Craniological differentiation between European wildcats (Felis silvestris silvestris), African wildcats (F. s. lybica) and Asian wildcats (F. s. ornata): implications for their evolution and conservation

Intraspecific diversification of the wildcat (Felis silvestris), including the European wildcat (F. s. silvestris), the Asian wildcat (F. s. ornata) and the African wildcat (F. s. lybica), was examined based on 39 cranial morphology variables. The samples of free‐ranging cats originated from Britain, Europe, Central Asia and southern Africa, consisting of both nominal wildcat specimens (referred to henceforth as ‘wildcats’) and nominal non‐wildcat specimens (‘non‐wildcats’) based on museum labels. The skull morphology of ‘wildcats’ from Britain and Europe is clearly different from that of ‘wildcats’ of Central Asia and southern Africa. The latter are characterized especially by their proportionately larger cheek teeth. On the basis of principal component, discriminant function and canonical variate analyses, the skull morphology of British ‘non‐wildcats’ is less distinct than is that of British ‘wildcats’ from the skull morphologies of ‘wildcats’ of Central Asia and southern Africa. On the other hand, the skull morphology of southern African ‘non‐wildcats’ is as distinct from those of ‘wildcats’ of Britain and Europe as is that of southern African ‘wildcats’. We suggest that the evolution of the modern wildcat probably consisted of at least three different distribution expansions punctuated by two differentiation events: the exodus from Europe during the late Pleistocene, coinciding with the emergence of the steppe wildcat lineage (phenotype of Asian–African wildcat), followed by its rapid range expansion in the Old World. The second differentiation event was the emergence of the domestic cat followed by its subsequent colonization of the entire world with human assistance. Considering the recent evolutionary history of, and morphological divergence in, the wildcat, preventing hybridization between the European wildcat and the domestic cat is a high conservation priority. © 2004 The Linnean Society of London, Biological Journal of the Linnean Society, 2004, 83 , 47–63.     

Evolution to the extreme: origins of the highly modified apical system in pourtalesiid echinoids

The apical system of the genus Pourtalesia displays a plate architecture that falls so far outside that typical of other echinoids that plate homologies remain problematic. A new approach using the Extraxial–Axial Theory (EAT) that develops homologies for the Echinodermata is proposed. The exploration of apical plate patterns throughout ontogenetic sequences shows that the typical holasteroid pattern found in the youngest specimens undergoes a series of disturbances that result in a multiple disjunction accompanied by isolation or disappearance of certain genital plates. We propose a new interpretation of the apical architecture of the genus that agrees with: (1) the plate addition processes as predicted by the EAT; (2) patterns observed in other genera of the Pourtalesiidae as well as in its sister‐group (plexechinids); and (3) the patterns known from Palaeocene holasteroids. In the context of the EAT, the genus Pourtalesia appears to represent the extreme in a reduction of the extraxial part of the body wall. © 2004 The Linnean Society of London, Zoological Journal of the Linnean Society, 2004, 140 , 137–155.     

An experimental study of the influence of periphytic algae on invertebrate abundance in a Hong Kong stream

1. Small cages (294cm²) containing unglazed clay quarry tiles were used to investigate the influence of periphytic algae on macroinvertebrate abundance in a Hong Kong stream. Algal biomass was manipulated by shading cages with plastic sheets. Individual cages were assigned to one of three treatment groups: unshaded, shaded and deeply shaded. Invertebrate densities and algal biomass within cages were monitored after 23, 37 and 65 days. 2. Multiple-regression analysis revealed that algal biomass, invertebrate morphospecies richness and total abundance declined with greater shading intensity. The responses of individual invertebrate taxa varied: some (especially Trichoptera) were unaffected by shading, whereas grazers (Baetidae, Psephenidae and Elmidae) declined as shading increased. 3. Significant regressions of the densities of individual taxa upon algal and detrital standing stocks in cages had positive slopes, but algal biomass increased during the study while detrital standing stocks declined. Abundance of invertebrates declined or remained rather stable over time. Density increases resulting from a positive association with algae were apparently offset by declines in abundance correlated with reductions in detritus. 4. Declines in algal biomass were associated with greater shading to which animals may respond directly. To uncouple the link between scarcity of algae and reduction of light intensity, the plastic covers on two groups of cages (deeply shaded and unshaded) which had been placed in the stream for 28 days were reversed so that cages which had been shaded became unshaded and vice versa. The cages were recovered on day 33, Only Coleoptera demonstrated a positive association with atgae inside cages; no relationship between population densities and algal biomass or light intensity was apparent for other taxa. However, the design may have been confounded by deposition of sediment in the cages (due to declining stream discharge) which reduced population densities of colonizers. 5. This study documents changes in invertebrate abundance and morphospecies richness in response periphyton and detritus standing stocks within patches. Summation of such responses may account for observed variations in benthic communities among Hong Kong streams which differ in the extent of shading by riparian vegetation.     

Does the tsetse parturition rhythm have a circadian basis?

Abstract. Under an LD 12:12h photoregime at constant temperature, parturition in Glossina morsitans centralis is a gated event occurring late in the afternoon. When flies are switched to continuous light the rhythm quickly dampens, but its persistence for at least two 24-h cycles beyond the final scotophase suggests the rhythm has a circadian basis. A weak rhythm appears after 7 days of continuous light, perhaps in response to the daily disturbance caused by feeding. Return of the flies to LD 12:12h restores the rhythm after exposure to a single scotophase.     

An Assessment of Gibberellin Structure-activity Relationships

Information on the biological activities of gibberellins (GAs)in the barley aleurone, Tangin-bozu dwarf rice, dwarf pea, lettucehypocotyl and cucumber hypocotyl bioassays is reviewed and discussedin the context of GA structure-activity relationships. The barley aleurone bioassay exhibits a limited response toGAs and it is suggested that this may be because the aleuronecells are able to carry out few GA interconversions. Consequentlyactivity is determined by the degree of compatibility betweenthe GAs and a receptor site. In this assay high biological activityis associated with GAs having a 3ß-hydroxy--lactonestructure. This activity is substantially enhanced by the additionalpresence of a 13-hydroxyl group. The substitution of a -lactoneor a -lactol for a -lactone results in reduced activity while3ß,13-dihydroxy GAs with either 20-carboxyl or 20-methylfunctions are completely inactive. The Tanginbozu dwarf ricebioassay responds to many more GAs than the barley aleuronesystem possibly because the rice seedlings can carry out extensiveGA interconversions. Under these circumstances GAs that areinactive per se can be metabolically converted to active forms.There is no interaction between the 3ß- and 13-hydroxyfunctions of GA molecules in the rice assay. Activity appearsto be determined by the degree oxidation of the C-20 group.The order of activity is usually -lactone > -lactol >-lactone > methyl > carboxyl. It is suggested this mayindicate that in rice seedlings C₂₀-GAs are converted to C₁₉-GAsvia a Baeyer-Villiger type oxidation. Activity in the dwarfpea bioassay is dependent upon GAs possessing both 3ß-and 13-hydroxyl groups and is again related to the state ofoxidation at the C-20 locus. In the lettuce bioassay activityis restricted to GAs with a -lactone function. In some instancesa -lactone, but not a -lactol, can substitute effectively. Thismay imply that the applied C₂₀-GAs are not converted to C₁₉-GAsand that the response to the -lactone results from the six-memberedring mimicking the -lactone at the receptor site. Only GAs havinga 19,10 or a 19,20 lactonic bridge show substantial activityin the cucumber bioassay. The additional presence of eithera 12- or a 13-hydroxyl group severely reduces activity.     

Site of Nitrogenase Activity in the Blue-Green Alga <Emphasis Type="Italic">Anabaena</Emphasis> sp. L-31

MANY blue-green algae fix nitrogen, assimilate carbon dioxide and evolve oxygen and as algal nitrogenase is inhibited^1–3 by high oxygen pressure, enhanced nitrogen fixation accompanying photosynthesis is surprising. Heterocysts do not contain⁴ or have comparatively less amounts^4–7 of photosystem II (PS II) pigments, which are responsible for the evolution of oxygen. This tends to favour the suggestion of Fay et al.⁸ that these cells are the sites of nitrogenase activity. Until now, however, attempts at obtaining unequivocal evidence for heterocysts as principal loci for nitrogenase activity have yielded conflicting results. Stewart et al.⁷ first demonstrated nitrogenase activity in heterocysts incubated aerobically, a finding confirmed by Wolk and Wojciuch⁹ and Van Gorkom and Donze¹⁰. By contrast, Smith and Evans^3,11 and Kurz and La Rue¹² reported results favouring vegetative cells as the major site of nitrogenase activity. Other evidence^2,13 showed high nitrogenase activity in cell-free preparations of Anabaena cylindrica and the non-heterocystous alga Plectonema boryanum strain 594.     

Helical Structure of <Emphasis Type="Italic">Myxicola</Emphasis> Axoplasm

Dissection and polarizing microscopy of the giant axon of Myxicola reveal fibrous protein arranged in three levels of helical configurations, all of which may arise from torques about the axes of individual proteins.     

Synthesis of Carcinoembryonic Antigen <Emphasis Type="Italic">in vitro</Emphasis>

NORMAL and neoplastic mammalian cells cultivated in vitro retain a number of functions that characterize their cellular origin, even after extensive passage¹. It therefore seems reasonable to expect that cell products such as tumour-associated antigens could, if present from the outset, be retained in a demonstrable state when the tumour cells are cultivated outside the original host organism. The discovery by Gold and Freedman² of an antigenic substance specific for entodermally-derived cancers of the digestive system, carcinoembryonic antigen (CEA), provides a suitable candidate for studying one such property related to a particular type of human cancer. It has been proposed, however, that tumour-specific antigens such as CEA are not indigenous to the tumours, but are glycoproteins produced elsewhere in the body and coating the tumour cells secondarily³. If this were the case, then human colonic cancer cells in long-term propagation in vitro should not synthesize this material. We now present evidence to the contrary.     

Involvement of <Emphasis Type="Italic">H</Emphasis>-2 Locus in a Multigenically-determined Immune Response

IT has been known for a number of years that specific immune responses can be under genetic control. In some cases the immunological phenotype is controlled by a single Mendelian genetic factor^1–3, while in other cases a more complex mode of inheritance determines the animal's ability to mount a specific immune response^4–7. An intriguing feature of this line of investigation is that in many cases a gene controlling a specific immune response is genetically linked to a histocompatibility locus^3,8–13. We now report that a specific immune response which has been shown to be under complex genetic control⁷ can be explained by the segregation of two genetic loci, one of which is closely linked or identical to the H-2 locus.