The Effect of Water Depth on the Structure and Allocation of Waterlily (Nymphaea pubescens Willd) Biomass in Lebak Swampland in Kalimantan Selatan
Abstract
Nymphaea pubescens is found in the swamplands of Kalimantan Selatan, where it lives in the shape of a basin with divergent levels of water. From February to June 2019, the environment and its development were studied in four zones, with depth differences ranging from 28 to 95 meters in the zone I, 28 to 99 meters in zone II, 54 to 112 meters in zone III, and 55 to 124 meters in zone IV. A transect system is used to zone the area, with fluctuating degrees of water depth reflected in each zone as one moves closer to a basin. Geomorphology in a basin has an essential relief, causing different levels of water surface depth in lebak swampland. The GPS was used to determine the distance traveled.
The purposive sampling technique determines the number of observation stations in each zone. In zone I, waterlily growth generated smaller and more frequent leaves than plants in zone II, which produced smaller and fewer leaves than plants in zone III, which produced smaller and fewer leaves than plants in zone IV. However, the area of the leaves expanded greatly with the depth of water, although the number of leaves fell dramatically with water depth. The organization of the percentage of biomass for the development of shoots and roots was different, even though the total biomass was not statistically different. Waterlily growing in shallower water depths had larger biomass allocations for seeds and lower biomass allocations for roots. Root biomass increased significantly as the depth of the water body increased.
This experiment showed that the deeper the water, the lesser the nutrients and the greater the extent the roots must spread to meet their nutritional requirements. Even though the relationship between leaf area and bloom number weakened as water depth increased, the relationship between leaf number and root number was significantly positive concerning biomass and water depth. Groundwater depth has a significant effect on the allocation of underground biomass (A), with the biomass proportion decreasing as water depth increases from 28 to 95 cm in zone I = 53.1 percent to 28–99 cm in zone II = 53.7 percent to 55–124 cm in zone III = 48.6 percent in zone IV = 42.4 percent. Because water depth has a considerable effect on the average aboveground biomass–to–underground biomass ratio, the average root crown ratio decreases as water depth increases. Among the lowest average ratios found are those found at a water depth of 55–124 cm in zone IV (ratio of 0.54 ± 0.2), while the highest average percentage found is that found at a water depth of 28–95 cm in the zone I (ratio of 1.25 ± 0.61).
References
[1] Alwi, M., and Tapakrisnanto C., 2017. Potensi dan karakteristik lahan rawa lebak in: Fatah, L., Noor, M., Masganti, H., Subagio, Alwi, M., Simatupang, S., Ar–Riza I., 2017. Lahan rawa lebak: Sistem pertanian dan pengembangannya. IAARD Press 160 pp. (in Indonesian)
[2] Atwell, B.J., Kreidermann, P.E., and Turnbull, C.G.N., 2003. Plants in action: Adaptation in nature, performance in cultivation. Macmillan, South Yarra, Australia.
[3] Baastrup–Spohr, L., Møller, C.L., and Sand–Jensen, K., 2016. Water–level fluctuations affect sediment properties, carbon flux and growth of the isoetid littorella uniflo rain oligotrophic lakes. Freshw. Biol. 61, 301–315. DOI: https://doi.org/ 10.1111/fwb.127044
[4] Baastrup–Spohr, L., Sand–Jensen, K., Nicolajsen, S.V., and Bruun, H.H., 2015. From soaking wet to bone dry: Predicting plant community composition along a steep hydrological gradient. J. Veg. Sci. 26, 619–630. DOI: https://doi.org/10.1111/jvs.12280
[5] Badan Pusat Statistik Kabupaten Hulu Sungai Utara (BPS–HSU), 2020. Kecamatan Sungai Pandan dalam angka. Available at: https://hulusungaiutara.bps.go.id/publication.html. (in Indonesian)
[6] Bai, X., Chen, K., Zhao, H., and Chen, X., 2015. Impact of water depth and sediment type on root morphology of the submerged plant Vallisneria natans. J. Freshw. Ecol. 30: 75–84. DOI:http://dx.doi.org/10.1080/02705060. 2014.970672
[7] Balai Penelitian Tanah (BPT–Bogor), 2009. Petunjuk teknis: Analisis kimia tanah, tanaman, air, dan pupuk. Balai Penelitian Tanah, Bogor, Jawa Barat, Indonesia. (in Indonesian)
[8] Baldwin, D.S, and Mitchell, A.M. 2000. The effects of drying and re–flooding on the sediment and soil nutrient dynamics of lowland river–floodplain systems: A synthesis. River Research and Applications: an international journal devoted to river research and management, 16: 457–467.
[9] Bando, F.M., Michelan, T.S., Cunha, E.R., Figueiredo, B.R.S., and Thomaz, S.M., 2015. Macrophyte species richness and composition are correlated with canopy openness and water depth in tropical floodplain lakes. Rev. Bras. Bot. 38: 289–294. DOI: https://doi.org/10.1007/s40415 –015–0137–y
[10] Barko, J.W., Gunnison D., and Carpenter S.R. 1991. Sediment interacters with submerged macrophyte growth and community dynamics. Aquat. Bot. 41. DOI: https://doi.org/10.1016/0304–3770(91)90038–7
[11] Barko, J.W. and Smart, R.M. 1981. Comparative influences of light and temperature on the growth and metabolism of selected submersed freshwater macrophytes. Ecol. Monogr. 51: 219–236. DOI: https://doi.org/ 10.2307/2937264
[12] Barko, J.W., and Smart, R.M. 1983. Effects of organic matter additions to sediment on the growth of aquatic plants. J. Ecol. 71: 161–175. DOI: https://doi.org/10.2307/2259969
[13] Bini, L.M., Thomaz, S.M., Murphy, K.J. and Camargo, A.F.M. 1999. Aquatic macrophyte distribution in relation to water and sediment conditions in the Itaipu Reservoir, Brazil. Hydrobiologia, 415: 147–154. Available at: https://repositorio.unesp.br/handle/11449/20426
[14] Blanch, S.J., Ganf, G.G., and Walker, K.F, 1999. Growth and resource allocation in response to flooding in the emergent sedge Bolboschoenus medianus. Aquat. Bot. 63: 145–160. DOI:https://dx.doi.org/10.1007/s10452–010–9334–8
[15] Bloom, A.J., Chapin, F.S. and Mooney, H.A., 1985. Resource limitation in plants an economic analogue. Annu. Rev. Ecol. Syst. 16: 363–392. DOI: https://doi.org/10.1146/annurev.es.16.110185.002051
[16] Boar, R. 2006. Responses of a fringing Cyperus papyrus L. swamp to changes in water level. Aquat. Bot., 84: 85–92. DOI: https://dx.doi.org/10.1016/j.aquabot.2005.07.008
[17] Brock, Th.C.M., Arts, G.H.P., Goossen, L.L.M. Rutenfrans, A.H.M., 1983. Structure and annual biomass production of Nymphoides peltata (Gmel.) O. Kuntze (Menyanthaceae). Aquat. Bot. 17: 167–188. DOI:https://doi.org/10.1016/0304–3770(83)90056–6
[18] Brouwer, R. 1963. Some aspects of the equilibrium between overground and underground plant parts. Jaarboek van het instituut voor biologisch en scheikundig onderzoek van landbouwgewassen, Wageningen 31–39. Available at: https://edepot.wur.nl/361707
[19] Casanova, M.T., and Brock, M.A., 2000. How do depth, duration and frequency of flooding influence the establishment of wetland plant communities?. Plant Ecol. 147: 237–250. DOI: https://doi.org/10.1023/
[20] Cazzanelli, M., Warming, T.P., and Christoffersen, K.S., 2008. Emergent and floating–leaved macrophytes as refuge for zooplankton in a eutrophic temperate lake without submerged vegetation. Hydrobiologia 605: 113–122. DOI: https://doi.org/10.1007/s10750–008–9324–1
[21] Chapin, F.S. 1980. The mineral nutrition of wild plants. Ann. Rev. Ecol. Syst. 11: 233–260. DOI:https://doi.org/10.1146/annurev.es.11.110180.001313
[22] Chen, F., et al. 2017. Water lilies as emerging models for Darwin’s abominable mystery. Hortic. Res. 4. DOI:10.1038/hortres,2017.51
[23] Chen, W., et al. 2007. Root growth of wetland plants with different root types. Acta Ecol. Sinica, 27: 450–457. DOI: https://doi.org/10.1016/s1872–2032(07)60017
[24] Chernova, A.M., 2015. Seasonal dynamics of yellow water lily Nuphur lutea (L.) Smith (Nymphaeaceae) in the small Ild River (Yaroslavl oblast). Inland Water Biol., 8: 157–165. DOI: https://doi.org/10.1134/ S1995082915020042.
[25] Čížková–Končalová, H., Květ, J., and Thompson, K., 1992. Carbon starvation: A key to reed decline in eutrophic lakes. Aquat. Bot. 43: 105–113. DOI: https://doi.org/10.1016/0304–3770(92)90036–I
[26] Coops, H., and Hosper, S.H. 2002. Water–Level management as a tool for the restoration of shallow lakes in the Netherlands. Lake Reserv. Manage., 18: 293–298. DOI: https://doi.org/10.1080/07438140209353935
[27] Coops, H., van den Brink, F.W.B., and van der Velde, G., 1996. Growth and morphological responses of four Helophytes species in an experimental water–depth gradient. Aquat. Bot., 54: 11–24. DOI:https://doi.org/10.1016/0304–3770(96)01025–X
[28] Crawford, R.M.M. 1992. Oxygen availability as an ecological limit to plant distribution. Adv. Ecol. Res., 23: 93–185. DOI: https://doi.org/10.1016/S0065–2504(08)60147–6
[29] Cronk, J.K., and Fennessy, M.S. 2001. Wetland plants: Biology and ecology. Washington, New York. Lewis Publishers 462 p.
[30] Deegan, B.M., White, S.D., and Ganf, G.G. 2007. The influence of water level fluctuations on the growth four emergent macrophyte species. Aquat. Bot. 86: 309–315. DOI: https://doi.org/10.1016/j.aquabot.2006.11.006
[31] Deegan, B.M., White, S.D., and Ganf, G.G. 2012. Nutrients and water level fluctuations: A study of three aquatic plants. River Res. Appl. 28: 359–368. DOI: https://doi.org/10.1002/rra.14611
[32] Dong, B., Qin, B., Li, W., and Gao, G., 2017. Growth and community composition of submerged macrophytes in Lake Taihu (China): Assessment of changes in response to sediment characteristics. Wetlands. 37: 233–243. DOI: 10.1007/s13157–016–0861–5
[33] Duarte, C.M., and Kalff, J., 1986. Littoral slope as a predictor of the maximum biomass of submerged microphyte communities. Limnol. Oceanogr., 31: 1072–1080. DOI: https://doi.org/10.4319/lo.1986. 31.5.1072
[34] Fares, A.L.B., et al. 2020. Environmental factors affect macrophyte diversity on Amazonian aquatic ecosystems inserted in an anthropogenic landscape. Ecol. Indic., 113: 106–231. DOI:https://doi.org/10.1016/j.ecolind.2020.106231.
[35] Felle, H.H. 2005. pH regulation in anoxic plants. Ann. Bot. 96: 519–532. DOI: 10.1093/aob/mci207.
[36] Ford, K.A., and Champion, P.D. 2019. Flora of New Zealand: Seed plants Nymphaeales. Manaaki Whenue Press. DOI: http://dx.doi.org/10.7931/b1jh–cp50
[37] Fossey, M. and Rousseau, A.N. 2016. Can isolated and riparian wetlands mitigate the impact of climate change on watershed hydrology? A case study approach. J. Environ. Manage., 184: 327–339. DOI:http://dx.doi.org/10.1016/j.jenvman.2016.09.043
[38] Givnish, T.J. 1987. Comparative studies of leaf form: Assessing the relative roles of selective pressures and phylogenetic constraints. New Phytol., 106: 131–160. DOI: https://doi.org/10.1111/j.1469–8137.1987.tb04687.x
[39] Gopal, B. and Harma, K.P. 1990. Ecology of plant populations. In: Ecology and management of aquatic vegetation in the Indian subcontinent. Edited by B. Gopal. Kluwer Academic Publishers, Dordrecht 79–106 pp.
[40] Huang, X. et al. 2018. The root structures of 21 aquatic plants in a macrophyte–dominated lake in China. J. Plant Ecol., 11: 39–46. DOI: https://doi.org/10.1093/jpe/rtx018
[41] Huber, H., et al. 2012. Plasticity as a plastic response: how submergence–induced leaf elongation in Rumex palustris depends on light and nutrient availability in its early life stage. New Phytol. 194: 572–582. DOI:https://doi:10.1111/j.1469-8137.2012.04075.x
[42] Ismuhajaroh, B.N., Indradewa, D., Kurniasih, B., and Utami, S.N.H., 2022. Interrelationships of Air Canal Adaptation in the Leaves of Water Lilies and Water Depth of Lebak Swampland in Kalimantan Selatan. JEMT, 1(57): 197-210.
[43] Jian, Z., Ma, F., Guo, Q., Qin, A., and Xiao, W., 2018. Long–term responses of riparian plant’s composition to water level fluctuation in China’s three gorges reservoir. PLoS ONE. 13: e0207689. DOI:https://doi.org/10.1371/journal.pone.0207689
[44] Kennedy, M.P., Milne, J.M., and Murphy, K.J., 2003. Experimental growth responses to groundwater level variation and competition in five British wetland plant species. Wetl. Ecol. Manage. 11: 383–396. DOI:10.1023/b:wetl.0000007194.01073.6b
[45] Kleindl, P.M., and Steinman, A.D. 2021. Contrasting trajectories in macrophyte community development after shoreline restoration: water level obscures trends. Aquat. Bot. 169, 103327. DOI: https://doi.org/10.1016/ j.aquabot.2020.103327
[46] Klok, P.F., and van der Velde, G., 2017. Plant traits and environment: Floating leaf blade production and turnover of waterlilies. PeerJ., DOI:10.7717/peerj.3212
[47] Kordyum, E., Mosyakin, S., Ivanenko, G., Ovcharenko, Y., and Brykov, V., 2021. Hydropotes of young and mature leaves in Nuphar lutea and Nymphaea alba (Nymphaeaceae): Formation, functions and phylogeny. Aquat. Bot. 169, 103342. DOI: https://doi.org/10.1016/j.aquabot.2020.103342
[48] Kornijów, R., Measey, G.J., and Moss, B., 2016. The structure of the littoral: Effects of waterlily density and perch predation on sediment and plant–associated macroinvertebrate communities. Freshw. Biol. 61: 32–50. DOI: https://.org/10.1111/fwb.12674
[49] Kunii, H. and Aramaki, M., 1992. Annual net production and life span of floating leaves in Nymphaea tetragona Georgi: a comparison with other floating–leaved macrophytes. Hydrobiologia, 242: 185–193. DOI:https://doi.org/10.1007/BF00019967
[50] Kutschker, A.M., Epele, L.B., and Miserendino M.L., 2014. Aquatic plant composition and environmental relationships in grazed Northwest Patagonian wetlands, Argentina. Ecol. Eng. 64: 37–48. DOI:https://doi.org/10.1016/ j.ecoleng.2013.12.007
[51] Lacoul, P. and Fredman, B., 2006. Envionmental influences on aquatic plants in freshwater ecosystems. Environ. Rev. 14: 89–136. DOI:10.1139/aO6–001
[52] Larcher, W. 1995. Photosynthesis as a tool for indicating temperature stress events In: Schulze, E.D., Caldwell, M.M., Ecophysiology of photosynthesis. Springer, Berlin Heidelberg New York, 261–277 pp.
[53] Les, D.H. 2018. Aquatic Dicotyledons of North America: Ecology, life history and systematics, CRC Press. 1351p.
[54] Li, Q., Zeng, Y., and Zha, W. 2020. Velocity distribution and turbulence structure of open channel flow with floating–leaved vegetation. J. Hydrol. 590, 125298. DOI: https://doi.org/10.1016/j.jhydrol.2020.125298
[55] Liu, Y.L., and Kumar, M. 2016. Role of meteorological controls on interannual variations in wet–period characteristics of wetlands. Water Resour. Res. 52: 5056–5074. DOI:https://doi.org/10.1002/2015WR018493
[56] Long, S.P., Farage, P.K., Nie, G.Y., and Osborne, C.P. 1995. Photosynthesis and rising CO2 concentration. In: Mathis P. Photosynthesis: from light to biosphere. Kluwer Amsterdam V, 729– 736.
[57] Lu, J., Bunn, S.E. and Burford, M.A. 2018. Nutrient release and uptake by littoral macrophytes during water level fluctuations. Sci. Total Environ., 622: 29–40. DOI: https://doi.org/10.1016/j.scitotenv.2017.11.199
[58] Lu, X.M., and Chen, J.J., 2012. Effects of the diurnal variation of sunlight on water quality and the physiology of Nymphaea tetragona. Environ. Toxicol. Chem., 94: 294–309. DOI:https://doi.org/10.1080/02772248.2011.648939
[59] Lynn, D.E. and Waldren, S. 2003. Survival of Ranunculus repens L. (Creeping Buttercup) in an amphibious habitat. Ann. Bot. 91: 75–84. DOI: https://doi.org/10.1093/aob/mcg011
[60] Macek, P., Rejmánková, E. and Houdková, K. 2006. The effect of long–term submergence on functional properties of Eleocharis cellulosa Torr. Aquat. Bot. 84: 251–258. DOI:http://dx.doi.org/0.1016/j.aquabot.2005.11.003
[61] Madsen, T., and Brix, H. 1997. Growth, photosynthesis and acclimation by two submerged macrophytes in relation to temperature. Oecologia, 110: 320–327. DOI: https://doi.org/10.1007/s004420050165
[62] Magee, T.K., Ernst, T.L., Kentula, M.E., and Dwire, K.A. 1999. Floristic comparison of freshwater wetlands in an urbanizing environment. Wetlands, 19: 477–489. DOI: http://dx.doi.org/10.1007/BF03161690
[63] Maurer, D.A., and Zedler, J.B. 2002. Differential invasion of a wetland grass explained by tests of nutrients and light availability on the establishment and clonal growth. Oecologia, 131: 279–288. DOI:https://doi.org/10.1007/s00442–002–0886–8
[64] Miao, S.L., Newman, S., and Sklar, F.H., 2000. Effects of habitat nutrients and seed sources on growth and expansion of Typha domingensis. Aquat. Bot. 68: 297–311. DOI: https://doi.org/10.1016/S0304–3770(00)00127–3
[65] Molles, M.C.Jr., and Sher, A.A. 2019. Ecology: Concepts and applications. 8th Edition. Mc. Grow Hill.
[66] Mommer, L. et al. 2005. Submergence–induced morphological, anatomical, and biochemical responses in a terrestrial species affect gas diffusion resistance and photosynthetic performance. Plant Physiol. 139: 497–508. DOI: https://doi.org/10.1104/pp.105.064725
[67] Müller, I., Schmid, B., and Weiner, J. 2000. The effect of nutrient availability on biomass allocation patterns in 27 species of herbaceous plants. Perspect. Plant Ecol. Evol. Syst., 3: 115–127. DOI:https://doi.org/10.1078/1433–8319–00007
[68] Neill, C. 1990. Effects of nutrient and water levels on emergent macrophyte biomass in a prairie marsh. Can. J. Bot. 68: 1007–1014.
[69] Nohara, S. and Tsuchiya, T. 1990. Effects of water level fluctuation on the growth of Nelumbo nucifera Gaertn. In lake Kasmigaura, Japan. Ecol. Res. 5: 237–252. DOI: https://doi.org/10.1139/b90–127
[70] Paillisson, J.M. and Marion, L. 2011. Water level fluctuations for managing excessive plant biomass in shallow lakes. Ecol. Eng. 37: 241–247. DOI: https://doi.org/10.1016/j.ecoleng.2010.11.017
[71] Phillips, G., Willby, N. and Moss, B. 2016. Submerged macrophyte decline in shallow lakes: What have we learnt in the last forty years?. Aquat. Bot. 135: 37–45. DOI: https://doi.org/10.1016/j.aquabot.2016.04.004
[72] Pinay, G., Clément, J.C., and Naiman, R.J., 2002. Basic principles and ecological consequences of changing water regims on nitrogen sycling in fluvial systems. Environ. Manage. 30: 481–491. DOI: 10.1007/s00267–002–2736–1
[73] Pip, E. 1989. Water temperature and freshwater macrophyte distribution. Aquat. Bot. 34: 367–373. DOI:https://doi.org/10. 1016/0304–3770(89)90079–X
[74] Poorter, H., and Nagel, O. 2000. The role of biomass allocation in the growth response of plants to different levels of light, CO2, nutrients and water: A quantitative review. Aust. J. Plant Physiol., 27: 595–607. DOI:http://dx.doi.org/ 10.1071/pp99173_co
[75] Poorter, H., et al. 2012. Biomass allocation to leaves, stems and roots: Meta–analyses of interspecific variation and environmental control. New Phytol. 193: 30–50. DOI: https://doi.org/10.1111/j.1469–8137.2011.03952.x
[76] Puijalon, S., et al. 2008. Phenotypic plasticity in response to mechanical stress: hydrodynamic performance and fitness of four aquatic plant species. New Phytol., 177: 907–917. DOI: https://doi.org/10.1111/j.1469–8137.2007.02314.x
[77] Raulings, E.J., Morris, K., Roache, M.C. and Boon, P.I. 2010. The importance of water regimes operating at small spatial scales for the diversity and structure of wetland vegetation. Freshwater Biol., 55: 701–715. DOI:https://doi.org/10.1111/j.1365–2427.2009.02311.x
[78] Ribaudo, C., et al. 2012. CO2 and CH4 fluxesa crossa Nuphar lutea (L.) Sm. stand. J. Limnol., 71: 200–210. DOI: https://doi.org/10.4081/mnol.2012.e21
[79] Richards, J.F., Troxler, T.G., Lee, D.W., and Zimmerman, M.S. 2011. Experimental determination of effects of water depth on Nymphaea odorata growth, morphology and biomass allocation. Aqua. Bot., 95: 9–16. DOI: 10.1016/j.aquabot.2011.03.002
[80] Richards, J.H., and Cao, C., 2012. Germination and early growth of Nymphaea odorata at different water depths. Aquat. Bot., 98: 12–19. DOI:10.1016/j.aquabot.2011.12.003
[81] Riis, T., and Hawes, I. 2002. Relationships between water level fluctuations and vegetation diversity in shallow water of New Zealand lakes. Aquat. Bot., 74: 133–148. DOI: https://doi.org/10.1016/S0304–3770(02)00074–8
[82] Riis, T., et al. 2012. Growth and morphology in relation to temperature and light availability during the establishment of three invasive aquatic plant species. Aquat. Bot., 102: 56–64. DOI:https://doi.org/10.1016/j.aquabot.2012.05.002
[83] Ritchie, R.J. 2012. Photosynthesis in the blue waterlily (Nymphaea caerulea Saligny) using pulse amplitude modulation fluoromentry. Int. J. Plant Sci., 173: 124–136. DOI:10.1086/663168
[84] Rossenberry, D.O., and Hayashi, M., 2013. Assessing and measuring wetland hydrology in: Anderson, J.T., Davis, C.A., Wetland techniques: Volume I: Foundations. DOI: 10.1007/978–94–007–6860–4_3
[85] Sasidharan, R., et al. 2018. Signal dynamics and interactions during flooding stress. Plant Physiol., 176: 1106–1117. DOI: http://dx.doi.org/10.1104/pp.17.01232
[86] Scheffer, M. 2004. Ecology of shallow lakes, Population and community biology series. Champman and Hall. London. 378p.
[87] Scheffer, M., Hosper, S.H., Meijer, M.L., Moss, B., and Jeppesen, E. 1993. Alternative equilibria in shallow lakes. Trends Ecol. Evol., 8: 275–279. DOI: https://doi.org/10.1016/0169–5347(93)90254–M
[88] Shipley, B., and Meziane, D. 2002. The balanced–growth hypothesis and the allometry of leaf and root biomass allocation. Funct. Ecol., 16: 326–331. DOI: https://doi.org/10.1046/j.1365–2435.2002.00626.x
[89] Smith, R.G.B., and Brock, M.A. 2007. The ups and downs of life on the edge: The influence of water level fluctuation on biomass allocation in two contrasting aquatic plants. Plant Ecol., 188: 103–116. DOI:10.1007/sl 1258–006–9151–2
[90] Snir, A., Gurevitz, M., and Marcus, Y. 2006 Alterations in Rubisco activity and in stomatal behavior induce a daily rhythm in photosynthesis of aerial leaves in the amphibious–plant Nuphar lutea. Photosynth. Res., 90: 233–242. DOI: 10.1007/s11120–007–9142–8
[91] Solórzano, J.V., Gallardo–Cruz, J.A., Peralta–Carreta, C., Martínez–Camilo, R., and de Oca, A.F.M. 2020. Plant community composition patterns in relation to microtopography and distance to water bodies in a tropical forested wetland. Aquat. Bot. 167: 103295. DOI: https://doi.org/10.1016/j.aquabot.2020.103295
[92] Sudiarto, S.I.A., Renggaman, A., and Choi, H.L. 2019. Floating aquatic plants for total nitrogen and phosphorus removal from treated swine wastewater and their biomass characteristics. J. Environ. Manage., 231: 763–769. DOI: 10.1016/ j.jenvman.2018.10.070
[93] Torres–Fernández del Campo, J., Olvera–Vargas, M., Figueroa–Rangel, B.L., Cuevas–Guzmán, R., and Iñiguez–Dávalos, L.I., 2018. Patterns of spatial diversity and structure of mangrove vegetation in pacific West–Central Mexico. Wetlands. DOI: https://doi.org/10.1007/s13157–018–1041–6
[94] Tsuchiya, T. 1991. Leaf life span of floating–leaved plants. Kluwer Academic Publishers, Belgium. Vegetation 97: 149–160. DOI: 10.1007/BF00035388
[95] Twilley, R.R., Blanton, L.R., Brinson, M.M., and Davis, G.J. 1985. Biomass production and nutrient cycling in aquatic macrophyte communities of the Chowan River, North Carolina. Aquat. Bot., 22: 231–252. DOI:https://doi.org/10.1016/0304–3770(85)90002–6
[96] van der Valk, A., and Mushet, D.M. 2016. Interannual water–level fluctuations and the vegetation of Prairie Potholes: Potential impacts of climate change. Wetlands, 36: 397–406. DOI: https://doi.org/10.1007/s13157–016–0850–8
[97] van der Valk, A.G. 2005. Water–level fluctuations in North American prairie wetlands. Hydrobiologia, 539: 171–188. DOI: 10.1007/s10750–004–4866–3
[98] van Geest, G.J., et al. 2005. Water–level fluctuations affect macrophyte richness in floodplain lakes. Hydrobiologia, 539: 239–248. DOI: 10.1007/s10750–004–4879–y
[99] van Wijk, M.T., Williams, M., Gough, L., Hobbie, S.E., and Shaver, G.R., 2003. Luxury consumption of soil nutrients: A possible competitive strategy in above–ground and below–ground biomass allocation and root morphology for slow–growing arctic vegetation?. J. Ecol., 91: 664–676. DOI: https://doi.org/10.1046/j.1365–2745.2003.00788.x
[100] Vartapetian, B.B., and Jackson, M.B. 1997. Plant adaptations to anaerobic stress. Ann. Bot., 79: 3–20. DOI: https://doi.org/10.1093/oxfordjournals.aob.a010303
[101] Voesenek, E.J.W., et al. 2003. Interaction between plant hormones regulate submergence–induced shoot elongation in the flooding–tolerant dicot Rumex palustris. Ann. Bot., 91: 205–211.
[102] Vymazal, J., and Kröpfelová, L. 2008. Wastewater treatment in constructed wetlands with horizontal sub–surface flow. Springer. 579p.
[103] Wang, P., Zhang, Q., Xu, Y.S., and Yu, F.H., 2016. Effects of water level fluctuation on the growth of submerged macrophyte communities. Flora–Morphol. Distrib. Funct. Ecol. Plants., 223: 83–89. DOI:http://dx.doi.org/10.1016/j/flora.2016.05.005
[104] Wang, Q., Chen, I., Liu, F., and Li, W., 2014. Morphological changes and resource allocation of Zizania latifolia (Griseb.) Stapf in response to different submergence depth and duration. Flora, 209: 279–284. DOI:10.1016/j.flora.2014.03.006
[105] Webb, M.A., Ott, R.A.Jr., and Bonds, C.C. 2012. Propagation and establishment of native aquatic plants in reservoirs. Management data series, No. 273. Inland fisheries division, Austin, Texas 78744. Available at: https://tpwd.texas.gov/publications/pwdpubs/media/pwd_rp_t3200_1770.pdf
[106] Webb, R.H., and Leake, S.A. 2006. Ground–watersurface–waterinteractions and long–term change in riverine riparian vegetation in the southwestern United States. J. Hydrol., 320: 302–323. DOI:https://doi.org/10.1016/j.jhydrol.2005.07.022
[107] Wei, G.W., et al. 2019. Growth responses of eight wetland species to water level fluctuation with different ranges and frequencies. PLOS ONE., 14, e0220231. DOI:https://doi.org/10.1371/journal.pone.0220231
[108] Wetsel, R.G., and Likens, G.E. 2000. Limnological analyses. San Diego, California. Academic Press 3rd Edition.
[109] White, M.S., et al. 2008. Natural lake level fluctuation and associated concordance with water quality and aquatic communities within small lakes of the Laurentian Great Lakes region. Hydrobiologia, 613: 21 –31. DOI:10.1007/s10750–008–9469–y
[110] Wu, J., Zhao, H–B., Yu, D. and Xu, X., 2017. Transcriptome profiling of the floating leaved aquatic plant Nymphoides peltata in response to flooding stress. BMC Genom. 18. DOI:10.1186/s12864–017–3515–y
[111] Yamamoto, I., Tsuchiya, T., and Ikusima, I. 1999. Relationship between net photosynthetic rate and leaf life span of six submerged plants in experimental ponds. Japanase J. Limnologi, 60: 257–263. DOI:https://doi.org/10.3739/rikusui.60.257
[112] Yang, F., and Guo, Z. 2015. Characterization of micro–morphology and wettability of lotus leaf, waterlily leaf and biomimetic ZnO surface. J. Bionic Eng., 12: 88–97. DOI: https://doi.org/10.1016/S1672–6529(14)60103–7
[113] Yu, H., Niu, Y., Hu, Y., and Du, D. 2014. Photosynthetic response of the floating–leaved macrophyte Nymphoides peltata to a temporary terrestrial habitat and its implications for ecological recovery of lake side zones. Knowl. Managt. Aquatic Ecosyst. 412, 08. DOI: https://doi.org/10.1051/kmae/2013090
[114] Zhang, A.Y., et al. 2019. Dam effect on soil nutrients and potentially toxic metals in a reservoir riparian zone. Clean–Soil Air Water. 47, 1700497. DOI: https://doi.org/10. 1002/clen.201700497
[115] Zhonghua, W., Dan, Y., Manghui, T., Qiang, W., and Wen, X. 2007. Interference between two floating–leaved aquatic plants: Nymphoides peltata and Trapa bispinosa. Aquat. Bot., 86: 316–320. DOI:https://doi.org/10.1016/j.aquabot. 2006.11.008
[116] Zhu, J., et al. 2017. Modeling the potential impacts of climate change on the water table level of selected forested wetlands in the southeastern United States. Hydrol. Earth Syst. Sci., 21: 6289–6305. DOI:https://doi.org/10.5194/hess–21–6289–2017
[2] Atwell, B.J., Kreidermann, P.E., and Turnbull, C.G.N., 2003. Plants in action: Adaptation in nature, performance in cultivation. Macmillan, South Yarra, Australia.
[3] Baastrup–Spohr, L., Møller, C.L., and Sand–Jensen, K., 2016. Water–level fluctuations affect sediment properties, carbon flux and growth of the isoetid littorella uniflo rain oligotrophic lakes. Freshw. Biol. 61, 301–315. DOI: https://doi.org/ 10.1111/fwb.127044
[4] Baastrup–Spohr, L., Sand–Jensen, K., Nicolajsen, S.V., and Bruun, H.H., 2015. From soaking wet to bone dry: Predicting plant community composition along a steep hydrological gradient. J. Veg. Sci. 26, 619–630. DOI: https://doi.org/10.1111/jvs.12280
[5] Badan Pusat Statistik Kabupaten Hulu Sungai Utara (BPS–HSU), 2020. Kecamatan Sungai Pandan dalam angka. Available at: https://hulusungaiutara.bps.go.id/publication.html. (in Indonesian)
[6] Bai, X., Chen, K., Zhao, H., and Chen, X., 2015. Impact of water depth and sediment type on root morphology of the submerged plant Vallisneria natans. J. Freshw. Ecol. 30: 75–84. DOI:http://dx.doi.org/10.1080/02705060. 2014.970672
[7] Balai Penelitian Tanah (BPT–Bogor), 2009. Petunjuk teknis: Analisis kimia tanah, tanaman, air, dan pupuk. Balai Penelitian Tanah, Bogor, Jawa Barat, Indonesia. (in Indonesian)
[8] Baldwin, D.S, and Mitchell, A.M. 2000. The effects of drying and re–flooding on the sediment and soil nutrient dynamics of lowland river–floodplain systems: A synthesis. River Research and Applications: an international journal devoted to river research and management, 16: 457–467.
[9] Bando, F.M., Michelan, T.S., Cunha, E.R., Figueiredo, B.R.S., and Thomaz, S.M., 2015. Macrophyte species richness and composition are correlated with canopy openness and water depth in tropical floodplain lakes. Rev. Bras. Bot. 38: 289–294. DOI: https://doi.org/10.1007/s40415 –015–0137–y
[10] Barko, J.W., Gunnison D., and Carpenter S.R. 1991. Sediment interacters with submerged macrophyte growth and community dynamics. Aquat. Bot. 41. DOI: https://doi.org/10.1016/0304–3770(91)90038–7
[11] Barko, J.W. and Smart, R.M. 1981. Comparative influences of light and temperature on the growth and metabolism of selected submersed freshwater macrophytes. Ecol. Monogr. 51: 219–236. DOI: https://doi.org/ 10.2307/2937264
[12] Barko, J.W., and Smart, R.M. 1983. Effects of organic matter additions to sediment on the growth of aquatic plants. J. Ecol. 71: 161–175. DOI: https://doi.org/10.2307/2259969
[13] Bini, L.M., Thomaz, S.M., Murphy, K.J. and Camargo, A.F.M. 1999. Aquatic macrophyte distribution in relation to water and sediment conditions in the Itaipu Reservoir, Brazil. Hydrobiologia, 415: 147–154. Available at: https://repositorio.unesp.br/handle/11449/20426
[14] Blanch, S.J., Ganf, G.G., and Walker, K.F, 1999. Growth and resource allocation in response to flooding in the emergent sedge Bolboschoenus medianus. Aquat. Bot. 63: 145–160. DOI:https://dx.doi.org/10.1007/s10452–010–9334–8
[15] Bloom, A.J., Chapin, F.S. and Mooney, H.A., 1985. Resource limitation in plants an economic analogue. Annu. Rev. Ecol. Syst. 16: 363–392. DOI: https://doi.org/10.1146/annurev.es.16.110185.002051
[16] Boar, R. 2006. Responses of a fringing Cyperus papyrus L. swamp to changes in water level. Aquat. Bot., 84: 85–92. DOI: https://dx.doi.org/10.1016/j.aquabot.2005.07.008
[17] Brock, Th.C.M., Arts, G.H.P., Goossen, L.L.M. Rutenfrans, A.H.M., 1983. Structure and annual biomass production of Nymphoides peltata (Gmel.) O. Kuntze (Menyanthaceae). Aquat. Bot. 17: 167–188. DOI:https://doi.org/10.1016/0304–3770(83)90056–6
[18] Brouwer, R. 1963. Some aspects of the equilibrium between overground and underground plant parts. Jaarboek van het instituut voor biologisch en scheikundig onderzoek van landbouwgewassen, Wageningen 31–39. Available at: https://edepot.wur.nl/361707
[19] Casanova, M.T., and Brock, M.A., 2000. How do depth, duration and frequency of flooding influence the establishment of wetland plant communities?. Plant Ecol. 147: 237–250. DOI: https://doi.org/10.1023/
[20] Cazzanelli, M., Warming, T.P., and Christoffersen, K.S., 2008. Emergent and floating–leaved macrophytes as refuge for zooplankton in a eutrophic temperate lake without submerged vegetation. Hydrobiologia 605: 113–122. DOI: https://doi.org/10.1007/s10750–008–9324–1
[21] Chapin, F.S. 1980. The mineral nutrition of wild plants. Ann. Rev. Ecol. Syst. 11: 233–260. DOI:https://doi.org/10.1146/annurev.es.11.110180.001313
[22] Chen, F., et al. 2017. Water lilies as emerging models for Darwin’s abominable mystery. Hortic. Res. 4. DOI:10.1038/hortres,2017.51
[23] Chen, W., et al. 2007. Root growth of wetland plants with different root types. Acta Ecol. Sinica, 27: 450–457. DOI: https://doi.org/10.1016/s1872–2032(07)60017
[24] Chernova, A.M., 2015. Seasonal dynamics of yellow water lily Nuphur lutea (L.) Smith (Nymphaeaceae) in the small Ild River (Yaroslavl oblast). Inland Water Biol., 8: 157–165. DOI: https://doi.org/10.1134/ S1995082915020042.
[25] Čížková–Končalová, H., Květ, J., and Thompson, K., 1992. Carbon starvation: A key to reed decline in eutrophic lakes. Aquat. Bot. 43: 105–113. DOI: https://doi.org/10.1016/0304–3770(92)90036–I
[26] Coops, H., and Hosper, S.H. 2002. Water–Level management as a tool for the restoration of shallow lakes in the Netherlands. Lake Reserv. Manage., 18: 293–298. DOI: https://doi.org/10.1080/07438140209353935
[27] Coops, H., van den Brink, F.W.B., and van der Velde, G., 1996. Growth and morphological responses of four Helophytes species in an experimental water–depth gradient. Aquat. Bot., 54: 11–24. DOI:https://doi.org/10.1016/0304–3770(96)01025–X
[28] Crawford, R.M.M. 1992. Oxygen availability as an ecological limit to plant distribution. Adv. Ecol. Res., 23: 93–185. DOI: https://doi.org/10.1016/S0065–2504(08)60147–6
[29] Cronk, J.K., and Fennessy, M.S. 2001. Wetland plants: Biology and ecology. Washington, New York. Lewis Publishers 462 p.
[30] Deegan, B.M., White, S.D., and Ganf, G.G. 2007. The influence of water level fluctuations on the growth four emergent macrophyte species. Aquat. Bot. 86: 309–315. DOI: https://doi.org/10.1016/j.aquabot.2006.11.006
[31] Deegan, B.M., White, S.D., and Ganf, G.G. 2012. Nutrients and water level fluctuations: A study of three aquatic plants. River Res. Appl. 28: 359–368. DOI: https://doi.org/10.1002/rra.14611
[32] Dong, B., Qin, B., Li, W., and Gao, G., 2017. Growth and community composition of submerged macrophytes in Lake Taihu (China): Assessment of changes in response to sediment characteristics. Wetlands. 37: 233–243. DOI: 10.1007/s13157–016–0861–5
[33] Duarte, C.M., and Kalff, J., 1986. Littoral slope as a predictor of the maximum biomass of submerged microphyte communities. Limnol. Oceanogr., 31: 1072–1080. DOI: https://doi.org/10.4319/lo.1986. 31.5.1072
[34] Fares, A.L.B., et al. 2020. Environmental factors affect macrophyte diversity on Amazonian aquatic ecosystems inserted in an anthropogenic landscape. Ecol. Indic., 113: 106–231. DOI:https://doi.org/10.1016/j.ecolind.2020.106231.
[35] Felle, H.H. 2005. pH regulation in anoxic plants. Ann. Bot. 96: 519–532. DOI: 10.1093/aob/mci207.
[36] Ford, K.A., and Champion, P.D. 2019. Flora of New Zealand: Seed plants Nymphaeales. Manaaki Whenue Press. DOI: http://dx.doi.org/10.7931/b1jh–cp50
[37] Fossey, M. and Rousseau, A.N. 2016. Can isolated and riparian wetlands mitigate the impact of climate change on watershed hydrology? A case study approach. J. Environ. Manage., 184: 327–339. DOI:http://dx.doi.org/10.1016/j.jenvman.2016.09.043
[38] Givnish, T.J. 1987. Comparative studies of leaf form: Assessing the relative roles of selective pressures and phylogenetic constraints. New Phytol., 106: 131–160. DOI: https://doi.org/10.1111/j.1469–8137.1987.tb04687.x
[39] Gopal, B. and Harma, K.P. 1990. Ecology of plant populations. In: Ecology and management of aquatic vegetation in the Indian subcontinent. Edited by B. Gopal. Kluwer Academic Publishers, Dordrecht 79–106 pp.
[40] Huang, X. et al. 2018. The root structures of 21 aquatic plants in a macrophyte–dominated lake in China. J. Plant Ecol., 11: 39–46. DOI: https://doi.org/10.1093/jpe/rtx018
[41] Huber, H., et al. 2012. Plasticity as a plastic response: how submergence–induced leaf elongation in Rumex palustris depends on light and nutrient availability in its early life stage. New Phytol. 194: 572–582. DOI:https://doi:10.1111/j.1469-8137.2012.04075.x
[42] Ismuhajaroh, B.N., Indradewa, D., Kurniasih, B., and Utami, S.N.H., 2022. Interrelationships of Air Canal Adaptation in the Leaves of Water Lilies and Water Depth of Lebak Swampland in Kalimantan Selatan. JEMT, 1(57): 197-210.
[43] Jian, Z., Ma, F., Guo, Q., Qin, A., and Xiao, W., 2018. Long–term responses of riparian plant’s composition to water level fluctuation in China’s three gorges reservoir. PLoS ONE. 13: e0207689. DOI:https://doi.org/10.1371/journal.pone.0207689
[44] Kennedy, M.P., Milne, J.M., and Murphy, K.J., 2003. Experimental growth responses to groundwater level variation and competition in five British wetland plant species. Wetl. Ecol. Manage. 11: 383–396. DOI:10.1023/b:wetl.0000007194.01073.6b
[45] Kleindl, P.M., and Steinman, A.D. 2021. Contrasting trajectories in macrophyte community development after shoreline restoration: water level obscures trends. Aquat. Bot. 169, 103327. DOI: https://doi.org/10.1016/ j.aquabot.2020.103327
[46] Klok, P.F., and van der Velde, G., 2017. Plant traits and environment: Floating leaf blade production and turnover of waterlilies. PeerJ., DOI:10.7717/peerj.3212
[47] Kordyum, E., Mosyakin, S., Ivanenko, G., Ovcharenko, Y., and Brykov, V., 2021. Hydropotes of young and mature leaves in Nuphar lutea and Nymphaea alba (Nymphaeaceae): Formation, functions and phylogeny. Aquat. Bot. 169, 103342. DOI: https://doi.org/10.1016/j.aquabot.2020.103342
[48] Kornijów, R., Measey, G.J., and Moss, B., 2016. The structure of the littoral: Effects of waterlily density and perch predation on sediment and plant–associated macroinvertebrate communities. Freshw. Biol. 61: 32–50. DOI: https://.org/10.1111/fwb.12674
[49] Kunii, H. and Aramaki, M., 1992. Annual net production and life span of floating leaves in Nymphaea tetragona Georgi: a comparison with other floating–leaved macrophytes. Hydrobiologia, 242: 185–193. DOI:https://doi.org/10.1007/BF00019967
[50] Kutschker, A.M., Epele, L.B., and Miserendino M.L., 2014. Aquatic plant composition and environmental relationships in grazed Northwest Patagonian wetlands, Argentina. Ecol. Eng. 64: 37–48. DOI:https://doi.org/10.1016/ j.ecoleng.2013.12.007
[51] Lacoul, P. and Fredman, B., 2006. Envionmental influences on aquatic plants in freshwater ecosystems. Environ. Rev. 14: 89–136. DOI:10.1139/aO6–001
[52] Larcher, W. 1995. Photosynthesis as a tool for indicating temperature stress events In: Schulze, E.D., Caldwell, M.M., Ecophysiology of photosynthesis. Springer, Berlin Heidelberg New York, 261–277 pp.
[53] Les, D.H. 2018. Aquatic Dicotyledons of North America: Ecology, life history and systematics, CRC Press. 1351p.
[54] Li, Q., Zeng, Y., and Zha, W. 2020. Velocity distribution and turbulence structure of open channel flow with floating–leaved vegetation. J. Hydrol. 590, 125298. DOI: https://doi.org/10.1016/j.jhydrol.2020.125298
[55] Liu, Y.L., and Kumar, M. 2016. Role of meteorological controls on interannual variations in wet–period characteristics of wetlands. Water Resour. Res. 52: 5056–5074. DOI:https://doi.org/10.1002/2015WR018493
[56] Long, S.P., Farage, P.K., Nie, G.Y., and Osborne, C.P. 1995. Photosynthesis and rising CO2 concentration. In: Mathis P. Photosynthesis: from light to biosphere. Kluwer Amsterdam V, 729– 736.
[57] Lu, J., Bunn, S.E. and Burford, M.A. 2018. Nutrient release and uptake by littoral macrophytes during water level fluctuations. Sci. Total Environ., 622: 29–40. DOI: https://doi.org/10.1016/j.scitotenv.2017.11.199
[58] Lu, X.M., and Chen, J.J., 2012. Effects of the diurnal variation of sunlight on water quality and the physiology of Nymphaea tetragona. Environ. Toxicol. Chem., 94: 294–309. DOI:https://doi.org/10.1080/02772248.2011.648939
[59] Lynn, D.E. and Waldren, S. 2003. Survival of Ranunculus repens L. (Creeping Buttercup) in an amphibious habitat. Ann. Bot. 91: 75–84. DOI: https://doi.org/10.1093/aob/mcg011
[60] Macek, P., Rejmánková, E. and Houdková, K. 2006. The effect of long–term submergence on functional properties of Eleocharis cellulosa Torr. Aquat. Bot. 84: 251–258. DOI:http://dx.doi.org/0.1016/j.aquabot.2005.11.003
[61] Madsen, T., and Brix, H. 1997. Growth, photosynthesis and acclimation by two submerged macrophytes in relation to temperature. Oecologia, 110: 320–327. DOI: https://doi.org/10.1007/s004420050165
[62] Magee, T.K., Ernst, T.L., Kentula, M.E., and Dwire, K.A. 1999. Floristic comparison of freshwater wetlands in an urbanizing environment. Wetlands, 19: 477–489. DOI: http://dx.doi.org/10.1007/BF03161690
[63] Maurer, D.A., and Zedler, J.B. 2002. Differential invasion of a wetland grass explained by tests of nutrients and light availability on the establishment and clonal growth. Oecologia, 131: 279–288. DOI:https://doi.org/10.1007/s00442–002–0886–8
[64] Miao, S.L., Newman, S., and Sklar, F.H., 2000. Effects of habitat nutrients and seed sources on growth and expansion of Typha domingensis. Aquat. Bot. 68: 297–311. DOI: https://doi.org/10.1016/S0304–3770(00)00127–3
[65] Molles, M.C.Jr., and Sher, A.A. 2019. Ecology: Concepts and applications. 8th Edition. Mc. Grow Hill.
[66] Mommer, L. et al. 2005. Submergence–induced morphological, anatomical, and biochemical responses in a terrestrial species affect gas diffusion resistance and photosynthetic performance. Plant Physiol. 139: 497–508. DOI: https://doi.org/10.1104/pp.105.064725
[67] Müller, I., Schmid, B., and Weiner, J. 2000. The effect of nutrient availability on biomass allocation patterns in 27 species of herbaceous plants. Perspect. Plant Ecol. Evol. Syst., 3: 115–127. DOI:https://doi.org/10.1078/1433–8319–00007
[68] Neill, C. 1990. Effects of nutrient and water levels on emergent macrophyte biomass in a prairie marsh. Can. J. Bot. 68: 1007–1014.
[69] Nohara, S. and Tsuchiya, T. 1990. Effects of water level fluctuation on the growth of Nelumbo nucifera Gaertn. In lake Kasmigaura, Japan. Ecol. Res. 5: 237–252. DOI: https://doi.org/10.1139/b90–127
[70] Paillisson, J.M. and Marion, L. 2011. Water level fluctuations for managing excessive plant biomass in shallow lakes. Ecol. Eng. 37: 241–247. DOI: https://doi.org/10.1016/j.ecoleng.2010.11.017
[71] Phillips, G., Willby, N. and Moss, B. 2016. Submerged macrophyte decline in shallow lakes: What have we learnt in the last forty years?. Aquat. Bot. 135: 37–45. DOI: https://doi.org/10.1016/j.aquabot.2016.04.004
[72] Pinay, G., Clément, J.C., and Naiman, R.J., 2002. Basic principles and ecological consequences of changing water regims on nitrogen sycling in fluvial systems. Environ. Manage. 30: 481–491. DOI: 10.1007/s00267–002–2736–1
[73] Pip, E. 1989. Water temperature and freshwater macrophyte distribution. Aquat. Bot. 34: 367–373. DOI:https://doi.org/10. 1016/0304–3770(89)90079–X
[74] Poorter, H., and Nagel, O. 2000. The role of biomass allocation in the growth response of plants to different levels of light, CO2, nutrients and water: A quantitative review. Aust. J. Plant Physiol., 27: 595–607. DOI:http://dx.doi.org/ 10.1071/pp99173_co
[75] Poorter, H., et al. 2012. Biomass allocation to leaves, stems and roots: Meta–analyses of interspecific variation and environmental control. New Phytol. 193: 30–50. DOI: https://doi.org/10.1111/j.1469–8137.2011.03952.x
[76] Puijalon, S., et al. 2008. Phenotypic plasticity in response to mechanical stress: hydrodynamic performance and fitness of four aquatic plant species. New Phytol., 177: 907–917. DOI: https://doi.org/10.1111/j.1469–8137.2007.02314.x
[77] Raulings, E.J., Morris, K., Roache, M.C. and Boon, P.I. 2010. The importance of water regimes operating at small spatial scales for the diversity and structure of wetland vegetation. Freshwater Biol., 55: 701–715. DOI:https://doi.org/10.1111/j.1365–2427.2009.02311.x
[78] Ribaudo, C., et al. 2012. CO2 and CH4 fluxesa crossa Nuphar lutea (L.) Sm. stand. J. Limnol., 71: 200–210. DOI: https://doi.org/10.4081/mnol.2012.e21
[79] Richards, J.F., Troxler, T.G., Lee, D.W., and Zimmerman, M.S. 2011. Experimental determination of effects of water depth on Nymphaea odorata growth, morphology and biomass allocation. Aqua. Bot., 95: 9–16. DOI: 10.1016/j.aquabot.2011.03.002
[80] Richards, J.H., and Cao, C., 2012. Germination and early growth of Nymphaea odorata at different water depths. Aquat. Bot., 98: 12–19. DOI:10.1016/j.aquabot.2011.12.003
[81] Riis, T., and Hawes, I. 2002. Relationships between water level fluctuations and vegetation diversity in shallow water of New Zealand lakes. Aquat. Bot., 74: 133–148. DOI: https://doi.org/10.1016/S0304–3770(02)00074–8
[82] Riis, T., et al. 2012. Growth and morphology in relation to temperature and light availability during the establishment of three invasive aquatic plant species. Aquat. Bot., 102: 56–64. DOI:https://doi.org/10.1016/j.aquabot.2012.05.002
[83] Ritchie, R.J. 2012. Photosynthesis in the blue waterlily (Nymphaea caerulea Saligny) using pulse amplitude modulation fluoromentry. Int. J. Plant Sci., 173: 124–136. DOI:10.1086/663168
[84] Rossenberry, D.O., and Hayashi, M., 2013. Assessing and measuring wetland hydrology in: Anderson, J.T., Davis, C.A., Wetland techniques: Volume I: Foundations. DOI: 10.1007/978–94–007–6860–4_3
[85] Sasidharan, R., et al. 2018. Signal dynamics and interactions during flooding stress. Plant Physiol., 176: 1106–1117. DOI: http://dx.doi.org/10.1104/pp.17.01232
[86] Scheffer, M. 2004. Ecology of shallow lakes, Population and community biology series. Champman and Hall. London. 378p.
[87] Scheffer, M., Hosper, S.H., Meijer, M.L., Moss, B., and Jeppesen, E. 1993. Alternative equilibria in shallow lakes. Trends Ecol. Evol., 8: 275–279. DOI: https://doi.org/10.1016/0169–5347(93)90254–M
[88] Shipley, B., and Meziane, D. 2002. The balanced–growth hypothesis and the allometry of leaf and root biomass allocation. Funct. Ecol., 16: 326–331. DOI: https://doi.org/10.1046/j.1365–2435.2002.00626.x
[89] Smith, R.G.B., and Brock, M.A. 2007. The ups and downs of life on the edge: The influence of water level fluctuation on biomass allocation in two contrasting aquatic plants. Plant Ecol., 188: 103–116. DOI:10.1007/sl 1258–006–9151–2
[90] Snir, A., Gurevitz, M., and Marcus, Y. 2006 Alterations in Rubisco activity and in stomatal behavior induce a daily rhythm in photosynthesis of aerial leaves in the amphibious–plant Nuphar lutea. Photosynth. Res., 90: 233–242. DOI: 10.1007/s11120–007–9142–8
[91] Solórzano, J.V., Gallardo–Cruz, J.A., Peralta–Carreta, C., Martínez–Camilo, R., and de Oca, A.F.M. 2020. Plant community composition patterns in relation to microtopography and distance to water bodies in a tropical forested wetland. Aquat. Bot. 167: 103295. DOI: https://doi.org/10.1016/j.aquabot.2020.103295
[92] Sudiarto, S.I.A., Renggaman, A., and Choi, H.L. 2019. Floating aquatic plants for total nitrogen and phosphorus removal from treated swine wastewater and their biomass characteristics. J. Environ. Manage., 231: 763–769. DOI: 10.1016/ j.jenvman.2018.10.070
[93] Torres–Fernández del Campo, J., Olvera–Vargas, M., Figueroa–Rangel, B.L., Cuevas–Guzmán, R., and Iñiguez–Dávalos, L.I., 2018. Patterns of spatial diversity and structure of mangrove vegetation in pacific West–Central Mexico. Wetlands. DOI: https://doi.org/10.1007/s13157–018–1041–6
[94] Tsuchiya, T. 1991. Leaf life span of floating–leaved plants. Kluwer Academic Publishers, Belgium. Vegetation 97: 149–160. DOI: 10.1007/BF00035388
[95] Twilley, R.R., Blanton, L.R., Brinson, M.M., and Davis, G.J. 1985. Biomass production and nutrient cycling in aquatic macrophyte communities of the Chowan River, North Carolina. Aquat. Bot., 22: 231–252. DOI:https://doi.org/10.1016/0304–3770(85)90002–6
[96] van der Valk, A., and Mushet, D.M. 2016. Interannual water–level fluctuations and the vegetation of Prairie Potholes: Potential impacts of climate change. Wetlands, 36: 397–406. DOI: https://doi.org/10.1007/s13157–016–0850–8
[97] van der Valk, A.G. 2005. Water–level fluctuations in North American prairie wetlands. Hydrobiologia, 539: 171–188. DOI: 10.1007/s10750–004–4866–3
[98] van Geest, G.J., et al. 2005. Water–level fluctuations affect macrophyte richness in floodplain lakes. Hydrobiologia, 539: 239–248. DOI: 10.1007/s10750–004–4879–y
[99] van Wijk, M.T., Williams, M., Gough, L., Hobbie, S.E., and Shaver, G.R., 2003. Luxury consumption of soil nutrients: A possible competitive strategy in above–ground and below–ground biomass allocation and root morphology for slow–growing arctic vegetation?. J. Ecol., 91: 664–676. DOI: https://doi.org/10.1046/j.1365–2745.2003.00788.x
[100] Vartapetian, B.B., and Jackson, M.B. 1997. Plant adaptations to anaerobic stress. Ann. Bot., 79: 3–20. DOI: https://doi.org/10.1093/oxfordjournals.aob.a010303
[101] Voesenek, E.J.W., et al. 2003. Interaction between plant hormones regulate submergence–induced shoot elongation in the flooding–tolerant dicot Rumex palustris. Ann. Bot., 91: 205–211.
[102] Vymazal, J., and Kröpfelová, L. 2008. Wastewater treatment in constructed wetlands with horizontal sub–surface flow. Springer. 579p.
[103] Wang, P., Zhang, Q., Xu, Y.S., and Yu, F.H., 2016. Effects of water level fluctuation on the growth of submerged macrophyte communities. Flora–Morphol. Distrib. Funct. Ecol. Plants., 223: 83–89. DOI:http://dx.doi.org/10.1016/j/flora.2016.05.005
[104] Wang, Q., Chen, I., Liu, F., and Li, W., 2014. Morphological changes and resource allocation of Zizania latifolia (Griseb.) Stapf in response to different submergence depth and duration. Flora, 209: 279–284. DOI:10.1016/j.flora.2014.03.006
[105] Webb, M.A., Ott, R.A.Jr., and Bonds, C.C. 2012. Propagation and establishment of native aquatic plants in reservoirs. Management data series, No. 273. Inland fisheries division, Austin, Texas 78744. Available at: https://tpwd.texas.gov/publications/pwdpubs/media/pwd_rp_t3200_1770.pdf
[106] Webb, R.H., and Leake, S.A. 2006. Ground–watersurface–waterinteractions and long–term change in riverine riparian vegetation in the southwestern United States. J. Hydrol., 320: 302–323. DOI:https://doi.org/10.1016/j.jhydrol.2005.07.022
[107] Wei, G.W., et al. 2019. Growth responses of eight wetland species to water level fluctuation with different ranges and frequencies. PLOS ONE., 14, e0220231. DOI:https://doi.org/10.1371/journal.pone.0220231
[108] Wetsel, R.G., and Likens, G.E. 2000. Limnological analyses. San Diego, California. Academic Press 3rd Edition.
[109] White, M.S., et al. 2008. Natural lake level fluctuation and associated concordance with water quality and aquatic communities within small lakes of the Laurentian Great Lakes region. Hydrobiologia, 613: 21 –31. DOI:10.1007/s10750–008–9469–y
[110] Wu, J., Zhao, H–B., Yu, D. and Xu, X., 2017. Transcriptome profiling of the floating leaved aquatic plant Nymphoides peltata in response to flooding stress. BMC Genom. 18. DOI:10.1186/s12864–017–3515–y
[111] Yamamoto, I., Tsuchiya, T., and Ikusima, I. 1999. Relationship between net photosynthetic rate and leaf life span of six submerged plants in experimental ponds. Japanase J. Limnologi, 60: 257–263. DOI:https://doi.org/10.3739/rikusui.60.257
[112] Yang, F., and Guo, Z. 2015. Characterization of micro–morphology and wettability of lotus leaf, waterlily leaf and biomimetic ZnO surface. J. Bionic Eng., 12: 88–97. DOI: https://doi.org/10.1016/S1672–6529(14)60103–7
[113] Yu, H., Niu, Y., Hu, Y., and Du, D. 2014. Photosynthetic response of the floating–leaved macrophyte Nymphoides peltata to a temporary terrestrial habitat and its implications for ecological recovery of lake side zones. Knowl. Managt. Aquatic Ecosyst. 412, 08. DOI: https://doi.org/10.1051/kmae/2013090
[114] Zhang, A.Y., et al. 2019. Dam effect on soil nutrients and potentially toxic metals in a reservoir riparian zone. Clean–Soil Air Water. 47, 1700497. DOI: https://doi.org/10. 1002/clen.201700497
[115] Zhonghua, W., Dan, Y., Manghui, T., Qiang, W., and Wen, X. 2007. Interference between two floating–leaved aquatic plants: Nymphoides peltata and Trapa bispinosa. Aquat. Bot., 86: 316–320. DOI:https://doi.org/10.1016/j.aquabot. 2006.11.008
[116] Zhu, J., et al. 2017. Modeling the potential impacts of climate change on the water table level of selected forested wetlands in the southeastern United States. Hydrol. Earth Syst. Sci., 21: 6289–6305. DOI:https://doi.org/10.5194/hess–21–6289–2017
Published
2022-09-02
How to Cite
ISMUHAJAROH, Bakti Nur et al.
The Effect of Water Depth on the Structure and Allocation of Waterlily (Nymphaea pubescens Willd) Biomass in Lebak Swampland in Kalimantan Selatan.
Journal of Environmental Management and Tourism, [S.l.], v. 13, n. 5, p. 1374 - 1395, sep. 2022.
ISSN 2068-7729.
Available at: <https://journals.aserspublishing.eu/jemt/article/view/7206>. Date accessed: 21 nov. 2024.
doi: https://doi.org/10.14505/jemt.v13.5(61).14.
Section
Article
Copyright© 2024 The Author(s). Published by ASERS Publishing 2024. This is an open access article distributed under the terms of CC-BY 4.0 license.