46,535 research outputs found
Psychoda serraorobonensis Bravo, Cordeiro & Chagas
No full textPsychoda serraorobonensis Bravo, Cordeiro & Chagas (Figs 32–33) Psychoda serraorobonensis Bravo, Cordeiro & Chagas, 2006: 10. Type locality: Brazil (Bahia, Serra do Orobó). Diagnosis. Eyes separated by 1.5 –2.0 facet diameters; antenna with 14 flagellomeres, the 3 apical subequal, 11 th, 12 th and 13 th fused, 14 th flagellomere separated and spherical; ascoids in Y; median fork incomplete; female subgenital plate pilose on distal half and with lateral margins convex. Additional characters. hair patch of frons extending to facet row 1, almost reaching hair patch of vertex; eyes separated by 1.5 –2.0 facet diameters; 5–6 supra-ocular setae; interocular suture absent; clypeus with 2 or 3 stronger lateral alveoli; frontoclypeal suture absent; 11 th, 12 th and 13 th flagellomeres fused (only 11 th and 12 th on original description), spines present on 11 th and 13 th; palpal formula 1: 1.2 (1.1–1.3): 1.1 (1.1–1.3): 1.4 (1.3–1.5); labellum with 3 apical teeth, 1 subapical tooth and 2 lateral setae; distitarsus without apical projection (Fig. 32); female subgenital plate pilose on distal half, internally with a micropilose structure goblet shaped and a pair of lateral sclerotized lines just lateral to the digit (Fig. 33); genital chamber oval, with posterior apodeme. Male. Unknown. Material examined. Type material: holotype Ƥ BRAZIL, Bahia, Serra do Orobó, 29.xii. 2004, col. F. Bravo (MZUEFS). Others specimens: 2 Ƥ BRAZIL, Amazonas, Pitinga, Grota (c), 29.vi.1991, 12cdc/m, no collector name, (1 Ƥ INPA, 1 Ƥ MZUEFS); 1 Ƥ Amazonas, Silves, Saracá, área alterada, 17.xii.1997, 6 cdc - m, col. RF / FLS/LMC (INPA); 1 Ƥ Bahia, Senhor do Bonfim, Serra de Santana, 28.viii. 2006, col. R. Vieira & C. Chagas (MZUEFS); 1 Ƥ Bahia, Senhor do Bonfim, Serra de Santana, 29.viii. 2006, col. R. Vieira & C. Chagas (MZUEFS); 1 Ƥ Bahia, Cachoeira, Faz. Villa Rial, 13–27.vi. 2007, Malaise trap, col. E. Alvim & I. Castro (MZUEFS); 1 Ƥ BRAZIL, Paraná, Antonina, Res. Sapitanduva, 02.iii. 1987, Malaise trap, Profaupar 4.5 (DZUP). Distribution. Brazil (Amazonas, Bahia and Paraná). Comments. This species is morphologically similar to species of the subgenus Psycha, mainly in the number of flagellomeres and the type of fusion of the last flagellomeres, but different from Psycha by the globular format of the apical flagellomere, which in all species of Psycha is drop shaped. This is the first record of this species to Amazonas and Paraná.Published as part of Cordeiro, Danilo, Bravo, Freddy & De, Claudio J. B., 2011, Taxonomy of Brazilian Psychoda Latreille, 1796 (Diptera, Psychodidae) with the description of thirteen new species, pp. 1-37 in Zootaxa 3101 on pages 15-16, DOI: 10.5281/zenodo.20524
Philosepedon oblongolum Bravo, Chagas & Cordeiro, sp. nov.
No full textPhilosepedon oblongolum Bravo, Chagas & Cordeiro, sp. nov. (Figs. 1–9) Type material BRAZIL, Bahia, Porto Seguro (16 º 23 ’S 39 º 10 ’W), male holotype, 0 5.12. 2002, F. Bravo col. (MZUEFS). Bahia, Jussarí (Serra do Teimoso, 15 º09’S 39 º 31 ’W), 1 paratype male, 27.04. 2001, F. Bravo col. (MZUEFS). Etymology The species name oblongolum is from Latin, and refers to the long parameres. Description Male. Eye bridge with 4 facet rows (Fig. 1); eyes separated by 1.0 facet diameter (Fig. 1); interocular suture without median spur (Fig. 1). Palpus formula = 1.0: 1.5: 1.9: 2.4; first palpomere without pit with sensorial rods (Fig. 2). Antenna with 13 flagellomeres, flagellomeres nodiform (Figs. 3, 4), flagellomeres 11, 12, and 13 reduced, 11 and 12 broadly fused, 13 separate (Fig. 4); scape cylindrical, 1.2 X length of pedicel (Fig. 3); pedicel spherical (Fig. 3); ascoids Yshaped (Fig. 3). Labellum not flattened (Fig. 5). Wing with short Sc; radial fork apical to medial fork; radial fork complete and M 2 incomplete; base of C wider and little sclerotized; R 2 and M 3 with oval apical enlargement; CuA wide in basal 2 / 3 and thin in apical 1 / 3 (Fig. 6). Male terminalia (Figs. 7–9): Gonostyle with pointed apex 1.5 X length of gonocoxite. Epandrium rectangular with central aperture. Sternite 10 with triangular apex. Cercus with 2 apical tenacula with rounded tips. Parameres triangular, straight, with apex reaching end of aedeagus. Aedeagus symmetrical, with same length as aedeagal apodeme. Aedeagal apodeme uniformly thin. Female. Unknown. Distribution Brazil, Bahia, Porto Seguro, Serra do Teimoso. FIGURES 1–9. Philosepedon oblongolum Bravo, Chagas & Cordeiro, sp. nov., holotype male. 1. Head. 2. Palpus. 3. Base of antenna; scape and pedicel and basal flagellomeres. 4. Terminal lobe of labium. 5. Antenna; 9 th, 10 th, 11 th, 12 th, and 13 th flagellomeres. 6. Wing. 7. Male terminalia, dorsal. 8. Male terminalia, lateral. 9. Epandrium. Philosepedon uncinatum Bravo, Chagas & Cordeiro, sp. nov. (Figs. 10–19) Type material BRAZIL, Bahia, Santa Terezinha (Serra da Jibóia, 12 º 50 ’S 39 º 28 ’W), holotype male, 27.07. 2000, F. Bravo col. (MZUEFS); 1 paratype male, same locality, date and collector as holotype (MZUEFS); Bahia, Cachoeira (Fzda Villa Rial, 15 º09’S 39 º 32 ’S), 2 paratype males, 20.05. 2004, F. Bravo col. (MZUEFS) and 1 paratype male, 20.07. 2004, F. Bravo col. (MZUEFS); Bahia, Ituberá (13 º 42 ’S 39 º 11 ’W), 4 paratype males, 0 1.07. 2003, F. Bravo col. (MZUEFS). Etymology The species name uncinatum is from Latin, and refers to the curved parameres. Description Male. Eye bridge with 4 facet rows (Fig. 10); eyes separated by 1.0 facet diameter (Fig. 10); interocular suture with very short spur (Fig. 10) Palpus formula = 1.0: 1.7: 1.9: 2.6 (Fig. 9); first palpomere with pit with sensorial rods. Antenna with 13 flagellomeres, flagellomeres nodiform (Figs. 12, 13), flagellomeres 11, 12, and 13 reduced, 11 and 12 broadly fused, 13 separate (Fig. 13); scape cylindrical, 1.2 X length of pedicel (Fig. 12); pedicel spherical (Fig. 12); ascoids Yshaped (Fig. 12). Labellum not flattened (Fig. 14). Wing (Fig. 15) with short Sc; radial fork apical to medial fork; radial fork complete and M 2 incomplete; base of C wider and little sclerotized and other specimen with C evenly wide; R 2 and M 3 with oval apical enlargement, but R 2 can present, in some specimens, a smaller enlargement; CuA wide in basal 2 / 3 and thin in apical 1 / 3. Male terminalia (Figs. 16–19): gonostyle with pointed apex having same length as gonocoxite. Epandrium rectangular with central aperture. Sternite 10 wider distally. Cercus with 2 tenacula with rounded tips, 1 apical and the other subapical. Parameres triangular and curved, ½ length of aedeagus. Aedeagus symmetrical, same length as aedeagal apodeme. Aedeagal apodeme wider in posterior 2 / 3; anterior 1 / 3 very thin. Female. Unknown. Distribution Brazil, Bahia, Serra da Jibóia, Cachoeira, Ituberá. Comments The two new species of Philosepedon were collected in the wet forests of the Atlantic Coastal Rain Forest of Bahia in northeastern Brazil. These two new species from Brazil, with two tenacula on the cercus, are different from the two southern Brazilian species of Philosepedon (Ph. plaumanni and Ph. spathipenis), which have only one tenaculum on the cercus. Philosepedon uncinatum sp. nov. was collected at various localities in the Atlantic Rain Forest of Bahia, except from southern Bahia, while Ph. oblongolum sp. nov. was collected only from southern Bahia (Porto Seguro and Jussarí). The two new species are morphologically similar and are probably related. These new species can be distinguished from the other species of Philosepedon by the presence of 13 flagellomeres with the 11 th and 12 th fused, the oval apical enlargement of R 2 and M 3, an incomplete M 2, and two tenacula on the cercus. Likewise, Ph. uncinatum sp. nov. can be distinguished from Ph. oblongolum sp. nov. because the apices of the parameres of the former reach only to the middle of the aedeagus, whereas the apices of the parameres of Ph. oblongolum sp. nov. almost reach the apex of the aedeagus. No known species of Philosepedon has been described with this oval apical enlargement of the R 2 and M 3 veins; these characteristics could be a synapomorphy of these new Brazilian species. The New Guinea species Ph. torosa Quate & Quate and Ph. pectinata Quate & Quate have a similarly enlarged vein area, but this enlargement is near the center of R 2 + 3 and in the base of M 4. Only one previously described species of Philosepedon, Ph. aliciae IbáñezBernal & Cáceres, has a cercus with 2 tenacula and 13 flagellomeres, but it differs from the two new species from Brazil by the foliar arms of the ascoids, and by the separated flagellomeres 11 and 12. FIGURES 10–19. Philosepedon uncinatus Bravo, Chagas & Cordeiro, sp. nov., holotype male. 10. Head. 11. Palpus. 12. Base of antenna; scape and pedicel and basal flagellomeres. 13. Antenna; 10 th, 11 th, 12 th, and 13 th flagellomeres. 14. Terminal lobe of labium. 15. Wing. 16. Cercus, apex with two tenacula. 17. Male terminalia, dorsal. 18. Male terminalia, lateral. 19. Epandrium.Published as part of Bravo, Freddy, Chagas, Cinthia & Cordeiro, Danilo, 2006, Two new species of Philosepedon Eaton (Diptera: Psychodidae: Psychodinae) from the Atlantic Coastal Rain Forest of northeastern Brazil, pp. 63-68 in Zootaxa 1206 on pages 64-67, DOI: 10.5281/zenodo.17239
Erratum to: Effect of moderate red wine intake on cardiac prognosis after recent acute myocardial infarction of subjects with Type 2 diabetes mellitus (Diabetic Medicine, (2006), 23, 9, (974-981), 10.1111/j.1464-5491.2006.01886.x)
No full textIn an article by Marfella et al, the author name C. Saron is incorrect and should be listed as C. Sardu. Therefore the correct author list is: R. Marfella, F. Cacciapuoti, M. Siniscalchi, F. C. Sasso, F. Marchese, F. Cinone, E. Musacchio, M. A. Marfella, L. Ruggiero, G. Chiorazzo, D. Liberti, G. Chiorazzo, G. F. Nicoletti, C. Sardu, F. D'Andrea, C. Ammendola, M. Verza and L. Coppola.In an article by Marfella et al, the author name C. Saron is incorrect and should be listed as C. Sardu. Therefore the correct author list is: R. Marfella, F. Cacciapuoti, M. Siniscalchi, F. C. Sasso, F. Marchese, F. Cinone, E. Musacchio, M. A. Marfella, L. Ruggiero, G. Chiorazzo, D. Liberti, G. Chiorazzo, G. F. Nicoletti, C. Sardu, F. D'Andrea, C. Ammendola, M. Verza and L. Coppola
Alepia janjezeki Cordeiro & Bravo 2015, sp. nov.
No full textAlepia janjezeki Cordeiro & Bravo, sp. nov. (Figs 28–36) Type material. HOLOTYPE: ♁, BRAZIL: BAHIA: Piatã, Cachoeira do Patrício, light trap, 5.xi.2013, cols. Menezes E., Nascimento F., Carvalho J., Cordeiro D. & Bravo F. (MZFS). PARATYPE: 1 ♀, same place, data and collectors as holotype (MZFS). Diagnosis. Eyes widely separated; wing membrane with setae on base of costal cell; cercus conical, with dark area at base bearing 25 long clavate tenacula; pair of well sclerotized parameres lateral to aedeagus. Description. Head. Frons seta patch slightly divided (Figs 28 and 29); eye bridge short, eyes widely separated; no larger alveoli on area of supraocular setae and occipital setae (Figs 28–30); interocular suture present; clypeus wider than long; antenna with cylindrical scape 2× (male, Fig. 28) or 2.5× (female, Fig. 29) length of spherical pedicel, 14 flagellomeres with pair of digitiforme ascoids on the same side, apical flagellomere with apiculus around 0.4× length of whole flagellomere (Fig. 31); palpal formula 1.0: 2.1: 2.1: 2.3. Labellum bulbous, with short spines on inner margin and several lateral setae. Thorax (Fig. 32). Pre-sutural setae separated from supraalar setae; seta patch of anepisternum divided. Wing (Fig. 33). Wing membrane bare except on veins and base of cell C, with pattern of infuscation as illustrated; vein Sc short; R1 ending beyond level of CuA2; radial fork complete and basal to complete medial fork; base of M 2 weakened. Legs. Distitarsi with apical projection (Fig. 34). Male terminalia (Fig. 35). Hypandrium straight, separating gonocoxites; gonostylus spatulate with several small setae sparsely distributed throughout its length; gonocoxal apodemes large, expanding anteriorly and meeting at midline to form gonocoxal bridge; cercus conical, with dark area at base bearing 25 long clavate tenacula; aedeagus symmetric; aedeagal apodeme large; pair of well sclerotized parameres lateral to aedeagus; parameres have continuous apodemes at base, dorsally to aedeagus. Female terminalia (Fig. 36). Subgenital plate bilobed; ovipositor almost reaching 1.4 length of subgenital plate; genital chamber with expansion on lateral margin. Differential diagnosis. This species is morphologically close to Alepia copelata Quate, 1999, in the eyes widely separated, and the shape of aedeagal complex, with two large well sclerotized parameres, but they can be differentiated by the shape of gonostylus and the number of tenacula in the dark area at the base of cercus. Etymology. The species epithet is given in honor to Dr. Jan Ježek for his enormous contribution to the taxonomy of family Psychodidae. Distribution. Brazil (Bahia).Published as part of Cordeiro, Danilo, Bravo, Freddy & Chagas, Cínthia, 2015, Four new species of Psychodinae (Diptera: Psychodidae) from the Brazilian semiarid region, with contributions to supraspecific classification of Trichopsychodina and a redefinition of Feuerborniella, pp. 457-472 in Acta Entomologica Musei Nationalis Pragae 55 (2) on pages 469-470, DOI: 10.5281/zenodo.450387
Feuerborniella jezeki Cordeiro & Bravo 2015, sp. nov.
No full textFeuerborniella jezeki Cordeiro & Bravo, sp. nov. (Figs 7–13) Type material. HOLOTYPE: ♁, BRAZIL: BAHIA: Pindobaçú, 10°39 ′ S 40°21 ′ W, 26.ix. 2009, 500 m a.s.l., light trap, F. Bravo col. (MZFS). Diagnosis. Dorsal extension of frons seta patch not reaching eye bridge; scape of about same length of pedicel, flagellomeres 11–13 fused together; subapical enlargement on veins R2 and M3, infuscation on veins R5, CuA1 and basal half of CuA2; cerci short, not longer than epandrium, with two tenacula; gonocoxal bridge W-shaped. Description. Male. Head. Frons seta patch slightly divided basally but extending upwards in thin stripe, not reaching eye bridge (Fig. 7); eye bridge with 4 facet rows, separated by half facet diameter, vertex seta patch continuous laterally with setae of posterior margin of eye (Fig. 8); 8 supraocular setae, 1 larger occipital alveolus; interocular suture present with short dorsal extension; clypeus wider than long with lateral row of 4 larger alveoli; frontoclypeal suture present; antenna with cylindrical scape, about same length as subspherical pedicel, and apparently 14 flagellomeres (terminal flagellomere probably lost during preparation), 12 and 13 reduced, 11, 12 and 13 fused together (Fig. 9); ascoids Y-shaped; palpal formula 1.0: 1.8: 1.8: 1.9 (Fig. 10); labellum with 3 spines and 3 lateral setae. Thorax (Fig. 11). Presutural setae join supraalar setae; pteropleutite longer than wide, anterior margin around 1.5× shorter than posterior margin; long and complete transverse suture on upper margin of katepisternum. Wing membrane bare except on veins; second costal node absent; sc vein short; radial fork complete and apical to incomplete medial fork; subapical enlargement of vein M3; costal cell slightly darkened. Legs. Distitarsi with apical projection. Male terminalia. Epandrium subquadrate with concave posterior margin and one small foramen; hypandrium narrow, separating gonocoxites (Fig. 13); gonostylus about length of gonocoxite, with group of setae on external side of base of gonocoxite and several setae sparsely distributed throughout its length with one longer seta at apex; gonocoxal apodemes meet medially to form W-shaped gonocoxal bridge; cercus about same length as epandrium, with two apical tenacula and two subapical papillae (Fig. 12); epiproct not projecting posteriorly; hypoproct simple; aedeagus symmetrical, aedeagal apodeme simple and short, around 1/3 length of aedeagus; pair of conical parameres latero-ventral to aedeagus, with apex slightly pointing to outer side (Fig. 13); parameres are continuous with large stripe dorsal to aedeagus, forming aedeagal ‘ring’; parameres articulated basally with base of aedeagus and gonocoxal apodemes. Female. Unknown. Differential diagnosis. Wing is not illustrated as both wings are damaged on holotype, but the described characteristics can be seen on the parts of wings mounted on the slide. F. jezeki is very similar to F. opposita but it can be separated from it by the shape of aedeagus, which is spatulate in the new species and very narrow and rod-like on F. opposita. Etymology. The species epithet is given in honor of Dr. Jan Ježek for his enormous contribution to the taxonomy of the family Psychodidae. Distribution. Brazil (Bahia).Published as part of Cordeiro, Danilo, Bravo, Freddy & Chagas, Cínthia, 2015, Four new species of Psychodinae (Diptera: Psychodidae) from the Brazilian semiarid region, with contributions to supraspecific classification of Trichopsychodina and a redefinition of Feuerborniella, pp. 457-472 in Acta Entomologica Musei Nationalis Pragae 55 (2) on page 463, DOI: 10.5281/zenodo.450387
[Memo from Lieutenant Colonel M. F. Hass, Civil Affairs Division, with amendments to an evacuation proposal]
No full textA memorandum sent form Lieutenant General M. F. Hass, Civil Affairs Division, which has two corrections from a an evacuation proposal originally sent on May 13, 1942. The correction changes the destination to the Merced Assembly Center.The War Relocation Authority (WRA), together with the Wartime Civil Control Administration (WCCA), the Civil Affairs Division (CAD) and the Office of the Commanding General (OFG) of the Western Defense Command (WDC) operated together to segregate and house some 110,000 men women and children from 1942 to 1945. The collection contains documents and photographs relating to the establishment and administrative workings of the (WDC), the (WRA) and the (WCCA) for the year 1942
Feuerborniella pilosella Cordeiro & Bravo 2015, sp. nov.
No full textFeuerborniella pilosella Cordeiro & Bravo, sp. nov. (Figs 21–27) Type material. HOLOTYPE: ♁, BRAZIL: PARAÍBA: Areias, Brejo paraibano, 06°58 ′ S 39°44 ′ W, 567 m a.s.l., 25.–29. ix.2011, Nascimento, E. & Silva-Neto, A. Cols (MZFS). PARATYPES: 1 ♁, same data as holotype (MZFS); 1 ♀, BRAZIL: PARAÍBA: Santa Terezinha, Faz. dos Franceses, 07°00 ′ 57.2 ″ S 37°24 ′ 29.8 ″ W 258 m a.s.l., 6.v.2011, Lima & Brito cols. (MZFS). Diagnosis. Wing membrane pilose at veins and on midline between veins; hypoproct subquadrate posteriorly; pair of asymmetric conical parameres latero-ventral to aedeagus which are continuous basally with dorsal sheath to aedeagus. Description. Head. Frons seta patch extending in thin stripe between eyes, reaching second row of facets on eye bridge (Fig. 21); eye bridge with 4 facet rows, separated by half facet diameter, vertex seta patch weakly continuous laterally with setae of posterior margin of eye (Fig. 22); 6–8 supraocular setae, 3–4 (1–2 in female) larger occipital alveoli; interocular suture present; clypeus wider than long with lateral row of 3 larger alveoli; frontoclypeal suture present; antenna with cylindrical scape, slightly longer than subspherical pedicel, flagellomeres apical to 8 th lost during preparation; ascoids Y-shaped; palpal formula 1.0: 1.4: 1.6: 1.9 (Fig. 23); labellum with 2–3 spines and 6 lateral setae. Thorax (Fig. 24). Pre-sutural setae join supraalar setae; pteropleurite longer than wide, anterior margin shorter than posterior margin; long transverse suture on upper margin of katepisternum. Wing (Fig. 25). Wing membrane pilose at veins and on midline between veins; second costal node absent; sc vein short, not extending beyond line of base of veins Rs, M and CuA1; R1 ending beyond level of CuA2; radial fork complete and apical to incomplete medial fork. Legs. Distitarsi with apical projection. Male terminalia. Epandrium subquadrate with concave posterior margin (almost V-shaped) and one small foramen; hypandrium narrow, separating proximate gonocoxites (Fig. 27); gonostylus slightly longer than gonocoxite, with several setae sparsely distributed throughout its length; gonocoxal bridge bilobed anteriorly; cercus conical, long, almost 2× length of epandrium (Fig. 26), with one apical tenacula and three subapical papillae, epiproct triangular; hypoproct subquadrate posteriorly; aedeagus asymmetric, aedeagal apodeme simple, short, less than half length of aedeagus; pair of asymmetric conical parameres latero-ventral to aedeagus, one shorter and the other longer, with truncate apex; one dorsal shaft to aedeagus, connected to one paramere by membrane (Fig. 27); base of parameres continuous dorsally to aedeagus; parameres articulating baso-dorsally with aedeagus and baso-ventrally with gonocoxal apodemes. Female terminalia. Subgenital plate wider than long, bilobed posteriorly; ovipositor long, around 1.5 width of subgenital plate at base. Differential diagnosis. This species is similar to F. paramuna in the characteristic vestiture of the wing, asymmetric aedeagus, large subconical parameres and the presence of a dorsal shaft to aedeagus, but it can be differentiated from it by the asymmetrical parameres, and the subquadrate hypoproct. Etymology. The species epithet is derived from Greek pilos, in allusion to the pilose wing; adjective. Distribution. Brazil (Paraíba).Published as part of Cordeiro, Danilo, Bravo, Freddy & Chagas, Cínthia, 2015, Four new species of Psychodinae (Diptera: Psychodidae) from the Brazilian semiarid region, with contributions to supraspecific classification of Trichopsychodina and a redefinition of Feuerborniella, pp. 457-472 in Acta Entomologica Musei Nationalis Pragae 55 (2) on page 468, DOI: 10.5281/zenodo.450387
Corrigendum to “Presence and function of kisspeptin/KISS1R system in swine ovarian follicles” (Theriogenology (2018) 115 (1–8), (S0093691X1830147X), (10.1016/j.theriogenology.2018.04.006))
No full textThe authors regret the following changes to the author group G. Basinia, F. Grassellia, S. Bussolatia, R. Ciccimarraa, M. Maranesib, A. Bufalarib, C. Dall'Agliob, F. Parilloc,#, M. Zeranib,c,*. a Dipartimento di Scienze Mediche Veterinarie, Università di Parma, 43126 Parma, Italy. b Dipartimento di Medicina Veterinaria, Università di Perugia, 06126 Perugia Italy. c Scuola di Bioscienze e Medicina Veterinaria, Università di Camerino, 62024 Matelica Italy. # Deceased. * Corresponding author: tel.: +39 0755857642; fax +39 0755857654. E-mail address: [email protected] (M. Zerani). And to the acknowledgements and figures
[Memo from Lieutenant Colonel M. F. Hass, Civil Affairs Division, with amendments to an evacuation proposal]
No full textA memorandum sent form Lieutenant General M. F. Hass, Civil Affairs Division, which has two corrections from a an evacuation proposal originally sent on May 11, 1942. The first correction changes the number of evacuees to 275 people, and the second correction changes the destination to Tanforan Assembly Center.The War Relocation Authority (WRA), together with the Wartime Civil Control Administration (WCCA), the Civil Affairs Division (CAD) and the Office of the Commanding General (OFG) of the Western Defense Command (WDC) operated together to segregate and house some 110,000 men women and children from 1942 to 1945. The collection contains documents and photographs relating to the establishment and administrative workings of the (WDC), the (WRA) and the (WCCA) for the year 1942
[Memo from Lietnenant Colonel M. F. Hass, Civil Affairs Division, regarding the destination for Exclusion Order No. 98]
No full textA one page memo from Lieutenant Colonel M. F. Hass, Civil Affairs Division, that declares the destination for evacuees affected by Exclusion Order No. 98. The evacuees from all three movements were sent to the Portaln Assembly Center in Oregon.The War Relocation Authority (WRA), together with the Wartime Civil Control Administration (WCCA), the Civil Affairs Division (CAD) and the Office of the Commanding General (OFG) of the Western Defense Command (WDC) operated together to segregate and house some 110,000 men women and children from 1942 to 1945. The collection contains documents and photographs relating to the establishment and administrative workings of the (WDC), the (WRA) and the (WCCA) for the year 1942
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