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Anastrepha mitaraka Norrbom, new species Figs. 11, 54, 109, 134 urn:lsid:zoobank.org:act: E1986F6E-DE16-4F86-9D18-7E392CFAB135 Diagnosis. Anastrepha mitaraka can be distinguished from other species of Anastrepha by the following combination of characters: V-band complete, connected to S-band; subapical hyaline area in radial cells distal to crossvein r-m extending anteriorly into cell r 1; oviscape 0.79 times as long as mesonotum; aculeus 2.34 mm long, ventrally curved; tip 0.25 mm long, nonserrate. In the key of Zucchi et al. (2011) it runs to A. flavipennis Greene, from which it differs in having cell bm hyaline and the aculeus more than 2.0 mm long, or A. belenensis Zucchi, from which it differs in having the V-band complete and connected to the S-band, the subapical hyaline area in the radial cells extending into cell r 1, and lacking a constriction near midlength on the aculeus tip. One sequence of A. mitaraka (MT 763869), from the holotype from French Guiana, was included in the COI barcode analysis of Moore et al. (in prep.). The smallest interspecific K2P distance was 5.6% with A. flavipennis Greene. Description. Mostly yellow to orange. Setae orange brown to red brown. Head: Yellow to orange except brown ocellar tubercle. 3 frontal setae; 2 orbital setae, posterior seta well developed. Ocellar seta weak, approximately as long as ocellar tubercle. Facial carina, in profile, straight on dorsal twothirds. Antenna not extended to ventral facial margin. Palpus in lateral view dorsally curved, evenly setulose. Thorax: Mostly yellow to orange, most of scutum orange; with following areas white to pale yellow (poorly differentiated in holotype): postpronotal lobe and lateral margin of scutum bordering it; medial scutal vitta, broadly quadrate posteriorly, extending laterally to dorsocentral seta; sublateral scutal vitta from transverse suture to posterior margin, including base of intra-alar seta; scutellum; dorsal margins of anepisternum and katepisternum; katepimeron; and most of anatergite and katatergite. Scuto-scutellar suture without brown spot medially. Subscutellum and mediotergite entirely orange. Mesonotum 3.32 mm long. Postpronotal lobe, notopleuron, scutum and scutellum entirely microtrichose; scutal setulae orange, evenly distributed sublaterally. Chaetotaxy typical for genus. Katepisternal seta absent. Legs: Entirely yellow to orange. Wing (Fig. 54): Length 7.09 mm, width 3.08 mm, ratio 2.30. Apex of vein R 1 at 0.55 wing length, proximal to level of anterior end of crossvein r-m. Cell c 1.19 times as long as pterostigma; pterostigma 3.41 times as long as wide. Vein R 2+3 slightly sinuous. Crossvein r-m at 0.64 distance from bm-m to dm-m on vein M 1. Vein M 1 strongly curved apically; cell r 4+5 at apex 0.90 times as wide as at level of dm-m, 0.69 times as wide as maximum subapical width. Cell cu a with distal lobe moderately long, length of cu a 1.66 times as long as anterior margin, lobe 0.87 times as long as vein CuA+CuP. Wing pattern mostly orange and moderate brown. C-band mostly orange, cells bc and c orange, pterostigma mostly brown, distal margin in cells r 1 and r 2+3 narrowly brown, with small ovoid dark brown spot on fork of vein Rs, and with elongate faint brown marking in cell br opposite cell bm and with posterior margin of band in cell br narrowly brown. C-band and S-band broadly connected along vein R 4+5; hyaline marginal spot in cell r 1 subtriangular, with apex aligned proximal to anterior end of crossvein r-m. Basal hyaline area in cell dm relatively small. Basal half of S-band relatively broad, mostly orange, anterobasal margin mostly narrowly brown in cells r 1, r 2+3 and br, posterodistal margin mostly narrowly brown, but broadly posteriorly in cell m 4 extending to apex of lobe of cell cu a, with weak incision in cell m 4 (this area with teneral streak in holotype, perhaps normally without incision); distal section mostly orange, with margins in cells r 1 and r 2+3 and all of part in cell r 4+5 moderate brown; medium width, at apex of vein R 2+3 0.56 times width of cell r 2+3, slightly broader along vein R 4+5, barely extended to apex of vein M 1, without marginal hyaline areas; hyaline area proximal to apex of band extended into cell r 1. V-band with proximal arm moderately broad, mostly brown except for most of part in cell r 4+5, except proximal margin, and bordering most of crossvein dm-m; broadly connected to S-band along vein R 4+5; on posterior margin extended approximately three-fourths distance to vein CuA+CuP; distal arm slender, brown except anteriorly, connected to proximal arm; hyaline area between arms of V-band and vein M 1 approximately one-third width of cell cell r 4+5. Abdomen: Mostly orange, without brown markings. Female terminalia: Oviscape 2.61 mm long, 0.79 times as long as mesonotum; entirely orange; spiracle at basal 0.33. Eversible membrane not everted, partially visible through oviscape, with approximately 20 dorsobasal denticles in subtriangular pattern. Aculeus (Fig. 109) slightly ventrally curved in lateral view, 2.34 mm long, 0.90 times oviscape length; in ventral view base distinctly expanded, triangular, 0.23 mm wide, shaft 0.12 mm wide at midlength; tip (Fig. 134) 0.25 mm long, 0.11 times aculeus length, 0.08 mm wide at base and preapically, 3.13 times as long as wide; in ventral view gradually tapered, nonserrate; 0.07 mm wide in lateral view, 0.88 times ventral width. Spermathecae not examined. Distribution. Anastrepha mitaraka is known only from French Guiana. Biology. The host plants and other aspects of the biology of this species are unknown. Type data. Holotype ♀ (MNHNP USNMENT00875225), FRENCH GUIANA: [Saint-Laurent du Maroni: Maripasoula,] Mitaraka, site MIT-DZ, 2°14’1.8”N 54°27’1”W, 306 m, 1 Mar 2015, SLAM, J. Touroult & E. Poirier / MITARAKA/218 La Planète Revisitée —MNHN/PNI Guyane 2015. Etymology. The name of this species is a noun in apposition, the name of the region where the holotype was collected. Comments. This species has not been placed in a species group. In the COI analysis of Moore et al. (in prep.) it was placed as the sister group of A. flavipennis Greene., Published as part of Norrbom, Allen L., Muller, Alies, Gangadin, Anielkoemar, Sutton, Bruce D., Rodriguez, Erick J., Savaris, Marcoandre, Lampert, Silvana, Rodriguez, Pedro A., Steck, Gary J., Moore, Matthew R., Nolazco, Norma, Troya, Henry, Keil, Clifford B., Padilla, Anabel, Wiegmann, Brian M., Cassel, Brian, Branham, Marc & Ruiz-Arce, Raul, 2021, New species and host plants of Anastrepha (Diptera: Tephritidae) primarily from Suriname and Pará, Brazil, pp. 1-74 in Zootaxa 5044 (1) on pages 28-29, DOI: 10.11646/zootaxa.5044.1.1, http://zenodo.org/record/5532026, {"references":["Zucchi, R. A., Uramoto, K. & Souza-Filho, M. F. de (2011) Chave ilustrada para as especies de Anastrepha da regiao Amazonia brasileira. In: Adaime da Silva, R., Lemos, W. P. & Zucchi, R. A. (Eds.), Moscas-das-frutas na Amazonia brasileira: Diversidade, hospedeiros e inimigos naturais. Embrapa Amapa, Macapa, pp. 71 - 90."]}

Anastrepha curvivenis Norrbom, new species Figs. 5, 6, 35–39, 79–81, 101–102, 125–126, 151–152 urn:lsid:zoobank.org:act: 4E08C8D0-5E5A-44B5-AE48-80D898AE6F89 Diagnosis. Anastrepha curvivenis can be distinguished from other species of Anastrepha by the following combination of characters: Setae dark redbrown to black; C-band and S-band separated; V-band complete, separated from S-band; vein M 1 very strongly curved apically (cell r 4+5 at apex 0.67–0.76 times as wide as at level of dm-m), reaching or almost reaching apex of S-band; oviscape 4.83–5.48 mm long, 1.32–1.41 times as long as mesonotum; aculeus tip nonserrate, relatively long (0.54–0.61 mm), and tapered most strongly subbasally; lateral surstylus short, with basolateral lobe; phallus> 5 mm long. It resembles A. costalimai Autuori, A. leptozona Hendel and A. barnesi Aldrich in wing pattern and venation and surstylus shape but differs from them in terminalia length and the shape of the aculeus tip. It also differs from the latter two species in lacking serrations on the aculeus tip. It resembles A. galbina Stone in the shape and length of the aculeus tip, but differs in having the V-band complete, vein M 1 more strongly curved apically, and the terminalia slightly longer. It also resembles A. scobinae Stone in wing pattern and the length of the aculeus tip, but differs in having vein M 1 more strongly curved apically, the oviscape brown apically, fewer dorsobasal denticles on the eversible membrane, and the aculeus tip more strongly tapered subbasally. In the key of Zucchi et al. (2011) A. curvivenis runs to A. furcata Lima or A. hendeliana Lima, from which it differs in having the C-band and S-band separated, A. leptozona, from which it differs as indicated above, or A. dissimilis, from which it differs in having vein M 1 more strongly curved apically, longer terminalia, and a longer aculeus tip. Five sequences of A. curvivenis, from four adult specimens from Suriname (MT672181 – MT672184) and one from Ecuador (BCE1117688), were included in the COI barcode analysis of Moore et al. (in prep.). There were four unique sequences. The five sequences of A. curvivenis formed a separate cluster (i.e., with a COI barcode gap), with a range in intraspecific K2P distance of 0.0–0.6%. The smallest interspecific K2P distance was 5.9% with A. leptozona. Description. Mostly yellow to orange. Setae dark red brown to black. Head: Yellow to orange except brown ocellar tubercle. 3–5 frontal setae; 2 orbital setae, posterior seta well developed. Ocellar seta weak, 1–2 times as long as ocellar tubercle. Facial carina, in profile, straight or concave on dorsal two-thirds. Antenna not extended to ventral facial margin. Palpus in lateral view dorsally curved, evenly setulose. Thorax: Mostly yellow to orange, most of scutum orange to dark orange; with following areas white to pale yellow: postpronotal lobe and lateral margin of scutum bordering it; medial scutal vitta, narrow anteriorly, quadrate posteriorly, extending laterally to dorsocentral seta; sublateral scutal vitta from transverse suture to posterior margin, including base of intra-alar seta; scutellum; dorsal margins of anepisternum and katepisternum; katepimeron; and most of anatergite and katatergite. Scutum usually with narrow orange brown to brown band on posterior margin, often darkest laterally, not extended laterally to intra-alar seta; in Brazilian and Peruvian females absent or present only as diffusely brownish area between dorsocentral and intra-alar lines. Subscutellum and mediotergite entirely orange. Mesonotum 3.50–4.23 mm long. Postpronotal lobe, notopleuron, scutum and scutellum entirely microtrichose; scutal setulae orange, sometimes brownish on lateral margin, evenly distributed sublaterally. Chaetotaxy typical for genus. Katepisternal seta weak, orange, less than one-third length of anepisternal seta. Legs: Entirely yellow to orange. Wing (Figs. 35–39): Length 7.09–8.84 mm, width 2.91–3.65 mm, ratio 2.42–2.56. Apex of vein R 1 at 0.53–0.55 wing length, proximal to level of anterior end of crossvein r-m. Cell c 1.06–1.20 times as long as pterostigma; pterostigma 3.76–4.44 times as long as wide. Vein R 2+3 not sinuous. Crossvein r-m at 0.66–0.70 distance from bm-m to dm-m on vein M 1. Vein M 1 very strongly curved apically; cell r 4+5 at apex 0.67–0.76 times as wide as at level of dm-m, 0.55–0.59 times as wide as maximum subapical width. Cell cu a with distal lobe relatively long, length of cu a 1.65–1.82 times as long as anterior margin, lobe 0.71–0.83 times as long as vein CuA+CuP. Wing pattern mostly orange and moderate brown. C-band mostly orange, cells bc and c paler, bc and posterior part of cell c often subhyaline, pterostigma mostly moderate brown, distal margin of band in cells r 1 and r 2+3 narrowly brown, with small dark brown mark on fork of vein Rs, and in cell br usually with small to elongate irregular brown area in part anterior to cell bm and with elongate brown mark on distal margin of band. C-band and S-band broadly separated by hyaline band from cell bm to costa, usually slightly narrowed along vein R 4+5. Basal hyaline area in cell dm relatively large. Basal half of S-band relatively narrow, mostly orange, anterobasal margin mostly narrowly brown in cells br, r 1, and r 2+3, posterodistal margin narrowly brown anteriorly, more broadly posteriorly in cell m 4, extending to or usually into lobe of cell cu a, with weak or no incision in cell m 4; distal section orange, with most of margins and part in cell r 4+5 moderate brown; relatively broad, at apex of vein R 2+3 0.72–0.87 times width of cell r 2+3, extended to or almost to apex of vein M 1, without marginal hyaline areas; hyaline area proximal to apex of band extended to vein R 2+3. V-band with proximal arm relatively broad, mostly brown, orange medially in cell r 4+5 and bordering anterior part of crossvein dm-m; separated from S-band along vein R 4+5; on posterior margin extended two-thirds to three-fourths distance to vein CuA+CuP; distal arm mostly to entirely brown, connected to proximal arm; hyaline area between arms of V-band and vein M 1 one-third to two-thirds width of cell cell r. 4+5 Abdomen: Mostly orange, without brown markings. Female terminalia: Oviscape 4.83–5.56 mm long, 1.30–1.41 times as long as mesonotum; orange basally, distal two-thirds darker orange brown to brown; spiracle at basal 0.25–0.29. Eversible membrane (Figs. 79–81) withdorsobasal denticles in short but very broad pattern, with 70–80 relatively stout hooklike denticles in more than 10 V-shaped rows. Aculeus (Figs. 101–102) ventrally curved in lateral view, 4.57–5.24 mm long, 0.93–0.99 times oviscape length; in ventral view base distinctly expanded, triangular, 0.24–0.26 mm wide, shaft 0.100 – 0.135 mm wide at midlength; tip (Figs. 125–126) 0.54–0.62 mm long, 0.11–0.12 times aculeus length, 0.11–0.14 mm wide at base, 0.114 –0.135 preapically, 4.43–5.09 times as long as wide; in ventral view tapered subbasally, then gradually, nonserrate; 0.06–0.09 mm wide in lateral view, 0.50–0.67 times ventral width. Spermathecae not examined. Male terminalia (Figs. 151–152): Epandrium slightly shorter than high in lateral view, in posterior view with posterodorsal margin without medial V-shaped indentation. Lateral surstylus without basolateral lobe, relatively short, extended beyond prensisetae by 0.50 times length of prensiseta; in lateral view short, truncate, with small posterodistal lobe; in posterior view short, apex somewhat truncate, with subapical lateral lobe, medial margin convex. Proctiger with ventral and lateral sclerotized areas connected. Phallus 5.5 mm long, 1.54 times as long as mesonotum; glans 0.4 mm long. Distribution. Anastrepha curvivenis is known from Brazil (Amazonas), Ecuador (Zamora-Chinchipe), Peru (San Martín), and Suriname. In Suriname it was collected at Berg en Dal, Brownsberg and Nassau, although in relatively small numbers. Biology. The host plants and other aspects of the biology of this species are unknown. Type data. Holotype ♀ (USNM USNMENT01527082), SURINAME: Brokopondo: Berg en Dal, Bergendal Resort, [exit road, hilltop, 5.14908°N 55.07515°W, 29 m,] trap BD-ML-12, [24 May –] 6 Jun 2019, A. Muller. Paratypes: BRAZIL: Amazonas: Coari, Rio Urucu, RUC-27, 4°49’34”S 65°15’37”W, at mercury vapor light, 5–18 Mar 1994, P. F. Bührnheim et alia, 2♀ (INPA USNMENT01526557–58). ECUADOR: Zamora-Chinchipe: Soapaca, 3.91114°S 78.8299°W, 854 m, 21 Mar 2017, D. Elizalde, 1♀ (CNREE-AGROCALIDAD E11-17688). PERU: San Martín: Tarapoto, trampa 2,2,6,2, 9 Feb 2006, 1♀ (SENASA USNMENT00744647). SURINAME: Brokopondo: Brownsberg Nature Park, Leo Val trail, 4.95234°N 55.18755°W, 472 m, trap BNP-ML-29, 21 Jul–20 Aug 2016, A. Gangadin, 1♀ (NZCS USNMENT00875205). Sipaliwini: Nassau, 4.81445°N 54.61536°W, mercury vapor light, black light blue (HPL /BLB), 22–31 Jul 2016, A. J. Hielkema, 1♂ 1♀ (USNM USNMENT00875206 USNMENT00875208); same, 23–30 Jul 2016, 1♀ (USNM USNMENT00875207). Etymology. The name of this species is a Latin adjective, from curvus, meaning curved, and vena, meaning vein, in reference to the strongly curved vein M 1. Comments. This species belongs to the leptozona species group as indicated by its wing pattern (C-band and S-band separated), venation (vein M 1 very strongly curved apically), and male surstylus shape (short, with lateroapical lobe). In the COI analysis of Moore et al. (in prep.), the five sequences of A. curvivenis form a separate cluster which is grouped with A. barnesi Aldrich and A. leptozona Hendel, other members of the leptozona group., Published as part of Norrbom, Allen L., Muller, Alies, Gangadin, Anielkoemar, Sutton, Bruce D., Rodriguez, Erick J., Savaris, Marcoandre, Lampert, Silvana, Rodriguez, Pedro A., Steck, Gary J., Moore, Matthew R., Nolazco, Norma, Troya, Henry, Keil, Clifford B., Padilla, Anabel, Wiegmann, Brian M., Cassel, Brian, Branham, Marc & Ruiz-Arce, Raul, 2021, New species and host plants of Anastrepha (Diptera: Tephritidae) primarily from Suriname and Pará, Brazil, pp. 1-74 in Zootaxa 5044 (1) on pages 15-17, DOI: 10.11646/zootaxa.5044.1.1, http://zenodo.org/record/5532026, {"references":["Zucchi, R. A., Uramoto, K. & Souza-Filho, M. F. de (2011) Chave ilustrada para as especies de Anastrepha da regiao Amazonia brasileira. In: Adaime da Silva, R., Lemos, W. P. & Zucchi, R. A. (Eds.), Moscas-das-frutas na Amazonia brasileira: Diversidade, hospedeiros e inimigos naturais. Embrapa Amapa, Macapa, pp. 71 - 90."]}

29. Anastrepha grandis (Macquart) Distribution in Bolivia: Chuquisaca (Norrbom 1991, Lobos 1997), Cochabamba (this publication), La Paz (Hendel 1914, Stone 1942, Foote 1967, Norrbom 1991, Hern��ndez-Ortiz & Aluja 1994, Lobos 1997, Conde Blanco et al. 2018), Santa Cruz (this publication), Tarija (Barr et al. 2017, this publication). New specimen data: BOLIVIA: Cochabamba: Carrasco, Bulo Bulo, McPhail trap R1-1, 19 Jul 2005, E. Quisberth, G. Z��rate & A. Salda��a, 1♀ (USNM USNMENT00212065). Santa Cruz: Florida, Samaipata, Dec 1998, F. A. Langer, 1♀ (MNKM). Tarija: Aniceto Arce, Bermejo, [22��39���S 64��22���W], McPhail trap, 14 Aug 2005, R. Urban, 1♀ (USNM USNMENT00212785); Bermejo, Candado Grande, 22��42���55���S 64��22���53���W, McPhail trap, 23 Aug 2005, E. Becerra, 1��� (SENASAG)., Published as part of Ramos, Elizabeth Quisberth, Norrbom, Allen L., Marinoni, Luciane, Sutton, Bruce D., Steck, Gary J. & S��nchez, Juan Jos�� Lagrava, 2021, The Bolivian fauna of the genus Anastrepha Schiner (Diptera: Tephritidae), pp. 43-64 in Zootaxa 4926 (1) on page 53, DOI: 10.11646/zootaxa.4926.1.3, http://zenodo.org/record/4500587, {"references":["Lobos, A. C. (1997) Distribucion y registros de principales especies de moscas de las frutas (Diptera: Tephritidae) en los paises suramericanos. Instituto de Cooperacion para la Agricultura IICA, Lima, 62 pp. [http: // repiica. iica. int / docs / B 1487 e / B 1487 e. pdf]","Hendel, F. (1914) Die Bohrfliegen S ʾ damerika. Abhandlungen und Berichte des Koniglichen Zoologischen und Anthropologisch- Ethnographischen Museums zu Dresden, 14 (3), 1 - 84. [1912]","Stone, A. (1942) The fruit flies of the genus Anastrepha. United States Department of Agriculture Miscellaneous Publication, 439, 1 - 112.","Foote, R. H. (1967) Family Tephritidae (Trypetidae, Trupaneidae). In: Papavero, N. (Ed.), A catalogue of the Diptera of the Americas south of the United States. Departamento de Zoologia da Secretaria de Agricultura de Sao Paulo, Brasil, 57, 1 - 91.","Hernandez-Ortiz, V. & Aluja, M. (1994) Listado de especies del genero Neotropical Anastrepha (Diptera: Tephritidae) con notas sobre su distribucion y plantas hospederas. Folia Entomologica Mexicana, 88 (1993), 89 - 105.","Conde Blanco, E. A., Loza-Murguia, G., Asturizaga-Aruquipa, L. B., Ugarte-Anaya, D. & Kimenes-Espinoza, R. (2018) Modelo de fluctuacion poblacional de moscas de la fruta (Ceratitis capitata (Wiedemann 1824) y Anastrepha spp. (Diptera: Tephritidae) en dos rutas en el municipio de Caranavi, Bolivia. Journal of the Selva Andina Research Society, 9, 2 - 24. [http: // www. scielo. org. bo / pdf / jsars / v 9 n 1 / v 9 n 1 _ a 02. pdf] https: // doi. org / 10.36610 / j. jsars. 2018.090100003","Barr, N. B., Ruiz-Arce, R., Farris, R. E., Silva, J. G., Lima, K. M., Dutra, V. S., Ronchi-Teles, B., Kerr, P. H., Norrbom, A. L., Nolazco, N. & Thomas, D. B. (2017) Identifying Anastrepha (Diptera; Tephritidae) species using DNA barcodes. Journal of Economic Entomology, 111, 405 - 421. [2018] https: // doi. org / 10.1093 / jee / tox 300"]}

49. Anastrepha schultzi Blanchard Distribution in Bolivia: Chuquisaca (this publication), La Paz (Conde Blanco 2018), Tarija (this publication). New specimen data: BOLIVIA: Chuquisaca: Hernando Siles, Monteagudo, 05-03-01, McPhail trap, Jul 2009, 1♀ (SENASAG) 1♁ 3♀ (USNM USNMENT01526623-26). Tarija: Aniceto Arce, Bermejo, [22°39’S 64°22’W], 06-06-01, McPhail trap, 2009, 2 ♁ 2♀ (SENASAG) 2♁ 3♀ (USNM USNMENT01526618-22)., Published as part of Ramos, Elizabeth Quisberth, Norrbom, Allen L., Marinoni, Luciane, Sutton, Bruce D., Steck, Gary J. & Sánchez, Juan José Lagrava, 2021, The Bolivian fauna of the genus Anastrepha Schiner (Diptera: Tephritidae), pp. 43-64 in Zootaxa 4926 (1) on page 56, DOI: 10.11646/zootaxa.4926.1.3, http://zenodo.org/record/4500587, {"references":["Conde Blanco, E. A., Loza-Murguia, G., Asturizaga-Aruquipa, L. B., Ugarte-Anaya, D. & Kimenes-Espinoza, R. (2018) Modelo de fluctuacion poblacional de moscas de la fruta (Ceratitis capitata (Wiedemann 1824) y Anastrepha spp. (Diptera: Tephritidae) en dos rutas en el municipio de Caranavi, Bolivia. Journal of the Selva Andina Research Society, 9, 2 - 24. [http: // www. scielo. org. bo / pdf / jsars / v 9 n 1 / v 9 n 1 _ a 02. pdf] https: // doi. org / 10.36610 / j. jsars. 2018.090100003"]}

22. Anastrepha daciformis Bezzi Distribution in Bolivia: Chuquisaca (this publication), La Paz (Stone 1939, Foote 1967, Hernández-Ortiz & Aluja 1994, Lobos 1997, Norrbom et al. 1999, Norrbom 2004a). New specimen data: BOLIVIA: Chuquisaca: Luis Calvo, Muyupampa, 05-04-03, McPhail trap, 2009, 1♁ 1♀ (SENASAG) 2♁ 3♀ (USNM USNMENT01526589-93)., Published as part of Ramos, Elizabeth Quisberth, Norrbom, Allen L., Marinoni, Luciane, Sutton, Bruce D., Steck, Gary J. & Sánchez, Juan José Lagrava, 2021, The Bolivian fauna of the genus Anastrepha Schiner (Diptera: Tephritidae), pp. 43-64 in Zootaxa 4926 (1) on page 50, DOI: 10.11646/zootaxa.4926.1.3, http://zenodo.org/record/4500587, {"references":["Stone, A. (1939) A revision of the genus Pseudodacus Hendel (Dipt. Trypetidae). Revista de Entomologia (Rio de Janeiro), 10, 282 - 289.","Foote, R. H. (1967) Family Tephritidae (Trypetidae, Trupaneidae). In: Papavero, N. (Ed.), A catalogue of the Diptera of the Americas south of the United States. Departamento de Zoologia da Secretaria de Agricultura de Sao Paulo, Brasil, 57, 1 - 91.","Hernandez-Ortiz, V. & Aluja, M. (1994) Listado de especies del genero Neotropical Anastrepha (Diptera: Tephritidae) con notas sobre su distribucion y plantas hospederas. Folia Entomologica Mexicana, 88 (1993), 89 - 105.","Lobos, A. C. (1997) Distribucion y registros de principales especies de moscas de las frutas (Diptera: Tephritidae) en los paises suramericanos. Instituto de Cooperacion para la Agricultura IICA, Lima, 62 pp. [http: // repiica. iica. int / docs / B 1487 e / B 1487 e. pdf]","Norrbom, A. L., Carroll, L. E., Thompson, F. C., White, I. M. & Freidberg, A. (1999) Systematic database of names. In: Thompson, F. C. (Ed.) Fruit Fly Expert Identification System and Systematic Information Database. Myia (1998), 9, 65 - 251 & Diptera Data Dissemination Disk (CD-ROM) (1998), 1.","Norrbom, A. L. (2004 a) Updates to Biosystematic Database of World Diptera for Tephritidae through 1999. Diptera Data Dissemination Disk (CD-ROM), 2."]}

57. Anastrepha woodleyi Norrbom & Korytkowski Distribution in Bolivia: Santa Cruz (Norrbom & Korytkowski 2011, Mengual et al. 2017, this publication). New specimen data: BOLIVIA: Santa Cruz: Andrés Ibáñez, Potrerillo del Guendá, 17°40’S 63°27’W, 300-400 m, light trap, 22-24 Sep 2014, P. Skelley & J. Wappes, 1♀ (FSCA AP042213.01); Potrerillo del Guendá, entrance road, across river, trail near 2nd gate, 17.67635°S 63.44664°W, 385 m, trap ML-PG-35, 9-17 Oct 2014, B. D. Sutton, A. L. Norrbom & E. Quisberth, 1♁ (USNM); same, entrance road, past open area, 17.67183°S 63.45576°W, 417 m, trap ML-PG-02, 18-30 Dec 2014, E. Quisberth, 2♀ (USNM USNMENT01526516-17); same, N trail, 17.66312°S 63.45842°W, 410 m, trap ML-PG-26, 18-30 Dec 2014, E. Quisberth, 1♀ (DSASC) 1♀ (MNKM); same, N trail, 17.66117°S 63.4594°W, 396 m, trap ML-PG-41, 18-30 Dec 2014, E. Quisberth, 1♁ 1♀ (SENASAG); same, next to cabins, 17.67078°S 63.45741°W, 401 m, trap ML-PG-11, 9-17 Oct 2014, B. D. Sutton, A. L. Norrbom & E. Quisberth, 2♁ (FSCA); same, trail to Quebrada Las Conchas, between fence and small grassy clearing, 17.67045°S 63.46011°W, 403 m, on undersides of leaves of plant 14-Bol-20, 16-17 Oct 2014, B. D. Sutton, A. L. Norrbom & E. Quisberth, 1♁ 1♀ (USNM USNMENT01526507-08); same, trail to water tower, 17.67038°S 63.45763°W, 387 m, on undersides of leaves of plant 14-Bol-18, “leche leche”, 9-12 Oct 2014, B. D. Sutton, A. L. Norrbom & E. Quisberth, 1♀ (FSCA). Ichilo Prov., 4-6 km. SSE of Buena Vista, Hotel Flora y Fauna, dirt road, 17.49645°S 63.64900°W, 384 m, emerged 30-31 Mar 2014 reared ex fruit of Pacouria boliviensis collected 8 Mar 2014, G. J. Steck, B. D. Sutton, A. L. Norrbom & A. Saravia, 10♁ 9♀ (FSCA) 1♀ (FSCA AP121014.46) 5♁ 5♀ (SENASAG) 4♁ 4♀ (USNM); same, emerged 1-4 Apr 2014, 5♁ 13♀ (FSCA) 23♁ 13♀ (MNKM) 2♁ 5♀ (SENASAG) 5♁ 3♀ (USNM) 10♀ (USNM USNMENT00744948-49, USNMENT01526506, USNMENT01526509-15); Hotel Flora y Fauna, E of dirt road, 17.49878°S 63.64615°W, 407 m, trap FF-ML-12, 6-9 Mar 2014, G. J. Steck, B. D. Sutton, A. L. Norrbom & A. Saravia, 1♁ (FSCA) 1♁ (USNM USNMENT00744952). New host plant data: Pacouria boliviensis (Markgr.) A. Chev. (Apocynaceae), known locally as “tutumillo”., Published as part of Ramos, Elizabeth Quisberth, Norrbom, Allen L., Marinoni, Luciane, Sutton, Bruce D., Steck, Gary J. & Sánchez, Juan José Lagrava, 2021, The Bolivian fauna of the genus Anastrepha Schiner (Diptera: Tephritidae), pp. 43-64 in Zootaxa 4926 (1) on page 58, DOI: 10.11646/zootaxa.4926.1.3, http://zenodo.org/record/4500587, {"references":["Norrbom, A. L. & Korytkowski, C. A. (2011) New species of and taxonomic notes on Anastrepha (Diptera: Tephritidae). Zootaxa, 2740 (1), 1 - 23. https: // doi. org / 10.11646 / zootaxa. 2740.1.1","Mengual, X., Kerr, P., Norrbom, A. L., Barr, N. B., Lewis, M. L., Stapelfeldt, A. M., Scheffer, S. J., Woods, P., Islam, M. - S., Korytkowski, C. A., Uramoto, K., Rodriguez, E. J., Sutton, B. D., Nolazco, N., Steck, G. J. & Gaimari, S. (2017) Phylogenetic relationships of the tribe Toxotrypanini (Diptera: Tephritidae) based on molecular characters. Molecular Phylogenetics and Evolution, 113, 84 - 112. https: // doi. org / 10.1016 / j. ympev. 2017.05.011"]}

47. Anastrepha rheediae Stone Distribution in Bolivia: Santa Cruz (Ledezma et al. 2013, Quisberth et al. 2016a, Barr et al. 2017, this publication). New specimen data: BOLIVIA: Santa Cruz: Ichilo Prov., 4-6 km. SSE of Buena Vista, Hotel Flora y Fauna, 2nd river trail, 17.50261°S 63.64743°W, 355 m, trap FF-ML-21, 9-10 Mar 2014, G. J. Steck, B. D. Sutton, A. L. Norrbom & A. Saravia, 1♀ (USNM USNMENT00744962); same, E of dirt road, 17.49878°S 63.64615°W, 407 m, trap FF-ML-12, 9-10 Mar 2014, G. J. Steck, B. D. Sutton, A. L. Norrbom & A. Saravia, 1♁ (FSCA); Hotel Flora y Fauna, R. Vargas orchard, 17.49465°S 63.65425°W, 349 m, trap FF-ML- 26 in tomatillo tree, 9-10 Mar 2014, G. J. Steck, B. D. Sutton, A. L. Norrbom & A. Saravia, 1♁ (USNM USNMENT00744964)., Published as part of Ramos, Elizabeth Quisberth, Norrbom, Allen L., Marinoni, Luciane, Sutton, Bruce D., Steck, Gary J. & Sánchez, Juan José Lagrava, 2021, The Bolivian fauna of the genus Anastrepha Schiner (Diptera: Tephritidae), pp. 43-64 in Zootaxa 4926 (1) on page 56, DOI: 10.11646/zootaxa.4926.1.3, http://zenodo.org/record/4500587, {"references":["Ledezma Arias, J., Quisberth Ramos, E., Amaya Ledezma, M., Magne Salazar, C., Ramos Conde, A. C. & Torrico Sanchez, J. (2013) Parasitoides para el control biologico de las moscas de la fruta en Santa Cruz. Tinkazos, 33, 93 - 117. [http: // www. scielo. org. bo / scielo. php? script = sci _ arttext & pid = S 1990 - 74512013000200006]","Quisberth, E., Torrez, B. J. & Torrico, S. J. (2016 a) Natural host of Garcinia humilis (Vahl) associated with Anastrepha rheediae Stone (Diptera, Tephritidae) Santa Cruz, Bolivia. Abstract, 9 th Meeting of Tephritid Workers of the Western Hemisphere, Buenos Aires, Argentina.","Barr, N. B., Ruiz-Arce, R., Farris, R. E., Silva, J. G., Lima, K. M., Dutra, V. S., Ronchi-Teles, B., Kerr, P. H., Norrbom, A. L., Nolazco, N. & Thomas, D. B. (2017) Identifying Anastrepha (Diptera; Tephritidae) species using DNA barcodes. Journal of Economic Entomology, 111, 405 - 421. [2018] https: // doi. org / 10.1093 / jee / tox 300"]}