Der Einfluss des Wirtes in der Massenzucht auf die Qualität des EiparasitenTrichogramma evanescens bei der Bekämpfung des Maiszünslers,Ostrinia nubilalis

Zusammenfassung In vier Feldversuchen wurde die Wirksamkeit eines an den Maiszünsler besonders angepassten Stammes vonTrichogramma evanescens Westw. bei der Bek?mpfung des MaiszünslersOstrinia nubilalis Hübner geprüft. Die Parasiten wurden entweder auf Eiern der GetreidemotteSitotroga cerealella (Oliv.) oder auf Eiern der MehlmotteEphestia kuehniella Zell. gezüchtet. Die Freilassung erfolgte in den Versuchsparzellen durch Anbringen von Eikarten mit jeweils etwa 1000 parasitierten Wirtseiern an Bl?ttern von Maispflanzen in Abst?nden von 14 Metern. VierTrichogramma-Freilassungen in w?chentlichen Abst?nden mit jeweils 45000 Parasiten pro Hektar ergaben hohe Parasitierungsraten bei denO. nubilalis-Eiern und starke Verminderungen des Larvenbefalls. In den Parzellen, in denen aufS. cerealella-Eiern gezüchtete Parasiten freigelassen wurden, lagen die Parasitierungsraten zwischen 81,7 und 82,3% im Vergleich zu 63,0 und 84,3% bei den aufE. kuehniella gezüchteten Trichogrammen. Die Verminderung des bei der Ernte festgestelltenO. nubilalis-Larvenbefalls im Vergleich zur unbehandelten Kontrolle lag bei den aufS. cerealella gezüchteten Parasiten zwischen 75,5 und 94,8% verglichen mit 77,6 und 89,9% bei den aufE. kuehniella gezüchteten Tieren. Es gab somit keine signifikanten Unterschiede zwischen den beiden getestetenTrichogramma-St?mmen.

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Summary The effectiveness of a strain ofTrichogramma evanescens Westw. especially adapted to the European corn borerOstrinia nubilalis Hübner was examined in 4 field experiments. The parasites were reared on either the Angoumois grain mothSitotroga cerealella (Oliv.) or the Mediterranean flour mothEphestia kuehniella Zell. and were released in separate experimental plots by attaching egg cards, each containing about 1000 parasitized host eggs, to corn leaves at distances of 14 meters in the field. FourTrichogramma treatments at 1 week intervals using 45000 parasites per hectar per treatment resulted in high parasitization rates ofO. nubilalis-eggs and large reductions in larval damage. In experimental plots whereT. evanescens, reared onS. cerealella-eggs, were released, the parasitization rates ofO. nubilalis-eggs varied between 81,7 and 82,3%, compared with 63,0 and 84,3% forT. evanescens reared onE. kuehniella. The reduction inO. nubilalis larval infestation at the harvest in the treated plots, compared to untreated controls varied between 75,5 and 94,8% forT. evanescens that was reared onS. cerealella, compared with 77,6 and 89,8% forT. evanescens that was reared onE. kuehniella. There were no significant differences in efficiency between the two tested methods of rearingTrichogramma.

     

Disease lesion mimics in maize: I. Effect of genetic background,temperature, developmental age,and wounding on necrotic spot formation with Les1

Les1, a dominant gene of maize (Zea mays L.), results in the production of necrotic leaf spots. Expression of this trait is temperature sensitive, and the nonpermissive temperature for expression is determined by the genetic background in which the gene is placed. Exposure to nonpermissive conditions for 24–48 hr will induce lesion production in the most sensitive genotype. Lesions form first at the leaf tip, the oldest part of the leaf, and progress basipetally through fully expanded tissue. Leaves excised from plants grown at either permissive or nonpermissive temperatures and placed in water, gibberellic acid, or abscisic acid solutions form no new lesions at either 20 or 30°C, and the leaves senesce rapidly. However, when leaves excised from normal and Les1 plants are placed in kinetin, senescence is delayed and numerous lesions develop at 20°C on Les1 plants. Our results suggest that there is a developmental time window during which maize leaf cells can be induced to form lesions: cells must be fully elongated but not yet senescent. This hypothesis is strengthened by the observation that pinprick wounding of leaves induces lesions only in a band of tissue approximately 2 days younger than the area of the leaf currently producing lesions. Various models for the action of Les1 in causing discrete lesion formation are discussed.     

Molecular evolution of P transposable elements in the genus Drosophila. III. The melanogaster species group

Phylogenetic relationships were determined for 76 partial P-element sequences from 14 species of the melanogaster species group within the Drosophila subgenus Sophophora. These results are examined in the context of the phylogeny of the species from which the sequences were isolated. Sequences from the P-element family fall into distinct subfamilies, or clades, which are often characteristic for particular species subgroups. When examined locally among closely related species, the evolution of P elements is characterized by vertical transmission, whereby the P-element phylogeny traces the species phylogeny. On a broader scale, however, the P-element phylogeny is not congruent with the species phylogeny. One feature of P-element evolution in the melanogaster group is the presence of more than one P-element subfamily, differing by as much as 36%, in the genomes of some species. Thus, P elements from several individual species are not monophyletic, and a likely explanation for the incongruence between P-element and species phylogenies is provided by the comparison of paralogous sequences. In certain instances, horizontal transfer seems to be a valid alternative explanation for lack of congruence between species and P-element phylogenies. The canonical P-element subfamily, which represents the active, autonomous transposable element, is restricted to D. melanogaster. Thus, its origin clearly lies outside of the melanogaster species group, consistent with the earlier conclusion of recent horizontal transfer.      

Nuclear, Virescent Mutants of Zea mays L. with High Levels of Chlorophyll (a/b) Light-Harvesting Complex during Thylakoid Assembly

We have found nuclear, recessive mutants in Zea mays L. where assembly of the major chlorophyll (a/b) light-harvesting complex (LHC) was not delayed relative to most other thylakoid protein complexes during thylakoid biogenesis. This contrasts with the normal development of maize chloroplasts (NR Baker, R Leech 1977 Plant Physiol 60: 640-644). All four mutants examined were allelic and virescent, and displayed visibly higher yields of leaf Chl fluorescence during greening. Fully greened mutants had normal leaf Chl fluorescence yield and normal levels of LHC, and grew to maturity under field conditions. Therefore, delayed LHC assembly is not an obligate feature of thylakoid differentiation.

Assigning the molecular basis for the mutation should provide information concerning reguation of LHC assembly. Several possibilities are discussed. The pleiotropic mutant phenotype is not attributable to defects in thylakoid glycerolipid synthesis. Thylakoids isolated from greening mutant leaf sections had elevated glycerolipid/Chl ratios. In addition, both the molar distribution and acyl composition of four major glycerolipids were normal for developing mutant thylakoids.

     

Biosynthesis of lysosomal hydrolases: their synthesis in bound polysomes and the role of co- and post-translational processing in determining their subcellular distribution

By in vitro translation of mRNA’s isolated from free and membrane-bound polysomes, direct evidence was obtained for the synthesis of two lysosomal hydrolases, β-glucuronidase of the rat preputial gland and cathespin D of mouse spleen, on polysomes bound to rough endoplasmic reticulum (ER) membranes. When the mRNA’s for these two proteins were translated in the presence of microsomal membranes, the in vitro synthesized polypeptides were cotranslationally glycosylated and transferred into the microsomal lumen. Polypeptides synthesized in the absence of microsomal membranes were approximately 2,000 daltons larger than the respective unglycosylated microsomal polypeptides found after short times of labeling in cultured rat liver cells treated with tunicamycin. This strongly suggests that nascent chains of the lysosomal enzymes bear transient amino terminal signals which determine synthesis on bound polysomes and are removed during the cotranslational insertion of the polypeptides into the ER membranes. In the line of cultured rat liver cells used for this work, newly synthesized lysosomal hydrolases showed a dual destination; approximately 60 percent of the microsomal polypeptides detected after short times of labeling were subsequently processed proteolytically to lower molecular weight forms characteristic of the mature enzymes. The remainder was secreted from the cells without further proteolytic processing. As previously observed by other investigations in cultured fibroblasts (A. Gonzalez-Noriega, J.H. Grubbs, V. Talkad, and W.S. Sly, 1980, J Cell Biol. 85: 839-852; A. Hasilik and E.F. Neufeld, 1980, J. Biol. Chem., 255:4937-4945.) the lysosomotropic amine chloroquine prevented the proteolytic maturation of newly synthesized hydrolases and enhanced their section. In addition, unglycosylated hydrolases synthesized in cells treated with tunicamycin were exclusively exported from the cells without undergoing proteolytic processing. These results support the notions that modified sugar residues serve as sorting out signals which address the hydrolases to their lysosomal destination and that final proteolytic cleavage of hydrolase precursors take place within lysosome itself. Structural differences in the carbohydrate chains of intracellular and secreted precursors of cathespin D were detected from their differential sensitivity to digestion with endoglycosidases H and D. These observations suggest that the hydrolases exported into the medium follow the normal secretory route and that some of their oligosaccharides are subject to modifications known to affect many secretory glycoproteins during their passage through the Golgi apparatus.     

Variation of growth form parameters inCapsella (Cruciferae)

Growth form parameters ofCapsella bursa-pastoris populations, including a wide range of different environments, have been analyzed from random block field and growth chamber experiments. Changes in one character are often correlated with changes in another. Of special interest are correlations detected with the onset of first flowering. Variation in each of the characters is clearly influenced by both phenotypic and genotypic components. However, genotype — environment interactions are also subject to variation. Therefore, the adaptive significance of a given parameter is not found to be constant over the entire geographical range of the genus. Alpine populations tend to shift from annual to biannual life cycles.Part of a series Adaptation in life history traits of colonizing plant species. Part of a doctoral thesis by the first author. Dedicated to Prof. Dr.Karl Mägdefrau on the occasion of his 80th birthday.     

Noisy-threshold control of cell death

Background  

Cellular responses to death-promoting stimuli typically proceed through a differentiated multistage process, involving a lag phase, extensive death, and potential adaptation. Deregulation of this chain of events is at the root of many diseases. Improper adaptation is particularly important because it allows cell sub-populations to survive even in the continuous presence of death conditions, which results, among others, in the eventual failure of many targeted anticancer therapies.     

A simple method for staining nuclei of mature and germinated maize pollen

A sugar acetocarmine staining technique has been developed for staining the sperm and vegetative nucleus of mature and germinated maize pollen grains. This procedure is simple, stable and highly repeatable. The physiological properties of the mature maize pollen grains are first adjusted by using an in vitro germinating culture solution. This solution is 15% sucrose and contains 360 ppm calcium chloride dihydrate, and 120 ppm boric acid. One part fresh pollen grains is uniformly mixed with nine parts of the solution and left at room temperature for at least 5 hr. One part of this solution is then mixed with two parts of regular acetocarmine stain and left overnight. The color of this mixture is pinkish red or raspberry. The sugar in the mixture helps to increase color contrast between the pollen cytoplasm (light pink) and the nuclei (reddish purple), decreases the frequency of burst pollen, increases pollen expansion, stabilizes pollen figures and automatically seals the coverglass.     

Hybridisation between oilseed rape (Brassica napus) and tetraploid Brassica rapa under field conditions

Cross-compatible relatives of crop species contribute to the uncertainty regarding the potential risk of transgene escape from genetically modified varieties. The most successful crossing partner of oilseed rape (Brassica napus L.) is diploid Brassica rapa L. Variation of ploidy level among B. rapa cultivars has, until recently, been neglected in the context of gene flow and hybridisation with oilseed rape. We estimated the extent of hybridisation between autotetraploid B. rapa varieties (female) and B. napus (pollen donor) under experimental field conditions. Morphology, variation of relative DNA amount, and microsatellite markers were used to distinguish between intraspecific offspring of tetraploid B. rapa and interspecific hybrids with B. napus. Of 517 seed progenies of tetraploid B. rapa, 45 juvenile plants showed species specific morphological traits of oilseed rape. The detection of putative hybrids based on variation in relative DNA amounts was problematic due to the occurrence of aneuploidy. In total, 84 offspring showed relative DNA amounts deviating from tetraploid B. rapa, four of which were hexaploids. Of the 205 offspring analysed at three microsatellite loci, 67 had oilseed rape alleles. Based on molecular evidence a minimum hybridisation rate of 13.0% was estimated. A few mother plants accounted for the majority of hybrids. The mean pollen viability of hybrids between B. napus and tetraploid B. rapa (80.6%) was high in comparison with mean pollen viability of triploid hybrids between B. napus and diploid B. rapa. Therefore, the occurrence of tetraploid B. rapa should be taken into consideration when estimating the likelihood of gene flow from oilseed rape to close relatives at the landscape level. Tetraploid B. rapa is a common component of several seed mixtures and establishes feral populations in northwest Germany. Assuming a similar abundance of diploid and tetraploid B. rapa, gene flow from B. napus to tetraploid may be more likely than gene flow to diploid B. rapa.