Life history studies of the predaceous mite Phytoseius hawaiiensis

Phytoseius hawaiiensis (Acari: Phytoseiidae) had relatively long periods of preoviposition, oviposition and postoviposition (4.6, 46.9 and 52.0 days, respectively, at 24 °C), and a relatively low fecundity (31.4 eggs per female), compared to other phytoseiid species. The most favorable food tested was all stages of Oligonychus punicae (Hirst), but various other species of mite prey as well as pollen also promoted oviposition. Extreme variation was observed in hatching time of the eggs, from 10 min (rare) to over 4 days (common). Occasionally, females apparently retain their eggs until just before larvae hatch, as eggs containing developed larvae were observed inside some females. Results of experiments suggested that unsuitable substrate (e.g. for oviposition) is a factor which induces longer egg retention prior to oviposition.

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Résumé Chez Phytoseius hawaiiensis, les durées des périodes précédant la ponte, correspondant à la ponte et succédant à la ponte, sont relativement longues; respectivement 4, 6; 31, 4 et 52 jours à 24 °C; dans ces conditions, la fécondité est relativement basse: 31, 4 oeufs par femelle. Oligonychus punicae (aux différents stades) a constitué le meilleur aliment essayé, mais diverses autres espèces d'acariens ainsi que le pollen induisent la ponte. La date d'éclosion des oeufs a présenté une très grande variabilité, de 10 min (rare) à plus de 4 jours (fréquent). Souvent, les femelles semblent retenir leurs oeufs jusqu'au moment précédant l'éclosion des larves, car des oeufs contenant des larves développées on été observés dans quelques femelles. Les résultats des expériences ont suggére qu'un substrat défavorable (pour la ponte) induit une plus longue rétention de la ponte.

     

The uptake of a polyvalent cation and its distribution in the root apices of Allium cepa: Tracer and autoradiographic studies

Summary Observations on the inhibition of root elongation and cell division in Allium cepa showed that the toxic effects of scandium and aluminium were very similar. Tracer uptake studies using ⁴⁶Sc indicated that the rate of uptake in the apical 3.0 mm of the axis was more rapid than elsewhere in the root and proceeded in two distinct phases; Phase 1, probably superficial adsorption, was characterised by a rapid initial rate which was little affected by low temperature, the rate of Phase 2 was slower but remained constant for 24 hours and was highly dependent on temperature.Autoradiographs from roots treated for 30 min with ⁴⁶Sc showed that most of the isotope in the root tip was concentrated in a peripheral belt corresponding with the mucigel layer of the root cap and it is suggested that this is the site of Phase 1 adsorption. The underlying root cap and epidermal cells retained little scandium but interior to them some isotope was associated with dividing cells; this increased steadily over 6 hour to an estimated concentration of 30 mM, and possibly represents Phase 2 uptake. Differentiation and secondary wall formation in the cortex restricted the rate of radial penetration of scandium. The primary endodermis restricted the entry of scandium into the stele at a very early stage in its development, which leads to the conclusion that migration of the ion across the root is primarily in the free space.Scandium enters the dividing cells in advance of observable effects on cell division, a situation compatible with the direct involvement of this ion in the inhibition of the mitotic cycle. Suggestions are made on the mechanisms by which polyvalent cations might disturb cell division and extension.     

Inversions over the terminus region in Salmonella and Escherichia coli: IS200s as the sites of homologous recombination inverting the chromosome of Salmonella enterica serovar typhi

Genomic rearrangements (duplications and inversions) in enteric bacteria such as Salmonella enterica serovar Typhimurium LT2 and Escherichia coli K12 are frequent (10(-3) to 10(-5)) in culture, but in wild-type strains these genomic rearrangements seldom survive. However, inversions commonly survive in the terminus of replication (TER) region, where bidirectional DNA replication terminates; nucleotide sequences from S. enterica serovar Typhimurium LT2, S. enterica serovar Typhi CT18, E. coli K12, and E. coli O157:H7 revealed genomic inversions spanning the TER region. Assuming that S. enterica serovar Typhimurium LT2 represents the ancestral genome structure, we found an inversion of 556 kb in serovar Typhi CT18 between two of the 25 IS200 elements and an inversion of about 700 kb in E. coli K12 and E. coli O157:H7. In addition, there is another inversion of 500 kb in E. coli O157:H7 compared with E. coli K12. PCR analysis confirmed that all S. enterica serovar Typhi strains tested, but not strains of other Salmonella serovars, have an inversion at the exact site of the IS200 insertions. We conclude that inversions of the TER region survive because they do not significantly change replication balance or because they are part of the compensating mechanisms to regain chromosome balance after it is disrupted by insertions, deletions, or other inversions.     

Exploring the specificity of bacterial elongation factor Tu for different tRNAs

In order to identify amino acids in Thermus thermophilus elongation factor Tu which contribute to its specificity for different tRNAs, the binding affinities of 20 point mutations were compared to that of wild type protein using four tRNAs of differing affinities. The observed specificity for tRNA is the result of the varying contributions of five amino acids which make contacts with the T-stem and the 3' terminus of tRNA. For three of the amino acids the test tRNAs differ in sequence at the site of contact, presumably explaining the specificity. However, the remaining two amino acids contact tRNA at conserved positions, suggesting that more global structural or dynamic properties of the free tRNA contribute to specificity.     

Inferring angiosperm phylogeny from EST data with widespread gene duplication

Background

Most studies inferring species phylogenies use sequences from single copy genes or sets of orthologs culled from gene families. For taxa such as plants, with very high levels of gene duplication in their nuclear genomes, this has limited the exploitation of nuclear sequences for phylogenetic studies, such as those available in large EST libraries. One rarely used method of inference, gene tree parsimony, can infer species trees from gene families undergoing duplication and loss, but its performance has not been evaluated at a phylogenomic scale for EST data in plants.

Results

A gene tree parsimony analysis based on EST data was undertaken for six angiosperm model species and Pinus, an outgroup. Although a large fraction of the tentative consensus sequences obtained from the TIGR database of ESTs was assembled into homologous clusters too small to be phylogenetically informative, some 557 clusters contained promising levels of information. Based on maximum likelihood estimates of the gene trees obtained from these clusters, gene tree parsimony correctly inferred the accepted species tree with strong statistical support. A slight variant of this species tree was obtained when maximum parsimony was used to infer the individual gene trees instead.

Conclusion

Despite the complexity of the EST data and the relatively small fraction eventually used in inferring a species tree, the gene tree parsimony method performed well in the face of very high apparent rates of duplication.

     

The use of monoclonal antibodies to fragments of chicken type IV collagen in structural and localization studies

In previous experiments, three pepsin-resistant fragments of type IV collagen were isolated from chicken gizzards and designated 7S, F3, and (F1)2F2 (Mayne, R., and Zettergren, J. G. (1980) Biochemistry 19, 4065-4072). In the present experiments, a series of monoclonal antibodies to type IV collagen were prepared, each one of which recognized an epitope present in only one of the three fragments. A high molecular weight fraction of type IV collagen (designated 7S + arms (215 nm)) was isolated after agarose gel filtration and characterized by electron microscopy after rotary shadowing and by gel electrophoresis. Analysis of 7S + arms (215 nm) by inhibition enzyme-linked immunosorbent assay demonstrated the presence of the epitopes for 7S and F3 but not for (F1)2F2. This result, therefore, provides additional evidence that the order of the pepsin-resistant fragments of chicken type IV collagen is 7S-F3-(F1)2F2.     

The XbaI-BlnI-CeuI genomic cleavage map of Salmonella enteritidis shows an inversion relative to Salmonella typhimurium LT2

We have established the genomic cleavage map of Salmonella enteritidis strain SSU7998 using pulsed-field gel electrophoresis. The chromosome of 4600kb was analysed by XbaI (16 fragments), I-CeuI (7 fragments) and BlnI (12 fragments); the genome also contains a plasmid of 60 kb. Cleavage sites of I-CeuI, in the large subunit ribosomal RNA gene, are conserved from Salmonella typhimurium and Escherichia coli K-12, and the XbaI and BinI sites in glt-tRNA are also conserved, but other sites are less conserved. Transposon Tn10, located at 60 different positions in the chromosome of S. typhimurium, was transduced by bacteriophage P22 into S. enteritidis and the insertion mapped using the XbaI and BlnI sites on Tn10. Gene order in S. enteritidis is identical to S. typhimurium LT2 and similar to E. coli K-12 except for an inversion of 815 kb, which covers the terminus region including T1 and T2. Endpoints are in the NDZs, or non-divisible zones, in which inversion endpoints were not detected in experiments in E. coli K-12 and S. typhimurium LT2. This inversion resembles the inversion between S. typhimurium and E. coli, but is longer at both ends.