Soil temperature and the energy balance of vegetative mulch in the semi-arid tropics. II. Dynamic analysis of the total energy balance

Soil Research ◽  
1985 ◽  
Vol 23 (4) ◽  
pp. 515 ◽  
Author(s):  
PJ Ross ◽  
J Williams ◽  
RL Mccown

Soil temperatures and water losses under killed vegetative mulch canopies are examined in the context of no-tillage crop production, using a numerical dynamic model of the soil, canopy and lower atmosphere. Both liquid and vapour movement in the soil are included, as are free and forced convection in the canopy. The predictions of the model for a clay loam soil are as follows. Medium and heavy mulches reduce the water loss over six days by 1.4 and 2.7 mm respectively, the reduction occurring while the soil surface is wet. This small effect is important in giving seedlings an extra 2 or 3 days for establishment. Water loss from bare soil and under a medium mulch is limited by soil resistance even on the first day of evaporation from initially wet soil. Mulch canopies that intercept 80 and 50% of incoming radiation can keep surface soil temperatures within 10 and 20�C respectively of ambient, whereas bare soil temperatures may rise 30�C above ambient. A moderate wind reduces soil temperatures under a mulch only a few degrees, but cools the canopy much more. A rough soil surface helps cool the soil. Water losses and soil temperatures are little affected by a 50% change in soil water diffusivity or thermal conductivity. An extensive mulched area results in temperatures well above those observed on small plots surrounded by transpiring vegetation, which maintains cool air above the mulch. A simplified form of the model, which incorporates only a single mulch layer and which ignores effects of wind, yields soil temperatures which are not greatly different from those generated by the more complex model for wind speeds below 1 ms-1 at canopy height.

Author(s):  
Fernando Gomes de Souza ◽  
Valdinar Ferreira Melo ◽  
Wellington Farias Araújo ◽  
Thiago Henrique de Castro Araújo

Currently in Brazil, the main form of erosion is caused by the impact of raindrops on the soil surface, triggering the process of water erosion and causing serious damage to agricultural areas. This study evaluated losses of soil, water, organic carbon and nutrients in different cultures, bare soil and savanna under natural rain. The experimental design was completely randomized with five treatments (bare soil - BS, cowpea bean - CB, Brachiaria brizantha - BB, corn - CO and natural savanna – SN) with three replications; The treatment of bare soil (BS), followed by the treatment cultivated with cowpea bean  (CB) showed higher losses of soil, water, organic carbon and nutrients; The highest losses of soil, water, organic carbon and nutrients in the treatment of bare soil (BS) occurred during the period of greatest erosivity; but for treatments CB, BB and CO, the highest losses occurred during the establishment of the crop, in view of the lower soil cover. Soils cultivated with Brachiaria brizantha - BB, corn - CO and in the Natural Savana - SN area were more efficient in reducing soil and water losses during all months evaluated. Plant cover produced by the (SN) treatment and by the (BB) and (CO) treatments acted to reduce the harmful effects of erosion, minimizing losses of nutrients and organic carbon. The soil should be well protected during periods when rainfall presents the highest values of erosivity index.


2008 ◽  
Vol 9 (5) ◽  
pp. 936-950 ◽  
Author(s):  
Tushar Sinha ◽  
Keith A. Cherkauer

Abstract Seasonal cycles of freezing and thawing influence surface energy and water cycle fluxes. Specifically, soil frost can lead to the reduction in infiltration and an increase in runoff response, resulting in a greater potential for soil erosion. An increase in the number of soil freeze–thaw cycles may reduce soil compaction, which could affect various hydrologic processes. In this study, the authors test for the presence of significant trends in soil freeze–thaw cycles and soil temperatures at several depths and compare these with other climatic variables including air temperature, snowfall, snow cover, and precipitation. Data for the study were obtained for three research stations located in northern, central, and southern Indiana that have collected soil temperature observations since 1966. After screening for significant autocorrelations, testing for trends is conducted at a significance level of 5% using Mann–Kendall’s test. Observations from 1967 to 2006 indicate that air temperatures during the cold season are increasing at all three locations, but there is no significant change in seasonal and annual average precipitation. At the central and southern Indiana sites, soil temperatures are generally warming under a bare soil surface, with significant reductions in the number of days with soil frost and freeze–thaw cycles for some depths. Meanwhile, 5-cm soils at the northernmost site are experiencing significant decreases in cold season temperatures, as an observed decrease in annual snowfall at the site is counteracting the increase in air temperature. Seasonal mean maximum soil temperatures under grass cover are increasing at the southernmost site; however, at the central site, it appears that seasonal minimum soil temperatures are decreasing and the number of freeze–thaw cycles is increasing.


2009 ◽  
Vol 35 (5) ◽  
pp. 232-240
Author(s):  
Michael Arnold ◽  
Garry McDonald

Three experiments investigated the effects of various groundcovers on establishment of redbuds [Cercis canadensis L. var. texensis (S. Watson) M. Hopkins ‘Alba’] and baldcypress [Taxodium distichum (L.) Rich.]. The first experiment involved eight surface treatments. Controls were bare soil. Remaining treatments were pine bark mulch; Asian jasmine [Trachelospermum asiaticum (Siebold & Zucc.) Nakai]; St. Augustinegrass [Stenotaphrum secundatum (Walt.) Kuntze]; decorative gravel; recycled paper mulch; decorative brick pavers; or seasonal rotations of herbaceous annuals. Other experiments compared brick-on-sand treatments ranging in color from light blonde to dark charcoal with bare soil on establishment of redbuds or baldcypress. Most organic and living soil surface covers were preferable to bare soils, however, some inorganic surface covers were detrimental to tree growth. Paving surfaces adversely affected survival, shoot or root growth, but differences were species dependent. Soil moisture, pH, and bulk density did not appear to be limiting under pavers, but substantial seasonal fluctuations in soil temperatures were observed. Light and medium bricks reflected more photosynthetically active radiation than dark bricks or bare soil. Atmospheric temperatures were greatest above dark and medium bricks. Root growth decreased as darkness of brick color increased. Redbud survival and growth were more adversely affected than with baldcypress


1996 ◽  
Vol 10 (2) ◽  
pp. 247-252 ◽  
Author(s):  
Erik D. Wilkins ◽  
Robin R. Bellinder

Field studies determined the influence of developmental stage on mow-killing of winter wheat and rye. Both crops were clipped at either three or four different growth stages in 1992 and 1993. When mowed at first node, wheat biomass was 4350 and 1970 kg/ha in 1992 and 1993, respectively. At this stage, primary tiller apices were below 10 cm and regrowth was vigorous. Mowing prior to 75% heading consistently yielded more than 1000 kg/ha regrowth 8 wk later. Wheat cut after flowering produced 15 460 and 9160 kg/ha dry matter in 1992 and 1993, respectively, but less than 30 kg/ha total regrowth. At first and second node, rye produced 4440 and 1800 kg/ha biomass in 1992 and 1993. When mowed belore boot, more than 50% of the total rye biomass was due to regrowth. Rye mowed at boot yielded 6940 and 3740 kg/ha in 1992 and 1993 respectively, and regrowth measured 780 and 910 kg/ha 8 wk later. Mowing after flowering resulted in no measurable regrowth. Soil temperature and PAR were affected by mow-kill date and biomass. Biomass at first mowings (first and second node) in both wheat and rye reduced seasonal soil temperatures 3.5 C compared to bare soil temperatures; while biomass at kernal-filling lowered temperatures 6.0 C. Measured 8 wk after mowing, first node mowings absorbed between 55% and 70% PAR, while plants mowed at kernal-filling absorbed less than 5%.


Weed Science ◽  
2003 ◽  
Vol 51 (6) ◽  
pp. 876-885 ◽  
Author(s):  
H. R. Huarte ◽  
R. L Benech Arnold

Field experiments were carried out at the Facultad de Agronomía, Universidad de Buenos Aires, Argentina (34°25′S, 58°25′W), to evaluate the possibility of reducing weed seedling emergence through the use of alfalfa cultivars with low levels of winter dormancy and by increasing plant density from 200 to 400 plants m−2. It was hypothesized that these treatments would alter the temperature regime and the red (R)–far-red (FR) ratio of radiation to which seeds were exposed. Responses to management treatments were recorded for bull thistle, cotton thistle, plumeless thistle, tall rocket, mustard, curly dock, and pigweed. During the alfalfa establishment year, pigweed and curly dock emergence was reduced by the nondormant cultivar established at high density. This reduction disappeared when soil beneath the canopy was fitted with heaters that mimicked bare-soil temperatures. Crop canopy presence during the establishment year was not effective in reducing mustard, cotton thistle, bull thistle, plumeless thistle, and tall rocket emergence. During the second and third years after crop establishment, the canopy of the nondormant alfalfa cultivar was effective in reducing germination of weed seeds placed on the soil surface during fall and winter. In contrast, the winter-dormant cultivar allowed the establishment of weeds during the winter period. These reductions in weed emergence were associated with a modification in the R–FR ratio perceived by the seeds located at the soil surface and could largely be removed by using FR filters to increase the R–FR ratio. These results suggest that the selection of a nondormant cultivar combined with an increase in plant density could effectively reduce weed populations in alfalfa.


2015 ◽  
Vol 50 (4) ◽  
pp. 336-348
Author(s):  
Mohamed H. Ahmed ◽  
Saud Gutub

Modern irrigation techniques use automated systems where irrigation schedules are controlled according to certain criteria. The objective of this study is to numerically estimate irrigation events, water content and temperature distributions, evaporation, drainage, and soil water under closed loop automated irrigation systems of a bare soil. The automated irrigation system is activated and deactivated according to the water content value. The governing equations for transient one-dimensional liquid water flow and heat transfer of unsaturated porous media are applied. The energy balance equation at the soil surface is used as an upper boundary condition based on measured meteorological data of Jeddah City. The results show that the current procedure can be applied to simulate different variables under automated irrigation systems. The water content shows periodic behavior, as well as time lags and decreases in amplitude with soil depth. The timing of applied irrigation has an important impact on evaporation and soil temperature. Applying irrigation water during the daytime leads to increased evaporation. The soil surface temperature decreases suddenly when water is supplied in the afternoon, while a slight increase is observed when irrigation is applied at midnight.


2002 ◽  
Vol 138 (2) ◽  
pp. 135-152 ◽  
Author(s):  
S. R. GAZE ◽  
M. A. STALHAM ◽  
E. J. ALLEN

The neutron probe (NP) is used widely to measure changes in soil water storage in research and more recently to aid irrigation scheduling. Its accuracy is rarely questioned and most of the relationships between soil water changes and productivity are based on its use. A field experiment was conducted at Cambridge University Farm in 1999 to address whether the NP could accurately measure changes in soil water content (SWC) under irrigation or substantial rain (>10 mm). The experiment was a replicated split-plot design with four irrigation treatments allocated to the main plots, and surface profile (ridge, flat) and crop (potato cv. Saturna, bare soil) treatments allocated to the subplots. The mean results from four NP access tubes per plot installed to measure soil moisture deficit (SMD) across the row-width were analysed. The NP was inconsistent in measuring known irrigation or rainfall input. In relatively dry soil (SMD>40 mm), the NP generally measured 93 to 110% of 18 mm of irrigation within 4 h of irrigation. The NP recorded much less water applied as irrigation in wetter soil, and often only 40 to 70% of the applied irrigation (18 or 36 mm) was measured. There were occasions when the NP did not measure all the water input even when the SMDs before irrigation were greater than the water subsequently applied. Some of the ‘missing’ water might be attributed to drainage, however, results from an additional experiment using an open-topped tank of soil showed that the NP was unable to detect all the water added to the soil, particularly where the water was largely confined close to the soil surface. Replicated measurements of the change in SMD in the field experiment were precise for a given event and treatment (mean S.E. = 1·3 mm) but were not accurate when compared against the input measured in rain gauges. It was concluded, that the NP could not be used reliably to measure changes in soil water storage after irrigation or substantial rain. For periods when there were minimal inputs of water, there was a closer correlation between changes in SMD measured by the NP and those predicted by a modified Penman–Monteith equation than after substantial inputs of water. However, for predicted changes in SMD of c. 20 mm, there was a range of c. ±5 mm in the changes in SMD measured by the neutron probe.The value of the NP for monitoring SMDs where there is irrigation, or substantial rain, must be seriously doubted. Consequently, its limitations for scheduling irrigation, testing models or quantifying the effects of treatments on crop water use in potatoes must be appreciated, especially where the areal sampling limitations of single access tubes positioned only in the ridge centre have not been addressed.


Plant Disease ◽  
2001 ◽  
Vol 85 (7) ◽  
pp. 723-730 ◽  
Author(s):  
K. D. Cox ◽  
H. Scherm

Pseudosclerotia (infected, mummified fruit) on the orchard floor act as oversummering and overwintering structures and the sole source of primary inoculum of Monilinia vaccinii-corymbosi, the causal agent of mummy berry disease of blueberry. Survival of pseudosclerotia may be affected by their maturity (degree of stromatization), which can vary considerably at the time of fruit abscission in early summer, and by variations in the soil surface environment. From July through October in 2 years, survival of pseudosclerotia of varying initial maturity (expressed as the proportion of fruit containing mature, melanized entostromata; immature, nonmelanized entostromata; or undifferentiated mycelia) was investigated in the laboratory relative to soil surface temperature and soil moisture content and in the field in relation to shading (full sun versus 50% shade) and ground cover (bare soil versus grass). In the laboratory, oversummer survival, expressed as the percentage of intact pseudosclerotia at the end of the experiment, was higher for cool soil temperatures (approximately 15°C), soils drier than field capacity, and pseudosclerotia containing mature entostromata. In the field, survival was related solely to initial maturity of pseudosclerotia and was highest for pseudosclerotia containing mature entostromata. Shading or grass ground cover did not significantly (P > 0.05) affect oversummer survival, presumably because they did not greatly modify soil temperature or soil moisture. When individual, intact pseudosclerotia were tested for viability using fluorescein diacetate staining, a linear relationship (r = 0.982, P < 0.0001, n = 90) between viable and intact pseudosclerotia was observed, supporting the use of the percentage of intact pseudosclerotia as a measure of oversummer survival.


Sign in / Sign up

Export Citation Format

Share Document