123,143 research outputs found
FIGURE 9. Nevrorthus reconditus Monserrat & Gavira n in A new European species of Nevrorthus in the Iberian Peninsula (Insecta, Neuropterida)
No full textFIGURE 9. Nevrorthus reconditus Monserrat & Gavira n. sp., general appearance of the larva.Published as part of Monserrat, V. J. & Gavira, O., 2014, A new European species of Nevrorthus in the Iberian Peninsula (Insecta, Neuropterida), pp. 349-360 in Zootaxa 3796 (2) on page 354, DOI: 10.11646/zootaxa.3796.2.7, http://zenodo.org/record/22557
Myrmeleon almohadarum Badano, Acevedo, Pantaleoni & Monserrat, 2016, sp. nov.
No full textMyrmeleon almohadarum sp. nov. Diagnosis. Small-sized Myrmeleon with a dark brown, variegated habitus (Figs 1, 2); pronotum with a diagnostic pattern (Fig. 3 B); wings hyaline with dark-and-pale dashed veins (Fig. 4 A); male hindwing with pilula axillaris; abdomen with conspicuous paler markings, creating an annulated pattern. Larva with an ochre habitus (Fig. 7), characterized by a particularly dense arrangement of digging setae on sternite IX (Fig. 8). Description of the adult. Size. Average body length 20.43 mm (min-max 16.03–26.82); forewing male length 21.56 mm (19.20–23.33), female length 23.05 mm (19.84–26.5), ratio width/length (both sexes) 0.23; hind wing male length 19.57 mm (16.35–21.42), female length 20.81 mm (17.77–25.55), ratio width/length (both sexes) 0.22. General colouring. Dark brown with large ochre markings on thorax and abdomen (Fig. 2). Head. Vertex and occiput dark brown, with a contrasting ochre pattern (Fig. 3 B). Frons dark brown with paler lateral margins. Ocular rim pale. Clypeus pale with fainted median marking. Labrum pale. Maxillary palpus brown. Labial palpus pale, with the distal segment fusiform and dark brown, palpimacula elliptical. Scape brown, paler distally, pedicellum dark brown, flagellum brown. (Fig. 3 A). Thorax. Pronotum brown, with anterior and lateral margins pale; dorsal side with a complex pattern composed by: a narrow median pale stripe, a pair of poorly defined pale spots in the apical half and a pair of usually well contrasted pale spots in the basal half (Fig. 3 B). Mesonotum and metanotum brown, lateral and ventral sclerite margins ochre, particularly evident on mesoscutum, mesoscutellum, metascutum and metascutellum (Fig. 2). Legs. Coxae brown in all legs (Fig. 2). Pro- and mesothoracic legs with extensive brown markings on the femur and tibia. Metathoracic leg with brown markings on the femur and the inner face of the tibia brown (Fig. 2). Tibial spurs as long as the first tarsomere. Wings. Relatively broad with a rounded apex (Fig. 4 A). Membrane hyaline. Pterostigma distinct, proximally brown and distally whitish. Venation predominantly dark brown with alternating pale dashes. Radius sector of forewing with on average 5–7 (less frequently 8) crossveins, thus the cells of Rs are few and elongated. Cubital fork of forewing slightly more basal than Media posterior fork. Hind wing with on average 5 presectoral crossveins. Male hind wing equipped with pilula axillaris (Fig. 4 A). Abdomen. Shorter than wings (Fig. 2). Tergites brown with large dorso-proximal ochre markings. Sternites brown with ventro-proximal pale markings. Interpleural membrane brown with paler markings. Ectoproct ochre. Male terminalia as in Fig. 5 A, B; male genitalia, complex of gonocoxites 9+11 sensu Aspöck & Aspöck 2008 (gonarcus-paramere complex) as in Fig. 6. Female terminalia as in Fig. 5 C, D. Variability. M. almohadarum sp. nov. is a relatively variable species in term of body pattern, like other congeners. Body colour varies from brown to dark brown but it is never pale ochre or blackish, like M. mariaemathildae and M. inconspicuus respectively. Some specimens are characterized by a partial fusion or fading of the pronotal pattern (e.g. specimen depicted in Fig. 2). The markings on the clypeus are also relatively variable. Description of the third instar larva. Size. Average body length 9.20 mm; head length 1.78 mm (min-max 1.67–1.87), head width 1.53 mm (1.47–1.57), mandible length 1.83 mm (1.75–1.87), ratio head width/length 0.86, ratio mandible length/head length 1.03. General colouring. Pale brown, with a dark brown pattern, ventral side of the body paler, with conspicuous dark markings (Fig. 7). Dorsal side of the head capsule with dark brown markings on the clypeo-labrum and a posterior V-shaped, fainted marking, lateral side with dark brown markings. Ventral side pale, with a pair of large dark brown spots (Fig. 7). Mandible pale brown. Some preserved Spanish larvae are characterized by the presence of a dark marking in the median section of the mandible. Legs pale brown, unspotted. Body chaetotaxy black. Head. Sub-rectangular, longer than wide. Ocular tubercle sessile. Mandible as long as the head capsule, provided with 3 equidistant teeth not abruptly differentiated in size. Interdental mandibular setae: (5)(2)(2)(1). External margin with a fringe of long setae, dorsal and ventral side almost hairless except a few short setae near the margin. Labial palpus 4-segmented. Abdomen. VIII abdominal sternite with small odontoid processes, posterior margin with stout setae. IX abdominal sternite with many ventral digging setae, unevenly arranged or irregularly aligned in rows, mostly sub-equal in size and interspersed with smaller ones (Fig. 8). Rastra sessile, each bearing 4 digging setae, of which the external pairs are longer (Fig. 8). Examined specimens. HOLOTYPE: Spain: Cádiz: Bolonia / 30 STE 59 / 10 m / ex larva 13.VII.2015 / F. Acevedo leg., 1 ♂ in alcohol [VM] (Fig. 1). PARATYPES. Spain: Almería: Las Casillas de Atochares, Rambla del Artal / 210 m / ex l. 20.VIII.2012 / F. Acevedo leg., 1 ♀ dry pinned [DB]; San Roque / 300 m / 2.IX.1993 / J. Ramírez leg., 1 ♀ dry pinned [VM]; Tabernas, Rambla Roja / 360 m / ex l. 16.VII.2012 / F. Acevedo leg., 1 ♂ dry pinned [DB]; Baleares: Ibiza, Las Salinas / 10 m / ex l. 3.VIII.2011 / V. J. Monserrat leg., 1 ♀ dry pinned [VM]; Cádiz: Barbate, Cerro del Pinar / 130 m / 20.VIII.1976 / V. J. Monserrat leg., 1♀ * dry pinned [VM]; Pinar de la Duquesa 26.VIII.77 E.L. / V. Monserrat 1♀ * [RAP]; Bolonia / 10 m / ex l. 13.VIII.2012 / F. Acevedo leg., 1♂ * dry pinned [VM]; Bolonia / 10 m / ex l. 25.VIII.2012 / F. Acevedo leg., 1 ♂ dry pinned [VM]; Bolonia / 10 m / ex l. 13.VII.2015 / F. Acevedo leg., 1♂ [VM]; Bolonia / 10 m / ex l. 13.VII.2015 / F. Acevedo leg., 1♂ [VM]; Bonanza / 18 m / ex l. 2.VII.2012 / F. Acevedo leg., 1 ♂ * dry pinned [DB]; Bonanza / 18 m / ex l. 3.VII.2012 / F. Acevedo leg., 1 ♂ * dry pinned [VM]; Bonanza / 18 m / ex l. 23.VII.2012 / F. Acevedo leg., 1 ♂ * dry pinned [VM]; Bonanza / 18 m / ex l. 13.VIII.2012 / F. Acevedo leg., 1 ♀ * dry pinned [DB]; Cádiz, Castillo de San Sebastián / 10 m / 10.VII.1976 / V. J. Monserrat leg., 1 ♂ * dry pinned [VM]; Caños de Meca / 10 m / ex l. 23.VII.2012 / F. Acevedo leg., 1 ♂ * dry pinned [VM]; Caños de Meca / 10 m / ex l. 4.VIII.2012 / F. Acevedo leg., 1 ♂ * dry pinned [VM]; Chiclana / 10 m /ex l. 13.VII.2012 / F. Acevedo leg., 1 ♂ * dry pinned [DB]; Playa de Los Lances / 10 m / ex l. 13.VIII.2012 / V. J. Monserrat leg., 1 ♂ * dry pinned [DB]; Playa Los Lances / 10 m / ex l. 27.VIII.2012 / V. J. Monserrat leg., 1 ♀ * dry pinned [DB]; Puerto Santa María, La Puntilla / 10 m / 29.VI.1976 / V. J. Monserrat leg., 1 ♂ * dry pinned [VM]; Venta del Retín/ 40 m / 5.VIII.1976 / I. Reviejo leg., 1 ♀ * dry pinned [DB]; Huelva: Punta Umbría / 10 m / ex l. 16.VII.2012 / F. Acevedo leg., 1 ♀ * dry pinned [VM]; Punta Umbría / 10 m / ex l. 4.VIII.2012 / F. Acevedo leg., 1 ♀ * dry pinned [VM]; Jaén: El Centenillo / 600 m / ex l. 6.VII.1986 / V. J. Monserrat leg., 1 ♂ [VM]; El Centenillo / 600 m / ex l. 10.VII.1986 / V. J. Monserrat leg., 1 ♂ [VM]; El Centenillo / 600 m / ex l. 10.VII.1986 / V. J. Monserrat leg., 1 ♀ [VM]; El Centenillo / 600 m / ex l. 11.VII.1986 / V. J. Monserrat leg., 1 ♀ [VM]; El Centenillo / 600 m / ex l. VIII.1986 / V. J. Monserrat leg., 1 ♀ [VM]; Málaga: Estepona, Sierra Bermeja, Rio Padrón / 140 m / 9.VII.2013 V. J. Monserrat leg., 1 ♂ dry pinned [DB]. Tunisia: Tunis, Gammarth / VII.2010 / INRGREF leg. / 1♀, ex larva, in alcohol [DB]; Tunis, Gammarth / VII.2010 / INRGREF leg. / 2♂, 2♀, ex larvae, in alcohol [RAP]; Forêt de Dar Chichou 36° 57,733N 10° 59,445E / VIII.2010 / INRGREF leg. 1♂, 4♀ ex larvae, in alcohol [RAP]; Al Sawasi (=Souassi) 35° 21,953N 10° 36,689E / VIII.2010 / INRGREF leg. 1♀ ex larva, in alcohol [RAP]; Tunis, Gammarth 36°55’10”N 10°17’38”E / 9.IV.2014 / R. A. Pantaleoni leg., 1 ♀, ex larva, dry pinned [DB]; Tunis, Gammarth 36°55’10”N 10°17’38”E / 9.IV.2014 / R. A. Pantaleoni leg. 1♂, 2♀, ex larvae, in alcohol [DB]; Tunis, Gammarth 36°55’10”N 10°17’38”E / 9.IV.2014 / R. A. Pantaleoni leg., 3♂, 2 ♀, ex larvae, in alcohol [RAP]. Larvae. Spain: Cádiz: Bolonia / 10 m / 24.V.2012 / F. Acevedo leg., 3 third instar larvae [VM]; Bolonia/ 10 m / 5.IV.2015 / F. Acevedo leg., 2 third instar larvae [VM]; Bonanza/ 18 m / 21.VI.2012 / F. Acevedo leg., 2 third instar larvae [VM]; Huelva: Punta Umbría / 10 m / 24.V.2012 / V. J. Monserrat leg., 3 third instar larvae [VM]; Málaga: Las Cañillas / 160 m / 25.V.2012 / F. Acevedo leg., 6 third instar larvae [VM]; Monda, Llanos de Purla / 370 m / 18.VIII.2013 / V. J. Monserrat leg., 2 third instar larvae [VM]. Tunisia: Tunis, Gammarth 36°55’10”N 10°17’38”E / 9.IV.2014 / R. A. Pantaleoni leg., 2 third instar larvae, in alcohol [DB]; Tunis, Gammarth 36°55’10”N 10°17’38”E / 9.IV.2014 / R. A. Pantaleoni leg.,over 20 larvae, in alcohol [RAP] Derivatio nominis. The name of this new species is a noun in the genitive case, referring to the Almohad dynasty, which dominated North Africa and the south of the Iberian Peninsula between the 12th and 13th centuries. DNA taxonomy and phylogeny. The six putative species of the genus Myrmeleon, included in the analysed data set, were all supported by Bayesian posterior probabilities of 1.0 (Fig. 10). The Bayesian Poisson tree process algorithm applied on the Bayesian consensus tree also supported the existence of six species, reinforcing the morphology-based assumptions. The status of M. almohadarum as a new species was confirmed by a posterior probability of 0.97, given the input phylogeny and the bPTP model. The Bayesian phylogenetic analysis reconstructed M. almohadarum as sister to M. inconspicuus with a posterior probability of 1.0 (Fig. 10). Ecological notes and distribution. In Tunisia, the pit-building larvae of M. almohadarum were collected in old coastal sand dunes with tree vegetation, including pine plantations. In Spain, besides the above mentioned environments, this species was also found in river banks and dry ephemeral riverbeds, suggesting that this antlion shares the same habitat preferences with M. inconspicuus (Nicoli Aldini 2007; Gepp 2010; Pantaleoni et al. 2010; Badano & Pantaleoni 2014) but it is more thermophilous. M. almohadarum is presently known from relatively few localities in Spain, mostly in the southernmost part of the Iberian Peninsula (Andalusia: Huelva, Jaén, Cádiz, Málaga and Almería). An isolated record from the Balearic Islands (Ibiza) is also known (Fig. 9). At least some of the numerous records of M. inconspicuus from the Iberian Peninsula (see list in Monserrat & Acevedo 2013), especially from its southernmost part and/or the Balearic Islands, very likely belong to the new species. In North Africa, this antlion was collected in Tunisia, but it is probably widespread along the south-western Mediterranean coast, in areas influenced by the Mediterranean climate and avoiding desert environments. Comparative notes. The Myrmeleon inconspicuus -group of species, firstly delimited by Pantaleoni et al. (2010), includes the Turano-European M. inconspicuus, the Mediterranean M. mariaemathildae and the Asiatic-E- European M. immanis Walker. These species differ from other Palaearctic congeners in a set of adult characters: forewing Cubital fork more basal than Media posterior fork (Fig. 4), male hind wing with pilula axillaris and male genitalia with a large, lamellar mediuncus (Fig. 6). Moreover, the larvae of this species-group are characterized by the IX abdominal sternite with the anterior row of digging setae composed by at least 6 bristles (Badano & Pantaleoni 2014). M. almohadarum also fits within this species group, based on adult and larval morphology and the DNA-based phylogenetic reconstruction. The new species and M. immanis are easily distinguished by the unmistakable habitus of the latter (i.e. blackish body colour and yellowish, hyaline wings with pointed apex). M. inconspicuus is also darker than M. almohadarum and it is characterized by a blackish pronotum with a thin median line and an isolated pale spot per side (Fig. 3 C). On the other hand, M. mariaemathildae is a highly variable species, with distinct pale and dark morphs, though most specimens are pale ochre. The pronotum of M. mariaemathildae is usually characterized by large pale markings and paired dark areas, with a large median, pale stripe connected with a pair of posterior spots (Fig. 3 D), though in very dark specimens the pronotum closely resembles that of M. inconspicuus, see Pantaleoni et al. (2010) for further details. M. almohadarum is best distinguished from these closely related species due to the overall brown habitus and the dark brown pronotum with two pale markings per side connected to a median stripe (but see Variability). The new species is usually characterized by the Radius sector of forewing with about 5–7 transversal crossveins, therefore the cells of the Rs are few and comparatively long (Fig. 4 A). In other species (including the other members of the M. inconspicuus group) the Rs crossveins are usually 10 or more, thus the cells appear more numerous but shorter (Fig. 4 B, C). M. almohadarum closely resembles the African species M. caliginosus Hölzel & Ohm. The most obvious difference, besides genitalia, between these species is represented by the presence of pilula axillaris on male hind wing, always lacking in M. caliginosus. Moreover, M. caliginosus is overall darker, with pronotal spots well separated and not connected by a median line. The larva of M. almohadarum is very similar in body pattern and relative proportions to those of M. inconspicuus and M. mariaemathildae (see Badano & Pantaleoni 2014). The larva of the new species is characterized by the IX sternite with the anterior row of digging setae comprising numerous and irregularly arranged bristles, mostly of similar size (Fig. 8). M. inconspicuus has a lower number of setae on the anterior row, while M. mariaemathildae is recognizable due to its combination of large setae disorderly interspersed with smaller ones (Badano & Pantaleoni 2014).Published as part of Badano, Davide, Acevedo, Fernando, Pantaleoni, Roberto A. & Monserrat, Víctor J., 2016, Myrmeleon almohadarum sp. nov., from Spain and North Africa, with description of the larva (Neuroptera Myrmeleontidae), pp. 210-220 in Zootaxa 4196 (2) on pages 212-218, DOI: 10.11646/zootaxa.4196.2.2, http://zenodo.org/record/16796
Período de auge y desmantelamiento de la Industria Militar argentina
No full textDocumento de trabajo N ̊17Fil: Monserrat, XimenaMonserrat, X. (2013). Período de auge y desmantelamiento de la Industria Militar argentina. Recuperado de: http://www.cefadigital.edu.ar/handle/1847939/151
Rosario's workers organizations and the State: conflicts and union practices. (1912-1930)
No full textFil: Monserrat, María Alejandra. Universidad Nacional de Rosario; Argentin
Joan Miralles i Monserrat, Corpus d'antropònims mallorquins del segle XIV, 1997
No full textBilly Pierre-Henri. Joan Miralles i Monserrat, Corpus d'antropònims mallorquins del segle XIV, 1997. In: Nouvelle revue d'onomastique, n°31-32, 1998. pp. 293-294
Chemoprotection of Amazonian Mauritia flexuosa fruit pulp against ammonia and nitrite toxicity to juvenile shrimps Litopenaeus vannamei: A hormetic response?
No full textThe effects of the inclusion (0-control group; 1.25; 2.50; 5.00; and 10.00% W/W) during 43 days of Amazonian Mauritia flexuosa fruit pulp in diets for feeding Litopenaeus vannamei postlarvae (PL) (weight: 5.0 ± 0.3 mg) were investigated. Measured response variables included growth performance, total carotenoid content, total antioxidant capacity (ACAP), and lipid peroxidation (TBARS). After 43 days juvenile shrimps were exposed for 96 h to ammonia (0.48 mg NH3-N L-1) and nitrite (40 mg NO3 L-1). and total antioxidant capacity (ACAP), and lipid peroxidation (TBARS), reduced glutathione and protein sulfhydryl group
Presentation of the "Identidades políticas y sindicales en la Argentina del siglo XX. Ciudadanía y cultura en contextos regionales" dossier
No full textFil: Martín, María Pía. Universidad Nacional de Rosario; ArgentinaFil: Monserrat, María Alejandra. Universidad Nacional de Rosario; Argentin
Javier Monserrat, Existencia, mundanidad, cristianismo. Introducción filosófico antropológica a la teología fundamental
No full textReix André. Javier Monserrat, Existencia, mundanidad, cristianismo. Introducción filosófico antropológica a la teología fundamental. In: Revue Philosophique de Louvain. Quatrième série, tome 74, n°24, 1976. pp. 675-676
Javier Monserrat, Existencia, mundanidad, cristianismo. Introducción filosófico antropológica a la teología fundamental
No full textReix André. Javier Monserrat, Existencia, mundanidad, cristianismo. Introducción filosófico antropológica a la teología fundamental. In: Revue Philosophique de Louvain. Quatrième série, tome 74, n°24, 1976. pp. 675-676
Hemerobiella oswaldi Monserrat 1998
No full text<i>Hemerobiella oswaldi</i> Monserrat, 1998 <p>(Figs. 4–7)</p> <p> <b>Remarks</b>. Monserrat (1998) described <i>H. oswaldi</i> with accuracy and provided figures of the male and female genitalia. Herein, some details and images of the species are added (Figs. 4–6), which are useful for identification of the species and comparison with <i>Hemerobiella periotoi</i> <b>sp</b>. <b>nov</b>.: Head: light brown, as high as wide; frons slightly raised medially, covered by sparse, light brown pilosity; maxillary and labial palpi light brown, unmarked; scape 1.6 times as high as wide; pronotum longer than wide (length/smaller width:1.6; length /larger width: 0.8); forewing ovoid, length 9.3 mm, 2.0 times as long as wide, costal area wide (0.3 times wing width), five outer and four inner gradates; hindwing: length 7.3 mm, 2.0 times as long as wide, four outer gradates.</p> <p> <b>Material examined</b>. <b>VENEZUELA</b>. <i>Amazonas state</i>: Parque Nacional Duida Marahuaka, Macizo Central, 30º40’ N / 65º28’ W, 1040 m, 8.iii.1985, 1♂, no collector data (MIZA); <i>Aragua state</i>: Parque Nacional Henri Pittier (formerly Rancho Grande), 1100 m, 4.xii.1967, 1♀, J. Salcedo Leg. (MIZA); Idem, 30.iv.1968, 1♀, F. FernándezYépez Leg.(MIZA), determined as <i>Hemerobiella</i> sp. by Oswald in 1992. <i>Yaracuy state</i>: Chivacoa County, La Cumbre, 10º16’N / 68º54’W, 1200 m, 1♂, 12.iv.2013, F. Sosa, F. Díaz & C. Martins Leg. (MJMO); Cocorote County, El Candelo, 10.36886º N / 68.82628º W, 1650 m, 20–27.iv.2001, 1♂, R. Briceño, A. Chacón, J. Clavijo, F. Díaz and F. Paz Leg. (MIZA), Project S1-2000000479.</p> <p> <b>Known geographical distribution</b>. Venezuela (Lara state) and Mexico (Chiapas) (Monserrat 1998).</p> <p> <b>New records</b>. Venezuela (Amazonas, Aragua and Yaracuy states) (Fig. 7).</p>Published as part of <i>Sosa, Francisco, Lara, Rogéria I. R. & Martins, Caleb C., 2015, A new species of Hemerobiella Kimmins (Neuroptera, Hemerobiidae) from Venezuela with notes on the genus, pp. 421-429 in Zootaxa 4028 (3)</i> on page 425, DOI: 10.11646/zootaxa.4028.3.7, <a href="http://zenodo.org/record/253672">http://zenodo.org/record/253672</a>
- …
