Uneven moisture patterns in water repellent soils

In the Netherlands, water repellent soils are widespread and they often show irregular moisture patterns, which lead to accelerated transport of water and solutes to the groundwater and surface water. Under grasscover, spatial variability in soil moisture content is high due to fingered flow, in arable land vegetation and microtopography play a dominant role. Examples are given of uneven soil moisture patterns in water repellent sand, loam, clay and peat soils with grasscover, and in cropped water repellent sandy soils. In addition, the influence of fungi on inducing soil moisture patterns is illustrated as well.     

用RAPD标记检测与杨树生长和物候期有关的QTLs

取美洲黑杨（母本）和青杨（父本）杂交获得的Ｆ２群体样本８０株,应用ＲＡＰＤ标记检测与Ｆ２群体３个数量性状（苗高、地径和封顶期）有关的ＱＴＬｓ。在Ｆ２九体中,一年生苗高、地径和封顶期性状表现显著分离,基本符合正态分布。单因子方差分析检测出与苗高、地径和封顶期性状相关的７个、６个和３个标记座位。并计算了各标记对相关性状变异的贡献率。与数量性状相关的标记有不同的亲本来源。ｔ检查结果各标记显带型和不显带型     

Nighttime transpiration in woody plants from contrasting ecosystems

It is commonly assumed that transpiration does not occur at night because leaf stomata are closed in the dark. We tested this assumption across a diversity of ecosystems and woody plant species by various methods to explore the circumstances when this assumption is false. Our primary goals were: (1) to evaluate the nature and magnitude of nighttime transpiration, E(n), or stomatal conductance, g(n); and (2) to seek potential generalizations about where and when it occurs. Sap-flow, porometry and stable isotope tracer measurements were made on 18 tree and eight shrub species from seven ecosystem types. Coupled with environmental data, our findings revealed that most of these species transpired at night. For some species and circumstances, nighttime leaf water loss constituted a significant fraction of total daily water use. Our evidence shows that E(n) or g(n) can occur in all but one shrub species across the systems we investigated. However, under conditions of high nighttime evaporative demand or low soil water availability, stomata were closed and E(n) or g(n) approached zero in eleven tree and seven shrub species. When soil water was available, E(n) or g(n) was measurable in these same species demonstrating plasticity for E(n) or g(n). We detected E(n) or g(n) in both trees and shrubs, and values were highest in plants from sites with higher soil water contents and in plants from ecosystems that were less prone to atmospheric or soil water deficits. Irrespective of plant or ecosystem type, many species showed E(n) or g(n) when soil water deficits were slight or non-existent, or immediately after rainfall events that followed a period of soil water deficit. The strongest relationship was between E(n) or g(n) and warm, low humidity and (or) windy (> 0.8 m s(-1)) nights when the vapor pressure deficit remained high (> 0.2 kPa in wet sites, > 0.7 kPa in dry sites). Why E(n) or g(n) occurs likely varies with species and ecosystem type; however, our data support four plausible explanations: (1) it may facilitate carbon fixation earlier in the day because stomata are already open; (2) it may enhance nutrient supply to distal parts of the crown when these nutrients are most available (in wet soils) and transport is rapid; (3) it may allow for the delivery of dissolved O(2) via the parenchyma to woody tissue sinks; or (4) it may occur simply because of leaky cuticles in older leaves or when stomata cannot close fully because of obstructions from stomatal (waxy) plugs, leaf endophytes or asymmetrical guard cells (all non-adaptive reasons). We discuss the methodological, ecophysiological, and theoretical implications of the occurrence of E(n) or g(n) for investigations at a variety of scales.