首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   155篇
  免费   7篇
  国内免费   3篇
林业   10篇
农学   1篇
基础科学   1篇
  28篇
综合类   11篇
农作物   3篇
水产渔业   18篇
畜牧兽医   69篇
园艺   2篇
植物保护   22篇
  2022年   1篇
  2020年   4篇
  2019年   2篇
  2018年   3篇
  2017年   3篇
  2016年   4篇
  2015年   2篇
  2014年   6篇
  2013年   5篇
  2012年   13篇
  2011年   15篇
  2010年   9篇
  2009年   8篇
  2008年   8篇
  2007年   15篇
  2006年   10篇
  2005年   7篇
  2004年   9篇
  2003年   2篇
  2002年   5篇
  2001年   2篇
  2000年   7篇
  1999年   3篇
  1998年   4篇
  1997年   1篇
  1996年   1篇
  1995年   1篇
  1992年   3篇
  1991年   2篇
  1989年   2篇
  1987年   1篇
  1985年   1篇
  1984年   1篇
  1981年   1篇
  1971年   1篇
  1969年   1篇
  1968年   1篇
  1958年   1篇
排序方式: 共有165条查询结果,搜索用时 15 毫秒
161.
In 2010, the populations of Fusarium sp. and Microdochium sp. were monitored in Belgium and 16 strains were identified as Fusarium langsethiae on wheat in Belgium. The other species identified from the sampling were F. poae, F. tritinctum, F. graminearum, F. avenaceum and Microdochium nivale. The pathogenicity potential of the F. langsethiae strains was assessed via an in vitro coleoptile growth rate test on wheat seedlings and compared with strains of F. poae, F. tritinctum, F. graminearum and F. avenaceum known to cause Fusarium head blight. The results showed the ability of F. langsethiae to cause retardation in the wheat coleoptile growth rate, but at a lower rate than F. graminearum, F. avenaceum, F. poae and F. tricinctum. A test for mycotoxin production in vitro showed the ability of the four strains tested to produce T-2 and HT-2 toxins at a rate of up to 290 mg kg?1. This is the first report on the potential pathogenicity of F. langsethiae on wheat in Belgium, a species known to produce T-2 and HT-2 toxins, which are highly toxic for humans and animals.  相似文献   
162.
A PCR diagnostic test for detection of Ralstonia solanacearum at the infraspecific level was developed, based on polymorphisms within the 16S rRNA gene sequence. Partial sequences of this gene were determined for three French isolates which showed the characteristics of R. solanacearum subdivision 2a described by Taghavi et al. (1996). Oligonucleotide primers were designed to incorporate the nucleotide triplet (at positions 458–460 of the 16S rRNA gene) which differs between divisions 1 and 2 16S rRNA sequences of R. solanacearum isolates. A simple PCR test unambiguously revealed the division of each isolate. The PCR test was useful for identification of isolates of R. solanacearum from Europe.  相似文献   
163.
Thiffault  Nelson  Picher  Geneviève  Auger  Isabelle 《New Forests》2012,43(5-6):849-868
New Forests - In the Canadian boreal forest, conifer plantations are mainly used to overcome poor natural regeneration following harvesting or wildfires. However, competitive interactions can...  相似文献   
164.
165.
Drainage-induced diffuse pollution and erosion are key water quality problems in peatland forestry. A major part of the pollutant load is transported during peak runoff periods after snowmelt or intense rainfall. This study investigated possibilities to increase retention time of runoff waters in drained peatland catchments on purpose to diminish peak runoff and improve settling conditions of suspended solids (SS). To create retention, a peak runoff control (PRC) structure was developed and its functioning, dimensioning and practical applications were studied in five partly or completely ditch-drained catchments in Central Finland. The method reduced runoff peaks by 10–73% or 5.07–57.63 l−1 s−1 km−2, and functioned especially well during largest runoff peaks. The effectiveness of the PRC method depended on (i) catchment topography (slope) and available detention volume, (ii) dimensioning and location of the PRC structure, and (iii) runoff rates. The PRC structure is cheap and can easily be created with forest drainage machinery during the ditching and ditch network maintenance operations. Different issues relating to the structural design, water quality benefits, and impacts on forestry are discussed.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号