Carbon Production of Sunflower Cultivars in Field and Controlled Environment. II. Leaf Growth

1980 ◽  
Vol 7 (5) ◽  
pp. 575 ◽  
Author(s):  
HM Rawson ◽  
GA Constable ◽  
GN Howe
Keyword(s):  
Water Stress ◽  
Leaf Area ◽  
Leaf Growth ◽  
Field Studies ◽  
Leaf Number ◽  
Area Index ◽  
Average Growth ◽  
Unit Leaf Area ◽  
Unit Leaf ◽  
Stomatal Apparatus

In field studies of several cultivars of sunflower grown on stored soil moisture or with irrigation, yield was positively related to leaf area at anthesis. The regression which described this relationship stated that 1370 kg seed ha-1 were associated with a unit increment in leaf area index. Cultivars differed in final leaf number, rate of leaf appearance, and in the vertical distribution of leaf area in the profiles. Final leaf number of plants grown on stored moisture remained the same as in irrigated plants, but the period for which each leaf grew was reduced from 19 to 16 days while the average growth rate was reduced from 13 to 6 cm2 day-1. These changes reduced the final leaf area from 5700 to 1900 cm2 per plant. As water stress increased, the period when leaves grew fastest became progressively earlier, from approximately 35% Amax to when leaves were less than 5 cm2. Water stress increased stomatal frequencies but reduced the area of individual stomata so that the area of the stomatal apparatus per unit leaf area was unchanged. This may partially explain the constancy of peak gas exchange per unit leaf area of sunflower grown under different water regimes. There was evidence that leaves could recommence growth when the stress was alleviated.

Analysis of Carbon Sequestration and Oxygen Release Capabilities of 25 Afforestation Plants in Tianjin

2014 ◽  
Vol 641-642 ◽  
pp. 1087-1092
Author(s):  
Fang Wang ◽  
Hong Yuan Li ◽  
Xin Li ◽  
Jia Nan Yang
Keyword(s):  
Carbon Sequestration ◽  
Leaf Area ◽  
Test System ◽  
Diospyros Kaki ◽  
Oxygen Release ◽  
Ulmus Pumila ◽  
Area Index ◽  
Unit Leaf Area ◽  
Unit Leaf ◽  
Platanus Orientalis

CI-340 portable photosynthesis test system and JYM-B leaf area meter were employed to observe the physiological velocity and leaf area index of 25 widely used afforestation plants in Tianjin. The results indicate that the diurnal change curve of net photosynthesis rates of 25 experimental species has one or two peaks. The daily carbon sequestration and oxygen release per unit leaf area are respectively 3.98-13.01 g/( m2·d) and 2.9-9.46 g/( m2·d). Among arbors, the order of carbon sequestration and oxygen release capabilities per unit leaf area is Ulmus pumila >Fraxinus velutina>Sophora japonica>Salix matsudana f. pendula>Malus micromalus cv.‘American’>Koelreuteria paniculata>Acer truncatum>Ulmus pumila cv. ‘jinye’>Prunus davidiana>Malus micromalus>Cotinus coggygria > Rhus typhina> Platanus orientalis>Catalpa speciosa>Diospyros kaki> Morus alba cv. ‘Tortuosa’. Among shrubs, the order is Weigela florida>Euonymus japonicus>Cercis chinensis>Ligustrum vicaryi >Sorbaria sorbifolia> Syringa oblata > Lonicera maackii >Cornus alba>Lonicera japonica.

FIELD EVALUATION OF GROWTH AND NITROGEN FIXATION IN PEAS SELECTED FOR HIGH AND LOW PHOTOSYNTHETIC CO2 EXCHANGE

1982 ◽  
Vol 62 (1) ◽  
pp. 5-17 ◽  
Author(s):  
J. D. MAHON
Keyword(s):  
Leaf Area ◽  
Field Measurements ◽  
Field Evaluation ◽  
Co2 Exchange ◽  
Physiological Age ◽  
Area Index ◽  
Large Variability ◽  
Unit Leaf Area ◽  
Unit Leaf ◽  
Area Basis

Six genotypes of pea (Pisum sativum L.), selected for either high or low CO2 exchange rate per unit leaf area (CER) on the basis of field measurements, were grown in field plots during 1978 and 1979. During two growing seasons, CER was determined in leaves of different physiological age at several times of the day and season. Dry weights, leaf areas and node numbers were determined 4, 7 and 10 wk after planting, and again after pod ripening. C2H2 reduction by detached roots was measured 5, 6, 8 and 9 wk after planting. Despite the large variability in CER with years, leaf numbers, and times of measurement, the mean CER of the three genotypes selected for high rates was always greater than that of the low selected group. CER was significantly correlated with growth per unit leaf area (E) and the high to low group ratios averaged 1.4 for CER and 1.3 for E. C2H2 reduction on an equivalent leaf area basis was not different in the two groups. On a land area basis, the low CER group had a significantly greater leaf area index which compensated for the decreased CER, and estimates of total CO2 exchange, growth and C2H2 reduction were similar in the two groups. Total aboveground dry matter and seed yields were greater in the low CER group, but harvest index was generally greater in those genotypes selected for high CER.

scholarly journals Leaf growth in early development is key to biomass heterosis in Arabidopsis

2020 ◽  
Vol 71 (8) ◽  
pp. 2439-2450 ◽  
Author(s):  
Pei-Chuan Liu ◽  
W James Peacock ◽  
Li Wang ◽  
Robert Furbank ◽  
Anthony Larkum ◽  
...  
Keyword(s):  
Leaf Area ◽  
Photosynthetic Efficiency ◽  
Unit Area ◽  
Leaf Growth ◽  
Co2 Assimilation ◽  
Photosynthetic Parameters ◽  
Fresh Weight Basis ◽  
Unit Leaf Area ◽  
Unit Leaf ◽  
Stage Of Development

Abstract Arabidopsis thaliana hybrids have similar properties to hybrid crops, with greater biomass relative to the parents. We asked whether the greater biomass was due to increased photosynthetic efficiency per unit leaf area or to overall increased leaf area and increased total photosynthate per plant. We found that photosynthetic parameters (electron transport rate, CO2 assimilation rate, chlorophyll content, and chloroplast number) were unchanged on a leaf unit area and unit fresh weight basis between parents and hybrids, indicating that heterosis is not a result of increased photosynthetic efficiency. To investigate the possibility of increased leaf area producing more photosynthate per plant, we studied C24×Landsberg erecta (Ler) hybrids in detail. These hybrids have earlier germination and leaf growth than the parents, leading to a larger leaf area at any point in development of the plant. The developing leaves of the hybrids are significantly larger than those of the parents, with consequent greater production of photosynthate and an increased contribution to heterosis. The set of leaves contributing to heterosis changes as the plant develops; the four most recently emerged leaves make the greatest contribution. As a leaf matures, its contribution to heterosis attenuates. While photosynthesis per unit leaf area is unchanged at any stage of development in the hybrid, leaf area is greater and the amount of photosynthate per plant is increased.

scholarly journals Coffee crop coefficient for precision irrigation based on leaf area index

Bragantia ◽  
2011 ◽  
Vol 70 (4) ◽  
pp. 946-951 ◽  
Author(s):  
Antonio Roberto Pereira ◽  
Marcelo Bento Paes de Camargo ◽  
Nilson Augusto Villa Nova
Keyword(s):  
Leaf Area Index ◽  
Leaf Area ◽  
Crop Coefficient ◽  
Initial Guess ◽  
Planting Density ◽  
Reference Surface ◽  
Area Index ◽  
Unit Leaf Area ◽  
Unit Leaf ◽  
Canopy Volume

Crop coefficient (Kc) for coffee plantations was found to be linearly related to the leaf area index (L) up to 3, i.e., Kc = b L. The basic assumption is that for irrigated trees the water use per unit leaf area (ET LA) is equal to the reference evapotranspiration (ETo) expressed also on a unit leaf area basis of the reference surface (ET LA = ETo/Lo). As recommended by FAO-56 the leaf area index (Lo) for the hypothetical reference surface (grass) is equal to 2.88, then the most likely value is b = Lo-1 = 2.88-1 = 0.347. However, for L > 3 (completely covered ground surface) Kc decreased from a peak value (~1.05) tending to an asymptotic low value around 0.7 for L > 6, but the linear model gives unrealistic Kc estimates; tentatively the empirical function Kc = 1.8 L-0.5 is offered here as an initial guess due to the lack of experimental results for the interval 3.5 <L < 5.5. To become operational under commercial fields it is necessary to estimate the leaf area per coffee tree (LA, m² tree-1), and based on a very limited set of data, LA was estimated as a function of planting density (PD, trees ha-1), i.e., LA = 88.38 - 8.63 Ln (PD). Alternatively, L (< 3.4) can be computed directly as a function of canopy volume (for V < 1.2 m³).

Stomatal Development During Leaf Expansion in Tobacco and Sunflower

1975 ◽  
Vol 23 (2) ◽  
pp. 253 ◽  
Author(s):  
HM Rawson ◽  
CL Craven
Keyword(s):  
Leaf Area ◽  
Stomatal Density ◽  
Stomatal Development ◽  
Developmental Patterns ◽  
Full Size ◽  
Unit Leaf Area ◽  
Unit Leaf ◽  
Wide Range ◽  
Young Leaves ◽  
Different Levels

Changes in stomatal density and size were followed in tobacco and sunflower leaves expanding from 10% of final area (10% Amax) to Amax under different levels of radiation. Lower radiation increased final leaf area, reduced stomatal densities, and increased area per stoma but had little effect on stomatal area per unit leaf area at Amax. In very young leaves (20% Amax) there was a wide range in the sizes of individual stomata, some stomata being close to full size, but by Amax differences were small. The possible relationship between the developmental patterns described and photosynthesis is briefly discussed.

Influence of different organic manures on growth, yield and mineral nutrient accumulation in lettuce (Lactuca sativa L.)

2021 ◽  
Vol 30 (2) ◽  
pp. 159-168
Author(s):  
Shabnur Chowdhury ◽  
MK Rahman
Keyword(s):  
Leaf Area Index ◽  
Leaf Area ◽  
Lactuca Sativa ◽  
Dry Weight ◽  
Organic Manure ◽  
Leaf Number ◽  
Nutrient Accumulation ◽  
Area Index ◽  
Organic Manures ◽  
Lactuca Sativa L

Effects of organic manures on growth and yield of lettuce (Lactuca sativa L.) and nutrient accumulation in its leaves was examined. The experiment was conducted in a completely randomized design (CRD) replicated thrice with ten treatments involving nine organic manures and a control treatment. Growth parameters viz. plant height, leaf number, leaf length, leaf area, leaf area index and fresh and dry weight of leaf, stem and root were assessed. The highest height (23.69 cm), longest leaf (32.18cm), leaf area (5883.43cm2), leaf area index (6.434), fresh weight (85.41 g) and dry weight (42.73 g) were found in Payel organic manure. The maximum leaf number (27) was recorded in Approshika organic manure. The maximum content of nitrogen (6.12%), phosphorus (1.83%), potassium (4.11%) and Sulphur (1.69%) were observed in Payel organic manure. The best growth performance and nutrient accumulation was observed in Payel organic manure. Dhaka Univ. J. Biol. Sci. 30(2): 159-168, 2021 (July)

Effect of Interspecific Interference, Light Intensity, and Soil Moisture on Soybean (Glycine max), Common Cocklebur (Xanthium strumarium), and Sicklepod (Cassia obtusifolia) Water Uptake

Weed Science ◽  
1993 ◽  
Vol 41 (4) ◽  
pp. 534-540 ◽  
Author(s):  
Ronald E. Jones ◽  
Robert H. Walker
Keyword(s):  
Soil Moisture ◽  
Light Intensity ◽  
Leaf Area ◽  
Water Uptake ◽  
Root Weight ◽  
Pressure Potential ◽  
Unit Leaf Area ◽  
Unit Leaf ◽  
Shoot Weight ◽  
The Relationship

Greenhouse and growth chamber experiments with potted plants were conducted to determine the effects of interspecific root and canopy interference, light intensity, and soil moisture on water uptake and biomass of soybean, common cocklebur, and sicklepod. Canopy interference and canopy plus root interference of soybean with common cocklebur increased soybean water uptake per plant and per unit leaf area. Root interference with soybean decreased common cocklebur water uptake per plant. Canopy interference of soybean with sicklepod increased soybean water uptake per unit leaf area, while root interference decreased uptake per plant. Combined root and canopy interference with soybean decreased water uptake per plant for sicklepod. Soybean leaf area and shoot weight were reduced by root interference with both weeds. Common cocklebur and sicklepod leaf area and shoot weight were reduced by root and canopy interference with soybeans. Only common cocklebur root weight decreased when canopies interfered and roots did not. The relationship between light intensity and water uptake per unit leaf area was linear in both years with water uptake proportional to light intensity. In 1991 water uptake response to tight was greater for common cocklebur than for sicklepod. The relationship between soil moisture level and water uptake was logarithmic. Common cocklebur water uptake was two times that of soybean or sicklepod at −2 kPa of pressure potential. In 1991 common cocklebur water uptake decreased at a greater rate than soybean or sicklepod in response to pressure potential changes from −2 to −100 kPa.

scholarly journals Simulated insect defoliation and duration of weed interference affected soybean growth

Weed Science ◽  
2006 ◽  
Vol 54 (4) ◽  
pp. 735-742 ◽  
Author(s):  
Travis C. Gustafson ◽  
Stevan Z. Knezevic ◽  
Thomas E. Hunt ◽  
John L. Lindquist
Keyword(s):  
Leaf Area ◽  
Defense Mechanism ◽  
Field Studies ◽  
Area Index ◽  
Early Season ◽  
Weed Interference ◽  
Insect Defoliation ◽  
Weed Growth ◽  
Simultaneous Control ◽  
Vegetative And Reproductive Growth

An improved understanding of crop stress from multiple pests is needed for better implementation of integrated pest management (IPM) strategies. Field studies were conducted in 2003 and 2004 at two locations in eastern Nebraska to describe the effects of simulated early-season insect defoliation of soybean and duration of weed interference on soybean growth. Three levels of simulated defoliation (undefoliated, 30, and 60%) and seven durations of weed interference (weedy and weed free; weed removal at V2, V4, V6, R3, and R5) were evaluated in a split-plot design. Defoliation significantly reduced soybean leaf-area index (LAI), total dry matter (TDM), and crop height in season-long weedy treatments only. Biomass partitioning during vegetative and reproductive growth was affected by both defoliation and weed interference. Increase in soybean relative growth rate (RGR) and biomass production soon after defoliation occurred (e.g., V5 stage) indicated potential defense mechanism by which soybean is able to adjust its physiology in response to the loss of leaf area. Weed interference combined with defoliation caused the greatest yield losses up to 97%. Results from this study indicate the need for monitoring early-season insect density and weed growth to determine if simultaneous control of both pests may be needed.

Carbon Isotope Discrimination and Gas Exchange in Coffea arabica During Adjustment to Different Soil Moisture Regimes

1992 ◽  
Vol 19 (2) ◽  
pp. 171 ◽  
Author(s):  
FC Meinzer ◽  
NZ Saliendra ◽  
C Crisosto
Keyword(s):  
Soil Moisture ◽  
Gas Exchange ◽  
Leaf Area ◽  
Coffea Arabica ◽  
Carbon Isotope Discrimination ◽  
Total Leaf Area ◽  
Unit Leaf Area ◽  
Unit Leaf ◽  
Moisture Regimes ◽  
Area Basis

Although carbon isotope discrimination (Δ) has been reported to decline in plants growing under reduced soil moisture, there is little information available concerning the dynamics of adjustments in Δ and gas exchange following a change in soil water availability. In this study Δ, photosynthetic gas exchange, and growth were monitored in container-grown coffee (Coffea arabica L.) plants for 120 days under three soil moisture regimes. At the end of 120 d, total leaf area of plants irrigated twice weekly was one half that of plants irrigated twice daily, although their assimilation rates on a unit leaf area basis were nearly equal throughout the experiment. This suggested that maintenance of nearly constant photosynthetic characteristics on a unit leaf area basis through maintenance of a smaller total leaf area may constitute a major mode of adjustment to reduced soil moisture availability in coffee. Intrinsic water-use efficiency (WUE) predicted from foliar Δ values was highest in plants irrigated weekly, intermediate in plants irrigated twice weekly and lowest in plants irrigated twice daily. When instantaneous WUE was estimated from independent measurements of total transpiration per plant and assimilation on a unit leaf area basis, the reverse ranking was obtained. The lack of correspondence between intrinsic and instantaneous WUE was attributed to adjustments in canopy morphology and leaf size in the plants grown under reduced water supply which enhanced transpiration relative to assimilation. Values of Δ predicted from the ratio of intercellular to ambient CO2 partial pressure determined during gas exchange measurements were not always consistent with measured foliar Δ. This may have resulted from a patchy distribution of stomatal apertures in plants irrigated weekly and from a lag period between adjustment in gas exchange and subsequent alteration in Δ of expanding leaves. The importance of considering temporal and spatial scales, and previous growth and environmental histories in comparing current single leaf gas exchange behaviour with foliar Δ values is discussed.

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