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Journal articles on the topic 'Atopomelidae'

Author: Grafiati

Published: 3 June 2025

Last updated: 5 July 2025

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1

Bochkov, Andre V., and Alex Fain. "Revision of the subgenus Marquesania (Acari : Atopomelidae : Listrophoroides)." Invertebrate Systematics 17, no. 4 (2003): 575. http://dx.doi.org/10.1071/it01050.

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The subgenus Marquesania Womersley (Acari : Atopomelidae : Listrophoroides) is revised. The species of this subgenus are permanent parasites living in the fur of rats (Rodentia : Murinae) in the Oriental region, Australia and New Guinea. Most of the type material has been examined. Two new species, Listrophoroides melomys, sp. nov. from Melomys moncktoni (Thomas) and L. mordax, sp. nov. from Rattus mordax (Thomas) are described from New Guinea. A new diagnosis of the subgenus Marquesania, detailed descriptions, and a key for all species is provided. The phylogenetic reconstruction of the subgenus Marquesania was effected by the method of parsimonius cladistics. The monophyly of the subgenus is strongly supported by this analysis, and most species from the Oriental region fall at the base of the cladogram. The distribution of Marquesania species on their hosts is discussed. It is suggested that these mites originated in the Oriental region and then migrated to Australia and New Guinea. The distribution of Marquesania species in the Australian and New Guinean regions is noticeably complicated, reflecting the complex settling history of their hosts.

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BOCHKOV, ANDRE V., ALEXEI V. ABRAMOV, and JEAN-PIERRE HUGOT. "Five new species of fur mites (Acariformes: Sarcoptoidea) from small mammals in Laos." Zootaxa 2980, no. 1 (2011): 1. http://dx.doi.org/10.11646/zootaxa.2980.1.1.

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Five new fur-inhabiting mites of the superfamily Sarcoptoidea (Acariformes: Astigmata) are described from small mammals associated with tower karstic landscape in Khammouane Province of Laos: Listrophoroides oconnori sp. n. from Saxatilomys paulinae Musser et al. (Rodentia: Muridae) and Atopomelus megalotis sp. n. from Hylomys megalotis Jenkins and Robbinson (Erinaceomorpha: Erinaceidae)—Atopomelidae; Afrolistrophoroides laonastes sp. n. from Laonastes aenigmamus Jenkins et al. (Rodentia: Diatomyidae), A. saxatilomys sp. n. from Saxatilomys paulinae, and Pteromychirus menetes from Menetes berdmorei (Blyth) (Rodentia: Sciuridae)—Listrophoridae.

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3

Domrow, R. "Acari Astigmata (excluding Feather Mites) parasitic on Australian vertebrates: an annotated checklist, keys and bibliography." Invertebrate Systematics 6, no. 6 (1992): 1459. http://dx.doi.org/10.1071/it9921459.

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The astigmatic mites (excluding feather mites) parasitic on, or associated with Australian vertebrates are reviewed, and keys and illustrations provided to enable separation of all 77 genera and 204 species recognised. Murichirus anabiotus, sp. nov. (Atopomelidae) is described from Pseudocheirus peregrinus (Boddaert) (Marsupialia: Petauridae). New synonymy in Echimyopodidae: Marsupiopus leporilli Fain, 1969a = M. l. pseudomys Fain & Lukoschus, 1976; in Acaridae: Thyreophagus Rondani, 1874 = Michaelopus Fain & Johnston, 1974; in Hypoderatidae: Hypodectes de Filippi, 1861 = Hypodectoides Fain & Bafort, 1966; Hypodectes propus (Nitzsch in Giebel, 1861) = H. p. bubulci Fain, 1967a = H. p. similimus Cerny, 1969; Neottialges Fain, 1966d = Suladectes Fain, 1969b; Tytodectes Fain, 1966d = Caprimuldectes Janssen Duijghuijsen, Lukoschus & Fain, 1979; in Laminosioptidae: Fainocoptes Lukoschus & Lombert, 1979 = Calamicoptes Lukoschus & Lombert, 1979 = Streetacarus Lukoschus & Lombert, 1979; Laminosioptes cisticola (Vizioli, 1868) = Acarus depilis Brown, 1897; in Listrophoridae: Leporacarus Fain, 1970b = Listracarus Domrow, present paper; in Chirodiscidae: Alabidocarpus recurvus (Womersley, 1943) = A. yandinae intersitus Fain & Lukoschus, 1981a; Dentocarpus Dusbabek & Cruz, 1966 = Paradentocarpus Fain, 1976a = Labidocarpellus Fain, 1976a; in Atopomelidae: Austrochirus Womersley, 1943 = Austrochiroides Fain, 1970e; Campylochirus Trouessart, 1893 = Campylochiroides Fain, 1971a; Dasyurochirus Fain, 1970e = Neodasyurochirus Fain, 1972a = Atopomelopsis Fain, 1972a; Dasyurochirus longipilis Fain, 1971a = Atopomelopsis gibberosa Fain, 1972a; D. sminthopsis (Womersley, 1954) = D. s. leucopus Fain & Lukoschus, 1981b; Murichirus Fain, 1971a = Murichiroides Fain, 1971a = Teinocheirus Fain & Lukoschus, 1981c; Murichirus a. alatus Fain & Lukoschus, 1981c = M. a. prosquamatus Fain & Lukoschus, 1981c. A host-parasite list and bibliography are included, and corrigenda and addenda to earlier parts of this checklist are provided. Laelaps elegans Canestrini, 1898 (Laelapidae) is a primary homonym of L. elegans Domrow, 1980a (= L. lampetes, nom. nov.); and L. manguinhosi calvescens Furman, 1972 of L. calvescens Domow, 1980b (= L. deanei, norn. nov.). Liponyssoides adsonis, sp. nov. (Dermanyssidae) is described from Climacteris leucophaea (Latham) (Passeriformes: Climacteridae).

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4

Troyo, Adriana, Mayra E. Solano, Olger Calderón-Arguedas, Misael Chinchilla, Ronald Sánchez, and Gustavo A. Gutiérrez-Espeleta. "Fur mite,Listrocarpus alouattaeFain (Acari: Atopomelidae), fromAlouatta palliataGray (Primates: Cebidae) in Costa Rica." International Journal of Acarology 28, no. 3 (2002): 251–55. http://dx.doi.org/10.1080/01647950208684299.

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5

TAKADA, Ayumi. "Records of Myocoptidae, Listrophoridae, Chirodiscidae, and Atopomelidae skin and fur mites in Japan." Journal of the Acarological Society of Japan 26, no. 2 (2017): 83–88. http://dx.doi.org/10.2300/acari.26.83.

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6

Canto-Osorio, Juan Miguel, Alan Cuxim-Koyoc, Hugo A. Ruiz-Piña, Juan B. Morales-Malacara, and Enrique Reyes-Novelo. "Ectoparasites of Didelphis virginiana From Yucatan, Mexico." Journal of Medical Entomology 57, no. 6 (2020): 1821–29. http://dx.doi.org/10.1093/jme/tjaa106.

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Abstract A faunal study is presented to determine the species of ectoparasites found in the opossum Didelphis virginiana (Kerr) (Marsupialia: Didelphidae). For this, Tomahawk traps were placed in the peridomiciles of a rural town in Yucatán, to capture individuals of this marsupial and proceed to the collection of their ectoparasites. A total of 3,023 arthropods were collected from 145 opossums. The most frequent ectoparasites were the acarines Ornithodoros (Alectorobius) nr. talaje (64.8%) (Argasidae); Ornithonyssus wernecki Fonseca (53.8%) (Macronyssidae) and Didelphilicus serrifer Fain (25.5%) (Atopomelidae); the ticks Amblyomma parvum Aragão (8.3%) and A. mixtum Koch (10.3%) (Ixodidae); and the fleas Ctenocephalides felis (Bouché) (20.7%) and Pulex simulans Baker (8.3%) (Pulicidae). It is concluded that the ectoparasite fauna of this marsupial is mainly composed of euryxenous organisms, which have been documented as vectors of diseases caused by rickettsial bacteria. Since D. virginiana is widely adapted to the peridomiciliary environment in the region, this study allows recognizing those that represent a potential risk for the transmission of vector-borne zoonotic diseases.

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7

Bochkov, Andre V., and Sergey V. Mironov. "Phylogeny and systematics of mammal-associated psoroptidian mites (Acariformes:Astigmata:Psoroptidia) derived from external morphology." Invertebrate Systematics 25, no. 1 (2011): 22. http://dx.doi.org/10.1071/is10023.

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We used morphological characters to explore the phylogeny of mammal-associated psoroptidian mites. In both maximum parsimony and Bayesian analyses, the clades uniting Psoroptoidea and Analgoidea–Sarcoptoidea (higher Psoroptidia) were strongly supported, and monophyly of most sarcoptoid families was confirmed. However, the relationships among families of the higher Psoroptidia (Analgoidea and Sarcoptoidea) remained poorly resolved. Two most parsimonious trees were obtained after successive weighting. In these trees, higher Psoroptidia split into two main clusters with Sarcoptoidea in the traditional sense shown as diphyletic. Cluster I consists of two superfamilies: Analgoidea, including Dermationidae, and Psoroptoidea, stat. res.: Psoroptoidinae (Turbinoptidae–Paracoroptinae); (Pandalurinae (Pyroglyphidae–Lobalgidae); Paralgopsidae, stat. nov.–Ptyssalgidae (Epidermoptidae–Psoroptidae). Cluster II consists of the superfamily Sarcoptoidea represented by two lineages: Listropsoralgidae, stat. nov. (Myocoptidae (Rhyncoptidae–Sarcoptidae)) and Dromiciocoptidae, stat. nov. ((Listrophoridae–Atopomelidae) (Chirodiscidae (Gastronyssidae (Pneumocoptidae–Lemurnyssidae)))). We hypothesised that mites of the superfamilies Pterolichoidea, Analgoidea and Psoroptoidea have independently colonised birds with subsequent ancestral shifts of the families Lobalgidae and Psoroptidae and subfamily Paracoroptinae from birds to mammals. Mites of the superfamily Sarcoptoidea switched from nidicoly to parasitism on ancestors of therian mammals and evolved exclusively on this host group.

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8

Bochkov, Andre V., and Barry M. OConnor. "Phylogeny and host associations of the fur-mite subgenus Listrophoroides (sensu stricto) Hirst (Acari:Atopomelidae) with an intriguing example of synhospitality on rats of the genus Maxomys." Invertebrate Systematics 19, no. 5 (2005): 437. http://dx.doi.org/10.1071/is05017.

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Phylogenetic relationships among species of the parasitic mite subgenus Listrophoroides Hirst (Atopomelidae), fur-mites of Asian and African murine rodents, are reconstructed on the basis of parsimony analysis of morphological characters. This group is polyphyletic with respect to the outgroup, subgenera Marquesania Womersley and Paklistrophoroides Fain & Hyland. The mite phylogeny partially reflects the host phylogeny and several groups of closely related species associated with particular rodent groups are recognised. The rajah-group, with 34 species associated with rats of the genus Maxomys Sody, is most diverse. Most Maxomys species are parasitised by a single mite species but some of them harbour a complex of several species. Maxomys surifer (Miller), the most widespread species of the genus, hosts unique species combinations comprising 23 species in different parts of its range. This synhospitality is hypothesised to have originated during Pleistocene isolation of different host populations in multiple rain forest refugia. The current species complexes also reflect later host range expansions. These data are consistent with a hypothesis of Pliocene vicariance in some Sunda Shelf rodents and not with the traditional view of widespread migration across the Late Pleistocene Sunda Shelf. The rajah species-group is revised, 16 species are described as new and three are synonymised.

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9

Thille, Katelyn Noelle, Nia Francesca Rametta, Daniel Mark Fitzpatrick, et al. "Ectoparasites of brown rats (Rattus norvegicus) in Grenada, West Indies." Veterinary World 12, no. 9 (2019): 1390–94. http://dx.doi.org/10.14202/vetworld.2019.1390-1394.

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Background and Aim: Arthropod ectoparasites (mites, lice, ticks, and fleas) on common house rats or brown rats (Rattus norvegicus) are known to transmit zoonotic pathogens and diminish rat health. To the best of our knowledge, there is no published information regarding the prevalence of ectoparasites on R. norvegicus in Grenada. This study aimed to determine the prevalence and types of ectoparasites present on brown rats from Grenada. Materials and Methods: One hundred sixty-eight rats were collected live from the parishes of St. George and St. David, Grenada, from May to July 2017. Following euthanasia, external parasites were collected using fine combs, thumb forceps, and paper tape. Tape samples and free specimens were placed in containers with 70% ethanol. External parasites were evaluated using dissection microscopy. Results: Over 2000 ectoparasites were collected from 149 of the 168 trapped rats (88.7%). Ectoparasites identified included mesostigmatid mites (found on 84.6% of infested rats), fur mites in the families Atopomelidae and Listrophoridae (67.1%), Polyplax spp. lice (6.7%), fleas (3.4%), an unidentified larval tick (0.7%), and a mite in the family Myobiidae (0.7%). Infestation rates were higher in St. David Parish (86/89; 96.6%) than in St. George Parish (63/79; 79.7%) (p=0.001). When comparing sex and age, males had a marginal increase in infestation rate (83/89; 93.3%) compared to females (66/79; 83.5%) (p=0.054), and adults had an infestation rate of 90.7% (97/107) compared to juvenile rats who had a 66.7% (14/21) infestation rate. Conclusion: Brown rats in Grenada are heavily infested with ectoparasites, including known vectors of pathogens. Future studies will examine the prevalence of zoonotic pathogens in these arthropods.

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10

Bochkov, Andre V., Alexei V. Abramov, and Jean-Pierre Hugot. "Five new species of fur mites (Acariformes: Sarcoptoidea) from small mammals in Laos." Zootaxa 2980 (December 31, 2011): 1–22. https://doi.org/10.5281/zenodo.278298.

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11

LIU, DONG, TIAN-CI YI, YUN XU, and ZHI-QIANG ZHANG. "Hotspots of new species discovery: new mite species described during 2007 to 2012." Zootaxa 3663, no. 1 (2013): 1–102. https://doi.org/10.11646/zootaxa.3663.1.1.

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LIU, DONG, YI, TIAN-CI, XU, YUN, ZHANG, ZHI-QIANG (2013): Hotspots of new species discovery: new mite species described during 2007 to 2012. Zootaxa 3663 (1): 1-102, DOI: 10.11646/zootaxa.3663.1.1, URL: http://dx.doi.org/10.11646/zootaxa.3663.1.1

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12

Perez-Gelabert, Daniel E. "Arthropods of Hispaniola (Dominican Republic and Haiti): A checklist and bibliography." Zootaxa 1831, no. 1 (2008): 1–530. https://doi.org/10.11646/zootaxa.1831.1.1.

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Perez-Gelabert, Daniel E. (2008): Arthropods of Hispaniola (Dominican Republic and Haiti): A checklist and bibliography. Zootaxa 1831 (1): 1-530, DOI: 10.11646/zootaxa.1831.1.1, URL: https://biotaxa.org/Zootaxa/article/view/zootaxa.1831.1.1

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13

Bochkov, Andre V., and Michel P. Valim. "New species and records of mites of the superfamily Sarcoptoidea (Acariformes: Psoroptidia) from mammals in Brazil." Acta Parasitologica 61, no. 1 (2016). http://dx.doi.org/10.1515/ap-2016-0003.

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AbstractSixteen species of the superfamily Sarcoptoidea (Acariformes: Psoroptidia) belonging to 10 genera of the families Atopomelidae, Listrophoridae, Chirodiscidae, and Listropsoralgidae are recorded in Brazil. Among them, three species, Prolistrophorus hylaeamys sp. nov. from Hylaeamys laticeps (Lund, 1840) (Cricetidae: Sigmodontinae) from Minas Gerais, Lynxacarus serrafreirei sp. nov. from Galictis cuja (Molina, 1782) (Carnivora: Mustelidae) from Rio de Janeiro (Listrophoridae), and Didelphoecius micoureus sp. nov. (Atopomelidae) from Micoureus paraguayanus (Tate, 1931) (Didelphimorphia: Didelphidae) from Minas Gerais are described as new for science. Three species of the family Listrophoridae, Prolistrophorus bidentatus Fain et Lukoschus, 1984 from Akodon cursor (Winge, 1887) (Rodentia: Cricetidae) (new host), Prolistrophorus ctenomys Fain, 1970 from Ctenomys torquatus Lichtenstein, 1830 (Rodentia: Ctenomyidae) (new host), and Leporacarus sylvilagi Fain, Whitaker et Lukoschus, 1981 from Sylvilagus brasiliensis (Linnaeus, 1758) (Lagomorpha: Leporidae) (new host) -from Minas Gerais and Rio Grande do Sul, and one species of the family Chirodiscidae, Parakosa tadarida McDaniel and Lawrence, 1962 from Molossus molossus (Pallas, 1766) (Chiroptera: Molossidae) are recorded for the first time in Brazil. The previously unknown female of Didelphoecius validus Fain, Zanatta-Coutinho et Fonseca, 1996 (Atopomelidae) from Metachirus nudicaudatus (Geoffroy, 1803) (Didelphimorphia: Didelphidae) from Minas Gerais is described. All data on host-parasite associations of sarcoptoids in Brazil are summarized. Totally, 61 sarcoptoid species of 8 families are recorded in Brazil.

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14

Kolesnikov, Vasiliy B., and Barry M. OConnor. "TAXONOMY OF MADAGASCAN ATOPOMELIDAE (ACARI, ASTIGMATA, PSOROPTIDIA) I: DESCRIPTION OF A NEW SPECIES OF LISTROPHOROIDES ASSOCIATED WITH ORYZORICTES HOVA (AFROSORICIDA, TENRECIDAE)." Acarina, 2024, 191–98. https://doi.org/10.21684/0132-8077-2024-32-2-191-198.

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This is the first work in a series of taxonomic investigations of Madagascan Atopomelidae, associated with Tenrecidae. Here, a new species—Listrophoroides (Madlistrophoroides) bochkovi sp. n. (male and female)—associated with Oryzorictes hova (Afrosoricida, Tenrecidae), is described. The new species is similar to Listrophoroides (Madlistrophoroides) fortis, but differs from the latter in a number of morphological features in both males and females, as well as in host specificity. Two species of Listrophoroides were found on Oryzorictes hova: Listrophoroides (Madlistrophoroides) uniformis and the new species.

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15

Troyo, Adriana, Mayra E. Solano, Ólger Calderón Arguedas, Misael Chinchilla, Rónald Sánchez, and Gustavo A. Gutiérrez Espeleta. "Prevalence of fur mites (Acari: Atopomelidae) in non-human primates of Costa Rica." Revista de Biología Tropical 57, no. 1-2 (2013). http://dx.doi.org/10.15517/rbt.v57i1-2.11326.

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16

Corpuz-Raros, Leonila A. "Addendum to the Checklist and Bibliography of Philippine Acari (Arachnida) with Notes on Nomenclatural Changes in Some Previously Recorded Species." Philippine Entomologist - Volume 30 Issue 2 30, no. 2 (2016). https://doi.org/10.59852/tpe-a656v30i2.

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A checklist of 196 acarine species recorded from the Philippines from 2006- 2015 is presented, including some species that were missed in a checklist published earlier, covering 1844-2005. These belong to 98 genera and 50 families, of which 55 genera and 15 families were reported as new to the Philippines during the former period. The number of added species is greatest for the free-living families, Otocepheidae (29), Cunaxidae (17), Haplozetidae (16), [superfamily] Galumnoidea (15), Hermanniidae (13) and Macrochelidae (13). There were also noteable increases in records of parasitic Astigmata, particularly fur mites of the family Atopomelidae (13 spp.) and internal parasitic Gastronyssidae (11 spp.). As in the 2005 checklist, the added species originated mainly from the largest islands of Luzon (84), Mindanao (46) and Samar (31). Altogether, the known Philippine fauna from 1844 to 2015 now amounts to 1,417 species, 565 genera and 180 families. The species are distributed to the major groups of the Superclass Acari as follows: Oribatida 441, Prostigmata 423, Mesostigmata 338, Astigmata 178, and lxodida 37. Slightly over half (52.3%) are known to occur only in or endemic to the Philippines at present. Changes in nomenclature of 136 previously listed species are provided, with notes on reasons for and references to their respective changes. These are mainly due to generic transfers consequent to erection of new genera, downgrading of genera to subgenera, synonymies and even resurrection of previous junior generic synonyms. Additional bibliographic references are provided for faunal records, nontaxonomic works, and world revisions, keys and checklists including species that were originally described from the Philippines.

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17

TROYO, ADRIANA, MAYRA E. SOLANO, and OLGER CALDERÓN-ARGUEDAS. "Two new species of Listrocarpus Fain (Acari: Atopomelidae) from Cebus capucinus Linnaeus and Saimiri oerstedii Reinhardt (Primates: Cebidae) in Costa Rica." Systematic and Acarology Acarology Special Publications 18, no. 1 (2004). http://dx.doi.org/10.11158/saasp.18.1.1.

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