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Neoseiulus viticolus Trincado & Martin, n. sp. (Figs 11–17) Diagnosis: This species is most similar to Neoseiulus brigarinus Beard, 2001, Neoseiulus cucumeris (Oudemans, 1930) and Neoseiulus noosae (McMurtry & Schicha, 1987). They all differ from the new species here described by having distinct atrium, and ventrianal shield much wider at level at ZV 2 than at level of anus. The former two species further differ by having three teeth on the fixed digit and one tooth on movable digit, while the latter further differs by having shorter Z 5. FEMALE : (4 specimens measured) Dorsum (Fig. 11). Dorsal shield reticulated, except for a transverse band between setae S 4 and S 5; with seven distinguishable pairs of pores and 11 pairs of lyrifissures; 398 (375– 412) long, 210 (205–218) wide; j 1 24 (23–25), j 3 26 (25–28), j 4 18, j 5 16 (15–18), j 6 19 (18–20), J 2 20, J 5 13, z 2 21 (20–23), z 4 23 (23–25), z 5 16 (15–18), Z 1 20, Z 4 43 (40–48), Z 5 56 (55–58), s 4 32 (30–35), S 2 29 (28–32), S 4 23 (20–25), S 5 23, r 3 24 (23–25), R 1 23 (20–25). All setae smooth, except for Z 4 and Z 5, serrate. Peritreme (Fig. 11). Extending forward almost to level of j 1. Venter (Fig. 12). Sternal shield smooth over most of its extent, with scant anterolateral striae; with three pairs of setae, and two pairs of lyrifissures; distances between St 1– St 3 71 (68–73), St 2– St 2 73 (68–78). Genital shield smooth; distance between St 5– St 5 81 (75–85). Ventrianal shield transversely striate in the anterior half and irregularly striate elsewhere, vase-shaped 136 (133–140) long, 92 (88–100) wide at ZV 2 level and 88 (85–90) at anus level, with three pairs of pre-anal setae and a pair of small, rounded pre-anal pores posteromesad of JV 2. Seta JV 5 41 (38–45). All ventral setae smooth. Two pairs of slender metapodal shields, the posterior distinctly larger. Chelicera (Fig. 13). Antiaxial lyrifissure distinct. Fixed digit 28 (25–30) long, with five teeth in addition to apical tooth and setiform pilus dentilis. Movable digit 31 (30–33) long, with two teeth in addition to apical tooth. Legs (Fig. 14). Macrosetae present only on leg IV, with tiny distal knob: Sge 29 (28–30), Sti 23, St 41 (38–45). Chaetotaxy of genu II 2 2/0, 2/0 1; genu III 1 2/1, 2/0 1. Spermatheca (Fig. 15). Calyx bell-shaped, 18 long. Atrium discrete. Male: (3 specimens measured) Dorsum. Dorsal shield similar to female; 311 (305–315) long, 212 (200–222) wide; j 1 21 (21–22), j 3 25 (23–26), j 4 16 (13–16), j 5 17 (15–18), j 6 17 (16–17), J 2 16 (16–17), J 5 11 (10–11), z 2 18 (17–18), z 4 24 (21–26), z 5 15 (14– 15), Z 1 19 (17–23), Z 4 34 (31–37), Z 5 42 (39–46), s 4 32 (27–36), S 2 22 (19–25), S 4 20 (19–21), S 5 20, r 3 22 (20–24), R 1 18 (16–20). All setae smooth, except for Z 4 and Z 5, serrated. Peritreme. Extending forward almost to level of j 3. Venter (Fig. 16). Sternogenital shield mostly smooth, with scant lateral striae; with five pairs of setae, and two pairs of liryfissures; distances between St 1– St 3 66 (66–67), St 2–St2 62 (61–62). Ventrianal shield reticulate, subtriangular, 188 (185–192) long, 141 (137–145) wide at anterior corners, with five pairs of pre-anal setae and a pair of small, rounded pre-anal pores posteromesad of JV 2. Metapodal shields indistinct. Chelicera (Fig. 17). Fixed digit 22 (21–22) long, with five teeth in addition to apical tooth and setiform pilus dentilis. Movable digit 20 (19–21) long, with one tooth in addition to apical tooth; spermadactyl with shaft 19 (15–21) and foot 8 (7–9) long. Legs. Macrosetae present only on leg IV, with tiny distal knob: Sge 21 (19–25), Sti 18 (15–19), St 33 (30–35). Etymology. The specific name viticolus refers to Vitis vinifera L., the plant species from which the types of this new species were collected. Type locality. Holotype female collected on 29 September 2009, from Pirque, Santiago Region, Chile, on Vitis vinifera L., associated with Brevipalpus chilensis Baker. Deposited at Departamento de Entomologia e Acarologia, Escola Superior de Agricultura “Luiz de Queiroz”, Universidade de São Paulo. One paratype female and one paratype male, same collection records as holotype; deposited at Departamento de Entomologia e Acarologia, Escola Superior de Agricultura “Luiz de Queiroz”, Universidade de São Paulo; two paratype females and one paratype male, same collection data as holotype, deposited at Museo Nacional de Historia Natural, Santiago to Chile.

Neoseiulus bicaudus (Wainstein) Amblyseius bicaudus Wainstein, 1962: 146. Neoseiulus bicaudus.��� Moraes et al., 1986: 72; 2004: 108; Wang et al., 2015: 456. Specimens examined. Santiago Region. Municipality of La Pintana, on Malva nicaensis All, April 2002, associated with Tetranychus desertorum Banks; on Vitis vin��fera L., June 2002, associated with Brevipalpus chilensis Baker. Measurements of a collected female: dorsal shield 400 long, 160 maximum width; j 1 25, j 3 28, j 4 10, j 5 15, j 6 17, J 2 18, J 5 12, z 2 17, z 4 15, z 5 7, Z 1 18, Z 4 35, Z 5 110, s 4 30, S 2 32, S 4 33, S 5 40, r 3 29, R 1 25, St IV 61. Remarks. Measurements of the specimens collected fit the redescription of the species provided by Ferragut et al. (2010)., Published as part of Trincado, R. D., Martin, J. P. I., M��ndez Rosa, D. D., Lopes, P. C. & De Moraes, G. J., 2018, Phytoseiid mites (Acari: Phytoseiidae) from Chile, with descriptions of three new species and a redescription of Chileseius camposi, pp. 322-340 in Zootaxa 4482 (2) on page 328, DOI: 10.11646/zootaxa.4482.2.5, http://zenodo.org/record/1440610, {"references":["Wainstein, B. A. (1962) Some new predatory mites of the family Phytoseiidae (Parasitiformes) of the USSR fauna. Entomologicheskoe Obozrenie, 41, 230 - 240. [translation in Entomological Review, 41, 139 - 146]","Moraes, G. J. de, McMurtry, J. A. & Denmark, H. A. (1986) A Catalog of the Mite Family Phytoseiidae. References to Taxonomy, Synonymy, Distribution and Habitat. EMBRAPA - DDT, Brasilia, 353 pp.","Wang, B. - M., Wang, Z. - H., Jiang, X. - H., Zhang, J. - P. & Xu, X. - N., (2015) Re-description of Neoseiulus bicaudus (Acari: Phytoseiidae) newly recorded from Xinjiang, China. Systematic and Applied Acarology, 20 (4), 455 - 461. https: // doi. org / 10.11158 / saa. 20.4.11","Ferragut, F., Perez Moreno, I., Iraola, V. & Escudero, A. (2010) Acaros depredadores em las plantas cultivadas. Familia Phytoseiidae. Ediciones Agrotecnicas, Madrid, 202 pp."]}

Galendromus (Galendromus) occidentalis (Nesbitt) Typhlodromus occidentalis Nesbitt, 1951: 29. Galendromus (Galendromus) occidentalis.��� Moraes et al. 1986: 190; 2004: 268. Specimens examined. Santiago Region. Municipality of La Pintana, on Convolvulus arvensis L., March 2000, associated with Tetranychus urticae Koch; on Ficus carica L., March 2000, associated with Eriophyes fici Essig; on Malus domestica Borkh, February 2002, associated with Tydeidae; on Pelargonium hortorum L. H. Bailey, June 2002, associated with Tydeidae; on Phaseolus vulgaris L., March 2002, associated with Tetranychus desertorum Banks; Prunus salicina, April 2002, associated with Oligonychus sp.; on Trifolium sp., March 2002, associated with T.. urticae; Buin, on Malus domestica Borkh, April 1990, associated with Panonychus ulmi (Koch); on Prunus avium (L.), April 1990, associated with Panonychus ulmi (Koch) and T. urticae. Measurements of two collected females: dorsal shield 315, 342 long, 170, 180 width; j 1 20; j 3 52; j 4 31; j 5 37, 46; j 6 56, 62; j 2 55, 68; J 5 9, 10; z 2 53, 59; z 3 47, 54; z 4 52, 58; z 5 37, 47; Z 4 58, 67; z 5 57, 62; s 4 54, 62; s 6 62, 71; S 2 62, 72; S 5 57, 65; r 3 42, 49. Remarks. The two females with the same collection data were found to have very different sizes, and for this reason, both were measured. Both of them are distinctly smaller than reported by Chant & Yoshida-Shaul (1984) for a type specimen (dorsal shield 380 long); concurrently, most setae of the larger specimens are about 10���20% shorter than reported by those authors for that type specimen., Published as part of Trincado, R. D., Martin, J. P. I., M��ndez Rosa, D. D., Lopes, P. C. & De Moraes, G. J., 2018, Phytoseiid mites (Acari: Phytoseiidae) from Chile, with descriptions of three new species and a redescription of Chileseius camposi, pp. 322-340 in Zootaxa 4482 (2) on pages 331-332, DOI: 10.11646/zootaxa.4482.2.5, http://zenodo.org/record/1440610, {"references":["Nesbitt, H. H. J. (1951) A taxonomic study of the Phytoseiidae (Family Laelaptidae) predaceous upon Tetranychidae of economic importance. Zoologische Verhandelingen, 12, 1 - 64, 32 pls.","Moraes, G. J. de, McMurtry, J. A. & Denmark, H. A. (1986) A Catalog of the Mite Family Phytoseiidae. References to Taxonomy, Synonymy, Distribution and Habitat. EMBRAPA - DDT, Brasilia, 353 pp.","Chant, D. A. & Yoshida-Shaul, E. (1984) A world review of four species groups in the genus Typhlodromus Scheuten (Acari: Phytoseiidae): brevicollis, luculentis, carinulatus, and pinnatus. Canadian Journal of Zoology, 62, 2631 - 2642. https: // doi. org / 10.1139 / z 84 - 383"]}

Metaseiulus (Metaseiulus) relictus Trincado & Martin, n. sp. (Figs 18–24) Diagnosis. This species is most similar to Metaseiulus brevicollis Gonzalez & Schuster, 1962, also described from Chile. However, the latter differs by having fixed cheliceral digit with only two teeth in addition to the apical tooth, R 1 on dorsal shield and about as long as s 6, and dorsal shield lightly reticulate. FEMALE : (4 specimens measured) Dorsum (Fig. 18). Dorsal shield smooth; with seven distinguishable pairs of pores and 13 distinguishable pairs of lyrifissures; 360 (335– 370) long, maximum width 185 (175–205); j 1 25 (23–27), j 3 30 (29–34), j 4 12 (12–20), j 5 15 (14–15), j 6 16 (15–20), J 2 20 (12–20), J 5 13 (12–14), z 2 17 (16–27), z 3 27 (25–30), z 4 30 (30–32), z 5 12 (10–13), Z 4 52 (51–60), Z 5 74 (65–77), s 4 47 (41–47), s 6 47 (43–50), S 5 18 (18–19), R 1 20 (17–22). All setae smooth. Peritreme (Fig. 18). Extending forward almost to level of j 1. Venter (Fig. 18). Sternal shield smooth; with three pairs of setae, and two pairs of lyrifissures; distances between St 1– St 3 71 (68–73), St 2– St 2 65 (60–73). Genital shield smooth; distance between St 5– St 5 60 (55–74). Ventrianal shield smooth, shield-shaped, slightly constricted at level of JV 2; 120 (120–128) long, 95 (95–100) wide at ZV 2 level and 90 (84–90) at anus level, with four pairs of pre-anal setae and a pair of small, rounded pre-anal pores mesad and slightly posterior of JV 3. Seta JV 5 60 (60–65). Two pairs of slender metapodal plates, the posterior distinctly larger. Chelicera (Fig. 20). Antiaxial lyrifissure distinct. Fixed digit 43 (40–45) long, with seven teeth in addition to apical tooth and setiform pilus dentilis. Movable digit 36 (35–40) long, with two teeth in addition to apical tooth. Legs (Fig. 21). Macrosetae present only on legs III and IV, all with a very tiny distal knob: Sge III 22 (21–23), Sge IV 48 (47–48), Sti IV 36, St IV 46 (44–46). Chaetotaxy of genu II 2 2/1, 2/0 1; genu III 1 2/1, 2/0 1. Spermatheca (Fig. 22). Calyx bell-shaped, 9 (8–10) long. Atrium discrete. Male: (3 specimens measured) Dorsum. Dorsal shield similar to female; 310 (300– 310) long, maximum width 165 (160–165); j 1 20 (16–22), j 3 29 (28–30), j 4 16 (15–17), j 5 15, j 6 15 (15–16), J 2 16 (16–17), J 5 11 (10–12), z 2 16 (14–20), z 4 27 (25–28), z 5 11 (10–12), Z 4 27 (25–28), Z 5 60 (59–65), s 4 38 (32–40), S 5 16 (16–18), R 1 18 (16–20). All setae smooth. Peritreme. Extending between j 1 and j 3. Venter (Fig. 23). Sternogenital shield smooth with five pairs of setae and two pairs of liryfissures; distances between St 1– St 3 68 (66–71), St 2– St 2 52 (52–55). Ventrianal shield transversely striate, subtriangular, 140 (137– 150) long, 150 (150–155) wide at anterior corners, with five pairs of pre-anal setae and a pair of round pre-anal pores. Metapodal shields indistinct. Chelicera (Fig. 24). Fixed digit 35 (30–40) long, with five teeth in addition to apical tooth and a setiform pilus dentilis. Movable digit 25 (25–35) long, with one tooth in addition to apical tooth; spermadactyl with shaft 19 (18– 21) and foot 12 (9–12) long. Legs. Macrosetae present only on legs III and IV, but differently from female, distal knob not distinct: Sge III 17 (16–18), Sge IV 33 (30–33), Sti IV 25, St IV 35 (35–37). Etymology: The specific name relictus refers to the type locality of this species, a humid relict forest located at the southern extreme of the coastal desert of north-central Chile. Type locality. Holotype female, collected on 24 March 2014, from Parque National Fray Jorge, Coquimbo, Chile, on Escallonia illinita C. Presl, associated with Brevipalpus sp. Deposited at Departamento de Entomologia e Acarologia, Escola Superior de Agricultura “Luiz de Queiroz”, Universidade de São Paulo. One paratype female and three paratype males, same collection records as holotype; all deposited at Departamento de Entomologia e Acarologia, Escola Superior de Agricultura “Luiz de Queiroz”, Universidade de São Paulo; 11 paratype females and 6 paratype males, on Senecio sp., other collection records same as holotype, deposited at Museo Nacional de Historia Natural, Santiago to Chile.

Chileseius camposi Gonzalez & Schuster Chileseius camposi Gonzalez & Schuster, 1962: 7. Chileseius camposi.— Moraes et al., 1986: 182, 2004: 58. Avioseius pennatus Karg 1976: 513 (synonymy according to Chant & McMurtry, 2003: 11). Chileseius pennatus.— Chant & McMurtry, 2003: 11. Specimens examined. Holotype female: Curicó, Chile, on Vitis vinífera L., associated with Brevipalpus chilensis Baker, 8 April 1961, collected by L. E. Campos; deposited at USNM United States National Insect & Mite Collection, US National Museum of Natural History (Smithsonian), held at Systematic Entomology Laboratory (SEL), Beltsville Agricultural Research Center West (BARC West), United States Department of Agriculture (USDA), Beltsville, Maryland, USA. Paratype female: Vilcún, Temuco, Chile, on apple, associated with Tetranychidae, 28 April 1961, collected by L. M. Smith; deposited at Museo Luis Peña Guzmán, Facultad de Agronomía, Universidad de Chile, Santiago. Other specimens: Santiago Region. Municipality of La Pintana, on Punica granatum L., February 2008, associated with Eriophyes granati (Canestrini & Massalongo); on Rubus ulmifolius Schott., September 2002, associated with Tydeidae. Municipality of Curacaví, on Schinus latifolius (Gill. ex Lindl.), February 2000, associated with Tydeidae. FEMALE : (holotype, paratype and 4 additional specimens measured) Dorsum (Fig. 6). Dorsal shield with seven distinguishable pairs of pores and 11 distinguishable pairs of lyrifissures; 377 369 (344–405) long, 208 215 (187–230) maximum width; j 1 22 27 (20–30), j 3 22 31 (25–37), j 4 17 20 (15–25), j 5 17 20 (15–27), j 6 18 23 (15–32), J 2 22 31 (20–39), J 4 22 32 (20–32), J 5 12 15 (12–18), z 2 22 32 (25–40), z 4 24 35 (24–44), z 5 19 25 (18–32), z 6 23 30 (22–38), Z 1 27 37 (30–43), Z 3 23 32 (25–40), Z 4 45 55 (45– 58), Z 5 58 62 (55–70), s 4 27 42 (34–50), S 2 32 43 (31–50), S 4 34 48 (40–63), S 5 34 46 (37–53), r 3 23 31 (28–37), R 1 22 34 (28–39). Holotype with J 4, J 5, Z 4, Z 5, S 2 S 4 and S 5 serrate; other setae, smooth. All setae relatively stout; setae on the opisthonotal region of the dorsal shield setae on small tubercles. Peritreme (Fig. 6). Extending forward to level of j 1. Venter (Fig. 7). Sternal shield smooth; with two pairs of lyrifissures; distances between St 1– St 3 66 66 (64–67), St 2– St 2 62 68 (63–75). Genital shield smooth; distance between St 5– St 5 67 71 (67–75). Ventrianal shield striate, shield-shaped 129 127 (117–135) long, 89 98 (89–100) wide at ZV 2 level and 56 75 (56–80) at anus level, with three pairs of pre-anal setae and a pair of small, rounded pre-anal pores posteromesad of JV 2. Seta JV 5 35 48 (35– 55). All ventral setae smooth. Two pairs of slender metapodal plates, the posterior distinctly larger. Chelicera (Fig. 8). Antiaxial lyrifissure distinct. Fixed digit 35 35 long, with five or six teeth in addition to apical tooth and setiform pilus dentilis. Movable digit 32 32 long, with two teeth in addition to apical tooth. Legs (Fig. 9). Macrosetae present only on leg IV, blunt (in some specimens collected in this study, slightly knobbed). Sti IV 18 24 and St IV 28 34. Chaetotaxy of genu II 2 2/0, 2/0 1; genu III 1 2/1, 2/0 1. Spermatheca (Fig. 10). Calyx dish-shaped, 5 4 (3–5) long. Atrium discrete. Remarks. In the original description of the species, the ventrianal shield is shown smooth, but our examination of the holotype showed it to be reticulate, as also observed in the additional specimens examined. The spermatheca was illustrated, but not described in the original description. The illustration could suggest the calyx to be trumpetshaped. However, our examination of the holotype and of the additional specimens examined suggests the calyx to be dish-shaped and the atrium being difficult to discern. In this publication, this species is considered to have most dorsal shield setae highly variable in length; measurements of the holotype are within the range determined for most setae of the specimens collected in this study, but j 3, J 5, Z 1, s 4, S 4, S 5, r 3 and R 1 of the holotype are shorter than observed in the specimens collected. In addition, differently from the holotype, in some of the specimens collected in this study Z 3 is distinctly serrate.

Metaseiulus (Metaseiulus) camelliae Chant & Yoshida-Shaul Typhlodromus camelliae Chant & Yoshida-Shaul, 1983: 1053. Typhlodromina camelliae.��� Moraes et al., 1986: 236. Metaseiulus (Metaseiulus) camelliae.��� Moraes et al., 2004: 278. Specimens examined. Santiago Region. Municipality of La Pintana, on Citrus aurantium L., July 2002, associated with Planococcus citri. Municipality of Buin, on Vitis vinifera L., February 1994, associated with Brevipalpus chilensis Barker and June 2002, associated with Tydeidae. Measurements of a collected female: dorsal shield 350 long, 200, maximum width; j 1 20, j 3 20, j 4 15, j 5 12, j 6 17, J2 22, J5 12, z 2 20, z 3 20, z 4 22, z 5 12, Z 4 35, z 5 45, s 4 25, s 6 26, S 5 20, r 3 22, R 1 29. These measurements are similar to those of the original description of the species., Published as part of Trincado, R. D., Martin, J. P. I., M��ndez Rosa, D. D., Lopes, P. C. & De Moraes, G. J., 2018, Phytoseiid mites (Acari: Phytoseiidae) from Chile, with descriptions of three new species and a redescription of Chileseius camposi, pp. 322-340 in Zootaxa 4482 (2) on page 332, DOI: 10.11646/zootaxa.4482.2.5, http://zenodo.org/record/1440610, {"references":["Chant, D. A. & Yoshida-Shaul, E. (1983) A world review of five similar species groups in the genus Typhlodromus Scheuten. Part II. The conspicuus and cornus groups (Acarina: Phytoseiidae). Canadian Journal of Zoology, 61, 1041 - 1057. https: // doi. org / 10.1139 / z 83 - 138","Moraes, G. J. de, McMurtry, J. A. & Denmark, H. A. (1986) A Catalog of the Mite Family Phytoseiidae. References to Taxonomy, Synonymy, Distribution and Habitat. EMBRAPA - DDT, Brasilia, 353 pp.","Moraes, G. J. de, McMurtry, J. A. & Denmark, H. A. (2004) A revised catalog of the mite family Phytoseiidae. Zootaxa, 434 (1), 1 - 494. https: // doi. org / 10.11646 / zootaxa. 434.1.1"]}

Amblyseius tamatavensis Blommers Amblyseius (Amblyseius) tamatavensis Blommers, 1974: 144. Amblyseius tamatavensis.��� Moraes et al., 1986: 31; 2004: 52; Abo-Shnaf et al., 2016: 610. Specimens examined. Isla de Pascua, on Thespesia populnea (L.), April 2008, associated with Brevipalpus sp.; on Citrus Limon (L.), April 2008, associated with Brevipalpus sp.. Measurements of a collected female: dorsal shield 350 long, maximum width 210. Setae: j 1 34, j 3 54, j 4 5, j 5 5, j 6 5, J2 4, J5 5, z 2 5, z 4 5, z 5 6, Z 1 6, Z 4 123, Z 5 250, s 4 93, S 2 5, S 4 5, r 3 6, R 1 6, Sge IV 104, Sti IV 84, St IV 71. Remarks. These measurements are similar to those of the original description of the species., Published as part of Trincado, R. D., Martin, J. P. I., M��ndez Rosa, D. D., Lopes, P. C. & De Moraes, G. J., 2018, Phytoseiid mites (Acari: Phytoseiidae) from Chile, with descriptions of three new species and a redescription of Chileseius camposi, pp. 322-340 in Zootaxa 4482 (2) on page 323, DOI: 10.11646/zootaxa.4482.2.5, http://zenodo.org/record/1440610, {"references":["Blommers, L. (1974) Species of the genus Amblyseius Berlese, 1914, from Tamatave, east Madagascar (Acarina: Phytoseiidae). Bulletin Zoologisch Museum Universiteit van Amsterdam, 3, 143 - 155.","Moraes, G. J. de, McMurtry, J. A. & Denmark, H. A. (1986) A Catalog of the Mite Family Phytoseiidae. References to Taxonomy, Synonymy, Distribution and Habitat. EMBRAPA - DDT, Brasilia, 353 pp.","Abo-Shnaf, R. I. A., Sanchez, L. & de Moraes, G. J. (2016) Plant inhabiting Gamasina mites (Acari: Mesostigmata) from the Dominican Republic, with descriptions of four new species of Lasioseius (Blattisociidae) and complementary descriptions of other species. Systematic & Applied Acarology, 21 (5), 607 - 646. https: // doi. org / 10.11158 / saa. 21.5.5"]}

Metaseiulus (Metaseiulus) brevicollis Gonzalez & Schuster Metaseiulus brevicollis Gonzalez & Schuster, 1962: 19. Galendromus (Cursoriseius) brevicollis.��� Moraes et al., 1986: 186. Metaseius (Metaseius) brevicollis.��� Moraes et al., 2004: 278. Specimens examined. Santiago Region. Municipality of La Pintana, on Buddleja globosa Hope, July 2002, associated with Brevipalpus sp. Measurements of a collected female: dorsal shield 377 long, 200 maximum width; j 1 25, j 3 35, j 4 20, j 5 20, j 6 27, J 2 30, J 5 13, z 2 27, z 3 27, z 4 30, z 5 20, Z 4 52, Z 5 72, s 4 42, s 6 37, S 5 50, r 3 32, R 1 35. Remarks. These measurements are similar to those reported for the holotype in the original description and in the redescription by Chant &Yoshida-Shaul (1984)., Published as part of Trincado, R. D., Martin, J. P. I., M��ndez Rosa, D. D., Lopes, P. C. & De Moraes, G. J., 2018, Phytoseiid mites (Acari: Phytoseiidae) from Chile, with descriptions of three new species and a redescription of Chileseius camposi, pp. 322-340 in Zootaxa 4482 (2) on page 332, DOI: 10.11646/zootaxa.4482.2.5, http://zenodo.org/record/1440610, {"references":["Gonzalez, R. H. & Schuster, R. O. (1962) Especies de la familia Phytoseiidae en Chile I. (Acarina: Mesostigmata). Boletin Tecnico. Estacion Experimental Agronomica. Universidad de Chile, Facultad de Agronomia, Chile, 16, 1 - 35.","Moraes, G. J. de, McMurtry, J. A. & Denmark, H. A. (1986) A Catalog of the Mite Family Phytoseiidae. References to Taxonomy, Synonymy, Distribution and Habitat. EMBRAPA - DDT, Brasilia, 353 pp.","Moraes, G. J. de, McMurtry, J. A. & Denmark, H. A. (2004) A revised catalog of the mite family Phytoseiidae. Zootaxa, 434 (1), 1 - 494. https: // doi. org / 10.11646 / zootaxa. 434.1.1","Chant, D. A. & Yoshida-Shaul, E. (1984) A world review of four species groups in the genus Typhlodromus Scheuten (Acari: Phytoseiidae): brevicollis, luculentis, carinulatus, and pinnatus. Canadian Journal of Zoology, 62, 2631 - 2642. https: // doi. org / 10.1139 / z 84 - 383"]}

Euseius fructicolus (Gonzalez & Schuster) Amblyseius fructicolus Gonzalez & Schuster, 1962: 12 Euseius fructicolus.— Moraes et al., 1986: 45; 2004: 69; Lopes et al., 2015: 182; Ferragut & Navia, 2015: 542. Specimens examined. Santiago Region. Municipality of Buin, on Prunus avium (L.), April 1990, associated with Panonychus ulmi (Koch) and February 1991, associated with Bryobia rubrioculus (Scheuten); on Quillaja saponaria Mol., August 2002 and Rafanus sativus L., July 2002, associated with Brevipalpus sp.. Municipality of San José de Maipo: on Aristotelia chilensis (Mol.), February 2000, associated with Tetranychus urticae Koch; on Citrus limon L., September 2002, associated with Panonychus citri (McGregor). Municipality of Curacaví, on Cissus striata (Ruiz & Pav.), March 1994, associated with Tydeidae; on Persea lingue (Ruiz et Pav.), February 2002 associated with Oligonychus yothersi (McGregor). Municipality La Pintana: on Aloysia triphylla Palau, July 2002 and Corylus avellana L., March 2000, associated with T. urticae; on Aristotelia chilensis (Mol.), August 2002, associated with Tydeidae; on Azara serrata Ruiz & Pav., September 2002; on Melia azedarach Mill., March 2000, Pelargonum hortorum L. H. Bailey, April 2001, Malva nicaensis All., July 2002, Buddleja globosa Hope, July 2002 and Ligustrum sinense Lour., August 2002, associated with Brevipalpus sp.; on Corylus sativa Poit. & Turpin, April 2002 and Schinus poligamus (Cav.), July 2002, associated with Oligonychus sp.; on Crinodendron patagua Mol., July 2002 and Schinus molle L., August 2002, associated with Eriophyidae; on Juglans regia L., March 2000, associated with Oligonychus yothersi (McGregor); on Maytenus boaria Mol., July 2002, associated with Saissetia oleae Oliver; on Malus domestica Borkh., March 2000, associated with Aculus schlechtendali (Nalepa); on Prunus domestica L., March 2002, associated with Panonychus ulmi (Koch) and April 2001, associated with Aculus fockeui (Nalepa & Trouessart); on Prunus salicina Lindl., March 2002, associated with Bryobia rubrioculus (Scheuten); on Vitis vinifera L., April 2001, associated with Oligonychus vitis Zaher & Shehata and February 2002, associated with Colomerus vitis (Pagenstecher). Municipality of Renca, on Solanum lycopersicum L., March 2000, associated with Aculops lycopersici (Masse). Valparaiso Region—Municipality of Los Andes, on V. vinifera L., January1991, associated with Drepanothrips reuteri (Uzel). Municipality of Valparaiso: knoll Miraflores, on Ricinus communis L., August 1999, associated with Tetranychidae. Measurements of a collected female: dorsal shield 325 long, 210 maximum width; j 1 27, j 3 37, j 4 17, j 5 12, j 6 10, J 2 15, J 5 8, z 2 22, z 4 30, z 5 17, Z 1 17, Z 4 20, Z 5 47, s 4 37, S 2 22, S 4 17, S 5 22, r 3 17, R 1 11, Sge IV 32, Sti IV 31, St IV 50. Remarks. These measurents are similar to those of the original description.

Amblyseius herbicolus (Chant) Typhlodromus (Amblyseius) herbicolus Chant, 1959: 84. Amblyseius herbicolus.��� Daneshvar & Denmark, 1982: 5; Moraes et al., 1986: 14; 2004: 27. Specimens examined. Isla de Pascua, on Thespesia populnea (L.), April 2008, associated with Brevipalpus sp.; on Mangifera indica L., April 2008, associated with Tydeidae; on Citrus limon (L.), August 2008, associated with Brevipalpus sp.. Measurements of a collected female: dorsal shield 370 long, maximum width 239. Setae j 1 39, j 3 41, j 4 9, j 5 6, j 6 6, J 2 8, J5 11, z 2 14, z 4 10, z 5 6, Z 1 9, Z 4 94, Z 5 47, s 4 98, S 2 11, S 4 10, S 5 9, r 3 14, R 1 10, Sge IV 110, S ti IV 82, St IV 74. Remarks. These measurements are similar to those of Guanilo et. al. (2008) for specimens from Peru., Published as part of Trincado, R. D., Martin, J. P. I., M��ndez Rosa, D. D., Lopes, P. C. & De Moraes, G. J., 2018, Phytoseiid mites (Acari: Phytoseiidae) from Chile, with descriptions of three new species and a redescription of Chileseius camposi, pp. 322-340 in Zootaxa 4482 (2) on page 323, DOI: 10.11646/zootaxa.4482.2.5, http://zenodo.org/record/1440610, {"references":["Chant, D. A. (1959) Phytoseiid mites (Acarina: Phytoseiidae). Part I. Bionomics of seven species in southeastern England. Part II. A taxonomic review of the family Phytoseiidae, with descriptions of thirty-eight new species. The Canadian Entomologist, 12 (Supplement), 1 - 166.","Daneshvar, H. & Denmark, H. A. (1982) Phytoseiids of Iran (Acarina: Phytoseiidae). International Journal of Acarology, 8, 3 - 14. https: // doi. org / 10.1080 / 01647958208683272","Moraes, G. J. de, McMurtry, J. A. & Denmark, H. A. (1986) A Catalog of the Mite Family Phytoseiidae. References to Taxonomy, Synonymy, Distribution and Habitat. EMBRAPA - DDT, Brasilia, 353 pp."]}

Arrenoseius robertogonzalezi Trincado & Martin, n. sp. Diagnosis. This species is most similar to Arrenoseius morgani (Chant, 1957), but the latter differs by having much longer j 1, j 3, s 4, Z 4 and Z 5 and the much shorter z 2 and z 4, and by having no teeth on the movable cheliceral digit. Female: (4 specimens measured) Dorsum (Fig. 1). With seven distinguishable pairs of pores and 11 distinguishable pairs of lyrifissures; 389 (360–407) long, 320 (300–330) maximum width; j 1 17 (16–18), j 3 25 (24–26), j 4 8 (7–9), j 5 8 (6–9), j 6 8 (6–9), J 2 8 (7–9), J 5 10 (8–11), z 2 16 (14–18), z 4 24 (23–25), z 5 6 (6–7), Z 1 11 (10–12), Z 4 71 (68–75), Z 5 89 (85–96), s 4 54 (50–57), S 2 17 (15–18), S 4 15 (14–16), S 5 17 (15–19), r 3 21 (20–22), R 1 16 (15–17). All setae smooth. Peritreme (Fig. 1). Extending forward to level of j 1. Venter (Fig. 2). Sternal shield reticulate; with two pairs of lyrifissures; distances between St 1– St 3 61 (60–64), St 2– St 2 64 (60–65). Genital shield with striae forming an inverted U-shaped pattern; distance between St 5– St 5 92 (89–94). Ventrianal shield reticulate, shield-shaped 123 (120–130) long and 142 (100–165) wide at ZV 2 level, with three pairs of pre-anal setae and a very pair of small, rounded pre-anal pores posteromesad of JV 2. Seta JV 5 50 (50–51). All ventral setae smooth. Two pairs of metapodal plates, the inner rounded and much smaller than the elongate outer pair. Chelicera (Fig. 3). Antiaxial lyrifissure distinct. Fixed digit 34 (33–35) long, with eight teeth in addition to apical tooth and setiform pilus dentilis. Movable digit 35 (35–36) long, with two teeth in addition to apical tooth. Legs (Fig. 4). Macroseta present only on tarsus IV, 61 (60–64). Chaetotaxy of genu II 2 2/1, 2/0 1; genu III 1 2/ 1, 2/0 1. Spermatheca (Fig. 5). Calyx saccular, 18 (17–20) long. Atrium distinct. Etymology. This species is named after Prof. Roberto H. González, eminent Chilean acarologist and entomologist, who regretfully passed away recently. Type locality: Holotype female collected on 2 April 1991, from Municipality of Buin, Santiago Region, Chile, on Festuca sp. Deposited at Departamento de Entomologia e Acarologia, Escola Superior de Agricultura “Luiz de Queiroz”, Universidade de São Paulo. Three paratype females collected on 9 July 2012, from Quinta de Tilcoco, O’Higgins Region, Chile, on Viburnum tinus L., associated with Tydeidae; all deposited at Departamento de Entomologia e Acarologia, Escola Superior de Agricultura “Luiz de Queiroz”, Universidade de São Paulo. Two paratype females collected on 5 November 2002, from San Pedro, Santiago Region, on Passiflora incarnata L, associated with Tydeidae, deposited at Museo Nacional de Historia Natural, Santiago to Chile.

Neoseiulus anonymus (Chant & Baker) Amblyseius anonymus Chant & Baker, 1965: 21. Neoseiulus anonymus.��� Moraes et al., 1986: 68; 2004: 102. Specimens examined. Santiago Region. Municipality of Pudahuel, on Convulvulus arvensis L., March 2011 and Marrubium vulgare L., May 2011, associated with Tetranychus urticae Koch. Measurements of a studied female: dorsal shield 341 long, 154 maximum width; j 1 25, j 3 56, j 4 50, j 5 50, j 6 62, J 2 56, J 5 12, z 2 53, z 4 50, z 5 37, Z 1 56, Z 4 75, Z 5 76, s 4 55, S 2 68, S 4 35, S 5 30, r 3 37, R 1 43, St IV 50. Remarks. Most of these measurements of the specimen studied in this work are slightly longer than reported by Schicha & Elshafie (1980) for the holotype of N. anonymus, which is compatible with the larger size of the former; the exceptions are the slightly shorter S 4 and macroseta of tarsus IV (respectively 43 and 54���67 in the holotype)., Published as part of Trincado, R. D., Martin, J. P. I., M��ndez Rosa, D. D., Lopes, P. C. & De Moraes, G. J., 2018, Phytoseiid mites (Acari: Phytoseiidae) from Chile, with descriptions of three new species and a redescription of Chileseius camposi, pp. 322-340 in Zootaxa 4482 (2) on page 328, DOI: 10.11646/zootaxa.4482.2.5, http://zenodo.org/record/1440610, {"references":["Chant, D. A. & Baker, E. W. (1965) The Phytoseiidae (Acarina) of Central America. Memoirs of the Entomological Society of Canada, 41, 1 - 56.","Moraes, G. J. de, McMurtry, J. A. & Denmark, H. A. (1986) A Catalog of the Mite Family Phytoseiidae. References to Taxonomy, Synonymy, Distribution and Habitat. EMBRAPA - DDT, Brasilia, 353 pp.","Schicha, E. & Elshafie, M. (1980) Four new species of phytoseiid mites from Australia, and three species from America redescribed (Acari: Phytoseiidae). Journal of the Australian Entomological Society, Australia, 19, 27 - 36."]}

Chileseius paracamposi Yoshida-Shaul & Chant Chileseius paracamposi Yoshida-Shaul & Chant, 1991: 95. Chileseius paracamposi.��� Moraes et al., 2004: 58; Ferragut & Navia, 2015: 527. Specimens examined. Magallanes Region. Municipality of Punta Arenas, on Nothophagus pumilio (P. et. E.), November 2012., Published as part of Trincado, R. D., Martin, J. P. I., M��ndez Rosa, D. D., Lopes, P. C. & De Moraes, G. J., 2018, Phytoseiid mites (Acari: Phytoseiidae) from Chile, with descriptions of three new species and a redescription of Chileseius camposi, pp. 322-340 in Zootaxa 4482 (2) on page 327, DOI: 10.11646/zootaxa.4482.2.5, http://zenodo.org/record/1440610, {"references":["Moraes, G. J. de, McMurtry, J. A. & Denmark, H. A. (2004) A revised catalog of the mite family Phytoseiidae. Zootaxa, 434 (1), 1 - 494. https: // doi. org / 10.11646 / zootaxa. 434.1.1","Ferragut, F. & Navia, D. (2015) Phytoseiid mites (Acari: Phytoseiidae) from Patagonia and Tierra del Fuego. Zootaxa, 3990 (4), 525 - 550. https: // doi. org / 10.11646 / zootaxa. 3990.4.3"]}

A total of 40 phytoseiid species has been reported from Chile, including the two species (Neoseiulus californicus (McGregor) and Phytoseiulus persimilis (Athias-Henriot) most widely used worldwide for the biological control of the two-spotted spider mite, Tetranychus urticae Koch (Tetranychidae). In this paper we report nine other species found in new collecting conducted since 1989, including three new species: Amblyseius herbicolus (Chant), Amblyseius tamatavensis Blommers, Arrenoseius robertogonzalezi Trincado & Martin n. sp., Neoseiulus anonymus (Chant & Baker), Neoseiulus bicaudus (Wainstein), Neoseiulus viticolus Trincado & Martin n. sp., Metaseiulus (Metaseiulus) camelliae (Chant & Yoshida-Shaul), Metaseiulus (Metaseiulus) neoflumenis Moraes & Kreiter and Metaseiulus (Metaseiulus) relictus Trincado & Martin n. sp.. Chileseius camposi Gonzalez & Schuster, 1962 is redescribed, and a list of all species presently known from Chile and a key to help in their separation are given. A new name, Proprioseiopsis kargi Trincado nom. nov., is a replacement name for Proprioseiopsis globosus Karg, 1976, a junior homonym of Proprioseiopsis globosus (Gonzalez & Schuster, 1962).

La parroquia Panaquire del estado Miranda, suele inundarse cuando aumenta el caudal del Río Tuy. Los Sistemas de Alerta Temprana (SAT) permiten alertar y dirigir acciones apropiadas en caso de desastres, reduciendo pérdidas y daños, cultura preventiva necesaria que puede crearse gracias al apoyo de las instituciones educativas. El objetivo de investigación fue diseñar una propuesta educativa ambiental para incorporar los SAT en las comunidades educativas como en la U.E.N "Liceo Bolivariano Panaquire", proyecto factible que permitirá mejorar la calidad de vida de la comunidad. La investigación se llevó a cabo en tres fases: (a) diagnóstico, aplicando una encuesta a 13 docentes de la U.E.N "Liceo Bolivariano Panaquire", (b) diseño y elaboración de la propuesta, (c) validación y estudio de factibilidad. Los resultados demuestran la relevancia de la propuesta porque los participantes desconocían los SAT. Recomendamos continuar con la investigación apoyando a la comunidad educativa para consolidar la creación del SAT. The state of Miranda Panaquire parish, usually flooded with increasing flow Tuy River. Early Warning System (EWS) allow appropriate alert and direct disaster actions, reducing loss and damage, preventive culture needed to be created through the support of educational institutions. The research objective was to design an environmental education proposal to incorporate the EWS in the educational communities and the N.E.U. "Bolivarian High School Panaquire" feasible project that will improve the quality of life of the community. The research was conducted in three phases: (a) diagnosis, through a survey of 13 teachers from the N.E.U. "Bolivarian High School Panaquire", (b) design and development of the proposal, (c) validation and feasibility study. The results demonstrate the relevance of the proposal because participants unknown the EWS. We recommend continued research supporting the educational community to consolidate the creation of the EWS.

Se evaluó la precisión y exactitud en la estimación de la grasa corporal (%) por absorciometría dual de rayos X (DXA Lunar-DPX-MD) comparado con el modelo de cuatro compartimentos (4C) en 32 púberes (F=16) de 9 a 14 años. El sesgo entre la DXA y el modelo de 4C fue de -3.5% de grasa (r=0.25; p=0.171) con un intervalo de confianza de -1.9 a -5.1 (p=0.050). Los límites de concordancia al 95% fueron de +5% a -12% de grasa. El coeficiente de correlación de concordancia fue de pc=0.85. La prueba de exactitud por análisis de regresión mostró que el intercepto y la pendiente de las estimaciones de grasa corporal por DXA fueron diferentes al modelo de 4C (p>0.05). La precisión evaluada con el valor de R2 mostró que la DXA explicó el 83% de la varianza de la grasa corporal por el modelo de 4C con un error de 4.1%. El error total como medida de exactitud fue de 5.6%. La exactitud grupal evaluada por análisis de varianza no mostró interacción entre el método (DXA-4C) y el análisis por separado del sexo, el estado puberal y la presencia de sobrepeso. No obstante, hubo efecto del método (p=0.043) en presencia de sobrepeso (p

En este artículo se pretende dar cuenta de algunas de las conclusiones de una investigación realizada sobre “Las actitudes de los estudiantes hacia la Universidad como indicador de calidad”. Para ello, procedemos a articular el discurso en cuatro apartados: en primer lugar, establecemos el papel del estudiante universitario en el marco del discurso sobre los retos que plantea el EEES; en segundo lugar, presentamos de forma muy breve el trabajo de investigación realizado; en tercer lugar informamos sobre las conclusiones a las que hemos llegado y que contribuyen a describir el grado de (des)orientación estudiantil ante los nuevos retos que plantea el EEES, y finalmente planteamos una serie de recomendaciones para la mejora de este ámbito, pues es importante para la consecución de un desarrollo integral de los estudiantes en el marco de la convergencia.

Validerat; 20101217 (root)

[ES] Se plantea este estudio sobre el chorizo rojo de Teror, debido a la falta total y absoluta de definición de este alimento tradicional. Muchos elaboradores comercializan este alimento sin un referente de calidad y seguridad alimentaria básico, existiendo la necesidad de ofertar un producto de calidad contrastada al consumidor canario que demanda alimentos tradicionales para incorporar a su dieta. Por ello, se ha estudiado el proceso de elaboración, la evolución de los parámetros químicos y los parámetros de estabilidad (aw y pH), así como de los principales grupos microbianos presentes en dicho producto y la evaluación de los posibles riesgos asociados a la formulación de aditivos.

Validerat; 20101217 (root)

La dieta en países en vías de desarrollo está constituida por cereales y legumbres que si bien aportan cantidades importantes de hierro (Fe) y zinc (Zn), resultan ser minerales de baja disponibilidad. Los objetivos del presente trabajo fueron: 1) cuantificar el contenido total y dializable de Fe y Zn en alimentos del norte (Sonora) y del sur (Oaxaca) de México; 2) evaluar el efecto de la presencia de carne sobre los valores de Fe y Zn dializables. La cuantificación de Fe y Zn total y dializable se hizo por el método de la AOAC y de Shen et al, respectivamente. Los resultados obtenidos para Fe total en alimentos de Sonora presentaron un rango de 0.78±0.0 a 11.59±0.03 mg/100g (base seca, BS); y en los de Oaxaca de 0.86±0.18 a 8.8±0.57 mg/100g (BS). Para Zn total los valores variaron de 0.91± 0.00 a 13.58± 0.05 mg/100g (BS) en Sonora y de 0.64±0.18 a 20.80±0.33 mg/100 g (BS) en Oaxaca. En los alimentos de Sonora se tuvieron valores de 0.1± 0.04% a 10.6± 0.36% para Fe dializable y de 4.0± 0.21 % a 55.32± 0.14% para Zn dializable. En los de Oaxaca el rango fue de 0.22± 0.06 % a 9.40± 0.14% para Fe dializable y de 2.41± 0.26% a 54.27± 1.49% para Zn dializable. Se obtuvo un promedio mayor en el contenido de Fe dializable en los alimentos que contenían carne, respecto a los que no la contenían y entre el frijol pinto y las tortillas de maíz de Sonora respecto al frijol negro y tortillas de maíz rurales de Oaxaca. El contenido de Zn dializable no mostró diferencias significativas entre los alimentos de las dos regiones. Developing countries diets are based on a variety of plant foods that often are the main suppliers of important amounts of iron (Fe) and zinc (Zn). The objectives of this study were 1) to measure the total and dialyzable amounts of Fe and Zn in foods from Northern Mexico (Sonora) and from Southern Mexico (Oaxaca) and 2) to evaluate the effect of meat content of diets on the dialyzable amount of Fe and Zn. Methods to calculate the total dialyzable amount of Fe and Zn, were those of the AOAC and of Shen et al. Total Fe in e northern Mexican foods went from 0.78 ± 0.0 to 11.59 ± to 0.03 mg/100g (dry weight, DW); in southern Mexican foods the same micronutrient amounts were 0.86 ± 0.18 to 8.8 ± 0.57 mg/100g (BS). Total Zn values were 0.91 ± 0.00 to 13.58 ± 0.05 mg/100g (DW) in Sonora, and 0.64 ± 0.18 to 20.80± 0.33 mg/100 g (DW) in Oaxaca. In northern Mexico, foods dialyzable Fe had values from 0.1 ± 0.04 % to 10.6 ± 0.36% and for Zn from 4.0 ± 0.21% to 55.32 ± 0.14%. Meanwhile, the range of values of dialyzable Fe for foods from Oaxaca were from 0.22 ± 0.06% to 9.40 ± 0.14% for and from 2.41 ± 0.26% to 54.27 ± 1.49% for dialyzable Zn. The average value for dialyzable Fe was higher in the foods that contained meat or meat products (p= 0.001).

El trabajo se realizó en el bosque seco caducifolio localizado en Rio Escalante del Refugio de Vida Silvestre de Chacocente. El objetivo es tener una primera descripción de las características ... edafológicas y florística de las cuatro parcelas de muestreo ,permanente. El estudio se efectuó en parcelas de 1 ha cada una, se determinó su composición florística existente, como tambien la ubicación, descripción y toma de muestras de los perfiles de suelos para su análisis físicos y químicos obteniendo así su clasificación. En las cuatro parcelas se encontraron diferentes tipos de suelos, la PMP-1 con un tipo de suelo Typic Cromusthers, PMP-2 Typic Ustropepts, en la PMP-3 Durorthidic Ustortents y la PMP-4 Udic Haplustalts. Se identificaron 76 especies arbóreas con diecinueve especies comúnes para las cuatros parcelas sobresaliendo la familia: fabaceae.