177,673 research outputs found
R. P. Brou, S. L, Saint François-Xavier : Lettres spirituelles, 1937
No full textVansteenberghe Edmond. R. P. Brou, S. L, Saint François-Xavier : Lettres spirituelles, 1937. In: Revue des Sciences Religieuses, tome 18, fascicule 4, 1938. pp. 547-548
R. P. Brou, S. L, Saint François-Xavier : Lettres spirituelles, 1937
No full textVansteenberghe Edmond. R. P. Brou, S. L, Saint François-Xavier : Lettres spirituelles, 1937. In: Revue des Sciences Religieuses, tome 18, fascicule 4, 1938. pp. 547-548
Lithophane abita Brou & Lafontaine 2009, sp. n.
No full textLithophane abita Brou & Lafontaine, sp. n. urn:lsid:zoobank.org:act: 346FF58C-13A6-42AF-8560-71D612F30B98 Figs 1, 2, 5, 6, 7 Type material. Holotype ♁ (Fig.1): USA, Louisiana, St. Tammany Parish, 4.2 miles (6.8 km) NE of Abita Springs, Sec [tion] 24, T [ownship] 6 S[outh], R [ange] 12 E[ast], 14 Feb. 2002, Vernon A. Brou Jr. Deposited in Canadian National Collection of Insects, Arachnids, and Nematodes (CNC), Ottawa, Canada. Allotype ♀ (Fig. 2): same locality and collector, 6 Dec. 2003. Deposited in CNC. Paratypes: 145 ♁, 162 ♀. Alabama: Baldwin Co., Bon Secour National Wildlife Refuge, Sec. 24, T9 S, R2 E, 18 Jan. 1993, Richard L. Brown (1 ♁). Florida: Alachua Co., Gainesville, 19 Dec. 1982, Edward C. Knudson (1 ♀); Alachua Co., Gainesville, 14 Feb. 2004, Jeffrey R. Slotten (1 ♀); Baker Co., Baxter, 29 Dec. 1990, John S. Kutis (1 ♀), Pinhook Swamp, 24 Feb. 2001, Hugo L. Kons Jr. (1 ♁); Collier Co., Golden Gate Estates 26 Jan. 1991, John S. Kutis (1 ♁); Duval Co., Jacksonville, 11 Mar. 1977, H.D. Baggett (1 ♀); Hernando Co., 1 Mar. 2007, James T. Vargo (1 ♁); Hillsborough Co., Lutz, Florida, 13 & 22 Mar. 1911, F. W. Friday (2 ♀); Marion Co., Bay Lake, 0.5 mi. west of CR315, 7 Feb. 1991, John S. Kutis (1 ♁); Pasco Co., Clay Sink, Withlacoochee St. Forest, 6 Feb. 1991, John S. Kutis (1 ♀); Putnam Co., Putnam Hall Post Office, 3 Mar. 2004, Jeffrey R. Slotten (1 ♁); Sumpter Co., Withlacoochee St. Forest, 5 Feb. 1991, John S. Kutis (1 ♀), same location and collector, 9 Feb. 1991 (1 ♀), same location, 9 Feb. 1991, Richard M. Gillmore (1 ♀); Volusia Co., Cassadaga, 11 Feb. 1963, S. V. Fuller (1 ♁), 15 Feb. 1964, same location and collector (1 ♁), 23 Feb. 1966, same location and collector (1 ♁, 1 ♀). Georgia: Long Co., Griffin Ridge Wildlife Management Area, NE of Altamaha River, 3 mi. SW of Ludowici, 3–4 Mar. 2004, James K. Adams (1 ♀). Louisiana: same locality and collector as for holotype, 21 Nov.–29 Mar. 1982 –2009 (128 ♁, 138 ♀). Maryland: Calvert Co., Battle Creek Cypress Swamp, D. Williams/ A. Brown, 14 Feb. 1990, H. Godwin Stevensen (2 ♁); same locality and collector, Dwight F. Williams, 22 Oct. 1989 (1 ♁); Worcester Co., Pokomoke State Forest, 17 Oct. 1996 and 18 Oct. 1998, J. Glaser (3 ♀); Worcester Co., Sturges Creek Cypress Swamp, 18 Oct. 1998, J. Glaser (1 ♀). Mississippi: Tishomingo Co., Tishomingo State Park, 34° 35’ 54” N, 88° 10’ 43” W, 3 Apr. 1998, Richard L. Brown (1 ♁). North Carolina: Carteret Co., Junction of Hwy 101 and Mill Creek Road, 22 Nov. 1973, J. Bolling Sullivan (1 ♀); Craven Co., North Harlow, 25 and 31 Mar. and 12 Nov. 1990, 13 and 18 Feb. and 20 Mar. 1991, J. Bolling Sullivan (3 ♁, 5 ♀); Jones Co., Haywood Landing, 3 Apr. 1996 and 8 Mar. 2000, J. Bolling Sullivan (1 ♁, 1 ♀); Pender Co., Shelter Gamelands, 5 Apr. 1996, J. Bolling Sullivan (1 ♀). Paratypes deposited in CNC; Florida State Collection of Arthropods, Gainesville; Louisiana State Arthropod Museum, Baton Rouge; Mississippi Entomological Museum; Cornell University Collection, Ithaca, New York; National Museum of Natural History [USNM], Washington, DC; and the private collections of: James K. Adams, Robert J. Borth, Richard M. Gillmore, Edward C. Knudson, Hugo L. Kons Jr., Jeffrey R. Slotten, J. Bolling Sullivan, and the senior author. Primary types are designated with the words Holotype and Allotype in black text on red labels; paratypes are designated with the word Paratype in black text on yellow labels. Etymology. The epithet is derived from the type locality near which all of the known Louisiana specimens have been taken, the town of Abita Springs, St. Tammany Parish, Louisiana, USA. Diagnosis. Lithophane abita is a medium-sized species of Lithophane with a gray forewing and pinkish-fuscous hindwing. Th e forewing maculation tends to be pale and muted, except for a contrasting black line in the fold connecting the deeply zigzagged antemedial and postmedial lines. In these superficial characters, it has the appearance of some species in the Lithophane lepida Grote species-group of which only Lithophane adipel (Benjamin) (Fig. 3) occurs in southeastern United States. It is even more similar to Lithophane thaxteri Grote (Fig. 4), which like L. abita, has a brown flush to the area around the reniform spot and a black line defining the lower edge of the reniform spot, but L. thaxteri occurs in the boreal zone of Canada and in eastern United States as far south as New Jersey, but probably will not be found within the range of L. abita. The male genitalia of L. abita, however, are unique within the genus and the characteristic shape of the apices of the valves can be seen by brushing away some scales from the end of the abdomen. Th e digitus of the right valve projects beyond the apex of the valve as a long, curved, saber-like spine that is almost ⅔ as long as the valve (Fig. 5); that of the left valve is short, stout, and apically blunt with the part of the digitus extending beyond the valve about ¼ of the length of that of the right valve. Th e spine-like process at the apex of the right valve can often be seen with the naked eye protruding from the end of the abdomen. The association of L. abita with bald cypress (Taxodium distichum Rich.), the probable larval host, is also unique within Lithophane. Description. Males and females similar in all external characters except size. Head: color usually light to medium slate gray, occasional specimens dark gray; pronounced frontal tuft; a wide lateral black band of scales on center of head between eyes defined above and below by a bright white line of scales, upper line at a position above eye and below antenna: antenna filiform, simple, slender, and acuminate, similar gray in color, more so dorsally and near base of shaft; labial palp with black scales laterally and gray scales ventrally and dorsally; labial palp peppered with either black or gray scales with white tips; ventral surface of palp with long scales forming a pointed tuft projecting anteroventrally slightly beyond apex of palp. Thorax: dorsal color similar to that of head and forewing ground color except for wide transverse dark brown band on prothoracic collar with upper margin defined by distinct black line with upper scales forming a bright white line; anterior part of thorax with dorsal partially divided tuft of scales; ventral color of thorax light pinkish brown, gray, or fuscous, with area between legs and wings entirely black; outer side of foreleg coxa a mixture of black and white scales (appearing gray to naked eye), with a short group of longitudinal black scales emanating from base; scales on the inner side of coxa brownish gray with a fine longitudinal line of black scales; femur covered with black and white scales (appearing gray to naked eye) with black scales more concentrated near trochanter; scales on coxa of midleg a mixture of gray and white, except near trochanter, where scales form a band of black followed by a band of white; similar black and white bands continue along remainder of midleg femur, tibia, and tarsus; hindleg similar in color and appearance to midleg. Abdomen: dorsal color fuscous with pink suffusion throughout; ventral color same as dorsal. Forewing: dorsal ground color matching that on dorsum of head and thorax; maculation varying from strongly marked to barely distinguishable; weakly marked specimens appear to have been on the wing longer, but do not necessarily appear exceptionally worn; most specimens with very faint, sometimes barely distinguishable, bifurcating black basal dash; antemedial (am) line mostly faint, deeply zigzagged, defined in paler gray and partly bordered on outer edge by black, except in area of fold where am line sharply defined in black forming an outward projecting “V” that extends into prominent, black dash in fold parallel to lower margin of wing and extends to postmedial (pm) line; pm line deeply serrated but faint, partly defined by pale gray and dark gray scales; subterminal line also faintly defined in pale and dark gray but usually bordered in subterminal area by series of diffuse, dark-gray, wedge-shaped spots; terminal area concolorous with medial area, or very slightly darker with wing veins partly defined in black; terminal line incomplete, dark gray, usually stronger between veins; orbicular spot a rounded or slightly oblong paler gray shade defined mainly by the darker gray shading surrounding it; a prominent crescentic black line extends from outer lower edge of orbicular spot and around lower margin of reniform spot; reniform spot barely distinguishable as a paler gray outline above black line on lower margin of spot; forewing with fuscous-brown scales in area between reniform and orbicular spots, and in lower part of reniform. Ventral color of forewing pale luteous brown on basal half of wing, pinkish brown on distal half and forming a darker marginal shade; reniform spot diffuse, dark brown, usually crescent-shaped; terminal line defined by faint black scales accentuated with conspicuous black scales forming v-shaped wedges between veins; fringe gray. Wing length: male: 16.7 mm (15.7–18.0, n = 25); female: 17.1 mm (15.6–18.4, n = 25). Hindwing: dorsal color fuscous with pinkish suffusion throughout; fringe contrastingly lighter slate gray, especially at base of fringe; terminal line usually expressed as diffuse darker brown lines most often only between veins on outer margin of wing; discal spot crescentic, darker than ground color but barely discernable. Ventral color entirely light pink with numerous tiny brown scales sprinkled over entire surface; terminal line generally similar to that on dorsal surface; discal spot very large, brownish-black spot in center of wing; postmedial line a faint but discernable dark, broad line. Male genitalia (n = 6): genital capsule (Fig. 5) with supporting ring modified, so enlarged vinculum and pleural sclerite occupy basal ⅔ of ring, presumably to support greatly enlarged base of valve; tegumen proportionally reduced to dorsal ⅓ of ring; uncus short, cylindrical, expanded at apex; juxta a very large diamond-shaped plate oc- cupying most of area inside genital ring; valves short and triangular, very large at base and tapering to narrow apex; valves asymmetrical; right sacculus large, twice as long as cucullus; cucullus reduced with sclerotized finger-like process at base of cucullus on dorsal margin of valve; apical part of cucullus reduced to rounded, almost membranous flap without any trace of a corona; digitus massive, arising from costal margin of valve, covering basal b of cucullus, then bending dorsally to project posterodorsally from end of valve as a long, tapered, saber-like spine; clasper reduced to Y-shaped sclerite at apex of valve with ampulla projecting beyond costal margin of valve as lightly sclerotized, finger-like process; left valve similar to right valve, except sacculus not as enlarged dorsally at base, costal process at base of cucullus triangular, part of left digitus projecting from valve ¼ as long as saber-like extension of right digitus, and apex of left digitus blunt and rounded. Aedeagus (Fig. 6) cylindrical, heavily sclerotized, about 6 × as long as wide; vesica about 1½ × as long as aedeagus; basal 1/6 as wide as aedeagus; apical part inflated and sac-like, curving in an arc 180° to project anteriorly; vesica with two short diverticula, one short preapical on dorsal surface and one on ventral surface at apex; apex of vesica with two subapical patches of spine-like cornuti, one dorsal and one ventral. Female genitalia (n = 5) (Fig. 7): corpus bursae with prominent postmedial constriction giving it a figure 8-shape; without signa; posterior part of corpus bursae with short, lightly sclerotized, appendix bursae to left of ductus bursae; ductus bursae about ⅓ as long as corpus bursae, sclerotized posteriorly but more lightly sclerotized anteriorly and wider at corpus bursae; ostium bursae sclerotized, tapered anteriorly, truncated abruptly at membranous connection with ductus bursae; anterior apophyses slightly shorter, but much stouter, than posterior apohyses, about ¼ × longer than ring of abdominal segment VIII; anal papillae lightly sclerotized, rounded at apex, about as long as membranous connection to abdominal segment VIII; covered by mixture of short and longer hair-like setae. Biology and distribution. Within Louisiana, Lithophane abita is single brooded with adults on the wing from November 21 to March 29 (Fig. 8). Elsewhere the flight season extends from 17 October (Maryland) to early April (Mississippi and North Carolina). Lithophane abita has been confirmed from the states of Alabama, Florida, Georgia, Louisiana, Maryland, Mississippi, and North Carolina. Th e suspected host plant is bald cypress, Taxodium distichum Rich. In Maryland the three known localites are in bald cypress swamps within a few kilometers of the northernmost site of natu- rally occurring bald cypress trees. In Florida, this moth is often found in or very close to pond cypress domes (R. M. Gillmore, pers. comm.). A single Florida specimen was labeled as captured at fruit bait. Remarks. R. M. Gillmore provided the authors with numerous additional Florida records acquired from various sources, from the counties already listed in the paratype series. Th ese specimens are not included as paratypes due to their poor quality. Within Louisiana, L. abita was captured using ultraviolet light traps only at the Abita Springs location despite 39 continuous years of collecting using the same collecting methods throughout the State. No species of Lithophane was previously recorded for Louisiana by Chapin and Callahan (1967), who published the only list of Noctuidae for the state. However, intensive collecting by the senior author at the type locality of L. abita has turned up about 10 Lithophane species, some requiring further study to confirm their identity.[move this and the next paragraph to beginning of Discussion section] Reference to this undescribed species can be found dating back 44 years to Kimball’s (1965) book on the Lepidoptera of Florida. Under the heading Lithophane sp., Kimball (1965: 93) states that [John G.] Franclemont is describing it. Kimball listed six specimens from the Florida counties of Alachua, Escambia, Hillsborough, and Jefferson with collecting dates on three of the specimens from Lutz, Hillsborough Co., dating back 93 years. Th e oldest specimens of L. abita we were able to find were captured 98 years ago in 1911, also at Lutz, Florida.Published as part of Brou Jr., Vernon & Lafontaine, Donald, 2009, A new species of Lithophane Hbn. (Lepidoptera, Noctuidae, Xyleninae), pp. 11-20 in ZooKeys 9 (9) on pages 12-17, DOI: 10.3897/zookeys.9.158, http://zenodo.org/record/57644
Appropriate Similarity Measures for Author Cocitation Analysis
No full textWe provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis
"Closing the R&D Gap, Evaluating the Sources of R&D Spending"
No full textBoth spending and tax policies have been implemented in the United States with the goal of stimulating private sector research and development (R&D). Karier questions whether current R&D policy, especially the research and experimentation tax credit, can contribute to closing the gap between nondefense expenditures on R&D in the United States and such expenditures in other countries, such as Japan and Germany. He also explores possible changes to our current R&D policy to make it more effective.
Going Beyond Counting First Authors in Author Co-citation Analysis
No full textThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Letter from R. R. Zellick, Assistant Trust Officer, Anglo California National Bank of San Francisco, to Joseph R. Goodman, October 2, 1942
No full textLetter from R. R. Zellick, Assistant Trust Officer at The Anglo California National Bank of San Francisco, to Joseph R. Goodman, regarding property owned by Dave Tatsuno. Zellick mentions a dispute between current tenants and Tatsuno, and that Tatsuno has asked Goodman to help locate trustworthy tenants.Personal correspondence, organizational records, government documents, publications, and other papers created or collected by Joseph R. Goodman documenting the forced removal and incarceration of Japanese Americans during World War II, as well as organized resistance to incarceration. Included in the collection are records of the Japanese Young Men's Christian Association and the Japanese American Citizens' League in San Francisco, including papers of the Japanese YMCA's executive secretary Lincoln Kanai; Sakai family papers; Goodman's correspondence to and from Japanese American incarcerees, organizations opposing forced removal and incarceration of Japanese Americans, the War Relocation Authority, and others; publications, photographs, and ephemera from the Topaz Relocation Center, where Goodman taught high school; War Relocation Authority records and publications; and newspaper clippings, pamphlets, and reports about forced removal and incarceration created by various government, religious, and civic organizations, in California and nationwide
Dispelling the Myths Behind First-author Citation Counts
No full textWe conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued
use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation
counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more
sophisticated methods
Liftings for noncomplete probability spaces
No full textThe current state of knowledge concerning liftings for noncomplete probability spaces is discussed. This is a somewhat expanded version of the author's talk given at the 1991 Summer Conference on General Topology and Applications in Honor of Mary Ellen Rudin and Her Work.PT: S; CR: BURKE MR, IN PRESS P AM MATH S BURKE MR, 1991, ISRAEL J MATH, V73, P33 BURKE MR, 1992, ISRAEL J MATH, V79, P289 CARLSON T, THEOREM LIFTING CHRISTENSEN JPR, 1974, TOPOLOGY BOREL STRUC FREMLIN DH, 1989, HDB BOOLEAN ALGEBRAS, P877 INOESCUTULCEA A, 1966, 5TH P BERK S MATH ST, V2 IONESCUTULCEA A, 1967, CONTRIBUTIONS PROB 1, P63 IONESCUTULCEA A, 1969, TOPICS THEORY LIFTIN JECH TJ, 1978, SET THEORY JOHNSON RA, 1980, P AM MATH SOC, V80, P234 JUST W, IN PRESS T AM MATH S KUPKA J, 1983, INDIANA U MATH J, V32, P717 LOSERT V, 1983, LNM, V1080, P95 MAHARAM D, 1958, P AM MATH SOC, V9, P987 SHELAH S, 1983, ISRAEL J MATH, V45, P90 TALAGRAND M, 1982, P AM MATH SOC, V84, P379 VONNEUMANN J, 1931, CRELLES J MATH, V165, P109; NR: 18; TC: 0; J9: ANN N Y ACAD SCI; PG: 4; GA: BZ86BSource type: Electronic(1
Hansen, Lee (Lee R.). Union, non-union, and managerial pay plan state employees, 2008-2019
No full text1 online resource (2 pages)"July 1, 2021."Provides the number of union and non-union state employees in each of the last 14 years. Also provides the number of state employees paid under the state's managerial pay plan during each of those years. Updates OLR research report 2019-R-011
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