ENHANCED BUD REGENERATION AND BULB FORMATION OF SPRING SNOWFLAKES LEUCOJUM VERNUM IN LIQUID CULTURES

2009 ◽  
pp. 195-200
Author(s):  
M. Ziv
Agriculture ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 292
Author(s):  
Ilie Bodale ◽  
Gabriela Mihalache ◽  
Vladut Achiţei ◽  
Gabriel-Ciprian Teliban ◽  
Ana Cazacu ◽  
...  

Nutrient consumption by plants depends on the growth stage and environmental conditions. In general, plants take up species of elements at different speeds. We monitored and recorded the electrical charge flow through xylem sap of tomato plants (Brillante F1) using femto/picoammeter equipment (Keysight B2981A). This technique evaluates the nutrient uptake of tomato treated with the most common macronutrients (KNO3; KH2PO4; Ca(NO3)2; KCl) by monitoring the electrical conductivity for 24 h. The electrical conductivity of each treatment correlated with the plant growth and development stages. The results showed that the tomato plants had a high consumption of nutrients in the vegetative stage, while in other stages, they had a specific consumption, like phosphorus for bulb formation, potassium for increasing the number of flowers and water for the ripening of fruits. The quantitative evaluation of the ions absorbed by the plant was based on the magnitude and shape of the electrical conductivity curves. Our technique is an efficient method to determine nutrient consumption and is useful in predicting the deficiency of a certain element in tomato plants.


2021 ◽  
Vol 297 ◽  
pp. 123744
Author(s):  
Zhengyao Qu ◽  
Shuaiqi Guo ◽  
Yifeng Zheng ◽  
Emma C. Giakoumatos ◽  
Qingliang Yu ◽  
...  

2006 ◽  
Vol 86 (2) ◽  
pp. 211-218 ◽  
Author(s):  
Denise Russowski ◽  
Natasha Maurmann ◽  
Sandra Beatriz Rech ◽  
Arthur Germano Fett-Neto

1965 ◽  
Vol 162 (989) ◽  
pp. 555-566 ◽  

Growth in the presence of inhibitory concentrations of copper enhances the tendency of yeast to flocculate. Many yeasts will not flocculate unless calcium is included in the growth medium and Guinness strain 522 used in the present work required a relatively large amount. Single cell cultures may undergo variation during subculture, resulting in the production of a large number of variants (Chester 1963). The cells of these variants differ considerably in their ability to adhere together. Flocculation variants of strain 522 differed among themselves in the amount of calcium necessary for flocculation, the most flocculent variants requiring least calcium. Washed cells of the more flocculent yeasts removed more calcium from a calcium chloride solution than did those with lesser powers of adhesion. In a copper medium con­taining calcium the more flocculent variants replaced the less flocculent. Calcium protected cells from copper and the more flocculent variants enjoyed most protection. All variants acquired resistance to copper during growth in the copper medium. Despite the selection of the more flocculent yeasts during growth in liquid medium, their copper resistance was less than that of the less flocculent yeasts. When calcium was added to the liquid copper medium, cultures developed less resistance. It is concluded that the less flocculent cells, having less protection by calcium, were exposed to what was effectively a greater concentration of copper and therefore became more resistant. This greater resistance did not enable these cells to compete with the flocculent cells in liquid cultures.


1967 ◽  
Vol 13 (6) ◽  
pp. 629-633 ◽  
Author(s):  
E. B. Lillehoj ◽  
A. Ciegler ◽  
H. H. Hall

Aflatoxin G1was removed from liquid cultures by growing and resting cells of Flavobacterium aurantiacum NRRL B-184. In inoculated culture media containing toxin levels of 7.5 p.p.m. and above, there was a protracted growth lag which was subsequently overcome; toxin removal then occurred, concomitant with growth. Only a few cells demonstrated aberrant morphological forms when cultured in the presence of aflatoxin G1. A comparison of the effects of aflatoxin G1with B1on growth and morphology showed that B1was distinctly more toxic. Three hundred and thirty micrograms of aflatoxin G1was removed per 1 × 1013resting cells during a 4-hour incubation period. Preincubation of resting cells with aflatoxin B1did not interfere with subsequent uptake of G1.


1994 ◽  
Vol 57 (6) ◽  
pp. 839-841 ◽  
Author(s):  
William A. Ayer ◽  
Latchezar S. Trifonov

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