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Motyxia Chamberlin is comprised of eight species of bioluminescent xystocheirine millipeds in which the gonopodal solenomere arises at different positions, from basally and subbasally on the acropodite to being fused with the companion acropodal branch and detaching proximad or near midlength. Previous synonymies of Amplocheir Chamberlin and LuminodeslnllS Loomis and Davenport under Motyxia are confirmed as is its assignment to the tribe Xystocheirini, which is redefined. Component species are 111. Iwnw Chamberlin, the type species, monica Chamberlin, sequoiae (Loomis and Davenport), tularea (Chamberlin), sequoia (Chamberlin), pior Chamberlin, porrecta Causey and Tiemann, and tiemanni Causey. Motyxia sequoia is comprised oftwo races, the nominate and sequoia alia Causey and Tiemann; sequoia ollae Causey and Tiemann is properly a subspecies of tularea. 1I1otyxiapiorform secea is an invalid name without standing in nomenclature, and M. tejona Chamberlin, and M. expansa and exilis, both by Loomis, are placed in synonymy under M. monica, the oldest name for the southernmost species, as Polydesllws dissectus Wood is referrable to Xystocheir Cook. The bioluminescence is a continuous, neon-white glow of the entire dorsal surface including the antennae and legs. Its visibility at night suggests a warning function analogous to aposematic coloration. The phenomenon may observe a circadian rhythm, and controlled photoperiod experimentation may be productive.
The Sclerocoelus galapagensis group is defined and revised, including the description of S. galapagensis new species from the Galapagos Islands; S. caribensis new species from the Caribbean and adjacent areas; S. brasilensis new species from Brazil, Ecuador, Colombia, and Panama; S. hemorrhoidal is new species from Ecuador and Venezuela; and S. andensis new species from Argentina, Bolivia, and Venezuela. The south Atlantic species Sclerocoelus subbrevipennis (Frey), new combination, is redescribed as a member of the S. galapagensis group, and is considered the sister species to the rest of the species group. A key to species, character matrix, and cladogram are provided.
Explaining cross-country differences in growth rates requires not only an understanding of the link between growth and public policies, but also an understanding of why countries choose different public policies. This paper shows that ethnic diversity helps explain cross-country differences in public policies and other economic indicators. In the case of Sub-Ssharan Africa, economic growth is associated with low schooling, political instability, underdeveloped financial systems, distorted foreign exchange markets, high government deficits, and insufficient infrastructure. Africa's high ethnic fragmentation explains a significant part of most of these characteristics.
The endomychid beetle genera Anidrytus Gerstaecker and Epopterus Chevrolat have been confused for many years. This paper discusses the similarities and differences of these genera, describes new species, makes some nomenclatural changes, and illustrates the genitalia for many species. New species described: Epopterus picticollis, E. bioculatus, E. confusus, E. gracilis, E. loretensis, E. anomalus, E. aravacus, E. atriventris, E. crypticus, E. quechuanus, E. callerianus, E. flavonotatus, E. submaculatus, E. parvus, Anidrytus nimbiferus, A. parki, A. compactus, A. gibbosus, A. circumcinctus, A. bechyneorum, A. batesi, A. mexicanus, A. trinitatis, A. major, A. humerosus, A. grandis, A. cardiosoma. New synonymies: E. vacuus Gerstaecker (= E. scalaris Gorham); E. decempunctatus Gerstaecker (= E. bifasciatus Pic); E. variegatus Erichson (= E. decoratus Kirsch); A. contractus Gerstaecker (= A. dolosus Gorham); A. helvolus Gerstaecker (= Ephebus ignobilis Gorham); A. parallelus Gerstaecker (= Ephebus depressus Gorham). Changes in nomenclatural status or combination: Epopterus kirshi Strohecker is reduced to a subspecies of E. partitus Gerstaecker; E. angustatus Strohecker is reduced to a subspecies of E. fasciatus (Fabricius); E. fuliginosus Guerin-Meneville is transferred to Anidrytus.
The subfamily Epiphloeinae is defined to include fourteen genera as follows: Epiphloeus Spinola; Pilosirus, new genus; Plocamocera Spinola; Iontoclerus, new genus; Arenaria, new genus; Ichnea Laporte; Diapromeces, new genus; Pyticeroides Kuwert; Ellipotoma Spinola; J{atamyurus, new genus; Megatrachys, new genus; Madoniella Pic; Hapsidopteris, new genus; and Teutonia, new genus. The following type-species are described: Pilosirus brunoi, new species; Arenaria chiapas, new species; Diapromeces aclydis, new species; Katamyurus paxillus, new species; Megatrachys paniculus, new species; Hapsidopteris diastenus, new species; and Teutonia nova, new species. Elloplium humerale Klug is designated as the typespecies of Iontoclerus. The genus Madolliella is removed from the subfamily Korynetinae andis declared a senior synonym of Phlogistosternus Wolcott. Neiclmea is synonymized with Pyticeroides. This treatise includes a key to the genera of Epiphloeinae, descriptions of the genera and new type-species, and distribution map for each genus.
A lot of interest has recently been paid to constraint-based definitions and extensions of Tree Adjoining Grammars (TAG). Examples are the so-called quasi-trees, D-Tree Grammars and Tree Description Grammars. The latter are grammars consisting of a set of formulars denoting trees. TDGs are derivation based where in each derivation step a conjunction is built of the old formular, a formular of the grammar and additional equivalences between node names of the two formulars. This formalism is more powerfull than TAGs. TDGs offer the advantages of MC-TAG and D-Tree Grammars for natural languages and they allow underspecification. However the problem is that TDGs might be unnecessarily powerfull for natural languages. To solve this problem, in this paper, I will propose a local TDGs, a restricted version of TDGs. Local TDGs still have the advantages of TDGs but they are semilinear and therefore more appropriate for natural languages. First, the notion of the semilinearity is defined. Then local TDGs are introduced, and, finally, semilinearity of local Tree Description Languages is proven.
Four new species of Ommatius Wiedemann, the female of O. stramineus Scarbrough, and the male of 0. nigellus Scarbrough from Hispaniola are described. A lectotype for O. gwenae Scarbrough and a neotype for O. cinnamomeus are selected. Notes of previously named species, new records, illustrations of terminalia, and a key to the species are included.
Several Coleopterists have been asked to revise the family sections, working from diskettes modified and provided from the original "Beetles of the United States." They will rewrite these sections, and will be recognized as the author of the section. They are asked to sign a writing contract with the publisher. Other Coleopterists have been asked to review the family sections of the new book. These persons are acknowledged in the family section text.
Six species of the genus Polyplectropns are recorded from the People's Republic of China. All the species are new to science. A key to the males is given. The larva of Polyplectropns nanjingensis sp. nov. is illustrated. The phylogenetic relationships among these species and with Polyplectropns species of the New World are discussed.
The shape of the facial carina in Altastreplia is discussed. Although taxonomically useful, the protrudent form probably occurs by convergence in different species groups. Two species groups in which the carina is usually produced are revised. The belljamini species group includes: belljamini Lima (from southeastern Brazil), gigantea Stone (from Panama), magna, n. sp. (from Colombia and Venezuela), and superj1ua Stone (from Panama). Host data for this group are limited to only one record of benjamilli from a species of Pouteria (Sapotaceae). The pallidipennis complex, which is included in the pseudoparallela species group, is recognized to include: amnis Stone (from southern Brazil and possibly Trinidad), curitis Stone (from Colombia, Peru, and northern Brazil), pallida, n. sp. (from Panama), pallidipennis Greene (from Colombia and Venezuela), and vele::i, n. sp. (from Colombia). These species breed in fruit of Passij10ra (Passifloraceae) (P. ambigua Hems., ligularis Juss., Idtida H.B.K., quadrallgularis L., and seemannii Griseb.). The relationships of these Anastrepliaspecies are discussed, and diagnoses and ill ustrations are provided to permit their identification. A neotype is designated for A. consobrina (Loew), and the identity of this species is clarified.
Six new species ofTrichoptera are described and figured, belonging to the families Goeridae and Leptoceridae. The goerid species are Goera baishanzuensis new species and Goera recta new species. The leptocerid species are Setodes chlorinus new species, Ceraclea (Athripsodina) semicircularis new species, Ceraclea (Athripsodina) brachyclada new species, and Ceraclea (Athripsodina) vaciva new species (Leptoceridae).
Based on his studies of the genus Rubus in the Czech Republic, the author describes classification of brambles from Rubus subgen. Rubus in Europe, its recent history, present state, and current problems. In general, the author follows the adherents of "Weberian batology" which in the last 25 years has assumed European responsibility for attempting to ciassify that particular genus. The thesis that not every bramble plant can be inciuded in the ciassification is accepted. The objective reasons for taxonomic difficulties within Rubus subgen. Rubus are connected with special features of taxogenesis of its members, especially with incomplete apomixis, frequent hybridization, splitting of the progeny into different morphotypes, resexualization, transitory existence of segregants, etc. The progress of the evolution of a new taxon in the given taxonomic group can be ranked: individual bush - local type - regional species - species with an extensive distribution area. When classifying a taxon, alongside sufficient morphological characteristics,
great emphasis should be put on the distribution area; its extent can render possible the taxon to be accepted into the classification scheme. On the basis of experience gained from the Czech Republic, the author has accepted some modifications of the scale for acceptance of plants as species. The basic difference is in lowering the low limit of the extent of the distribution area for regional species, to be acceptable for their lnclusion to the classification, i.e. to 20 km in diameter. In contrast to taxa of other plant groups, species of apomictic brambles with more extensive distribution areas are phytogeographically more important than those with small distribution areas. In spite of the use of stricter requirements for the description of new species in Rubus, it appears that many (distinct) species have been neglected until now, and that the number of species in Rubus subgen. Rubus is continuously increasing. The author stresses the necessity of studying the group ser. Glandulosi in Central Europe and points out the usefulness of cooperation with population ecologists to describe the quantitative representation of taxonomically unclassified bramble plants in the field.
The sting apparatus and pygidium are described for eight of 20 Lordomyrma species and one of five Mayriella species. The apparatus of L. epinotaiis is distinctly different from that of other Lordomyrma species. Comparisons with other genera suggest affinities of species of Lordomyrma to species of Cyphoidris and Lachnomyrmex, while Mayriella abstinens Forel shares unusual features with those of Proatta butteli.
The following changes in nomenclature of some species of Amblyeems Thunberg, 1815, are proposed: A) Elevated to new taxonomic status- A. insuturatus (pic, 1902) from (Spennophagus subflavidus var.insuturatus); A. luteolineatus (pic, 1929) from (Spennophagus luteonotatus var .luteolineatus);A. paulonotatus (pic, 1906) from (Spennophagus luteonotatus var.paulonotatus). B) New synonymy-A. dispar(Sharp, 1885)(=Spermophagus longissimus Pic, 1902; =S. earyoborifonnis Pic, 1910; =S. guyanensis Pic, 1917; S.pieeosuturalis Pic, 1927; =S. earaeasensis Pic, 1954); A. gounellei (pic. 1902)(=S. eurtus Pic, 1911; =S. basipennis Pic, 1936); A. insuturatus (pic, 1902)(=A. woleotti Kingsolver, 1970;A.jatayensis (Pic, 1902)(=S.jatayensis var. bieolorieeps Pic, 1955; =S.jatayensis var. hahnelli Pic, 1955; A. IIwltimaculatus (pic, 1902)( =S. minasensis Pic, 1918); A. perfectus (Sharp, 1885)(=S. maeulatopygus Pic, 1927); A. reticulatus (Jekel, 1855)(=S. rufotestaeeus Pic, 1912);A.luteolineatus (pic, 1929)(=S. multisignatus Pic, 1954). C). Lectotype/s and paralectotype/s are designated for: S. luteonotatus Pic, 1902; S. multimaeulatus Pic, 1902; S. maeulatopygus Pic, 1927; S. subflavidus Pic, 1902; S. trisignatus Sharp, 1885; S.jatayensis Pic, 1902; S. longissimus Pic, 1902; S. earyoborifonnis Pic, 1910; S. dispar Sharp, 1885; S. subflavidusvar. insuturatus Pic, 1902. For all species listed in this paper, we provide a bibliography, label data on type material, sex of types and their repository.