Abstract
Excessively water saturates the soil pores and creates waterlogging when there is indeed no or very thin coating of water present on the soil. Waterlogging typically causes changes in gene expression that affect a plant’s physiology, metabolism, and anatomy. Crops respond to and adapt to waterlogging stress in a variety of ways, including the development of aerenchyma, adventitious root development, metabolism of energy, and plant-hormone signaling. One of the most damaging abiotic stresses that annually destroys 17 million km2 of land, along with drought, is floods. Recent studies have found that increased extreme weather events, like flooding and soil waterlogging, brought on by climate change are having a substantial influence on agricultural productivity. Because of this, it is essential to understand how crops are impacted by flooding stresses and to develop better production methods that boost cropping systems’ resistance and ability to endure extreme climate events. Potential management strategies that can be utilized to alleviate the stress brought on by soil waterlogging include the adoption of waterlogging-tolerant varieties, altering administration practices, improving permeability, and putting adaptive nutritional monitoring systems into place. These management approaches, which may be crop- or site-specific, should be assessed for their commercial feasibility before developing future implementation strategies that enable sustainable agricultural output from waterlogged soils.
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1 Introduction
Water facilitates plant development and functions, making it essential to a plant’s life. However, plants are put in danger by flooding or waterlogging (Normile 2008). As seen in Fig. 1, the condition known as “waterlogging” occurs when a whole or a plant portion is completely under water (Bailey-Serres et al. 2012). As a result, air pockets in the earth are simply filled, leading to wet conditions. In many plant communities around the world, soil waterlogging is an abiotic (non-living) stress which impacts species composition as well as its production (Jackson and Colmer 2005). Seasonal precipitation as a whole, as well as the differences between and among seasonal precipitation events, have changed due to climatic variations. Extremes in the availability of water have grown more severe globally in farming areas during the past 50 years (Aderonmu 2015; Bailey-Serres et al. 2012). The main causes of waterlogging in Pakistan include inadequate irrigation management techniques, a scarcity of suitable infrastructure for drainage of soils, and the use of low-quality water for irrigation purposes (Hossain 2010). Due to the threat to food security, it is urgent to find low-cost, ecologically friendly ways for managing and reclaiming these soils (Qadir and Oster 2002).
Flooding has a devastating effect on society and the environment. As terrestrial plant species including cultivated crops are susceptible to flood conditions, there is a decline in biodiversity of plants, natural species distribution, and production of food worldwide (Normile 2008). Each year, flooding damages about 17 million km2 of land worldwide, resulting in losses in crop production and serious damage to plants (Voesenek and Sasidharan 2013). Waterlogging or serious soil drainage issues harm between 10% and 12% of the world’s agricultural land (Shabala 2011). The projected annual cost of damage from severe floods that occur all over the world is much more than $74 billion (www.dartmouth.edu/∼floods/Archives/2005sum.htm). According to existing fluctuations in changing climate globally, showing harsh climatic events, the National Aeronautics and Space Administration (NASA) simulation models estimated losses worth $3 billion annually in food production by 2030 (Rosenzweig et al. 2002). Pakistan has experienced exceptional monsoon conditions since June 2022, this month alone received rainfall which was 67% above average levels. As of August 27, the nation had received 2.9-fold as much rain as the 30-year average. A total of two million acres of crops and orchards have also been damaged at this point, including 1.54 million acres in Sindh, Baluchistan is 304,475 acres, and 178,186 acres in Punjab (OCHA 2022). Anatomical, physiological, and metabolic alterations are typically reported as plant responses to wet and flooding situations (Voesenek et al. 2006). Water diffusion, a mode of transportation in a biological system, is thought to be very low for terrestrial plants’ survival for a long duration, which is why flooding causes damage. Essential nutrient deficits and toxicities from micronutrients like Copper (Cu), Iron (Fe), and Manganese (Mn) have an impact on plants (Setter et al. 2006). The primary source of potential energy for plant roots to absorb nutrients is aerobic respiration (Ferreira et al. 2008). These waterlogging effected roots resort to an ineffective anaerobic fermentation, using their present glucose reserves to produce the ATP they require to survive and operate. Continued hypoxia or anoxia impairs root growth and function due to reduced integrity of the membrane, hunger, and phytotoxic chemical diffusion into the root cells (Sauter 2013). Under hypoxic circumstances, the functions of shoots are compromised and may show apparent symptoms like senescence, wilting, and death because the roots are unable to transfer water and nutrients effectively (Sasidharan and Voesenek 2015). In addition, photosynthesis, carbohydrate partitioning, and the production and transport of growth regulators are all significantly impacted (Ferrer et al. 2005). Under waterlogged conditions, these physiological impedances ultimately result in a decreased crop yield.
To maintain root activity and plant survival in susceptible genotypes, waterlogged circumstances may induce and initiate crop tolerance traits or adaptation features that might enhance aeration and mitigate root hypoxia or anoxia. Plant tissues soaked with water produce ethylene (El-Esawi 2016a, b). The activation of genes related to aerenchyma production and adventitious root formation is crucial among the well-explained roles that ethylene plays in waterlogged conditions (Vidoz et al. 2010; Sasidharan and Voesenek 2015). In the shoot, the transport of auxin is reprogrammed by increased ethylene level in the stem, which causes a flow of auxin to be directed toward the submerged stem to start the growth of adventitious roots. Auxin transport inhibition reduces adventitious root development (Vidoz et al. 2010). The formation of suberin or lignin barrier, among other things, in roots in order to prevent loss of O2, and direct its transportation to the tip of the root, were other adaptive traits displayed by resistant crops (Shiono et al. 2011).
Grain growers employ a wide range of crop management techniques to mitigate the impacts of waterlogging. Selection of crops, crop varieties that can withstand waterlogging, bio-drainage, and various agronomic techniques, like sowing season, nutrient application, engineering methods for surface and subsurface drainage, etc., and use of plant growth regulators (PGRs), are among them (Manik et al. 2019).
2 Causes of Soil Waterlogging
The oxygen concentration drops quickly in waterlogged soils because in water diffusion of a gas is several times slower than in air, causing a series of events that are detrimental to the survival of the majority of plant species (Colmer and Greenway 2011). In Asia and America, flooding is the main reason for yield losses, and waterlogging is thought to damage between 10% and 16% of the planet’s cultivable soils (Yaduvanshi et al. 2012). In addition, in response to changing climate, flooding events are anticipated to occur more frequently and more intensely in every part of the planet (Westra et al. 2014). More than 21 Mha of Pakistan’s 79.61 Mha total geographic area where agricultural practices take place. Almost 25% of irrigated area in Punjab province is seriously under waterlogging, but about 60% in Sindh (WAPDA 2007). Soil waterlogging in the plant-rooting zone can be caused by many variables, including the amount of water that enters the soil, the amount that flows over/through the soil’s surface, and the amount of water that is absorbed by plants and other species (Kunkel 2003). Numerous factors, such as soil type, geography, meteorological circumstances, lateral ground water flows, and rising/perched water tables, can cause waterlogging (Fig. 2).
2.1 Extreme Precipitation
The frequency of heavy precipitation events and several rains is a significant factor in an increase in waterlogging or flooding (Kunkel 2003). Extremely rainy years are distinguished from dry years by the amount, frequency, size, and spacing of precipitation events (Knapp et al. 2015). The Intergovernmental Panel on Climate Change (IPCC) predicts that rising emission of greenhouse gas will probably result in more instances of extreme precipitation ahead (Cubasch et al. 2001).
2.2 Human Alteration in Land Use
In addition to rising precipitation frequency and severity, human modifications to stream channels, and land use are other factors contributing to rises in waterlogging (Kunkel 2003).
2.3 Over Irrigation/Rainfall after Irrigation
Soil waterlogging or floods may also be caused by over-irrigation or subsequent rains (Kirkpatrick et al. 2006). Shallow water table, compaction of soil, insufficient internal drainage as well as surface drainage are some of the issues (Kirkpatrick et al. 2006), in soils like heavy clay soils, clay pan, or duplex soil with coarse textured topsoil over compacted clay subsoil (Batey 2009).
2.4 Increased Runoff From Slope
Waterlogging in low-lying areas can result from excessive runoff from steep slope topographical regions, especially if soils there are inadequately drained (Singh et al. 2016).
2.5 Soil Compaction
Waterlogging is caused by poor soil structure resulting from natural processes or human activities, like compaction of soil due to puddling or heavy traffic, which results in shallow elevated ground water within the top few centimeters of soil or the subsurface (Batey 2009). Flooding can occur as a result of soil compaction brought on by tractor wheels movement in a field because it reduces water infiltration, permeability, and flow through the soil profile. Soil compaction can impact crop emergence, germination of seed, and its growth in addition to making roots more resistant to growth. Air movement inside the soil profile is affected by compaction because it rearranges soil particles, changes aggregate stability, bulk density, or arrangement, and affects the structure of soil (Samad et al. 2001).
2.6 Claypan
In situations of heavy precipitation or irrigation, soils with swelling–shrinking clay kinds (heavy clay soils) are vulnerable to soil waterlogging. Heavy clay soils with a high-water retention capacity and poor drainage may swell as the soil reaches its maximum water retention capacity, preventing penetration into the soil profile (Blessitt 2007). Constrictive clay subsoil horizons can be found on over 290 million ha of soil worldwide (USDA-NRCS 2006). In soils with clay pans, the subsoil horizon often suffers a fast, 100% rise in clay concentration in comparison to the soil layers above it over a small vertical distance (Motavalli et al. 2003). Depending on the topography, the claypan layer’s depth could range, from 10 cm at the back slope locations to 40 cm at the front slope locations (Jiang et al. 2007).
2.7 Soil Preparation for Rice
The yield of successive non-rice crops in the rotation is negatively impacted by the breakdown of aggregates of soil also the creation of a hardpan during puddling, and these crops also demand more effort for land preparation (Kumar and Ladha 2011). Additionally, where the field had been puddled for rice, the soil infiltration rates during the wheat season are lower than they were whenever the land had been dry-drilled or maintained in no (Singh et al. 2011). Preparation of soil for rice (Oryza sativa L.) cultivate causes compaction of subsurface, leading to low drainage, as a result, waterlogging issues in crops like wheat in Asian countries (Samad et al. 2001).
3 Why Did Waterlogging Conditions Develop in Pakistan?
Pakistan is blessed with an abundance of water sources, including enormous rivers, tributaries, rivulets, and hill torrents, as well as significant underground water reservoirs that are known for their tall snow- and ice-covered mountain summits. The Indus irrigation system utilizes a large river and rainwater, which may help irrigate vast amounts of potentially fertile agricultural land (Aslam et al. 2015). Pakistan’s economy is largely agrarian just because of that. Major crop yields, however, are much lower than any of those attained by other developing nations worldwide. Table 1 provides information on crop output (year) deficiency in the Indus Basin. Various soil, water, and management techniques, inadequate floods and spoor water management procedures, inadequate irrigation inputs of good quality water, and an insufficient drainage system could all be to blame for this (Aslam et al. 2015).
In Pakistan, irrigated agriculture is primarily limited to the Indus plains, where it has grown as a result of utilizing the main water resources the nation has to offer. Adjoining Indus Basin irrigates a total of 16 million acres. In the 1960, Indus Water Treaty, Pakistan has access to 181 × 109 m3 of water, or around 75% of the yearly available flow, from the Indus River system (Reinsch and Pearce 2005). Due to the rising depth of groundwater levels (>15 m), growers must transition, from tiny tubewells operated by diesel to powerful engines run by electricity or diesel. The majority of tubewell was driven by electricity, installations took place in the 1970s and 1980s, a time when the government offered installation cost incentives. Early in the 1990s, the government stopped providing subsidies due to rising energy costs, which caused the development of electric tubewells to stop and the number of diesel-powered tubewells to rise. Recent estimates indicate that tubewells powered by electricity are just 13%, with the remaining 85% being powered by diesel engines of various sizes (Qureshi et al. 2003). Fresh groundwater is readily available on demand, which has helped farmers attain stable and predictable yields while coping with the fluctuations in surface water supply (WAPDA 2003). To prevent a rise in the groundwater table in semiarid and arid areas, draining is seen as a complementary activity to irrigation. However, even though irrigation development has advanced significantly, Pakistan has never prioritized the building of drainage infrastructure. Due to the constant seepage over time from unlined clay canals, a wide number of distributing channels, irrigated fields infiltration losses, groundwater levels are rising in most of the canal command regions as a result of this carelessness. In large irrigated regions, the groundwater table quickly increased within about 1.5 m of the surface of the soil (WAPDA 2007).
4 Waterlogging Stress: Physiological and Metabolic Processes in Plants
Waterlogging has been related to the number of responses shown by plants that are frequently speculative (Parent et al. 2008; Shaw et al. 2013). Oxygen transport rate in root tissues is significantly slowed down (104 times) by waterlogging in mesophytes. Ethylene, which is produced from its precursor ACC transferred from roots, regulates apoptosis induction in specific tissues and cells, nodal adventitious root formation, the creation of air chambers, metabolic variations during anaerobesis, also several other tasks (Subbaiah and Sachs 2003).
4.1 Oxygen Deprivation
Lack of oxygen caused by excessive water negatively impacts root and shoot development, photosynthesis, hydraulic conductivity, and nutrient uptake. The flow of oxygen to the soil, roughly 3 lac 20 thousand folds lesser pore spaces filled with water when compared to one filled with gas, and in water the oxygen diffusion rate compared to air is about 1/10,000th (Armstrong and Drew 2002; Colmer and Flowers 2008). Compared to air, gas diffusion in water is 104 folds slower, and O2 deprivation is a primary barrier to waterlogging stress (Bailey-Serres and Voesenek 2008). Reduced O2 availability slows down plant respiration and ATP synthesis, which inhibits root development (Bailey-Serres and Voesenek 2010). Decreased respiration and Adenosine Tri Phosphate production loss in wet roots are the causes of plant wilting (Sairam et al. 2008). Glycolysis uses glucose as its main fuel to provide energy for plant reproduction and growth through downstream processes including respiration (Galant et al. 2015). During respiration, glucose enters the pathway of glycolysis to create two molecules of ATP and pyruvate. Then, as a component of the TCA cycle (tricarboxylic acid), pyruvate burns to produce CO2 and H2O and high energy (36 ATP) in the mitochondria. Figure 3 illustrates the formation of ethanol on cytoplasm from pyruvate under hypoxic conditions, generating two ATP molecules (Sauter 2013). Waterlogged maize, rice, wheat, and barley showed energy deficiency-related restriction of root development. A study on barley and wheat for 11 days (waterlogged treatment) indicated that the growth of roots and shoots considerably decreased (Steffens et al. 2005). In comparison to plants with good drainage, wet shoots, and roots had significantly lower dry weights and root/shoot ratios (Araki et al. 2012). Waterlogging in maize slowed root senescence, which significantly reduced the roots and shoots dry weight (Ren et al. 2016a, b, c). In addition, both lowland and highland rice types’ dry weight and root elongation were reduced by hypoxia (Liu et al. 2020b). Waterlogged plants’ poor root development also reduced their ability to absorb water and nutrients (Ren et al. 2016a, b, c).
4.2 Photosynthesis Rate
Waterlogging stress on crops reduces their photosynthetic rate because of closure of stomata, the conductance of mesophyll, degradation of chlorophyll, disruption to photosystem II, also decreased activity of photosynthetic enzymes (Ploschuk et al. 2018). Photosynthetic enzyme activity is further decreased with a prolonged waterlogging duration. Reduction in photosynthesis during flooding circumstances was shown to be caused by stomatal closure, which was found to be associated with the CO2 exchange rate and transpiration (Irfan et al. 2010). Chlorophyll fluorescence metrics can be used to determine the various photosynthesis activities that took place in PS II including light absorption, photochemical reactions, and energy transfer (Ashraf et al. 2011). Normal leaf photosynthesis depends on the function of the chloroplast structure in mesophyll cells, which has been discovered to be damaged in waterlogged maize (Ren et al. 2016a, b, c). This damage persistently prevents photosynthetic electron transport (Yordanova and Popova 2007). After 6 h of waterlogging treatment, the photosynthesis rate of barley plants (waterlogged) initially fell by 40% (Ploschuk et al. 2018).Waterlogged treatment for 5 days, a substantial reduction of photosynthetic rate occurred and RuBisCo activity (ribulose-1.5-bisphosphate carboxylase) in barley (Yordanova and Popova 2001). Although rice is a crop that can withstand flooding, it also showed a 50% reduction in the rate of photosynthesis following an anoxic treatment of four days (Mustroph and Albrecht 2003). Flooding stress decreased soybean chlorophyll concentration by 18–34%. (Mutava et al. 2015). The maize leaf area index decreased as the period of waterlogging increased (Liu et al. 2013). Respiratory activity of wheat roots, photosynthetic rate, leaf greenness (SPAD reading), transpiration rate, grain production, number of grains per spike, stomatal conductance, and weight of 1000 grain significantly decreased due to flooding during the post-anthesis stage. Yet, the intercellular amount of CO2 rose (Wu et al. 2012). In addition, flooded maize plants had lower chlorophyll (a + b) content and were around 20% smaller than control plants (Yordanova and Popova 2007). During the treatment for waterlogging, RuBisCo activity decreased in maize plants by 20–30% (Yordanova and Popova 2007).
4.3 Root Hydraulic Conductance
Wilting, which results from decreased root water intake and decreased root hydraulic conductance (Lp), is a frequent reaction against waterlogging stress (Herzog et al. 2016). Water absorption capacity is determined by Lp, which is connected with transpiration rate (Tan et al. 2018). Under prolonged waterlogged conditions, the death of root cells decreases Lp through erecting barriers (physical) to the flow of water (Bramley et al. 2010). Aquaporin gating and anaerobic respiration caused by a lack of oxygen are additional causes of a large shift in Lp (Tournaire-Roux et al. 2003). Energy production and cytosolic pH control aquaporin, an essential protein of membrane allowing uptake of water by the development of proteinaceous membrane pores (Aroca et al. 2012). Cellular acidosis, which is brought on by CO2 buildup through respiration and ATP depletion, and aquaporin phosphorylation, which results from these processes, control the reduction of aquaporin gating of wet plant roots (Aroca et al. 2012; Tan et al. 2018). Low-ambient oxygen and waterlogging diminish Lp in plants, but species-specific responses differ based on the water transport channel (Bramley et al. 2010).
There are three methods for transporting water:
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Apoplastic method that is around the protoplasts.
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Synthetic method that is by plasmodesmata.
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Transmembrane/across the membranes.
The transmembrane system is regulated by aquaporins, whereas the apoplastic pathway depends on the structure of the root and the characteristics of the cell wall (Maurel et al. 2015). Under hypoxic conditions, lower hydraulic conductance was discovered in Arabidopsis, maize, and wheat as cellular acidosis impairs the activity of aquaporin (Tan et al. 2018). However, the primary route in other species is apoplastic, thus root Lp is not significantly affected by the decrease in the activity of aquaporin in flooding stress (Tournaire-Roux et al. 2003; Bramley et al. 2010). In addition, morphological modifications in Oryza sativa (rice), like the creation of barriers that prevent O2 transport through roots, may have a deleterious impact on roots’ hydraulic systems (Aroca et al. 2012).
4.4 Nutrient Absorption
Leaf chlorosis is a frequent symptom of waterlogging stress, which encourages early senescence in the leaf to remobilize N (nitrogen) to new leaves. Reduced nitrogen uptake and transport from roots results in the lower nutritional content of waterlogged shoots (Herzog et al. 2016). It accomplishes this by reduced surface, compromised function, decreased PMF (proton motive force), decreased potential of the membrane also decreased loading of xylem (Steffens et al. 2005). Particularly, wheat and barley under waterlogging stress have significantly lower amounts of magnesium (Mg), copper (Cu), phosphorous (P), potassium (K), zinc (Zn), nitrogen (N), and manganese (Mn) (Steffens et al. 2005). When compared to aerated circumstances, wheat seminal roots took up fewer nutrients from stagnant solutions (Wiengweera and Greenway 2004). Within a few minutes, the hypoxia in the barley roots’ mature zone reduced net K+ uptake (Shabala and Pottosin 2014). At various phases of maize growth, Nitrogen assimilation, as well as metabolism, is reduced due to flooding stress (Ren et al. 2017). A physical barrier is created in rice in response to flooding stress in order to prevent O2 passage form the roots, which might reduce roots nutrition absorption capacity, in contrast to waterlogging vulnerable barley, wheat, and maize that exhibited a significant loss in nutrient content (Rubinigg et al. 2002). For roots to absorb nutrients, there are three possible routes (Reichardt and Timm 2012):
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Interception of roots’ haphazard expansion into new soil areas in search of nutrients.
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Mass flow, which represents water movement caused by evaporation and transpiration together with ion transfer to the root surface.
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Diffusion, which is the gradient in chemical potential that encourages the flow of nutrients.
By reducing nutrient interception, in waterlogging stress reduction of growth of roots drastically reduced the potential intake of nutrients (Mancuso and Shabala 2010). The majority of roots of maize (apart from adventitious roots) were not able to take nutrients from ambient soil under waterlogging treatment for 6 days (Qiu et al. 2007). The majority of nutritional absorption relies on diffusion and is fueled by proton motive force and membrane potential, both of which are suppressed during conditions of waterlogging stress. Limited ATP supply resulted in a depolarized plasma membrane, reduced proton motive force, and impaired activity of the plasma membrane proton-pumping ATPase, all of which lowered the cytoplasmic pH. (Mancuso and Shabala 2010). With the help of plasma membrane H + -ATPase, ions that the roots have taken up are transferred to the shoot through the xylem. Waterlogged situations, inhibit xylem transport due to a decrease in H + - ATPase in the parenchyma of the xylem, which constantly lowers the shoot’s nutritional content in waterlogged plants (Colmer and Greenway 2011).
5 Anatomical Adaptation
5.1 Formation of Aerenchyma
An air tissue in some plants’ adventitious roots creates gaps between cells and does gaseous transportation between roots and shoots, a typical adaptive characteristic linked to the ability to withstand waterlogging (Colmer 2003). Two distinct forms of aerenchyma, schizogenous, and lysigenous, are produced when cells are separated and then lysed, respectively. The cortex of roots of the majority of cereal crops, such as wheat, maize, barley, and rice develops lysigenous aerenchyma (Yamauchi et al. 2013). Lysigenous aerenchyma for wetland plant rice develops constitutively including well soil conditions and rises in wet situations. However, the aerenchyma production in barley, maize, wheat, and other terrestrial plants is only brought on due to moisture stress (Yamauchi et al. 2011). Following 7 days of flood treatment, aerenchyma was found in mature root zones of barley in the tolerant cultivars at a distance of around 6 cm from the root apex (Zhang et al. 2015). According to a study on maize, under conditions of waterlogging, cell death began at 10 mm from the tips and was fully developed at 30–40 mm from the tips (Evans 2004). Higher root porosity and the production of aerenchyma are significant adaptive features that contribute to the ability to withstand waterlogging (Setter and Waters 2003). By starting planned death in cells of particular cell types, ROS abbreviated as reactive oxygen species and the phytohormone ethylene in gaseous form are associated with lysigenous aerenchyma formation. Due to obstruction of gas transport to the rhizosphere and the increased ethylene production caused by waterlogging stress, ethylene builds up in roots (Yamauchi et al. 2018). In response to the stress of waterlogging, antioxidant defense systems are used to combat the harmful consequences of ROS build up (Ashraf et al. 2011).
5.2 Adventitious Root Growth
Seminal root growth is inhibited in wet plants, which results in a lower root/shoot ratio. There are two main plant root types: seminal roots and adventitious roots. Comparatively to seminal roots, which only have a fully developed main root axis, adventitious roots have much more core metaxylem and cortical cell layers (Knipfer and Fricke 2011). As seen in Fig. 4, waterlogged plants frequently respond by forming adventitious roots, which can substitute the damaged seminal roots and produce more aerenchyma to increase the capacity for inner O2 delivery. In trials conducted in greenhouses, seedlings of Zea mays ssp. huehuetenangensis displayed higher adaptation toward submersion with adventitious root formation (Mano et al. 2005). The number of adventitious roots in barley genotypes (tolerant) after 21 days of waterlogging treatment was significantly higher than that in genotypes that were sensitive (Luan et al. 2018a, b). Aerenchyma was found to occupy 20–22% and 19%, respectively, of adventitious roots of wheat and barley (Ploschuk et al. 2018). A study on rice discovered that the hormone auxin gradient in root tips determines the adventitious root growth direction (Lin and Sauter 2019). Adventitious roots extend upward to get closer to the oxygen-rich water surface to help with water and nutrient absorption from the top layer of the moist soil (Jia et al. 2021; Steffens and Rasmussen 2016). Additionally, as it develops at the stem nodes, adventitious roots can shorten the distance that oxygen is transported between shoots and roots (Steffens and Sauter 2009). Epidermal cell death induced by ROS and ethylene promotes the formation of adventitious roots from the epidermis of the node (Nguyen et al. 2018a, b).
5.3 Radial Oxygen Loss (ROL) Barrier
Radial Oxygen Loss barrier, yet some other crucial response characteristic in order to deal with stresses like waterlogging in addition to aerenchyma formation. An apoplastic barrier called the ROL barrier, which is found in the outer root cell layer stops oxygen from escaping into the anaerobic environment (Yamauchi et al. 2018). In general, rice generates ROL barriers in waterlogged or stagnant conditions, whereas flooding-sensitive cereals like barley, wheat, and maize don’t (Ejiri et al. 2021). Under hypoxic soil, the ROL barrier enables a plant to maintain high quantities of oxygen at the tips of its roots (Abiko et al. 2012). The development of lignified sclerenchyma and suberized hypodermis in roots regulates ROL (Watanabe et al. 2013). Light ROL barrier development was stimulated for flooding-resistant Zea nicaraguensis (wild maize), and lignin and suberin, found in inner and outer layers, orderly (Watanabe et al. 2017). Rice roots’ basal region can be shown to have both suberized and lignified cells after two to three weeks of waterlogging (Soukup et al. 2007). Figure Microarray analysis on rice adventitious roots showed during the construction of the ROL barrier, numerous putative genes connected to suberin biosynthesis were highly elevated, while only a small number of genes related to lignin production were induced (Shiono et al. 2011). Malic acid and long-chain fatty acids are connected to the production of suberin, according to metabolite analyses of rice adventitious roots. Malic acid and long-chain fatty acids accumulated during ROL growth (Kulichikhin et al. 2014). Lysigenous aerenchyma is continuously produced under drained soil conditions, but barriers to ROL are not established, which lowers O2 diffusion towards the apical portion. On the other hand, lysigenous aerenchyma development is accelerated, and the construction of the barrier to ROL is stimulated in wet soil conditions, which promotes longitudinal O2 diffusion to the root apex. Figure 5 shows how the basal region of the roots constitutively produces lysigenous aerenchyma (a) under drained circumstances of soil, typically not produced at the apical root part (b). At the basal region, lysigenous aerenchyma is formed (c) and the apical part (d) of roots in wet soil conditions. The roots’ basal (a, c) compared to its apical portion, the lysigenous aerenchyma is much more developed (b, d). The O2 availability is shown by the thickness of the arrow. In barley waterlogging tolerant cultivars, lignin deposition under waterlogging stressors greatly increased the activity of the enzyme caffeic acid o-methyltransferase (COMT), which is associated with the formation of lignin (Luan et al. 2018a).
6 Signaling and Response to the Stress of Waterlogging
6.1 Phytohormone Signaling
Under conditions of waterlogging, ethylene, an essential phytohormone that controls plant development and senescence, was shown to accumulate (Iqbal et al. 2017). The development of a plant root barrier that restricts ethylene diffusion leads to ethylene buildup (Voesenek and Sasidharan 2013). In addition, it has been discovered that the activity of two enzymes, ACC oxidase, and synthase (1-amino-cyclopropane-1-carboxylic acid), increases due to waterlogging stress (Dat et al. 2004; Broekaert et al. 2006;). Ethephon, an agrochemical that releases ethylene, increased aerenchyma development at the tips of roots and prevented wilting due to waterlogging in barley after pretreatment (Shiono et al. 2019). In order to facilitate plants’ movement of O2 from shoots to roots when there is a lack of oxygen, ethylene controls the creation of gas spaces (aerenchyma) in roots (Steffens and Sauter 2009). In waterlogged maize and barley roots, a transcription level of XET expression was shown to be increased (Luan et al. 2018b). Thus, XET expression and cellulase are induced by ethylene and aid in the production of aerenchyma in roots by dissolving cell walls. Gibberellin (GA), ethylene, and abscisic acid (ABA), significantly play a role in the survival of waterlogged plants by inducing elongation of the shoot. Gibberellic acid encourages elongation between nodes through the breakdown of proteins that are growth inhibitory (Hedden and Sponsel 2015), also through the breaking of starch, releasing cell walls in order to mobilize dietary resources thus enhancing the growth of plants (Else et al. 2009). GA significantly boosts the growth of shoots whereas elongation of roots is inhibited by ABA, acting as antagonists in plants’ reactions to growth stimuli (Dat et al. 2004). After 3 h of the flooded plants receiving the ethylene treatment, GA1 increased four-fold and ABA decreased by 75% in deep-water rice (Vaahtera et al. 2014). The stem node ABA content and gene expression level in ABA production were both decreased in the adventitious roots of flooded wheat. After 3 weeks of waterlogging treatment, ABA content was observed to be reduced in the roots and leaves of varieties of barley (tolerant & sensitive), with a greater decrease in tolerant species (Luan et al. 2018a, b).
6.2 Reactive Oxygen Species Accumulation (ROS)
For crop stress conditions like droughts, salinity, freezing, and mechanical stress, ROS plays a crucial supplementary messenger role, even though they can be harmful to plants because they unrestrictedly oxidize cell components (Mittler 2002; Mhamdi and Van Breusegem 2018). Figure 6 illustrates the primary metabolic adaptations of flooding tolerance of plants as well as stress responses to waterlogging. Different organelles in plants, such as chloroplasts for photosynthesis, mitochondria for respiration, and peroxisomes for photorespiration, all participate in the metabolism of ROS (Foyer and Shigeoka 2011). The breakdown in mitochondria of the electron transport chain during oxygen deprivation results in the production of hydrogen peroxide (H2O2), It acts as a stimulus for epidermal cell death to generate aerenchyma, protecting plants from anaerobic environment stress (Fukao and Bailey-Serres 2004; Steffens et al. 2011; Rajhi et al. 2011). H2O2 treatment increased lysigenous aerenchyma production by processes of cell death in flooded Oryza sativa (rice) (Blokhina et al. 2001). Similarly, under wet conditions, H2O2 accumulation was discovered in the roots of wheat and barley (Yamauchi et al. 2014). ROS accumulation, a trigger for wheat seedlings to respond to waterlogging by controlling gene expression, is associated with fermentation of ethanol (ADH and PDC) and aerenchyma formation (Sumimoto 2008). Respiratory Burst Oxidase Homolog (RBOH), which genes for an NADPH oxidase found in the plasma membrane for the production of H2O2, controls the accumulation of ROS (Steffens 2014).
7 Agronomic Practices to Grow the Crop in Waterlogged Soil
Given how weather-sensitive agronomic crop production is, global climate change has an impact on the agricultural industry (Aderonmu 2015). The amount of seasonal precipitation as a whole, as well as the differences between and within seasonal precipitation events, have changed due to climatic fluctuations. Extremes in water availability, particularly waterlogging, have increased during the past 50 years in agricultural districts all over the globe (Aderonmu 2015; Bailey-Serres et al. 2012). Whenever all or a portion of a plant is submerged in water, the condition is referred to as “flooding” (Bailey-Serres et al. 2012). Figure 7 illustrates suggested procedures for various wet environments. The measures listed below can help you deal with the effects of waterlogging:
8 Modeling of Crops and Decision-Making Systems
Numerous models, such as DRAINMOD, can simulate how crops respond to waterlogging in the soil in terms of growth and yield (Skaggs 2008). These models can be used to determine which places or circumstances will result in a decrease in yield and to evaluate the effect of management practice modifications on the reduction of flooding stress on crop plants. For instance, the Agricultural Production Systems Simulator (APSIM-Wheat) was used in order to predict impacts on wheat due to waterlogging at various dates of the plantation. It was discovered, only in places with a minimal to medium risk of waterlogging will an earlier planting date boost crop output, yet had no effect in areas that frequently experienced waterlogging (Bassu et al. 2009). However, the effectiveness of these simulation models for use in evaluating waterlogging stress depends on how well the processes are represented in them (Shaw et al. 2013). Additionally, remote sensing and GIS are utilized to locate fields’ sensitive areas to soil flooding or dry conditions and can assist in the precise positioning of crops or strategies of management of nutrients thus lessening waterlogging stress. Selectively regions with the greatest nutrient losses, employment of cover crops may lower the cost of planting cover crops and result in financial savings for farmers. For producers to make decisions on the precise placement of various crop management measures to reduce the stress caused by soil waterlogging, they need decision support tools. The Right, Practice, Right, Place (RPRP) Toolbox, which consists of collection preservation strategizing tools online that connect at the local, watersheds, and field level, applying the “right practice of conservation “ to the “right spot” can help increase the efficacy as well as efficiency of efforts to improve quality of the water. (McLellan et al. 2018). Using several BMPs (Best Management Practices), individually /collectively, to reduce the loss of nutrients in crop fields is evaluated using the SWAT (Water Assessment Tool) model (Merriman et al. 2019). Although these decision-support systems have been tested for identifying BMPs for improving the quality of water, yet not been examined in determining how well BMPs mitigate stresses like flooding in various situations. Crop producers can use these models as tools to help them make well-informed choices about the use of techniques of crop management for locations where the chances of waterlogging stress are high. Still no information regarding how to apply these systems for deploying methods for management at individual sites are available (Kaur et al. 2020).
9 Crop Management Practices
9.1 Application of Nutrients
Nutrient deficiency is among the main impacts of waterlogging upon plants, which reduces net carbon fixation and photosynthesis and, eventually, growth and production (Bange et al. 2004). Increased productivity will result from the application of vital nutrients, which will help to lessen the effects of abiotic pressures such as waterlogging (Noreen et al. 2018). N fertilizer applications may increase and speed up a plant’s ability to adapt to waterlogging stress, including root regrowth and adventitious root growth following a flooding event. This may raise a plant’s tolerance to waterlog stress. Due to low O2 during flooding, which may prevent plants from absorbing N, its loss through leaching and denitrification may result in N deficits, decrease nitrogen availability, and restrict root function (Nielsen 2015), as seen in Fig. 8. The application of enhanced-efficiency N fertilizers, such as slow-release or controlled-release (SR/CR) fertilizers, under wet conditions, is crucial for enhancing plant growth and development (Shaviv 2001; Varadachari and Goertz 2010). By coordinating nitrogen release with crop needs, throughout growing crops, slow-release fertilizers can emit nitrogen across a long duration of time, maximizing (NUE) nitrogen use efficiency (Trenkel 2021). Externally applied fertilizers may be effective if the nutrient ions infiltrate the root architecture, enabling plants to heal from waterlogging-related damage, claims many research studies (Ashraf et al. 2011; Habibzadeh et al. 2012; Najeeb et al. 2015). Wheat (Pereira et al. 2017; Zheng et al. 2017), barley (Pang et al. 2007), corn (Kaur et al. 2018), canola (Kaur et al. 2017), and cotton (Wu et al. 2012; Li et al. 2013) are among the crops that are (Habibzadeh et al. 2012). Application of fertilizer also extends the time that the canopy is open and speeds up the development of photo-assimilates that are transferred to grain rather than straw, raising HI (harvest index) (Kisaakye et al. 2015, 2017). Additionally noted that potassium fertilizer can mitigate the negative impacts of waterlogging in a variety of crops, including rapeseed and cotton (Cong et al. 2009; Ashraf et al. 2011). In phosphorous deficiency, during a rainy growing season, external application of different phosphorus (P) sources, such as Meat & Bone Meal (MBM) and Dairy Cow Manure (DCM), is beneficial for providing the highest yields (Ylivainio et al. 2008, 2018). Under flooded conditions, the administration of FYM (Farm Yard Manure), greatly enhanced iron, zinc and copper concentrations in grain (Masunaga and Fong 2018).
Even with high-value crops, the application of fertilizer to prevent waterlogging loss in extensive farming is limited due to the lack of research on their potential benefits for improving crop performance in waterlogged circumstances (Trenkel 2021). To prevent tissue toxicities (such as manganese) and nutrient imbalance from harming soil ecology, it is important to examine the application techniques, nutrient types, timing, and rate that are acceptable (Rochester et al. 2001; Jackson and Ricard 2003).
9.2 Plant Growth Regulator
Applying PGRs at the proper growth stage can reduce the damage that waterlogging causes to plants (Wu et al. 2018; Ren et al. 2018). Plant growth under wet conditions is improved by plant growth regulator administration (Pang et al. 2007; Ren et al. 2016a, b, c). In waterlogged barley, auxin (synthetic) 1-NAA (1-naphthalene acetic acid) encourages adventitious roots formation (Pang et al. 2007), while the external administration of cytokinin 6-BA (6-benzyl adenine) can reduce the effects of waterlogging and boost maize output (Ren et al. 2016a, b, c, 2018). By enhancing leaf photosynthesis, pre-waterlogging ABA foliar treatment enhanced the resistance of cotton plants to subsequent waterlogging-related damage (Pandey et al. 2002; Kim et al. 2018). Triazole is recognized to be a fungus-toxicants, and they also affect how plants respond to stress and regulate their growth (Rademacher 2015). For instance, paclobutrazol reduces the harm caused by waterlogging in sweet potato plants and canola (Lin et al. 2008). 5-methyl-1,2,4-triazole (3,4-b) benzothiazole (Tricyclazole) treatment reduces plant damage when there is waterlogging (Habibzadeh et al. 2013). However, there hasn’t been much usage of plant growth regulators to lessen waterlogging damage due to inconsistent results at the commercial level (Manik et al. 2019).
9.3 Pretreatment with Hydrogen Peroxide
Pre-treating plants with an agent could be a successful method to boost their tolerance to various stresses as shown in Fig. 9. For instance, pretreating crops with H2O2 can shield them from oxidative harm brought on by waterlogging, intense light, chilly weather, salt stress, drought, and heavy metal exposure (Gechev et al. 2002; Rajaeian and Ehsanpour 2015; Andrade et al. 2018). Increases in the diameter of the stem, high accumulation of biomass, the volume of the root, and photosynthetic pigments were also brought about by H2O2 pretreatment (Andrade et al. 2018). H2O2 pretreatment resistant against waterlogging, despite substantial research being done on treatments against both biotic and abiotic stresses, is still in its infancy (Mustafa et al. 2017; Lal et al. 2018; Ashraf et al. 2018).
9.4 Utilization of Tolerant Varieties and Species
Waterlogging tolerance is one of the most effective ways to reduce the loss brought on by flooding in available plant species (Zhou 2010; Wani et al. 2018). There are genetic variations in waterlogging resistance among several crops, including wheat and barley (Zhang et al. 2015; Huang et al. 2015; Herzog et al. 2016; Wu et al. 2018; Nguyen et al. 2018a, b). Waterlogging tolerance, however, is a dynamic condition that is regulated by a diverse range of mechanisms, including the maintenance of membrane potential (Gill et al. 2018), the control of ROS production under stress conditions, resilience to metabolites (Pang et al. 2006), toxicity of ion (Huang et al. 2018), aerenchyma formation in roots under waterlogging stress, and many quantitative trait loci (QTL) (Gill et al. 2018). The identification of genes that are associated with different tolerance mechanisms is crucial for the success of breeding programs because it enables producers to elevate tolerance genes. Depending on the region and the weather, flooding can happen at any stage of the crop’s growth. Waterlogging brought on by heavy rains in the fall can delay crop harvesting, so it’s critical to breeding crop varieties with traits like strong stems, superior seed quality, and reduced sensitivity to diseases and pests. It is important to create variety with tolerance both to cold and floods stress since flooding in the early part of the growing season often subjects crops to cold soil temperatures. In conclusion, it’s critical to create and test novel varieties of crops that are resistant to a variety of biotic or abiotic stresses, such as heat, drought, and waterlogging stress, along with disease vectors (Kaur et al. 2020).
9.5 Adjusting Dates of Planting
In order to encourage favorable crop emergence and development during the initial spring season, planting dates might be modified to minimize waterlogging circumstances. The emergence of crop and plant development vigor can be delayed by cool, damp soils. A short growth period and exposure to dryness subsequently in the planting season may result in decreased crop yields, while later sowing dates may prevent potential initial extreme rainfall events and saturated soil conditions. Droughts that occur over the summer have pushed the dates of the plantation, sooner into the spring (Kucharik 2006). The creation of cultivars resistant to unfavorable weather conditions and diseases, treatment of seed, enhanced plantation tools, crop protection products, and the use of time-saving crop management techniques like conservation tillage are further variables that contribute to early planting dates (Kucharik 2006). By extending the time for solar radiation absorption and biomass accumulation, early planting dates enable a longer growing period and larger yields (Kucharik 2006). Crop varieties chosen for early planting ought to be resistant to a low temperature of soil that develops after or during planting because there is a danger of plant injuries due to inadequate soil temperature at these early planting dates. Changing planting dates to reduce soil waterlogging depends on when and how long the waterlogging lasts (Kaur et al. 2020).
9.6 Use of Cover Crops
By enhancing soil structure, lowering compaction, and boosting the rate of water infiltration, the use of cover crops may not just improve soil health but also reduce waterlogging (Blanco-Canqui et al. 2015). Cover crop roots can create more macropores, which will result in more water moving through the soil. Increased cover crop transpiration during the spring may potentially dry the soil in time for earlier crop planting. Through larger evapotranspiration (ET) losses, cover crops with higher water requirements and warmer springtime temperatures can assist in eliminating extra moisture from the waterlogged soils. Numerous studies have documented how cover crops can reduce soil moisture content (Monteiro and Lopes 2007; Zhang and Schilling 2006). Reed canary grass (Phalaris arundinacea) had a reduced water table and soil moisture content due to increased ET losses, which decreased groundwater recharge, according to research on the impact of land cover on these variables (Zhang and Schilling 2006). Utilizing cover crops during the winter fallow season is another possible strategy for preventing soil waterlogging. However, depending on the soil type, climate, and cover crop species employed, the impact of cover crops on the water distribution in the soil profile can be beneficial, negative, or neutral (Blanco-Canqui et al. 2015). Therefore, further research should be done on the utilization of different types of cover crops for fields that are prone to flooding or drought. Topography, which can affect nutrient and water dynamics within a field and provide variability biomass synthesis of cover crop and cash crop yields, is not always present in agricultural fields. Therefore, it is crucial to better assess how topography and cover crops interact to lessen the stress caused by waterlogging in big agricultural areas. Using spatial modeling and remote sensing techniques from the geographic information system (GIS), it may be possible to spot parts of an agricultural field that are prone to flooding (Kaur et al. 2020).
9.7 Using Conservation Tillage Techniques
Conservation tillage techniques include mulch tillage, minimal (reduced) tillage, ridge tillage, and contour tillage. The term “minimum tillage” (MT) refers to soil manipulation with only a minimal amount of plowing utilizing primary tillage tools. No-tillage (NT) refers to field cultivation with little to no soil surface disturbance. Mulch tillage involves preparing or tilling the soil in a way that allows plant wastes or other materials that cover the surface to the greatest possible amount. In ridge tillage, crops are planted in rows either on top of or along the ridges that are formed at the start of a cropping season. Variations in conservation tillage’s effects on soil characteristics rely on the specific system selected. The soil qualities, particularly in the top few centimeters, have changed significantly as a result of no-till (NT) methods, that achieve high top soil coverage (Anikwe and Ubochi 2007). NT technologies are particularly successful at minimizing erosion losses, decreasing the amount of residue disturbance, and moderating soil evaporation (Lal et al. 2007). No-till soils have been linked to much more stable aggregates mostly in the soil’s upper surface than tilled soils, which leads to high permeability under NT plots. Over 37–40 years of tillage operations in Gottingen, Germany, minimum tillage (MT) enhanced both levels of SOC and nitrogen inside the aggregate in the upper 5–8 cm soil depth as well as aggregate stability (Jacobs et al. 2009). In tropical and sub-humid tropics, no-till has been proven to be more beneficial in terms of water saving. Contrary to tilled plots, untilled plots hold more water (Kargas et al. 2012).
Compared to normal plowing, minimum tillage increased the soil pores (0.5–50 mm), also many elongated transmission pores (50–500 mm), which improved the soil’s pore system (Pagliai et al. 2004). The upper layer of soil (0–10 cm) under NT has been observed to have a greater holding capacity for water (McVay et al. 2006). Therefore, to improve soil water storage and increase water use efficiency (WUE), the majority of research has recommended shifting to conservation tillage rather than just traditional tillage (Fabrizzi et al. 2005; Silburn et al. 2007). Table 2 lists many benefits and drawbacks of crop management techniques.
10 Adaptive Water Management
Numerous initiatives have been launched to address the issue of waterlogging since the early 1960s. Farmers made no investments in the majority of these initiatives because they were subsidized by the government. Despite significant investment, progress in resolving land degradation issues has been slow. Waterlogging issues were not as easily handled as originally thought. A high groundwater level is a problem for 20–30% of the population as a result of excessive surface water use (Smedema 2000).
10.1 Drainage Systems
One of the key strategies for increasing yields per available agricultural area is land drainage (Malano and Van Hofwegen 2018; Singh 2018b). The two major goals of agricultural drainage are to decrease soil submergence and open up a new areas for agriculture (Singh 2018b). When compared to irrigation, drainage is a more effective agriculture engineering solution to fight to waterlog; nevertheless, neither individual farmers nor governmental organizations have given it the same priority as irrigation. Around the world, drainage is utilized to reduce waterlogging (Milroy et al. 2009). Numerous research from North America, Europe, and England show that draining can successfully lower the water table and boost crop production (Gramlich et al. 2018). Many techniques to lessen the waterlogging problems have been proposed (Kazmi et al. 2012; Singh 2012, 2016). These techniques are explained below:
10.1.1 Surface Drainage
Surface drainage is the method of employing manufactured channels to safely remove surplus water from the surface of the ground (Ritzema et al. 2008; Ayars and Evans 2015). Surface drainage systems have been proven to be cost-effective, with cost-benefit ratios ranging from 1.2–3.2, average return rates from 20 to 58%, and payoff times of 3 to 9 years (Ritzema et al. 2008). The simplest and most affordable option is to keep the surface drains that already exist and build additional ones across edges or via depressions while considering their proper size and placement. Using cut-off drains to stop water from flowing from higher to lower paddocks is also a smart option (Palla et al. 2018). However, inadequate lateral water flow or internal soil drainage qualities frequently limit the effectiveness of surface drainage, resulting in poor drainage near the drains (Saadat et al. 2018). This means that the solutions to these issues may involve both subsurface and surface drainage.
10.1.1.1 Raised Beds
In semi-arid and arid areas, these are re-utilized to address hurdles like irrigation requirements and also waterlogging (Govaerts et al. 2007). By preserving a suitable moisture level in soil via enhanced seepage and acting as a channel to distribute irrigation water, raised seedbeds can improve crop yields (Velmurugan et al. 2016). It increases drainage, and aggregate stability and reduces bulk density (Hassan et al. 2005). To prevent compaction of soil, which promotes penetration of soil, development of roots, and surface and subsurface infiltration, traffic in the furrows should be kept to a minimum. In comparison to flat seedbed planting, raised bed planting has been shown in several studies to increase crop yields in soil that is saturated with water (Blessitt 2007). Soil structure enhancement as seen by infiltration rate and lower bulk densities in clay soil (duplex), which decreased the likelihood of waterlogging and promotes rates of runoff seen in raised beds due to the availability of furrows (Bakker et al. 2005a). As the top 15 centimeters are kept dry during planting in raised beds, as shown in Fig. 10, raised bed planting minimized waterlogging stress. Raised beds have helped to lessen the consequences caused by flooding, but it also has some demerits. These include the price of modifying and adapting machinery, the difficulty of managing drainage water, the use is restricted where the water table is too high, handling stubble and preserving fodder, firefighting and mobilizing livestock, the possibility of pesticide contamination of waterways and leaching into the water table, ineffectiveness of machinery, and weed management in furrows (Bakker et al. 2005b; Gibson 2014).
10.1.2 Subsurface Drainage
Due to the thick soil composition, compact layers, and naturally occurring or artificial hard pan as well as water flowing downhill from springs or from higher slopes, which raises the water table, poor subsurface water mobility occurs (Ward et al. 2018). Subsurface drainage reduces the water table or perched water and creates an environment that is conducive to waterlogging in the root region (Christen and Skehan 2001; Xian et al. 2017). Open and pipe drains with varying drain depths and spacing constitute subsurface drainage systems (Ritzema et al. 2008). The sort of drain that should be installed often relies on the topography, the soil, and the needed drainage rate.
10.1.2.1 Horizontal Subsurface Drainage
The crop root zone is drained of excess water via horizontal subsurface drainage (Teixeira et al. 2018). The drainage system is made up of pathways of perforated pipes below the surface of the earth. Higher agricultural yields can be achieved by draining surplus soil moisture, to enhance root emergence and growth (Nelson et al. 2009, 2011). Flooded soil drainage can be improved globally through subsurface drainage technology (Nelson et al. 2012; Sharma et al. 2016). Using tiny pipes constructed of concrete that is placed at a predetermined depth, tile drainage is a form of horizontal subsurface drainage. In agricultural fields where subsurface excess water is a regular issue, tile drainage is widely used (Williams et al. 2015). In places with shallow groundwater and dense soil conditions, to strengthen the system typically gravel is utilized as a backfill material just above tile seepage (Filipović et al. 2014). This method might not be acceptable for agricultural locations where the top soils are prone to seasonal waterlogging due to inadequate hydraulic conductivity and the need to find a suitable outfall for drained water (Christen and Skehan 2001; Singh 2018a).
10.1.2.2 Tile Drainage
Agricultural fields with tile drainage may lose nitrate due to factors such as precipitation volume and time, initial soil moisture, season, tile depth, and tile distance (Drury et al. 2009). Figure 11 illustrates a study finding that this method enhanced moisture in the soil. In contrast to nondrained plots, it enabled soybean planting earlier at least 17 days and enhanced its output from 9% to 22%. Reducing nitrate that enters surface or groundwater systems, crop output can be increased using subsurface drainage systems that include controlled drainage and sub-irrigation (CDSI), increase the effectiveness with which nitrogen is used, and lessen the likelihood of adverse impacts on the quality of water (Drury et al. 2009; Frankenberger et al. 2004). Another possible strategy for addressing the water quality challenges while also offering crop production systems with flood and drought resilience is to connect subsurface tile-drainage to the irrigation reservoirs. However, this requires more analysis.
10.1.2.3 Vertical Subsurface Drainage
Sand compaction piles prefabricated vertical drains (PVDs), gravel piles, stone columns, and sand drains are a few examples of vertical subsurface drainage (Indraratna et al. 2005; Indraratna 2017). Compared to other subsurface drainage systems, the VD system has a few advantages. For instance, VDs are frequently chosen over other types of drainage because of their comparatively inexpensive cost of construction, also the surface drains shorter length that they provide (Christen and Skehan 2001). However, because operating a network of tube wells requires a lot of energy, the operating and maintenance expense compared to horizontal drainage is more (Food and Agriculture Organization [FAO] 2002; Prathapar et al. 2018). Vertical drainage is more effective for areas with a high water table.
10.1.2.4 Mole Drains
Subsurface drainage also includes mole drainage. In terms of design and functionality, mole drains are comparable to tile drainage as a semi-permanent solution (Dhakad et al. 2018; Tuohy et al. 2018). It is typically put in place to address issues with soil salinization and rising groundwater levels (Kolekar et al. 2014). Mole drainage depends on densely packed channels and subsoil fissures (Tuohy et al. 2015). The optimum applications for mole drains, which are put next to tile drains, are heavy soils with low permeability, such as clay (Monaghan et al. 2002; Monaghan and Smith 2004). We must put it, to the height of no more than 600 mm above the ground, forming a circle of drainage that is 40 to 50 mm in diameter (Gibson 2014). By dragging a metal object through the ground, such as a mole plow or a bullet with a blade-like foot, a mole drain can be created, as shown in Fig. 12. This method creates an open channel. The expense of installing mole drainage is less, but to maintain the integrity of the channel and improve system efficiency, the moles must be reformed every 2–5 years (Tuohy et al. 2018). To assist with drainage management in a flooded landscape and to successfully duplicate water balance and a drainage network system over a watershed, integrated drainage systems (tile and mole drainage) may be employed (Tuohy et al. 2018).
11 Strategies Adopted in Pakistan
In Pakistan, waterlogged soils have been repaired using reclamation, engineering, and bioremediation techniques. In addition to using subsurface drainage systems and industrial waste water conveyance lines, municipal surface drainage systems have been employed to remove extra water from agricultural areas. In fresh groundwater areas, Pakistan decided to construct tube wells in irrigated areas up to 14,000 in number that cover 2.6 Mha area, to lower the groundwater level to handle waterlogging and to boost irrigation resources at the gate of the farm via blending canal and pumped ground water. The above decision was made after a thorough survey of the depth and salinity of the groundwater table in the 1950s. 63 projects costing 2 billion US$ covering an area of a total of 8 Mha were completed underneath this Salinity Control and Reclamation Projects (SCARPs) over the past 40 years (Qureshi 2011). With the help of the SCARPs initiative, the waterlogging issues were successfully managed, if not reversed, and more water was made available for irrigation. Cropping intensities increased, as a result, rising from 84 to 115% in the majority of SCARP locations. However, as time went on, rising maintenance and operational costs as well as an increase in the salinity of the groundwater being pumped diminished the effectiveness of SCARPs, causing water tables to rise and crop yield to decline. With the belief that with the passage of time drainage water quality would improve, increasing the likelihood of using drainage water for irrigation, thinking switched to horizontal (pipe) drainage systems in the middle of the 1970s. There will also be less of an issue with the disposal. In Pakistan since then, around ten significant horizontal drainage projects collectively drainage pipes of 12,600 km been constructed (Qureshi et al. 2008). In order to address this issue, Pakistan constructed a 2000 km surface drainage on the left bank of the Indus River to transport drainage water from over 500,000 acres of soil to the sea (Qureshi et al. 2008). Although the drain’s initial results were highly positive, seepage quickly caused the neighboring communities to become flooded. This heightened interprovincial conflict between the Sindh and Punjab provinces led to a blockage of Punjab’s drainage water’s path through Sindh and ultimately into the sea. This makes Punjab’s waterlogging issues worse. The advantages and disadvantages of the aforementioned adaptive management techniques for waterlogged conditions are shown in Table 3.
11.1 Bioremediation Strategies/Bio-Drainage
Scientists and engineers began considering alternate solutions that are more sustainable and cost-effective as a result of the limited effectiveness in addressing waterlogging issues despite significant investments. Using biological methods to reduce the water table is one of the possible solutions. The idea of improved evapotranspiration serves as the foundation for the utilization of bioremediation in wet environments (Ram et al. 2011). Figure 13 illustrates the fundamental idea of transpiration, absorption, and movement involved in bio-drainage. Waterlogging may be decreased by using herbaceous perennial legumes that are suited to flooding and waterlogging, like Messina (Melilotus siculus), lucerne (Medicago sativa), and Clovers (Genus: Trifolium), in cropping systems (Cocks 2001; Nichols 2018). Typically, compared to other annual crops, these deeply rooted pasture species can drain water and cause the soil to dry to greater depths (McCaskill and Kearney 2016). The suitability of different pasture species for seed production technologies, also to merge them thus providing the greatest merits have been thought of as information gaps that call for further research (Cocks 2001) because different pasture species’ tolerance levels differ significantly from waterlogging. In order to deal with drainage congestion and environmental dangers, bio-drainage, or vertical drainage in soil water utilizing specialized forms of rapidly developing trees with a high evapotranspiration need (Kapoor 2000; Heuperman and Kapoor 2003; Sarkar et al. 2018). Trees in particular are often referred to as “biological pumps” and are crucial to the whole water cycle in a particular area. There is no need for us to:
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Stimulate soil water movement toward a pipe drain or tube well.
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Construct main and collector drains to remove water from the drainage area in bioremediation systems, which are advantageous compared to typical subsurface drainage systems.
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Run pumps to remove drained water, then transfer it to disposal facilities.
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Build disposal facilities (for example: through evaporation ponds).
Bioremediation’s durable viability has been heavily debated. As an alternative to conventional field drainage techniques, it has been suggested that bioremediation may be employed in “parallel field drainage” designs for canal leakage interception and flooded landscape depressions (Smedema 2000). The bottom line is that this is a “pro-poor” technique that increases the revenue of struggling producers who might otherwise leave their properties fallow.
In Pakistan, waterlogged soils have been restored via bioremediation. Poplar (Populus deltoides), Eucalyptus, Tamarix, Gum arabic tree (Acacia nilotica), and mesquite (Prosopis juliflora), are among the trees that belong to this category. Non-woody plants, like shrubs, sedges, grasses, and herbs, can have deeply rooted systems that come into contact with groundwater like that of woody plants (Choudhry and Bhutta 2000). A recent study found that 2.5% of the 200 million irrigated agricultural trees in Punjab province are eucalyptus trees (Shah et al. 2011). The water table wouldn’t be expected to be significantly affected by such a plantation until the plants occupy a sizable enough portion of the catchments so that their combined water demand equals the catchments’ whole recharge. In Pakistan, the capacity of productive tree plantations to drain shallow groundwater is seen as a vital tool for controlling rising water levels.
12 Conclusion
Waterlogging of the soil significantly reduces crop yields around the world and has a negative impact on plant growth. The fluctuating precipitation patterns and temperature brought on by climate change are expected to increase crop losses owing to soil waterlogging in many regions. Waterlogging is a major problem for Pakistan’s irrigated agriculture sector, depriving farmers of their productive resources and endangering their livelihoods. In general, plants can acquire some adaptive features, such as the expansion of adventitious roots or aerenchyma tissue to endure soil waterlogging stress. Commercial cultivars that are not resistant to waterlogging stress might anticipate experiencing yield losses. This article provides a summary of potential management techniques that land managers and farmers can use to increase production. However, the implementation of any management strategies will be region-specific depending on how simple it is to apply in the producers’ current management plans. There are still large gaps in our knowledge of the advantages and disadvantages of appropriate management techniques for various types of soil or crop types, the governance of additional micro as well as macronutrients, and the genetic basis of plant responses to hypoxia and elemental toxicity in flooded soils. Cost-benefit analyses of these management strategies should be the main focus of future research in order to confirm their commercial feasibility and to create management plans that will encourage sustainable crop production from intermittent and variable duration waterlogged soils.
References
Abiko T, Kotula L, Shiono K, Malik AI, Colmer TD, Nakazono M (2012) Enhanced formation of aerenchyma and induction of a barrier to radial oxygen loss in adventitious roots of Zea nicaraguensis contribute to its waterlogging tolerance as compared with maize (Zea mays ssp. mays). Plant Cell Environ 35(9):1618–1630
Acuña TB, Dean G, Riffkin P (2011) Constraints to achieving high potential yield of wheat in a temperate, high-rainfall environment in South-Eastern Australia. Crop Past Sci 62(2):125–136
ADB [Asian Development Bank] (2002) Water resources strategy study. Draft report vol 1. Islamabad, Pakistan ADB
Aderonmu AT (2015) Assessing the impact of changing climate on agriculture in Missouri and the use of crop insurance as an adaptation strategy (1980–2010). University of Missouri-Kansas City
Andrade CA, de Souza KRD, de Oliveira Santos M, da Silva DM, Alves JD (2018) Hydrogen peroxide promotes the tolerance of soybeans to waterlogging. Scient Hort 232:40–45
Anikwe MAN, Ubochi JN (2007) Short-term changes in soil properties under tillage systems and their effect on sweet potato (Ipomea batatas L.) growth and yield in an Ultisol in South-Eastern Nigeria. Soil Res 45(5):351–358
Araki H, Hossain MA, Takahashi T (2012) Waterlogging and hypoxia have permanent effects on wheat root growth and respiration. J Agron Crop Sci 198(4):264–275
Armstrong W, Drew MC (2002) Root growth and metabolism under oxygen deficiency. In: Plant roots. CRC Press, pp 1139–1187
Aroca R, Porcel R, Ruiz-Lozano JM (2012) Regulation of root water uptake under abiotic stress conditions. J Exp Bot 63(1):43–57
Ashraf MA, Ahmad MSA, Ashraf M, Al-Qurainy F, Ashraf MY (2011) Alleviation of waterlogging stress in upland cotton (Gossypium hirsutum L.) by exogenous application of potassium in soil and as a foliar spray. Crop Past Sci 62(1):25–38
Ashraf MA, Akbar A, Askari SH, Iqbal M, Rasheed R, Hussain I (2018) Recent advances in abiotic stress tolerance of plants through chemical priming: an overview. Adv Seed Prim:51–79
Aslam K, Rashid S, Saleem R, Aslam RMS (2015) Use of geospatial technology for assessment of waterlogging & salinity conditions in the Nara Canal command area in Sindh, Pakistan. J Geogr Inf Syst 7(04):438
Ayars JE, Evans RG (2015) Subsurface drainage—What’s next? Irrig Drain 64(3):378–392
Bailey-Serres J, Voesenek LACJ (2008) Flooding stress: acclimations and genetic diversity. Annu Rev Plant Biol 59:313
Bailey-Serres J, Voesenek LA (2010) Life in the balance: a signaling network controlling survival of flooding. Curr Opin Plant Biol 13(5):489–494
Bailey-Serres J, Lee SC, Brinton E (2012) Waterproofing crops: effective flooding survival strategies. Plant Physiol 160(4):1698–1709
Bakker DM, Hamilton GJ, Houlbrooke DJ, Spann C (2005a) The effect of raised beds on soil structure, waterlogging, and productivity on duplex soils in Western Australia. Soil Res 43(5):575–585
Bakker D, Houlbrooke D, Hamilton G, Spann C (2005b) A manual for raised bed farming in Western Australia
Bakker DM, Hamilton GJ, Houlbrooke DJ, Spann C, Van Burgel A (2007) Productivity of crops grown on raised beds on duplex soils prone to waterlogging in Western Australia. Aust J Exp Agric 47(11):1368–1376
Bange MP, Milroy SP, Thongbai P (2004) Growth and yield of cotton in response to waterlogging. Field Crop Res 88(2–3):129–142
Bassu S, Asseng S, Motzo R, Giunta F (2009) Optimising sowing date of durum wheat in a variable Mediterranean environment. Field Crop Res 111(1–2):109–118
Batey T (2009) Soil compaction and soil management–a review. Soil Use Manag 25(4):335–345
Bennett D (2022) Mole drainage in Western Australia, Department of Primary Industries and Regional development, Available at: https://www.agric.wa.gov.au/waterlogging/mole-drainage-western-australia
Blanco-Canqui H, Shaver TM, Lindquist JL, Shapiro CA, Elmore RW, Francis CA, Hergert GW (2015) Cover crops and ecosystem services: insights from studies in temperate soils. Agron J 107(6):2449–2474
Blessitt JB (2007) Productivity of raised seedbeds for soybean [Glycine max.(L.) Merr.] production on clayey soils of the Mississippi Delta. Mississippi State University
Blokhina OB, Chirkova TV, Fagerstedt KV (2001) Anoxic stress leads to hydrogen peroxide formation in plant cells. J Exp Bot 52(359):1179–1190
Bramley H, Turner NC, Turner DW, Tyerman SD (2010) The contrasting influence of short-term hypoxia on the hydraulic properties of cells and roots of wheat and lupin. Funct Plant Biol 37(3):183–193
Broekaert WF, Delauré SL, De Bolle MF, Cammue BP (2006) The role of ethylene in host-pathogen interactions. Annu Rev Phytopathol 44:393–416
Choudhry MR, Bhutta MN (2000) Problems impeding the sustainability of drainage systems in Pakistan. In: Proceedings and recommendations of the national seminar on drainage in Pakistan, pp 16–18
Christen E, Skehan D (2001) Design and management of subsurface horizontal drainage to reduce salt loads. J Irrig Drain Eng 127(3):148–155
Cocks PS (2001) Ecology of herbaceous perennial legumes: a review of characteristics that may provide management options for the control of salinity and waterlogging in dryland cropping systems. Aust J Agric Res 52(2):137–151
Colmer TD (2003) Long-distance transport of gases in plants: a perspective on internal aeration and radial oxygen loss from roots. Plant Cell Environ 26(1):17–36
Colmer TD, Flowers TJ (2008) Flooding tolerance in halophytes. New Phytol 179(4):964–974
Colmer TD, Greenway H (2011) Ion transport in seminal and adventitious roots of cereals during O2 deficiency. J Exp Bot 62(1):39–57
Cong Y, Li YJ, Zhou CJ, Zou CS, Zhang XK, Liao X, Zhang CL (2009) Effect of application of nitrogen, phosphorus and potassium fertilizers on yield in rapeseed (Brassica napus L.) under the waterlogging stress. Plant Nutrit Fertiliz Sci 15(5):1122–1129
Cubasch U, Meehl GA, Boer GJ, Stouffer RJ, Dix M, Noda A, Yap KS (2001) Projections of future climate change. In: Climate change 2001: the scientific basis. Contribution of WG1 to the third assessment report of the IPCC (TAR). Cambridge University Press, pp 525–582
Dash JP, Sarangi A, Singh AK, Dahiya S (2005) Bio-drainage: an alternate drainage technique to control waterlogging and salinity. J Soil Water Conserv India 4(3&4):149–155
Dat JF, Capelli N, Folzer H, Bourgeade P, Badot PM (2004) Sensing and signalling during plant flooding. Plant Physiol Biochem 42(4):273–282
Dhakad SS, Ambawatia GR, Verma G, Patel S, Rao KR, Verma S (2018) Performance of Mole drain system for soybean (glycine max)-wheat (Triticum aestivum) cropping system of Madhya Pradesh
Drury CF, Tan CS, Reynolds WD, Welacky TW, Oloya TO, Gaynor JD (2009) Managing tile drainage, subirrigation, and nitrogen fertilization to enhance crop yields and reduce nitrate loss. J Environ Qual 38(3):1193–1204
Ejiri M, Fukao T, Miyashita T, Shiono K (2021) A barrier to radial oxygen loss helps the root system cope with waterlogging-induced hypoxia. Breed Sci 71(1):40–50
El-Esawi MA (2016a) Nonzygotic embryogenesis for plant development. In: Plant tissue culture: propagation, conservation and crop improvement, pp 583–598
El-Esawi MA (2016b) Micropropagation technology and its applications for crop improvement. In: Plant tissue culture: propagation, conservation and crop improvement. Springer, Singapore, pp 523–545
Else MA, Janowiak F, Atkinson CJ, Jackson MB (2009) Root signals and stomatal closure in relation to photosynthesis, chlorophyll a fluorescence and adventitious rooting of flooded tomato plants. Ann Bot 103(2):313–323
Engineer Moid (2021) Waterlogging its 5 types and causes. Civilclick.com. Available at: https://www.civilclick.com/waterlogging/
Evans DE (2004) Aerenchyma formation. New Phytolog 161(1):35–49
Fabrizzi KP, Garcıa FO, Costa JL, Picone LI (2005) Soil water dynamics, physical properties and corn and wheat responses to minimum and no-tillage systems in the southern Pampas of Argentina. Soil Tillage Res 81(1):57–69
Ferreira JL, Coelho CHM, Magalhães PC, Santána GC, Borém A (2008) Evaluation of mineral content in maize under flooding. Embrapa Milho e Sorgo-Artigo em periódico indexado (ALICE)
Ferrer JLR, Magalhaes PC, Alves JD, Vasconcellos CA, Delu Filho N. Fries DD, Purcino AAC. (2005) Calcium partially relieves the deleterius effects of hypoxia on a maize cultivar selected for waterlogging tolerance
Filipović V, Mallmann FJK, Coquet Y, Šimůnek J (2014) Numerical simulation of water flow in tile and mole drainage systems. Agric Water Manag 146:105–114
Food and Agriculture Organization [FAO] (2002) Food and Agriculture Organization of the United Nations. Available at: http://www.fao.org/3/abc600e.pdf
Foyer CH, Shigeoka S (2011) Understanding oxidative stress and antioxidant functions to enhance photosynthesis. Plant Physiol 155(1):93–100
Frankenberger J, Kladivko E, Sands G, Jaynes DB, Fausey N, Helmers MJ, Brown L (2004) Drainage water management for the midwest. Agricultural and Biosystems Engineering Extension and Outreach Publications: West Lafayette, IN
Fukao T, Bailey-Serres J (2004) Plant responses to hypoxia–is survival a balancing act? Trends Plant Sci 9(9):449–456
Galant AL, Kaufman RC, Wilson JD (2015) Glucose: detection and analysis. Food Chem 188:149–160
Gechev TS, Gadjev I, Van Breusegem F, Inzé D, Dukiandjiev S, Toneva V, Minkov I (2002) Hydrogen peroxide protects tobacco from oxidative stress by inducing a set of antioxidant enzymes. Cell Mol Life Sci 59(4):708–714
Gibson G (2014) Utilising innovative management techniques to reduce waterlogging. Nuffield Australia Farming Scholars, Moama, NSW
Gill MB, Zeng F, Shabala L, Böhm J, Zhang G, Zhou M, Shabala S (2018) The ability to regulate voltage-gated K+-permeable channels in the mature root epidermis is essential for waterlogging tolerance in barley. J Exp Bot 69(3):667–680
Govaerts B, Sayre KD, Lichter K, Dendooven L, Deckers J (2007) Influence of permanent raised bed planting and residue management on physical and chemical soil quality in rain fed maize/wheat systems. Plant Soil 291(1):39–54
Gramlich A, Stoll S, Stamm C, Walter T, Prasuhn V (2018) Effects of artificial land drainage on hydrology, nutrient and pesticide fluxes from agricultural fields–a review. Agric Ecosyst Environ 266:84–99
Habibzadeh F, Sorooshzadeh A, Pirdashti H, Sanavy SAMM (2012) Effect of nitrogen compounds and tricyclazole on some biochemical and morphological characteristics of waterlogged-canola. Int Res J Appl Basic Sci 3(1):77–84
Habibzadeh F, Sorooshzadeh A, Pirdashti H, Modarres-Sanavy SAM (2013) Alleviation of waterlogging damage by foliar application of nitrogen compounds and tricyclazole in canola. Aust J Crop Sci 7(3):401–406
Hassan I, Hussain Z, Akbar G (2005) Effect of permanent raised beds on water productivity for irrigated maize–wheat cropping system. Evaluation and performance of permanent raised bed cropping systems in Asia, Australia and Mexicop, p 121
Hedden P, Sponsel V (2015) A century of gibberellin research. J Plant Growth Regul 34(4):740–760
Herzog M, Striker GG, Colmer TD, Pedersen O (2016) Mechanisms of waterlogging tolerance in wheat–a review of root and shoot physiology. Plant Cell Environ 39(5):1068–1086
Heuperman AF, Kapoor AS (2003) Biodrainage status in India and other countries. Indian National Committee on Irrigation and Drainage, New Delhi, pp 1–47
Hossain MA (2010) Global warming induced sea level rise on soil, land and crop production loss in Bangladesh. In: 19th world congress of soil science, soil solutions for a changing world, Brisbane
Htet Y, Lu Z, Trauger SA, Tennyson AG (2019) Hydrogen peroxide as a hydride donor and reductant under biologically relevant conditions. Chem Sci 10(7):2025–2033
Huang X, Shabala S, Shabala L, Rengel Z, Wu X, Zhang G, Zhou M (2015) Linking waterlogging tolerance with Mn2+ toxicity: a case study for barley. Plant Biol 17(1):26–33
Huang X, Fan Y, Shabala L, Rengel Z, Shabala S, Zhou MX (2018) A major QTL controlling the tolerance to manganese toxicity in barley (Hordeum vulgare L.). Mol Breed 38(2):1–9
Indraratna B (2017) Recent advances in vertical drains and vacuum preloading for soft ground stabilisation. In: Proceedings of 19th international conference on soil mechanics and geotechnical engineering, Seou. International Society for Soil Mechanics and Geotechnical Engineering, London, pp 145–170
Indraratna B, Rujikiatkamjorn C, Sathananthan I (2005) Analytical and numerical solutions for a single vertical drain including the effects of vacuum preloading. Can Geotech J 42(4):994–1014
Iqbal N, Khan NA, Ferrante A, Trivellini A, Francini A, Khan MIR (2017) Ethylene role in plant growth, development and senescence: interaction with other phytohormones. Front Plant Sci 8:475
Irfan M, Hayat S, Hayat Q, Afroz S, Ahmad A (2010) Physiological and biochemical changes in plants under waterlogging. Protoplasma 241(1):3–17
Ishibashi Y, Yamaguchi H, Yuasa T, Iwaya-Inoue M, Arima S, Zheng SH (2011) Hydrogen peroxide spraying alleviates drought stress in soybean plants. J Plant Physiol 168(13):1562–1567
Jackson MB, Colmer T (2005) Response and adaptation by plants to flooding stress. Ann Bot 96(4):501–505
Jackson MB, Ricard B (2003) Physiology, biochemistry and molecular biology of plant root systems subjected to flooding of the soil. Root Ecol:193–213
Jacobs A, Rauber R, Ludwig B (2009) Impact of reduced tillage on carbon and nitrogen storage of two Haplic Luvisols after 40 years. Soil Tillage Res 102(1):158–164
Jia W, Ma M, Chen J, Wu S (2021) Plant morphological, physiological and anatomical adaption to flooding stress and the underlying molecular mechanisms. Int J Mol Sci 22(3):1088
Jiang P, Anderson SH, Kitchen NR, Sadler EJ, Sudduth KA (2007) Landscape and conservation management effects on hydraulic properties of a claypan-soil toposequence. Soil Sci Soc Am J 71(3):803–811
Kapoor AS (2000) Bio-drainage feasibility and principles of planning and design. In: Role of drainage and challenges in 21st century. Vol. IV. Proceedings of the eighth ICID international drainage workshop, New Delhi, India, 31 January–4 February 2000. International Commission on Irrigation and Drainage, pp 17–32
Kargas G, Kerkides P, Poulovassilis A (2012) Infiltration of rain water in semi-arid areas under three land surface treatments. Soil Tillage Res 120:15–24
Kaur G, Zurweller BA, Nelson KA, Motavalli PP, Dudenhoeffer CJ (2017) Soil waterlogging and nitrogen fertilizer management effects on corn and soybean yields. Agron J 109(1):97–106
Kaur G, Nelson KA, Motavalli PP (2018) Early-season soil waterlogging and N fertilizer sources impacts on corn N uptake and apparent N recovery efficiency. Agronomy 8(7):102
Kaur G, Singh G, Motavalli PP, Nelson KA, Orlowski JM, Golden BR (2020) Impacts and management strategies for crop production in waterlogged or flooded soils: a review. Agron J 112(3):1475–1501
Kazmi SI, Ertsen MW, Asi MR (2012) The impact of conjunctive use of canal and tube well water in Lagar irrigated area, Pakistan. Phys Chem Earth, Parts A/B/C 47:86–98
Kijne JW (2006) Abiotic stress and water scarcity: identifying and resolving conflicts from plant level to global level. Field Crop Res 97(1):3–18
Kim Y, Seo CW, Khan AL, Mun BG, Shahzad R, Ko JW, Lee IJ (2018) Ethylene mitigates waterlogging stress by regulating glutathione biosynthesis-related transcripts in soybeans. bioRxiv, 252312
Kirkpatrick MT, Rothrock CS, Rupe JC, Gbur EE (2006) The effect of Pythium ultimum and soil flooding on two soybean cultivars. Plant Dis 90(5):597–602
Kisaakye E, Botwright Acuna T, Johnson P, Shabala S (2015) Effect of water availability and nitrogen source on wheat growth and nitrogen-use efficiency. In: 17th Australian Society of Agronomy conference, pp 1–4
Kisaakye E, Acuña TB, Johnson P, Shabala S (2017) Improving wheat growth and nitrogen-use efficiency under waterlogged conditions. In: 18th Australian agronomy conference 2017, pp 1–4
Knapp AK, Hoover DL, Wilcox KR, Avolio ML, Koerner SE, La Pierre KJ, Smith MD (2015) Characterizing differences in precipitation regimes of extreme wet and dry years: implications for climate change experiments. Glob Chang Biol 21(7):2624–2633
Knipfer T, Fricke W (2011) Water uptake by seminal and adventitious roots in relation to whole-plant water flow in barley (Hordeum vulgare L.). J Exp Bot 62(2):717–733
Kolekar O, Patil S, Rathod S (2014) Effects of different mole drain spacings on the yield of summer groundnut. Int J Res Eng Technol 3:2321–7308
Kucharik CJ (2006) A multidecadal trend of earlier corn planting in the Central USA. Agron J 98(6):1544–1550
Kulichikhin K, Yamauchi T, Watanabe K, Nakazono M (2014) Biochemical and molecular characterization of rice (Oryza sativa L.) roots forming a barrier to radial oxygen loss. Plant Cell Environ 37(10):2406–2420
Kumar V, Ladha JK (2011) Direct seeding of rice: recent developments and future research needs. Adv Agron 111:297–413
Kunkel KE (2003) North American trends in extreme precipitation. Nat Hazards 29(2):291–305
Lal R, Reicosky DC, Hanson JD (2007) Evolution of the plow over 10,000 years and the rationale for no-till farming. Soil Tillage Res 93(1):1–12
Lal SK, Kumar S, Sheri V, Mehta S, Varakumar P, Ram B, Reddy MK (2018) Seed priming: an emerging technology to impart abiotic stress tolerance in crop plants. In: Advances in seed priming. Springer, Singapore, pp 41–50
Lerch RN, Lin CH, Goyne KW, Kremer RJ, Anderson SH (2017) Vegetative buffer strips for reducing herbicide transport in runoff: effects of buffer width, vegetation, and season. J Am Water Resour Assoc 53(3):667–683
Li MF, Zhu JQ, Jiang ZH (2013) Plant growth regulators and nutrition applied to cotton after waterlogging. In: 2013 third international conference on intelligent system design and engineering applications. IEEE, pp 1045–1048
Lin C, Sauter M (2019) Polar auxin transport determines adventitious root emergence and growth in rice. Front Plant Sci 10:444
Lin KH, Tsou CC, Hwang SY, Chen LFO, Lo HF (2008) Paclobutrazol leads to enhanced antioxidative protection of sweetpotato under flooding stress. Bot Stud 49(1):9–18
Lin CH, Lerch RN, Goyne KW, Garrett HE (2011) Reducing herbicides and veterinary antibiotics losses from agroecosystems using vegetative buffers. J Environ Qual 40(3):791–799
Liu Z, Liu Z, Xiao J, Nan J, Gong W (2013) Waterlogging at seedling and jointing stages inhibits growth and development, reduces yield in summer maize. Trans Chin Soc Agric Eng 29(5):44–52
Liu K, Harrison MT, Shabala S, Meinke H, Ahmed I, Zhang Y, Zhou M (2020a) The state of the art in modeling waterlogging impacts on plants: what do we know and what do we need to know. Earth’s Fut 8(12):e2020EF001801
Liu J, Hasanuzzaman M, Sun H, Zhang J, Peng T, Sun H, Zhao Q (2020b) Comparative morphological and transcriptomic responses of lowland and upland rice to root-zone hypoxia. Environ Exp Bot 169:103916
Luan H, Guo B, Pan Y, Lv C, Shen H, Xu R (2018a) Morpho-anatomical and physiological responses to waterlogging stress in different barley (Hordeum vulgare L.) genotypes. Plant Growth Regul 85(3):399–409
Luan H, Shen H, Pan Y, Guo B, Lv C, Xu R (2018b) Elucidating the hypoxic stress response in barley (Hordeum vulgare L.) during waterlogging: a proteomics approach. Sci Rep 8(1):1–13
Malano HM, Van Hofwegen PJ (2018) Management of irrigation and drainage systems–a service approach. CRC Press
Mancuso S, Shabala S (2010) Waterlogging signalling and tolerance in plants. Springer, Heidelberg. ISBN 9783642103049
Manik SM, Pengilley G, Dean G, Field B, Shabala S, Zhou M (2019) Soil and crop management practices to minimize the impact of waterlogging on crop productivity. Front Plant Sci 10:140
Mano Y, Muraki M, Fujimori M, Takamizo T, Kindiger B (2005) Identification of QTL controlling adventitious root formation during flooding conditions in teosinte (Zea mays ssp. huehuetenangensis) seedlings. Euphytica 142(1):33–42
Masunaga T, Fong JDM (2018) Strategies for increasing micronutrient availability in soil for plant uptake. In: Plant micronutrient use efficiency. Academic Press, pp 195–208
Maurel C, Boursiac Y, Luu DT, Santoni V, Shahzad Z, Verdoucq L (2015) Aquaporins in plants. Physiol Rev 95(4):1321–1358
McCaskill MR, Kearney GA (2016) Control of water leakage from below the root zone by summer-active pastures is associated with persistence, density and deep rootedness. Crop Past Sci 67(6):679–693
McDonald G (2022) Raised beds – design, layout, construction and renovation. Department of Primary Industries and Regional development, Available at: https://www.agric.wa.gov.au/waterlogging/raised-beds-_-design-layout-construction-andrenovation#skip-link
McLellan EL, Schilling KE, Wolter CF, Tomer MD, Porter SA, Magner JA, Prokopy LS (2018) Right practice, right place: a conservation planning toolbox for meeting water quality goals in the Corn Belt. J Soil Water Conserv 73(2):29A–34A
McVay KA, Budde JA, Fabrizzi K, Mikha MM, Rice CW, Schlegel AJ, Thompson C (2006) Management effects on soil physical properties in long-term tillage studies in Kansas. Soil Sci Soc Am J 70(2):434–438
Merriman KR, Daggupati P, Srinivasan R, Hayhurst B (2019) Assessment of site-specific agricultural best management practices in the upper East River watershed, Wisconsin, using a field-scale SWAT model. J Great Lakes Res 45(3):619–641
Mhamdi A, Van Breusegem F (2018) Reactive oxygen species in plant development. Development 145(15):dev164376
Milroy SP, Bange MP, Thongbai P (2009) Cotton leaf nutrient concentrations in response to waterlogging under field conditions. Field Crop Res 113(3):246–255
Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7(9):405–410
Monaghan RM, Smith LC (2004) Minimising surface water pollution resulting from farm-dairy effluent application to mole-pipe drained soils. II. The contribution of preferential flow of effluent to whole-farm pollutant losses in subsurface drainage from a West Otago dairy farm. N Z J Agric Res 47(4):417–428
Monaghan RM, Paton RJ, Drewry JJ (2002) Nitrogen and phosphorus losses in mole and tile drainage from a cattle-grazed pasture in eastern Southland. N Z J Agric Res 45(3):197–205
Monteiro A, Lopes CM (2007) Influence of cover crop on water use and performance of vineyard in Mediterranean Portugal. Agric Ecosyst Environ 121(4):336–342
Motavalli PP, Anderson SH, Pengthamkeerati P (2003) Surface compaction and poultry litter effects on corn growth, nitrogen availability, and physical properties of a claypan soil. Field Crop Res 84:303–318
Munoz-Carpena R, Fox GA, Ritter A, Perez-Ovilla O, Rodea-Palomares I (2018) Effect of vegetative filter strip pesticide residue degradation assumptions for environmental exposure assessments. Sci Total Environ 619:977–987
Mustafa HSB, Mahmood T, Ullah A, Sharif A, Bhatti AN, Nadeem M, Ali R (2017) Role of seed priming to enhance growth and development of crop plants against biotic and abiotic stresses. Sect Plant Sci 2(2):1–11
Mustroph A, Albrecht G (2003) Tolerance of crop plants to oxygen deficiency stress: fermentative activity and photosynthetic capacity of entire seedlings under hypoxia and anoxia. Physiol Plant 117(4):508–520
Mutava RN, Prince SJK, Syed NH, Song L, Valliyodan B, Chen W, Nguyen HT (2015) Understanding abiotic stress tolerance mechanisms in soybean: a comparative evaluation of soybean response to drought and flooding stress. Plant Physiol Biochem 86:109–120
Najeeb U, Bange MP, Tan DK, Atwell BJ (2015) Consequences of waterlogging in cotton and opportunities for mitigation of yield losses. AoB Plants 7:plv080
Nelson KA, Paniagua SM, Motavalli PP (2009) Effect of polymer coated urea, irrigation, and drainage on nitrogen utilization and yield of corn in a claypan soil. Agron J 101(3):681–687
Nelson KA, Smoot RL, Meinhardt CG (2011) Soybean response to drainage and subirrigation on a claypan soil in Northeast Missouri. Agron J 103(4):1216–1222
Nelson KA, Meinhardt CG, Smoot RL (2012) Soybean cultivar response to subsurface drainage and subirrigation in Northeast Missouri. Crop Manag 11(1):1–9
Nguyen HC, Lin KH, Ho SL, Chiang CM, Yang CM (2018a) Enhancing the abiotic stress tolerance of plants: from chemical treatment to biotechnological approaches. Physiol Plant 164(4):452–466
Nguyen TN, Tuan PA, Mukherjee S, Son S, Ayele BT (2018b) Hormonal regulation in adventitious roots and during their emergence under waterlogged conditions in wheat. J Exp Bot 69(16):4065–4082
Nichols P (2018) Yanco subterranean clover. Department of Primary Industries and Regional Development (DPIRD), Orange
Nielsen RL (2015) Effects of flooding or ponding on corn prior to tasseling. In: Corny news network. Purdue University, West Lafayette, IN
Nishiuchi S, Yamauchi T, Takahashi H, Kotula L, Nakazono M (2012) Mechanisms for coping with submergence and waterlogging in rice. Rice 5(1):1–14
Noreen S, Fatima Z, Ahmad S, Athar HUR, Ashraf M (2018) Foliar application of micronutrients in mitigating abiotic stress in crop plants. In: Plant nutrients and abiotic stress tolerance. Springer, Singapore, pp 95–117
Normile D (2008) Reinventing rice to feed the world
OCHA, Pakistan (2022) Floods response plan: 01 Sep 2022–28 Feb 2023 (Issued 30 Aug 2022), Relief web, Available at: https://reliefweb.int/report/pakistan/pakistan-2022-floods-response-plan-01-sep-2022-28-feb-2023-issued-30-aug-2022
Pagliai M, Vignozzi N, Pellegrini S (2004) Soil structure and the effect of management practices. Soil Tillage Res 79(2):131–143
Palla A, Colli M, Candela A, Aronica GT, Lanza LG (2018) Pluvial flooding in urban areas: the role of surface drainage efficiency. J Flood Risk Manag 11:S663–S676
Pandey DM, Goswami CL, Kumar B, Jain S (2002) Effect of growth regulators on photosynthetic metabolites in cotton under water stress. Biol Plant 45(3):445–448
Pang JY, Newman IAN, Mendham N, Zhou M, Shabala S (2006) Microelectrode ion and O2 fluxes measurements reveal differential sensitivity of barley root tissues to hypoxia. Plant Cell Environ 29(6):1107–1121
Pang J, Ross J, Zhou M, Mendham N, Shabala S (2007) Amelioration of detrimental effects of waterlogging by foliar nutrient sprays in barley. Funct Plant Biol 34(3):221–227
Parent C, Capelli N, Berger A, Crèvecoeur M, Dat JF (2008) An overview of plant responses to soil waterlogging. Plant Stress 2(1):20–27
Pereira EI, Nogueira ARA, da Cruz CC, Guimarães GG, Foschini MM, Bernardi AC, Ribeiro C (2017) Controlled urea release employing nanocomposites increases the efficiency of nitrogen use by forage. ACS Sustain Chem Eng 5(11):9993–10001
Ploschuk RA, Miralles DJ, Colmer TD, Ploschuk EL, Striker GG (2018) Waterlogging of winter crops at early and late stages: impacts on leaf physiology, growth and yield. Front Plant Sci 9:1863
Poulisw (2011) Anaerobic respiration (fermentation), Biology form 6, Available at: http://biomhs.blogspot.com/2011/04/anaerobic-respiration-fermentation.html
Prathapar SA, Rajmohan N, Sharma BR, Aggarwal PK (2018) Vertical drains to minimize duration of seasonal waterlogging in eastern Ganges Basin flood plains: a field experiment. Nat Hazards 92(1):1–17
Qadir M, Oster J (2002) Vegetative bioremediation of calcareous sodic soils: history, mechanisms, and evaluation. Irrig Sci 21(3):91–101
Qiu F, Zheng Y, Zhang Z, Xu S (2007) Mapping of QTL associated with waterlogging tolerance during the seedling stage in maize. Ann Bot 99(6):1067–1081
Qureshi AS (2011) Water management in the Indus Basin in Pakistan: challenges and opportunities. Mountain Res Develop 31(3):252–260
Qureshi AS, Akhtar M, Sarwar A (2003) Effect of electricity pricing policies on groundwater management in Pakistan
Qureshi AS, McCornick PG, Qadir M, Aslam Z (2008) Managing salinity and waterlogging in the Indus Basin of Pakistan. Agric Water Manag 95(1):1–10
Rademacher W (2015) Plant growth regulators: backgrounds and uses in plant production. J Plant Growth Regul 34(4):845–872
Rajaeian SO, Ehsanpour AA (2015) Physiological responses of tobacco plants (Nicotiana rustica) pretreated with ethanolamine to salt stress. Russ J Plant Physiol 62(2):246–252
Rajhi I, Yamauchi T, Takahashi H, Nishiuchi S, Shiono K, Watanabe R, Nakazono M (2011) Identification of genes expressed in maize root cortical cells during lysigenous aerenchyma formation using laser microdissection and microarray analyses. New Phytol 190(2):351–368
Ram J, Dagar JC, Lal K, Singh G, Toky OP, Tanwar VS, Chauhan MK (2011) Biodrainage to combat waterlogging, increase farm productivity and sequester carbon in canal command areas of Northwest India. Curr Sci:1673–1680
Rao R, Bryan HH, Reed ST (2002) Assessment of foliar sprays to alleviate flooding injury in corn (Zea mays L.). In: Proceedings of the Florida State Horticultural Society, vol 115, pp 208–211
Reichardt K, Timm LC (2012) Soil, plant and atmosphere. Springer, Cham. ISBN 9783030193218
Reinsch M, Pearce D (2005) Pakistan-country water resources assistance strategy: water economy running dry
Ren B, Zhang J, Dong S, Liu P, Zhao B (2016a) Effects of waterlogging on leaf mesophyll cell ultrastructure and photosynthetic characteristics of summer maize. PLoS One 11(9):e0161424
Ren B, Zhang J, Dong S, Liu P, Zhao B (2016b) Root and shoot responses of summer maize to waterlogging at different stages. Agron J 108(3):1060–1069
Ren B, Zhu Y, Zhang J, Dong S, Liu P, Zhao B (2016c) Effects of spraying exogenous hormone 6-benzyladenine (6-BA) after waterlogging on grain yield and growth of summer maize. Field Crop Res 188:96–104
Ren B, Dong S, Zhao B, Liu P, Zhang J (2017) Responses of nitrogen metabolism, uptake and translocation of maize to waterlogging at different growth stages. Front Plant Sci 8:1216
Ren B, Zhang J, Dong S, Liu P, Zhao B (2018) Exogenous 6-benzyladenine improves antioxidative system and carbon metabolism of summer maize waterlogged in the field. J Agron Crop Sci 204(2):175–184
Ritzema HP, Satyanarayana TV, Raman S, Boonstra J (2008) Subsurface drainage to combat waterlogging and salinity in irrigated lands in India: lessons learned in farmers’ fields. Agric Water Manag 95(3):179–189
Rochester IJ, Peoples MB, Hulugalle NR, Gault R, Constable GA (2001) Using legumes to enhance nitrogen fertility and improve soil condition in cotton cropping systems. Field Crop Res 70(1):27–41
Rosenzweig C, Tubiello FN, Goldberg R, Mills E, Bloomfield J (2002) Increased crop damage in the US from excess precipitation under climate change. Glob Environ Chang 12(3):197–202
Rubinigg M, Stulen I, Elzenga JTM, Colmer TD (2002) Spatial patterns of radial oxygen loss and nitrate net flux along adventitious roots of rice raised in aerated or stagnant solution. Funct Plant Biol 29(12):1475–1481
Saadat S, Bowling L, Frankenberger J, Kladivko E (2018) Nitrate and phosphorus transport through subsurface drains under free and controlled drainage. Water Res 142:196–207
Sairam RK, Kumutha D, Ezhilmathi K, Deshmukh PS, Srivastava GC (2008) Physiology and biochemistry of waterlogging tolerance in plants. Biol Plant 52(3):401–412
Samad A, Meisner CA, Saifuzzaman M, van Ginkel M (2001) Waterlogging tolerance. In: Reynolds MP, Ortiz-Monasterio JI, McNab A (eds) Application of physiology in wheat breeding, pp 136–144. ISBN:970-648-077-3
Sarkar A, Banik M, Ray R, Patra SK (2018) Soil moisture and groundwater dynamics under bio drainage vegetation in a waterlogged land
Sasidharan R, Voesenek LA (2015) Ethylene-mediated acclimations to flooding stress. Plant Physiol 169(1):3–12
Sauter M (2013) Root responses to flooding. Curr Opin Plant Biol 16(3):282–286
Savvides A, Ali S, Tester M, Fotopoulos V (2016) Chemical priming of plants against multiple abiotic stresses: mission possible? Trends Plant Sci 21(4):329–340
Setter TL, Waters I (2003) Review of prospects for germplasm improvement for waterlogging tolerance in wheat, barley and oats. Plant Soil 253(1):1–34
Setter TL, Khabaz-Saberi H, Waters I, Singh KN, Kulshreshtha N, Sharma SK (2006). Review of waterlogging tolerance in wheat in India: involvement of element/microelement toxicities, relevance to yield plateau and opportunities for crop management. In: International symposium on balanced fertilization. Ludhiana, India, pp 22–25
Shabala S (2011) Physiological and cellular aspects of phytotoxicity tolerance in plants: the role of membrane transporters and implications for crop breeding for waterlogging tolerance. New Phytol 190(2):289–298
Shabala S, Pottosin I (2014) Regulation of potassium transport in plants under hostile conditions: implications for abiotic and biotic stress tolerance. Physiol Plant 151(3):257–279
Shah AH, Gill KH, Syed NI (2011) Sustainable salinity management for combating desertification in Pakistan. Int J Water Res Arid Environ 1(5):312–317
Sharma PC, Kaledhonkar MJ, Thimmappa K, Chaudhari SK (2016) Reclamation of waterlogged saline soils through subsurface drainage technology
Shaviv A (2001) Advances in controlled-release fertilizers
Shaw RE, Meyer WS, McNeill A, Tyerman SD (2013) Waterlogging in Australian agricultural landscapes: a review of plant responses and crop models. Crop Past Sci 64(6):549–562
Shiono K, Ogawa S, Yamazaki S, Isoda H, Fujimura T, Nakazono M, Colmer TD (2011) Contrasting dynamics of radial O2-loss barrier induction and aerenchyma formation in rice roots of two lengths. Ann Bot 107(1):89–99
Shiono K, Ejiri M, Shimizu K, Yamada S (2019) Improved waterlogging tolerance of barley (Hordeum vulgare) by pretreatment with ethephon. Plant Prod Sci 22(2):285–295
Silburn DM, Freebairn DM, Rattray DJ (2007) Tillage and the environment in sub-tropical Australia—tradeoffs and challenges. Soil Tillage Res 97(2):306–317
Singh A (2012) Development and application of a watertable model for the assessment of waterlogging in irrigated semi-arid regions. Water Resour Manag 26(15):4435–4448
Singh A (2016) Hydrological problems of water resources in irrigated agriculture: a management perspective. J Hydrol 541:1430–1440
Singh A (2018a) Managing the salinization and drainage problems of irrigated areas through remote sensing and GIS techniques. Ecol Indic 89:584–589
Singh A (2018b) Salinization of agricultural lands due to poor drainage: a viewpoint. Ecol Indic 95:127–130
Singh Y, Singh VP, Singh G, Yadav DS, Sinha RKP, Johnson DE, Mortimer AM (2011) The implications of land preparation, crop establishment method and weed management on rice yield variation in the rice–wheat system in the Indo-Gangetic plains. Field Crop Res 121(1):64–74
Singh G, Williard KW, Schoonover JE (2016) Spatial relation of apparent soil electrical conductivity with crop yields and soil properties at different topographic positions in a small agricultural watershed. Agronomy 6(4):57
Skaggs RW (2008) DRAINMOD: a simulation model for shallow water table soils
Smedema L (2000) Irrigation-induced river salinization: five major irrigated basins in the arid
Soukup A, Armstrong W, Schreiber L, Franke R, Votrubová O (2007) Apoplastic barriers to radial oxygen loss and solute penetration: a chemical and functional comparison of the exodermis of two wetland species, Phragmites australis and Glyceria maxima. New Phytol 173(2):264–278
Steffens B (2014) The role of ethylene and ROS in salinity, heavy metal, and flooding responses in rice. Front Plant Sci 5:685
Steffens B, Rasmussen A (2016) The physiology of adventitious roots. Plant Physiol 170(2):603–617
Steffens B, Sauter M (2009) Epidermal cell death in rice is confined to cells with a distinct molecular identity and is mediated by ethylene and H2O2 through an autoamplified signal pathway. Plant Cell 21(1):184–196
Steffens D, Hutsch BW, Eschholz T, Losak T, Schubert S (2005) Water logging may inhibit plant growth primarily by nutrient deficiency rather than nutrient toxicity. Plant Soil Environ 51(12):545
Steffens B, Geske T, Sauter M (2011) Aerenchyma formation in the rice stem and its promotion by H2O2. New Phytol 190(2):369–378
Subbaiah CC, Sachs MM (2003) Molecular and cellular adaptations of maize to flooding stress. Ann Bot 91(2):119–127
Sumimoto H (2008) Structure, regulation and evolution of Nox-family NADPH oxidases that produce reactive oxygen species. FEBS J 275(13):3249–3277
Sundgren TK, Uhlen AK, Lillemo M, Briese C, Wojciechowski T (2018) Rapid seedling establishment and a narrow root stele promotes waterlogging tolerance in spring wheat. J Plant Physiol 227:45–55
Tan X, Xu H, Khan S, Equiza MA, Lee SH, Vaziriyeganeh M, Zwiazek JJ (2018) Plant water transport and aquaporins in oxygen-deprived environments. J Plant Physiol 227:20–30
Teixeira DL, de Matos AT, de Matos MP, Miranda ST, Vieira DP (2018) Evaluation of the effects of drainage and different rest periods as techniques for unclogging the porous medium in horizontal subsurface flow constructed wetlands. Ecol Eng 120:104–108
Tong C, Hill CB, Zhou G, Zhang XQ, Jia Y, Li C (2021) Opportunities for improving waterlogging tolerance in cereal crops—physiological traits and genetic mechanisms. Plan Theory 10(8):1560
Tournaire-Roux C, Sutka M, Javot H, Gout E, Gerbeau P, Luu DT et al (2003) Cytosolic pH regulates root water transport during anoxic stress through gating of aquaporins. Nature 425(6956):393–397
Trenkel ME (2021) Slow-and controlled-release and stabilized fertilizers: an option for enhancing Nutrient use effiiency in agriculture. International Fertilizer Industry Association (IFA)
Tuohy P, Humphreys J, Holden N, Fenton O (2015) Mole drainage performance in a clay loam soil. In: NJF congress: Nordic view to sustainable rural development, 25, Riga (Latvia), 16–18 Jun 2015. NJF Latvia
Tuohy P, O’Loughlin J, Fenton O (2018) Modeling performance of a tile drainage system incorporating mole drainage. Trans ASABE 61(1):169–178
USDA-NRCS (2006) Land resource regions and major land resource areas of the United States, the Caribbean, and the Pacific Basin. USDA Handbook 296. Retrieved from https://www.fertilizer.org/images/Library_Downloads/2010_Trenkel_slow%20release%20book.pdf
Vaahtera L, Brosché M, Wrzaczek M, Kangasjärvi J (2014) Specificity in ROS signaling and transcript signatures. Antioxid Redox Signal 21(9):1422–1441
Varadachari C, Goertz HM (2010) Slow-release and controlled-release nitrogen fertilizers. Indian Nitrogen Group, Society
Velmurugan A, Swarnam TP, Ambast SK, Kumar N (2016) Managing waterlogging and soil salinity with a permanent raised bed and furrow system in coastal lowlands of humid tropics. Agric Water Manag 168:56–67
Vidoz ML, Loreti E, Mensuali A, Alpi A, Perata P (2010) Hormonal interplay during adventitious root formation in flooded tomato plants. Plant J 63(4):551–562
Voesenek LACJ, Sasidharan R (2013) Ethylene–and oxygen signalling–drive plant survival during flooding. Plant Biol 15(3):426–435
Voesenek LACJ, Colmer TD, Pierik R, Millenaar FF, Peeters AJM (2006) How plants cope with complete submergence. New Phytol 170(2):213–226
Wani SH, Choudhary M, Kumar P, Akram NA, Surekha C, Ahmad P, Gosal SS (2018) Marker-assisted breeding for abiotic stress tolerance in crop plants. In: Biotechnologies of crop improvement, vol 3. Springer, Cham, pp 1–23
WAPDA (2007) Waterlogging, salinity and drainage situation. SCARP Monitoring Organization, Water and Power Development Authority, Lahore
WAPDA (Water and Power Development Authority) (2003) Salinity and Reclamation Department. SCARP Monitoring Organization, Lahore
Ward A, Sharpley A, Miller K, Dick W, Hoorman J, Fulton J, LaBarge GA (2018) An assessment of in-field nutrient best management practices for agricultural crop systems with subsurface drainage. J Soil Water Conserv 73(1):5A–10A
Watanabe K, Nishiuchi S, Kulichikhin K, Nakazono M (2013) Does suberin accumulation in plant roots contribute to waterlogging tolerance? Front Plant Sci 4:178
Watanabe K, Takahashi H, Sato S, Nishiuchi S, Omori F, Malik AI, Nakazono M (2017) A major locus involved in the formation of the radial oxygen loss barrier in adventitious roots of teosinte Zea nicaraguensis is located on the short-arm of chromosome 3. Plant Cell Environ 40(2):304–316
Westra S, Fowler HJ, Evans JP, Alexander LV, Berg P, Johnson F, Roberts N (2014) Future changes to the intensity and frequency of short-duration extreme rainfall. Rev Geophys 52(3):522–555
Wiengweera A, 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. J Exp Bot 55(405):2121–2129
Williams MR, King KW, Fausey NR (2015) Drainage water management effects on tile discharge and water quality. Agric Water Manag 148:43–51
Wollmer AC, Pitann B, Mühling KH (2018) Nutrient deficiencies do not contribute to yield loss after waterlogging events in winter wheat (Triticum aestivum). Ann Appl Biol 173(2):141–153
Wu QX, Zhu JQ, Liu KW, Chen LG (2012) Effects of fertilization on growth and yield of cotton after surface waterlogging elimination. Adv J Food Sci Technol 4(6):398–403
Wu H, Xiang J, Chen HZ, Zhang YP, Zhang YK, Zhu F (2018) Effects of exogenous growth regulators on plant elongation and carbohydrate consumption of rice seedlings under submergence. J Appl Ecol 29(1):149–157
Xian C, Qi Z, Tan CS, Zhang TQ (2017) Modeling hourly subsurface drainage using steady-state and transient methods. J Hydrol 550:516–526
Yaduvanshi NPS, Setter TL, Sharma SK, Singh KN, Kulshreshtha N (2012) Influence of waterlogging on yield of wheat (Triticum aestivum), redox potentials, and concentrations of microelements in different soils in India and Australia. Soil Res 50(6):489–499
Yamauchi T, Rajhi I, Nakazono M (2011) Lysigenous aerenchyma formation in maize root is confined to cortical cells by regulation of genes related to generation and scavenging of reactive oxygen species. Plant Signal Behav 6(5):759–761
Yamauchi T, Shimamura S, Nakazono M, Mochizuki T (2013) Aerenchyma formation in crop species: a review. Field Crop Res 152:8–16
Yamauchi T, Watanabe K, Fukazawa A, Mori H, Abe F, Kawaguchi K, Nakazono M (2014) Ethylene and reactive oxygen species are involved in root aerenchyma formation and adaptation of wheat seedlings to oxygen-deficient conditions. J Exp Bot 65(1):261–273
Yamauchi T, Colmer TD, Pedersen O, Nakazono M (2018) Regulation of root traits for internal aeration and tolerance to soil waterlogging-flooding stress. Plant Physiol 176(2):1118–1130
Ylivainio K, Uusitalo R, Turtola E (2008) Meat bone meal and fox manure as P sources for ryegrass (Lolium multiflorum) grown on a limed soil. Nutr Cycl Agroecosyst 81(3):267–278
Ylivainio K, Jauhiainen L, Uusitalo R, Turtola E (2018) Waterlogging severely retards P use efficiency of spring barley (Hordeum vulgare). J Agron Crop Sci 204(1):74–85
Yordanova RY, Popova LP (2001) Photosynthetic response of barley plants to soil flooding. Photosynthetica 39(4):515–520
Yordanova RY, Popova LP (2007) Flooding-induced changes in photosynthesis and oxidative status in maize plants. Acta Physiol Plant 29(6):535–541
Zhang S (2005) Soil hydraulic properties and water balance under various soil management regimes on the Loess Plateau, China, vol 2005, no 2005, p 126
Zhang YK, Schilling KE (2006) Effects of land cover on water table, soil moisture, evapotranspiration, and groundwater recharge: a field observation and analysis. J Hydrol 319(1–4):328–338
Zhang X, Shabala S, Koutoulis A, Shabala L, Johnson P, Hayes D, Zhou M (2015) Waterlogging tolerance in barley is associated with faster aerenchyma formation in adventitious roots. Plant Soil 394(1):355–372
Zheng W, Liu Z, Zhang M, Shi Y, Zhu Q, Sun Y, Geng J (2017) Improving crop yields, nitrogen use efficiencies, and profits by using mixtures of coated controlled-released and uncoated urea in a wheat-maize system. Field Crop Res 205:106–115
Zhou M (2010) Improvement of plant waterlogging tolerance. In: Waterlogging signalling and tolerance in plants. Springer, Berlin, Heidelberg, pp 267–285
Zhou MX, Li HB, Mendham NJ (2007) Combining ability of waterlogging tolerance in barley. Crop Sci 47(1):278–284
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Qamar, R., Atique-ur-Rehman, Shafaat, S., Javeed, H.M.R. (2023). Management of Crops in Water-Logged Soil. In: Ahmed, M., Ahmad, S. (eds) Disaster Risk Reduction in Agriculture. Disaster Resilience and Green Growth. Springer, Singapore. https://doi.org/10.1007/978-981-99-1763-1_12
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