190,115 research outputs found
SALGADO, Adán R.
Correspondence between Mr. Adán R. Salgado and Gen. Alvaro Obregón, in which the former supports and congratulates Gen. Obregón on his election victory. File S-3. / Correspondencia entre el Sr. Adán R. Salgado y el Gral. Alvaro Obregón en la que el primero da su apoyo y felicita al Gral. Obregón por su triunfo electoral. Exp. S-
Factura, 1916 oct. 25, Madrid, de Salvador R. Salgado a D. Luis Olleros
Factura impresa en color azul, manuscrita en tinta negraAlcance y contenido: Versa sobre el arreglo de varias luces en el domicilio de la Calle Mayor, nº 41, así como la adquisición de un enchufe y seis lámparasEn el membrete: "Aparatos, Globos, Tulipas, Estufas, Ventiladores é Instalaciones eléctricas / Salvador R. Salgado / Luna, 6 / Madrid / Teléfono 2.602"Aparece el destinatario con dirección: "Mayor, nº 41"Recibí con firma impresa de S. R. SalgadoMembrete en azul formado por la actividad, el nombre y la dirección del establecimiento en la parte superior del documento en diferentes líneas y tipografía variada. En el lado izquierdo, publicidad enmarcada en una especie de pergaminoPapel en color crema con rayas por las dos caras, al verso sin cumplimentarEn laparte inferior derecha del membrete, datos de la gráfica: "J. Layunta, Araña, 24
SOTOMAYOR, Francisco L. y Estanislao R. SALGADO
Communique from Mr. Francisco L. Sotomayor, Mr. Estanislao R. Salgado, President and Secretary, respectively, from the Nationalist Board of Culiacán, Sinaloa, informing of the change of the Board of directors / Circular de los Srs. Francisco L. Sotomayor y Estanislao R. Salgado, Presidente y Secretario, respectivamente, de la Junta Nacionalista de Culiacán, Sin., informando del cambio de mesa directiva de la misma
SOTOMAYOR, Francisco L. y Estanislao R. SALGADO
Communique from Mr. Francisco L. Sotomayor, Mr. Estanislao R. Salgado, President and Secretary, respectively, from the Nationalist Board of Culiacán, Sinaloa, informing of the change of the Board of directors / Circular de los Srs. Francisco L. Sotomayor y Estanislao R. Salgado, Presidente y Secretario, respectivamente, de la Junta Nacionalista de Culiacán, Sin., informando del cambio de mesa directiva de la misma
Amphidraus draconicaudatus Salgado & Ruiz 2017
Amphidraus draconicaudatus Salgado & Ruiz, 2017 Figs 26 A–D, 26G, 27A–E, 28A, 29A–B, 30 Amphidraus draconicaudatus Salgado & Ruiz, 2017: 427, figs 22–24 (Holotype ♂ from Pium, 09°58'38.7"S, 50°02'05.0"W, Tocantins, Brazil, 11–26.V.2016, Serrão et al. leg., deposided in MPEG 32689; 1♂ and 2♀ paratypes, same data as holotype, deposited in IBSP 211843–211844, MPEG 32690); World Spider Catalog 2018. Additional material examined. BRAZIL: Tocantins: Caseara, 9°18'15.6"S, 49°57'28.4"W: 2♂, 11.V.2016, A.B. Bonaldo et al. leg. (MPEG 35018); Pium, 09°58'38.7"S, 50°02'05.0"W: 1♂, 19.V.2016, A.B. Bonaldo et al. leg. (MPEG 35019). Revised diagnosis. A. draconicaudatus is similar to A. shenlong sp. nov. by having an elongate and stout projection on the retrolateral border of the embolic disc that extends towards the retrolateral tegulum border and bears several branches (Figs 21D, 26A, 26C, 27A); also, by having the RvTA pointing ventrally, with projections on its border (Figs 21F, 22B, 26G). However, the male of A. draconicaudatus can be distinguished by having the RvTA with a single serrated projection, and a RTA reduced to spikes (Figs 26G, 27 B–D), whereas in A. shenlong sp. nov. the RvTA has four projections (three with acute tip and one with serrated tip), and the RTA serrated tip reaches the same height of the RvTA tip along palp axis (Figs 21F, 22B, 26H). The female of A. shenlong sp. nov. is unknown, but among the currently known females of Amphidraus, A. draconicaudatus sp. nov. is most similar to those of A. draconitupan sp. nov., both with spermathecae kidney-shaped, with glands near copulatory openings and with a narrow dorsal pocket placed posteriorly on epigynal plate (Figs 24D, 25D, 27E). However, the female of A. draconicaudatus sp. nov. can be distinguished from that of A. draconitupan sp. nov. by having longer copulatory ducts connected to the inner posterior border of spermathecae (see Salgado & Ruiz 2017: fig. 24F), whereas they connect to the outer border of the spermathecae in A. draconitupan (Fig. 25D). Description. See Salgado & Ruiz (2017). Variation. Among the males examined, we observed the following variation in palpal structures (Figs 26 A–D, 26G): the superior border of the branched projection of embolic disc can be smooth (Figs 26 A–B) or occupied by large serial spikes (similar to a comb) (Figs 26 C–D). We decided to refrain from describing this variation as a new species and all these forms are considered conspecific. Also, the number and shape of branches on the RvTA is variable (Fig. 26G; see Salgado & Ruiz 2017: figs 23B, 24B, 24D). Note. Amphidraus draconicaudatus, A. shenlong sp. nov. and A. draconitupan sp. nov. clearly compose a particular group within the genus. The males in this group have one stout projection that emerges from the retrolateral border of the embolic disc and extends towards to retrolateral border of tegulum (Figs 22A, 25A, 26A, 27A). Moreover, males also have pockets on outer faces of chelicerae (Figs 28 A–C, 29A–B), of unknown use. Distribution. Known only from the state of Tocantins (Brazil) (Fig. 30).Published as part of Salgado, Alexandre & Ruiz, Gustavo R. S., 2019, Seven new species of Amphidraus Simon, 1900 (Araneae: Salticidae: Euophryini), pp. 451-481 in Zootaxa 4563 (3) on pages 474-477, DOI: 10.11646/zootaxa.4563.3.3, http://zenodo.org/record/260134
Amphidraus caxiuanan Salgado & Ruiz 2017
Amphidraus caxiuanan Salgado & Ruiz, 2017 Figs 18 A–H, 19C–D, 19F–G, 20 Amphidraus caxiuanan Salgado & Ruiz, 2017: 408, figs 5A–B, 6A–D (Holotype ♂ from Melgaço, [01°42'24"S, 51°27'34.3"W], Pará, Brazil, 14.IV.2006, J.A.P. Barreiros leg., deposited in MPEG 29052); World Spider Catalog 2018. Additional material examined. BRAZIL: Pará: 1♂ from Floresta Estadual do Trombetas, Rio Acapu (along about 25 km on the North margin), [01°06'10.10"S, 56°26'04.00"W], Oriximiná, 10–18.X.2014, M.B. Aguiar-Neto et al. leg. (MPEG 35013). Revised diagnosis. Amphidraus caxiuanan Salgado & Ruiz, 2017 and A. manauara sp. nov. have the embolic disc with one long, prolaterally projected, distal process (dPED) with rounded tip, and one short, ventrally projected ventral process (vPED) (Figs 17A, 19C); also, the same pattern of tibial apophyses: the RvTA is short and rounded and the RTA emerges from retrodorsal portion of tibia, being curved and projected to the apex of palp (Figs 19 E–G); proximal dorso-prolateral portion of cymbium is prominent in both species, and there is a proximal retro-dorsal cavity on cymbium (Figs 17B, 19B, 19D). However, Amphidraus caxiuanan can be distinguished by having a longer proximal dorso-prolateral projection of cymbium (Figs 19B, 19D) and longer RTA (Figs 19 E–G). Moreover, the embolus shaft and the embolic filament are longer in proportion to the embolic disc in A. caxiuanan (Figs 19A, 19C). The female of A. caxiuanan is still unknown. Description. See Salgado & Ruiz (2017). Variation. Based on comparisons between the type specimen of A. caxiuanan from Melgaço, Pará, Brazil, and this new male from Oriximiná, Pará, Brazil (about 550 km from the type locality; Fig. 20), we observed several similarities, including in tibial apophyses and especially in the embolic disc, which made us refrain from describing a new species from Oriximiná. That male is herein recognized as being a variant form of A. caxiuanan. Hence, palpal variation within the species is summarized as follows (Figs 18 B–D, 18F–H, 19C–D, 19F–G): the RTA has a slight (Figs 18G, 19F) or accentuated curvature (Figs 18C, 19G); the dorso-prolateral, proximal cymbial projection varies in length (Figs 18D, 18H); RTA length is also variable (Figs 18 C–D, 18G–H, 19F–G). However, the proportions of these structures in the male from Oriximiná are intermediate when comparing the holotype of A. caxiuanan and the holotype of A. manauara (whose type locality is about 450 km away from Oriximiná; Fig. 20), which could indicate a cline across the Amazon River. Nevertheless, the embolic disc of the male palp of A. manauara is different enough to convince us to describe it as a new species (see diagnoses above). Distribution. Known only from the state of Pará, Brazil (Fig. 20). It is worth mentioning that, if the specimens from Oriximiná and Melgaço are indeed conspecific, this small species of jumping spider occurs in preserved forests on both margins of the old Amazon River, which is between two and eight kilometers wide in that portion of South America. This provides evidence for the high ability of dispersal present in this species.Published as part of Salgado, Alexandre & Ruiz, Gustavo R. S., 2019, Seven new species of Amphidraus Simon, 1900 (Araneae: Salticidae: Euophryini), pp. 451-481 in Zootaxa 4563 (3) on page 468, DOI: 10.11646/zootaxa.4563.3.3, http://zenodo.org/record/260134
Amphidraus araripe Salgado & Ruiz 2019, sp. nov.
Amphidraus araripe sp. nov. Figs 11–14 Type material. Holotype: Ƌ from Floresta Nacional do Araripe-Apodi, 7°18'39.6"S, 39°26'49.2"W, Crato, Ceará, Brazil, 06.II.2011, L.S. Carvalho et al. leg. (MPEG 35011); Paratypes: 1 Ƌ and 1♀ from Parque Nacional de Ubajara, Trilha da Samambaia, 3°50'19.4"S, 40°53'58.6"W, Ubajara, Ceará, Brazil, 14.V.2013, L.S. Carvalho et al. leg. (UFMG 14887). Etymology. The specific epithet is a noun in apposition taken from the locality of the holotype. Diagnosis. Among all species of Amphidraus, A. araripe sp. nov. is most similar to A. pulvinus Salgado & Ruiz, 2017 by having the tegulum with small retrolateral spermophore loop (RSPL) (Figs 11D, 13B; see Salgado & Ruiz 2017: fig. 8C) and the same tibial apophysis pattern: the retroventral tibial apophysis (RvTA) and intercalary tibial apophysis (ITA) are short and blade-shaped (the ITA with an internal basal projection; black arrow in Fig. 11E; see also Salgado & Ruiz 2017: fig. 8D) and the RTA is linked to an inflated membrane (Figs 11 E–G, 13B–C; see Salgado & Ruiz: figs 8B, 8D). These species also have an embolic disc with a distal process projected to prolateral side and a ventral process projected to retrolateral side (Figs 11C, 13A; see Salgado & Ruiz 2017: fig. 8C). However, A. araripe sp. nov. can be distinguished by having the RvTA and ITA more separated from each other (Figs 11F, 13B), whereas these are almost fused in A. pulvinus (see Salgado & Ruiz 2017: fig. 8D). In addition, A. araripe sp. nov. has a vPED placed near the distal processes (Figs 11C, 13A), whereas in A. pulvinus the vPED is placed on the prolateral border of embolic disc (see Salgado & Ruiz 2017: fig. 8C). The female of A. pulvinus is unknown, but among the Amphidraus species currently known, the epigyne of A. araripe sp. nov. is most similar to that of A. manaura sp. nov., both with glands near copulatory openings and with epigynal plate with border slightly bilobed (Figs 12C, 13D, 16D, 17D). However, the female of A. araripe sp. nov. differs by having a longer copulatory duct (with one loop ventrally projected) and by having the less expanded border of epigynal plate (Figs 13D, 17D). Description. Male holotype (MPEG 35011). Total length: 2.73. Carapace 1.32 long, 0.88 wide and 0.65 high. Ocular quadrangle 0.54 long. Anterior eye row 0.93 wide, posterior 0.81 wide. Legs 4312. Length of leg: I 2.09 (0.63 + 0.77 + 0.69); II 2.04 (0.62 + 0.70 + 0.72); III 2.50 (0.75 + 0.82 + 0.93); IV 2.78 (0.79 + 0.94 + 1.05). Palp (Figs 11 C–G, 13A–C): femur and patella without modifications; cymbium oval (Fig. 13C); tegulum with thick lobe curved to prolateral side (Figs 11C, 13A); embolus shaft (e) strongly arched to prolateral side, with tip retrolaterally projected (Fig. 13A); embolic filament (ef) short, with nearly half the length of embolus shaft (Fig. 13A). Color in alcohol (Figs 11 A–B): cephalic area black; thoracic area brown with pale longitudinal stripe; abdomen dorsally variegated with brown, and with a pale longitudinal stripe bearing white setae; ventrally pale with posterior portion dark; legs pale. Description. Female paratype (UFMG 14887). Total length: 2.95. Carapace 1.40 long, 0.97 wide and 0.67 high. Ocular quadrangle 0.68 long. Anterior eye row 1.02 wide, posterior 0.90 wide. Legs 4312. Length of leg: I 2.18 (0.71 + 0.82 + 0.65); II 2.06 (0.66 + 0.76 + 0.64); III 2.50 (0.79 + 0.86 + 0.85); IV 2.88 (0.81+ 0.99 + 1.08). Epigyne/vulva (Figs 12 C–D, 13D: copulatory openings separated by about two diameters of copulatory duct; spermathecae kidney-shaped; fertilization ducts anteriorly placed and laterally projected. Color in alcohol (Figs 12 A–B): cephalic area black; thoracic area dark brown with a longitudinal light brown stripe; abdomen dorsally black with longitudinal interrupted pale stripe; ventrally pale; femora pale with black spots; other leg segments light brown with black spots. Distribution. Known only from the type locality (state of Ceará, Brazil) (Fig. 14).Published as part of Salgado, Alexandre & Ruiz, Gustavo R. S., 2019, Seven new species of Amphidraus Simon, 1900 (Araneae: Salticidae: Euophryini), pp. 451-481 in Zootaxa 4563 (3) on pages 460-465, DOI: 10.11646/zootaxa.4563.3.3, http://zenodo.org/record/260134
Amphidraus draconitupan Salgado & Ruiz 2019, sp. nov.
<i>Amphidraus draconitupan</i> sp. nov. <p>Figs 23 A–G, 24A–D, 25A–D, 30</p> <p> <b>Type material. Holotype:</b> ♂ from Fazenda Palma, Varpa, 22°05'44.4"S, 50°30'07.9"W, Tupã, São Paulo, Brazil, XII.2016, G.R.S Ruiz leg. (MPEG 35022). <b>Paratypes:</b> 1♂ from Cachoeira Eubiose, 21°43'33.9"S, 44°57'36.0"W, São Thomé das Letras, Minas Gerais, Brazil, XII.2017, A. Salgado leg. (MPEG 35016) and 2♀, same data as holotype (MPEG 35017, 35028).</p> <p> <b> Additional material examined. BRAZIL: <i>Mato Grosso do Sul</i>:</b> 1♂, Brasilândia, Usina Hidrelétrica Sérgio Motta [21°16’22.7”S, 51°55’52.5”W], 2000, Equipe IBSP leg. (IBSP 30911); <b> <i>Minas Gerais</i>:</b> 1♀, São Thomé das Letras, Vale das Borboletas, 21°43'24.4"S, 45°00'24.4"W, XII.2017, A. Salgado leg. (MPEG 35023); 1♂ and 2♀ from São Thomé das Letras, Cachoeira Eubiose, 21°43'33.9"S, 44°57'36.0"W, XII.2017, A. Salgado leg. (MPEG 35024); <b> <i>São Paulo</i>:</b> 9♀, Tupã, Fazenda Palma, Varpa, 22°05'44.4"S, 50°30'07.9"W, XII.2016, G.R.S Ruiz leg. (MPEG 35029–35031).</p> <p> <b>Etymology.</b> The specific epithet is a compound name that refers to the large projection of embolic disc (homologous to projection with dragon's tail shape of <i>A. draconicaudatus</i>) and the type locality (Tupã). The final - n is added in order to mimic phonetics of the name of the locality.</p> <p> <b>Diagnosis.</b> The male of <i>Amphidraus draconitupan</i> <b>sp. nov.</b> is most similar to those of <i>A. draconicaudatus</i> Salgado & Ruiz, 2017 and <i>A. shenlong</i> <b>sp. nov.</b> by having an elongate and stout projection on the retrolateral border of the embolic disc that extends towards the retrolateral tegulum border (Figs 22A, 25A, 26A). However, the male of <i>A. draconitupan</i> <b>sp. nov.</b> differs from the males of these two species by having the superior border of its elongate projection of embolic disc with a rounded projection followed by several reduced spikes (Figs 23D, 25A), whereas in <i>A. draconicaudatus</i> and <i>A. shenlong</i> <b>sp. nov.</b> the rounded projection is absent and the elongate projections have several branches (Figs 26 A–F). The epigyne of <i>A. draconitupan</i> <b>sp. nov.</b> is similar to that of <i>A. draconicaudatus</i>, both with spermathecae kidney-shaped, with glands near to copulatory openings and with a narrow dorsal pocket placed posteriorly on epigynal plate (Figs 25D, 27E) (the female of <i>A. shenlong</i> <b>sp. nov.</b> is still unknown). However, the female of <i>A. draconitupan</i> <b>sp. nov</b>. can be distinguished from that of <i>A. draconicaudatus</i> by having shorter copulatory ducts connected to spermathecae on its outer border (Fig. 25D), whereas they connect to the inner posterior border in <i>A. draconicaudatus</i> (see Salgado & Ruiz 2017: fig. 24F).</p> <p> <b>Description. Male holotype (MPEG 35022).</b> Total length: 2.87. Carapace 1.79 long, 1.18 wide and 0.95 high. Ocular quadrangle 0.82 long. Anterior eye row 1.33 wide, posterior 1.14 wide. Legs 3412. Length of leg: I 2.93 (0.92 + 1.14 + 0.87); II 2.61 (0.86 + 0.93 + 0.82); III 3.42 (1.18 + 1.16 + 1.08); IV 3.39 (1.09 + 1.10 + 1.20). Chelicerae with pockets, as in <i>A. shenlong</i> <b>sp. nov.</b> (Fig. 28C). Palp (Figs 23 D–G, 25A–C): femur with medianproventral region prominent (Fig. 25B); RvTA ventrally projected with one single projection pointed to apex of palp (Figs 23G, 25C); cymbium oval; cymbial conductor leaf-shaped (Fig. 25A); tegular lobe dorsally curved (Fig. 23F); embolic disc with membranous prolateral portion, with two short distal processes (dPED) almost fused, and one triangular ventral process (vPED) distally placed (Figs 23D, 25A); straight embolus shaft, with its basal portion covered by the stout projection of embolic disc (Figs 23D, 25A); embolic filament with nearly half the length of embolus shaft (Fig. 25A). Color in alcohol (Figs 23 A–C): carapace black; abdomen black, dorsally variegated with brown; ventrally black; legs generally black; legs III and IV with pale metatarsi and tarsi.</p> <p> <b>Female paratype (MPEG 35028).</b> Total length: 3.07. Carapace 1.63 long, 1.08 wide and 0.75 high. Ocular quadrangle 0.87 long. Anterior eye row 1.17 wide, 1.00 posterior wide. Legs 4312. Length of leg: I 2.39 (0.79 + 0.88 + 0.72); II 2.32 (0.76 + 0.86 + 0.70); III 3.12 (1.04 + 1.10 + 0.98); IV 3.32 (0.98 + 1.11 + 1.23). Epigyne/vulva (Figs 24D, 25D): epigynal plate with lateral depressions. Color in alcohol (Fig. 24 A–B): cephalic area black; thoracic area dark brown; abdomen dorsally variegated with black and brown; ventrally pale; legs pale with black spots. Compare this with color of live specimen in Fig. 24C.</p> <p> <b>Distribution.</b> Known from the states of Mato Grosso do Sul, Minas Gerais and São Paulo (Brazil) (Fig. 30).</p> <p> <b>Natural History.</b> The specimens were collected in leaf-litter and tree trunk, close to waterfalls and lakes.</p>Published as part of <i>Salgado, Alexandre & Ruiz, Gustavo R. S., 2019, Seven new species of Amphidraus Simon, 1900 (Araneae: Salticidae: Euophryini), pp. 451-481 in Zootaxa 4563 (3)</i> on pages 472-474, DOI: 10.11646/zootaxa.4563.3.3, <a href="http://zenodo.org/record/2601342">http://zenodo.org/record/2601342</a>
Amphidraus cornipalpis Salgado & Ruiz 2019, sp. nov.
Amphidraus cornipalpis sp. nov. Figs 1–6, 14 Type material. Holotype: Ƌ from Parque Nacional da Serra das Confusões, [09°10'31.4"S, 43°33'20.8"W], Guaribas, Piauí, Brazil, 15.XII.10, L.S. Carvalho et al. leg. (MPEG 35014). Paratypes: 1 ♀, same data as holotype [MPEG 35015]; 1♂ and 1♀ from Caruaru, [08°17'08.6"S, 35°58'06.7"W], Pernambuco, Brazil, 2009–2010, H.P. Amorim leg. [IBSP 160615 (♂), 160616 (♀)]. Etymology. The specific epithet is a compound adjective in Latin (cornus + palpus) and refers to the shape of distal process on the embolic disc (Fig. 3A). Diagnosis. Males of Amphidraus cornipalpis sp. nov. share similarities with those of Amphidraus loxodontillus Salgado & Ruiz, 2017, both with an embolic disc with one poorly-sclerotized, distal lamella that covers part of dPED ventral view (white arrows in Figs 3 A–B). However, males of A. cornipalpis sp. nov. can be distinguished from those of A. loxodontillus by having a longer and acute distal process on embolic disc (dPED) with the tip curved distally (shaped like a cow horn) (Figs 2C, 3A, 5A, 5D, 6 D–E), whereas in A. loxodontillus the dPED is short and rounded (Fig. 3B; see also Salgado & Ruiz 2017: fig. 26C). In addition, A. cornipalpis sp. nov. has a reduced RTA (as large as RvTA in A. loxodontillus) and a small ITA in the male palp (Figs 5B, 5E), which is absent in A. loxodontillus (see Salgado & Ruiz 2017: figs 26B, 26D). Also, males of A. cornipalpis sp. nov. differ from those of all other species of Amphidraus by having a tubercle placed on proximal dorso-retrolateral portion of the cymbium (black arrows in Figs 2 C–F, 5A–B, 5E, 6C) (present also in Yacuitella nana Galiano, 1999). Females of A. cornipalpis sp. nov. are similar to those of Y. nana by the arrangement of copulatory ducts and spermathecae in the epigyne, but differ from that species by having more separate copulatory openings, longer copulatory ducts and no tubercle on the epigynal plate (Fig. 5F), which is medially placed in Y. nana (see Galiano 1999: figs 12–14). Description. Male holotype (MPEG 35014). Total length: 3.33. Carapace 1.78 long, 1.23 wide and 0.89 high. Ocular quadrangle 0.83 long. Anterior eye row 1.25 wide, posterior 1.13 wide. Legs 4312. Length of leg: I 2.65 (0.83 + 1.00 + 0.82); II 2.54 (0.81 + 0.93 + 0.80); III 3.12 (1.01 + 1.09 + 1.02); IV 3.40 (0.97 + 1.19 + 1.24). Palp (Figs 2 C–F, 3A, 5A–E, 6A–E): femur with large and low bump on median-ventral portion (Fig. 5C); patella with no modifications; tibia with a prolateral rounded expansion and a ventro-distal depression (Figs 2 D–F, 5A, 5E, 6A); large RvTA with acute tip (Figs 2D, 5B, 6C); short, poorly-sclerotized ITA retrolaterally projected (Figs 2F, 5E, 6C); cymbium oval (Figs 2F, 5E), with conductor (cc) wider than long with sinuous proximal border (Figs 2E, 6 A–B); tegulum with slender lobe curved to prolateral side (Figs 2C, 3A, 5A, 5D); embolus shaft (e) with tip strongly curved to retrolateral side (Figs 2C, 3A, 5A); embolic filament (ef) longer than embolus shaft (Figs 3A, 5A, 5D). Color in alcohol (Figs 1, 2 A–B): cephalic area black; thoracic area light brown with a black procurved arc; chelicera light brown; palp light brown, with black mark ventrally on femur and with dark brown cymbium; mouthparts and sternum light brown; abdomen dorsally and ventrally light brown variegated with dark brown; legs light brown with a distal black ring on metatarsi III and two black rings on metatarsi IV, one proximal and another distal. Female paratype (MPEG 35015). Total length: 3.77. Carapace 1.66 long, 1.15 wide and 0.81 high. Ocular quadrangle 0.80 long. Anterior eye row 1.13 wide, posterior 1.00 wide. Legs 4312. Length of leg: I 2.54 (0.83 + 1.00 + 0.71); II 2.25 (0.73 + 0.88 + 0.64); III 3.08 (1.05 + 1.05 + 0.98); IV 3.55 (1.08 + 1.23 + 1.24). Epigyne/vulva (Figs 4C, 5F): epigynal plate with posterior border slightly bilobed; copulatory openings separated by approximately two diameters of copulatory ducts; long and convoluted copulatory ducts, forming a pair of rounded masses with spermathecae; oval spermathecae diagonally projected; fertilization ducts anteriorly placed and laterally projected. Color in alcohol (Figs 4 A–B): cephalic area black; thoracic area dorso-laterally dark brown and centrally light brown; abdomen dorsally and laterally variegated with brown; ventrally pale; pale legs with black spots, being more intense on metatarsi III and IV (same pattern as in male). Distribution. Known from the states of Pernambuco and Piauí (Brazil) (Fig. 14).Published as part of Salgado, Alexandre & Ruiz, Gustavo R. S., 2019, Seven new species of Amphidraus Simon, 1900 (Araneae: Salticidae: Euophryini), pp. 451-481 in Zootaxa 4563 (3) on pages 452-453, DOI: 10.11646/zootaxa.4563.3.3, http://zenodo.org/record/260134
Entrenamiento en métodos de estudio de varroosis, evaluación del comportamiento higiénico, grooming en colonias de Apis mellifera en apiarios de Corrientes
La apicultura del Nordeste Argentino posee un desarrollo promisorio, debido en parte a las condiciones favorables de la región. Su clima subtropical favorece la disponibilidad de flores durante todo el año (Salgado & Pire, 1998; 1999, Salgado et al. 2014, 2017; Salgado 2016), generando que la trashumancia de las colmenas no sea un factor decisivo para el éxito comercial de la actividad como sucede en zonas de clima templado. Por otra parte, el predominio de la vegetación nativa ofrece amplia oferta de néctar y polen tanto en cantidad como en calidad. La riqueza y posibles formas de producción sustentable en la Ecorregión Chaco Húmedo han sido mencionada por Morello et al. (2012)
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