The distribution and abundance of species of Danthonia DC on the New England Tablelands (Australia)

The distribution and percent frequency of the 13 species and one variety of Danthonia recorded on the New England Tablelands were examined in a survey of 110 predominantly pastoral sites. The relationships between site factors and the presence and percent frequency of the different Danthonia species were subjected to canonical correlation analysis. Individual species were found to have particular sets of environmental factors associated with their distribution and percent frequency; a fact not well recognized in the past. The most common factor associated with the abundance of Danthonia was either a long time since the last cultivation or no cultivation at all. Other factors such as altitude, drainage, soil parent material, soil texture and total soil phosphorus status were also of some importance. The six species most commonly recorded throughout the New England Tablelands were D. racemosa RBr, D. pilosa RBr, D. laevis J. Vickery, D. linkii Kunth., D. richardsonii Cashmore and D. tenuior (Steud.) Conert. Of these the first three are ecologically wide species. The first two can coexist with other naturalized species under grazing while D. laevis tends to disappear with disturbance. D. linkii and D. richardsonii require fairly narrow habitat conditions but these conditions and consequently these species are common. Both species respond positively to disturbance. Danthonia linkii increases with cultivation and D. richardsonii colonizes eroded soil surfaces. Danthonia tenuior has more restricted requirements and is not so frequent The other seven species and one variety did not occur often enough for detailed study and the occurrence of two of these species, D. carphoides and D. caespitosa must be considered as rare.     

Field techniques for assessing the reaction of winter wheat cultivars to Septoria nodorum

Methods of assessing the reaction of winter wheat cultivars to Septoria nodorum were compared in nine field trials. Plots were inoculated either by scattering naturally infected wheat debris or by spraying with a suspension of conidia at different growth stages, and were subsequently kept damp by several methods. Disease development was monitored by assessing the percentage cover of different organs by lesions, or by measuring the maximum height of lesions above ground. Major differences between cultivars were evident with all methods of inoculation and assessment, but time of assessment was critical for best differentiation. Inoculation with conidia soon after ear emergence, followed by assessment of lesions on flag leaves and ears, was a simple and effective method. Yield loss due to disease was measured by making comparisons either between inoculated and uninoculated plots, with various degrees of separation, or between inoculated plots with and without fungicidal treatment: the first of these methods was more effective in maintaining a disease differential. Yield loss was positively correlated with severity of disease and there was little evidence that cultivars differed in tolerance of disease. Disease was measured more easily and with less error than yield loss.     

Phyletic coevolution between subterranean rodents of the genus Ctenomys (Rodentia: Hystricognathi) and nematodes of the genus Paraspidodera (Heterakoidea: Aspidoderidae) in the Neotropics: temporal and evolutionary implications

Coevolution was studied in six species of rodents of the genus Ctenomys and their parasitic nematodes of the genus Paraspidodera , collected in Bolivia. Representatives of the families Octodontidae and Caviidae were used as outgroups for the mammals, and nematodes from caviids were used as outgroups of the nematodes from ctenomyids. For the nematodes, quantitative and qualitative morphological characteristics of both males and females and electrophoretic characters of both sexes were used to generate phylogenetic hypotheses of evolutionary relationships of the OTUs occurring in hosts of different species. Concordance estimates of cladograms generated from biochemical—genetic and morphological data of the nematodes show a percentage incongruence (Mickevich-Farris Incongruence Statistic or I _MF) of 8.23% in the character sets. Parsimony mapping, testing concordance of topologies between the trees derived from both analysis of both morphological and biochemical—genetic data indicates an overall agreement of 82.3°. Comparisons of topologies of the host and parasite cladograms, as measured with parsimony mapping, showed 70.8% concordance, indicating substantially more cospeciation than host-switching in the Ctenomys-Paraspidodera host-parasite system. Nematodes of the genus Paraspidodera appear to have invaded the Ctenomys lineage from an origin in caviids sometime before the ctenomyids began to diversify in early Pleistocene time.     

Phylogeny and classification of the Asteroidea (Echinodermata)

Post-Palaeozoic asteroids share a large number of derived characters of the ambulacral column and the mouth frame, and constitute the crown group of the monophyletic group Asteroidea. This crown group is here called the Neoasteroidea (new subclass). The stem species of the crown group lived in the Permian or early Triassic and so the evolution of the asteroids parallels that of the echinoids. Character distribution within the Neoasteroidea, especially morphology of the skeleton, digestive system, larvae and tube feet, allows subdivision into four orders (Paxillosida, Notomyotida, Valvatida, Forcipulatida). The latter three orders possess the synapomorphy of suckered tube feet and are united as the Surculifera (new superorder); the Paxillosida are their primitive sister group. Palaeozoic asteroids represent the stem group of the class, and may be divided into plesions according to the order of appearance of synapomorphies with the crown group. Classification of Palaeozoic asteroids requires much further study. The appearance of new characters within the crown group asteroids, such as suckered tube feet, implies that these were absent in the stem group. The range of life-habits possible in Palaeozoic asteroids can thus be partly deduced from evidence provided by living asteroids. Palaeozoic asteroids are deduced to have lacked suckered tube feet and were presumably unable to evert the stomach; hence they were precluded from life on hard substrates and extraoral feeding on epifaunal organisms. It is suggested that they lived on soft substrates by deposit feeding, scavenging and predation on small benthos.     

EVIDENCE FOR CHEMICAL BORING IN PETRICOLA LAPICIDA (GMELIN, 1791) (BIVALVIA: PETRICOLIDAE)

Specimens of the dead coral-boring bivalve Petri-cola lapicidahave been obtained from Thailand and Jamaica. Although formerlyconcluded to be a mechanical borer, examination of the burrowand the shell strongly suggests chemical boring. Two glandslocated in the inner mantle folds around the antero-ventr'alpedal gape are thought to be involved in this, although onemay secrete the calcareous material cemented to the posteriorshell margin Less specialised petricolids are mechanical borers of stiffmuds, shales and calcareous rocks. A few are nestlers, e.g.,Claudiconcha. As has been recently suggested for other familiesof borers, the Petricolidae constitute another example of theevolution of a specialised chemical borer from a less specialisedmechanically-boring ancestor (Received 20 July 1987;     

Genetic Characterization and Use of a Restriction Fragment Length Variant in the Hypotrichous Ciliate Euplotes crassus1

Two forms of a macronuclear DNA molecule differing in the presence or absence of a restriction endonuclease recognition site have been detected in the hypotrichous ciliate Euplotes crassus. Through a series of genetic crosses the two forms were shown to be allelic, being derived from a single micronuclear genetic locus. This restriction fragment length variant (RFLV) was used as a genetic marker to determine that the migratory and stationary pronuclei generated during mating can be genetically non-identical. In addition, the RFLV was used to investigate the efficiency of processing of the alternate alleles during macronuclear development and their subsequent transmission during vegetative growth. Little or no bias in the processing and/or amplification of the two alleles was observed during macronuclear development. During vegetative growth, however, changes in the relative amounts of the two alleles were observed.