scholarly journals Intraspecific Competition in Honey Mesquite: Leaf and Whole Plant Responses

1998 ◽  
Vol 51 (3) ◽  
pp. 345 ◽  
Author(s):  
R. J. Ansley ◽  
B. A. Trevino ◽  
P. W. Jacoby
2019 ◽  
Vol 223 (3) ◽  
pp. 1073-1105 ◽  
Author(s):  
Hendrik Poorter ◽  
Ülo Niinemets ◽  
Nikolaos Ntagkas ◽  
Alrun Siebenkäs ◽  
Maarit Mäenpää ◽  
...  

1994 ◽  
Vol 36 (2) ◽  
pp. 301-307 ◽  
Author(s):  
A. Gulati ◽  
P. K. Jaiwal

1981 ◽  
Vol 8 (3) ◽  
pp. 267 ◽  
Author(s):  
MK Smith ◽  
JA Mccomb

The effect of NaCl on growth was examined for whole plants and callus cultures of a salt-sensitive glycophyte (Phaseolus vulgaris L.), a salt-tolerant glycophyte (Beta vulgaris L.) and two halophytes (Atriplex undulata D. Dietr., which has salt glands, and Suaeda australis (R. Br.) Moq., a succulent). Whole plants were grown in nutrient solution culture at NaCl concentrations of 0.1-250 mM. Callus cultures were initiated from the same seed stock, and similar saline regimes were imposed. Whole plant responses were characteristic for the various types of plants: P. vulgaris showed a decrease in growth with increasing salinity; B. vulgaris showed a slight increase in growth at the intermediate salt level and a decrease at higher levels; A. undulata and S. australis showed well defined growth optima at 62.5 mM and 125 mM NaCl, respectively. Callus cultures of P. vulgaris and the two halophytes grew very poorly when salinity was increased. Callus of B. vulgaris showed the same tolerance to salt as did the whole plants. Thus salt tolerance of the halophytes depends on the anatomical and physiological complexity of the intact plant while callus from B. vulgaris appears to have a mechanism(s) of salt tolerance which operates at the cellular level.


1986 ◽  
Vol 13 (1) ◽  
pp. 143 ◽  
Author(s):  
R Munns ◽  
A Termaat

This paper discusses whole-plant responses to salinity in order to answer the question of what process limits growth of non-halophytes in saline soils. Leaf growth is more sensitive to salinity than root growth, so we focus on the process or processes that might limit leaf expansion. Effects of short-term exposure (days) are considered separately from long-term exposure (weeks to years). The answer in the short term is probably the water status of the root and we suggest that a message from the root is regulating leaf expansion. The answer to what limits growth in the long term may be the maximum salt concentration tolerated by the fully expanded leaves of the shoot; if the rate of leaf death approaches the rate of new leaf expansion, the photosynthetic area will eventually become too low to support continued growth.


HortScience ◽  
1994 ◽  
Vol 29 (6) ◽  
pp. 693-694 ◽  
Author(s):  
Mary Ann Rose ◽  
Mark A. Rose

A closed-loop photosynthesis system and a heat-balance sap-flow gauge independently confirmed oscillatory transpiration in a greenhouse-grown Rosa hybrids L. Repetitive sampling revealed 60-minute synchronized oscillations in CO2-exchange rate, stomatal conductance, and whole-plant sap-flow rate. To avoid confusing cyclical plant responses with random noise in measurement, we suggest that gas-exchange protocols begin with frequent, repetitive measurements to determine whether transpiration is stable or oscillating. Single measurements of individual plants would be justified only when transpiration is steady state.


2020 ◽  
Vol 25 (4) ◽  
pp. 611-626 ◽  
Author(s):  
Latif Ahmad Peer ◽  
Zahoor A. Dar ◽  
Aijaz A. Lone ◽  
Mohd Yaqub Bhat ◽  
Nusrat Ahamad

Weed Science ◽  
1997 ◽  
Vol 45 (1) ◽  
pp. 22-30 ◽  
Author(s):  
J. Boyd Carey ◽  
Donald Penner ◽  
James J. Kells

Greenhouse and laboratory studies were conducted to determine the physiological basis for selectivity of nicosulfuron and primisulfuron in 5 plant species. Differential sensitivity of the species was quantified by determining GR50values (herbicide rate required to reduce plant growth 50%) for each species/herbicide combination. GR50data indicated the following levels of sensitivity: corn—tolerant to both herbicides; seedling johnsongrass—sensitive to both herbicides; barnyardgrass—sensitive to nicosulfuron and tolerant to primisulfuron; giant foxtail—sensitive to nicosulfuron and tolerant to primisulfuron; and eastern black nightshade—tolerant to nicosulfuron and sensitive to primisulfuron. Studies using14C-radiolabeled herbicides were conducted to determine whether differential herbicide absorption, translocation, or metabolism contributed to whole plant responses. Nicosulfuron and primisulfuron selectivity in corn, johnsongrass, barnyardgrass, and giant foxtail was primarily due to differential herbicide metabolism rate. Tolerant species metabolized the herbicide more rapidly and extensively than sensitive species. Differential herbicide absorption, translocation, or metabolism did not explain differential sensitivity of eastern black nightshade to the herbicides. Further studies indicated that the tolerance of eastern black nightshade to nicosulfuron and its sensitivity to primisulfuron was directly related to lower sensitivity of the acetolactate synthase (ALS) to nicosulfuron than to primisulfuron. Eastern black nightshade translocated very little (3%) of the nicosulfuron applied. The ALS sensitivity of johnsongrass and eastern black nightshade was similar in the presence of nicosulfuron. A combination of a higher ALS level and less herbicide translocation contributes to tolerance of eastern black nightshade and to sensitivity of johnsongrass to nicosulfuron.


HortScience ◽  
2017 ◽  
Vol 52 (5) ◽  
pp. 706-712 ◽  
Author(s):  
John Erwin ◽  
Esther Gesick

The impact of irradiance (0–1200 μmol·m−2·s−1) and carbon dioxide concentration (CO2; 50–1200 ppm) on kale (Brassica oleracea and B. napus pabularia; three cultivars), Swiss chard (chard, Beta vulgaris; four cultivars), and spinach (Spinacea oleracea; three cultivars) photosynthetic rate (Pn; per area basis) was determined to facilitate maximizing yield in controlled environment production. Spinach, chard, and kale maximum Pn were 23.8, 20.3, and 18.2 μmol CO2·m−2·s−1 fixed, respectively, across varieties (400 ppm CO2). Spinach and kale had the highest and lowest light compensation points [LCPs (73 and 13 μmol·m−2·s−1, respectively)] across varieties. The light saturation points (LSPs) for chard and kale were similar at 884–978 μmol·m−2·s−1, but for spinach, the LSP was higher at 1238 μmol·m−2·s−1. Dark respiration was lowest on kale and highest on spinach (−0.83 and −5.00 μmol CO2·m−2·s−1, respectively). The spinach CO2 compensation point (CCP) was lower (56 ppm) than the chard or kale CCP (64–65 ppm). Among varieties, ‘Red Russian’ kale Pn saturated at the lowest CO2 concentration (858 ppm), and ‘Bright Lights’ chard saturated at the highest (1266 ppm; 300 μmol·m−2·s−1). Spinach Pn was more responsive to increasing irradiance than to CO2. Kale Pn was more responsive to increasing CO2 than to irradiance, and chard Pn was equally responsive to increasing CO2 or irradiance. Implications and limitations of this work when “upscaling” to whole-plant responses are discussed.


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