Redescription of a brooding nemertine,Cyanophthalma obscura (Schultze) gen. et comb.n., with observations on its biology and discussion of the species of Prostomatella and related taxa*†

A new genus, Cyanophthalma, is erected with the type species Tetrastemma obscura Schultze, 1851. Cyanophthalma obscura is transferred from Prostomatella and is redescribed from observations of more than 300 living specimens and serial sections of 59 specimens from the northeast coast of North America. Comparison is made with serial sections of C. obscura from the Baltic and with serially sectioned specimens of three other described species of Prostomatella. Two of these, P. enteroplecta and P. merula, do not fit either genus and are provisionally placed in the aggregate genus Tetrastemma, whose present diagnosis they do fit. Prostomatella remains with only its type species, P. arenicola. Amphiporus cordiceps is also transferred to Cyanophthalma. Some of the characters that form the basis for classifying Monostilifera are assessed for phylogenetic significance. Cyanophthalma obscura in Nova Scotia lives in salt marshes. Young are brooded through the winter while ice covers most of the marsh.     

Life-history patterns in British Umbelliferae: a review

British Umbelliferae form a natural cohesive taxon, having patterns of habitat distribution, reproductive biology and life-history that distinguish them from other British dicotyledons. They are usually found in open sites, and are local or rare in distribution. Almost half of British species have the andromonoecious sex habit. Perfect flowers are usually protandrous. The floral composition of umbels, and the pattern of opening of the inflorescence combine to produce a protogynous effect. These have been interpreted as mechanisms which decrease competition for resources between male and female functions in the plant, such that separate maternal and paternal fitness can become optimal. Seeds often require a chilling treatment, alternating temperatures, or a period of after-ripening before they are capable of germination. Schizocarps are of low weight. This seems to relate to the relative openness of habitat wherein unbellifers are found. Patterns of dry matter distribution reflect the life-history strategies of various umbellifer species. Agromyzid leaf miners parasitize the more widespread species, and those which are found in a greater number of different habitats.     

Short note Report of diurnal acid metabolism in two aquatic Australian species of Isoetes

Previous studies have demonstrated the presence of crassulacean acid metabolism in the North American submerged aquatic Isoetes howellii (Isoetaceae). Diurnal changes in titratable acidity and malic acid levels indicate the presence of this pathway in two Australian species of Isoetes.     

Physical and Chemical Properties of Cilia Isolated from Tetrahymena pyriformis*

SYNOPSIS. Cilia devoid of their basal granules and isolated from Tetrahymena pyriformis strain W, by the method of Watson et al. (66) have been characterized in terms of physical, chemical and immunologic properties. The general chemical composition of cilia, based on mean values from these determinations is 66.3% protein, 24.3%“lipid,” 3.7 or 4.8% carbohydrate, and 0.4% nucleic acid. The amino acid composition of cilia includes hydroxyproline and is not significantly different from the amino acid composition of whole cells. Chloroformmethanol extracts of ciliary material contain free amino acids as well as neutral lipids and phospholipids. The lipid composition of cilia also is not significantly different from that of whole cells. Pentose, hexose and small but significant amounts of adenine nucleotide and ribonucleic acid are present. Cilia are a greater stimulus for the production of antibody than an equivalent amount of cellular antigen, and the ciliary antigen is strain specific.     

Ventilation and the origin of jawed vertebrates: a new mouth

This study investigates the origin of jaws by re-assessing homologies between the oropharyngeal regions of Agnatha and Chondrichthyes. In accordance with classical theory, jaws are interpreted as the most anterior arches of the ventilatory branchial basket. It is proposed that jaws first enlarged for a ventilatory function, i.e. closing the jaws prevented reflux of water through the mouth during forceful expiration. Next, they enlarged further to grasp prey in feeding. As they enlarged, the jaws tilted forward, squeezing the ancestral oral cavity in front of them ('old mouth') into a slit between the jaws and lips. Simultaneously, the anterior part of the pharynx behind the jaws was pulled forward and became a 'new mouth' (the buccal part of the buccopharyngeal cavity of gnathostomes). During the transition to gnamostomes, the premandibular cheeks and lips of the old mouth remained in place, and are represented in ammocoete lampreys, chimaeroids, and sharks. The stages in the evolution of gnathostomes, driven by selection for increasing activity, are modelled as: ancestral vertebrate (with unjointed branchial arches) to early pre-gnathostome (jointed internal arches and stronger ventilation) to late pre-gnadiostome (with mouth-closing, ventilatory 'jaws') to early gnathostome (feeding jaws).