2021
DOI: 10.3390/insects12050452
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The Taxonomic History of Ochlerotatus Lynch Arribálzaga, 1891 (Diptera: Culicidae)

Abstract: A review of all taxonomic actions within the subgenus Ochlerotatus Lynch Arribálzaga, 1891 (Diptera: Culicidae) sensu Reinert et al. (2008) is provided. In particular, the complex historical taxonomic treatment of the type species of this group is dissected and explained in detail. Additionally, current challenges with the definition of the subgenus and its constituents are discussed, as are the requisite steps for a successful revision of the taxon. Going forward, we conclude that a taxonomic revision of the … Show more

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Cited by 4 publications
(2 citation statements)
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“…For consistency, Culex pipiens was used for studies reporting Culex pipiens complex and Culex pipiens sensu lato [ 37 , 38 ]. Likewise, Ochlerotatus caspius and Ochlerotatus scapularis were denoted as Aedes caspius and Aedes scapularis , respectively, as both genus names were used in the literature [ 39 ]. Virus detection methods were classified into four categories: 1) sequencing, for samples that were directly analyzed by next-generation sequencing, 2) PCR, for samples in which viruses of a particular virus taxon or species were detected by PCR, 3) culture-sequencing, when mosquito homogenate was cultured on mosquito cell lines, after which viruses were detected by next-generation sequencing, and 4) culture-PCR, when mosquito homogenate was cultured on cell lines and virus was detected by PCR using virus taxon or species specific PCR primers.…”
Section: Methodsmentioning
confidence: 99%
“…For consistency, Culex pipiens was used for studies reporting Culex pipiens complex and Culex pipiens sensu lato [ 37 , 38 ]. Likewise, Ochlerotatus caspius and Ochlerotatus scapularis were denoted as Aedes caspius and Aedes scapularis , respectively, as both genus names were used in the literature [ 39 ]. Virus detection methods were classified into four categories: 1) sequencing, for samples that were directly analyzed by next-generation sequencing, 2) PCR, for samples in which viruses of a particular virus taxon or species were detected by PCR, 3) culture-sequencing, when mosquito homogenate was cultured on mosquito cell lines, after which viruses were detected by next-generation sequencing, and 4) culture-PCR, when mosquito homogenate was cultured on cell lines and virus was detected by PCR using virus taxon or species specific PCR primers.…”
Section: Methodsmentioning
confidence: 99%
“…In previous studies, morphological and biological aspects were targeted for phylogenetic reconstruction; however, this method has drawbacks, especially in cases with diverse and ancient taxa [ 39 ]. Various studies have demonstrated that mtDNA sequences are valuable genetic markers for phylogenetic studies of members of Nematoda [ 39 , 40 ], and the advent of molecular tools has allowed a deeper investigation of the taxonomic relationships between organisms [ 41 ]. To date, only a few species have been confirmed to be infected by Neofoleyellides parasites, and more data are needed to understand their diversity and distribution, especially in wild animals [ 9 ].…”
Section: Resultsmentioning
confidence: 99%