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Sigmodontine rats are one of the most diverse components of the Neotropical mammal fauna. They exhibit a wide ecological diversity and a variety of locomotor types that allow them to occupy different environments. To explore the relationship between morphology and locomotor types, we analyzed traits of the postcranial osteology (axial and appendicular skeletons) of 329 specimens belonging to 51 species and 29 genera of sigmodontines exhibiting different locomotor types. In this work, postcranial skeletal characters of these rats are considered in an ecomorphological study for the first time. Statistical analyses showed that of the 34 osteological characters considered, 15 were related to the locomotor types studied, except for ambulatory. However, character mapping showed that climbing and jumping sigmodontines are the only taxa exhibiting clear adaptations in their postcranial osteology, which are highly consistent with the tendencies described in many other mammal taxa. Climbing, digging and swimming rats presented statistically differences in traits associated with their vertebral column and limbs, whereas jumping rats showed modifications associated with all the skeletal regions. Our data suggest that sigmodontine rats retain an all-purpose morphology that allows them to use a variety of habitats. This versatility is particularly important when considering the lack of specialization of sigmodontines for a specific locomotor mode. Another possible interpretation is that our dataset probably did not consider relevant information about these groups and should be increased with other types of characters (e.g. characters from the external morphology, myology, etc.). [ABSTRACT FROM AUTHOR]

The Miridae (Hemiptera: Heteroptera) are one of the most species rich families of insects, with about 11 100 described species. Mirinae is the largest subfamily and its endemism becomes evident at the tribal level and below. Mirines of the tribe Restheniini are found throughout America, with most of the diversity confined to the Neotropics. Prepops Reuter is the largest genus in Restheniini with 198 described species and its geographical range is similar to that of the tribe. The study of the distribution and areas of endemism in Miridae are scarce and non-existent for Prepops. We analyzed all the geographic records of Prepops (707 records for 181 species) in order to identify diversity patterns and areas of endemism, using network analysis. Locality data were assigned using museum specimens and geographic records in the literature. Additionally we used spatial data to propose habitat preferences and geoclimatic variables important for each group of co-occurring species. The results indicate high species richness in subtropical regions, while the tropical belt and high latitudes appear impoverished. The Neotropical region contains 86% of the species, and the Nearctic about 11 % (but with larger species ranges); the Andean region is sparingly represented. Twenty-three areas of endemism (and two diads), formed by 2 or more endemic species, are distributed in the Nearctic (3), Mexican Transition Zone and Caribbean subregion (5), South American Transition Zone and Amazonian, Chacoan and Paranaense subregions (15). Overlap between some of the areas indicates regions with high species richness and complex history. The lack of records from the Andean region (except for P. nigrus in Southern Patagonia) and dominance of strictly Neotropical species (86 %) supports the hypothesis of a Neotropical origin for the tribe Restheniini. The general arrangement of the units of co-occurrence of Prepops species shows a close correlation with known biogeographic regions and subregions. Broad physiographic characteristics most commonly associated with Prepops geographical records are, in order of importance: broad leaf forests (wet and dry), grasslands and xeric habitats. [ABSTRACT FROM AUTHOR]

Background: Identifying hereditary parkinsonism is valuable for diagnosis, genetic counseling, patient prioritization in trials, and studying the disease for personalized therapies. However, most studies were conducted in Europeans, and limited data exist on admixed populations like those from Latin America., Objectives: This study aims to assess the frequency and distribution of genetic parkinsonism in Latin America., Methods: We conducted a systematic review and meta-analysis of the frequency of parkinsonian syndromes associated with genetic pathogenic variants in Latin America. We defined hereditary parkinsonism as those caused by the genes outlined by the MDS Nomenclature of Genetic Movement Disorders and heterozygous carriers of GBA1 pathogenic variants. A systematic search was conducted in PubMed, Web of Science, Embase, and LILACS in August 2022. Researchers reviewed titles and abstracts, and disagreements were resolved by a third researcher. After this screening, five researchers reanalyzed the selection criteria and extracted information based on the full paper. The frequency for each parkinsonism-related gene was determined by the presence of pathogenic/likely pathogenic variants among screened patients. Cochran's Q and I 2 tests were used to quantify heterogeneity. Meta-regression, publication bias tests, and sensitivity analysis regarding study quality were also used for LRRK2-, PRKN-, and GBA1-related papers., Results: We included 73 studies involving 3014 screened studies from 16 countries. Among 7668 Latin American patients, pathogenic variants were found in 19 different genes. The frequency of the pathogenic variants in LRRK2 was 1.38% (95% confidence interval [CI]: 0.52-2.57), PRKN was 1.16% (95% CI: 0.08-3.05), and GBA1 was 4.17% (95% CI: 2.57-6.08). For all meta-analysis, heterogeneity was high and publication bias tests were negative, except for PRKN, which was contradictory. Information on the number of pathogenic variants in the other genes is further presented in the text., Conclusions: This study provides insights into hereditary and GBA1-related parkinsonism in Latin America. Lower GBA1 frequencies compared to European/North American cohorts may result from limited access to gene sequencing. Further research is vital for regional prevalence understanding, enabling personalized care and therapies. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society., (© 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.)