“…Exceptionally, some Gaeolaelaps, at least one species associated with cockroaches, have a triangular, denticulate gnathotectum (Faraji & Halliday, 2009). More distant laelapid genera such as Mesolaelaps have somewhat triangular gnathotecta although more extended anteriorly (Tenorio & Radovsky, 1974).…”
Section: Discussionmentioning
confidence: 99%
“…In addition to the attributes mentioned in the introduction, the well-developed internal malae of Persicolaelaps are indicative of Laelapidae in general, and their thick, elongate filaments show a resemblance (or possible relation) to some laelapids species such as Cosmolaelaps cuneifer (Michael) (Evans & Till, 1966) Karg, 1982, (which, at least superficially, resemble some Laelaspisella species). The internal malae of Mesolaelaps accessoria Tenorio & Radovsky, 1974 also have thick projections, but they appear shorter and originate from the lateral margin of the main, median processes. Some Laelaspisella and the apparently related Pogonolaelaps species have elongate fringed internal malae, but composed of hair-like and thinner filaments, based on illustrations and personal examination of some species (Marais & Loots, 1969;Nemati & Gowiazdowicz, 2016;SK pers.…”
A new monotypic mite genus of the family Laelapidae, Persicolaelaps gen. nov., is described to accommodate a new species, P. hallidayi sp. nov., on the basis of adult female specimens collected from decaying wood, soil and litter in northern Iran, Golestan and Mazandaran provinces, respectively. The new genus can be distinguished from other members of the family by a combination of morphological attributes, some of which are unique or rarely observed in laelapids, such as (1) a series of small subrectangular sclerites flanking dorsally coxae I and gnathosomal base and adjoining podal plates anterolaterally, which are extending from and fused with sternal shield between coxae I and II; (2) an epigynal shield, so broad as to reach or even overlap acetabula III-IV, posteriorly axe-shaped; (3) metasternal setae absent; (4) a typical anal shield, though capturing pair of opisthogastric setae JV3; (5) gnathotectum triangular and acuminate; (6) the presence of six setae on trochanter IV; (7) genu IV with two ventral setae (occasional in Laelapidae); (8) internal malae with a series of thick, elongate filaments.
“…Exceptionally, some Gaeolaelaps, at least one species associated with cockroaches, have a triangular, denticulate gnathotectum (Faraji & Halliday, 2009). More distant laelapid genera such as Mesolaelaps have somewhat triangular gnathotecta although more extended anteriorly (Tenorio & Radovsky, 1974).…”
Section: Discussionmentioning
confidence: 99%
“…In addition to the attributes mentioned in the introduction, the well-developed internal malae of Persicolaelaps are indicative of Laelapidae in general, and their thick, elongate filaments show a resemblance (or possible relation) to some laelapids species such as Cosmolaelaps cuneifer (Michael) (Evans & Till, 1966) Karg, 1982, (which, at least superficially, resemble some Laelaspisella species). The internal malae of Mesolaelaps accessoria Tenorio & Radovsky, 1974 also have thick projections, but they appear shorter and originate from the lateral margin of the main, median processes. Some Laelaspisella and the apparently related Pogonolaelaps species have elongate fringed internal malae, but composed of hair-like and thinner filaments, based on illustrations and personal examination of some species (Marais & Loots, 1969;Nemati & Gowiazdowicz, 2016;SK pers.…”
A new monotypic mite genus of the family Laelapidae, Persicolaelaps gen. nov., is described to accommodate a new species, P. hallidayi sp. nov., on the basis of adult female specimens collected from decaying wood, soil and litter in northern Iran, Golestan and Mazandaran provinces, respectively. The new genus can be distinguished from other members of the family by a combination of morphological attributes, some of which are unique or rarely observed in laelapids, such as (1) a series of small subrectangular sclerites flanking dorsally coxae I and gnathosomal base and adjoining podal plates anterolaterally, which are extending from and fused with sternal shield between coxae I and II; (2) an epigynal shield, so broad as to reach or even overlap acetabula III-IV, posteriorly axe-shaped; (3) metasternal setae absent; (4) a typical anal shield, though capturing pair of opisthogastric setae JV3; (5) gnathotectum triangular and acuminate; (6) the presence of six setae on trochanter IV; (7) genu IV with two ventral setae (occasional in Laelapidae); (8) internal malae with a series of thick, elongate filaments.
“…Given that most Gaeolaelaps species and species of many hypoaspidine and laelapine genera possess Px2-3, as well as Mesolaelaps and Myonyssus (e.g. Tenorio & Radovsky, 1974), the presence of Px2-3 is probably plesiomorphic in Laelapidae (Walter & Campbell, 2003), and therefore is not very meaningful; the absence of one or both Px setae, might, however, indicate close relationships in some cases, if combined with other shared characters. Tarsal spines on legs II and IV are the main feature defining the aculeifer species group (see group concepts and keys in Karg, 1979Karg, , 1982also key in Karg 1989a).…”
Section: Discussionmentioning
confidence: 99%
“…that we know of have most dorsal and some opisthogastric setae pilose or barbed: H. longichaetus Ma, 1996, H. pinnae Karg, 1987, as well as H. kassai Van Aswegen & Loots, 1970, which has feathered or bipectinate setae. Barbs on the posterior dorsomarginal and/or opisthogastric setae are also present in variously distant laelapids such as some Cosmolaelaps (Moriera et al, 2014), Coleolaelaps, Pseudoparasitus, many Laelaspis (Kazemi & Beaulieu, personal observations; see also Joharchi et al, 2012), Androlaelaps (personal observations; see also , Bisternalis (Baker et al, 1983); Nidilaelaps, Laelapsella (Shaw, 2012), Notolaelaps (Shaw, 2011), Juxtalaelaps (Domrow, 1978, Dowling et al, 2007, and more extensively on the idiosoma and legs of at least some Mesolaelaps (Tenorio & Radovsky, 1974), haemogamasines and acanthochelines (Radovksy & Gettinger, 1999). Accounting for the presence and the extent of barbs on idiosomal, gnathosomal and leg setae in species description may later help to shed light on the phylogenetic significance of these attributes in laelapids.…”
Two new species of laelapid mites of the genus Gaeolaelaps Evans & Till are described based on adult females collected from soil and litter in Kerman Province, southeastern Iran, and Mazandaran Province, northern Iran. Gaeolaelaps jondishapouri Nemati & Kavianpour is redescribed based on the holotype and additional specimens collected in southeastern Iran. The concept of the genus is revised to incorporate some atypical characters of recently described species. Finally, some morphological attributes with potential to define natural species groupings as well as hypoaspidine genera are discussed, particularly idiosomal gland pores and poroids.
“…R. exulans, the Polynesian rat, was probably introduced by Polynesian seafarers some centuries ago; the Norway rat gained entry from a shipwreck in 1921 (Watt 1975). Tenorio & Radovsky (1974) list a mite collected from the common house mouse (Mus musculus) on Raoul in 1962. Mice have not previously been recorded from the Kermadecs, and are not known to be established there now, so if this is not a misidentification of a young Polynesian rat, the animal must have been a chance invader.…”
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