Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 8 de 8
Filtrar
1.
Nature ; 605(7909): 285-290, 2022 05.
Artículo en Inglés | MEDLINE | ID: mdl-35477765

RESUMEN

Comprehensive assessments of species' extinction risks have documented the extinction crisis1 and underpinned strategies for reducing those risks2. Global assessments reveal that, among tetrapods, 40.7% of amphibians, 25.4% of mammals and 13.6% of birds are threatened with extinction3. Because global assessments have been lacking, reptiles have been omitted from conservation-prioritization analyses that encompass other tetrapods4-7. Reptiles are unusually diverse in arid regions, suggesting that they may have different conservation needs6. Here we provide a comprehensive extinction-risk assessment of reptiles and show that at least 1,829 out of 10,196 species (21.1%) are threatened-confirming a previous extrapolation8 and representing 15.6 billion years of phylogenetic diversity. Reptiles are threatened by the same major factors that threaten other tetrapods-agriculture, logging, urban development and invasive species-although the threat posed by climate change remains uncertain. Reptiles inhabiting forests, where these threats are strongest, are more threatened than those in arid habitats, contrary to our prediction. Birds, mammals and amphibians are unexpectedly good surrogates for the conservation of reptiles, although threatened reptiles with the smallest ranges tend to be isolated from other threatened tetrapods. Although some reptiles-including most species of crocodiles and turtles-require urgent, targeted action to prevent extinctions, efforts to protect other tetrapods, such as habitat preservation and control of trade and invasive species, will probably also benefit many reptiles.


Asunto(s)
Conservación de los Recursos Naturales , Extinción Biológica , Reptiles , Caimanes y Cocodrilos , Anfibios , Animales , Biodiversidad , Aves , Mamíferos , Filogenia , Reptiles/clasificación , Medición de Riesgo , Tortugas
2.
Conserv Biol ; 35(5): 1388-1395, 2021 10.
Artículo en Inglés | MEDLINE | ID: mdl-33484006

RESUMEN

Some conservation prioritization methods are based on the assumption that conservation needs overwhelm current resources and not all species can be conserved; therefore, a conservation triage scheme (i.e., when the system is overwhelmed, species should be divided into three groups based on likelihood of survival, and efforts should be focused on those species in the group with the best survival prospects and reduced or denied to those in the group with no survival prospects and to those in the group not needing special efforts for their conservation) is necessary to guide resource allocation. We argue that this decision-making strategy is not appropriate because resources are not as limited as often assumed, and it is not evident that there are species that cannot be conserved. Small population size alone, for example, does not doom a species to extinction; plants, reptiles, birds, and mammals offer examples. Although resources dedicated to conserving all threatened species are insufficient at present, the world's economic resources are vast, and greater resources could be dedicated toward species conservation. The political framework for species conservation has improved, with initiatives such as the UN Sustainable Development Goals and other international agreements, funding mechanisms such as The Global Environment Facility, and the rise of many nongovernmental organizations with nimble, rapid-response small grants programs. For a prioritization system to allow no extinctions, zero extinctions must be an explicit goal of the system. Extinction is not inevitable, and should not be acceptable. A goal of no human-induced extinctions is imperative given the irreversibility of species loss.


Asignación de Recursos para la Conservación, Resiliencia de Poblaciones Pequeñas y la Falacia del Triaje de Conservación Resumen Algunos métodos de priorización de la conservación están basados en el supuesto de que las necesidades de la conservación superan a los actuales recursos y que no todas las especies pueden ser conservadas; por lo tanto, se necesita un esquema de triaje (esto es, cuando el sistema está abrumado, las especies deben dividirse en tres grupos con base en su probabilidad de supervivencia y los esfuerzos deben enfocarse en aquellas especies dentro del grupo con las mejores probabilidades de supervivencia y a aquellas en el grupo sin probabilidades de supervivencia o aquellas en el grupo que no necesita esfuerzos especializados para su conservación se les deben reducir o negar los esfuerzos de conservación) para dirigir la asignación de recursos. Discutimos que esta estrategia para la toma de decisiones no es apropiada porque los recursos no están tan limitados como se asume con frecuencia y tampoco es evidente que existan especies que no puedan ser conservadas. Por ejemplo, tan sólo un tamaño poblacional pequeño no es suficiente para condenar a una especie a la extinción; contamos con ejemplos en plantas, reptiles, aves y mamíferos. Aunque actualmente todos los recursos dedicados a la conservación de todas las especies amenazadas son insuficientes, los recursos económicos mundiales son vastos y se podrían dedicar mayores recursos a la conservación de especies. El marco de trabajo político para la conservación de especies ha mejorado, con iniciativas como los Objetivos de Desarrollo Sustentable de la ONU y otros acuerdos internacionales, el financiamiento de mecanismos como el Fondo para el Medio Ambiente Mundial, y el surgimiento de muchas organizaciones no gubernamentales mediante programas de subsidios pequeños hábiles y de respuesta rápida. Para que un sistema de priorización no permita las extinciones, las cero extinciones deben ser un objetivo explícito del sistema. La extinción no es inevitable y no debería ser aceptable. El objetivo de cero extinciones inducidas por humanos es imperativo dada la irreversibilidad de la pérdida de especies.


Asunto(s)
Conservación de los Recursos Naturales , Triaje , Animales , Biodiversidad , Especies en Peligro de Extinción , Extinción Biológica , Mamíferos , Asignación de Recursos
3.
Curr Biol ; 30(12): R721-R735, 2020 06 22.
Artículo en Inglés | MEDLINE | ID: mdl-32574638

RESUMEN

Turtles and tortoises (chelonians) have been integral components of global ecosystems for about 220 million years and have played important roles in human culture for at least 400,000 years. The chelonian shell is a remarkable evolutionary adaptation, facilitating success in terrestrial, freshwater and marine ecosystems. Today, more than half of the 360 living species and 482 total taxa (species and subspecies combined) are threatened with extinction. This places chelonians among the groups with the highest extinction risk of any sizeable vertebrate group. Turtle populations are declining rapidly due to habitat loss, consumption by humans for food and traditional medicines and collection for the international pet trade. Many taxa could become extinct in this century. Here, we examine survival threats to turtles and tortoises and discuss the interventions that will be needed to prevent widespread extinction in this group in coming decades.


Asunto(s)
Conservación de los Recursos Naturales , Tortugas , Animales , Especies en Peligro de Extinción , Extinción Biológica , Dinámica Poblacional
4.
Mol Ecol ; 18(6): 1252-62, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-19222749

RESUMEN

Using ancient DNA sequences of subfossil European pond turtles (Emys orbicularis) from Britain, Central and North Europe and accelerator mass spectrometry radiocarbon dating for turtle remains from most Swedish sites, we provide evidence for a Holocene range expansion of the pond turtle from the southeastern Balkans into Britain, Central Europe and Scandinavia, according to the 'grasshopper pattern' of Hewitt. Northeastern Europe and adjacent Asia were colonized from another refuge located further east. With increasing annual mean temperatures, pond turtles reached southern Sweden approximately 9800 years ago. Until approximately 5500 years ago, rising temperatures facilitated a further range expansion up to Ostergötland, Sweden (approximately 58 degrees 30'N). However, around 5500 years ago pond turtle records suddenly terminate in Sweden, some 1500 years before the Holocene thermal maximum ended in Scandinavia and distinctly earlier than previously thought. This extinction coincides with a temporary cooling oscillation during the Holocene thermal maximum and is likely related to lower summer temperatures deteriorating reproductive success. Although climatic conditions improved later again, recolonization of Sweden from southern source populations was prevented by the Holocene submergence of the previous land connection via the Danish Straits that occurred approximately 8500 years ago.


Asunto(s)
Clima , Extinción Biológica , Tortugas/genética , Animales , Secuencia de Bases , Datos de Secuencia Molecular , Datación Radiométrica , Análisis de Secuencia de ADN , Suecia
5.
Curr Biol ; 25(10): R431-8, 2015 May 18.
Artículo en Inglés | MEDLINE | ID: mdl-25989087

RESUMEN

Humans depend on biodiversity in myriad ways, yet species are being rapidly lost due to human activities. The ecosystem services approach to conservation tries to establish the value that society derives from the natural world such that the true cost of proposed development actions becomes apparent to decision makers. Species are an integral component of ecosystems, and the value they provide in terms of services should be a standard part of ecosystem assessments. However, assessing the value of species is difficult and will always remain incomplete. Some of the most difficult species' benefits to assess are those that accrue unexpectedly or are wholly unanticipated. In this review, we consider recent examples from a wide variety of species and a diverse set of ecosystem services that illustrate this point and support the application of the precautionary principle to decisions affecting the natural world.


Asunto(s)
Biodiversidad , Ecosistema , Animales , Agentes de Control Biológico , Bivalvos , Secuestro de Carbono , Conservación de los Recursos Naturales , Cultura , Ecología/economía , Humanos , Calidad del Agua , Humedales
6.
Evolution ; 57(1): 119-28, 2003 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-12643572

RESUMEN

The painted turtle, Chrysemys picta, is currently recognized as a continentally distributed polytypic species, ranging across North America from southern Canada to extreme northern Mexico. We analyzed variation in the rapidly evolving mitochondrial control region (CR) in 241 turtles from 117 localities across this range to examine whether the painted turtle represents a continentally distributed species based on molecular analysis. We found strong support for the novel hypothesis that C. p. dorsalis is the sister group to all remaining Chrysemys, with the remaining Chrysemys falling into a single, extremely wide-ranging and genetically undifferentiated species. Given our goal of an evolutionarily accurate taxonomy, we propose that two evolutionary lineages be recognized as species within Chrysemys: C. dorsalis (Agassiz 1857) in the southern Mississippi drainage region, and C. picta (Schneider 1783) from the rest of the range of the genus. Neither molecular nor recent morphological analyses argue for the hybrid origin of C. p. marginata as previously proposed. Within C. picta, we find evidence of at least two independent range expansions into previously glaciated regions of North America, one into New England and the other into the upper Midwest. We further find evidence of a massive extinction/recolonization event across the Great Plains/Rocky Mountain region encompassing over half the continental United States. The timing and extent of this colonization is consistent with a recently proposed regional aridification as the Laurentide ice sheets receded approximately 14,000 years ago, and we tentatively propose this paleoclimatological event as a major factor shaping genetic variation in Chrysemys.


Asunto(s)
Geografía , Filogenia , Tortugas/genética , Animales , Secuencia de Bases , Cartilla de ADN , Tortugas/clasificación
7.
Thomson, Scott A; Pyle, Richard L; Ahyong, Shane T; Alonso-Zarazaga, Miguel; Ammirati, Joe; Araya, Juan Francisco; Ascher, John S; Audisio, Tracy Lynn; Azevedo-Santos, Valter M; Bailly, Nicolas; Baker, William J; Balke, Michael; Barclay, Maxwell V. L; Barrett, Russell L; Benine, Ricardo C; Bickerstaff, James R. M; Bouchard, Patrice; Bour, Roger; Bourgoin, Thierry; Boyko, Christopher B; Breure, Abraham S. H; Brothers, Denis J; Byng, James W; Campbell, David; Ceriaco, Luis M. P; Cernak, Istvan; Cerretti, Pierfilippo; Chang, Chih-Han; Cho, Soowon; Copus, Joshua M; Costello, Mark J; Cseh, Andras; Csuzdi, Csaba; Culham, Alastair; D'Elia, Guillermo; d'Acoz, Cedric d'Udekem; Daneliya, Mikhail E; Dekker, Rene; Dickinson, Edward C; Dickinson, Timothy A; van Dijk, Peter Paul; Dijkstra, Klaas-Douwe B; Dima, Balint; Dmitriev, Dmitry A; Duistermaat, Leni; Dumbacher, John P; Eiserhardt, Wolf L; Ekrem, Torbjorn; Evenhuis, Neal L; Faille, Arnaud; Fernandez-Trianam, Jose L; Fiesler, Emile; Fishbein, Mark; Fordham, Barry G; Freitas, Andre V. L; Friol, Natalia R; Fritz, Uwe; Froslev, Tobias; Funk, Vicki A; Gaimari, Stephen D; Garbino, Guilherme S. T; Garraffoni, Andre R. S; Geml, Jozsef; Gill, Anthony C; Gray, Alan; Grazziotin, Felipe Gobbi; Greenslade, Penelope; Gutierrez, Eliecer E; Harvey, Mark S; Hazevoet, Cornelis J; He, Kai; He, Xiaolan; Helfer, Stephan; Helgen, Kristofer M; van Heteren, Anneke H; Garcia, Francisco Hita; Holstein, Norbert; Horvath, Margit K; Hovenkamp, Peter H; Hwang, Wei Song; Hyvonen, Jaakko; Islam, Melissa B; Iverson, John B; Ivie, Michael A; Jaafar, Zeehan; Jackson, Morgan D; Jayat, J. Pablo; Johnson, Norman F; Kaiser, Hinrich; Klitgard, Bente B; Knapp, Daniel G; Kojima, Jun-ichi; Koljalg, Urmas; Kontschan, Jeno; Krell, Frank-Thorsten; Krisai-Greilhuberm, Irmgard; Kullander, Sven; Latelle, Leonardo; Lattke, John E; Lencioni, Valeria; Lewis, Gwilym P; Lhano, Marcos G; Lujan, Nathan K; Luksenburg, Jolanda A; Mariaux, Jean; Marinho-Filho, Jader; Marshall, Christopher J; Mate, Jason F; McDonough, Molly M; Michel, Ellinor; Miranda, Vitor F. O; Mitroiulm, Mircea-Dan; Molinari, Jesus; Monks, Scott; Moore, Abigail J; Moratelli, Ricardo; Muranyi, David; Nakano, Takafumi; Nikolaeva, Svetlana; Noyes, John; Ohl, Michael; Oleas, Nora H; Orrell, Thomas; Pall-Gergele, Barna; Pape, Thomas; Papp, Viktor; Parenti, Lynne R; Patterson, David; Pavlinov, Igor Ya; Pine, Ronald H; Poczai, Peter; Prado, Jefferson; Prathapan, Divakaran; Rabeler, Richard K; Randall, John E; Rheindt, Frank E; Rhodin, Anders G. J; Rodriguez, Sara M; Rogers, D. Christopher; Roque, Fabio de O; Rowe, Kevin C; Ruedas, Luis A; Salazar-Bravo, Jorge; Salvador, Rodrigo B; Sangster, George; Sarmiento, Carlos E; Schigel, Dmitry S; Schmidt, Stefan; Schueler, Frederick W; Segers, Hendrik; Snow, Neil; Souza-Dias, Pedro G. B; Stals, Riaan; Stenroos, Soili; Stone, R. Douglas; Sturm, Charles F; Stys, Pavel; Teta, Pablo; Thomas, Daniel C; Timm, Robert M; Tindall, Brian J; Todd, Jonathan A; Triebel, Dagmar; Valdecasas, Antonio G; Vizzini, Alfredo; Vorontsova, Maria S; de Vos, Jurriaan M; Wagner, Philipp; Watling, Les; Weakley, Alan; Welter-Schultes, Francisco; Whitmore, Daniel; Wilding, Nicholas; Will, Kipling; Williams, Jason; Wilson, Karen; Winston, Judith E; Wuster, Wolfgang; Yanega, Douglas; Yeates, David K; Zaher, Hussam; Zhang, Guanyang; Zhang, Zhi-Qiang; Zhou, Hong-Zhang.
PLoS. Biol. ; 16(3): e2005075, 2018.
Artículo en Inglés | SES-SP, SES SP - Instituto Butantan, SES-SP | ID: but-ib15045
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA