11 results on '"Balducci, Ezequiel"'
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2. Breeding Strategy for the Cedrela Genus in Argentina
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Grignola, Josefina, Balducci, Ezequiel, Trápani, Adrián, Saravia, Pablo, Montero, Mario Hernán Feyling, Gatto, Miguel, Cuello, Roberto, Perez, Gonzalo Antonio, de Gonzalez, Liliana Ríos, Ruiz, Verónica Eugenia, Meloni, Diego, Saez, Julio Victor, Pastorino, Mario J., Pastorino, Mario J., editor, and Marchelli, Paula, editor
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- 2021
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3. Peteribí (Cordia trichotoma), Lapacho Rosado (Handroanthus impetiginosus), and Cebil Colorado (Anadenanthera colubrina var. cebil): Three Valuable Species with Incipient Breeding Programs
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Fornes, Luis F., Inza, Virginia, García, María Victoria, Barrandeguy, María Eugenia, Soldati, María Cristina, Barth, Sara, Ledesma, Tilda, Saravia, Pablo, Tarnowski, Christian, Rodríguez, Gustavo, Balducci, Ezequiel, Grignola, Josefina, Schmid, Patricia, Galíndez, Guadalupe, Trápani, Adrián, Pastorino, Mario J., editor, and Marchelli, Paula, editor
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- 2021
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4. Changes in soil organic carbon in native forests of Argentina related to land use change and environmental factors.
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Nosetto, Marcelo Daniel, Balducci, Ezequiel, Gaitán, Juan, Mastrángelo, Matías, Pastur, Guillermo Martínez, Pinazo, Martín, Villagra, Pablo, Roglich, Mariano Gonzalez, Kowaljow, Esteban, Colazo, Juan Cruz, Perez‐Harguindeguy, Natalia, Naldini, María Betania, de Dios Herrero, Juan, Quiroga, Alberto, Wilson, Marcelo, Whitworth‐Hulse, Juan, Jobbágy, Esteban, Ballesteros, Silvina, Polo, Marina González, and von Müller, Axel
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SOIL texture ,LAND use ,TREE crops ,REGRESSION trees ,FORESTS & forestry - Abstract
Native forests host important pools of soil organic carbon (SOC). This is a key element not only for ecosystem functioning but also for the global carbon cycle. Globally, and particularly in Argentina, native forests are being rapidly replaced by other land uses, raising questions about the impact of these transformations on SOC and its environmental controls. Based on the construction of the largest SOC database in Argentina to date, we investigated the patterns and controls of changes in SOC stocks associated with the replacement of native forests by other land uses. We constructed the database with a total of 818 sites with SOC data (0–30 cm depth), covering the main ecoregions, to which we added environmental information (e.g. satellite data, soil database and climate database), to study the environmental controls on SOC change after deforestation and on the original SOC content of native forests. Considering all ecoregions and all land use alternatives together, we found an average decrease in SOC stock of 18.2 Mg C ha−1, which represents a loss of more than a quarter of the original SOC stock of the native forest sites. A boosted regression tree explained 89% of the variation in SOC stock change and indicated that the initial forest SOC stock and the post‐deforestation land use were the most important variables explaining this variation (relative influence of 30.9% and 18.2%, respectively). The replacement of native forests by rainfed annual crops resulted in the largest decrease in SOC (−28 Mg C ha−1), which was twice as large as the decrease observed in rangelands (−14 Mg C ha−1). On the contrary, neither irrigated croplands nor tree plantations of fast‐growing species caused a decrease in SOC stocks (p >.10). Climate and soil texture had an indirect effect on SOC changes through a strong influence on the initial SOC stocks in native forests (p <.01). Our study highlighted the significant impact of land use change on SOC stocks, overshadowing other relevant environmental controls. Understanding how the SOC pool responds to land use change, environmental conditions and management practices is essential to increase the effectiveness of practices implemented to improve soil properties and mitigate climate change. [ABSTRACT FROM AUTHOR]
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- 2024
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5. Breeding Strategy for the Cedrela Genus in Argentina
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Grignola, Josefina, primary, Balducci, Ezequiel, additional, Trápani, Adrián, additional, Saravia, Pablo, additional, Montero, Mario Hernán Feyling, additional, Gatto, Miguel, additional, Cuello, Roberto, additional, Perez, Gonzalo Antonio, additional, de Gonzalez, Liliana Ríos, additional, Ruiz, Verónica Eugenia, additional, Meloni, Diego, additional, Saez, Julio Victor, additional, and Pastorino, Mario J., additional
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- 2020
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6. Peteribí (Cordia trichotoma), Lapacho Rosado (Handroanthus impetiginosus), and Cebil Colorado (Anadenanthera colubrina var. cebil): Three Valuable Species with Incipient Breeding Programs
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Fornes, Luis F., primary, Inza, Virginia, additional, García, María Victoria, additional, Barrandeguy, María Eugenia, additional, Soldati, María Cristina, additional, Barth, Sara, additional, Ledesma, Tilda, additional, Saravia, Pablo, additional, Tarnowski, Christian, additional, Rodríguez, Gustavo, additional, Balducci, Ezequiel, additional, Grignola, Josefina, additional, Schmid, Patricia, additional, Galíndez, Guadalupe, additional, and Trápani, Adrián, additional
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- 2020
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7. Estudio de la dinámica poblacional y alternativas de manejo de Hypsipyla grandella Zéller (Lepidoptera, Piralydae) en plantaciones de Cedrela balansae en el norte de Salta : Proyecto de investigación aplicada (SAFO 203)
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Lucía, Alejandro, Balducci, Ezequiel, Sanchez, Estefanía, Baca, Verónica, Bulak, Karina, Gutierrez Brower, Jimena, Romero, A., Aquino, Daniel Alejandro, Tavares, M. T., Quintana De Quinteros, Sara, and Malizia, Lucio
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Ingeniería Forestal ,Yungas ,Dinámica poblacional - Abstract
Las especies de cedros nativos de las Yungas (Cedrela balansae, C.saltensis y C.an- gustifolia), presentan un gran potencial para el desarrollo de plantaciones forestales, dadas sus tasas de crecimiento, la calidad de su madera y su presencia en el mercado. La principal limitante está dada por la incidencia de Hypsipyla grandella (Lep. Pyra- lidae), una de las plagas forestales más severas conocidas en el trópico. El principal daño es causado por la larva que destruye el brote terminal principal y lateral, barrenando los ápices y haciendo túneles en los tallos jóvenes de árboles del genero Cedrela (cedros). Los rebrotes de las plantas afectadas por repetidos ataques del insecto, dan como resultado numerosas ramas laterales y, consecuentemente, árboles mal formados, indeseables para la producción de madera (Briceño Vergara, A., 1997). El objetivo fue estudiar la dinámica poblacional de adultos, el patrón de ataques sobre renovales, para determinar cuál es el momento oportuno de control y establecer una periodicidad de aplicación para la evaluación de productos potencialmente registrables para uso forestal, en el marco del Manejo Integrado de Plagas. Facultad de Ciencias Agrarias y Forestales Facultad de Ciencias Naturales y Museo
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- 2016
8. Brachymeria Westwood
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Aquino, Daniel Alejandro, Tavares, Marcelo Texeira, Balducci, Ezequiel, Baca, Verónica, and Quinteros, Sara Quintana De
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Insecta ,stomatognathic system ,Arthropoda ,Brachymeria ,Animalia ,Chalcididae ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Brachymeria Westwood Brachymeria was recently diagnosed by Andrade & Tavares (2009) and is based on the following characteristics: hind tarsal claw with a falciform process (Brachymeriini); scrobal-malar carina absent; mandibular formula 2: 3 or 2: 2, in the later instance upper tooth at least half as long as lower tooth and never distant from the mandible apex; occipital carina not converging to occipital foramen; and diameter of mesonotal umbilicated fovea at least 0.25 �� as large as mid ocellar diameter., Published as part of Aquino, Daniel Alejandro, Tavares, Marcelo Texeira, Balducci, Ezequiel, Baca, Ver��nica & Quinteros, Sara Quintana De, 2015, The microlepidopterous natural enemy Brachymeria subrugosa Blanchard, 1942 (Hymenoptera, Chalcididae): identity, hosts and geographic distribution, pp. 293-300 in Zootaxa 4013 (2) on page 294, DOI: 10.11646/zootaxa.4013.2.10, http://zenodo.org/record/245592, {"references":["Andrade, T. V. de & Tavares, M. T. (2009) Revisao de Ceyxia Girault. stat. rev. (Hymenoptera, Chalcididae, Brachymeriini). Revista Brasileira de Entomologia, 53 (4), 511 - 548. http: // dx. doi. org / 10.1590 / S 0085 - 56262009000400004"]}
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- 2015
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9. Brachymeria subrugosa Blanchard 1942
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Aquino, Daniel Alejandro, Tavares, Marcelo Texeira, Balducci, Ezequiel, Baca, Verónica, and Quinteros, Sara Quintana De
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Insecta ,Arthropoda ,Brachymeria ,Animalia ,Chalcididae ,Biodiversity ,Hymenoptera ,Taxonomy ,Brachymeria subrugosa - Abstract
Brachymeria subrugosa Blanchard, 1942 (Figs 1���8) Trigonura annulipes Costa Lima 1919: 57 ���58 [preoccupied by Chalcis annulipes Walker 1834, a junior synonym of Brachymeria annulata (Fabricius)]. Brasil: Maranh��o. Brachymeria subrugosa Blanchard 1942: 116 ���117, Fig. 11. Argentina: Charata. Syn. nov. Brachymeria subrugosa: Parker, Berry & Guido 1953: 49 (hosts). Brachymeria (Pseudobrachymeria) conica (Ashmead): Burks 1960: 270 ���271 (part, misidentification, hosts); De Santis 1979: 64 (part, misidentification, hosts); Ter��n 1980: 292 (part, misidentification, hosts); De Santis 1989: 13 (part, catalogue). Brachymeria (Brachymeria) subrugosa: De Santis 1967: 209 (catalogue); 1979: 62 (catalogue); 1980: 253 (catalogue). Trigonura annulipes Costa Lima: De Santis 1980: 249 (catalogue). Brachymeria annulipes: Bouček 1992: 88 (combination). Brachymeria subconica: Delvare 1993: 351, 361, Figs 5���7 (misidentification, key). Diagnosis. Preorbital carinae present along upper third of orbit, curving in front of lateral ocelli to meet each other just on posterior margin of median ocellus (Figs 1, 2); scrobal margin completely carinate and carinae touching lateral margin of median ocellus (Figs 1, 2); area enclosed by scrobal margin and preorbital carinae flat to slightly concave; lower face with scrobal-orbital ruga delimiting upper and lower face, conspicuous and usually reaching orbit (Fig. 3); torularclypeal ruga conspicuous and complete (Fig. 3); interantennal projection as a short carina (Fig. 3); fore wing with cubital fold glabrous and basal fold with a line of hairs (Fig. 5); metafemur subelliptic, ventral margin with 8���10 teeth, the basal one small, the medial ones the largest, outer surface coriaceous with dense and small piliferous punctures (Fig. 6); hypopygium at apex conspicuously emarginate (Figs 7, 8). Redescription. FEMALE. Lectotype: 5.25 mm. Color. Mainly black except as follows: eyes and ocelli brown; yellow on tegula, distal fifth of mesofemur, distal spot on external surface of metafemur, fore and mesotibiae, proximal and distal quarters of metatibia, and tarsi. Wings hyaline. Pilosity mainly white, brown on syntergum 7 + 8. Head. Preorbital carinae present along upper third of orbit, the carinae curving in front of lateral ocelli and meeting each other just on posterior margin of median ocellus (Figs 1, 2). Scrobal margin carinate, dorsally carinae touching lower margin of median ocellus, close or virtually tangent to median ocellus (Figs 1, 2); area enclosed by scrobal margin and preorbital carinae flat. Frons dorsally and vertex usually with umbilicate foveae, interstices coriaceous, foveae at most 0.3 �� median ocellar diameter; lower face with piliferous punctures, interstices coriaceous; scrobal-orbital ruga separating the lower face from frons, conspicuous and reaching orbit (Fig. 3); a torular-clypeal ruga conspicuous and complete. Lower margin of torulus at lower eye level. Interantennal projection as a short carina (Fig. 3). Malar carinae curving posteriorly towards genal carina. Mandibular formula 2: 3. Genal carina running towards lateral ocellus, upper portion not curving toward occiput. Antenna clavate, scape just reaching lower margin of median ocellus. Measurements: head height:width:length = 1.07: 1.68: 0.79; frontovertex = 0.82; DAO = 0.17; POL = 0.42; OOL = 0.10; malar space = 0.31; oral fossa = 0.42; eye height:width = 0.93: 0.69; antennal segments (length:width) = scape 0.65: 0.15; pedicel 0.10: 0.10; anellus 0.10: 0.3; Fu 1 0.16: 0.15; Fu 2 ���Fu 3 0.15: 0.16; Fu 4 ���Fu 6 0.13: 0.17; Fu 7 0.13: 0.18; clava 0.27: 0.18. Mesosoma. Pronotum, mid lobe of mesoscutum and scutellum with umbilicate foveae, foveae diameter 0.3���0.4 �� mid ocellar diameter; interstices coriaceous, as wide as 0.5 ���1.0�� diameter of foveae; scutellum with a smooth and slightly elevated medial stripe (Fig. 4), usually inconspicuously coriaceous; lateral lobe of mesoscutum on inner half with shallow, scattered and smaller umbilicate foveae. Setation as long as 2 �� diameter of foveae. Frenal carinae medially slightly emarginate. Epicnemial carina ventromedially straight. Fore wing with basal cell and cubital fold glabrous; basal fold with a line of setae (Fig. 5); subcubital fold basally with line of fine setae. Metafemur subelliptic; on ventral margin with 8���10 teeth, the basal one small, the medial ones the largest; outer surface coriaceous with dense and small piliferous punctures (Fig. 6). Measurements (length or length:width): mesosoma = 2.31; mesoscutum = 0.98: 1.64; scutellum = 1.00: 0.90; fore wing = 3.35: 1.42; submarginal vein = 1.69; marginal vein = 0.65; postmarginal vein = 0.17; stigmal vein = 0.08; metacoxa = 0.86: 0.62; metafemur = 1.93: 0.95. Metasoma. Gaster acuminate (Fig. 7), at least 1.1 �� as long as head plus mesosoma; Tg 1 smooth and shiny, except for a few fine dorsolateral punctures; Tg 2 ���Tg 5 coriaceous with 1 or 2 lateral rows of piliferous punctures; Tg 6 coriaceous with shallow umbilicate foveae on side, dorsal foveae irregular; syntergum 7 + 8 coriaceous with piliferous punctures, 1.5 �� as long as wide. Exerted part of ovipositor sheaths as long as high. Hypopygium at apex broadly emarginate (Figs 7, 8). Measurements (length or length:width): gaster = 3.65: 1.35; Gt 1 = 1.15; Gt 7 + 8 = 0.72: 0.33. MALE. Length: 3.6���4.8 mm. Very similar to female, except area around median ocellus slightly concave; apex of gaster not acuminate. Variation. Female: Body length 4.0��� 7.2 mm; area around median ocellus flat to slightly concave; umbilicated foveae on former area sometimes shallow and irregular; scrobal-orbital ruga reaching orbits or not; Tg 7 + 8 from 1.3 ���2.0�� as long as wide. Type material. Brachymeria subrugosa: Lectotype (here designated), ♀, labelled ���s/ A. argillaceae, Charata, Parker, iii. 40 ��� ��� Brachymeria subrugosa sp.n., det. E. E. Blanchard��� (MLPA). Blanchard (1942) described B. subrugosa based on two syntypes. The specimen here designated as lectotype was received on loan by one of the authors (MTT) from Manfredo A. Fritz (Institute of Entomology of Salta, Salta Argentina). The specimen labels data (date, place and host) agree with the original description, except for the collector (indicated as ���Roberto G. Mallo��� in original description, but as ���Parker��� on the lectotype label). In addition to the specimen agreeing with the original description, the typical Blanchard's identification label with his handwriting and the indication "sp. n." reinforce it as one of the original syntypes. Trigonula annulipes: holotype, ♀ (damaged on right side of mesoscutum and scutellum), labelled ��� Trigonura annulata C.L.��� ���G. de Entom. Esc. Sup. Agri. ��� Nictheroy ��� E. Rio, No 3266 ��� (UFRR). Costa Lima (1919) mentioned that the holotype of B. annulipes was deposited in the collection of Gabinete de Entomologia da Escola Superior de Agricultura (Niter��i, Rio de Janeiro State, Brazil), but that collection is now in the Costa Lima Collection at the Instituto de Biologia of Universidade Federal Rural do Rio de Janeiro (Serop��dica, Rio de Janeiro State, Brazil). The holotype has a red label written " Trigonura annulata C.L." (Costa Lima's handwriting) and a Niter��i cabinet label with the number 3266. In the former collection's record book, under that number is registered: " Hymenoptera / Chalcididae / Trigonura annulata, C.L./box # 63 / Maranh��o. ii. 919 / I removed it from inside a chrysalis of Pectinophora gossypiella ". The type specimen was found into box # 63 and the record book data corroborates the original description. The specific epithet annulata on the type label and in the book record clearly are mistakes. Other studied material. USA. Texas: 1 ♀, 1 ♂, Victoria, ix. 1920, J. D. Mitchell col. (USNM). MEXICO. 1 ♀, 28.iii. 1934, O. C. Morris col. (USNM); 1 ♀, 10.ix. 1952 [without collecting data] (USNM). Sinaloa: 1 ♀, 2,5 miles N. Mazatlan, 12.viii. 1970, J. S. & M. S. Wasbauer colls. (EMEC). Nuevo Leon: 1 ♂, Villa del Carmen, 24.i. 1972, ex. webworm on pecan [sic.], J. J. Ortiz col. (USNM); 1 ♀, Villa Garcia, iii. 1964, ex. Lespeyresia caryana, Guajardo col. (USNM). Colima: 1 ♀, 21 miles N. Manzanillo, 25.vii. 1970, M. S. & J. S.Wasbauer cols. (EMEC). Veracruz: 1 ♀, Cotaxtla, 03.viii. 1958, ex. Stenomidae pupa on Annona fruits (USNM). HONDURAS. 1 ♀, 1 ♂, 10.v. 1934, J. A. Ramos col. (USNM); 1 ♀, Punta Castilla, 29.iii. 1924 (USNM). COSTA RICA. 1 ♀, [without collecting data] (USNM). Guanacaste: 1 ♀, Playas del Coco, 05.viii. 1964, G. C. Eickwort col. (SEMC). Cartago: 1 ♀, Turrialba, 10.ix. 1964 (M. G. Naumann) (SEMC); 1 ♀, Turrialba, 11.vii. 1971, ex. Anadasmus pupa, Becker col. (MLPA); 1 ♀, Turrialba, 20.x. 1972, on Cedrella odorata L., Grisjma col. (MLPA); 1 ♀, 640 m [without collecting data] ex. H. grandella, V. O. Becker col. (MLPA). PANAMA. Canal Zone: 1 ♀, Las Cascadas, 01.v. 1911, on pyralid in cocoa poa [sic.] (USNM); 1 ♀, Porto Bello, 09.iii. 1911, A. Brusck col. (USNM). TRINIDAD Y TOBAGO. 1 ♀, Sagre Grande, 28.v. 1958, ex. Philornis puparium, T. Aitken col. (USNM). COLOMBIA. Cesar: 2 ♀, 2 ♂, San Alberto, 23.v. 1989, ex. pupae Stenoma cecropia, P. Genty col. (CIRAD). Tolina: 2 ♀, Armero, 26.i��� 05.ii. 1977, E. L. Peyton & Suarez cols. (USNM). VENEZUELA. Zulia: 1 ♀, Carasquero, 29���30.v. 1976, A. S. Menke & D. Vincent col. (USNM); 1 ♀, Rosario, 14.vi. 1976, A. S. Menke & D. Vincent col. (USNM); 1 ♀, Puerto de Cata, 10���11.vi. 1976, A. S. Menke & D. Vincent col. (USNM). Aragua: 1 ♀, Ocumare de La Costa, 12.vi. 1976, A. S. Menke & D. Vincent cols. (USNM); 1 ♀, Maracay, 24.ix. 1952, ex. Stenomidae pupa on almond, F. Fernandez col. (USNM). EQUADOR. Napo: 2 ♀, Coca, iv. 1985 e i. 86, G. Onore col. (QCAZ). BRAZIL. 2 ♀, attacking material # 11045 [without collecting data] (IBUS). Acre: 1 ♀, Rio Branco, 25.x���08.xi. 1991, F. Ramos e eq. col. (MPEG). Amazonas: 1 ♀, Manaus, Reserva Ducke, 19.x. 1981, J. A. Rafael col. (INPA); 1 ♀, idem, 05.xi. 1986, B. Klein col. (INPA). Federal District: 1 ♀, Reserva Ecol��gica do IBGE, 06.x. 1978, Malaise trap (IBGE). Mato Grosso: 1 ♀, Chapada dos Guimar��es, 08��� 13.ii. 1986, Malaise, I. Gorayeb col. (MPEG). Par��: 1 ♀, Bel��m, 25.viii. 1935, ex. Gnorimoschema sp (FIOC); 1 ♀, Oriximin��, 07��� 25.x. 1982, Malaise, J. A. Rafael & eq. cols. (INPA); 1 ♀, Tucurui, Vila Brava, 27.vi. 1980, Nunes de Mello & eq. cols. (INPA). Pernambuco: 1 ♀, Recife, 08.vii. 1935, J. A. Albuquerque col. (IBUS). Esp��rito Santo: 2 ♀, Vit��ria, urban area, 03.vii.2004, 20.x��� 5.xii.2004, 20�� 17 ��� 27 ��� S, 40 �� 17 ��� 30 ��� W, R. Kawada col. (UFES). Rio de Janeiro: 2 ♀, 1 ♂, Rio de Janeiro, viii. 1943, ex. Stenoma annonella, C. H. Ribbs col. (IBUS); 4 ♀, 1 ♂, Belfort Roxo, 11.ii. 1935, # 3191, ex. Cerconota anonella pupa in sugar���apple [Anonna squamosa], M. Marques col. (IBUS); 2 ♀, 2 ♂, Guaratiba, 23.vi. 1942, # 6223, ex. Cerconota anonella pupa, A. Silva col. (IBUS); 1 ♀, Rio de Janeiro, Horto Florestal, vi. 1942, A. Silva col. (IBUS); 1 ♀, 1 ♂, Rio de Janeiro, vii. 1925, ex. Cerconota anonella pupa, J. Alves col. (MNRJ); 2 ♀, 2 ♂, S��o Bento, i. 1943, ex. Cerconota anonella pupa, L. Portela col. (IBUS). S��o Paulo: 1 ♀, Campinas, ix. 1992, ex. Stenoma catenifer pupa, H. Z. Firsher col. (UFES). ARGENTINA. Salta: 1 ♀, 14 km S. Urundel, ex. Calpodes ethlius pupae (IFML); 1 ♀, Valle Morado, 18.ii. 2013, ex. H. grandella on Cedrela balansae, E. Balducci (MLPA); Tucum��n: 1 ♀, i. 1929 (IFML); 1 ♀, San Miguel de Tucum��n, x. 1973, parasite of Ceroplastes sp on Tabebuia [probably attacking eggs predator lepidoptera] (IFML). Biology. Brachymeria subrugosa usually is a solitary, primary parasitoid of Lepidoptera pupae, mainly microlepidoptera. It has also been recorded as hyperparasitoid of Lepidoptera and Cassidini (Coleoptera) beetles through Tachinidae (Parker, Berry & Guido 1953). The following host records for B. subconica actually refer to B. subrugosa: Melitara dentata (Grote) (Burks 1960); Anadasmus porinodes (Meyrick) (De Santis 1979); Stenomidae (Ter��n 1980); and Stenoma cecropia Meyrick (Delvare 1993). Costa Lima (1945) mentioned that the specimens of B. pseudovata, identified by Jamirez Gomes, were obtained from pupae of Cerconota annonella (Sepp) (Lepidoptera: Oecophoridae), but this record corresponds to B. subrugosa. Of the examined specimens, one female is point mounted with a puparium of Philornis sp. (Diptera: Sarcophagidae) and one female of B. podagrica F. The latter was obtained from inside the puparium that was opened, suggesting that both specimens developed from the same host. These data suggest that beyond lepidopterans B. subrugosa may attack dipterans, not as a secondary parasitoid. Distribution. USA * (Texas), Mexico *, Honduras *, Costa Rica *, Panama *, Trinidad and Tobago *, Colombia *, Venezuela *, Ecuador *, Argentina * (Salta and Tucum��n), Brasil (Acre*, Amazonas*, Federal District*, Maranh��o, Minas Gerais, Mato Grosso do Sul*, Par��*, Rio de Janeiro*, Roraima* and S��o Paulo*) and Uruguay. Hosts. LEPIDOPTERA: Pectinophora gossypiella (Saunders) (Gelechiidae); Calpodes ethlius * (Stoll) (Hesperiidae); Megalopyge chacona * (Schaus) (Megalopygidae); Alabama argillacea (H��bner) (as primary and secondary host) (Noctuidae); Anadasmus porinodes * (Meyrick), Cerconota annonella * (Sepp), Stenoma cecropia * Meyrick and S. catenifer * Walsingham (Oecophoridae); Hypsipyla grandella * (Zeller), Melitara dentata * (Grote) (Pyralidae); Laspeyresia caryana * (Tortricidae). DIPTERA: Eucelatoriopsis parkeri Sabrosky and Patelloa sp. (Tachinidae). COLEOPTERA (secondary host): Chelymorpha variabilis Boheman (Chrysomelidae). Comments. Bouček (1992) pointed out that B. annulipes (Costa Lima) was a junior homonym of Chalcis annulipes Walker, 1834, a junior synonym under B. annulata (Fabricius), but he did not replace the former name. Once B. subrugosa Blanchard is considered a synonym of B. annulipes (Costa Lima), the former replaces the later one according to ICZN (1999) (Art. 60.2). Brachymeria subrugosa belongs to a species group that would agree with the subgenus Pseudobrachymeria Burks 1960 because it is extremely close to B. subconica, the type species of that subgenus. Both species have a cross carina in front of the lateral ocelli (regarded here as an extension of the preorbital carinae) (Figs 1, 2, 9) in addition to the following: the preorbital carinae are absent at least along the lower half of orbit; the scrobal-ocular carinae are present (Fig. 3); and the metafemur on the outer surface has dense pilliferous punctures and conspicuous coriaceous interstices (Fig. 6). Brachymeria subrugosa differs from B. subconica by the following: the scrobal margin virtually reaches the lower margin of the median ocellus, whereas the upper scrobal margin is somewhat distant from the median ocellus in B. subconica (Fig. 9); the fore wing has the cubital fold glabrous and the basal fold with a line of setae, whereas a line of setae are present on the cubital fold and 2���3 lines on the basal fold in B. subconica (Fig. 10); and the hypopygium is broadly emarginate medially at its apex conversely to being narrowly emarginate in B. subconica (Figs 11, 12). The geographic distribution of B. subconica is similar to that of B. subrugosa (Paraguay, from south to north of Brazil, Ecuador, El Salvador and Mexico). Specimens of B. subrugosa have been frequently misidentified. One of the authors (MTT) found specimens identified as B. subconica, B. pseudovata Blanchard and B. producta (Olivier). Consequently, at least part of the following citations of B. subconica refers to B. subrugosa: Burks (1960), De Santis (1980, 1989), Ter��n (1980), and Delvare (1993) (see the items Hosts and Studied material). The illustrations of B. subconica provided by Delvare (1993) clearly refer to B. subrugosa., Published as part of Aquino, Daniel Alejandro, Tavares, Marcelo Texeira, Balducci, Ezequiel, Baca, Ver��nica & Quinteros, Sara Quintana De, 2015, The microlepidopterous natural enemy Brachymeria subrugosa Blanchard, 1942 (Hymenoptera, Chalcididae): identity, hosts and geographic distribution, pp. 293-300 in Zootaxa 4013 (2) on pages 294-299, DOI: 10.11646/zootaxa.4013.2.10, http://zenodo.org/record/245592, {"references":["Blanchard, E. E. (1942) Parasitos de Alabama argillacea Hbn. en la Republica Argentina. Anales de la Sociedad Cientifica Argentina, 134, 94 - 128.","Costa Lima, A. M. (1919) Contribucao as conhecimento dos microhymenopteros parasitos de lagarta rosea de Pectinophora gossypiella (Saunders) no Brasil. Archivos da Escuela Superior de Agricultura e Medicina Veterinaria, Nictheroy, Rio de Janeiro, New Series, 3 (1 - 2), 57.","Walker, F. (1834) Monographia Chalciditum. (Continued.) Entomological Magazine, 2 (1), 13 - 39.","Parker, H. L., Berry, P. A. & Guido, A. S. (1953) Host - parasite and parasite - host lists of insects reared in the South American Parasite Laboratory during the period 1940 - 1946. Revista de la Asociacion Agronomia Uruguay, 93, 1 - 101.","Burks, B. D. (1960) A revision of the genus Brachymeria Westwood in America north of Mexico (Hymenoptera: Chalcididae). Transactions of the American Entomological Society, 86, 225 - 273, pls. 12 - 14.","De Santis, L. (1979) Catalogo de los Himenopteros Calcidoideos de America al sur de los Estados Unidos. Publicacion Especial Provincia de Buenos Aires. Comision de Investigaciones Cientificas, La Plata, 488 pp.","Teran, J. B. (1980) Lista preliminar de Hymenoptera parasitos de otros insectos en Venezuela. Revista de la Facultad de Agronomia (Maracay), 11 (1 - 4), 283 - 389.","De Santis, L. (1989) Catalogo de los Himenopteros Calcidoideos (Hymenoptera) al Sur de los Estados Unidos - Segundo suplemento. Acta Entomologica Chilena, 15, 9 - 90.","De Santis, L. (1967) Catalogo de los Himenopteros Argentinos de la serie Parasitica, incluyendo Bethyloidea. Provincia de Buenos Aires Gobernacion. Comision de Investigacion Cientifica, La Plata, 337 pp.","De Santis, L. (1980) Catalogo de los Himenopteros Brasilenos de la serie parasitica: incluyendo Bethyloidea. Universidade Federal do Parana, Curitiba, 395 pp.","Delvare, G. (1993) Les Chalcididae d'importance economique dans les palmeraies d'Amerique tropicale (Hymenoptera). Bulletin de la Societe Entomologique de France, 94 (4), 349 - 372.","Costa Lima, A. M. (1945) Insetos do Brasil: Lepidopteros. 5 ° Tomo. Escola Nacional de Agronomia, Serie Didatica n. º 7, 1 - 376."]}
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- 2015
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10. The microlepidopterous natural enemy Brachymeria subrugosa Blanchard, 1942 (Hymenoptera, Chalcididae): identity, hosts and geographic distribution
- Author
-
Aquino, Daniel Alejandro, Tavares, Marcelo Texeira, Balducci, Ezequiel, Baca, Verónica, and Quinteros, Sara Quintana De
- Subjects
Insecta ,Arthropoda ,Animalia ,Chalcididae ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Aquino, Daniel Alejandro, Tavares, Marcelo Texeira, Balducci, Ezequiel, Baca, Verónica, Quinteros, Sara Quintana De (2015): The microlepidopterous natural enemy Brachymeria subrugosa Blanchard, 1942 (Hymenoptera, Chalcididae): identity, hosts and geographic distribution. Zootaxa 4013 (2): 293-300, DOI: http://dx.doi.org/10.11646/zootaxa.4013.2.10
- Published
- 2015
11. The microlepidopterous natural enemy Brachymeria subrugosa Blanchard, 1942 (Hymenoptera, Chalcididae): identity, hosts and geographic distribution
- Author
-
AQUINO, DANIEL ALEJANDRO, primary, TAVARES, MARCELO TEXEIRA, additional, BALDUCCI, EZEQUIEL, additional, BACA, VERÓNICA, additional, and QUINTEROS, SARA QUINTANA DE, additional
- Published
- 2015
- Full Text
- View/download PDF
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