37 results on '"Ruokolainen, K."'
Search Results
2. A Comparison of Fine-Scale Distribution Patterns of Four Plant Groups in an Amazonian Rainforest
- Author
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Vormisto, J., Phillips, O. L., Ruokolainen, K., Tuomisto, H., and Vásquez, R.
- Published
- 2000
3. Estimating Number of Pteridophyte and Melastomataceae Species from Satellite Images in Western Amazonian Rain Forests
- Author
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Rajaniemi, S., Tomppo, E., Ruokolainen, K., Tuomisto, H., Corona, Piermaria, editor, Köhl, Michael, editor, and Marchetti, Marco, editor
- Published
- 2003
- Full Text
- View/download PDF
4. Amazon tree dominance across forest strata
- Author
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Draper, F.C., Costa, F.R.C., Arellano, G., Phillips, O.L., Duque, A., Macía, M.J., ter Steege, H., Asner, G.P., Berenguer, E., Schietti, J., Socolar, J.B., de Souza, F.C., Dexter, K.G., Jørgensen, P.M., Tello, J.S., Magnusson, W.E., Baker, T.R., Castilho, C.V., Monteagudo-Mendoza, A., Fine, P.V.A., Ruokolainen, K., Coronado, E.N.H., Aymard, G., Dávila, N., Sáenz, M.S., Paredes, M.A.R., Engel, J., Fortunel, C., Paine, C.E.T., Goret, J.-Y., Dourdain, A., Petronelli, P., Allie, E., Andino, J.E.G., Brienen, R.J.W., Pérez, L.C., Manzatto, Â.G., Zambrana, N.Y.P., Molino, J.-F., Sabatier, D., Chave, J., Fauset, S., Villacorta, R.G., Réjou-Méchain, M., Berry, P.E., Melgaço, K., Feldpausch, T.R., Sandoval, E.V., Martinez, R.V., Mesones, I., Junqueira, A.B., Roucoux, K.H., de Toledo, J.J., Andrade, A.C., Camargo, J.L., del Aguila Pasquel, J., Santana, F.D., Laurance, W.F., Laurance, S.G., Lovejoy, T.E., Comiskey, J.A., Galbraith, D.R., Kalamandeen, M., Aguilar, G.E.N., Arenas, J.V., Guerra, C.A.A., Flores, M., Llampazo, G.F., Montenegro, L.A.T., Gomez, R.Z., Pansonato, M.P., Moscoso, V.C., Vleminckx, J., Barrantes, O.J.V., Duivenvoorden, J.F., de Sousa, S.A., Arroyo, L., Perdiz, R.O., Cravo, J.S., Marimon, B.S., Junior, B.H.M., Carvalho, F.A., Damasco, G., Disney, M., Vital, M.S., Diaz, P.R.S., Vicentini, A., Nascimento, H., Higuchi, N., Van Andel, T., Malhi, Y., Ribeiro, S.C., Terborgh, J.W., Thomas, R.S., Dallmeier, F., Prieto, A., Hilário, R.R., Salomão, R.P., Silva, R.C., Casas, L.F., Vieira, I.C.G., Araujo-Murakami, A., Arevalo, F.R., Ramírez-Angulo, H., Torre, E.V., Peñuela, M.C., Killeen, T.J., Pardo, G., Jimenez-Rojas, E., Castro, W., Cabrera, D.G., Pipoly, J., de Sousa, T.R., Silvera, M., Vos, V., Neill, D., Vargas, P.N., Vela, D.M., Aragão, L.E.O.C., Umetsu, R.K., Sierra, R., Wang, O., Young, K.R., Prestes, N.C.C.S., Massi, K.G., Huaymacari, J.R., Gutierrez, G.A.P., Aldana, A.M., Alexiades, M.N., Baccaro, F., Céron, C., Muelbert, A.E., Rios, J.M.G., Lima, A.S., Lloyd, J.L., Pitman, N.C.A., Gamarra, L.V., Oroche, C.J.C., Fuentes, A.F., Palacios, W., Patiño, S., Torres-Lezama, A., Baraloto, C., Draper, F.C., Costa, F.R.C., Arellano, G., Phillips, O.L., Duque, A., Macía, M.J., ter Steege, H., Asner, G.P., Berenguer, E., Schietti, J., Socolar, J.B., de Souza, F.C., Dexter, K.G., Jørgensen, P.M., Tello, J.S., Magnusson, W.E., Baker, T.R., Castilho, C.V., Monteagudo-Mendoza, A., Fine, P.V.A., Ruokolainen, K., Coronado, E.N.H., Aymard, G., Dávila, N., Sáenz, M.S., Paredes, M.A.R., Engel, J., Fortunel, C., Paine, C.E.T., Goret, J.-Y., Dourdain, A., Petronelli, P., Allie, E., Andino, J.E.G., Brienen, R.J.W., Pérez, L.C., Manzatto, Â.G., Zambrana, N.Y.P., Molino, J.-F., Sabatier, D., Chave, J., Fauset, S., Villacorta, R.G., Réjou-Méchain, M., Berry, P.E., Melgaço, K., Feldpausch, T.R., Sandoval, E.V., Martinez, R.V., Mesones, I., Junqueira, A.B., Roucoux, K.H., de Toledo, J.J., Andrade, A.C., Camargo, J.L., del Aguila Pasquel, J., Santana, F.D., Laurance, W.F., Laurance, S.G., Lovejoy, T.E., Comiskey, J.A., Galbraith, D.R., Kalamandeen, M., Aguilar, G.E.N., Arenas, J.V., Guerra, C.A.A., Flores, M., Llampazo, G.F., Montenegro, L.A.T., Gomez, R.Z., Pansonato, M.P., Moscoso, V.C., Vleminckx, J., Barrantes, O.J.V., Duivenvoorden, J.F., de Sousa, S.A., Arroyo, L., Perdiz, R.O., Cravo, J.S., Marimon, B.S., Junior, B.H.M., Carvalho, F.A., Damasco, G., Disney, M., Vital, M.S., Diaz, P.R.S., Vicentini, A., Nascimento, H., Higuchi, N., Van Andel, T., Malhi, Y., Ribeiro, S.C., Terborgh, J.W., Thomas, R.S., Dallmeier, F., Prieto, A., Hilário, R.R., Salomão, R.P., Silva, R.C., Casas, L.F., Vieira, I.C.G., Araujo-Murakami, A., Arevalo, F.R., Ramírez-Angulo, H., Torre, E.V., Peñuela, M.C., Killeen, T.J., Pardo, G., Jimenez-Rojas, E., Castro, W., Cabrera, D.G., Pipoly, J., de Sousa, T.R., Silvera, M., Vos, V., Neill, D., Vargas, P.N., Vela, D.M., Aragão, L.E.O.C., Umetsu, R.K., Sierra, R., Wang, O., Young, K.R., Prestes, N.C.C.S., Massi, K.G., Huaymacari, J.R., Gutierrez, G.A.P., Aldana, A.M., Alexiades, M.N., Baccaro, F., Céron, C., Muelbert, A.E., Rios, J.M.G., Lima, A.S., Lloyd, J.L., Pitman, N.C.A., Gamarra, L.V., Oroche, C.J.C., Fuentes, A.F., Palacios, W., Patiño, S., Torres-Lezama, A., and Baraloto, C.
- Abstract
The forests of Amazonia are among the most biodiverse plant communities on Earth. Given the immediate threats posed by climate and land-use change, an improved understanding of how this extraordinary biodiversity is spatially organized is urgently required to develop effective conservation strategies. Most Amazonian tree species are extremely rare but a few are common across the region. Indeed, just 227 ‘hyperdominant’ species account for >50% of all individuals >10 cm diameter at 1.3 m in height. Yet, the degree to which the phenomenon of hyperdominance is sensitive to tree size, the extent to which the composition of dominant species changes with size class and how evolutionary history constrains tree hyperdominance, all remain unknown. Here, we use a large floristic dataset to show that, while hyperdominance is a universal phenomenon across forest strata, different species dominate the forest understory, midstory and canopy. We further find that, although species belonging to a range of phylogenetically dispersed lineages have become hyperdominant in small size classes, hyperdominants in large size classes are restricted to a few lineages. Our results demonstrate that it is essential to consider all forest strata to understand regional patterns of dominance and composition in Amazonia. More generally, through the lens of 654 hyperdominant species, we outline a tractable pathway for understanding the functioning of half of Amazonian forests across vertical strata and geographical locations.
- Published
- 2021
5. Estimating Number of Pteridophyte and Melastomataceae Species from Satellite Images in Western Amazonian Rain Forests
- Author
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Rajaniemi, S., primary, Tomppo, E., additional, Ruokolainen, K., additional, and Tuomisto, H., additional
- Published
- 2003
- Full Text
- View/download PDF
6. Beta-diversity in tropical forests
- Author
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Ruokolainen, K., Tuomisto, H., Chave, J., Muller-Landau, H., Condit, R., Pitman, N., Duivenvoorden, J.F., Svenning, J.-C., and Wright, S.J.
- Published
- 2002
7. Phytogéographie tropicale : réalités et perspectives
- Author
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Ruokolainen, K., Guillaumet, Jean-Louis (ed.), Belin, M. (ed.), and Puig, H. (ed.)
- Subjects
FORET DENSE ,PHYTOSOCIOLOGIE ,PHYTOGEOGRAPHIE ,PHYTOECOLOGIE - Abstract
Les modèles de distribution des plantes de la forêt pluvieuse de l'Amazonie sont peu connus à cause d'une recherche botanique inadéquate et géographiquement inégale. Si les espèces végétales forment de manière récurrente des communautés écologiquement restreintes, il devrait y avoir des modèles de distribution récurrents qui pourraient être découverts en étudiant seulement une partie de la flore. Les comparaisons de la flore de douze terrains d'étude différents dans l'Amazonie péruvienne sur la base d'arbres supérieurs à 2,5 cm de diamètre à la hauteur de la poitrine, fougères terrestres et #Melastomataceae$, indiquent qu'il existe des communautés de plantes récurrentes et que les fougères et #Melastomataceae$ sont de très bons indicateurs de plusieurs modèles phytogéographiques généraux en Amazonie. (Résumé d'auteur)
- Published
- 1996
8. Estimating and mapping pteridophyte and Melastomataceae species richness in western Amazonian rainforests
- Author
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Rajaniemi, S., primary, Tomppo, E., additional, Ruokolainen, K., additional, and Tuomisto, H., additional
- Published
- 2005
- Full Text
- View/download PDF
9. Beta-Diversity in Tropical Forests
- Author
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Ruokolainen, K., primary
- Published
- 2002
- Full Text
- View/download PDF
10. Phylogenetic classification of the world's tropical forests
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Slik, J. W. F., Franklin, J., Arroyo-Rodríguez, V., Field, R., Aguilar, S., Aguirre, N., Ahumada, J., Aiba, S.-I., Alves, L. F., Anitha, K., Avella, A., Mora, F., Aymard, G. A. C., Báez, S., Balvanera, P., Bastian, M. L., Bastin, J.-F., Bellingham, P. J., Van Den Berg, E., Da Conceição Bispo, P., Boeckx, P., Boehning-Gaese, K., Bongers, F., Boyle, B., Brambach, F., Brearley, F. Q., Brown, S., Chai, S.-L., Chazdon, R. L., Chen, S., Chhang, P., Chuyong, G., Ewango, C., Coronado, I. M., Cristóbal-Azkarate, J., Culmsee, H., Damas, K., Dattaraja, H. S., Davidar, P., DeWalt, S. J., DIn, H., Drake, D. R., Duque, A., Durigan, G., Eichhorn, K., Eler, E. S., Enoki, T., Ensslin, A., Fandohan, A. B., Farwig, N., Feeley, K. J., Fischer, M., Forshed, O., Garcia, Q. S., Garkoti, S. C., Gillespie, T. W., Gillet, J.-F., Gonmadje, C., Granzow-De La Cerda, I., Griffith, D. M., Grogan, J., Hakeem, K. R., Harris, D. J., Harrison, R. D., Hector, A., Hemp, A., Homeier, J., Hussain, M. S., Ibarra-Manríquez, G., Hanum, I. F., Imai, N., Jansen, P. A., Joly, C. A., Joseph, S., Kartawinata, K., Kearsley, E., Kelly, D. L., Kessler, M., Killeen, T. J., Kooyman, R. M., Laumonier, Y., Laurance, S. G., Laurance, W. F., Lawes, M. J., Letcher, S. G., Lindsell, J., Lovett, J., Lozada, J., Lu, X., Lykke, A. M., Bin Mahmud, K., Mahayani, N. P. D., Mansor, A., Marshall, A. R., Martin, E. H., Matos, D. C. L., Meave, J. A., Melo, F. P. L., Mendoza, Z. H. A., Metali, F., Medjibe, V. P., Metzger, J. P., Metzker, T., Mohandass, D., Munguía-Rosas, M. A., Muñoz, R., Nurtjahy, E., De Oliveira, E. L., Onrizal, Parolin, P., Parren, M., Parthasarathy, N., Paudel, E., Perez, R., Pérez-García, E. A., Pommer, U., Poorter, L., Qi, L., Piedade, M. T. F., Pinto, J. R. R., Poulsen, A. D., Poulsen, J. R., Powers, J. S., Prasad, R. C., Puyravaud, J.-P., Rangel, O., Reitsma, J., Rocha, D. S. B., Rolim, S., Rovero, F., Rozak, A., Ruokolainen, K., Rutishauser, E., Rutten, G., Mohd Said, M. N., Saiter, F. Z., Saner, P., Santos, B., Dos Santos, J. R., Sarker, S. K., Schmitt, C. B., Schoengart, J., Schulze, M., Sheil, D., Sist, P., Souza, A. F., Spironello, W. R., Sposito, T., Steinmetz, R., Stevart, T., Suganuma, M. S., Sukri, R., Sultana, A., Sukumar, R., Sunderland, T., Supriyadi, Suresh, H. S., Suzuki, E., Tabarelli, M., Tang, J., Tanner, E. V. J., Targhetta, N., Theilade, I., Thomas, D., Timberlake, J., De Morisson Valeriano, M., Van Valkenburg, J., Van Do, T., Van Sam, H., Vandermeer, J. H., Verbeeck, H., Vetaas, O. R., Adekunle, V., Vieira, S. A., Webb, C. O., Webb, E. L., Whitfeld, T., Wich, S., Williams, J., Wiser, S., Wittmann, F., Yang, X., Yao, C. Y. A., Yap, S. L., Zahawi, R. A., Zakaria, R., and Zang, R.
- Subjects
15. Life on land
11. Distribution and diversity of pteridophytes and melastomataceae along edaphic gradients in Yasuní National Park, Ecuadorian Amazonia
- Author
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Tuomisto, H., Ruokolainen, K., Poulsen, A. D., Moran, R. C., Quintana, C., Cañas, G., and Jorge Celi
12. Parameters for global ecosystem models [8] (multiple letters)
- Author
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Crutzen, P. J., Fall, R., Galbally, I., Lindinger, W., Schulman, L., Ruokolainen, K., Hanna Tuomisto, Tian, H., Melillo, J. M., Kicklighter, D. W., Mcguire, A. D., Moore Iii, B., and Vorosmarty, C. J.
13. Evolutionary heritage influences Amazon tree ecology
- Author
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Coelho De Souza, F, Dexter, KG, Phillips, OL, Brienen, RJW, Chave, J, Galbraith, DR, Lopez Gonzalez, G, Monteagudo Mendoza, A, Pennington, TR, Poorter, L, Alexiades, M, Álvarez-Dávila, E, Andrade, A, Aragão, LEOC, Araujo-Murakami, A, Arets, E, Aymard, GA, Baraloto, C, Barroso, JG, Bonal, D, Boot, RGA, Camargo, JLC, Comiskey, JA, Cornejo Valverde, F, de Camargo, PB, Di Fiore, A, Elias, F, Erwin, TL, Feldpausch, TR, Ferreira, L, Fyllas, NM, Gloor, E, Herault, B, Herrera, R, Higuchi, N, Honorio Coronado, EN, Killeen, T, Laurance, WF, Laurance, S, Lloyd, J, Lovejoy, TE, Malhi, Y, Maracahipes, L, Marimon, BS, Marimon-Junior, BH, Mendoza, C, Morandi, P, Neill, DA, Núñez Vargas, P, Oliveira, EA, Lenza, E, Palacios, WA, Peñuela-Mora, M, Pipoly III, JJ, Pitman, NCA, Prieto, A, Quesada, CA, Ramirez-Angulo, H, Rudas, A, Ruokolainen, K, Salomão, RP, Silveira, M, Stropp, J, ter Steege, H, Thomas-Caesar, R, van der Hout, P, van der Heijden, GMF, van der Meer, PJ, Vasquez, RV, Vieira, SA, Vilanova, E, Vos, VA, Wang, O, Young, KR, Zagt, RJ, Baker, TR, Chercheur indépendant, Ecologie et Ecophysiologie Forestières [devient SILVA en 2018] (EEF), Institut National de la Recherche Agronomique (INRA)-Université de Lorraine (UL), and The Royal Society
- Subjects
Life Sciences & Biomedicine - Other Topics ,Convergent Evolution ,WOOD DENSITY ,[SDV]Life Sciences [q-bio] ,Trait ,Forests ,Trees ,BIOMASS ,Angiosperm ,Divergence ,Divergent selection ,Natural Selection ,tropical tree ,Phylogeny ,Research Articles ,Ecology ,PRODUCTIVITY ,trait ,phylogenetic signal ,RAIN-FOREST ,11 Medical And Health Sciences ,Biological Evolution ,Phylogenetics ,GROWTH ,divergent selection ,Life Sciences & Biomedicine ,Environmental Sciences & Ecology ,Life History Trait ,Forest Inventory ,Magnoliophyta ,Amazonia ,Tropical Forest ,Tropical tree ,convergent evolution ,Mortality ,Biology ,Tropical Climate ,Evolutionary Biology ,Science & Technology ,South America ,PHYLOGENETIC NICHE CONSERVATISM ,06 Biological Sciences ,SIGNAL ,SIZE ,FUNCTIONAL TRAITS ,Ecosystem Function ,07 Agricultural And Veterinary Sciences ,COMMUNITY ECOLOGY - Abstract
Lineages tend to retain ecological characteristics of their ancestors through time. However, for some traits, selection during evolutionary history may have also played a role in determining trait values. To address the relative importance of these processes requires large-scale quantification of traits and evolutionary relationships among species. The Amazonian tree flora comprises a high diversity of angiosperm lineages and species with widely differing life-history characteristics, providing an excellent system to investigate the combined influences of evolutionary heritage and selection in determining trait variation. We used trait data related to the major axes of life-history variation among tropical trees (e.g. growth and mortality rates) from 577 inventory plots in closed-canopy forest, mapped onto a phylogenetic hypothesis spanning more than 300 genera including all major angiosperm clades to test for evolutionary constraints on traits. We found significant phylogenetic signal (PS) for all traits, consistent with evolutionarily related genera having more similar characteristics than expected by chance. Although there is also evidence for repeated evolution of pioneer and shade tolerant lifehistory strategies within independent lineages, the existence of significant PS allows clearer predictions of the links between evolutionary diversity, ecosystem function and the response of tropical forests to global change. © 2016 The Authors.
14. An estimate of the number of tropical tree species
- Author
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Slik, J.W.F., Arroyo-Rodríguez, V., Aiba, Shin-Ichiro, Álvarez Loayza, P., Alvese, L.F., Ashton, P., Balvanera, Patricia, Bastian, M.L., Bellingham, P.J., Berg, E. van den, Bernacci, L., Conceição Bispo, P.da, Blanc, Lilian, Bohning-Gaese, K., Boeckx, P., Bongers, F., Boyle, B., Bradford, M., Brearley, F.Q., Hockemba, M.B.-N., Bunyavejchewin, S., Matos, D.C.L., Castillo-Santiago, M., Catharino, E.L.M., Chai, S.L., Chen, Y., Colwell, R.K., Robin, C.L., Clark, C., Clark, D.B., Clark, D.A., Culmsee, H., Damas, K., Dattaraja, H.S., Dauby, G., Davidar, P., DeWalt, S.J., Doucet, J.L., Duque, A., Durigan, G., Eichhorn, K.A.O., Eisenlohr, P.V., Eler, E., Ewango, C.E.N., Farwig, N., Feeley, K.J., Ferreira, L., Field, R., Oliveira Filho, A.T. de, Fletcher, C., Forshed, O., Franco, G., Fredriksson, G., Gillespie, T., Gillet, J.F., Amarnath, Giriraj, Griffith, D.M., Grogan, J., Gunatilleke, N., Harris, D., Harrison, R., Hector, A., Homeier, J., Imai, N., Itoh, A., Jansen, P.A., Joly, C.A., Jong, B.H.J. de, Kartawinata, K., Kearsley, E., Kelly, D.L., Kenfack, D., Kessler, M., Kitayama, K., Kooyman, R., Larney, E., Laumonier, Y., Laurance, S.G.W., Laurance, W.F., Lawes, M.J., Amaral, I.L.do, Letcher, S.G., Lindsell, J., Lu, X., Mansor, A., Marjokorpi, A., Martin, E.H., Meilby, H., Melo, F.P.L., Metcalfea, D.J., Medjibe, V.P., Metzger, J.P., Millet, J., Mohandass, D., Montero, J.C., Morisson Valeriano, M. de, Mugerwa, B., Nagamasu, H., Nilus, R., Onrizal, S.O.G., Page, N., Parolin, P., Parren, M., Parthasarathy, N., Paudel, E., Permana, A., Piedade, M.T.F., Pitman, N.C.A., Poorter, L., Poulsen, A.D., Poulsen, J., Powers, J., Prasad, R.C., Puyravaud, J.-P., Razafimahaimodison, J.C., Reitsma, J., Santos, J.R. dos, Spironello, W.R., Romero Saltos, H., Rovero, F., Rozak, A.H., Ruokolainen, K., Rutishauser, E., Saiter, F., Saner, P., Santos, B.A., Santos, F., Sarker, S.K., Satdichanh, M., Schmitt, C.B., Schongart, J., Schulze, M., Suganuma, M.S., Sheil, Douglas, Silva Pinheiro, E.da, Sist, P., Stevart, T., Sukumar, R., Sun, I.-F., Sunderland, Terry C.H., Suresh, H.S., Suzuki, E., Tabarelli, M., Tang, J., Targhetta, N., Theilade, I., Thomas, D.W., Tchouto, P., Hurtado, J., Valencia, R., Valkenburg, J.L.C.H. van, Van Do, T., Vásquez, R., Verbeeck, H., Adekunle, V., Vieira, S.A., Webb, C.O., Whitfeld, T., Wich, S.A., Williams, J., Wittmann, F., Woll, H., Yang, X., Yao, C.Y.A., Yap, S.L., Yoneda, T., Zahawi, R.A., Zakaria, R., Zang, R., Assis, R.L. de, Luize, B.G., Venticinque, E.M., Slik, J.W.F., Arroyo-Rodríguez, V., Aiba, Shin-Ichiro, Álvarez Loayza, P., Alvese, L.F., Ashton, P., Balvanera, Patricia, Bastian, M.L., Bellingham, P.J., Berg, E. van den, Bernacci, L., Conceição Bispo, P.da, Blanc, Lilian, Bohning-Gaese, K., Boeckx, P., Bongers, F., Boyle, B., Bradford, M., Brearley, F.Q., Hockemba, M.B.-N., Bunyavejchewin, S., Matos, D.C.L., Castillo-Santiago, M., Catharino, E.L.M., Chai, S.L., Chen, Y., Colwell, R.K., Robin, C.L., Clark, C., Clark, D.B., Clark, D.A., Culmsee, H., Damas, K., Dattaraja, H.S., Dauby, G., Davidar, P., DeWalt, S.J., Doucet, J.L., Duque, A., Durigan, G., Eichhorn, K.A.O., Eisenlohr, P.V., Eler, E., Ewango, C.E.N., Farwig, N., Feeley, K.J., Ferreira, L., Field, R., Oliveira Filho, A.T. de, Fletcher, C., Forshed, O., Franco, G., Fredriksson, G., Gillespie, T., Gillet, J.F., Amarnath, Giriraj, Griffith, D.M., Grogan, J., Gunatilleke, N., Harris, D., Harrison, R., Hector, A., Homeier, J., Imai, N., Itoh, A., Jansen, P.A., Joly, C.A., Jong, B.H.J. de, Kartawinata, K., Kearsley, E., Kelly, D.L., Kenfack, D., Kessler, M., Kitayama, K., Kooyman, R., Larney, E., Laumonier, Y., Laurance, S.G.W., Laurance, W.F., Lawes, M.J., Amaral, I.L.do, Letcher, S.G., Lindsell, J., Lu, X., Mansor, A., Marjokorpi, A., Martin, E.H., Meilby, H., Melo, F.P.L., Metcalfea, D.J., Medjibe, V.P., Metzger, J.P., Millet, J., Mohandass, D., Montero, J.C., Morisson Valeriano, M. de, Mugerwa, B., Nagamasu, H., Nilus, R., Onrizal, S.O.G., Page, N., Parolin, P., Parren, M., Parthasarathy, N., Paudel, E., Permana, A., Piedade, M.T.F., Pitman, N.C.A., Poorter, L., Poulsen, A.D., Poulsen, J., Powers, J., Prasad, R.C., Puyravaud, J.-P., Razafimahaimodison, J.C., Reitsma, J., Santos, J.R. dos, Spironello, W.R., Romero Saltos, H., Rovero, F., Rozak, A.H., Ruokolainen, K., Rutishauser, E., Saiter, F., Saner, P., Santos, B.A., Santos, F., Sarker, S.K., Satdichanh, M., Schmitt, C.B., Schongart, J., Schulze, M., Suganuma, M.S., Sheil, Douglas, Silva Pinheiro, E.da, Sist, P., Stevart, T., Sukumar, R., Sun, I.-F., Sunderland, Terry C.H., Suresh, H.S., Suzuki, E., Tabarelli, M., Tang, J., Targhetta, N., Theilade, I., Thomas, D.W., Tchouto, P., Hurtado, J., Valencia, R., Valkenburg, J.L.C.H. van, Van Do, T., Vásquez, R., Verbeeck, H., Adekunle, V., Vieira, S.A., Webb, C.O., Whitfeld, T., Wich, S.A., Williams, J., Wittmann, F., Woll, H., Yang, X., Yao, C.Y.A., Yap, S.L., Yoneda, T., Zahawi, R.A., Zakaria, R., Zang, R., Assis, R.L. de, Luize, B.G., and Venticinque, E.M.
15. An estimate of the number of tropical tree species
- Author
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Slik, J.W.F., Arroyo-Rodríguez, V., Aiba, Shin-Ichiro, Álvarez Loayza, P., Alvese, L.F., Ashton, P., Balvanera, Patricia, Bastian, M.L., Bellingham, P.J., Berg, E. van den, Bernacci, L., Conceição Bispo, P.da, Blanc, Lilian, Bohning-Gaese, K., Boeckx, P., Bongers, F., Boyle, B., Bradford, M., Brearley, F.Q., Hockemba, M.B.-N., Bunyavejchewin, S., Matos, D.C.L., Castillo-Santiago, M., Catharino, E.L.M., Chai, S.L., Chen, Y., Colwell, R.K., Robin, C.L., Clark, C., Clark, D.B., Clark, D.A., Culmsee, H., Damas, K., Dattaraja, H.S., Dauby, G., Davidar, P., DeWalt, S.J., Doucet, J.L., Duque, A., Durigan, G., Eichhorn, K.A.O., Eisenlohr, P.V., Eler, E., Ewango, C.E.N., Farwig, N., Feeley, K.J., Ferreira, L., Field, R., Oliveira Filho, A.T. de, Fletcher, C., Forshed, O., Franco, G., Fredriksson, G., Gillespie, T., Gillet, J.F., Amarnath, Giriraj, Griffith, D.M., Grogan, J., Gunatilleke, N., Harris, D., Harrison, R., Hector, A., Homeier, J., Imai, N., Itoh, A., Jansen, P.A., Joly, C.A., Jong, B.H.J. de, Kartawinata, K., Kearsley, E., Kelly, D.L., Kenfack, D., Kessler, M., Kitayama, K., Kooyman, R., Larney, E., Laumonier, Y., Laurance, S.G.W., Laurance, W.F., Lawes, M.J., Amaral, I.L.do, Letcher, S.G., Lindsell, J., Lu, X., Mansor, A., Marjokorpi, A., Martin, E.H., Meilby, H., Melo, F.P.L., Metcalfea, D.J., Medjibe, V.P., Metzger, J.P., Millet, J., Mohandass, D., Montero, J.C., Morisson Valeriano, M. de, Mugerwa, B., Nagamasu, H., Nilus, R., Onrizal, S.O.G., Page, N., Parolin, P., Parren, M., Parthasarathy, N., Paudel, E., Permana, A., Piedade, M.T.F., Pitman, N.C.A., Poorter, L., Poulsen, A.D., Poulsen, J., Powers, J., Prasad, R.C., Puyravaud, J.-P., Razafimahaimodison, J.C., Reitsma, J., Santos, J.R. dos, Spironello, W.R., Romero Saltos, H., Rovero, F., Rozak, A.H., Ruokolainen, K., Rutishauser, E., Saiter, F., Saner, P., Santos, B.A., Santos, F., Sarker, S.K., Satdichanh, M., Schmitt, C.B., Schongart, J., Schulze, M., Suganuma, M.S., Sheil, Douglas, Silva Pinheiro, E.da, Sist, P., Stevart, T., Sukumar, R., Sun, I.-F., Sunderland, Terry C.H., Suresh, H.S., Suzuki, E., Tabarelli, M., Tang, J., Targhetta, N., Theilade, I., Thomas, D.W., Tchouto, P., Hurtado, J., Valencia, R., Valkenburg, J.L.C.H. van, Van Do, T., Vásquez, R., Verbeeck, H., Adekunle, V., Vieira, S.A., Webb, C.O., Whitfeld, T., Wich, S.A., Williams, J., Wittmann, F., Woll, H., Yang, X., Yao, C.Y.A., Yap, S.L., Yoneda, T., Zahawi, R.A., Zakaria, R., Zang, R., Assis, R.L. de, Luize, B.G., Venticinque, E.M., Slik, J.W.F., Arroyo-Rodríguez, V., Aiba, Shin-Ichiro, Álvarez Loayza, P., Alvese, L.F., Ashton, P., Balvanera, Patricia, Bastian, M.L., Bellingham, P.J., Berg, E. van den, Bernacci, L., Conceição Bispo, P.da, Blanc, Lilian, Bohning-Gaese, K., Boeckx, P., Bongers, F., Boyle, B., Bradford, M., Brearley, F.Q., Hockemba, M.B.-N., Bunyavejchewin, S., Matos, D.C.L., Castillo-Santiago, M., Catharino, E.L.M., Chai, S.L., Chen, Y., Colwell, R.K., Robin, C.L., Clark, C., Clark, D.B., Clark, D.A., Culmsee, H., Damas, K., Dattaraja, H.S., Dauby, G., Davidar, P., DeWalt, S.J., Doucet, J.L., Duque, A., Durigan, G., Eichhorn, K.A.O., Eisenlohr, P.V., Eler, E., Ewango, C.E.N., Farwig, N., Feeley, K.J., Ferreira, L., Field, R., Oliveira Filho, A.T. de, Fletcher, C., Forshed, O., Franco, G., Fredriksson, G., Gillespie, T., Gillet, J.F., Amarnath, Giriraj, Griffith, D.M., Grogan, J., Gunatilleke, N., Harris, D., Harrison, R., Hector, A., Homeier, J., Imai, N., Itoh, A., Jansen, P.A., Joly, C.A., Jong, B.H.J. de, Kartawinata, K., Kearsley, E., Kelly, D.L., Kenfack, D., Kessler, M., Kitayama, K., Kooyman, R., Larney, E., Laumonier, Y., Laurance, S.G.W., Laurance, W.F., Lawes, M.J., Amaral, I.L.do, Letcher, S.G., Lindsell, J., Lu, X., Mansor, A., Marjokorpi, A., Martin, E.H., Meilby, H., Melo, F.P.L., Metcalfea, D.J., Medjibe, V.P., Metzger, J.P., Millet, J., Mohandass, D., Montero, J.C., Morisson Valeriano, M. de, Mugerwa, B., Nagamasu, H., Nilus, R., Onrizal, S.O.G., Page, N., Parolin, P., Parren, M., Parthasarathy, N., Paudel, E., Permana, A., Piedade, M.T.F., Pitman, N.C.A., Poorter, L., Poulsen, A.D., Poulsen, J., Powers, J., Prasad, R.C., Puyravaud, J.-P., Razafimahaimodison, J.C., Reitsma, J., Santos, J.R. dos, Spironello, W.R., Romero Saltos, H., Rovero, F., Rozak, A.H., Ruokolainen, K., Rutishauser, E., Saiter, F., Saner, P., Santos, B.A., Santos, F., Sarker, S.K., Satdichanh, M., Schmitt, C.B., Schongart, J., Schulze, M., Suganuma, M.S., Sheil, Douglas, Silva Pinheiro, E.da, Sist, P., Stevart, T., Sukumar, R., Sun, I.-F., Sunderland, Terry C.H., Suresh, H.S., Suzuki, E., Tabarelli, M., Tang, J., Targhetta, N., Theilade, I., Thomas, D.W., Tchouto, P., Hurtado, J., Valencia, R., Valkenburg, J.L.C.H. van, Van Do, T., Vásquez, R., Verbeeck, H., Adekunle, V., Vieira, S.A., Webb, C.O., Whitfeld, T., Wich, S.A., Williams, J., Wittmann, F., Woll, H., Yang, X., Yao, C.Y.A., Yap, S.L., Yoneda, T., Zahawi, R.A., Zakaria, R., Zang, R., Assis, R.L. de, Luize, B.G., and Venticinque, E.M.
16. Distribution of Pteridophyta and Melastomataceae along an edaphic gradient in an Amazonian rain forest
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Ruokolainen, K. and Tuomisto, H.
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MELASTOMATACEAE ,PTERIDOPHYTA ,RAIN forests - Published
- 1994
17. The role of ecological knowledge in explaining biogeography and biodiversity in Amazonia
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Ruokolainen, K. and Tuomisto, H.
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BIODIVERSITY ,RAIN forests - Abstract
Biogeographical studies in Amazonia have commonly taken a historical, rather than an ecological approach. General patterns have been sought in the distribution maps of different species, and these have beenexplained in terms of past or present distribution barriers, especially past climates an large rivers. Implicitly, and often also explicitly, it is assumed that Amazonia is ecologically so uniform that present-day ecological conditions are rather insignificant in determiningspecie distribution patterns and speciation. However, this assumption is more based on the lack of relevant data than on actual observations of environmental uniformity or ecological unspecialization of thespecies. Recent studies have indeed documented ecological heterogeneity and floristic difference among sites that were previously thoughtsimilar. In the absence of direct knowledge of the past, more complete ecological and environmental understanding of the present-day Amazonia are needed for evaluating the relative roles of historical and ecological factors in Amazonian biogeography and biodiversity. [ABSTRACT FROM AUTHOR]
- Published
- 1997
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18. Understanding different dominance patterns in western Amazonian forests.
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Matas-Granados L, Draper FC, Cayuela L, de Aledo JG, Arellano G, Saadi CB, Baker TR, Phillips OL, Honorio Coronado EN, Ruokolainen K, García-Villacorta R, Roucoux KH, Guèze M, Sandoval EV, Fine PVA, Amasifuen Guerra CA, Gomez RZ, Stevenson Diaz PR, Monteagudo-Mendoza A, Martinez RV, Socolar JB, Disney M, Del Aguila Pasquel J, Llampazo GF, Arenas JV, Huaymacari JR, Grandez Rios JM, and Macía MJ
- Subjects
- Humans, Trees, Brazil, Biodiversity, Ecosystem, Forests
- Abstract
Dominance of neotropical tree communities by a few species is widely documented, but dominant trees show a variety of distributional patterns still poorly understood. Here, we used 503 forest inventory plots (93,719 individuals ≥2.5 cm diameter, 2609 species) to explore the relationships between local abundance, regional frequency and spatial aggregation of dominant species in four main habitat types in western Amazonia. Although the abundance-occupancy relationship is positive for the full dataset, we found that among dominant Amazonian tree species, there is a strong negative relationship between local abundance and regional frequency and/or spatial aggregation across habitat types. Our findings suggest an ecological trade-off whereby dominant species can be locally abundant (local dominants) or regionally widespread (widespread dominants), but rarely both (oligarchs). Given the importance of dominant species as drivers of diversity and ecosystem functioning, unravelling different dominance patterns is a research priority to direct conservation efforts in Amazonian forests., (© 2023 The Authors. Ecology Letters published by John Wiley & Sons Ltd.)
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- 2024
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19. Does environmental adaptation or dispersal history explain the geographical distribution of Ixodes ricinus and Ixodes persulcatus ticks in Finland?
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Kulha N, Ruokolainen K, Vesterinen EJ, Lamppu M, Klemola T, and Sormunen JJ
- Abstract
In Finland, the distribution area of the taiga tick, Ixodes persulcatus (Schulze, 1930), is nested within a broader area of distribution of a congeneric species, the sheep tick, Ixodes ricinus (Linnaeus, 1758) (Acari: Ixodidae). We assess whether distinct environmental adaptations or dispersal history provides a more parsimonious explanation for the differences in the distributions of the two common and medically important ixodids in Finland. We used an innovative spatially constrained randomization procedure to analyze whether crowdsourced occurrence data points of the two tick species had statistically different associations with any of the 28 environmental variables. Using points of presence in a region of species co-occurrence, we built Maxent models to examine whether environmental factors or dispersal history could explain the absence of I. persulcatus in a part of the range of I. ricinus in Finland. Five environmental variables-number of inhabitants, road length, elevation above sea level, proportion of barren bedrock and boulders, and proportion of unsorted glacial deposits-were significant at p ≤ .05, indicating greater between-species difference in original than in the randomized data. Of these variables, only the optimum value for unsorted glacial deposits was higher for I. persulcatus than for I. ricinus . Maxent models also predicted high relative habitat suitability (suitability >80%) for I. persulcatus south of its current, sharply bounded distribution range, suggesting that the species has not fulfilled its distribution potential in Finland. The two most common and medically relevant ixodids in Finland may colonize habitats with different environmental conditions. On the contrary, the recent establishment and ongoing dispersion of I. persulcatus in Fennoscandia rather than environmental conditions cause the southernmost distribution limit of the species in Finland., Competing Interests: The authors declare that the research was conducted in the absence of any commercial, financial, or other relationships that could be construed as a potential conflict of interest., (© 2022 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd.)
- Published
- 2022
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20. Amazon tree dominance across forest strata.
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Draper FC, Costa FRC, Arellano G, Phillips OL, Duque A, Macía MJ, Ter Steege H, Asner GP, Berenguer E, Schietti J, Socolar JB, de Souza FC, Dexter KG, Jørgensen PM, Tello JS, Magnusson WE, Baker TR, Castilho CV, Monteagudo-Mendoza A, Fine PVA, Ruokolainen K, Coronado ENH, Aymard G, Dávila N, Sáenz MS, Paredes MAR, Engel J, Fortunel C, Paine CET, Goret JY, Dourdain A, Petronelli P, Allie E, Andino JEG, Brienen RJW, Pérez LC, Manzatto ÂG, Zambrana NYP, Molino JF, Sabatier D, Chave J, Fauset S, Villacorta RG, Réjou-Méchain M, Berry PE, Melgaço K, Feldpausch TR, Sandoval EV, Martinez RV, Mesones I, Junqueira AB, Roucoux KH, de Toledo JJ, Andrade AC, Camargo JL, Del Aguila Pasquel J, Santana FD, Laurance WF, Laurance SG, Lovejoy TE, Comiskey JA, Galbraith DR, Kalamandeen M, Aguilar GEN, Arenas JV, Guerra CAA, Flores M, Llampazo GF, Montenegro LAT, Gomez RZ, Pansonato MP, Moscoso VC, Vleminckx J, Barrantes OJV, Duivenvoorden JF, de Sousa SA, Arroyo L, Perdiz RO, Cravo JS, Marimon BS, Junior BHM, Carvalho FA, Damasco G, Disney M, Vital MS, Diaz PRS, Vicentini A, Nascimento H, Higuchi N, Van Andel T, Malhi Y, Ribeiro SC, Terborgh JW, Thomas RS, Dallmeier F, Prieto A, Hilário RR, Salomão RP, Silva RDC, Casas LF, Vieira ICG, Araujo-Murakami A, Arevalo FR, Ramírez-Angulo H, Torre EV, Peñuela MC, Killeen TJ, Pardo G, Jimenez-Rojas E, Castro W, Cabrera DG, Pipoly J, de Sousa TR, Silvera M, Vos V, Neill D, Vargas PN, Vela DM, Aragão LEOC, Umetsu RK, Sierra R, Wang O, Young KR, Prestes NCCS, Massi KG, Huaymacari JR, Gutierrez GAP, Aldana AM, Alexiades MN, Baccaro F, Céron C, Muelbert AE, Rios JMG, Lima AS, Lloyd JL, Pitman NCA, Gamarra LV, Oroche CJC, Fuentes AF, Palacios W, Patiño S, Torres-Lezama A, and Baraloto C
- Subjects
- Biodiversity, Brazil, Humans, Forests, Trees
- Abstract
The forests of Amazonia are among the most biodiverse plant communities on Earth. Given the immediate threats posed by climate and land-use change, an improved understanding of how this extraordinary biodiversity is spatially organized is urgently required to develop effective conservation strategies. Most Amazonian tree species are extremely rare but a few are common across the region. Indeed, just 227 'hyperdominant' species account for >50% of all individuals >10 cm diameter at 1.3 m in height. Yet, the degree to which the phenomenon of hyperdominance is sensitive to tree size, the extent to which the composition of dominant species changes with size class and how evolutionary history constrains tree hyperdominance, all remain unknown. Here, we use a large floristic dataset to show that, while hyperdominance is a universal phenomenon across forest strata, different species dominate the forest understory, midstory and canopy. We further find that, although species belonging to a range of phylogenetically dispersed lineages have become hyperdominant in small size classes, hyperdominants in large size classes are restricted to a few lineages. Our results demonstrate that it is essential to consider all forest strata to understand regional patterns of dominance and composition in Amazonia. More generally, through the lens of 654 hyperdominant species, we outline a tractable pathway for understanding the functioning of half of Amazonian forests across vertical strata and geographical locations.
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- 2021
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21. Bamboo, climate change and forest use: A critical combination for southwestern Amazonian forests?
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Ferreira E, Kalliola R, and Ruokolainen K
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- Brazil, Ecosystem, Forests, Peru, Trees, Climate Change, Fires
- Abstract
About 160 000 km
2 of forests in the border zone between Brazil and Peru are dominated by semi-scandent bamboos (Guadua spp.). We argue that both predicted decreased precipitation during the dry season and widespread anthropogenic disturbances will significantly increase the distribution and biomass of bamboos in the area. Seasonal dryness favours the growth of evergreen bamboos in relation to trees that shed their leaves during the dry season. Disturbance can be beneficial for the bamboo because, as a clonal plant, it is often able to recover more rapidly than trees. It also withstands dry season better than many trees. The bamboo life cycle ends in a mass mortality event every 28 years, producing potential fuel for a forest fire. Presently, natural forest fires hardly exist in the area. However, in the projected future climate with more pronounced dry season and with increased fuel load after bamboo die-off events the forests may start to catch fire that has escaped from inhabited areas or even started naturally. Fires can kill trees, thus further increasing the fuel load of the forest. As a result, the landscape may start to convert to a savanna ecosystem.- Published
- 2020
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22. White sand vegetation in an Amazonian lowland under the perspective of a young geological history.
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Rossetti DF, Moulatlet GM, Tuomisto H, Gribel R, Toledo PM, Valeriano MM, Ruokolainen K, Cohen MCL, Cordeiro CLO, Rennó CD, Coelho LS, and Ferreira CAC
- Subjects
- Brazil, Geography, Sand, Geologic Sediments, Geological Phenomena, Melastomataceae, Tracheophyta
- Abstract
What controls the formation of patchy substrates of white sand vegetation in the Amazonian lowlands is still unclear. This research integrated the geological history and plant inventories of a white sand vegetation patch confined to one large fan-shaped sandy substrate of northern Amazonia, which is related to a megafan environment. We examined floristic patterns to determine whether abundant species are more often generalists than the rarer one, by comparing the megafan environments and older basement rocks. We also investigated the pattern of species accumulation as a function of increasing sampling effort. All plant groups recorded a high proportion of generalist species on the megafan sediments compared to older basement rocks. The vegetation structure is controlled by topographic gradients resulting from the smooth slope of the megafan morphology and microreliefs imposed by various megafan subenvironments. Late Pleistocene-Holocene environmental disturbances caused by megafan sedimentary processes controlled the distribution of white sand vegetation over a large area of the Amazonian lowlands, and may have also been an important factor in species diversification during this period. The integration of geological and biological data may shed new light on the existence of many patches of white sand vegetation from the plains of northern Amazonia.
- Published
- 2019
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23. Evolution within a language: environmental differences contribute to divergence of dialect groups.
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Honkola T, Ruokolainen K, Syrjänen KJJ, Leino UP, Tammi I, Wahlberg N, and Vesakoski O
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- Adaptation, Physiological, Culture, Finland, Genetic Variation, Geography, Humans, Linguistics, Models, Theoretical, Biological Evolution, Environment, Language
- Abstract
Background: The processes leading to the diversity of over 7000 present-day languages have been the subject of scholarly interest for centuries. Several factors have been suggested to contribute to the spatial segregation of speaker populations and the subsequent linguistic divergence. However, their formal testing and the quantification of their relative roles is still missing. We focussed here on the early stages of the linguistic divergence process, that is, the divergence of dialects, with a special focus on the ecological settings of the speaker populations. We adopted conceptual and statistical approaches from biological microevolution and parallelled intra-lingual variation with genetic variation within a species. We modelled the roles of geographical distance, differences in environmental and cultural conditions and in administrative history on linguistic divergence at two different levels: between municipal dialects (cf. in biology, between individuals) and between dialect groups (cf. in biology, between populations)., Results: We found that geographical distance and administrative history were important in separating municipal dialects. However, environmental and cultural differences contributed markedly to the divergence of dialect groups. In biology, increase in genetic differences between populations together with environmental differences may suggest genetic differentiation of populations through adaptation to the local environment. However, our interpretation of this result is not that language itself adapts to the environment. Instead, it is based on Homo sapiens being affected by its environment, and its capability to adapt culturally to various environmental conditions. The differences in cultural adaptations arising from environmental heterogeneity could have acted as nonphysical barriers and limited the contacts and communication between groups. As a result, linguistic differentiation may emerge over time in those speaker populations which are, at least partially, separated., Conclusions: Given that the dialects of isolated speaker populations may eventually evolve into different languages, our result suggests that cultural adaptation to local environment and the associated isolation of speaker populations have contributed to the emergence of the global patterns of linguistic diversity.
- Published
- 2018
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24. Phylogenetic classification of the world's tropical forests.
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Slik JWF, Franklin J, Arroyo-Rodríguez V, Field R, Aguilar S, Aguirre N, Ahumada J, Aiba SI, Alves LF, K A, Avella A, Mora F, Aymard C GA, Báez S, Balvanera P, Bastian ML, Bastin JF, Bellingham PJ, van den Berg E, da Conceição Bispo P, Boeckx P, Boehning-Gaese K, Bongers F, Boyle B, Brambach F, Brearley FQ, Brown S, Chai SL, Chazdon RL, Chen S, Chhang P, Chuyong G, Ewango C, Coronado IM, Cristóbal-Azkarate J, Culmsee H, Damas K, Dattaraja HS, Davidar P, DeWalt SJ, Din H, Drake DR, Duque A, Durigan G, Eichhorn K, Eler ES, Enoki T, Ensslin A, Fandohan AB, Farwig N, Feeley KJ, Fischer M, Forshed O, Garcia QS, Garkoti SC, Gillespie TW, Gillet JF, Gonmadje C, Granzow-de la Cerda I, Griffith DM, Grogan J, Hakeem KR, Harris DJ, Harrison RD, Hector A, Hemp A, Homeier J, Hussain MS, Ibarra-Manríquez G, Hanum IF, Imai N, Jansen PA, Joly CA, Joseph S, Kartawinata K, Kearsley E, Kelly DL, Kessler M, Killeen TJ, Kooyman RM, Laumonier Y, Laurance SG, Laurance WF, Lawes MJ, Letcher SG, Lindsell J, Lovett J, Lozada J, Lu X, Lykke AM, Mahmud KB, Mahayani NPD, Mansor A, Marshall AR, Martin EH, Calderado Leal Matos D, Meave JA, Melo FPL, Mendoza ZHA, Metali F, Medjibe VP, Metzger JP, Metzker T, Mohandass D, Munguía-Rosas MA, Muñoz R, Nurtjahy E, de Oliveira EL, Onrizal, Parolin P, Parren M, Parthasarathy N, Paudel E, Perez R, Pérez-García EA, Pommer U, Poorter L, Qie L, Piedade MTF, Pinto JRR, Poulsen AD, Poulsen JR, Powers JS, Prasad RC, Puyravaud JP, Rangel O, Reitsma J, Rocha DSB, Rolim S, Rovero F, Rozak A, Ruokolainen K, Rutishauser E, Rutten G, Mohd Said MN, Saiter FZ, Saner P, Santos B, Dos Santos JR, Sarker SK, Schmitt CB, Schoengart J, Schulze M, Sheil D, Sist P, Souza AF, Spironello WR, Sposito T, Steinmetz R, Stevart T, Suganuma MS, Sukri R, Sultana A, Sukumar R, Sunderland T, Supriyadi, Suresh HS, Suzuki E, Tabarelli M, Tang J, Tanner EVJ, Targhetta N, Theilade I, Thomas D, Timberlake J, de Morisson Valeriano M, van Valkenburg J, Van Do T, Van Sam H, Vandermeer JH, Verbeeck H, Vetaas OR, Adekunle V, Vieira SA, Webb CO, Webb EL, Whitfeld T, Wich S, Williams J, Wiser S, Wittmann F, Yang X, Adou Yao CY, Yap SL, Zahawi RA, Zakaria R, and Zang R
- Subjects
- Biodiversity, Conservation of Natural Resources, Environmental Monitoring, Forests, Phylogeny, Plants classification, Plants genetics, Tropical Climate
- Abstract
Knowledge about the biogeographic affinities of the world's tropical forests helps to better understand regional differences in forest structure, diversity, composition, and dynamics. Such understanding will enable anticipation of region-specific responses to global environmental change. Modern phylogenies, in combination with broad coverage of species inventory data, now allow for global biogeographic analyses that take species evolutionary distance into account. Here we present a classification of the world's tropical forests based on their phylogenetic similarity. We identify five principal floristic regions and their floristic relationships: ( i ) Indo-Pacific, ( ii ) Subtropical, ( iii ) African, ( iv ) American, and ( v ) Dry forests. Our results do not support the traditional neo- versus paleotropical forest division but instead separate the combined American and African forests from their Indo-Pacific counterparts. We also find indications for the existence of a global dry forest region, with representatives in America, Africa, Madagascar, and India. Additionally, a northern-hemisphere Subtropical forest region was identified with representatives in Asia and America, providing support for a link between Asian and American northern-hemisphere forests., Competing Interests: Conflict of interest statement: V.A.-R., K.B.-G., B.B., F.Q.B., N.F., M.K., W.F.L., S. G. Letcher, C.B.S., D.S., T. Stevart, and S. Wiser have coauthored papers with Jens-Christian Svenning in the past 48 months. A.M.L. and Jens-Christian Svenning are both affiliated with Aarhus University., (Copyright © 2018 the Author(s). Published by PNAS.)
- Published
- 2018
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25. Using digital soil maps to infer edaphic affinities of plant species in Amazonia: Problems and prospects.
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Moulatlet GM, Zuquim G, Figueiredo FOG, Lehtonen S, Emilio T, Ruokolainen K, and Tuomisto H
- Abstract
Amazonia combines semi-continental size with difficult access, so both current ranges of species and their ability to cope with environmental change have to be inferred from sparse field data. Although efficient techniques for modeling species distributions on the basis of a small number of species occurrences exist, their success depends on the availability of relevant environmental data layers. Soil data are important in this context, because soil properties have been found to determine plant occurrence patterns in Amazonian lowlands at all spatial scales. Here we evaluate the potential for this purpose of three digital soil maps that are freely available online: SOTERLAC, HWSD, and SoilGrids. We first tested how well they reflect local soil cation concentration as documented with 1,500 widely distributed soil samples. We found that measured soil cation concentration differed by up to two orders of magnitude between sites mapped into the same soil class. The best map-based predictor of local soil cation concentration was obtained with a regression model combining soil classes from HWSD with cation exchange capacity (CEC) from SoilGrids. Next, we evaluated to what degree the known edaphic affinities of thirteen plant species (as documented with field data from 1,200 of the soil sample sites) can be inferred from the soil maps. The species segregated clearly along the soil cation concentration gradient in the field, but only partially along the model-estimated cation concentration gradient, and hardly at all along the mapped CEC gradient. The main problems reducing the predictive ability of the soil maps were insufficient spatial resolution and/or georeferencing errors combined with thematic inaccuracy and absence of the most relevant edaphic variables. Addressing these problems would provide better models of the edaphic environment for ecological studies in Amazonia.
- Published
- 2017
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26. Evolutionary heritage influences Amazon tree ecology.
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Coelho de Souza F, Dexter KG, Phillips OL, Brienen RJ, Chave J, Galbraith DR, Lopez Gonzalez G, Monteagudo Mendoza A, Pennington RT, Poorter L, Alexiades M, Álvarez-Dávila E, Andrade A, Aragão LE, Araujo-Murakami A, Arets EJ, Aymard C GA, Baraloto C, Barroso JG, Bonal D, Boot RG, Camargo JL, Comiskey JA, Valverde FC, de Camargo PB, Di Fiore A, Elias F, Erwin TL, Feldpausch TR, Ferreira L, Fyllas NM, Gloor E, Herault B, Herrera R, Higuchi N, Honorio Coronado EN, Killeen TJ, Laurance WF, Laurance S, Lloyd J, Lovejoy TE, Malhi Y, Maracahipes L, Marimon BS, Marimon-Junior BH, Mendoza C, Morandi P, Neill DA, Vargas PN, Oliveira EA, Lenza E, Palacios WA, Peñuela-Mora MC, Pipoly JJ 3rd, Pitman NC, Prieto A, Quesada CA, Ramirez-Angulo H, Rudas A, Ruokolainen K, Salomão RP, Silveira M, Stropp J, Ter Steege H, Thomas-Caesar R, van der Hout P, van der Heijden GM, van der Meer PJ, Vasquez RV, Vieira SA, Vilanova E, Vos VA, Wang O, Young KR, Zagt RJ, and Baker TR
- Subjects
- Biological Evolution, Ecology, South America, Forests, Phylogeny, Trees classification, Tropical Climate
- Abstract
Lineages tend to retain ecological characteristics of their ancestors through time. However, for some traits, selection during evolutionary history may have also played a role in determining trait values. To address the relative importance of these processes requires large-scale quantification of traits and evolutionary relationships among species. The Amazonian tree flora comprises a high diversity of angiosperm lineages and species with widely differing life-history characteristics, providing an excellent system to investigate the combined influences of evolutionary heritage and selection in determining trait variation. We used trait data related to the major axes of life-history variation among tropical trees (e.g. growth and mortality rates) from 577 inventory plots in closed-canopy forest, mapped onto a phylogenetic hypothesis spanning more than 300 genera including all major angiosperm clades to test for evolutionary constraints on traits. We found significant phylogenetic signal (PS) for all traits, consistent with evolutionarily related genera having more similar characteristics than expected by chance. Although there is also evidence for repeated evolution of pioneer and shade tolerant life-history strategies within independent lineages, the existence of significant PS allows clearer predictions of the links between evolutionary diversity, ecosystem function and the response of tropical forests to global change., (© 2016 The Authors.)
- Published
- 2016
- Full Text
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27. Urban Power Line Corridors as Novel Habitats for Grassland and Alien Plant Species in South-Western Finland.
- Author
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Lampinen J, Ruokolainen K, and Huhta AP
- Subjects
- Conservation of Natural Resources, Ecosystem, Finland, Linear Models, Soil chemistry, Urbanization, Grassland, Introduced Species, Plant Physiological Phenomena, Plants classification, Power Plants
- Abstract
Regularly managed electric power line corridors may provide habitats for both early-successional grassland plant species and disturbance-dependent alien plant species. These habitats are especially important in urban areas, where they can help conserve native grassland species and communities in urban greenspace. However, they can also provide further footholds for potentially invasive alien species that already characterize urban areas. In order to implement power line corridors into urban conservation, it is important to understand which environmental conditions in the corridors favor grassland species and which alien species. Likewise it is important to know whether similar environmental factors in the corridors control the species composition of the two groups. We conducted a vegetation study in a 43 kilometer long urban power line corridor network in south-western Finland, and used generalized linear models and distance-based redundancy analysis to determine which environmental factors best predict the occurrence and composition of grassland and alien plant species in the corridors. The results imply that old corridors on dry soils and steep slopes characterized by a history as open areas and pastures are especially suitable for grassland species. Corridors suitable for alien species, in turn, are characterized by productive soils and abundant light and are surrounded by a dense urban fabric. Factors controlling species composition in the two groups are somewhat correlated, with the most important factors including light abundance, soil moisture, soil calcium concentration and soil productivity. The results have implications for grassland conservation and invasive alien species control in urban areas.
- Published
- 2015
- Full Text
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28. An estimate of the number of tropical tree species.
- Author
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Slik JW, Arroyo-Rodríguez V, Aiba S, Alvarez-Loayza P, Alves LF, Ashton P, Balvanera P, Bastian ML, Bellingham PJ, van den Berg E, Bernacci L, da Conceição Bispo P, Blanc L, Böhning-Gaese K, Boeckx P, Bongers F, Boyle B, Bradford M, Brearley FQ, Breuer-Ndoundou Hockemba M, Bunyavejchewin S, Calderado Leal Matos D, Castillo-Santiago M, Catharino EL, Chai SL, Chen Y, Colwell RK, Chazdon RL, Clark C, Clark DB, Clark DA, Culmsee H, Damas K, Dattaraja HS, Dauby G, Davidar P, DeWalt SJ, Doucet JL, Duque A, Durigan G, Eichhorn KA, Eisenlohr PV, Eler E, Ewango C, Farwig N, Feeley KJ, Ferreira L, Field R, de Oliveira Filho AT, Fletcher C, Forshed O, Franco G, Fredriksson G, Gillespie T, Gillet JF, Amarnath G, Griffith DM, Grogan J, Gunatilleke N, Harris D, Harrison R, Hector A, Homeier J, Imai N, Itoh A, Jansen PA, Joly CA, de Jong BH, Kartawinata K, Kearsley E, Kelly DL, Kenfack D, Kessler M, Kitayama K, Kooyman R, Larney E, Laumonier Y, Laurance S, Laurance WF, Lawes MJ, Amaral IL, Letcher SG, Lindsell J, Lu X, Mansor A, Marjokorpi A, Martin EH, Meilby H, Melo FP, Metcalfe DJ, Medjibe VP, Metzger JP, Millet J, Mohandass D, Montero JC, de Morisson Valeriano M, Mugerwa B, Nagamasu H, Nilus R, Ochoa-Gaona S, Onrizal, Page N, Parolin P, Parren M, Parthasarathy N, Paudel E, Permana A, Piedade MT, Pitman NC, Poorter L, Poulsen AD, Poulsen J, Powers J, Prasad RC, Puyravaud JP, Razafimahaimodison JC, Reitsma J, Dos Santos JR, Roberto Spironello W, Romero-Saltos H, Rovero F, Rozak AH, Ruokolainen K, Rutishauser E, Saiter F, Saner P, Santos BA, Santos F, Sarker SK, Satdichanh M, Schmitt CB, Schöngart J, Schulze M, Suganuma MS, Sheil D, da Silva Pinheiro E, Sist P, Stevart T, Sukumar R, Sun IF, Sunderland T, Suresh HS, Suzuki E, Tabarelli M, Tang J, Targhetta N, Theilade I, Thomas DW, Tchouto P, Hurtado J, Valencia R, van Valkenburg JL, Van Do T, Vasquez R, Verbeeck H, Adekunle V, Vieira SA, Webb CO, Whitfeld T, Wich SA, Williams J, Wittmann F, Wöll H, Yang X, Adou Yao CY, Yap SL, Yoneda T, Zahawi RA, Zakaria R, Zang R, de Assis RL, Garcia Luize B, and Venticinque EM
- Subjects
- Conservation of Natural Resources, Databases, Factual, Ecosystem, Phylogeography, Rainforest, Species Specificity, Statistics, Nonparametric, Biodiversity, Forests, Trees classification, Tropical Climate
- Abstract
The high species richness of tropical forests has long been recognized, yet there remains substantial uncertainty regarding the actual number of tropical tree species. Using a pantropical tree inventory database from closed canopy forests, consisting of 657,630 trees belonging to 11,371 species, we use a fitted value of Fisher's alpha and an approximate pantropical stem total to estimate the minimum number of tropical forest tree species to fall between ∼ 40,000 and ∼ 53,000, i.e., at the high end of previous estimates. Contrary to common assumption, the Indo-Pacific region was found to be as species-rich as the Neotropics, with both regions having a minimum of ∼ 19,000-25,000 tree species. Continental Africa is relatively depauperate with a minimum of ∼ 4,500-6,000 tree species. Very few species are shared among the African, American, and the Indo-Pacific regions. We provide a methodological framework for estimating species richness in trees that may help refine species richness estimates of tree-dependent taxa.
- Published
- 2015
- Full Text
- View/download PDF
29. Hyperdominance in Amazonian forest carbon cycling.
- Author
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Fauset S, Johnson MO, Gloor M, Baker TR, Monteagudo M A, Brienen RJ, Feldpausch TR, Lopez-Gonzalez G, Malhi Y, ter Steege H, Pitman NC, Baraloto C, Engel J, Pétronelli P, Andrade A, Camargo JL, Laurance SG, Laurance WF, Chave J, Allie E, Vargas PN, Terborgh JW, Ruokolainen K, Silveira M, Aymard C GA, Arroyo L, Bonal D, Ramirez-Angulo H, Araujo-Murakami A, Neill D, Hérault B, Dourdain A, Torres-Lezama A, Marimon BS, Salomão RP, Comiskey JA, Réjou-Méchain M, Toledo M, Licona JC, Alarcón A, Prieto A, Rudas A, van der Meer PJ, Killeen TJ, Marimon Junior BH, Poorter L, Boot RG, Stergios B, Torre EV, Costa FR, Levis C, Schietti J, Souza P, Groot N, Arets E, Moscoso VC, Castro W, Coronado EN, Peña-Claros M, Stahl C, Barroso J, Talbot J, Vieira IC, van der Heijden G, Thomas R, Vos VA, Almeida EC, Davila EÁ, Aragão LE, Erwin TL, Morandi PS, de Oliveira EA, Valadão MB, Zagt RJ, van der Hout P, Loayza PA, Pipoly JJ, Wang O, Alexiades M, Cerón CE, Huamantupa-Chuquimaco I, Di Fiore A, Peacock J, Camacho NC, Umetsu RK, de Camargo PB, Burnham RJ, Herrera R, Quesada CA, Stropp J, Vieira SA, Steininger M, Rodríguez CR, Restrepo Z, Muelbert AE, Lewis SL, Pickavance GC, and Phillips OL
- Abstract
While Amazonian forests are extraordinarily diverse, the abundance of trees is skewed strongly towards relatively few 'hyperdominant' species. In addition to their diversity, Amazonian trees are a key component of the global carbon cycle, assimilating and storing more carbon than any other ecosystem on Earth. Here we ask, using a unique data set of 530 forest plots, if the functions of storing and producing woody carbon are concentrated in a small number of tree species, whether the most abundant species also dominate carbon cycling, and whether dominant species are characterized by specific functional traits. We find that dominance of forest function is even more concentrated in a few species than is dominance of tree abundance, with only ≈1% of Amazon tree species responsible for 50% of carbon storage and productivity. Although those species that contribute most to biomass and productivity are often abundant, species maximum size is also influential, while the identity and ranking of dominant species varies by function and by region.
- Published
- 2015
- Full Text
- View/download PDF
30. Interspecific variation in functional traits in relation to species climatic niche optima in Andean Polylepis (Rosaceae) tree species: evidence for climatic adaptations.
- Author
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Toivonen JM, Horna V, Kessler M, Ruokolainen K, and Hertel D
- Abstract
Plant functional traits can be genetically determined or phenotypically plastic. We assessed the degree of genetic determinism in the functional traits of Andean Polylepis tree species among 14 important traits that enable the species to withstand cold and dry conditions. We conducted a common garden experiment and related the species-specific means of the functional traits to the variables of climatic niche optima of the species (mean annual temperature and annual precipitation), deducing that if the interspecific variation in the functional trait is related to the species climatic niche optima according to the theoretically-expected pattern of climate-trait relationship, the variation of the trait must be genetically determined. In general, the traits were related either to species temperature or precipitation optima. For example, leaf size, maximum photosynthesis rate and root tip abundance were related to temperature, whereas light compensation and light saturation points were related to precipitation. Only leaf size showed a significant phylogenetic signal, indicating that most of the manifested climate-trait relationships are not caused purely by phylogeny, but are mainly a result of species specialisation along an environmental gradient. However, in many cases the relationships were rather weak. This suggests that important functional traits of Polylepis species involve both genetic and phenotypic components aiming to maximise the overall fitness of the species at high elevations.
- Published
- 2014
- Full Text
- View/download PDF
31. Comment on "Disentangling the drivers of β diversity along latitudinal and elevational gradients".
- Author
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Tuomisto H and Ruokolainen K
- Subjects
- Altitude, Biodiversity, Ecosystem, Environment, Plants, Trees
- Abstract
Kraft et al. (Report, 23 September 2011, p. 1755) argued that the latitudinal trend in β diversity is spurious and just reflects a trend in γ diversity. Their results depend on the idiosyncrasies of their data, especially the latitudinally varying degree of undersampling and a local sampling setup that is not suitable for analyzing drivers of β diversity.
- Published
- 2012
- Full Text
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32. Geological control of floristic composition in Amazonian forests.
- Author
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Higgins MA, Ruokolainen K, Tuomisto H, Llerena N, Cardenas G, Phillips OL, Vásquez R, and Räsänen M
- Abstract
AIM: Conservation and land-use planning require accurate maps of patterns in species composition and an understanding of the factors that control them. Substantial doubt exists, however, about the existence and determinants of large-area floristic divisions in Amazonia. Here we ask whether Amazonian forests are partitioned into broad-scale floristic units on the basis of geological formations and their edaphic properties. LOCATION: Western and central Amazonia. METHODS: We used Landsat imagery and Shuttle Radar Topography Mission (SRTM) digital elevation data to identify a possible floristic and geological discontinuity of over 300 km in northern Peru. We then used plant inventories and soil sampling to document changes in species composition and soil properties across this boundary. Data were obtained from 138 sites distributed along more than 450 km of road and river. On the basis of our findings, we used broad-scale Landsat and SRTM mosaics to identify similar patterns across western and central Amazonia. RESULTS: The discontinuity identified in Landsat and SRTM data corresponded to a 15-fold change in soil cation concentrations and an almost total change in plant species composition. This discontinuity appears to be caused by the widespread removal of cation-poor surface sediments by river incision to expose cation-rich sediments beneath. Examination of broad-scale Landsat and SRTM mosaics indicated that equivalent processes have generated a north-south discontinuity of over 1500 km in western Brazil. Due to similarities with our study area, we suggest that this discontinuity represents a chemical and ecological limit between western and central Amazonia. MAIN CONCLUSIONS: Our findings suggest that Amazonian forests are partitioned into large-area units on the basis of geological formations and their edaphic properties. The evolution of these units through geological time may provide a general mechanism for biotic diversification in Amazonia. These compositional units, moreover, may correspond to broad-scale functional units. The existence of large-area compositional and functional units would suggest that protected-area, carbon sequestration, and other land-use strategies in Amazonia be implemented on a region-by-region basis. The methods described here can be used to map these patterns, and thus enable effective conservation and management of Amazonian forests.
- Published
- 2011
- Full Text
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33. A novel facility for ageing materials with narrow-band ultraviolet radiation exposure.
- Author
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Kärhä P, Heikkilä A, Ruokolainen K, and Kaunismaa M
- Abstract
A facility for exploring wavelength dependencies in ultraviolet (UV) radiation induced degradation in materials has been designed and constructed. The device is essentially a spectrograph separating light from a lamp to spectrally resolved UV radiation. It is based on a 1 kW xenon lamp and a flat-field concave holographic grating 10 cm in diameter. Radiation at the wavelength range 250-500 nm is dispersed onto the sample plane of 1.5 cm in height and 21 cm in width. The optical performance of the device has been characterized by radiometric measurements. Using the facility, test samples prepared of regular newspaper have been irradiated from 1 to 8 h. Color changes on the different locations of the aged samples have been quantified by color measurements. Yellowness indices computed from the color measurements demonstrate the capability of the facility in revealing wavelength dependencies of the material property changes in reasonable time frames.
- Published
- 2011
- Full Text
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34. ANALYZING OR EXPLAINING BETA DIVERSITY? REPLY.
- Author
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Tuomisto H and Ruokolainen K
- Published
- 2008
- Full Text
- View/download PDF
35. Analyzing or explaining beta diversity? Understanding the targets of different methods of analysis.
- Author
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Tuomisto H and Ruokolainen K
- Subjects
- Population Density, Biodiversity, Ecology methods, Models, Biological, Models, Statistical
- Abstract
It has been actively discussed recently what statistical methods are appropriate when one is interested in testing hypotheses about the origin of beta diversity, especially whether one should use the raw-data approach (e.g., canonical analysis such as RDA and CCA) or the distance approach (e.g., Mantel test and multiple regression on distance matrices). Most of the confusion seems to stem from uncertainty as to what is the response variable in the different approaches. Here our aim is to clarify this issue. We also show that, although both the raw-data approach and the distance approach can often be used to address the same ecological hypothesis, they target fundamentally different predictions of those hypotheses. As the two approaches shed light on different aspects of the ecological hypotheses, they should be viewed as complementary rather than alternative ways of analyzing data. However, in some cases only one of the approaches may be appropriate. We argue that S. P. Hubbell's neutral theory can only be tested using the distance approach, because its testable predictions are stated in terms of distances, not in terms of raw data. In all cases, the decision on which method is chosen must be based on which addresses the question at hand, it cannot be based on which provides the highest proportion of explained variance in simulation studies.
- Published
- 2006
- Full Text
- View/download PDF
36. Dispersal, environment, and floristic variation of western Amazonian forests.
- Author
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Tuomisto H, Ruokolainen K, and Yli-Halla M
- Subjects
- Colombia, Ecuador, Geography, Peru, Seasons, Soil, Ecosystem, Environment, Ferns classification, Ferns growth & development, Melastomataceae classification, Melastomataceae growth & development, Trees
- Abstract
The distribution of plant species, the species compositions of different sites, and the factors that affect them in tropical rain forests are not well understood. The main hypotheses are that species composition is either (i) uniform over large areas, (ii) random but spatially autocorrelated because of dispersal limitation, or (iii) patchy and environmentally determined. Here we test these hypotheses, using a large data set from western Amazonia. The uniformity hypothesis gains no support, but the other hypotheses do. Environmental determinism explains a larger proportion of the variation in floristic differences between sites than does dispersal limitation; together, these processes explain 70 to 75% of the variation. Consequently, it is important that management planning for conservation and resource use take into account both habitat heterogeneity and biogeographic differences.
- Published
- 2003
- Full Text
- View/download PDF
37. Dissecting amazonian biodiversity.
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Tuomisto H, Ruokolainen K, Kalliola R, Linna A, Danjoy W, and Rodriguez Z
- Abstract
Biogeographical and biodiversity studies in Iowland Amazonian rain forests typically refer to observed or postulated distribution barriers such as past unfavorable climates, mountains, rivers, and river floodplains that divide the uniform tierra firme (noninundated) forest. Present-day ecological heterogeneity within tierra firme has hardly been discussed in this context, although edaphic differences are known to affect species distribution patterns in both inundated areas and tierra firme. Quantification of landscape heterogeneity in Peruvian Iowland Amazonia (500,000 kilometers squared), based on field studies and satellite image analysis, shows that Peruvian Amazonia is considerably more heterogeneous than previously reported. These observations have implications for the research, management, and conservation of Amazonian biodiversity.
- Published
- 1995
- Full Text
- View/download PDF
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