Using Allium alien monosomic addition lines to study chlorophyll degradation in stored Japanese bunching onion

Summary

Chlorophyll (Chl) degradation and the formation of Chl derivatives in stored leaves of Japanese bunching onion (JBO; Allium fistulosum L., genome FF) were determined to elucidate the mechanism of Chl degradation by using alien monosomic addition lines (AMALs; FF+1A to FF+8A) of JBO from shallot (A. cepa L. Aggregatum group, genome AA). Year-round changes in Chl content in JBO and in the AMALs were also detected over 2 years. The Chl content in FF was significantly influenced by the alien chromosomes from shallot. In particular, the Chl contents of FF+4A or FF+5A, were higher in Winter than in FF, which suggests that chromosomes 4A and 5A from shallot had a larger influence on the formation of Chl than the other chromosomes. Chl contents in FF+3A and FF+5A decreased greatly in the leaves of AMALs and JBO during storage at 25°C, whereas in FF+4A the Chl content was the lowest compared to the control, FF. Chlorophyllide (Chlide) a, C13²-hydroxychlorophyll (OHChl) a, pheophorbide a, and pheophytin (Phy) a, as derivatives of Chl a, were present mainly during storage of JBO and the AMALs. Phy alevels increased with Chl degradation, especially in FF+3A, while OHChl alevels in FF and FF+3A showed a decline during storage. In addition, Chlide alevels in all lines diminished during storage.Thus, Chl amay be degraded, in part, through Phy a, as well as Chlide aand OHChl a, in JBO and the AMALs during storage.     

Direct seeding as an alternative to transplanting for guayule in southeast Queensland

Guayule (Parthenium argentatum Gray) is a source of high quality rubber and low-allergenic latex. Commercial potential of guayule to produce high value latex products has increased due to the increased incidence of deadly diseases in humans. The objective of this study was to investigate the potential of direct seeding in southeast Queensland as an alternative to establishment by the current high cost transplanting method. Experiments were conducted for 2 years at Gatton, Queensland using physical and chemical seed treatments. NaOCl plus GA₃, osmo-priming with polyethylene glycol, seed pelleting and seed tape planting were tested. Planting depth had a significant influence on seedling emergence. Emergence at 18 mm depth (1.5 seedlings/m) was significantly reduced compared with 10 mm depth (2.9 seedlings/m). Osmo-priming was effective in increasing germination from 36 to 47%. It also improved seedling emergence and vigour. Osmo-priming significantly increased establishment (7.5 seedlings/m) compared with untreated seed (3.3 seedlings/m). NaOCl plus GA₃ did not have a significant influence on germination (38%) or seedling emergence (5.0 seedlings/m) but increased survival at 42 days after planting. Establishment as a percentage of emerged seedlings was high for both osmo-primed and NaOCl plus GA₃ treatments with 89 and 88% respectively, whereas untreated seed had only 70% survival. Osmo-priming also increased vigour as indicated by increased root length (101 mm), shoot height (123 mm), and seedling dry matter (379 mg/seedling) compared with the control (83, 107 mm and 206 mg/seedling, respectively).     

Combined effect of biochar and soil moisture on soil chemical properties and microbial community composition in microplastic-contaminated agricultural soil

Accumulation of microplastics (MPs) in agricultural environments has caused growing concern in recent years because of its detrimental impacts on soil quality, crop productivity and ecosystem function. This study was conducted to assess the impact of biochar on soil chemical and microbial properties in a MP-contaminated soil under two moisture regimes. Soil was contaminated with 1% (w/w) of low-density polyethylene MPs. Four types of standard biochar, that is, oil seed rape (OSR) biochar produced at 550°C (OSR 550) and 700°C (OSR 700) and soft wood pellet (SWP) biochar produced at 550°C (SWP 550) and 700°C (SWP 700), were applied at a rate of 5% (w/w). The control was maintained without MP addition. The samples were incubated in soil with two moisture regimes, that is, at 30% and 70% of the water holding capacity, and the soil chemical and microbiological properties were assessed after 100 days of incubation. OSR biochar application significantly increased soil pH (8.53–8.81) and electrical conductivity (0.51–0.58 dS/m) in both moisture regimes. The effect of biochar application on soil enzyme activity and microbial community composition did not show a clear trend. However, SWP 700 biochar improved soil enzyme activity compared with that of the control and improved bacterial diversity and evenness compared with those of other biochars, which was attributed to the high surface area available for microbial colonization. Low soil moisture content significantly reduced enzyme activity and bacterial richness even with biochar amendment, except for SWP 550 biochar. This study implies the suitability of biochar for improvement of soil quality in MP contaminated soil under both moisture regimes. However, further long-term studies are needed to get a clear understanding on the impact of different types of biochar on MP-contaminated soil.     

Atmospheric residence time of CH3Br estimated from the junge spatial variability relation

The atmospheric residence time for methyl bromide (CH3Br) has been estimated as 0.8 +/- 0.1 years from its empirical spatial variability relative to C2H6, C2Cl4, CHCl3, and CH3Cl. This evaluation of the atmospheric residence time, based on Junge's 1963 general proposal, provides an estimate for CH3Br that is independent of source and sink estimates. Methyl bromide from combined natural and anthropogenic sources furnishes about half of the bromine that enters the stratosphere, where it plays an important role in ozone destruction. This residence time is consistent with the 0.7-year value recently calculated for CH3Br from the combined strength estimates for its known significant sinks.     

Distribution of lipopolysaccharide core types among avian pathogenic Escherichia coli in relation to the major phylogenetic groups

Five distinct lipopolysaccharide (LPS) core types, namely R1-R4 and K12 have been identified in Escherichia coli. The aims of this study were to determine, primarily by means of PCR, the distribution of those oligosaccharide core types among avian pathogenic E. coli and their relationship to phylogenetic groups. To identify putative avian pathogenic E. coli, serum resistance and the presence of three virulence genes encoding temperature sensitive haemagglutinin (tsh), increased serum survival (iss) and colicin V (cvaC) were determined. Of the 143 clinical isolates examined 62% possessed the R1 core, 22% were R3, 13% were R4 and 3% were R2. Fifty commensal isolates consisted of 58% with R1 core, 38% with R3 core, 4% with R4 core, and none with R2. None of the isolates were of K12 core type. The distribution of core oligosaccharide types in clinical and commensal isolates were not statistically significant (P=0.51). Three genes, tsh, iss and cvaC were found in E. coli of all four core types. The genes tsh (P<0.001) and iss (P=0.03412) were significantly associated with the R4 core oligosaccharide type. The isolates containing R4 core type LPS were mainly confined to phylogenetic group D. The widespread R1 core type showed less ability to possess virulence genes and 83% were in the phylogenetic group A. Results of this study indicated that E. coli with R1, R2, R3 and R4 were important in causing infections in chickens and further, the E. coli with R4 core type were less common among commensals, possessed more virulence genes and were related to phylogenetic groups pathogenic for poultry.     

Assessment of the potential toxicity of a poison for rabbits, pindone (2-pivalyl 1, 3 indandione), to domestic animals

The toxicity of pindone, a rabbit poison, to horses, cattle, goats, chickens, dogs and cats was investigated, using extension of prothrombin time (PT) as an index of poisoning. The daily dose of pindone, administered for 5 days, ranged from 0.3 mg/kg for dogs to 2.5 mg/kg for chickens. This range of dose rates was considered to be indicative of the worst possible case that could arise following a campaign of baiting for rabbits. Although significant elevations in PT (more than double baseline values) were noted in all species other than horses, clinical signs of anticoagulant poisoning were not observed in any of the species tested. From the observed PT, cattle and cats appeared to be the most susceptible, and horses the least susceptible, to pindone toxicity. The half-lives of the elevated PT were calculated as 3.1 days for cattle, 2.8 days for goats and chickens, 1.9 days for horses and dogs and less than one day for cats. It is proposed that these half-lives can be used as a guide for determining the duration of treatment of pindone-affected animals.     

如何提高仔猪饲料中小麦的利用率

<正>用最具成本效益的方法配制猪饲料是提高养猪场经济利润的一种重要手段。但是,具有最低成本的饲料配制方法往往会就几种主要饲料原料的饲喂价值进行过于简单的假设,同时还假定各饲料原料的养分具有相加性。这种情况会因饲料添加剂的加入而进一步混乱,或受到潜在的损害,因为饲料添加剂旨在使饲料释放更多的能量和/或氨基酸。因此,饲料配方师不得不充分确保某种添加剂将持     

Population structure and virulence content of avian pathogenic Escherichia coli isolated from outbreaks in Sri Lanka

Avian pathogenic Escherichia coli (APEC) causes economically significant infections in poultry. The genetic diversity of APEC and phylogenetic relationships within and between APEC and other pathogenic E. coli are not yet well understood. We used multilocus sequence typing (MLST), PCR-based phylogrouping and virulence genotyping to analyse 75 avian E. coli strains, including 55 isolated from outbreaks of colisepticaemia and 20 from healthy chickens. Isolates were collected from 42 commercial layer and broiler chicken farms in Sri Lanka. MLST identified 61 sequence types (ST) with 44 being novel. The most frequent ST, ST48, was represented by only six isolates followed by ST117 with four isolates. Phylogenetic clusters based on MLST sequences were mostly comparable to phylogrouping by PCR and MLST further differentiated phylogroups B1 and D into two subgroups. Genotyping of 16 APEC associated virulence genes found that 27 of the clinical isolates and one isolate from a healthy chicken belonged to highly virulent genotype according to previously established classification schemes. We found that a combination of four genes, ompT, hlyF, iroN and papC, gave a comparable prediction to that of using five and nine genes by other studies. Four STs (ST10, ST48, ST117 and ST2016) contained APEC isolates from this study and human UPEC isolates reported by others, suggesting that these STs are potentially zoonotic. Our results enhanced the understanding of APEC population structure and virulence association.