An integrated approach to control glyphosate‐resistant Ambrosia trifida with tillage and herbicides in glyphosate‐resistant maize

Glyphosate‐resistant Ambrosia trifida is a competitive and difficult‐to‐control annual broad‐leaved weed in several agronomic crops in the Midwestern United States and Ontario, Canada. The objectives of this study were to compare treatments for control of glyphosate‐resistant A. trifida with tillage followed by pre‐emergence (PRE) and/or post‐emergence (POST) herbicides in glyphosate‐resistant maize and to determine the impact of A. trifida escapes on maize yield. Field experiments were conducted in 2013 and 2014 in grower fields infested with glyphosate‐resistant A. trifida. Tillage prior to maize sowing resulted in 80–85% control compared with no tillage. Tillage followed by PRE application of saflufenacil plus dimethenamid‐P with or without atrazine resulted in 99% control compared with ≤86 and 96% control with PRE herbicides alone at 7 and 21 days after application respectively. Tillage or POST‐only herbicides resulted in 4–14 A. trifida plants m^?2, whereas a PRE and POST programme had <3 plants m^?2. Maize yield was greatest (13.1–14.2 tonnes ha^?1) with tillage followed by PRE and POST herbicide programme. The relationship between maize yield and late‐season density of A. trifida escapes showed a 50% maize yield reduction irrespective of control measures when A. trifida density was 8.4 plants m^?2. It was concluded that the combination of tillage with PRE and/or POST herbicides reduced A. trifida density and biomass accumulation early in the season and provided an integrated approach for effective management.     

氮素水平对茶树新梢叶片代谢谱及其昼夜变化的影响

茶树叶片中含有丰富的代谢产物,氨基酸、茶多酚和咖啡碱是决定茶叶品质的重要成分。本文结合基于1H-核磁共振(1H-NMR)的代谢组学非靶标分析与通过高效液相色谱法进行的定量靶标分析两种方法,比较白天和夜晚所取不同施氮水平的茶树新梢第2叶的代谢产物差异,探讨了基于1H-NMR的代谢组学研究方法应用于茶叶品质成分形成机理研究的可行性。结果表明,白天和夜晚所取茶树新梢第2叶代谢组差异较大,可以显著分离,区分两个样本的主要组分为茶氨酸、葡萄糖和蔗糖,而不同施氮水平下茶树新梢第2叶代谢组没有显著差异。高效液相色谱定量分析的结果表明,施氮水平对主要游离氨基酸组分和儿茶素组分均有影响,且存在昼夜差别。     

Vaccination and challenge studies with psittacine beak and feather disease virus

SUMMARY: Psittacine beak and feather disease virus (PBFDV) was administered to adult galahs ( Eolophusroselcapillus ) by mouth or by intramuscular injection. Concentration of PBFDV antibodies in serum and excretion of PBFDV were monitored by haemagglutlnation inhibition (HI) and haemagglutination (HA) respectively. After oral administration, 17 of 18 galahs remained clinically normal and a small rise in antibody titre was detected in 3 of 18 birds. After intramuscular administration, antibody was detected in all birds. PBFDV was not detected in the feather dander of birds in either group. One bird developed diarrhoea and high faecal HA titres within 4 days of oral administration and then died. Adult and nestling cockatoos were vaccinated with an experimental inactivated double-oil emulsion vaccine. PBFDV antibody responses are comparable to those induced by a primary-oil emulsion vaccination regimen using Freund's adjuvants. Both vaccines protected nestlings. Three sibling wild-caught sulphur-crested cockatoos were vaccinated but died of PBFD before experimental challenge despite antibody responses in all birds. Unvaccinated control chicks developed acute PBFD within 4 weeks of challenge, probably from PBFDV-induced hepatitis since high concentrations of PBFDV were detected in their livers.     

Epidemiological and clinical investigations into big liver and spleen disease of broiler breeder hens

SUMMARY The epidemiological and clinical features of big liver and spleen disease (BLS) in flocks on two broiler breeder farms were investigated by serology and gross pathology. The most common necropsy findings on farm 1 were splenomegaly and hepatomegaly, with kidney enlargement in some birds. In one flock (farm 1), a decline in egg production began at 40 weeks of age and lasted for 9 weeks. Seroconversion to BLS antigen was first detected at 45 weeks (3.1% of birds) and increased to 72% at 50 weeks, which coincided with clinical recovery in the flock. Antigen was detected before antibody at 44 weeks and persisted at low incidence (<15%). Farm egg production statistics and serology indicated that the disease affected all flocks on the farm. In three of eight flocks, seroconversion was detected in birds before peak production. The birds in the remaining sheds did not seroconvert or become sick until after peak production. On the second farm, sampling began within a flock already experiencing BLS. Clinical signs and pathology were similar to those seen in flocks on farm 1. However, the lesions that were seen in the pancreas in 15% of birds have not been reported previously. BLS antibody was detected in 78%, and circulating antigen in 14%, of sick birds.     

Clinicopathologic analysis of herpesvirus-induced urinary tract infection in specific-pathogen-free cats given methylprednisolone

The clinicopathologic manifestations of bovid herpesvirus-4 (BHV-4; FCAHV strain)-induced infection of the lower portion of the urinary tract were characterized in 12 adult neutered male and 6 female specific-pathogen-free cats, and were compared with those in 12 neutered male control cats. Six neutered male and 6 female cats were given immunosuppressive doses of methylprednisolone acetate prior to inoculation of their urinary bladders with BHV-4. Six neutered male control cats were given immunosuppressive doses of methylprednisolone acetate prior to inoculation of their urinary bladders with uninfected tissue culture control inoculum. Six additional neutered male control cats were exposed only to uninfected tissue culture control inoculum. All cats were observed for 90 days following inoculation. Dysuria and gross hematuria were observed in only 1 BHV-4-exposed cat. Radiographic abnormalities of the lower portion of the urinary tract were not observed. Microscopic hematuria, crystalluria, and lipiduria were identified with similar frequency in BHV-4-exposed and control cats. Results of urine culturing for bacteria, mycoplasma, ureaplasma, and viruses were negative. Viruses were not isolated from blood leukocytes collected from exposed or control cats. Three to 6 weeks after inoculation, high concentrations of BHV-4 serum antibodies were detected in all exposed cats by an indirect fluorescent antibody test. Light microscopic examination of the urinary tract revealed multifocal lymphoid cystitis in 2 BHV-4-exposed cats. Except for suppurative bronchitis in 1 BHV-4-exposed cat given glucocorticoids, morphologic differences in urinary and extraurinary tissues were not observed. In urinary bladder tissue collected 90 days after inoculation, BHV-4 was reisolated from urinary bladder explants of all but 1 exposed cat. Virus was also isolated from a kidney explant of 1 exposed male cat, and spleen cell co-cultures of 1 exposed female cat given glucocorticoids.(ABSTRACT TRUNCATED AT 250 WORDS)     

水稻丝氨酸蛋白酶S8基因家族的分布及分析

水稻丝氨酸蛋白酶S8基因家族在水稻的生长发育过程中起着重要的调控作用。本研究利用公共数据库资源,分析水稻中丝氨酸蛋白酶S8基因家族,在水稻12条染色体上找到46个该类基因。通过其结构分析发现,每个基因的内含子数目从0到10各不相同,但氨基酸序列是非常保守的,都有催化活性位点和底物结合位点。系统进化树分析显示,这46个基因分为3个亚家族,S8-1亚家族最大。该家族基因的进化主要是通过基因重复复制的方式进行,其表达模式发生了变化,并且多个基因在穗部具有表达。     

Effect of Roller Mill Extraction Rate on the Chapatti-Making Quality of Canadian Flours

The effect of roller mill extraction rate on the chapatti-making potential of Canadian wheat from six different classes was assessed. Objective measurement of texture including pliability, puncturability, and tearing force, in conjunction with color, discerned significant differences due to flour extraction rate as well as wheat class. The 85% extraction yield was determined by sensory panelists to yield the best chapatti. Analyses of objective measurements, HunterLab values L*, a*, and b*, in conjunction with sensory assessments, suggested that the optimum chapatti have a brightness (L*) of 75–79, redness (a*) of 1.5–4.0, and a yellowness (b*) >17. Sensory scoring compared with objective measurement indicated that a tearing force of <4.0 kg was necessary to achieve optimum panelist evaluation of tearing and chewability. The primary reasons for a fair rating were attributable to either a too white and nonwheaty taste for the low extraction flours or, in the case of the 95% extraction material, dark chapattis with a slightly off flavor. No chapatti prepared from any of the wheat classes or varying extraction rate flours resulted in an unacceptable rating. Evidence suggests that removal of low-extraction mill-streams, up to 40%, from a 85% extraction yield flour did not have a detrimental effect on chapatti quality.     

Cross-resistance of horseweed (Conyza canadensis) populations with three different ALS mutations

BACKGROUND: Horseweed is a weed commonly found in agronomic crops, waste areas and roadsides. Resistance to ALS‐inhibiting herbicides in horseweed was first reported in 1993 in a population from Israel. Resistance to ALS‐inhibiting herbicides in horseweed is now widespread, but, as of now, the resistance mechanism has not been reported. RESULTS: Two of three populations evaluated (P116 and P13) were found to be uniform for resistance (>98% of individuals survived 8.8 g AI ha^?1 of cloransulam), whereas a third population, P525, contained about 85% resistant individuals. Cross‐resistance to cloransulam, chlorimuron, imazethapyr and bispyribac was observed in the P116 population. P525 and P13 were both sensitive to imazethapyr but resistant to chlorimuron, imazethapyr and bispyribac. Enzyme activity assays indicated that resistance in P13 was due to an altered target site. Southern blot analysis indicated that the ALS target site is encoded by a single copy gene. Overlapping ALS gene regions were amplified and sequenced from each population. Amino acid substitutions of Ser for Pro at position 197 (P197S) was detected from P13, Ala for Pro (P197A) was identified from P525 and substitution of Glu for Asp (D376E) at position 376 was found in P116. Molecular markers were developed to differentiate between wild‐type and resistant codons at positions 197 and 376 of horseweed ALS. CONCLUSION: Resistance to ALS‐inhibiting herbicides in horseweed is conferred by target‐site mutations that have also been identified in other weed species. Identification of the mutations within horseweed ALS gene sequence enables molecular assays for rapid detection and resistance diagnosis. Copyright © 2011 Society of Chemical Industry