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In the field of mycology at the present time, many of the fungi which are most frustrating to attempt to classify are the Ascomycetes of pyrenomycetous nature. While it is possible to identify many species from descriptions in the literature, the position of these species in respect to one another is difficult to assign. A major step toward a modern classification was provided by Luttrell (1951b, 1955), where he expanded Miller's (1928) and Nannfeldt's (1932) recognition of differences between the subclasses Loculoascomycetes and Euascomycetes and utilized the basic characteristics of the ascus and of centrum development to delimit major groups. Currently, studies of generic types by a number of investigators are providing a firm base for the assignment of taxa to the correct genus. Several systems of classification are available, but none of these is entirely satisfactory. The following synopsis is offered as an alternative arrangement of one order in the Loculoascomycetes. For the present, the system applies to fungi known from temperate North America. The classification probably will have to be expanded and emended as tropical and temperate fungi from other continents are studied. My intention is to continue with similar studies of taxa in the other orders of both Loculoascomycetes and Euascomycetes.
The avifauna of the island of Flores and its satellite islands from Komodo to Alor is reviewed, combining historical data with recent observations. Recent surveys have added substantially to the data base, especially of the resident forest species, and endangered and endemic taxa, as well as adding a number of migrant and maritime species to the island list. Of particular interest are the rare forest endemics Wallace's Hanging-parrot Loriculus flosculus, the almost unknown Flores Scopsowl Otus alfredi, Flores Monarch Monarcha sacerdotum and Flores Crow Corvus florensis. An appeal is made for further surveys over the eastern part of the island and the eastern island chain.
A new genus is proposed within the family Geophilidae: Hyphydrophilus n. gen., for H. adisi n.sp. Four additional new species are described, i.e. the ballophilids ltyphilus crabilli n.sp. and Taeniolinllm arborum n.sp. and the schendylids Pecfiniunguis ascendens n.sp. and Schendyluflls amazonicl/s n.sp. The geophilid species Ribautia centralis (SILVESTRI, 1907) is redescribed, after material from Brazil compared with the holotype. The ballophilid Thalthybil/s perrieri BROLEMANN, 1909 is transferred to the genus ltyphi/us COOK, 1889 and a lectotype is designated here for it.
This paper is an annotated catalogue of the geophilomorph centipedes known from Mexico, Central America, West Indies, South America and the adjacent islands. 310 species and 4 subspecies in 91 genera in 111 families are listed, not including 6 additional taxa of uncertain generic identity and 4 undescribed species provisionally listed as 'n.sp.' under their respective genera. Sixteen new combinations are proposed: Garrina pujola (CHAMBERLIN, 1943) and G. vera (CHAMBERLIN, 1943), both from Pycnona; Nesidiphilus plusiopol'us (ATTEMS, 1947), from Mesogeophilus VERHOEFF, 1901; Polycricus bredini (CRABILL, 1960), P. cordoballensis (VERHOEFF, 1934), P. hailiensis (CHAMBERLIN, 1915) and P. nesiotes (CHAMBERLIN, 1915), all from Lestophilus; Tuoba baeckstroemi (VERHOEFF, 1924), from Geophilus (Nesogeophilus); T. culebrae (SILVESTRI, 1908), from Geophilus; T. laticollis (ATTEMS, 1903), from Geophilus (Nesogeophilus); Titanophilus hasei (VERHOEFF, 1938), from Notiphilides (Venezuelides); T. incus (CHAMBERLIN, 1941), from Incorya; Schendylops nealotus (CHAMBERLIN, 1950), from Nesondyla nealota; Diplethmus porosus (ATTEMS, 1947), from Cyclorya porosa; Chomatobius craterus (CHAMBERLIN, 1944) and Cil. orizabae (CHAMBERLIN, 1944), both from Gosiphilus. The new replacement name Schizonampa Iibera is proposed pro Schizonampa prognatha (CRABILL, 1964) ex Schizotaellia prognatha CRABILL, 1964 nec Schizotaenia prognatha COOK, 1896.
A new family (Macronicophilidae) is established for Macronicophilus Silvestri, 1909, currently placed in Geophilidae. Seven new species of Neotropical Geophilomorpha are described: Ilyphilus saudus n.sp. and I. sensibilis n.sp. (Baliophilidae), Hyphydrophilus projeclUs n.sp. and Ribautia onycophaena n.sp. (Geophilidae), Macronicophilus abbrevialus n.sp., M. unguiseta n.sp. and M. venezolanus n.sp. (Macronicophilidae). The hitherto unknown male of Schendylops marchantariae (PEREIRA, MINELLI & BARBIERI, 1995) is described and two species (Pectiniunguis geayi (BROLEMANN & RIBAUT, 1911) and Ityphilus calinus CHAMBERLIN, 1957 are redescribed from the type and new material. A key to the species of Macronicophilus is provided.
This review lists Agama smithii Boulenger 1896 as a synonym of Agama agama (Linnaeus 1758), Agama trachypleura Peters 1982 as a synonym of Acanthocercus phillipsii (Boulenger 1895) and describes for the first time Acanthocercus guentherpetersi n. sp. Without more convincing evidence, Chamaeleon ruspolii Boettger 1893 cannot be accepted as specifically distinct from Chamaeleo dilepis Leach 1819, nor Chamaeleo calcaricarens Böhme 1985 from C. africanus Laurenti 1768. Consequently, 101 species of lizard are currently recognised in Ethiopia, of which some 40% appear to be denizens of the Somali-arid zone. This significant proportion is attributable in part to the importance of the Horn of Africa as a centre for reptilian diversification and endemicity, in part to the fact that this lowland fauna was rather extensively sampled during the 1930s, but also to the conspicuous neglect of lizards in other regions of the country. Mountain and forested habitats are widespread in Ethiopia, so it seems extraordinary to record only five saurian species which are believed to be endemic in such environments. The inference that there are many more still to be discovered has important implications for conservation, because montane forest is known to be among the most threatened of Ethiopian biomes and there is clearly an urgent need for its herpetofauna to be more thoroughly researched and documented.
La distribuzione geografica delle 21 specie di Zygaena e 8 specie di Adscitinae viventi nelle Alpi Liguri è stata analizzata sia nei suoi rapporti col resto della fauna paleartica, sia a livello italiano e ligure. Tale indagine ha consentito di evidenziare l'esistenza di numerosi centri di rifugio e speciazione e di mettere in luce diverse aree di transizione primaria e secondaria intese secondo il senso di Thorpe (1983). Il significato adattativo del cosiddetto melanismo littorale (Burgeff 1950) è discusso in termini di conquista di una nuova nicchia ecologica e di caduta nel valore aposematico.
It has been the goal of this review to describe the functional interrelations between Deiters' vestibular nucleus and numerous brain structures. Emphasis is placed on dynamic and integrative properties of linkages between the neurons of Deiters' nucleus and many other brain structures in order to begin considering the capabilities of the loops in the light of motor control and coordination of movement. The problem of somatotopy within the loops is also considered. Putting this information together, the possible roles of Deiters' nucleus in the control of movements are described. It is suggested that Deiters' nucleus in co-operation with cerebral cortex, cerebellum, subcortical and brainstem structures are responsible for the integration and realization of different movements.
Aus dem Dogger Norddeutschlands und des nordwestlichen Polens sowie aus Dogger-Geschieben werden 1 Art der Neritimorpha und 30 Arten der Caenogastropoda beschrieben. Neu sind 7 Arten. 14 Arten werden bereits beschriebenen Arten zugeordnet und 10 unter offener Nomenklatur beschrieben. Neu sind die Gattung Bicorempterus (Aporrhaidae) und die Familien Naricopsinidae, Tripartellidae und Maturifusidae. Die beschriebenen Caenogastropoden zeigen mehr Gemeinsamkeiten zu bisher aus dem Dogger Mittel- und Westeuropas bekannt gemachten Faunen als es bei den Archaeogastropoda und den Heterostropha der Fall war. Die Gleichsetzung der hier vorgestellten Arten mit aus der Literatur bekannten ist oftmals problematisch. Taxonomisch relevante Details besonders der Frühontogenese wurden bisher kaum beschrieben. Auch Fragen der innerartlichen Variation wurden nur gelegentlich angesprochen. Vatopsis antiquus n. sp. ist der älteste genauer bekannte Vertreter der Cerithiopsoidea. Pictavia und Oonia konnten als Vertreter der Ampullospiridae erkannt werden (Ausbildung des Protoconchs). Naricopsina repräsentiert eine Gruppe, die möglicherweise zu den echten Naticidae führte. Einige Gattungen der Aporrhaidae können genauer gefaßt werden. Maturifusus ist der älteste sichere Vertreter der höheren Caenogastropoda (Neomesogastropoda).
A review of biological control efforts against Diptera of medical and veterinary importance includes pertinent literature of major dipterous taxonomic groups where some success has been achieved or where work is currently being conducted on species breeding in aquatic (e.g., mosquitoes, blackflies, tabanids) and terrestrial habitats (muscids, tsetse, etc.). Most effort has been directed against aquatic Diptera because of the human and animal disease agents they transmit. Research has established that the natural enemy component frequently is responsible for significant population reduction and indispensable to integrated control which seeks to maintain populations below annoyance or disease transmission levels. The manipulation of natural enemies through introduction and/or augmentation has in some cases provided satisfactory control, and sustained releases of natural enemies over several years may overcome the relative high cost of massive release rates. Ultimately, to guarantee the existence and maximum expression of resident natural enemies has become almost universally accepted, and challenging, to sound control practices. Indeed, chemical industry recognizing this, has sought to manufacture products such as Bacillus toxins, juvenile hormones, and baits that are minimally disruptive to existing natural controls. Although such easily applied products have been widely adopted, their cost continues to become prohibitive with developing resistance, as was observed earlier with many organophosphate and chlorinated hydrocarbon insecticides. Further advancements in the control ofthese Diptera should continue to embrace a sound appreciation for the natural control component and nurture ways to allow its maximum expression. Keyword Index: Biological Control, Diptera, Medical, Veterinary.
Arthropods use fluid medium motion-sensing filiform hairs on their exoskeleton to detect aerodynamic or hydrodynamic stimuli in their surroundings that affect their behaviour. The hairs, often of different lengths and organized in groups or arrays, respond to particular fluid motion amplitudes and frequencies produced by prey, predators, or conspecifics, even in the presence of background noise peculiar to the environment. While long known to biologists and experimentally investigated by them, it is only relatively recently that comprehensive physical-mathematical models have emerged offering an alternative methodology for investigating the biomechanics of filiform hair motion. These models have been developed and applied to quantitatively predict the performance characteristics of filiform hairs in air and water as a function of the relevant parameters that affect their physical behaviour. They even allow the exploration of possible biological evolutionary paths for filiform hair changes resulting from physical selection pressures. In this chapter we review the state of knowledge of filiform hair biomechanics and discuss two physical-mathematical models to predict hair dynamical behaviour. One modelling approach is analytically exact, serving for quantitative purposes, while the other, derived from it, is approximate, serving for qualitative guidance concerning the parameter dependencies of hair motion. Using these models we look in turn at the influence of these parameters and the fluid media physical properties on hair motion, including the possibility of medium-facilitated viscous coupling between hairs. The models point to areas where data is currently lacking and future research could be focused. In addition, new results are presented pertaining to transient tlows. We qualitatively explore the possibility of an overlapping water-air niches adaptation potential that may explain how, over many generations, the filiform hairs of an arthropod living in water could have evolved to function in air. Because flow-sensing hairs have served to inspire corresponding artificial medium motion microsensors, we discuss recent advances in this area. Significant challenges remain to be overcome, especially with respect to the materials and fabrication techniques used. In spite of the impressive technological advances made, nature still remains unrivalled.
The birds of Billiton Island
(1937)
Resume 1) The egg of Squilla oratoria DE HAAN is centrolecithal and undergoes partial cleavages resulting in rudimentary primary yolk pyramids. 2) The germinal disk is first represented by a pair of optic lobes and a ventral plate, which are afterward connected by paired, lateral ectoderm thickenings to form a V-shape. The V is then transformed into an O by the appearance of a transverse band between the optic lobes of both sides. 3) A small blastopore is formed. Of the mesendoderm cells derived from the blastopore by cell immigrations, those attached to the lower surface of the lateral ectoderm thickenings are differentiated into a U-shaped, naupliar mesoderm band. This inesoderm band joins the preante:mulary mesoderm derived from the optic lobe, and grows into a complete ring conforming to the shape of the germinal disk. 4) The extra-blastoporic immigrants consist of a preantennulary mesoderm, mesodermal yolk cells and a part of the naupliar mesoderm. The greater part of the preantennulary mesoderm cells disintegrate sooner or later, without forming any distinct structure. The mesodermal yolk cells also degenerate after taking part in the dissolution of the deutoplasm. A discussion as regards the mutual relationship between these elements, with the conclusion that the formation of the preantennulary mesoderm represents the initial step of the extra-blastoporic cell sinking from the whole egg surface, is included. 5) The endodermal elements consist of a compact cell mass differentiated from the posterior part of the mesendoderm layer and the endodermal yolk cells immigrated from the blastopore. The yolk cells, after migrating through the most peripheral part of the yolk, scatter all over its surface. The endoderm plate is nothing but a mass of yolk cells. which remain without scattering. 6) Eight mesoteloblasts derived from the blastoporic lip are attached to the inner surface of the thoracico-abdominal process, making four groups. The ectoteloblasts are differentiated from the ordinary blastoderm cells in a later stage than the mesoteloblasts. In the final condition they consist of 21 cells forming a complete ring around the thoracico-abdominal process. 7) Both the ectoderm and the mesoderm are derived from the teloblasts in all of the post-naupliar segments.· The dorsal ectoderm, however, is non-teloblastic in only a few anterior segments. Differentiation of segments proceeds from the front toward the back. 8) The telson mesoderm is formed by the cells sunk from the telson ectoderm which is derived from the peri-blastoporic ectoderm . 9) The anus is the remnant of the blastopore. In accordance with the change of the caudal furca, the anus is displaced from the dorsal side of the telson to the ventral border between this and the last abdominal segment. 10) There is a distinct nauplius stage. Of the meta-naupliar segments, those from the m:txillula to the second maxilliped are laid on the germinal disk, the following segments together forming a thoracico-abdominal process. Two maxiliiped segments, however, are later separated from the cephalon with the development of the carapace fold, and join the trunk segments. Externally, six abdominal segments are formed. 11) The ganglionic cells are proliferated from the neuroblasts occupying the most superficial part of the centra1 nervous system. The giant ganglionic cells arise from the ordinary ganglionic cells and not directly from neuroblasts. The development of the cerebrum is described. The tritocerebra of both sides are conne~ted by a transverse nerve-fibre bundle behind the stomodaeum. The ganglia of the segments from the mandible to the second maxilliped first exhibit a typical ladder-like shape. Of these ganglia, the anterior three constitute a sub-resophageal ganglion by more or less complete fusion, while the posterior two are transferred from the cephalon to the thoracico-abdomimil process with the constriction of the segments. The inter-ganglionic cell groups take part in the constriction of the consecutive segments. The seventh abdominal ganglion is clearly indicated by the presence of such a cell group as well as of a pair of nerve fibre masses. 12) The development of the compound eye is traced. The ganglion opticum is derived from the ectoderm of the optic lobe lateral to the protocerebrum; it is not an outgrowth of the cerebrum. 13) The ganglion visceralum is differentiated from the anterior wall of the stomodaeum. 14) A median dorsal organ is formed. In close connection with the activity of this organ, the embryo undergoes one ecdysis. 15) The mid-gut epithelium is formed by the gradual expansion of the anterior and posterior endoderm plates over the yolk sac. These plates, however, extend only on the ventral side of the yolk sac before hatching. The posterior plate is produced by the concentration of the scattered yolk cells toward the periphery of the. plate differentiated from the mesendoderm, while the anterior plate is formed by yolk cells alone. 16) The greater part of the intestine develops from the outgrowth of the posterior endoderm epithelium, the proctodaeum occupying only the rectum. 17) The posterior liver lobes are produced from the posterior endoderm plate as a pair of blind tubes and extend as far backward as the telson. The anterior liver lobes and the lateral mid-gut cceca are rather incompletely developed, being ~eparated by shallow superficial grooves of the yolk sac. These two pairs of diverticula are only partially covered by the endoderm epithelium, and develop into more or less distinct coeca during larval life. They later seem to be completely absorbed again by the mid-gut. 18) The product of each division of the mesoteloblast is equivalent to one mesodermal-segment. The mesoderm of the seventh abdominal segment is derived from the posteriorly situated daughter cell produced by the last division of the teloblast. In' accordance with the grouping of teloblasts, the trunk mesoderm is separated into two ventral and two dorsal bands. Each band is further separated into segmentally arranged blocks, the somites. The ccelom develops in no stage and in no segment. 19) The dorsal mesoderm gives rise to the extensor and the oblique muscles of the trunk, the anterior and posterior limb muscles, as well as to the mesodermal inclusion of the limb. The -ventral mesoderm grows into the flexor. The connective tissue investing the intestine -and the liver lobes are principally constructed from the dorsal mesoderm. The germ cell does not appear until hatching. A brief account is also given of the fate of the naupliar mesoderm. 20) The heart wall and the pericardial floor are morphologically one unit. They arise from the dorsal mesoderm as a pair of membranes stretching between it and the intestine. The dilated and elongated parts of the heart are formed by the subsequent union of these paired rudiments. 21) The anterior dorsal vessel has a two-fold origin; it is formed by the fusion of an anterior rudiment extending backward from the rostrum and a posterior one developing as a tubular outgrowth of the heart. The former is derived from the rearrangement of mesenchymatous cells which migrated from the anterior end of the naupliar mesoderm. 22) By the time of hatching, two pairs of lateral vessels are formed as hollow linear thickenings of the pericardial floor in front and behind the dilated part of the heart. 23) The antennal gland remains rudimentary without acquiring any intercellular lumen. The maxillar gland is not laid until hatching. The labral and anal glands are derived from the peristomodaeal and the telson mesoderm respectively. 23) Comparisons are made bewteen Squilla and other orders of Malacostraca as regards the salient points of the embryonic development. These have led to the conclusion that the Stomatopoda are most closely related in their embryonic development to Nebaliacea, and further that Stomatopoda represent a rather primitive group separated from the main stem of Malacostraca very early, only next in order to Nebaliacea.