Prevention of potato top-roll by aphicide and its effect on leaf area and photosynthesis

In a field of potatoes, top-roll, which is induced by the aphid Macrosiphum euphorbiae feeding on the leaves, was restricted to two rows of plants which accidentally received no phorate aphicide granules at planting. The photo-synthetic rate per unit leaf area and the ground cover of top-rolled leaves were respectively 50% and 20% less than those of normal plants which may account for the smaller yields of affected plants observed in previous experiments.     

Sperm structure and ultrastructure in the Hymenoptera (Insecta)

A light and electron microscopical survey of spermatozoan gross morphology and ultrastructure in the Hymenoptera is presented. Details are provided for the first time for members of the families Xyelidae, Argidae, Tenthredinidae, Diprionidae, Cephidae, Figitidae, Proctotrupidae, Diaprii- dae, Heloridae, Eurytomidae, Leucospidae, Perilampidae, Torymidae, Braconidae, Dryinidae, Sphecidae, Pompilidae and Vespidae. Spermatozoan length ranged from 8 μ m in some Braconidae to 500 μm in one chalcidoid. Considerable variation in gross morphology and ultrastructure were observed between taxa. Several phylogenetically informative characters were noted. Very small spermatozoa characterized most of the non-cyclostome subfamilies of Braconidae; spirally twisted axoneme and mitochondrial derivatives occur in the Eulophidae, Eurytomidae and Pteromalidae; spermatozoa with virtually indistinguishable head (nucleus and acrosome) regions characterized the Vespinae and Polistinae. The presence of well-developed spermatodesmata in the vas deferens and seminal vesicle characterize the Symphyta and were largely absent from other groups though they are occasionally present in some bees.     

Uptake, translocation and metabolism of fluazifop-butyl in Setaria viridis

The uptake and translocation of fluazifop-butyl was investigated in Setaria viridis. Young plants (three to four leaves) with a portion of the second, third or fourth leaf covered, were sprayed with a dose equivalent to 0.25 kg a.i. ha-¹. ¹⁴C-fluazifop-butyl was subsequently applied to the unsprayed area and the treatment resulted in plant death within 2 wk. Uptake by leaf 3 was rapid, with less than 5% of the applied dose remaining on the leaf surface after 24 h. The highest proportion of ^14C-activity was retained in the treated portion of the leaf. Only 2% of the applied dose was translocated from leaf 3 and 0. 76% accumulated in the apical meristem. Uptake by the younger leaf 4 was more rapid and the pattern of translocation differed in that more ¹⁴-^-activity accumulated in apical meristematic tissue. 6–30% of the applied dose was undetected and this was greatest when foliar uptake was slow. Artificial leaf surface experiments indicated that this undetected activity may have been due to volatility of fluazifop-butyl or degradation to volatile products. ^14C-activity extracted from treated leaves was identified as fluazifop-butyl, fluazifop acid and polar conjugates. The major ¹⁴C-activity extracted from the apical meristem was fluazifop acid and no fluazifop-butyl was detected in this extract.     

Identification of soybean mosaic, southern bean mosaic and tobacco ringspot viruses from soybean in the People's Republic of China

Samples of soybean plants with virus-like symptoms were collected from several locations in the People's Republic of China in 1981. These samples were used to prepare inocula for mechanical inoculation to soybean. Twenty-one virus cultures were obtained, the identities of which were determined by serology, symptomatology and host range. Sixteen cultures contained only soybean mosaic virus, four of which were more pathogenic than any previously studied; one culture contained only tobacco ringspot virus, another only southern bean mosaic virus, and three other cultures mixed infections of soybean mosaic and southern bean mosaic viruses. This is the first report of the occurrence of tobacco ringspot virus and southern bean mosaic virus in soybean in the People's Republic of China.     

Transformation-defective Strains of <Emphasis Type="Italic">Haemophilus influenzae</Emphasis>

THE mechanism of genetic transformation and recombination can be studied with mutants deficient in various stages of transformation and recombination, but their isolation has often proved to be difficult and time-consuming. We have developed a method for selectively removing cells which transform normally from cultures of Haemophilus influenzae. Mutants isolated from such cultures have been tested for DNA uptake, integration, ultraviolet and X-ray sensitivities and ultraviolet induced DNA synthesis delay.     

NEMATOCYSTS OF THE SEA ANEMONE METRIDIUM

Six types of nematocysts and their nematocytes in tentaclesand acontia of the sea anemone Metridium senile fimbriatum werestudied by electron microscopy. Microbasic b-mastigophores, microbasic amastigophores, and basitrichshave one fundamental feature in common: a straight, complexly-foldedshaft with dense spines pointing apically. An additional resemblancebetween a b-mastigophore and a basitrich is the possession ofa long, narrow, coiled thread bearing spines. An amastigophoreis characterized by a short, looped, unspined thread and a cup-shapedgranular matrix. Atrich and holotrich nematocysts have a coiled, spined tubeof uniform diameter which lies in an evenly granular matrixfilling the entire capsule. The above five nematocysts have three flaps at the apex of thecapsule which open upon discharge, and each nematocyte possessesa flagellum with which is associated one or two centrioles anda striated rootlet. The long rootlet of the b-mastigophorebearingnematocyte passes through a circular band of fibrils surroundingthe neck region of the capsule, and the short rootlet of theatrich lies in a dense fibrous sheath surrounding all but theapex of the capsule. The spirocyst differs from the other nematocysts in having athin, ridged, singlewalled capsule; an inverted tube containingbundles of tubules; an apical disk covered only by a thin layerof granular material and the nematocyst membrane; and the absenceof a flagellum in its nematocyte. Theories of excitation and mechanism of discharge of nematocystsand the function of spirocysts are discussed in the light ofthis and other recent studies of the fine structure of nematocysts.Special attention is drawn to the probable role of the foldsin the walls of shaft and thread in increasing the length ofthe tube upon discharge.     

Aminopeptidases from Plasmodium falciparum, Plasmodium chabaudi chabaudi and Plasmodium berghei

ABSTRACT. Using fluorogenic substrates and polyacrylamide gels we detected in cell-free extracts of Plasmodium falciparum, Plasmodium chabaudi chabaudi and Plasmodium berghei only a single aminopeptidase. A comparative study of the aminopeptidase activity in each extract revealed that the enzymes have similar specificities and kinetics, a near-neutral pH optima of 7.2 and are moderately thermophilic. Each has an apparent molecular weight of 80,000 ± 10,000, determined by high performance liquid chromatography on a calibrated SW500 column. Whilst the P. c. chabaudi and P. berghei activity co-migrate in native polyacrylamide gels, that of P. falciparum migrates more slowly. The three enzymes can be selectively inhibited by ortho -phenanthroline and are thus metallo-aminopeptidases; however, in contrast to other aminopeptidases the metal co-factor does not appear to be Zn²⁺.