3,446 research outputs found
Gabriel H. Cohn : Das Buch Jona im Lichte der biblischen Erzählkunst — Studia Semitica Neerlandica 12, 1969
No full textJacob Edmond. Gabriel H. Cohn : Das Buch Jona im Lichte der biblischen Erzählkunst — Studia Semitica Neerlandica 12, 1969. In: Revue d'histoire et de philosophie religieuses, 51e année n°3-4,1971. pp. 379-380
Purification of human butyrylcholinesterase from frozen Cohn fraction IV-4 by ion exchange and Hupresin affinity chromatography.
No full textHuman butyrylcholinesterase (HuBChE) is being developed as a therapeutic for protection from the toxicity of nerve agents. An enriched source of HuBChE is Cohn fraction IV-4 from pooled human plasma. For the past 40 years, purification of HuBChE has included affinity chromatography on procainamide-Sepharose. The present report supports a new affinity sorbent, Hupresin, for purification of HuBChE from Cohn fraction IV-4. Nine batches of 70-80 kg frozen Cohn fraction were extracted with water, filtered, and chromatographed on 30 L of Q-Ceramic ion exchange sorbent at pH 4.5. The 4% pure Q-eluent was pumped onto 4.2 L Hupresin, where contaminants were washed off with 0.3 M NaCl in 20 mM sodium phosphate pH 8.0, before 99% pure HuBChE was eluted with 0.1 M tetramethylammonium bromide. The average yield was 1.5 g of HuBChE from 80 kg Cohn paste. Recovery of HuBChE was reduced by 90% when the paste was stored at -20°C for 1 year, and reduced 100% when stored at 4°C for 24h. No reduction in HuBChE recovery occurred when paste was stored at -80°C for 3 months or 3 years. Hupresin and procainamide-Sepharose were equally effective at purifying HuBChE from Cohn fraction. HuBChE in Cohn fraction required 1000-fold purification to attain 99% purity, but 15,000-fold purification when the starting material was plasma. HuBChE (P06276) purified from Cohn fraction was a 340 kDa tetramer of 4 identical N-glycated subunits, stable for years in solution or as a lyophilized product
Patterns of Variation in Jakarta Indonesian: Linguistic and Social Dimensions
No full textColloquial varieties of Indonesian are increasingly becoming the native languages of a significant portion of the Indonesian population. Notable in this regard is Jakarta Indonesian
(JI). We seek to examine the nature of variation in this increasingly widely spoken variety based on the Betawi-Jakarta Indonesian corpus (Gil & Tadmor 2014). We investigate variation within a subset of speakers comparing the phonological variables Kurniawan (2018) examined (word-final [a] ~ [e], word-final [h] ~ [ʔ] ~ Ø, and active prefix N- ~ [ŋə]) with the
additional variables word-initial [s] ~ Ø and [h] ~ Ø (Cohn & Vogel 2019) and first person singular (1SG) pronouns (Abtahian, Cohn, Djenar & Vogel 2021). Investigation of this new emerging variety demonstrates both inter- and intra-speaker variation for the variables analyzed, but shows that the variables are not all conditioned by the same linguistic and social factors
A Conversation on Tamara Cohn Eskenazi's Ezra: A New Translation with Introduction and Commentary, Anchor Yale Bible 14A
No full textThis special collection contains revised essays from a 2023 SBL panel on Tamara Cohn Eskenazi’s Anchor Bible commentary on Ezra. Contributors assess her portrayal of Ezra’s political artistry and formation of “peoplehood,” engage major debates in Ezra–Nehemiah scholarship, and reflect on the role and limits of the commentator in reconstructing history and interpreting the text amid contemporary resonances
Inspección médica de las escuelas : conclusiones del profesor H. Cohn, de Breslau, aceptadas por el Congreso Internacional de Higiene, reunido en Ginebra en setiembre de 1882
No full textErioloides longinoi Naskrecki and Cohn, n. sp.
No full textErioloides longinoi Naskrecki and Cohn, n. sp. Figs. 22 B-C, 23A, 23F-G, 36B, 50A, Map 14 Type locality: Costa Rica, Guanacaste Prov., Estac. Pitilla; type depository: Academy of Natural Sciences, Philadelphia – holotype male Diagnostic description.— Very similar to the previous species. Body slender, small for the genus; wings in both sexes surpassing apices of hind femora by about half their length (Fig. 37 B). Fastigium of vertex evenly tapered, its apex narrowly rounded, about as long as eye diameter and as wide as scapus (Fig. 23 F). Face flat, smooth; genal carinae of head poorly developed, hardly discernible. Dorsal surface of pronotum relatively rugose, flat; anterior margin of pronotum straight, posterior one weakly convex (Fig. 23 G); lateral lobes of pronotum about 1.7 times longer than high, their posterior angles right. Male stridulatory file straight, 1.2 mm long, 130 μm wide, with 239 closely spaced and relatively very wide, lamelliform teeth; teeth in proximal half of file thinner and more closely arranged than in distal part (Fig. 50 A); mirror approximately rectangular, slightly longer than wide; secondary veinlet next to AA1 well developed and forming actual margin of mirror; stridulatory area of left wing devoid of secondary venation, distal margin of left mirror convex; secondary veinlet next to AA1 present, somewhat divergent from AA1. Male 10th tergite with two short, rounded, usually more or less parallel lobes (Fig. 22 B); female 10th tergite with deep, narrowly triangular incision. Male cercus robust, somewhat inflated, with large, blunt, hook-like dorsal spine; apex of cercus constricted (Figs. 22 B-C). Female cercus simple, elongately conical, distinctly curved. Titillators flattened, squamose, distinctly dilated apically, apices multidentate, divergent (Fig. 23 A). Male subgenital plate with distinct ventral keel and deep triangular incision apically; female subgenital plate broadly triangular, with small, semicircular incision at apex. Ovipositor relatively slender, with distinct lamella along midline of upper valvula; ratio ovipositor/hind femur 0.61-0.67. Coloration.— General coloration light green (Fig. 37 B). Face pale green, mandibles brightly emerald green, labrum dark brown. Tegmina green, with contrastingly yellow venation. Legs green; abdomen light green; ovipositor light brown, with darker apex. Measurements.— Table 15. Distribution.— This species seems to have a wide distribution, ranging from Mexico, through Costa Rica (Map 14), to Panama. Material examined.— COSTA RICA: Guanacaste Prov., Estac. Pitilla, 9 km S. Santa Cecilia, elev. 700 m, 3 May 1993 (coll. C. Moraga) - 1 female (paratype) (INBio); same locality, 15 June 1994 (coll. C. Moraga) - 1 male (paratype) (INBio); same locality, 15 July 1994 (coll. C. Moraga) - 1 male (holotype) (ANSP); Estac. Pitilla, 9 km S. Santa Cecilia, P.N. Guanacaste, elev. 700 m, 3 June 1993 (coll. C. Moraga) - 1 female (allotype) (ANSP); Estac. Pitilla, 9 km St. Cecilia, elev. 700 m, 15 January 1989 (coll. GNP Biodiversity Survey) - 1 female (paratype) (INBio); Heredia Prov., Finca Naranjo Valenciana, 2 km S Pueblo Nuevo, Sarapiquí, elev. 90 m, 22 August 1992 (coll. M. Ortiz) - 1 male (paratype) (INBio); same locality, elev. 90 m, 9 - 30 September 1992 (coll. M. Ortiz) - 1 female (paratype) (INBio); PANAMA: Canal Zone, Barro Colorado Is., 22 May 1977 (coll. Silberglied/Aiello) - 1 male (paratype) (UMMZ).; MEXICO: 20 mi W Tamazunchale, 19 September 1974 (coll. G. Bohart and W. Hanson) - 1 male (paratype) (EMUS). Etymology.— This species is named in honor of John (Jack) Longino, one of the founders of the project ALAS, the first large scale inventory of the Arthropoda of the tropical rain forest. Erioloides acutidentis Naskrecki and Cohn, n. sp. Figs. 22 F-G, 23C, 23H, 50C, Map15 Type locality: Costa Rica, Puntarenas Prov., Estac. Pittier; type depository: Academy of Natural Sciences, Philadelphia – holotype male Diagnostic description.— Very similar to the previous species; fastigium of vertex more pointed than in other species of the genus (Fig. 23 H). Male stridulatory file straight, 1.0 mm long, 103 μm wide, with 179 closely spaced and very wide, lamelliform teeth; teeth in proximal half of file thinner and more closely arranged than in distal part (Fig. 50 C); mirror elongately rectangular, distinctly longer than wide; secondary veinlet next to AA1 well developed, strongly divergent from AA1; stridulatory area of left wing devoid of secondary venation. Male 10th tergite with small, narrow incision on posterior margin (Fig. 22 F). Male cercus relatively slender, cylindrical, with small, spur-like dorsal spine; apex of cercus blunt (Fig. 22 F-G). Female cercus simple, elongately conical, distinctly curved. Titillators not clearly differentiated from phallic membrane, squamose (Fig. 23 C). Male subgenital plate with distinct ventral keel and deep triangular incision apically; female subgenital plate broadly triangular, with small, triangular incision at apex. Ovipositor relatively slender, with irregular lamella along midline of upper valvula; ratio ovipositor/hind femur 0.81. Coloration.— General coloration light green. Face pale green, mandibles brightly emerald green, labrum dark brown. Tegmina green, with contrastingly yellow venation. Legs green; abdomen light green dorsally; purple ventrally; ovipositor light brown, with darker apex. Measurements.— Table 15. Distribution.— So far, this species is known from only a one locality in southern Puntarenas Prov. (Map 15). Material examined.— COSTA RICA: Puntarenas Prov., Estac. Pittier, elev. 1670 m, 23 August - 13 September 1995 (coll. E. Navarro) - 1 female (allotype) (ANSP); same locality, 26 September - 5 October 1995 (coll. E. Navarro) - 1 male (holotype) (ANSP). Etymology.— The specific epithet refers to the sharp, spur-like spine on the male cercus. Erioloides sikesi Naskrecki and Cohn, n. sp. Figs. 22 I-H, 23D, 50B, Map 15 Type locality: Costa Rica, Puntarenas Prov., Res. Biol. Monteverde, Estac. La Casona; type depository: Academy of Natural Sciences, Philadelphia – holotype male Diagnostic description (male, female unknown).— Very similar to the previous species; fastigium of vertex more pointed than in other species of the genus. Male stridulatory file straight, 1.4 mm long, 146 μm wide, with 198 closely spaced and very wide, lamelliform teeth; teeth in proximal half of file thinner and more closely arranged than in distal part (Fig. 50 B); mirror nearly perfectly square; secondary veinlet next to AA1 present, parallel to AA1; stridulatory area of left wing devoid of secondary venation. Male 10th tergite with deep incision on posterior margin, resulting in two large, pointed lobes (note: Fig. 22 H shows the lobes from above, when the pointed ends of the lobes cannot be seen). Male cercus relatively slender, cylindrical, with small, blunt dorsal spine; apex of cercus blunt (Fig. 22I). Titillators flat, squamose, somewhat narrowed towards their apices (Fig. 23 D). Male subgenital plate with distinct ventral keel and deep triangular incision apically; female subgenital plate broadly triangular, with small, triangular incision at apex. Coloration.— General coloration light green. Face pale green, mandibles brightly emerald green, labrum yellow. Tegmina green, with contrastingly yellow venation. Legs green; abdomen light green dorsally; purple ventrally. Measurements.— Table 15. Distribution.— This species is known only from its type locality (Map 15). Material examined.— COSTA RICA: Puntarenas Prov., Estac. La Casona, Res. Biol. Monteverde, 1 - 30 April 1992 (coll. K. Flores) - 1 male (holotype) (ANSP). Etymology.— This species was named in honor of Derek S. Sikes, a fine coleopterist and good friend. Erioloides latiscobinus Naskrecki and Cohn, n. sp. Figs. 22 J-K, 23E, 49E, Map 15 Type locality: Costa Rica, Alajuela Prov., Sector Colonia Palmareña; type depository: Academy of Natural Sciences, Philadelphia – holotype male Diagnostic description.— Very similar to previous species. Male stridulatory file straight, 1.1 mm long, 145 μm wide, with 220 closely spaced and extremely wide, lamelliform teeth; teeth in proximal half of file thinner and more closely arranged than in distal part (Fig. 49 E); mirror approximately rectangular, distinctly longer than wide; secondary veinlet next to AA1 well developed, slightly divergent from AA1; stridulatory area of left wing devoid of secondary venation, distal margin of left mirror concave; secondary veinlet next to AA1 present, strongly divergent from AA1. Male 10th tergite with small, triangular apical incision (Fig. 22 J). Male cercus relatively slender, cylindrical, with thin, finger-like dorsal spine; apex of cercus somewhat constricted (Fig. 22 K). Female cercus simple, elongately conical, distinctly curved. Titillators flattened, squamose, apices multidentate, strongly divergent. Male subgenital plate with distinct ventral keel and deep triangular incision apically; female subgenital plate broadly triangular, with small, semicircular incision at apex. Ovipositor relatively slender, with file of pegs along midline of upper valvula; ratio ovipositor/hind femur 0.74-0.78. Coloration.— General coloration light green. Face pale green, mandibles brightly emerald green, labrum dark brown. Tegmina green, with contrastingly yellow venation. Legs green; abdomen light green dorsally; purple ventrally; ovipositor light brown, with darker apex. Measurements.— Table 15. Distribution.— This new species seems to be widely distributed in Costa Rica, with most records from low or mid elevation forest habitats (Map 15). Material examined.— COSTA RICA: Alajuela Prov., Estac. San Ramón Oeste, elev. 620 m, 19 April 1994 (coll. F. Quesada) - 1 male (paratype) (INBio); Sect. San Ramón de Dos Rios, elev. 620 m, 18 March - 13 April 1995 (coll. F.A. Quesada) - 1 female (paratype) (INBio); Sector Colonia Palmareña, 9 km SO de Bajo Rodríguez, elev. 700 m, 1 - 30 April 1995 (coll. G. Carballo) - 1 female (allotype) (ANSP); same locality, 1 - 31 May 1997 (coll. G. Carballo) - 1 male (holotype) (ANSP); Guanacaste Prov., Estac. Pitilla, 9 km S. Santa Cecilia, elev. 700 m, 18 - 23 July 1993 (coll. C. Moraga) - 3 males (paratypes) (INBio); same locality, 15 June 1994 (coll. C. Moraga) - 1 male (paratype) (INBio); same locality, 15 July 1994 (coll. C. Moraga) - 1 male (paratype) (INBio); Estac. Pitilla, 9 km St. Cecilia, elev. 700 m, 15 May 1988 (coll. GNP Biodiversity Survey) - 3 males (paratypes) (INBio); same locality, 15 January 1989 (coll. GNP Biodiversity Survey) - 2 males, 2 females (paratypes) (INBio); Estac. Mengo, SW side Volcán Cacao, elev. 1100 m, 15 February 1989 (coll. GNP Biodiversity Survey) - 1 female (paratype) (INBio); Estac. Pitilla, 9 km S Santa Cecilia, elev. 700 m, 15 March 1990 (coll. P. Rios, C. Moraga and R. Blanco) - 1 female (paratype) (INBio); Heredia Prov., Finca Naranjo Valenciana, 2 km S Pueblo Nuevo, Sarapiquí, elev. 90 m, 9 - 30 September 1992 (coll. M. Ortiz) - 1 female (paratype) (INBio); Puntarenas Prov., Las Cruces, 1 July - 31 August 1991 (coll. J. Doubles) - 1 male (paratype) (UMMZ); Sirena, Corcovado N.P., elev. 0 - 100 m, 15 April 1989 (coll. R. Blanco and G. Fonseca) - 1 female (paratype) (INBio); Valle de Coto Brus, Las Cruces, Wilson Botanical Gardens, 22 March 1994 (coll. P. Naskrecki) - 1 male (paratype) (PN collection). Etymology.— Named in reference to the extremely wide teeth of the stridulatory file of the male. Erioloides acutidentis Naskrecki and Cohn, n. sp. Figs. 22 F-G, 23C, 23H, 50C, Map15 Type locality: Costa Rica, Puntarenas Prov., Estac. Pittier; type depository: Academy of Natural Sciences, Philadelphia – holotype male Diagnostic description.— Very similar to the previous species; fastigium of vertex more pointed than in other species of the genus (Fig. 23 H). Male stridulatory file straight, 1.0 mm long, 103 μm wide, with 179 closely spaced and very wide, lamelliform teeth; teeth in proximal half of file thinner and more closely arranged than in distal part (Fig. 50 C); mirror elongately rectangular, distinctly longer than wide; secondary veinlet next to AA1 well developed, strongly divergent from AA1; stridulatory area of left wing devoid of secondary venation. Male 10th tergite with small, narrow incision on posterior margin (Fig. 22 F). Male cercus relatively slender, cylindrical, with small, spur-like dorsal spine; apex of cercus blunt (Fig. 22 F-G). Female cercus simple, elongately conical, distinctly curved. Titillators not clearly differentiated from phallic membrane, squamose (Fig. 23 C). Male subgenital plate with distinct ventral keel and deep triangular incision apically; female subgenital plate broadly triangular, with small, triangular incision at apex. Ovipositor relatively slender, with irregular lamella along midline of upper valvula; ratio ovipositor/hind femur 0.81. Coloration.— General coloration light green. Face pale green, mandibles brightly emerald green, labrum dark brown. Tegmina green, with contrastingly yellow venation. Legs green; abdomen light green dorsally; purple ventrally; ovipositor light brown, with darker apex. Measurements.— Table 15. Distribution.— So far, this species is known from only a one locality in southern Puntarenas Prov. (Map 15). Material examined.— COSTA RICA: Puntarenas Prov., Estac. Pittier, elev. 1670 m, 23 August - 13 September 1995 (coll. E. Navarro) - 1 female (allotype) (ANSP); same locality, 26 September - 5 October 1995 (coll. E. Navarro) - 1 male (holotype) (ANSP). Etymology.— The specific epithet refers to the sharp, spur-like spine on the male cercus. Erioloides sikesi Naskrecki and Cohn, n. sp. Figs. 22 I-H, 23D, 50B, Map 15 Type locality: Costa Rica, Puntarenas Prov., Res. Biol. Monteverde, Estac. La Casona; type depository: Academy of Natural Sciences, Philadelphia – holotype male Diagnostic description (male, female unknown).— Very similar to the previous species; fastigium of vertex more pointed than in other species of the genus. Male stridulatory file straight, 1.4 mm long, 146 μm wide, with 198 closely spaced and very wide, lamelliform teeth; teeth in proximal half of file thinner and more closely arranged than in distal part (Fig. 50 B); mirror nearly perfectly square; secondary veinlet next to AA1 present, parallel to AA1; stridulatory area of left wing devoid of secondary venation. Male 10th tergite with deep incision on posterior margin, resulting in two large, pointed lobes (note: Fig. 22 H shows the lobes from above, when the pointed ends of the lobes cannot be seen). Male cercus relatively slender, cylindrical, with small, blunt dorsal spine; apex of cercus blunt (Fig. 22I). Titillators flat, squamose, somewhat narrowed towards their apices (Fig. 23 D). Male subgenital plate with distinct ventral keel and deep triangular incision apically; female subgenital plate broadly triangular, with small, triangular incision at apex. Coloration.— General coloration light green. Face pale green, mandibles brightly emerald green, labrum yellow. Tegmina green, with contrastingly yellow venation. Legs green; abdomen light green dorsally; purple ventrally. Measurements.— Table 15. Distribution.— This species is known only from its type locality (Map 15). Material examined.— COSTA RICA: Puntarenas Prov., Estac. La Casona, Res. Biol. Monteverde, 1 - 30 April 1992 (coll. K. Flores) - 1 male (holotype) (ANSP). Etymology.— This species was named in honor of Derek S. Sikes, a fine coleopterist and good friend. Erioloides latiscobinus Naskrecki and Cohn, n. sp. Figs. 22 J-K, 23E, 49E, Map 15 Type locality: Costa Rica, Alajuela Prov., Sector Colonia Palmareña; type depository: Academy of Natural Sciences, Philadelphia – holotype male Diagnostic description.— Very similar to previous species. Male stridulatory file straight, 1.1 mm long, 145 μm wide, with 220 closely spaced and extremely wide, lamelliform teeth; teeth in proximal half of file thinner and more closely arranged than in distal part (Fig. 49 E); mirror approximately rectangular, distinctly longer than wide; secondary veinlet next to AA1 well developed, slightly divergent from AA1; stridulatory area of left wing devoid of secondary venation, distal margin of left mirror concave; secondary veinlet next to AA1 present, strongly divergent from AA1. Male 10th tergite with small, triangular apical incision (Fig. 22 J). Male cercus relatively slender, cylindrical, with thin, finger-like dorsal spine; apex of cercus somewhat constricted (Fig. 22 K). Female cercus simple, elongately conical, distinctly curved. Titillators flattened, squamose, apices multidentate, strongly divergent. Male subgenital plate with distinct ventral keel and deep triangular incision apically; female subgenital plate broadly triangular, with small, semicircular incision at apex. Ovipositor relatively slender, with file of pegs along midline of upper valvula; ratio ovipositor/hind femur 0.74-0.78. Coloration.— General coloration light green. Face pale green, mandibles brightly emerald green, labrum dark brown. Tegmina green, with contrastingly yellow venation. Legs green; abdomen light green dorsally; purple ventrally; ovipositor light brown, with darker apex. Measurements.— Table 15. Distribution.— This new species seems to be widely distributed in Costa Rica, with most records from low or mid elevation forest habitats (Map 15). Material examined.— COSTA RICA: Alajuela Prov., Estac. San Ramón Oeste, elev. 620 m, 19 April 1994 (coll. F. Quesada) - 1 male (paratype) (INBio); Sect. San Ramón de Dos Rios, elev. 620 m, 18 March - 13 April 1995 (coll. F.A. Quesada) - 1 female (paratype) (INBio); Sector Colonia Palmareña, 9 km SO de Bajo Rodríguez, elev. 700 m, 1 - 30 April 1995 (coll. G. Carballo) - 1 female (allotype) (ANSP); same locality, 1 - 31 May 1997 (coll. G. Carballo) - 1 male (holotype) (ANSP); Guanacaste Prov., Estac. Pitilla, 9 km S. Santa Cecilia, elev. 700 m, 18 - 23 July 1993 (coll. C. Moraga) - 3 males (paratypes) (INBio); same locality, 15 June 1994 (coll. C. Moraga) - 1 male (paratype) (INBio); same locality, 15 July 1994 (coll. C. Moraga) - 1 male (paratype) (INBio); Estac. Pitilla, 9 km St. Cecilia, elev. 700 m, 15 May 1988 (coll. GNP Biodiversity Survey) - 3 males (paratypes) (INBio); same locality, 15 January 1989 (coll. GNP Biodiversity Survey) - 2 males, 2 females (paratypes) (INBio); Estac. Mengo, SW side Volcán Cacao, elev. 1100 m, 15 February 1989 (coll. GNP Biodiversity Survey) - 1 female (paratype) (INBio); Estac. Pitilla, 9 km S Santa Cecilia, elev. 700 m, 15 March 1990 (coll. P. Rios, C. Moraga and R. Blanco) - 1 female (paratype) (INBio); Heredia Prov., Finca Naranjo Valenciana, 2 km S Pueblo Nuevo, Sarapiquí, elev. 90 m, 9 - 30 September 1992 (coll. M. Ortiz) - 1 female (paratype) (INBio); Puntarenas Prov., Las Cruces, 1 July - 31 August 1991 (coll. J. Doubles) - 1 male (paratype) (UMMZ); Sirena, Corcovado N.P., elev. 0 - 100 m, 15 April 1989 (coll. R. Blanco and G. Fonseca) - 1 female (paratype) (INBio); Valle de Coto Brus, Las Cruces, Wilson Botanical Gardens, 22 March 1994 (coll. P. Naskrecki) - 1 male (paratype) (PN collection). Etymology.— Named in reference to the extremely wide teeth of the stridulatory file of the male. Erioloides sikesi Naskrecki and Cohn, n. sp. Figs. 22 I-H, 23D, 50B, Map 15 Type locality: Costa Rica, Puntarenas Prov., Res. Biol. Monteverde, Estac. La Casona; type depository: Academy of Natural Sciences, Philadelphia – holotype male Diagnostic description (male, female unknown).— Very similar to the previous species; fastigium of vertex more pointed than in other species of the genus. Male stridulatory file straight, 1.4 mm long, 146 μm wide, with 198 closely spaced and very wide, lamelliform teeth; teeth in proximal half of file thinner and more closely arranged than in distal part (Fig. 50 B); mirror nearly perfectly square; secondary veinlet next to AA1 present, parallel to AA1; stridulatory area of left wing devoid of secondary venation. Male 10th tergite with deep incision on posterior margin, resulting in two large, pointed lobes (note: Fig. 22 H shows the lobes from above, when the pointed ends of the lobes cannot be seen). Male cercus relatively slender, cylindrical, with small, blunt dorsal spine; apex of cercus blunt (Fig. 22I). Titillators flat, squamose, somewhat narrowed towards their apices (Fig. 23 D). Male subgenital plate with distinct ventral keel and deep triangular incision apically; female subgenital plate broadly triangular, with small, triangular incision at apex. Coloration.— General coloration light green. Face pale green, mandibles brightly emerald green, labrum yellow. Tegmina green, with contrastingly yellow venation. Legs green; abdomen light green dorsally; purple ventrally. Measurements.— Table 15. Distribution.— This species is known only from its type locality (Map 15). Material examined.— COSTA RICA: Puntarenas Prov., Estac. La Casona, Res. Biol. Monteverde, 1 - 30 April 1992 (coll. K. Flores) - 1 male (holotype) (ANSP). Etymology.— This species was named in honor of Derek S. Sikes, a fine coleopterist and good friend. Erioloides latiscobinus Naskrecki and Cohn, n. sp. Figs. 22 J-K, 23E, 49E, Map 15 Type locality: Costa Rica, Alajuela Prov., Sector Colonia Palmareña; type depository: Academy of Natural Sciences, Philadelphia – holotype male Diagnostic description.— Very similar to previous species. Male stridulatory file straight, 1.1 mm long, 145 μm wide, with 220 closely spaced and extremely wide, lamelliform teeth; teeth in proximal half of file thinner a
MiRNA profile in stage 1, surgically staged endometrial cancer and predicted downstream targets
No full textExotica in the Globular Cluster M4, Studied with Chandra, HST, and the VLA
No full textUsing the Hubble Ultraviolet Globular Cluster Survey (HUGS) and additional
HST archival data, we have carried out a search for optical counterparts to the
low-luminosity Chandra X-ray sources in the globular cluster M4 (NGC 6121). We
have also searched for optical or X-ray counterparts to radio sources detected
by the VLA. We find 24 new confident optical counterparts to Chandra sources
for a total of 40, including the 16 previously identified. Of the 24 new
identifications, 18 are stellar coronal X-ray sources (active binaries, ABs),
the majority located along the binary sequence in a V-I colour-magnitude
diagram and generally showing an H-alpha excess. In addition to confirming the
previously detected cataclysmic variable (CV, CX4), we identify one confident
new CV (CX76), and two candidates (CX81 and CX101). One MSP is known in M4
(CX12), and another strong candidate has been suggested (CX1); we identify some
possible MSP candidates among optical and radio sources, such as VLA20, which
appears to have a white dwarf counterpart. One X-ray source with a sub-subgiant
optical counterpart and a flat radio spectrum (CX8, VLA31) is particularly
mysterious. The radial distribution of X-ray sources suggests a relaxed
population of average mass ~ 1.2 - 1.5 Msun. Comparing the numbers of ABs,
MSPs, and CVs in M4 with other clusters indicates that AB numbers are
proportional to cluster mass (primordial population), MSPs to stellar encounter
rate (dynamically formed population), while CVs seem to be produced both
primordially and dynamically.Comment: 30 pages, 12 figures, 2 pages of supplementary material containing
finding chart
David S. Vanderhooft (ed.), In Conversation with Oded Lipschits, The Fall and Rise of Jerusalem.
No full text This conversation with O. Lipschits, The Fall and Rise of
Jerusalem (Winona Lake, Ind.: Eisenbrauns, 2005) began at a session of the
“Literature and History of the Persian Period” group at the 2005 Annual Meeting
of the Society of Biblical Literature in Philadelphia. It includes an
introduction by the editor and contributions by Rainer Albertz, Tamara Cohn
Eskenazi, Daniel Master, Gary N. Knoppers, Hugh G.M. Williamson and a response
by Oded Lipschits. </jats:p
Correction to: Dahl-Popolizio, S., Carpenter, H., Coronado, M., Popolizio, N. J., & Swanson, C. (2020). Telehealth for the provision of occupational therapy: Reflections on experiences during the COVID-19 pandemic
No full textCorrection to: Dahl-Popolizio, S., Carpenter, H., Coronado, M., Popolizio, N. J., & Swanson, C. (2020). Telehealth for the provision of occupational therapy: Reflections on experiences during the COVID-19 pandemic. International Journal of Telerehabilitation, 12(2), 77–92. https://doi.org/10.5195/ijt.2020.632
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