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467 results on '"Rossetto, Maurizio"'

1. Building meaningful collaboration in conservation genetics and genomics

Author

Shaw, Robyn E., Brockett, Brittany, Pierson, Jennifer C., Sarre, Stephen D., Doyle, Paula, Cliff, Hannah B., Eldridge, Mark D. B., Miller, Kimberly A., Ottewell, Kym, Parrott, Marissa L., Rossetto, Maurizio, Sunnucks, Paul, Banks, Sam C., Byrne, Margaret, Campbell, Bridget L., Chong, Caroline, Ens, Emilie J., Ferraro, Paul A., Grueber, Catherine E., Harrison, Peter A., Hogg, Carolyn, Hutton, Marlee, Roycroft, Emily, Sowersby, Will, Karajarri Rangers, Kiwirrkurra Rangers, Ngurrara Rangers, Nyangumarta Rangers, Ngururrpa Rangers, and Neaves, Linda E.

Published
2024
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6. Publisher Correction: Open Science principles for accelerating trait-based science across the Tree of Life

Author

Gallagher, Rachael V, Falster, Daniel S, Maitner, Brian S, Salguero-Gómez, Roberto, Vandvik, Vigdis, Pearse, William D, Schneider, Florian D, Kattge, Jens, Poelen, Jorrit H, Madin, Joshua S, Ankenbrand, Markus J, Penone, Caterina, Feng, Xiao, Adams, Vanessa M, Alroy, John, Andrew, Samuel C, Balk, Meghan A, Bland, Lucie M, Boyle, Brad L, Bravo-Avila, Catherine H, Brennan, Ian, Carthey, Alexandra JR, Catullo, Renee, Cavazos, Brittany R, Conde, Dalia A, Chown, Steven L, Fadrique, Belen, Gibb, Heloise, Halbritter, Aud H, Hammock, Jennifer, Hogan, J Aaron, Holewa, Hamish, Hope, Michael, Iversen, Colleen M, Jochum, Malte, Kearney, Michael, Keller, Alexander, Mabee, Paula, Manning, Peter, McCormack, Luke, Michaletz, Sean T, Park, Daniel S, Perez, Timothy M, Pineda-Munoz, Silvia, Ray, Courtenay A, Rossetto, Maurizio, Sauquet, Hervé, Sparrow, Benjamin, Spasojevic, Marko J, Telford, Richard J, Tobias, Joseph A, Violle, Cyrille, Walls, Ramona, Weiss, Katherine CB, Westoby, Mark, Wright, Ian J, and Enquist, Brian J

Subjects
Biological Sciences, Environmental Management, Ecology, Evolutionary Biology, Environmental Sciences, Evolutionary biology, Environmental management
Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Published
2020

7. Open Science principles for accelerating trait-based science across the Tree of Life

Author

Gallagher, Rachael V, Falster, Daniel S, Maitner, Brian S, Salguero-Gómez, Roberto, Vandvik, Vigdis, Pearse, William D, Schneider, Florian D, Kattge, Jens, Poelen, Jorrit H, Madin, Joshua S, Ankenbrand, Markus J, Penone, Caterina, Feng, Xiao, Adams, Vanessa M, Alroy, John, Andrew, Samuel C, Balk, Meghan A, Bland, Lucie M, Boyle, Brad L, Bravo-Avila, Catherine H, Brennan, Ian, Carthey, Alexandra JR, Catullo, Renee, Cavazos, Brittany R, Conde, Dalia A, Chown, Steven L, Fadrique, Belen, Gibb, Heloise, Halbritter, Aud H, Hammock, Jennifer, Hogan, J Aaron, Holewa, Hamish, Hope, Michael, Iversen, Colleen M, Jochum, Malte, Kearney, Michael, Keller, Alexander, Mabee, Paula, Manning, Peter, McCormack, Luke, Michaletz, Sean T, Park, Daniel S, Perez, Timothy M, Pineda-Munoz, Silvia, Ray, Courtenay A, Rossetto, Maurizio, Sauquet, Hervé, Sparrow, Benjamin, Spasojevic, Marko J, Telford, Richard J, Tobias, Joseph A, Violle, Cyrille, Walls, Ramona, Weiss, Katherine CB, Westoby, Mark, Wright, Ian J, and Enquist, Brian J

Subjects
Climate Change Impacts and Adaptation, Biological Sciences, Environmental Sciences, Networking and Information Technology R&D (NITRD), Generic health relevance, Biodiversity, Biological Evolution, Ecology, Phenotype, Research, Evolutionary biology, Environmental management
Abstract

Synthesizing trait observations and knowledge across the Tree of Life remains a grand challenge for biodiversity science. Species traits are widely used in ecological and evolutionary science, and new data and methods have proliferated rapidly. Yet accessing and integrating disparate data sources remains a considerable challenge, slowing progress toward a global synthesis to integrate trait data across organisms. Trait science needs a vision for achieving global integration across all organisms. Here, we outline how the adoption of key Open Science principles-open data, open source and open methods-is transforming trait science, increasing transparency, democratizing access and accelerating global synthesis. To enhance widespread adoption of these principles, we introduce the Open Traits Network (OTN), a global, decentralized community welcoming all researchers and institutions pursuing the collaborative goal of standardizing and integrating trait data across organisms. We demonstrate how adherence to Open Science principles is key to the OTN community and outline five activities that can accelerate the synthesis of trait data across the Tree of Life, thereby facilitating rapid advances to address scientific inquiries and environmental issues. Lessons learned along the path to a global synthesis of trait data will provide a framework for addressing similarly complex data science and informatics challenges.

Published
2020

10. Ecology and Conservation of a Living Fossil: Australia’s Wollemi Pine (Wollemia nobilis)

Author

Mackenzie, Berin D.E., primary, Clarke, Steve W., additional, Zimmer, Heidi C., additional, Liew, Edward C.Y., additional, Phelan, Maureen T., additional, Offord, Catherine A., additional, Menke, Lisa K., additional, Crust, David W., additional, Bragg, Jason, additional, McPherson, Hannah, additional, Rossetto, Maurizio, additional, Coote, David M., additional, Yap, Jia-Yee Samantha, additional, and Auld, Tony D., additional

Published
2022
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12. AusTraits, a curated plant trait database for the Australian flora

Author

Falster, Daniel, Gallagher, Rachael, Wenk, Elizabeth H., Wright, Ian J., Indiarto, Dony, Andrew, Samuel C., Baxter, Caitlan, Lawson, James, Allen, Stuart, Fuchs, Anne, Monro, Anna, Kar, Fonti, Adams, Mark A., Ahrens, Collin W., Alfonzetti, Matthew, Angevin, Tara, Apgaua, Deborah M. G., Arndt, Stefan, Atkin, Owen K., Atkinson, Joe, Auld, Tony, Baker, Andrew, von Balthazar, Maria, Bean, Anthony, Blackman, Chris J., Bloomfield, Keith, Bowman, David M. J. S., Bragg, Jason, Brodribb, Timothy J., Buckton, Genevieve, Burrows, Geoff, Caldwell, Elizabeth, Camac, James, Carpenter, Raymond, Catford, Jane A., Cawthray, Gregory R., Cernusak, Lucas A., Chandler, Gregory, Chapman, Alex R., Cheal, David, Cheesman, Alexander W., Chen, Si-Chong, Choat, Brendan, Clinton, Brook, Clode, Peta L., Coleman, Helen, Cornwell, William K., Cosgrove, Meredith, Crisp, Michael, Cross, Erika, Crous, Kristine Y., Cunningham, Saul, Curran, Timothy, Curtis, Ellen, Daws, Matthew I., DeGabriel, Jane L., Denton, Matthew D., Dong, Ning, Du, Pengzhen, Duan, Honglang, Duncan, David H., Duncan, Richard P., Duretto, Marco, Dwyer, John M., Edwards, Cheryl, Esperon-Rodriguez, Manuel, Evans, John R., Everingham, Susan E., Farrell, Claire, Firn, Jennifer, Fonseca, Carlos Roberto, French, Ben J., Frood, Doug, Funk, Jennifer L., Geange, Sonya R., Ghannoum, Oula, Gleason, Sean M., Gosper, Carl R., Gray, Emma, Groom, Philip K., Grootemaat, Saskia, Gross, Caroline, Guerin, Greg, Guja, Lydia, Hahs, Amy K., Harrison, Matthew Tom, Hayes, Patrick E., Henery, Martin, Hochuli, Dieter, Howell, Jocelyn, Huang, Guomin, Hughes, Lesley, Huisman, John, Ilic, Jugoslav, Jagdish, Ashika, Jin, Daniel, Jordan, Gregory, Jurado, Enrique, Kanowski, John, Kasel, Sabine, Kellermann, Jürgen, Kenny, Belinda, Kohout, Michele, Kooyman, Robert M., Kotowska, Martyna M., Lai, Hao Ran, Laliberté, Etienne, Lambers, Hans, Lamont, Byron B., Lanfear, Robert, van Langevelde, Frank, Laughlin, Daniel C., Laugier-Kitchener, Bree-Anne, Laurance, Susan, Lehmann, Caroline E. R., Leigh, Andrea, Leishman, Michelle R., Lenz, Tanja, Lepschi, Brendan, Lewis, James D., Lim, Felix, Liu, Udayangani, Lord, Janice, Lusk, Christopher H., Macinnis-Ng, Cate, McPherson, Hannah, Magallón, Susana, Manea, Anthony, López-Martinez, Andrea, Mayfield, Margaret, McCarthy, James K., Meers, Trevor, van der Merwe, Marlien, Metcalfe, Daniel J., Milberg, Per, Mokany, Karel, Moles, Angela T., Moore, Ben D., Moore, Nicholas, Morgan, John W., Morris, William, Muir, Annette, Munroe, Samantha, Nicholson, Áine, Nicolle, Dean, Nicotra, Adrienne B., Niinemets, Ülo, North, Tom, O’Reilly-Nugent, Andrew, O’Sullivan, Odhran S., Oberle, Brad, Onoda, Yusuke, Ooi, Mark K. J., Osborne, Colin P., Paczkowska, Grazyna, Pekin, Burak, Guilherme Pereira, Caio, Pickering, Catherine, Pickup, Melinda, Pollock, Laura J., Poot, Pieter, Powell, Jeff R., Power, Sally A., Prentice, Iain Colin, Prior, Lynda, Prober, Suzanne M., Read, Jennifer, Reynolds, Victoria, Richards, Anna E., Richardson, Ben, Roderick, Michael L., Rosell, Julieta A., Rossetto, Maurizio, Rye, Barbara, Rymer, Paul D., Sams, Michael A., Sanson, Gordon, Sauquet, Hervé, Schmidt, Susanne, Schönenberger, Jürg, Schulze, Ernst-Detlef, Sendall, Kerrie, Sinclair, Steve, Smith, Benjamin, Smith, Renee, Soper, Fiona, Sparrow, Ben, Standish, Rachel J., Staples, Timothy L., Stephens, Ruby, Szota, Christopher, Taseski, Guy, Tasker, Elizabeth, Thomas, Freya, Tissue, David T., Tjoelker, Mark G., Tng, David Yue Phin, de Tombeur, Félix, Tomlinson, Kyle, Turner, Neil C., Veneklaas, Erik J., Venn, Susanna, Vesk, Peter, Vlasveld, Carolyn, Vorontsova, Maria S., Warren, Charles A., Warwick, Nigel, Weerasinghe, Lasantha K., Wells, Jessie, Westoby, Mark, White, Matthew, Williams, Nicholas S. G., Wills, Jarrah, Wilson, Peter G., Yates, Colin, Zanne, Amy E., Zemunik, Graham, and Ziemińska, Kasia

Published
2021
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14. Environmental and Biogeographic Drivers behind Alpine Plant Thermal Tolerance and Genetic Variation.

Author

Danzey, Lisa M., Briceño, Verónica F., Cook, Alicia M., Nicotra, Adrienne B., Peyre, Gwendolyn, Rossetto, Maurizio, Yap, Jia-Yee S., and Leigh, Andrea

Subjects
GENETIC variation, MOUNTAIN plants, POPULATION differentiation, GLOBAL warming, LAST Glacial Maximum
Abstract

In alpine ecosystems, elevation broadly functions as a steep thermal gradient, with plant communities exposed to regular fluctuations in hot and cold temperatures. These conditions lead to selective filtering, potentially contributing to species-level variation in thermal tolerance and population-level genetic divergence. Few studies have explored the breadth of alpine plant thermal tolerances across a thermal gradient or the underlying genetic variation thereof. We measured photosystem heat (Tcrit-hot) and cold (Tcrit-cold) thresholds of ten Australian alpine species across elevation gradients and characterised their neutral genetic variation. To reveal the biogeographical drivers of present-day genetic signatures, we also reconstructed temporal changes in habitat suitability across potential distributional ranges. We found intraspecific variation in thermal thresholds, but this was not associated with elevation, nor underpinned by genetic differentiation on a local scale. Instead, regional population differentiation and considerable homozygosity within populations may, in part, be driven by distributional contractions, long-term persistence, and migrations following habitat suitability. Our habitat suitability models suggest that cool-climate-distributed alpine plants may be threatened by a warming climate. Yet, the observed wide thermal tolerances did not reflect this vulnerability. Conservation efforts should seek to understand variations in species-level thermal tolerance across alpine microclimates. [ABSTRACT FROM AUTHOR]

Published
2024
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15. Using molecular and morphometric data as operational criteria for the analysis of a threatened rainforest species complex shows interspecific variation, with implications for cryptic-species delimitation and conservation.

Author

Brunton, Aaron J., Forster, Paul I., Ogbourne, Steven M., Rossetto, Maurizio, Schoeman, David S., and Conroy, Gabriel C.

Subjects
ENDANGERED species, MORPHOMETRICS, CONSERVATION genetics
Abstract

Resolution of systematic associations and species boundaries is vital for developing conservation priorities for threatened taxa. A complex of Fontainea (Euphorbiaceae) populations, endemic to rainforest communities in central-eastern Australia, comprises several taxonomically challenging species. Fontainea oraria is Critically Endangered, with only one natural population of 10 mature individuals, with the closely related species F. australis being listed as Vulnerable. A recently discovered Fontainea population (currently nominated as F. sp. Coffs Harbour) with taxonomic similarities to F. oraria has been provisionally listed as Critically Endangered, with fewer than 40 individuals. This study employed an integrative approach, combining genetic data and morphometrics to determine species boundaries for three threatened Fontainea population groups as a model system for an integrative approach to delimiting cryptic species. Although our results suggest the potential subdivision of the population groups into three taxa, caution is warranted because this hypothesis remains inconclusive. Taxonomic challenges demand a careful approach, acknowledging the possibility of alternative interpretations. Contrary to supporting distinct species, our morphological and genetic data may also be interpreted as indicative of a single species with geographic variation, a phenomenon observed in genetically linked populations experiencing isolation by distance. Overall, we highlight the need for further research to establish species limits to guide conservation actions. [ABSTRACT FROM AUTHOR]

Published
2024
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26. Publish openly but responsibly

Author

Lowe, Andrew J., Smyth, Anita K., Atkins, Ken, Avery, Ron, Belbin, Lee, Brown, Noleen, Budden, Amber E., Gioia, Paul, Guru, Siddeswara, Hardie, Mel, Hirsch, Tim, Hobern, Donald, La Salle, John, Loarie, Scott R., Miles, Matt, Milne, Damian, Nicholls, Miles, Rossetto, Maurizio, Smits, Jennifer, Sparrow, Ben, Terrill, Gregston, Turner, David, and Wardle, Glenda M.

Published
2017

29. Genetic diversity and structure of the Australian flora

Author

Broadhurst, Linda, Breed, Martin, Lowe, Andrew, Bragg, Jason, Catullo, Renee, Coates, David, Encinas-Viso, Francisco, Gellie, Nick, James, Elizabeth, Krauss, Siegfried, Potts, Brad, Rossetto, Maurizio, Shepherd, Mervyn, and Byrne, Margaret

Published
2017

30. The genome of the Wollemi pine, a critically endangered “living fossil” unchanged since the Cretaceous, reveals extensive ancient transposon activity

Author

Stevenson, Dennis Wm., primary, Ramakrishnan, Srividya, additional, Alves, Cristiane de Santis, additional, Coelho, Laís Araujo, additional, Kramer, Melissa, additional, Goodwin, Sara, additional, Ramos, Olivia Mendevil, additional, Eshel, Gil, additional, Sondervan, Veronica M., additional, Frangos, Samantha, additional, Zumajo-Cardona, Cecilia, additional, Jenike, Katherine, additional, Ou, Shujun, additional, Wang, Xiaojin, additional, Lee, Yin Peng, additional, Loke, Stella, additional, Rossetto, Maurizio, additional, McPherson, Hannah, additional, Nigris, Sebastiano, additional, Moschin, Silvia, additional, Little, Damon P., additional, Katari, Manpreet S., additional, Varala, Kranthi, additional, Kolokotronis, Sergios-Orestis, additional, Ambrose, Barbara, additional, Croft, Larry J., additional, Coruzzi, Gloria M., additional, Schatz, Michael, additional, McCombie, W. Richard, additional, and Martienssen, Robert A., additional

Published
2023
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34. Araucaria bidwillii genomics suggest Indigenous Peoples broadened translocation practices in response to settler colonialism.

Author

Fahey, Monica, Rossetto, Maurizio, Ens, Emilie, and Kerkhove, Ray

Subjects
INDIGENOUS peoples, COLONIES, SPECIES distribution, INDIGENOUS Australians, TRADITIONAL knowledge, GENOMICS, AUSTRALIAN history, ETHNOHISTORY
Abstract

Retracing past anthropogenic dispersal of culturally important taxa offers insights to the biogeographic history of species, as well as the history of the people who interacted with them. Bunya Pine (Araucaria bidwillii Hook.) is a culturally and spiritually significant conifer tree for several Indigenous groups in eastern Australia. Sharing the edible nuts and attending Bunya gatherings is an important way for these groups to maintain their cultural connections and it has been hypothesized that prior to European colonization, Indigenous Peoples facilitated the dispersal of Bunya Pine as part of these ancient traditions.We used ethnohistorical information on the use of Bunya Pine by Indigenous Peoples to interpret genomic patterns within and between disjunct distributions of Bunya Pine.We found signatures of long‐term isolation within the Australian Wet Tropics (AWT) and extensive gene flow within southeast Queensland (SEQ) that does not fit models of faunal or passive dispersal. Within SEQ, we found greater population structure amongst sites known to pre‐date European colonization, than when colonial‐era planted sites were included in our analyses, suggesting that pre‐colonial translocation was sporadic or localized rather than systematic and widespread. Increased Indigenous translocations in conjunction with plantings by European settlers appears to have erased the natural pre‐colonial population structure of SEQ Bunya Pine. Our stairway plot models suggest sharp population decline of SEQ Bunya Pine in the early and late Pleistocene, though we did not find evidence that anthropogenic dispersal facilitated effective population size growth of the species in the Holocene.We concluded that pre‐colonial translocation of SEQ Bunya Pine was likely restricted by kinship‐based custodial rights, and that when Indigenous Peoples were displaced by European settlers, translocation was intensified to maintain cultural connectivity. This study is an example of how Indigenous Australian groups adapt plant management strategies to meet socio‐cultural needs and demonstrates the potential for plant genomics to supplement Indigenous Biocultural Knowledge that has been impacted by colonial dispossession. Read the free Plain Language Summary for this article on the Journal blog. Read the free Plain Language Summary for this article on the Journal blog. [ABSTRACT FROM AUTHOR]

Published
2024
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