92 results on '"Berenguer, E."'
Search Results
2. Resultados de un programa de descolonización de Staphylococcus aureus en cirugía protésica primaria de cadera y rodilla
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Yuste Berenguer, E., Colomina Morales, J., Señor Revuelto, P., Drudis Morell, R., Torra Riera, M., Pilares Ortega, E.P., and Trujillano Cabello, J.
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- 2023
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3. The global abundance of tree palms
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Muscarella, R, Emilio, T, Phillips, OL, Lewis, SL, Slik, F, Baker, WJ, Couvreur, TLP, Eiserhardt, WL, Svenning, JC, Affum-Baffoe, K, Aiba, SI, de Almeida, EC, de Almeida, SS, de Oliveira, EA, Álvarez-Dávila, E, Alves, LF, Alvez-Valles, CM, Carvalho, FA, Guarin, FA, Andrade, A, Aragão, LEOC, Murakami, AA, Arroyo, L, Ashton, PS, Corredor, GAA, Baker, TR, de Camargo, PB, Barlow, J, Bastin, JF, Bengone, NN, Berenguer, E, Berry, N, Blanc, L, Böhning-Gaese, K, Bonal, D, Bongers, F, Bradford, M, Brambach, F, Brearley, FQ, Brewer, SW, Camargo, JLC, Campbell, DG, Castilho, CV, Castro, W, Catchpole, D, Cerón Martínez, CE, Chen, S, Chhang, P, Cho, P, Chutipong, W, Clark, C, Collins, M, Comiskey, JA, Medina, MNC, Costa, FRC, Culmsee, H, David-Higuita, H, Davidar, P, del Aguila-Pasquel, J, Derroire, G, Di Fiore, A, Van Do, T, Doucet, JL, Dourdain, A, Drake, DR, Ensslin, A, Erwin, T, Ewango, CEN, Ewers, RM, Fauset, S, Feldpausch, TR, Ferreira, J, Ferreira, LV, Fischer, M, Franklin, J, Fredriksson, GM, Gillespie, TW, Gilpin, M, Gonmadje, C, Gunatilleke, AUN, Hakeem, KR, Hall, JS, Hamer, KC, Harris, DJ, Harrison, RD, Hector, A, Hemp, A, Herault, B, Pizango, CGH, Coronado, ENH, Hubau, W, Hussain, MS, Ibrahim, FH, Imai, N, Joly, CA, Joseph, S, Anitha, K, Kartawinata, K, Kassi, J, and Killeen, TJ
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above-ground biomass ,abundance patterns ,Arecaceae ,local abiotic conditions ,Neotropics ,pantropical biogeography ,tropical rainforest ,wood density ,Ecology ,Physical Geography and Environmental Geoscience ,Ecological Applications - Abstract
Aim: Palms are an iconic, diverse and often abundant component of tropical ecosystems that provide many ecosystem services. Being monocots, tree palms are evolutionarily, morphologically and physiologically distinct from other trees, and these differences have important consequences for ecosystem services (e.g., carbon sequestration and storage) and in terms of responses to climate change. We quantified global patterns of tree palm relative abundance to help improve understanding of tropical forests and reduce uncertainty about these ecosystems under climate change. Location: Tropical and subtropical moist forests. Time period: Current. Major taxa studied: Palms (Arecaceae). Methods: We assembled a pantropical dataset of 2,548 forest plots (covering 1,191 ha) and quantified tree palm (i.e., ≥10 cm diameter at breast height) abundance relative to co-occurring non-palm trees. We compared the relative abundance of tree palms across biogeographical realms and tested for associations with palaeoclimate stability, current climate, edaphic conditions and metrics of forest structure. Results: On average, the relative abundance of tree palms was more than five times larger between Neotropical locations and other biogeographical realms. Tree palms were absent in most locations outside the Neotropics but present in >80% of Neotropical locations. The relative abundance of tree palms was more strongly associated with local conditions (e.g., higher mean annual precipitation, lower soil fertility, shallower water table and lower plot mean wood density) than metrics of long-term climate stability. Life-form diversity also influenced the patterns; palm assemblages outside the Neotropics comprise many non-tree (e.g., climbing) palms. Finally, we show that tree palms can influence estimates of above-ground biomass, but the magnitude and direction of the effect require additional work. Conclusions: Tree palms are not only quintessentially tropical, but they are also overwhelmingly Neotropical. Future work to understand the contributions of tree palms to biomass estimates and carbon cycling will be particularly crucial in Neotropical forests.
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- 2020
4. Brazil’s environmental leadership at risk
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Ferreira, J., Aragão, L. E. O. C., Barlow, J., Barreto, P., Berenguer, E., Bustamante, M., Gardner, T. A., Lees, A. C., Lima, A., Louzada, J., Pardini, R., Parry, L., Peres, C. A., Pompeu, P. S., Tabarelli, M., and Zuanon, J.
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- 2014
5. ENVIRONMENT AND DEVELOPMENT: Brazilʼs environmental leadership at risk
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Ferreira, J., Aragão, L. E. O. C., Barlow, J., Barreto, P., Berenguer, E., Bustamante, M., Gardner, T. A., Lees, A. C., Lima, A., Louzada, J., Pardini, R., Parry, L., Peres, C. A., Pompeu, P. S., Tabarelli, M., and Zuanon, J.
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- 2014
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6. An unexpected finding: identification of the first complete shell of the Franco-Belgian middle Eocene littoral pleurodiran turtle Eocenochelus eremberti in Spain.
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Pérez-García, A., Díaz-Berenguer, E., Badiola, A., and Canudo, J.I.
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EOCENE Epoch , *TURTLES , *SPECIES distribution - Abstract
Pleurodiran turtles are relatively abundant in the Eocene record of Europe, being mostly represented by Podocnemididae. Two genera have been identified. The most abundant and diverse is the well-known freshwater Neochelys. The other is Eocenochelus. The record of this poorly-known genus is very scarce. It is the only representative of the Upper Cretaceous to extant Erymnochelyini (i.e., a new tribe proposed here for the 'Erymnochelys group of turtles') interpreted as a littoral form, and the only one known outside Africa. The finding of the only complete shell of Eocenochelus hitherto identified is presented here. It comes from the Castejón de Sobrarbe-41 site, in the middle Eocene (Lutetian) of the Sobrarbe Formation of the Ainsa Basin (Huesca, Spain). The sedimentary environment of the site is compatible with its attribution to a littoral form. It is attributed to the type species of the genus, Eocenochelus eremberti, so far exclusively known by two partial shells from the middle Eocene of the Franco-Belgian Basin. Therefore, the paleobiogeographic distribution of this species is markedly increased, from the southern area of the North Sea to the Bay of Biscay. This finding provides new anatomical data on the species Eocenochelus eremberti and on its poorly known genus. [ABSTRACT FROM AUTHOR]
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- 2021
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7. Inyección accidental de contraste hidrosoluble tras colocación de una sonda de nutrición enteral
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Morales-Berenguer, E., Pastor, F., Navarro-Martínez, J., and Company, R.
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- 2009
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8. Characterization of the EPR new generation polycrystalline silicon flat plates
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Hamoud, M., Sof, S., Kolic, Y., Lemiti, M., Berenguer, E., Gauthier, R., and Pinard, P.
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- 1992
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9. The biogeography of the Amazonian tree flora.
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Luize BG, Tuomisto H, Ekelschot R, Dexter KG, Amaral ILD, Coelho LS, Matos FDA, Lima Filho DA, Salomão RP, Wittmann F, Castilho CV, Carim MJV, Guevara JE, Phillips OL, Magnusson WE, Sabatier D, Cardenas Revilla JD, Molino JF, Irume MV, Martins MP, Guimarães JRDS, Ramos JF, Bánki OS, Piedade MTF, Cárdenas López D, Pitman NCA, Demarchi LO, Schöngart J, de Leão Novo EMM, Núñez Vargas P, Silva TSF, Venticinque EM, Manzatto AG, Reis NFC, Terborgh J, Casula KR, Honorio Coronado EN, Mendoza AM, Montero JC, Costa FRC, Feldpausch TR, Quaresma AC, Castaño Arboleda N, Zartman CE, Killeen TJ, Marimon BS, Marimon BH, Vasquez R, Mostacedo B, Assis RL, Baraloto C, do Amaral DD, Engel J, Petronelli P, Castellanos H, de Medeiros MB, Simon MF, Andrade A, Camargo JL, Laurance WF, Laurance SGW, Rincón LM, Schietti J, Sousa TR, Mori GB, Farias ES, Lopes MA, Magalhães JLL, Nascimento HEM, de Queiroz HL, Vasconcelos CC, Aymard C GA, Brienen R, Stevenson PR, Araujo-Murakami A, Cintra BBL, Baker TR, Feitosa YO, Mogollón HF, Duivenvoorden JF, Peres CA, Silman MR, Ferreira LV, Lozada JR, Comiskey JA, de Toledo JJ, Damasco G, Dávila N, Draper FC, García-Villacorta R, Lopes A, Vicentini A, Valverde FC, Alonso A, Arroyo L, Dallmeier F, Gomes VHF, Jimenez EM, Neill D, Peñuela Mora MC, Noronha JC, de Aguiar DPP, Barbosa FR, Bredin YK, Carpanedo RS, Carvalho FA, Souza FC, Feeley KJ, Gribel R, Haugaasen T, Hawes JE, Pansonato MP, Pipoly JJ 3rd, Paredes MR, Rodrigues DJ, Barlow J, Berenguer E, da Silva IB, Ferreira MJ, Ferreira J, Fine PVA, Guedes MC, Levis C, Licona JC, Villa Zegarra BE, Vos VA, Cerón C, Durgante FM, Fonty É, Henkel TW, Householder JE, Huamantupa-Chuquimaco I, Silveira M, Stropp J, Thomas R, Daly D, Milliken W, Molina GP, Pennington T, Vieira ICG, Albuquerque BW, Campelo W, Fuentes A, Klitgaard B, Pena JLM, Tello JS, Vriesendorp C, Chave J, Di Fiore A, Hilário RR, Pereira LO, Phillips JF, Rivas-Torres G, van Andel TR, von Hildebrand P, Balee W, Barbosa EM, Bonates LCM, Dávila Doza HP, Zárate Gómez R, Gonzales T, Gallardo Gonzales GP, Hoffman B, Junqueira AB, Malhi Y, Miranda IPA, Pinto LFM, Prieto A, Rudas A, Ruschel AR, Silva N, Vela CIA, Zent S, Zent EL, Endara MJ, Cano A, Carrero Márquez YA, Correa DF, Costa JBP, Monteiro Flores B, Galbraith D, Holmgren M, Kalamandeen M, Lobo G, Torres Montenegro L, Nascimento MT, Oliveira AA, Pombo MM, Ramirez-Angulo H, Rocha M, Scudeller VV, Umaña MN, van der Heijden G, Vilanova Torre E, Vargas TM, Ahuite Reategui MA, Baider C, Balslev H, Cárdenas S, Casas LF, Farfan-Rios W, Ferreira C, Linares-Palomino R, Mendoza C, Mesones I, Parada GA, Torres-Lezama A, Urrego Giraldo LE, Villarroel D, Zagt R, Alexiades MN, de Oliveira EA, Fortier RP, Garcia-Cabrera K, Hernandez L, Palacios Cuenca W, Pansini S, Pauletto D, Ramirez Arevalo F, Sampaio AF, Valderrama Sandoval EH, Valenzuela Gamarra L, Hirota M, Palma-Silva C, and Ter Steege H
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- Brazil, Biodiversity, Forests, Soil chemistry, Geography, Phylogeography, Trees
- Abstract
We describe the geographical variation in tree species composition across Amazonian forests and show how environmental conditions are associated with species turnover. Our analyses are based on 2023 forest inventory plots (1 ha) that provide abundance data for a total of 5188 tree species. Within-plot species composition reflected both local environmental conditions (especially soil nutrients and hydrology) and geographical regions. A broader-scale view of species turnover was obtained by interpolating the relative tree species abundances over Amazonia into 47,441 0.1-degree grid cells. Two main dimensions of spatial change in tree species composition were identified. The first was a gradient between western Amazonia at the Andean forelands (with young geology and relatively nutrient-rich soils) and central-eastern Amazonia associated with the Guiana and Brazilian Shields (with more ancient geology and poor soils). The second gradient was between the wet forests of the northwest and the drier forests in southern Amazonia. Isolines linking cells of similar composition crossed major Amazonian rivers, suggesting that tree species distributions are not limited by rivers. Even though some areas of relatively sharp species turnover were identified, mostly the tree species composition changed gradually over large extents, which does not support delimiting clear discrete biogeographic regions within Amazonia., (© 2024. The Author(s).)
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- 2024
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10. Small molecule inhibitors of human LRRK2 enhance in vitro embryogenesis and microcallus formation for plant regeneration of crop and model species.
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Carneros E, Berenguer E, Pérez-Pérez Y, Pandey S, Welsch R, Palme K, Gil C, Martínez A, and Testillano PS
- Abstract
In vitro plant embryogenesis and microcallus formation are systems which are required for plant regeneration, a process during which cell reprogramming and proliferation are critical. These systems offer many advantages in breeding programmes, such as doubled-haploid production, clonal propagation of selected genotypes, and recovery of successfully gene-edited or transformed plants. However, the low proportion of reprogrammed cells in many plant species makes these processes highly inefficient. Here we report a new strategy to improve in vitro plant cell reprogramming using small molecule inhibitors of mammalian leucine rich repeat kinase 2 (LRRK2), which are used in pharmaceutical applications for cell reprogramming, but never used in plants before. LRRK2 inhibitors increased in vitro embryo production in three different systems and species, microspore embryogenesis of oilseed rape and barley, and somatic embryogenesis in cork oak. These inhibitors also promoted plant cell reprogramming and proliferation in Arabidopsis protoplast cultures. The benzothiazole derivative JZ1.24, a representative compound of the tested molecules, modified the expression of the brassinosteroid (BR)-related genes BIN2, CPD, and BAS1, correlating with an activation of BR signaling. Additionally, the LRRK2 inhibitor JZ1.24 induced the expression of the embryogenesis marker gene SERK1-like. The results suggest that the use of small molecules from the pharmaceutical field could be extended to promote in vitro reprogramming of plant cells towards embryogenesis or microcallus formation in a wider range of plant species and in vitro systems. This technological innovation would help to develop new strategies to improve the efficiency of in vitro plant regeneration, a major bottleneck in plant breeding., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier GmbH.. All rights reserved.)
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- 2024
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11. Author Correction: One sixth of Amazonian tree diversity is dependent on river floodplains.
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Householder JE, Wittmann F, Schöngart J, Piedade MTF, Junk WJ, Latrubesse EM, Quaresma AC, Demarchi LO, de S Lobo G, Aguiar DPP, Assis RL, Lopes A, Parolin P, Leão do Amaral I, Coelho LS, de Almeida Matos FD, Lima Filho DA, Salomão RP, Castilho CV, Guevara-Andino JE, Carim MJV, Phillips OL, Cárdenas López D, Magnusson WE, Sabatier D, Revilla JDC, Molino JF, Irume MV, Martins MP, Guimarães JRDS, Ramos JF, Rodrigues DJ, Bánki OS, Peres CA, Pitman NCA, Hawes JE, Almeida EJ, Barbosa LF, Cavalheiro L, Dos Santos MCV, Luize BG, Novo EMML, Núñez Vargas P, Silva TSF, Venticinque EM, Manzatto AG, Reis NFC, Terborgh J, Casula KR, Costa FRC, Honorio Coronado EN, Monteagudo Mendoza A, Montero JC, Feldpausch TR, Aymard C GA, Baraloto C, Castaño Arboleda N, Engel J, Petronelli P, Zartman CE, Killeen TJ, Rincón LM, Marimon BS, Marimon-Junior BH, Schietti J, Sousa TR, Vasquez R, Mostacedo B, Dantas do Amaral D, Castellanos H, Medeiros MB, Simon MF, Andrade A, Camargo JL, Laurance WF, Laurance SGW, Farias ES, Lopes MA, Magalhães JLL, Mendonça Nascimento HE, Queiroz HL, Brienen R, Stevenson PR, Araujo-Murakami A, Baker TR, Cintra BBL, Feitosa YO, Mogollón HF, Noronha JC, Barbosa FR, de Sá Carpanedo R, Duivenvoorden JF, Silman MR, Ferreira LV, Levis C, Lozada JR, Comiskey JA, Draper FC, Toledo JJ, Damasco G, Dávila N, García-Villacorta R, Vicentini A, Cornejo Valverde F, Alonso A, Arroyo L, Dallmeier F, Gomes VHF, Jimenez EM, Neill D, Peñuela Mora MC, Carvalho FA, Coelho de Souza F, Feeley KJ, Gribel R, Pansonato MP, Ríos Paredes M, Barlow J, Berenguer E, Dexter KG, Ferreira J, Fine PVA, Guedes MC, Huamantupa-Chuquimaco I, Licona JC, Pennington T, Villa Zegarra BE, Vos VA, Cerón C, Fonty É, Henkel TW, Maas P, Pos E, Silveira M, Stropp J, Thomas R, Daly D, Milliken W, Pardo Molina G, Vieira ICG, Albuquerque BW, Campelo W, Emilio T, Fuentes A, Klitgaard B, Marcelo Pena JL, Souza PF, Tello JS, Vriesendorp C, Chave J, Di Fiore A, Hilário RR, Pereira LO, Phillips JF, Rivas-Torres G, van Andel TR, von Hildebrand P, Balee W, Barbosa EM, Bonates LCM, Doza HPD, Gómez RZ, Gonzales T, Gonzales GPG, Hoffman B, Junqueira AB, Malhi Y, Miranda IPA, Mozombite-Pinto LF, Prieto A, Rudas A, Ruschel AR, Silva N, Vela CIA, Zent S, Zent EL, Cano A, Carrero Márquez YA, Correa DF, Costa JBP, Flores BM, Galbraith D, Holmgren M, Kalamandeen M, Nascimento MT, Oliveira AA, Ramirez-Angulo H, Rocha M, Scudeller VV, Sierra R, Tirado M, Umaña MN, van der Heijden G, Vilanova Torre E, Ahuite Reategui MA, Baider C, Balslev H, Cárdenas S, Casas LF, Farfan-Rios W, Ferreira C, Linares-Palomino R, Mendoza C, Mesones I, Parada GA, Torres-Lezama A, Urrego Giraldo LE, Villarroel D, Zagt R, Alexiades MN, de Oliveira EA, Garcia-Cabrera K, Hernandez L, Palacios Cuenca W, Pansini S, Pauletto D, Ramirez Arevalo F, Sampaio AF, Valderrama Sandoval EH, Valenzuela Gamarra L, and Ter Steege H
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- 2024
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12. One sixth of Amazonian tree diversity is dependent on river floodplains.
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Householder JE, Wittmann F, Schöngart J, Piedade MTF, Junk WJ, Latrubesse EM, Quaresma AC, Demarchi LO, de S Lobo G, Aguiar DPP, Assis RL, Lopes A, Parolin P, Leão do Amaral I, Coelho LS, de Almeida Matos FD, Lima Filho DA, Salomão RP, Castilho CV, Guevara-Andino JE, Carim MJV, Phillips OL, Cárdenas López D, Magnusson WE, Sabatier D, Revilla JDC, Molino JF, Irume MV, Martins MP, Guimarães JRDS, Ramos JF, Rodrigues DJ, Bánki OS, Peres CA, Pitman NCA, Hawes JE, Almeida EJ, Barbosa LF, Cavalheiro L, Dos Santos MCV, Luize BG, Novo EMML, Núñez Vargas P, Silva TSF, Venticinque EM, Manzatto AG, Reis NFC, Terborgh J, Casula KR, Costa FRC, Honorio Coronado EN, Monteagudo Mendoza A, Montero JC, Feldpausch TR, Aymard C GA, Baraloto C, Castaño Arboleda N, Engel J, Petronelli P, Zartman CE, Killeen TJ, Rincón LM, Marimon BS, Marimon-Junior BH, Schietti J, Sousa TR, Vasquez R, Mostacedo B, Dantas do Amaral D, Castellanos H, Medeiros MB, Simon MF, Andrade A, Camargo JL, Laurance WF, Laurance SGW, Farias ES, Lopes MA, Magalhães JLL, Mendonça Nascimento HE, Queiroz HL, Brienen R, Stevenson PR, Araujo-Murakami A, Baker TR, Cintra BBL, Feitosa YO, Mogollón HF, Noronha JC, Barbosa FR, de Sá Carpanedo R, Duivenvoorden JF, Silman MR, Ferreira LV, Levis C, Lozada JR, Comiskey JA, Draper FC, Toledo JJ, Damasco G, Dávila N, García-Villacorta R, Vicentini A, Cornejo Valverde F, Alonso A, Arroyo L, Dallmeier F, Gomes VHF, Jimenez EM, Neill D, Peñuela Mora MC, Carvalho FA, Coelho de Souza F, Feeley KJ, Gribel R, Pansonato MP, Ríos Paredes M, Barlow J, Berenguer E, Dexter KG, Ferreira J, Fine PVA, Guedes MC, Huamantupa-Chuquimaco I, Licona JC, Pennington T, Villa Zegarra BE, Vos VA, Cerón C, Fonty É, Henkel TW, Maas P, Pos E, Silveira M, Stropp J, Thomas R, Daly D, Milliken W, Pardo Molina G, Vieira ICG, Albuquerque BW, Campelo W, Emilio T, Fuentes A, Klitgaard B, Marcelo Pena JL, Souza PF, Tello JS, Vriesendorp C, Chave J, Di Fiore A, Hilário RR, Pereira LO, Phillips JF, Rivas-Torres G, van Andel TR, von Hildebrand P, Balee W, Barbosa EM, Bonates LCM, Doza HPD, Gómez RZ, Gonzales T, Gonzales GPG, Hoffman B, Junqueira AB, Malhi Y, Miranda IPA, Mozombite-Pinto LF, Prieto A, Rudas A, Ruschel AR, Silva N, Vela CIA, Zent S, Zent EL, Cano A, Carrero Márquez YA, Correa DF, Costa JBP, Flores BM, Galbraith D, Holmgren M, Kalamandeen M, Nascimento MT, Oliveira AA, Ramirez-Angulo H, Rocha M, Scudeller VV, Sierra R, Tirado M, Umaña MN, van der Heijden G, Vilanova Torre E, Ahuite Reategui MA, Baider C, Balslev H, Cárdenas S, Casas LF, Farfan-Rios W, Ferreira C, Linares-Palomino R, Mendoza C, Mesones I, Parada GA, Torres-Lezama A, Urrego Giraldo LE, Villarroel D, Zagt R, Alexiades MN, de Oliveira EA, Garcia-Cabrera K, Hernandez L, Palacios Cuenca W, Pansini S, Pauletto D, Ramirez Arevalo F, Sampaio AF, Valderrama Sandoval EH, Valenzuela Gamarra L, and Ter Steege H
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- Brazil, Forests, Biodiversity, Trees, Rivers, Floods
- Abstract
Amazonia's floodplain system is the largest and most biodiverse on Earth. Although forests are crucial to the ecological integrity of floodplains, our understanding of their species composition and how this may differ from surrounding forest types is still far too limited, particularly as changing inundation regimes begin to reshape floodplain tree communities and the critical ecosystem functions they underpin. Here we address this gap by taking a spatially explicit look at Amazonia-wide patterns of tree-species turnover and ecological specialization of the region's floodplain forests. We show that the majority of Amazonian tree species can inhabit floodplains, and about a sixth of Amazonian tree diversity is ecologically specialized on floodplains. The degree of specialization in floodplain communities is driven by regional flood patterns, with the most compositionally differentiated floodplain forests located centrally within the fluvial network and contingent on the most extraordinary flood magnitudes regionally. Our results provide a spatially explicit view of ecological specialization of floodplain forest communities and expose the need for whole-basin hydrological integrity to protect the Amazon's tree diversity and its function., (© 2024. The Author(s).)
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- 2024
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13. Corrigendum: Mining the Utricularia gibba genome for insulator-like elements for genetic engineering.
- Author
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Laspisa D, Illa-Berenguer E, Bang S, Schmitz RJ, Parrott W, and Wallace J
- Abstract
[This corrects the article DOI: 10.3389/fpls.2023.1279231.]., (Copyright © 2024 Laspisa, Illa-Berenguer, Bang, Schmitz, Parrott and Wallace.)
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- 2024
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14. Critical transitions in the Amazon forest system.
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Flores BM, Montoya E, Sakschewski B, Nascimento N, Staal A, Betts RA, Levis C, Lapola DM, Esquível-Muelbert A, Jakovac C, Nobre CA, Oliveira RS, Borma LS, Nian D, Boers N, Hecht SB, Ter Steege H, Arieira J, Lucas IL, Berenguer E, Marengo JA, Gatti LV, Mattos CRC, and Hirota M
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- Droughts statistics & numerical data, Feedback, Wildfires statistics & numerical data, Uncertainty, Environmental Restoration and Remediation trends, Forests, Global Warming prevention & control, Global Warming statistics & numerical data, Trees growth & development
- Abstract
The possibility that the Amazon forest system could soon reach a tipping point, inducing large-scale collapse, has raised global concern
1-3 . For 65 million years, Amazonian forests remained relatively resilient to climatic variability. Now, the region is increasingly exposed to unprecedented stress from warming temperatures, extreme droughts, deforestation and fires, even in central and remote parts of the system1 . Long existing feedbacks between the forest and environmental conditions are being replaced by novel feedbacks that modify ecosystem resilience, increasing the risk of critical transition. Here we analyse existing evidence for five major drivers of water stress on Amazonian forests, as well as potential critical thresholds of those drivers that, if crossed, could trigger local, regional or even biome-wide forest collapse. By combining spatial information on various disturbances, we estimate that by 2050, 10% to 47% of Amazonian forests will be exposed to compounding disturbances that may trigger unexpected ecosystem transitions and potentially exacerbate regional climate change. Using examples of disturbed forests across the Amazon, we identify the three most plausible ecosystem trajectories, involving different feedbacks and environmental conditions. We discuss how the inherent complexity of the Amazon adds uncertainty about future dynamics, but also reveals opportunities for action. Keeping the Amazon forest resilient in the Anthropocene will depend on a combination of local efforts to end deforestation and degradation and to expand restoration, with global efforts to stop greenhouse gas emissions., (© 2024. The Author(s).)- Published
- 2024
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15. Consistent patterns of common species across tropical tree communities.
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Cooper DLM, Lewis SL, Sullivan MJP, Prado PI, Ter Steege H, Barbier N, Slik F, Sonké B, Ewango CEN, Adu-Bredu S, Affum-Baffoe K, de Aguiar DPP, Ahuite Reategui MA, Aiba SI, Albuquerque BW, de Almeida Matos FD, Alonso A, Amani CA, do Amaral DD, do Amaral IL, Andrade A, de Andrade Miranda IP, Angoboy IB, Araujo-Murakami A, Arboleda NC, Arroyo L, Ashton P, Aymard C GA, Baider C, Baker TR, Balinga MPB, Balslev H, Banin LF, Bánki OS, Baraloto C, Barbosa EM, Barbosa FR, Barlow J, Bastin JF, Beeckman H, Begne S, Bengone NN, Berenguer E, Berry N, Bitariho R, Boeckx P, Bogaert J, Bonyoma B, Boundja P, Bourland N, Boyemba Bosela F, Brambach F, Brienen R, Burslem DFRP, Camargo JL, Campelo W, Cano A, Cárdenas S, Cárdenas López D, de Sá Carpanedo R, Carrero Márquez YA, Carvalho FA, Casas LF, Castellanos H, Castilho CV, Cerón C, Chapman CA, Chave J, Chhang P, Chutipong W, Chuyong GB, Cintra BBL, Clark CJ, Coelho de Souza F, Comiskey JA, Coomes DA, Cornejo Valverde F, Correa DF, Costa FRC, Costa JBP, Couteron P, Culmsee H, Cuni-Sanchez A, Dallmeier F, Damasco G, Dauby G, Dávila N, Dávila Doza HP, De Alban JDT, de Assis RL, De Canniere C, De Haulleville T, de Jesus Veiga Carim M, Demarchi LO, Dexter KG, Di Fiore A, Din HHM, Disney MI, Djiofack BY, Djuikouo MK, Do TV, Doucet JL, Draper FC, Droissart V, Duivenvoorden JF, Engel J, Estienne V, Farfan-Rios W, Fauset S, Feeley KJ, Feitosa YO, Feldpausch TR, Ferreira C, Ferreira J, Ferreira LV, Fletcher CD, Flores BM, Fofanah A, Foli EG, Fonty É, Fredriksson GM, Fuentes A, Galbraith D, Gallardo Gonzales GP, Garcia-Cabrera K, García-Villacorta R, Gomes VHF, Gómez RZ, Gonzales T, Gribel R, Guedes MC, Guevara JE, Hakeem KR, Hall JS, Hamer KC, Hamilton AC, Harris DJ, Harrison RD, Hart TB, Hector A, Henkel TW, Herbohn J, Hockemba MBN, Hoffman B, Holmgren M, Honorio Coronado EN, Huamantupa-Chuquimaco I, Hubau W, Imai N, Irume MV, Jansen PA, Jeffery KJ, Jimenez EM, Jucker T, Junqueira AB, Kalamandeen M, Kamdem NG, Kartawinata K, Kasongo Yakusu E, Katembo JM, Kearsley E, Kenfack D, Kessler M, Khaing TT, Killeen TJ, Kitayama K, Klitgaard B, Labrière N, Laumonier Y, Laurance SGW, Laurance WF, Laurent F, Le TC, Le TT, Leal ME, Leão de Moraes Novo EM, Levesley A, Libalah MB, Licona JC, Lima Filho DA, Lindsell JA, Lopes A, Lopes MA, Lovett JC, Lowe R, Lozada JR, Lu X, Luambua NK, Luize BG, Maas P, Magalhães JLL, Magnusson WE, Mahayani NPD, Makana JR, Malhi Y, Maniguaje Rincón L, Mansor A, Manzatto AG, Marimon BS, Marimon-Junior BH, Marshall AR, Martins MP, Mbayu FM, de Medeiros MB, Mesones I, Metali F, Mihindou V, Millet J, Milliken W, Mogollón HF, Molino JF, Mohd Said MN, Monteagudo Mendoza A, Montero JC, Moore S, Mostacedo B, Mozombite Pinto LF, Mukul SA, Munishi PKT, Nagamasu H, Nascimento HEM, Nascimento MT, Neill D, Nilus R, Noronha JC, Nsenga L, Núñez Vargas P, Ojo L, Oliveira AA, de Oliveira EA, Ondo FE, Palacios Cuenca W, Pansini S, Pansonato MP, Paredes MR, Paudel E, Pauletto D, Pearson RG, Pena JLM, Pennington RT, Peres CA, Permana A, Petronelli P, Peñuela Mora MC, Phillips JF, Phillips OL, Pickavance G, Piedade MTF, Pitman NCA, Ploton P, Popelier A, Poulsen JR, Prieto A, Primack RB, Priyadi H, Qie L, Quaresma AC, de Queiroz HL, Ramirez-Angulo H, Ramos JF, Reis NFC, Reitsma J, Revilla JDC, Riutta T, Rivas-Torres G, Robiansyah I, Rocha M, Rodrigues DJ, Rodriguez-Ronderos ME, Rovero F, Rozak AH, Rudas A, Rutishauser E, Sabatier D, Sagang LB, Sampaio AF, Samsoedin I, Satdichanh M, Schietti J, Schöngart J, Scudeller VV, Seuaturien N, Sheil D, Sierra R, Silman MR, Silva TSF, da Silva Guimarães JR, Simo-Droissart M, Simon MF, Sist P, Sousa TR, de Sousa Farias E, de Souza Coelho L, Spracklen DV, Stas SM, Steinmetz R, Stevenson PR, Stropp J, Sukri RS, Sunderland TCH, Suzuki E, Swaine MD, Tang J, Taplin J, Taylor DM, Tello JS, Terborgh J, Texier N, Theilade I, Thomas DW, Thomas R, Thomas SC, Tirado M, Toirambe B, de Toledo JJ, Tomlinson KW, Torres-Lezama A, Tran HD, Tshibamba Mukendi J, Tumaneng RD, Umaña MN, Umunay PM, Urrego Giraldo LE, Valderrama Sandoval EH, Valenzuela Gamarra L, Van Andel TR, van de Bult M, van de Pol J, van der Heijden G, Vasquez R, Vela CIA, Venticinque EM, Verbeeck H, Veridiano RKA, Vicentini A, Vieira ICG, Vilanova Torre E, Villarroel D, Villa Zegarra BE, Vleminckx J, von Hildebrand P, Vos VA, Vriesendorp C, Webb EL, White LJT, Wich S, Wittmann F, Zagt R, Zang R, Zartman CE, Zemagho L, Zent EL, and Zent S
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- Biodiversity, Africa, Asia, Southeastern, Forests, Trees anatomy & histology, Trees classification, Trees growth & development, Tropical Climate
- Abstract
Trees structure the Earth's most biodiverse ecosystem, tropical forests. The vast number of tree species presents a formidable challenge to understanding these forests, including their response to environmental change, as very little is known about most tropical tree species. A focus on the common species may circumvent this challenge. Here we investigate abundance patterns of common tree species using inventory data on 1,003,805 trees with trunk diameters of at least 10 cm across 1,568 locations
1-6 in closed-canopy, structurally intact old-growth tropical forests in Africa, Amazonia and Southeast Asia. We estimate that 2.2%, 2.2% and 2.3% of species comprise 50% of the tropical trees in these regions, respectively. Extrapolating across all closed-canopy tropical forests, we estimate that just 1,053 species comprise half of Earth's 800 billion tropical trees with trunk diameters of at least 10 cm. Despite differing biogeographic, climatic and anthropogenic histories7 , we find notably consistent patterns of common species and species abundance distributions across the continents. This suggests that fundamental mechanisms of tree community assembly may apply to all tropical forests. Resampling analyses show that the most common species are likely to belong to a manageable list of known species, enabling targeted efforts to understand their ecology. Although they do not detract from the importance of rare species, our results open new opportunities to understand the world's most diverse forests, including modelling their response to environmental change, by focusing on the common species that constitute the majority of their trees., (© 2024. The Author(s).)- Published
- 2024
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16. Valuing the functionality of tropical ecosystems beyond carbon.
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Aguirre-Gutiérrez J, Stevens N, and Berenguer E
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- Conservation of Natural Resources, Biodiversity, Trees, Ecosystem, Carbon
- Abstract
Land-based carbon sequestration projects, such as tree planting, are a prominent strategy to offset carbon emissions. However, we risk reducing natural ecosystems to one metric - carbon. Emphasis on restoring ecosystems to balance ecosystem services, biodiversity conservation, and carbon sequestration is a more appropriate strategy to protect their functioning., Competing Interests: Declaration of interests No interests are declared., (Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2023
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17. Mining the Utricularia gibba genome for insulator-like elements for genetic engineering.
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Laspisa D, Llla-Berenguer E, Bang S, Schmitz RJ, Parrott W, and Wallace J
- Abstract
Introduction: Gene expression is often controlled via cis-regulatory elements (CREs) that modulate the production of transcripts. For multi-gene genetic engineering and synthetic biology, precise control of transcription is crucial, both to insulate the transgenes from unwanted native regulation and to prevent readthrough or cross-regulation of transgenes within a multi-gene cassette. To prevent this activity, insulator-like elements, more properly referred to as transcriptional blockers, could be inserted to separate the transgenes so that they are independently regulated. However, only a few validated insulator-like elements are available for plants, and they tend to be larger than ideal., Methods: To identify additional potential insulator-like sequences, we conducted a genome-wide analysis of Utricularia gibba (humped bladderwort), one of the smallest known plant genomes, with genes that are naturally close together. The 10 best insulator-like candidates were evaluated in vivo for insulator-like activity., Results: We identified a total of 4,656 intergenic regions with expression profiles suggesting insulator-like activity. Comparisons of these regions across 45 other plant species (representing Monocots, Asterids, and Rosids) show low levels of syntenic conservation of these regions. Genome-wide analysis of unmethylated regions (UMRs) indicates ~87% of the targeted regions are unmethylated; however, interpretation of this is complicated because U. gibba has remarkably low levels of methylation across the genome, so that large UMRs frequently extend over multiple genes and intergenic spaces. We also could not identify any conserved motifs among our selected intergenic regions or shared with existing insulator-like elements for plants. Despite this lack of conservation, however, testing of 10 selected intergenic regions for insulator-like activity found two elements on par with a previously published element (EXOB) while being significantly smaller., Discussion: Given the small number of insulator-like elements currently available for plants, our results make a significant addition to available tools. The high hit rate (2 out of 10) also implies that more useful sequences are likely present in our selected intergenic regions; additional validation work will be required to identify which will be most useful for plant genetic engineering., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision., (Copyright © 2023 Laspisa, llla-Berenguer, Bang, Schmitz, Parrott and Wallace.)
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- 2023
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18. Mapping density, diversity and species-richness of the Amazon tree flora.
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Ter Steege H, Pitman NCA, do Amaral IL, de Souza Coelho L, de Almeida Matos FD, de Andrade Lima Filho D, Salomão RP, Wittmann F, Castilho CV, Guevara JE, Veiga Carim MJ, Phillips OL, Magnusson WE, Sabatier D, Revilla JDC, Molino JF, Irume MV, Martins MP, da Silva Guimarães JR, Ramos JF, Bánki OS, Piedade MTF, Cárdenas López D, Rodrigues DJ, Demarchi LO, Schöngart J, Almeida EJ, Barbosa LF, Cavalheiro L, Dos Santos MCV, Luize BG, de Leão Novo EMM, Vargas PN, Silva TSF, Venticinque EM, Manzatto AG, Reis NFC, Terborgh J, Casula KR, Honorio Coronado EN, Monteagudo Mendoza A, Montero JC, Costa FRC, Feldpausch TR, Quaresma AC, Castaño Arboleda N, Zartman CE, Killeen TJ, Marimon BS, Marimon-Junior BH, Vasquez R, Mostacedo B, Assis RL, Baraloto C, do Amaral DD, Engel J, Petronelli P, Castellanos H, de Medeiros MB, Simon MF, Andrade A, Camargo JL, Laurance WF, Laurance SGW, Maniguaje Rincón L, Schietti J, Sousa TR, de Sousa Farias E, Lopes MA, Magalhães JLL, Nascimento HEM, de Queiroz HL, Aymard C GA, Brienen R, Stevenson PR, Araujo-Murakami A, Baker TR, Cintra BBL, Feitosa YO, Mogollón HF, Duivenvoorden JF, Peres CA, Silman MR, Ferreira LV, Lozada JR, Comiskey JA, Draper FC, de Toledo JJ, Damasco G, García-Villacorta R, Lopes A, Vicentini A, Cornejo Valverde F, Alonso A, Arroyo L, Dallmeier F, Gomes VHF, Jimenez EM, Neill D, Peñuela Mora MC, Noronha JC, de Aguiar DPP, Barbosa FR, Bredin YK, de Sá Carpanedo R, Carvalho FA, de Souza FC, Feeley KJ, Gribel R, Haugaasen T, Hawes JE, Pansonato MP, Ríos Paredes M, Barlow J, Berenguer E, da Silva IB, Ferreira MJ, Ferreira J, Fine PVA, Guedes MC, Levis C, Licona JC, Villa Zegarra BE, Vos VA, Cerón C, Durgante FM, Fonty É, Henkel TW, Householder JE, Huamantupa-Chuquimaco I, Pos E, Silveira M, Stropp J, Thomas R, Daly D, Dexter KG, Milliken W, Molina GP, Pennington T, Vieira ICG, Weiss Albuquerque B, Campelo W, Fuentes A, Klitgaard B, Pena JLM, Tello JS, Vriesendorp C, Chave J, Di Fiore A, Hilário RR, de Oliveira Pereira L, Phillips JF, Rivas-Torres G, van Andel TR, von Hildebrand P, Balee W, Barbosa EM, de Matos Bonates LC, Dávila Doza HP, Zárate Gómez R, Gonzales T, Gallardo Gonzales GP, Hoffman B, Junqueira AB, Malhi Y, de Andrade Miranda IP, Pinto LFM, Prieto A, Rudas A, Ruschel AR, Silva N, Vela CIA, Zent EL, Zent S, Cano A, Carrero Márquez YA, Correa DF, Costa JBP, Flores BM, Galbraith D, Holmgren M, Kalamandeen M, Lobo G, Torres Montenegro L, Nascimento MT, Oliveira AA, Pombo MM, Ramirez-Angulo H, Rocha M, Scudeller VV, Sierra R, Tirado M, Umaña MN, van der Heijden G, Vilanova Torre E, Reategui MAA, Baider C, Balslev H, Cárdenas S, Casas LF, Endara MJ, Farfan-Rios W, Ferreira C, Linares-Palomino R, Mendoza C, Mesones I, Parada GA, Torres-Lezama A, Urrego Giraldo LE, Villarroel D, Zagt R, Alexiades MN, de Oliveira EA, Garcia-Cabrera K, Hernandez L, Cuenca WP, Pansini S, Pauletto D, Ramirez Arevalo F, Sampaio AF, Valderrama Sandoval EH, Gamarra LV, Levesley A, Pickavance G, and Melgaço K
- Subjects
- Forests, Soil, Temperature, Trees, RNA, Long Noncoding
- Abstract
Using 2.046 botanically-inventoried tree plots across the largest tropical forest on Earth, we mapped tree species-diversity and tree species-richness at 0.1-degree resolution, and investigated drivers for diversity and richness. Using only location, stratified by forest type, as predictor, our spatial model, to the best of our knowledge, provides the most accurate map of tree diversity in Amazonia to date, explaining approximately 70% of the tree diversity and species-richness. Large soil-forest combinations determine a significant percentage of the variation in tree species-richness and tree alpha-diversity in Amazonian forest-plots. We suggest that the size and fragmentation of these systems drive their large-scale diversity patterns and hence local diversity. A model not using location but cumulative water deficit, tree density, and temperature seasonality explains 47% of the tree species-richness in the terra-firme forest in Amazonia. Over large areas across Amazonia, residuals of this relationship are small and poorly spatially structured, suggesting that much of the residual variation may be local. The Guyana Shield area has consistently negative residuals, showing that this area has lower tree species-richness than expected by our models. We provide extensive plot meta-data, including tree density, tree alpha-diversity and tree species-richness results and gridded maps at 0.1-degree resolution., (© 2023. The Author(s).)
- Published
- 2023
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19. More than 10,000 pre-Columbian earthworks are still hidden throughout Amazonia.
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Peripato V, Levis C, Moreira GA, Gamerman D, Ter Steege H, Pitman NCA, de Souza JG, Iriarte J, Robinson M, Junqueira AB, Trindade TB, de Almeida FO, Moraes CP, Lombardo U, Tamanaha EK, Maezumi SY, Ometto JPHB, Braga JRG, Campanharo WA, Cassol HLG, Leal PR, de Assis MLR, da Silva AM, Phillips OL, Costa FRC, Flores BM, Hoffman B, Henkel TW, Umaña MN, Magnusson WE, Valderrama Sandoval EH, Barlow J, Milliken W, Lopes MA, Simon MF, van Andel TR, Laurance SGW, Laurance WF, Torres-Lezama A, Assis RL, Molino JF, Mestre M, Hamblin M, Coelho LS, Lima Filho DA, Wittmann F, Salomão RP, Amaral IL, Guevara JE, de Almeida Matos FD, Castilho CV, Carim MJV, Cárdenas López D, Sabatier D, Irume MV, Martins MP, Guimarães JRDS, Bánki OS, Piedade MTF, Ramos JF, Luize BG, Novo EMML, Núñez Vargas P, Silva TSF, Venticinque EM, Manzatto AG, Reis NFC, Terborgh J, Casula KR, Demarchi LO, Honorio Coronado EN, Monteagudo Mendoza A, Montero JC, Schöngart J, Feldpausch TR, Quaresma AC, Aymard C GA, Baraloto C, Castaño Arboleda N, Engel J, Petronelli P, Zartman CE, Killeen TJ, Marimon BS, Marimon-Junior BH, Schietti J, Sousa TR, Vasquez R, Rincón LM, Berenguer E, Ferreira J, Mostacedo B, do Amaral DD, Castellanos H, de Medeiros MB, Andrade A, Camargo JL, Farias ES, Magalhães JLL, Mendonça Nascimento HE, de Queiroz HL, Brienen R, Cardenas Revilla JD, Stevenson PR, Araujo-Murakami A, Barçante Ladvocat Cintra B, Feitosa YO, Barbosa FR, Carpanedo RS, Duivenvoorden JF, de Noronha JDC, Rodrigues DJ, Mogollón HF, Ferreira LV, Householder JE, Lozada JR, Comiskey JA, Draper FC, de Toledo JJ, Damasco G, Dávila N, García-Villacorta R, Lopes A, Cornejo Valverde F, Alonso A, Dallmeier F, Gomes VHF, Jimenez EM, Neill D, Peñuela Mora MC, de Aguiar DPP, Arroyo L, Antunes Carvalho F, Coelho de Souza F, Feeley KJ, Gribel R, Pansonato MP, Ríos Paredes M, Brasil da Silva I, Ferreira MJ, Fine PVA, Fonty É, Guedes MC, Licona JC, Pennington T, Peres CA, Villa Zegarra BE, Parada GA, Pardo Molina G, Vos VA, Cerón C, Maas P, Silveira M, Stropp J, Thomas R, Baker TR, Daly D, Huamantupa-Chuquimaco I, Vieira ICG, Weiss Albuquerque B, Fuentes A, Klitgaard B, Marcelo-Peña JL, Silman MR, Tello JS, Vriesendorp C, Chave J, Di Fiore A, Hilário RR, Phillips JF, Rivas-Torres G, von Hildebrand P, Pereira LO, Barbosa EM, de Matos Bonates LC, Doza HPD, Zárate Gómez R, Gallardo Gonzales GP, Gonzales T, Malhi Y, de Andrade Miranda IP, Mozombite Pinto LF, Prieto A, Rudas A, Ruschel AR, Silva N, Vela CIA, Zent EL, Zent S, Cano A, Carrero Márquez YA, Correa DF, Costa JBP, Galbraith D, Holmgren M, Kalamandeen M, Lobo G, Nascimento MT, Oliveira AA, Ramirez-Angulo H, Rocha M, Scudeller VV, Sierra R, Tirado M, van der Heijden G, Vilanova Torre E, Ahuite Reategui MA, Baider C, Balslev H, Cárdenas S, Casas LF, Farfan-Rios W, Ferreira C, Linares-Palomino R, Mendoza C, Mesones I, Urrego Giraldo LE, Villarroel D, Zagt R, Alexiades MN, de Oliveira EA, Garcia-Cabrera K, Hernandez L, Palacios Cuenca W, Pansini S, Pauletto D, Ramirez Arevalo F, Sampaio AF, Valenzuela Gamarra L, and Aragão LEOC
- Subjects
- Humans, Brazil, Forests, Archaeology
- Abstract
Indigenous societies are known to have occupied the Amazon basin for more than 12,000 years, but the scale of their influence on Amazonian forests remains uncertain. We report the discovery, using LIDAR (light detection and ranging) information from across the basin, of 24 previously undetected pre-Columbian earthworks beneath the forest canopy. Modeled distribution and abundance of large-scale archaeological sites across Amazonia suggest that between 10,272 and 23,648 sites remain to be discovered and that most will be found in the southwest. We also identified 53 domesticated tree species significantly associated with earthwork occurrence probability, likely suggesting past management practices. Closed-canopy forests across Amazonia are likely to contain thousands of undiscovered archaeological sites around which pre-Columbian societies actively modified forests, a discovery that opens opportunities for better understanding the magnitude of ancient human influence on Amazonia and its current state.
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- 2023
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20. Giants of the Amazon: How does environmental variation drive the diversity patterns of large trees?
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de Lima RB, Görgens EB, da Silva DAS, de Oliveira CP, Batista APB, Caraciolo Ferreira RL, Costa FRC, Ferreira de Lima RA, da Silva Aparício P, de Abreu JC, da Silva JAA, Guimaraes AF, Fearnside PM, Sousa TR, Perdiz R, Higuchi N, Berenguer E, Resende AF, Elias F, de Castilho CV, de Medeiros MB, de Matos Filho JR, Sardinha MA, Freitas MAF, da Silva JJ, da Cunha AP, Santos RM, Muelbert AE, Guedes MC, Imbrózio R, de Sousa CSC, da Silva Aparício WC, da Silva E Silva BM, Silva CA, Marimon BS, Junior BHM, Morandi PS, Storck-Tonon D, Vieira ICG, Schietti J, Coelho F, Alves de Almeida DR, Castro W, Carvalho SPC, da Silva RDSA, Silveira J, Camargo JL, Melgaço K, de Freitas LJM, Vedovato L, Benchimol M, de Oliveira de Almeida G, Prance G, da Silveira AB, Simon MF, Garcia ML, Silveira M, Vital M, Andrade MBT, Silva N, de Araújo RO, Cavalheiro L, Carpanedo R, Fernandes L, Manzatto AG, de Andrade RTG, Magnusson WE, Laurance B, Nelson BW, Peres C, Daly DC, Rodrigues D, Zopeletto AP, de Oliveira EA, Dugachard E, Barbosa FR, Santana F, do Amaral IL, Ferreira LV, Charão LS, Ferreira J, Barlow J, Blanc L, Aragão L, Sist P, de Paiva Salomão R, da Silva ASL, Laurance S, Feldpausch TR, Gardner T, Santiago W, Balee W, Laurance WF, Malhi Y, Phillips OL, da Silva Zanzini AC, Rosa C, Tadeu Oliveira W, Pereira Zanzini L, José Silva R, and Mangabeira Albernaz AL
- Subjects
- Brazil, Rainforest, Biodiversity, Wind, Acclimatization
- Abstract
For more than three decades, major efforts in sampling and analyzing tree diversity in South America have focused almost exclusively on trees with stems of at least 10 and 2.5 cm diameter, showing highest species diversity in the wetter western and northern Amazon forests. By contrast, little attention has been paid to patterns and drivers of diversity in the largest canopy and emergent trees, which is surprising given these have dominant ecological functions. Here, we use a machine learning approach to quantify the importance of environmental factors and apply it to generate spatial predictions of the species diversity of all trees (dbh ≥ 10 cm) and for very large trees (dbh ≥ 70 cm) using data from 243 forest plots (108,450 trees and 2832 species) distributed across different forest types and biogeographic regions of the Brazilian Amazon. The diversity of large trees and of all trees was significantly associated with three environmental factors, but in contrasting ways across regions and forest types. Environmental variables associated with disturbances, for example, the lightning flash rate and wind speed, as well as the fraction of photosynthetically active radiation, tend to govern the diversity of large trees. Upland rainforests in the Guiana Shield and Roraima regions had a high diversity of large trees. By contrast, variables associated with resources tend to govern tree diversity in general. Places such as the province of Imeri and the northern portion of the province of Madeira stand out for their high diversity of species in general. Climatic and topographic stability and functional adaptation mechanisms promote ideal conditions for species diversity. Finally, we mapped general patterns of tree species diversity in the Brazilian Amazon, which differ substantially depending on size class., (© 2023 John Wiley & Sons Ltd.)
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- 2023
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21. Pervasive gaps in Amazonian ecological research.
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Carvalho RL, Resende AF, Barlow J, França FM, Moura MR, Maciel R, Alves-Martins F, Shutt J, Nunes CA, Elias F, Silveira JM, Stegmann L, Baccaro FB, Juen L, Schietti J, Aragão L, Berenguer E, Castello L, Costa FRC, Guedes ML, Leal CG, Lees AC, Isaac V, Nascimento RO, Phillips OL, Schmidt FA, Steege HT, Vaz-de-Mello F, Venticinque EM, Guimarães Vieira IC, Zuanon J, and Ferreira J
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- 2023
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22. Soil microbes under threat in the Amazon Rainforest.
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M Venturini A, B Gontijo J, A Mandro J, Berenguer E, Peay KG, M Tsai S, and Bohannan BJM
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- Rainforest, Biodiversity, Climate Change, Soil, Ecosystem
- Abstract
Soil microorganisms are sensitive indicators of land-use and climate change in the Amazon, revealing shifts in important processes such as greenhouse gas (GHG) production, but they have been overlooked in conservation and management initiatives. Integrating soil biodiversity with other disciplines while expanding sampling efforts and targeted microbial groups is crucially needed., Competing Interests: Declaration of interests The authors declare no conflicts of interest., (Copyright © 2023 Elsevier Ltd. All rights reserved.)
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- 2023
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23. Editing efficiencies with Cas9 orthologs, Cas12a endonucleases, and temperature in rice.
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Illa-Berenguer E, LaFayette PR, and Parrott WA
- Abstract
The advent of CRISPR-Cas technology has made it the genome editing tool of choice in all kingdoms of life, including plants, which can have large, highly duplicated genomes. As a result, finding adequate target sequences that meet the specificities of a given Cas nuclease on any gene of interest remains challenging in many cases. To assess target site flexibility, we tested five different Cas9/Cas12a endonucleases (SpCas9, SaCas9, St1Cas9, Mb3Cas12a, and AsCas12a) in embryogenic rice calli from Taipei 309 at 37°C (optimal temperature for most Cas9/Cas12a proteins) and 27°C (optimal temperature for tissue culture) and measured their editing rates under regular tissue culture conditions using Illumina sequencing. StCas9 and AsCas12 were not functional as tested, regardless of the temperature used. SpCas9 was the most efficient endonuclease at either temperature, regardless of whether monoallelic or biallelic edits were considered. Mb3Cas12a at 37°C was the next most efficient endonuclease. Monoallelic edits prevailed for both SaCas9 and Mb3Cas12a at 27°C, but biallelic edits prevailed at 37°C. Overall, the use of other Cas9 orthologs, the use of Cas12a endonucleases, and the optimal temperature can expand the range of targetable sequences., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2023 Illa-Berenguer, LaFayette and Parrott.)
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- 2023
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24. Unraveling Amazon tree community assembly using Maximum Information Entropy: a quantitative analysis of tropical forest ecology.
- Author
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Pos E, de Souza Coelho L, de Andrade Lima Filho D, Salomão RP, Amaral IL, de Almeida Matos FD, Castilho CV, Phillips OL, Guevara JE, de Jesus Veiga Carim M, López DC, Magnusson WE, Wittmann F, Irume MV, Martins MP, Sabatier D, da Silva Guimarães JR, Molino JF, Bánki OS, Piedade MTF, Pitman NCA, Mendoza AM, Ramos JF, Hawes JE, Almeida EJ, Barbosa LF, Cavalheiro L, Dos Santos MCV, Luize BG, de Leão Novo EMM, Vargas PN, Silva TSF, Venticinque EM, Manzatto AG, Reis NFC, Terborgh J, Casula KR, Coronado ENH, Montero JC, Marimon BS, Marimon-Junior BH, Feldpausch TR, Duque A, Baraloto C, Arboleda NC, Engel J, Petronelli P, Zartman CE, Killeen TJ, Vasquez R, Mostacedo B, Assis RL, Schöngart J, Castellanos H, de Medeiros MB, Simon MF, Andrade A, Camargo JL, Demarchi LO, Laurance WF, Laurance SGW, de Sousa Farias E, Lopes MA, Magalhães JLL, Nascimento HEM, de Queiroz HL, Aymard GAC, Brienen R, Revilla JDC, Costa FRC, Quaresma A, Vieira ICG, Cintra BBL, Stevenson PR, Feitosa YO, Duivenvoorden JF, Mogollón HF, Ferreira LV, Comiskey JA, Draper F, de Toledo JJ, Damasco G, Dávila N, García-Villacorta R, Lopes A, Vicentini A, Noronha JC, Barbosa FR, de Sá Carpanedo R, Emilio T, Levis C, de Jesus Rodrigues D, Schietti J, Souza P, Alonso A, Dallmeier F, Gomes VHF, Lloyd J, Neill D, de Aguiar DPP, Araujo-Murakami A, Arroyo L, Carvalho FA, de Souza FC, do Amaral DD, Feeley KJ, Gribel R, Pansonato MP, Barlow J, Berenguer E, Ferreira J, Fine PVA, Guedes MC, Jimenez EM, Licona JC, Mora MCP, Peres CA, Zegarra BEV, Cerón C, Henkel TW, Maas P, Silveira M, Stropp J, Thomas-Caesar R, Baker TR, Daly D, Dexter KG, Householder JE, Huamantupa-Chuquimaco I, Pennington T, Paredes MR, Fuentes A, Pena JLM, Silman MR, Tello JS, Chave J, Valverde FC, Di Fiore A, Hilário RR, Phillips JF, Rivas-Torres G, van Andel TR, von Hildebrand P, Barbosa EM, de Matos Bonates LC, Doza HPD, Fonty É, Gómez RZ, Gonzales T, Gonzales GPG, Guillaumet JL, Hoffman B, Junqueira AB, Malhi Y, de Andrade Miranda IP, Pinto LFM, Prieto A, Rudas A, Ruschel AR, Silva N, Vela CIA, Vos VA, Zent EL, Zent S, Albuquerque BW, Cano A, Correa DF, Costa JBP, Flores BM, Holmgren M, Nascimento MT, Oliveira AA, Ramirez-Angulo H, Rocha M, Scudeller VV, Sierra R, Tirado M, Umaña MN, van der Heijden G, Torre EV, Vriesendorp C, Wang O, Young KR, Reategui MAA, Baider C, Balslev H, Cárdenas S, Casas LF, Farfan-Rios W, Ferreira C, Linares-Palomino R, Mendoza C, Mesones I, Torres-Lezama A, Giraldo LEU, Villarroel D, Zagt R, Alexiades MN, Garcia-Cabrera K, Hernandez L, Milliken W, Cuenca WP, Pansini S, Pauletto D, Arevalo FR, Sampaio AF, Sandoval EHV, Gamarra LV, Boenisch G, Kattge J, Kraft N, Levesley A, Melgaço K, Pickavance G, Poorter L, and Ter Steege H
- Subjects
- Entropy, Forests, Plants, Ecology, Tropical Climate, Ecosystem, Biodiversity
- Abstract
In a time of rapid global change, the question of what determines patterns in species abundance distribution remains a priority for understanding the complex dynamics of ecosystems. The constrained maximization of information entropy provides a framework for the understanding of such complex systems dynamics by a quantitative analysis of important constraints via predictions using least biased probability distributions. We apply it to over two thousand hectares of Amazonian tree inventories across seven forest types and thirteen functional traits, representing major global axes of plant strategies. Results show that constraints formed by regional relative abundances of genera explain eight times more of local relative abundances than constraints based on directional selection for specific functional traits, although the latter does show clear signals of environmental dependency. These results provide a quantitative insight by inference from large-scale data using cross-disciplinary methods, furthering our understanding of ecological dynamics., (© 2023. The Author(s).)
- Published
- 2023
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25. The drivers and impacts of Amazon forest degradation.
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Lapola DM, Pinho P, Barlow J, Aragão LEOC, Berenguer E, Carmenta R, Liddy HM, Seixas H, Silva CVJ, Silva-Junior CHL, Alencar AAC, Anderson LO, Armenteras D, Brovkin V, Calders K, Chambers J, Chini L, Costa MH, Faria BL, Fearnside PM, Ferreira J, Gatti L, Gutierrez-Velez VH, Han Z, Hibbard K, Koven C, Lawrence P, Pongratz J, Portela BTT, Rounsevell M, Ruane AC, Schaldach R, da Silva SS, von Randow C, and Walker WS
- Subjects
- Biodiversity, Carbon Cycle, Brazil, Carbon, Conservation of Natural Resources, Rainforest
- Abstract
Approximately 2.5 × 10
6 square kilometers of the Amazon forest are currently degraded by fire, edge effects, timber extraction, and/or extreme drought, representing 38% of all remaining forests in the region. Carbon emissions from this degradation total up to 0.2 petagrams of carbon per year (Pg C year-1 ), which is equivalent to, if not greater than, the emissions from Amazon deforestation (0.06 to 0.21 Pg C year-1 ). Amazon forest degradation can reduce dry-season evapotranspiration by up to 34% and cause as much biodiversity loss as deforestation in human-modified landscapes, generating uneven socioeconomic burdens, mainly to forest dwellers. Projections indicate that degradation will remain a dominant source of carbon emissions independent of deforestation rates. Policies to tackle degradation should be integrated with efforts to curb deforestation and complemented with innovative measures addressing the disturbances that degrade the Amazon forest.- Published
- 2023
- Full Text
- View/download PDF
26. AtEXT3 is not essential for early embryogenesis or plant viability in Arabidopsis.
- Author
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Doll NM, Berenguer E, Truskina J, and Ingram G
- Subjects
- Gene Expression Regulation, Plant, Embryonic Development, Cell Wall metabolism, Arabidopsis genetics, Arabidopsis metabolism, Arabidopsis Proteins genetics, Arabidopsis Proteins metabolism
- Published
- 2022
- Full Text
- View/download PDF
27. The DNA methylation landscape of the root-knot nematode-induced pseudo-organ, the gall, in Arabidopsis, is dynamic, contrasting over time, and critically important for successful parasitism.
- Author
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Silva AC, Ruiz-Ferrer V, Müller SY, Pellegrin C, Abril-Urías P, Martínez-Gómez Á, Gómez-Rojas A, Berenguer E, Testillano PS, Andrés MF, Fenoll C, Eves-van den Akker S, and Escobar C
- Subjects
- Animals, Protein-Tyrosine Kinases genetics, Protein-Tyrosine Kinases metabolism, Gene Expression Regulation, Plant, DNA Methylation genetics, Plant Roots genetics, Plant Roots metabolism, Proto-Oncogene Proteins genetics, Proto-Oncogene Proteins metabolism, DNA (Cytosine-5-)-Methyltransferases genetics, DNA (Cytosine-5-)-Methyltransferases metabolism, Arabidopsis metabolism, Tylenchoidea physiology, Arabidopsis Proteins genetics, Arabidopsis Proteins metabolism
- Abstract
Root-knot nematodes (RKNs) induce giant cells (GCs) within galls which are characterized by large-scale gene repression at early stages. However, the epigenetic mechanism(s) underlying gene silencing is (are) still poorly characterized. DNA methylation in Arabidopsis galls induced by Meloidogyne javanica was studied at crucial infection stages (3 d post-infection (dpi) and 14 dpi) using enzymatic, cytological, and sequencing approaches. DNA methyltransferase mutants (met1, cmt2, cmt3, cmt2/3, drm1/2, ddc) and a DNA demethylase mutant (ros1), were analyzed for RKN resistance/tolerance, and galls were characterized by confocal microscopy and RNA-seq. Early galls were hypermethylated, and the GCs were found to be the major contributors to this hypermethylation, consistent with the very high degree of gene repression they exhibit. By contrast, medium/late galls showed no global increase in DNA methylation compared to uninfected roots, but exhibited large-scale redistribution of differentially methylated regions (DMRs). In line with these findings, it was also shown that DNA methylation and demethylation mutants showed impaired nematode reproduction and gall/GC-development. Moreover, siRNAs that were exclusively present in early galls accumulated at hypermethylated DMRs, overlapping mostly with retrotransposons in the CHG/CG contexts that might be involved in their repression, contributing to their stability/genome integrity. Promoter/gene methylation correlated with differentially expressed genes encoding proteins with basic cell functions. Both mechanisms are consistent with reprogramming host tissues for gall/GC formation. In conclusion, RNA-directed DNA methylation (RdDM; DRM2/1) pathways, maintenance methyltransferases (MET1/CMT3) and demethylation (ROS1) appear to be prominent mechanisms driving a dynamic regulation of the epigenetic landscape during RKN infection., (© 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation.)
- Published
- 2022
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- View/download PDF
28. An Agrobacterium strain auxotrophic for methionine is useful for switchgrass transformation.
- Author
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Prías-Blanco M, Chappell TM, Freed EF, Illa-Berenguer E, Eckert CA, and Parrott WA
- Subjects
- Transformation, Genetic, Methionine genetics, Agrobacterium tumefaciens genetics, Transgenes, Plants, Genetically Modified genetics, Plants, Genetically Modified microbiology, Panicum genetics
- Abstract
Auxotrophic strains of Agrobacterium tumefaciens can contribute to the development of more efficient transformation systems, especially for crops historically considered recalcitrant. Homologous recombination was used to derive methionine auxotrophs of two common A. tumefaciens strains, LBA4404 and EHA105. The EHA105 strains were more efficient for switchgrass transformation, while both the EHA105 and LBA4404 strains worked equally well for the rice control. Event quality, as measured by transgene copy number, was not affected by auxotrophy, but was higher for the LBA4404 strains than the EHA105 strains. Ultimately, the use of auxotrophs reduced bacterial overgrowth during co-cultivation and decreased the need for antibiotics., (© 2022. The Author(s).)
- Published
- 2022
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- View/download PDF
29. Heterologous expression of a lycophyte protein enhances angiosperm seedling vigor.
- Author
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Koh SWH, Diaz-Ardila HN, Bascom CS, Berenguer E, Ingram G, Estelle M, and Hardtke CS
- Subjects
- Seedlings genetics, Gene Expression Regulation, Plant genetics, Plant Roots metabolism, Arabidopsis Proteins genetics, Arabidopsis Proteins metabolism, Magnoliopsida metabolism, Arabidopsis metabolism
- Abstract
Seedling vigor is a key agronomic trait that determines juvenile plant performance. Angiosperm seeds develop inside fruits and are connected to the mother plant through vascular tissues. Their formation requires plant-specific genes, such as BREVIS RADIX (BRX) in Arabidopsis thaliana roots. BRX family proteins are found throughout the euphyllophytes but also occur in non-vascular bryophytes and non-seed lycophytes. They consist of four conserved domains, including the tandem BRX domains. We found that bryophyte or lycophyte BRX homologs can only partially substitute for Arabidopsis BRX (AtBRX) because they miss key features in the linker between the BRX domains. Intriguingly, however, expression of a BRX homolog from the lycophyte Selaginella moellendorffii (SmBRX) in an A. thaliana wild-type background confers robustly enhanced root growth vigor that persists throughout the life cycle. This effect can be traced to a substantial increase in seed and embryo size, is associated with enhanced vascular tissue proliferation, and can be reproduced with a modified, SmBRX-like variant of AtBRX. Our results thus suggest that BRX variants can boost seedling vigor and shed light on the activity of ancient, non-angiosperm BRX family proteins., Competing Interests: Competing interests The authors declare no competing or financial interests., (© 2022. Published by The Company of Biologists Ltd.)
- Published
- 2022
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- View/download PDF
30. Increased soil moisture intensifies the impacts of forest-to-pasture conversion on methane emissions and methane-cycling communities in the Eastern Amazon.
- Author
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Venturini AM, Dias NMS, Gontijo JB, Yoshiura CA, Paula FS, Meyer KM, Nakamura FM, da França AG, Borges CD, Barlow J, Berenguer E, Nüsslein K, Rodrigues JLM, Bohannan BJM, and Tsai SM
- Subjects
- Climate, Forests, Soil Microbiology, Methane analysis, Soil chemistry
- Abstract
Climatic changes are altering precipitation patterns in the Amazon and may influence soil methane (CH
4 ) fluxes due to the differential responses of methanogenic and methanotrophic microorganisms. However, it remains unclear if these climate feedbacks can amplify land-use-related impacts on the CH4 cycle. To better predict the responses of soil CH4 -cycling microorganisms and emissions under altered moisture levels in the Eastern Brazilian Amazon, we performed a 30-day microcosm experiment manipulating the moisture content (original moisture; 60%, 80%, and 100% of field capacity - FC) of forest and pasture soils. Gas samples were collected periodically for gas chromatography analysis, and methanogenic archaeal and methanotrophic bacterial communities were assessed using quantitative PCR and metagenomics. Positive and negative daily CH4 fluxes were observed for forest and pasture, indicating that these soils can act as both CH4 sources and sinks. Cumulative emissions and the abundance of methanogenesis-related genes and taxonomic groups were affected by land use, moisture, and their interaction. Pasture soils at 100% FC had the highest abundance of methanogens and CH4 emissions, 22 times higher than forest soils under the same treatment. Higher ratios of methanogens to methanotrophs were found in pasture than in forest soils, even at field capacity conditions. Land use and moisture were significant factors influencing the composition of methanogenic and methanotrophic communities. The diversity and evenness of methanogens did not change throughout the experiment. In contrast, methanotrophs exhibited the highest diversity and evenness in pasture soils at 100% FC. Taken together, our results suggest that increased moisture exacerbates soil CH4 emissions and microbial responses driven by land-use change in the Amazon. This is the first report on the microbial CH4 cycle in Amazonian upland soils that combined one-month gas measurements with advanced molecular methods., (Copyright © 2022 Elsevier Inc. All rights reserved.)- Published
- 2022
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- View/download PDF
31. Linking land-use and land-cover transitions to their ecological impact in the Amazon.
- Author
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Nunes CA, Berenguer E, França F, Ferreira J, Lees AC, Louzada J, Sayer EJ, Solar R, Smith CC, Aragão LEOC, Braga DL, de Camargo PB, Cerri CEP, de Oliveira RC Jr, Durigan M, Moura N, Oliveira VHF, Ribas C, Vaz-de-Mello F, Vieira I, Zanetti R, and Barlow J
- Subjects
- Agriculture, Brazil, Carbon, Humans, Anthropogenic Effects, Biodiversity, Conservation of Natural Resources, Rainforest
- Abstract
Human activities pose a major threat to tropical forest biodiversity and ecosystem services. Although the impacts of deforestation are well studied, multiple land-use and land-cover transitions (LULCTs) occur in tropical landscapes, and we do not know how LULCTs differ in their rates or impacts on key ecosystem components. Here, we quantified the impacts of 18 LULCTs on three ecosystem components (biodiversity, carbon, and soil), based on 18 variables collected from 310 sites in the Brazilian Amazon. Across all LULCTs, biodiversity was the most affected ecosystem component, followed by carbon stocks, but the magnitude of change differed widely among LULCTs and individual variables. Forest clearance for pasture was the most prevalent and high-impact transition, but we also identified other LULCTs with high impact but lower prevalence (e.g., forest to agriculture). Our study demonstrates the importance of considering multiple ecosystem components and LULCTs to understand the consequences of human activities in tropical landscapes.
- Published
- 2022
- Full Text
- View/download PDF
32. Functional susceptibility of tropical forests to climate change.
- Author
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Aguirre-Gutiérrez J, Berenguer E, Oliveras Menor I, Bauman D, Corral-Rivas JJ, Nava-Miranda MG, Both S, Ndong JE, Ondo FE, Bengone NN, Mihinhou V, Dalling JW, Heineman K, Figueiredo A, González-M R, Norden N, Hurtado-M AB, González D, Salgado-Negret B, Reis SM, Moraes de Seixas MM, Farfan-Rios W, Shenkin A, Riutta T, Girardin CAJ, Moore S, Abernethy K, Asner GP, Bentley LP, Burslem DFRP, Cernusak LA, Enquist BJ, Ewers RM, Ferreira J, Jeffery KJ, Joly CA, Marimon-Junior BH, Martin RE, Morandi PS, Phillips OL, Bennett AC, Lewis SL, Quesada CA, Marimon BS, Kissling WD, Silman M, Teh YA, White LJT, Salinas N, Coomes DA, Barlow J, Adu-Bredu S, and Malhi Y
- Subjects
- Forests, Trees, Water, Climate Change, Ecosystem
- Abstract
Tropical forests are some of the most biodiverse ecosystems in the world, yet their functioning is threatened by anthropogenic disturbances and climate change. Global actions to conserve tropical forests could be enhanced by having local knowledge on the forests' functional diversity and functional redundancy as proxies for their capacity to respond to global environmental change. Here we create estimates of plant functional diversity and redundancy across the tropics by combining a dataset of 16 morphological, chemical and photosynthetic plant traits sampled from 2,461 individual trees from 74 sites distributed across four continents together with local climate data for the past half century. Our findings suggest a strong link between climate and functional diversity and redundancy with the three trait groups responding similarly across the tropics and climate gradient. We show that drier tropical forests are overall less functionally diverse than wetter forests and that functional redundancy declines with increasing soil water and vapour pressure deficits. Areas with high functional diversity and high functional redundancy tend to better maintain ecosystem functioning, such as aboveground biomass, after extreme weather events. Our predictions suggest that the lower functional diversity and lower functional redundancy of drier tropical forests, in comparison with wetter forests, may leave them more at risk of shifting towards alternative states in face of further declines in water availability across tropical regions., (© 2022. The Author(s), under exclusive licence to Springer Nature Limited.)
- Published
- 2022
- Full Text
- View/download PDF
33. Strong floristic distinctiveness across Neotropical successional forests.
- Author
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Jakovac CC, Meave JA, Bongers F, Letcher SG, Dupuy JM, Piotto D, Rozendaal DMA, Peña-Claros M, Craven D, Santos BA, Siminski A, Fantini AC, Rodrigues AC, Hernández-Jaramillo A, Idárraga A, Junqueira AB, Zambrano AMA, de Jong BHJ, Pinho BX, Finegan B, Castellano-Castro C, Zambiazi DC, Dent DH, García DH, Kennard D, Delgado D, Broadbent EN, Ortiz-Malavassi E, Pérez-García EA, Lebrija-Trejos E, Berenguer E, Marín-Spiotta E, Alvarez-Davila E, de Sá Sampaio EV, Melo F, Elias F, França F, Oberleitner F, Mora F, Williamson GB, Colletta GD, Cabral GAL, Derroire G, Fernandes GW, van der Wal H, Teixeira HM, Vester HFM, García H, Vieira ICG, Jiménez-Montoya J, de Almeida-Cortez JS, Hall JS, Chave J, Zimmerman JK, Nieto JE, Ferreira J, Rodríguez-Velázquez J, Ruíz J, Barlow J, Aguilar-Cano J, Hernández-Stefanoni JL, Engel J, Becknell JM, Zanini K, Lohbeck M, Tabarelli M, Romero-Romero MA, Uriarte M, Veloso MDM, Espírito-Santo MM, van der Sande MT, van Breugel M, Martínez-Ramos M, Schwartz NB, Norden N, Pérez-Cárdenas N, González-Valdivia N, Petronelli P, Balvanera P, Massoca P, Brancalion PHS, Villa PM, Hietz P, Ostertag R, López-Camacho R, César RG, Mesquita R, Chazdon RL, Muñoz R, DeWalt SJ, Müller SC, Durán SM, Martins SV, Ochoa-Gaona S, Rodríguez-Buritica S, Aide TM, Bentos TV, de S Moreno V, Granda V, Thomas W, Silver WL, Nunes YRF, and Poorter L
- Abstract
Forests that regrow naturally on abandoned fields are important for restoring biodiversity and ecosystem services, but can they also preserve the distinct regional tree floras? Using the floristic composition of 1215 early successional forests (≤20 years) in 75 human-modified landscapes across the Neotropic realm, we identified 14 distinct floristic groups, with a between-group dissimilarity of 0.97. Floristic groups were associated with location, bioregions, soil pH, temperature seasonality, and water availability. Hence, there is large continental-scale variation in the species composition of early successional forests, which is mainly associated with biogeographic and environmental factors but not with human disturbance indicators. This floristic distinctiveness is partially driven by regionally restricted species belonging to widespread genera. Early secondary forests contribute therefore to restoring and conserving the distinctiveness of bioregions across the Neotropical realm, and forest restoration initiatives should use local species to assure that these distinct floras are maintained.
- Published
- 2022
- Full Text
- View/download PDF
34. Global relationships in tree functional traits.
- Author
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Maynard DS, Bialic-Murphy L, Zohner CM, Averill C, van den Hoogen J, Ma H, Mo L, Smith GR, Acosta ATR, Aubin I, Berenguer E, Boonman CCF, Catford JA, Cerabolini BEL, Dias AS, González-Melo A, Hietz P, Lusk CH, Mori AS, Niinemets Ü, Pillar VD, Pinho BX, Rosell JA, Schurr FM, Sheremetev SN, da Silva AC, Sosinski Ê, van Bodegom PM, Weiher E, Bönisch G, Kattge J, and Crowther TW
- Subjects
- Biodiversity, Forests, Plant Bark physiology, Plant Leaves physiology, Plant Roots physiology, Seeds physiology, Wood physiology, Trees physiology
- Abstract
Due to massive energetic investments in woody support structures, trees are subject to unique physiological, mechanical, and ecological pressures not experienced by herbaceous plants. Despite a wealth of studies exploring trait relationships across the entire plant kingdom, the dominant traits underpinning these unique aspects of tree form and function remain unclear. Here, by considering 18 functional traits, encompassing leaf, seed, bark, wood, crown, and root characteristics, we quantify the multidimensional relationships in tree trait expression. We find that nearly half of trait variation is captured by two axes: one reflecting leaf economics, the other reflecting tree size and competition for light. Yet these orthogonal axes reveal strong environmental convergence, exhibiting correlated responses to temperature, moisture, and elevation. By subsequently exploring multidimensional trait relationships, we show that the full dimensionality of trait space is captured by eight distinct clusters, each reflecting a unique aspect of tree form and function. Collectively, this work identifies a core set of traits needed to quantify global patterns in functional biodiversity, and it contributes to our fundamental understanding of the functioning of forests worldwide., (© 2022. The Author(s).)
- Published
- 2022
- Full Text
- View/download PDF
35. Small molecule inhibitors of mammalian GSK-3β promote in vitro plant cell reprogramming and somatic embryogenesis in crop and forest species.
- Author
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Berenguer E, Carneros E, Pérez-Pérez Y, Gil C, Martínez A, and Testillano PS
- Subjects
- Animals, Embryonic Development, Forests, Glycogen Synthase Kinase 3 beta genetics, Cellular Reprogramming, Glycogen Synthase Kinase 3 genetics
- Abstract
Plant in vitro regeneration systems, such as somatic embryogenesis, are essential in breeding; they permit propagation of elite genotypes, production of doubled-haploids, and regeneration of whole plants from gene editing or transformation events. However, in many crop and forest species, somatic embryogenesis is highly inefficient. We report a new strategy to improve in vitro embryogenesis using synthetic small molecule inhibitors of mammalian glycogen synthase kinase 3β (GSK-3β), never used in plants. These inhibitors increased in vitro embryo production in three different systems and species, microspore embryogenesis of Brassica napus and Hordeum vulgare, and somatic embryogenesis of Quercus suber. TDZD-8, a representative compound of the molecules tested, inhibited GSK-3 activity in microspore cultures, and increased expression of embryogenesis genes FUS3, LEC2, and AGL15. Plant GSK-3 kinase BIN2 is a master regulator of brassinosteroid (BR) signalling. During microspore embryogenesis, BR biosynthesis and signalling genes CPD, GSK-3-BIN2, BES1, and BZR1 were up-regulated and the BAS1 catabolic gene was repressed, indicating activation of the BR pathway. TDZD-8 increased expression of BR signalling elements, mimicking BR effects. The findings support that the small molecule inhibitors promoted somatic embryogenesis by activating the BR pathway, opening up the way for new strategies using GSK-3β inhibitors that could be extended to other species., (© The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Experimental Biology.)
- Published
- 2021
- Full Text
- View/download PDF
36. Identification of blossom-end rot loci using joint QTL-seq and linkage-based QTL mapping in tomato.
- Author
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Topcu Y, Sapkota M, Illa-Berenguer E, Nambeesan SU, and van der Knaap E
- Subjects
- Chromosome Mapping methods, Disease Resistance genetics, Gene Expression Regulation, Plant, Genetic Linkage, Solanum lycopersicum growth & development, Solanum lycopersicum microbiology, Plant Diseases genetics, Plant Diseases microbiology, Plant Proteins genetics, Ascomycota physiology, Chromosomes, Plant genetics, Disease Resistance immunology, Solanum lycopersicum genetics, Plant Diseases immunology, Plant Proteins metabolism, Quantitative Trait Loci
- Abstract
Key Message: Blossom-End Rot is Quantitatively Inherited and Maps to Four Loci in Tomato. Blossom-end rot (BER) is a devastating physiological disorder that affects tomato and other vegetables, resulting in significant crop losses. To date, most studies on BER have focused on the environmental factors that affect calcium translocation to the fruit; however, the genetic basis of this disorder remains unknown. To investigate the genetic basis of BER, two F
2 and F3:4 populations along with a BC1 population that segregated for BER occurrence were evaluated in the greenhouse. Using the QTL-seq approach, quantitative trait loci (QTL) associated with BER Incidence were identified at the bottom of chromosome (ch) 3 and ch11. Additionally, linkage-based QTL mapping detected another QTL, BER3.1, on ch3 and BER4.1 on ch4. To fine map the QTLs identified by QTL-seq, recombinant screening was performed. BER3.2, the major BER QTL on ch3, was narrowed down from 5.68 to 1.58 Mbp with a 1.5-LOD support interval (SI) corresponding to 209 candidate genes. BER3.2 colocalizes with the fruit weight gene FW3.2/SlKLUH, an ortholog of cytochrome P450 KLUH in Arabidopsis. Further, BER11.1, the major BER QTL on ch11, was narrowed down from 3.99 to 1.13 Mbp with a 1.5-LOD SI interval comprising of 141 candidate genes. Taken together, our results identified and fine mapped the first loci for BER resistance in tomato that will facilitate marker-assistant breeding not only in tomato but also in many other vegetables suffering for BER., (© 2021. The Author(s).)- Published
- 2021
- Full Text
- View/download PDF
37. The contribution of insects to global forest deadwood decomposition.
- Author
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Seibold S, Rammer W, Hothorn T, Seidl R, Ulyshen MD, Lorz J, Cadotte MW, Lindenmayer DB, Adhikari YP, Aragón R, Bae S, Baldrian P, Barimani Varandi H, Barlow J, Bässler C, Beauchêne J, Berenguer E, Bergamin RS, Birkemoe T, Boros G, Brandl R, Brustel H, Burton PJ, Cakpo-Tossou YT, Castro J, Cateau E, Cobb TP, Farwig N, Fernández RD, Firn J, Gan KS, González G, Gossner MM, Habel JC, Hébert C, Heibl C, Heikkala O, Hemp A, Hemp C, Hjältén J, Hotes S, Kouki J, Lachat T, Liu J, Liu Y, Luo YH, Macandog DM, Martina PE, Mukul SA, Nachin B, Nisbet K, O'Halloran J, Oxbrough A, Pandey JN, Pavlíček T, Pawson SM, Rakotondranary JS, Ramanamanjato JB, Rossi L, Schmidl J, Schulze M, Seaton S, Stone MJ, Stork NE, Suran B, Sverdrup-Thygeson A, Thorn S, Thyagarajan G, Wardlaw TJ, Weisser WW, Yoon S, Zhang N, and Müller J
- Subjects
- Animals, Carbon Sequestration, Climate, Ecosystem, Geographic Mapping, International Cooperation, Carbon Cycle, Forests, Insecta metabolism, Trees metabolism
- Abstract
The amount of carbon stored in deadwood is equivalent to about 8 per cent of the global forest carbon stocks
1 . The decomposition of deadwood is largely governed by climate2-5 with decomposer groups-such as microorganisms and insects-contributing to variations in the decomposition rates2,6,7 . At the global scale, the contribution of insects to the decomposition of deadwood and carbon release remains poorly understood7 . Here we present a field experiment of wood decomposition across 55 forest sites and 6 continents. We find that the deadwood decomposition rates increase with temperature, and the strongest temperature effect is found at high precipitation levels. Precipitation affects the decomposition rates negatively at low temperatures and positively at high temperatures. As a net effect-including the direct consumption by insects and indirect effects through interactions with microorganisms-insects accelerate the decomposition in tropical forests (3.9% median mass loss per year). In temperate and boreal forests, we find weak positive and negative effects with a median mass loss of 0.9 per cent and -0.1 per cent per year, respectively. Furthermore, we apply the experimentally derived decomposition function to a global map of deadwood carbon synthesized from empirical and remote-sensing data, obtaining an estimate of 10.9 ± 3.2 petagram of carbon per year released from deadwood globally, with 93 per cent originating from tropical forests. Globally, the net effect of insects may account for 29 per cent of the carbon flux from deadwood, which suggests a functional importance of insects in the decomposition of deadwood and the carbon cycle., (© 2021. The Author(s), under exclusive licence to Springer Nature Limited.)- Published
- 2021
- Full Text
- View/download PDF
38. Tracking the impacts of El Niño drought and fire in human-modified Amazonian forests.
- Author
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Berenguer E, Lennox GD, Ferreira J, Malhi Y, Aragão LEOC, Barreto JR, Del Bon Espírito-Santo F, Figueiredo AES, França F, Gardner TA, Joly CA, Palmeira AF, Quesada CA, Rossi LC, de Seixas MMM, Smith CC, Withey K, and Barlow J
- Subjects
- Brazil, Forests, Humans, Carbon Cycle, Droughts, El Nino-Southern Oscillation, Forestry statistics & numerical data, Plant Physiological Phenomena, Trees growth & development, Wildfires
- Abstract
With humanity facing an unprecedented climate crisis, the conservation of tropical forests has never been so important - their vast terrestrial carbon stocks can be turned into emissions by climatic and human disturbances. However, the duration of these effects is poorly understood, and it is unclear whether impacts are amplified in forests with a history of previous human disturbance. Here, we focus on the Amazonian epicenter of the 2015-16 El Niño, a region that encompasses 1.2% of the Brazilian Amazon. We quantify, at high temporal resolution, the impacts of an extreme El Niño (EN) drought and extensive forest fires on plant mortality and carbon loss in undisturbed and human-modified forests. Mortality remained higher than pre-El Niño levels for 36 mo in EN-drought-affected forests and for 30 mo in EN-fire-affected forests. In EN-fire-affected forests, human disturbance significantly increased plant mortality. Our investigation of the ecological and physiological predictors of tree mortality showed that trees with lower wood density, bark thickness and leaf nitrogen content, as well as those that experienced greater fire intensity, were more vulnerable. Across the region, the 2015-16 El Niño led to the death of an estimated 2.5 ± 0.3 billion stems, resulting in emissions of 495 ± 94 Tg CO
2 Three years after the El Niño, plant growth and recruitment had offset only 37% of emissions. Our results show that limiting forest disturbance will not only help maintain carbon stocks, but will also maximize the resistance of Amazonian forests if fires do occur., Competing Interests: The authors declare no competing interest., (Copyright © 2021 the Author(s). Published by PNAS.) - Published
- 2021
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39. Two efficient CRISPR/Cas9 systems for gene editing in soybean.
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Carrijo J, Illa-Berenguer E, LaFayette P, Torres N, Aragão FJL, Parrott W, and Vianna GR
- Subjects
- Genetic Vectors genetics, Genome, Plant genetics, Promoter Regions, Genetic genetics, RNA, Guide, CRISPR-Cas Systems genetics, Glycine max growth & development, CRISPR-Cas Systems genetics, Gene Editing, Genetic Engineering, Glycine max genetics
- Abstract
Genome editing using CRISPR/Cas9 has been highlighted as a powerful tool for crop improvement. Nevertheless, its efficiency can be improved, especially for crops with a complex genome, such as soybean. In this work, using the CRISPR/Cas9 technology we evaluated two CRISPR systems, a one-component vs. a two-component strategy. In a simplified system, the single transcriptional unit (STU), SpCas9 and sgRNA are driven by only one promoter, and in the conventional system, the two-component transcriptional unit (TCTU), SpCas9, is under the control of a pol II promoter and the sgRNAs are under the control of a pol III promoter. A multiplex system with three targets was designed targeting two different genes, GmIPK1 and GmIPK2, coding for enzymes from the phytic acid synthesis pathway. Both systems were tested using the hairy root soybean methodology. Results showed gene-specific edition. For the GmIPK1 gene, edition was observed in both configurations, with a deletion of 1 to 749 base pairs; however, the TCTU showed higher indel frequencies. For GmIPK2 major exclusions were observed in both systems, but the editing efficiency was low for STU. Both systems (STU or TCTU) have been shown to be capable of promoting effective gene editing in soybean. The TCTU configuration proved to be preferable, since it was more efficient. The STU system was less efficient, but the size of the CRISPR/Cas cassette was smaller.
- Published
- 2021
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40. Identification and characterization of GLOBE, a major gene controlling fruit shape and impacting fruit size and marketability in tomato.
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Sierra-Orozco E, Shekasteband R, Illa-Berenguer E, Snouffer A, van der Knaap E, Lee TG, and Hutton SF
- Abstract
Within large-fruited germplasm, fruit size is influenced by flat and globe shapes. Whereas flat fruits are smaller and retain better marketability, globe fruits are larger and more prone to cuticle disorders. Commercial hybrids are often developed from crosses between flat and globe shaped parents because flat shape is thought to be dominant and fruit size intermediate. The objectives of this study were to determine the genetic basis of flat/globe fruit shape in large-fruited fresh-market tomato germplasm and to characterize its effects on several fruit traits. Twenty-three advanced single plant selections from the Fla. 8000 × Fla. 8111B cross were selectively genotyped using a genome-wide SNP array, and inclusive composite interval mapping identified a single locus on the upper arm of chromosome 12 associated with shape, which we termed globe. A 238-plant F
2 population and 69 recombinant inbred lines for this region from the same parents delimited globe to approximately 392-kilobases. A germplasm survey representing materials from multiple breeding programs demonstrated that the locus explains the flat/globe shape broadly. A single base insertion in an exon of Solyc12g006860, a gene annotated as a brassinosteroid hydroxylase, segregated completely with shape in all populations tested. CRISPR/Cas9 knock out plants confirmed this gene as underlying the globe locus. In silico analysis of the mutant allele of GLOBE among 595 wild and domesticated accessions suggested that the allele arose very late in the domestication process. Fruit measurements in three genetic backgrounds evidenced that globe impacts fruit size and several fruit shape attributes, pedicel length/width, and susceptibility of fruit to weather check. The mutant allele of GLOBE appears mostly recessive for all traits except fruit size where it acts additively.- Published
- 2021
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41. 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.
- Published
- 2021
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42. Assessing invertebrate herbivory in human-modified tropical forest canopies.
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Barreto JR, Berenguer E, Ferreira J, Joly CA, Malhi Y, de Seixas MMM, and Barlow J
- Abstract
Studies on the effects of human-driven forest disturbance usually focus on either biodiversity or carbon dynamics but much less is known about ecosystem processes that span different trophic levels. Herbivory is a fundamental ecological process for ecosystem functioning, but it remains poorly quantified in human-modified tropical rainforests.Here, we present the results of the largest study to date on the impacts of human disturbances on herbivory. We quantified the incidence (percentage of leaves affected) and severity (the percentage of leaf area lost) of canopy insect herbivory caused by chewers, miners, and gall makers in leaves from 1,076 trees distributed across 20 undisturbed and human-modified forest plots in the Amazon.We found that chewers dominated herbivory incidence, yet were not a good predictor of the other forms of herbivory at either the stem or plot level. Chewing severity was higher in both logged and logged-and-burned primary forests when compared to undisturbed forests. We found no difference in herbivory severity between undisturbed primary forests and secondary forests. Despite evidence at the stem level, neither plot-level incidence nor severity of the three forms of herbivory responded to disturbance. Synthesis . Our large-scale study of canopy herbivory confirms that chewers dominate the herbivory signal in tropical forests, but that their influence on leaf area lost cannot predict the incidence or severity of other forms. We found only limited evidence suggesting that human disturbance affects the severity of leaf herbivory, with higher values in logged and logged-and-burned forests than undisturbed and secondary forests. Additionally, we found no effect of human disturbance on the incidence of leaf herbivory., Competing Interests: None declared., (© 2021 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd.)
- Published
- 2021
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43. Rainforest-to-pasture conversion stimulates soil methanogenesis across the Brazilian Amazon.
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Kroeger ME, Meredith LK, Meyer KM, Webster KD, de Camargo PB, de Souza LF, Tsai SM, van Haren J, Saleska S, Bohannan BJM, Rodrigues JLM, Berenguer E, Barlow J, and Nüsslein K
- Subjects
- Brazil, Methane, Soil Microbiology, Rainforest, Soil
- Abstract
The Amazon rainforest is a biodiversity hotspot and large terrestrial carbon sink threatened by agricultural conversion. Rainforest-to-pasture conversion stimulates the release of methane, a potent greenhouse gas. The biotic methane cycle is driven by microorganisms; therefore, this study focused on active methane-cycling microorganisms and their functions across land-use types. We collected intact soil cores from three land use types (primary rainforest, pasture, and secondary rainforest) of two geographically distinct areas of the Brazilian Amazon (Santarém, Pará and Ariquemes, Rondônia) and performed DNA stable-isotope probing coupled with metagenomics to identify the active methanotrophs and methanogens. At both locations, we observed a significant change in the composition of the isotope-labeled methane-cycling microbial community across land use types, specifically an increase in the abundance and diversity of active methanogens in pastures. We conclude that a significant increase in the abundance and activity of methanogens in pasture soils could drive increased soil methane emissions. Furthermore, we found that secondary rainforests had decreased methanogenic activity similar to primary rainforests, and thus a potential to recover as methane sinks, making it conceivable for forest restoration to offset greenhouse gas emissions in the tropics. These findings are critical for informing land management practices and global tropical rainforest conservation.
- Published
- 2021
- Full Text
- View/download PDF
44. The COVID-19 pandemic as an opportunity to weaken environmental protection in Brazil.
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Vale MM, Berenguer E, Argollo de Menezes M, Viveiros de Castro EB, Pugliese de Siqueira L, and Portela RCQ
- Abstract
This paper examines the effects of the COVID-19 pandemic on environmental protection and legislation in Brazil. We evaluate major legislative actions, environmental fines and deforestation since January 2019. We show that 57 legislative acts aimed at weakening environmental protection in Brazil during the current administration, almost half of which in the seven-month period of the pandemic in Brazil, with September 2020 as the month with the most legislative acts (n = 16). These acts either deregulated or weakened current environmental legislation, with a number of them aimed at dismantling the main federal institutions in charge of environmental protection. We also found a 72% reduction in environmental fines during the pandemic, despite an increase in Amazonian deforestation during this period. We conclude that the current administration is taking advantage of the COVID-19 pandemic to intensify a pattern of weakening environmental protection in Brazil. This has the potential to intensify ongoing loss of biodiversity, greenhouse gas emissions, and the likelihood of other zoonotic disease outbreaks, and inflict substantial harm to traditional and indigenous peoples. We highlight the key role of the scientific community, media and civil society, national and international levels, in order to reverse these harmful actions., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (© 2021 Elsevier Ltd. All rights reserved.)
- Published
- 2021
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- View/download PDF
45. Suppression of Metacaspase- and Autophagy-Dependent Cell Death Improves Stress-Induced Microspore Embryogenesis in Brassica napus.
- Author
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Berenguer E, Minina EA, Carneros E, B R Ny I, Bozhkov PV, and Testillano PS
- Subjects
- Brassica napus physiology, Gene Expression Regulation, Plant, Seeds physiology, Stress, Physiological, Autophagic Cell Death, Brassica napus growth & development, Caspases metabolism, Plant Proteins metabolism, Pollen physiology, Seeds growth & development
- Abstract
Microspore embryogenesis is a biotechnological process that allows us to rapidly obtain doubled-haploid plants for breeding programs. The process is initiated by the application of stress treatment, which reprograms microspores to embark on embryonic development. Typically, a part of the microspores undergoes cell death that reduces the efficiency of the process. Metacaspases (MCAs), a phylogenetically broad group of cysteine proteases, and autophagy, the major catabolic process in eukaryotes, are critical regulators of the balance between cell death and survival in various organisms. In this study, we analyzed the role of MCAs and autophagy in cell death during stress-induced microspore embryogenesis in Brassica napus. We demonstrate that this cell death is accompanied by the transcriptional upregulation of three BnMCA genes (BnMCA-Ia, BnMCA-IIa and BnMCA-IIi), an increase in MCA proteolytic activity and the activation of autophagy. Accordingly, inhibition of autophagy and MCA activity, either individually or in combination, suppressed cell death and increased the number of proembryos, indicating that both components play a pro-cell death role and account for decreased efficiency of early embryonic development. Therefore, MCAs and/or autophagy can be used as new biotechnological targets to improve in vitro embryogenesis in Brassica species and doubled-haploid plant production in crop breeding and propagation programs., (� The Author(s) 2020. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists.)
- Published
- 2021
- Full Text
- View/download PDF
46. Improving the spatial-temporal analysis of Amazonian fires.
- Author
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Berenguer E, Carvalho N, Anderson LO, Aragão LEOC, França F, and Barlow J
- Subjects
- Climate, Forests, Spatio-Temporal Analysis, Fires, Trees
- Abstract
There is a growing interest in Amazonian fires, accompanied by a substantial increase in research in the subject. Here, we list five common misunderstandings about Amazonian climate, vegetation, fires and the deforestation process to help to support future research., (© 2020 John Wiley & Sons Ltd.)
- Published
- 2021
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47. Belowground changes to community structure alter methane-cycling dynamics in Amazonia.
- Author
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Meyer KM, Morris AH, Webster K, Klein AM, Kroeger ME, Meredith LK, Brændholt A, Nakamura F, Venturini A, Fonseca de Souza L, Shek KL, Danielson R, van Haren J, Barbosa de Camargo P, Tsai SM, Dini-Andreote F, de Mauro JMS, Barlow J, Berenguer E, Nüsslein K, Saleska S, Rodrigues JLM, and Bohannan BJM
- Subjects
- Animals, Brazil, Cattle, Forests, Soil Microbiology, Methane, Soil
- Abstract
Amazonian rainforest is undergoing increasing rates of deforestation, driven primarily by cattle pasture expansion. Forest-to-pasture conversion has been associated with increases in soil methane (CH
4 ) emission. To better understand the drivers of this change, we measured soil CH4 flux, environmental conditions, and belowground microbial community structure across primary forests, cattle pastures, and secondary forests in two Amazonian regions. We show that pasture soils emit high levels of CH4 (mean: 3454.6 ± 9482.3 μg CH4 m-2 d-1 ), consistent with previous reports, while forest soils on average emit CH4 at modest rates (mean: 9.8 ± 120.5 μg CH4 m-2 d-1 ), but often act as CH4 sinks. We report that secondary forest soils tend to consume CH4 (mean: -10.2 ± 35.7 μg CH4 m-2 d-1 ), demonstrating that pasture CH4 emissions can be reversed. We apply a novel computational approach to identify microbial community attributes associated with flux independent of soil chemistry. While this revealed taxa known to produce or consume CH4 directly (i.e. methanogens and methanotrophs, respectively), the vast majority of identified taxa are not known to cycle CH4 . Each land use type had a unique subset of taxa associated with CH4 flux, suggesting that land use change alters CH4 cycling through shifts in microbial community composition. Taken together, we show that microbial composition is crucial for understanding the observed CH4 dynamics and that microorganisms provide explanatory power that cannot be captured by environmental variables., (Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.)- Published
- 2020
- Full Text
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48. Integrated terrestrial-freshwater planning doubles conservation of tropical aquatic species.
- Author
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Leal CG, Lennox GD, Ferraz SFB, Ferreira J, Gardner TA, Thomson JR, Berenguer E, Lees AC, Hughes RM, Mac Nally R, Aragão LEOC, de Brito JG, Castello L, Garrett RD, Hamada N, Juen L, Leitão RP, Louzada J, Morello TF, Moura NG, Nessimian JL, Oliveira-Junior JMB, Oliveira VHF, de Oliveira VC, Parry L, Pompeu PS, Solar RRC, Zuanon J, and Barlow J
- Subjects
- Animals, Biodiversity, Brazil, Aquatic Organisms, Conservation of Natural Resources, Rivers
- Abstract
Conservation initiatives overwhelmingly focus on terrestrial biodiversity, and little is known about the freshwater cobenefits of terrestrial conservation actions. We sampled more than 1500 terrestrial and freshwater species in the Amazon and simulated conservation for species from both realms. Prioritizations based on terrestrial species yielded on average just 22% of the freshwater benefits achieved through freshwater-focused conservation. However, by using integrated cross-realm planning, freshwater benefits could be increased by up to 600% for a 1% reduction in terrestrial benefits. Where freshwater biodiversity data are unavailable but aquatic connectivity is accounted for, freshwater benefits could still be doubled for negligible losses of terrestrial coverage. Conservation actions are urgently needed to improve the status of freshwater species globally. Our results suggest that such gains can be achieved without compromising terrestrial conservation goals., (Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.)
- Published
- 2020
- Full Text
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49. Smoke pollution's impacts in Amazonia.
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de Oliveira G, Chen JM, Stark SC, Berenguer E, Moutinho P, Artaxo P, Anderson LO, and Aragão LEOC
- Subjects
- Brazil epidemiology, COVID-19, Humans, Pandemics, Air Pollution, Conservation of Natural Resources, Coronavirus Infections epidemiology, Forests, Pneumonia, Viral epidemiology, Smoke
- Published
- 2020
- Full Text
- View/download PDF
50. Biased-corrected richness estimates for the Amazonian tree flora.
- Author
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Ter Steege H, Prado PI, Lima RAF, Pos E, de Souza Coelho L, de Andrade Lima Filho D, Salomão RP, Amaral IL, de Almeida Matos FD, Castilho CV, Phillips OL, Guevara JE, de Jesus Veiga Carim M, Cárdenas López D, Magnusson WE, Wittmann F, Martins MP, Sabatier D, Irume MV, da Silva Guimarães JR, Molino JF, Bánki OS, Piedade MTF, Pitman NCA, Ramos JF, Monteagudo Mendoza A, Venticinque EM, Luize BG, Núñez Vargas P, Silva TSF, de Leão Novo EMM, Reis NFC, Terborgh J, Manzatto AG, Casula KR, Honorio Coronado EN, Montero JC, Duque A, Costa FRC, Castaño Arboleda N, Schöngart J, Zartman CE, Killeen TJ, Marimon BS, Marimon-Junior BH, Vasquez R, Mostacedo B, Demarchi LO, Feldpausch TR, Engel J, Petronelli P, Baraloto C, Assis RL, Castellanos H, Simon MF, de Medeiros MB, Quaresma A, Laurance SGW, Rincón LM, Andrade A, Sousa TR, Camargo JL, Schietti J, Laurance WF, de Queiroz HL, Nascimento HEM, Lopes MA, de Sousa Farias E, Magalhães JLL, Brienen R, Aymard C GA, Revilla JDC, Vieira ICG, Cintra BBL, Stevenson PR, Feitosa YO, Duivenvoorden JF, Mogollón HF, Araujo-Murakami A, Ferreira LV, Lozada JR, Comiskey JA, de Toledo JJ, Damasco G, Dávila N, Lopes A, García-Villacorta R, Draper F, Vicentini A, Cornejo Valverde F, Lloyd J, Gomes VHF, Neill D, Alonso A, Dallmeier F, de Souza FC, Gribel R, Arroyo L, Carvalho FA, de Aguiar DPP, do Amaral DD, Pansonato MP, Feeley KJ, Berenguer E, Fine PVA, Guedes MC, Barlow J, Ferreira J, Villa B, Peñuela Mora MC, Jimenez EM, Licona JC, Cerón C, Thomas R, Maas P, Silveira M, Henkel TW, Stropp J, Paredes MR, Dexter KG, Daly D, Baker TR, Huamantupa-Chuquimaco I, Milliken W, Pennington T, Tello JS, Pena JLM, Peres CA, Klitgaard B, Fuentes A, Silman MR, Di Fiore A, von Hildebrand P, Chave J, van Andel TR, Hilário RR, Phillips JF, Rivas-Torres G, Noronha JC, Prieto A, Gonzales T, de Sá Carpanedo R, Gonzales GPG, Gómez RZ, de Jesus Rodrigues D, Zent EL, Ruschel AR, Vos VA, Fonty É, Junqueira AB, Doza HPD, Hoffman B, Zent S, Barbosa EM, Malhi Y, de Matos Bonates LC, de Andrade Miranda IP, Silva N, Barbosa FR, Vela CIA, Pinto LFM, Rudas A, Albuquerque BW, Umaña MN, Carrero Márquez YA, van der Heijden G, Young KR, Tirado M, Correa DF, Sierra R, Costa JBP, Rocha M, Vilanova Torre E, Wang O, Oliveira AA, Kalamandeen M, Vriesendorp C, Ramirez-Angulo H, Holmgren M, Nascimento MT, Galbraith D, Flores BM, Scudeller VV, Cano A, Ahuite Reategui MA, Mesones I, Baider C, Mendoza C, Zagt R, Urrego Giraldo LE, Ferreira C, Villarroel D, Linares-Palomino R, Farfan-Rios W, Farfan-Rios W, Casas LF, Cárdenas S, Balslev H, Torres-Lezama A, Alexiades MN, Garcia-Cabrera K, Valenzuela Gamarra L, Valderrama Sandoval EH, Ramirez Arevalo F, Hernandez L, Sampaio AF, Pansini S, Palacios Cuenca W, de Oliveira EA, Pauletto D, Levesley A, Melgaço K, and Pickavance G
- Subjects
- Brazil, Biodiversity, Classification methods, Forests, Rivers, Trees classification
- Abstract
Amazonian forests are extraordinarily diverse, but the estimated species richness is very much debated. Here, we apply an ensemble of parametric estimators and a novel technique that includes conspecific spatial aggregation to an extended database of forest plots with up-to-date taxonomy. We show that the species abundance distribution of Amazonia is best approximated by a logseries with aggregated individuals, where aggregation increases with rarity. By averaging several methods to estimate total richness, we confirm that over 15,000 tree species are expected to occur in Amazonia. We also show that using ten times the number of plots would result in an increase to just ~50% of those 15,000 estimated species. To get a more complete sample of all tree species, rigorous field campaigns may be needed but the number of trees in Amazonia will remain an estimate for years to come.
- Published
- 2020
- Full Text
- View/download PDF
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