, N'Dja JK, Phillips OL, Rivas-Torres G, Sklenář P, Speziale K, Strohbach BJ, Vásquez Martínez R, Wang HF, Wesche K, and Bruelheide H
- Subjects
- Ecosystem, Plants, Biodiversity, Tracheophyta
- Abstract
Global patterns of regional (gamma) plant diversity are relatively well known, but whether these patterns hold for local communities, and the dependence on spatial grain, remain controversial. Using data on 170,272 georeferenced local plant assemblages, we created global maps of alpha diversity (local species richness) for vascular plants at three different spatial grains, for forests and non-forests. We show that alpha diversity is consistently high across grains in some regions (for example, Andean-Amazonian foothills), but regional 'scaling anomalies' (deviations from the positive correlation) exist elsewhere, particularly in Eurasian temperate forests with disproportionally higher fine-grained richness and many African tropical forests with disproportionally higher coarse-grained richness. The influence of different climatic, topographic and biogeographical variables on alpha diversity also varies across grains. Our multi-grain maps return a nuanced understanding of vascular plant biodiversity patterns that complements classic maps of biodiversity hotspots and will improve predictions of global change effects on biodiversity., (© 2022. The Author(s).)
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- 2022
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18. Distance decay 2.0 - A global synthesis of taxonomic and functional turnover in ecological communities.
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Graco-Roza C, Aarnio S, Abrego N, Acosta ATR, Alahuhta J, Altman J, Angiolini C, Aroviita J, Attorre F, Baastrup-Spohr L, Barrera-Alba JJ, Belmaker J, Biurrun I, Bonari G, Bruelheide H, Burrascano S, Carboni M, Cardoso P, Carvalho JC, Castaldelli G, Christensen M, Correa G, Dembicz I, Dengler J, Dolezal J, Domingos P, Erös T, Ferreira CEL, Filibeck G, Floeter SR, Friedlander AM, Gammal J, Gavioli A, Gossner MM, Granot I, Guarino R, Gustafsson C, Hayden B, He S, Heilmann-Clausen J, Heino J, Hunter JT, Huszar VLM, Janišová M, Jyrkänkallio-Mikkola J, Kahilainen KK, Kemppinen J, Kozub Ł, Kruk C, Kulbiki M, Kuzemko A, Christiaan le Roux P, Lehikoinen A, Teixeira de Lima D, Lopez-Urrutia A, Lukács BA, Luoto M, Mammola S, Marinho MM, Menezes LS, Milardi M, Miranda M, Moser GAO, Mueller J, Niittynen P, Norkko A, Nowak A, Ometto JP, Ovaskainen O, Overbeck GE, Pacheco FS, Pajunen V, Palpurina S, Picazo F, Prieto JAC, Rodil IF, Sabatini FM, Salingré S, De Sanctis M, Segura AM, da Silva LHS, Stevanovic ZD, Swacha G, Teittinen A, Tolonen KT, Tsiripidis I, Virta L, Wang B, Wang J, Weisser W, Xu Y, and Soininen J
- Abstract
Aim: Understanding the variation in community composition and species abundances (i.e., β-diversity) is at the heart of community ecology. A common approach to examine β-diversity is to evaluate directional variation in community composition by measuring the decay in the similarity among pairs of communities along spatial or environmental distance. We provide the first global synthesis of taxonomic and functional distance decay along spatial and environmental distance by analysing 148 datasets comprising different types of organisms and environments., Location: Global., Time Period: 1990 to present., Major Taxa Studied: From diatoms to mammals., Method: We measured the strength of the decay using ranked Mantel tests (Mantel r ) and the rate of distance decay as the slope of an exponential fit using generalized linear models. We used null models to test whether functional similarity decays faster or slower than expected given the taxonomic decay along the spatial and environmental distance. We also unveiled the factors driving the rate of decay across the datasets, including latitude, spatial extent, realm and organismal features., Results: Taxonomic distance decay was stronger than functional distance decay along both spatial and environmental distance. Functional distance decay was random given the taxonomic distance decay. The rate of taxonomic and functional spatial distance decay was fastest in the datasets from mid-latitudes. Overall, datasets covering larger spatial extents showed a lower rate of decay along spatial distance but a higher rate of decay along environmental distance. Marine ecosystems had the slowest rate of decay along environmental distances., Main Conclusions: In general, taxonomic distance decay is a useful tool for biogeographical research because it reflects dispersal-related factors in addition to species responses to climatic and environmental variables. Moreover, functional distance decay might be a cost-effective option for investigating community changes in heterogeneous environments., Competing Interests: The authors declare no conflicts of interest., (© 2022 The Authors. Global Ecology and Biogeography published by John Wiley & Sons Ltd.)
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- 2022
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19. Using historical spy satellite photographs and recent remote sensing data to identify high-conservation-value forests.
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Munteanu C, Senf C, Nita MD, Sabatini FM, Oeser J, Seidl R, and Kuemmerle T
- Subjects
- Biodiversity, Forests, Remote Sensing Technology, Conservation of Natural Resources methods, Ecosystem
- Abstract
High-conservation-value forests (HCVFs) are critically important for biodiversity and ecosystem service provisioning, but they face many threats. Where systematic HCVF inventories are missing, such as in parts of Eastern Europe, these forests remain largely unacknowledged and therefore often unprotected. We devised a novel, transferable approach for detecting HCVFs based on integrating historical spy satellite images, contemporary remote sensing data (Landsat), and information on current potential anthropogenic pressures (e.g., road infrastructure, population density, demand for fire wood, terrain). We applied the method to the Romanian Carpathians, for which we mapped forest continuity (1955-2019), canopy structural complexity, and anthropogenic pressures. We identified 738,000 ha of HCVF. More than half of this area was identified as susceptible to current anthropogenic pressures and lacked formal protection. By providing a framework for broad-scale HCVF monitoring, our approach facilitates integration of HCVF into forest conservation and management. This is urgently needed to achieve the goals of the European Union's Biodiversity Strategy to maintain valuable forest ecosystems., (© 2021 The Authors. Conservation Biology published by Wiley Periodicals LLC on behalf of Society for Conservation Biology.)
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- 2022
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20. Natural disturbance impacts on trade-offs and co-benefits of forest biodiversity and carbon.
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Mikoláš M, Svitok M, Bače R, Meigs GW, Keeton WS, Keith H, Buechling A, Trotsiuk V, Kozák D, Bollmann K, Begovič K, Čada V, Chaskovskyy O, Ralhan D, Dušátko M, Ferenčík M, Frankovič M, Gloor R, Hofmeister J, Janda P, Kameniar O, Lábusová J, Majdanová L, Nagel TA, Pavlin J, Pettit JL, Rodrigo R, Roibu CC, Rydval M, Sabatini FM, Schurman J, Synek M, Vostarek O, Zemlerová V, and Svoboda M
- Subjects
- Biodiversity, Carbon Sequestration, Conservation of Natural Resources, Forests, Trees, Carbon analysis, Climate Change
- Abstract
With accelerating environmental change, understanding forest disturbance impacts on trade-offs between biodiversity and carbon dynamics is of high socio-economic importance. Most studies, however, have assessed immediate or short-term effects of disturbance, while long-term impacts remain poorly understood. Using a tree-ring-based approach, we analysed the effect of 250 years of disturbances on present-day biodiversity indicators and carbon dynamics in primary forests. Disturbance legacies spanning centuries shaped contemporary forest co-benefits and trade-offs, with contrasting, local-scale effects. Disturbances enhanced carbon sequestration, reaching maximum rates within a comparatively narrow post-disturbance window (up to 50 years). Concurrently, disturbance diminished aboveground carbon storage, which gradually returned to peak levels over centuries. Temporal patterns in biodiversity potential were bimodal; the first maximum coincided with the short-term post-disturbance carbon sequestration peak, and the second occurred during periods of maximum carbon storage in complex old-growth forest. Despite fluctuating local-scale trade-offs, forest biodiversity and carbon storage remained stable across the broader study region, and our data support a positive relationship between carbon stocks and biodiversity potential. These findings underscore the interdependencies of forest processes, and highlight the necessity of large-scale conservation programmes to effectively promote both biodiversity and long-term carbon storage, particularly given the accelerating global biodiversity and climate crises.
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- 2021
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21. An integrated framework of plant form and function: the belowground perspective.
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Weigelt A, Mommer L, Andraczek K, Iversen CM, Bergmann J, Bruelheide H, Fan Y, Freschet GT, Guerrero-Ramírez NR, Kattge J, Kuyper TW, Laughlin DC, Meier IC, van der Plas F, Poorter H, Roumet C, van Ruijven J, Sabatini FM, Semchenko M, Sweeney CJ, Valverde-Barrantes OJ, York LM, and McCormack ML
- Subjects
- Phenotype, Plant Leaves, Ecosystem, Plants
- Abstract
Plant trait variation drives plant function, community composition and ecosystem processes. However, our current understanding of trait variation disproportionately relies on aboveground observations. Here we integrate root traits into the global framework of plant form and function. We developed and tested an overarching conceptual framework that integrates two recently identified root trait gradients with a well-established aboveground plant trait framework. We confronted our novel framework with published relationships between above- and belowground trait analogues and with multivariate analyses of above- and belowground traits of 2510 species. Our traits represent the leaf and root conservation gradients (specific leaf area, leaf and root nitrogen concentration, and root tissue density), the root collaboration gradient (root diameter and specific root length) and the plant size gradient (plant height and rooting depth). We found that an integrated, whole-plant trait space required as much as four axes. The two main axes represented the fast-slow 'conservation' gradient on which leaf and fine-root traits were well aligned, and the 'collaboration' gradient in roots. The two additional axes were separate, orthogonal plant size axes for height and rooting depth. This perspective on the multidimensional nature of plant trait variation better encompasses plant function and influence on the surrounding environment., (© 2021 The Authors. New Phytologist © 2021 New Phytologist Foundation.)
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- 2021
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22. Author Correction: European primary forest database v2.0.
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Sabatini FM, Bluhm H, Kun Z, Aksenov D, Atauri JA, Buchwald E, Burrascano S, Cateau E, Diku A, Duarte IM, Fernández López ÁB, Garbarino M, Grigoriadis N, Horváth F, Keren S, Kitenberga M, Kiš A, Kraut A, Ibisch PL, Larrieu L, Lombardi F, Matovic B, Melu RN, Meyer P, Midteng R, Mikac S, Mikoláš M, Mozgeris G, Panayotov M, Pisek R, Nunes L, Ruete A, Schickhofer M, Simovski B, Stillhard J, Stojanovic D, Szwagrzyk J, Tikkanen OP, Toromani E, Volosyanchuk R, Vrška T, Waldherr M, Yermokhin M, Zlatanov T, Zagidullina A, and Kuemmerle T
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- 2021
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23. European primary forest database v2.0.
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Sabatini FM, Bluhm H, Kun Z, Aksenov D, Atauri JA, Buchwald E, Burrascano S, Cateau E, Diku A, Duarte IM, Fernández López ÁB, Garbarino M, Grigoriadis N, Horváth F, Keren S, Kitenberga M, Kiš A, Kraut A, Ibisch PL, Larrieu L, Lombardi F, Matovic B, Melu RN, Meyer P, Midteng R, Mikac S, Mikoláš M, Mozgeris G, Panayotov M, Pisek R, Nunes L, Ruete A, Schickhofer M, Simovski B, Stillhard J, Stojanovic D, Szwagrzyk J, Tikkanen OP, Toromani E, Volosyanchuk R, Vrška T, Waldherr M, Yermokhin M, Zlatanov T, Zagidullina A, and Kuemmerle T
- Subjects
- Databases, Factual, Europe, Conservation of Natural Resources, Forests
- Abstract
Primary forests, defined here as forests where the signs of human impacts, if any, are strongly blurred due to decades without forest management, are scarce in Europe and continue to disappear. Despite these losses, we know little about where these forests occur. Here, we present a comprehensive geodatabase and map of Europe's known primary forests. Our geodatabase harmonizes 48 different, mostly field-based datasets of primary forests, and contains 18,411 individual patches (41.1 Mha) spread across 33 countries. When available, we provide information on each patch (name, location, naturalness, extent and dominant tree species) and the surrounding landscape (biogeographical regions, protection status, potential natural vegetation, current forest extent). Using Landsat satellite-image time series (1985-2018) we checked each patch for possible disturbance events since primary forests were identified, resulting in 94% of patches free of significant disturbances in the last 30 years. Although knowledge gaps remain, ours is the most comprehensive dataset on primary forests in Europe, and will be useful for ecological studies, and conservation planning to safeguard these unique forests., (© 2021. The Author(s).)
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- 2021
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24. Root traits explain plant species distributions along climatic gradients yet challenge the nature of ecological trade-offs.
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Laughlin DC, Mommer L, Sabatini FM, Bruelheide H, Kuyper TW, McCormack ML, Bergmann J, Freschet GT, Guerrero-Ramírez NR, Iversen CM, Kattge J, Meier IC, Poorter H, Roumet C, Semchenko M, Sweeney CJ, Valverde-Barrantes OJ, van der Plas F, van Ruijven J, York LM, Aubin I, Burge OR, Byun C, Ćušterevska R, Dengler J, Forey E, Guerin GR, Hérault B, Jackson RB, Karger DN, Lenoir J, Lysenko T, Meir P, Niinemets Ü, Ozinga WA, Peñuelas J, Reich PB, Schmidt M, Schrodt F, Velázquez E, and Weigelt A
- Subjects
- Climate, Phenotype, Water, Forests, Plant Dispersal
- Abstract
Ecological theory is built on trade-offs, where trait differences among species evolved as adaptations to different environments. Trade-offs are often assumed to be bidirectional, where opposite ends of a gradient in trait values confer advantages in different environments. However, unidirectional benefits could be widespread if extreme trait values confer advantages at one end of an environmental gradient, whereas a wide range of trait values are equally beneficial at the other end. Here, we show that root traits explain species occurrences along broad gradients of temperature and water availability, but model predictions only resembled trade-offs in two out of 24 models. Forest species with low specific root length and high root tissue density (RTD) were more likely to occur in warm climates but species with high specific root length and low RTD were more likely to occur in cold climates. Unidirectional benefits were more prevalent than trade-offs: for example, species with large-diameter roots and high RTD were more commonly associated with dry climates, but species with the opposite trait values were not associated with wet climates. Directional selection for traits consistently occurred in cold or dry climates, whereas a diversity of root trait values were equally viable in warm or wet climates. Explicit integration of unidirectional benefits into ecological theory is needed to advance our understanding of the consequences of trait variation on species responses to environmental change., (© 2021. The Author(s), under exclusive licence to Springer Nature Limited.)
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- 2021
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25. Trade-offs between carbon stocks and biodiversity in European temperate forests.
- Author
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Sabatini FM, de Andrade RB, Paillet Y, Ódor P, Bouget C, Campagnaro T, Gosselin F, Janssen P, Mattioli W, Nascimbene J, Sitzia T, Kuemmerle T, and Burrascano S
- Subjects
- France, Hungary, Italy, Biodiversity, Carbon analysis, Climate Change, Forests
- Abstract
Policies to mitigate climate change and biodiversity loss often assume that protecting carbon-rich forests provides co-benefits in terms of biodiversity, due to the spatial congruence of carbon stocks and biodiversity at biogeographic scales. However, it remains unclear whether this holds at the scales relevant for management, and particularly large knowledge gaps exist for temperate forests and for taxa other than trees. We built a comprehensive dataset of Central European temperate forest structure and multi-taxonomic diversity (beetles, birds, bryophytes, fungi, lichens, and plants) across 352 plots. We used Boosted Regression Trees (BRTs) to assess the relationship between above-ground live carbon stocks and (a) taxon-specific richness, (b) a unified multidiversity index. We used Threshold Indicator Taxa ANalysis to explore individual species' responses to changing above-ground carbon stocks and to detect change-points in species composition along the carbon-stock gradient. Our results reveal an overall weak and highly variable relationship between richness and carbon stock at the stand scale, both for individual taxonomic groups and for multidiversity. Similarly, the proportion of win-win and trade-off species (i.e., species favored or disadvantaged by increasing carbon stock, respectively) varied substantially across taxa. Win-win species gradually replaced trade-off species with increasing carbon, without clear thresholds along the above-ground carbon gradient, suggesting that community-level surrogates (e.g., richness) might fail to detect critical changes in biodiversity. Collectively, our analyses highlight that leveraging co-benefits between carbon and biodiversity in temperate forest may require stand-scale management that prioritizes either biodiversity or carbon in order to maximize co-benefits at broader scales. Importantly, this contrasts with tropical forests, where climate and biodiversity objectives can be integrated at the stand scale, thus highlighting the need for context-specificity when managing for multiple objectives. Accounting for critical change-points of target taxa can help to deal with this specificity, by defining a safe operating space to manipulate carbon while avoiding biodiversity losses., (© 2018 John Wiley & Sons Ltd.)
- Published
- 2019
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26. Global trait-environment relationships of plant communities.
- Author
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Bruelheide H, Dengler J, Purschke O, Lenoir J, Jiménez-Alfaro B, Hennekens SM, Botta-Dukát Z, Chytrý M, Field R, Jansen F, Kattge J, Pillar VD, Schrodt F, Mahecha MD, Peet RK, Sandel B, van Bodegom P, Altman J, Alvarez-Dávila E, Arfin Khan MAS, Attorre F, Aubin I, Baraloto C, Barroso JG, Bauters M, Bergmeier E, Biurrun I, Bjorkman AD, Blonder B, Čarni A, Cayuela L, Černý T, Cornelissen JHC, Craven D, Dainese M, Derroire G, De Sanctis M, Díaz S, Doležal J, Farfan-Rios W, Feldpausch TR, Fenton NJ, Garnier E, Guerin GR, Gutiérrez AG, Haider S, Hattab T, Henry G, Hérault B, Higuchi P, Hölzel N, Homeier J, Jentsch A, Jürgens N, Kącki Z, Karger DN, Kessler M, Kleyer M, Knollová I, Korolyuk AY, Kühn I, Laughlin DC, Lens F, Loos J, Louault F, Lyubenova MI, Malhi Y, Marcenò C, Mencuccini M, Müller JV, Munzinger J, Myers-Smith IH, Neill DA, Niinemets Ü, Orwin KH, Ozinga WA, Penuelas J, Pérez-Haase A, Petřík P, Phillips OL, Pärtel M, Reich PB, Römermann C, Rodrigues AV, Sabatini FM, Sardans J, Schmidt M, Seidler G, Silva Espejo JE, Silveira M, Smyth A, Sporbert M, Svenning JC, Tang Z, Thomas R, Tsiripidis I, Vassilev K, Violle C, Virtanen R, Weiher E, Welk E, Wesche K, Winter M, Wirth C, and Jandt U
- Subjects
- Forests, Grassland, Life History Traits, Plant Dispersal, Plants
- Abstract
Plant functional traits directly affect ecosystem functions. At the species level, trait combinations depend on trade-offs representing different ecological strategies, but at the community level trait combinations are expected to be decoupled from these trade-offs because different strategies can facilitate co-existence within communities. A key question is to what extent community-level trait composition is globally filtered and how well it is related to global versus local environmental drivers. Here, we perform a global, plot-level analysis of trait-environment relationships, using a database with more than 1.1 million vegetation plots and 26,632 plant species with trait information. Although we found a strong filtering of 17 functional traits, similar climate and soil conditions support communities differing greatly in mean trait values. The two main community trait axes that capture half of the global trait variation (plant stature and resource acquisitiveness) reflect the trade-offs at the species level but are weakly associated with climate and soil conditions at the global scale. Similarly, within-plot trait variation does not vary systematically with macro-environment. Our results indicate that, at fine spatial grain, macro-environmental drivers are much less important for functional trait composition than has been assumed from floristic analyses restricted to co-occurrence in large grid cells. Instead, trait combinations seem to be predominantly filtered by local-scale factors such as disturbance, fine-scale soil conditions, niche partitioning and biotic interactions.
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- 2018
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27. Ground layer plant species turnover and beta diversity in southern-European old-growth forests.
- Author
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Sabatini FM, Burrascano S, Tuomisto H, and Blasi C
- Subjects
- Europe, Plant Development, Species Specificity, Forests, Plants classification
- Abstract
Different assembly processes may simultaneously affect local-scale variation of species composition in temperate old-growth forests. Ground layer species diversity reflects chance colonization and persistence of low-dispersal species, as well as fine-scale environmental heterogeneity. The latter depends on both purely abiotic factors, such as soil properties and topography, and factors primarily determined by overstorey structure, such as light availability. Understanding the degree to which plant diversity in old-growth forests is associated with structural heterogeneity and/or to dispersal limitation will help assessing the effectiveness of silvicultural practices that recreate old-growth patterns and structures for the conservation or restoration of plant diversity. We used a nested sampling design to assess fine-scale species turnover, i.e. the proportion of species composition that changes among sampling units, across 11 beech-dominated old-growth forests in Southern Europe. For each stand, we also measured a wide range of environmental and structural variables that might explain ground layer species turnover. Our aim was to quantify the relative importance of dispersal limitation in comparison to that of stand structural heterogeneity while controlling for other sources of environmental heterogeneity. For this purpose, we used multiple regression on distance matrices at the within-stand extent, and mixed effect models at the extent of the whole dataset. Species turnover was best predicted by structural and environmental heterogeneity, especially by differences in light availability and in topsoil nutrient concentration and texture. Spatial distances were significant only in four out of eleven stands with a relatively low explanatory power. This suggests that structural heterogeneity is a more important driver of local-scale ground layer species turnover than dispersal limitation in southern European old-growth beech forests.
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- 2014
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28. Evidence for a recent increase in forest growth is questionable.
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Foster JR, Burton JI, Forrester JA, Liu F, Muss JD, Sabatini FM, Scheller RM, and Mladenoff DJ
- Subjects
- Carbon Dioxide analysis, Climate Change, Trees chemistry, Biomass, Trees growth & development
- Published
- 2010
- Full Text
- View/download PDF
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