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1.
Genome ; 55(3): 194-204, 2012 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-22360780

RESUMEN

The nearly complete mitochondrial (mt) genome of an egg parasitoid, Trissolcus basalis (Wollaston), was sequenced using both 454 and Illumina next-generation sequencing technologies. A portion of the noncoding region remained unsequenced, possibly owing to the presence of repeats. The sequenced portion of the genome is 15,768 bp and has a high A+T content (84.2%), as is typical for hymenopteran mt genomes. A total of 36 of the 37 genes normally present in animal mt genomes were located. The one exception was trnR; a truncated version of this gene is present between trnS(1) and nd5, but it is unclear whether this gene fragment could code for the entire trnR gene. The mt gene arrangement of T. basalis is different from other Proctotrupomorpha mt genomes, with a number of trn genes in different positions. However, no shared derived gene rearrangements were identified in the present study. Bayesian analyses of mt genomes from 29 hymenopteran taxa and seven other orders of holometabolous insects support some uncontroversial evolutionary relationships, but indicate that much higher levels of taxonomic sampling are necessary for the resolution of family and superfamily relationships.


Asunto(s)
Genoma Mitocondrial/genética , Filogenia , Avispas/genética , Secuencia de Aminoácidos , Animales , Composición de Base , Secuencia de Bases , Teorema de Bayes , Codón/genética , Modelos Genéticos , Datos de Secuencia Molecular , Alineación de Secuencia , Análisis de Secuencia de ADN
2.
Zookeys ; (778): 1-95, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30104914

RESUMEN

The genus Chromoteleia Ashmead is revised. Twenty-seven species are recognized, of which six species are redescribed: C.congoana (Risbec), C.connectens Kieffer, C.fuscicornis Kieffer, C.longitarsis Kieffer, C.semicyanea Ashmead, C.tricarinata Kieffer; and twenty-one species are described as new: C.aequalis Chen & Johnson, sp. n., C.alternata Chen & Johnson, sp. n., C.bidens Chen & Masner, sp. n., C.copiosa Chen & Johnson, sp. n., C.cuneus Chen & Johnson, sp. n., C.curta Chen & Johnson, sp. n., C.depilis Chen & Johnson, sp. n., C.dispar Chen & Masner, sp. n., C.feng Chen & Johnson, sp. n., C.fossa Chen & Johnson, sp. n., C.ingens Chen & Masner, sp. n., C.levitas Chen & Johnson, sp. n., C.longa Chen & Johnson, sp. n., C.maura Chen & Masner, sp. n., C.parvitas Chen & Johnson, sp. n., C.pilus Chen & Johnson, sp. n., C.plana Chen & Johnson, sp. n., C.rara Chen & Johnson, sp. n., C.robusta Chen & Johnson, sp. n., C.semilutea Chen & Johnson, sp. n., C.sparsa Chen & Johnson, sp. n.Chromoteleiarufithorax Kieffer remains a valid species, but its identity and status are unclear. All species are known only from the Neotropical region except for Chromoteleiacongoana (Resbec) which only occurs in Africa.

3.
Zootaxa ; 4137(3): 425-31, 2016 Jul 12.
Artículo en Inglés | MEDLINE | ID: mdl-27470734

RESUMEN

A new species, Evaniodes costatus Valerio sp. nov., belonging to the tribe Evanoidini is described and illustrated. The new species is compared with the five species currently known to occur in the genus Evaniodes Szépligeti.


Asunto(s)
Avispas/anatomía & histología , Avispas/clasificación , Animales , Brasil , Femenino , Especificidad de la Especie
4.
Rev Biol Trop ; 53(1-2): 63-71, 2005.
Artículo en Español | MEDLINE | ID: mdl-17354420

RESUMEN

We indirectly evaluated the selective pressures on dispersal and establishment of Campsiandra angustifolia, a common water-dispersed tree from the Peruvian Amazon, analyzing the variation in the relationship between the volume occupied by dispersal and establishment structures in a total of 535 seeds from 13 trees located at three different habitats. The seeds differed one order of magnitude in their total volume. However, independently of their size and the location of the maternal tree, the relationship between the volume occupied by dispersal and establishment structures was relatively constant (approximately 1) and showed a normal distribution with low skewness, indicating stabilizing selection. These results suggest that, in the habitats studied, dispersal and establishment processes may have similar importance to C. agustifolia. In species with seeds confined in pods, and therefore strongly space-limited, the relative volume of their seeds occupied by dispersal and establishment structures could be a better measure of the trade-off between these two processes than the variation in seed size.


Asunto(s)
Ecosistema , Fabaceae/fisiología , Germinación/fisiología , Semillas/fisiología , Selección Genética , Tamaño Corporal/fisiología , Cotiledón/fisiología , Desastres , Fabaceae/anatomía & histología , Relámpago , Perú , Estaciones del Año , Plantones/fisiología , Semillas/anatomía & histología
5.
Zootaxa ; 3904(4): 501-40, 2015 Jan 08.
Artículo en Inglés | MEDLINE | ID: mdl-25660797

RESUMEN

Thirteen new species belonging to the genus Triraphis Ruthe are described and illustrated: Triraphis baios sp. nov., T. balteus sp. nov., T. chinusi sp. nov., T. cortazari sp. nov., T. defectus sp. nov., T. guarusa sp. nov., T. huidobroi sp. nov., T. ikelosops sp. nov., T. melasops sp. nov., T. paraholos sp. nov., T. proxilus sp. nov., T. simphlex sp. nov. and T. willei sp. nov. The lepidopteran hosts were feeding on 17 genera of plants within 16 families. Two families of Lepidoptera are reported as new hosts for Triraphis: Acraga sp. (Dalceridae) parasitized by T. paraholos sp. nov. and Norape sp. (Megalopygidae) by T. guarusa sp. nov. Moreover, four Triraphis species are treated as new combinations under the genus Triraphis sensu van Achterberg: Triraphis areatus (Cresson) comb. n., T. fasciipennis (Cresson) comb. n., T. fusciceps (Cresson) comb. n. and T. ornatus (Cresson) comb. n.. 


Asunto(s)
Avispas/anatomía & histología , Avispas/clasificación , Animales , Costa Rica , Femenino , Masculino
6.
Rev Biol Trop ; 52(3): 665-77, 2004 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-17361560

RESUMEN

The current taxonomic status of the species and subspecies belonging to the genus Alouatta is addressed by combined phylogenetic analysis using morphological, kariotipyc and molecular data (mitochondrial genes cytocrome oxidase II and cytochrome B). Our result demonstrated that Alouatta palliata is the most basal taxon for the genus in concordance with previous studies, as well as showing the validity of the taxon Alouatta sara as a species. Also our analysis shows that the sex chromosome has evolved from a XY/XX system to a X1X2Y1Y2/X1X1X2X2 system within the genus, as well as an increase in the size and complexity of the hioideal bone.


Asunto(s)
Alouatta/genética , ADN Mitocondrial/genética , Filogenia , Cromosomas Sexuales/genética , Alouatta/anatomía & histología , Alouatta/clasificación , Animales , Grupo Citocromo b/genética , Complejo IV de Transporte de Electrones/genética , Evolución Molecular , Cariotipificación , Alineación de Secuencia
7.
Zookeys ; (380): 1-188, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24624012

RESUMEN

The genus Scelio is a cosmopolitan and speciose group of solitary parasitoids of the eggs of short-horned grasshoppers (Orthoptera: Acrididae). A number of these hosts are important pests, including plague locusts of the genus Schistocerca. Species of Scelio are recognized as potentially important biological control agents, but this possibility has yet to be fully realized, in part because the species-level taxonomy is still incompletely developed. The species of the pulchripennis group have been recently revised. As a continuation of this effort, here we revise the Afrotropical species of Scelio, excluding the pulchripennis species group. Sixty two (62) species are treated, 48 of which are new. Species are classified into the following species groups: ernstii (12 species, 9 new), howardi (23 species, 19 new), ipomeae (6 species, 5 new), irwini (4 species, 3 new), simoni (3 new species) and walkeri (12 species, 9 new). Keys to species groups and to the species within each group are provided. New species described are: S. albatus Yoder, sp. n., S. aphares Yoder, sp. n., S. apospastos Yoder, sp. n., S. ardelio Yoder, sp. n., S. aurantium Yoder, sp. n., S. balo Valerio & Yoder, sp. n., S. bayanga Yoder, sp. n., S. bubulo Yoder, sp. n., S. cano Yoder, sp. n., S. clypeatus Yoder, sp. n., S. concavus Yoder, sp. n., S. copelandi Yoder, sp. n., S. crepo Yoder, sp. n., S. destico Yoder, sp. n., S. dupondi Yoder, sp. n., S. effervesco Yoder, sp. n., S. erugatus Yoder, sp. n., S. exophthalmus Yoder, sp. n., S. fremo Valerio & Yoder, sp. n., S. gemo Yoder, sp. n., S. grunnio Yoder, sp. n., S. harinhalai Yoder, sp. n., S. igland Yoder, sp. n., S. impostor Yoder, sp. n., S. irwini Yoder, sp. n., S. janseni Yoder, sp. n., S. latro Yoder, sp. n., S. memorabilis Yoder, sp. n., S. modulus Yoder, sp. n., S. mutio Yoder, sp. n., S. ntchisii Yoder, sp. n., S. parkeri Yoder, sp. n., S. phaeoprora Yoder, sp. n., S. pilosilatus Yoder, sp. n., S. pipilo Yoder, sp. n., S. quasiclypeatus Yoder, sp. n., S. retifrons Yoder, sp. n., S. ructo Yoder, sp. n., S. scomma Yoder, sp. n., S. simoni Yoder, sp. n., S. simonolus Yoder, sp. n., S. somaliensis Yoder, sp. n., S. susurro Yoder, sp. n., S. tono Yoder, sp. n., S. transtrum Yoder, sp. n., S. tritus Yoder, sp. n., S. ululo Yoder, sp. n., S. vannoorti Valerio & Yoder, sp. n. The following species are redescribed: S. afer Kieffer, S. chapmani Nixon, S. howardi Crawford, S. ipomeae Risbec, stat. n., S. mauritanicus Risbec, S. philippinensis Ashmead, S. remaudierei Ferrière, S. striatus Priesner,S. taylori Nixon, and S. zolotarevskyi Ferrière. The genus Lepidoscelio Kieffer is treated as a junior synonym of Scelio Latreille, syn. n.; its type species, Lepidoscelio fuscipennis Kieffer, 1905 is transferred to Scelio, renamed Scelio obscuripennis Johnson, nom. n. (preoccupied by Scelio fuscipennis Ashmead, 1887), and redescribed. The following additional species are transferred from Lepidoscelio to Scelio: S. cayennensis (Risbec), comb. n., S. insularis Ashmead, rev. comb., S. luteus (Cameron), comb. n., S. thoracicus Ashmead, rev. comb. Lectotypes are designated for S. africanus Risbec, S. ipomeae Risbec, S. mauritanicus Risbec, S. remaudierei Ferrière, S. sudanensis Ferrière, and S. zolotarevskyi Ferrière. Scelio gaudens Nixon is a junior synonym of Scelio striatus Priesner, syn. n.; Scelio africanus Risbec and Scelio clarus Fouts are both junior synonyms of Scelio afer Kieffer, syn. n.; Scelio sudanensis Ferrière and Scelio cheops Nixon are both junior synonyms of Scelio zolotarevskyi Ferrière, syn. n.; Scelio cahirensis Priesner is a junior synonym of Scelio mauritanicus Risbec, syn. n. The name Scelio chapmanni Nixon is an incorrect original spelling, requiring an emendation to S. chapmani. Digital versions of the identification keys are available at http://www.waspweb.org/Platygastroidea/Keys/index.htm.

8.
Zookeys ; (314): 1-151, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23878506

RESUMEN

The genera Odontacolus Kieffer and Cyphacolus Priesner are among the most distinctive platygastroid wasps because of their laterally compressed metasomal horn; however, their generic status has remained unclear. We present a morphological phylogenetic analysis comprising all 38 Old World and four Neotropical Odontacolus species and 13 Cyphacolus species, which demonstrates that the latter is monophyletic but nested within a somewhat poorly resolved Odontacolus. Based on these results Cyphacolus syn. n. is placed as a junior synonym of Odontacolus which is here redefined. The taxonomy of Old World Odontacolus s.str. is revised; the previously known species Odontacolus longiceps Kieffer (Seychelles), Odontacolus markadicus Veenakumari (India), Odontacolus spinosus (Dodd) (Australia) and Odontacolus hackeri (Dodd) (Australia) are re-described, and 32 new species are described: Odontacolus africanus Valerio & Austin sp. n. (Congo, Guinea, Kenya, Madagascar, Mozambique, South Africa, Uganda, Zimbabwe), Odontacolus aldrovandii Valerio & Austin sp. n. (Nepal), Odontacolus anningae Valerio & Austin sp. n. (Cameroon), Odontacolus australiensis Valerio & Austin sp. n. (Australia), Odontacolus baeri Valerio & Austin sp. n. (Australia), Odontacolus berryae Valerio & Austin sp. n. (Australia, New Zealand, Norfolk Island), Odontacolus bosei Valerio & Austin sp. n. (India, Malaysia, Sri Lanka), Odontacolus cardaleae Valerio & Austin sp. n. (Australia), Odontacolus darwini Valerio & Austin sp. n. (Thailand), Odontacolus dayi Valerio & Austin sp. n. (Indonesia), Odontacolus gallowayi Valerio & Austin sp. n. (Australia), Odontacolus gentingensis Valerio & Austin sp. n. (Malaysia), Odontacolus guineensis Valerio & Austin sp. n. (Guinea), Odontacolus harveyi Valerio & Austin sp. n. (Australia), Odontacolus heratyi Valerio & Austin sp. n. (Fiji), Odontacolus heydoni Valerio & Austin sp. n. (Malaysia, Thailand), Odontacolus irwini Valerio & Austin sp. n. (Fiji), Odontacolus jacksonae Valerio & Austin sp. n. (Cameroon, Guinea, Madagascar), Odontacolus kiau Valerio & Austin sp. n. (Papua New Guinea), Odontacolus lamarcki Valerio & Austin sp. n. (Thailand), Odontacolus madagascarensis Valerio & Austin sp. n. (Madagascar), Odontacolus mayri Valerio & Austin sp. n. (Indonesia, Thailand), Odontacolus mot Valerio & Austin sp. n. (India), Odontacolus noyesi Valerio & Austin sp. n. (India, Indonesia), Odontacolus pintoi Valerio & Austin sp. n. (Australia, New Zealand, Norfolk Island), Odontacolus schlingeri Valerio & Austin sp. n. (Fiji), Odontacolus sharkeyi Valerio & Austin sp. n. (Thailand), Odontacolus veroae Valerio & Austin sp. n. (Fiji), Odontacolus wallacei Valerio & Austin sp. n. (Australia, Indonesia, Malawi, Papua New Guinea), Odontacolus whitfieldi Valerio & Austin sp. n. (China, India, Indonesia, Sulawesi, Malaysia, Thailand, Vietnam), Odontacolus zborowskii Valerio & Austin sp. n. (Australia), and Odontacolus zimi Valerio & Austin sp. n. (Madagascar). In addition, all species of Cyphacolus are here transferred to Odontacolus: Odontacolus asheri (Valerio, Masner & Austin) comb. n. (Sri Lanka), Odontacolus axfordi (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus bhowaliensis (Mani & Mukerjee) comb. n. (India), Odontacolus bouceki (Austin & Iqbal) comb. n. (Australia), Odontacolus copelandi (Valerio, Masner & Austin) comb. n. (Kenya, Nigeria, Zimbabwe, Thailand), Odontacolus diazae (Valerio, Masner & Austin) comb. n. (Kenya), Odontacolus harteni (Valerio, Masner & Austin) comb. n. (Yemen, Ivory Coast, Paskistan), Odontacolus jenningsi (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus leblanci (Valerio, Masner & Austin) comb. n. (Guinea), Odontacolus lucianae (Valerio, Masner & Austin) comb. n. (Ivory Coast, Madagascar, South Africa, Swaziland, Zimbabwe), Odontacolus normani (Valerio, Masner & Austin) comb. n. (India, United Arab Emirates), Odontacolus sallyae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus tessae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus tullyae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus veniprivus (Priesner) comb. n. (Egypt), and Odontacolus watshami (Valerio, Masner & Austin) comb. n. (Africa, Madagascar). Two species of Odontacolus are transferred to the genus Idris Förster: Idris longispinosus (Girault) comb. n. and Idris amoenus (Kononova) comb. n., and Odontacolus doddi Austin syn. n. is placed as a junior synonym of Odontacolus spinosus (Dodd). Odontacolus markadicus, previously only known from India, is here recorded from Brunei, Malaysia, Sri Lanka, Thailand and Vietnam. The relationships, distribution and biology of Odontacolus are discussed, and a key is provided to identify all species.

9.
Biol Direct ; 6: 50, 2011 Oct 05.
Artículo en Inglés | MEDLINE | ID: mdl-21974828

RESUMEN

BACKGROUND: Volutin granules appear to be universally distributed and are morphologically and chemically identical to acidocalcisomes, which are electron-dense granular organelles rich in calcium and phosphate, whose functions include storage of phosphorus and various metal ions, metabolism of polyphosphate, maintenance of intracellular pH, osmoregulation and calcium homeostasis. Prokaryotes are thought to differ from eukaryotes in that they lack membrane-bounded organelles. However, it has been demonstrated that as in acidocalcisomes, the calcium and polyphosphate-rich intracellular "volutin granules (polyphosphate bodies)" in two bacterial species, Agrobacterium tumefaciens, and Rhodospirillum rubrum, are membrane bound and that the vacuolar proton-translocating pyrophosphatases (V-H+PPases) are present in their surrounding membranes. Volutin granules and acidocalcisomes have been found in organisms as diverse as bacteria and humans. RESULTS: Here, we show volutin granules also occur in Archaea and are, therefore, present in the three superkingdoms of life (Archaea, Bacteria and Eukarya). Molecular analyses of V-H+PPase pumps, which acidify the acidocalcisome lumen and are diagnostic proteins of the organelle, also reveal the presence of this enzyme in all three superkingdoms suggesting it is ancient and universal. Since V-H+PPase sequences contained limited phylogenetic signal to fully resolve the ancestral nodes of the tree, we investigated the divergence of protein domains in the V-H+PPase molecules. Using Protein family (Pfam) database, we found a domain in the protein, PF03030. The domain is shared by 31 species in Eukarya, 231 in Bacteria, and 17 in Archaea. The universal distribution of the V-H+PPase PF03030 domain, which is associated with the V-H+PPase function, suggests the domain and the enzyme were already present in the Last Universal Common Ancestor (LUCA). CONCLUSION: The importance of the V-H+PPase function and the evolutionary dynamics of these domains support the early origin of the acidocalcisome organelle. In particular, the universality of volutin granules and presence of a functional V-H+PPase domain in the three superkingdoms of life reveals that the acidocalcisomes may have appeared earlier than the divergence of the superkingdoms. This result is remarkable and highlights the possibility that a high degree of cellular compartmentalization could already have been present in the LUCA.


Asunto(s)
Bacterias/enzimología , Gránulos Citoplasmáticos/metabolismo , Evolución Molecular , Pirofosfatasa Inorgánica/metabolismo , Vacuolas/enzimología , Ácidos/metabolismo , Archaea/clasificación , Archaea/enzimología , Bacterias/clasificación , Bacterias/ultraestructura , Teorema de Bayes , Calcio/metabolismo , Bases de Datos de Proteínas , Eucariontes/clasificación , Eucariontes/enzimología , Microscopía Electrónica , Filogenia , Polifosfatos/metabolismo , Estructura Terciaria de Proteína , Alineación de Secuencia , Vacuolas/metabolismo
10.
Rev. biol. trop ; 53(1/2): 63-71, mar.-jun 2005. ilus, graf
Artículo en Español | LILACS | ID: lil-455487

RESUMEN

We indirectly evaluated the selective pressures on dispersal and establishment of Campsiandra angustifolia, a common water-dispersed tree from the Peruvian Amazon, analyzing the variation in the relationship between the volume occupied by dispersal and establishment structures in a total of 535 seeds from 13 trees located at three different habitats. The seeds differed one order of magnitude in their total volume. However, independently of their size and the location of the maternal tree, the relationship between the volume occupied by dispersal and establishment structures was relatively constant (~1) and showed a normal distribution with low skewness, indicating stabilizing selection. These results suggest that, in the habitats studied, dispersal and establishment processes may have similar importance to C.angustifolia. In species with seeds confined in pods, and therefore strongly space-limited, the relative volume of their seeds occupied by dispersal and establishment structures could be a better measure of the trade-off between these two processes than the variation in seed size


Evaluamos indirectamente las presiones selectivas sobre la dispersión y el establecimiento en Campsiandra angustifolia, un árbol de la Amazonía Peruana dispersado por agua, analizando variaciones de la relación entre el volumen ocupado por las estructuras de dispersión y de establecimiento en sus semillas. Medimos un total de 535 semillas de 13 árboles ubicados en tres hábitats diferentes, las cuales presentaron una gran variación en su volumen total. Independientemente del tamaño de la semilla y de la ubicación del árbol de origen, la relación entre el volumen asignado a estructuras de establecimiento y a estructuras de dispersión fue relativamente constante (~1) y presentó una distribución normal con baja asimetría, indicando selección estabilizante. Este resultado sugiere que los procesos de dispersión y establecimiento poseen una importancia relativa similar para C.angustifolia en los hábitats estudiados. En especies con semillas empaquetadas, el volumen relativo ocupado por estructuras relacionadas con la dispersión o el establecimiento podría ser una medida más adecuada de la solución de compromiso entre estos dos procesos que la variación del tamaño de la semilla


Asunto(s)
Ecosistema , Fabaceae/fisiología , Germinación/fisiología , Selección Genética , Semillas/fisiología , Árboles/fisiología , Tamaño Corporal/fisiología , Cotiledón/fisiología , Desastres , Fabaceae/anatomía & histología , Relámpago , Perú , Estaciones del Año , Plantones/fisiología , Semillas/anatomía & histología
11.
Rev. biol. trop ; 52(3): 665-677, sept. 2004. tab, ilus
Artículo en Inglés | LILACS | ID: lil-501714

RESUMEN

The current taxonomic status of the species and subspecies belonging to the genus Alouatta is addressed by combined phylogenetic analysis using morphological, kariotipyc and molecular data (mitochondrial genes cytocrome oxidase II and cytochrome B). Our result demonstrated that Alouatta palliata is the most basal taxon for the genus in concordance with previous studies, as well as showing the validity of the taxon Alouatta sara as a species. Also our analysis shows that the sex chromosome has evolved from a XY/XX system to a X1X2Y1Y2/X1X1X2X2 system within the genus, as well as an increase in the size and complexity of the hioideal bone.


Asunto(s)
Animales , Alouatta/genética , Cromosomas Sexuales/genética , ADN Mitocondrial/genética , Filogenia , Alineación de Secuencia , Alouatta/anatomía & histología , Alouatta/clasificación , Cariotipificación , Complejo IV de Transporte de Electrones/genética , Evolución Molecular , Grupo Citocromo b/genética
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