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1.
    
Parsimony analysis of endemicity (PAE) was used to analyse the distributional patterns of 124 species of Mexican gymnosperms, using two different sample units: grid-cells and biogeographical provinces. PAE analyses were based on distributional data from herbarium specimens and specialized literature. Two data matrices were constructed for 60 grid-cells of 2° and 14 biogeographical provinces. The analysis of the 2° grid-cell matrix led to 7084 cladograms. The strict consensus cladogram showed several clades equivalent to the results obtained with the biogeographical provinces. Three clades agree with some principal regions of distribution of Mexican pines, previously identified by several authors, located at the northern portion of the Baja California peninsula, the Sierra Madre Occidental, and the Sierra Madre Oriental. These areas represent important centres of species diversity and endemism for Mexican gymnosperms. The analysis of the province matrix led to two most parsimonious cladograms, which only differed in the position of the Sierra Madre Occidental province. The iterative procedure PAE with progressive character elimination was applied to identify generalized tracks, where clades of provinces were considered equivalent to generalized tracks, and each time a cladogram was obtained, species defining its clades were deleted and a new run was undertaken. We found five generalized tracks, mainly located in montane provinces. The distribution patterns of gymnosperms agree with the existence of several Mexican biogeographical provinces, and a different historical biogeography of the Mexican peninsulas from the rest of the country is evident.  © 2007 The Linnean Society of London, Biological Journal of the Linnean Society , 2007, 92 , 405–417.  相似文献   

2.
Here we present a complete revision of the species of Baconia. Up until now there have been 27 species assigned to the genus (Mazur, 2011), in two subgenera (Binhister Cooman and Baconia s. str.), with species in the Neotropical, Nearctic, Palaearctic, and Oriental regions. We recognize all these species as valid and correctly assigned to the genus, and redescribe all of them. We synonymize Binhister, previously used for a polyphyletic assemblage of species with varied relationships in the genus. We move four species into Baconia from other genera, and describe 85 species as new, bringing the total for the genus to 116 species. We divide these into 12 informal species groups, leaving 13 species unplaced to group. We present keys and diagnoses for all species, as well as habitus photos and illustrations of male genitalia for nearly all. The genus now contains the following species and species groups: Baconia loricata group [Baconia loricata Lewis, 1885, B. patula Lewis, 1885, Baconia gounellei (Marseul, 1887a), Baconia jubaris (Lewis, 1901), Baconia festiva (Lewis, 1891), Baconia foliosoma sp. n., Baconia sapphirina sp. n., Baconia furtiva sp. n., Baconia pernix sp. n., Baconia applanatis sp. n., Baconia disciformis sp. n., Baconia nebulosa sp. n., Baconia brunnea sp. n.], Baconia godmani group [Baconia godmani (Lewis, 1888), Baconia venusta (J. E. LeConte, 1845), Baconia riehli (Marseul, 1862), comb. n., Baconia scintillans sp. n., Baconia isthmia sp. n., Baconia rossi sp. n., Baconia navarretei sp. n., Baconia maculata sp. n., Baconia deliberata sp. n., Baconia excelsa sp. n., Baconia violacea (Marseul, 1853), Baconia varicolor (Marseul, 1887b), Baconia dives (Marseul, 1862), Baconia eximia (Lewis, 1888), Baconia splendida sp. n., Baconia jacinta sp. n., Baconia prasina sp. n., Baconia opulenta sp. n., Baconia illustris (Lewis, 1900), Baconia choaspites (Lewis, 1901), Baconia lewisi Mazur, 1984], Baconia salobrus group [Baconia salobrus (Marseul, 1887b), Baconia turgifrons sp. n., Baconia crassa sp. n., Baconia anthracina sp. n., Baconia emarginata sp. n., Baconia obsoleta sp. n.], Baconia ruficauda group [Baconia ruficauda sp. n., Baconia repens sp. n.], Baconia angusta group [Baconia angusta Schmidt, 1893a, Baconia incognita sp. n., Baconia guartela sp. n., Baconia bullifrons sp. n., Baconia cavei sp. n., Baconia subtilis sp. n., Baconia dentipes sp. n., Baconia rubripennis sp. n., Baconia lunatifrons sp. n.], Baconia aeneomicans group [Baconia aeneomicans (Horn, 1873), Baconia pulchella sp. n., Baconia quercea sp. n., Baconia stephani sp. n., Baconia irinae sp. n., Baconia fornix sp. n., Baconia slipinskii Mazur, 1981, Baconia submetallica sp. n., Baconia diminua sp. n., Baconia rufescens sp. n., Baconia punctiventer sp. n., Baconia aulaea sp. n., Baconia mustax sp. n., Baconia plebeia sp. n., Baconia castanea sp. n., Baconia lescheni sp. n., Baconia oblonga sp. n., Baconia animata sp. n., Baconia teredina sp. n., Baconia chujoi (Cooman, 1941), Baconia barbarus (Cooman, 1934), Baconia reposita sp. n., Baconia kubani sp. n., Baconia wallacea sp. n., Baconia bigemina sp. n., Baconia adebratti sp. n., Baconia silvestris sp. n.], Baconia cylindrica group [Baconia cylindrica sp. n., Baconia chatzimanolisi sp. n.], Baconia gibbifer group [Baconia gibbifer sp. n., B. piluliformis sp. n., Baconia maquipucunae sp. n., Baconia tenuipes sp. n., Baconia tuberculifer sp. n., Baconia globosa sp. n.], Baconia insolita group [Baconia insolita (Schmidt, 1893a), comb. n., Baconia burmeisteri (Marseul, 1870), Baconia tricolor sp. n., Baconia pilicauda sp. n.], Baconia riouka group [Baconia riouka (Marseul, 1861), Baconia azuripennis sp. n.], Baconia famelica group [Baconia famelica sp. n., Baconia grossii sp. n., Baconia redemptor sp. n., Baconia fortis sp. n., Baconia longipes sp. n., Baconia katieae sp. n., Baconia cavifrons (Lewis, 1893), comb. n., Baconia haeterioides sp. n.], Baconia micans group [Baconia micans (Schmidt, 1889a), Baconia carinifrons sp. n., Baconia fulgida (Schmidt, 1889c)], Baconia incertae sedis [Baconia chilense (Redtenbacher, 1867), Baconia glauca (Marseul, 1884), Baconia coerulea (Bickhardt, 1917), Baconia angulifrons sp. n., Baconia sanguinea sp. n., Baconia viridimicans (Schmidt, 1893b), Baconia nayarita sp. n., Baconia viridis sp. n., Baconia purpurata sp. n., Baconia aenea sp. n., Baconia clemens sp. n., Baconia leivasi sp. n., Baconia atricolor sp. n.]. We designate lectotypes for the following species: Baconia loricata Lewis, 1885,Phelister gounellei Marseul, 1887, Baconia jubaris Lewis, 1901, Baconia festiva Lewis, 1891, Platysoma venustum J.E. LeConte, 1845, Phelister riehli Marseul, 1862, Phelister violaceus Marseul, 1853, Phelister varicolor Marseul, 1887b, Phelister illustris Lewis, 1900, Baconia choaspites Lewis, 1901, Epierus festivus Lewis, 1898, Phelister salobrus Marseul, 1887, Baconia angusta Schmidt, 1893a, Phelister insolitus Schmidt, 1893a, Pachycraerus burmeisteri Marseul, 1870, Phelister riouka Marseul, 1861, Homalopygus cavifrons Lewis, 1893, Phelister micans Schmidt, 1889a, Phelister coeruleus Bickhardt, 1917, and Phelister viridimicans Schmidt, 1893b. We designate neotypes for Baconia patula Lewis, 1885 and Hister aeneomicans Horn, 1873, whose type specimens are lost.  相似文献   

3.
  总被引：2，自引：0，他引：2  
Abstract.  1. Patterns of simuliid species richness were examined over a variety of scales at 532 stream sites in the Nearctic (394) and Neotropical (138) regions. In Nearctic streams, species richness of immature blackflies both within and across ecoregions and over two seasons was examined. Stream variables at each site included seston, width, depth, velocity, discharge, conductivity, pH, dissolved oxygen, water temperature, dominant streambed-particle size, canopy cover, and riparian vegetation. These variables were subjected to a principal component analysis and derived principal components were related back to richness, using regression analysis. At the level of the stream reach, richness was not highly correlated with single-point measurements of stream conditions.
2. Using data from both Nearctic and Neotropical sites, the effect of regional richness on local richness was examined. As regional richness increased, local diversity reached an asymptote in which further increases in regional richness were not matched by increases in local richness. Hence, simuliid communities are best described as saturated (type II) communities, consistent with the current view of lotic communities as non-equilibrium systems.
3. The well-established pattern of greater species richness in tropical regions was not observed in this study. To the contrary, blackfly richness is higher in temperate streams than in tropical streams at both local and regional scales.  相似文献   

4.
    
Most Neotropical colubrid snakes belong to a single, well‐supported lineage. Relationships between the major constituents of this clade remain. Here, we explore the phylogenetic relationships of Mastigodryas and its affinities to other Neotropical colubrid genera by combining DNA and morphological data. Analyses demonstrate that the concatenation of multiple individuals into a single terminal can mask the detection of new taxa. Further, non‐random missing data and/or taxa in some empirical datasets can bias species tree analyses more than concatenation approaches. Our results place Mastigodryas in a strongly supported clade that includes Drymarchon, Rhinobothryum, Drymoluber, Simophis and Leptodrymus. Mastigodryas bifossatus is more closely related to species of Drymoluber and Simophis than to its congeners. Thus, we erect a new genus to accommodate it and recover a monophyletic Mastigodryas. We highlight the importance of the use of morphological characters to diagnose suprageneric clades by showing that some key external and hemipenial characteristics are phylogenetically informative.  相似文献   

5.
    
Aim The Mexican transition zone is a complex area where Neotropical and Nearctic biotic elements overlap. A previous study on mammal species has shown a great diversification in the area. We analyse the diversification of their flea species (Insecta: Siphonaptera), in order to determine if a diversification similar to their mammal host species has occurred. Location The area analysed corresponds to Mexico. Methods The panbiogeographical or track analysis was based on the comparison of the individual tracks of 112 species belonging to 48 genera and eight families of the order Siphonaptera. Generalized tracks were obtained based on the comparison of the individual tracks. Nodes were found in the areas where generalized tracks overlapped. Results Thirty‐four generalized tracks were obtained, distributed within the Mexican transition zone (20), the Nearctic region plus the Mexican transition zone (8), the Nearctic region (4) and the Neotropical region plus the Mexican transition zone (2). In the areas where they intersected, 26 nodes were identified: 23 in the Mexican transition zone and 3 in the Nearctic region. Main conclusions The nodes are concentrated in the Transmexican Volcanic Belt (14), Sierra Madre Oriental (5) and Sierra Madre del Sur (4) provinces of the Mexican transition zone. These results show a significant diversification of the flea taxa, in parallel with the diversification of their mammal hosts.  相似文献   

6.
The effects of vertebrate predation have been monitored since 1989 on 16 replicated 0.56 ha study plots in a semiarid thorn scrub community in north-central Chile. Using fences of different heights with and without holes and suspended game netting to alter principal predator (foxes and raptors) and large rodent herbivore (Octodon degus) access, four grids each have been assigned to the following treatments: 1) low fencing and holes allowing free access of predators and small mammals; 2) low fencing without holes to exclude degus only; 3) high fencing and netting with holes to exclude predators only; and 4) high fencing and netting without holes to exclude predators and degus. Small mammal population censuses are conducted monthly using mark-recapture techniques. Degu population trends during 1989 and 1990 showed strongly but nonsignificantly lower numbers in control plots during months when densities were characteristically low (September–November) for this seasonally reproductive species; since March 1991, differences have become persistent and increasingly significant. Predators appear to have greater numerical effects when their prey populations are low. Survival times of degus, particularly established adults, were significantly longer in predator exclusion grids during the 2 1/2 years of observation; thus, predation also affects prey population structure.  相似文献   

7.
    
Aim The main drainages of the Plata Basin – the Paraná, Paraguay and Uruguay rivers – begin in tropical latitudes and run in a north–south direction into subtropical–temperate latitudes. Consequently, the biota of these rivers has tropical elements that contrast with temperate biomes through which the rivers run. We apply a panbiogeographical approach, to test whether the large rivers of the Plata Basin have a differential influence on distributional patterns of tropical snakes in subtropical and temperate latitudes of South America. Location Subtropical and temperate sections of the major Plata Basin rivers, South America. Methods We compared the individual tracks of 94 snake taxa. The track analysis consisted of: (1) plotting the localities of each taxon on maps, (2) connecting the localities of each taxon using a minimal geographical proximity determinant of the ‘individual tracks’, and (3) superimposing the individual tracks to determine generalized tracks. To detect tropical snakes that reach higher latitudes through the rivers we used the preferential direction of distribution concept. For each taxon we measured the angular deviations between the line of its individual track and the course of the rivers in a 100 × 100 km scaled grid. Average angular values < 45° indicated a positive association with the rivers. Results Thirty‐five of 94 taxa showed distributions associated with the major rivers of the Plata Basin, including fauna from distinct biogeographical lineages, supported by the occurrence of five generalized tracks as follows: (1) the Paraguay–Middle Paraná, (2) the Paraguay–Paraná fluvial axis, Upper Paraná and Middle Paraná to Upper Delta, (3) the Lower Paraguay, Paraná and Uruguay rivers, excluding the sectors High Paraná and High Uruguay, (4) the Uruguay River and Upper Paraná, and (5) the High Paraná. The Atlantic species occurred with significantly higher frequency in the Uruguay River and High Paraná river sections, the Amazon species were found with significantly higher frequency in the Paraguay and Middle Paraná sections, and the species with a Pantanal distribution were found in all sections. Main conclusions The observed distributional patterns may be explained by the interaction of ecological, geographical and historical factors. Previous authors have developed ecological (hydrological or environmental similarity) or dispersalist (effect of rivers as migration routes) explanations. The coincidence between generalized tracks and past geomorphological events that caused displacements and changed relationships between the Paraguay, Paraná and Uruguay river sections supports hypotheses involving the strong influence of historical factors in the present configuration of tropical snake distribution in temperate latitudes.  相似文献   

8.
    
In the identification key proposed by Mantilleri in 2016 for the genus Pertusius, some mistakes were introduced in references to figures. They are corrected here.  相似文献   

9.
    
Aim The large rivers of the Neotropics are considered areas of high diversity and endemism, which play an important role in the distribution patterns and evolution of Neotropical biota. Several methods have been proposed for prioritizing terrestrial conservation areas, but there has been little effort to develop models for river systems. We propose a panbiogeographical approach to identify priority areas for conservation along rivers. Location The Plata Basin rivers. Methods We compared the individual tracks (IT) of 96 snake taxa and identified the species associated with rivers using the concept of preferential direction of distribution. For each taxon, we measured the angular deviations between the line of its IT and the course of the rivers on a 100 × 100 km scaled grid. Average angular values < 45° indicated a positive association with rivers. We detected 35 taxa associated with rivers, and their IT were used to determine the generalized tracks (GT) and nodes. We applied a complementarity algorithm to identify the minimum set of nodes required to represent all species. Results Six nodes were found. The region where the High and Upper Paraná Rivers converge (Node 1) is of first priority, with 60 of 96 species. The second priority is the Lower Paraguay River and northern section of Middle Paraná River (Node 2). The third is the High Paraná, which together with Nodes 1 and 2, comprises 94% of the total species. The fourth and fifth are the High and Middle Uruguay, and the western section of the Upper Paraná and Iberá Marsh system, respectively. These five nodes include all species. Main conclusions Our results highlight the areas of particular interest for the conservation of rivers and provide a biogeographical algorithm for detecting priority conservation areas. The nodes are a biogeographical approach that allows evolutionary and ecological traits to be included in conservation assessment.  相似文献   

10.
    
Aim To uncover and describe patterns of biogeography of helminth parasites in freshwater fishes of Mexico, and to understand processes that determine them. Three predictions about host‐specificity, faunal exchange in transitional areas, and the biogeographical ‘core’ fauna, are evaluated, all of which follow from a fundamental hypothesis: that parasites show characteristic associations with particular host clades. The parasite fauna of the southern Mexican cichlids and of the fishes of the Mesa Central are examined as case studies that reflect Neotropical and Nearctic historical influences. Location The region covered in this study includes most of Mexico, with emphasis on six biogeographical areas: the Yucatán Peninsula (area 1), the Grijalva‐Usumacinta drainage (area 2), the Papaloapan and Pánuco drainages (area 3), the Balsas drainage (area 4), the Lerma‐Santiago drainage (area 5), and the Bravo drainage (area 6). Methods A parasite data base containing all the records of helminth parasites of freshwater fishes of Mexico was filtered to extract records of adult helminth parasites in freshwater fishes from the six biogeographical areas designated in this study. Jaccard's similarity coefficients and cluster analyses (using upgma ) were used to analyse the extent of faunal similarity between the designated biogeographical areas and between host (fish) families. Taxonomic composition of parasite assemblages in different host groups was also qualitatively compared from summary data. These data were used to test the three main predictions. Results To date, 184 species of helminths (120 as adults) have been recorded from 127 freshwater fishes in Mexico (almost 33% of the total fish diversity of Mexico). Of these parasite species, 69 are digenetic flukes, 51 are nematodes, 33 are monogeneans, 25 are tapeworms, and only six are acanthocephalans. The data and analyses from the six biogeographical areas corroborate the predictions that: (1) the adult parasite fauna is largely circumscribed by higher levels of monophyletic host taxa (families, orders, etc.), and that this pattern is independent of areas; (2) areas within a certain biogeographical region, and consequently with similar fish composition (e.g. areas 1, 2 and 3) have more similar parasite faunas compared to areas with less similar fish faunal composition; and (3) ‘core’ parasite faunas persist to some extent in transitional areas with limited host‐sharing. Main conclusions Helminth biodiversity in Mexican freshwater fishes is determined by the historical and contemporary biogeography of their hosts. Host lineage specificity, mainly at the level of the host family, appears to be an important factor in the distribution of the parasites. Most fish families (Characidae, Cichlidae, Pimelodidae, Ictaluridae, Catsotomidae, Goodeidae, Atherinidae) possess their own characteristic ‘core’ helminth fauna, with limited host‐sharing in transitional areas (e.g. areas 3 and 4). A re‐evaluation of the helminth fauna of Mexican cichlids questions the hypothesis that cichlids lost parasites during the colonization of Mexico from South America. The evidence supports the idea that they acquired new parasites by host switching, possibly from marine or brackish‐water percomorphs. In contrast, the parasite fauna of the Mesa Central remains enigmatic and reflects the region's history of endemicity with historical marine and Nearctic connections.  相似文献   

11.
    
Aim  We analysed the geographical distributions of species of Buprestidae (Coleoptera) in Mexico by means of a panbiogeographical analysis, in order to identify their main distributional patterns and test the complex nature of the Mexican Transition Zone, located between the Nearctic and Neotropical regions.
Location  Mexico.
Methods  The geographical distributions of 228 species belonging to 33 genera of Buprestidae were analysed. Localities of the buprestid species were represented on maps and their individual tracks were drawn. Based on a comparison of the individual tracks, generalized tracks were detected and mapped. Nodes were identified as the areas where generalized tracks converged.
Results  Thirteen generalized tracks were obtained: one was restricted to the Mexican Transition Zone and five to the Neotropical region (Antillean and Mesoamerican dominions), a further two occurred in both the Nearctic region (Continental Nearctic dominion) and the Mexican Transition Zone, and a further five in both the Neotropical region (Mesoamerican dominion) and the Mexican Transition Zone. Seven nodes were identified at the intersections of the generalized tracks – in the Mesoamerican dominion (Mexican Pacific Coast, Mexican Gulf and Chiapas biogeographical provinces) and the Mexican Transition Zone (Trans-Mexican Volcanic Belt, Balsas Basin and Sierra Madre Oriental biogeographical provinces).
Main conclusions  We conclude that the geographical distribution of Buprestidae is mainly Neotropical, corresponding to the Mesoamerican dominion and the Antillean dominion of the Neotropical region, and the Mexican Transition Zone. Most of the generalized tracks and nodes correspond to the Mexican Transition Zone, thus confirming its complex nature. We suggest that the nodes we have identified could be particularly important areas to choose for conservation prioritization.  相似文献   

12.
    
Brazil has a variety of aquatic ecosystems and rich freshwater biodiversity, but these components have been constantly damaged by the expansion of unsustainable activities. An array of different conservation strategies is needed, especially the creation of protected areas (PAs, hereafter). However, Brazil's PAs are biased towards terrestrial ecosystems and we argue that current PAs have limited efficacy in the protection of freshwater biodiversity. New PAs should better consider aquatic environments, covering entire basins, rivers and other freshwater habitats. We recommend ways to implement these PAs and provide guidance to avoid social impacts. Freshwater systems in Brazil provide essential goods and services but these ecosystems are being rapidly degraded and will be lost if not adequately protected.  相似文献   

13.
Forty one new records of species of Bombyliidae are reported for Coahuila in northeastern Mexico. Nine of these species are reported for the first time for the country. The specimens were collected in the Cuatro Ciénegas Basin and Sierra La Madera mountains during 2007–2013. The modified distributions of species are discussed. The gaps in the distribution of many species suggest an undersampling of this group of insects in the north of Mexico.  相似文献   

14.
Eldridge KT 《ZooKeys》2010,(53):17-24
Myrmedonota helianthasp. n. is described from eastern Kansas (USA). All specimens were collected from dung. A modified new key to the species of Myrmedonota of America north of Mexico is provided.  相似文献   

15.
    
The Nearctic region is located on the North American plate. However, its tectonic history is related to convergence with other plates, which has promoted a complex topography. This complexity should be reflected by the distributional patterns of the biota. We used track analysis with 574 species of mammals to identify generalized tracks and panbiogeographic nodes in the Nearctic region and to propose an updated point of view of complex areas and their boundaries in North America. Seven generalized tracks with nested patterns (California, Columbia Plateau, Mesoamerican, Mexican Plateau, Neotropic, Southern Rocky Mountains, and Western Coast of USA) were identified using a parsimony analysis of endemicity with progressive character elimination. Nine panbiogeographic nodes were identified at the intersections of the generalized tracks, all of which were located in the Sierra of Chiapas and Central America physical features. A total of 192 nodes were identified for the nested patterns, located in only eight physical features. Our analysis revealed evolutionary patterns in generalized tracks, and the panbiogeographic nodes predicted areas with high evolutionary–geologic complexity, shared by other taxonomic groups.  相似文献   

16.
    
The Middle America is located in the Nearctic–Neotropical boundary. The combination of temperate and tropical biota of these two biogeographic regions, plus an area of biotic overlap propitiates unusually high species diversity and endemism. We present the first general assessment based on the IUCN Red List of Threatened Species that provides evidence of widespread decline in the conservation status of land mammals from southern U.S.A. to Panama. One in every three species considered in our study (n = 273) is classified as threatened, and the rate of biodiversity loss increased 0.64% between 2008 and 2012. Endangered species of the Middle America represents 11.8% of the global endangered mammal species, and 7.9% of the threatened species. Habitat loss and the introduction of alien species are the major threats; however, the relative impact of these threats varies among habitats. For continental species, habitat loss is prevalent, while for insular species the introduction of alien species has devastating effects. Our results suggest that if no integral multi-species conservation actions are applied in the short-term, more than 20% of the extant mammal species in the region could become extinct in the near future (10–50 years).  相似文献   

17.
    
The length-weight relationship (LWRs) was estimated for eight fish species collected from oxbow lakes on the floodplain of the middle Purus River in western Brazilian Amazonia in January, May, and September 2012. The specimens were collected using 12 gillnets (80 m in length × 4 m in height, meshes of between 1.5 cm and 12.0 cm), which were set during both diurnal and nocturnal periods. The species had allometric coefficients (b) of between 2.92 and 3.37, and correlation coefficients (r2) ranging from 0.954 to 0.993 and we highlight that the work presents new data for literature.  相似文献   

18.
    
Understanding the biology and conducting effective conservation of migratory species requires an understanding of migratory connectivity – the geographic linkages of populations between stages of the annual cycle. Unfortunately, for most species, we are lacking such information. The North American Bird Banding Laboratory (BBL) houses an extensive database of marking, recaptures and recoveries, and such data could provide migratory connectivity information for many species. To date, however, few species have been analyzed for migratory connectivity largely because heterogeneous re‐encounter probabilities make interpretation problematic. We accounted for regional variation in re‐encounter probabilities by borrowing information across species and by using effort covariates on recapture and recovery probabilities in a multistate capture–recapture and recovery model. The effort covariates were derived from recaptures and recoveries of species within the same regions. We estimated the migratory connectivity for three tern species breeding in North America and over‐wintering in the tropics, common (Sterna hirundo), roseate (Sterna dougallii), and Caspian terns (Hydroprogne caspia). For western breeding terns, model‐derived estimates of migratory connectivity differed considerably from those derived directly from the proportions of re‐encounters. Conversely, for eastern breeding terns, estimates were merely refined by the inclusion of re‐encounter probabilities. In general, eastern breeding terns were strongly connected to eastern South America, and western breeding terns were strongly linked to the more western parts of the nonbreeding range under both models. Through simulation, we found this approach is likely useful for many species in the BBL database, although precision improved with higher re‐encounter probabilities and stronger migratory connectivity. We describe an approach to deal with the inherent biases in BBL banding and re‐encounter data to demonstrate that this large dataset is a valuable source of information about the migratory connectivity of the birds of North America.  相似文献   

19.
Abstract Aim To examine how the genetic diversity of selected taxa of forest‐dwelling small mammals is distributed between and within the major rain forest domains of Amazonia and Atlantic Forest and the intervening interior forests of Brazil, as inferred by the relationships between gene genealogies and geography. I also addressed the historical importance of the central Brazilian forests in connecting Amazon and Atlantic Forest populations of rodents and marsupials. Methods I evaluated variation in the mitochondrial cytochrome b gene to estimate the levels of sequence divergence between those taxa occurring throughout the Amazon, Atlantic Forest, and forests in the Cerrado and Caatinga regions. I inferred the hierarchical relationships between haplotypes, populations and formal taxa using the cladistic approach of maximum parsimony. I compared areas and the clades identified by superimposing cladograms on the geographical distribution of samples. The degree of concordance both in phylogeny and the depth of the nodes in these phylogenies, in addition to patterns of geographical distribution of clades, permitted me to make inferences on how, when and where the taxa differentiated. Results Sequence similarity is often greater between samples from the Atlantic Forest and either Amazon or central Brazilian forests than it is within each of the two rain forest domains. The Atlantic Forest clades are either not reciprocally monophyletic or are the sister group to all the other clades. There is some indication of northern and southern components in the Atlantic Forest. Given the geographical distribution of clades and the relatively deep levels of divergence, the central Brazilian area does not behave as a separate region but is complementary to either Amazon or Atlantic Forest. Patterns of area relationships differ across taxa, suggesting that different processes and/or historic events affected the diversification within each lineage. Main conclusions The Amazon and the Atlantic forests are not exclusive in terms of their small mammal faunas; both overlap broadly with taxa occurring in gallery forests and dry forests in central Brazil. Central Brazilian forests are an integral part of the evolutionary scenario of lowland small mammals, playing an important role as present and past habitats for rain forest species. Therefore, representatives from this area should always be included in analyses of the evolutionary history of lowland rain forest faunas. The incongruence of branching patterns among areas is in agreement with recent results presented for Neotropical passerine birds and indicates that a single hypothesis of Neotropical area relationships is unlikely. These findings reinforce the idea that speciation in the Neotropics will not be explained by any single model of vicariance or climatic changes.  相似文献   

20.
    
White sand terra firme forests are unusual ecosystems scattered across Amazonia, covering just 3% of the basin. These forests differ from surrounding forests in their scleromorphic vegetation, low nutrient content, and propensity to harbor endemics. We report the capture of 62 Gray‐cheeked Thrushes (Catharus minimus) during a study of the understory avifauna of Amazonian white sand forests near Iquitos, Peru, conducted from 20 June to 8 December 2010–2012. We captured and banded Gray‐cheeked Thrushes in white sand (N = 57) and adjacent weathered clay (N = 5) terra firme forests. Sampling for three consecutive days at 19 different sites each year, the inter‐annual site fidelity rate of Gray‐cheeked Thrushes was 4.8% (N = 3). One bird banded in 2010 was recaptured in 2012. Of the 62 birds, 19.3% (N = 12) were recaptured on subsequent days. All recaptures were in white sand forests. The 19.3% recapture rate of Gray‐cheeked Thrushes from sites re‐sampled no more than 2 d in a given year suggests the presence of settled and perhaps territorial birds. Using rectrices from 12 Gray‐cheeked Thrushes, stable‐hydrogen isotope analyses (δ2H) suggest that the geographic breeding or natal origin of all sampled birds was likely northwestern North America. Our results suggest that Gray‐cheeked Thrushes exhibit site fidelity and may concentrate in white sand forests—an uncommon and scattered ecosystem type in western Amazonia. However, annual tracking of individual Gray‐cheeked Thrushes is needed to fully assess regional patterns of settlement and movement, and the connectivity between breeding and wintering areas.  相似文献   

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