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1.
J Insect Sci ; 17(1)2017 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-28130453

RESUMO

Many wild bee species are in global decline, yet much is still unknown about their diversity and contemporary distributions. National parks and forests offer unique areas of refuge important for the conservation of rare and declining species populations. Here we present the results of the first biodiversity survey of the bee fauna in the White Mountain National Forest (WMNF). More than a thousand specimens were collected from pan and sweep samples representing 137 species. Three species were recorded for the first time in New England and an additional seven species were documented for the first time in the state of New Hampshire. Four introduced species were also observed in the specimens collected. A checklist of the species found in the WMNF, as well as those found previously in Strafford County, NH, is included with new state records and introduced species noted as well as a map of collecting locations. Of particular interest was the relatively high abundance of Bombus terricola Kirby 1837 found in many of the higher elevation collection sites and the single specimen documented of Bombus fervidus (Fabricius 1798). Both of these bumble bee species are known to have declining populations in the northeast and are categorized as vulnerable on the International Union for Conservation of Nature's Red List.


Assuntos
Abelhas/fisiologia , Biodiversidade , Conservação dos Recursos Naturais , Altitude , Animais , Abelhas/classificação , Florestas , New Hampshire
2.
Sci Data ; 10(1): 747, 2023 11 02.
Artigo em Inglês | MEDLINE | ID: mdl-37919303

RESUMO

Species occurrence data are foundational for research, conservation, and science communication, but the limited availability and accessibility of reliable data represents a major obstacle, particularly for insects, which face mounting pressures. We present BeeBDC, a new R package, and a global bee occurrence dataset to address this issue. We combined >18.3 million bee occurrence records from multiple public repositories (GBIF, SCAN, iDigBio, USGS, ALA) and smaller datasets, then standardised, flagged, deduplicated, and cleaned the data using the reproducible BeeBDC R-workflow. Specifically, we harmonised species names (following established global taxonomy), country names, and collection dates and, we added record-level flags for a series of potential quality issues. These data are provided in two formats, "cleaned" and "flagged-but-uncleaned". The BeeBDC package with online documentation provides end users the ability to modify filtering parameters to address their research questions. By publishing reproducible R workflows and globally cleaned datasets, we can increase the accessibility and reliability of downstream analyses. This workflow can be implemented for other taxa to support research and conservation.


Assuntos
Abelhas , Animais , Editoração , Fluxo de Trabalho
3.
Zookeys ; 1110: 135-149, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36761452

RESUMO

This is a response to a preprint version of "A re-analysis of the data in Sharkey et al.'s (2021) minimalist revision reveals that BINs do not deserve names, but BOLD Systems needs a stronger commitment to open science", https://www.biorxiv.org/content/10.1101/2021.04.28.441626v2. Meier et al. strongly criticized Sharkey et al.'s publication in which 403 new species were deliberately minimally described, based primarily on COI barcode sequence data. Here we respond to these criticisms. The following points are made: 1) Sharkey et al. did not equate BINs with species, as demonstrated in several examples in which multiple species were found to be in single BINs. 2) We reiterate that BINs were used as a preliminary sorting tool, just as preliminary morphological identification commonly sorts specimens based on color and size into unit trays; despite BINs and species concepts matching well over 90% of species, this matching does not equate to equality. 3) Consensus barcodes were used only to provide a diagnosis to conform to the rules of the International Code of Zoological Nomenclature just as consensus morphological diagnoses are. The barcode of a holotype is definitive and simply part of its cellular morphology. 4) Minimalist revisions will facilitate and accelerate future taxonomic research, not hinder it. 5) We refute the claim that the BOLD sequences of Plesiocoelusvanachterbergi are pseudogenes and demonstrate that they simply represent a frameshift mutation. 6) We reassert our observation that morphological evidence alone is insufficient to recognize species within species-rich higher taxa and that its usefulness lies in character states that are congruent with molecular data. 7) We show that in the cases in which COI barcodes code for the same amino acids in different putative species, data from morphology, host specificity, and other ecological traits reaffirm their utility as indicators of genetically distinct lineages.

4.
Zootaxa ; 3946(1): 133-8, 2015 Apr 08.
Artigo em Inglês | MEDLINE | ID: mdl-25947678

RESUMO

Little work has been done with the African species of Cremnops since their original descriptions. Herein we propose new combinations for five species that are currently placed in Cremnops, i.e., C. atripennis Szépligeti 1914 and C. elegantissima Szépligeti 1908 are moved to Disophrys; C. borealis (Szépligeti 1914) and C. rubrigaster Masi 1944 are moved to Biroia; and C. pulchripennis Szépligeti 1905 is moved to and renamed Biroia neopulchipennis. These changes result in Disophrys atripennis (Szépligeti 1915) becoming a jr. homonym, which we change to Disophrys szatripennis. Additionally, two species are proposed as nomen dubia: C. rufitarsis Szépligeti 1913 and C. schubotzi Szépligeti 1915.


Assuntos
Vespas/classificação , África Subsaariana , Animais , Feminino , Masculino , Vespas/anatomia & histologia
5.
Zootaxa ; 3916: 1-83, 2015 Feb 09.
Artigo em Inglês | MEDLINE | ID: mdl-25662357

RESUMO

The New World species of the genus Cremnops are revised. Thirty-three species of Cremnops are treated; five are described as new, i.e., C. bertae sp. nov., C. cluttsis sp. nov., C. nymphius sp. nov., C. wileycoyotius sp. nov. and C. witkopegasus sp. nov. Six species are synonymized, i.e., Cremnops caribensis Berta, 1998, is synonymized under C. guanicanus Wolcott, 1924; C. nigrosternum (Morrison 1917) is synonymized under C. haematodes (Brullé 1846); C. punctatus Berta, 1998, is synonymized under C. marshi Berta, 1998; C. sharkei Berta, 1998, is synonymized under C. montrealensis (Morrison 1917); C. turrialbae Berta de Fernandez, 1998, is synonymized under C. ferrugineus (Cameron 1887); and C. misionensis Berta, 1987, is synonymized under C. slossonae (Morrison 1917). Cremnops florissanticola is transferred to its original combination Bracon florissanticola Cockerell, 1919, st. rev. Included are a molecular phylogeny, a dichotomous key, links to distribution maps, an electronic interactive key, and images of holotypes.


Assuntos
Vespas/classificação , Distribuição Animal , Estruturas Animais/anatomia & histologia , Estruturas Animais/crescimento & desenvolvimento , Animais , Tamanho Corporal , Ecossistema , Feminino , Masculino , Tamanho do Órgão , Vespas/anatomia & histologia , Vespas/crescimento & desenvolvimento
6.
Zookeys ; (130): 379-419, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-22259290

RESUMO

Twelve species of Costa Rican Lytopylus are treated; these include all species reared from Lepidoptera caterpillars in Area de Conservación Guanacaste, Costa Rica, over 32 years of caterpillar inventory, as well as two species recorded in the literature as occurring in Costa Rica. Ten new species are described, i.e., Lytopylus bradzlotnicki, Lytopylus colleenhitchcockae, Lytopylus gregburtoni, Lytopylus jessicadimauroae, Lytopylus jessiehillae, Lytopylus mingfangi, Lytopylus rebeccashapleyae, Lytopylus robpringlei, Lytopylus sandraberriosae, Lytopylus vaughntani. The following species are transferred to Lytopylus: Metriosoma flavicalcar Enderlein 1920 to Lytopylus flavicalcarcomb. n.; Bassus macadamiae Briceño and Sharkey 2000 to Lytopylus macadamiaecomb. n.; Metriosoma bicarinatum Enderlein 1920 to Lytopylus bicarinatumcomb. n.; Metriosoma brasiliense Enderlein 1920 to Lytopylus brasiliensecomb. n.; Bassus tayrona Campos 2007 to Lytopylus tayronacomb. n.; Microdus femoratus Cameron 1887 to Lytopylus femoratuscomb. n.; Microdus melanocephalus Cameron 1887 to Lytopylus melanocephaluscomb. n.; Bassus pastranai Blanchard 1952 to Lytopylus pastranaicomb. n.; Agathis nigrobalteata Cameron 1911 to Lytopylus nigrobalteatuscomb. n. Two keys to species of Lytopylus are presented, one interactive and the other static.

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