57 research outputs found

    Systematics of the Neotropical Genus Leptodactylus Fitzinger, 1826 (Anura: Leptodactylidae): Phylogeny, the Relevance of Non-molecular Evidence, and Species Accounts

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    A phylogeny of the species-rich clade of the Neotropical frog genus Leptodactylus sensu stricto is presented on the basis of a total evidence analysis of molecular (mitochondrial and nuclear markers) and non-molecular (adult and larval morphological and behavioral characters) sampled from > 80% of the 75 currently recognized species. Our results support the monophyly of Leptodactylus sensu stricto, with Hydrolaetare placed as its sister group. The reciprocal monophyly of Hydrolaetare and Leptodactylus sensu stricto does not require that we consider Hydrolaetare as either a subgenus or synonym of Leptodactylus sensu lato. We recognize Leptodactylus sensu stricto, Hydrolaetare, Adenomera, and Lithodytes as valid monophyletic genera. Our results generally support the traditionally recognized Leptodactylus species groups, with exceptions involving only a few species that are easily accommodated without proposing new groups or significantly altering contents. The four groups form a pectinate tree, with the Leptodactylus fuscus group diverging first, followed by the L. pentadactylus group, which is sister to the L. latrans and L. melanonotus groups. To evaluate the impact of non-molecular evidence on our results, we compared our total evidence results with results obtained from analyses using only molecular data. Although non-molecular evidence comprised only 3.5% of the total evidence matrix, it had a strong impact on our total evidence results. Only one species group was monophyletic in the molecular-only analysis, and support differed in 86% of the 54 Leptodactylus clades that are shared by the results of the two analyses. Even though no non-molecular evidence was included for Hydrolaetare, exclusion of that data partition resulted in that genus being nested within Leptodactylus, demonstrating that the inclusion of a small amount of non-molecular evidence for a subset of species can alter not only the placement of those species, but also species that were not scored for those data. The evolution of several natural history and reproductive traits is considered in the light of our phylogenic framework. Invasion of rocky outcrops, larval oophagy, and use of underground reproductive chambers are restricted to species of the Leptodactylus fuscus and L. pentadactylus groups. In contrast, larval schooling, larval attendance, and more complex parental care are restricted to the L. latrans and L. melanonotus groups. Construction of foam nests is plesiomorphic in Leptodactylus but their placement varies extensively (e.g., underground chambers, surface of waterbodies, natural or excavated basins). Information on species synonymy, etymology, adult and larval morphology, advertisement call, and geographic distribution is summarized in species accounts for the 30 species of the Leptodactylus fuscus group, 17 species of the L. pentadactylus group, eight species of the L. latrans group, and 17 species of the L. melanonotus group, as well as the three species that are currently unassigned to any species group.Se presenta una filogenia del gĂ©nero Leptodactylus, un ciado neotropical rico en especies, basada en anĂĄlises combinados de datos moleculares (marcadores nuclear y mitocondriales) y no moleculares (caracteres de la morfologĂ­a de adultos y larvas asĂ­ como de comportamiento) se muestrearon > 80% de las 75 especies reconocidas. Los resultados apoyan la monofĂ­lia de Leptodactylus sensu stricto, con Hydrolaetare como su grupo hermano. La monofĂ­lia recĂ­proca de Hydrolaetare y Leptodactylus no requiere considerar a Hydrolaetare como un subgĂ©nero o sinĂłnimo de Leptodactylus sensu lato. Se reconocen Leptodactylus sensu stricto, Hydrolaetare, Adenomera y Lithodytes como gĂ©neros monofilĂ©ticos vĂĄlidos. Los resultados en general resuelven los grupos tradicionalmente reconocidos de Leptodactylus, con excepciones de algunas especies que son reasignadas sin la necesidad de proponer nuevos grupos o alterar significativamente el contenido de los grupos tradicionales. Los cuatro grupos de especies forman una topologĂ­a pectinada donde el grupo de L. fuscus tiene una posiciĂłn basal, seguido por el grupo de L. pentadactylus que es el grupo hermano al clado formado por los grupo de L. latrans y L. melanonotus. Se estimĂł el impacto de los datos no moleculares en los resultados, comparĂĄndose los resultados de evidencia total con los de los anĂĄlises de datos moleculares solamente. Los datos no moleculares representan un 3.5% de la matriz de evidencia total, pero estos datos tuvieron un impacto significativo en los resultados del anĂĄlisis de evidencia total. En el anĂĄlisis estrictamente molecular solamente un grupo de especies resultĂł monofilĂ©tico, y el apoyo difiriĂł en 86% de los 54 ciados de Leptodactylus compartidos entre los dos anĂĄlises. A pesar que datos no moleculares no fueron incluidos para Hydrolaetare, la exclusiĂłn de evidencia no molecular resultĂł en el gĂ©nero estar dentro de Leptodactylus, demostrando que la inclusiĂłn de evidencia no molecular pequeña para un subgrupo de especies altera no solamente la posiciĂłn topolĂłgica de esas especies, sino tambien de las especies para las cuales dichos datos no fueron codificados. La evoluciĂłn de patrones de historia natural y reproduciĂłn se evalĂșan en el contexto filogenĂ©tico. La invasiĂłn de afloramientos rocosos y la construciĂłn de cĂĄmaras de reproduciĂłn subterraneas estĂĄ limitada a los grupos de Leptodactylus fuscus y L. pentadactylus, mientras que la oofagia larval estĂĄ restringida al grupo de L. pentadactylus. Por otro lado, los cĂĄrdumenes larvales, la proteciĂłn del cĂĄrdumen, y otros comportamientos parentales complejos carecterizan al clado formado por los grupos de especies de L. latrans y L. melanonotus. Los resĂșmenes de especies incluyen informaciĂłn de sinonimias, etimologĂ­a, morfologĂ­a de adultos y larvas, cantos, y distribuciĂłn geogrĂĄfica para las 30 especies del grupo de Leptodactylus fuscus, 17 especies del grupo L. pentadactylus, ocho especies del grupo de L. latrans, 17 especies del grupo de L. melanonotus, asĂ­ como para las tres especies que actualmente no se encuentran asociadas a ninguno de los grupos de especies.Taran Grant was supported by Conselho Nacional de Desenvolvimento CientĂ­fico e TecnolĂłgico Proc. 307001/2011-3 and Fundação de Amparo Ă  Pesquisa do Estado de SĂŁo Paulo Proc. 2012/10000-5

    Factors Associated with Revision Surgery after Internal Fixation of Hip Fractures

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    Background: Femoral neck fractures are associated with high rates of revision surgery after management with internal fixation. Using data from the Fixation using Alternative Implants for the Treatment of Hip fractures (FAITH) trial evaluating methods of internal fixation in patients with femoral neck fractures, we investigated associations between baseline and surgical factors and the need for revision surgery to promote healing, relieve pain, treat infection or improve function over 24 months postsurgery. Additionally, we investigated factors associated with (1) hardware removal and (2) implant exchange from cancellous screws (CS) or sliding hip screw (SHS) to total hip arthroplasty, hemiarthroplasty, or another internal fixation device. Methods: We identified 15 potential factors a priori that may be associated with revision surgery, 7 with hardware removal, and 14 with implant exchange. We used multivariable Cox proportional hazards analyses in our investigation. Results: Factors associated with increased risk of revision surgery included: female sex, [hazard ratio (HR) 1.79, 95% confidence interval (CI) 1.25-2.50; P = 0.001], higher body mass index (fo

    Open data from the third observing run of LIGO, Virgo, KAGRA, and GEO

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    The global network of gravitational-wave observatories now includes five detectors, namely LIGO Hanford, LIGO Livingston, Virgo, KAGRA, and GEO 600. These detectors collected data during their third observing run, O3, composed of three phases: O3a starting in 2019 April and lasting six months, O3b starting in 2019 November and lasting five months, and O3GK starting in 2020 April and lasting two weeks. In this paper we describe these data and various other science products that can be freely accessed through the Gravitational Wave Open Science Center at https://gwosc.org. The main data set, consisting of the gravitational-wave strain time series that contains the astrophysical signals, is released together with supporting data useful for their analysis and documentation, tutorials, as well as analysis software packages
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