187,562 research outputs found
Agonoscena pistaciae Burckhardt & Lauterer 1989
No full text<i>Agonoscena pistaciae</i> Burckhardt & Lauterer <p> <b>Material examined</b>. Iran: 15 ♂, 20 ♀, Kerman, Mahan, N 30°07’10”, E 57°10’35”, 6.x.2016, <i>P. vera</i> sp., M. Lashkari leg. (KGUT).</p> <p> <b>Published records.</b> Kerman: Mahan; Kerman (Burckhardt & Lauterer 1989, 1993).</p> <p> <b>Host plants.</b> <i>Pistacia mutica</i> Fisch. & C.A.Mey., <i>P. vera</i> L. (Anacardiaceae) (Burckhardt & Lauterer 1993).</p>Published as part of <i>Lashkari, Mohammadreza & Burckhardt, Daniel, 2020, Jumping plant-lice (Hemiptera: Psylloidea) of Kerman, Iran, with the description of one new Cacopsylla species, pp. 576-590 in Zootaxa 4803 (3)</i> on pages 582-583, DOI: 10.11646/zootaxa.4803.3.11, <a href="http://zenodo.org/record/3920207">http://zenodo.org/record/3920207</a>
Homotoma caroliquarti Burckhardt and Lauterer
No full text<i>Homotoma caroliquarti</i> Burckhardt and Lauterer <p> <b>Material examined</b>. Iran: 14 ♂, 20 ♀, Kerman, Arjasb, N 30°25’10”, E 56°32’15’’, 8.v.2016, <i>Ficus</i> sp., M. Lashkari leg. (KGUT).</p> <p> <b>Published records.</b> Kerman: Arjasb (Lashkari <i>et al</i>. 2016); Kerman (Davatchi 1958, as <i>H. ficus</i>; Burckhardt & Lauterer 1993).</p> <p> <b>Host plant.</b> <i>Ficus carica</i> L. (Moraceae) (Burckhardt & Lauterer 1993).</p>Published as part of <i>Lashkari, Mohammadreza & Burckhardt, Daniel, 2020, Jumping plant-lice (Hemiptera: Psylloidea) of Kerman, Iran, with the description of one new Cacopsylla species, pp. 576-590 in Zootaxa 4803 (3)</i> on page 583, DOI: 10.11646/zootaxa.4803.3.11, <a href="http://zenodo.org/record/3920207">http://zenodo.org/record/3920207</a>
Russelliana theresae Burckhardt 2008
No full text<i>Russelliana theresae</i> Burckhardt, 2008 <p>(Figs 10 J, 15E, 20D, 25D, 29D, 34B)</p> <p> <i>Russelliana theresae</i> Burckhardt, 2008a: 85.</p> <p> <b>Material examined.</b> Type material. <b>Holotype</b> ♂: <b>Chile</b>: V Region, Province Los Andes, El Juncal, 2200 m, 24.xii.1998, <i>Mulguraea scoparia</i> [<i>Diostea scoparia</i>], alpine scrub with low bushes (D. Burckhardt) #6(1) (NHMB, dry). <b>Paratypes: Chile</b>: 3 ♀, 9 immatures, 1 immature skin, V Region, Province Los Andes, Río Blanco to Portillo, route 60, Aconcagua Valley, 32°50'S 70°08'W, 2200–2400 m, 23.xi.1992, <i>Mulguraea scoparia</i> [<i>Diostea scoparia</i>], alpine scrub (D. Burckhardt) #12 (MHNG, dry); 1 ♂, 2 ♀, same but 25 km W Portillo, 1900–2100 m, 1.xii.1993, subalpine/alpine scrub (D. Burckhardt) #1 (MHNG, dry); 8 ♂, 15 ♀, same but Portillo, 1800 m, 31.xii.1993, <i>Mulguraea scoparia</i> [<i>Diostea scoparia</i>], alpine scrub (D. Burckhardt) #43 (MHNG, dry); 1 ♂, 2 ♀, 1 immature, same but 2200 m, <i>Mulguraea scoparia</i> [<i>Diostea scoparia</i>] (D. Burckhardt) #44 (MHNG, dry); 3 ♂, 7 ♀, same but km 10 Portillo to Río Blanco, 2300 m, 23.xii.1995, <i>Mulguraea scoparia</i> [<i>Diostea scoparia</i>] (D. Burckhardt) #18(1) (MHNG, dry); 4 ♂, 3 ♀, same but km 14 Portillo to Río Blanco, 2100 m, <i>Mulguraea scoparia</i> [<i>Diostea scoparia</i>], subalpine scrub (D. Burckhardt) #19(1) (MHNG, dry); 3 ♂, 3 ♀, same but km 19 Portillo to Río Blanco, 1900 m, <i>Mulguraea scoparia</i> [<i>Diostea scoparia</i>] (D. Burckhardt) #20(2) (MHNG, dry); 21 ♂, 22 ♀, same but along road from Portillo to Río Blanco, 24.xii.1998, <i>Mulguraea scoparia</i> [<i>Diostea scoparia</i>], gully with a few shrubs and small trees along river and subalpine scrub (D. Burckhardt) #7(2) (NHMB, dry, on slide, 70 % ethanol); 27 ♂, 19 ♀, 3 immatures, 1 immature skin, same as holotype (D. Burckhardt) #6(1) (NHMB, dry, on slide, 70 % ethanol).</p> <p> <b>Description.</b> Coloration. Head including genal processes yellow to brown, genal processes with dark tips, genae brown to dark brown, vertex with orange to brown pattern; clypeus dark brown to black. Eyes yellow to brown, ocelli orange to red. Antenna pale yellow, segments 1–2 yellow to brown, segments 3–8 with brown apices, segments 9–10 entirely dark brown. Pronotum of the same colour as vertex, dark brown on either side and yellow to brown spot in the middle; mesopraescutum pale yellow, with two orange to brown patches along the fore margin and three orange transverse stripes posteriorly; mesoscutum pale yellow, with four broad orange to brown and, in the middle, one narrow orange longitudinal stripes; mesoscutellum pale yellow along the margin, yellow to brown in the middle. Metanotum yellow to dark brown. Forewing with whitish to dark brown veins and semitransparent, colourless membrane with dark brown pattern, similar to <i>R. marionae</i>, consisting of two broad stripes: submarginal one stretching from apical part of costal vein to median part of vein Cu1a, along vein Cu1a and to base of vein M1+2, sometimes leaving light areas in cells m1 and m2 along the margin, and median one stretching from base of pterostigma, along the veins R, M+Cu and Cu, to base of vein Cu1b; membrane between stripes colourless, with dots varying in size and number. Legs dirty yellow to brown, with dark brown femora and distal tarsal segments, meracanthus of metacoxa pale yellow to orange. Abdomen and terminalia dark brown, sometimes black.</p> <p>Structure. Head, in profile, weakly inclined from longitudinal body axis (<45°). Vertex subtrapezoidal, flat with indented foveae, anteriorly produced into transverse lobe on either side of mid-line, hind margin around lateral ocelli not raised, covered with long setae; genal processes conical, slender, subacute apically, of the same length as vertex, covered with long setae. Pronotum bearing two pronounced lateral tubercles on either side. Forewing oblong-oval, broadly, evenly rounded apically; vein C+Sc weakly curved, pterostigma long, vein Rs weakly sinuous, curved to fore margin apically; vein M slightly longer than either of veins M1+2 and M3+4; surface spinules very dense, present in all cells, leaving no spinule-free stripes along the veins, irregularly spaced, less developed on unpigmented areas; radular spinules not pronounced. Metatibia with 6–7 apical spurs.</p> <p>Terminalia. Male. Proctiger tubular; densely covered with long setae. Subgenital plate short, subglobular; with sparsely spaced moderately long setae. Paramere narrowly lamellar; with finger-shaped apico-anterior process on long pedicel and long apico-posterior lobe, slightly convex posteriorly, evenly rounded apically; both process and lobe of subequal length; outer face sparsely covered with moderately long setae mostly in posterior half, inner face densely covered with moderately long setae in anterior part, few long setae along anterior margin, sparsely covered with moderately long setae in posterior part and with few long setae apically. Distal segment of aedeagus elongate, weakly, irregularly truncated towards apex; lateral lobes long, tubular, sclerotised.—Female. Proctiger cuneate, pointed apically; dorsal margin, in profile, with median indentation; relatively densely covered with moderately long setae. Subgenital plate subglobular, with moderately long apical process; densely covered with moderately long setae.</p> <p> <b>Host-plant.</b> <i>Mulguraea scoparia</i> (Gillies & Hook.) N.O'Leary & P.Peralta (Verbenaceae).</p> <p> <b>Distribution.</b> Reported from Chile (V Region) (Burckhardt 2008a).</p> <p> <b>Comments.</b> <i>Russelliana theresae</i> resembles <i>R. marionae</i>; see comments under <i>R. marionae</i>. <i>R. theresae</i> differs from <i>R. marionae</i> in a shorter forewing with a more extensive pattern in the basal half of its membrane, the presence of microscopical setae on the forewing veins, and a paramere bearing a broader apico-posterior lobe.</p>Published as part of <i>Serbina, Liliya & Burckhardt, Daniel, 2017, Systematics, biogeography and host-plant relationships of the Neotropical jumping plant-louse genus Russelliana (Hemiptera: Psylloidea), pp. 1-114 in Zootaxa 4266 (1)</i> on pages 54-55, DOI: <a href="http://zenodo.org/record/575325">10.5281/zenodo.575325</a>
Agonoscena pistaciae Burckhardt & Lauterer 1989
No full textAgonoscena pistaciae Burckhardt & Lauterer Material examined. GH: 1 ♀, Panyas, 33º14’55’ N 35º41’ 40’E, 8.v.2010 (A. Freidberg); UG: 1 ♂, 7 ♀, Ramot Naftali, 33º04.986’N 35º32.75’E, 490 m, 12.v.2010, Pistacia atlantica (D. Burckhardt); CR: 1 ♀, Nahal Oren, 24.vii.2001 (A. Freidberg); CCP: 2 ♀, Tel Aviv University Botanical Gardens, 10.v.2010, Pistacia palaestina (D. Burckhardt), 1 ♂, Tel Aviv University Botanical Gardens, 14.xi.2000, Rhus tripartita (O. Manheim); SCP: 2 ♂, 2 ♀, Bet Dagan, 1.xi.1996, Pistacia atlantica (PPIS); AV: 1 ♀, Elifaz fields, 29o48.106’N 35o02.037’E, 82 m, 13.v.2010 (D. Burckhardt). Published records in Israel. JH, LG, UG (Burckhardt & Lauterer 1989). Host plant. Pistacia atlantica, P. palaestina (Anacardiaceae).Published as part of Spodek, Malkie, Burckhardt, Daniel & Freidberg, Amnon, 2017, The Psylloidea (Hemiptera) of Israel, pp. 301-345 in Zootaxa 4276 (3) on pages 314-315, DOI: 10.11646/zootaxa.4276.3.1, http://zenodo.org/record/103910
Pseudophacopteron verrucifrons Burckhardt & Harten 2006
No full textPseudophacopteron verrucifrons Burckhardt & Harten, 2006 (Figs 63–69) Pseudophacopteron sp.: BURCKHARDT & MIFSUD (1998): 10. Pseudophacopteron verrucifrons Burckhardt & Harten, 2006: 191; MALENOVSKÝ & BURCKHARDT (2009): 30. Material examined. Numerous ♂♂ ♀♀, 4 fifth and 1 fourth instar immatures, central Socotra, Hagher mountains, Tudhen, 12°32′42″N 53°59′54″E, 1135 m, 18. and 22.vi.2012, on Commiphora planifrons, I. Malenovský & P. Kment leg.; 2 fourth and 1 third instar immatures, central Socotra, Dixam plateau, wadi Dirhor near Firmihin protected area, 12°28′00″N 54°00′30″E, 340 m, 15.vi.2012, open dry woodland with Boswellia ameero trees, on Commiphora parvifolia, I. Malenovský leg.; 2 ♂♂ 8 ♀♀, north-eastern Socotra, Homhil protected area, 12°34′30″N 54°18′30″E, 435 m, 10.–11.vi.2012, open dry woodland with Boswellia elongata and Dracaena cinnabari trees, on Commiphora parvifolia, I. Malenovský leg.; 1 ♂♂ 3 ♀♀, north-eastern Socotra, Kazazhan area, 12°33′48″N 54°19′48″E, 540 m, 10.vi.2012, open dry woodland, on Commiphora parvifolia, I. Malenovský leg. (MMBC, NMPC; dry- and slide- -mounted and preserved in alcohol). Description. Adult male and female described and figured by BURCKHARDT & HARTEN (2006) and MALENOVSKÝ & BURCKHARDT (2009). Fifth instar immature (Figs 63, 69). Pale yellow with numerous small dark brown markings on body dorsum. Body robust, oval. Body margin and dorsum with large truncate lanceolate setae in following numbers: margin (one side only, except abdomen): head 5–8, prothorax 5–7, forewing pad 12–16, hindwing pad 3–5, abdomen (both sides) 30–32; dorsum (one side only): cephaloprothorax 8–10, mesothorax including forewing pads 8–16, metathorax including hindwing pads 6–8, abdomen 18–22. Eye with 1 truncate lanceolate seta. Antenna straight, directed obliquely forwards, short, 2-segmented, basal segment with one and flagellum with five incomplete subdivisions, flagellum with two rhinaria (Fig. 64). Tarsal arolium membranous, fan-shaped, as large as claws (Fig. 65). Abdomen dorsally with four free sclerites and incompletely fused caudal plate; caudal plate margin broadly rounded. Anus in ventral position. Circumanal ring moderately large, with fore and hind margin close together; outer ring composed of a single row of pores, not sinuate (Fig. 66). Measurements (n = 4; in mm). BL 0.72–0.90, BW 0.53–0.59, AL 0.15–0.19, FL 0.28–0.31, TL 0.22–0.25, CPL 0.31–0.41, CPW 0.34–0.45, CRW 0.10–0.11. Ratios: BL/BW 1.31–1.53, AL/FL 0.50–0.61, CL/CW 0.86–0.91, CRW/CPW 0.22–0.29. Differential diagnosis. The fifth instar immature of P. verrucifrons resembles immatures of P. marmoratum Malenovský & Burckhardt, 2009 (sympatric with P. verrucifrons on Commiphora africana in Kenya) and P. stigmatum Malenovský & Burckhardt, 2009 (associated with Aucoumea klaineana in tropical West Africa and South Africa) in the relatively robust body (ratio BL/BW ≤ 1.50), ventral anus, and short, obliquely forwards directed antenna. Lanceolate setae in both these similar species are, however, confined only to the body margin (in P. marmoratum only to the apex of the caudal plate) and are completely missing on the body dorsum, in contrast to P. verrucifrons. The fifth instar immature of P. marmoratum is also larger than P. verrucifrons (BL> 1.0) (MALENOVSKÝ & BURCKHARDT 2009). Host plants. Found on Commiphora africana (A.Rich.) Endl. in Kenya (BURCKHARDT & HARTEN 2006, MALENOVSKÝ & BURCKHARDT 2009); in Socotra associated with Commiphora parvifolia (Balf.f.) Engl. and C. planifrons (Balf.f.) Engl. (Burseraceae) (Fig. 70). Biology. Immatures were found free-living on lower surface of leaves of Commiphora parvifolia and C. planifrons which are quite small in size (only one immature individual of P. verrucifrons per leaf was observed each time). No deformations were observed on the hosts which could be associated with the development or feeding activity of P. verrucifrons. Occurrence in Socotra. Probably widespread, although quite local on Commiphora parvifolia in open dry woodland on limestone plateaus in central and eastern Socotra and on C. planifrons in montane shrubland on southern slopes of the Hagher Mts. (Fig. 70). Distribution. Kenya, mainland Yemen (BURCKHARDT & HARTEN 2006, MALENOVSKÝ & BURCKHARDT 2009); Oman (unpublished record; A. Al-Wahaibi, pers. comm.), Socotra (new record). One of the known host plants, Commiphora africana, is widely distributed in the Afrotropical Region and the Arabian Peninsula (HASSLER 2014) while C. parvifolia and C. planifrons are endemics of Socotra (MILLER & MORRIS 2004, BROWN & MIES 2012).Published as part of Malenovský, Igor & Burckhardt, Daniel, 2014, Jumping plant-lice of Socotra Island (Hemiptera: Psylloidea), pp. 23-61 in Acta Entomologica Musei Nationalis Pragae 54 on pages 45-48, DOI: 10.5281/zenodo.531435
Triozoida ingens Burckhardt 1988
No full text<p> <i>Triozoida ingens</i> Burckhardt, 1988</p> <p>Distribution. Panama, Paraguay.— Brazil: MG (Brown & Hodkinson 1988, Burckhardt 1988).</p> <p> Host plant. Adult specimens were collected on <i>Pimenta</i> sp. (Myrtaceae) which is a possible host.</p>Published as part of <i>Burckhardt, Daniel & Queiroz, Dalva Luiz De, 2012, Checklist and comments on the jumping plant-lice (Hemiptera: Psylloidea) from Brazil, pp. 26-48 in Zootaxa 3571</i> on page 42, DOI: 10.11646/zootaxa.3571.1.2, <a href="http://zenodo.org/record/208484">http://zenodo.org/record/208484</a>
Tainarys sordida Burckhardt
No full text<i>Tainarys sordida</i> Burckhardt <p>(Figs 18, 32, 46, 60, 74, 98, 111, 124, 137, 148, 158, 169, 178, 182)</p> <p> <i>Tainarys sordida</i> Burckhardt, 1987: 314.</p> <p> <b>Material examined.</b> Argentina (Mendoza, Río Negro), Chile (Regions III‒VIII [without Región Metropolitana]) (MHNG, NHMB).</p> <p> <b>Descriptions</b> of adult by Burckhardt (1987) and of immature by Burckhardt & Basset (2000).</p> <p> <b>Distribution</b>. Argentina (Cordoba, Mendoza, Río Negro), Chile (Regions III‒IX and Metropolitana) (Burckhardt 1987; Flores <i>et al.</i> 1989; Flores 1990; Sáiz & Nuñez 1997; Burckhardt & Basset 2000, Malcom <i>et al</i>. 2015). The record from Argentina (Buenos Aires) by Kuzmanich <i>et al.</i> (2015) is doubtful and may concern another, related species.</p> <p> <b>Host plants</b>. <i>S. fasciculata</i> (Grieseb.) Johnston, <i>Schinus johnstonii</i> F.A. Barkley, <i>S. latifolia</i> (Gillies) Engler, <i>S. montana</i> (Philippi) Engler, <i>S. patagonica</i> (Phil.) I.M.Johnst. ex Cabrera, <i>S. polygama</i> (Cav.) Cabrera, <i>S. velutinus</i> (Turcz.) I.M. Johnst. (Anacardiaceae). Forming irregular leaf roll galls or crumpling of young leaves. The reexamination of the plant voucher specimens showed that the record of <i>Schinus fasciculata</i> (Grieseb.) Johnston by Burckhardt & Basset (2000) concerns <i>S. johnstonii</i> (C. L. da Silva, in litt.). Kuzmanich <i>et al</i>. (2015) reported galls on the leaves of <i>S. longifolia</i> (Lindl.) Speg. from Argentina (Buenos Aires) which they attributed to <i>T. sordida</i>. This record is doubtful and may concern another, related species.</p> <p> <b>Comments</b>. Flores <i>et al</i>. (1989) observed two generations per year in a population on <i>S. polygama</i> in Central Chile. The emergence of adults coincided with the growth of new twigs.</p>Published as part of <i>Burckhardt, Daniel & Queiroz, Dalva L., 2017, The jumping plant-lice of the Neotropical genus Tainarys (Hemiptera: Psylloidea) associated with Anacardiaceae, pp. 535-567 in Zootaxa 4232 (4)</i> on page 563, DOI: 10.11646/zootaxa.4232.4.5, <a href="http://zenodo.org/record/313114">http://zenodo.org/record/313114</a>
Craspedolepta remaudierei Burckhardt & Lauterer 1993
No full text<i>Craspedolepta remaudierei</i> Burckhardt & Lauterer <p> <b>Material examined</b>. Iran: 8 ♂, 6 ♀, Kerman, Arjasb, N 30°25’22”, E 56°32’03”, 8.iv.2015, <i>Artemisia</i> sp., M. Lashkari leg. (KGUT).</p> <p> <b>Published records.</b> Kerman: Arjasb (Lashkari <i>et al</i>. 2016).</p> <p> <b>Host plant.</b> <i>Artemisia cina</i> Berg ex Poljakov. (Compositae) (Burckhardt & Lauterer 1993).</p>Published as part of <i>Lashkari, Mohammadreza & Burckhardt, Daniel, 2020, Jumping plant-lice (Hemiptera: Psylloidea) of Kerman, Iran, with the description of one new Cacopsylla species, pp. 576-590 in Zootaxa 4803 (3)</i> on page 580, DOI: 10.11646/zootaxa.4803.3.11, <a href="http://zenodo.org/record/3920207">http://zenodo.org/record/3920207</a>
Russelliana capsici Burckhardt 1987
No full text<i>Russelliana capsici</i> Burckhardt, 1987 <p>(Figs 8 H, 11I, 16H, 21H, 26H, 30H)</p> <p> <i>Russelliana capsici</i> Burckhardt, 1987: 387.</p> <p> <b>Material examined.</b> Type material. <b>Paratypes: Brazil</b>: 2 ♂, 1 ♀, same as holotype (H. Catling) (MHNG, dry).</p> <p> Additional material. <b>Argentina</b>: 1 ♂, Province Buenos Aires, Zelaya, i.1943 (J. B. Daguerre) (MHNG, on slide); 8 ♂, 9 ♀, 10 immatures, same but Province Entre Ríos, Concordia, Ciudad de Concordia, 10.iii.2010, <i>Capsicum annuum</i> (J. P. Bouvet) (NHMB, dry, on slide, 70 % ethanol). <b>Brazil</b>: 13 ♂, 23 ♀, 8 immatures, 2 immature skins, State Minas Gerais, Río Verde do Mato Grosso, BR163, 18°55.7/57.1' S 54°50.1 /56.0'W, 35 0–440 m, 13.xi.2012, <i>Capsicum annuum</i>, Cerrado vegetation, park (D. Burckhardt & D. L. Queiroz) #68(6) (NHMB, 70 % ethanol); 3 ♂, 4 ♀, same but State Paraná, Curitiba, Parque Bacacheri, 25°19.2–20.1' S 49°09.4 –10.1'W, 920 m, 6.iv.2013, <i>Capsicum annuum</i>, park, remnants of Atlantic forest (D. Burckhardt & D. L. Queiroz) #98(3) (NHMB, 70 % ethanol); 1 ♀, same but Parque Barigui, 25°24.9/25.6' S 49°18.6' W, 900 m, 19.vii.2012, park with remnant of natural <i>Araucaria</i> forest (D. Burckhardt & D. L. Queiroz) #43 (NHMB, 70 % ethanol); 23 ♂, 17 ♀, 24 immatures, 2 skins, same but Jardim Botânico, 25°26.5/6' S 49°14.2 /3'W, 930 m, 19.vii.2012, <i>Capsicum annuum</i>, planted park vegetation and remnant of <i>Araucaria</i> forest edge (D. Burckhardt & D. L. Queiroz) #44(2) (NHMB, 70 % ethanol); 4 ♂, 5 ♀, same but 15.ii.2013, <i>Capsicum annuum</i>, forest reserve, edge of Atlantic forest (D. Burckhardt & D. L. Queiroz) #94A(9) (NHMB, 70 % ethanol); 105 ♂, 55 ♀, 30 immatures, 22 immature skins, same but 25°26.476'S 49°14.271'W, 915 m, 12.iii.2013 (D. L. Queiroz) #462 (NHMB, on slide, 70 % ethanol); 1 ♂, 4 ♀, same but Parque Passaúna, 25°28.5'S 49°22.7'W, 930 m, 27–30.xi.2012, <i>Capsicum annuum</i>, planted park vegetation and edge of <i>Araucaria</i> forest remnant (D. Burckhardt & D. L. Queiroz) #78(2) (NHMB, dry); 1 ♂, 3 ♀, same but 25°28.5'S 49°22.6'W, 940 m, 5.ii.2013, <i>Capsicum annuum</i> (D. Burckhardt & D. L. Queiroz) #89(8) (NHMB, 70 % ethanol); 4 ♂, 13 ♀, same but Parque Tanguá, 25°22.9'S 49°17.1'W, 930 m, 6.ii.2013, <i>Capsicum annuum</i>, old mine redone as park with seminatural biotopes, mixed Atlantic <i>Araucaria</i> forest (D. Burckhardt & D. L. Queiroz) #90(16) (NHMB, 70 % ethanol); 2 ♂, 1 ♀, same but Parque Tingui, 25°23.2/7' S 49°18.4' W, 910–920 m, 31.i.2016, <i>Capsicum annuum</i>, planted park vegetation and remnants of <i>Araucaria</i> forest edge (D. Burckhardt & D. L. Queiroz) #189 (9) (NHMB, 70 % ethanol).</p> <p> <b>Description.</b> Coloration. General colour of body yellow. Head yellow to brown, genal processes pale to bright yellow; clypeus pale brown to black. Eyes red to dark brown, ocelli orange. Antenna pale yellow, segments 3–8 with more or less distinct brown apices, segments 9–10 entirely dark brown. Thorax entirely pale to bright yellow; mesopraescutum with two bright yellow to orange patches along the fore margin; mesoscutum with four broad bright yellow to orange longitudinal stripes. Forewing with whitish to dark brown veins and membrane with brown to dark brown pattern consisting of two broad transverse stripes: submarginal one stretching from apical part of costal vein to median part of cell cu1 leaving light areas in cells r2, m1, m2 and cu1 along the margin, and median one stretching from median part of vein C+Sc to apical part of anal vein; membrane between two bands colourless, sometimes with few dark brown dots in cells and sometimes on veins. Legs pale to dirty yellow, sometimes with brownish femora, meracanthus of metacoxa pale yellow. Abdomen yellow to brown; terminalia pale yellow to orange. Female proctiger with dark apex. Females with slightly lighter head and abdomen.</p> <p>Structure. Head, in profile, weakly inclined from longitudinal body axis (<45°). Vertex trapezoidal, flat, anteriorly produced into transverse lobe on either side of mid-line, hind margin around lateral ocelli not raised, covered with microscopical setae; genal processes short, swollen, slightly conical apically, covered with short setae. Pronotum with two pronounced lateral and one relatively shallow sublateral tubercles on either side. Forewing rhomboidal; vein C+Sc strongly, unevenly curved, pterostigma long, vein Rs almost straight, strongly curved to fore margin apically; vein M about as long as either of veins M1+2 and M3+4; surface spinules large, very dense, present in all cells, leaving narrow spinule-free stripes along the veins, forming hexagons, less developed on unpigmented areas; radular spinules not pronounced. Metatibia with 5–7 apical spurs.</p> <p>Terminalia. Male. Proctiger tubular; sparsely covered with moderately long setae in apical half. Subgenital plate elongate; with sparsely spaced moderately long setae in apical half. Paramere narrowly lamellar; with recurved apico-anterior process on pedicel and long apico-posterior lobe with inwards directed sclerotised anterior tooth situated at base of the lobe; lobe about twice longer than process; outer face sparsely covered with moderately long setae mostly in apical half, inner face densely covered with long thick bristles apically. Distal segment of aedeagus massive, broadly evenly expanding towards apex; with one small apico-posterior tubercle; lateral lobes moderately long, dilated towards apex which is irregularly rounded and with frayed margin.—Female. Proctiger subglobular, pointed apically; dorsal margin, in profile, strongly bent downwards; densely covered with moderately long setae. Subgenital plate subglobular, rounded apically, with tiny apical process; densely covered with long setae in apical half.</p> <p> <b>Host-plant.</b> <i>Capsicum annuum</i> L. (Solanaceae).</p> <p> <b>Distribution.</b> Reported from Argentina (Buenos Aires, Entre Ríos), Brazil (Minas Gerais, Paraná, Santa Catarina, São Paulo) (Burckhardt 1987; Burckhardt & Queiroz 2012; Burckhardt <i>et al.</i> 2012). Holotype ♂ from São Paulo, Piracicaba, viii–ix.1969, <i>Capsicum annuum</i> (M. de Menezes) (BMNH, dry), not examined here; Burckhardt 1987. Material examined. Argentina (Buenos Aires, Entre Ríos), Brazil (Minas Gerais, Paraná).</p> <p> <b>Comments.</b> <i>Russelliana capsici</i> resembles <i>R. dimorpha</i> and <i>lycii</i> in a weakly inclined head (<45°), in short swollen genal processes, in a forewing with a brown pattern, a strongly curved vein C+Sc and a vein Rs strongly curved to the fore margin apically, in a tubular male proctiger, in a cuneate male subgenital plate, in a narrowly lamellar paramere bearing a short apico-anterior process and a long apico-posterior lobe with a tooth, in a distal segment of the aedeagus broadly expanded towards apex and bearing lateral lobes with a frayed margin apically, in a subglobular female proctiger with its dorsal margin bent downwards, and a subgenital plate densely covered by setae. <i>R. capsici</i> differs from the two species in the absence of sexual dimorphism. It differs from <i>R. dimorpha</i> in shorter setae on the female subgenital plate, and from <i>R. lycii</i> in a recurved apico-anterior process of the paramere and a female subgenital plate bearing an apical process.</p>Published as part of <i>Serbina, Liliya & Burckhardt, Daniel, 2017, Systematics, biogeography and host-plant relationships of the Neotropical jumping plant-louse genus Russelliana (Hemiptera: Psylloidea), pp. 1-114 in Zootaxa 4266 (1)</i> on pages 19-21, DOI: <a href="http://zenodo.org/record/575325">10.5281/zenodo.575325</a>
Calophya terebinthifolii Burckhardt and Basset 2000
No full text<i>*</i> <i>Calophya terebinthifolii</i> Burckhardt and Basset, 2000 <p> <b>Materials examined. USA</b>: <b>Florida</b>: <b>St. Lucie County</b>: Ft. Pierce, University of Florida Biological Research and Containment Laboratory, <i>Schinus terebinthifolia</i> (FSCA, NHMB).</p> <p> <b>Diagnosis.</b> Description by Burckhardt et al. (2018).</p> <p> <b>Distribution.</b> Brazil (Burckhardt et al. 2018). Reared in quarantine in Florida as possible biological control for Brazilian peppertree.</p> <p> <b>Host plants.</b> <i>Schinus terebinthifolia</i> Raddi (Anacardiaceae).</p> <p> <b>Mastigimatinae Bekker-Migdisova, 1973</b></p> <p> <b> <i>Mastigimas</i> Enderlein, 1921</b> </p>Published as part of <i>Halbert, Susan E. & Burckhardt, Daniel, 2020, The psyllids (Hemiptera: Psylloidea) of Florida: newly established and rarely collected taxa and checklist, pp. 1-88 in Insecta Mundi 2020 (788)</i> on page 31, DOI: <a href="http://zenodo.org/record/4564694">10.5281/zenodo.4564694</a>
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