Multiple paternity and mating group size in the European earwig,Forficula auricularia

1. The patterns of multiple paternity among the progeny of females are key properties of genetic mating systems. Female multiple mating should evolve due to direct or indirect benefits, but it may also partly be driven by the encounter rate with different potential mates. 2. In this study this hypothesis was experimentally tested in the European earwig (Forficula auricularia L.) by establishing experimental mating groups that differed in the number of males and females (i.e. density). The number of sires and mean sibling relatedness in each clutch were estimated using microsatellite‐based paternity analysis. 3. As predicted, the mean number of sires per clutch was significantly increased, and sibling relatedness decreased, in the higher density treatment where more potential male mates were available. This change was less than proportional to the number of males in the mating groups, indicating that mechanisms limiting multiple paternity in large mating groups were involved. There were no significant relationships between female reproductive success or male siring success with morphology (body size, weight, and forceps size). 4. The present results show that multiple paternity in F. auricularia clutches is partly determined by the availability of male mates and suggest that this effect is modulated by mechanisms in males and/or females that limit multiple paternity.     

H-Y Antigen Expression in Temperature Sex-Reversed Turtles (Emys orbicularis)

H-Y antigen has been used as a marker for the heterogametic sex and is assumed to be an organizing factor for the heterogametic gonad. In the turtle Emys orbicularis , H-Y antigen is restricted to the female cells, indicating a female heterogamety (ZZ/ZW) sex-determining mechanism. Moreover, the sexual differentiation of the gonads is temperature sensitive, and complete sex reversal can be obtained at will. In this framework the relationships between H-Y antigen, temperature, and gonadal phenotype were studied. Mouse H-Y antiserum was absorbed with blood and gonadal cells of control wild male and female adults, and with blood and gonadal cells from three lots of young turtles from eggs incubated at 25–26°C (100% phenotypic males), at 30–30.5°C (100% phenotypic females), or at 28.5–29°C (majority of females with some males and intersexes). The residual activity of H-Y antiserum was then estimated using an immunobacterial rosette technique. In adults, both blood cells and gonadal cells were typed as H-Y negative in males and as H-Y positive in females. In each of the three lots of young, blood cells were H-Y negative in some individuals and H-Y positive in others. The proposed interpretation is that the H-Y negative individuals were genotypic males (ZZ) and the H-Y positive were genotypic females (ZW). The gonads of these animals were then pooled in different sets according to their sexual phenotype and to the presumed genotypic sex (i.e., blood H-Y phenotype). Testicular cells were typed as H-Y negative in genotypic males as well as in the presumed sex-reversed genotypic females; likewise, ovarian cells were typed as H-Y positive in genotypic females as well as in the presumed sex-reversed genotypic males. These results provide additional evidence that H-Y antigen expression is closely associated with ovarian structure in vertebrates displaying a ZZ/ZW sex-determining mechanism.     

A genomic walking method for screening sequence length polymorphism

We adapted a recently developed nonrestrictional, nonligational genome walking method, Universal Fast Walking (UFW), for detection of length polymorphism in the proximal promoter region of genes. We demonstrate its efficacy at discovering naturally occurring transposition into heat‐shock genes of wild Drosophila and show that it surmounts limitations of simple polymerase chain reaction (PCR) approaches. We further present modifications to the standard UFW protocol and provide some guidelines to improve specificity. Although the resultant banding pattern of a standard UFW can be regarded as a DNA fingerprint, many amplicons result from false priming and not real polymorphisms. We describe ways to distinguish between UFW amplicons and false priming products in a high‐throughput assay.     

Differential Staining Patterns of Heterochromatin in Man

QUINACRINE staining¹ can be used to distinguish between different heterochromatic segments in various organisms and Giemsa staining has been used to locate constitutive heterochromatin in human chromosomes². In using both these techniques on human chromosome preparations we have found certain specific staining properties of hetero-chromatic segments which suggest the existence of at least two different constitutive heterochromatins.     

Pathogenicity of Spiroplasma taiwanense for larval Aedes aegypti mosquitoes

Helical replicative forms, but not the persistent non-replicative forms, of Spiroplasma taiwanense Abalain-Colloc et al. (isolated from the mosquito Anopheles sinensis Wiedemann in Taiwan) were shown to reduce significantly the survival of Aedes aegypti (L.) mosquito larvae reared in 10 ml of water with 0.3 ml of S.taiwanense suspensions added on days 0 and 3. The suspensions contained, respectively, helical forms at a concentration of 10(9) Colour Change Units (CCU)/ml and persistent forms at 10(6) CCU/ml. It is suggested that S.taiwanense, or toxins produced from it, are potentially useful for use in integrated mosquito control programmes.     

Quantitative biochronology of Devonian ammonoids from Morocco and proposals for a refined unitary association method

Monnet, C., Klug, C., Goudemand, N., De Baets, K. & Bucher, H. 2011: Quantitative biochronology of Devonian ammonoids from Morocco and proposals for a refined unitary association method. Lethaia, Vol. 44, pp. 469–489. Based on a rich dataset, the biostratigraphy of the late Emsian and the Eifelian (Early–Middle Devonian) ammonoids from the Moroccan Tafilalt is re‐evaluated. We processed this dataset (comprising 53 species from 15 sections) with the unitary association method (UAM), by means of the UA‐graph freeware. This led to the construction of a sequence of 17 UAs (maximal sets of actually or virtually coexisting taxa), which are grouped into 10 laterally reproducible association zones. This biostratigraphical subdivision of this interval is in some parts finer than the classically used empirical stratigraphical scheme and than a previous graphic correlation analysis. It enabled us to measure regional ammonoid diversity of this interval in detail. The UAM is a powerful biochronological method, which benefits from complementary tools to analyse conflicting inter‐taxon stratigraphical relationships inherent to complex biostratigraphical datasets. In cases of under‐constrained superpositional relationships between the taxa, the UAM can yield results, which are not parsimonious in terms of reconstructed virtual coexistences. We suggest several additions to complement the algorithmic steps of the method. The most important is the exhaustive or heuristic reconstruction of possible solutions resolving the observed biostratigraphical contradictions (conflicting inter‐taxon superpositional relationships and cycles between maximal cliques) and the selection among the solutions of the most‐parsimonious one(s) in terms of reconstructed virtual coexistences. Multiple equivalent results may then be processed with standard consensus techniques. Finally, the robustness of the results can be tested by bootstrapping methods to provide confidence estimates on the ranges and associations of studied taxa. □Ammonites, Anti‐Atlas, biostratigraphy, correlation, zonation, diversity.     

Stolidobranch ascidians from the tropical western Indian Ocean

Coastal ascidians collected over two centuries from Suez to Mozambique have been successively deposited in the MNHN and are now described and figured. Some of them were already known from the Indian Ocean, others are common to the Pacific, and some others are new species. Even though the present taxonomic work notably increases our knowledge of the tropical eastern African coast, it comprises so many miscellaneous collections from such distant points that it can only begin to suggest the diversity of ascidians there. © 2002 The Linnean Society of London. Zoological Journal of the Linnean Society , 2002, 135 , 65–120.