scholarly journals Response to fertilizer nitrogen and water of post-rainy season sorghum on a Vertisol. 2. Biomass and water extraction

1998 ◽  
Vol 131 (4) ◽  
pp. 429-438 ◽  
Author(s):  
PIARA SINGH ◽  
J. L. MONTEITH ◽  
K. K. LEE ◽  
T. J. REGO ◽  
S. P. WANI

During rainless weather following a monsoon, sorghum (Sorghum bicolor cv. SPH–280) was grown on a Vertisol either unirrigated throughout growth or irrigated for 7 weeks after emergence and rainfed thereafter. Before sowing, ammonium sulphate was applied at six rates from 0 to 150 kg/ha N. Roots were sampled every 2 weeks to determine biomass and root length density as a function of depth. Every week, soil water content in all treatments was measured gravimetrically to a depth of 0·23 m and with a neutron probe from 0·3 to 1·5 m.Below 0·45 m, volumetric water content was a negative exponential function of time after roots arrived and the maximum depth of extraction moved downwards at 2–5 cm per day. In the dry treatment, the extraction ‘front’ lagged behind the deepest roots by c. 12 days initially but the two fronts eventually converged. Irrigation delayed the descent of the extraction front by c. 20 days but thereafter it appeared to descend faster than without irrigation. Averaged over N rates, the time constant of the exponential function was inversely related to the root length density, lv, decreasing with depth from about 20 to 10 days as lv increased from 2·5 to 4·0 km/m3.The biomass[ratio ]water ratio was almost independent of N but increased from a mean of 5·3 g dry matter per kg water in the dry treatments to 6·9 g/kg with irrigation. When normalized by the seasonal mean difference in vapour pressure deficit within irrigated and unirrigated plots, the ratios were 13·1 and 13·3 kPa g per kg water, respectively.

1988 ◽  
Vol 28 (2) ◽  
pp. 249 ◽  
Author(s):  
S Fukai ◽  
P Inthapan

Several physiological responses were compared, under irrigated and water-stressed conditions, in an attempt to explain the reasons for the greater reduction in dry matter production of rice compared with maize and sorghum in a water-limiting environment. Leaf water potential and leaf rolling were determined weekly, soil water profiles and root length density twice, and leaf osmotic potential once during a long dry period. Root length density of rice was at least as high as that of maize and sorghum in the top 0.6 m layer of soil in both the wet and dry trials. There was no difference in water extraction among the 3 species from this layer, while rice extracted less water than did the other species from below 0.6 m. High variability among replicates precluded any conclusion being drawn regarding root length in the deeper layer. Leaf water potential, measured in the early afternoon, was consistently lower in rice than in maize and sorghum, even when soil water content was high, indicating high internal resistance to the flow of water in the rice plants. The low leaf water potential in rice was accompanied by low osmotic potential, and this assisted in maintenance of turgor and dry matter growth when soil water content was relatively high. As soil water content decreased, however, leaf water potential became very low (less than - 2.5 MPa) and, for rice, leaves rolled tightly.


1979 ◽  
Vol 16 (1) ◽  
pp. 1-11 ◽  
Author(s):  
Eric Renshaw

This paper examines a model for ecological and epidemiological spread. Expressions are derived for mean waveforms and expectation velocities for two specific contact distributions. Whilst one distribution may be bounded above by a negative exponential function the other may not, and these two situations respectively give rise to finite and infinite asymptotic expectation velocities.


2009 ◽  
Vol 60 (3) ◽  
pp. 280 ◽  
Author(s):  
Peter S. Searles ◽  
Diego A. Saravia ◽  
M. Cecilia Rousseaux

Several studies have evaluated many above-ground aspects of olive production, but essential root system characteristics have been little examined. The objective of our study was to evaluate root length density (RLD) and root distribution relative to soil water content in three commercial orchards (north-west Argentina). Depending on the orchard, the different drip emitter arrangements included either: (1) emitters spaced continuously at 1-m intervals along the drip line (CE-4; 4 emitters per tree); (2) 4 emitters per tree spaced at 1-m intervals, but with a space of 2 m between emitters of neighbouring trees (E-4); or (3) 2 emitters per tree with 4 m between emitters of neighbouring trees (E-2). All of the orchards included either var. Manzanilla fina or Manzanilla reina trees (5–8 years old) growing in sandy soils, although the specific characteristics of each orchard differed. Root length density values (2.5–3.5 cm/cm3) in the upper soil depth (0–0.5 m) were fairly uniform along the drip line in the continuous emitter (CE-4) orchard. In contrast, roots were more concentrated in the E-4 and E-2 orchards, in some cases with maximum RLD values of up to 7 cm/cm3. Approximately 70% of the root system was located in the upper 0.5 m of soil depth, and most of the roots were within 0.5 m of the drip line. For each of the three orchards, significant linear relationships between soil water content and RLD were detected based on 42 sampling positions that included various distances from the trunk and soil depths. Values of RLD averaged over the entire rooting zone and total tree root length per leaf area for the three orchards were estimated to range from 0.19 to 0.48 cm/cm3 and from 1.8 to 3.5 km/m2, respectively. These results should reduce the uncertainty associated with the magnitude of RLD values under drip irrigation as intensively managed olive orchards continue to expand in established and new growing regions.


2020 ◽  
Author(s):  
Mohamed E Saleh ◽  
Zeinab Elmehdi Saleh

Background: The SEIR model or a variation of it is commonly used to study epidemic spread and make predictions on how it evolves. It is used to guide officials in their response to an epidemic. This research demonstrates an effective and simple approach that estimates the parameters of any variations of the SEIR model. This new technique will be demonstrated on the spread of COVID-19 in Libya. Methods: A five compartmental epidemic model is used to model the COVID-19 pandemic in Libya. Two sets of data are needed to evaluate the model parameters, the cumulative number of symptomatic cases and the total number of active cases. This data along with the assumption that the cumulative number of symptomatic cases grows exponentially, to determine most of the model parameters. Results: Libya epidemic start-date was estimated as t_o=-18.5 days, corresponding to May 5th. We mathematically demonstrated that the number of active cases follows two competing exponential distributions: a positive exponential function, measuring how many new cases are added, and a negative exponential function, measuring how many cases recovered. From this distribution we showed that the average recovery time is 48 days, and the incubation period is 15.2 days. Finally, the productive number was estimated as R0 = 7.6. Conclusions: With only the cumulative number of cases and the total number of active cases of COVID19, several important SEIR model parameters can be measured effectively. This approach can be applied for any infectious disease epidemic anywhere in the world.


1971 ◽  
Vol 24 (3) ◽  
pp. 805 ◽  
Author(s):  
LA Downey ◽  
TC Mitchell

The pair of lodicules situated at the base of the ovary and adjacent to the lemma of the wheat floret have long been known to be involved in the opening of the wheat floret at anthesis (see Arber 1965). At anthesis, the lodicules swell and force the lemma away from the palea, allowing the stamens to grow out from the floret. Some minutes later and presumably in response to a stimulus associated with pollination (male-sterile florets may remain open for many hours: Dr. A. T. Pugsley, personal communication) the lodicules collapse and the floret closes. We are studying the events which lead to this rapid swelling and degeneration of the lodicule in wheat and noticed that information about the nature of the vascular tissues in lodicules is very meagre.


2013 ◽  
Vol 59 (No. 7) ◽  
pp. 295-302 ◽  
Author(s):  
B. Ji ◽  
Y. Zhao ◽  
X. Mu ◽  
K. Liu ◽  
C. Li

Subsoil compaction can result in unfavourable soil physical conditions and hinder the root growth of maize. The effects of deep tillage and conventional tillage on soil physical properties and root growth of maize were studied during 2010–2011 at two sites (loam at Hebi and clay at Luohe) in central China. The results showed that soil penetration resistance, bulk density, water content and root length density were significantly affected by tillage, soil depth and year. Deep tillage had lower penetration resistance and lower soil bulk density, but higher soil water content than conventional tillage across years and depths. Averaged over the whole soil profile, deep tillage not only significantly decreased penetration resistance and soil bulk density, but significantly increased soil water content and root length density on loam, while deep tillage only significantly increased the root length density on clay. We conclude that deep tillage on the loam is more suitable for the root growth of summer maize.


1979 ◽  
Vol 16 (01) ◽  
pp. 1-11 ◽  
Author(s):  
Eric Renshaw

This paper examines a model for ecological and epidemiological spread. Expressions are derived for mean waveforms and expectation velocities for two specific contact distributions. Whilst one distribution may be bounded above by a negative exponential function the other may not, and these two situations respectively give rise to finite and infinite asymptotic expectation velocities.


1984 ◽  
Vol 14 (3) ◽  
pp. 466-467 ◽  
Author(s):  
J. Pastor ◽  
W. M. Post

A simple negative exponential function is presented which relates soil water storage to a maximum storage value (field capacity) and accumulated potential water loss. This formula summarizes 10 tables from Thornthwaite and Mather (Publications in Climatology, 10: 183–311, 1957) needed to calculate actual evapotranspiration (AET). Comparisons are presented for values predicted by this formula and Thornthwaite and Mather's tabulated values.


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