Hostname: page-component-cd9895bd7-dk4vv Total loading time: 0 Render date: 2024-12-23T09:44:13.519Z Has data issue: false hasContentIssue false

Differential Response of Palmer Amaranth (Amaranthus palmeri) Gender to Abiotic Stress

Published online by Cambridge University Press:  13 February 2017

Nicholas E. Korres*
Affiliation:
Postdoctoral Research Associate, Professor, Elms Farming Chair of Weed Science, Assistant Professor, and Distinguished Professor, University of Arkansas, Department of Crop, Soil and Environmental Sciences, 1366 West Altheimer Drive, Fayetteville, AR 72704
Jason K. Norsworthy
Affiliation:
Postdoctoral Research Associate, Professor, Elms Farming Chair of Weed Science, Assistant Professor, and Distinguished Professor, University of Arkansas, Department of Crop, Soil and Environmental Sciences, 1366 West Altheimer Drive, Fayetteville, AR 72704
Toby FitzSimons
Affiliation:
PepsiCo, C/O University of Minnesota, 1991 Upper Buford Circle, 411 Buford Hall, St. Paul, MN 55108
Trent L. Roberts
Affiliation:
Postdoctoral Research Associate, Professor, Elms Farming Chair of Weed Science, Assistant Professor, and Distinguished Professor, University of Arkansas, Department of Crop, Soil and Environmental Sciences, 1366 West Altheimer Drive, Fayetteville, AR 72704
Derrick M. Oosterhuis
Affiliation:
Postdoctoral Research Associate, Professor, Elms Farming Chair of Weed Science, Assistant Professor, and Distinguished Professor, University of Arkansas, Department of Crop, Soil and Environmental Sciences, 1366 West Altheimer Drive, Fayetteville, AR 72704
*
*Corresponding author’s E-mail: [email protected] or [email protected]

Abstract

Knowledge of Palmer amaranth biology and physiology is essential for the development of effective weed management systems. The aim of this study was to investigate the response of Palmer amaranth gender to nutrient deficiency and light stress. Differential gender responses were observed for all the growth, phenology, and photochemistry parameters measured. Female plants, for example, invested more in height, stem, and total dry weight, whereas male plants invested more in leaf area and leaf dry weight. The growth rate of females was higher than that of male Palmer amaranth plants, although both followed similar declining trends as the experimental period progressed. Initiation of flowering of female plants occurred 6 to 8 d earlier compared with male plants. Nitrogen and to a certain extent phosphorous were the most influential nutrients that affected measured parameters in both Palmer amaranth genders, particularly under high light intensity. Electron transport rate and chlorophyll content of female Palmer amaranth plants compared with male plants was lower at high light intensity in combination with nitrogen and phosphorous deficiencies. There is a potential to manipulate Palmer amaranth population structure by altering microenvironments at the field level.

Type
Physiology/Chemistry/Biochemistry
Copyright
© Weed Science Society of America, 2017 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

Associate Editor for this paper: Vijay Nandula, USDA–ARS

References

Literature Cited

Adams, S, Allen, T, Whitelam, GC (2009) Interaction between the light quality and flowering time pathways in Arabidopsis . Plant J 60:257267 CrossRefGoogle ScholarPubMed
Bawa, KS (1980) Evolution of dioecy in flowering plants. Annu Rev Ecol Syst 11:1539 CrossRefGoogle Scholar
Bjorkman, O, Demming, B (1987) Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77K among vascular plants of diverse origins. Planta 170:489504 Google Scholar
Blackshaw, RE, Brandt, RN, Jazen, HH, Entz, T, Grant, CA, Derksen, (2003) Differential response of weed species to added nitrogen. Weed Sci 52:532539 Google Scholar
Brainard, DC, Bellinder, RR, DiTommaso, A (2005) Effects of canopy shade on the morphology, phenology, and seed characteristics of Powell amaranth (Amaranthus powellii). Weed Sci 53:175186 Google Scholar
Buckley, TN, Farquhar, GD (2004) A new analytical model for whole-leaf potential electron transport rate. Plant Cell Environ 27:14871502 CrossRefGoogle Scholar
Cheng, L, Fuchigami, LH, Breen, PJ (2000) Light absorption and partitioning in relation to nitrogen content in “Fuji” apple leaves. J Am Soc Hort Sci 125:581587 CrossRefGoogle Scholar
Cheplick, GP (1995) Life history trade-offs in Amphibromus scabrivalvis (Poaceae): allocation to clonal growth, storage and cleistogamous reproduction. Am J Bot 82:621629 Google Scholar
Chinnusamy, V, Zhu, J, Zhu, JK (2006) Salt stress signaling and mechanisms of plant salt tolerance. Genet Eng (NY) 27:141177 Google Scholar
Culpepper, AS, Grey, T, Vencill, W, Kichler, J, Webster, T, Brown, S, York, A, Davis, J, Hanna, W (2006) Glyphosate-resistant Palmer amaranth (Amaranthus palmeri) confirmed in Georgia. Weed Sci 54:620626 CrossRefGoogle Scholar
Culpepper, AS, Webster, TM, Sosnoskie, LM, York, AC (2010) Glyphosate resistant Palmer amaranth in the United States. Pages 195212 in Nandula VK, ed. Glyphosate Resistance in Crops and Weeds: History, Development, and Management. Hoboken, NJ: Wiley Google Scholar
Dabney, SM, Delgado, JA, Reeves, DW (2001) Using winter cover crops to improve soil and water quality. Commun Soil Sci Plant Anal 32:12211250 Google Scholar
Dai, Y, Shen, Z, Liu, Y, Wang, L, Hannaway, D, Lu, H (2009) Effects of shade treatments on the photosynthetic capacity, chlorophyll fluorescence, and chlorophyll content of Tetrastigma hemsleyanum Diels et Gilg. Environ Exp Bot 65:177182 CrossRefGoogle Scholar
Das, BK, Sen, SP (1981) Effect of nitrogen, phosphorus and potassium deficiency on the uptake and mobilization of ions in Bengal gram (Cicer arietinum). J Biosci 3:249258 Google Scholar
Dawson, TE, Bliss, LC (1989) Patterns of water use and the tissue water relations in the dioecious shrub, Salix arctica: the physiological basis for habitat partitioning between the sexes. Oecologia 79:332343 CrossRefGoogle ScholarPubMed
Dawson, TE, Geber, MA (1999) Sexual dimorphism in physiology and morphology. Pages 175216 in Geber MA, Dawson TE & Delph LF, eds. Gender and Dimorphism of Flowering Plants. Berlin: Springer Google Scholar
De Groot, CC, Van den Boogaard, R, Marcelis, LFM, Harbinson, J, Lambers, H (2003) Contrasting effects of N and P deprivation on the regulation of photosynthesis in tomato plants in relation to feedback limitation. J Exp Bot 54:19571967 Google Scholar
Delph, LF (1999) Sexual dimorphism in life history. Pages 149173 in Geber MA, Dawson TE & Delph LF, eds. Gender and Dimorphism of Flowering Plants. Berlin: Springer CrossRefGoogle Scholar
Duke, ST, Powles, SB (2009) Glyphosate-resistant crops and weeds: now and in the future. AgBioForum 12:346357 Google Scholar
Duque, AS, de Almeida, AM, da Silva, AB, da Silva, JM, Farinha, AP, Santos, D, Fevereiro, P, de Sousa Araujo, S (2013) Abiotic stress responses in plants: unraveling the complexity of genes and networks to survive. Pages 49101 in Vahdati K & Lesli C, eds. Abiotic Stress-Plant Responses and Applications in Agriculture. Rijeka, Croatia: InTech Google Scholar
Flexas, J, Escalona, JM, Medrano, H (1999) Water stress induces different levels of photosynthesis and electron transport rate regulations in grapevines. Plant Cell Envir 22:3948 Google Scholar
Foyer, CH, Bloom, AJ, Queval, G, Noctor, G (2009) Photorespiratory metabolism: genes, mutants, energetics, and redox signaling. Ann Rev Plant Biol 60:455484 Google Scholar
Franssen, AS, Skinner, DZ, Al-Khatib, K, Horak, MJ, Kulakow, PA (2001) Interspecific hybridization and gene flow of ALS resistance in Amaranthus species. Weed Sci 49:598606 CrossRefGoogle Scholar
Gan, H, Jiao, Y, Jia, J, Wang, X, Li, H, Shi, W, Peng, C, Polle, A, Luo, ZB (2013) Phosphorus and nitrogen physiology of two contrasting poplar genotypes when exposed to phosphorus and/or nitrogen starvation. Tree Physiol 36:2238 Google Scholar
Geber, MA (1990) The cost of meristem limitation in Polygonum arenastrum: negative genetic correlations between fecundity and growth. Evolution 44:799819 Google Scholar
Ghersa, CM, Benech-Arnoldb, RL, Satorre, EH, Martinez-Ghersa, MA (2000) Advances in weed management strategies. Field Crops Res 67:95104 Google Scholar
Hall, DO, Rao, KK (1994) Photosynthesis. 5th edn. Cambridge, UK: Cambridge University Press. 211 pGoogle Scholar
Hatayama, T, Takeno, K (2003) The metabolic pathway of salicylic acid rather than of chlorogenic acid is involved in the stress-induced flowering of Pharbitis nil . J Plant Physiol 160:461467 Google Scholar
Hidaka, A, Kitayama, K (2013) Relationship between photosynthetic phosphorus-use efficiency and foliar phosphorus fractions in tropical tree species. Ecol Evol 3:48724880 Google Scholar
Hirai, N, Kojima, Y, Koshimizu, K, Shinozaki, M, Takimoto, A (1993) Accumulation of phenylpropanoids in cotyledons of morning glory (Pharbitis nil) seedlings during the induction of flowering by poor nutrition. Plant Cell Physiol 34:10391044 Google Scholar
Hirai, N, Kuwano, Y, Kojima, Y, Koshimizu, K, Shinozaki, M, Takimoto, A (1995) Increase in the activity of phenylalanine ammonia-lyase during the non-photoperiodic induction of flowering in seedlings of morningglory (Pharbitis nil). Plant Cell Physiol 36:291297 CrossRefGoogle Scholar
Hopkins, WG, Hüner, NPA (2009) Introduction to Plant Physiology. 4th edn. Hoboken, NJ: Wiley. 489 pGoogle Scholar
Jacob, J, Lawlor, DW (1992) Dependence of photosynthesis of sunflower and maize on phosphate supply, ribulose-1, 5-bisphosphate carboxylase/oxygenase activity, and ribulose-1,5-bisphosphate pool size. Plant Physiol 98:801807 Google Scholar
Jha, P, Norsworthy, JK, Riley, MB, Bielenberg, DG, Bridges, W Jr (2008) Acclimation of Palmer amaranth (Amaranthus palmeri) to shading. Weed Sci 56:729734 Google Scholar
Kaspar, TC, Kladivko, EJ, Singer, JW, Morse, S, Mutch, DR (2008) Potential and limitations of cover crops, living mulches, and perennials to reduce nutrient losses to water sources from agricultural fields in the Upper Mississippi River Basin. Gulf Hypoxia and Local Water Quality Concerns Workshop. St. Joseph, Michigan: ASABE. Pp 127148 Google Scholar
Keeley, PE, Carter, CH, Thullen, RJ (1987) Influence of planting date on growth of Palmer amaranth (Amaranthus palmeri). Weed Sci 35:199204 Google Scholar
Korres, NE (2005) Encyclopaedic Dictionary of Weed Science: Theory and Digest. Paris: Lavoisier. 789 pGoogle Scholar
Korres, NE, Norsworthy, JK, Bagavathiannan, MV, Mauromoustakos, A (2015a) Distribution of arable weed populations along eastern Arkansas Mississippi Delta roadsides: factors affecting weed occurrence. Weed Technol 29:596604 CrossRefGoogle Scholar
Korres, NE, Norsworthy, JK, Brye, KR, Skinner, V Jr, Mauromoustakos, A, Bagavathiannan, MV (2017) Relationships between soil properties and the occurrence of the most agronomically important weed species in the field margins of eastern Arkansas. Implications on weed management. Weed Res (under review)CrossRefGoogle Scholar
Korres, NE, Norsworthy, JK, Green, JK, Godwin, JA, Martin, SM, Lancaster, ZD (2015b) Effects of soybean row spacing and population on Palmer amaranth biological characteristics and sex expression. Proceedings of the Arkansas Crop Protection Association, Vol. 19. Fayetteville, Arkansas, November 30–December 1, 2015. https://acpanews.com/dev/wp-content/uploads/2017/01/ACPA-ABSTRACTS-2015.pdf. Accessed: January 27, 2017Google Scholar
Korres, NE, Norsworthy, JK, Green, JK, Godwin, JA, Martin, SM, Lancaster, ZD (2016a) Palmer amaranth demographics in wide row soybean. Proceedings of the Weed Science Society of America Annual Meeting. San Juan, Puerto Rico, February 8–11, 2016. http://wssaabstracts.com/public/38/proceedings.html. Accessed: December 9, 2016Google Scholar
Korres, NE, Norsworthy, JK, Tehranchian, P, Gitsopoulos, TC, Loka, DA, Oosterhuis, DM, Moss, S, Gealy, D, Burgos, NR, Miller, R, Palhano, M (2016b) Cultivars to face climate change effects on crops and weeds: a review. Agron Sust Dev 36: 10.1007/s13593-016-0350-5CrossRefGoogle Scholar
Koshio, A, Hasegawa, T, Okada, R, Takeno, K (2015) Endogenous factors regulating poor-nutrition stress-induced flowering in pharbitis: The involvement of metabolic pathways regulated by aminooxyacetic acid. J Plant Physiol 173:8288 CrossRefGoogle ScholarPubMed
Liebman, M, Davis, AS (2000) Integration of soil, crop and weed management in low-external-input farming systems. Weed Res 40:2747 Google Scholar
Liu, K, Fu, H, Bei, Q, Luan, S (2000) Inward potassium channel in guard cells as a target for polyamine regulation of stomatal movements. Plant Physiol 124:13151326 Google Scholar
Long, JR, Ma, GH, Wan, YZ, Song, CF, Sun, J, Qin, RJ (2013) Effects of nitrogen fertilizer level on chlorophyll fluorescence characteristics in flag leaf of super hybrid rice at late growth stage. Rice Sci 20:220228 Google Scholar
Marschner, H (1995) Mineral Nutrition of Higher Plants. London: Academic. 889 pGoogle Scholar
Massinga, RA, Currie, R, Horak, MJ, Boyer, J Jr (2001) Interference of Palmer amaranth in corn. Weed Sci 49:202208 Google Scholar
Maxwell, K, Johnson, GN (2000) Chlorophyll fluorescence-a practical guide. J Exp Bot 51:659668 CrossRefGoogle ScholarPubMed
McLachlan, SM, Swanton, CJ, Weise, SF, Tollenaar, M (1993) Effect of corn-induced shading and temperature on rate of leaf appearance in redroot pigweed (Amaranthus retroflexus L.). Weed Sci 41:590593 Google Scholar
Montesinos, D, Villar-Salvador, P, Garcia-Fayos, P, Verdu, M (2012) Genders in Juniperus thurifera have different functional responses to variations in nutrient availability. New Phytol 193:705712 CrossRefGoogle ScholarPubMed
Moran, PJ, Showler, AT (2005) Plant responses to water deficit and shade stresses in pigweed and their influence on feeding and oviposition by the beet armyworm (Lepidoptera: Noctuidae). Environ Entomol 34:929937 CrossRefGoogle Scholar
Morgan, DC, Smith, H (1976) Linear relationship between phytochrome photoequilibrium and growth in plants under simulated natural radiation. Nature 262:210212 Google Scholar
Morgan, GD, Bauman, PA, Chandler, JM (2001) Competitive impact of Palmer amaranth (Amaranthus palmeri) on cotton (Gossypium hirsutum) development and yield. Weed Technol 15:408412 CrossRefGoogle Scholar
Mortensen, DA, Egan, JF, Maxwell, BD, Ryan, MR, Smith, RG (2012) Navigating a critical juncture for sustainable weed management. BioScience 62:7584 Google Scholar
Motohashi, R, Myouga, F (2015) Chlorophyll fluorescence measurements in Arabidopsis plants using a pulse-amplitude-modulated (PAM) fluorometer. Bio-protocol 5:e1464. http://www.bio-protocol.org/e1464. Accessed: January 27, 2017Google Scholar
Norsworthy, JK, Korres, NE, Walsh, MJ, Powles, SB (2016) Integrating herbicide programs with harvest weed seed control and other fall management practices for the control of glyphosate-resistant Palmer amaranth (Amaranthus palmeri). Weed Sci 64:540550 Google Scholar
Oberhuber, W, Dai, Z, Edwards, GE (1993) Light dependence of quantum yields of photosystem II and CO2 fixation in C3 and C4 plants. Photosynth Res 35:265274 CrossRefGoogle Scholar
Obeso, JR (2002) The costs of reproduction in plants. New Phytol 155:321348 Google Scholar
Puricelli, E, Orioli, G, Sabbatini, MR (2002) Demography of Anoda cristata in wide- and narrow-row soybean. Weed Res 42:456463 Google Scholar
Qu, C, Liu, C, Ze, Y, Gong, X, Hong, M, Wang, L, Hong, F (2011) Inhibition of nitrogen and photosynthetic carbon assimilation of maize seedlings by exposure to a combination of salt stress and potassium-deficient stress. Biol Trace Elem Res 144:11591174 Google Scholar
Radin, JW, Eidenbock, MP (1984) Hydraulic conductance as a factor limiting leaf expansion of phosphorus‐deficient cotton plants. Plant Physiol 75:372377 Google Scholar
Ramegowdaa, V, Senthil-Kumar, M (2015) The interactive effects of simultaneous biotic and abiotic stresses on plants: mechanistic understanding from drought and pathogen combination. J Plant Physiol 176:4754 Google Scholar
Rebeiz, CA, Montazer-Zouhoor, A, Hopen, HJ, Wu, SM (1984) Photodynamic herbicides: 1. concept and phenomenology. Enzyme Micro Technol 6:390396 CrossRefGoogle Scholar
Reddy, KJ (2006) Nutrient stress. Pages 187219 in Rao MS, Raghavendra AS & Reddy KJ, eds. Physiology and Molecular Biology of Stress Tolerance in Plants. Dordrecht, Netherlands: Springer Google Scholar
Renner, SS, Ricklefts, RE (1995) Dioecy and its correlates in the flowering plants. Amer J Bot 82:596606 Google Scholar
Riar, DS, Norworthy, JK, Steckel, LE, Stephenson, DO, Eubank, TW, Scott, RC (2013) Assessment of weed management practices and problem weeds in the Midsouth United States-soybean: a consultant’s perspective. Weed Technol 27:612622 Google Scholar
Richardson, AD, Duigan, SP, Berlyn, GP (2002) An evaluation of noninvasive methods to estimate foliar chlorophyll content. New Phytol 153:185194 Google Scholar
Rowland, DL, Johnson, NC (2001) Sexual demographics of riparian populations of Populus deltoides: can mortality be predicted from change in reproductive status? Can J Bot 79:702710 Google Scholar
Sage, RF, Pearcy, RW (1987) The nitrogen use efficiency of C3 and C4 plants. II. Leaf nitrogen effects on the gas exchange characteristics of Chenopodium album (L.) and Amaranthus retroflexus (L.). Plant Physiol 84:959963 Google Scholar
Salisbury, FB, Ross, CW (1992) Plant Physiology. 4th edn. Belmont, CA: Wadsworth. Pp. 207222 Google Scholar
Sanchez-Vilas, J, Retuerto, R (2012) Response of the sexes of the sub-dioecious plant Honckenya peploides to nutrients under different salt spray conditions. Ecol Res 27:163171 CrossRefGoogle Scholar
Schreiber, U (2004) Pulse-amplitude-modulation (PAM) fluorometry and saturation pulse method. Pages 279319 in Papaqeorgiou G, Govindjee, eds. Chlorophyll a Fluorescence: A Signature of Photosynthesis. Dordrecht, Netherlands: Springer Google Scholar
Shinozaki, M (1985) Organ correlation in long day flowering of Pharbitis nil . Biol Plant 27:382385 CrossRefGoogle Scholar
Shinozaki, M, Takimoto, A (1982) The role of cotyledons in flower initiation of Phabitis nil at low temperatures. Plant Cell Physiol 23:403408 CrossRefGoogle Scholar
Solbrig, OT (1981) Studies on the population biology of the genus Viola. II. The effect of plant size on fitness in Viola sororia . Evolution 35:10801093 Google Scholar
Steckel, LE (2007) The dioecious Amaranthus spp.: here to stay. Weed Technol 21:567570 Google Scholar
Takeno, K (2012) Stress induced flowering. Pages 331345 in Ahmad P & Prasad MNV, eds. Abiotic Stress Responses in Plants: Metabolism, Productivity and Sustainability. London: Springer Science+Business Media CrossRefGoogle Scholar
Tanaka, O, Nakayama, Y, Emori, K, Takeba, G, Sato, K, Sugino, M (1997) Flower-inducing activity of lysine in Lemna paucicostata . Plant Cell Physiol 38:124128 CrossRefGoogle Scholar
Teaster, ND, Hoagland, RE (2014) Characterization of glyphosate resistance in cloned Amaranthus palmeri plants. Weed Biol Manag 14:110 Google Scholar
Teyker, RH, Hoelzer, HD, Liebl, RA (1991) Maize and pigweed response to nitrogen supply and form. Plant Soil 135:287292 Google Scholar
Thompson, H (2012) War on weeds loses ground. Nature 485:430 Google Scholar
Wada, KC, Kondo, H, Takeno, K (2010) Obligatory short-day plant Perilla frutescens var. crispa can flower in response to low-intensity light stress under long-day conditions. Physiol Plant 138:339345 Google Scholar
Wada, KC, Takeno, K (2010) Stress-induced flowering. Plant Signal Behav 5:944947 Google Scholar
Ward, SM, Webster, TM, Steckel, LE (2013) Palmer amaranth (Amaranthus palmeri): a review. Weed Technol 27:1227 Google Scholar
Webster, TM, Grey, TL (2015) Glyphosate-resistant Palmer amaranth (Amaranthus palmeri) morphology, growth, and seed production in Georgia. Weed Sci 63:264272 Google Scholar
Webster, TM, Nichols, RL (2012) Changes in the prevalence of weed species in the major agronomic crops of the Southern United States: 1994/1995 to 2008/2009. Weed Sci 60:145157 Google Scholar
Weiner, J (1988) The influence of competition on plant reproduction. Pages 228245 in Doust JL & Doust LL, eds. Plant Reproductive Ecology: Patterns and Strategies. New York: Oxford University Press Google Scholar
Wilson, PJ, Thompson, K, Hodgson, JG (1999) Specific leaf area and leaf dry matter content as alternative predictors of plant strategies. New Phytol 143:155162 Google Scholar
Yan, N, Zhang, YL, Xue, HM, Zhang, XH, Wang, ZD, Shi, LY, Guo, DP (2015) Changes in plant growth and photosynthetic performance of Zizania latifolia exposed to different phosphorus concentrations under hydroponic condition. Photosynthetica 53:630635 CrossRefGoogle Scholar
Yoshida, S, Forno, DA, Cock, JH, Gomez, KA (1976) Laboratory Manual for Physiological Studies of Rice. 3rd edn. Los Banos, Laguna, Philippines: International Rice Research Institute. Pp. 6165 Google Scholar
Zhang, K, Liu, H, Tao, P, Chen, H (2014) Comparative proteomic analyses provide new insights into low phosphorus stress responses in maize leaves. PLoS One 9. doi: 10.1371/journal.pone.0098215 Google Scholar
Zhang, S, Jiang, H, Peng, S, Korpelainen, H, Li, C (2011) Sex-related differences in morphological, physiological, and ultrastructural responses of Populus cathayana to chilling. J Exp Bot 62:675686 Google Scholar
Zhao, D, Reddy, KR, Kakani, VG, Reddy, VR (2005) Nitrogen deficiency effects on plant growth, leaf photosynthesis, and hyperspectral reflectance properties of sorghum. Europ J Agron 22:391403 Google Scholar
Zhua, Y, Fana, X, Houa, X, Wua, J, Wang, T (2014) Effect of different levels of nitrogen deficiency on switchgrass seedling growth. Crop J 2:223234 Google Scholar