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Thatched cottage
Thatched cottage. 'S. Prout at Jde. London, Pubd,, Jany. 1, 1819, at R. Ackermann's Repository of Arts, 101 Strand.
Rhodostrophia plesiochora Prout 1917
Rhodostrophia plesiochora Prout, 1917 Rhodostrophia plesiochora Prout, 1917, Novit. zool., 24: 306. Holotype ♁, China (west): Pu-tsu-fong, 9820 ft (NHM). Diagnosis. The species is very similar to R. yunnanaria, and only can be distinguished by the less rounded wings and the wavy antemedial line of the forewing (Prout (1934 –1939), p. 24, pl. 3: i). Distribution. China (Sichuan). Remarks. Prout (1934 –1939) mentioned R. yunnanaria is a possible more heavily marked form of R. plesiochora. Unfortunately, we have no chance to examine the specimens. The differential diagnosis of R. yunnanaria and R. plesiochora needs further attention and study.Published as part of Cui, Le, Xue, Dayong & Jiang, Nan, 2019, Description of two new species of Rhodostrophia Hübner, 1823 from China (Lepidoptera, Geometridae), pp. 337-353 in Zootaxa 4563 (2) on page 341, DOI: 10.11646/zootaxa.4563.2.7, http://zenodo.org/record/260126
Rhodostrophia tremiscens Prout 1918
Rhodostrophia tremiscens Prout, 1918 Rhodostrophia tremiscens Prout, 1918, Novit. zool., 25: 77. Syntypes 2 ♁, China (west): Sichuan (south), Nanchuen (NHM). Diagnosis. The species is similar to R. bisinuata on external characters. However, the wings are broader and darker; the transverse lines of the wings are darker and thinner; the antemedial line of the forewing is absent, but it is distinct in R. bisinuata; the medial line of the forewing is more sinuous; the postmedial line is less wavy than in R. bisinuata (Prout (1934 –1939), p. 25, pl. 4: b). Distribution. China (Sichuan).Published as part of Cui, Le, Xue, Dayong & Jiang, Nan, 2019, Description of two new species of Rhodostrophia Hübner, 1823 from China (Lepidoptera, Geometridae), pp. 337-353 in Zootaxa 4563 (2) on page 345, DOI: 10.11646/zootaxa.4563.2.7, http://zenodo.org/record/260126
[Report : Petition of Holden W. Prout]
R-P of H. Prout. 25 Feb. SD 49, 17-1, vl, lp. [59] Creek Indians; 1815-1816
Rhodostrophia bisinuata subsp. wilemani Prout 1938
Rhodostrophia bisinuata wilemani Prout, 1938 Rhodostrophia bisinuata wilemani Prout, 1938, in Seitz, Macrolepid. World, 12: 145. Syntypes 4 ♁, 3♀, China: Taiwan: Rantaizan; Arizan (NHM). Diagnosis. The wings of R. bisinuata wilemani are larger than those of R. bisinuata bisinuata; the postmedial lines of the two wings are tinged with more greyish brown colour, the grey shade outside is darker terminally (Prout 1920 –1941; Wang 1998). Distribution. China (Taiwan). Remarks. Material is available at ZFMK.Published as part of Cui, Le, Xue, Dayong & Jiang, Nan, 2019, Description of two new species of Rhodostrophia Hübner, 1823 from China (Lepidoptera, Geometridae), pp. 337-353 in Zootaxa 4563 (2) on pages 343-344, DOI: 10.11646/zootaxa.4563.2.7, http://zenodo.org/record/260126
Rhodostrophia anchotera Prout 1935
<i>Rhodostrophia anchotera</i> Prout, 1935 <p>Fig. 13</p> <p> <i>Rhodostrophia anchotera</i> Prout, 1935, <i>in</i> Seitz, <i>Macrolepid. World</i>, 4 (Suppl.): 25, pl. 4: a. Holotype <i>♁</i>, China: Sichuan, S of Muli, 8850 ft (NHM).</p> <p> <b>Diagnosis.</b> The species is similar to <i>R. acidaria</i> Staudinger, 1892, but can be distinguished by the following characters: the male hind tibia has three spurs, but it has four spurs in <i>R. acidaria</i>; the antemedial line of the forewing is less sharply angled near the costa in <i>R. anchotera</i> than that in <i>R. acidaria</i>, the postmedial line of the hind wing is less sinuous (Prout 1920 –1941).</p> <p> <b>Material examined. CHINA: Yunnan</b> (ZFMK): 1 <i>6</i>, Li-kiang, 22.III.1935, coll. H. Höne. More material is available at ZFMK.</p> <p> <b>Distribution.</b> China (Sichuan, Yunnan).</p>Published as part of <i>Cui, Le, Xue, Dayong & Jiang, Nan, 2019, Description of two new species of Rhodostrophia Hübner, 1823 from China (Lepidoptera, Geometridae), pp. 337-353 in Zootaxa 4563 (2)</i> on page 350, DOI: 10.11646/zootaxa.4563.2.7, <a href="http://zenodo.org/record/2601267">http://zenodo.org/record/2601267</a>
Holarctias Prout 1913
Holarctias Prout, 1913 Type species: Haematopis sentinaria Geyer, 1837. Diagnosis. Venation. On forewing one single areole present, close to or slightly remote from closed cell apex, exceeding distal margin of cell; R l and R 2 –R 5 on common stalk, origins of R l and R 5 close to each other. Eyes small. Palpi extremely bushy and long (about twice diameter of eye). Proboscis well developed. Frons convex. Thorax and legs with long hairy scales. Hindtibia without hair pencil, with two long spurs in male. Tympanal cave large, sclerotized. Central sclerite and setose patch absent in male sternum A 2. Male genitalia. Genitalia strongly sclerotized, including socii. Socii lobe-like, with terminal or ventro-terminal triangular or pointed extension. Aedeagus broadened basally, with long basal process and with long, groove-like, more or less twisted distal process. Vesica with plate-shaped sclerotization at proximal end of ductus ejaculatorius. Sternum A 8 ovoid with cerata very short and placed posteriorly, or lacking. Mappa small or completely reduced. Female genitalia. Apophyses anteriores short, sometimes almost reduced. Ductus bursae short and broad, strongly sclerotized. Antrum posteriorly extended over the vaginal plate, with wide spade-like extension ventrally. Corpus bursae membranous, covered with minute spines on inner surface, signum absent.Published as part of Beljaev, Evgeny A., 2011, Redescription of Holarctias rufinularia (Staudinger, 1901), with notes on the taxonomy and relationships of Holarctias Prout, 1913 (Lepidoptera: Geometridae: Sterrhinae), pp. 57-67 in Zootaxa 3097 on page 63, DOI: 10.5281/zenodo.27913
Eueupithecia Prout 1910
Genus Eueupithecia Prout, 1910 Type species. Eueupithecia cisplatensis Prout, 1910 by monotypy. Until recently, the genus Eueupithecia Prout, 1910 had been considered to be monotypic (Scoble 1999; Scoble & Hausmann 2007). Genus diagnosis. Females with frenulum developed as one single stout bristle, similar to that of the male. So far, this was known only from male geometrids (sister genus Euacidalia, however, exhibits transitions to that same unusual character). Male antennae ciliate-fasciculate, in female filiform, in the type species very shortly ciliate. Palpi very small in both sexes. Proboscis absent in the type species, very short in E. vollonoides sp. n.. Male hindtibia and tarsus narrow, without spurs, in female with two spurs. Venation of forewing with one single, long areole, R 3 +R 4 usually connate with R 5, arising from tip of areole; hindwing with Sc+R 1 and Rs distinctly stalked. In male genitalia valva simple, tegumen smooth, aedeagus with two large cornuti. In female genitalia papillae anales and lateral lobi large, apophyses anteriores vestigial, ductus bursae short, with a small ‘colliculum’, corpus bursae with two smoothly sclerotized posterior sclerites, signum absent. Differential diagnosis against Euacidalia Packard, 1873 with currently 12 described species of which eight seem to be restricted to North America and Mexico (possibly extending their range to other countries of central America), two others occurring slightly further south (E. externata (Walker, 1863) from Dominican Republic and E. oroandes (Druce, 1893) from Guatemala), and the last two having their type localities further south: E. angusta (Warren, 1906) from Peru (with synonym oriochares Prout, 1922), E. rosea (Warren, 1897) from Surinam. Euacidalia species with male antennae ciliate-setose or ciliate-fasciculate, female antennae filiform or ciliate setose, palpi short or medium-sized, proboscis well developed, male hindtibia in some species strongly dilated and tarsus weak or vestigial, in other species normal but hindfemur strongly dilated. Female hindtibia with two spurs. Female frenulum consisting of 3–6 stout bristles, sometimes almost appearing to be fused. Venation of forewing of Euacidalia with double areole, R 3 +R 4 connate with R 5, arising from tip of second areole; hindwing with Sc+R 1 and Rs distinctly stalked (examined in E. orbelia). E. oroandes in male genitalia differing from Eueupithecia by distinctly forked tip of valva, lateral stout bristles from tegumen tip of aedeagus with 4 rows of microcornuti, base of aedeagus with a rectangular, furrowed sclerite. In male genitalia differing by smaller papillae anales and lateral lobes, apophyses anteriores developed, antrum broader, alate, ductus bursae long, corpus bursae with spinulose sclerites. Variation of morphological traits in the genitalia of the different Euacidalia species still awaits further study. See also differential diagnoses and genetic data under Eueupithecia vollonoides sp. n..Published as part of Hausmann, Axel, Chainey, John, Heard, Tim A., Kay, Fernando Mc & Raghu, S., 2016, Revision of the genus Eueupithecia Prout, 1910 from Argentina (Lepidoptera, Geometridae, Sterrhinae), pp. 392-400 in Zootaxa 4138 (2) on page 393, DOI: 10.11646/zootaxa.4138.2.11, http://zenodo.org/record/26221
Prasinocyma perpulverata Prout 1916
Prasinocyma perpulverata Prout, 1916 Prasinocyma perpulverata Prout (1916): 143. Locus typicus: Somalia, Mandera (Holotype ♂ NHM, examined). Material. In NHM there is a long series from Ethiopia, 'Dire Daoua', mentioned also in Prout (1930). Redescription (P. p e r p ul v er at a). Adult small, wingspan in male 14 – 17 mm, in female 16 – 18 mm. Forewing narrow, hindwing termen rounded. Ground colour pale ochre, irrorated with dark brown scales, mainly on forewing. Male usually with much stronger forewing irroration, sometimes with very dar medial area, reminiscent of the coloration of P. l o ve r i dg e i (Prout, 1926), cf. Fig. 11. Dark brown discal spot conspicuous, elongate on all wings, on forewing often blackish and not rarely curved. Length of male and female (!) palpi 0.9 – 1.1 times diameter of eye, pale ochre. Frons pale ochre, with some dark brown scales. Antennae bipectinate in male, filiform in female. Antennal branches ochre, markedly darker at base. Male frenulum present. Male hindtibia with four spurs, with pencil and with terminal process covering first tarsomere. Male and female genitalia not studied from P. perpulverata, but probably very close to those of P. l overi dgei (cf. Figs 52, 88). Male genitalia of P. loveri dgei (Fig. 52). Uncus short. Socii developed as short setose patches. Gnathos weakly sclerotized. Valva narrow, subapical ventral lobe at rather central position. Harpe short and broad. Aedeagus bent twice at centre, with sclerotized edge at 2 / 3, length 1.25 mm. Sternum A 8 with two sub-truncate projections, sclerotized and concave between. In male genitalia reminiscent of those of P. hailei, mainly in the shape of aedeagus and sternum A 8. Female genitalia (Fig. 87) Sterigma with two tapering posterior projections. Ductus bursae short, corpus bursae very small, membranous. Remarks. Closely related to P. loveridgei (Prout, 1926) described from Tanzania and examined from a series from Kenya (ZSM). P. loveridgei may reveal to need to be downgraded to a subspecies of P. perpulverata, some Ethiopian specimens from the NHM series (' P. perpulverata ') are indistinguishable from our Kenyan P. loveridgei in habitus. Genetic data. Not yet barcoded.Published as part of Hausmann, Axel, Sciarretta, Andrea & Parisi, Francesco, 2016, The Geometrinae of Ethiopia II: Tribus Hemistolini, genus Prasinocyma (Lepidoptera: Geometridae, Geometrinae), pp. 1-63 in Zootaxa 4065 (1) on pages 17-18, DOI: 10.11646/zootaxa.4065.1.1, http://zenodo.org/record/27049
Lithostege ancyrana Prout
L. ancyrana Prout (Figs. 23, 49; Map 5) Lithostege ancyrana Prout, 1938: 239, pl. 6: i. Holotype 3, paratype 3, BMNH (examined). Type locality: Ankara (Turkey). Lithostege ancyrana: Viidalepp, 1996: 47; Parsons et al., 1999: 545. Material examined. Type material: Holotype and paratype (both 3); ‘ Turkey, Angora [Ankara] 1930 Sureya Bay’, ‘ Lithostege ancyrana male Prout type; Geom 1937 – 316 ’, ‘Pres. Imp. Inst. Ent. Brit. Mus. 1933 – 172 ’; in BMNH. Additional material: 7 3, 11 Ƥ: 1 3, 4 Ƥ: Türkei, Konya, Taurus, Aladag, 25.5. 1986, 1000m, leg. P. Kuhna; 5 3, 3 Ƥ, preps Ƥ 1627, 3 1629 / 2011 H. R.: same data, 30.5. 1975, preps 3 1625, 1626, / 2011 H. R.; 2 Ƥ: Türkei, Taurus, Aladag, Göksu-tal, 30.5. 1976, leg. P. Kuhna, gen. prep. 3 1628 / 2011 H. R.; 2 Ƥ: Ost-Türkei, Gürün, 1400m, 11.6. 1985, leg. P. Kuhna, gen. prep. 1607 / 2010 H. R.; all in ZFMK. 1 3: Asia Min., Gürün, 19.- 30. Juni 1976, leg. Friedel, gen. prep. 1013 / 2010 H. R.; in ZSM. Preparations of genitalia: 5 3, 2 Ƥ. Description & Diagnosis. Wingspan 24–26 mm, in general smaller than the externally similar L. farinata which also occurs in Turkey. Forewings a little narrower than those of farinata, greyish white, without discal dot, grey underneath, with the basal and central area brown. Hindwings on upper- and underside like forewings (Fig. 23). Male genitalia (Fig. 49) similar to those in L. griseata griseata, with short sclerotized costa with weakly marked distal tip (not a free process like in farinata and coassata), differing in the much larger harpe with a pointed, tooth-like apex and the longer dorsal arm.Juxta in L. ancyrana vase-shaped, nearly two times longer than in L. griseata griseata. Saccus much shorter than in farinata, but longer compared to griseata; aedaegous longer and more distinctly curved compared to griseata (Figs 47 –53). Bionomics. Collected in May and June at 1400m. Distribution. Turkey (Map 5). May also occur in W. Iran.Published as part of Sh, Hossein Rajaei, Stüning, Dieter & Viidalepp, Jaan, 2011, A review of the species of Lithostege Hübner, [1825] 1816 (Lepidoptera: Geometridae, Larentiinae), occurring in Iran and adjacent countries, with description of two new species from Iran and Pakistan, pp. 1-46 in Zootaxa 3105 on page 19, DOI: 10.5281/zenodo.27920
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