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Invasive alien species (IAS) are a major global challenge requiring urgent action, and the Strategic Plan for Biodiversity (2011–2020) of the Convention on Biological Diversity (CBD) includes a target on the issue. Meeting the target requires an understanding of invasion patterns. However, national or regional analyses of invasions are limited to developed countries. We identified 488 IAS in China’s terrestrial habitats, inland waters and marine ecosystems based on available literature and field work, including 171 animals, 265 plants, 26 fungi, 3 protists, 11 procaryots, and 12 viruses. Terrestrial plants account for 51.6% of the total number of IAS, and terrestrial invertebrates (104 species) for 21.3%. Of the total numbers, 67.9% of plant IAS and 34.8% of animal IAS were introduced intentionally. All other taxa were introduced unintentionally despite very few animal and plant species that invaded naturally. In terms of habitats, 64.3% of IAS occur on farmlands, 13.9% in forests, 8.4% in marine ecosystems, 7.3% in inland waters, and 6.1% in residential areas. Half of all IAS (51.1%) originate from North and South America, 18.3% from Europe, 17.3% from Asia not including China, 7.2% from Africa, 1.8% from Oceania, and the origin of the remaining 4.3% IAS is unknown. The distribution of IAS can be divided into three zones. Most IAS are distributed in coastal provinces and the Yunnan province; provinces in Middle China have fewer IAS, and most provinces in West China have the least number of IAS. Sites where IAS were first detected are mainly distributed in the coastal region, the Yunnan Province and the Xinjiang Uyghur Autonomous Region. The number of newly emerged IAS has been increasing since 1850. The cumulative number of firstly detected IAS grew exponentially.
The hypnorum-complex of bumblebees (in the genus Bombus Latreille, 1802) has been interpreted as consisting of a single widespread Old-World species, Bombus hypnorum (Linnaeus, 1758) s. lat., and its closely similar sister species in the New World, B. perplexus Cresson, 1863. We examined barcodes for evidence of species’ gene coalescents within this species complex, using the closely related vagans-group to help calibrate Poisson-tree-process models to a level of branching appropriate for discovering species. The results support seven candidate species within the hypnorum-complex (Bombus taiwanensis Williams, Sung, Lin & Lu, 2022, B. wolongensis Williams, Ren & Xie sp. nov., B. bryorum Richards, 1930, B. hypnorum, B. koropokkrus Sakagami & Ishikawa, 1972, and B. hengduanensis Williams, Ren & Xie sp. nov., plus B. perplexus), which are comparable in status to the currently accepted species of the vagans-group. Morphological corroboration of the coalescent candidate species is subtle but supports the gene coalescents if these candidates are considered near-cryptic species.
Bumblebees (Bombus Latreille, 1802), because of their large body size, bright colours and activity at times and places that coincide with biologists, are an example of a group of insects that is particularly well represented in museum collections. This is important if taxonomic revisions are to achieve greater comparability among species. Bumblebees have also attracted particular attention because they are especially ecologically and economically valuable for pollination in north temperate regions, where they are now becoming increasingly threatened. I argue that the what, the where, and the how of effective conservation management may be informed by understanding the divergent characteristics that have affected their biogeographical past: by helping us to see ‘the woods’, not just ‘the trees’, of their habitat needs. Identifying suitable habitat should be part of reconstructing historical biogeography within taxonomic revisions. For bumblebees, for example, biogeographical analysis associates major taxonomic groups either with flower-rich lowland grasslands or with flower-rich montane grasslands, highlighting their contrasting requirements for: nest sites, flowers of different depths, pollen-plant families, and especially the differing importance of early spring and late summer flowers for breeding success. This broad view of species groups helps filter the less important idiosyncrasies from local case studies in order to focus conservation actions.
Five new state records for Idaho in the genera Agrilus Curtis, Anthaxia Eschscholtz, and Buprestis Linnaeus (Coleoptera: Buprestidae) are included herein, with brief comments thereon. Two of the species are believed to be introduced. Agrilus liragus Barter and Brown is elevated to a full species, resurrected status.
ZooBank registration. urn:lsid:zoobank.org:pub:3AE72784-F368-45A2-AC90-B31E48D0D5CC
Centris xanthomelaena Moure & Castro, 2001 is a relict species, endemic to northeastern Brazil and broadly recorded within the semiarid region of Caatinga xerophilous open vegetation. It was originally included in the subgenus Paracentris Cameron, 1903 but posteriorly interpreted as remotely related to it or to the subgenus Centris s. str. Fabricius, 1804. In this paper it is proposed to recognize this species as the single member of the monotypic Relicthemisia, a new subgenus which belongs to the ‘Centris group’, one of the main internal lineages of the genus. The proposition of this new subgenus is based on both, morphological and molecular data which indicate its long history as a distinct lineage. Distribution records, floral hosts as well as photographs of both sexes of C. xanthomelaena are also provided.
An annotated list, including information on type species, distribution, and number of species, is provided for all of the non-flea-beetle galerucine genera known to occur in the New World (tribes Galerucini, Metacyclini, and Luperini). A diagnostic key to the genera is provided. Habitus illustrations are provided for most genera. The following new genera are proposed: Amplioluperus gen. nov., Cornuventer gen. nov., Geethaluperus gen. nov., Megarhabda gen. nov., Mexiluperus gen. nov., Monoaster gen. nov., Pyesexora gen. nov., Texiluperus gen. nov., Trachyelytron gen. nov. and Yingabruxia gen. nov. The following new taxonomic placements are proposed: Microbrotica Jacoby, 1887 is transferred from the tribe Metacyclini to the section Diabroticites Chapuis, 1875 (tribe Luperini, subtribe Diabroticina Chapuis, 1875); Pteleon Jacoby, 1888 is transferred from the section Exosomites Wilcox, 1973 (tribe Luperini, subtribe Luperina Gistel, 1848) to the section Scelidites Chapuis, 1875 (subtribe Luperina). The following new combinations are proposed: Luperodes histrio Horn, 1895, Luperus maculicollis LeConte, 1884, and Scelolyperus cyanellus Horn, 1895 are transferred from Pseudoluperus Beller & Hatch, 1932 to Amplioluperus; Luperodes tuberculatus Blake, 1942 is transferred from Pseudoluperus to Cornuventer; Luperus flavofemoratus Jacoby, 1888 is transferred from Pseudoluperus to Geethaluperus; Trirhabda obscurovittata Jacoby, 1886 is transferred from Trirhabda LeConte, 1865 to Megarhabda; Cneorane nigripes Allard, 1889 is transferred from Scelida Chapuis, 1875 to Metacycla Baly, 1861; Luperodes wickhami Horn, 1893 and Luperus dissimilis Jacoby, 1888 are transferred from Pseudoluperus to Mexiluperus; Scelolyperus tenuimarginatus Bowditch, 1925, is transferred from Scelida to Mimastra Baly, 1865 and is synonymized with Mimastra semimarginata Jacoby, 1886 syn. nov.; Pseudoluperus fulgidus Wilcox, 1965 and Pseudoluperus linus Wilcox, 1965 are transferred from Pseudoluperus to Monoaster; Crioceris detrita detrita Fabricius, 1801, Malacosoma detrita laevicollis Jacoby, 1887, Pyesia detrita meridionalis Bechyné, 1958, Pyesia elytropleuralis elytropleuralis Bechyné, 1958, and Pyesia elytropleuralis subalutacea Bechyné, 1958 are transferred from Pyesia Clark, 1865 to Pyesexora; Luperodes spretus Horn, 1893 and Luperodes texanus Horn, 1893 are transferred from Pseudoluperus to Texiluperus; Chthoneis smaragdipennis Jacoby, 1888 is transferred from Platymorpha Jacoby, 1888 to Trachyelytron; Luperus albomarginatus Jacoby, 1888 is transferred from Pseudoluperus to Trichobrotica Bechyné, 1956; and Galleruca sordida LeConte, 1858, Monoxia apicalis Blake, 1939, Monoxia batisia Blatchley, 1917, and Monoxia brisleyi Blake, 1939 are transferred from Monoxia LeConte, 1865 to Yingabruxia; all comb. nov. Pseudoluperus decipiens (Horn, 1893), originally described in Scelolyperus Crotch, 1874, is reduced to a junior synonym of Pseudoluperus longulus (LeConte, 1857), syn. nov. Trachyscelida dichroma Viswajyothi & Clark is proposed as a nom. nov. for Racenisa bicolor Bechyné, 1958 (not Agelastica bicolor LeConte, 1884), as both species are currently placed in the genus Trachyscelida Horn, 1893.
The West African region possesses one of the largest knowledge gaps in the distribution and taxonomy of all species, especially inconspicuous ones. This work presents one of the few bat studies ever carried out in the Cabo Verde Islands. Knowledge on the distribution of the seven species recorded in this remote archipelago is still very scarce and with very low resolution (many at island level), so new records are expectable and invaluable for the establishment of conservation policies. A review on the scattered and digitally unavailable (due to the old date of publication) knowledge of the Cabo Verde bat fauna with the first bat records for two islands and new occurrence data for two species on three islands is presented. It is expected that this work can constitute a reference for future bat works in the region, while providing acoustic data that can easily be updated upon future taxonomic revisions.
The olive ridley sea turtle Lepidochelys olivacea has been recorded in the Cape Verde Islands, but the most recent published data (1998-2000) are of stranded individuals and remains only. This article presents new data on olive ridleys recorded during the years 2001-2011 on Boavista and Sal islands. The presence of this species does not appear to be related to nesting activity. The possible geographical origin of these turtles is discussed. In addition, we propose some studies that could help to reinforce the conservation of sea turtles in West Africa.
Two new species of Palpimanus Dufour, 1820 are described from India: P. godawan Tripathi & Sankaran sp. nov. (♂♀), collected from the Thar Desert in Rajasthan, and P. maldhok Kuni, Tripathi & Sankaran sp. nov. (♂♀), collected from Maharashtra. Images of the endogyne and male palp of the holotype and paratype of P. narsinhmehtai Parajapati, Hun & Raval, 2021 are presented to facilitate its identification. A key to Indian species of Palpimanus and a catalogue of Indian palpimanid spiders are provided. The current distribution of all the known Indian palpimanid spiders is mapped.
On 31 August 2003, at 11:40 local time, c. 5 nm southwest of São Nicolau (16º33.1N, 024º27.7W), Cape Verde Islands, GT and PLS observed c. 20 Fraser’s Dolphins Lagenodelphis hosei Fraser, 1956 (Fig.1). The sighting was made under excellent weather conditions (sea state Beaufort 2 with sun) from the 39.6 m diesel engine powered oceanographic research vessel Taliarte during a two week cetacean survey conducted as part of the Hydrocarpo project.
Pitfall trapping in the National Park Thy, north-western Jutland, Denmark, in 2011 and 2013 revealed 3654 specimens of the harvestman Nelima gothica. In most European countries, including Denmark, this species has been considered rare and little information is available on its biology. The species was found predominantly in the yellow dune habitat close to the North Sea coast. Here it could be either very abundant or completely absent at localities only a few kilometres apart. It also occurred in lower numbers in the grey dunes and the dune heathland, and was rare in managed grassland; it disappeared from habitats further inland. In the yellow dunes high numbers were recorded especially in rather dense Ammophila arenaria vegetation not disturbed by sand shifting. The phenology follows the typical pattern of North-European Phalangiidae and Leiobuninae: an annual life-cycle with juveniles developing through late spring and summer months, reproduction in autumn and hibernation in the egg stage. The findings suggest that N. gothica may be found all along the coastal dunes of western Denmark and possibly the Wadden Sea area, though it may only locally reach high abundances. Earlier records also included the coasts of eastern Denmark.
A survey of butterfly species was carried out on 12 islands of the Cape Verde archipelago (Brava, Cima, Fogo, Santiago, Maio, Boa Vista, Sal, São Nicolau, Raso, Santa Luzia, São Vicente, Santo Antão) during almost eight weeks in 2013. Results include the discovery of six species not previously recorded from the islands: Vanessa atalanta, V. vulcania, Junonia oenone, Danaus plexippus, Eurema brigitta and Azanus ubaldus. Known island distribution of some resident species is extended. Status of some long-standing (and questionable) historical records and probable misidentifications are discussed in detail. Data are presented with regard to habitat, habits and host-plants of all taxa, together with a table of species, islands, status and probable original geographical source. Entomological data from Cambridge University ornithological research on Raso between 2006 and 2014 are also included. Comment is made with regard to whether butterfly studies support inclusion of the Cape Verde Islands in ‘Macaronesia’ sensu lato.
The authors carried out a survey of butterflies on 12 of the Cape Verde Islands from 29 October to 18 December 2013. During the survey records were also made of the few hawk-moths (Lepidoptera: Sphingidae) encountered during the day, or feeding at flowers at dusk and dawn. None was collected at light. Since several of our records are believed to be new island records, we present them here. The few voucher specimens collected have been deposited in the Natural History Museum, London.
The taxonomic status of the nominal taxon Dryophis prasinus flavescens Wall, 1910 is reevaluated herein. Based on molecular data generated from fresh collections of Ahaetulla prasina (H. Boie in F. Boie, 1827) auctorum from Northeast India and, additionally, morphological data from museum specimens originating from the same areas, we resurrect this taxon as Ahaetulla flavescens (Wall, 1910) comb. nov. We clarify the status, identity and locations of its type specimens, rediscover, redescribe and illustrate those specimens and also designate a lectotype in order to effect a proper taxonomic redefinition of this nominal taxon. We provide further details on the morphology and diagnosis of this species and elucidate its phylogenetic position. We also provide a summary of the natural history and distribution of this species. Adding to the known cryptic diversity and genetic divergence within Southeast Asian populations, this work also hints at the need for a taxonomic revision of the A. prasina complex. This work complements a previous study on the A. prasina complex focusing on populations in Indonesia. Taken together, these two studies represent phylogenetic reconstructions from different populations of the A. prasina complex across its distribution range, on the Asian mainland and the surrounding islands.
Thanks to newly collected material from the Terra Nova Bay area (Ross Sea, Antarctica), we discuss the taxonomy of the ampharetid genera Amage Malmgren, 1866 and Amythas Benham, 1921. A new species of Amage, A. giacomobovei sp. nov., is described based on morpho-anatomical data. This is the second new species described from an area which appears to be rich in ampharetids, a coastal embayment at ~500 m depth near the Italian “Mario Zucchelli” research station. The new species is characterized by having 16 abdominal uncinigers and four pairs of branchiae that readily distinguish it from its congeners. Tubes of A. giacomobovei sp. nov. are also characteristic in showing a large amount of embedded sponge spicules, suggesting a possible close association to spicule mats. Based on the amended diagnoses of the two genera, Amage septemdecima Schüller & Jirkov, 2013 is transferred to the genus Amythas. Finally, to simplify the task of ampharetid genera recognition for untrained people, we provide a dichotomic key for ampharetid genera found in Antarctica and a checklist of species occurring in Terra Nova Bay.
Allomyia renoa (Milne, 1935) (Trichoptera: Apataniidae) was described from six females. The male association is verified in this paper. The original type locality information is limited: “Reno, Nev.,‘78, Morrison”. An Allomyia Banks population found at Mount Rose in Washoe County, Nevada, was compared to the A. renoa type material and found to be the conspecific. Figures, descriptions and distribution of male, female, pupal and larval A. renoa are provided.
Mobulinae rays are part of Cabo Verde native biodiversity and belong to two extant genera, Manta and Mobula (Paig-Tran et al. 2013, Ward-Paige et al. 2013). Mobula spp. can be distinguished from Manta spp. by the mouth position, the shape of the cephalic fins and body size (Stevens 2011). Despite their large size, little is known about their population trends and precise distribution. They are particularly difficult to study in the wild and have restricted distributions (Ward-Paige et al. 2013, Croll et al. 2015).
New state records for 33 species of Eucnemidae (Coleoptera) are reported from the eastern United States based on the examination and identifications of specimens from four institutional and personal collections over the past several years. Images of 12 eucnemid species are also provided.
ZooBank registration. urn:lsid:zoobank.org:pub:DAFE70DF-394F-4ECF-A518-3EF5DD8B8B6F
Abstract. New state records for 35 species of Eucnemidae (Coleoptera: Elateroidea) are reported from the eastern United States based on examination and identification of specimens from several institutional and two private collections in the last year. Images of 18 eucnemid species are provided.
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New records for a new species and other exotic Dirrhagofarsus Fleutiaux (Coleoptera: Eucnemidae: Melasinae: Dirhagini) species are reported from throughout much of the northeastern and southern areas of the United States. Dirrhagofarsus brevis, new species, is hereby described in this study. Two other exotic species, Dirrhagofarsus modestus (Fleutiaux) and Dirrhagofarsus unicolor (Hisamatsu), new country records, are redescribed and diagnosed as they were compared with other Dirrhagofarsus species present in the Nearctic region. All Dirrhagofarsus species in this study are imaged, highlighting essential character states to facilitate better diagnosis in conjunction to the new identification key provided in this study.
ZooBank registration. urn:lsid:zoobank.org:pub:24DCE05F-14CE-465B-AB11-A2F34012FAB6