Analysing the patterning of a sequence of discrete behavioural events

Existing techniques for analysing the organization of behavioural events are discussed. Cluster analysis, mutual replaceability, ‘melody’ detection and Markov analyses are examined in order to discover the validity and usefulness of the concepts searched for by each technique, and the mathematical and statistical background of the techniques is scrutinized. Some new techniques, designed to search for and detect possible important sequential organization patterns, are described in the light of the previous criticisms. Of these techniques, the Pre-post-state Histogram (PPSH)—a multi-order Markov graphical analysis—would appear to be the most important for future work, especially when used in conjunction with the other techniques described.     

Secretion of lysosomal enzymes by human placental villi in vitro

Summary Chorionic villi from first trimester and term human placentas have been incubated in vitro and shown to release the lysosomal enzymes, -hexosaminidase, -glucosidase and -gluctlronidase. There was negligible release of the cytoplasmic enzyme, lactate dehydrogenase, under the same conditions. The first trimester villi released proportionally more of their lysosomal enzyme content than did the term villi. Extracellular levels of -hexosaminidase were raised and those of -glucosidase and, -glucuronidase were lowered when tissue was incubated with 1 M colchicine, suggesting that microtubules are involved in the control of lysosomal enzyme release from placental villi.     

Response of deep-sea benthic foraminifera to Miocene paleoclimatic events, DSDP Site 289

Changes in the Miocene deep-sea benthic foraminifera at DSDP Site 289 closely correlate to the climatically induced variations in deep and bottom waters in the Pacific Ocean. In early Miocene time, oxygen and carbon isotopes indicate that bottom waters were relatively warm and poorly oxygenated. Benthic foraminiferal assemblages are characterized by various species inherited from the Oligocene. Expansion of the Antarctic icecap in the early middle Miocene, 14–16 m.y. ago, increased oxygen isotope values, produced cold, more oxygenated bottom waters and lead to a turnover in the benthic foraminifera. An Oligocene—early Miocene assemblage was replaced by a cibicidoid-dominated assemblage. Some species became extinct and benthic faunas became more bathymetrically restricted with the increased stratification of deep waters in the ocean. In mid-Miocene time, Epistominella exigua and E. umbonifera, indicative of young, oxygenated bottom waters, are relatively common at DSDP Site 289. Further glacial expansion 5–9 m.y. ago lowered sealevel, increased oceanic upwelling and associated biological productivity and intensified the oxygen minima. Abundant hispid and costate uvigerines become a dominant faunal element at shallow depths above 2500 m as E. umbonifera becomes common to abundant below 2500 m. By late Miocene time, benthic faunas similar in species composition and proportion to modern faunas on the Ontong-Java plateau, had become established.     

A cytological basis for the separation of Geropogon from Tragopogon (Compositae: Lactuceae)

The single species ofGeropogon, G. hybridus (L.) Schultz-Bip., is sometimes submerged in the morphologically similarTragopogon. A comparative study of the karyotypes ofGeropogon andTragopogon sensu stricto clarified their relationship. The karyotype ofG. hydridus (2n=14) was compared with that ofT. dubius Scop. (2n=12). The karyotypes are distinct, offering a compelling reason to recognizeGeropogon as a separate genus.     

Effect of food-deprivation on rat pancreatic islet cells

Somatostatin, insulin and glucagon concentrations in rat pancreas were measured following various intervals of food-deprivation. Tissue concentrations, as measured by radioimmunoassay, were correlated with A-, B-, and D-cell number and size using a scanning integrating image analyzer (Quantimet 720). Alterations in total islet hormone content were not correlated to changes in size or distribution of cells. This implies that changes in tissue content reflect changes in turnover of peptides rather than changes in cell size or number.