A recent discussion of the evolution of the amniotic egg (Laurin and Reisz, 1997) was criticized by Wilkinson and Nussbaum (1998), and these criticisms provoked a rebuttal (Laurin et al., 2000). Here we show that the objections raised by Laurin et al. (2000) do not substantiate the conclusions of Laurin and Reisz (1997). Wealso discuss additional evidence on the ancestral ontogeny of caecilians from the literature. This evidence is inconsistent with the view that extended embryo retention is the ancestral condition for caecilians and that it is a parsimonious interpretation of the condition of the ancestral amniote as argued by Laurin and Reisz (1997) and by Laurin et al. (2000). The available data are more consistent with the traditional hypothesis that the amniotic egg originated as an adaptation of eggs to the terrestrial environment. We also discuss problems in the definition of ontogenetic characters reflecting variation with respect to extended embryo retention, and we present new observations on the early development of the caecilian Gegeneophis ramaswamii Taylor. 相似文献
Summary Marking experiments, seasonal variations in the population density and observations on the breeding cycle indicated that healthy adult Littorina saxatilis tenebrosa (Mont.) migrate down to the lower supralittoral fringe in order to give birth to the young in July–August and in January–February. The young and adults then migrate up towards the upper supralittoral fringe. Specimens infected with Parvatrema homoeotecnum, unlike those infected with two other digenean species investigated, migrate in the same way as healthy specimens. This ensures that although initial infestation takes place in the lower supralittoral fringe, parasitized specimens occur throughout the supralittoral fringe. Only juvenile hosts, below 7·0 mm long and usually below 5·0 mm long are infected, highest percentages occurring in specimens measuring 1·1–2·0 mm long. The seasonal variations in percentage infection are corellated with the breeding cycle, growth, mortality and migration of the host. 相似文献
1. A morphological study of five body regions of the Lepidoptera has been made, these being (a) the radial system of the mesothoracic wing, (b) the mesothoracic sternopleural region, (c) the ventral thoraco-abdominal articulative (and adjacent) structures, including the integumental components of the tympanum where present, (d) the dorsal thoraco-abdominal articulation, etc., and (e) the metathoracic furca or endosternite. These regions were selected because the nature of the variation they exhibit suggested that, of the much larger number of regions primarily investigated, they are the most likely to provide information on the evolution of the higher taxa in the order. None of these regions had been investigated at all fully previously, and therefore a considerable amount of basic morphological study was necessary as a preliminary to phylogenetic discussion. This morphological work has been extended to include the primitive Lepidoptera (with the Trichoptera) in the case of the mesosternopleural region, and in the regions of thoraco-abdominal articulation, in order to clarify basic homologies where these were obscure in the Ditrysia.
2. Included also in the preliminary morphological treatment are two other body regions, the variation of which is not complex, and can be more briefly described. These regions are the prothoracic sclerites and the metanotal subdivisions—both of these showing interesting variation throughout the order which can be easily interpreted from the phylogenetic standpoint.
3. Following reference to the basic morphology of each region studied, a broad outline of the evolutionary dynamics of each character complex is given in order to provide a basis for discussion of the evolutionary trends manifested within the superfamilies.
4. In sections four and five of this work, the character complexes which were the subject of morphological study earlier are examined further with regard to their dynamics as manifested within each of the Ditrysian superfamilies. The formation of the concepts which are outlined here is based on consideration of all information derivable from all of these character complexes along with previously published information on other aspects of Lepidopterous anatomy. Resulting from this, a re-organization of the superfamilies has been possible on a phylogenetic basis. The chaotic state of the past literature on the classification of the Lepidoptera, the result of superficial taxonomic work, renders the comparison of the present system with previous ones clearly impossible within the scope of the present paper, but it is noted that many of the superfamily groupings do not differ very widely from those in some of the more comprehensive early studies, such as Forbes (1923). Through lack of material, no radical re-organization of the primitive Ditrysian superfamilies included in the Tinaeoid complex has been attempted, and for the same attempting to convey a very great deal of information by means of varied labelling of the two components of the suture. Reference both to the text, and to the figures given in the introductory (morphological) section of this paper, should however, enable anyone to appreciate these factors from the figures given. (3) Abbreviations used with reference to wing veins and pupal tracheae follow the standard Comstock-Needham system, apart from the identification of Cu2, which follows Tillyard's (1969) interpretation.
Note also that a few of the less common structures have been explained with the captions to the figures. 相似文献