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UV-Effects on Young Seedlings of Soybean: Effects in Early Development and Long-Term Effects

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UV Radiation in Global Climate Change

Abstract

Young plants are the most susceptible to ultraviolet (UV) radiation, due to the large number of growing and dividing cells. Incident UV radiation to earth has increased, even at temperate latitudes. Chronic exposure to UV light, especially UV-B (290 nm – 320 nm) radiation, causes damage to land plants including reduced photosynthetic capacity, biomass yield, nutritional quality of the seed, altered patterns of species competition, plant ultrastructure and pigment production, and increased incidence of disease. Hence it is important to know how exposures early in the life cycle of the plant affect the establishment of the seedling and the production of viable seed. We found that the greatest affects of UV-B occurred very early in the plant’s life cycle, notably in the first week post planting. Aside from increased mortality with increasing UV energy, UV-B treated seedlings had increased deformity, decreased ability to produce viable seeds and dysregulation of phenylpropanoid synthesis, which is dependent upon phenylalanine. Responses to high energy UV-B cause noticeably different effects in different varieties of soybean. If soybean experience higher energy UV in the early stages of growth, the effects can cause heritable changes, which will in turn effect yield and impact the viability of the next generation of seed.

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References

  • Ajavon AN, Albritton DL, Megie G and Watson RT (2003) Scientific assessment of Ozone Depletion: 2002. Global Ozone and Monitoring Project—Report # 47. World Meteorological Organization, Geneva

    Google Scholar 

  • Beerhues L, Robeneck H, and Wiermann R (1988) Chalcone synthesis from spinach (Spinacia aleracea L.). Immunofluorescence and immunogold localization. Planta 173, 544–553

    Article  CAS  Google Scholar 

  • Bieza K and Lois R (2001) An Arabidopsis mutant tolerant to lethal ultraviolet-B levels shows constitutively elevated accumulation of flavonoids and other phenolics. Plant Physiology 126, 1105–1115

    Article  CAS  Google Scholar 

  • Biggs RH, Kossuth SV, and Teramura AH (1981) Response of 19 cultivars of soybeans to ultraviolet-B irradiance. Physiol. Plant. 53, 19–26

    Article  Google Scholar 

  • Bilger W, Hohnsen T and Schreiber U (2001) UV-excited chlorophyll fluorescence as a tool for the assessment of UV-protection by the epidermis of plants. Journal of Experimental Botany 52, 2007–2014

    Article  CAS  Google Scholar 

  • Bird SM, and Gray JE (2003) Signals from the cuticle affect epidermal cell differentiation. New Phytologist 157, 9–23

    Article  CAS  Google Scholar 

  • Blanding C, Simmons SJ, Casati P, Walbot V and Stapleton AE (2007) Coordinated regulation of maize genes during increasing exposure to ultraviolet radiation: identification of ultravioletresponsive genes, functional processes and associated potential promoter motifs. Plant Biotechnology Journal 5, 677–695

    Article  CAS  Google Scholar 

  • Brown BA, Cloix C, Jiang GH, Kaiserli E, Herzyk P, Kliebenstein DJ, and Jenkins GI (2005) A UV-B-specific signaling component orchestrates plant UV protection. Proceedings of the National Academy of Science U.S.A. 102, 18225–18230

    Article  CAS  Google Scholar 

  • Brown BA and Jenkins GI (2008) UV-B signaling pathways with different fluence-rate response profiles are distinguished in mature Arabidopsis leaf tissue by requirement for UVR8, HY5, and HYH. Plant Physiology 146, 576–588

    Article  CAS  Google Scholar 

  • Burchard P, Bilger W and Weissenbock G (2000) Contribution of hydroxycinnamates and flavonoids to epidermal shielding of UV-A and UV-B radiation in developing rye primary leaves as assessed by ultraviolet-induced chlorophyll fluorescence measurements. Plant, Cell & Environment 23, 1373–1380

    Article  CAS  Google Scholar 

  • Caldwell MM, and Flint SD (1994) Stratospheric ozone reduction, solar UV-B radiation and terrestrial ecosystems. Climatic Change 28, 375–394

    Article  CAS  Google Scholar 

  • Caldwell M, Teramura AH, Tevini M, Bornman JF, Bjorn LO and Kulandevalu G (1995) Effects of increased solar ultraviolet radiation on terrestrial plants. AMBIO 24, 166–173

    Google Scholar 

  • Caldwell MM, Ballare CL, Bornman JF, Flint SD, Bjorn LO, Teramura AH, Kulandaivelu G and Tevini M (2003) Terrestrial ecosystems, increased solar ultraviolet radiation and interactions with other climatic change factors. Photochemical and Photobiological Sciences 2, 29–38

    Article  CAS  Google Scholar 

  • Caldwell MM, Bornman JF, Ballare CL, Flint SD and Kulandaivelu G (2007) Terrestrial ecosystems, increased solar ultraviolet radiation, and interactions with other climate change factors. Photochemical and Photobiological Sciences 6, 252–266

    Article  CAS  Google Scholar 

  • Cartwright HN, Baucom C, Singh P, Smith KL and Stapleton AE (2001) Intraspecific comparisons reveal differences in the pattern of ultraviolet radiation responses in four maize (Zea mays L.) varieties. Journal of Photochemistry and Photobiology B: Biology 62, 88–96

    Article  CAS  Google Scholar 

  • Casati P and Walbot V (2005) Differential accumulation of maysin and rhamnosylisoorientin in leaves of high-altitude landraces of maize after UV-B exposure. Plant, Cell & Environment 28, 788–799

    Article  CAS  Google Scholar 

  • Chappell J, and Hahlbrock K (1984) Transcription of plant defense genes in response to UV light or fungal elicitor. Nature 311, 76–78

    Article  CAS  Google Scholar 

  • Chapple CCS, Shirley BW, Zook M, Hammerschmidt R and Somerville SC (1994) Secondary metabolism in Arabidopsis. In E M Meyerowitz and C R Somerville, eds, Arabidopsis, CSH laboratory Press, Plainview, New York, pp. 989–1030

    Google Scholar 

  • Christie JM and Jenkins GI (1996) Distinct UV-B and UV-A/blue light signal transduction pathways induce chalcone synthase gene expression in Arabidopsis cells. Plant Cell 8, 1555–1567

    Article  CAS  Google Scholar 

  • Christie PJ, Alfenito MR and Walbot V (1994) Impact of low-temperature stress on general phenylpropanoid and anthocyanin pathways: Enhancement of transcript abundance and anthocyanin pigmentation in maize seedlings. Planta 194, 541–549

    Article  CAS  Google Scholar 

  • Cosio EG and McClure JW (1984) Kaempferol glycosides and enzymes of the flavonol biosynthesis in leaves of a soybean strain with low photosynthetic rates. Plant Physiology 74, 877–881

    Article  CAS  Google Scholar 

  • Davin LB and Lewis NG (1992) In HA Stafford and RK Ibrahim, eds Recent Advances in Phytochemistry, Plenum Press, New York 26, 325–375

    Google Scholar 

  • Frohnmeyer H and Staiger D (2003) Ultraviolet-B radiation-mediated responses in plants. Balancing damage and protection. Plant Physiology 133, 1420–1428

    Article  CAS  Google Scholar 

  • Frohnmeyer H, Bowler C and Schafer E (1997) Evidence for some signal transduction elements involved in UV-light-dependent responses in parsley protoplasts. Journal of Experimental Botany 48, 739–750

    Article  CAS  Google Scholar 

  • Fuglevand G, Jackson JA and Jenkins GI (1996) UV-B, UV-A, and blue light signal transduction pathways interact synergistically to regulate chalcone synthase gene expression in Arabidopsis. Plant Cell 8, 2347–2357

    Article  CAS  Google Scholar 

  • Gilchrist DG and Kosuge T (1980) Aromatic amino acid biosynthesis and its regulation. In PK Stumpf, EE Conn, eds, The Biochemistry of Plants, Vol 5, B J Miflin, Academic Press, New York, pp 507–531

    Google Scholar 

  • Gonzalez R, Paul ND, Percy K, Ambrose M, McLaughlin CK, Barnes JD, Areses M and Wellburn AR (1996) Responses to ultraviolet-B radiation (280 nm–315 nm) of pea (Pisum sativum) lines differing in leaf surface wax. Physiologia Plantarum 98, 852–860

    Article  CAS  Google Scholar 

  • Grammatikopoulos G, Kyparissis A, Drilias P, Petropoulou Y and Manetas Y (1998) Effects of UV-B radiation on cuticle thickness and nutritional value of leaves in two mediterranean evergreen sclerophylls. Journal of Plant Physiology 153, 506–512

    CAS  Google Scholar 

  • Gritz DC, Liu-Gritz L, Britz SJ, and Sullivan J H (2005) Ultraviolet B effects on stomatal density, water use efficiency and stable carbon isotope discrimination in four glasshousegrown soybean (Glycine max) cultivars. Environ. Exp. Bot. 53, 343–355

    Article  Google Scholar 

  • Hahlbrock K and Scheel D (1989) Physiology and molecular biology of phenylpropanoid metabolism. Annual Review of Plant Physiology and Plant Molecular Biology 40, 347–369

    Article  CAS  Google Scholar 

  • Jansen MAK, Gaba V and Greenberg BM (1998) Higher plants and UV radiation: balancing damage repair and acclimation. Trends in Plant Sciences 3, 131–135

    Article  Google Scholar 

  • Jenkins GI and Brown BA (2007) UV-B perception and signal transduction. In Light and Plant Development, G.C. Whitelam and K.J. Halliday, eds (Oxford, UK: Blackwell Publishing), pp. 155–182

    Chapter  Google Scholar 

  • Kaiserli E and Jenkins GI (2007) UV-B promotes rapid nuclear translocation of the Arabidopsis UV-B-specific signaling component UVR8 and activates its function in the nucleus. Plant Cell 19, 2662–2673

    Article  CAS  Google Scholar 

  • Kim KS, Park SH, Kim DK and Jenks MA (2007) Influence of water deficit on leaf cuticular waxes of soybean (Glycine max [L.] Merr.) International Journal of Plant Science 168, 307–316

    Article  CAS  Google Scholar 

  • Kliebenstein DJ (2004) Secondary metabolites and plant/environment interactions: a view through Arabidopsis thaliana tinged glasses. Plant, Cell Environment 27, 675–684

    Article  CAS  Google Scholar 

  • Koti S, Reddy KR, Reddy VR, Kakani VG and Zhao DL (2005) Interactive effects of carbon dioxide, temperature, and ultraviolet-B radiation on soybean (Glycine max L.) flower and pollen morphology, pollen production, germination, and tube lengths. Journal of Experimental Botany 56, 725–736

    Article  CAS  Google Scholar 

  • Koti S, Reddy KR, Kakani VG, Zhao VG and Gao W (2007) Effects of carbon dioxide, temperature and ultraviolet-B radiation and their interactions on soybean (Glycine max L.) growth development. Environmental and Experimental Botany 60, 1–10

    Article  CAS  Google Scholar 

  • Landry LG, Chapple CCS and Last RL (1995) Arabidopsis mutants lacking phenolic sunscreens exhibit enhanced Ultraviolet-B injury and oxidative damage. Plant Physiology 109, 1159–1166

    Article  CAS  Google Scholar 

  • Lapik Y and Kaufman LS (2003) The Arabidopsis cupin domain protein AtPirin1 and AtGPA1, the Arabidopsis G subunit interact with each other and regulate seed germination and early seedling development. Plant Cell, 15, 1578–1590

    Article  CAS  Google Scholar 

  • Lepiniec L, Debeaujon I, Routaboul JM, Baudry A, Pourcel L, Nesi N and Caboche M (2006) Genetics and biochemistry of seed flavonoids. Annual Review of Plant Biology 57, 405–430

    Article  CAS  Google Scholar 

  • Lewis NG and Yamamoto E (1989) In RW Hemingway, JJ Karchesy, eds, Chemistry and significance of condensed tannins. Plenum Press, New York, pp 23–47

    Google Scholar 

  • Leyva A, Jarillo JA, Salinas J and Martinez-Zapater JM (1995) Low temperature induces the accumulation of phenylalanine ammonia lyase and chalcone synthase mRNAs of Arabidopsis thaliana in a light dependent manner. Plant Physiology 108, 39–46

    CAS  Google Scholar 

  • Li J, Ou-Lee I-M, Raba R, Amundson RG and Last RL (1993) Arabidopsis flavonoid mutants are hypersensitive to UV-B irradiation. Plant Cell 5, 171–179

    Article  CAS  Google Scholar 

  • Li Y, Zu YQ, Chen HY and Chen JJ (2003) Intraspecific differences in physiological response of 20 soybean cultivars to enhanced ultraviolet-B radiation under field conditions. Environmental and Experimental Botany 50, 87–97

    Google Scholar 

  • Liu L and McClure JW (1995) Effects of UV-B on activities of enzymes of secondary phenolic metabolism in barley primary leaves. Physiologia Plantarum 93, 734–739

    Article  CAS  Google Scholar 

  • Liu L, Gitz DC and McClure JW (1995) Effects of UV-B on flavonoids, ferulic acid, growth and photosynthesis in barley primary leaves. Physiologia Plantarum 93, 725–733

    Article  CAS  Google Scholar 

  • Long LM, Patel HP, Cory WC and Stapleton AE (2003) The maize epicuticular wax layer provides UV protection. Functional Plant Biology 30, 75–81

    Article  Google Scholar 

  • Mahmoodzadeh H (2007) Effect of salinity stress on structural and ultrastructural features of apical meristems of two cultivars of canola (Brassica napus L.c.v.). Comparative biochemistry and Physiology A 146, S261–S262

    Google Scholar 

  • Margna U (1977) Control at the level of substrate supply — An alternative in the regulation of phenylpropanoid accumulation in plant cells. Phytochemistry 16, 419–426

    Article  CAS  Google Scholar 

  • Margna U, VainJarv T and Laanest L (1989) Different L-Phenylalanine pools available for the biosynthesis of phenolics in buckwheat seedling tissues. Phytochemistry 28, 469–475

    Article  CAS  Google Scholar 

  • Mazza CA, Boccalandro HE, Giordano CV, Battista D, Scopel AL and Ballare CL (2000) Functional significance and induction by solar radiation of ultraviolet-absorbing sunscreens in field-grown soybean crops. Plant Physiology 122, 117–125

    Article  CAS  Google Scholar 

  • Middleton EM, Kim MS, Krizek DT, and Bajwa RKS (2005) Symposium-in-Print: Ultraviolet Radiation and Terrestrial Ecosystems Evaluating UV-B Effects and EDU Protection in Soybean Leaves. Photochem. Photobiol. 81, 1075–1085

    Article  CAS  Google Scholar 

  • Nawrath C (2006) Unraveling the complex network of cuticular structure and function. Current Opinion Plant Biology 9, 281–287

    Article  CAS  Google Scholar 

  • Ohl S, Hahlbrock K and Schafer E (1989) A stable blue-light-derived signal modulates ultraviolet-light-induced activation of the chalcone-synthase gene in cultured parsley cells. Planta 177, 228–236

    Article  CAS  Google Scholar 

  • Oravecz A, Baumann A, Mate Z, Brzezinska A, Molinier J, Oakeley EJ, Adam E, Schafer E, Nagy F and Ulm R (2006) Constitutively Photomorphogenic1 is required for the UV-B response in Arabidopsis. Plant Cell 18, 1975–1990

    Article  CAS  Google Scholar 

  • Reed HE, Teramura AH, and Kenworthy WJ (1992) Ancestral U.S. soybean cultivars characterized for tolerance to ultraviolet-B radiation. Crop Science 32, 1214–1219

    Article  Google Scholar 

  • Reuber S, Bornman JF and Weissenböck G (1996) Phenylpropanoid compounds in primary leaf tissues of rye (Secale cereale): light response of their metabolism and the possible role in UV-B protection. Physiologia Plantarum 97, 160–168

    Article  CAS  Google Scholar 

  • Ries G, Heller W, Puchta H, Sandermann H, Seidlitz HK and Hohn B (2000) Elevated UV-B radiation reduces genome stability in plants. Nature 406, 98–1010

    Article  CAS  Google Scholar 

  • Robberecht R and Caldwell MM (1978) Leaf epidermal transmittance of ultraviolet radiation and its implications for plant sensitivity to ultraviolet radiation. Photochemistry and Photobiology 41, 95–99

    Google Scholar 

  • Rozema J, vandeStaaij J, Bjorn LO and Caldwell M (1997) UV-B as an environmental factor in plant life: Stress and regulation. Trends in Ecology & Evolution 12, 22–28

    Article  Google Scholar 

  • Rozema J, Bjorn LO, Bornman JF, Gaberscik A, Hader D-P, Trost T, Germ M, Klisch M, Groniger A, Sinha RP, Lebert M, He Y-Y, Buffoni-Hall R, de Bakker NVJ, van de Stajj J and Meijkamp BB (2002) The role of UV-B radiation in aquatic and terrestrial ecosystems—an experimental and functional analysis of the evolution of UV-absorbing compounds. J. Photochem. Photobiol. B: Biology 66, 2–12

    Article  CAS  Google Scholar 

  • Rozema J, Boelen P and Blokker P (2005) Depletion of stratospheric ozone over the Antarctic and Arctic: Responses of plants of polar terrestrial ecosystems to enhanced UV-B. Environmental Pollution 137, 428–442

    Article  CAS  Google Scholar 

  • Sato T, Kang HS and Kumagai T (1994) Genetic study of resistance to inhibitory effects of UV-radiation in Rice (Oryza sativa). Physiologia Plantarum 91, 234–238

    Article  CAS  Google Scholar 

  • Sacks MM, Silk WK, and Burman P (1997) Effect of water stress on cortical cell division rates within the apical meristem of primary roots of maize. Plant Physiol. 114, 519–527

    CAS  Google Scholar 

  • Sheahan JJ and Rechnitz GA (1993) Differential visualization of transparent testa mutants in Arabidopsis thaliana. Analytical Chemistry 65, 961–963

    Article  CAS  Google Scholar 

  • Sieber P, Schorderet M, Ryser U, Buchala A, Kolattukudy P, Metraux JP, and Nawrath C (2000) Transgenic Arabidopsis plants expressing a fungal cutinase show alterations in the structure and properties of the cuticle and postgenital organ fusions. Plant Cell 12, 721–737

    Article  CAS  Google Scholar 

  • Stapleton AE and Walbot V (1994) Flavonoids can protect maize DNA from induction of ultraviolet radiation damage. Plant Physiology 105, 881–889

    Article  CAS  Google Scholar 

  • Stapleton AE, Thornber CS and Walbot V (1997) UV-B component of sunlight causes measurable damage in field-grown maize (Zea mays L): Developmental and cellular heterogeneity of damage and repair. Plant, Cell & Environment 20, 279–290

    Article  CAS  Google Scholar 

  • Strid A, Chow WS and Anderson JM (1994) UV-B damage and protection at the molecular level in plants. Photosynthesis Research 39, 475–489

    Article  CAS  Google Scholar 

  • Sullivan JH (2005) Possible impacts of changes in UV-B radiation on North American trees and forests. Environmental Pollution 137, 380–389

    Article  CAS  Google Scholar 

  • Sullivan JH and Rozema J (1999) UV-B effects on terrestrial plant growth and photosynthesis. In, Stratospheric ozone depletion: the effects of enhanced UV-B radiation on terrestrial ecosystems (edited by J. Rozema), pp. 39–57. Backhays Publishers, Leiden, The Netherlands.

    Google Scholar 

  • Sullivan JH and Teramura AH (1988) The effects of ultraviolet-B irradiation on seedling growth in the Pinaceae. American Journal of Botany 75, 225–230

    Article  Google Scholar 

  • Sullivan JH, Gitz DC, Peek MS, and McElrone AJ (2003) Response of three eastern tree species to supplemental UV-B radiation: leaf chemistry and gas exchange. Agricultural and Forest Meteorology. 120, 219–228

    Article  Google Scholar 

  • Sullivan JH, Gitz DC III, Liu-Gitz L, Xu C, Gao W and Slusser J (2007) Coupling short-term changes in ambient UV-B levels with induction of UV-screening compounds. Photochemistry and Photobiology 83, 863–870

    Article  CAS  Google Scholar 

  • Tattini M, Gravano E, Pinelli P, Mulinacci N and Romani A (2000) Flavonoids accumulate in leaves and glandular trichomes of Phillyrea latifolia exposed to excess solar radiation. New Phytologist 148, 69–77

    Article  CAS  Google Scholar 

  • Teramura AH and Murali NS (1986) Intraspecific differences in growth and yield of soybean exposed to ultraviolet-B radiation under greenhouse and field conditions. Environ. and Experi. Botany. 26, 89–95

    Article  Google Scholar 

  • Teramura AH and Sullivan JH (1987) Soybean growth response to enhanced levels of ultraviolet-B radiation. American Journal of Botany 74, 975–979

    Article  Google Scholar 

  • Teramura AH, and Sullivan JH (1991) Potential effects of increased solar UV-B on global plant productivity. In: Riklis E (Ed.), Photobiology, Plenum Press, New York, pp 625–634

    Google Scholar 

  • Teramura AH, Sullivan JH, and Lydon J (1990) Effects of solar UV-B radiation on Soybean yield and seed quality: a six-year field study. Physiologia Plantarum. 80, 5–11

    Article  Google Scholar 

  • Torabinejad J and Caldwell MM (2000) Inheritance of UV-B tolerance in seven ecotypes of Arabidopsis thaliana L. Heynh. and their F1 hybrids. Heredity 91, 228–233

    Article  CAS  Google Scholar 

  • Ulm R and Nagy F (2005) Signaling and gene regulation in response to ultraviolet light. Current Opinion in Plant Biology 8, 477–482

    Article  CAS  Google Scholar 

  • van Heerden PS, Neil Towers GH, and Lewis NG (1996) Nitrogen Metabolism in Lignifying Pinus taeda Cell Cultures. Journal of Biological Chemistry 271, 12350–12355

    Article  Google Scholar 

  • Wade HK, Bibikova TN, Valentine WJ and Jenkins G I (2001) Interactions within a network of phytochrome, cryptochrome, and UV-B phototransduction pathways regulate chalcone synthase gene expression in Arabidopsis leaf tissue. Plant Journal 25, 675–685

    Article  CAS  Google Scholar 

  • Warpeha KMF, and Kaufman LS (1990) Two distinct blue-light responses regulate the levels of transcripts of specific nuclear-coded genes in pea. Planta 182, 553–558

    Article  CAS  Google Scholar 

  • Warpeha KMF, Hamm HE, Rasenick MM, and Kaufman LS (1991) A blue-light activated GTP binding protein in the plasma membrane of etiolated pea. Proc. Natl. Acad. Sci. U.S.A. 88, 8925–8929

    Article  CAS  Google Scholar 

  • Warpeha KM, Lateef SS, Lapik Y, Anderson MB, Lee BS and Kaufman LS (2006) G-Protein-Coupled Receptor1, G-Protein G-Subunit1, and Prephenate Dehydratase1 Are Required for Blue Light-Induced Production of Phenylalanine in Etiolated Arabidopsis. Plant Physiology 140, 844–855

    Article  CAS  Google Scholar 

  • Warpeha KM, Gibbons J, Carol A, Slusser J, Tree R, Durham W, and Kaufman LS (2008) Presence of adequate phenylalanine mediated by G-protein is Critical for Protection from UV Radiation Damage in young etiolated Arabidopsis thaliana seedlings. Plant Cell and Env.

    Google Scholar 

  • Warpeha KM, Sullivan JH, and Kaufman LS (2009) Phenylalanine provides critical protection from UV Radiation Damage in young soybean (Glycine max) seedlings. Submitted

    Google Scholar 

  • Weinig C, Gravuer KA, Kane NC and Schmitt J (2004) Testing adaptive plasticity to UV: Costs and benefits of stem elongation and light-induced phenolics. Evolution 58, 2645–2656

    CAS  Google Scholar 

  • West G, Inze D, and Beemster GTS (2004) Cell cycle modulation in the response of the primary root of Arabidopsis to salt stress. Plant Physiology 135, 1050–1058

    Article  CAS  Google Scholar 

  • Winkel-Shirley B (2002) Biosynthesis of flavonoids and effects of stress, Current Opinion in Plant Biology 5, 218–223

    Article  CAS  Google Scholar 

  • Yamada T, Matsuda F, Kasai K, Fukuoka S, Kitamura K, Tozawa Y, Miyagawa H and Wakasa K (2008) Mutation of a rice gene encoding a phenylalanine biosynthetic enzyme results in accumulation of phenylalanine and tryptophan. Plant Cell 20, 1316–1329

    Article  CAS  Google Scholar 

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Warpeha, K.M., Kaufman, L.S. (2010). UV-Effects on Young Seedlings of Soybean: Effects in Early Development and Long-Term Effects. In: Gao, W., Slusser, J.R., Schmoldt, D.L. (eds) UV Radiation in Global Climate Change. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-03313-1_17

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