Cladistic analysis of polytene chromosome rearrangements in anopheline mosquitoes, subgenus Cellia, series Neocellia

1985 ◽  
Vol 27 (2) ◽  
pp. 123-133 ◽  
Author(s):  
C. A. Green ◽  
B. A. Harrison ◽  
T. Klein ◽  
V. Baimai

New data on rearrangements of ovarian polytene chromosomes from mosquitoes are presented for the following species in the series Neocellia of Anopheles (Cellia): annularis, philippinensis, nivipes, splendidus, jamesii, and ramsayi. Rearrangement has involved fixation of alternatives for paracentric inversions. Two fixed inversion differences allow for the first time the direct identification of wild-caught females of philippinensis and nivipes. There is a suggestion that the latter nominal species may include two genetic species. These data and those published for close relatives are drawn together in a cladistic analysis to suggest relationships between the species. The data are limited and total relationships are not clear within the group.Key words: cladistic analysis, polytene chromosomes, Anopheles, mosquito, speciation.

ZooKeys ◽  
2021 ◽  
Vol 1025 ◽  
pp. 91-137
Author(s):  
Marília Pessoa-Silva ◽  
Marcos Ryotaro Hara ◽  
Ricardo Pinto-da-Rocha

Species of the genus Sadocus Sørensen, 1886 are conspicuous gonyleptids that occur in Chile and Argentina. Here, the genus is revised for the first time and the cladistic analysis based on morphological characters does not corroborate its monophyly unless a phylogenetically unrelated species is excluded (explained further on). A new classification is proposed for the seven species left in the genus and considered valid, of the 13 nominal species previously recognized. Two out of the seven valid species are considered as species inquirendae: Sadocus allermayeri (Mello-Leitão, 1945) [= Carampangue allermayeri Mello-Leitão, 1945] and Sadocus nigronotatus (Mello-Leitão, 1943) [= Carampangue nigronotatum Mello-Leitão, 1943]. The following synonymies are proposed: Sadocus bicornis (Gervais, 1849) [original combination = Gonyleptes bicornis Gervais, 1849] is a junior synonym of Sadocus asperatus (Gervais, 1847) [= Gonyleptes asperatus Gervais, 1847]; Sadocus conspicillatus Roewer, 1913, Sadocus exceptionalis (Mello-Leitão, 1946) [= Araucanoleptes exceptionalis Mello-Leitão, 1946] and Sadocus guttatus Sørensen, 1902 are junior synonyms of the valid name Sadocus polyacanthus (Gervais, 1847) [= Gonyleptes polyacanthus Gervais, 1847]; and Sadocus calcar (Roewer, 1913) [= Lycomedes calcar Roewer, 1913] is a junior synonym of the valid name Gonyleptes horridus Kirby, 1819. Sadocus brasiliensis Soares & Soares, 1949 is not congeneric with Argentinean/Chilean species of the genus according to the cladistic analysis and is here synonymized with Discocyrtus catharinensis (Mello-Leitão, 1923 [= Sadocus catharinensis Mello-Leitão, 1923]).


Genome ◽  
1991 ◽  
Vol 34 (2) ◽  
pp. 267-272 ◽  
Author(s):  
Jan Conn

The larval polytene chromosomes of Anopheles triannulatus are described for the first time in this report. The population from western Venezuela was chosen arbitrarily as the chromosome standard and is the basis for the photomap presented here. Anopheles triannulatus displays whole-arm associations distinct from other members of the subgenus Nyssorhynchus that have been examined cytogenetically. The association pattern for An. triannulatus is 2R–3R and 2L–3L, rather than the more common 2R–2L and 3R–3L. The possible role of whole-arm translocations in speciation is briefly discussed.Key words: Anopheles triannulatus, polytene chromosome photomap, whole-arm translocation, Venezuela.


1991 ◽  
Vol 123 (S160) ◽  
pp. 3-341 ◽  
Author(s):  
Jean-François Landry

AbstractGenera and previously described species of Nearctic Scythrididae are revised for the first time, based on the study of adult structures. About 90 percent of the Nearctic fauna known in collections consists of undescribed species. The supraspecific taxa treated in this work encompass less than half of the Nearctic species diversity. Only six new species are described, all within the largest and structurally most diverse genus. The status of all nominal species is revised. Valid species are redescribed and their features illustrated. General problems in the systematics of the Scythrididae are discussed. A description of adult features of the family Scythrididae is providad. Extra-limital genera are briefly reviewed. A key to the Nearctic genera and informal supraspecific lineages is provided.Six genera, including three new, are treated: Areniscythris Powell, 1976, Arotrura Walsingham, 1888, Asymmetrura gen. nov., Neoscythris gen. nov., Rhamphura gen. nov., and Scythris s. str. Hübner, [1825]. Areniscythris includes a single described species, Areniscythris brachypteris Powell, but is defined more broadly to account for a number of undescribed species. Arotrura is divided into nine informal species groups with the following included species: Arotrura atascosa sp. nov., Arotrura balli sp. nov., Arotrura divaricata (Braun) comb, nov., Arotrura eburnea Walsingham, Arotrura formidabilis sp. nov., Arotrura hymenata sp. nov., Arotrura longissima sp. nov., Arotrura oxyplecta (Meyrick) comb, nov., Arotrura powelli sp. nov., and Arotrura sponsella (Busck) comb. nov. Asymmetrura includes: Asymmetrura albilineata (Walsingham) comb. nov., Asymmetrura graminivorella (Braun) comb. nov., Asymmetrura impositella (Zeller) comb. nov. and type species, Asymmetrura matutella (Clemens) comb, nov., Asymmetrura reducta (Braun) comb, nov., and Asymmetrura scintillifera (Braun) comb. nov. Neoscythris includes: Neoscythris confinis (Braun) comb, nov., Neoscythris euthia (Walsingham) comb. nov., Neoscythris fissirostris (Meyrick) comb. nov. and type species, and Neoscythris planipenella (Chambers) comb. nov. Rhamphura includes: Rhamphura altisierrae (Keifer) comb, nov., Rhamphura ochristriata (Walsingham) comb. nov. and type species, Rhamphura perspicillella (Walsingham) comb. nov., Rhamphura suffusa (Walsingham) comb. nov., and the extra-limital Rhamphura immunis (Meyrick) comb. nov. from Peru. Scythris s. str. includes: Scythris immaculatella (Chambers) rev. stat., Scythris limbella (Fabricius), Scythris mixaula Meyrick, Scythris trivinctella (Zeller), and Scythris ypsilon Braun. A further eight species are phylogenetically distinct from Scythris s. str. but provisionally are only assigned to five informal monophyletic lineages until their cladistic relationships are more firmly established. These are: the Scythris basilaris lineage including Scythris basilaris (Zeller), Scythris eboracensis (Zeller), and Scythris fuscicomella (Clemens); the Scythris interrupta lineage including Scythris interrupta Braun; the Scythris inspersella lineage including Scythris inspersella (Hübner) and Scythris noricella (Zeller); the Scythris anthracina lineage including Scythris anthracina Braun; and the Scythris charon lineage including Scythris charon Meyrick. Three species are incertae sedis: Scythris inornatella (Chambers) comb, nov., Scythrispilosella (Zeller), and Scythris piratica Meyrick.Coleophora albacostella Chambers and Coleophora inornatella Chambers are transferred from the Coleophoridae. Scythris arizoniella (Kearfott) is transferred to the Coleophoridae [Coleophora arizoniella (Kearfott) comb. nov.].The following new synonymy is proposed: Colinita Busck, 1907 = Arotrura Walsingham, 1888; Gelechia aterrimella Walker, 1864 and Scythris epilobiella McDunnough, 1942 = Scythris inspersella [Hübner, (1817)]; Scythris magnatella Busck, 1904 = Scythris noricella (Zeller, 1843); Scythris pacifica McDunnough, 1927 = Scythris immaculatella (Chambers, 1875); Coleophora albacostella Chambers, 1875 and Scythris hemidictyas Meyrick, 1928 = Neoscythris planipenella (Chambers, 1875).A cladistic definition of the family is presented for the first time. The monophyly of the Scythrididae is supported by the following synapomorphies: very narrow ductus bursae, broad ductus seminalis anastomosed with the oviduct and the corpus bursae, lack of signum, unique shape of the apophyses of the metathoracic furca, tarsomeres 1–4 with two subapical spurs, aedeagus ankylosed, and origin of forewing veins R4 and R5 on a common stalk with R4 extended to the costa and R5 to the termen. Relationships of the Scythrididae within the Gelechioidea are discussed. Based on the cladistic analysis of 52 structural characters, phylogenetic relationships of supraspecific taxa are inferred. Two cladograms, one for the genera and one for the species groups of Arotrura, are presented and used in deriving the classification.


Zootaxa ◽  
2012 ◽  
Vol 3280 (1) ◽  
pp. 1 ◽  
Author(s):  
AMAZONAS CHAGAS-JÚNIOR

Three new species of Otostigmus Porat, 1876 from Brazilian Atlantic Forest are described. Otostigmus beckeri sp. n. andO. lanceolatus sp. n. are described from the state of Bahia and O. giupponii sp. n. from the state of Espírito Santo. InBrazil, the otostigmine scolopendrid genus Otostigmus comprises 22 species. A summary of Brazilian Otostigmus speciesis presented with new distribution records, taxonomic remarks when appropriate and an identification key. Otostigmus sul-catus Meinert, 1886 is recorded for the first time from Brazil; the Andean Otostigmus silvestrii Kraepelin 1903, previouslyrecorded from Brazil, is here considered not to be present in this country. Eight nominal species are regarded here as newsynonyms. Five of them—Otostigmus pradoi Bücherl, 1939, O. longistigma Bücherl, 1939, O. longipes Bücherl, 1939,O. langei Bücherl, 1946 and O. dentifusus Bücherl, 1946—are based on females of O. tibialis Brölemann, 1902. O. latipesBücherl, 1954 is conspecific with and is considered a junior synonym of O. sulcatus Meinert, 1886; O. limbatus diminutusBücherl, 1946 is a junior synonym of O. limbatus Meinert, 1886 and O. fossulatus Attems, 1928 is a junior synonym of O. goeldii Brölemann, 1898. A lectotype is designated for O. goeldii.


Genetics ◽  
1983 ◽  
Vol 103 (3) ◽  
pp. 465-482
Author(s):  
Hampton L Carson

ABSTRACT Of 103 picture-winged Drosophila species endemic to the high Hawaiian islands, all but three are endemic to single islands or island complexes. They are presumed to have evolved in situ on each island. The banding pattern sequences of the five major polytene chromosomes of these species have been mapped to a single set of Standard sequences. Sequential variation among these chromosomes is due to 213 paracentric inversions. An atlas of their break points is provided. Geographical, morphological and behavioral data may be used to supplement the cytological information in tracing ancestry. Starting at the newer end of the archipelago, the 26 species of the Island of Hawaii (less than 700,000 years old) are inferred to have been derived from 19 founders, 15 from the Maui complex, three from Oahu and one from Kauai. The existence of 40 Maui complex species is explicable as resulting from 12 founders, ten from Oahu and two from Kauai. The 29 Oahu species can be explained by 12 founder events, five from Kauai and seven from Maui complex (summary in Figure 5). Although the ancestry of two Kauai species can be traced to newer islands, the ten remaining ones on this island (age about 5.6 million years) are apparently ancient elements in the fauna, relating ultimately to Palearctic continental sources.


2007 ◽  
Vol 7 (2) ◽  
pp. 281-285 ◽  
Author(s):  
Cristina de Oliveira Dias ◽  
Sérgio Luiz Costa Bonecker

During a series of zooplankton surveys carried out from 2001 through 2005 off the coast of the state of Bahia, Brazil, 98 individuals of monstrilloid copepods were collected. These belong to five species (Monstrilla grandis, Cymbasoma cf. longispinosum, Cymbasoma cf. rigidum, Cymbasoma gracilis, and Cymbasoma quadridens). The first three are recorded for the first time in the Bahia coastal region. The geographical range of C. quadridens is expanded to the Brazilian northeastern coast. The results presented herein increase to nine the number of nominal species of Monstrilloida known from off Bahia; the environmental diversity of Caravelas Channel with highly productive areas and coral reef zones harbor an abundant and diverse monstrilloid fauna that should be surveyed in more detail.


2021 ◽  
Author(s):  
Dingxi Zhou ◽  
Mariana Borsa ◽  
Daniel J. Puleston ◽  
Susanne Zellner ◽  
Jesusa Capera ◽  
...  

CD4+ T cells orchestrate both humoral and cytotoxic immune responses. While it is known that CD4+ T cell proliferation relies on autophagy, direct identification of the autophagosomal cargo involved is still missing. Here, we created a transgenic mouse model, which, for the first time, enables us to directly map the proteinaceous content of autophagosomes in any primary cell by LC3 proximity labelling. IL-7Rα, a cytokine receptor mostly found in naive and memory T cells, was reproducibly detected in autophagosomes of activated CD4+ T cells. Consistently, CD4+ T cells lacking autophagy showed increased IL-7Rα surface expression, while no defect in internalisation was observed. Mechanistically, excessive surface IL-7Rα sequestrates the common gamma chain, impairing the IL-2R assembly and downstream signalling crucial for T cell proliferation. This study provides proof-of-principle that key autophagy substrates can be reliably identified with this model to help mechanistically unravel autophagy's contribution to healthy physiology and disease.


Development ◽  
1999 ◽  
Vol 126 (2) ◽  
pp. 293-303 ◽  
Author(s):  
K.J. Dej ◽  
A.C. Spradling

Polytene chromosomes exhibit intricate higher order chromatin structure that is easily visualized due to their precisely aligned component strands. However, it remains unclear if the same factors determine chromatin organization in polyploid and diploid cells. We have analyzed one such factor, the cell cycle, by studying changes in Drosophila nurse cell chromosomes throughout the 10 to 12 endocycles of oogenesis. We find that nurse cells undergo three distinct types of endocycle whose parameters are correlated with chromosome behavior. The first four endocycles support complete DNA replication; poorly banded polytene euchromatin progressively condenses during the late S phases to produce blob-like chromosomes. During the unique fifth endocycle, an incomplete late S phase is followed by a mitosis-like state during which the 64C chromosomes dissociate into 32 chromatid pairs held together by unreplicated regions. All the subsequent endocycles lack any late S phase; during these cycles a new polytene chromosome grows from each 2C chromatid pair to generate 32-ploid polytene nuclei. These observations suggest that euchromatin begins to condense during late S phase and that nurse cell polytene chromosome structure is controlled by regulating whether events characteristic of late S and M phase are incorporated or skipped within a given endocycle.


Zootaxa ◽  
2020 ◽  
Vol 4806 (1) ◽  
pp. 1-144
Author(s):  
STEFFEN BAYER ◽  
HUBERT HÖFER ◽  
HEIKO METZNER

We propose a revision of the spider genus Corythalia C.L. Koch, 1850 (Salticidae: Euophryini) with a revised genus diagnosis based on examination of all species available to us. In this paper we redescribe all previously described species from South America with revised species diagnoses and describe 20 new species from South America (and the nearby islands). For C. latipes, the type species of the genus Corythalia, a neotype is designated. In total, 52 nominal species of the genus are herein treated, 46 species are recognized as valid. The females of C. waleckii Taczanowski, 1871, C. luctuosa Caporiacco, 1954 and C. latipes (C.L. Koch, 1846) are described for the first time. Corythalia sellata Simon, 1901, erroneously considered as nomen nudum in the present version of the World Spider Catalog, is here recognised as a valid species. Corythalia fulgipedia Crane, 1948 is also considered a valid species and is removed from the synonymy of C. tropica (Mello-Leitão, 1939). One name is considered a nomen dubium (Corythalia variegata Caporiacco, 1954), two are nomina nuda (C. major Simon, 1901; C. dimidiata Simon, 1901). Two species are transferred to other genera: C. argyrochrysos (Mello-Leitão, 1946) to Pachomius Peckham & Peckham, 1896 as Pachomius argyrochrysos (Mello-Leitão, 1946), comb. nov. and C. heliophanina (Taczanowski, 1871) to Neonella Gertsch, 1936, as Neonella heliophanina (Taczanowski, 1871), comb. nov. under incertae sedis. One species is synonymised: C. barbipes (Mello-Leitão, 1939) is a junior synonym of C. cincta (Badcock, 1932), syn. nov. The new Corythalia species are: C. conferta sp. nov. (♂♀, Brazil), C. concinna sp. nov. (♀, Brazil), C. drepane sp. nov. (♂♀, Brazil), C. drepanopsis sp. nov. (♀, Brazil), C. antepagmenti sp. nov. (♂♀, Brazil), C. ricti Bayer, sp. nov. (♂, Guyana), C. protensa sp. nov. (♂, Brazil), C. gasnieri sp. nov. (♂, Brazil), C. verhaaghi sp. nov. (♀, Brazil), C. scutellaris Bayer, sp. nov. (♂♀, Ecuador), C. dakryodes Bayer, sp. nov. (♀, Colombia), C. foelixi Bayer, sp. nov. (♂♀, French Guiana), C. longiducta sp. nov. (♀, Brazil), C. latior sp. nov. (♂, Bolivia), C. trochophora Bayer, sp. nov. (♂, Ecuador), C. lineata Bayer, sp. nov. (♂, Guyana), C. hamulifera Bayer, sp. nov. (♂, Ecuador), C. tribulosa sp. nov. (♂, Colombia), C. flagrans sp. nov. (♂, Brazil) and C. fragilis sp. nov. (♂♀, Brazil). Illustrations are provided for all of the new species and for all (primary) type specimens of the species re-described. Hypotheses of possible relationships among the different species of Corythalia are discussed. 


Zootaxa ◽  
2009 ◽  
Vol 2318 (1) ◽  
pp. 552-565 ◽  
Author(s):  
PIERFILIPPO CERRETTI ◽  
THOMAS PAPE

A cladistic analysis of the genus Melanophora Meigen, 1803 (type-species: Musca grossificationis Linnaeus, 1758 [= Musca roralis Linnaeus, 1758]) is presented and the generic delimitation is critically redefined. The nominal genus-group taxon Bequaertiana Curran, 1929 (type-species: Bequaertiana argyriventris Curran, 1929) is synonymised with Melanophora Meigen syn. nov. The following new combinations are proposed: Melanophora argyriventris (Curran, 1929) comb. nov. and Melanophora basilewskyi (Peris, 1957) comb. nov. Melanophora chia sp. nov. from SW Sardinia is described, illustrated and compared with the other known species of the genus. The male of Melanophora asetosa Kugler, 1978 is described for the first time. Melanophora basilewskyi (Peris, 1957) is recorded from Kenya for the first time.


Sign in / Sign up

Export Citation Format

Share Document