Distributions of Ephemeroptera, Plecoptera, and Trichoptera of three maritime catchments differing in pH

1. Two broad-scale environmental influences affecting species of Ephemeroptera, Trichoptera and Plecoptera inhabiting riffle habitat of three study catchments in New Brunswick and Nova Scotia were stream size-temperature-related variables and acidity-related variables. 2. Species richness was most affected by acidity in tributaries of intermediate size <0.001<0.1m³s^?1). 3. Of the three insect orders investigated, mayfly species richness was affected most by acidity, and stonefly species richness affected least by this factor. 4. Zoogeographical isolation of the Nova Scotian catchments resulted in absence of some species of low general abundance, but these species had little influence on the site classification by TWINSPAN analysis. 5. Predaceous stoneflies were collected in greater numbers from circumneutral sites and predaceous caddisflies in greater numbers from the Nova Scotian sites. 6. Although the Nova Scotian catchments have probably been historically acidic, due to high concentrations of organic acids, pH currently limits the distributions of many indigenous invertebrate species. These species may be vulnerable to the more recent, additional, anthropogenic acidification of these catchments.     

Kinetic Analysis of Chemokinesis of Paramecium1

Paramecia detect and accumulate in or disperse from some chemicals. Cells do this by changing frequency of turning and speed of swimming. There are at least two mechanisms by which cells respond: one dependent on ability to turn, one dependent on speed modulation. There are also two classes of chemicals: those that require the cells' ability to turn in order to cause accumulation and dispersal (type I), and those that apparently require only speed modulation (type II). Attractants of type I cause qualitatively similar changes in behavior to repellents of type II and the converse; therefore, assays are needed to distinguish between these two classes of chemicals, despite qualitatively similar behavior of some attractants and repellents. We examined two assays of paramecium chemoresponse, T-maze assay and well test, to understand how the T-maze distinguishes between attractants of type I and repellents of type II and why the well test does not.     

Multiphasic accumulation of nutrients by plants

Seedlings of rice (Oryza sativa), soybean (Glycine max) and sour orange (Citrus aurantium) were grown for 20 to 125 days under controlled conditions in nutrient solutions wiht up to 16 different concentrations of NH⁴₊, H₂PO₄^-, K⁺, Ca²⁺, Mg²⁺ or Zn²⁺. Nutrient concentrations differed by up to 4 orders of magnitude (H₂PO₄^- and Zn²⁺) and were kept constant or within certain limits by changing solutions daily. Dry weights and concentrations of N, P, K, Ca, Mg or Zn were determined for roots and tops (or roots, stems and leaves). The relationship between tissue concentration of an element and external concentration of the corresponding nutient ion was invariably multiphasic, with phases separated by sharp breaks or jumps. The kinetics of accumulation were similar to those of short-term uptake of the same ions. Reanalysis of previously published data (including data for Mn²⁺) for other plants yielded, similarly, bi- or multiphasic isotherms for accumulation. Accumulation patterns and growth were in several instances correlated, with separate phases coinciding with regions of poverty adjustment, luxury consumption and toxicity. Implications of multiphasic kinetics of long-term nutrient accumulation for membrane properties, fluxes and regulation include: (i) Membranes and uptake mechanisms must remain relatively constant throughout the life of the plant with respect to affinities for ions and concentrations at which transitions occur. (ii) Rate-limitation occurs at the plasmalemma of the root cortical cells. (iii) Uptake is at all times under multiphasic control by the external solution.     

Chemical Forms of Manganese and Zinc in Phloem Exudates

Investigations were performed to study the chemical form in which manganese and zinc are transported in sieve tubes. As a test plant Ricinus communis was used. From this plant phloem sap can be obtained in a rather pure state. The plants received labelled manganese or zinc. In the experiments on manganese translocation a radioactive phosphorus isotope was added to the nutrient solution to test if complex compounds of the cation contain also phosphorus. Components of the phloem exudate were determined by means of physicochemical separation methods. Almost all zinc but only a part of the manganese were bound to organic compounds. The major part of the manganese was in ionic form. The molecular weight of the complexing com-pound(s) of manganese was estimated to be between 1000 and 5000 and of zinc between 1000 and 1500. The complexes probably contain some phosphorus. The charge of the zinc complex is negative.     

Hormonal Regulation of Phototropism in the Light-grown Sunflower Seedling, Helianthus annuus L.: Immobility of Endogenous Indoleacetic Acid and Inhibition of Hypocotyl Growth by Illuminated Cotyledons

Light-grown sunflower seedlings contain 10^–7–3 x10^–7 M indoleacetic acid (IAA). The even distributionof this endogenous IAA in straight hypocotyls does not changeduring phototropic curvature. The diffusate from hypocotylscontains substance(s) influencing the elongation rate of Avenacoleoptile segments but hardly any IAA. Phototropic curvature of the hypocotyl requires the presenceof illuminated cotyledons. Illumination of cotyledons inhibitshypocotyl growth. It is concluded that the phototropic response of the sunflowerhypocotyl is regulated by factors promoting and inhibiting cellelongation other than IAA.     

Cell Wall Solubilization in Pedicel Abscission of Begonia Flower Buds

Effects of metabolic inhibitors and growth regulators on the course of abscission and on the activities of cell wall solubilizing enzymes were studied in pedicel explants of Begonia flower buds. Actinomycin D, chloramphenicol and 2,4-dinitrophenol slightly retarded abscission, whereas cycloheximide exerted a strong inhibition if applied until 10.5 h after explant excision. Indoleacetic acid retarded and ethylene promoted abscission and cell wall solubilization. However, the activities of cell wall solubilizing enzymes did not correspond with the course of abscission. No polygalacturonase and pectic acid and pectin transeliminases could be detected in the abscission zone during abscission, whereas a low pectin methylesterase activity did not change. Endo- and exocellulase activities did not increase until about 10 h after the onset of abscission, indicating that they are the result rather than the cause of abscission.     

Hormonal Regulation of Pedicel Abscission in Begonia Flower Buds

In order to analyse the hormonal regulation of flower bud shedding in Begonia, levels of indoleacetic acid (IAA), abscisic acid (ABA) and ethylene were determined in buds and pedicels. The translocation and metabolism of ¹⁴C-labeled IAA in pedicel segments were also studied. In a monoecious Begonia fuchsioides hybrid, abscising male flower buds contain about 1% of the IAA present in non-abscising female flowers. In a male Begonia davisii hybrid, the seasonal variation in bud drop coincides with changes in the IAA content of the buds, while also the release of IAA from the bud to the pedicel is hampered. Abscission zones of these pedicels always contain abscission promoting ethylene concentrations. The tissue is prevented from responding with abscission by IAA from the flower buds. The buds also contain ABA but without influencing abscission considerably. Pretreatment with ethylene or ABA does not affect IAA transport in pedicel segments. The rate of this transport is 4–6 mm × h^–1:; the capacity increases with the transverse area. In young segments, IAA is decarboxylated and also otherwise metabolized.     

Respiration Rate and Mitochondrial Activity in Iris Bulbs

The oxygen uptake of iris bulbs (Iris×hollandica‘Wedgwood’) which had been stored dry at 30 C (“retarded’ bulbs) was low (10 μmol O₂ per h and bulb), the oxygen uptake of the intact bulb, the three outer fleshy scales and the remaining central part of the bulb increased three- to fourfold, nearly twofold and fourfold, respectively. Mitochondria were isolated from the scales of retarded and activated bulbs and their oxygen consumption with succinate, l -malate (plus pyruvate). x-ketoglutarate and NADH as substrate was measured polarographically. The oxidative capacity of mitochondria isolated from the scales of activated bulbs was only slightly higher than that from retarded bulbs when calculated on a tissue basis. No difference was found between the phosphorylation efficiency, respiratory control, cytochrome c deficiency, succinate dehydrogenase, malate dehydrogenase, succinate-cytochrome c rductase, NADH-cytochrome c reductase and cytochrome oxidase activity of the retarded and activated bulbs. The increase in the in vitro oxygen uptake of the scales after transition from 30 to 13 C was not accompanied by an equal increase in the oxidative capacity of their mitochondria suggesting that they are not responsible for this rise in oxygen uptake.