Chaetetid growth form and its controlling factors

Chactetid sponge morphology is examined to provide details on growth styles and their controlling factors. Chactetid growth forms range from laminar to domical. bulbous. columnar and complex branching in a variety of sizes. The chactetid skeleton began as a laminar unit comprising growth of many calicles across the substrate at the same time. Several styles of early growth. involving differential calicle growth rates and varying directions of adjacent calicle growth. are recognized. and result in complex arrangements of caliclcs in the skeleton. Despite this. the cross-sectional protile of the gross morphology at any stage of growth is usually a simple outline. implying that internal complexities of calicle development are modulated to produce an optimum cross-sectional outline for the individual chactetid. The morphological range of chactetids is similar to stromatoporoids. some tabulate. heliolitid and colonial rugose corals. some bryozoans. stromatolites. encrusting foraminifera and calcareous algae: the common environmental controlling factors of sedimentation and turbulence profoundly influenced growth form in all these organisms by virtue of their common sessile shallow marine habit. Chactetid growth forms show a general relationship to the environment: columnar and branching forms grew in quiet water. while laminar and domical were better adapted to environments of higher energies. The environmental adaptations of laminar forms. however. remain problematic. because they are found in both high and low energy facies. and interpretation depends strongly on facies study. Also. interpretation of all growth forms is suspected to relate to taxonomic aspects. as has been recognized for other groups. Unfortunately. chaetetid taxonomy is in need of revision. and at present no certain relationship has been demonstrated between taxonomy and growth form. Some modern calcareous sponges with a chaetetiform architccture also show similarities in growth form to fossil types. and may be subject to similar controls. □Chaetetid. calcified sponge. growth form. Pennsyloanian. North America.     

In Vitro Characteristics of the Microsporidian: Enterocytozoon salmonis

ABSTRACT. Enterocytozoon salmonis , an intranuclear microsporidian of salmonid fish, was propagated in vitro using chinook salmon mononuclear leukocytes. Characteristic morphology and infectivity of the cultured parasites were evaluated to determine the effect of in vitro maintenance and passage on the parasites. Cultured parasites developed through several stages from meronts to infectious spores. Parasites obtained from in vitro passages tested up to the 17th subculture, retained their morphological characteristics and pathogenicity for chinook salmon ( Oncorhynchus tshawytscha) . The disease induced by experimental infections with parasites from in vitro cultures was ideniical to that observed in naturally infected chinook salmon. An examination of supernatants obtained from the infected cultures revealed evidence of soluble factor(s) produced by E. salmonis -infected cells that stimulated uninfected target cells in vitro. This observation may explain in part the proliferative disease of hematopoietic tissues which characterizes the disease in infected chinook salmon.     

Cold Acclimation, Freezing Resistance and Protein Synthesis in Alfalfa (Medicago sativaL. cv. Saranac)

Mohapatra, S. S., Poole, R. J. and Dhindsa, R. S. 1987. Coldacclimation, freezing resistance and protein synthesis in alfalfa(Medicago sativa L. cv. Saranac).—J. exp. Bot. 38: 1697–1703. Changes in freezing resistance (percent survival at —10°C), pattern of protein synthesis and translatable mRNApopulation during cold acclimation of alfalfa (Medicago sativaL. cv. Saranac) have been examined. Two days of cold acclimationat 4 °C increased freezing resistance from about 6% to 40%,protein content by 200% and total RNA content by 100%. Acclimationfor longer periods did not cause further increases in freezingresistance, protein content or RNA content. Examination of proteinchanges by sodium dodecyl sulphate-polyacrylamide gel electrophoresis(SDS-PAGE) coupled with protein staining, and by fluorographyof in vivo labelled proteins separated by SDS-PAGE, showed thatseveral proteins are increasingly or newly synthesized duringcold acclimation. Analysis of in vitro translation productsby SDS-PAGE and fluorography shows changes in the populationof translatable mRNAs. It is concluded that in this varietyof alfalfa cold acclimation for only 2 d is sufficient to confermaximum freezing resistance, and that changes in proteins duringcold acclimation are regulated most probably at the transcnptionallevel. Key words: Freezing resistance, protein synthesis, cold acclimation, SDS-PAGE, Medicago sativa L.     

Spatial and temporal variation in the diet of a predaceous stonefly (Plecoptera: Perlodidae)

SUMMARY. 1. Spatial and temporal variation in the diet of the univoltine predatory stonefly, Kogotus nonus , was studied over 3 years in a small Alberta stream to determine whether the relative abundance of prey types in the diet of Kogotus reflected relative prey densities in the stream and whether the variation in absolute feeding rate was related to either prey or predator density.
2. The seasonal shift from sole utilization of Orthocladiinae to inclusion of Baetis in the diet could not be attributed to seasonal changes in prey density, but was probably related to predator size and ability to handle very active prey. Most of the spatial variation in diet could be related to differences in background prey densities, but very high densities of Baetis caused the predator to specialize on this prey.
3. Feeding rate on Baetis . as assessed by per capita gut contents, showed a seasonal shift from a positive correlation with Baetis density in winter to a negative relationship with predator density in spring. This suggested that feeding by small Kogotus is a function of prey density. while feeding by later instars is influenced by between predator interactions such as interference.     

DNA Biosynthesis in Chloroplasts: II. DEVELOPMENTAL VARIATION IN TTP INCORPORATION INTO DNA BY PLASTID EXTRACTS

Incorporation of [³H]TTP into DNA by pea chloroplast extractswas highly dependent on the age of the tissue from which plastidswere prepared. Catalytic activity was greatest in samples from6- to 9-d-old plants; preparations from more mature tissueswere much less effective. Moreover, activity was 3 to 10 timesgreater in younger tissues regardless of whether chlorophyll,protein or plastid number was used as the index of comparison.Enzymes from the first (oldest), second, third, and fourth (youngest)leaves of the same plants were also studied. Again, activitywas 4 to 10 times greater in samples from the youngest tissues.When plastid extracts from older leaves were mixed with thosefrom younger tissues, they did not reduce synthesis. Thus, thedecline in activity does not appear to be due to the productionof an inhibitor during plant development. One explanation forthese data is that enzymes of ctDNA replication, such as DNApolymerase, vary in activity during leaf development; thereforechanges in enzyme levels may be an important factor in controllingchloroplast DNA replication during development. We have alsoexamined the incorporation of [³H]TTP into DNA by isolated intactpea chloroplasts; in general, labelled TTP was less readilyincorporated into chloroplast DNA than was [³H]thymidine. Key words: Chloroplast DNA replication, chloroplast DNA polymerase     

Mimosa pudica: Electrical and mechanical stimulation of plant movements

Thigmonastic movements in the sensitive plant Mimosa pudica L., associated with fast responses to environmental stimuli, appear to be regulated through electrical and chemical signal transductions. The thigmonastic responses of M. pudica can be considered in three stages: stimulus perception, electrical signal transmission and induction of mechanical, hydrodynamical and biochemical responses. We investigated the mechanical movements of the pinnae and petioles in M. pudica induced by the electrical stimulation of a pulvinus, petiole, secondary pulvinus or pinna by a low electrical voltage and charge. The threshold value was 1.3–1.5 V of applied voltage and 2 to 10 µC of charge for the closing of the pinnules. Both voltage and electrical charge are responsible for the electro‐stimulated closing of a leaf. The mechanism behind closing the leaf in M. pudica is discussed. The hydroelastic curvature mechanism closely describes the kinetics of M. pudica leaf movements.