Microorganisms associated with the retting of flax treated with the herbicide glyphosate

Greater numbers of fungi were isolated from stems of flax following treatment with the herbicide glyphosate than from untreated stems although there was also a general increase in numbers with time. The fungal genera isolated were the same from both treated and untreated plants, the most common being Cladosporium, Aureobasidium, Epicoccum and Botrytis with Cladosporium being predominant. Populations of bacteria were generally not enhanced after glyphosate treatment. Partial dew-retting of crops resulted in the reduction in numbers of Cladosporium compared with conventionally-treated flax. The increase in numbers of fungi was associated with an increase in retting. Overretting also occurred, particularly in discrete pale areas on the stem. These were associated with colonisation by Botrytis cinerea and the tensile strength of fibres from these areas was 15 times weaker than from surrounding darker areas of the stem. Light microscopy showed death of cells after glyphosate application, followed by invasion and degradation of the epidermis and cortex by fungi and other microorganisms. Fibre bundles were partially dissociated but the individual fibres remained largely intact as did the xylem and medulla.     

Localization of sequences regulating ancestral and acquired sites of esterase6 activity in Drosophila melanogaster

We have broadly defined the DNA regions regulating esterase6 activity in several life stages and tissue types of D. melanogaster using P- element-mediated transformation of constructs that contain the esterase6 coding region and deletions or substitutions in 5' or 3' flanking DNA. Hemolymph is a conserved ancestral site of EST6 activity in Drosophila and the primary sequences regulating its activity lie between -171 and -25 bp relative to the translation initiation site: deletion of these sequences decrease activity approximately 20-fold. Hemolymph activity is also modulated by four other DNA regions, three of which lie 5' and one of which lies 3' of the coding region. Of these, two have positive and two have negative effects, each of approximately twofold. Esterase6 activity is present also in two male reproductive tract tissues; the ejaculatory bulb, which is another ancestral activity site, and the ejaculatory duct, which is a recently acquired site within the melanogaster species subgroup. Activities in these tissues are at least in part independently regulated: activity in the ejaculatory bulb is conferred by sequences between -273 and -172 bp (threefold decrease when deleted), while activity in the ejaculatory duct is conferred by more distal sequences between -844 and -614 bp (fourfold decrease when deleted). The reproductive tract activity is further modulated by two additional DNA regions, one in 5' DNA (-613 to -284 bp; threefold decrease when deleted) and the other in 3' DNA (+1860 to +2731 bp; threefold decrease when deleted) that probably overlaps the adjacent esteraseP gene. Collating these data with previous studies suggests that expression of EST6 in the ancestral sites is mainly regulated by conserved proximal sequences while more variable distal sequences regulate expression in the acquired ejaculatory duct site.      

Phylogenetic diversification of immunoglobulin genes and the antibody repertoire

Immunoglobulins are encoded by a large multigene system that undergoes somatic rearrangement and additional genetic change during the development of immunoglobulin-producing cells. Inducible antibody and antibody-like responses are found in all vertebrates. However, immunoglobulin possessing disulfide-bonded heavy and light chains and domain-type organization has been described only in representatives of the jawed vertebrates. High degrees of nucleotide and predicted amino acid sequence identity are evident when the segmental elements that constitute the immunoglobulin gene loci in phylogenetically divergent vertebrates are compared. However, the organization of gene loci and the manner in which the independent elements recombine (and diversify) vary markedly among different taxa. One striking pattern of gene organization is the "cluster type" that appears to be restricted to the chondrichthyes (cartilaginous fishes) and limits segmental rearrangement to closely linked elements. This type of gene organization is associated with both heavy- and light-chain gene loci. In some cases, the clusters are "joined" or "partially joined" in the germ line, in effect predetermining or partially predetermining, respectively, the encoded specificities (the assumption being that these are expressed) of the individual loci. By relating the sequences of transcribed gene products to their respective germ-line genes, it is evident that, in some cases, joined-type genes are expressed. This raises a question about the existence and/or nature of allelic exclusion in these species. The extensive variation in gene organization found throughout the vertebrate species may relate directly to the role of intersegmental (V<==>D<==>J) distances in the commitment of the individual antibody-producing cell to a particular genetic specificity. Thus, the evolution of this locus, perhaps more so than that of others, may reflect the interrelationships between genetic organization and function.      

Control of potato cyst-nematode, Globodera pallida, on tomatoes grown under glass, by applying steam or chemical nematicides to the soil

In a sandy loam under glass, potato cyst-nematode, Globodera pallida, was controlled in soil to 20 cm deep, and tomato yields were greatly increased by sheet steaming for 4 h, by 977 kg methyl bromide ha^-1 or by 448 kg Telone (1,3-dichloropropene mixture or Di-Trapex CP (20% methyl isothiocyanate: 15% chloropicrin:65% dichloropropene-dichloropropane mixture) ha^-1 followed by 441 kg dazomet or 11.2 kg oxamyl ha^-1. Sheet steaming, unlike the other treatments, had relatively little effect on the nematode in soil 20 to 40 cm deep. Until the apices of the plants were cut off production of fruit was curvilinear against time in all treated soil but linear against time in untreated soil.     

A Rapid and Simple Radioassay for Abscisic Acid using 14C-Diazomethane

A simple physical method for measuring abscisic acid concentrationin plant material is described. Abscisic acid in partially purifiedextracts was radiolabelled by reaction with ¹⁴C-diazomethaneto give ¹⁴C-methyl abscisate, which was purified from otherradiolabelled products by thin layer chromatography. Abscisicacid concentration was measured by comparison of the ¹⁴C radioactivityincorporated into plant abscisic acid with that in standard¹⁴-C-methyl abscisate prepared under the same conditions fromknown amounts of pure abscisic acid. Losses of abscisic acidwhich occurred during purification were corrected by measuringthe recovery of ³H-abscisic acid added to initial extracts. Abscisic acid concentration was measured by radioassay and byconventional electron capture-gas chromatography in oat, bean,and turgid or wilted tobacco leaves. Results from the two methodswere closely comparable. Radioassay is as rapid and sensitiveas existing procedures for measuring abscisic acid, but requiresonly simple and inexpensive chromatographic equipment.