Occurrence of Bucephaloides gracilescens metacercariae in three species of gadoid fish

Bucephaloides gracilescens metacercaria is a common encysted trematode parasite of whiting, Merlangius merlangus (L), haddock, Melanogrammus aeglefinus (L), and hake, Merluccius merluccius (L), in the Irish Sea. The incidence of infection over an 18-month period was uniformly high (whiting, 95%; haddock and hake, 100%). The major site of infection in all three hosts was the cranial fluid surrounding the brain. Large numbers of cysts were also found embedded in the spinal nerves posterior to the anus in haddock and hake and in the auditory capsules in whiting and haddock. Other sites of infection included the spinal canal, cranial nerves (V, VII, VIII, X), eye muscles, orbits and nasal region. Results are discussed in the light of previous records of gasterostome trematodes in the Gadidae.     

Cranial morphology of the early tertiary Phenacolemur and its bearing on primate phylogeny

An early Eocene skull of the paromomyid Phenacolemur, a plesiadapoid primate, is described with particular emphasis on the ear region. The auditory bulla is composed of the petrosal and of a large ectotympanic plate which is outside of the bulla. The preserved morphology of the middle ear is distinctly more primitive than that of the older Plesiadapis. It cannot be determined with certainty whether Phenacolemur had the carotid circulation enclosed in bony tubes or not. The auditory bulla of early primates and relevant living ones is discussed and it is suggested that an extrabullar ectotympanic, as seen in all non-lemuriform fossil and extant primates, was probably the primitive ordinal condition, rather than the intrabullar ring-like ectotympanic in the Lemuriformes. Aspects of the carotid circulation are discussed as they pertain to the relationship of early Tertiary primates, living Tarsiiformes, Lemuriformes and Lorisiformes.     

Ultrastructure of the spermatozoon ofElenchus japonicus and its bearing on the phylogeny of strepsiptera

The fine structure of the mature spermatozoon of the strepsipteranElenchus japonicus Esaki and Hashimoto (Elenchidae) is described using transmission electron microscopy. The spermatozoon was seen to have an elongated head, a tail containing a 9 + 9 + 2 axoneme, two mitochondrial derivatives and two accessory sheaths. The monolayered acrosome is conical in shape while the nucleus exhibits an internal channel of uncondensed chromatin. The tail is long, and in its final portion, the axoneme, loses its elements progressively. These results are compared with the sperm ultrastructure ofXenos moutoni De Buysson (Stylopidae) and with those of other insect orders, particularly the Coleoptera.     

The evolution of the amphibian lateral line system and its bearing on amphibian phylogeny

In modern amphibians that are aquatic the lateral line system is organized, by order, as follows: caecilians have electroreceptive ampullary organs and single rows of mechanoreceptive neuromast organs; generalized anurans have single rows of neuromasts that divide in a transverse plane to form secondary neuromasts or stitches, they do not have ampullary organs; generalized urodeles have ampullary organs, transverse stitches, and double or triple rows of neuromasts. Fossil evidence indicates that early amphibians had both ampullary organs and single rows of neuromasts embedded in bone. With time, receptors became epidermal in all three orders. Modern caecilians have retained the primitive receptor arrangement. I propose that the common ancestor of anurans and urodeles had transverse stitches, and that this character allies these two groups. Subsequent to the anuranurodele split, anurans lost their ampullary organs, perhaps concomitant with developing specializations for herbivory. Urodeles developed orthogonal neuromast couplets und triplets. In modern anurans und urodeles, transverse stitches are correlated with pond dwelling, while ampullary organs are correlated with carnivory, suggesting that the anuran-urodele ancestor(s) was a (were) pond-dwelling carnivore(s).     

Haploid meiosis and its bearing on the phylogeny of pearl millet,Pennisetum typhoides stapf et hubb.

Meiotic chromosome associations in a spontaneously originated haploid plant of pearl millet have been studied and their phyletic significance discussed. Chromosome pairing could be observed at pachytene and diplotene. Out of a total of 285 PMC's studied at diakinesis-metaphase 1, 43 showed one bivalent and 7 had two bivalents per cell. Both rod- and ring-bivalents were observed. Apart from synapsis accompanied by chiasma formation, close associations of univalent chromosomes were observed. Out of 150 cells without true bivalents, 41 showed 1 s-s association and five, 2 s-s pairs per cell. On the basis of the realization of a maximum of two bivalents per cell, as also of a maximum of 2 s-s pairs, it has been inferred that the chromosome complement ofP. typhoides (n=7) has evolved from a basic set ofn=5 chromosomes. Other available evidence supporting this inference is also discussed.     

The palatine bone and its associations in gadoid fishes

The articulation of the palatine bone in gadoid fishes has been thought of as a specialization of that group. It is shown that there are, in fact, three principal types of articulation, two of which are shared with other gadiform groups. The type of palatine articulation in other paracanthopterygians is briefly described and compared with that of various acanthopterygians. The supposed relationships of some gadoids are commented upon in the light of the specialized nature of some types of palatine articulation.     

Spinal nerves and their bearing on,salamander phylogeny

Examination of the vertebral columns of representatives of all families of salamanders revealed that, in contrast to the condition found in most other vertebrates, salamander spinal nerves often pass through foramina in the vertebrae. Two kinds of spinal nerve foramina were found: those in the anterior halves of vertebrae, and those in the posterior halves. In addition, many salamanders retain intervertebral nerves. However, within each family or, in a few cases, subfamily there is a characteristic pattern of spinal nerve-vertebral relationships. The first spinal nerve of all salamanders exits through a foramen in the anterior half of the atlas. All more posterior nerves are intervertebral in the families Cryptobranchidae, Hynobiidae and Proteidae. The posterior caudal nerves exit through the posterior halves of the caudal vertebrae in the family Amphiumidae, while in the subfamilies Dicamptodontinae and Rhyacotritoninae all post-sacral nerves exit through the posterior halves of the vertebrae. All but the first three nerves exit through posterior foramina in the family Plethodontidae and the subfamily Ambystomatinae, while all but the first two nerves pass through posterior foramina in the families Salamandridae and Sirenidae. Several fossil salamanders were also examined. These showed that the amphiumid and dicamptodontine-rhyacotritonine nerve patterns had evolved by the Late Cretaceous, and the sirenid pattern had probably evolved by that time. Other Cretaceous genera associated with the Ambystomatoidea still possessed the primitive intervertebral pattern. Using spinal nerve patterns and several other previously described morphological characters, a new hypothesis of the phylogeny of recent and fossil salamanders is presented and compared to earlier proposed phylogenies of the group. A new classification of salamander families is presented.     

The distribution of Australian relict plants and its bearing on angiosperm evolution

The distribution of relict plants in the Australian flora shows a bimodal distribution of genera with relict vegetative characters and a unimodal distribution centred on N.E. Queensland for floral characters. Archaic features of the vegetative group link them with the Glossopteridae of Permian age. The geophysical history of the continent is reviewed and indicates only minor climatic changes since the Permian, which would permit the survival of primitive vegetative features. The bimodal distribution of this group is accounted for by the Cretaceous marine invasion of the continent and the unimodal distribution of the floral relicts by a preponderance of genera of Indo-Malaysian affinity, which could not have entered Australia until contact was made with New Guinea about 45 m. y. B.P. Two different cycles of evolutionary diversification are responsible for the two elements. Vegetative features of the Proteaceae relate to the Glossopteridae and are supported by Permian fossils scarcely distinguishable from modern leaves of Epacridaceae. If recent discoveries of Glossopteris fructifications are accepted as pro-angiosperms, it is shown that some anomalies in the vascular supply to the androecium in the Proteaceae can be accounted for.