ECONOMIC THRESHOLDS AND ECONOMIC INJURY LEVELS OF CEREAL APHIDS ON BARLEY IN SOUTHWESTERN QUEBEC

1980 ◽  
Vol 112 (8) ◽  
pp. 759-764 ◽  
Author(s):  
S. A. Ba-Angood ◽  
R. K. Stewart

AbstractArtificial infestations of cereal aphids in caged plants were made at different growth stages of barley in the field in 1978 and 1979. Forty, 80, 160, and 200 aphids/tiller reduced grain yield significantly (P < 0.01) when introduced into caged plants at flowering and milky stages for 2 weeks. Only the 150 and 200 aphids/tiller-treatments gave significant reductions in yield when introduction was at the mealy ripe stage. Twenty aphids/tiller gave a significant reduction in yield only when they were introduced at the beginning of ear emergence and flowering, but not at the milky ripe stage. Significant reduction in percentage protein was obtained only when 160 and 200 aphids/tiller were introduced at flowering and milky ripe stages. The economic injury and threshold levels were calculated as 10–18 and 8–16 aphids/tiller, respectively, depending on rate of increase of aphids, costs of chemical control, and the value of the crop in 1978 and 1979.

Agronomy ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 106 ◽  
Author(s):  
Ke Zhang ◽  
Xiaojun Liu ◽  
Syed Tahir Ata-Ul-Karim ◽  
Jingshan Lu ◽  
Brian Krienke ◽  
...  

Accurate estimation of the nitrogen (N) spatial distribution of rice (Oryza sativa L.) is imperative when it is sought to maintain regional and global carbon balances. We systematically evaluated the normalized differences of the soil and plant analysis development (SPAD) index (the normalized difference SPAD indexes, NDSIs) between the upper (the first and second leaves from the top), and lower (the third and fourth leaves from the top) leaves of Japonica rice. Four multi-location, multi-N rate (0–390 kg ha−1) field experiments were conducted using seven Japonica rice cultivars (9915, 27123, Wuxiangjing14, Wunyunjing19, Wunyunjing24, Liangyou9, and Yongyou8). Growth analyses were performed at different growth stages ranging from tillering (TI) to the ripening period (RP). We measured leaf N concentration (LNC), the N nutrition index (NNI), the NDSI, and rice grain yield at maturity. The relationships among the NDSI, LNC, and NNI at different growth stages showed that the NDSI values of the third and fourth fully expanded leaves more reliably reflected the N nutritional status than those of the first and second fully expanded leaves (LNC: NDSIL3,4, R2 > 0.81; NDSIothers, 0.77 > R2 > 0.06; NNI: NDSIL3,4, R2 > 0.83; NDSIothers, 0.76 > R2 > 0.07; all p < 0.01). Two new diagnostic models based on the NDSIL3,4 (from the tillering to the ripening period) can be used for effective diagnosis of the LNC and NNI, which exhibited reasonable distributions of residuals (LNC: relative root mean square error (RRMSE) = 0.0683; NNI: RRMSE = 0.0688; p < 0.01). The relationship between grain yield, predicted yield, and NDSIL3,4 were established during critical growth stages (from the stem elongation to the heading stages; R2 = 0.53, p < 0.01, RRMSE = 0.106). An NDSIL3,4 high-yield change curve was drawn to describe critical NDSIL3,4 values for a high-yield target (10.28 t ha−1). Furthermore, dynamic-critical curve models based on the NDSIL3,4 allowed a precise description of rice N status, facilitating the timing of fertilization decisions to optimize yields in the intensive rice cropping systems of eastern China.


2010 ◽  
Vol 41 (No. 4) ◽  
pp. 158-164 ◽  
Author(s):  
E.A. Egwurube ◽  
O. Ogunlana M ◽  
C. Dike M ◽  
I. Onu

Population studies and tests on the relationship between density and damage were conducted in 1999 to 2001 to determine the pest status of <I>Empoasca dolichi</I> on groundnut (<I>Arachis hypogaea </I>L.) in the Zaria area of northern Nigeria. Analyses showed that <I>Empoasca</I> numbers varied significantly from one year to another, and within each year the numbers of leafhoppers observed at the different growth stages of the plant were significantly different (<I>P</I> = 0.01). There was an inverse and highly significant relationship between the mean kernel yield and the <I>Empoasca </I>damage at the different growth stages of the plant. When natural population densities were plotted against economic injury level (EIL), the densities did not reach the EIL throughout the groundnut growing seasons. The insect was thus not an economic pest on groundnut in Zaria during the period of the study.


1980 ◽  
Vol 112 (7) ◽  
pp. 681-686 ◽  
Author(s):  
S. A. Ba-Angood ◽  
R. K. Stewart

AbstractNatural infestations of cereal aphids caused significant reductions in grain yield in field plots of early and late cultivars of barley, wheat, and oats in southwestern Quebec. Severely reduced grain yields resulted when caged plants of wheat and late cultivars of barley and oats were artificially infested, but early cultivars of barley and oats were less affected. The percentage protein of grain was significantly reduced in all crops, but wheat and late oats were most affected.


2002 ◽  
Vol 73 (2-3) ◽  
pp. 67-79 ◽  
Author(s):  
Hiroyuki Shimono ◽  
Toshihiro Hasegawa ◽  
Kazuto Iwama

Weed Science ◽  
2009 ◽  
Vol 57 (6) ◽  
pp. 584-592 ◽  
Author(s):  
Uliana B. Bashtanova ◽  
K. Paul Beckett ◽  
Timothy J. Flowers

Japanese knotweed is an aggressive alien species in Europe, North America, and Australia, causing a range of environmental problems. Eradication of Japanese knotweed is proving to be a difficult task, because the plant is able to propagate generatively by intra- and interspecific hybridization, and vegetatively from shoot and tiny rhizome pieces. Despite the economic consequences of Japanese knotweed on natural and built environments, its physiology is not yet fully understood; especially important are sink-source relations between old and young parts of the rhizome and growth of lateral and latent rhizome buds. Current methods of chemical control include three types of phloem-mobile herbicides, such as glyphosate, imazapyr, and synthetic auxins. These herbicides have limitations on their use, and all fail to eradicate the plant completely, for the reasons discussed in this review. Our aim is to suggest prospective approaches to enable chemical eradication: use of signals to induce controlled growth and development of quiescent rhizome buds; use of phytohormones, sugars, and light to increase allocation of phloem-mobile herbicides to the rhizome; use of xylem-mobile herbicides to exterminate the old rhizome parts; and use of different phloem-mobile herbicides at different growth stages.


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