DIATOM MINERALIZATION OF SILICIC ACID IV. KINETICS OF SOLUBLE Si POOL FORMATION IN EXPONENTIALLY GROWING AND SYNCHRONIZED NAVICULA PELLICULOSA1

Silicic acid taken up from the growth medium by Navicula pelliculosa (Bréb.) Hilse was shown to enter at least two compartments: i) soluble pools; ii) insoluble fraction comprised predominantly of the silica frustule. Soluble Si pools were extracted by a variety of agents from cells uniformly labeled for ten generations in medium containing ⁶⁸Ge-Si(OH)₄. 100 C water soluble and 0 C perchloric acid (PCA) soluble Si pools of 680 mM Si·l^?1 and 490 mM Si·l^?1 cell water represented 13 and 9%, respectively, of total, cell Si in exponential growth phase cells. Uniformly labeled cells synchronized by the combined synchronization technique accumulate at the cell cycle stage where silica frustule development is initiated. These cells contain water and PCA soluble pools of 10 nmol Si·10⁶ cells^?1 and-8.8 nmol Si·10⁶ cells^?1, respectively. On addition of Si(OH)₄, a rapid uptake ensues allowing the Si pool to expand 2.5-fold, apparently to provide precursors of the silica frustule.     

Modification of soil aggregation by watering regime and roots growing through beds of large aggregates

The influence of root growth and soil watering regime on aggregation was studied under controlled conditions. The study examined the influence of pea (Pisum sativum cv Greenfeast), ryegrass (Lolium rigidum cv Wimmera) and wheat (Triticum aestivum cv Kite) roots on changes in aggregation and on the properties of the aggregates. The soil was a non swelling red-brown earth which was either kept wet or was allowed to wet and dry during the experiment. Root growth increased the percentage of small sized aggregates (<18 mm diameter), organic carbon, tensile strength and stability of aggregates in comparison with a non planted soil. Changes in aggregate size distribution and properties of the aggregates were related to root length density of the species and also to the soil watering regime. Root length density was in the order ryegrass>pea>wheat. Wetting and drying of soil increased the strength and stability of aggregates. Incubating aggregates allowed some roots to decompose but did not increase the strength or stability of aggregates compared with unincubated soil. The results of this experiment are of practical significance in soil structural management, and in studies of soil aggregation dynamics. It may be possible to use plant roots to alter the size and properties of aggregates.     

Limiting response alternatives in time-intensity scaling: an examination of the halo-dumping effect

Time-related measurements pose some challenges to psychophysicsand to applied sensory testing methods including control ofpsychological biases which have been found in single-point scaling.This research examined enhancement of ratings when responsealternatives were limited in time-intensity scaling tasks usingrepeated category ratings. Panelists rated a pseudo-beveragecontaining sweetener and flavor and one with sweetener onlyover a 90-s period. The aromatic flavor caused an increase insweetness intensity and especially so when the panelists werelimited to sweetness responses only. The odor-induced enhancementof sweetness was smaller when panelists were given both flavorand sweetness response options than when the panelists weregiven only a sweetness scale. Prior use of both scales in aprevious experimental session did not lessen the halo-dumpingenhancement effect. In one study, sweetness ratings of sucrosealone were depressed when the additional scale for flavor wasprovided, perhaps due to inappropriate partitioning of responses.     

Plasma prostaglandin levels and circulating fuel levels in rats with diabetic ketoacidosis: Effects of cyclooxygenase inhibitors and of alpha and beta adrenergic blockade

We studied the effects of two structurally unrelated inhibitors of the fatty acid cyclooxygenase and of alpha and beta adrenergic blockade on the elevated plasma levels of 13,14-dihydro-15-keto-prostaglandin (PG)E₂, 6-keto-PGF_1α and thromboxane(TX)B₂, the stable derivatives of PGE₂, PGI₂ (prostacyclin) and TXA₂, respectively, in rats with streptozotocin-induced diabetic ketoacidosis (DKA). Meclofenamic acid and indomethacin each produced a significant decrease in the elevated plasma levels of 13,14-dihydro-15-keto-PGE₂, 6-keto-PGF_1α and TXB₂. Phentolamine significantly reduced the plasma level of TXB₂ but had no effect on the elevated circulating levels of glucose, free fatty acids, total ketones, 13,14,-dihydro-15-keto-PGE₂ or 6-keto-PGF_1α. Propranolol significantly reduced the elevated circulating levels of glucose, free fatty acids and total ketones but had no effect on the levels of the three prostaglandin derivatives. The ability of meclofenamic acid and indomethacin to reduce the plasma levels of 13,14-dihydro-15-keto-PGE₂, 6-keto-PGF_1α and TXB₂ confirms that the plasma levels of these three derivatives are elevated in rats with DKA. Since abnormalities in the production of PGI₂ and perhaps other cyclooxygenase derivatives may contribute to the pathogenesis of certain important hemodynamic and gastrointestinal features of DKA, cyclooxygenase inhibitors may play a role in the management of selected patients with this disorder. Alpha adrenergic activity is essential for the maintenance of the elevated plasma TXB₂ level in rats with DKA. The fall in the plasma TXB₂ level during alpha adrenergic blockade appears to reflect inhibition of platelet aggregation and platelet TXA₂ production, but other sources of the elevated plasma TXB₂ level in DKA are not excluded. Beta adrenergic activity contributes to the maintenance of elevated circulating levels of glucose, free fatty acids and total ketones in experimental DKA but not to the elevated plasma levels of the prostaglandin derivatives.     

Effect of water stress on subsequent uptake of chloride by wheat plants

Summary Wheat plants that were grown for 30 days in flowing nutrient solution were transferred to CaSO₄ solution, and water stress was developed by increasing the evaporative demand on the tops and decreasing the amount of the root system in the solution. The stress was maintained for 3 or 9 h. Uptake of³⁶Cl by the plants was measured immediately after removal of the stress and at intervals up to 36 h later.The water potential of the leaves ranged from –5 bar in the control to –12 bar in stressed plants. Stressed plants transpired less water after removal of the stress than did unstressed plants.Chloride uptake immediately after the removal of water stress was unaffected by the stress, but when measurements were made 36 h later previously stressed plants absorbed only 2 M h^–1 chloride compared to 7 M h^–1 for unstressed plants.     

Chemosystematic studies in the saxifragaceae sensu lato. 8. The flavonoids of elmera racemosa (Watson) Rydberg

The flavonoid glycosides of both varieties of Elmera racemosa were isolated and identified. The compounds were the monoglucosides of kaempferol, quercetin and myricetin, the rutinosides of the same aglycones, and the rhamnosylrutinosides of kaempferol and quercetin. All glycosides were linked at position-3 of the flavonols. The two varieties (var. racemosa and var. puberulenta C. L. Hitchcock) were identical. A comparison of the flavonoid chemistry of Elmera, Heuchera, and Tellima supports the existence of Elmera as a genus. A survey of several collections of Tellima grandiflora, Heuchera micrantha, and H. cylindrica showed only minor quantitative differences in the two-dimensional thin layer chromatograms from collection to collection. The possible origin of Tellima and Elmera from ancestral stock having Heuchera-like flavonoid chemistry is discussed.     

A Batch Staining Method for Brain Slices Allowing Volume Measurements of Grey and White Matter Using an Image Analyzing Computer (Quanttmet 720)

Normal formalin-fixed gelatin-embedded cerebral hemispheres were serially sliced and the 25 to 30 slices from each hemisphere were batch stained by a modification of Mulligan's method. Following washing in water the slices were immersed in Mulligan's acid/copper sulfate/ phenol solution for 20 minutes at room temperature, treated with a xylene/Polyclens mixture for 20 seconds and immediately transferred to a 2% sodium hydroxide solution for 10 seconds. Final staining was by immersion in 2% potassium ferrocyanide which was followed by washing in tap water. The grey matter was stained a brick red color while the whiteness of the white matter was accentuated. Following staining the slices were stored between sheets of black paper in 2% aqueous formalin prior to measurement of the respective areas of grey and white matter using a Quantimet 720 image analyzing computer. The method is rapid and color stable, and reduces the risk of exposure to toxic fumes by eliminating the need for hot phenol solutions. This technique is also suitable for the macroscopic demonstration and quantitation of demyelinating conditions in the brain.     

Mutations in loop six of the large subunit of ribulose-1,5-bisphosphate carboxylase affect substrate specificity

Mutagenesis in vitro of the gene encoding the large subunit of ribulose-1,5-bisphosphate carboxylase/ oxygenase (EC 4.1.1.39) from Anacystis nidulans Synechococcus PCC 6301) was used to generate novel enzymes in Escherichia coli. Residues in C-terminal loop 6 of the / barrel structure of the large subunit were changed. Replacement of valine 331 with alanine caused a 90% reduction in V _max but did not alter the enzyme's relative specificity towards either of its gaseous substrates, CO₂ and O₂. However replacement of alanine 340 with glutamate decreased the enzyme's specificity for CO₂ but had no significant effect on either the K _m for ribulose-1,5-bisphosphate or CO₂ or on V _max. In contrast replacing a small cassette of residues 338-341 produced a small increase in the specificity factor.Abbreviations Rubisco ribulose-1,5-bisphosphate carboxylase/oxygenase - RuBP ribulose-1,5-bisphosphate - CABP 2-carbox-yarabinitol-1,5-bisphosphate We thank Karen Moore for the statistical analysis of the specificity factors. We acknowledge helpful discussions with Jim Pitts and Richard Pickersgill. This work was aided by the invaluable technical assistance of Iain Major.     

Diurnal Variations in Swimming Activity of Rutilus rutilus (Cyprinidae) in a Group under Tank Conditions

Measurements of the swimming activity of a group of roach (12–19 cm TL, average) in a circular swimming chamber revealed two distinct activity patterns: a diurnal and a nocturnal one. The experiments showed that, having the choice, two factors stimulated the rhythmicity of the swimming behaviour of the fish, i.e. light intensity and the presence of a current field in the proximity of the fish. During daytime (bright light conditions) the fish moved into the current field and swam on average at 0.4 BL/s (resting swimming). The roach remained swimming at this speed even if no current field was established, however, then distributed evenly in the basin. By contrast, during night (dim light conditions) the fish predominantly chose the still water section but swam on average with a cruising speed of 1.6 BL/s (night swimming). Accordingly, they did not seek the still water section for night swimming if the light was kept on. Then again, the fish distributed more or less evenly in the basin. The results support the hypothesis that the fish migrate during night-time and do this preferably in still water.     

Interaction of FXYD10 (PLMS) with Na,K-ATPase from shark rectal glands. Close proximity of Cys74 of FXYD10 to Cys254 in the a domain of the alpha-subunit revealed by intermolecular thiol cross-linking

FXYD domain-containing proteins are tissue-specific regulators of the Na,K-ATPase that have been shown to have significant physiological implications. Information about the sites of interaction between some FXYD proteins and subunits of the Na,K-ATPase is beginning to emerge. We previously identified an FXYD protein in plasma membranes from shark rectal gland cells and demonstrated that this protein (FXYD10) modulates shark Na,K-ATPase activity. The present study was undertaken to identify the location of the C-terminal domain of FXYD10 on the alpha-subunit of Na,K-ATPase, using covalent cross-linking combined with proteolytic cleavage. Treatment of Na,K-ATPase-enriched membranes with the homobifunctional thiol cross-linker 1,4-bismaleimidyl-2,3-dihydroxybutane resulted in cross-linking of FXYD10 to the alpha-subunit. Cross-linking was not affected by preincubation with sodium or potassium but was significantly reduced after pre-incubation with the non-hydrolyzable ATP analog beta,gamma-methyleneadenosine 5'-triphosphate (AMP-PCP). A peptic assay was developed, in which pepsin treatment of Na,K-ATPase at low pH resulted in extensive cleavage of the alpha-subunit while FXYD10 was left intact. Proteolytic fragments of control and cross-linked preparations were isolated by immunoprecipitation and analyzed by gel electrophoresis. A proteolytic fragment containing FXYD10 cross-linked to a fragment from the alpha-subunit could be localized on SDS gels. Sequencing of this fragment showed the presence of FXYD10 as well as a fragment within the A domain of the alpha-subunit comprising 33 amino acids, including a single Cys residue, Cys254. Thus, regulation of Na,K-ATPase by FXYD10 occurs in part via cytoplasmic interaction of FXYD10 with the A domain of the shark alpha-subunit.