Pseudotelphusa Janse
publication ID |
https://doi.org/ 10.5281/zenodo.182949 |
DOI |
https://doi.org/10.5281/zenodo.5036750 |
persistent identifier |
https://treatment.plazi.org/id/03FE87A3-FF8C-FF82-FF47-30FEFEC8E5F2 |
treatment provided by |
Plazi |
scientific name |
Pseudotelphusa Janse |
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Pseudotelphusa Janse View in CoL
Pseudotelphusa Janse, 1958: 68 View in CoL .
Type species: Telphusa probata Meyrick, 1909 , by original designation.
Sattleria Cãpuşe, 1968a: 19 View in CoL . Unnecessary replacement name for Pseudotelphusa Janse, 1958 View in CoL .
Note: Pseudotelphusa Janse, 1958 View in CoL is not a junior homonym of Pseudotelphusa Marschall, 1873 View in CoL , which is an incorrect subsequent spelling of Pseudothelphusa Saussure, 1857 (Crustacea) View in CoL , and is therefore invalid and unavailable for purposes of homonymy. Sattleria Cãpuşe View in CoL also is a homonym of Sattleria Povolný, 1965 View in CoL ( Lepidoptera View in CoL : Gelechiidae View in CoL ).
Klaussattleria Cãpuşe, 1968b: 80 View in CoL . Unnecessary replacement name for Sattleria Cãpuşe, 1968 View in CoL .
Klaussatleria Cãpuşe, 1968b: 80 View in CoL . Misspelling of Klaussattleria Cãpuşe, 1968 b .
Description. Imago (Fig. 60). Labial palpus with third segment slightly shorter than second. Clypeus with ventral margin rounded. Antenna longer than half forewing length. Ocellus present. Posterior area of sitophore with four campaniform sensilla in symmetrical trapezoid; anterior area with five, eight, or nine campaniform sensilla. Forewing (length/width ratio 4.3) with tufts of raised scales; M1, M2, and M3 separate, CuA1 and CuA2 present; median fascia transverse or directed from base of costa toward posterior margin. Hindwing (length/width ratio 3.9) with R5 and M1 connate, M2, M3, and CuA1 separate. Male abdomen with sternum VIII broadly subrectangular, slightly or deeply emarginate posteriorly; tergum VIII lingulate, with pair of anterolateral hair pencils.
Male genitalia ( Fig. 31 View FIGURES 30 – 33 ): uncus as long as length of tegumen, tapered apically; gnathos absent; valva with costal part developed, curved dorsad (outwards in slide preparations with vinculum rolled to one side); tegumen basal width/length ratio 1.0; vinculum with pair of processes; phallus slender, base slightly inflated, without cornuti.
Female genitalia ( Fig. 41 View FIGURES 40 – 43 ): apophyses posteriores about 3 x length of apophyses anteriores; ductus bursae shorter than that in species of Carpatolechia ; signum rhomboid with serrate margins, with transverse ridges, anterior ridge sinuous.
Larva. Body with black or brown pinacula; head and prothoracic shield pale brown, prothoracic shield with median sulcus ( Bland 2002; Braun 1930).
Pupa. Maxillary palpi touching or adjacent to genae; antennae adjacent to each other for about 3 x greater distance than the length of visible ends of metathoracic legs; pronotum with the midline length at least 1/3 its greatest length; prothoracic legs separated from oculi; if body less than 6 mm in length, abdomen usually lacking setae ( Mosher 1916; Patoèka and Turcáni 2005).
Diagnosis. Pseudotelphusa species are superficially similar to those of Carpatolechia . Males of Pseudotelphusa are distinguished by absence of a gnathos and an uncus that is as long as tegumen and tapered apically.
Hosts. Berberidaceae : Berberis vulgaris L. ( P. tessella ). Betulaceae : Betula spp. ( P. betulella , P. paripunctella ). Elaeagnaceae : Hippophae rhamnoides L. ( P. paripunctella ). Fagaceae : Quercus spp. ( P. fuscopunctella , P. istrella , P. palliderosacella , P. paripunctella , P. quercinigracella P. scalella ). Myricaceae : Myrica gale L. ( P. paripunctella ). Rosaceae : Amelanchier canadensis (L.) ( P. amelanchierella ), Malus spp. ( P. incana ). ( Bland 2002; Braun 1930; Chapman and Lienk 1971; Forbes 1923; Heinemann 1870; Kaitila 1996; Mann 1872; Patoèka 1987; Robinson et al. 2002; Sattler 1980; Zhang 1994).
Diversity and distribution. The 14 species of Pseudotelphusa occur in Europe, Asia, and eastern North America ( Huemer and Karsholt 1999; Park 1992; Patoèka 1987; Sattler 1960, 1982). Additional species occur in southern Africa ( Janse 1958) and possibly in other regions of the world.
Carpatolechia Cãpuşe, 1964: 12 View in CoL .
Type species: Carpatolechia dumitrescui Cãpuşe, 1964 , by original designation, a junior synonym of Tinea decorella Haworth, 1812 .
Description. Imago (Fig. 61). Labial palpus with third segment shorter than second. Clypeus with ventral margin rounded. Antenna and forewing subequal in length. Ocellus present. Posterior area of sitophore with four campaniform sensilla posterior area in line except right sensillum off-set; anterior area with three or ten campaniform sensilla. Forewing (length/width ratio 3.8) with tufts of raised scales; R5, M1, M2 and M3 separate, CuA1 and CuA2 present ( Fig. 8 View FIGURES 7 – 18 ); median fascia present or absent, if present, transverse or directed from base of costa toward posterior margin. Hindwing (length/width ratio 3.4) with R5 and M1 stalked, M2, M3, and CuA1 separate. Male abdominal tergum VIII short, lingulate, exceptionally bilobed, with pair of anterolateral hair pencils, some species with additional pair of posterolateral hair pencil, sternum VIII broad, distally rounded. Female abdominal segment VIII with posteriorly rounded lobes.
Male genitalia: uncus well developed, elongate, with numerous, large setae laterally; gnathos reduced or absent; tegumen deeply emarginate anteriorly with broadly rounded lateral arms, basal width/length ratio 1.4; costal part of valva slender and digitate or reduced, saccular part of valva 1/2 to 3/4 length of costal part; phallus without cornuti.
Female genitalia: apophyses posteriores about 3 x length of abdominal segment VIII; ostium bursae surrounded by suboval sclerotization; antrum reduced; ductus and corpus bursae well developed; signum subhexagonal to rhomboid, with strongly serrate margins and two transverse ridges.
Larva. Body light green, sometimes tinged with pink or red; head and prothoracic shield yellow, light brown, or black; pinacula black ( Emmet 2002).
Pupa. Less than 6 mm in length; maxillary palpi touching or adjacent to genae; antennae adjacent to each other for about 3 x greater distance than the length of visible ends of metathoracic legs; pronotum with the midline length at least 1/3 its greatest length; prothoracic legs separated from oculi; abdomen usually lacking setae ( Patoèka and Turcáni 2005).
Diagnosis. Carpatolechia species are superficially similar to those of Pseudotelphusa , Teleiodes , and Neotelphusa , but differ by the presence of a well-developed saccular part of the valva and a rounded uncus, which is tapered or notched in the other genera.
Hosts. Aceraceae : Acer sp. ( C. fugitivella ). Anacardiaceae : Cotinus coggygria Scop. ( C. decorella ), Pistacia spp. ( C. decorella ), Rhus sp. ( C. decorella ). Betulaceae : Alnus spp. ( C. belangerella , C. proximella ); Betula spp. ( C. alburnella , C. fugacella , C. notatella , C. proximella ). Cornaceae : Cornus mas L. ( C. decorella ), C. sanguinea (L.) ( C. decorella ). Corylaceae : Corylus sp. ( C. notatella , C. fugitivella ). Fagaceae : Quercus spp. ( C. decorella , C. fugitivella ). Oleaceae : Phillyrea sp. ( C. decorella ), Fraxinus sp. ( C. fugitivella ). Rosaceae : Prunus avium L. ( C. fugitivella ), Pyracantha coccinea L. ( C. fugitivella ). Salicaceae : Salix spp. ( C. notatella ). Tiliaceae : Tilia sp. ( C. fugitivella ). Ulmaceae : Ulmus spp. ( C. fugitivella , C. fugacella ). ( Bradford and Sokoloff 1988; Disqué 1901, 1908; Emmet 1988; Forbes 1923; Huemer 1988; Kasy 1979; Kaitila 1996; Lhomme, [1946]; Sattler 1980, 1982; Robinson et al. 2002). Lhomme ([1946]) also listed Abies alba Mill. (Pinaceae) as one of several hosts of C. decorella in his catalogue of Lepidoptera of France and Belgium. However, this record is questionable because other polyphagous species in Teleiodini are restricted to either coniferous or deciduous hosts, e.g., Exoteleia and Coleotechnites . Thus, Carpatolechia is not included as a coniferous feeder.
Diversity and distribution. The sixteen species of Carpatolechia occur in Europe and Asia ( Huemer and Karsholt 1999; Huisman and Koster 2000; Park 2000a). An undescribed species from eastern Canada was found in this study.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Pseudotelphusa Janse
Lee, Sangmi & Brown, Richard L. 2008 |
Sattleria Cãpuşe, 1968a : 19
Capuse 1968: 19 |
Klaussattleria Cãpuşe, 1968b : 80
Capuse 1968: 80 |
Klaussatleria Cãpuşe, 1968b : 80
Capuse 1968: 80 |
Carpatolechia Cãpuşe, 1964 : 12
Capuse 1964: 12 |
Pseudotelphusa
Janse 1958: 68 |