1,093 results on '"Porter, Charles"'
Search Results
202. The Centennial Trial of Steam Fire Engines
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Porter, Charles T.
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- 1876
203. Action of the Reciprocating Parts of Steam Engines
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Porter, Charles T.
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- 1871
204. Management of a Small Water Utility
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Porter, Charles L.
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- 1964
205. Documentary Research Methods Applied to Historic Sites and Buildings
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Porter,, Charles W.
- Published
- 1951
206. Managers forum focuses on competitive strategies and continuous improvement
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Kubinski, Ray, Bookhart, Sam, Callahan, Anita, Isles, Marvin L., Porter, Charles, Liotti, Anthony T., and Tomczak, Margie
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Conferences and Meetings ,Management Style ,Strategic Planning ,Competition ,Quality Control ,Ethics ,Information Systems ,Growth ,Performance Measurement ,Management by Objectives ,Industrial equipment and supplies industry -- Management ,Management by objectives -- Conferences, meetings and seminars - Abstract
"Continuous Improvement: Managing for Manufacturing Excellence," IIE's 14th annual IE Managers Forum, is coming up March 9-11 in Atlanta and is designed to make managers in manufacturing environments knowledgeable about […]
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- 1992
207. Number sequences
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Lanska, Douglas J., Dobbs, Henry, Kierstead, Friend H., Jr., and Porter, Charles F.
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Number theory -- Tests, problems and exercises ,Sequences (Mathematics) -- Tests, problems and exercises ,Calculus, Integral -- Tests, problems and exercises ,Mathematics - Published
- 1991
208. Sharing the Common Pool : Water Rights in the Everyday Lives of Texans
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Porter, Charles R. and Porter, Charles R.
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- Water rights--Texas
- Abstract
If all the people, municipalities, agencies, businesses, power plants, and other entities that think they have a right to the water in Texas actually tried to exercise those rights, there would not be enough water to satisfy all claims, no matter how legitimate. In Sharing the Common Pool: Water Rights in the Everyday Lives of Texans, water rights expert Charles Porter explains in the simplest possible terms who has rights to the water in Texas, who determines who has those rights, and who benefits or suffers because of it. The origins of Texas water law, which contains elements of the state's Spanish, English, and Republic heritages, contributed to the development of a system that defines water by where it sits, flows, or falls and assigns its ownership accordingly. Over time, this seemingly logical, even workable, set of expectations has evolved into a tortuous collection of laws, permits, and governing authorities under the onslaught of population growth and competing interests—agriculture, industry, cities—all with insatiable thirsts. In sections that cover ownership, use, regulation, real estate, and policy, Porter lays out in as straightforward a fashion as possible just how we manage (and mismanage) water in this state, what legal cases have guided the debate, and where the future might take us as old rivalries, new demands, and innovative technologies—such as hydraulic fracturing of oil shale formations (“fracking”)—help redefine water policy. To learn more about The Meadows Center for Water and the Environment, sponsors of this book's series, please click here.
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- 2014
209. Molecular operational taxonomic units of mosquitoes (Diptera: Culicidae) collected in high Andean mountain ecosystems of Antioquia, Colombia
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ROSERO-GARCÍA, DORIS, primary, BICKERSMITH, SARA A., additional, SUAZA-VASCO, JUAN DAVID, additional, PORTER, CHARLES, additional, CORREA, MARGARITA M., additional, CONN, JAN E., additional, and URIBE-SOTO, SANDRA, additional
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- 2017
- Full Text
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210. Phylogenetic signal at the Cytb-SertRNA-IG1-ND1 mitochondrial region in Anopheles (Kerteszia) neivai Howard, Dyar & Knab, 1913
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López-Rubio, Andrés, primary, Suaza, Juan David, additional, Porter, Charles, additional, Uribe, Sandra, additional, Bedoya, Gabriel, additional, and Vélez, Iván Darío, additional
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- 2017
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211. Species of sand flies (Diptera: Psychodidae) collected from natural reserves in the Pacific and Darien regions of Colombia
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Vivero, Rafael J., primary, Contreras, María Angélica, additional, Suaza, Juan D., additional, Vélez, Iván D., additional, Porter, Charles, additional, and Uribe, Sandra, additional
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- 2017
- Full Text
- View/download PDF
212. Optimal Accuracy Rocket Trajectories.
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Baker, George A., Ford, Kenneth W., and Porter, Charles E.
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- 1959
- Full Text
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213. Queensland Aboriginal policy (Full text by Queensland's Minister for Aboriginal and Island Affairs)
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Porter, Charles
- Published
- 1978
214. Lista actualizada de flebotomíneos (Diptera: Psychodidae: Phlebotominae) de la región cafetera colombiana
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Contreras-Gutiérrez, María Angélica, Vélez, Iván Darío, Porter, Charles, and Uribe, Sandra Inés
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Lutzomyia ,coffee ,café ,Psychodidae ,Colombia ,leishmaniasis - Abstract
Se presenta una lista actualizada de especies de flebotomíneos en zonas cafeteras de la región andina colombiana. Con base en la revisión y verificación taxonómica, se registraron 53 especies presentes en 12 departamentos. Además de los registros obtenidos con base en un muestreo intensivo en cinco departamentos, se recopilaron los datos existentes en trabajos publicados y en la revision taxonómica de los especímenes de la zona pertenecientes a la colección entomológica del Programa de Estudio y Control de Enfermedades Tropicales (PECET). El listado comprende los géneros Brumptomyia (2 especies), Lutzomyia (50 especies) y Warileya (1 especie). Con base en este trabajo se confirmaron 11 nuevos registros de especies en la región cafetera colombiana, entre los cuales es relevante Lutzomyia panamensis , especie de importancia médica no registrada previamente en esta zona. En total, 18 especies de las registradas poseen hábitos antropofílicos o están relacionadas con la transmisión de Leishmania spp. An updated list of phlebotomine sand flies species in coffee growing areas in the Colombian Andean region is presented. Fifty three species were reported from 12 departments. In addition, species distribution in the region was derived from specimens obtained during intensive field work in five departments, from previously published studies and from the taxonomic revision of specimens in the entomological collection of the Programa de Estudio y Control de Enfermedades Tropicales (PECET). The list includes the genera Brumptomyia (2 species), Lutzomyia (50 species) and Warileya (1 species). The updated list contains eleven new records in the region under study, including Lutzomyia panamensis , a species of medical importance not recorded previously in this zone. Eighteen of the species are considered to be anthropophilic, and many of them have been implicated in the transmission of leishmaniasis.
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- 2014
215. Partial Brain Tissue Oxygen Levels Predict Arrhythmia and Prognosis in Patients With Brain Injury
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Vanga, Subba Reddy, primary, Korlakunta, Hema, additional, Duthuluru, Sowjanya, additional, Bommana, Sudharani, additional, Narotam, Pradeep, additional, Ryschon, Kay, additional, Mohiuddin, Syed M., additional, Porter, Charles, additional, Dawn, Buddhadeb, additional, and Lakkireddy, Dhanunjaya, additional
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- 2016
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216. Use of DNA barcoding to distinguish the malaria vector Anopheles neivai in Colombia
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LÓPEZ-RUBIO, ANDRÉS, primary, SUAZA-VASCO, JUAN, additional, MARCET, PAULA L, additional, RUÍZ-MOLINA, NATALIA, additional, CÁCERES, LORENZO, additional, PORTER, CHARLES, additional, and URIBE, SANDRA, additional
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- 2016
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217. Tyrosine kinase inhibitors in hematologic malignancy: should we be concerned?
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Porter, Charles, primary
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- 2016
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218. Describe the moment/event when you knew collecting coins was going to be a serious hobby for you.
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Johnson, Rodney, Branch, Mike, Helmuth, Dwayne, Lavertu, Lorne, Jackson, Ken, Dave, Porter, Charles, Spivey, Robert, Kramer, Robert, Burdis, Dave, Butcher, Patrick, Robertson, Roy E., Joseph, Peek, John, Grant, Bob, and Vinton, Dru
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COIN collecting ,GRANDPARENTS ,CENT ,COIN dealers ,COIN errors ,PAPER money ,MEDALS - Abstract
The article focuses on individuals sharing the moments or events that sparked their serious interest in coin collecting, including receiving V nickels from a grandmother, finding an 1883 Indian cent on a bus, inheriting an 1851 half dime from a father, and discovering proof sets and valuable coins at a young age.
- Published
- 2023
219. Groundwater Conservation District Finance in Texas: Results of a Preliminary Study
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Porter, Charles R
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Finance ,Water supply for domestic and industrial purposes ,business.industry ,Bond ,Groundwater management ,groundwater conservation district finance ,Ad valorem tax ,Economics ,Revenue ,business ,groundwater management ,TD201-500 ,Groundwater ,Valuation (finance) - Abstract
The preferred method of groundwater management in Texas is by locally formed groundwater conservation districts (GCDs). However, not all of Texas groundwater is managed by a district; some areas have not voted to form a GCD. There are 99 GCDs in Texas with 2 pending; only 174 of the 254 counties are covered by a GCD. GCDs are financed by ad valorem taxes, fees, and grants. Not all GCDs have ad valorem tax support. Revenues from the responding GCDs in this study range from $20,000 annually to $2,632,982. Some cannot open their offices daily. All need money for research to determine the actual amount of groundwater in their district, its sources, and its characteristics. Tax rates for the GCDs with ad valorem tax authority in this study run from $.005/$100 valuation to $.035/$100 valuation, meaning a $200,000 home in these districts would pay from $10 to $70 annually, not as much as a few cups of Starbucks coffee cost annually. All Texans agree water is life and groundwater is one of our most precious resources, therefore GCDs deserve more financial resources. The Texas Water Code provides a number of tools for GCDs to finance their operations including ad valorem taxation levies, issuance of bonds, notes, and promulgation of fees to name a few. However, in many of the GCDs who responded to the study, these tools are not practical to use. Since ad valorem taxation and bond authority must be granted by local voter approval, these tools are unavailable in some GCDs as well., Texas Water Journal, Vol. 4 No. 1 (2013)
- Published
- 2013
220. Diversidad molecular de Anopheles (Kerteszia) neivai en el pacífico colombiano
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Rubio, Andrés López, Vasco, Juan David Suaza, Molina, Natalia Ruíz, Soto, Sandra Ines Uribe, Porter, Charles, Marcet, Paula, and García, Giovan Fernando Gómez
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- 2013
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221. South African medical congress, June, 1905
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Porter, Charles H.
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- 1905
- Full Text
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222. Tunable Linewidth Chip-Level Lasers Using Hybrid Integration Methods
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Porter, Charles
- Subjects
- Tunable Linewidth, Hybrid Integration, PIC, Electromagnetics and Photonics
- Abstract
Photonic integrated circuits (PICs) have significant value in today’s world of research. They enable devices to experience large reductions in size, weight, operation power, and cost (SWAPc), making photonic technology more accessible than ever. The functionality of PICs is greatly enhanced due to the realization of both active and passive devices within a single device structure. This is made possible through hybrid integration, which utilizes various coupling methods to transfer light from an active chip to a passive chip. Hybrid integration technology tremendously expands the capabilities of PICs, leading to a plethora of applications. One significant application is that of narrow linewidth lasers. Narrow linewidth lasers are necessary for many emerging applications including laser spectroscopy, light detection and ranging (LiDAR), optical communication, and other forms of optical measurement. Narrow linewidth lasers have a low phase noise, making them ideal for measurement applications. Achieving narrow linewidth within a semiconductor laser package is of increasing importance due to its smaller form factor, allowing such devices to be employed in a plethora of fields that require a small device footprint. External cavity lasers are usually employed to achieve these characteristics by using hybrid integration to couple light from an active source into a passive waveguide, the external cavity, which greatly extends the incident photon lifetime, thus decreasing linewidth. This passive device structure is highly dependent on micro-ring resonators to couple light to and from the waveguide, making the coupling coefficient an integral parameter to the success of external cavity lasers. The passive device structure in this work utilizes the thermo-optic effect of a passive waveguide within a Mach-Zehnder Interferometer integrated with a racetrack resonator to control how much light couples into a feedback waveguide, thus tuning the linewidth using a thermo-optic heater. This in turn shows the tuning of the ring resonator coupling coefficient. Devices of similar structure have previously been used to create widely tunable lasers and optical switches, but to our knowledge, have not been used to tune laser linewidth in such an application.
- Published
- 2023
223. LETTERS.
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LYON JR., JOE, MCREYNOLDS, CHARLES F., ANDERSON, WARREN E., HOWE, FREDERICK R., COLLIER, MILES, BARROW, ETHEL H., PORTER, CHARLES RODMAN, ADLERMANN, EMIL, ANDREWS, A.W., BLANCHARD III, NATHAN W., COMANDINI, ADELE, BLIVEN, BRUCE, HORTON, ROBERT W., and GENTZ, VIRGINIA
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ISOLATIONISM ,NATIONAL security ,HISTORY of women's rights ,WOMEN'S rights ,TWENTIETH century - Published
- 1940
224. Why the 'Peace Congressmen' Lost.
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Porter, Charles O.
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UNITED States politics & government ,POLITICAL parties ,PEACE movements ,POLITICAL campaigns ,POLITICAL participation - Abstract
A U.S. Congressman strivings for peace is hard to get across to his constituents and easy for his opponent to distort. The article analyzes why the activities of the author who is a Congressman led his opponent to say that the author defeated himself. His opponent was Republican Dr. Edwin C. Durno of Medford. Durno called the author an appeaser because he attended two world law conferences and three disarmament meetings in Europe. This kind of campaign was successful because foreign-policy issues are complex and remote from the experience of the average voter. Emotions are easily aroused when one's country and personal security are involved.
- Published
- 1960
225. LETTERS.
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LORANT, STEFAN, BACHRACH, LOUIS FABIAN, FALLON, ELAINE M., BARBEE, DAVID RANKIN, HIEATT, LOUISE M., HATCH, J., MIXON JR., A. M., CRANLEY, VICTOR B., FRANK, BERNARD K., LESOURD, LEONARD E., GOLDSMITH, GOLDWIN, COSMIC, R., PORTER, CHARLES H., FREMONT-SMITH, MAURICE, HARTNETT, ROSE N., MCMORROW, KATHERINE, STILL, G., WILCOX, JOSEPH V., KEGLEY, CHARLES W., and PHILLIPS, E. A.
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LETTERS to the editor ,WAR photography ,CIVIL war ,PHOTOGRAPHERS - Abstract
Several letters to the editor are presented in response to articles in previous issues including an article on a photograph taken by Civil War photographer Mathew Brady in the October 20, 1952 issue, a short story by Joyce Gary in the October 20, 1952 issue and the article "Unsuspected Cancer" in the October 20, 1952 issue.
- Published
- 1952
226. LETTERS.
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KROGER, DON, CONLON, JHON P., PAPROCKI, JOSEPH S., ROBERTS, CARL M., KIPLEY, MAXINE, GORMLEY, M. K., DOOLEY, G. K., DUNN, J. NORTON, DETLEFSEN, HAROLD H., Clark Jr, Harvey, MICHAEL, HAROLD L., REDMAN, CHARLES B., ROTH, ROBERT B., DE NOBRIGA, FRANK H., WALLACE, H. O., STEVENSON, FRED L., PORTER, CHARLES H., and STRAUSS, J. M.
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LETTERS to the editor ,LIQUORS ,DISABILITY laws - Abstract
Several letters to the editor are presented in response to articles in previous issues including one about liquor and Pearl Harbor in the August 20, 1951 issue, another about the disability bill in the August 27, 1951 issue, and the article "The Case Against Ike" in the August 20, 1951 issue.
- Published
- 1951
227. First neotropic record of Idiolispa with description of a new species from Honduras (Hymenoptera: Ichneumonidae)
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Porter, Charles C.
- Subjects
ddc:590 - Abstract
Idiolispa Foerster (Ichneumonidae: Phygadeuontinae: Mesostenini) has been known previously only from the Holarctic Region but an undescribed species now is reported in tropical cloud forest (1800 m) on Monte Uyuca near the Escuela Agricola Panamericana at Zamorano, Honduras.
- Published
- 2010
228. The Sabethines of Northern Andean Coffee-Growing Regions of Colombia
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Suaza-Vasco, Juan, primary, López-Rubio, Andrés, additional, Galeano, Juan, additional, Uribe, Sandra, additional, Vélez, Iván, additional, and Porter, Charles, additional
- Published
- 2015
- Full Text
- View/download PDF
229. New Phycitiplex Porter (Hymenoptera, Ichneumonidae) from Subandean Desert in northwest Argentina
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Porter, Charles C. and Center for Systematic Entomology, Inc.
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ddc:590 - Abstract
Six new species of Phycitiplex (P. obscurior, P. tricinctus, P. unicinctus, P. peralta, P. trichroma, and P. lepidus) are described from material taken by Malaise trap in a humid ravine at Santa Vera Cruz in the Subandean Desert (Monte) of La Rioja Province (Argentina). These are keyed along with several closely related described species. Except for P. eremnus from central Chile, this genus is known only from the semiarid Chaco and Subandean biogeographic provinces in the northern half of Argentina. The only available host record is of Phycitiplex doddi (Cushman) reared from larvae of Cactoblastis cactorum (Berg), a phycitid moth that attacks prickly pear cacti.
- Published
- 2009
230. Trachysphyrus uspallatae Porter
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Porter, Charles C.
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Insecta ,Arthropoda ,Trachysphyrus uspallatae ,Trachysphyrus ,Animalia ,Biodiversity ,Hymenoptera ,Ichneumonidae ,Taxonomy - Abstract
Trachysphyrus uspallatae Porter Material Examined. 2 females, Argentina, La Rioja Province, Sierra de Velasco, San Pedro, 1600 m, 30- IV-2000, P. Fidalgo (FSCA, IMLA) This species was previously known only from Uspallata in Mendoza Province some 500 km distant in the southern Subandean Desert (Porter 1967). The specimens now recorded from La Rioja Province differ from the type series only in lacking white bands on gastric tergites 4-7., Published as part of Porter, Charles C., 2008, New Trachysphyrus Haliday (Hymenoptera, Ichneumonidae) in the albomarginatus species group from northwestern Argentina, pp. 1-9 in Insecta Mundi 2008 (55) on page 9, DOI: 10.5281/zenodo.5170133, {"references":["Porter, C. C. 1967. A revision of the South American species of the South American species of Trachysphyrus. Memoirs of the American Entomological Institute 10: 368 p."]}
- Published
- 2008
- Full Text
- View/download PDF
231. New Trachysphyrus Haliday (Hymenoptera, Ichneumonidae) in the albomarginatus species group from northwestern Argentina
- Author
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Porter, Charles C.
- Subjects
Insecta ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Ichneumonidae ,Taxonomy - Abstract
Porter, Charles C. (2008): New Trachysphyrus Haliday (Hymenoptera, Ichneumonidae) in the albomarginatus species group from northwestern Argentina. Insecta Mundi 2008 (55): 1-9, DOI: http://doi.org/10.5281/zenodo.5170133, {"references":["Cabrera, A. L., and A. Willink. 1973. Biogeografia de America. Organizacion de los Estados Americanos, Serie de Biologia, Monografia 13: 120 p.","DeSantis, L. 1956. Anotaciones sobre Ichneumonoideos argentinos con descripcion de una especies nueva (Hymenoptera). Notas del Museo de La Plata 18(165): 303-312.","Porter, C. C. 1967. A revision of the South American species of the South American species of Trachysphyrus. Memoirs of the American Entomological Institute 10: 368 p.","Received September 29, 2008; accepted November 3, 2008."]}
- Published
- 2008
- Full Text
- View/download PDF
232. Trachysphyrus riojanus Porter 2008, new species
- Author
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Porter, Charles C.
- Subjects
Trachysphyrus riojanus ,Insecta ,Arthropoda ,Trachysphyrus ,Animalia ,Biodiversity ,Hymenoptera ,Ichneumonidae ,Taxonomy - Abstract
Trachysphyrus riojanus Porter, new species (Fig. 2) Description. Female Holotype. Color: antenna black with a white band above on flagellomeres 6-9; head, mesosoma and gaster black with dull white and reddish staining on mandible, a white line on upper half of facial orbit and much of frontal orbit, a white line on upper half of hind orbit, dull white on pronotal collar; fore and mid leg with coxa and trochanter black, femur orange, tibia duller orange with faint dusky staining, tarsus dull orange with dusky on tips of segments 1-4 and 5 th segment mostly black; hind leg similar except with some white on tarsomeres 3 and 4; wings dark brown with metallic reflections. Length of forewing: 8.1 mm. Flagellum slender, cylindric with first segment 3.7 times as long as deep at apex. Clypeus subnasute, weakly and asymmetrically raised in profile, basal face gently curved and apical face strongly concave, 0.3 times as long as base, the faces very distinct in anterior view, separated towards middle by a low ridge. Malar space 0.6 times as long as basal width of mandible. Fore tibia stout but scarcely inflated. Mesoscutum with notauli sharp and narrow, reaching 0.9 times length of mesoscutum; surface shining with some weak transverse wrinkling along notauli and with very dense but largely noncoalescent small, sharp punctures which are a little larger and more discrete on lateral lobes and a little smaller and more crowded on central lobe. Mesopleuron dully shining, densely puncto-reticulate; sternaulus becoming broad and shallow on its apical 0.5 but traceable throughout. Wing venation with areolet large, intercubiti moderately convergent above, second abscissa of radius 0.8 times as long as first intercubitus. Propodeum with spiracle 1.7 times as long as wide; basal transcarina delicate but traceable throughout; apical transcarina faintly developed toward middle, stronger laterally where it is developed into broad, low subcuneate cristae. First gastric tergite with postpetiole strongly expanded, 1.1 times as wide at apex as long from spiracle to apex; dorsal longitudinal carinae distinct but not sharp on apex of petiole and base of postpetiole; surface smooth and polished with very weak micro-reticulation and small widely scattered punctures which are most numerous laterad. Second gastric tergite dully shining with small very numerous tiny crowded punctures that are mostly subadjacent to a little confluent and which emit short, overlapping setae. Ovipositor sheathed portion 0.80 times as long as fore wing, straight, compressed; nodus well developed with a tiny notch at summit, dorsal valve in profile steeply and directly tapering from notch to apex, 0.33 times as long as high at apex. Variation. Color: white band on flagellomeres 5-9; white markings on head often very faint. Length of fore wing: 6.4-8.7 mm. Flagellum with first segment 3.5-4.0 times as long as deep at apex. Malar space 0.8 times as long as basal width of mandible. Wing venation: second abscissa of radius 0.7-0.9 times as long as first intercubitus. Ovipositor: sheathed portion 0.70 times as long as fore wing; tip 0.30-0.34 times as high a notch as long from notch to apex. Type Material. Holotype female, ARGENTINA, La Rioja Province, Sierra de Velasco, Santa Vera Cruz, 1700 m, XII-2001, P. Fidalgo, Malaise trap [IMLA]. Paratypes: 9 females, ARGENTINA, 3 females, La Rioja Province, Sierra de Velasco, Santa Vera Cruz, 1700 m, 15-31-XII-2003, I-2002, P. Fidalgo, Malaise trap [AEIC, FSCA, IMLA]; 2 females, Salta Province, Tacuil, 2400 m, 16-31-XII-1968,1- 15-I-1969, Willink, Terán, Stange, Malaise trap [IMLA]; 3 females, Salta Province, Yacochuya 1950 m, ca. Cafayate, 16-30- IX-1968, 1-15-X-1969, 16-31-X-1968, 16-31-XII-1969, Willink, Terán, Stange, Malaise trap [IMLA]. Relationships. This species is distinctive in its long ovipositor with the nodus conspicuously elevated, sharp and almost percurrent notauli, dully shining second gastric tergite with tiny crowded punctures and densely overlapping setae, and entirely black gaster. Only T. blanchardi has the ovipositor equally long but this is an adaptive character of little phylogenetic significance and, as indicated in the key, T. riojanus has several distinctive features which suggest that it is not closely related to any other species of its group., Published as part of Porter, Charles C., 2008, New Trachysphyrus Haliday (Hymenoptera, Ichneumonidae) in the albomarginatus species group from northwestern Argentina, pp. 1-9 in Insecta Mundi 2008 (55) on pages 5-6, DOI: 10.5281/zenodo.5170133
- Published
- 2008
- Full Text
- View/download PDF
233. Phycitiplex trichroma Porter 2008, new species
- Author
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Porter, Charles C.
- Subjects
Insecta ,Arthropoda ,Phycitiplex trichroma ,Animalia ,Biodiversity ,Hymenoptera ,Ichneumonidae ,Taxonomy ,Phycitiplex - Abstract
Phycitiplex trichroma Porter, new species (Fig. 5) Description. Female Holotype. Color: much as in P. peralta except with no white below on scape, white flagellar band on segments 4-7; only a small white spot on face, white on pronotal collar and again well below on front margin of pronotum, only a narrow white band on apex of postpetiole, a little white apico-laterally on tergite 2, no white on tergites 5-7; fore and mid legs red, their coxae marked also with black and white, their trochanters, trochantelli, and femora bright red, tibiae and tarsi duller with slight dusky staining; hind leg red with a large white blotch on coxa and tibia and tarsi rather dusky. Length of forewing 5.3 mm. Flagellum: first segment 6.6 times as long as deep at apex. Malar space 0.44 times as long as basal width of mandible. First gastric tergite: postpetiole rather weakly expanded, 1.2 times as wide at apex as long from spiracle to apex and with well developed micro-reticulation that fades out only near apex as well as with scattered faint punctures of small to medium size. Second gastric tergite: dully shining with very fine micro-reticulation throughout and with numerous obscure, well spaced medium sized to small punctures. Ovipositor: decurved, compressed, sheathed portion 0.63 a times s long as forewing; nodus well defined, a little raised; dorsal valve in profile falling off directly from nodus to apex; tip 0.20 times as high at notch as long from notch to apex. Type material. Holotype female, ARGENTINA, La Rioja Province, Sierra de Velasco, Santa Vera Cruz, 1700 m, I-2002, P. Fidalgo, Malaise trap [IMLA]. Relationships. This species may be recognized by its long, decurved ovipositor, relatively slender postpetiole, uniformly white upper metapleuron, and by its unusually long first flagellar segment (6.6 times as long as deep at apex). Specific name. From the Greek prefix tri- (three) and the Greek noun chroma (color). This name is treated as a Greek neuter noun in apposition., Published as part of Porter, Charles C., 2008, New Phycitiplex Porter (Hymenoptera, Ichneumonidae) from Subandean Desert in northwest Argentina, pp. 1-13 in Insecta Mundi 2008 (56) on pages 9-10, DOI: 10.5281/zenodo.5170147
- Published
- 2008
- Full Text
- View/download PDF
234. Phycitiplex peralta Porter 2008, new species
- Author
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Porter, Charles C.
- Subjects
Insecta ,Arthropoda ,Animalia ,Phycitiplex peralta ,Biodiversity ,Hymenoptera ,Ichneumonidae ,Taxonomy ,Phycitiplex - Abstract
Phycitiplex peralta Porter, new species (Fig. 4) Description. Female Holotype. Color: scape dull reddish brown with a white spot below near apex, flagellum black with a white band above on segments 6-9; head black with slight reddish staining toward clypeus and mandibles and with the following white: large blotch on basal 0.5 of mandible, most of clypeus, broad band throughout on orbits becoming very broad in and behind malar space but with a slight break just in front of malar space, and with a large blotch that covers most of face and is partly confluent with orbital white band above; mesosoma black with white broadly on anterior and humeral margins of pronotum, weakly on prepectus dorsad, dully on subalarum, faintly on upper end of mesepimeron, conspicuously on tegula and on basal 0.6 of scutellum, dull reddish white on upper metapleuron and on apex of lower metapleuron, propodeum with the usual white bars on each side of hind face from cristae to apex; gaster light red, faintly dusky on tergites 5 and following, with a very broad white band on apex of first tergite, a narrow white subapical band on tergite 2, a very broad apical band on tergite 4, and variably developed lateral bands on tergites 5-7; fore and mid leg as in P. tricinctus but with tarsi generally paler and without black on last tarsomere; hind leg with a small white spot above on base of coxa, more dusky on tibia and slightly so on tarsus. Length of forewing: 4.4 mm. Flagellum: first segment 5.1 times as long as deep at apex. Malar space 0.44 times as long as basal width of mandible. First gastric tergite: postpetiole strongly expanded, 2.0 times as wide at apex as long from spiracle to apex; dorsal carinae obsolete, surface of postpetiole shining, finely but rather strongly micro-reticulate on basal 0.6 and more weakly so toward apex and with a few very inconspicuous small, shallow punctures, especially laterad and on apical 0.3. Second gastric tergite: rather mat with fine, dense micro-reticulation and numerous small but well defined shallow punctures which are quite sparse near base but become subadjacent to adjacent rearward. Ovipositor decurved throughout, sheathed portion 0.40 times as long as forewing; nodus scarcely defined, its position indicated by a minute notch, with a long, straight taper between notch and apex, 0.14 times as high at notch as long from notch to apex. Type material. Holotype female, ARGENTINA, La Rioja Province, Sierra de Velasco, Santa Vera Cruz, 1700 m, 31-I-2004, P. Fidalgo, Malaise trap [IMLA]. Relationships. In its decurved, relatively short ovipositor and strongly expanded postpetiole this species resembles P. charieis (Porter 1967) from which it differs by having a complete subapical white band and shallow but well defined punctures on the second gastric tergite. Specific name. This species is named for Sr. Daniel Peralta who owns a farm at Santa Vera Cruz and in recognition of his enthusiastic help in maintaining our Malaise traps at this locality. The name is treated as a masculine Latin noun in apposition., Published as part of Porter, Charles C., 2008, New Phycitiplex Porter (Hymenoptera, Ichneumonidae) from Subandean Desert in northwest Argentina, pp. 1-13 in Insecta Mundi 2008 (56) on pages 8-9, DOI: 10.5281/zenodo.5170147, {"references":["Porter, C. C. 1967. A Revision of the South American Species of Trachysphyrus (Hymenoptera, Ichneumonidae). Memoirs of the American Entomological Institute 10: 368 p."]}
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235. Phycitiplex unicinctus Porter 2008, new species
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Porter, Charles C.
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Insecta ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Ichneumonidae ,Phycitiplex unicinctus ,Taxonomy ,Phycitiplex - Abstract
Phycitiplex unicinctus Porter, new species (Fig. 3) Description. Female Holotype. Color: scape light reddish brown, flagellum black with a white band above on segments 5 (at apex) to 9; head and mesosoma with faint reddish staining on mandibles and around clypeus and with white markings as in P. tricinctus except no white on center of face, tegula not wholly white (brownish behind), no white blotch on mesopleural disc, scutellum white only on basal 0.6 with black toward apex, and dorsal metapleuron entirely black; gaster as in P. tricinctus but with a broad white apical band only on tergite 4 and with a little white in and briefly above lower hind corners of tergites 5 and 6; legs red but without white markings, blackish toward base anteriorly on fore and mid coxa, tibiae and tarsi dull red with weak dusky staining. Length of forewing: 4.6 mm. Flagellum: first segment 5.2 times as long as deep at apex. First gastric tergite: postpetiole moderately expanded, 1.5 times as wide at apex as long from spiracle to apex, distinctly micro-reticulate and with many small and faint shallow punctures which are mostly sparser than subadjacent and emit short, slightly overlapping setae. Ovipositor straight, slender, strongly compressed, sheathed portion 0.50 times as long as forewing, nodus low and marked by a tiny notch, straight in profile between notch and apex, tip 0.26 times as high at notch as long from notch to apex. Type material. Holotype female, ARGENTINA, La Rioja Province, Sierra de Velasco, Santa Vera Cruz, 1700 m, 1-15-XI-2003, P. Fidalgo, Malaise trap [IMLA]. Relationships. This species is distinctive in its sparse white markings (e.g., gaster with a white apical band on fourth tergite only), faintly punctate second gastric tergite, and long, straight ovipositor., Published as part of Porter, Charles C., 2008, New Phycitiplex Porter (Hymenoptera, Ichneumonidae) from Subandean Desert in northwest Argentina, pp. 1-13 in Insecta Mundi 2008 (56) on pages 7-8, DOI: 10.5281/zenodo.5170147
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236. Phycitiplex Porter 1987
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Porter, Charles C.
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Insecta ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Ichneumonidae ,Taxonomy ,Phycitiplex - Abstract
Key to the Subandean species of Phycitiplex 1. Hind face of propodeum entirely black; ovipositor 0.3-0.6 times as long as forewing.................. 2 — Hind face of propodeum with a broad white band on each side from crista, inclusive, to hind margin; ovipositor 0.6-0.8 times as long as forewing............................................................... 5 2(1). Front tibia stout and inflated; ventral valve of ovipositor on tip with well spaced vertical ridges; gaster with dorsally complete or nearly complete white apical bands on tergites 4-7................ ........................................................................................ Phycitiplex eugrammus (Porter) — Front tibia stout but not inflated; ventral valve of ovipositor on tip with inclivously oblique ridges; gaster with white on dorsum of tergite 4 but on 5-7 with white only ventro-laterally............ 3 3(2). Notauli weak, 0.5 times or less length of mesoscutum; mesoscutum with fine micro-reticulation, its punctures adjacent to confluent; scutellum wider than long; wing membrane with a large hairless area beneath pterostigma; gaster black except white on tergite 4.............................................................................................................................. Phycitiplex eremnus (Porter) — Notauli fine but traceable 0.7-0.8 times length of mesoscutum; mesoscutum shining with sharp, mostly subadjacent to adjacent punctures; scutellum as long as or longer than wide; wing membrane mostly setose beneath pterostigma; gaster black and red or sometimes black with white on much of tergite 4 and less extensively on 5............................................................... 4 4(3). Humeral margin of pronotum white; legs mostly red; malar space 0.80 times length of basal width of mandible; ovipositor 0.8 times as long as forewing Phycitiplex doddi (Cushman) — Humeral margin of pronotum black, sometimes with a little white anteriorly; legs mostly black; malar space 0.50-0.60 times as long as basal width of mandible; postpetiole shining with delicate micro-aciculation; ovipositor 0.6-0.7 times as long as forewing................................................................................................................................................... Phycitiplex obscurior Porter 5(1). Ovipositor straight....................................................................................................................... 6 — Ovipositor decurved..................................................................................................................... 7 6(5). Gaster with a white apical band on tergites 1-3 but without white on 4; white blotch in lower front quadrant of mesopleuron; upper metapleuron pure white; coxae red and white; postpetiole 1.8- 2.2 times as wide at apex as as long from spiracle to apex; tergite 2 with dense but not confluent, sharply defined, medium sized punctures.............................. Phycitiplex tricinctus Porter — Gaster with a white band only on tergite 4; no white markings on lower mesopleuron or on upper metapleuron; coxae red; postpetiole 1.5 times as wide at apex as long from spiracle to apex; tergite 2 with many small, faint punctures.......................... Phycitiplex unicinctus Porter 7(5). Postpetiole 1.6-2.0 times as wide at apex as long from spiracle to apex; ovipositor 0.4-0.5 times as long as forewing........................................................................................................................ 8 — Postpetiole 1.2-1.7 times as wide at apex as long from spiracle to apex; ovipositor 0.6 times as long as forewing................................................................................................................................ 9 8(7). Gaster with a complete subapical white band on tergite 2; second gastric tergite with numerous medium sized very shallow but well defined punctures............. Phycitiplex peralta Porter — Gaster often without white on tergite 2 or with a dorsally incomplete white band; tergite 2 with sparser, smaller, very obscure punctures.............................. Phycitiplex charieis (Porter) 9(7). Upper metapleuron pure white throughout; first flagellomere 6.6 times as long as deep at apex at apex; malar space 0.44 times as long as basal width of mandible............................................................................................................................................. Phycitiplex trichroma Porter — Upper metapleuron entirely black or sometimes obscurely stained with brownish white; first flagellomere 4.5-5.4 as times long as deep at apex; malar space 0.66-0.75 times as long as basal width of mandible........................................................................ Phycitiplex lepidus Porter, Published as part of Porter, Charles C., 2008, New Phycitiplex Porter (Hymenoptera, Ichneumonidae) from Subandean Desert in northwest Argentina, pp. 1-13 in Insecta Mundi 2008 (56) on pages 2-3, DOI: 10.5281/zenodo.5170147
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237. Phycitiplex obscurior Porter 2008, new species
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Porter, Charles C.
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Insecta ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Ichneumonidae ,Phycitiplex obscurior ,Taxonomy ,Phycitiplex - Abstract
Phycitiplex obscurior Porter, new species (Fig. 1) Description. Female Holotype. Color: antenna blackish with a white band above on flagellar segments 6-9; head and mesosoma black with reddish on mandible and around clypeus, a narrow white band on facial and frontal orbits, a broad white band toward apex on vertical orbit and continued below to lower half of hind orbit, a tiny white spot in malar space, anterior margin of pronotum white only on collar, a little white anteriorly on humeral margin of pronotum, white spot on base of tegula, subalarum slightly tinged with whitish, and basal 0.6 of scutellum pure white; gaster red on first tergite, duller red on second tergite, mostly blackish on third tergite, fourth tergite black with a very broad white apical band, following tergites black with abbreviated white bands ventro-laterally on fifth and sixth; fore and mid leg with coxa black with a little white toward apex, trochanter black and white, trochantellus pale orange and whitish, femur and tibia light orange, the tarsus dull orange suffused with dusky; hind leg orange red on coxa, with trochanter black and white, trochantellus pale orange and whitish, femur and tibia light orange, and tarsus dull orange with weak blackish staining toward apices of segments 1-4 and blackish throughout on 5; wings hyaline with slight brownish staining. Length of forewing 4.6 mm. Flagellum long, slender, cylindric, first segment 5.0 times as long as deep at apex. Clypeus strongly nasute, basal face convexly raised in profile, the slightly shorter apical face steeply declivous and a little concave. Malar space 0.50 times as long as basal width of mandible. Fore tibia stout but not inflated. Pronotum: submarginal groove narrow but percurrent and foveolate; mesoscutum with notauli fine and sharp basally and shallower rearward but traceable 0.8 times the length of mesoscutum, surface shining with very many rather large subadjacent to adjacent or a little confluent strong, sharp punctures. Wing venation: areolet large with intercubiti strongly convergent above, second abscissa of radius 0.4 times as long as first intercubitus; second recurrent a little reclivous on lower half and slightly outcurved above. Propodeum: spiracle 3.0 times as long as wide; whole propodeum in profile strongly and smoothly sloping from base to apex, the apical face being confluent with the slightly shorter basal face; basal trans-carina fine and sharp throughout; apical trans-carina absent medially but developed laterally into low although sharp edged broadly crescentic cristae. First gastric tergite: petiole slender basad but toward apex widened into the short and broad postpetiole which is 1.2 times as wide at apex as long from spiracle to apex; surface of postpetiole shining with delicate microaciculation which fades out toward apex and with a few widely scattered small to moderately large, inconspicuous punctures which are most conspicuous apically. Second gastric tergite: dully shining with very fine micro-reticulation, and a few sparse, inconspicuous punctures toward apex which emit short, mostly well spaced setae. Ovipositor: sheathed portion 0.65 times as long as forewing; nodus scarcely defined, its position indicated by a tiny notch; tip 0.20 times as high at notch as long from notch to apex. Variation. Color: may be back with no red areas and reduced white markings: no white on humeral margin of pronotum; scutellum black except tinged with brownish white on each side near base; no white on sixth gastric tergite; fore and mid legs light brownish; hind leg with coxa and trochanter black, trochantellus brownish, femur black with dull brownish orange laterally below and near base and apex. Length of forewing 4.1-4.8 mm. First flagellomere 4.8 times as long as deep at apex. Malar space up to 0.60 times as long as basal width of mandible. Wing venation: second abscissa of radius up to 0.6 as long as first intercubitus. Propodeum: spiracle 2.5 times as long as wide. First gastric tergite: postpetiole 1.3 times as wide at apex as long from spiracle to apex. Ovipositor 0.68-0.72 times as long as forewing, its tip 0.16-0.18 times as high as notch as long from notch to apex. Type material. Holotype female, ARGENTINA, La Rioja Province, Sierra de Velasco, Santa Vera Cruz, 1700 m, X-2001, P. Fidalgo, Malaise trap [IMLA]. Paratypes: 2 females, same data as holotype [FSCA, IMLA]. Relationships. This species is related to the partially sympatric northwest and central Argentine P. doddi and to P. eremnus from central Chile. It differs from both these species in its longer notauli (0.7-0.8 times the length of mesoscutum) and additionally from P. doddi by its mostly black legs. Other distinguishing features are noted in the key and in the respective species descriptions., Published as part of Porter, Charles C., 2008, New Phycitiplex Porter (Hymenoptera, Ichneumonidae) from Subandean Desert in northwest Argentina, pp. 1-13 in Insecta Mundi 2008 (56) on page 4, DOI: 10.5281/zenodo.5170147
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238. New Phycitiplex Porter (Hymenoptera, Ichneumonidae) from Subandean Desert in northwest Argentina
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Porter, Charles C.
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Insecta ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Ichneumonidae ,Taxonomy - Abstract
Porter, Charles C. (2008): New Phycitiplex Porter (Hymenoptera, Ichneumonidae) from Subandean Desert in northwest Argentina. Insecta Mundi 2008 (56): 1-13, DOI: http://doi.org/10.5281/zenodo.5170147, {"references":["Cabrera, A. L., and A. Willink. 1973. Biogeografia de America Latina, Organizacion de los Estados Americanos, Serie de Biologia. Monografia No. 13. Washington, D.C. 120 p.","Cushman, R. A. 1927. Miscellaneous Notes and Descriptions of Ichneumon-flies. Proceedings of the United States National Museum 72(2709): 1-22.","Porter, C. C. 1967. A Revision of the South American Species of Trachysphyrus (Hymenoptera, Ichneumonidae). Memoirs of the American Entomological Institute 10: 368 p.","Porter, C. C. 1975. Relaciones Zoogeograficas y Origen de la Fauna de Ichneumonidae (Hymenoptera) en la Provincia Biografica del Monte del Noroeste Argentino. Acta Zoologica Lilloana 31(15): 125-252.","Porter, C. C. 1986. A Revision of the euprepes Species Group of Cosmiocryptus (Hymenoptera, Ichneumonidae). Journal of the New York Entomological Society 94: 467-471.","Porter, C. C. 1987. A Revision of the Chilean Mesostenini. (Hymenoptera, Ichneumonidae). Contributions of the American Entomological Institute 23(3): 1-164.","Received September 25, 2008; accepted November 3, 2008."]}
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- 2008
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239. A remarkable new species of Zethus Fabricius (Hymenoptera, Vespidae, Eumeninae) from Costa Rica
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Porter, Charles C.
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Insecta ,Eumenidae ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Porter, Charles C. (2008): A remarkable new species of Zethus Fabricius (Hymenoptera, Vespidae, Eumeninae) from Costa Rica. Insecta Mundi 2008 (27): 1-4, DOI: http://doi.org/10.5281/zenodo.4532801, {"references":["Bohart, R. M., and L. A. Stange. 1965. A revision of the genus Zethus Fabricius in the Western Hemisphere. University of California Publications in Entomology. Vol. 40. 208 p.","Porter, C. C. 1975. New records for Zethus (Hymenoptera, Eumenidae) from Texas. Florida Entomologist. 58: 303-6.","Porter, C. C. 1978. Ecology and taxonomy of Lower Rio Grande Valley Zethus (Hymenoptera, Eumenidae). Florida Entomologist 61: 157-167.","Zavattari, E. 1912. Materalien fur eine Monografie der neotropischen Eumeniden. Archiv fur Naturgeschichte 78 (Abt. A), Heft 4: 1-272."]}
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240. Habronyx punensis Porter 2007, new species
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Porter, Charles C.
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Habronyx punensis ,Insecta ,Arthropoda ,Habronyx ,Animalia ,Biodiversity ,Hymenoptera ,Ichneumonidae ,Taxonomy - Abstract
Habronyx punensis Porter, new species (Figure 4-6) Description. Female Holotype. Similar to H. citrinus from which it differs as follows. Color: second gastric tergite faintly blackish on dorsum toward middle; fourth tergite with black on much of its apical 0.5; fore and mid trochanters largely black with some orange above and apically; hind leg with trochantellus blackish with obscure orange staining, tibia rather dull orange on about its basal 0.3 but otherwise black, and first tarsomere dull orange with black on its apical 0.3; wings hyaline. Length of fore wing: 9.3 mm. First flagellomere 2.6 times as long as deep at apex. Front with a sharp carina running from median ocellus ventrad to between antennal scrobes. Vertex: line from hind ocellus to occipital carina about 0.4 times the width of ocellus. Mesopleural disc on its lower 0.5 with strong, medium sized to large not at all recticulately confluent punctures which are mostly subadjacent or a little sparser with smooth, shining interspaces. Wing venation: nervulus only 0.2 times its length postfurcal; discoidella traceable throughout but spectral, largely desclerotized. Hind leg with femur 5.8 times as long as deep, second tarsomere 2.6 times as long as deep. Gaster with postpetiole 1.4 times as long as wide at apex. Male Allotype. Differs from female as follows: Color: fore and mid trochanters more largely orange than in female; hind tibia orange with dusky staining on basal 0.4 and black on distal 0.6. Length of fore wing 8.6 mm. First flagellomere 3.0 times as long as deep at apex. Mesopleuron: lower 0.5 of disc with punctures a little larger and more crowded than in female but not reticulately coalescing. Wing venation: discoidella desclerotized and barely traceable on basal 0.5, a little better developed on distal 0.5. Second hind tarsomere 3.3 times as long as deep at apex. Type material. Holotype female, BOLIVIA, La Paz, Huaraco-Aroma, 23-III-1994, colectado en cultivos de quinua, sali�� de larvas de Noctuidae [FSCA]. Allotype male, BOLIVIA, La Paz, Murillo, Laboratorio de Entomolog��a en Cota Cota, 23-III-1994, colectado en cultivos de quinua, sali�� de larvas de Noctuidae [FSCA]. Relationships. This species is very similar to the Chilean H. citrinus but differs in its more nearly hyaline wings, more extensively black gaster and legs, presence of a sharp median carina on the front, strongly but not reticulately punctate mesopleural disc, more briefly postfurcal nervulus, and more weakly sclerotized or even in part spectral nervellus. Some of these characters may not hold up when more specimens are at hand to show a fuller range of variation. However it would be unusual for a single species to occur from central Chile all the way north into the Andean steppe of Bolivia, although many temperate South American genera are represented by closely related species in each area. For example, as described by Porter (1967), the ichneumonid genus Trachysphyrus Haliday has the Metallicus species group at 3000-4000 m in the highlands of Bolivia and Per��, while its presumed sister taxon, the Irinus species group, occurs in Neantarctic central Chile from Atacama to Malleco (27 th- 37 th parallel) and at altitudes of 300-3000 m, with most records from below 2300 m. Hosts. These specimens were reared from an unidentified noctuid moth larvae on Chenopodium quinoa Willd. (Angiospermae: Chenopodiaceae). Habitat Notes. The type series was collected near La Paz, Bolivia at more than 3000m in the high Andean steppe or Puna Biogeographic Province as defined by Cabrera and Willink (1973). Chenopodium quinoa, host plant of the noctuid larva from which H. punensis was reared, is a desertic halophyte, native to the Andean highlands of Bolivia and Per��, where it is cultivated for its edible seeds and leaves. Specific Name. An adjective derived from the Quechua word puna by addition of the Latin locative suffix -ensis., Published as part of Porter, Charles C., 2007, Habronyx Foerster (Hymenoptera: Ichneumonidae: Anomaloninae) in Andean and Neantarctic South America with description of new species from Bolivia and Chile, pp. 1-8 in Insecta Mundi 2007 (20) on pages 5-6, DOI: 10.5281/zenodo.5172484, {"references":["Porter, C. C. 1967. A revision of the South American species of Trachysphyrus (Hymenoptera: Ichneumonidae). Memoirs of the American Entomological Institute 10: 368 p.","Cabrera, A. L., and A. Willink. 1973. Biogeografia de America Latina. Organizacion de los Estados Americanos, Serie de Biologia. Monografia 13: 120 p."]}
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- 2007
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241. Habronyx Foerster (Hymenoptera: Ichneumonidae: Anomaloninae) in Andean and Neantarctic South America with description of new species from Bolivia and Chile
- Author
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Porter, Charles C.
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Insecta ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Ichneumonidae ,Taxonomy - Abstract
Porter, Charles C. (2007): Habronyx Foerster (Hymenoptera: Ichneumonidae: Anomaloninae) in Andean and Neantarctic South America with description of new species from Bolivia and Chile. Insecta Mundi 2007 (20): 1-8, DOI: http://doi.org/10.5281/zenodo.5172484, {"references":["Cabrera, A. L., and A. Willink. 1973. Biogeografia de America Latina. Organizacion de los Estados Americanos, Serie de Biologia. Monografia 13: 120 p.","Dasch, C. E. 1984. Ichneumon-flies of America north of Mexico. Pt. 9. Subfamilies Theriinae and Anomaloninae. Memoirs of the American Entomological Institute 36: 610 p.","Gauld, I. D. 1984. An Introduction to the Ichneumonidae of Australia. British Museum (Natural History); London. 413 p.","Gauld, I. D. 1997. The Ichneumonidae of Costa Rica. Part 2. Subfamilies Anomaloninae, Ctenopelmatinae, Diplazontinae, Lycorininae, Phrudinae, Xoridinae, with an appendix on Rhyssinae. Memoirs of the American Entomological Institute 57: 485 p.","Porter, C. C. 1967. A revision of the South American species of Trachysphyrus (Hymenoptera: Ichneumonidae). Memoirs of the American Entomological Institute10: 368 p.","Porter, C. C. 1987. A revision of the Chilean Mesostenini (Hymenoptera: Ichneumonidae). Contributions of the American Entomological Institute 23(3): 164 p.","Porter, C. C. 1997. Guia de los generos de Ichneumonidae en la Region Neantartica del Sur de Sudamerica. Fundacion Miguel Lillo; Tucuman, Argentina. Opera Lilloana, No. 42: 234 p."]}
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- 2007
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242. Electronic Health Records and Drugs Prescribed for Off-label Indications
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Porter, Charles B.
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- 2017
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243. The Business of Enlightenment: A Publishing History of the Encyclopedie 1775-1800. Robert Darnton
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Porter, Charles A.
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- 1980
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244. Lebenserinnerungen eines Ingenieurs
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Porter, Charles T., primary
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- 1912
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245. RAPID FIELD METHOD FOR THE COLLECTION OF RADIONUCLIDES FROM MILK
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PORTER, CHARLES R., primary, CARTER, MELVIN W., additional, KAHN, BERND, additional, and PEPPER, ESTIE W., additional
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- 1968
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246. Especies de flebotomíneos (Diptera: Psychodidae) recolectados en reservas naturales de las regiones del Darién y del Pacífico en Colombia.
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Vivero, Rafael J., Contreras, María Angélica, Suaza, Juan D., Vélez, Iván D., Porter, Charles, and Uribe, Sandra I.
- Abstract
Copyright of Biomédica: Revista del Instituto Nacional de Salud is the property of Instituto Nacional de Salud of Colombia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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- 2017
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247. Phylogenetic signal at the Cytb--Ser tRNA--IG1--ND1 mitochondrial region in Anopheles (Kerteszia) neivai Howard, Dyar & Knab 1913.
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López-Rubio, Andrés, Suaza, Juan David, Porter, Charles, Uribe, Sandra, Bedoya, Gabriel, and Vélez, Iván Darío
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CLADISTIC analysis ,INSECTS ,MITOCHONDRIAL DNA ,CYTOCHROME b ,SERINE ,ANOPHELES ,INSECT evolution ,INSECT genetics ,GENE expression - Abstract
Copyright of Biomédica: Revista del Instituto Nacional de Salud is the property of Instituto Nacional de Salud of Colombia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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- 2017
248. Wyeomyia (Hystatomyia) chocoensis Porter & Wolff, sp.n
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Porter, Charles H., Wolff, Marta I., and E
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Insecta ,Culicidae ,Arthropoda ,Diptera ,Animalia ,Biodiversity ,Wyeomyia chocoensis ,Wyeomyia ,Taxonomy - Abstract
Wyeomyia (Hystatomyia) chocoensis Porter & Wolff, sp.n. (Figs. 1, 2, 5, 6) MALE. Head: Vertex and adjoining lateral surface of head with broad, dark decumbent scales with bronze and bluegreen iridescence; no erect scales present; patch of white scales occurs basolaterally; scales along ocular line white or with at least their distal margin white resulting in distinct white line along edge of compound eye. Ocular setae dark brown, including 2 long approximated interocular setae. Interocular space without scales, narrows to width equal to or slightly less than that of single ommatidium. Clypeus and frons without setae or scales; frons with dense covering of fine aculeae (pubescence) between postfrontal suture and antennal socket; clypeus with less dense covering of minute aculeae. Palpus twosegmented (0.16–0.19 mm, mean 0.18, n 6); segment 1 short, rather quadrate; segment 2 elongate; both covered with dark scales. Proboscis slightly expanded in distal 0.3; dorsal surface with dark scales with bluegreen iridescence; ventral surface primarily with pale and white scales extending from base to about 0.7 length where they merge with prominent preapical patch of bright white scales at beginning of apical expansion; white scales end at about 0.8, replaced by dark scales to distal end. Proboscis (P) (1.46–1.55 mm, n 3) longer than antennae (flagellum [F] 1.27–1.34 mm, mean 1.31, n 4), mean P:F 1.13 (n 3), but shorter than forefemur (FeI), mean P:FeI 0.74 (n 3). Pedicel with 6 small setae dorsomesad. Flagellum moderately verticillate, whorls with 8–11 setae, longest setae about 0.35 flagellum length; flagellomere 1 with dorsomesad cluster of 7–12 scales; length of selected flagellomeres (Flm) derived from 3 specimens (6 antennae) as follows: Flm 5 0.08–0.09 mm, Flm 11 0.10–0.12 mm, Flm 12 0.12–0.15 mm, Flm 13 all 0.19 mm; mean Flm 13:Flm 5 2.31. Distal 2 flagellomeres not disproportionately longer than preceding flagellomeres. Thorax: Integument primarily light brown. Scutum with broad dark scales with bronze and bluegreen iridescence, anterior promontary region with a few white scales and about 9 dark brown setae, no acrostichal or dorsocentral setae present. Supraalar and antealar areas have combined sum of 25–31 (mean 28, n 3) dark brown setae. Scutellum covered with broad scales concolorous with those of scutum, margin of median lobe with 4 large and about 3 small dark brown setae, lateral lobes with 4 large and 4 or 5 small dark brown setae. Mesopostnotum brown with medial cluster of 8–11 brown setae. Antepronotal lobes widely separated dorsally, with dark scales dorsally and silvery white scales on portion adjoining pleura; each lobe with 7–12 dark brown setae. Postpronotum without setae; covered primarily with silvery white scales, those along dorsal margin concolorous with scales of scutum. Pleuron with silvery white scales although anterior half of mesokatepisternum and posterior onethird of mesanepimeron bare. Paratergite, meron, and metapleuron entirely bare. Pleural chaetotaxy as follows: prespiracular, 1 dark seta; postspiracular setae absent; upper proepisternal, 2–4 yellow setae; lower mesokatepisternal, 4–7 yellow setae; upper mesokatepisternal setae absent; prealar, 3–4 dark, occasionally pale, setae; lower mesepimeral setae absent; upper mesepimeral, 6– 9 yellow setae. Legs: forecoxa with silvery white scales on anterior margin, otherwise bare; midcoxa and hindcoxa with silvery white scales. Trochanters primarily with silvery white scales although few on dorsal surface, small dark scales on upper distal margin of midtrochanter and hindtrochanter, scattered dark scales on upper surface of foretrochanter. Dorsal surface of femora with dark scales with bronze reflection and dark blue and greenishblue iridescence depending upon angle of incident light. Posteroventral surface of forefemur covered with white scales over basal 0.3; white scaling gradually decreases to narrow posteroventral line at about 0.5, which extends distally and becomes slightly broader near distal end. Ventral surface of midfemur and hindfemur with white scaling over entire length. Forefemur slightly longer than foretibia (TiI) (mean FeI:TiI 1.08, n 3); forefemur somewhat shorter than midfemur (FeII) (mean FeI:FeII 0.87, n 3) but longer than hindfemur (FeIII) (mean FeI:FeIII 1.27, n 3); forefemur longer than proboscis (mean FeI:P 1.36, n 3). Dorsal surface of foretibia and foretarsomere 1 (TaI 1) concolorous with forefemur; scales on dorsal surface of TaI 2–5 dark, appearing dark blue at certain angles of incident light; foretibia with white scaling on posteroventral surface, diminished distally, seldom reaching distal end; ventral surface of TaI 15 primarily with dark scales with metallic reflection; ungues equal, simple, dark but pale basally. Midfemur distinctly longer than midtibia (TiII) (mean FeII:TiII 1.56, n 3), dorsal surface of midtibia, and midtarsomere 1 (TaII 1) concolorous with midfemur, posteroventral surface of midtibia and TaII 1 with broad white scaling over entire length. Midtarsomere 2 (TaII 2) entirely white scaled with exception of some grey to dark scales basally on anteroventral surface, seldom extending beyond 0.3 length of tarsomere; TaII 3–5 completely white scaled except for a few grey to dark scales at distal end of TaII 5. Ungues dissimilar; larger unguis stout, dark, curved to almost 90 ° angle, tip blunt, rounded; smaller unguis simple, dark. Hindfemur slightly longer than hindtibia (TiIII) (mean FeIII:TiIII 1.05, n 3), hindtarsomere 1 (TaIII 1) somewhat longer than hindfemur (mean TaIII 1:FeIII 1.13, n 3). Dorsal surface of hindtibia and TaIII 1 & 2 concolorous with hindfemur, dorsal surface of Ta III 3–5 with dark scales with metallic reflection. Ventral surface of hindtibia with white scales limited to about basal 0.1, remainder primarily with pale scales with metallic reflection; ventral surface of TaIII 1 with a few pale scales basally but predominately with dark scales having metallic reflection; ventral surface of TaIII 2 with predominately pale scaling; ventral surface of TaIII 3–5 with dark scales having metallic reflection. Ungues unequal; longer unguis very slender (0.07–0.08 mm) with fine tip, about 2 x length of shorter; both curved distally. Halteres with scabellum and pedicel pale (creamcolored), distal portion of pedicel and capitellum covered with dark scales with bronze and bluegreen iridescence. Wing: 2.10–2.40 mm, wing scales mostly decumbent and concolorous with scutum. Dorsal scales primarily spatulate, rather broad with rounded ends; R 2, R 3, R 4 + 5, M 1, and M 2 with typical broad spatulate scales over entire length. In addition to broad spatulate scales, R 1 has a row of smaller spatulate scales closely appressed to vein; 1 A with somewhat narrower spatulate scales, which are closely appressed to vein and extend over almost entire length of vein before ending near wing margin. Sparse row of relatively narrow scales (plume scales) occurs on dorsal surface of M and radial sector (Rs). Ventral wing scales similar to dorsal scales but with plume scales on following veins: M 3 + 4 except near distal end, distal 0.5–0.6 of CuA, and a few on basal 0.5 of R 4 + 5 and basal ~ 0.5 of R 1. Also, plume scales may be present on distal third of 1 A. CuA and 1 A without spatulate scales on ventral surface, thus only with distal plume scales. Ventral scales of M all spatulate. Vein R 2 about 4–5 times longer than vein R 2 + 3; vein 1 A ends somewhat before junction of mcu and CuA. Alula with 9 or 10 piliform setae. Abdomen: Abdominal terga primarily with dark scales similar in color to those of scutum; lateral margins with silvery white scales, which form an essentially straight line along abdomen; pale scales expand dorsally somewhat on tergum VII; sterna covered with silvery white scales. Tergum I covered with dark scales dorsally, lateral margins bare; diffuse group of about 20–25 prominent, ambercolored setae occur laterally on either side of meson. Laterotergite without scales. Distal margin of terga II–V with about 7–14 small pale setae; these setae more numerous along distal margin of terga VI and VII (~ 22); lateral margins of terga II–VI usually with 1–4 small pale setae. Distal margin of sterna II–V with about 10–20 small pale setae; distal margin of sterna VI and VII (~ 23) with more numerous and somewhat longer setae; sternum VII also with 2 or 3 setae medially and slightly basal to distal margin; lateral margins of sterna III–VII usually with 3–6 small pale setae. Tergum VIII and sternum VIII are included in description of genitalia. Genitalia (Fig. 1 C–G): Tergum VIII (ventral in position) narrow, 2.8–3.3 x as wide as long; covered with small spicules, which become minute and very numerous basally although basal 0.2–0.4 glabrous; distal margin somewhat concave; spatulate scales primarily along lateral margins. Tergum VIII with 72–90 (mean 78, n 6) relatively long setae with curved tips, longest about 1.4 x length of tergum VIII along median plane; setae located along and near distal margin but most numerous in mesal region where their presence is somewhat expanded basally to about 0.5 length of tergum VIII; a pair of tiny setae located about 0.33 from basal margin and laterad of median plane. Sternum VIII (dorsal in position) 2.0– 2.5 x as wide as long; distal margin somewhat convex; covered with small spicules, which become minute and very numerous basally although about basal 0.3 glabrous. Sternum VIII also covered with dark, decumbent spatulate scales and with 17–24 (mean 21, n 6) setae arranged primarily as single row along distal margin, longest setae similar in length to those on tergum VIII; pair of minute setae or punctures located sublaterad and about 0.4 from basal margin. Tergum and sternum IX fused laterally forming complete ring. Tergum IX bearing 3 or 4 stout but relatively short setae on either side of narrow median bridge, apices of setae bent slightly laterad. Sternum IX narrow but with medial triangularshaped expansion between base of gonocoxites; outer surface densely spiculate. Gonocoxite spiculate; elongate, expanded basally, distal 0.5 slender and slightly bowed; sternal surface with scattered setae; lateral margin from near base to apex with scales and scattered setae; long, recurved, yellowish setae along mesal margin of slender distal portion of gonocoxite from slightly above base of gonostylus to near apex; apex with dense cluster of long, slightly lanceolate, dark setae (about 0.4 length of gonocoxite). Three tergal setal groups: (1) proximal mesal group comprised of a dense cluster (golden in color) of 25–30 (mean 28, n 8) lanceolate setae (about 0.4 length of gonocoxite), most curved beyond midlength; (2) a tight group of 9–15 (mean 12, n 8) slender, pale setae (similar in length to lanceolate setae) at distal edge of lanceolate setal cluster; (3) slightly laterad of lanceolate setal cluster is a diffuse group of 13–17 (mean 16, n 9) very slender dark setae, curved near tip. Gonostylus (Fig. 1 D) about 0.4 length of gonocoxite, arises on mesal surface of gonocoxite near midlength, curved toward distal direction at about 0.3 length; glabrous but rugose near apex; broad over entire length but with short, acute tip. Aedeagus longer than wide; submedian tergal arms bend toward each other resembling an upsidedown V, narrowly joined at midline to form a tergal bridge; apical tergal arms flared laterally and joined apically to form narrow apical tergal bridge (ATB), posterior margin of ATB minutely crenulate; median sternal plate located within apical tergal arms, apical portion coarsely denticulate. Proctiger (in lateral view) with broad basal sclerotization of tergum X, paraproct rounded apically with adjacent subapical lobe and with 4 or 5 cercal setae. FEMALE. Like male except for sexual characters as follows. Head: Proboscis slightly expanded in distal 0.3, ventral surface with white scales from base to slightly beyond 0.7 length of proboscis (ending near base of apical expansion), about distal 0.3 of proboscis with dark scales. Thorax: Integument tan to light brown. Legs: Posteroventral surface of forefemur with white scaling over basal ~ 0.3, rather narrow line of white scales continues to distal end. Posteroventral surface of foretibia with white scales over entire length or to 0.7 and with scattered white scales to distal end. Foretarsomeres 1–5 (TaI 1–5) with dark scaling, scales on posteroventral surface with bright metallic reflection. Foretarsomere 1 (TaI 1) often with a few white scales basally. Midfemur and midtibia with white scales over entire length on posteroventral surface, although white scales may become scattered or absent toward distal end of midtibia. Dorsal surface of midtarsomere 1 (TaII 1) primarily dark scaled with a few white scales at distal end; in some specimens, narrow irregular row of white scales extends over entire anterodorsal surface. Posteroventral surface of TaII 1 with metallic reflection; white scales limited primarily to basal 0.3 but scattered white and pale scales extend to distal end. Dorsal surface of TaII 2 (Fig. 6 B) with white scaling, which gradually expands distally to anterior and posterior surfaces; ventral surface with dark scales with metallic reflection. midtarsomeres 3–5 (TaII 3–5) primarily with white scales, dark scales limited to ventral surface; TaII 5 with a few dark scales dorsally at distal end. Ventral surface of hindfemur with white scales over entire length. Ventral surface of hindtibia primarily with dark scales, some specimens have white scales on basal 0.2. Dorsal surface of hindtarsomeres 1–5 (TaIII 1–5) with dark scaling and metallic or blue iridescence depending upon angle of light. Presence of white scales on ventral surface of TaIII 1 variable; a few scattered white scales may be present or white scales may extend as line to about 0.6. Scales on ventral surface of TaIII 2–5 pale to dark with bright metallic reflection. Genitalia (Fig. 5 EH): Tergum VIII wider than long (width 0.41 mm, length along median plane 0.17 mm), covered with minute spicules and spatulate scales, lateral margins rounded, distal margin somewhat convex. Setae primarily limited to distal 0.33 of tergum VIII, most numerous near distal margin, extending somewhat basally on median plane, in total about 38–47 setae; many setae near distal margin quite long, some slightly exceeding length of tergum VIII; interspersed among long setae are short setae about 0.20–0.25 length of long setae; pair of tiny setae situated sublaterally near basal margin. Sternum VIII wider than long (width 0.37–0.43 mm, length along median plane 0.11–0.12 mm), covered with minute spicules and spatulate scales; distal margin broadly concave with numerous strong setae, which expand posteriorly to form broad Vshaped cluster over median plane, in total about 52–53 setae; length of many setae similar to that of sternum VIII (0.12 mm) although longest nearly twice that length; lateral margins with very few scales or setae; pair of tiny setae located sublaterally near basal margin. Tergum IX narrow (width 0.21–0.22 mm, length 0.03 mm), covered with small spicules, distal margin slightly convex with slight emargination at center, 1 or 2 prominent setae on either side of midline. Insula wider than long, covered with moderately long spicules, apex rounded, about 12 small setae near distal margin, basomesal semicircular depression present with spicules along lateral edges. Postgenital lobe similar in length to cerci, covered with minute spicules, apex slightly emarginate at center, ventral surface with numerous short setae over distal 0.6, dorsal surface with about 7 longer setae on either side of midline; dorsal postgenital lobe length 0.09 mm, dorsal postgenital lobe index 1.85 –2.00 (see Reinert, 1974). Cercus rather flat, covered with minute spicules, apex rounded to somewhat truncate; dorsal surface with about 10–13 setae, longest 0.7–0.8 length of dorsal postgenital lobe. Three spherical spermathecal capsules, all somewhat different in diameter. PUPA (Fig. 1 A,B). Position and character of setae as figured; numbers of branches presented in Table 1. Overall color pattern of pupal exuviae remains similar among different individuals but variation occurs in intensity of pigmentation. Cephalothorax (CT): Tan with very pale to clear patches. Most notable pale areas on scutum include small spot at base of trumpet, two pale areas adjacent to antenna, and pale areas along dorsal margin of scutal protrusion associated with base of trumpet. Seta 1 CT strongly developed, long, double, often slightly bent or curved submedially or medially; 4 CT usually with 2 or 3 branches; 5 CT strongly developed, long, single. Mesothoracic wing mottled basally with 2 distinct pale areas, very pale distally. Metathoracic wing tan but mottled with pale areas; distinct clear spot on each lateral margin; narrow portion of metathoracic wing beyond pale spot (adjacent to lateral margin of abdominal segment I) quite darkly pigmented. Trumpet: Tan, darker basally and near distal end, medial portion very pale (almost white), distal end slightly flared and paler at tip (length 0.80–1.06 mm, mean 0.93 mm, n 8). Abdomen: Coloration varies from very light to dark tan. Abdominal tergum I mottled with pale spots corresponding to positions of seta 3 I, 4 I, and 6,7I. Pale spot associated with seta 6,7I large, often very prominent. Abdominal sternum I frequently with submesal puncture. Abdominal tergum II dark tan with pale areas/spots laterally and distally; seta 2,3II within distal submesal pale area and seta 1,5II at distal edge of this pale area; seta 4 II within pale spot and seta 6 II within extensive lateral pale area. Abdominal tergum III similar in pigmentation to abdominal tergum II but with distinct submesal pale area, which extends to distal margin, seta 1– 3 III within this pale area; seta 4 III within pale spot; seta 6 III within extensive lateral pale area. Areas of darker coloration, most prominent as mesal and submesal longitudinal lines, are progressively diminished from abdominal terga IV to VII. Abdominal terga II–V with sublateral pale area separated by narrow dark line from relatively broad pale area along lateral margin. Abdominal tergum VIII tan but with basomesal region darker. Seta 1 I usually with 13–17 branches, 1 II–VI prominent, multibranched; seta 2 II very small, basal or basolateral to 1 II, 2 III–VII very small, basomesal or mesal to 1 III–VII; seta 3 I rather strong, usually single, 3 II,III single, long (approx. 0.8 mm), 3 IV–VI about 0.3 length of 3 III, 3 IV,VI usually 2 branched, 3 V usually with 3 or 4 branches; seta 5 I double, infrequently triple; seta 5 II,III relatively small (approx. 0.2 mm), 5 II 3 branched, less frequently 2 or 4 branched, 5 &sh
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249. Wyeomyia (Hystatomyia) intonca Dyar & Knab
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Porter, Charles H., Wolff, Marta I., and E
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Insecta ,Culicidae ,Wyeomyia intonca ,Arthropoda ,Diptera ,Animalia ,Biodiversity ,Wyeomyia ,Taxonomy - Abstract
Wyeomyia (Hystatomyia) intonca Dyar & Knab (Figs. 3���6) Wyeomyia intonca Dyar & Knab, 1910: 173. Holotype ��, Empire, Canal Zone, Panama (USNM); examined. Synonymy with Wyeomyia (Dendromyia) circumcincta Dyar & Knab by Lane, 1945: 146. Resurrected from synonymy and placed in subgenus Hystatomyia by Judd, 1998: 579. Hystatomyia intonca: Dyar, 1919: 141, Pl. V (Fig. �� G). Wyeomyia (Hystatomyia) intonca: Dyar, 1923: 170 (Panama: list); Dyar & Shannon, 1924: 91 (Panama; list); Bonne & Bonne��Wepster, 1925: 59,76 (Canal Zone; A key). Prosopolepis (Hystatomyia) intonca: Dyar & Shannon, 1924: 482 (list); Dyar, 1925: 120, 124 (Panama; collection records; L bionomics; �� G key). Dendromyia intonca: Dyar, 1926: 43, 44 (L description, bionomics); del Ponte, 1939: 540 (A). Dendromyia (Hystatomyia) intonca: Dyar, 1928: 84, Pl. XVIII (Fig. �� G, L; ��, ��, L; L bionomics). Wyeomyia (Dendromyia) intonca: Edwards, 1932: 88 (Panama; list); Lane & Cerqueira, 1942: 606 (tentative synonym of circumcincta Dyar & Knab); Lane, 1945: 146 (synonym of circumcincta Dyar & Knab); Lane, 1953: 975 (synonym of circumcincta Dyar & Knab). Knight & Stone, 1977: 328 (synonym of circumcincta Dyar & Knab; info. on type). Wyeomyia (Hystatomyia) sp. D =? intonca: Heinemann & Belkin, 1978: 124, 160, 166. 194 (Panama; collection records; L bionomics). Life stages as described for Wy. chocoensis with following exceptions: MALE. Head: Frons with prominent puncture slightly below postfrontal suture. Ventral surface of proboscis with bright white scales from base to about 0.6 length where white scaling expands slightly (preapical patch) to ventrolateral margin; white scaling ends at about 0.75, replaced by dark scales to distal end. In many specimens, white scales are absent or very reduced slightly basad of preapical patch of white scales. Proboscis (P) (1.37���1.58 mm, mean 1.50 mm, n 5) longer than antennae (flagellum [F] 1.13���1.35 mm, mean 1.27, n 5), mean P:F, 1.18 (n 5), but shorter than forefemur, mean P:Fe��I 0.79 (n 5). Pedicel with 4���8 small setae dorsomesad. Flagellomere 1 with a primarily dorsomesad cluster of 5���10 scales; among 5 specimens (10 antennae) flagellomere 5 (Flm 5) quite uniform in length (0.08 mm), flagellomeres 12 and 13 more variable (Flm 12 0.10���0.14 mm, mean, 0.12; Flm 13 0.16���0.20 mm, mean 0.19); mean Flm 13:Flm 5 2.29. Thorax: Integument brown. Supraalar and antealar areas have combined sum of 22���33 (mean 27, n 5) dark brown setae. Mesopostnotum brown with medial cluster of 6���9 (mode 8) pale, occasionally dark, setae. Prealar area with 3���5 yellow setae. Legs: Forefemur slightly longer than foretibia (mean Fe��I:Ti��I 1.04, n 5); forefemur somewhat shorter than midfemur (mean Fe�� I:Fe��II 0.89, n 5) but longer than hindfemur (mean Fe��I:Fe��III 1.25, n 5); forefemur longer than proboscis (mean Fe��I:P 1.26, n 5); ventral surface of forefemur with white scales over basal 0.2, white scaling tapers to rather narrow line at about 0.4 and continues as narrow line along posteroventral surface to apex; posteroventral surface of foretarsomere 1 (Ta��I 1) with white scales confined primarily to basal 0.5 and with darker scales with metallic reflection distally, in some specimens white scales extend as narrow line to distal end. Midfemur distinctly longer than midtibia (mean Fe��II:Ti��II 1.51, n 5); posteroventral surface of midtibia and basal 0.3���0.6 of midtarsomere 1 (Ta��II 1) with bright white scales; midtarsomere 2 (Ta��II 2) primarily with bright white scales, extent of basal dark scaling quite variable but more extensive on posteroventral surface (0.4���0.6 length of Ta��II 2) than on anteroventral surface (0.2���0.3 length of Ta��II 2), dorsal surface often with white scales over entire length, but may be diminished or even replaced by dark scales over basal 0.2. Ungues of midtarsomere 5 dissimilar; larger unguis stout, dark, curved sharply to about 90 �� angle, tip blunt with apical spur. Hindfemur slightly longer than hindtibia (mean Fe�� III:Ti��III 1.04, n 5), hindtarsomere 1 slightly longer than hindfemur (mean Ta��III 1:FeIII 1.08, n 5), ventral surface of Ta��III 1 often with narrow line of white scales to ~ 0.75 length or with scattered white scales to near distal end. Ungues of hindtarsomere 5 slender, unequal; longer unguis 0.08 mm, about 2 x length of shorter, with moderate to slight curvature; shorter unguis often strongly curved near base. Wing: 1.97���2.25 mm (mean 2.13 mm, n 5). Abdomen: Lateral margins of abdomen with creamy white scales, which form an essentially straight line along abdomen; sterna covered with creamy white scales. Distal margin of sterna II���V with about 7���12 small pale setae, more numerous and longer pale setae along distal margin of sterna VI (~ 19) and VII (~ 24). Genitalia (Fig. 3 C��G): Tergum VIII (ventral in position) narrow, 3.4���4.7 x as wide as long; covered with small spicules, which become minute and very numerous basally although basal 0.3���0.5 glabrous; distal margin straight, 3 irregular rows of long dark setae (range 38���41, mean 40, n 6) along and near distal margin, longest setae about 2.1���2.5 times length of tergum VIII along median plane. Sternum VIII (dorsal in position) with distal margin somewhat convex; setae (range 23���27, mean 25, n 6) dark, arranged primarily as single row along distal margin; a few scales along lateral margins pale, rest dark. Tergum IX bearing 3, rarely 2, stout but relatively short setae on either side of narrow median bridge, apices of setae bent slightly laterad. Sternum IX narrow but expanded medially, becoming bell��shaped between base of gonocoxites; appears to be fused basally to gonocoxites; with rather broad U��shaped mesal membranous area; quite densely spiculate. Gonocoxite elongate, expanded basally; sternal basal surface spiculate with rather sparse covering of scales, an irregular row of setae just proximal to basal mesal setal clusters of tergum. Distal 0.5 of gonocoxite slender, distinctly bowed; mesal surface with slender setae distally that merge with dense subapical/ apical cluster of dark setae (0.2���0.3 length of gonocoxite); setae on or near mesal margin curved distally toward median plane of genitalia. Tergal surface of gonocoxite with 4 prominent clusters of setae (3 occur close together in a basal mesal position): (1) basalmost cluster comprised of 10���13 (mean 11) unmodified, moderately developed pale setae; (2) adjacent to this cluster (slightly mesad and distal to it) is a group of 11���15 (mean 14) stout, rather long setae (~ 0.4 length of gonocoxite) with golden reflection, which terminate in curved spathe��like apex (a few smaller unmodified setae occur along edge of this cluster); (3) ventral (prerotation sense) and often slightly distal to these setae is a third group of 9 (rarely 10) somewhat longer (~ 0.5 length of gonocoxite), lanceolate��shaped setae with golden to copper reflection, these setae become slightly broader subapically before bending sharply and narrowing to a fine tip; (4) fourth prominent cluster of setae laterad to three basal mesal clusters, usually consists of 28���41 (mean, 34) unmodified pale setae, longest often extending slightly beyond tip of gonocoxite. Gonostylus (Fig. 3 D) arises basally on gonocoxite near mesal margin of lateral setal cluster; the glabrous and relatively transparent gonostylus extends mesally, then curves distally and becomes broader; expanded apical area about 3 x width of basal portion (stem). Aedeagus slightly longer than wide; submedian tergal arms bend toward each other resembling an upsidedown V, in some individuals the arms appear to be joined medially but in others they appear to remain slightly separated. Proctiger (in lateral view) with broad basal sclerotization of tergum X, paraproct with rounded apex and bearing 4���7 cercal setae. FEMALE. Like male except for sexual characters as follows. Head: Ventral surface of proboscis often entirely dark scaled with exception of small cluster of white scales (preapical patch) from 0.6���0.7 length of proboscis; less frequently a narrow line of white scales extends from base of proboscis to preapical patch. Thorax: Integument light brown to brown. Legs: Resembling male but with several differences. Dorsal surface of midtarsomere 1 (Ta��II 1) with dark scales, white scales limited to basal 0.3 of posteroventral surface, most numerous on basal 0.1; midtarsomeres 2���5 (Ta��II 2���5) (Fig. 6 A) with dark scales with metallic reflection, a few pale and white scales may be present near basal and/or distal end of Ta��II 2���4; Ta��II 5 with variable amount of pale scaling. Genitalia (Fig. 5 A��D): Tergum VIII wider than long (width 0.43���0.48 mm, length along median plane 0.17���0.19 mm, n 2); covered with minute spicules and spatulate scales; distal margin slightly concave; setae confined to distal 0.5, most numerous along and near distal margin, absent from lateral margins, in total about 46���54 setae. Distal margin of sternum VIII with numerous strong, straight to slightly curved setae, which expand basally to form a mesal V��shaped cluster; in total about 55���69 setae. Insula wider than long, covered with moderately long spicules; apex broadly rounded to rather truncate, irregular anterolateral row of 5 or 6 small setae on either side of midline; mesal semicircular depression or cavity opening onto basal margin, prominent spicules along lower edges of opening. Dorsal postgenital lobe length 0.11 mm, dorsal postgenital lobe index 1.83���1.87 (see Reinert, 1974). Cercus rather flat; covered with minute spicules; apex rather truncate; dorsal surface with 12���16 setae, longest 0.6��� 0.7 length of dorsal postgenital lobe. PUPA (Fig. 3 A,B). Position and character of setae as figured; numbers of branches presented in Table 3. Cephalothorax: Tan with very pale to clear patches, especially along dorsal margin of scutal protrusion at base of trumpet. Seta 4 ��CT usually with 3 or 4 branches. Metathoracic wing tan with pale markings comprised of submedial pale spot and a slightly pale spot on each lateral margin. Trumpet: Length 0.84���1.26 mm (mean 1.08 mm, n 8); tan, darkest basally, distal end not quite as dark and slightly flared, medial portion similar in color to distal end or slightly paler. Abdomen: Abdominal tergum I rather uniformly tan although seta 6,7��I and occasionally 4,5��I within a pale spot. Seta 1 ��I well developed, most often with 18 or 19 branches. Seta 3 ��I moderately developed, usually double; seta 3 ��IV���VI about one��third the length of 3 ��III, 3 ��IV with 3 or 4 branches, 3 ��V usually 4 ��branched, 3 ��VI 2���4 ��branched. Seta 5 ��I single, infrequently double; seta 5 ��II,III relatively small (approx. 0.2 mm), usually 4 ��branched; 5 ��IV���VI single, very long (approx. 1.1���1.2 mm). Puncture near seta 4 ��III���V, usually located distolaterad of seta 4 ��III,IV and basal mesal to seta 4 ��V. Paddle: Pale tan, somewhat darker along midrib. Male genital lobe: Large (length [l] 0.57���0.62 mm, mean 0.60 mm, n 8; width [w] 0.50���0.54 mm, mean 0.52 mm, n 8; mean l:w 1.14, range 1.11���1.16) with elliptical��shaped apex; distinctly broader than combined width of paddles. Cephalothorax Abdominal segments Seta no. CT I II III IV V VI VII VIII 0 ��� ��� 1 1 1 1 1 1 1 1 Range followed in parenthesis by mode; based on 8 specimens (16 setae). 2 One exception from number in parenthesis. 3 Very small, occasionally with seta with 1 or 2 branches. Head Thorax Abdominal segments 1 Range followed in parenthesis by mode; based on 8 specimens (16 setae). 2 One exception from number in parenthesis. FOURTH��INSTAR LARVA (Fig. 4). Position and character of setae as figured; numbers of branches presented in Table 4. Head: Dorsomentum with 1 large central tooth and 9���11 pairs of smaller lateral teeth. Maxilla: Maxillary brush quite long, maxillary brush spicules similar in length to seta 4 ��Mx (0.23 mm). Seta 1 ��Mx short, stout (0.015 mm); seta 2 ��Mx very slender, approx. 0.025 mm in length, basal to 1 ��Mx. Mandible: Mandibular rake comprised of approximately 8 stout spicules, each about 0.12 mm in length. Antenna: Short (mean 0.29 mm, n 10), slender; seta 1 ��A 2 ��branched (rarely single), borne dorsally about 0.68 (mean of 10) length and usually not quite reaching tip of antenna. Thorax: Seta 14 ��P single, sometimes forked or 2 ��branched. Seta 2 ��M less than 0.5 length of 3 ��M, base of 2 ��M slightly narrower than base of 3 ��M; 7 ��M about 0.25���0.33 length of 5 ��M; 9,10��M long, similar in length. Abdomen: Seta 2 ��I laterad of 1 ��I, stout, often 2 ��branched; 2 ��II usually single, basal to 1 ��II; 2 ��III���VII distinctly mesad of 1 ��III���VII. Seta 3 ��I more than twice length of 2,4��I; 6 ��VII 4���6 ��branched, rather short; 10 ��VI usually 4 ��branched. Seta 11 ��I prominent, stellate, branches similar in length to those of 13 ��I. Segment VIII: Comb scales in 4 or 5 irregular rows (mean number of scales 69, range 58���76, n 9). Seta 2 ��VIII single, rather long, about 0.5 length of siphon. Siphon: Long, slender (mean length 1.17 mm, range 1.04���1.28 mm, n 12) usually somewhat curved distally, wider at base, lightly pigmented with subapical region of darker pigmentation and basal edge quite dark, surface smooth; siphon index 7.8���8.9 (mean 8.2, n 11). Pecten comprised of 5���8 (mode 6, n 12) spine��like spicules, somewhat fringed apically; basal spicule close to seta 1 ��S, often slightly distal to it. Seta 1 ��S usually with 3 or 4 branches; located basally at about 0.13 (mean of 12) of siphon���s length. Ventral accessory setae (1 a��S) unbranched, arranged in 2 rows; number of setae in 2 rows combined 12���16 (mean 14, n 12); length of distal��most seta usually slightly shorter than distance of seta to distal end of siphon. Dorsal accessory setae (2 a��S) unbranched, infrequently a distal seta is forked; arranged in 2 rows; number of setae in 2 rows combined 11���19 (mean 17, n 14); basal��most seta approximately same length as third and fourth setae from base; distal seta not extending to tip of siphon. Segment X: Saddle tan, similar in color to darkened subapical area of siphon; extending near to ventral surface, mean length of 0.22 mm (n 12) measured dorsally. Setae 1��� 3 ��X well developed; setae 1,3�� X 2 ��branched, all long; 2 ��X 3 ��branched, smallest (upper) branch about 0.4���0.8 length of middle branch, which is quite variable, and about 0.25���0.33 length of lower branch; seta 4 ��X 7���10 ��branched (mode 8,9, n 23), about 0.30 mm in length. BIONOMICS. Wyeomyia intonca originally was described from a male, which had been collected as a larva or pupa from a bromeliad on a fallen tree at the edge of Comacho river, Canal Zone, Panama (Dyar & Knab, 1909). In 1925 Dyar indicated larvae of Wy. intonca occur in Tillandsia, and in 1926 published a brief description of the larval stage from specimens found in ���wild pineapple, Ananas magdalenae (Andr��) Standl. ��� These plants were found in ���jungle, some three miles back of Fort Randolph on the Atlantic side of the Isthmus.��� Heinemann & Belkin (1977 a, b, 1978) reported collections of Wy. ? intonca (3 different forms designated D, G and H) from 15 bromeliad samples (Panama, 5; Costa Rica, 9; and Nicaragua, 1), which were primarily from forested areas at elevations of 100 m and 500��� 700 m. However, only Wy. (Hystatomyia) sp. D appears to correspond with Wy. intonca, and it was encountered only in Panama. Our collections, upon which the redescription is largely based, were from the northern Pacific Coast of Colombia, specifically Ensenada de Utria and southward to Jurubida. In this region, Wy. intonca was closely associated with coastal mangroves, which tended to be quite variable with respect to dominant tree species. Pi��uelo mangrove dominated by Pelliciera rhizophorae Tr. & Pl. (Pellicieraceae) and with numerous tank bromeliads (dominants include: Werauhia ringens [Griseb.] J.R. Grant, W. sanguinolenta [Linden ex Cogniaux & Marchal] J.R. Grant, and W. gladioliflora [H. Wendland] J.R. Grant) appeared to be a particularly suitable habitat for Wy. intonca. This mosquito also was abundant in red mangrove dominated by Rhizophora harrisonii Leechm. and R. mangle L. (Rhizophoraceae); dominant tank bromeliads include W. sanguinolenta, W. gladioliflora, W. kupperiana (Suess.) J.R. Grant, and Aechmea pubescens Baker. Within these mangroves, larvae of Wy. intonca were found in tank bromeliads located from 0.6 to 2.5 m above ground and were found primarily in larger plants, i.e., those with 0.5 to 1 + liters of water. Wyeomyia intonca was not encountered in bromeliads from forested areas adjacent to these mangroves, even though sampling was quite extensive. DISTRIBUTION. Collection records from Panama suggest the distribution of Wy. intonca extends from the Canal Zone to Colombia. At present, the known distribution of this mosquito in Colombia is limited to our collections from the northern Pacific Coast of the Department of Choc�� (Ensenada de Utria and southward to Jurubida). MATERIAL EXAMINED. Sixty��seven specimens (22 ��, 4 ��, 10 ��G, 3 ��G, 4 Le, 15 Pe, 9 L), including 4 complete and 11 partial individual rearings. Holotype, ��, genitalia on microscope slide, PANAMA: DK, 5 ��09, Type No. 12744 U.S. N.M. (red tag). Non��types, PANAMA: Canal Zone, Gatun, Jan. 1928 (1 �� 1 ��G 1 LePe �� 11146 ��m with dissected genitalia), (C.H. Bath Coll.), (blue tag). COLOMBIA: Choc��, Ensenada de Utria (6 ��03.1'N 77 �� 21.5 'W), 18 ��II�� 1999 (3 �� 1 �� 1 ��G 2 LePe�� 1 Pe�� 1 L ��� CO 1143 �� 3, �� 4, �� 6, �� 101 with dissected genitalia, �� 102), 0���10 m, hbt: Werauhia sanguinolenta (Linden ex Cogniaux & Marchal) J.R. Grant, (Wolff & Porter); same locality, 18 ��II�� 1999 (1 L ��� CO 1144 �� 19), 0���10 m, hbt: Werauhia sanguinolenta (Linden ex Cogniaux & Marchal) J.R. Grant, (Wolff & Porter); same locality, 18 ��II�� 1999 (1 L ��� CO 1145 �� 8), 0���10 m, hbt: Guzmania scherzeriana Mez, (Wolff & Porter); same locality, 18 ��II�� 1999 (1 �� 1 ��G 1 Pe�� 1 L ��� CO 1147 �� 8, �� 103 adult on microscope slide with dissected genitalia), 0���10 m, hbt: Guzmania scherzeriana Mez, (Wolff & Porter); sam, Published as part of Porter, Charles H., Wolff, Marta I. & E, 2004, A new species of Wyeomyia (Hystatomyia) (Diptera: Culicidae) from Colombia and a redescription of Wy. (Hystatomyia) intonca Dyar & Knab, pp. 1-31 in Zootaxa 477 on pages 17-25, DOI: 10.5281/zenodo.157376, {"references":["Dyar, H. G. & Knab, F. [1910] Description of three new American mosquitoes (Diptera, Culicidae). Proceedings Entomological Society of Washington, 11 [1909], 173 - 174.","Lane, J. (1945) Os sabetineos da America. (Addenda e Corrigenda). Revista de Entomologia, 16, 132 - 157.","Judd, D. D. (1998) Review of a bromeliad-ovipositing lineage in Wyeomyia and the resurrection of Hystatomyia (Diptera: Culicidae). Annals of the Entomological Society of America, 91, 572 - 589.","Dyar, H. G. (1919) A revision of the American Sabethini of the Sabethes group by the male genitalia. Insecutor Inscitiae Menstruus, 7, 114 - 142.","Dyar, H. G. (1923) The mosquitoes of Panama (Diptera, Culicidae). Insecutor Inscitiae Menstruus, 11, 167 - 186.","Bonne, C. & Bonne-Wepster, J. (1925) Mosquitoes of Surinam, a study on Neotropical mosquitoes. Koninkijke Vereeniging het Koloniaal Instituut te Amsterdam Meddideeling No. 21, Afdeeling Tropische Hygiene No. 13. Druk De Bussy, Amsterdam, 558 pp.","Dyar, H. G. (1925) The mosquitoes of Panama (Diptera, Culicidae). Insecutor Inscitiae Menstruus, 13, 101 - 195.","Dyar, H. G. (1926) The larva of Dendromyia intonca Dyar & Knab (Diptera, Culicidae). Insecutor Inscitiae Menstruus, 14, 43 - 44.","del Ponte, E. (1939) Identificacion de Sabethini (Dip. Culicidae) por medio de tarjetas perforadas. Physis, 17, 535 - 541.","Dyar, H. G. (1928) The mosquitoes of the Americas. Part I. Carnegie Institute of Washington Publication 387, v, 1 - 616.","Edwards, F. W. (1932) Genera Insectorum. Diptera. Fam. Culicidae. Fascicle 194. Desmet-Verteneul, Bruxelles, 258 pp.","Lane, J. & Cerqueira, N. L. (1942) Os sabetineos da America (Diptera, Culicidae). Arquivos de Zoologia do Estado de Sao Paulo, 3, 473 - 849.","Lane, J. (1953) Neotropical Culicidae. Vol. II. University of Sao Paulo, Sao Paulo, 553 - 1112 pp.","Knight, K. L. & Stone, A. (1977) A catalog of the mosquitoes of the world (Diptera: Culicidae). Second edition. The Thomas Say Foundation 6, ix + 611 pp.","Heinemann, S. J. & Belkin, J. N. (1978) Collection records of the project \" Mosquitoes of Middle America \" 10. Panama, including Canal Zone (PA, GG). Mosquito Systematics, 10, 119 - 196.","Reinert, J. F. (1974) Terminology and preparation techniques of the female genitalia of aedine mosquitoes (Diptera: Culicidae). Mosquito Systematics, 6, 46 - 56.","Heinemann, S. J. & Belkin, J. N. (1977 a) Collection records of the project \" Mosquitoes of Middle America \" 7. Costa Rica (CR). Mosquito Systematics, 9, 237 - 287.","Heinemann, S. J. & Belkin, J. N. (1977 b) Collection records of the project \" Mosquitoes of Middle America \" 8. Central America: Belize (BH), Guatemala (GUA), El Salvador (SAL), Honduras (HON), Nicaragua (NI, NIC). Mosquito Systematics, 9, 403 - 454."]}
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- 2004
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250. A new species of Wyeomyia (Hystatomyia) (Diptera: Culicidae) from Colombia and a redescription of Wy. (Hystatomyia) intonca Dyar & Knab
- Author
-
Porter, Charles H., Wolff, Marta I., and E
- Subjects
Insecta ,Culicidae ,Arthropoda ,Diptera ,Animalia ,Biodiversity ,Taxonomy - Abstract
Porter, Charles H., Wolff, Marta I., E (2004): A new species of Wyeomyia (Hystatomyia) (Diptera: Culicidae) from Colombia and a redescription of Wy. (Hystatomyia) intonca Dyar & Knab. Zootaxa 477: 1-31, DOI: 10.5281/zenodo.157376
- Published
- 2004
- Full Text
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