A classic compilation

Kurtén, B. 1988: On Evolution and Fossil Mammals . XVII + 301 pp. Columbia University Press. ISBN 0–231–05868–3. Price: USD40.00 (bound).     

The Whales of August

de Muizon, C. 1988: Les Vertébrés Fossiles de la Formation Pisco (Pérou) III. Les Odontocètes (Cetacea, Mammalia) du Miocène . 244 pp. Institut Fran¸ais d'études Andines et Institut de Paléon-tologie du Museum National d'Histoíre Naturelle. éditions Recherche sur les Civilisations, A.D.P.F., Paris. ISBN 2–86538–187–0, ISSN 0291–1655. Price: 289.00 FF (paper).     

Evolution of morphological differences with moderate genetic correlations among traits as exemplified by two flycatcher species (Ficeduia; Muscicapidae)

Theoretical work on multivariate evolution predicts that genetic correlations can act to constrain the rate at which new adaptive peaks are reached, but there is very limited empirical information available on this issue so far. To evaluate the importance of genetic correlations for evolutionary change, we studied the morphological differences between two flycatcher species (Ficeduia albicollis and F. hypoleuca) using both univariate and multivariate quantitative genetic models. Comparison of the results obtained using these different models revealed that even relatively low genetic correlations between traits will considerably increase the net selection forces needed for evolutionary changes in morphology. In particular, the divergence in wing and tail length, which are positively genetically correlated, would require a considerable amount of antagonistic selection. Because of the genetic correlations, strong selection will be needed to retain certain traits unchanged while others are changing. Based on these results, we argue that it is unlikely that small morphological differences such as between these two species could have evolved during a short (200 years) time period, i.e. the period of sympatry of these species in Sweden. These findings support the hypothesis that even relatively low genetic correlations may constrain short-term adaptive evolution in natural populations.     

High Capacity Chemisorbents for Protein Immobilization

IMMOBILIZED proteins have been used successfully for the purification and isolation of specific natural products, particularly proteins such as antigens, antibodies, enzymes and enzyme inhibitors^1–3. They have also been used for the commercial production of biochemicals⁴ and as models for imitating enzymes bound to cellular components in vivo.     

Cytoskeleton and PCH-Induced Pigment Aggregation in Macrobrachium potiuna Erythrophores

Herein we report the effects of microtubule- and actin-like filament disrupting drugs, as well as the microtubule stabilizer taxol, on PCH-induced pigment granule aggregation within erythrophores of the freshwater crustacean Macrobrachium potiuna. Dose-response curves (DRCs) to the pigment-concentrating hormone PCH were determined under control and experimental conditions to evaluate the effects elicited by the cytoskeleton-affecting drugs. Colchicine, at temperatures 22°C and 4°C, and vinblastine significantly inhibited the aggregating response to PCH and affected the dynamics of the process, as shown by the change in the slope of the regression curve calculated from the DRCs. Lumicolchicine, a colchicine analogue with no affinity for tubulin, also inhibited pigment migration, though no change in the slope of the regression curve was observed. The inhibitory effects of lumicolchicine demonstrate that changes in sites other than cytoskeleton, such as membrane permeability, may also cause a decrease in the PCH-induced aggregating responses and that the colchicine effects may result from its action on cellular sites additional to the cytoskeleton. Taxol, a microtubule stabilizer, did not affect the DRC to PCH, and DMSO improved the PCH-evoked responses, pointing out to the maintenance of tubulin in the polymerized state as the appropriate condition for aggregation. Cytochalasin B, an actin-like filament disrupter, diminished the aggregating responses to the hormone, with no change in the slope of the regression curve, indicating that these elements take part in the process and that cytosolic calcium rise, sol/gel transformations and endoplasmic reticulum motility may well play an important role in granule migration. It is suggested that microtubules are steadily polymerized as a requirement for pigment aggregation and that the process is biphasic, the initial phase being dependent on the microtubule integrity.     

Studies of fossil hyaenas: affinities of Lycyaenops rhomboideae Kretzoi from Pestlorinc, Hungary

The holotype of the lower-middle Pliocene hyaenid Lycyaenops rhomboideae is redescribed and compared with contemporaneous hyaenids of the genera Lycyaena, Hyaenictis, Chasmaporthetes and Pliocmcuta. These comparisons show that the material represents a valid and distinct genus and species. The genus Lycyaenops is referred to the Chasmaporthetes lineage on the basis of its two-cusped m 1 talonid with reduced entoconid, reduced posterolingual cingulum cusp on p4 and premolar accessory cusps set in a straight line. It is distinguished from all other genera of that lineage by its smaller premolar accessory cusps, broad premolars and squared-off and very broad posterior premolar shelves. The species L. silberbergi, previously assigned to Chasmaporthetes, is also referred to Lycyaenops. It differs from L. rhomboideae in its greater development of the premolar accessory cusps and less developed posterior premolar shelves, but shares the broad, squared-off premolars. The interrelationships of Hyaenictis, Chasmaporthetes and Lycyaenops are at present best described by an unresolved trichotomy, with Lycyaena as its sister taxon.     

Phylogeny and classification of the extant basal lineages of the Hymenoptera (Insecta)

The phylogeny of the basal hymenopteran lineages, including representatives of all ‘symphytan’ families, is anal; In total, 236 morphological characters were scored for 44 exemplars, including six outgroup, two xyelic tenthredinoid, five pamphilioid, three cephoid, five ‘siricoid’, one orussid, and six apocritan taxa. The datas analysed with parsimony under equal weights and under implied weights. The monophyly of the Hymenopte strongly supported but the sistergroup of the Hymenoptera cannot be identified with confidence. The relations of the ‘symphytan’ lineages are Xyeloidea +(Tenthredinoidea+ (Pamphilioidea + (Cephoidea + (Ariaxyelic (Siricidae + (Xiphydriidae +(Orussoidea+Apocrita))))))). Many of the relationships between the superfamilies, especially in the basal branching pattern, are only weakly corroborated. The monophyly of most superfamilies is supported, and all may be monophyletic except the ‘Siricoidea’, which is clearly paraphyletic. It is difficult to di whether the Siricidae or the Anaxyelidae are the closest relatives of Xiphydriidae + (Orussoidea + Apocrita). support for the sistergroup relationship between the Orussoidea and the Apocrita is substantial, putative apomorphies being provided by most character systems. There is also good evidence in favour of the monophj the Apocrita. The internal phylogeny of the Tenthredinoidea differs considerably from the results of earlier anal The Blasticotomidae are the sistergroup of the Tenthredinoidea s.s. Relationships at the base of the Tenthredini s.s. are weakly supported. It is uncertain whether the Tenthredinidae are monophyletic or comprise a 1 paraphyletic grade within the Tenthredinoidea s.s. The Diprionidae may be the sistergroup to Cimbicidae +(Argidae+ Pergidae). Most relationships within the Cimbicidae + (Argidae + Pergidae) clade are corroborated, with the exception of the monophyly of the Argidae. It is proposed to elevate the Anaxyelidae the Xiphydriida both to superfamily status. The family‐level classification of the Tenthredinoidea will probably have to be changed, but this must await further clarification of the phylogeny of this superfamily.