scholarly journals The family Parasitidae (Acari: Mesostigmata) - history, current problems and challenges

Acarologia ◽  
2018 ◽  
Vol 58 (Suppl) ◽  
pp. 25-42
Author(s):  
Kamila Hrúzová ◽  
Peter Fenďa

The family Parasitidae comprises two subfamilies, Parasitinae and Pergamasinae. A generic concept of this family is not stable and requires a revision. The number of genera varies depending on authors and their view on the systematics of the family, especially on the rank of taxa. We recognize 23 genera within Parasitinae and 22 genera within Pergamasinae, 4 of them are subdivided into subgenera. A dichotomous key for separation of genera and subgenera is provided. A new genus, Coprocarpais n. g. with type species Parasitus copridis Costa, 1963 is proposed and a diagnosis is given. The genus Erithosoma is not assigned to any subfamily because a description of females is missing. The most pressing taxonomic problems at generic and subgeneric levels are discussed. Fourteen new combinations are proposed.

Zootaxa ◽  
2009 ◽  
Vol 2221 (1) ◽  
pp. 27-40 ◽  
Author(s):  
JIANG-LI TAN ◽  
BAO-ZHEN HUA

Bicaubittacus gen. nov., the second genus of the family Bittacidae from the Oriental Region, is erected with Bittacus appendiculatus Esben-Petersen, 1927 as its type species. A key to the 17 extant genera of Bittacidae is compiled to include the new genus. Two new species, Bicaubittacus yangi sp. nov. and Bi. mengyangicus sp. nov. are described and illustrated from China. Three new combinations, Bicaubittacus appendiculatus (Esben-Petersen, 1927) and Bi. longiprocessus (Huang & Hua, 2005) from China, and Bi. burmanus (Tjeder, 1974) from Myanmar (formerly Burma), are transferred from the genus Bittacus Latreille. A key to the five species of Bicaubittacus is provided. The validity of Neobittacus and Thyridates is briefly discussed


1983 ◽  
Vol 61 (1) ◽  
pp. 31-44 ◽  
Author(s):  
Frank Dicosmo ◽  
T. R. Nag Raj ◽  
Bryce Kendrick

An emendation of the Phacidiaceae is presented. Of 24 genera placed in the family by previous authors, only 2, Lophophacidium and Phacidium (=Phacidiostroma) are retained. Four new species are described, and three new combinations made, in Phacidium. The Apostrasseria or Ceuthospora anamorphs of six of these are also described. Phacidium symplocinum is made the type species of a new genus, Ascluella, tentatively maintained in the Dermateaceae. The new combinations, Coccomyces gaultheriae, Odontotrema sieversiae, Pseudophacidium kumaonense, and Schizoxylon hemisphaericum, are introduced.


2020 ◽  
Vol 70 (3) ◽  
pp. 2147-2154 ◽  
Author(s):  
Guang-Da Feng ◽  
Xian-Jiao Zhang ◽  
Song-Zhen Yang ◽  
An-Zhang Li ◽  
Qing Yao ◽  
...  

During a phylogenetic analysis of Sphingorhabdus and its closely related genera in the family Sphingomonadaceae , we found that the genus Sphingorhabdus and the species Sphingopyxis baekryungensis might not be properly assigned in the taxonomy. Phylogenetic, phenotypic and chemotaxonomic characterizations clearly showed that the genus Sphingorhabdus should be reclassified into two genera (Clade I and Clade II), for which the original genus name, Sphingorhabdus , is proposed to be retained only for Clade I, and a new genus named as Parasphingorhabdus gen. nov. is proposed for Clade II with four new combinations: Parasphingorhabdus marina comb. nov., Parasphingorhabdus litoris comb. nov., Parasphingorhabdus flavimaris comb. nov. and Parasphingorhabdus pacifica comb. nov. Moreover, Sphingopyxis baekryungensis should represent a novel genus in the family Sphingomonadaceae , for which the name Novosphingopyxis gen. nov. is proposed, with a combination of Novosphingopyxis baekryungensis comb. nov. The study provides a new insight into the taxonomy of closely related genera in the family Sphingomonadaceae .


2019 ◽  
Vol 323 (3) ◽  
pp. 369-372
Author(s):  
A.F. Emeljanov

A new genus, Euryburnia gen. nov. (type species: Megamelus magnifrons Crawford, 1914) is erected to accommodate the group of Nearctic species of the family Delphacidae erroneously placed by Hamilton (2002) in the genus Eurybregma Scott, 1875. The new genus differs from Eurybregma by narrower metope without intermediate carinae on eumetope (only median carina is developed). According to male genitalia structure the new genus is close to the genera Unkanodes Fennah, 1956 and Chilodelphax Vilbaste, 1968, but distinguished by angular (not rounded) latero-ventral lobes of pygofer and by pygofer phragme without teeth and processes. From the genus Eurybregma the new genus differs by the presence of latero-ventral lobes of male pygofer. According to presence of unique, well developed beak-shaped basal lobes of dorso-lateral plates of ovipositor (first valvifers) the new genus is distinguished within all Delphacidae. New combinations proposed: Euryburnia magnifrons (Crawford, 1914), comb. nov. (=Megamelus magnifrons Crowford, 1914), Euryburnia montana (Beamer, 1952), comb. nov., (=Eurysa montana Beamer, 1952), Euryburnia obesa (Beamer, 1952), comb. nov. (=Eurysaobesa Beamer, 1952), Euryburnia eurytion (Hamilton, 2002), comb. nov. (=Eurybregma eurytion Hamilton, 2002).


2007 ◽  
Vol 15 (2) ◽  
pp. 301-303
Author(s):  
V.M. Gnezdilov ◽  
M.R. Wilson

A new genus Pamphylium gen. n. (type species: Latematium cingulatum Dlabola, 1983) is erected. Irakopterum Dlabola, 1985 is placed in synonymy under Libanissum Dlabola, 1980 and Paratetrica Distant, 1916 is placed in synonymy under Thabenoides Distant, 1916. New combinations for 11 species are proposed.


1988 ◽  
Vol 62 (2) ◽  
pp. 218-233 ◽  
Author(s):  
John Mark Malinky

Concepts of the family Hyolithidae Nicholson fide Fisher and the genera Hyolithes Eichwald and Orthotheca Novak have been expanded through time to encompass a variety of morphologically dissimilar shells. The Hyolithidae is here considered to include only those hyolithid species which have a rounded (convex) dorsum; slopes on the dorsum are inflated, and the venter may be flat or slightly inflated. Hyolithes encompasses species which possess a low dorsum and a prominent longitudinal sulcus along each edge of the dorsum; the ligula is short and the apertural rim is flared. The emended concept of Orthotheca includes only those species of orthothecid hyoliths which have a subtriangular transverse outline and longitudinal lirae covering the shell on both dorsum and venter.Eighteen species of Hyolithes and one species of Orthotheca from the Appalachian region and Western Interior were reexamined in light of more modern taxonomic concepts and standards of quality for type material. Reexamination of type specimens of H. similis Walcott from the Lower Cambrian of Newfoundland, H. whitei Resser from the Lower Cambrian of Nevada, H. billingsi Walcott from the Lower Cambrian of Nevada, H. gallatinensis Resser from the Upper Cambrian of Wyoming, and H. partitus Resser from the Middle Cambrian of Alabama indicates that none of these species represents Hyolithes. Hyolithes similis is here included under the new genus Similotheca, in the new family Similothecidae. Hyolithes whitei is designated as the type species of the new genus Nevadotheca, to which H. billingsi may also belong. Hyolithes gallatinensis is referred to Burithes Missarzhevsky with question, and H. partitus may represent Joachimilites Marek. The type or types of H. attenuatus Walcott, H. cecrops Walcott, H. comptus Howell, H. cowanensis Resser, H. curticei Resser, H. idahoensis Resser, H. prolixus Resser, H. resseri Howell, H. shaleri Walcott, H. terranovicus Walcott, and H. wanneri Resser and Howell lack shells and/or other taxonomically important features such as a complete aperture, rendering the diagnoses of these species incomplete. Their names should only be used for the type specimens until better preserved topotypes become available for study. Morphology of the types of H.? corrugatus Walcott and “Orthotheca” sola Resser does not support placement in the Hyolitha; the affinities of these species are uncertain.


Phytotaxa ◽  
2014 ◽  
Vol 186 (4) ◽  
pp. 188 ◽  
Author(s):  
Ying-Ying Zhou ◽  
HONG-WEI ZHANG ◽  
JIANG-QIN HU ◽  
Xiao-Feng Jin

Sinalliaria is described here as a new genus of the family Brassicaceae from eastern China, based on the morphological characters and molecular sequences. Sinalliaria differs from the related genus Orychophragmus in having basal leaves petiolate, simple or rarely with 1‒3 lateral lobes (not pinnatisect); cauline leaves petiolate, cordate at base (not sessile, auriculate or amplexicaul at base); petals obovate to narrowly obovate, claw inconspicuous (not broadly obovate, with a claw as along as sepal); siliques truncate (not long-beaked) at apex. The microscopic characters of seed testa also show significant differences between Sinalliaria and Orychophragmus. Phylogenetic evidence from DNA sequences of nuclear ribosomal ITS and plastid region trnL-trnF indicates that Sinalliaria is a distinct group related to Orychophragmus and Raphanus, but these three genera do not form a clade. The new genus Sinalliaria is endemic to eastern China and has only one species and one variety. The new combinations, S. limprichtiana (Pax) X. F. Jin, Y. Y. Zhou & H. W. Zhang and S. limprichtiana var. grandifolia (Z. X. An) X. F. Jin, Y. Y. Zhou & H. W. Zhang are proposed here.


2021 ◽  
Vol 63 (3-4) ◽  
pp. 351-390
Author(s):  
S. Y. Kondratyuk ◽  
L. Lőkös ◽  
I. Kärnefelt ◽  
A. Thell ◽  
M.-H. Jeong ◽  
...  

Seven genera new to science, i.e.: Helmutiopsis, Huriopsis, Johnsheardia, Klauskalbia, Kudratovia, Kurokawia and Poeltonia of the Physciaceae are proposed for the ‘Rinodina’ atrocinerea, the ‘Rinodina’ xanthophaea, the ‘Rinodina’ cinnamomea, the ‘Heterodermia’ obscurata, the ‘Rinodina’ straussii, the ‘Anaptychia’ isidiata and the ‘Physconia’ grisea groups consequently that all form strongly supported monophyletic branches in a phylogeny analysis based on a combined matrix of nrITS and mtSSU sequences. Phylogenetic positions of species belonging to the genera Kashiwadia s. l., Leucodermia, Mischoblastia,Oxnerella, Phaeorrhiza s. l., Polyblastidium and Rinodinella s. l. are discussed. Oxnerella afghanica which for the first time recorded as parasitic lichen species from both epiphytic and saxicolous crustose lichens is designated as type species for the genus Oxnerella. Sequences of the recently described Physcia orientostellaris as well as Huriopsis xanthophaea and additional sequences of Kashiwadia aff. orientalis and Mischoblastia aff. oxydata are submitted to the GenBank. The positions of Polyblastidium casaterrinum from Costa Rica, ‘Rinodina’ efflorescens from Białowieża, Poland, and ‘Mischoblastia’ confragosula from Cambodia in the Physciaceae are confirmed in a phylogeny analysis based on the nrITS sequences. The presence of ‘extraneous mycobiont DNA’ in lichen associations is exemplified with earlier incorrect identifications of Heterodermia, Kashiwadia, Kurokawia,Oxnerella and Poeltonia specimens. Fifty-six new combinations are presented: Helmutiopsis alba (for Rinodina alba Metzler ex Arn.), Helmutiopsis aspersa (for Lecanora aspersa Borrer), Helmutiopsis atrocinerea (for Parmelia atrocinerea Fr.), Huriopsis chrysidiata (for Rinodina chrysidiata Sheard), Huriopsis chrysomelaena (for Rinodina chrysomelaena Tuck.), Huriopsis lepida (for Lecanora lepida Nyl.), Huriopsis luteonigra (for Rinodina luteonigra Zahlbr.), Huriopsis plana (for Rinodina plana H. Magn.), Huriopsis thiomela (for Lecanora thiomela Nyl.), Huriopsis xanthomelana (for Rinodina xanthomelana Müll. Arg.), Huriopsis xanthophaea (for Lecanora xanthophaea Nyl.), Johnsheardia cinnamomea (for Rinodina mniaroea var. cinnamomea Th. Fr.), Johnsheardia herteliana (for Rinodina herteliana Kaschik), Johnsheardia jamesii (for Rinodina jamesii H. Mayrhofer), Johnsheardia reagens (for Rinodina reagens Matzer et H. Mayrhofer), Johnsheardia zwackhiana (for Lecanora zwackhiana Kremp.), Kashiwadia austrostellaris (for Physcia austrostellaris Elix), Kashiwadia jackii (for Physcia jackii Moberg), Kashiwadia littoralis for Physcia littoralis Elix), Kashiwadia nubila (for Physcia nubila Moberg), and Kashiwadia tropica (for Physcia tropica Elix), Klauskalbia crocea (for Heterodermia crocea R. C. Harris), Klauskalbia flabellata (for Parmelia flabellata Fée), Klauskalbia obscurata (for Physcia speciosa (Wulfen) Nyl. *obscurata Nyl.), Klauskalbia paradoxa (for Heterodermia paradoxa Schumm et Schäfer-Verwimp), Kudratovia bohlinii (for Rinodina bohlinii H. Magn.), Kudratovia candidogrisea (for Rinodina candidogrisea Hafellner, Muggia et Obermayer), Kudratovia luridata (for Buellia luridata Körb.), Kudratovia metaboliza (for Rinodina metaboliza Vain.), Kudratovia pycnocarpa (for Rinodina pycnocarpa H. Magn.), Kudratovia roscida (for Lecanora roscida Sommerf.), Kudratovia straussii (for Rinodina straussii J. Steiner), Kudratovia terrestris (for Rinodina terrestris Tomin), Kurokawia bryorum (for Anaptychia bryorum Poelt), Kurokawia isidiata (for Anaptychia isidiata Tomin), Kurokawia mereschkowskii (for Physcia mereschkowskii Tomin), Kurokawia palmulata (for Psoroma palmulatum Michx.), Kurokawia runcinata (for Lichen runcinatus With.), Kurokawia stippea (for Parmelia aquila var. stippea Ach.), Lecania safavidiorum (for Oxnerella safavidiorum S. Y. Kondr., Zarei-Darki, Lőkös et Hur), Leucodermia erinacea (for Lichen erinaceus Ach.), Mischoblastia confragosula (for Lecanora confragosula Nyl.), Mischoblastia destituta (for Lecidea destituta Nyl.), Mischoblastia moziana (for Lecanora moziana Nyl.), Mischoblastia moziana subsp. parasitica (comb. et stat. nova for Rinodina moziana var. parasitica Kaschik et H. Mayrhofer), Mischoblastia ramboldii (for Rinodina ramboldii Kaschik), Mischoblastia vezdae (for Rinodina vezdae H. Mayrhofer), Oxnerella afghanica (for Rinodina afghanica M. Steiner et Poelt), Oxnerella castanomelodes (for Rinodina castanomelodes H. Mayrhofer et Poelt), Physciella nigricans (for Lecanora nigricans Flörke), Poeltonia elegantula (for Physconia elegantula Essl.), Poeltonia grisea (for Lichen griseus Lam.), Poeltonia isidiomuscigena (for Physconia isidiomuscigena Essl.), Poeltonia perisidiosa (for Physcia perisidiosa Erichsen), Poeltonia venusta (for Parmelia venusta Ach.), and Polyblastidium albicans (for Parmelia albicans Pers.) are proposed.


Zootaxa ◽  
2018 ◽  
Vol 4540 (1) ◽  
pp. 7
Author(s):  
BEVERLY S. GERDEMAN ◽  
RUFINO C. GARCIA ◽  
ANDREW HERCZAK ◽  
HANS KLOMPEN

The generic classification of millipede associated Heterozerconidae in the Oriental region is revised. The genus Allozercon Vitzthum is re-diagnosed and Asioheterozercon Fain is designated as an subjective junior synonym of Allozercon. Philippinozercon gen. nov., with the type species P. makilingensis sp. nov., is described for all instars. This genus may be endemic for the Philippines, but is quite widespread in that country. All immature instars are described, making this the second species of Heterozerconidae known for all instars. The morphology of the immatures is compared with that of immatures of the temperate species Narceoheterozercon ohioensis and unnamed species from Brazil and Thailand. All immatures were collected from millipede frass and litter, never from millipedes. Adults are associated with millipedes in the family Trigoniulidae (Spirobolida). 


Zootaxa ◽  
2013 ◽  
Vol 3616 (1) ◽  
pp. 1-21 ◽  
Author(s):  
C. A. VIRAKTAMATH ◽  
ANA CLARA GONÇALVES

Studies on the Agalliini leafhoppers collected from the Terrestrial Arthropods of Madagascar inventory project of the Cal-ifornia Academy of Sciences, resulted in the discovery of one new genus Agallidwipa gen. nov. (type-species: A. biramosa sp. nov.) with three new species, A. biramosa sp. nov., A. bispinosa sp. nov. and A. webbi sp. nov. and three new species of the genus Igerna Kirkaldy, I. delta sp. nov., I. flavocosta sp. nov. and I. malagasica sp. nov. Two new combinations proposed are Agallidwipa pauliana (Evans) comb. nov. (from genus Agalliana Oman) and Igerna neosa (Webb) comb. nov. (from genus Stonasla White), a species previously recorded from Aldabra Islands. A previous record of Igerna bi-maculicollis (Stål) from Madagascar is shown most likely to be a case of misidentification. All the taxa are described and illustrated. Keys to species of Agalliini from Madagascar are included along with notes on the distinction between Agal-liana and Agallidwipa.


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