Aerial Root Physiology: Reaching for the Sky or Down to Earth?
Amanda Rasmussen
Division of Agriculture and Environmental Science/School of Biosciences, The University of Nottingham, Sutton Bonington, UK
Search for more papers by this authorDaisy P. Dobrijevic
Division of Agriculture and Environmental Science/School of Biosciences, The University of Nottingham, Sutton Bonington, UK
Search for more papers by this authorAnne Ola
School of Biological Sciences, The University of Queensland, St Lucia, Queensland, Australia
Search for more papers by this authorFindimila Dio Ishaya
Division of Agriculture and Environmental Science/School of Biosciences, The University of Nottingham, Sutton Bonington, UK
Search for more papers by this authorCatherine E. Lovelock
School of Biological Sciences, The University of Queensland, St Lucia, Queensland, Australia
Search for more papers by this authorAmanda Rasmussen
Division of Agriculture and Environmental Science/School of Biosciences, The University of Nottingham, Sutton Bonington, UK
Search for more papers by this authorDaisy P. Dobrijevic
Division of Agriculture and Environmental Science/School of Biosciences, The University of Nottingham, Sutton Bonington, UK
Search for more papers by this authorAnne Ola
School of Biological Sciences, The University of Queensland, St Lucia, Queensland, Australia
Search for more papers by this authorFindimila Dio Ishaya
Division of Agriculture and Environmental Science/School of Biosciences, The University of Nottingham, Sutton Bonington, UK
Search for more papers by this authorCatherine E. Lovelock
School of Biological Sciences, The University of Queensland, St Lucia, Queensland, Australia
Search for more papers by this authorAbstract
Aerial roots have evolved in plants from diverse ecosystems, many facing specific environmental challenges associated with their natural or agricultural setting. In coastal species exposed to wind and waves, including mangroves, soft anoxic substrates have resulted in highly developed aerial root systems. In the rainforest, aerial roots of hemi-epiphytic figs enable life to begin higher in the canopy while climbing plants, such as ivy and Monsteras, depend on structurally very different aerial roots to climb vertical substrates. Maize, globally one of the three most important cereals, develops aerial roots presumably reducing lodging in high winds. In each of these cases, the dominant hypothesized role for aerial roots is to provide support and enabling greater heights to be reached. But do aerial roots of these plant groups also contribute to resource uptake and movement? This article explores the current knowledge of aerial root physiology and structure from each of these interesting and challenging environmental conditions and discusses how understanding these adaptations and niche requirements has value for improving crops, protecting our coastlines, improving our urban green spaces, and managing biodiversity conservation.
References
- Abasolo, W.P., Yoshida, M., Yamamoto, H., and Okuyama, T. (2009). Stress generation in aerial roots of Ficus elastica (Moraceae). IAWA Journal 30 (2): 216–224.
- Ahmed, M.A., Zarebanadkouki, M., Kaestner, A., and Carminati, A. (2016). Measurements of water uptake of maize roots: the key function of lateral roots. Plant and Soil 398 (1): 59–77.
- Ahmed, M.A., Zarebanadkouki, M., Meunier, F. et al. (2018). Root type matters: measurement of water uptake by seminal, crown, and lateral roots in maize. Journal of Experimental Botany 69 (5): 1199–1206.
- Alongi, D.M. (2008). Mangrove forests: resilience, protection from tsunamis, and responses to global climate change. Estuarine, Coastal and Shelf Science 76 (1): 1–13.
- Atkinson, J.A., Rasmussen, A., Traini, R. et al. (2014). Branching out in roots: uncovering form, function, and regulation. Plant Physiology 166 (2): 538–550.
- Avalos, G. and Fernández Otárola, M. (2010). Allometry and stilt root structure of the neotropical palm Euterpe precatoria (Arecaceae) across sites and successional stages. American Journal of Botany 97 (3): 388–394.
- Ba Thuy, N., Tanimoto, K., Tanaka, N. et al. (2009). Effect of open gap in coastal forest on tsunami run-up—investigations by experiment and numerical simulation. Ocean Engineering 36 (15): 1258–1269.
- Ball, M.C. (1988). Ecophysiology of mangroves. Trees 2 (3): 129–142.
10.1007/BF00196018 Google Scholar
- Bianchini, E., Emmerick, J.M., Messetti, A.V.L., and Pimenta, J.A. (2015). Phenology of two Ficus species in seasonal semi-deciduous forest in Southern Brazil. Brazilian Journal of Biology 75: 206–214.
- Biddick, M., Hutton, I., and Burns, K.C. (2018). An alternative water transport system in land plants. Proceedings of the Royal Society B: Biological Sciences 285 (1884).
- Böer, B. (1993). Anomalous pneumatophores and adventitious roots of Avicennia marina (Forssk.) Vierh. Mangroves two years after the 1991 Gulf War oil spill in Saudi Arabia. Marine Pollution Bulletin 27: 207–211.
- Brooks, R.A. and Bell, S.S. (2002). Mangrove response to attack by a root boring isopod root repair versus architectural modification. Marine Ecology Progress Series 231: 85–90.
- Charoenkit, S. and Yiemwattana, S. (2016). Living walls and their contribution to improved thermal comfort and carbon emission reduction: a review. Building and Environment 105: 82–94.
- Clausing, G. and Renner, S.S. (2001). Evolution of growth form in epiphytic Dissochaeteae (Melastomataceae). Organisms Diversity & Evolution 1 (1): 45–60.
- Coelho, L.F.M., Ribeiro, M.C., and Pereira, R.A.S. (2014). Water availability determines the richness and density of fig trees within Brazilian semideciduous forest landscapes. Acta Oecologica 57: 109–116.
- Cottee-Jones, H.E.W. and Whittaker, R.J. (2015). Felling Ficus: the cultural status of fig trees in a Rural Assamese Community, India. Ethnobiology Letters 6 (1): 89–98.
- Danjon, F., Fourcaud, T., and Bert, D. (2005). Root architecture and wind-firmness of mature Pinus pinaster. New Phytologist 168 (2): 387–400.
- Davis, M.J.M., Tenpierik, M.J., Ramirez, F.R., and Perez, M.E. (2017). More than just a Green Facade: the sound absorption properties of a vertical garden with and without plants. Building and Environment 116: 64–72.
- Deng, L.J. and Deng, Q.H. (2018). The basic roles of indoor plants in human health and comfort. Environmental Science and Pollution Research 25 (36): 36087–36101.
- Duke, N.C., Ball, M.C., and Ellison, J.C. (1998). Factors influencing biodiversity and distributional gradients in mangroves. Global Ecology and Biogeography Letters 7 (1): 27–47.
- Durigon, J., Durán, S.M., and Gianoli, E. (2013). Global distribution of root climbers is positively associated with precipitation and negatively associated with seasonality. Journal of Tropical Ecology 29 (4): 357–360.
- Eamus, D., Macinnis-Ng, C.M.O., Hose, G.C. et al. (2005). Ecosystem services: an ecophysiological examination. Australian Journal of Botany 53 (1): 1–19.
- Elster, C. and Perdomo, L. (1999). Rooting and vegetative propagation in Laguncularia racemosa. Aquatic Botany 63 (2): 83–93.
- Erndwein, L., Ganji, E., Killian, M.L., and Sparks, E.E. (2019). Comparative biomechanical characterization of maize brace roots within and between plants. bioRxiv 547794.
- Evans, L.S., Okawa, Y., and Searcy, D.G. (2005). Anatomy and morphology of red mangrove Rhizophora mangle plants in relation to internal airflow. Journal of the Torrey Botanical Society 132 (4): 537–550.
- Evans, L.S., de Leon, M.F., and Sai, E. (2008). Anatomy and morphology of Rhizophora stylosa in relation to internal airflow and Attim's plant architecture. Journal of the Torrey Botanical Society 135 (1): 114–125.
- Gao, Y. and Lynch, J.P. (2016). Reduced crown root number improves water acquisition under water deficit stress in maize (Zea mays L.). Journal of Experimental Botany 67 (15): 4545–4557.
- Gill, C.J. (1975). The ecological significance of adventitious rooting as a response to flooding in woody species, with special reference to Alnus glutinosa (L.) Gaertn. Flora 164 (1): 85–97.
- Gill, A.M. and Tomlinson, P.B. (1969). Studies on the growth of red mangrove (Rhizophora mangle L.) I. Habit and general morphology. Biotropica 1 (1): 1–9.
10.2307/2989744 Google Scholar
- Gill, A.M. and Tomlinson, P.B. (1971). Studies on the growth of red mangrove (Rhizophora mangle L.) 2. Growth and differentiation of aerial roots. Biotropica 3 (1): 63–77.
- Gill, A.M. and Tomlinson, P.B. (1977). Studies on the growth of red mangrove (Rhizophora mangle L.) 4. The Adult root system. Biotropica 9 (3): 145–155.
- Golley, F.B., Child, G.I., McGinnis, J.T. et al. (1969). The structure of tropical forests in Panama and Colombia. BioScience 19 (8): 693–696.
- Gotsch, S.G., Nadkarni, N., and Amici, A. (2016). The functional roles of epiphytes and arboreal soils in tropical montane cloud forests. Journal of Tropical Ecology 32 (5): 455–468.
- Groot, E.P., Sweeney, E.J., and Rost, T.L. (2003). Development of the adhesive pad on climbing fig (Ficus pumila) stems from clusters of adventitious roots. Plant and Soil 248 (1): 85–96.
- Hamada, A. and Hanya, G. (2016). Frugivore assemblage of Ficus superba in a warm-temperate forest in Yakushima, Japan. Ecological Research 31 (6): 903–911.
- Hao, G.-Y., Sack, L., Wang, A.-Y. et al. (2010). Differentiation of leaf water flux and drought tolerance traits in hemiepiphytic and non-hemiepiphytic Ficus tree species. Functional Ecology 24 (4): 731–740.
- Hao, G.-Y., Goldstein, G., Sack, L. et al. (2011). Ecology of hemiepiphytism in fig species is based on evolutionary correlation of hydraulics and carbon economy. Ecology 92 (11): 2117–2130.
- Hao, G.-Y., Wang, A.-Y., Sack, L. et al. (2013). Is hemiepiphytism an adaptation to high irradiance? Testing seedling responses to light levels and drought in hemiepiphytic and non-hemiepiphytic Ficus. Physiologia Plantarum 148 (1): 74–86.
- Harrison, R.D. (2005). Figs and the diversity of tropical rainforests. BioScience 55 (12): 1053–1064.
- Herwitz, S.R. (1991). Aboveground adventitious roots and stemflow chemistry of Ceratopetalum virchowii in an Australian montane tropical rain forest. Biotropica 23 (3): 210–218.
- Hinchee, M.A.W. (1981). Morphogenesis of aerial and subterranean roots of Monstera deliciosa. Botanical Gazette 142 (3): 347–359.
- Hochholdinger, F., Yu, P., and Marcon, C. (2018). Genetic control of root system development in maize. Trends in Plant Science 23 (1): 79–88.
- Holbrook, N.M. and Putz, F.E. (1996a). From epiphyte to tree: differences in leaf structure and leaf water relations associated with the transition in growth form in eight species of hemiepiphytes. Plant, Cell & Environment 19 (6): 631–642.
- Holbrook, N.M. and Putz, F.E. (1996b). Water relations of epiphytic and terrestrially-rooted strangler figs in a Venezuelan palm savanna. Oecologia 106 (4): 424–431.
- Holder, A.J., McCalmont, J.P., McNamara, N.P. et al. (2018). Evapotranspiration model comparison and an estimate of field scale Miscanthus canopy precipitation interception. Global Change Biology Bioenergy 10 (5): 353–366.
- Hoppe, D.C., McCully, M.E., and Wenzel, C.L. (1986). The nodal roots of Zea: their development in relation to structural features of the stem. Canadian Journal of Botany 64 (11): 2524–2537.
10.1139/b86-335 Google Scholar
- Hsu, C.-C., Horng, F.-W., and Kuo, C.-M. (2002). Epiphyte biomass and nutrient capital of a moist subtropical forest in north-eastern Taiwan. Journal of Tropical Ecology 18 (5): 659–670.
- Huggett, B. and Tomlinson, P.B. (2010). Aspects of vessel dimensions in the aerial roots of epiphytic Araceae. International Journal of Plant Sciences 171 (4): 362–369.
- Jebb, M. (1992). A Field Guide to Pandanus in New Guinea, the Bismarck Archipelago and the Solomon Islands. Madang, Papua New Guinea: Christensen Research Institute.
- Jose, B., Harikumar, K., Krishnan, P.N., and Satheeshkumar, K. (2016). In vitro mass multiplication of screw pines (Pandanus spp.) – an important costal bio- resource. Journal of Coastal Conservation 20 (6): 443–453.
- Kattan, G.H. and Valenzuela, L.A. (2013). Phenology, abundance and consumers of figs (Ficus spp.) in a tropical cloud forest: evaluation of a potential keystone resource. Journal of Tropical Ecology 29 (5): 401–407.
- King, D.A. (1996). Allometry and life history of tropical trees. Journal of Tropical Ecology 12 (1): 25–44.
- Kitaya, Y., Yabuki, K., Kiyota, M. et al. (2002). Gas exchange and oxygen concentration in pneumatophores and prop roots of four mangrove species. Trees 16 (2): 155–158.
- Köhler, L., Tobón, C., Frumau, K.F.A., and Bruijnzeel, L.A. (2007). Biomass and water storage dynamics of epiphytes in old-growth and secondary montane cloud forest stands in Costa Rica. Plant Ecology 193 (2): 171–184.
- Kohlmeyer, J. (1969). Ecological notes on fungi in Mangrove forests. Transactions of the British Mycological Society 53 (2): 237–250.
10.1016/S0007-1536(69)80058-6 Google Scholar
- Komiyama, A., Poungparn, S., and Kato, S. (2005). Common allometric equations for estimating the tree weight of mangroves. Journal of Tropical Ecology 21 (4): 471–477.
- Lopez-Portillo, J., Ewers, F.W., Angeles, G., and Fisher, J.B. (2000). Hydraulic architecture of Monstera acuminata: evolutionary consequences of the hemiepiphytic growth form. New Phytologist 145 (2): 289–299.
- Lovelock, C.E., Simpson, L.T., Duckett, L.J., and Feller, I.C. (2015). Carbon budgets for Caribbean mangrove forests of varying structure and with phosphorus enrichment. Forests 6 (10): 3528–3546.
- Machado, A.F.P., Rønsted, N., Bruun-Lund, S. et al. (2018). Atlantic forests to the all Americas: biogeographical history and divergence times of Neotropical Ficus (Moraceae). Molecular Phylogenetics and Evolution 122: 46–58.
- Maniou, F., Chorianopoulou, S.N., and Bouranis, D.L. (2014). New insights into trophic aerenchyma formation strategy in maize (Zea mays L.) organs during sulfate deprivation. Frontiers in Plant Science 5.
- Martínez-Vilalta, J., Prat, E., Oliveras, I., and Piñol, J. (2002). Xylem hydraulic properties of roots and stems of nine Mediterranean woody species. Oecologia 133 (1): 19–29.
- Matthews, T.J., Cottee-Jones, H.E.W., Bregman, T.P., and Whittaker, R.J. (2017). Assessing the relative importance of isolated Ficus trees to insectivorous birds in an Indian human-modified tropical landscape. Biodiversity and Conservation 26 (12): 2803–2819.
- McCully, M.E. and Canny, M.J. (1985). Localisation of translocated 14C in roots and root exudates of field-grown maize. Physiologia Plantarum 65 (4): 380–392.
- McKee, K.L. (1993). Soil physicochemical patterns and mangrove species distribution—reciprocal effects? Journal of Ecology 81 (3): 477–487.
- Melzer, B., Steinbrecher, T., Seidel, R. et al. (2010). The attachment strategy of English ivy: a complex mechanism acting on several hierarchical levels. Journal of the Royal Society Interface 7 (50): 1383–1389.
- Melzer, B., Seidel, R., Steinbrecher, T., and Speck, T. (2012). Structure, attachment properties, and ecological importance of the attachment system of English ivy (Hedera helix). Journal of Experimental Botany 63 (1): 191–201.
- Méndez-Alonzo, R., Moctezuma, C., Ordoñez, V.R. et al. (2015). Root biomechanics in Rhizophora mangle: anatomy, morphology and ecology of mangrove's flying buttresses. Annals of Botany 115 (5): 833–840.
- Meunier, F., Zarebanadkouki, M., Ahmed, M.A. et al. (2018). Hydraulic conductivity of soil-growth lupine and maize unbranched roots and maize root-shoot junctions. Journal of Plant Physiology 227: 31–44.
- Meyer, C.F.J. and Zotz, G. (2004). Do growth and survival of aerial roots limit the vertical distribution of hemiepiphytic aroids? Biotropica 36 (4): 483–491.
- Moore, P.D. (1989). Upwardly mobile roots. Nature 341: 188.
- Nadkarni, N.M. (1981). Canopy roots: convergent evolution in rainforest nutrient cycles. Science 214 (4524): 1023–1024.
- Nadkarni, N.M. and Primack, R.B. (1989). A comparison of mineral uptake and translocation by above-ground and below-ground root systems of Salix syringiana. Plant and Soil 113 (1): 39–45.
- Naidoo, G., Naidoo, Y., and Achar, P. (2010). Responses of the mangroves Avicennia marina and Bruguiera gymnorrhiza to oil contamination. Flora – Morphology, Distribution, Functional Ecology of Plants 205 (5): 357–362.
10.1016/j.flora.2009.12.033 Google Scholar
- Nicoll, B.C. and Ray, D. (1996). Adaptive growth of tree root systems in response to wind action and site conditions. Tree Physiology 16 (11–12): 891–898.
- Niklas, K.J. (1995). Size-dependent allometry of tree height, diameter and trunk-taper. Annals of Botany 75 (3): 217–227.
- Ola, A., Gauthier, A.R.G., Xiong, Y., and Lovelock, C.E. (2019). The roots of blue carbon: responses of mangrove stilt roots to variation in soil bulk density. Biology Letters 15 (3): 20180866. doi: 10.1098/rsbl.2018.0866.
- Ong, J.E., Gong, W.K., and Wong, C.H. (2004). Allometry and partitioning of the mangrove, Rhizophora apiculata. Forest Ecology and Management 188 (1): 395–408.
- Orians, C.M., van Vuuren, M.M.I., Harris, N.L. et al. (2004). Differential sectoriality in long-distance transport in temperate tree species: evidence from dye flow, 15N transport, and vessel element pitting. Trees 18 (5): 501–509.
- Pi, N., Tam, N.F.Y., Wu, Y., and Wong, M.H. (2009). Root anatomy and spatial pattern of radial oxygen loss of eight true mangrove species. Aquatic Botany 90 (3): 222–230.
- Plowden, C., Uhl, C., and Oliveira, F.A. (2003). The ecology and harvest potential of titica vine roots (Heteropsis flexuosa: Araceae) in the eastern Brazilian Amazon. Forest Ecology and Management 182 (1): 59–73.
- Rodriguez-Dominguez, C.M., Carins Murphy, M.R., Lucani, C., and Brodribb, T.J. (2018). Mapping xylem failure in disparate organs of whole plants reveals extreme resistance in olive roots. New Phytologist 218 (3): 1025–1035.
- Rollon, R.N., Villamayor, B.M.R., Oropesa, L.J.B., and Samson, M.S. (2017). Prop root production response of planted Rhizophora to abrupt subsidence-induced sea level rise. Ocean & Coastal Management 142: 198–208.
- Sandifer, P.A., Sutton-Grier, A.E., and Ward, B.P. (2015). Exploring connections among nature, biodiversity, ecosystem services, and human health and well-being: opportunities to enhance health and biodiversity conservation. Ecosystem Services 12: 1–15.
- Sanford, R.L. (1987). Apogeotropic roots in an Amazon rain forest. Science 235 (4792): 1062–1064.
- Santini, N.S., Schmitz, N., Bennion, V., and Lovelock, C.E. (2013). The anatomical basis of the link between density and mechanical strength in mangrove branches. Functional Plant Biology 40 (4): 400–408.
- Schenk, H.J., Espino, S., Goedhart, C.M. et al. (2008). Hydraulic integration and shrub growth form linked across continental aridity gradients. Proceedings of the National Academy of Sciences 105 (32): 11248–11253.
- Schmitz, N., Egerton, J.J.G., Lovelock, C.E., and Ball, M.C. (2012). Light-dependent maintenance of hydraulic function in mangrove branches: do xylary chloroplasts play a role in embolism repair? New Phytologist 195 (1): 40–46.
- Scholander, P.F., van Dam, L., and Scholander, S.I. (1955). Gas exchange in the roots of mangroves. American Journal of Botany 42 (1): 92–98.
- Schwarzbach, A.E. and Ricklefs, R.E. (2000). Systematic affinities of Rhizophoraceae and Anisophylleaceae, and intergeneric relationships within Rhizophoraceae, based on chloroplast DNA, nuclear ribosomal DNA, and morphology. American Journal of Botany 87 (4): 547–564.
- Shane, M.W. and McCully, M.E. (1999). Root xylem embolisms: implications for water flow to the shoot in single-rooted maize plants. Functional Plant Biology 26 (2): 107–114.
- Shane, M.W., McCully, M.E., and Canny, M.J. (2000a). Architecture of branch-root junctions in Maize: structure of the connecting xylem and the porosity of pit membranes. Annals of Botany 85 (5): 613–624.
- Shane, M.W., McCully, M.E., and Canny, M.J. (2000b). The vascular system of maize stems revisited: implications for water transport and xylem safety. Annals of Botany 86 (2): 245–258.
- Sideris, C.P., Krauss, B.H., and Young, H.Y. (1937). Assimilation of ammonium and nitrate nitrogen from solution cultures by roots of Pandanus veitchii Hort, and distribution of the various nitrogen fractions and sugars in the stele and cortex. Plant Physiology 12 (4): 899–928.
- Simard, M., Fatoyinbo, L., Smetanka, C. et al. (2019). Mangrove canopy height globally related to precipitation, temperature and cyclone frequency. Nature Geoscience 12 (1): 40–45.
- Soreanu, G., Dixon, M., and Darlington, A. (2013). Botanical biofiltration of indoor gaseous pollutants – a mini-review. Chemical Engineering Journal 229: 585–594.
- Steffens, B. and Rasmussen, A. (2016). The physiology of adventitious roots. Plant Physiology 170 (2): 603–617.
- Steinbrecher, T., Danninger, E., Harder, D. et al. (2010). Quantifying the attachment strength of climbing plants: a new approach. Acta Biomaterialia 6 (4): 1497–1504.
- Suresh, H.S. and Sukumar, R. (2018). Phenology of Ficus spp. in a tropical dry forest, Mudumalai, south India. Journal of Forestry Research 29 (4): 1129–1138.
- Swagel, E.N., Bernhard, A.V.H., and Ellmore, G.S. (1997). Substrate water potential constraints on germination of the strangler fig Ficus aurea (Moraceae). American Journal of Botany 84 (5): 716–722.
- Tanaka, N., Nandasena, N.A.K., Jinadasa, K. et al. (2009). Developing effective vegetation bioshield for tsunami protection. Civil Engineering and Environmental Systems 26 (2): 163–180.
- Thorn, A.M. and Orians, C.M. (2011). Patchy nitrate promotes inter-sector flow and 15N allocation in Ocimum basilicum: a model and an experiment. Functional Plant Biology 38 (11): 879–887.
- Tomlinson, P.B. (1986). The Botany of Mangroves. Cambridge, UK: Cambridge University Press.
- Twilley, R.R. and Chen, R. (1998). A water budget and hydrology model of a basin mangrove forest in Rookery Bay, Florida. Marine and Freshwater Research 49 (4): 309–323.
- Van Deynze, A., Zamora, P., Delaux, P.M. et al. (2018). Nitrogen fixation in a landrace of maize is supported by a mucilage-associated diazotrophic microbiota. PLoS Biology 16 (8).
- Vanhoutte, B., Schenkels, L., Ceusters, J., and De Proft, M.P. (2017). Water and nutrient uptake in Vriesea cultivars: trichomes vs. roots. Environmental and Experimental Botany 136: 21–30.
- Wanek, W., Hofmann, J., and Feller, I.C. (2007). Canopy interactions of rainfall in an off-shore mangrove ecosystem dominated by Rhizophora mangle (Belize). Journal of Hydrology 345 (1): 70–79.
- Wang, Y.F., Bakker, F., de Groot, R., and Wortche, H. (2014). Effect of ecosystem services provided by urban green infrastructure on indoor environment: a literature review. Building and Environment 77: 88–100.
- Werner, F.A., Homeier, J., Oesker, M., and Boy, J. (2011). Epiphytic biomass of a tropical montane forest varies with topography. Journal of Tropical Ecology 28 (1): 23–31.
- Wiengweera, A. and Greenway, H. (2004). Performance of seminal and nodal roots of wheat in stagnant solution: K+ and P uptake and effects of increasing O2 partial pressures around the shoot on nodal root elongation. Journal of Experimental Botany 55 (405): 2121–2129.
- Yang, X. and Deng, W. (2017). Morphological and structural characterization of the attachment system in aerial roots of Syngonium podophyllum. Planta 245 (3): 507–521.
- Youssef, T. and Saenger, P. (1996). Anatomical adaptive strategies to flooding and rhizosphere oxidation in mangrove seedlings. Australian Journal of Botany 44 (3): 297–313.
- Yu, P., Li, X., Yuan, L., and Li, C. (2014). A novel morphological response of maize (Zea mays) adult roots to heterogeneous nitrate supply revealed by a split-root experiment. Physiologia Plantarum 150 (1): 133–144.
- Yu, P., Hochholdinger, F., and Li, C. (2015). Root-type-specific plasticity in response to localized high nitrate supply in maize (Zea mays). Annals of Botany 116 (5): 751–762.
- Zanne, A.E., Sweeney, K., Sharma, M., and Orians, C.M. (2006). Patterns and consequences of differential vascular sectoriality in 18 temperate tree and shrub species. Functional Ecology 20 (2): 200–206.
- Zhang, M., Liu, M., Prest, H., and Fischer, S. (2008). Nanoparticles secreted from ivy rootlets for surface climbing. Nano Letters 8 (5): 1277–1280.
- Zheng, J., Fan, J.L., Zhang, F.C. et al. (2018). Mulching mode and planting density affect canopy interception loss of rainfall and water use efficiency of dryland maize on the Loess Plateau of China. Journal of Arid Land 10 (5): 794–808.
- Zheng, J., Fan, J.L., Zhang, F.C. et al. (2019). Throughfall and stemflow heterogeneity under the maize canopy and its effect on soil water distribution at the row scale. Science of the Total Environment 660: 1367–1382.
- Zotz, G. (2013). The systematic distribution of vascular epiphytes – a critical update. Botanical Journal of the Linnean Society 171 (3): 453–481.
- Zotz, G. and Winkler, U. (2013). Aerial roots of epiphytic orchids: the velamen radicum and its role in water and nutrient uptake. Oecologia 171 (3): 733–741.
- Zotz, G., Patiño, S., and Tyree, M.T. (1997). Water relations and hydraulic architecture of woody hemiepiphytes. Journal of Experimental Botany 48 (10): 1825–1833.
Citing Literature
Browse other articles of this reference work: