Bioassay of metalaxyl in plant tissue

A method for determining the concentration of metalaxyl in methanolic extracts of plant tissue is described. Extracts were applied to filter papers in Petri dishes and covered with small volumes of lima bean agar. The growth of an isolate of Pythium ultimum sensitive to metalaxyl was related to the quantity of fungicide applied. The bioassay could detect quantities as low as 0·025 μg in the filter paper, a sensitivity which was confirmed by using ¹⁴C-metalaxyl. Whilst untreated extracts of lettuce and brassicas were not fungitoxic to the isolate of P. ultimum employed, this was not the case with tobacco and grape-vine. Hence alternative test organisms may be required before the method can be generally applied to all species.     

A seed treatment for the control of Pythium damping-off diseases and Peronospora parasitica on brassicas

In soil inoculated with Pythium ultimum or Pythium irregulare, seed treatment with either Apron 70 (=1 g metalaxyl and 1 g captan/kg seed) or thiram gave control of pre-emergence damping-off of Brussels sprout and cabbage seedlings. On cauliflower, Apron 70 was significantly more effective than thiram. No post-emergence damping-off occurred in either of these crops or in oil-seed rape following seed treatment with Apron 70 whilst post-emergence losses from untreated seed ranged from 10·2–19·4% and from thiram treated seed from 5·7-7·4%. Apron 70 gave complete control of Peronospora parasitica on cauliflower inoculated 10 days after sowing; thiram was ineffective. Following seed treatment with Apron 70, metalaxyl was detected in the cotyledons, true leaves and roots of cabbage seedlings up to 4 wk from sowing.     

The Ultrastructure and Analytical Microscopy of Silicon Deposition in the Aleurone Layer of the Caryopsis of Setaria italica (L.) Beauv.

Silicon deposition in the caryopsis of foxtail millet (Setariaitalica (L.) Beauv.) from Lin Xian, Northern China was investigatedusing transmission electron microscopy and energy dispersiveX-ray analysis. The highest silicon count rates were obtained from the pericarpand outer aleurone cell walls, and particularly from a granularelectron-opaque layer external to the outer aleurone cell wall.Silicon was not detected in tissues interior to the aleurone. A possible mechanism for silicon deposition in the caryopsisis suggested, and the results are discussed with respect tothe high incidence of oesophageal cancer in Lin Xian, NorthernChina. Setaria italica (L.) Beauv., foxtail millet, silicon deposition, alcurone layer, caryopsis, ultrastructure, X-ray analysis     

Aminopeptidases Isolated from Cotyledons of Cowpea, Vigna unguiculata

Three aminopeptidases have been separated from cotyledon extractsfrom cowpea, Vigna unguiculata (L.) Walp., and numbered in orderof decreasing affinity for the anion exchange medium DEAE-Sephacel.API showed a wide acceptance of model substrates, with highestactivity under standard conditions against arginyl ß-naphthylamide(NA). AP2 did not act on basic substrates and preferred phenylalanylß-NA. AP3 displayed the narrowest substrate specificity,with strong activity against only alanyl ß-NA andglycyl ß-NA. The chelator 1,10-phenanthroline completelyor almost completely inhibited forms AP1 and AP3, whereas AP2was insensitive to phenanthroline at the same concentration(5 mM). All three aminopeptidases were totally inhibited byAg⁺ or Zn²⁺ ( 0.5 mM). Vigna unguiculata (L.) Walp., aminopeptidase, cotyledon, cowpea, isoenzyme, 1, 10-phenanthroline     

Scanning Electron Microscopy of Silica Deposits in the Culms, Floral Bracts and Awns of Barley (Hordeum sativum Jess.)

Deposits of silica in the culm internodes, floral bracts andawns of Hordeum sativum Jess (cv Deba Abed) have been investigatedusing the scanning electron microscope The deposits were isolatedfrom all organic matter by digestion with nitric and perchloricacids Two basic types of deposits were recognized, lumen andwall silicification, the latter with or without lumen infillings In the culm internodes, lumen deposits are derived from idioblasts(‘hats’), sclerenchyma and xylem vessels In thefloral bracts they are derived from idioblasts (‘hats’and astenform opals), epidermal long cells (dendriform opals),sclerenchyma and xylem vessels The shape of these deposits doesnot generally resemble the outline of the cell itself, but depositsderived from cell walls do closely resemble the infact cell.In the culm, the walls of stomatal cells, trichomes and, largelythe outer tangential walls of mature long epidermal cells, becomesilicified, together with some cork cells In the floral bracts,silica is found in most epidermal cell walls but is confinedto the trichomes, scutiform cells and costal epidermal cellsearly in their development At maturity concentrations of silicaare much higher in the floral bracts and awns than in the culmsand leaves The results are discussed in relation to the pattern of depositionand its possible functions. Hordeum sativum Jess, barley, silica deposits, opals, scanning electron microscopy     

Opaline Silica Deposition in Rye (Secale cereale L.)

The types of opaline silica-bodies (opal phytoliths) which occurin the mature prophylls, radical and culm leaves, culms, andinflorescence bracts of rye (Secale cereale L.) are describedand figured. Silica-bodies are absent from the coleoptile, andthe adaxial epidermis of the prophylls, leaf sheaths, and inflorescencebracts. The stages of silica-body formation in young radicalleaf sheaths are also described. Alternative hypotheses forthe origin of silica-bodies are discussed.     

Electron-probe Microanalysis of Silicon in the Roots of Oryza sativa L.

Employing the electron-probe microanalyser, the localizationof silicon in the different tissues of the mature root of ricehas been investigated. Deposition of silicon is specific tothe endodermis. The heaviest accumulation is associated withthe inner tangential walls and to some extent the radial wallsof the endodermal cells.     

C4-derived soil organic carbon decomposes faster than its C3 counterpart in mixed C3/C4 soils

The large difference in the degree of discrimination of stable carbon isotopes between C3 and C4 plants is widely exploited in global change and carbon cycle research, often with the assumption that carbon retains the carbon isotopic signature of its photosynthetic pathway during later stages of decomposition in soil and sediments. We applied long-term incubation experiments and natural ¹³C-labelling of C3 and C4-derived soil organic carbon (SOC) collected from across major environmental gradients in Australia to elucidate a significant difference in the rate of decomposition of C3- and C4-derived SOC. We find that the active pool of SOC (ASOC) derived from C4 plants decomposes at over twice the rate of the total pool of ASOC. As a result, the proportion of C4 photosynthesis represented in the heterotrophic CO₂ flux from soil must be over twice the proportional representation of C4-derived biomass in SOC. This observation has significant implications for much carbon cycle research that exploits the carbon isotopic difference in these two photosynthetic pathways.