131,164 research outputs found
D. Jonckers, La Société minyanka du Mali
Lallemand SuzanneLallemand Suzanne. D. Jonckers, La Société minyanka du Mali. In: L'Homme, 1990, tome 30 n°114. pp. 154-155
Amberana noualhieri Lallemand 1920
Amberana noualhieri (Lallemand, 1920) (Figs 86–90) Literna noualhieri Lallemand, 1920: 283, transferred to Amberana by Lallemand, 1949: 71, 72. Male genitalia (Figs 89–90). Pygofer with posterior margin rounded on upper 2 / 3 part, clear protrusion stopping this curve basally, a small extension on dorsal margin anteriorly to anal tube. Pygofer height: 1.9 mm. Subgenital plates gently curved, reducing slowly in diameter to apex that is still thick. Aedeagus developed anteriorly in twopointed protrusions, the lower being bigger than the one above. Dorsal extensions long, posterior dorsal protrusion reaching beyond dorsal pygofer margin, apex bifid, anterior dorsal protrusion shorter and club shaped at apex. Lectotype designation. In the original description, Lallemand wrote: “ Types: ma collection et Muséum de Paris”, which leads to believe that Lallemand described this species from at least two specimens (syntypes), one (or several) in his collection (MRAC) and the other(s) in the MNHN. The only specimen from the MRAC is labelled as following: R. det. 6663 E; Literna noualhieri Lall. [hand written] det. V. Lallemand 192?; 3; type; coll. Mus. Congo, coll. V. Lallemand, Baie d’Antongil, Madagascar; holotypus. We believe that the label “ holotypus ” was pinned with the specimen posteriorly to the original description especially when an older label “ type ” was also pinned to the specimen. In 1949, Lallemand transferred Literna noualhieri to Amberana. This new combination is the only nomenclatural act written since the description of the species. Nothing in the literature justifies that the specimen from MRAC was recognised as holotype. In the MNHN collection, two specimens were found with the following labels: Muséum Paris, Madagascar, Baie d’Antongil, A. Mocquerys, coll. Noualhier 1898. The first specimen also bears a hand written label “ Dauphina noualhieri Lallem. Types ” by Lallemand. The locality, the epithet name of the species and the mention “ types ”, on the label, correspond to the original description, along with the fact that the specimens belong to the Noualhier’s collection to whom the species is dedicated. But, the genus name is incorrect and no Dauphina noualhieri has ever been described by Lallemand. We believe that Lallemand meant to write Literna and not Dauphina on his label. Lallemand (1920) described D. brunnea followed by L. noualhieri. When he wrote the label, for the specimens corresponding to the description of L. noualhieri, he probably merged the two species names of his article: D. brunnea and L. noualhieri. It is not the first time that spelling mistakes and/or the wrong genus name on Lallemand’s labels are observed, this error being linked to the vicinity of two names in the literature. According to these observations, we think that the nomenclatural status of these syntype specimens should be clarified. Here, we designate the specimen from the MRAC as lectotype and subsequently the two specimens cited above from the MNHN become paralectotypes. Material examined. Lectotype 3, Madagascar Baie d’Antongil, coll. V. Lallemand, R. det. 6663 E (MRAC). Paralectotypes 2 Ƥ Madagascar, Baie d’Antongil, A. Mocquerys, coll. Noualhier 1898, MNHN (EH) 4811 [original label hand written by Lallemand], MNHN (EH) 4812 (MNHN). Madagascar, Diego-Suarez, Ch Alluaud 1893, MNHN (EH) 4813, 1 Ƥ (MNHN. Madagascar, Sahanbava, Fianarantsoa, 1934 R. Catala, MNHN (EH) 4814, 1 Ƥ (MNHN). Madagascar, Fenerive, E. Perrot, Oberthür 101 – 96, MNHN (EH) 4815, 1 Ƥ (MNHN). Madagascar, Ile Sainte Marie, forêt de Kallao, III. 60 R. Andria, I. G. 23.285, 1 Ƥ; I. G. 22.889, 1 Ƥ; H. Synave det., I. G. 22.889, 13 (RIScNB).Published as part of Soulier-Perkins, Adeline & Kunz, Gernot, 2012, Revision of the malagassy endemic genus Amberana Distant (Hemiptera, Cercopidae) with description of one new genus, pp. 1-42 in Zootaxa 3156 (1) on pages 27-29, DOI: 10.11646/zootaxa.3156.1.1, http://zenodo.org/record/27963
S. Ardener, ed., avec les contributions de E. Ardener, S. A., J. Okely, H. Callan, D. Williams, C. Ifeka-Moller, Perceiving Women
Lallemand Suzanne. S. Ardener, ed., avec les contributions de E. Ardener, S. A., J. Okely, H. Callan, D. Williams, C. Ifeka-Moller, Perceiving Women. In: L'Homme, 1979, tome 19 n°3-4. Les catégories de sexe en anthropologie sociale. pp. 241-242
Orléans (Loiret)
Petit D., Lallemand V. Orléans (Loiret). In: Revue archéologique du Centre de la France, tome 28, fascicule 1, 1989. pp. 105-106
Zuata segui Lallemand
Zuata segui (Lallemand), description of male. Tomaspis segui Lallemand, 1924: 378. Diagnosis. Color of male (Fig. 13 C) similar to that of female type (Carvalho & Webb 2005, fig. 554) but tegmina darker than pronotum. Description. Male pygofer with low, rounded, setose lobes surrounding base of anal tube, posterior margin sloping towards narrow subgenital plates, with tapered tips hooked ventrad (as in Fig. 44 A), ventrally calipterate between prominent pygofer lobes (as in Fig. 45 D); styles (Carvalho & Webb 2005, fig. 10c) as in Z. bipunctata (Lallemand); theca robust, with dentate median ridge near tip on anterior surface, apical gonopore flanked by divergent angles (as in Fig. 45 C). Length: 7.5–7.8 mm, width across eyes 1.8–1.9 mm, across pronotum 2.3–2.5 mm; length of eye 0.6 mm, of side margins of pronotum 0.6 mm. Remarks. A female was taken with the only known male specimen at Paramo de Anango in May or June, 1949 by Wm. C. Macintyre (NCSU). The genitalia are similar to those of Z. tettigoniella (see below) but the color pattern of both sexes are entirely different. The female type, also from Ecuador, has paler tegmina than the male but the additional female has tegmina entirely dark behind the transverse pale band, showing that this is variable.Published as part of Andrew Hamilton, K. G., 2016, Neotropical spittlebugs related to Neaenini (Hemiptera, Cercopidae) and the origins of subfamily Cercopinae, pp. 201-250 in Zootaxa 4169 (2) on page 237, DOI: 10.11646/zootaxa.4169.2.1, http://zenodo.org/record/26258
Tomaspisinella Lallemand
Tomaspisinella Lallemand, redefined Tomaspisinella Lallemand, 1927: 117. Type-species by original designation: T. parva Lallemand, 1927. Hemitomaspis Lallemand, 1949: 31, syn.nov. Type-species by original designation: Tomaspis caligata Jacobi, 1908. Distribution. Neotropical, from Costa Rica south to Venezuela. Diagnosis. Superficially similar to Menytes (Fig. 14 A) but without sulcate face; color usually black to brown (except jocosa sp. nov.), body shorter, broader across the head, with convex tegmina (Fig. 35) and distinctive antenna (Figs 19 A–C) with postpedicel retracted into pedicel, as in Orthoraphini (Aphrophorinae) and basiconic sensillum elongate and setiform, as in Menytes and Simorhina (Neaenini) and Sphenorhina Amyot & Serville (Ischnorhinini). Description. Head distinctly to slightly narrower than pronotum (Carvalho & Webb 2005, figs 280–281); eyes varying from globose to transverse; crown short, weakly concave; antennal ledge arched above coronal margin; frons convexly inflated. Pronotum with anterior margin steeply declivous (Fig. 5 C), anterior border weakly to distinctly bowed; lateral margins as long as eyes to much shorter than half length of eyes, surface variable from medially carinate and transversely rugulose (Fig. 26) to smooth with scattered pits (Fig. 27) or densely setose (Fig. 35, Merinx subg. nov.), the nominate subgenus having fine setae (Fig. 5 C). Tegmina convex, shiny to hirsute; hind wing with 3 apical cells (Cu is unbranched; appendix large, even width around tip of wing. Fore femora distinctly longer than hind femora. Hind tibiae with 2 spines on outer edge, both long in smallest species, but basal one tiny in largest species; hind tibial pectin with 8–9 spines; hind basitarsal pecten of 6–7 black-tipped spines, that of second tarsomere with 8–9 such spines (hind legs missing from type of T. parva); arolia variable from much shorter than claws (in the type-species) as in Ischnorhinini, to longer than the claws (in Merinx subg. nov.). Male pygofer usually elongate and deeply notched dorsally on each side of anal tube (Figs 28–35 A) as in Menytes; subgenital plates absent or broad, fused to pygofer, nearly vertical, upper angles with decurved, pointed tips, sometimes with long, median processes (Fig. 34 D); styles unarmed or absent; phallobase short, sometimes fused to theca to form aedeagus; shaft unarmed or with paired, retrorse processes (Figs 28 C, 34–35C). Included species. The original description included Tomaspisinella caligata (Jacobi) T. parva Lallemand, T. minuscula (Jacobi) and 2 species now assigned to Zuata. Carvalho & Webb (2005) added T. apicifasciata (Fowler), known only from the female type, and these identities (except that of minuscula) have been confirmed by examination of the antennae. T. punctatissima (Stål: Lepyronia) comb.nov. and T. ignobilis (Fowler), comb.nov. were formerly placed in Hemitomaspis Lallemand and are here transferred to Tomaspisinella. These together with 6 new species increase the genus to 12 species. The typical subgenus appears to be paraphyletic with respect to 3 other apomorphic subgenera, with T. lucifer sp. nov. intermediate in pronotal characters and T. diabolos sp. nov. intermediate in genital characters.Published as part of Andrew Hamilton, K. G., 2016, Neotropical spittlebugs related to Neaenini (Hemiptera, Cercopidae) and the origins of subfamily Cercopinae, pp. 201-250 in Zootaxa 4169 (2) on pages 223-224, DOI: 10.11646/zootaxa.4169.2.1, http://zenodo.org/record/26258
Beesoniella Lallemand 1933
<i>Beesoniella</i> Lallemand, 1933:2. <p> Type-species by monotypy: <i>B. sylvestris</i> Lallemand, 1933.</p> <p> <b>Distribution.</b> Mountainous regions of India to southeast Asia. Only the type-species of the genus is widespread. It was described from two specimens collected from “the foliage of sandal[wood],” <i>Santalum album</i> L. (Lallemand 1933) in India. One male and three females of the same species have also been found in Laos and Vietnam (BPBM).</p> <p> <b>Diagnosis.</b> Form slender but hump-backed (Fig. 1 B); head narrower than pronotum, face receding, almost concealed beneath pronotum; tylus absent (Fig. 6 C); eyes transverse; ocelli set further apart than distance to eyes; antennal ledges high, thin and nearly flat before antennal pits, with 3 preantennal bristles in a vertical row on rim on pit; antennal postpedicel a truncate cone with single coeloconic sensillum set in deep pit and placoid sensillum surrounded by narrow, septate groove (Fig. 21D). Lateral margins of pronotum much shorter than eyes; pronotum arched, fore border steeply declivous, densely punctate. Tegmina flat, densely punctate, venation obscure. Hind wings each with 6–8 hooks on costal margin, 3 mounted on triangular process; first cell as large as in Cercopidae. Fore and hind femora of similar length; hind tibiae each armed with 2 large spines on basal half; hind basitarsi as long as other tarsomeres together; pectens of hind tibiae with 8 black-tipped spines, those of basitarsomere with 5 such spines, those of second tarsomere with 7 such spines. Male with subgenital plates obscure, forming low sinuation on posterior edge of pygofer; 2 pairs of pygofer processes (Fig. 12 A, E): a digittate median pair and a dorsoventrally flattened lateral pair with 1 or 2 acute angles posteriorly (Fig. 12–14 B). Theca very broad, flattened (Fig. 12 C–D), apex broadly notched, endotheca absent, 2 gonopores for gonoducts separating at base of theca (Fig. 12 D). Length: 5–7 mm.</p> <p> <b>Included taxa.</b> Three species, two of which are described below.</p>Published as part of <i>Andrew Hamilton, K. G., 2015, A new tribe and species of Clastopterinae (Hemiptera: Cercopoidea: Clastopteridae) from Africa, Asia and North America, pp. 151-189 in Zootaxa 3946 (2)</i> on page 165, DOI: 10.11646/zootaxa.3946.2.1, <a href="http://zenodo.org/record/233167">http://zenodo.org/record/233167</a>
Récits rustiques, historiques et légendaires de Haute-Marne / Yvon Lallemand
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Amberana limbata Lallemand 1955
Amberana limbata Lallemand, 1955 (Figs 63 –69) Amberana limbata Lallemand, 1955: 408. Male genitalia (Figs 66–68). Pygofer larger on its half upper part than its lower part, posteriorly and basally with a narrow prolongation on which subgenital plates are inserted. Pygofer height: 1.3 mm. Subgenital plates long with curved apex oriented dorsally slim, rounded and bearing a pad of short setae, total length greater than pygofer height (1.7 mm); the plates narrowing regularly from base to apex. Aedeagus developed anteriorly in a single pointed protrusion, with two dorsal extensions moderately extended, apex nearly reaching level of pygofer in dorsal margin; anterior dorsal extension with apex tomahawk shaped and posterior dorsal extension cogged. Parameres with a clear indentation on most posterior margin. Note. The black pattern on the tegmina can easily separate A. limbata from A. pygmaea Schmidt, 1920 (Figs 69, 110). Material examined. Holotype 3, Madagascar, Tananarive, Lamberton rec., coll. V. Lallemand R. Det. 6663 K (MRAC). Sandrangato, Institut Scientifique Madagascar, I. G. 21.002, 23, 2 Ƥ; I. G. 23.285, 1 ex. (RIScNB). Madagascar Sud-Est, forêt de Befotaka (Midongy du sud), 950m, 3–7 –III– 1959, P. Viette & P. Griveaud rec., I. G. 23.285, 1 ex. (RIScNB). Madagascar, Tananarive, coll. le Moult, I. G. 12.595, 1 ex. (RIScNB). Madagascar Tam., Perinet, 22 –IX– 58, F. Keiser rec., I. G. 23.285, 1 Ƥ (RIScNB). Madagascar, province Fianaransoa, Parc National Ranomafana, Radio tower at forest edge, 1130m, 4–12 March 2002, 21° 15 ’05’’S 47 ° 24 ’ 43 ’’E, collector R. Hanin’Hala, malaise, mixed tropical forest, MA–02–09B– 19, CASENT 8078982, 13; 19–26 Mach 2002, MA–02–09B– 21, CASENT 8078684, 1 Ƥ; national park Talatakely, 900m, 21,25 °S 47,42 °E, 9–19 January 2001, D. H. & K. M. Kavanaugh, R. L. Brett, E. Elson & F. Vargas collector, malaise trap, CASENT 3000589, 1 Ƥ (CAS). Madagascar, province Fianaransoa, Parc National Ranomafana, Vabharanana river, 4.1km 231 °SW Ranomafana, 1100m, 27–31 Mar 2003 21 ° 17 ’ 24 ’’S 47 ° 26 ’00’’E, Fisher, Griswold et al. Collector, yellow pan trap, montane rainforest, code BLF 8399, CASENT 3007945, 1 Ƥ (CAS). Madagascar 2006, rég. Haute Matsiatra, M. Attié rec., 11 –III– 2006, forêt humide de Ranomafana, 1681m, 21 ° 14.113 ’S, 47 ° 25.415 ’E, MNHN (EH) 4769, 1 Ƥ (MNHN). Madagascar Tam., Perinet, F. Keiser rec., 20 –IX– 58, 1Ƥ, 1 ex.; 23 –IX– 58, 1Ƥ (NHMB).Published as part of Soulier-Perkins, Adeline & Kunz, Gernot, 2012, Revision of the malagassy endemic genus Amberana Distant (Hemiptera, Cercopidae) with description of one new genus, pp. 1-42 in Zootaxa 3156 (1) on page 21, DOI: 10.11646/zootaxa.3156.1.1, http://zenodo.org/record/27963
MeSH term explosion and author rank improve expert recommendations
Information overload is an often-cited phenomenon that reduces the productivity, efficiency and efficacy of scientists. One challenge for scientists is to find appropriate collaborators in their research. The literature describes various solutions to the problem of expertise location, but most current approaches do not appear to be very suitable for expert recommendations in biomedical research. In this study, we present the development and initial evaluation of a vector space model-based algorithm to calculate researcher similarity using four inputs: 1) MeSH terms of publications; 2) MeSH terms and author rank; 3) exploded MeSH terms; and 4) exploded MeSH terms and author rank. We developed and evaluated the algorithm using a data set of 17,525 authors and their 22,542 papers. On average, our algorithms correctly predicted 2.5 of the top 5/10 coauthors of individual scientists. Exploded MeSH and author rank outperformed all other algorithms in accuracy, followed closely by MeSH and author rank. Our results show that the accuracy of MeSH term-based matching can be enhanced with other metadata such as author rank
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