电机护环钢在硝酸盐溶液中应力腐蚀开裂的控制过程研究

本文在文献［１］基础上，运用金相，电化学方法研究了５０Ｍｎ１８Ｃｒ４电机护环钢依照ＱＨＪ－７９试验标准在硝酸盐介质中应力腐蚀开裂（即ＳＣＣ）的性质，结果指出，此体系中ＳＣＣ的控制过程为阳极溶解。     

无公害技术在防治春尺蠖上的应用

阐述了春尺蠖的危害、发生规律及防治方法。利用糖醋盘 ,灯光诱杀成虫 ,在树干上捆绑草绳 ,喷涂毒环阻止成虫上树产卵及使用无公害生物制剂防治幼虫效果较好     

Pelargonium flower-break and pelargonium line pattern viruses in the Netherlands; purification,antiserum preparation,serological identification,and detection in pelargonium by ELISA

Two viruses, detected frequently in the Netherlands in pelargonium, were identified by serology and test plant reactions. Antisera were prepared and an ELISA procedure was developed to detect the viruses in pelargonium.One of the viruses, PFBV-N, proved to be pelargonium flower-break virus. With the antiserum to PFBV-N, it could be detected reliably throughout the year inPelargonium zonale Springtime Irene.The other virus, PLPV-N, was serologically closely related to pelargonium line pattern virus (PLPV) and to pelargonium ring pattern virus (PRPV), as were an old virus isolate from Saturnus, collected in the Netherlands in 1971 (L128), and PLPV isolates from Yugoslavia (PLPV-Y) and Denmark (PLPV-D). There were only minor differences in host-plant reactions between the virus isolates. Based on these tests, PLPV and PRPV are considered as isolates of the same virus, for which, for practical reasons, the name pelargonium line pattern virus is proposed.PLPV could be reliably detected by ELISA inP. zonale Springtime Irene and Amanda throughout the year with only a few exceptions. InPelargonium peltatum Tavira, however, reslts were erratic due to uneven distribution of virus in the plant. Best results were obtained when petioles of fully expanded leaves were tested.     

Growth loss of Lebanon cedar (Cedrus libani) stands as related to periodic outbreaks of the cedar shoot moth (Dichelia cedricola)

An outbreak ofDichelia cedricola (Diakonoff) (Lep.: Tortricidae), the cedar shoot moth (CSM), began in spring 1998 and lasted 3 years. This was the first monitored outbreak of the CSM in Isparta, Turkey. Tree crowns recovered to near normal condition by the middle of each growing season (in early June) during the outbreak. Tree volume and volume element increments were examined throughout the outbreak cycle from 1954 to 2001. In the past, CSM activity in stands of Lebanon cedar (Cedrus libani A. Rich.) was assessed through radial increment analyses. Cedar tree ring chronologies were analyzed for evidence of the CSM. Tree-ring chronologies from nonhost cedar (nondefoliated sample trees) were used to estimate potential growth in the host cedar (defoliated sample trees) during current and past outbreaks; all trees selected were the same subspecies and varieties. Regional outbreaks of the CSM were identified by synchronous and sustained growth periods of the trees. In 2001, increment cores were collected from 17 host and 16 nonhost dominant or codominant trees and annual radial growth indices from 1954–2001 were calculated for each of two host and two nonhost sample plots. Growth functions were defined as the cumulative sum of radial, height, and volume increment, and were graphically compared between CSM host cedar and nonhost cedar trees. Tree ring evidence suggests that a large-scale outbreak occurred in 1955 (from 1955 to 1966) and a small outbreak occurred in 1985 (1985–1990) and in 1998 (1998-continued) in the study area. The average diameter growth reductions around 1955, 1985 and 1998 were 40%, 46% and 7% of potential, respectively. It was concluded that a narrow latewood band is significant indicator of defoliation by the CSM and the outbreaks appear to be associated with dry winter and spring weather prior to the autumn and winter in which wood feeding occurred. http://www.phytoparasitica.org posting Nov. 24, 2004.     

环切对糯米糍荔枝果实大小和裂果的影响

结果母枝和主枝环切处理导致糯米糍荔枝的果实大小显著减小,裂果率显著增加,环切圈以上叶片中可溶性糖和淀粉的含量显著增加,结果母枝中的可溶性糖含量增加,果实中的总糖与蔗糖含量则显著地降低。据此认为,近几年来,糯米糍的果个比20世纪80年代明显减小,裂果增加,很可能与生产中多年连续施行主枝环切(或环剥)技术有关,而碳水化合物运入果实量的减少可能是环切导致果实变小的原因之一。     

荞麦轮纹病抗性鉴定方法的建立及荞麦抗病种质资源的筛选

为建立荞麦轮纹病的抗性鉴定方法和筛选可利用的抗轮纹病的荞麦种质资源,本研究以TP2和KP14为供试材料,在健康荞麦叶片正面针刺处理,然后用荞麦轮纹病的病原菌菌饼进行接种;利用建立的抗性鉴定方法,对50份荞麦种质资源进行抗病性评价。结果显示:针刺5针接种叶片病斑出现较快,且比针刺1针、针刺3针的叶片病斑大,针刺5针的病情指数最高。50份荞麦种质资源的病情指数有差异,其中YZ-18的病情指数为29.63,为高抗种质资源,YZ-2、YZ-5、YZ-13和YZ-9的病情指数均低于40,为中抗种质资源,其余为感病种质资源。因此,接种前叶片正面针刺5针的方法为最佳的抗性鉴定方法。50份抗性评价的荞麦种质资源中,筛选出5份抗病种质资源。     

苹果种质资源枝干轮纹病抗性评价

将田间自然发病抗性鉴定法与利用苹果轮纹病菌ZZ26人工接种枝条鉴定法相结合,对189份栽培种苹果种质资源进行了苹果轮纹病综合抗性鉴定,并根据抗病性鉴定结果对其进行抗病类型分类和评价。结果表明:不同苹果种质资源抗病性表现存在差异,但参试种质中未发现免疫种质。通过人工接种,189份苹果种质资源的抗病类型可分为:高抗(16个);中抗(75个);中感(81个);高感(17个)。通过田间调查,2012年得到抗病类型3种,即高抗(144个);中抗(44个);中感(1个)。2013年同样是3个抗病类型:高抗(14个);中抗(162个);中感(13个)。两年调查均无高感品种。2017年再次调查,结果显示田间调查与人工接种鉴定结果有随种植年限增加一致率逐渐提高的趋势,2012年为13.23%,2013年为38.62%,2017年则超过一半,达到57.14%。经过综合抗性筛选,最终得到表现一致性较好的高抗种质2份:北之幸和秦冠。     

定西于家山黄土洞穴的分布特征与侵蚀临界研究

黄土洞穴与滑坡、沟蚀等侵蚀过程联系紧密并加剧了黄土高原的水土流失程度,但目前黄土洞穴发育的分布特征与侵蚀临界暂未明晰。利用无人机获得了研究区高分辨率影像与数字表面模型,基于影像标识了黄土洞穴并统计了其土地利用类型与洞穴直径,利用标识点在数字表面模型上提取了黄土洞穴的坡度、坡向、曲率和汇水面积等地形数据并分析了黄土洞穴的分布特征。结果表明,黄土洞穴直径大多4 m。黄土洞穴在耕地上发育较少,多发育于牧草地区域流水汇聚的凹形坡,且在阴坡更为发育。同时,黄土洞穴坡度正切值范围集中于0.4～1.0,汇水面积一般不超过3 000 m~2。依托统计的坡度正切值与汇水面积数据绘制了黄土洞穴的侵蚀临界图并对比了黄土洞穴与浅沟、切沟的侵蚀临界。黄土洞穴的侵蚀临界边界分别为SA~(0.150)=0.368与SA~(0.135)=7.580,分布较广且覆盖了浅沟与切沟的侵蚀临界。浅沟、切沟的演化与黄土洞穴的发育有关,黄土洞穴通过连通与坍塌促进了浅沟、切沟的发育、转换与扩展,并因此加剧了黄土高原的水土流失。研究量化了黄土洞穴发育的分布特征,建立了黄土洞穴与浅沟、切沟的联系并深化了对黄土洞穴侵蚀过程的认识。     

苹果抗轮纹病机制研究进展

在中国引起苹果轮纹病的病原菌为葡萄座腔菌（Botryosphaeria dothidea），其主要通过自然孔口直接侵染苹果，并分泌细胞降解酶等使苹果组织降解以促进病菌的进一步侵染，而苹果可通过增强细胞壁的木质化、释放抗菌化合物以及产生免疫蛋白等抑制病菌。通过对苹果轮纹病的危害及病原菌种类、病菌侵染机制、苹果的抗性机制等方面的详细综述，为有效防治苹果轮纹病提供理论依据。     

AR regulates porcine immature Sertoli cell growth via binding to RNF4 and miR-124a

Sertoli cells are the only somatic cells in the seminiferous epithelium which directly contact with germ cells. Sertoli cells exhibit polarized alignment at the basal membrane of seminiferous tubules to maintain the microenvironment for growth and development of germ cells, and therefore play a crucial role in spermatogenesis. Androgens exert their action through androgen receptor (AR) and AR signalling in the testis is essential for maintenance of spermatogonial numbers, blood–testis barrier integrity, completion of meiosis, adhesion of spermatids and spermiation. In the present study, we demonstrated that AR gene could promote the proliferation of immature porcine Sertoli cells (ST cells) and the cell cycle procession, and accelerate the transition from G1 phase into S phase in ST cells. Meanwhile, miR-124a could affect the proliferation and cell cycle procession of ST cells by targeting 3′-UTR of AR gene. Furthermore, AR bound to the RNF4 via AR DNA-binding domain (DBD) and we verified that RNF4 was necessary for AR to regulate the growth of ST cells. Above all, this study suggests that AR regulates ST cell growth via binding to RNF4 and miR-124a, which may help us to further understand the function of AR in spermatogenesis.