The world woodlouse flies (Diptera, Rhinophoridae)

Cerretti, Pierfilippo; Badano, Davide; Gisondi, Silvia; Giudice, Giuseppe Lo; Pape, Thomas

doi:10.3897/zookeys.903.37775

Cited by 11 publications

(26 citation statements)

References 71 publications

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“…This family includes 177 described species belonging to 33 genera (Cerretti et al ., 2020). Our data strongly support the monophyly of Rhinophoridae, which is consistent with the morphology of the first instar larvae (Pape, 1986; Pape & Arnaud, 2001) and phylogenetic estimations using molecular datasets (Singh & Wells, 2013; Winkler et al ., 2015; Kutty et al ., 2019, but see Kutty et al ., 2010).…”

Section: Discussionmentioning

confidence: 99%

Protein‐encoding ultraconserved elements provide a new phylogenomic perspective of Oestroidea flies (Diptera: Calyptratae)

Buenaventura

Lloyd

López

et al. 2020

Systematic Entomology

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The diverse superfamily Oestroidea with more than 15 000 known species includes among others blow flies, flesh flies, bot flies and the diverse tachinid flies. Oestroidea exhibit strikingly divergent morphological and ecological traits, but even with a variety of data sources and inferences there is no consensus on the relationships among major Oestroidea lineages. Phylogenomic inferences derived from targeted enrichment of ultraconserved elements or UCEs have emerged as a promising method for resolving difficult phylogenetic problems at varying timescales. To reconstruct phylogenetic relationships among families of Oestroidea, we obtained UCE loci exclusively derived from the transcribed portion of the genome, making them suitable for larger and more integrative phylogenomic studies using other genomic and transcriptomic resources. We analysed datasets containing 37–2077 UCE loci from 98 representatives of all oestroid families (except Ulurumyiidae and Mystacinobiidae) and seven calyptrate outgroups, with a total concatenated aligned length between 10 and 550 Mb. About 35% of the sampled taxa consisted of museum specimens (2–92 years old), of which 85% resulted in successful UCE enrichment. Our maximum likelihood and coalescent‐based analyses produced well‐resolved and highly supported topologies. With the exception of Calliphoridae and Oestridae all included families were recovered as monophyletic with the following conclusions: Oestroidea is monophyletic with Mesembrinellidae as sister to the remaining oestroid families; Oestridae is paraphyletic with respect to Sarcophagidae; Polleniidae is sister to Tachinidae; Rhinophoridae sister to (Luciliinae (Toxotarsinae (Melanomyinae + Calliphorinae))); Phumosiinae is sister to Chrysomyinae and Bengaliinae is sister to Rhiniidae. These results support the ranking of most calliphorid subfamilies as separate families.

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Section: Discussionmentioning

confidence: 99%

Protein‐encoding ultraconserved elements provide a new phylogenomic perspective of Oestroidea flies (Diptera: Calyptratae)

Buenaventura

Lloyd

López

et al. 2020

Systematic Entomology

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“…The group was then re-circumscribed by Rognes (1991a) to include Morinia Robineau-Desvoidy, Nesodexia Villeneuve and (tentatively) Wilhelmina Villeneuve, the latter being reassigned to the calliphorid subfamily Phumosiinae by Rognes (2011), which is followed here. More recently, Cerretti et al (2019) elevated the group to full family rank and gave morphological and molecular evidence to support both the monophyly of the Polleniidae and the inclusion of six taxa previously assigned to the Rhinophoridae, namely Alvamaja chlorometallica Rognes and five Afrotropical species moved from the genus Phyto Robineau-Desvoidy into Morinia (Cerretti et al 2020).…”

Section: Introductionmentioning

confidence: 88%

The world Polleniidae (Diptera, Oestroidea): key to genera and checklist of species

Gisondi¹,

Rognes²,

Badano³

et al. 2020

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A key to the world genera and a checklist of the world species for the family Polleniidae, including distributions, are provided. The following taxonomic and nomenclatural changes are proposed: Nitellia hermoniella Lehrer, 2007 = Pollenia mediterranea Grunin, 1966, syn. nov., Pollenia bentalia Lehrer, 2007 = Pollenia semicinerea Villeneuve, 1911, syn. nov., Dasypoda angustifrons Jacentkovský, 1941 = Pollenia tenuiforceps Séguy, 1928, syn. nov.; Anthracomyza Malloch, 1928, resurrected name (monotypic; type species Anthracomyia atratula Malloch) is considered a valid name and tentatively assigned to Polleniidae, giving Anthracomyza atratula (Malloch, 1927) as a resurrected combination; Morinia crassitarsis (Villeneuve, 1936), stat. rev. is considered a valid species, and Micronitellia Enderlein, 1936, stat. nov. is considered an available name.

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“…Digital images of the external morphology of the holotypes were taken using a Canon EOS 6D camera equipped with Canon Photo lens MP-E 65mm 1.2.8 and processed by Canon Digital Photo Professional (Canon, Ōta, Tokyo, Japan), Combine ZM by Alan Hadley and GIMP 2.10.4 by Alexandre Prokoudine. Terminology of the external morphology, and measurements and ratios of the head follow Cumming and Wood [ 12 ] and Cerretti et al [ 11 ], respectively. We follow Cerretti et al [ 11 ] in using the term “global apomorphy” for an uncontradicted and unreversed apomorphic character state, whereas “local apomorphy” is used for a character state that is homoplasious due to convergence or reversal.…”

Section: Methodsmentioning

confidence: 99%

“…Terminology of the external morphology, and measurements and ratios of the head follow Cumming and Wood [ 12 ] and Cerretti et al [ 11 ], respectively. We follow Cerretti et al [ 11 ] in using the term “global apomorphy” for an uncontradicted and unreversed apomorphic character state, whereas “local apomorphy” is used for a character state that is homoplasious due to convergence or reversal.…”

Section: Methodsmentioning

confidence: 99%

“…In recent years, research projects concerning rhinophorids have been flourishing, leading to the discovery of several new taxa [ 7 , 8 , 9 , 10 ] and the publication of a world catalogue with a key to genera [ 11 ]. The present paper aims to describe three new rhinophorid species, which are included in ongoing molecular studies (Gisondi et al).…”

Section: Introductionmentioning

confidence: 99%

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Growing the Rhinophorid Tree: Three New Species and Their Phylogenetic Implications (Diptera: Rhinophoridae)

Gisondi

Pape

Shima

et al. 2020

Insects

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Three new species of Rhinophoridae (Aporeomyia elaphocerasp. nov., Baniassa pennatasp. nov. from the Oriental Region, and Phyto mambillasp. nov. from the Afrotropical Region) are described, illustrated and compared with congeners. Genus-level affiliation of the new species is based on a morphology-based phylogeny, preliminarily accepting a paraphyletic Phyto Robineau-Desvoidy awaiting incorporation of molecular data. Keys to the species of the genus Aporeomyia Pape & Shima as well as to the Afrotropical species of the genus Phyto Robineau-Desvoidy are given.

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The world woodlouse flies (Diptera, Rhinophoridae)

Cited by 11 publications

References 71 publications

Protein‐encoding ultraconserved elements provide a new phylogenomic perspective of Oestroidea flies (Diptera: Calyptratae)

Protein‐encoding ultraconserved elements provide a new phylogenomic perspective of Oestroidea flies (Diptera: Calyptratae)

The world Polleniidae (Diptera, Oestroidea): key to genera and checklist of species

Growing the Rhinophorid Tree: Three New Species and Their Phylogenetic Implications (Diptera: Rhinophoridae)

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