56,426 research outputs found

    Amblyseius paulofariensis Demite, Lofego & Feres

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    Amblyseius paulofariensis Demite, Lofego & Feres Amblyseius paulofariensis Demite et al., 2007: 65. Specimens examined: Matão: A. communis, IV- 2008 (6), VII- 2008 (8), IV- 2009 (4), Heliconia sp. (Heliconiaceae), III- 2008 (1), M. nigra, III- 2009 (1); Novo Horizonte: A. communis, VII- 2007 (25), X- 2007 (1), I- 2008 (5), IV- 2008 (5), VII- 2008 (15), X- 2008 (1); S. J. de Iracema: A. communis, VII- 2007 (19), X- 2007 (1), I- 2008 (1), IV- 2008 (3), VII- 2008 (11), X- 2008 (3), IV- 2009 (4), P. arboreum, VI- 2007 (5), T. casaretti, VII- 2007 (8), VII- 2008 (2); Turmalina: A. communis, IV- 2008 (5), VII- 2008 (14), X- 2008 (1), IV- 2009 (4). Previous records: Brazil.Published as part of Demite, Peterson R., Lofego, Antonio C. & Feres, Reinaldo J. F., 2011, Phytoseiidae (Acari) in forest fragments in the State of São Paulo, Brazil, pp. 31-56 in Zootaxa 3086 on page 40, DOI: 10.5281/zenodo.20537

    Amazoniaseius imparisetosus n. sp., n. g.: an unusual new phytoseiid mite (Acari: Phytoseiidae) from the Amazon forest

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    Demite, Peterson R., Cruz, Wilton P., Moraes, Gilberto J. (2017): Amazoniaseius imparisetosus n. sp., n. g.: an unusual new phytoseiid mite (Acari: Phytoseiidae) from the Amazon forest. Zootaxa 4236 (2): 302-310, DOI: https://doi.org/10.11646/zootaxa.4236.2.

    Proprioseiopsis biologicus Lofego, Demite & Moraes, sp. nov.

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    Proprioseiopsis biologicus Lofego, Demite & Moraes sp. nov. (Figures 8–12) Specimens examined. Holotype female, Campinas (22 ° 54 ' S, 47 °01' W), on B. decumbens, August 2008, A.C. Lofego coll.; 1 paratype female, same data as holotype, and 2 paratype females, same locality and host as holotype, July 2008, P.R. Demite coll.; all deposited at Departamento de Zoologia e Botânica, Universidade Estadual Paulista (UNESP), São José do Rio Preto, State of São Paulo, Brazil (DZSJRP, http: // www.splink.cria.org.br). Two paratype females, same data as holotype, deposited at Departamento de Entomologia, Fitopatologia e Zoologia Agrícola, Escola Superior de Agricultura “Luiz de Queiroz”, Universidade de São Paulo, Piracicaba, State of São Paulo, Brazil. One paratype female, same locality and host as holotype, July 2008, P.R., Demite coll., deposited at Laboratório de Entomologia Econômica, Centro Experimental Central do Instituto Biológico (LEE/ CEIB) (http//www.biologico.sp. gov.br), Campinas, SP, Brazil. Description. FEMALE (7 specimens measured). Dorsum. Dorsal shield mostly smooth, with a few anterolateral striae, 378 (362–392) long and 227 (212– 255) wide; j 1 28 (25–30), j 3 28 (25–30), j 4 6 (5–7), j 5 5 (4–6), j 6 9 (6–7), J 5 8 (7–9), z 2 7 (7–8), z 4 10 (9–12), z 5 6 (5–6), Z 1 10 (10–11), Z 4 118 (105–130), Z 5 120 (105–132), s 4 103 (93–115), S 2 10 (10–12), S 4 10 (10– 12), S 5 10 (9–11), r 3 27 (26–28), R 1 9 (8–9). All setae smooth, except Z 4 and Z 5, serrate. Ve n t e r. Sternal and genital shields reticulated, distances between st 1 -st 3 71 (70–73), st 2 -st 2 79 (77–81) and st 5 -st 5 68 (67–70); ventri-anal shield pentagonal, striated anteriorly, transversally striated medially and smooth posteriorly, 131 (129–133) long, 107 (105–110) wide at level of ZV 2 and 86 (83–90) wide at level of anus; JV 5 92 (90–95). Peritreme. Extending forward to level of j 1. Chelicera. Movable cheliceral digit 33 long, with 3 teeth; fixed cheliceral digit 32 (31–32) long, with 13 teeth. Spermatheca. Calyx saccular, 11 (10–13) long; atrium punctated, not distinctly winder than adjacent section of major duct. Legs. Sge I 36 (33–40), Sge II 34 (30–38), Sge III 33 (30–36), Sti III 29, Sge IV 70 (60–80), Sti IV 59 (55–68), St IV 82 (70–90); all macrosetae sharp-tipped. Chaetotaxy: genu II 2 - 2 / 0-2 / 0-1; genu III 1-2 / 1-2 / 0-1. Etymology. This species is named in honor of “Instituto Biológico de São Paulo”, a renowned Brazilian institution where the type specimens of this species were collected and which has contributed for many years to the development of agriculture in Brazil. Remarks: This new species could be classified in the peruvianus species group (Chant & McMurtry 2005 b) by having a macroseta on genu I. However, it differs from the species listed by Chant & McMurtry (2005 b) in this group by having an elongate dorsal shield. It resembles several species of the belizensis subgroup of the belizensis species group (Chant & McMurtry 2005 b), mainly Proprioseiopsis asetus (Chant), P. caliensis (Moraes & Mesa), P. mexicanus (Garman), P. miconiae (Moraes & Mesa), P. lineatus (Wu & Lan) and P. weintraubi (Chant & Hansell), by the similar lengths of the dorsal shield setae and macrosetae of leg IV, shape of dorsal and ventral shields, smooth texture of dorsal shield and, except P. asetus and P. mexicanus, shape of the spermatheca. However, the new species differs from the former four species by having seta j 1 about as long as j 3 (j 3 distinctly longer than j 1 in those species). In addition, it differs from P. asetus and P. mexicanus by having calyx of spermatheca sacullar (cup-shaped in those species), from P. caliensis and P. miconiae by having setae s 4, Z 4 and Z 5 about 1.4 times longer and sternal and genital shields distinctly more reticulated, and from P. lineatus and P. weintraubi by having sternal and genital shields reticulated and preanal pores mesad and transversely aligned with the bases of setae JV 2 (sternal and genital shields smooth and pre-anal pores posterior and longitudinally aligned with the bases of setae JV 2 in those species).Published as part of Lofego, Antonio C., Demite, Peterson R., Kishimoto, Raquel G. & De, Gilberto J., 2009, Phytoseiid mites on grasses in Brazil (Acari: Phytoseiidae), pp. 41-59 in Zootaxa 2240 on pages 51-53, DOI: 10.5281/zenodo.19052

    Amazoniaseius imparisetosus Demite, Cruz & McMurtry

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    Amazoniaseius imparisetosus Demite, Cruz & McMurtry Female (n = 15). Figures 1–5. Dorsum. With 21 pairs of setae (j1, j3–j6, J2, J4, J5, z2–z6, Z4, Z5, s4, s6, S2, S4, r3, R1) and two unpaired setae (x and X); setae r3 and R1 on unsclerotised cuticle. Dorsal shield ornamented with nodular structures, one pair of pores and four pairs of lyrifissures distinguishable, 290 293 (275–310) long and 102 105 (100–112) wide. Setal length: j 1 25 27 (25–28), j3 35 37 (34–40), j4 44 42 (40–45), j5 58 60 (56–63), j6 75 77 (70–81), J2 72 75 (72–77), J4 48 50 (45–57), J5 57 57 (51–69), z 2 31 30 (25–33), z3 40 41 (40–43), z4 66 65 (61–70), z5 36 37 (35–39), z6 57 60 (55–65), Z4 48 50 (46–53), Z5 70 73 (70–80), s4 80 81 (76–89), s6 87 93 (87–100), S2 70 71 (68–77), S4 68 68 (65–74), r3 45 49 (44–54), R1 57 57 (52–60), x 60 62 (55–67), X 50 54 (48–61). Setae barbed and pointed. Venter. Ventral shields distinct. Sternal shield lightly reticulate, with three pairs of setae and two pairs of lyrifissures; distance between st1–st3 60 62 (54–65), st2–st2 61 61 (59–64). Seta st4 on metasternal plate. Genital shield smooth, with posterior margin broadly rounded; distance between st5–st5 67 66 (62–72). Anal shield ovoid, lightly reticulate and with a pair of pores on anterolateral margins; 67 64 (58–67) long, 50 51 (44–55) wide at anus level. With three pairs of opisthogastric setae (JV1, JV2 and JV5; all on unsclerotised cuticle) in addition to circumanal setae; JV5 47 50 (47–53). Ventral setae smooth. Metapodal plates indistinguishable. Peritreme extending to level of j3. Spermatheca. Calyx cup- to bell-shaped, 10 11 (10-13) long; atrium relatively small, but distinct. Chelicera. Fixed cheliceral digit 29 29 (27–30), with 2–3 distal teeth in addition to apical tooth and pilus dentilus; movable digit 25 26 (24–27) long, edentate. Legs. Macrosetae of the following lengths: Sge IV 60 59 (57–62), Sti IV 41 43 (40–46), St IV 110 109 (104– 115), all pointed; other legs without macrosetae. Chaetotatic formulae: genu II – 2 2/1 2/0 1; genu III – 1 2/1 2/0 1. Deutonymph (n = 2). Figures 6–7. Dorsum. Chaetotaxy as in adult female. Dorsal shield lightly reticulate, pores and lyrifissures not distinguishable, 244–247 long and 110–121 wide. Setal length: j1 21, j3 35–38, j4 41–44, j5 63–65, j6 89–91, J2 66–75, J4 38–39, J5 40–52, z2 28, z3 35–38, z4 70–78, z5 34–38, z6 52–57, Z4 37–38, Z5 52–54, s4 84 –88, s6 86 – 90, S2 70 – 79, S4 50 –53, r3 39–40, R1 41–42, x 58 –63, X 35 –40. Setae slightly barbed and pointed. Venter. Shields weakly sclerotised. Sternogenital shield with five pairs of setae (st1–st5) and only a pair of distinguishable lyrifissures. Anal shield indistinguishable. Opisthogastric region with two pairs of setae (JV1 and JV2), in addition to circumanal setae; JV5 35-36, visible dorsally in mounted specimen. Peritreme extending to level between z2 and z3. Chelicera. Not clearly visible. Legs. Macrosetae of the following length: Sge IV 50, Sti IV 58 –60, St IV 114–115, all pointed; other legs without macrosetae. Protonymph (n= 2). Figures 8–9. Dorsum. Dorsal shield barely distinguishable; pores and lyrifissures not distinguishable; 190–200 long and 100–108 wide. Setal length: j 1 19–22, j 3 30–31, j4 38–40, j5 69–70, j6 90–94, J2 52–54, J 5 21–25, z 2 28–32, z4 70–74, z 5 28–32, Z 4 26–28, Z5 36–38, s4 79–86, s6 44–45, S4 52, r 3 23–24, R 1 13–15. Setae slightly barbed and pointed, except R1 apparently smooth and pointed. Venter. Ventral shields indistinguishable. Venter with st1–st3, JV1, JV2, JV5 and circumanal setae. Peritreme short, extending to level of s6. Chelicera. Not clearly visible. Leg. Macrosetae of the following length: Sge IV 62 –67, Sti IV 65 –70, St IV 105–108, all pointed; other legs without macrosetae. Type material (15 females, 2 deutonymphs and 2 protonymphs) Holotype female, 8 paratype females, 2 paratype deutonymphs and 2 paratype protonymphs: Rio Preto da Eva (02°26’04” S; 59°33’46” W), Amazonas state, Brazil, collected by W.P. Cruz from Elaeis oleifera (Kunth) Cortés (Arecaceae) on January 22, 2013; deposited at Departamento de Entomologia e Acarologia, Universidade de São Paulo, Escola Superior de Agricultura ‘ Luiz de Queiroz ” (ESALQ / USP), Piracicaba, São Paulo state, Brazil. One paratype female collected on May 14, 2013 and one paratype female collected on October 30, 2012; other collection data and depository as for holotype; one paratype female, collected from Astrocaryum aculeatum G.F.W Meyer (Arecaceae) on March 26, 2013; other collection data and depository as for holotype; three paratype females, same collection data as holotype; all deposited at Departamento de Zoologia e Botânica, UNESP - Universidade Estadual Paulista, São José do Rio Preto, São Paulo state, Brazil. Etymology. The name imparisetosus refers to the presence of unpaired setae in the dorsal shield. Remarks. The identification of some dorsal shield setae in this study is provisional, because of their unique position within the phytoseiids. One of the uncertainties refers to the identity of the seta called x in this paper. Is that a podonotal or opisthonotal seta? That seta, observed in the examined deutonymphs and adult females, could actually correspond to J1. Supportive of this interpretation is the absence of this seta in some specimens and the occurrence of two x setae in one of the specimens collected. The very anteriad position of x in relation to what would be expected for the normal position of J1 argues against that interpretation. Also against this interpretation is the fact that in Ascidae sensu Lindquist & Evans (1963), a group taxonomically close to the phytoseiids (see Lindquist et al., 2009 and Famah-Sourassou et al., 2015), J1 normally first appears in the protonymphal stage, whereas in the taxon here described it appeared only in the deutonymphal stage. Thus, we could conclude that the most anterior unpaired seta is podonotal, occupying the same location as the unpaired podonotal setae found in Spadiseius calyptrogynae Lindquist & Moraza (Melicharidae) (Lindquist & Moraza, 2008). The fact that this seta is not found in Spadiseius spathiphyllae Lindquist & Moraza suggests its instability in different species of that genus (and perhaps in the genus here described). Alternatively, if that seta is really J1, it would be necessary to argue that the strong lateral compression of the dorsal shield caused disturbance to the normal chaetotactic pattern, leading to the appearance of J 1 in the deutonymphal rather than in the protonymphal stage. The tendency towards evolutionary loss of J1 could also explain its instability in the deutonymph and adult. It could be argued that the seta interpreted as S 2 in this work is actually S3, because of the position. A point against that interpretation is that S3 has never been reported for phytoseiids. Its first appearance in the deutonymphal stage makes its identification more difficult because in Ascidae sensu Lindquist & Evans (1965) S2 first appear in the protonymphal stage, whereas S3 first appear in the larval stage. The actual absence of S5 is supported by the fact that the usual position of this seta is posterolaterad of the pore located anterolaterally of Z5 (idm5 of Athias-Henriot, 1969). Wide variation is observed among Amazoniaseius imparisetosus n. sp. specimens in relation to the absence of some opisthonotal setae (all of which inserted behind J2): X in five specimens, one J 5 in two specimens, X and one J 5 in one specimen, one S 4 in two specimens, one Z 4 in three specimens, and one Z4 and one S 4 in one specimen. Intra-specific variations as presence or absence of setae, place of insertion of setae, lengths of setae etc., have been reported for other species (e.g. Kolodochka, 1995; Demite et al., 2008; Toyoshima & Amano, 2013; Tixier et al., 2016). The idiosomal setal pattern of the new taxon here described has never been reported in Phytoseiidae. On the ventral surface of the idiosoma, the absence of all ZV setae has not been previously reported. Thus, our interpretation of the dorsal idiosomal setae in the new taxa here described leads us to propose a new setal pattern for the phytoseiids: 13A+x:8F+X/JV-3,4:ZV-1–3.Published as part of Demite, Peterson R., Cruz, Wilton P. & Moraes, Gilberto J., 2017, Amazoniaseius imparisetosus n. sp., n. g.: an unusual new phytoseiid mite (Acari: Phytoseiidae) from the Amazon forest, pp. 302-310 in Zootaxa 4236 (2) on pages 304-305, DOI: 10.11646/zootaxa.4236.2.5, http://zenodo.org/record/32177

    Amazoniaseius Demite, Cruz & Moraes, 2017, new genus

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    <i>Amazoniaseius</i> new genus Demite, Cruz & McMurtry <p> <b>Diagnosis.</b> Protonymphs, deutonymphs and adult females with dorsal idiosomal setae long, distinctly barbed in adults (but slightly barbed in nymphal stages), dorsal shield narrowed, <i>J5</i> relatively long (over twice as long as distance <i>J5–J5</i>); fixed cheliceral digit with few teeth. Deutonymphs and adult females with an unpaired seta immediately behind <i>j6</i> (<i>x</i>) and another immediately behind <i>J2</i> (<i>X</i>); <i>z3</i>, <i>z6</i>, <i>s6</i>, <i>J4</i> present; macrosetae present only on genu, tibia and tarsus of leg IV; <i>Z1</i>, <i>S5</i>, <i>JV3</i>, <i>JV4</i>, <i>ZV1–ZV3</i> absent; anal shield with a pair of small pores on anterolateral margins.</p> <p> <i>Adult female</i>. Dorsum of idiosoma with 21 pairs of setae (<i>j1</i>, <i>j3–j6</i>, <i>J2</i>, <i>J4</i>, <i>J5</i>, <i>z2–z6</i>, <i>Z4</i>, <i>Z5</i>, <i>s4</i>, <i>s6</i>, <i>S2</i>, <i>S4</i>, <i>r3</i>, <i>R1</i>) and two unpaired setae (<i>x</i> and <i>X</i>). Setae <i>J5</i> and <i>S2</i> displaced respectively anteriad and posteriad of their usual position. Dorsal shield strongly narrowed. Ventral shields distinct. Sternal shield with three pairs of setae and two pairs of lyrifissures. Seta <i>st 4</i> set on metasternal plate. Posterior margin of genital shield broadly rounded. Anal shield ovoid, with a pair of pores on anterolateral margins. With three pairs of opisthogastric setae (<i>JV1</i>, <i>JV2</i> and <i>JV5</i>; all on unsclerotised cuticle) in addition to circumanal setae. Peritreme extending to level of <i>j3</i>. Fixed cheliceral digit with 2–3 teeth in addition to apical tooth; movable digit edentate. Macrosetae present only on genu, tibia and tarsus IV.</p> <p> <i>Adult male</i>. Unknown.</p> <p> <i>Deutonymph</i>. Dorsal idiosomal setae as in adult female. Sternogenital shield with five pairs of setae (<i>st1–st5</i>). Opisthogastric region with two pairs of setae (<i>JV1</i> and <i>JV2</i>) in addition to circumanals. Peritreme extending to level between <i>z2</i> and <i>z3</i>. Leg macrosetae as in adult female.</p> <p> <i>Protonymph</i>. Dorsum of idiosoma with 17 pairs of setae, distinguished from adult female and deutonymph by the absence of <i>j4</i>, <i>z3</i> and <i>z6</i>; seta <i>J5</i> also displaced anteriad of usual position. Ventral shields indistinguishable; with <i>st1–st3</i>, <i>JV1</i>, <i>JV2</i>, <i>JV5</i> and circumanal setae. Peritreme extending to the level of <i>s6</i>. Leg macrosetae as in deutonymph and adult female.</p> <p> <b>Etymology.</b> The name of this genus is a combination of <i>Amazonia</i> referring to Amazonia rainforest, plus <i>seius</i> (a Roman surname commonly used to compose names of mesostigmatic mites).</p> <p> <b>Remarks.</b> This taxon is placed in Typhlodrominae by having setae <i>z3</i>, <i>s6</i>, <i>S2</i> and <i>S4</i>. The presence of <i>J4</i> is reported for the first time in Typhlodrominae, whereas the absence of all <i>ZV</i> setae is reported for the first time in Phytoseiidae. Within this subfamily, this genus is placed in Paraseiulini (Wainstein, 1976) by the presence of <i>z6</i> and <i>S4</i>, but it differs from the other genera in this tribe by the presence of the unpaired setae and <i>J4</i>, by the absence of <i>S5</i>, <i>JV4</i> and <i>ZV</i>, by the narrow dorsal shield and the presence of anal shield.</p> <p> A long seta <i>J5</i> is not a common characteristic in this family; <i>J5</i> as long as <i>Z5</i> has been reported for <i>Macrocaudus</i> Moraes, McMurtry & Mineiro (Amblyseiinae), but even in that case, those setae are shorter than the distance between their bases (Moraes <i>et al</i>., 2003). A broadly rounded posterior margin of the genital shield has been reported for <i>Amblyseiella</i> Muma and <i>Phytoseiulus</i> Evans (Amblyseiinae), but apparently for none of the Typhlodrominae genera. Among the phytoseiids, the presence of extra unpaired dorsal setae of the idiosoma has not been reported. However, a single seta anteriad of <i>J2</i> has been reported in some specimens of <i>Australiseiulus angophorae</i> (Schicha) (Typhlodrominae), whereas in other specimens two setae or none have been found (Schicha, 1981); other species of the same genus do not have that seta, interpreted by Beard (1999) as <i>J1</i>. Other phytoseiids reported to have seta <i>J1</i> belong to the Amblyseiinae, namely <i>Chileseius</i> Gonzalez & Schuster, <i>Diaphoroseius</i> Chant & McMurtry, <i>Evansoseius</i> Sheals and <i>Rubuseius</i> Ragusa, as well as a few species of <i>Typhodromalus</i> Muma and <i>Typhlodromips</i> De Leon (Chant & McMurtry, 2007). <i>Australiseiulus poplar</i> Beard has a <i>J</i> seta interpreted by Beard (1999) as <i>J4</i>. In comparison with some specimens of <i>Arrenoseius palustris</i> (Chant) and with <i>Macrocaudus multisetatus</i> Moraes, McMurtry & Mineiro, the only phytoseiid species (Amblyseiinae) reported to have <i>J3</i> (Moraes <i>et al</i>., 2003; Chant & McMurtry, 2007), and with species of the closely related family Blattisociidae (Lindquist & Evans, 1965), it seems that this seta could instead be <i>J3</i>. Seta <i>J4</i> has been reported in several phytoseiid genera (all Amblyseiinae), namely <i>Evansoseius</i>, <i>Pararrenoseius</i> Chant & McMurtry, <i>Rubuseius</i>, as well as in <i>Chileseius camposi</i> Gonzalez & Schuster, <i>M</i>. <i>multisetatus</i>, <i>Typhloseiella perforata</i> (Wainstein) and some specimens of <i>A</i>. <i>palustris</i> (Chant & McMurtry, 2007).</p> <p> Extra setae are quite commonly found in other mesostigmatid mites, including species of Ascidae, Blattisociidae and Melicharidae (Moraes <i>et al</i>., 2016) and Laelapidae (Evans & Till, 1966). Most often, extra setae are found in only some of the species of each genus. Thus, other species of this new genus may lack the setae here referred to as <i>x</i> and <i>X</i>.</p>Published as part of <i>Demite, Peterson R., Cruz, Wilton P. & Moraes, Gilberto J., 2017, Amazoniaseius imparisetosus n. sp., n. g.: an unusual new phytoseiid mite (Acari: Phytoseiidae) from the Amazon forest, pp. 302-310 in Zootaxa 4236 (2)</i> on pages 303-304, DOI: 10.11646/zootaxa.4236.2.5, <a href="http://zenodo.org/record/321772">http://zenodo.org/record/321772</a&gt

    FIGURES 6–9. Amazoniaseius imparisetosus n in Amazoniaseius imparisetosus n. sp., n. g.: an unusual new phytoseiid mite (Acari: Phytoseiidae) from the Amazon forest

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    FIGURES 6–9. Amazoniaseius imparisetosus n. sp., n. g.. Deutonymph: 6. Dorsal idiosoma, 7. Ventral idiosoma. Protonymph: 8. Dorsal idiosoma, 9. Ventral idiosoma.Published as part of Demite, Peterson R., Cruz, Wilton P. & Moraes, Gilberto J., 2017, Amazoniaseius imparisetosus n. sp., n. g.: an unusual new phytoseiid mite (Acari: Phytoseiidae) from the Amazon forest, pp. 302-310 in Zootaxa 4236 (2) on page 307, DOI: 10.11646/zootaxa.4236.2.5, http://zenodo.org/record/32177

    Neoseiulus jeca Lofego & Demite & Calvalcante 2016, n. sp.

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    Neoseiulus jeca n. sp. (Figure 1) Diagnosis — Females with dorsal shield reticulate, except for a area next to Z4, setae Z4 and Z5 serrate; length of almost all dorsal setae subequal; peritreme extending anteriorly to j1; ventral shields smooth; ventrianal shield much longer than wide with a slight waist; calyx of spermatheca cup-shaped and atrium inconspicuous. Description. Female (n= 5). Dorsum — Idiosomal setal pattern (Chant and Yoshida-Shaul, 1991): 10A:9B/JV-3:ZV. Dorsal shield reticulate, except for a area next to Z4, 283 291 (283 – 300) long, 170 172 (170 – 175) wide at level of s4; with nine pairs of lyrifissures and six pairs of pores; setae: j1 19 20 (19 – 21), j3 34 34 (31 – 35), j4 24 26 (24 – 28), j5 26 26 (23 – 29), j6 41 41 (38 – 42), J2 45 48 (45 – 50), J5 8 9 (8 – 10), z2 29 32 (29 – 34), z4 36 40 (36 – 42), z5 39 37 (34 – 39), Z1 39 42 (39 – 45), Z4 47 46 (44 – 47), Z5 55 56 (53 – 58), s4 50 51 (50 – 55), S2 45 44 (41 – 46), S4 38 38 (37 – 40), S5 27 28 (26 – 30), r3 30 31 (30 – 32), R1 23 24 (23 – 25). All setae smooth, except Z4 and Z5 slightly serrate. Venter — Sternal shield with three pairs of setae and two pairs of lyrifissures; distances between st1-st3 60 60 (60 – 61), st2-st2 67 67 (65 – 67); st4 on metasternal plate; Genital shield smooth; distance between st5-st5 65 62 (61 – 65). Ventrianal shield constricted at level of JV2; smooth; 102 106 (102 – 113) long, 68 70 (68 – 71) wide at level of ZV2 and 55 57 (55 – 58) wide at level of anus; with three pairs of pre-anal setae (JV1, JV2 and ZV2) and a pair of minute pores postero-mesad of JV2. Four pairs of opisthogastric setae on unsclerotized cuticle (JV4, JV5, ZV1 and ZV3). Seta JV5 37 38 (36 – 40). All ventral setae smooth. Two metapodal plates visible. Peritreme — Extending anteriorly to j1. Spermatheca — Calyx cup-shaped 10 10 (9 – 10) long, atrium inconspicuous. Chelicera — Movable digit 27 28 (27 – 29) long, with two teeth in addition to apical tooth; fixed digit 29 29 (28 – 30), with 11 10 – 11 teeth in addition to apical tooth. Pilus dentilis not visible. Legs — Macrosetae present only on leg IV: SgeIV 32 33 (32 – 35), StiIV 26 26 (24 – 28), StIV 58 63 (58 – 67). SgeIV and StIV with knobbed tip. Chaetotatic formula of genu II: 2-2/0-2/0-1 and of genu III: 1- 2/1-2/0-1. Type deposition — Holotype female and three paratypes female: Natividade da Serra (21°21’28"S; 45°17’33"W), Sªo Paulo State, Brazil, on Cecropia sp. (Cecropiaceae), July 26, 2008, P.R. Demite and A.C. Lofego collectors, deposited at Departamento de Zoologia e Botânica, UNESP – Universidade Estadual Paulista, Sªo JosØ do Rio Preto, SP, Brazil; One paratype female, same locality, host, data and collectors as holotype, deposited at Departamento de Entomologia e Acarologia, Universidade de Sªo Paulo, Escola Superior de Agricultura "Luiz de Queiroz" (ESALQ/USP), Piracicaba, SP, Brazil. Etymology — The specific name refers to character "Jeca Tatu" created by the Brazilian writer Monteiro Lobato (1882-1948). This character, one of the most important of this writer, lived in rural areas of the region where this species was found. Remarks — This new species belongs to peruanus species group (Chant and McMurtry, 2003) which is characterized mainly by having almost all dorsal setae approximately subequal; the fixed digit of chelicerae with more than seven small teeth and movable digit bidentate; ventrianal shield much longer than wide with a slight waist, with three pairs of preanal setae arranged in a triangular pattern, and with a pair of minute pores posterior and mesad of setae JV2. This group was previously represented by two species, Neoseiulus peruanus (El-Banhawy, 1979) and Neoseiulus irungus (El-Banhawy and Knapp, 2011), with register in South America and Africa, respectively. The new species differs from both by having ventrianal shield smooth and calyx of spermatheca cupshaped. N. peruanus and N. irungus has a striated ventrianal shield and a trumpet-shaped and bellshaped calyx, respectively. Nothing is known about biology or ecology of this new species.Published as part of Lofego, A. C., Demite, P. R. & Calvalcante, A. C. C., 2016, A new species of Neoseiulus Hughes (Acari: Phytoseiidae) from Sªo Paulo State, Brazil, pp. 115-119 in Acarologia 56 (1) on pages 116-118, DOI: 10.1051/acarologia/20162194, http://zenodo.org/record/466737

    Typhloseiopsis dorsoreticulatus Lofego & Demite & Feres 2011, sp. nov.

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    <i>Typhloseiopsis dorsoreticulatus</i> sp. nov. <p>(Figure 2)</p> <p> <i>Diagnosis</i></p> <p> This new species and <i>Typhloseiopsis funiculatus</i> DeLeon, 1965 are unique in the genus by having the ventrianal shield completely formed. However, <i>T</i>. <i>dorsoreticulatus</i> differs from <i>T. funiculatus</i> by having the dorsal shield completely reticulated and setae Z4 and Z5 strongly serrate, whereas <i>T. funiculatus</i> has a smooth dorsal shield for the most part and Z4 and Z5 also smooth.</p> <p> <i>Specimens examined</i></p> <p> Holotype female, from <i>Piper</i> sp. (Piperaceae) leaves, 24 July 2008, Serra do Japí, Jundiaí, State of São Paulo, Brazil, 23 ◦ 11 ′ S, 46 ◦ 52 ′ W, P.R. Demite and J.C. de Souza colls. Paratypes: two females and one male, from same host, date and collectors as the holotype; one female and one male, from <i>Croton floribundus</i> Spreng. (Euphorbiaceae) leaves, 12 September 2008, V. de O. Lima and C. Vieira colls. All paratypes from same locality as the holotype.</p> <p> <i>Description of female (four specimens measured)</i></p> <p> <i>Dorsum</i> (Figure 2A). Dorsal shield distinctly reticulated; with seven pairs of lyrifissures and six pairs of pores; <b>317</b> 327 (317–340) long and <b>182</b> 189 (182–200) wide at s4 level; j1 <b>17</b> 18 (17–20), j3 <b>15</b> 17 (15–18), j4 <b>11</b> 12 (11–14), j5 <b>11</b> 12 (11–13), j6 <b>12</b> 14 (12–15), J2 <b>16</b> 18 (16–19), J5 <b>11</b> 12 (11–12), z2 <b>14</b> 15 (14–16), z3 <b>12</b> 14 (12–16), z4 <b>15</b> 16 (15–17), z5 <b>12</b> 14 (12–15), Z4 <b>21</b> 23 (21–24), Z5 <b>54</b> 57 (54–61), s4 <b>17</b> 19 (17–20), s6 <b>16</b> 18 (16–20), S5 <b>14</b> 15 (14–15), r3 <b>15</b> 16 (15–17), R1 <b>15</b> 16 (15–17). All setae smooth, except J5, Z4 and Z5, which are serrated.</p> <p> <i>Venter</i> (Figure 2B). Sternal and genital shields smooth, distance between st1–st3 <b>58</b> 59 (57–60), st2–st2 <b>61</b> 60 (59–61), st5–st5 <b>59</b> 61 (59–64). Ventrianal shield smooth, <b>106</b> 111 (106–117) long, <b>92</b> 94 (89–100) wide at level of ZV2 and <b>90</b> 94 (90–98) wide at the anus level; JV5 <b>31</b> 34 (31–35).</p> <p> <i>Peritreme</i>. Extending to the level of j1.</p> <p> <i>Chelicera</i> (Figure 2C). Movable cheliceral digit <b>22</b> 22 (21–23) long, with two teeth. Fixed cheliceral digit <b>23</b> 24 (23–25) long, with four teeth.</p> <p> <i>Spermatheca</i> (Figure 2D). Calyx tubular, short, <b>10</b> 10 (9–10). Atrium nodular.</p> <p> <i>Legs</i> (Figure 2E). Only legs III and IV with macrosetae: SgeIII <b>11</b> 13 (11–14), Sge IV <b>12</b> 15 (12–17), StiIV <b>15</b> 14 (13–15), StIV <b>30</b> 31 (28–35). All macrosetae knobbed. Chaetotaxy: genu II 2-2 <i>/</i> 0-2 <i>/</i> 0-1; genu III 1-2 <i>/</i> 1-2 <i>/</i> 0-1.</p> <p> <i>Description of male (two specimens measured)</i></p> <p> <i>Dorsum</i>. Dorsal shield distinctly reticulated, 250–260 long and 150–170 wide; j1 12– 15, j3 15, j4 11, j5 10–11, j6 10–11, J2 14–16, J5 10–11, z2 11–12, z3 11–13, z4 12–15, z5 10–13, Z4 16–19, Z5 39–40, s4 16, s6 16 –17, S5 13 – 15, r3 14–15, R1 15, All setae smooth, except J5, Z4 and Z5, which are serrate.</p> <p> <i>Venter</i> (Figure 2F). Sternogenital shield smooth. Ventrianal shield with striae on the anterior region and with lateral reticules at the level of JV1 and ZV2, fused to peritremal shield by a strip arising from the anterior margin near corners; 102–106 long, 138–150 wide at anterior corners level; with four pairs of pre-anal setae, one distinct pair of pores posterior to JV2 and three pairs of lyrifissures; JV5 18–19.</p> <p> <i>Peritreme</i>. Extending to the level of j1.</p> <p> <i>Spermatodactyl</i> (Figure 2G). T-shaped, shaft 15–16.</p> <p> <i>Legs</i>. SgeIII 9–10, SgeIV 12, StiIV 11–13, StIV 22–25. All macrosetae knobbed. Chaetotaxy: genu II 2-2 <i>/</i> 0-2 <i>/</i> 0-1; genu III 1-2 <i>/</i> 1-2 <i>/</i> 0-1.</p> <p> <i>Etymology</i></p> <p> The specific epithet is composed of the Latin noun <i>dorso</i> and the adjective <i>reticulatus</i>, referring to the completely reticulated dorsal shield.</p>Published as part of <i>Lofego, Antonio C., Demite, Peterson R. & Feres, Reinaldo J. F., 2011, Two new species of phytoseiid mites (Acari: Phytoseiidae) from the State of São Paulo, Brazil, pp. 2347-2354 in Journal of Natural History 45 (37 - 38)</i> on pages 2350-2353, DOI: 10.1080/00222933.2011.596950, <a href="http://zenodo.org/record/4652470">http://zenodo.org/record/4652470</a&gt

    Oligonychus steinhaueri Flechtmann & Baker 1970

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    Oligonychus steinhaueri Flechtmann & Baker, 1970 Origin of the specimens examined — S. J. do Rio Preto – Area 1: unidentified plant: VI-1990 (19♀ and 4♂). Previous records — Brazil.Published as part of Demite, P. R., Flechtmann, C. H. W. & Feres, R. J. F., 2016, Tetranychidae (Acari) in forest fragments in the State of Sªo Paulo, Brazil, pp. 435-449 in Acarologia 56 (4) on page 443, DOI: 10.1051/acarologia/20162245, http://zenodo.org/record/539786

    Kaliszewskia ochoai Lofego, Demite & Moraes, 2015, sp. nov.

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    Kaliszewskia ochoai sp. nov. (Figs. 1–6) Diagnosis. Adult females of this species can be distinguished from those of other tarsonemid species by the combination of characters given in the diagnosis of the genus. Female (three specimens measured). Gnathosoma: (Fig. 1 a and 2) sub-triangular, length 30 (29–31), maximum width 38 (36–40); dorsal apodeme indistinguishable. Setae dgs 11 (10–12) and vgs 9, smooth; seta pp absent or indistinguishable. Palpi short and robust, each with one subterminal seta and a small cone-shaped structure. Cheliceral stylets 10 (9–10). Pharynx fusiform 16 (15–18) long and 7 (6–7) wide at widest region, with discrete muscular layer and thinly sclerotized walls. Idiosoma (Figs. 1 and 2): Tergites and ventral plates punctated; length 208 (193–230), width at level of c 1 133 (130–138); prodorsal shield covering gnathosoma entirely. Stigma on discrete marginal projection of prodorsal shield, laterad of base of tubercle (40 long) bearing v 1. Seta sc 2 inserted anterolaterad of sc 1. Lengths of setae: v 1 40 (39–42), sc 1 17 (16–17), sc 2 35 (33–36), c 1 48 (46–50), c 2 22 (19–24), d 36 (33–39), e 6 (5–6), f 21 (20–22), h 8 (7–8). Distances between dorsal setae: v 1 –v 1 17 (16–18), sc 2 –sc 2 62 (61–62), v 1 –sc 2 34 (33–35), c 1 –c 1 81 (77– 83) c 2 –c 2 115 (110–118), c 1 –c 2 40 (38–41), d–d 45 (44–46), f–f 29 (27–30), e–f 5 (4–5), h–h 19 (18–19). Seta v 1 stout and strongly serrate; seta sc 1 knobbed and with tiny spines; setae sc 2, c 1, c 2 and d stout but flexible (tip bent to different directions in mounted specimens), barbed and knobbed; setae e, f and h barbed and sharp-tipped. Coxisternal seta 1a 7 (6–7), inserted near junction of apodeme 1 with prosternal apodeme; coxal pits 1 b hardly distinguishable, located anterolaterad seta 1 a; seta 2a 7 (6–7) inserted on distal end of apodeme 2; coxal pits 2 b posterolaterad 2 a; seta 3a 7 (7–8), inserted midway between sejugal apodeme and apodeme 3; seta 3 b 5, inserted on distal end of apodeme IV. Prosternal apodeme fused with apodemes 1, but not with apodeme 2, conspicuous from apodeme 1 to level of posterior ends of apodemes 2, widening and fading posteriorly to reach sejugal apodeme, which is continuous, but faded medially. Apodeme 3 slightly arched, transverse, extending from anterior end of trochanter III to level posterolaterad insertion of 3 a. Poststernal apodeme distinct, not bifurcate anteriorly, extending from level of apodeme 3 to level of posterior end of trochanter III. Tegula rounded, 11 (10–11) long and 12 (11–12) wide at base. Anterior edge of metapodosomal plate nearly straight. Posterolateral extensions of coxisternal plates IV approaching but not overlapping each other medially beneath tegula. Setae ps minute (2). Legs (Figs. 3–6): lengths (proximal end of trochanter to distal end of tarsus): leg I 52 (51–52), leg II 53 (52– 53), leg III 54 (51–57), leg IV 36 (36–37). Number of setae (solenidia in parentheses) on femur, genu, tibia and tarsus, respectively: leg I: 4 – 4–6 + 8 (+ 1 ω), leg II: 3 – 3–4 – 5 (+ 1 ω), leg III: 1 + 3–4 – 4. Tarsal solenidion ω of tibiotarsus I 7 (6–7), stout and slightly elongate. Sensory cluster of tibia I incomplete (φ 1 and φ 2 missing); eupathidion k (5) proximal to d 34 (32–35), serrate. Solenidion ω of tarsus II proximal, 7, stout and slightly elongate; seta pl'' absent. Seta d of tibia II 38 (36–40), serrate. Femurogenu IV 25; tibiotarsus IV 15. Lengths of leg IV setae: v´F 7, v´G 8, v'Ti 16 (16–17) and tc'' 22 (21–23); setae v'G and v'F slender and smooth, v'Ti lanceolate and smooth; tc"Ta slender and serrate. Larva and male: Unknown. Type material. Holotype ♀ (specimen number 9515): Serra do Conduru, Uruçuca, Bahia State, Brazil, on Plinia sp. (Myrtaceae), 16 March 2013, deposited at Departamento de Zoologia e Botânica, Universidade Estadual Paulista (UNESP), São José do Rio Preto, São Paulo State, Brazil. Paratypes: 2 ♀ (specimen numbers T-MZLQ 3013, T-MZLQ 3014): Ilha do Cardoso, Cananéia (25 °04S; 47 ° 55 W), São Paulo State, Brazil, on Blepharocalix salicifolius (Kunt) O. Berg (Myrtaceae), 16 July 2012, deposited at Departamento de Entomologia e Acarologia, Escola Superior de Agricultura “Luiz de Queiroz”(ESALQ), Universidade de São Paulo (USP), Piracicaba, São Paulo State, Brazil. All specimens collected by P. R. Demite. Etymology. This species is named after the eminent acarologist Ronald Ochoa, USDA, USA. Remarks. Nothing is known about the feeding behavior of this species. Tarsonemini species are known as egg parasitoids, algivores, fungivores or phytophages (Lindquist 1969, 1986; Lofego et al. 2005). The feeding habits of species of the genera morphologically most similar to Kaliszewskia are also inadequately known. Fungitarsonemus species have been speculated to feed on fungi, which could also be the case of the species here described, given that the habitats where the types were found are humid, allowing easy development of fungi on leaves. Species of Ceratotarsonemus, Daidalotarsonemus and Rynchotarsonemus are also thought to feed on algae, lichens or on plant leaves.Published as part of Lofego, Antonio C., Demite, Peterson R. & Moraes, Gilberto J., 2015, A new genus and species of Tarsonemidae (Acari: Heterostigmata) from the Atlantic Forest, Brazil, pp. 561-568 in Zootaxa 3986 (5) on pages 563-567, DOI: 10.11646/zootaxa.3986.5.3, http://zenodo.org/record/24296
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