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Kawagoe, James C, Abrams, Adelaine E, Lourie, Austin P, and Walse, Spencer S
- Pest Management Science; Jul2022, Vol. 78 Issue 7, p3090-3097, 8p
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STINKBUGS, BROWN marmorated stink bug, CARBON dioxide, FUMIGATION, ATMOSPHERIC carbon dioxide, HEMIPTERA, and DILUTION
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BACKGROUND: The brown marmorated stink bug (BMSB), Halyomorpha halys, has caused significant agricultural damage to numerous hosts, so agricultural producers seek to limit its spread. Where established, BMSB can also cause substantial urban and commercial disturbance, as overwintering adults may seek refuge inside dwellings, covered spaces, vehicles, and consignments. Phytosanitary authorities are most concerned with the importation of 'hitchhiking' adults in this refugia, with certain countries requiring a quarantine treatment to mitigate risk. This study explores fumigation with ethyl formate, applied as 16.7% by mass dilution in carbon dioxide, for control of adult BMSB. RESULTS: The induction of diapause, to simulate overwintering physiology, resulted in 2‐ and 3‐fold increases in the tolerance of adults toward this ethyl formate fumigation at 10 ± 0.5 °C (x¯±2s) lasting for 8 and 12 h, respectively. However, a decreased tolerance (0.7‐fold) of diapausing specimens was observed for a 4‐h duration. Diapausing and nondiapausing adult BMSB can be controlled at the probit 9 level if the headspace concentration of ethyl formate, [EF], in the carbon dioxide mixture is maintained ≥7.68 mg L−1 for 12 h at 10 ± 0.5 °C (x¯±2s). If the duration is shortened to 4 h, [EF] must be maintained ≥14.73 mg L−1 over the course of fumigation. CONCLUSION: The toxicity of ethyl formate in this mixture can be distinct for different physiological states of the same life stage, as evidenced by a ca. 3‐fold increase in the Haber's z parameter for adult BMSB when in diapause. Respective to the physiological state of adults, this study identifies how the applied dose and/or treatment duration can be modulated (i.e. tuned) to ensure adequate toxicological efficacy toward BMSB infesting hosts or refuge at temperatures ca. >10 °C. Published 2022. This article is a U.S. Government work and is in the public domain in the USA. [ABSTRACT FROM AUTHOR]
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Panizzi, A. R. and Lucini, T. L.
- Arthropod-Plant Interactions; Feb2022, Vol. 16 Issue 1, p1-14, 14p
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Most stink bugs (Pentatomidae) are polyphagous and feed on an array of cultivated and non-cultivated plants. Among the last, weed plants play an important role in their bioecology and pest status, particularly in the Neotropics, in where stink bugs are active during most of the year. In spite of this, the weeds role is, in general, underestimated. In this review article we present and discuss the importance of weed plants present in row crops and pasture lands, affecting stink bugs pests of major commodities in the Neotropics. We surveyed the literature and other sources (unpublished records) on the presence of stink bugs on weed plants. These plants were ranked as hosts (allowing nymph development and/or adult reproduction) or as associated plants (providing some nutrients/water/shelter, but not allowing nymph and/or adult performance). The following stink bug pest species were covered: The green-bellied stink bugs, Diceraeus furcatus (F.) and D. melacanthus Dallas; the Neotropical brown sink bug, Euschistus heros (F.); the brown-winged stink bug, Edessa meditabunda (F.); the southern green stink bug, Nezara viridula (L.); the rice stink bugs, Oebalus poecilus (Dallas) and O. ypsilongriseus (De Geer); the red-banded stink bug, Piezodorus guildinii (Westwood); the rice stalk stink bug, Tibraca limbativentris Stål; and the red-shouldered stink bug, Thyanta perditor (F.). The survey showed plants from 16 different families interacting with the 10 species of pest pentatomids analyzed, with the greater number of species of Fabaceae (16+), Poaceae (14+), and Asteraceae (7). Data demonstrated that, in the modern landscape scenario of agricultural areas in the Neotropics, highly polyphagous species, such as N. viridula, tend to suffer greater impact, while the oligophagous species, E. heros, D. furcatus, and D. melacanthus, in contrast, tend to be favored. The management of weed plants through the increase use of herbicides, multiple cropping, and the non-tillage cultivation systems seems to be the major factors influencing the interactions of stink bugs and weeds, changing the population dynamics of pest stink bugs in the Neotropics, and, consequently their pest status. [ABSTRACT FROM AUTHOR]
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Abrams, Adelaine E, Alvarez, Alfredo, Rodriguez, Matthew S, Kron, Cindy R, Bellamy, Dave E, and Walse, Spencer S
- Journal of Economic Entomology; Dec2021, Vol. 114 Issue 6, p2297-2306, 10p
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BROWN marmorated stink bug, STINKBUGS, HEMIPTERA, GREENHOUSES, ADULTS, and COWPEA
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Brown marmorated stink bug (BMSB), Halyomorpha halys (Stål) (Hemiptera: Pentatomidae), is a pest of concern that must be controlled for market access of host material and regulated articles to certain countries. This work outlines a rearing system for BMSB on live cowpea plants, Vigna unguiculata (L.) Walp. (Fabales: Fabaceae), including methods to induce adults to both enter and exit diapause. This scalable system affords continuous access to >600 specimens per week of each life stage and/or age group, which is particularly advantageous when developing treatment efficacy data. [ABSTRACT FROM AUTHOR]
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Kaptein, F H J, Stals, M A M, Klaase, E, Kapteijn, M Y, Cannegieter, S C, Taphoorn, M J B, Dirven, L, Huisman, M V, Koekkoek, J A F, and Klok, F A
- Neuro-Oncology; 2021 Supplement, Vol. 23, pii38-ii38, 1p
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F H J Kaptein, M A M Stals, E Klaase, M Y Kapteijn, S C Cannegieter, M J B Taphoorn, L Dirven, M V Huisman, J A F Koekkoek, and F A Klok
- Neuro-Oncology. 23:ii38-ii38
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Cancer Research, Clinical Neurology, and Oncology
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BACKGROUND Patients with glioblastoma are considered to be at high risk of venous thromboembolism (VTE) and major bleeding (MB), although reliable incidence estimates are lacking. The aim of this study was to assess the cumulative incidence, risk factors and prognostic impact of VTE and MB in a large cohort of glioblastoma patients. MATERIAL AND METHODS Patients diagnosed with glioblastoma between 2004–2020 from the Leiden University Medical Center and Haaglanden Medical Center were included and followed from 6 months before date of histopathological glioblastoma diagnosis up to two years after, or until an outcome of interest (VTE and MB) or death occurred. Cumulative incidences were estimated using Kaplan-Meier and cumulative incidence competing risk methods. Outcome predictors were determined with multivariable (time-dependent) Cox models. RESULTS Of the 967 included patients, 631 died, 101 were diagnosed with VTE and 130 with MB during a median follow-up of 15 months (IQR 9–22). The majority of MBs were intracranially (94%), of which half was within 4 weeks post-surgery (51%). Ambulant patients did not routinely receive pharmacological thromboprophylaxis. The adjusted 2.5-year-cumulative incidence of VTE was 12% (95%CI 10–14) and of MB 16% (95%CI 13–18). One year increase in age (HR 1.03, 95%CI 1.01–1.05), tumor resection (vs. biopsy: HR 0.56, 95%CI 0.35–0.89) and performance status (ECOG >1 vs ≤1: HR 1.8, 95%CI 1.2–2.7) were independent predictors of VTE (a biopsy rather than resection was performed in patients with the worst prognosis). MB and VTE predicted all-cause mortality (adjusted HR 1.7, 95%CI 1.3–2.1 and 1.3, 95%CI 0.99–1.6 respectively). CONCLUSION The incidences of VTE and MB in patients with glioblastoma are high, with both complications associated with a poor prognosis. Our observations emphasize the need for prospective studies to determine optimal thromboprophylaxis and VTE treatment strategy in these patients.
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Rider, David A. and Swanson, Daniel R.
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Biodiversity, Taxonomy, Animalia, Arthropoda, Insecta, Hemiptera, Pentatomidae, Thyanta, Thyanta custator, and Thyanta custator accerra mcatee, 1919
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Thyanta custator accerra McAtee, 1919 Distribution: Canada: MB (Maw et al. 2000), ON (Maw et al. 2000, Roch 2020), QC, SK (Scudder 2013). United States: AL, AR, AZ, CA (Van Duzee 1917, Johnson & Ledig 1918, Norland 1931, Goeden 1971, Rider & Chapin 1992), CO, CT (Van Duzee 1917, Parshley 1923 a, O’Donnell & Schaefer 2012), DE (Rider & Chapin 1992), DC (Rider & Chapin 1992), FL, GA, IA (Osborn, 1892, Stoner 1915, Van Duzee 1917, Hendrickson 1930, Knight 1936, Rider & Chapin 1992), IL, IN, KS, KY (Rider & Chapin 1992), LA (Rider & Chapin 1992, Temple, Davis, Micinski et al. 2013), MA (Uhler 1878, Parshley 1917, Van Duzee 1917), MD (Rider & Chapin 1992), ME (Phipps 1930, Rider & Chapin 1992, Roch 2020), MI, MN (Rider & Chapin 1992, Koch et al. 2014), MO, MS, MT, NC, ND, NE (Uhler 1872, 1876; Van Duzee 1917; Rider & Chapin 1992), NH (Rider & Chapin 1992, Roch 2020), NJ (Van Duzee 1917, Rider & Chapin 1992), NM, NV, NY, OH (Osborn 1900, Adkins 1917, Balduf 1923, Furth 1974, Rider & Chapin 1992), OK (Ortenburger 1927; Carpenter 1937; Smith 1940a, b; Fenton & Howell 1957; Stoner et al. 1962; Arnold & Drew 1988; Rider & Chapin 1992; Kondratieff et al. 2005), PA (Van Duzee 1917, Rider & Chapin 1992), SC (Jones & Sullivan 1981, Rider & Chapin 1992), SD, TN (Stål 1872, Van Duzee 1917, Howden & Crossley 1961, Rider & Chapin 1992, Lambdin et al. 2003), TX, UT, VA (Hoffman 1971; Allen & Hoffman 1975, 1976; Rider & Chapin 1992; Basnet et al. 2014), WV (Rider & Chapin 1992), WI (Rider & Chapin 1992), WY. (Mexico, Guatemala, Hawaii) Comments: At the time of the Froeschner (1988) catalog, the status of the different U.S. forms within Thyanta was confused. Rider & Chapin (1992) determined that Thyanta custator is composed of two subspecies - the nominate subspecies occurs along the Atlantic and Gulf coasts, whereas Thyanta custator accerra occurs throughout the rest of the U.S., except it is replaced by Thyanta pallidovirens in the western U.S. This form was listed in Froeschner (1988) as Thyanta accerra and also the records for Thyanta pallidovirens spinosa Ruckes refer to this form. Additionally, most records of Thyanta perditor from the desert southwestern states should be referred here. The Idaho record for this species should be referred to Thyanta pallidovirens.
Published as part of Rider, David A. & Swanson, Daniel R., 2021, A distributional synopsis of the Pentatomidae (Heteroptera) north of Mexico, including new state and provincial records, pp. 1-69 in Zootaxa 5015 (1) on pages 38-39, DOI: 10.11646/zootaxa.5015.1.1, http://zenodo.org/record/5159085
{"references":["McAtee, W. L. (1919) Notes on Nearctic Hemiptera. Bulletin of the Brooklyn Entomological Society, 14, 8 - 16.","Maw, H. E. L., Foottit, R. G., Hamilton, K. G. A. & Scudder, G. G. E. (2000) Checklist of the Hemiptera of Canada and Alaska. National Research Council of Canada, NRC Research Press, Ottawa, 220 pp. Canada,","Roch, J-F. (2020) Entomofaune du Quebec. Liste des Punaises du Quebec et des Regions Adjacentes (Hemiptera: Heteroptera). Document Faunique 27. Version 2.3. Entomofaune du Quebec Inc., Saguenay, 41 pp.","Scudder, G. G. E. (2013) Additional provincial and state records for Heteroptera (Hemiptera) in Canada and the United States. Journal of the Entomological Society of British Columbia, 109, 55 - 69.","Van Duzee, E. P. (1917) Catalogue of the Hemiptera of America North of Mexico, Excepting the Aphididae, Coccidae and Aleurodidae. University of California Publications Entomology 2. University of California press, Berkeley, California, xiv + 902 pp. https: // doi. org / 10.5962 / bhl. title. 29381","Johnson, C. & Ledig, R. (1918) Tentative list of Hemiptera from the Claremont-Laguna region. Journal of Entomology and Zoology, 10, 3 - 8.","Norland, C. (1931) List of California Pentatomidae, especially from the south. Journal of Entomology and Zoology, 23, 45 - 46.","Goeden, R. D. (1971) Insect ecology of silverleaf nightshade. Weed Science, 19 (1), 45 - 51. https: // doi. org / 10.1017 / S 0043174500048244","Rider, D. A. & Chapin, J. B. (1992) Revision of the genus Thyanta Stal, 1862 (Heteroptera: Pentatomidae) II. North America, Central America, and the West Indies. Journal of the New York Entomological Society, 100 (1), 42 - 98.","Parshley, H. M. (1923 a) Family Pentatomidae, Cydnidae, Scutelleridae. In: Britton, W. E. (Ed.), Guide to the Insects of Connecticut. Part IV. The Hemiptera or Sucking Insects of Connecticut. Connecticut State Geological and Natural History Survey Bulletin, 34, pp. 753 - 783, pls. XVIII - XX","Wheeler, A. G. Jr. & Krimmel, B. A. (2012) Banasa sordida (Uhler) (Hemiptera: Pentatomidae): Monterey cypress and Gowen cyprus (Cupressus macrocarpa, C. goveniana; Cupressaceae) as host plants in coastal California. Proceedings of the Entomological Society of Washington, 114 (2), 263 - 268. https: // doi. org / 10.4289 / 0013 - 8797.114.2.263","Osborn, H. (1892) Catalogue of the Hemiptera of Iowa. Proceedings of the Iowa Academy of Sciences, 1 (2), 120 - 131.","Stoner, D. (1915) Preliminary notes on Iowa Pentatomoidea (Heterop.). Entomological News, 26, 353 - 355.","Hendrickson, G. O. (1930) Studies on the insect fauna of Iowa praries. Iowa State College Journal of Science, 4 (2), 49 - 179.","Knight, H. H. (1936) Records of southern insect species moving northward during the drouth years of 1930 and 1934. Annals of the Entomological Society of America, 29 (4), 578 - 580. https: // doi. org / 10.1093 / aesa / 29.4.578","Temple, J. H., Davis, J. A., Micinski, S., Hardke, J. T., Price, P. & Leonard, B. R. (2013) Species composition and seasonal abundance of stink bugs (Hemiptera: Pentatomidae) in Louisiana soybean. Environmental Entomology, 42 (4), 648 - 657. https: // doi. org / 10.1603 / EN 11135","Uhler, P. R. (1878) On the Hemiptera collected by Dr. Elliott Coues, U. S. A., in Dakota and Montana, during 1873 - 74. Bulletin of the United States Geological and Geographical Survey of the Territories, 4, 503 - 512.","Parshley, H. M. (1917) Fauna of New England. 14. List of the Hemiptera-Heteroptera. Occasional Papers of the Boston Society of Natural History, 7, 1 - 125.","Phipps, C. R. (1930) Blueberry and huckleberry insects. Bulletin of the Maine Agricultural Experiment Station, 356, 107 - 232.","Koch, R. L., Rider, D. A., Tinerella, P. P. & Rich, W. A. (2014) Stink bugs (Hemiptera: Heteroptera: Pentatomidae) of Minnesota: An annotated checklist and new state records. The Great Lakes Entomologist, 47 (3 - 4), 171 - 185.","Uhler, P. R. (1872) Notices of the Hemiptera of the Western Territories of the United States, chiefly from the surveys of Dr. F. V. Hayden. In: Hayden, F. V. (Ed.), Preliminary Report of the United States Geological Survey of Montana and Portions of Adjacent Territories, Being a Fifth Annual Report of Progress. Government Printing Office, Washington, D. C, pp. 392 - 423.","Uhler, P. R. (1876) List of the Hemiptera of the region west of the Mississippi River, including those collected during the Hayden explorations of 1873. Bulletin of the United States Geological and Geographical Survey of the Territories, 1, 267 - 361.","Osborn, H. (1900) Remarks on the hemipterous fauna of Ohio with a preliminary record of species. Annual Report of the Ohio State Academy of Science, 8, 60 - 79.","Adkins, W. S. (1917) Some Ohio Heteroptera records. Ohio Journal of Science, 18 (2), 58 - 61.","Balduf, W. V. (1923) The insects of the soybean in Ohio. Bulletin of the Ohio Agricultural Experiment Station, 366, 147 - 181.","Furth, D. G. (1974) The stink bugs of Ohio (Hemiptera: Pentatomidae). Bulletin of the Ohio Biological Survey, 5 (1), 1 - 62.","Ortenburger, A. I. (1927) Some Oklahoma Hemiptera. Proceedings of the Oklahoma Academy of Science, 6, 184 - 192.","Carpenter, J. R. (1937) Fluctuations in biotic communities, III. Aspection in a ravine sere in central Oklahoma. Ecology, 18 (1), 80 - 92. https: // doi. org / 10.2307 / 1932704","Smith, C. C. (1940 a) Biotic and physiographic succession on abandoned eroded farmland. Ecological Monographs, 10 (3), 421 - 484. https: // doi. org / 10.2307 / 1948513","Fenton, F. A. & Howell, D. E. (1957) A comparison of five methods of sampling alfalfa fields for arthropod populations. Annals of the Entomological Society of America, 50 (6), 606 - 611. https: // doi. org / 10.1093 / aesa / 50.6.606","Stoner, A., Bryan, D. E. & Drew, W. A. (1962) A partial inventory of insect populations in tallgrass prarie pastures in north central Oklahoma. Proceedings of the Oklahoma Academy of Science, 42, 143 - 157.","Arnold, D. C. & Drew, W. A. (1988) The Pentatomoidea (Hemiptera) of Oklahoma. Agricultural Experiment Station, Oklahoma State University, Technical Bulletin T - 166. Norman, Oklahoma, 42 pp.","Kondratieff, B. C., Schmidt, J. P., Opler, P. A. & Garhart, M. C. (2005) Survey of selected arthropod taxa of Fort Sill, Comanche County, Oklahoma. III. Arachnida: Ixodidae, Scorpiones, Hexapoda: Ephemeroptera, Hemiptera, Homoptera, Coleoptera, Neuroptera, Trichoptera, Lepidoptera, and Diptera. Contributions of the C. P. Gillette Museum of Arthropod Diversity, 2005, 72 - 265.","Jones, W. A. Jr. & Sullivan, M. J. (1981) Overwintering habitats, spring emergence patterns, and winter mortality of some South Carolina Hemiptera. Environmental Entomology, 10 (3), 409 - 414. https: // doi. org / 10.1093 / ee / 10.3.409","Stal, C. (1872) Enumeratio Hemipterorum. Bidrag till en forteckning ofver alla hittels kanda Hemiptera, Jemte Systematiska meddelanden. 2. Kongliga Svenska Vetenskaps-Akademiens Handlingar, 10 (4), 1 - 159.","Howden, H. F. & Crossley, D. A. Jr. (1961) Insect Species on Vegetation of the White Oak Lake Bed, Oak Ridge, Tennessee. No. ORNL- 3094. Oak Ridge National Laboratory, Oak Ridge, Tennessee, 38 pp. https: // doi. org / 10.2172 / 4041200","Lambdin, P. L., Grant, J. F., Wiggins, G. J. & Saxton, A. (2003) Diversity of the true bugs (Hemiptera: Heteroptera) on Arnold Air Force Base, Tullahoma, Tennessee. Journal of the Tennessee Academy of Science 78 (3), 76 - 84.","Hoffman, R. L. (1971) The Insects of Virginia: No. 4. Shield Bugs (Hemiptera; Scutelleroidea, Corimelaenidae, Cydnidae, Pentatomidae). Virginia Polytechnic Institute and State University, Research Division Bulletin, 67, i - v + 1 - 61, 7 maps, 1 pl.","Allen, W. A. & Hoffman, R. L. (1975) Distribution records of several Virginia shield bugs (Hemiptera: Scutelleridae, Corimelaenidae, Cydnidae, Pentatomidae). USDA Cooperative Economic Insect Report, 25 (12), 233 - 236.","Allen, W. A. & Hoffman, R. L. (1976) New geographical and seasonal distribution records for thiry-one species of Virginia shield bugs (Hemiptera: Scutelleridae, Cydnidae, and Pentatomidae. USDA Cooperative Plant Pest Report, 1 (41), 747 - 751.","Basnet, S., Maxey, L. M., Laub, C. A., Kuhar, T. P. & Pfeiffer, D. G. (2014) Stink bugs (Hemiptera: Pentatomidae) in primocanebearing raspberries in southwestern Virginia. Journal of Entomological Science, 49 (3), 304 - 312. https: // doi. org / 10.18474 / 0749 - 8004 - 49.3.304","Froeschner, R. C. (1988) Family Pentatomidae Leach, 1815. The stink bugs. In: Henry, T. J. & Froeschner, R. C. (Eds.), Catalog of the Heteroptera, or True Bugs, of Canada and the Continental United States. E. J. Brill, Leiden, New York, pp. 544 - 607. https: // doi. org / 10.1201 / 9781351070447 - 30"]}
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7. Platyvelia brachialis [2021]
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Rodrigues, Juliana Mourão Dos Santos, Nery, Leticia, Rodrigues, Higor D. D., and Moreira, Felipe Ferraz Figueiredo
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Biodiversity, Taxonomy, Animalia, Arthropoda, Insecta, Hemiptera, Veliidae, Platyvelia, and Platyvelia brachialis
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Platyvelia brachialis (Stål, 1860) (Figs 100, 104) Geographical distribution: Argentina (Torres et al. 2008), Belize (Floriano et al. 2017a), Brazil (Stål 1860), Colombia (Roback & Nieser 1974), Costa Rica (Polhemus & Polhemus 1993), Cuba (Uhler 1894a), Dominican Republic (Drake & Maldonado-Capriles 1956), El Salvador (Floriano et al. 2017a), Grenada (Uhler 1894a), Guatemala (Champion 1898), Haiti (Perez-Gelabert & Floriano 2016), Jamaica (Lanigan & Hyslop 2011), Mexico (Uhler 1894b), Nicaragua (Polhemus & Polhemus 1993), Panama (Champion 1898), Peru (Polhemus & Polhemus 1993), Suriname (Polhemus & Polhemus 1993), Trinidad & Tobago (Hynes 1948), United States of America (Snow 1905), Venezuela (Floriano et al. 2017a). Distribution in Brazil: AL*, ES (Nieser & Melo 1997; Moreira et al. 2010; Crumière et al. 2016), GO (Polhemus & Polhemus 1993), MG (Nieser & Melo 1997; Melo & Nieser 2004; Souza et al. 2006), MS (Floriano et al. 2013), MT (Dias-Silva et al. 2013; Dias-Silva et al. 2020), PE (Rodrigues et al. 2012), PI (Cordeiro & Moreira 2015), RJ (Stål 1860; Ribeiro et al. 2010), SC (Polhemus & Polhemus 1993), SE*. Material examined: BRAZIL • Alagoas • 1 female, 4 nymphs; Campo Grande, rio; -9.955930, -36.837280; 07 Jul. 2018; C.F.B. Floriano, J.M.S. Rodrigues & J.F. Barbosa col.; CEIOC 81257. • 1 male; Igaci, Rodovia BR-316, Rio Lunga; -9.531060, -36.533150; 06 Jul. 2018; C.F.B. Floriano, J.M.S. Rodrigues & J.F. Barbosa col.; CEIOC 79728. • 1 male; Maragogi, APACC; -8.930730, -35.210490; 29 Apr. 2018; C.F.B. Floriano, J.M.S. Rodrigues & O.M. Magalhães col.; CEIOC 79727. • 1 female; Murici, EEM; -9.220460, -35.870290; 28 Apr. 2018; C.F.B. Floriano, J.M.S. Rodrigues & O.M. Magalhães col.; CEIOC 79726. • 1 male, 3 females, 1 nymph; Quebrangulo, RBPT, riacho em um pasto; -9.260420, -36.416020; 04 Jul. 2018; C.F.B. Floriano, J.M.S. Rodrigues & J.F. Barbosa col.; CEIOC 79730. • 3 males, 1 female; same data, except: Rio Cafuringa; -9.259130, -36.417430; CEIOC 79731. • 1 male, 1 female, 2 nymphs; same data, except: Sítio Juliana, rio; -9.234030, -36.448860; 05 Jul. 2018; CEIOC 79733. • 1 female; Taquarana, Coité do Noá, queda d´água; -9.67230, -36.49871; 06 Jul. 2018; C.F.B. Floriano, J.M.S. Rodrigues & J.F. Barbosa col.; CEIOC 81256. • 1 male; Viçosa, Cachoeira do Anel; -9.3174619, -36.2943674; alt. 333 m; 21 May 2019; J.M.S. Rodrigues, H. Rodrigues, W. Sousa & F.F.F. Moreira col.; CEIOC 79781. • 1 male, 1 female; same data, except: Fazenda Baixa Funda, riacho; -9.3242712, -36.2829933; CEIOC 79784. • 1 male, 1 female; Viçosa, Fazenda Baixa Funda; -9.323889, -36.282500; alt. 284 m; 21 Mar. 2019; H. Rodrigues col.; MZUSP. • 1 male; Viçosa, Fazenda Baixa Funda; -9.324022, -36.282647; alt. 284 m; 14 Sep. 2017; L-0001; H. Rodrigues & K. Paresque col.; MZUSP. • Sergipe • 1 male, 4 females, 2 nymphs; Japoatã, Estrada SE- 335; -10.367910, -36.807400; 03 May 2018; C.F.B. Floriano, J.M.S. Rodrigues & O.M. Magalhães col.; CEIOC 79732. • 2 females; São Cristóvão, Estrada Rita Cacete; -10.985110, -37.286830; 04 May 2018; C.F.B. Floriano, J.M.S. Rodrigues & O.M. Magalhães col.; CEIOC 79729.
Published as part of Rodrigues, Juliana Mourão Dos Santos, Nery, Leticia, Rodrigues, Higor D. D. & Moreira, Felipe Ferraz Figueiredo, 2021, Survey of the semiaquatic bugs (Hemiptera: Heteroptera: Gerromorpha) from Alagoas and Sergipe, Northeast Brazil, pp. 103-159 in Zootaxa 4958 (1) on pages 143-144, DOI: 10.11646/zootaxa.4958.1.9, http://zenodo.org/record/4693243
{"references":["Stal, C. (1860) Bidrag till Rio Janeiro-Traktens Hemipter-Fauna. Kongliga Svenska Vetenskaps Akademiens Handlingar, 2 (7), 1 - 84.","Torres, P. L. M., Mazzuconi, S. A., Michat, M. C. & Bachmann, A. O. (2008) Los coleopteros y heteropteros acuaticos del Parque Nacional Calilegua (Provincia de Jujuy, Argentina). Revista de la Sociedad Entomologica Argentina, 67 (1 - 2), 127 - 144.","Floriano, C. F. B., Moreira, F. F. F. & Bispo, P. C. (2017 a) New records of Gerromorpha (Insecta: Hemiptera: Heteroptera) from the Neotropical Region. Transactions of the American Entomological Society, 143 (2), 103 - 117. https: // doi. org / 10.3157 / 061.143.0202","Roback, S. S. & Nieser, N. (1974) Aquatic Hemiptera (Heteroptera) from the Llanos of Colombia. Proceedings of the Academy of Natural Sciences of Philadelphia, 126, 29 - 49.","Polhemus, J. T. & Polhemus, D. A. (1993) Two new genera for New World Veliinae (Heteroptera: Veliidae). Journal of the New York Entomological Society, 101 (3), 391 - 398.","Uhler, P. R. (1894 a) On the Hemiptera- Heteroptera of the Island of Grenada, West Indies. Proceedings of the Zoological Society of London, 1894, 167 - 224.","Drake, C. J. & Maldonado-Capriles, J. (1956) Some Pleids and Water-Striders from the Dominican Republic (Hemiptera). Bulletin of the Brooklyn Entomological Society, 51, 53 - 56.","Champion, G. C. (1898) Hemiptera - Heteroptera. Biologia Centrali-Americana. Rhynchota, 2, 1 - 416.","Perez-Gelabert, D. E. & Floriano, C. F. B. (2016) New Records of the Water Strider Platyvelia brachialis (Stal, 1860) (Hemiptera: Heteroptera: Veliidae) from the Dominican Republic and Haiti, with a Checklist of the West Indian Veliidae. Proceedings of the Entomological Society of Washington, 118 (3), 471 - 476. https: // doi. org / 10.4289 / 0013 - 8797.118.3.471","Lanigan, A. C. & Hyslop, E. J. (2011) The aquatic and semiaquatic Hemiptera of Jamaica. Journal of Freshwater Ecology, 26 (2), 295 - 297. https: // doi. org / 10.1080 / 02705060.2011.559335","Uhler, P. R. (1894 b) Observations upon the Heteropterous Hemiptera of Lower California, with descriptions of new species. Proceedings of the California Academy of Sciences, 2 (4), 223 - 295.","Hynes, H. B. N. (1948) Notes on the aquatic Hemiptera-Heteroptera of Trinidad and Tobago, B. W. I., with a description of a new species of Martarega B. White (Notonectidae). Transactions of the Royal Entomologist Society of London, 99 (10), 341 - 360. https: // doi. org / 10.1111 / j. 1365 - 2311.1948. tb 01225. x","Snow, F. H. (1905) Some Results of the University of Kansas Entomological Expeditions to Arizona in 1904 and 1905. Transactions of the Kansas Academy of Science, 20, 155 - 181. https: // doi. org / 10.2307 / 3624697","Nieser, N. & Melo, A. L. (1997) Os heteropteros aquaticos de Minas Gerais. Guia introdutorio com chave de identificacao para as especies de Nepomorpha e Gerromorpha. Universidade Federal de Minas Gerais, Belo Horizonte, 180 pp.","Moreira, F. F. F., Nessimian, J. L., Rudio, J. A. & Salles, F. F. (2010) New species and new records of Veliidae from Espirito Santo State and adjacent Minas Gerais state, Brazil, with notes on nomenclature (Insecta: Heteroptera: Gerromorpha). Journal of Natural History, 44 (45), 2761 - 2801. https: // doi. org / 10.1080 / 00222933.2010.512423","Crumiere, A. J. J., Santos, M. E., Semon, M., Armisen, D., Moreira, F. F. F. & Khila, A. (2016) Diversity in Morphology and Locomotory Behavior Is Associated with Niche Expansion in the Semiaquatic Bugs. Current Biology, 26, 1 - 7. https: // doi. org / 10.1016 / j. cub. 2016.09.061","Melo, A. L. & Nieser, N. (2004) Faunistical notes on aquatic and semiaquatic Heteroptera of Minas Gerais (Brazil): an annotated list of Gerromorpha and Nepomorpha collected near Januaria. Lundiana, 5, 43 - 49.","Souza, M. A. A., Melo, A. L. & Vianna, G. J. C. (2006) Heteropteros aquaticos oriundos do Municipio de Mariana, MG. Neotropical Entomology, 35, 803 - 810. https: // doi. org / 10.1590 / S 1519 - 566 X 2006000600013","Floriano, C. F. B., Oliveira, I. A. D. V. & Melo, A. L. (2013) New records and checklist of aquatic and semi-aquatic Heteroptera (Insecta: Hemiptera: Gerromorpha and Nepomorpha) from the Southern region of Mato Grosso do Sul, Brazil. Biota Neotropica, 13 (1), 210 - 219. https: // doi. org / 10.1590 / S 1676 - 06032013000100022","Dias-Silva, K., Moreira, F. F. F., Giehl, N. F. S., Nobrega, C. C. & Cabette, H. S. R. (2013) Gerromorpha (Hemiptera: Heteroptera) of eastern Mato Grosso State, Brazil: checklist, new records, and species distribution modeling. Zootaxa, 3736 (3), 201 - 235. https: // doi. org / 10.11646 / zootaxa. 3736.3.1","Dias-Silva, K., Brasil, L. S., Juen, L., Cabette, H. S. R., Freitas, P. V. & De Marco Jr. P. (2020) Influence of Local Variables and Landscape Metrics on Gerromorpha (Insecta: Heteroptera) Assemblages in Savanna Streams, Brazil. Neotropical Entomology, 49, 191 - 202. https: // doi. org / 10.1007 / s 13744 - 019 - 00748 - 8","Rodrigues, H. D. D., Melo, A. L. & Ferreira-Keppler, R. L. (2012) New records of Gerromorpha (Insecta: Hemiptera: Heteroptera) from Brazil. Check List, 8 (5), 908 - 913. https: // doi. org / 10.15560 / 8.5.908","Cordeiro, I. R. S. & Moreira, F. F. F. (2015) New distributional data on aquatic and semiaquatic bugs (Hemiptera: Heteroptera: Gerromorpha & Nepomorpha) from South America. Biodiversity Data Journal, 3, e 4913. https: // doi. org / 10.3897 / BDJ. 3. e 4913","Ribeiro, J. R. I., Moreira, F. F. F., Alecrim, V. P., Barbosa, J. F. & Nessimian, J. L. (2010) Especies de heteropteros dulciaquicolas (Hemiptera, Heteroptera, Gerromorpha e Nepomorpha) registradas no Estado do Rio de Janeiro, Brazil. Arquivos do Museu Nacional, 67, 303 - 312."]}
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Cornelius, Mary L, Herlihy, Megan V, Vinyard, Bryan T, Weber, Donald C, and Greenstone, Matthew H
- Journal of Economic Entomology; Apr2021, Vol. 114 Issue 2, p590-596, 7p
- Subjects
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STINKBUGS, BROWN marmorated stink bug, PREDATION, HEMIPTERA, SPECIES, and LANDSCAPES
- Abstract
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This study evaluated parasitism and predation on sentinel egg masses of three stink bug species, the spined soldier bug, Podisus maculiventris (Say), the brown stink bug, Euschistus servus (Say), and the invasive brown marmorated stink bug (BMSB), Halyomorpha halys (Stål), in ornamental landscapes composed of either native or exotic plants. This study also compared the species composition of parasitoids attacking two native stink bug species (P. maculiventris and E. servus) with those attacking the invasive BMSB on the same tree species in the same habitat. Overall, egg parasitism and predation were much higher on the two native stink bug species compared with BMSB, with an average parasitism rate of 20.6% for E. servus , 12.7% for P. maculiventris , and only 4.2% for H. halys and an average predation rate of 8.2% for E. servus, 17.7% for P. maculiventris, and 2.3% for H. halys. Egg predation was also significantly higher on P. maculiventris than on E. servus eggs. Eight parasitoid species attacked sentinel stink bug eggs in the ornamental landscaped plots. Trissolcus euschisti (Ashmead) (Hymenoptera: Scelionidae) was the predominant parasitoid for all three stink bug species. There were no significant differences in parasitism and predation rates on any of the stink bug species between native and exotic plots. Therefore, there is no evidence that ornamental landscapes composed of native plants increased parasitism or predation rates of sentinel egg masses of two native stink bug species or the invasive BMSB, compared with those composed entirely of exotic plants. [ABSTRACT FROM AUTHOR]
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Leopoldo J. Álvarez, Adela M. Bernardis, Bárbara S. Defea, Pablo M. Dellapé, María G. Del Río, Cecilia G. Gittins López, Analía A. Lanteri, María F. López Armengol, Ana M. Marino de Remes Lenicov, Eugenia Minghetti, Susana L. Paradell, and María E. Rizzo
- Revista de la Sociedad Entomológica Argentina. 80:48-69
- Subjects
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Insect Science, Ecology, and Ecology, Evolution, Behavior and Systematics
- Abstract
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The knowledge of the entomological fauna in productive systems is important for the agroecological management since beneficial insects are a key resource for pest management in horticultural systems. Scientific information on the biodiversity present in a given area is essential as well as the ecological function and/or feeding habits of the insects. In Alto Valle de Río Negro and Neuquén, horticultural production systems can be described as highly dependent on chemical inputs for pest management and fertilization. The aim of this study is to carry out an inventory of the biodiversity of some families of Hemiptera, Coleoptera (Curculionidae) and Hymenoptera present in peri-urban and rural farms located in Neuquén and Río Negro, respectively. Insects were collected through pitfall and sweeping net on tomato and pepper crops and the surrounding non-cultivated areas. Idiosystatus Berg (Auchenorrhyncha) was cited for the first time from Argentina. Species cited for the first time from Neuquén: Hemiptera: Auchenorrhyncha: Acanalonia chloris (Berg), Syncharina punctatissima (Signoret), Amplicephalus dubius Linnavuori, Exitianus obscurinervis (Stål), Agalliana ensigera Oman and Bergallia signata (Stål); Hemiptera: Heteroptera: Harmostes (Harmostes) prolixus Stål and Atrachelus (Atrachelus) cinereus (Fabricius); Coleoptera: Curculionidae: Hypurus bertrandi (Perris), Naupactus leucoloma Boheman, Otiorhynchus rugosostriatus (Goeze) and Sitona discoideus Gyllenhal and Hymenoptera: Xylocopa (Neoxylocopa) augusti Lepeletier and Pseudagapostemon (Neagapostemon) singularis Jörgensen. Species cited for the first time from Río Negro: Hemiptera: Auchenorrhyncha: Amplicephalus dubius Linnavuori, Amplicephalus marginellanus Linnavuori, Circulifer tenellus (Baker) and Xerophloea viridis (Fabricius); Hemiptera: Heteroptera: Tupiocoris cucurbitaceus (Spinola), Atrachelus (Atrachelus) cinereus (Fabricius), Dichelops furcatus (Fabricius) and Harmostes (Harmostes) prolixus Stål; Coleptera: Curculionidae: Naupactus xanthographus (Germar) and Hymenoptera: Diadasia pereyrae (Holmberg) and Dialictus autranellus (Vachal)
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Bryan T. Vinyard, Megan V. Herlihy, Donald C. Weber, Matthew H. Greenstone, and Mary L. Cornelius
- Journal of Economic Entomology. 114:590-596
- Subjects
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Insect Science, Ecology, General Medicine, Biological pest control, Spined soldier bug, biology.organism_classification, biology, Pentatomidae, Hemiptera, Zoology, Predation, Parasitism, Scelionidae, and Brown marmorated stink bug
- Abstract
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This study evaluated parasitism and predation on sentinel egg masses of three stink bug species, the spined soldier bug, Podisus maculiventris (Say), the brown stink bug, Euschistus servus (Say), and the invasive brown marmorated stink bug (BMSB), Halyomorpha halys (Stål), in ornamental landscapes composed of either native or exotic plants. This study also compared the species composition of parasitoids attacking two native stink bug species (P. maculiventris and E. servus) with those attacking the invasive BMSB on the same tree species in the same habitat. Overall, egg parasitism and predation were much higher on the two native stink bug species compared with BMSB, with an average parasitism rate of 20.6% for E. servus, 12.7% for P. maculiventris, and only 4.2% for H. halys and an average predation rate of 8.2% for E. servus,17.7% for P. maculiventris, and 2.3% for H. halys. Egg predation was also significantly higher on P. maculiventris than on E. servus eggs. Eight parasitoid species attacked sentinel stink bug eggs in the ornamental landscaped plots. Trissolcus euschisti (Ashmead) (Hymenoptera: Scelionidae) was the predominant parasitoid for all three stink bug species. There were no significant differences in parasitism and predation rates on any of the stink bug species between native and exotic plots. Therefore, there is no evidence that ornamental landscapes composed of native plants increased parasitism or predation rates of sentinel egg masses of two native stink bug species or the invasive BMSB, compared with those composed entirely of exotic plants.
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