The ectoparasitization of Coleophora alticolella (Lepidoptera) in relation to its aititudinal distribution

Abstract. 1. The parasitization of the larvae of Coleophora alticolella . feeding on Juncus squarrosus , was investigated at a series of altitudes from 15 to 520m above sea-level in northern England during 1977 and 1978.
2. Six species of primary parasitoid and one hyperparasitoid were reared from this host. Five of the primary parasitoids were ectophagous; only two specimens of the endoparasitoid, Gonotypus melanostoma , were reared.
3. All of the parasitoid species were recorded at 15 m but fewer at sites of higher altitude. Only one species, Scambus brevicomis , was recorded above 305 m, and none above 395 m. The hyperparasitoid, Tetrastichus endemus, was present only at 15 m.
4. Percentage parasitization was highest at 15 m; it was reduced from 51% to only 2% between 215 and 305 m in 1978. There was an increase in host density over this altitudinal range.
5. Three species, Scambus brevicomis. Elachertus olivaceus and Euderus viridis , accounted for most of the parasitization, but their relative proportions vaned at different altitudes.
6. The sex-ratios of the parasitoids reared from Coleophora alticolella ranged from 3.2% females for Scambus brevicomis , which is considered to also use larger hosts, to 99.4% females for Elachertus olivaceus , which develops by thelytokous parthenogenesis.
7. Euderus viridis and Scambus brevicomis started to attack the Coleophora alticolella larvae at a later date at 245 m than at 15 m, but attack by Elachertus olivacats was not delayed at the higher site.     

Functional organization and plasticity of the photosynthetic unit of the cyanobacterium Anacystis nidulans

Anacystis nidulans grown under high and low light, 100 and 10 μE m^?2 s^?1, respectively, was analyzed with respect to chlorophyll/P700, phycobiliproteins/P700, chlorophyll/cell, and oxygen evolution parameters. The photosynthetic unit sizes of this cyanobacterium, measured as the ratio of total chromophores (chlorophyll and bilin) to P700, were shown to be similar to those of higher plants and green algae. High light grown cells possessed a photosynthetic unit consisting of a core of 157 ± 6 chlorophyll a molecules per P700 associated with a light harvesting system of 95 ± 3.5 biliprotein chromophores. Low light grown cells had substantially more biliprotein chromophores per P700 (125 ± 3.1) than high light cells, but showed no significant difference in the numbers of chlorophyll a molecules per P700 (149 ± 4). Analyses of aqueous biliprotein extracts indicate that low light grown cells produce proportionately more phycocyanin relative to allophycocyanin than high light cells. Calculations of the molecular weight of biliproteins per P700 suggest that there is less than one phycobilisome per reaction center I under both growth conditions. Differences in chlorophyll/cell ratios and oxygen evolution characteristics were also observed. High light cells contain 6.3 × 10^?12 mg chlorophyll cell^?1, while low light grown cells contain 12.8 × 10^?12 mg chlorophyll cell^?1. Photosynthetic oxygen evolution rate vs. light intensity curves indicate that high light grown cells reach maximal levels of oxygen evolution at higher light intensity than low light grown cells. Maximal rates of oxygen evolution were 16.6 μmol oxygen min^?1 (mg chlorophyll)^?1 for high and 8.4 μmol oxygen min^?1 (mg chlorophyll)^?1 for low light cells. Maximal oxygen evolution rates per cell were equivalent for both cell types, although the amount of P700 per cell was lower in high light cells. High light grown cells are therefore capable of producing more oxygen per reaction center I than low light grown cells.     

The "Goldilocks Effect" in Cystic Fibrosis: identification of a lung phenotype in the <Emphasis Type="Italic">cftr</Emphasis> knockout and heterozygous mouse

Background  

Cystic Fibrosis is a pleiotropic disease in humans with primary morbidity and mortality associated with a lung disease phenotype. However, knockout in the mouse of cftr, the gene whose mutant alleles are responsible for cystic fibrosis, has previously failed to produce a readily, quantifiable lung phenotype.     

Molecular genetic variation and geographical structuring in Fusarium graminearum

Inter‐simple sequence repeat markers were employed to study the genetic structure of Fusarium graminearum populations collected from three Canadian provinces. Our study suggested high genetic diversity and frequent gene flow among population samples analysed. The analysis of molecular variance indicated that most of the gene diversity (91.78% to 97.23%) was distributed within populations. Frequent gene flow among the western prairie provinces and cluster analysis results indicated that the population sample from Alberta was closer to Saskatchewan than Manitoba, which could be the result of movement of the pathogen via infected grain or through wind‐borne ascospore dispersal. Analysis of multilocus associations showed that all populations were in linkage equilibrium, indicating that sexual recombination is a frequent phenomenon in F. graminearum populations from western Canada.     

Ryanodine receptors, a family of intracellular calcium ion channels, are expressed throughout early vertebrate development

Background

We developed a new version of the open source software package Peptrix that can yet compare large numbers of Orbitrap? LC-MS data. The peptide profiling results for Peptrix on MS1 spectra were compared with those obtained from a small selection of open source and commercial software packages: msInspect, Sieve? and Progenesis?. The properties compared in these packages were speed, total number of detected masses, redundancy of masses, reproducibility in numbers and CV of intensity, overlap of masses, and differences in peptide peak intensities. Reproducibility measurements were taken for the different MS1 software applications by measuring in triplicate a complex peptide mixture of immunoglobulin on the Orbitrap? mass spectrometer. Values of peptide masses detected from the high intensity peaks of the MS1 spectra by peptide profiling were verified with values of the MS2 fragmented and sequenced masses that resulted in protein identifications with a significant score.

Findings

Peptrix finds about the same number of peptide features as the other packages, but peptide masses are in some cases approximately 5 to 10 times less redundant present in the peptide profile matrix. The Peptrix profile matrix displays the largest overlap when comparing the number of masses in a pair between two software applications. The overlap of peptide masses between software packages of low intensity peaks in the spectra is remarkably low with about 50% of the detected masses in the individual packages. Peptrix does not differ from the other packages in detecting 96% of the masses that relate to highly abundant sequenced proteins. MS1 peak intensities vary between the applications in a non linear way as they are not processed using the same method.

Conclusions

Peptrix is capable of peptide profiling using Orbitrap? files and finding differential expressed peptides in body fluid and tissue samples. The number of peptide masses detected in Orbitrap? files can be increased by using more MS1 peptide profiling applications, including Peptrix, since it appears from the comparison of Peptrix with the other applications that all software packages have likely a high false negative rate of low intensity peptide peaks (missing peptides).