Genetic polymorphism (ABO, Rh, Kell) in Kabul (Afghanistan)

ABO, rhesus and Kell blood group data on 1327 donors in Kabul are analysed by ethnic affinity and compared with existing data on Afghanistan peoples. Blood group frequencies are very similar in Pushtu and Tadjik, despite their different historical, linguistic, and cultural backgrounds. Inclusion of the small sample of Hazara in the analysis shows overall heterogeneity in rhesus D, E, and e frequencies, suggesting the existence of a broader pattern of genetic variation among the peoples of Afghanistan.     

Spermiogenesis in Anaspides tasmaniae (Thomson) (Crustacea,Malacostraca, Syncarida)

Spermiogenesis of the syncarid Anaspides tasmaniae (subclass Eumalacostraca) was investigated by transmission electron microscopy. The spermatozoan of Anaspides is an ovoid cell with an acrosome covering the anterior pole and a lobulated nucleus and mitochondria occupying the rest of the cell. A long subacrosomal filament bypasses the nucleus and forms a spiral that supports a thin extension of the posterior cytoplasm, giving the spermatozoan a bell-shaped appearance. No flagellum is present at any stage. The immobile spermatozoans are embedded in a hard capsule, secreted by the cells of the wall of the vas deferens.     

Ecomorphology ofCrassostrea cucullata (Born, 1778) (Ostreidae) in a mangrove creek (Gazi,Kenya)

Variations of shell form and shell length were studied for oysters growing in the mangroves of Gazi Creek, Kenya, and related to different environmental factors.For the study of the form, Fourier analysis was performed on the circumference of 85 oysters. The resulting coefficients were compared among specimens using cluster analysis. The correspondence between this classification and substrate diameter is virtually perfect (only one misclassification out of 85 oysters). For the clusters based on height above chart datum, 9 specimens, all on intermediate height levels, were misclassified. Orientation with respect to tidal current had 13 misclassifications. Mangrove species seemed to influence form only marginally, if at all.In the study of the size ofCrassostrea cucullata, the length of 956 oysters, growing along two transects were measured, and correlated with several environmental factors. Oyster length was not related to substrate diameter or its orientation with respect to the main current. Length was not influenced by density up to a cover of 70%. For densities higher than 70%, there was a fairly strong negative correlation (r ² = 0.634,n = 217). Length was not correlated with height above bottom (base of the tree) for heights lower than 20 cm, while oysters growing closer to the bottom were smaller. The correlation with height above chart datum was negative but very low (r ² = 0.060,n = 957). However, if all measurements of oysters closer than 20 cm to the bottom, and all from a density of more than 70% cover are deleted from the data set, the correlation with height increased dramatically, the slope still being negative (r ² = 0.859,n = 543).     

Antidiuretic mechanism in Rhodnius prolixus (Stal, 1859) (Hemiptera, Reduviidae)

An antidiuretic mechanism is proposed for Rhodnius prolixus, whose activity is manifested when the diuretic phase has terminated and is maintained until the insect has fed again. Presumably this mechanism acts at the level of the proximal rectal sphincter and is inhibited by ingestion, mechanical distension of the gut and central disinhibition by decapitation. It is suggested that the antidiuretic activity is maintained by the nervous system and is modified when there is distention of the gut or when the nervous signal is interrupted by decapitation. It is demonstrated that the excretion of urine in R. prolixus is not controlled exclusively by the diuretic hormone, but rather that factors not linked to the haemolymph maintain the insects in a diuretic or nondiuretic state.     

Mating behaviour in Moina brachiata (Jurine, 1820) (Crustacea,Anomopoda)

Information on mating behaviour in Anomopoda isavailable for very few species only, though matelocation and recognition certainly play an importantrole in maintaining reproductive isolation betweenspecies. Ephippial females and males of Moinabrachiata were observed in a drop of water under amicroscope for 10–20 minutes. Different combinationsof specimens were used, but copulation was onlyobserved when two males and two ephippial females wereplaced together. Males were very active, and oftentried to grasp a female, whereas females usually madeattempts to escape during the entire period of mating.Three phases were recognized: capture, positioning andcopulation. The male captured the female from thedorsal side, then moved to the ventral side and tooka position with its length axis being perpendicular tothat of the female, forming a sort of cross.Thereafter the pair started rotating around the lengthaxis of the female, while the male pushed thepostabdomen into the females brood pouch. Copulationlasted from 16 to 25 seconds. When different kinds offemales were used, males showed preference forephippial females with an empty ephippium and enlargedovaries. Our results indicate that not only visual andtactile cues may be important in identifying speciesidentity and receptivity of the female, but alsochemical signals.     

A new nematode species (Seuratoidea, Cucullanidae) parasitizing Parauchenipterus striatulus (Steindachner, 1876) (Pisces, Auchenipteridae) in Brazil

A new species of a cucullanid nematode is described, illustrated and compared with Cucullanus brevispiculus Moravec, Kohn & Fernandes, 1993 and C. rhamphichthydis Moravec, Kohn & Fernandes, 1997, two species previously reported as parasitizing freshwater fish in South America. The new species is characterized mainly by markedly short spicules, deirids and excretory pore situated posterior to the oesophago-intestinal junction, presence of strongly sclerotized plates in the oesophastome and oesophagus divided into two distinct portions.     

On the Knowledge of Coprophilus (Zonyptilus) pennifer (Motschulsky, 1845) and Coprophilus (Zonyptilus) marginalis (Reitter, 1894) (Coleoptera,Staphylinidae)

Entomological Review - The type and other extensive material of Coprophilus (Zonyptilus) pennifer (Motschulsky, 1845) and some of its synonyms was examined. Coprophilus (Zonyptilus) marginalis...     

Distribution of Boros schneideri (Panzer, 1796) (Coleoptera, Boridae) in Lithuania

The distribution of the endangered species Boros schneideri was studied by checking the presence of larvae and adults under the bark of dead Pinus sylvestris trees in 13 pine forests in Lithuania. B. schneideri was found in 10 biggest pine forests, the area of which exceeded 20,000 ha. However, it was not detected in smaller isolated forests. In Kazlų Rūda, Šimonys, Pabradė and Rūdiškės forests this species was recorded for the first time. The part of localities in which B. schneideri was found and the percentage of trees with B. schneideri were significantly higher in the main parts of the biggest forests than in satellite or smaller forests. Both these parameters were significantly lower in forests located in the close vicinity of urban territories than in forests further from them. Consequently, the forest size and the distance of the forest from urban territories were found to be of critical importance for the survival and density of the B. schneideri population. These distribution regularities are important for the establishment of protected areas for this species conservation.     

Chromosome numbers in antlions (Myrmeleontidae) and owlflies (Ascalaphidae) (Insecta,Neuroptera)

A short review of main cytogenetic features of insects belonging to the sister neuropteran families Myrmeleontidae (antlions) and Ascalaphidae (owlflies) is presented, with a particular focus on their chromosome numbers and sex chromosome systems. Diploid male chromosome numbers are listed for 37 species, 21 genera from 9 subfamilies of the antlions as well as for seven species and five genera of the owlfly subfamily Ascalaphinae. The list includes data on five species whose karyotypes were studied in the present work. It is shown here that antlions and owlflies share a simple sex chromosome system XY/XX; a similar range of chromosome numbers, 2n = 14-26 and 2n = 18-22 respectively; and a peculiar distant pairing of sex chromosomes in male meiosis. Usually the karyotype is particularly stable within a genus but there are some exceptions in both families (in the genera Palpares and Libelloides respectively). The Myrmeleontidae and Ascalaphidae differ in their modal chromosome numbers. Most antlions exhibit 2n = 14 and 16, and Palparinae are the only subfamily characterized by higher numbers, 2n = 22, 24, and 26. The higher numbers, 2n = 20 and 22, are also found in owlflies. Since the Palparinae represent a basal phylogenetic lineage of the Myrmeleontidae, it is hypothesized that higher chromosome numbers are ancestral for antlions and were inherited from the common ancestor of Myrmeleontidae + Ascalaphidae. They were preserved in the Palparinae (Myrmeleontidae), but changed via chromosomal fusions toward lower numbers in other subfamilies.     

Genetic variation in the soil phthiracarid mite, Steganacarus (S.) magnus (Nicolet, 1855) (Acarida, Oribatida) (Notulae Oribatologicae XL)

Genetic divergence and variability at 14 enzyme loci were examined in and between Italian populations of two edaphic Oribatid (Acarida, Oribatida) species, Steganacarus (Steganacarus) magnus (8 populations) and S. (S.) hirsutus (1 population). The seven populations belonging to S. (S.) magnus can be divided into two groups according to their phenotype, form anomala (A) (MON, ARG, AST, CDO) and form magna (M) (MAL, MAM, RIF) while another can be considered as hybrid between the two preceding groups (ZOC). Genetic identity (I) values between the S. (S.) magnus populations in spite of their morphological differences ranged from 0.977 to 1.000 showing the great genetic similarity of simple local populations while those of S. (S.) hirsutus indicated two distinct morphological species. The genetic distances between all the populations examined were very low despite the ecological differences and geographical distances between the collecting sites. Genetic variability estimates in all the populations of both species were very low when compared to those reported for most arthropods. Some explanatory considerations are suggested.     

On the Synonymy of Coprophilus (Zonyptilus) pennifer (Motschulsky, 1845) (Coleoptera,Staphylinidae, Oxytelinae)

Entomological Review - The type material of several synonyms of Coprophilus (Zonyptilus) pennifer (Motschulsky, 1845) is revised. Both Coprophilus (Zonyptilus) striatipennis (Eppelsheim, 1894) and...     

Multizooidal Budding in Parasmittina trispinosa (Johnston) (Bryozoa,Cheilostomata)

Two principally different wall types occur in the bryozoan colony: Exterior walls delimiting the super-individual, the colony, against its surroundings and interior walls dividing the body cavity of the colony thus defined into units which develop into sub-individuals, the zooids. In the gymnolaemate bryozoans generally, whether uniserial or multiserial, the longitudinal zooid walls are exterior, the transverse (proximal and distal) zooid walls interior ones. The radiating zooid rows grow apically to form “tubes” each surrounded by exterior walls but subdivided by interior (transverse) walls. The stenolaemate bryozoans show a contrasting mode of growth in which the colony swells in the distal direction to form one confluent cavity surrounded by an exterior wall but internally subdivided into zooids by interior walls. In the otherwise typical gymnolaemate Parasmittina trispinosa the growing edge is composed of a series of “giant buds” each surrounded by exterior walls on its lateral, frontal, basal and distal sides and forming an undifferentiated chamber usually 2–3 times as broad and 3 or more times as long as the final zooid. Its lumen is subdivided by interior walls into zooids 2–3, occasionally 4, in breadth. This type of zooid formation is therefore similar to the “common bud” or, better-named, “multizooidal budding” characteristic of the stenoleamates but has certainly evolved independently as a special modification of the usual gymnolaemate budding.     

Electronic structures of collagen model polymers: (Gly-Pro)n, (Gly-Hyp)n, (Ala-Pro)n, (Ala-Hyp)n, (Gly-Pro-Gly)n, (Gly-Hyp-Gly)n, (Gly-Pro-Pro)n, and (Gly-Pro-Hyp)n

In order to investigate the relationship existing between the electronic structures of collagen and its biochemical functions in vivo, the semiempirical CNDO/2 SCF MO calculations were carried out on several model polymers of collagen, (Gly-Pro)_n, (Gly-Hyp)_n, (Ala-Pro)_n, (Ala-Hyp)_n, (Gly-Pro-Gly)_n, (Gly-Hyp-Gly)_n, (Gly-Pro-Pro)_n and (Gly-Pro-Hyp)_n. Geometries of the skeleton of these polymers were assumed to be the same as those of poly(l-proline) I (cis) and II (trans) and the calculations were performed only on infinite polymers in a single chain. The results show that the cis form is always more stable than the trans form for all the polymers treated. This energy difference between the cis and trans forms depends, for example, on the kind of amino acid residue, Gly or Ala, but this could not be seen in the Pro or Hyp residue. The flexibility or mobility of the collagen structure was explained using the energy difference between the cis and trans forms of the polymers, i.e. the cis-trans conversion of the collagen was discussed in connection with the energy difference. The reason why the collagen has the constitution of (Gly-Pro-Hyp)_n is briefly discussed.