Two-pion production in deuteron-deuteron collisions at low energies

The cross section for the dd -> 4He pi pi reaction is estimated near threshold in a two-step model where a pion created in a first interaction produces a second pion in a subsequent interaction. This approach, which describes well the rates of 2pi and eta production in the pd -> 3He pi pi and dd -> 4He eta reactions, leads to predictions that are much too low compared to experiment. Alternatives to this and the double-Delta model will have to be sought to explain these data.Comment: 5 pages with 4 postscript figure

Eta-Helium Quasi-Bound States

The cross section and tensor analysing power t_20 of the d\vec{d}->eta 4He reaction have been measured at six c.m. momenta, 10 < p(eta) < 90 MeV/c. The threshold value of t_20 is consistent with 1/\sqrt{2}, which follows from parity conservation and Bose symmetry. The much slower momentum variation observed for the reaction amplitude, as compared to that for the analogous pd->eta 3He case, suggests strongly the existence of a quasi-bound state in the eta-4He system and optical model fits indicate that this probably also the case for eta-3He.Comment: LaTeX, uses elsart.sty, 10 pages, 3 Postscript figures, Submitted to Physics Letters

The pd --> ^3He eta pi0 reaction at T_p = 1450 MeV

The cross section for the pd --> ^3He eta pi0 reaction has been measured at a beam energy of 1450 MeV using the WASA detector at the CELSIUS storage ring and detecting one ^3He and four photons from the decays of the two photons. The data indicate that the production mechanism involves the formation of the Delta(1232) isobar. Although the beam energy does not allow the full peak of this resonance to be seen, the invariant masses of all three pairs of final state particles are well reproduced by a phase space Monte Carlo simulation weighted with the p-wave factor of the square of the pi^0 momentum in the ^3Hepi^0 system.Comment: 10 pages, 5 figure

Differential Expression of miRNAs in Response to Topping in Flue-Cured Tobacco (Nicotiana tabacum) Roots

Topping is an important cultivating measure for flue-cured tobacco, and many genes had been found to be differentially expressed in response to topping. But it is still unclear how these genes are regulated. MiRNAs play a critical role in post-transcriptional gene regulation, so we sequenced two sRNA libraries from tobacco roots before and after topping, with a view to exploring transcriptional differences in miRNAs.Two sRNA libraries were generated from tobacco roots before and after topping. Solexa high-throughput sequencing of tobacco small RNAs revealed a total of 12,104,207 and 11,292,018 reads representing 3,633,398 and 3,084,102 distinct sequences before and after topping. The expressions of 136 conserved miRNAs (belonging to 32 families) and 126 new miRNAs (belonging to 77 families) were determined. There were three major conserved miRNAs families (nta-miR156, nta-miR172 and nta-miR171) and two major new miRNAs families (nta-miRn2 and nta-miRn26). All of these identified miRNAs can be folded into characteristic miRNA stem-loop secondary hairpin structures, and qRT-PCR was adopted to validate and measure the expression of miRNAs. Putative targets were identified for 133 out of 136 conserved miRNAs and 126 new miRNAs. Of these miRNAs whose targets had been identified, the miRNAs which change markedly (>2 folds) belong to 53 families and their targets have different biological functions including development, response to stress, response to hormone, N metabolism, C metabolism, signal transduction, nucleic acid metabolism and other metabolism. Some interesting targets for miRNAs had been determined.The differential expression profiles of miRNAs were shown in flue-cured tobacco roots before and after topping, which can be expected to regulate transcripts distinctly involved in response to topping. Further identification of these differentially expressed miRNAs and their targets would allow better understanding of the regulatory mechanisms for flue-cured tobacco response to topping

A comparison of biodegradation caused by Teredinidae (Mollusca:Bivalvia), Limnoriidae (Crustacea:Isopoda), and C. terebans (Crustacea:Amphipoda) across 4 shipwreck sites in the English Channel

The need to protect underwater cultural heritage from biodegradation is paramount, however with many sites needing funding and support, it is hard to prioritise, thus the ability to identify high risk sites is crucial to ensure resources are best placed. In doing so a clear understanding of environmental conditions acting upon a site and abundance and composition of species present is essential to this identification. Therefore, the aim of this study was to assess the rate of biodegradation on four underwater cultural heritage sites in different marine environments by placing a series of wooden test panels in direct contact with the exposed structure on the sites. Upon recovery, test panels were photographed, X-rayed, and wood boring and sessile fouling species were identified and counted. The damage attributed to each species was recorded with CAD software. Results indicated a significant difference between sites, with HMS Invincible having the highest abundance of marine wood borers and the highest rate of surface area and volume degradation; whilst vestigial evidence of marine wood borers was found on the London, it would appear the environmental conditions had significantly impeded their survival. The study indicated further factors such as sediment type and coverage, availability of wood and the proximity of other colonised sites were also determining factors controlling the abundance of marine wood borers and the rate of biodegradation

Developmental dynamics of myogenesis in the shipworm Lyrodus pedicellatus (Mollusca: Bivalvia)

Background: The shipworm Lyrodus pedicellatus is a wood-boring bivalve with an unusual vermiform body. Although its larvae are brooded, they retain the general appearance of a typical bivalve veliger-type larva. Here, we describe myogenesis of L. pedicellatus revealed by filamentous actin labelling and discuss the data in a comparative framework in order to test for homologous structures that might be part of the bivalve (larval) muscular ground pattern. Results: Five major muscle systems were identified: a velum retractor, foot retractor, larval retractor, a distinct mantle musculature and an adductor system. For a short period of larval life, an additional ventral larval retractor is present. Early in development, a velum muscle ring and an oral velum musculature emerge. In late stages the lateral and dorsal mantle musculature, paired finger-shaped muscles, an accessory adductor and a pedal plexus are formed. Similar to other bivalve larvae, L. pedicellatus exhibits three velum retractor muscles, but in contrast to other species, one of them disappears in early stages of L. pedicellatus. The remaining two velum retractors are considerably remodelled during late larval development and are most likely incorporated into the elaborate mantle musculature of the adult. Conclusions: To our knowledge, this is the first account of any larval retractor system that might contribute to the adult bodyplan of a (conchiferan) mollusk. A comparative analysis shows that a pedal plexus, adductors, a larval velum ring, velum retractors and a ventral larval retractor are commonly found among bivalve larvae, and thus most likely belong to the ground pattern of the bivalve larval musculature

Developmental dynamics of myogenesis in the shipworm Lyrodus pedicellatus (Mollusca: Bivalvia) - Additional files

Additional files to: Wurzinger-Mayer, Andrea, J Shipway, Alen Kristof, Thomas Schwaha, Simon M Cragg, and Andreas Wanninger. 2014. "Developmental Dynamics of Myogenesis in the Shipworm Lyrodus Pedicellatus (Mollusca: Bivalvia)." Frontiers in Zoology 11 (1): 90. doi:10.1186/s12983-014-0090-9. Additional file 1: Figure S1.: Scanning electron micrographs of late-stage Lyrodus pedicellatus larvae. Additional file 2: Description of the methods used to generate the scanning electron micrograph shown in Supplemental Figure 1