In soybeans, a leaf area index (LAI) of 3.5 at reproductive stage is consideredcritical for maximum yield. This critical LAI corresponds to about 90% canopy lightinterception. Reduction of the LAI below 3.5, or light interception below 90%,results in significant yield loss. 44, 75 When growing conditions are optimal for soybeans,including sufficient precipitation or irrigation water, soybeans can produce aleaf area index as high as 7. Consequently, these soybeans with ample water supplycan tolerate a significant defoliation injury without a significant yield loss. Forinstance, if the canopy has attained an LAI of 7, removal of half of the leaf area maynot result in a significant yield reduction.Although optimal moisture supply may enhance the level of tolerance to insectinjury, excess moisture can be harmful for plant growth. 76, 77 In some areas wherethere is excessive precipitation, drainage becomes a challenge to overcome waterlogging. Therefore, optimal water supply that favors rapid plant growth is desirable.The more vigorous the plants are, the more tolerant they can be to injuries by insectpests. Therefore, optimizing the supply of resources required for plant growth is onealternative to increasing the level of plant tolerance to insect injury <strong>and</strong> consequentlyreducing yield loss.In agricultural ecosystems, moisture stress can interact with arthropod injury toaffect plant gas exchange, dry-matter, <strong>and</strong> yield. 62, 63, 77, 78 Agronomic factors, suchas soil moisture available for plant growth, affect plant vigor altering the level of toleranceto arthropod injury. Therefore, consideration of agronomic inputs in a pestmanagement plan may be essential to increase plant tolerance to arthropod injury.8.9 CONCLUSIONSSeldom are environmental requisites in optimal supply for plants to achieve theirgenetic yield potential. In natural <strong>and</strong> agricultural systems, plants experience stressfrom both biotic <strong>and</strong> abiotic factors that can disrupt normal plant physiologicalprocesses <strong>and</strong> growth. As a result, stressed plants experience reduced fitness or yield.Moisture stress is one of the major abiotic factors that limit agricultural productivity.Plants experiencing moisture stress have reduced physiological processes suchas photosynthesis, transpiration, <strong>and</strong> reduced biomass <strong>and</strong> reduced yield. If there isextreme moisture stress, particularly at early growth stages, plants may not recoverfrom moisture stress <strong>and</strong> can die. However, if the level of moisture stress is notsevere, plants deploy different strategies to maintain fitness. Some of the adaptationsto moisture stress include increases in some hormone concentration to regulate stomatalconductance limiting transpirational water loss. In addition, moisture-stressedplants tend to increase root growth to absorb more water from the soil.Plants face multiple stressors that can limit their growth, development, <strong>and</strong> fitness.Because little research has focused on the interactions of abiotic stress <strong>and</strong>insect injury, the broad importance of the interaction is not clear. Few studies indicatethat abiotic factors can alter plant response to insect injury. In agricultural ecosystems,yield loss occurs from both moisture stress <strong>and</strong> insect injury. However, themagnitude of yield loss from the interaction of the two stressors could be differentfrom the magnitude of yield loss if these stressors were acting independently. This
implies that, at least in some systems, the impact of insect injury depends on moisturestress <strong>and</strong> other abiotic factors. <strong>Yield</strong> loss from insect injury is most likelygreater in plants subjected to moisture stress than in unstressed plants. This is becauseplants provided with optimum resources may tolerate insect injury more than plantswithout optimum resources. Consequently, there may be opportunities to increaseplant tolerance to insect injury <strong>and</strong> reduce yield losses by cultural practices thatincrease plant vigor.REFERENCES1. Boyer, J. S., Plant productivity <strong>and</strong> environments, Science, 218, 443, 1982.2. Roades, D. F., Herbivore population dynamics <strong>and</strong> plant chemistry, in Variable Plants <strong>and</strong>Herbivores in Natural <strong>and</strong> Managed Systems, Denno, R. F., <strong>and</strong> McClure, M. S., Eds.,Academic Press, New York, 1983, chap. 6.3. Isichaikul, S., Fujimura, K., <strong>and</strong> Ichikawa, T., Humid microenvironment prerequisite forthe survival <strong>and</strong> growth of nymphs of the rice brown planthopper, Nilaparvata lugens(Stal) (Homoptera: Delphacidae), Res. Popul. Ecol., 36, 23, 1994.4. Lummus, P. F., Smith, J. C., <strong>and</strong> Powell, N. L., Soil moisture <strong>and</strong> texture effects on survivalof immature Southern corn rootworm, Diabrotica undecimpunctata howardi Barber(Coleoptera: Chrysomelidae), Environ. Entomol., 12, 1529, 1983.5. Burst, G. E., <strong>and</strong> House, G. J., Effects of soil moisture, texture, <strong>and</strong> rate of soil drying onegg <strong>and</strong> larval survival of the Southern corn rootworm (Coleoptera: Chrysomelidae),Environ. Entomol., 19, 697, 1990.6. Rosenberg, N. J., Blad, B. L., <strong>and</strong> Verma. S. B., Microclimate, The BiologicalEnvironment, 2nd Ed., Wiley-Interscience, New York, 1983.7. Stoutjesdijk, P. H., <strong>and</strong> Barkman, J. J., Microclimate Vegetation <strong>and</strong> Fauna, Opulus Press,Uppsala, 1992.8. Perring, T. M., Holtzer, T. O., Toole, J. L., <strong>and</strong> Norman, J. M., Temperature <strong>and</strong> humidityeffects on ovipositional rates, fecundity, <strong>and</strong> longevity of adult female Banks grass mites(Acari: Tetranychidae), Ann. Entomol. Soc. Am., 77, 581, 1984.9. Perring, T. M., Holtzer, T. O., Toole, J. L., <strong>and</strong> Norman, J. M., Relationships between corncanopymicroenvironments <strong>and</strong> Banks grass mite (Acari: Tetranychidae) abundance,Environ. Entomol., 15, 79, 1986.10. Toole, J. L., Norman, J. M., Holtzer, T. O., <strong>and</strong> Perring, T. M., Simulating Banks grass mitepopulation dynamics as a subsystem of a crop canopy-microenvironment model, Environ.Entomol., 13, 329, 1984.11. Mattson, W. J., <strong>and</strong> Haack, R. A., The role of drought in outbreaks of plant-eating insects,Bioscience, 37, 110, 1987.12. Marc<strong>and</strong>ier S., <strong>and</strong> Khachatourians, G. G., Susceptibility of the migratory grasshopper,Melanoplus sanguinipes (Fab.) (Orthoptera: Acrididae), to Beauveria bassiana (Bals.)Vuillemin (Hyphomycete): influence of relative humidity, Can. Entomol., 119, 901, 1987.13. Trichilo, P. J., Wilson, L. T., <strong>and</strong> Grimes, D. W., Influence of irrigation management on theabundance of leafhoppers (Homoptera: Cicadellidae) on grapes, Environ. Entomol., 19,1803, 1990.14. Biladdawa, C. W., The effect of crop microenvironment on the pea leaf weevil’s behavior:an explanation for weevil departure from diverse cropping systems, Insect Sci. Appl., 9,509, 1988.
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Biotic Stressand Yield Loss
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Library of Congress Cataloging-in-P
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PrefaceThe idea for this book came
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EditorsRobert K. D. Peterson, Ph.D.
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ContentsChapter 1Illuminating the B
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1Illuminating the Black Box:The Rel
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increase plant tolerance, through p
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the action of a stressor on a plant
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The magnitude and duration of injur
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Plant part injuredrefers to the pla
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cific competition, while agricultur
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2Yield Loss and PestManagementLeon
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direct relationships between the ac
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In keeping with the theme of this b
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egressions. Actually, the title “
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REFERENCES1. Teng, P. S., Crop Loss
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3Techniques for EvaluatingYield Los
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number of species and stage of cutw
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especially if buried in soil, can d
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elationships for some pests. When m
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injury can be precisely controlled
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day. 81, 99 However, except for an
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the literature most likely are actu
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20. Ba-Angood, S. A., and Stewart,
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60. Stewart, J. G., McRae, K. B., a
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99. Shields, E. J., and Wyman, J. A
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4.3.3.1.3 Third generation European
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ing on the developmental stage at t
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4.2.2.1.2 Temperature stressPlant s
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chronic injury. Acute injury result
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ows, roadsides, or small grain fiel
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numbers are present. Stink bugs, Eu
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Oligonychus pratensis, feed on corn
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ECB2. 224.3.3.1.4 The impacts of Eu
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stalk borer, Papaipema nebris, is a
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period prolonged with sufficient co
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Arthropod injuries to developing ea
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esponses to herbivory have been obs
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Midwest, Purdue University CES and
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59. Bailey, W. C., and Pedigo, L. P
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5Phenological Disruptionand Yield L
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ity by animal consumers is the agro
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- Page 168 and 169: 10Stephen C. WelterCONTENTSContrast
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53. Panda, N., and Heinrichs, E. A.
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97. Gross, K. L., and Soule, J. D.,
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143. Davidson, J. L., and Milthorpe
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11Crop Disease andYield LossBrian D
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The conditions listed above are opt
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to associate the effects of disease
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general relationship between LAI an
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Biomassproduction(total dryweight)R
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Y RUE(t)RI(t)[1 X]dt [11.12]wher
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sue. The most accurate prediction o
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tion. Two weeks before harvest, the
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15. Spitters, C. J. T., Van Roermun
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57. Richardson, A. J., Wiegand, C.
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they were cheap, convenient, and ef
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dW / W dtcauses and consequences of
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(a)(b)Maize yield (Mg ha -1 )987654
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Recall that c is a constant, so by
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where the subscripts c and w repres
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0.6Fraction yield loss0.40.2Eq. 16,
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the leaf area index (LAI). Incorpor
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can no longer be tolerated and, the
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cide. Steckel et al. 68 showed that
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A eq ∑ jN eq,ji 1YL n,j [12.31]1
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samples per field. Thomas 85 sugges
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external factors such as annual wea
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38. Boznic, A. C., and Swanton, C.
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weeds, Weed Sci., 44, 856, 1996.79.
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competition and weed management. 3-
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per unit biomass (1/W i)(dW i/dt) o
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of light interception). Algorithms
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where G a,iis the water limited pla
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13.4 COMPETITION FOR SOIL NITROGENA
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As with soil water, Equations 13.10
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partitioning of nitrogen to leaves.
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and stems to optimize photosyntheti
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influence of enhanced UV-B conditio
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Systems Approaches at the Field Lev