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Review Article

Cascading Impacts of Change in Carbon Dioxide Concentration, Temperature and Precipitation on Horticulture Crops: A Review

Pandurang Pawar1,*, Bhagwan Sakhale1
1Gopinathrao Munde National Institute of Rural Development and Research, Dr. Babasaheb Ambedkar Marathawada University Campus, Aurangabad-431 004, Maharashtra, India.

ABSTRACT

The impacts of an increase in carbon dioxide concentration, temperature and precipitation on physiology, yield and biochemical contents of horticulture crops including its mitigation measures are evident globally. This study mainly focuses on South-East Asia and Africa. We have reviewed crop-wise published literature mainly from 2000-2021 regarding the impacts of rising carbon dioxide concentration, temperature and precipitation on horticulture. Visible phenophase changes in horticultural crops such as budburst, leaf initiation, flowering, fruiting, seedling and the overall development stages of the crops are evident from the available literature. The prevalence of many diseases like blight, mildew, abaca, black sigatoka and Pierce’s disease are the results of climate change. Changes in the biochemical content of the horticulture crops such as tannins, flavonol, alcohol level, acidic content, starch, amino acids, lipids, chloroplasts, sugar, organic acids and antioxidants were observed. The recommended mitigation measures throughout the literature are delayed sowing dates, efficient seed varieties, controlled fertilizer use, soil moisture conservation and other biotechnological measures. Salinity, moisture and environmental stress-tolerant crops need to develop for better management of climate change. Breeding of short-duration and heat-tolerant varieties, vulnerability quantification and early warning disease forecasting are some of the important research areas.

INTRODUCTION

Sustainable production of fruit and vegetables is the challenge of the horticulture sector posed by uncertain climate change and environmental degradation (FAO, 2015). Total greenhouse gas (GHG) emission from anthropogenic sources was estimated to be 23% derived from Agricultural, Forestry and Other Land Use (AFOLU) from 2007 to 2016. The AFOLU activities accounted for around 13% (CO2), 44% (CH4) and 81% (N2O)emissions from anthropogenic activities globally (IPCC, 2019). In 2019, the concentrations of atmospheric CO2 were higher compared to at least the last 2 million years. Concentrations of CH4 and N2O  were also found to be higher than in the last 0.8 million years (IPCC, 2019). Simulations by global climate models have projected an increase in average global warming between 1.5-5.8°C and a 5 to 15% increase in the mean precipitation pattern by the end of the 21st century (IPCC, 2001). Food security risks due to global warming are high to very high if the average temperature rises in the range of 2°C to 2.7°C (IPCC, 2019). The major impacts of climate change are temperature rise, frost-free seasons and growing seasons will lengthen, change in precipitation patterns, an increase in drought, heatwaves, intense and stronger hurricanes, sea-level rise (1-8 feet by 2100) and the Arctic region likely to become ice-free (IPCC, 2007; IPCC, 2013).  Livestock farming and rice production directly contribute to GHG emissions and thereby fuel climate change. 

Globally, the semiarid region comprises approximately 90% of the area with a 99% human population and it is mainly a low-crop productivity region (Hiwale, 2015). A rise in temperature affects pollination, flowering and harvesting dates. In Arctic habitats, some plants are blooming earlier and then flower for longer periods (Gimenez-Benavides et al., 2010). In the last 50 years, extreme weather events like cyclones, floods, landslides and cloud bursts may decrease the production of horticulture by 40% (Sivakumar, 2019). The yield and product quality may reduce due to heat stress and heat waves (Gruda, 2005). Carbon dioxide in the C3 pathway of photosynthesis promotes growth and productivity and is an example of a positive effect on C3 plants. However, it cannot compensate for the rise in temperature and reduced yield of the horticultural crops. In 2007, floods in England reported very high financial losses in the horticulture sector. Direct losses caused by crop and yield decline and some indirect losses like an increase in livestock feeding costs were reported (Posthumus et al., 2009). Soil fertility may get altered due to the impacts of the microbial activity of soil. In bananas, stunting is a common symptom if it is flooded for more than 48 hours continuously; waterlogging for 72-96 hours may be irrecoverable and at this stage, the banana plant often dies (Stover, 1972). The agriculture sector was adversely affected by El Nino from 1997 to 1998, especially in Indonesia, Nordeste and Brazil (Rosenzweig et al., 2001).  Food security risk differs between regions (Gregory et al., 2005). The horticulture sector has tremendous potential to reduce the problem of hunger to a large extent (FAO, 2015). Overall, climate change threatens the agriculture system mainly due to the prevalence of pests and insects, weeds and diseases, heat stress, extreme weather events, soil fertility and erosion. The horticulture sector plays a crucial role in enriching diets, promoting gender equality, employment generation, nutritional security and income increase.
 
Impacts of climate change on major horticultural crops
 
Fruit crops
 
The range and abundance of major pollinators like butterflies, bats, bees and moths are shrinking with climate change. Some of the major factors like high temperature, changing rainfall patterns and increasing CO2 levels are responsible for the impacts on fruit crops.
 
Citrus (Citrus species)
 
The optimum level of temperature and rainfall are 16-27°C and 1400-1800 mm respectively (Nath et al., 2019). Water scarcity may lead to less leaf initiation, leaf size reduction and leathery and thick leaves with unfavourable root growth. The detailed study of temperature sensitivity in the phenological stages of citrus showed that a mean temperature of 20°C is required for flowering. Fruit set development may be hampered if the temperature exceeds 38°C and 50% losses can be seen at 48°C temperature. Cool temperature leads to the breakdown of green chlorophylls and heat may result in re-greening (Mechlia and Carroll, 1989). Temperature determines the fruit growth, phenophase and growing days. Fruits attain early flowering and fruit set in warmer temperatures (Nawaz et al., 2020). The water requirement changes due to the potential climate change were reported for citrus from major citrus-producing regions of the world like Asia, Africa, Australia, the Mediterranean and America. In response to increasing atmospheric CO2, the projected decrease in future citrus irrigation requirements is by up to 37% and evapotranspiration was also projected to decrease by up to 12%. However, a negative correlation has been observed between annual rainfall changes and citrus irrigation requirements. However, the prediction showed an increase in drainage and canopy interception for the 2055s and 2090s compared to the baseline period. Many authors showed that the increase in atmospheric CO2 influences the stomatal opening and thereby decreases evapotranspiration. Moreover, the increase in temperature with constant CO2 concentration increases the evapotranspiration and gross irrigation requirement (Fares et al., 2017). In addition to the temperature and CO2, severe droughts, extreme weather events and flooding also influence the citriculture sector. A reduction in yield, fruit size, photosynthesis and CO2 uptake was observed.
            
Mango (Mangifera indica L.)
 
The optimum level of rainfall is 900-1100 mm and the temperature is 24-30°C, temperatures above 42°C and below 10°C may affect the growth (Nath et al., 2019). Flowering phenology may get influenced and hot and cold waves can cause considerable damage (Singh et al., 1966). Premature ripening, flowering delay, discrepancy in fruit maturity and unusual fruit sets are the major effects of temperature rise (Rajan et al., 2011). Moreover, the higher temperature leads to multiple reproductive flushes and alteration of reproductive buds into vegetative buds (Rajan et al., 2013). The high temperature affects the cell wall enzyme activity, delayed ripening and changes in chemical composition (Haokip et al., 2020). The suitable area for mango may shift due to an increase in the temperature of 0.7-1.0°C for Alphonso and Dashehari varieties of mango (Haokip et al., 2020).
      
Banana (Musa spp)
 
Banana requires 20-30°C temperature and 500-3000 mm rainfall for ideal growth (Nath et al., 2019). An increase in plant maturity at about 31-32°C temperature results in a shortening of the bunch development period. The sunburn damage in fruits may be seen on exposure to >38°C temperature. Soil moisture deficit and water stress lead to poor bunch formation, small-sized fingers besides low numbers, poor filling of fingers and less bunch weight (Turner et al., 2007). Since 1961, the annual yield has increased by 1.37 t ha-1 in a changing climate that shows temporary positive effects. However, by 2050, the global yield gains would reduce by 0.59 t ha-1 (Varma and Bebber, 2019). The infections of Black Sigatoka increased due to the increased risk of climate change in the Caribbean and Latin America. The temperature increase has resulted in a wetter crop canopy and spore germination with growth (Bebber 2019). The maximum tolerable temperature for the growth of leaf area, leaf production and dry weight increment is 33.50 to 39.20°C for bananas (Ravi and Mustaffa, 2013).
     
Guava (Psidium guajava L.)
 
The optimum temperature range is 23°C to 28°C and the requirement of about 1000 mm of rainfall for guava (Nath et al., 2019). The temperature increase may lead to disease and pest outbreaks and fruit fly abundance (Hazarika, 2013). The increase of 0.2°C temperature may reduce the suitable area for the development of the red colour guava (Haokip et al., 2020). Even though guava is an environmental stress-tolerant species, drought and cold can cause harm to younger plants.

Grape (Vitis vinifera L.)
 
It is originally from temperate regions. Higher temperature leads to higher sugar content and less amount of tartaric acid. The rise in temperature triggers an advance in phenology and harvest dates. The increase in the alcohol level by more than 2% by volume, pH by 0.2 units and decrease in acidity level by 1 g tartrate per litre. It may be the result of a rise in atmospheric CO2, radiation and more hang time. Some of the predictable effects showed that flowering would be advanced by 15 days until 2050 and by 30 days by the twenty-first century. Similarly, ripening will also advance by 25 and 45 days, respectively. The increased evapotranspiration led to the drier vintage due to the temperature rise, while negligible effects were observed for amino acid synthesis. In red grapes, the higher UV-B radiation intensifies colour, tannin synthesis and flavonol. However, in white grapes, it may induce off-flavours and sunburn (Leeuwen and Darriet, 2016). The temperature increase affected the physiological activities of the grapes like a decrease in net photosynthesis at >25°C and starch getting replaced by lipids in leaf chloroplasts. Further warming of >30°C may reduce the weight and berry size, including the stoppage of metabolism and sugar accumulation. At elevated CO2 levels, 40-50% biomass may increase as total biomass and dry fruit weight. Even though the level of acid and sugar equally increased at the stage of maturity, none of the variables was found to be affected due to elevated CO2 levels (Bindi et al., 2001; Mira de Orduna, 2010). The various pests and diseases and their vectors are also affected due to climate change. Some diseases may move poleward like Pierce’s disease caused by Xylella fastidiosa.
 
Pomegranate (Punica granatum L.)
 
The optimum rainfall and temperature are 600-1200 mm and 18-36°C respectively. The drought situation results in the cracking of pomegranate fruits and reduces the fruit set. The temperature increase hampers the processes like photosynthesis, alteration in sugars, flavonoid content, organic acids, firmness and antioxidant activity (Haokip et al., 2020). 

Litchi (Litchi chinensis)
 
The fruit cracking may be observed during drought situations. It requires cold dry winters but not less than zero degrees Celsius and warm humid summers. The optimum requirement of temperature is 25-35°C and rainfall is 1200-2500 mm (Nath et al., 2019). Drought may lead to stomatal closure, reducing CO2 assimilation, leaf expansion, fruit growth and stem extension; it also hampers the process of photosynthesis (Menzel, 2005). The high temperature causes sunburn on fruits and leaves and growth inhibition of shoots and roots. The fruit’s discolouration, cracking, dropping and underdevelopment of the fruits are the result of an unfavourable climate (Kumar, 2016) (Fig 1 and 2).

Fig 1: Litchi fruit cracking and Litchi fruit growth retardation. Both images from Kumar, 2016.



​

Fig 2: Litchi fruit cracking and Litchi fruit growth retardation. Both images from Kumar, 2016.


 
Papaya (Carica papaya L.)
 
The activities like stigma and sterility activities get enhanced due to an increase in temperature which also results in the flower drop and sex change in flowers (Haokip et al., 2020). The optimum range of rainfall, temperature and soil moisture are 800-1500 mm, 18-27°C and 20% respectively. The environmental stress may lead to photosynthetic carbon assimilation, water deficit and lower biomass production. In turn, growth, fruit quality and yield will be affected. Soil moisture plays a crucial role in controlling the growth and yield; the 10% soil moisture reduction may decrease the leaf dry weight, central leaflet length and several leaves; a 12% soil moisture decrease may result in a shrinking of the trunk diameter, dry matter and plant height (Mahouachi et al., 2006). The high air temperature increases the leaf temperature up to 42°C and decreases the transpiration to 0.20 L m-2 leaf h-1 (Ferraz et al., 2015; Campostrini et al., 2018).
 
Apple (Malus domestica L)
 
In Western Himalayas, changes in the pattern of blossom, fruit yield and quality of apples including early flowering, have been reported. Temperate fruits like apples are very sensitive to frosts; temperatures below zero can damage the flower buds and also worsens the quality of the fruits. A shift in the range of cultivation towards the higher altitude in the apple-growing region of Himachal Pradesh, India, where the temperature trend is increasing and the precipitation decreasing over the period (Rana et al., 2011).
 
Custard apple (Annona reticulata L.)
 
Less than zero degrees Celsius and more than 40°C temperature are harmful and may lead to a poor fruit set. The optimum range of rainfall and temperature is 800-1800 mm and 18-27 mm respectively (Nath et al., 2019). The higher rain and temperature may lead to the dropping of fruits and black spots respectively (Rajatiya et al., 2018).   
 
Plantation crops
 
Cashew
 
The optimum temperature and rainfall requirement for cashew are 20-27.5°C and 600-1500 mm respectively. A temperature >34°C and less than 20% relative humidity results in the drying of flowers and yield reduction. Unseasonal rain leads to more pest attacks and diseases, a decline in pollinator insect activity, poor setting, blackening and poor quality of nuts. The nut yield was reduced by 50-65% due to unseasonal rain. The salinity level (e.g. Tamilnadu, India) and rising sea water level due to the tsunami in coastal areas affect the cashew crops production (Yadukumar et al., 2010; Rupa et al., 2013).
 
Coconut
 
The production and productivity of nuts get affected due to cyclones and droughts. However, over the last 50 years, coconut production has increased in some parts of India (Kumar and Aggarwal, 2013; Singh, 2013).  The coconut is mainly a rainfed plantation and drought reduces nut yield. The deficit in soil and atmospheric water leads to reduced carbon assimilation. The reduction of net carbon assimilation rate from 7% to 47% for the dwarf genotypes and from 12% to 67 for the tall genotype was reported (Repellin et al., 1994; Repellin et al., 1997). The biomass at elevated CO2 concentration varies based on the exposure level of CO2, at 550 ppm and 700 ppm biomass increases by 8 and 25% respectively (Hebbar et al., 2013).
   
Black pepper
 
Kerala Agricultural University’s Agricultural Market Intelligence Centre reported a rapid decline (50%) in Indian pepper production in the past 10 years. A decline (24%) in the total area under the pepper plantation was also observed (Malhotra, 2017). High temperature impedes the fruit set and fertilisation progression (Erickson and Markhart, 2002). The black pepper requires an average of 200-300 cm rainfall and 23-32°C temperature for ideal growth. The increase in rainfall from December to January decreases productivity while rainfall from March to April increases productivity. This is a thermosensitive crop and high temperatures may inhibit fruit set, especially in the post-pollination stage (Das and Sharangi, 2018). 
 
Vegetables
 
Onion (Allium cepa L)
 
In the early stages, soil water stress may reduce bulb size and about 26% yield (Lawande, 2010). Flooding may decrease the yield by up to 30-40% (Singh, 2013). An increase in atmospheric CO2 concentration also improves the yield of the onion by 25-30% (Wurr et al., 1998).
 
Tomato (Solanum lycopersicum L.)
 
The optimum daily mean temperature for tomato fruit set is 21-24°C (Geisenberg and Stewart, 1986). Water stress supplemented by more than 28°C temperature may result in a 30-45% flower drop (Rao, 1995). Accumulation of endogenous ethylene under flooding conditions leads to an epinastic leaf response. Low fruit quality, smaller size and reduction in fruit set may be observed due to an increase in temperature. Deficient pollen growth and irregularities in the endothecium and epidermis were reported to be associated with temperature stress (Sato et al., 2002). 
 
Hot pepper (Capsicum annuum L.)
 
A detailed study was carried out by Lee et al., 2017, on Capsicum annuum L. under two climate change scenarios. (Table 1).

Table 1: Shows two climate change scenarios.



At RCP 4.5 treatments, the mean plant height was the highest of all treatments. At RCP 8.5, treatments, decreased leaf length, fruit length, fruit width, dry fruit weight and fresh fruit weight, by 40.7%, 22.3%, 62.5%, 0.8/fruit and 4.1/fruit respectively. The increase in the percentage of dry matter and number of leaves were 1.3 and 2.2 times, respectively. The maximum carbon dioxide assimilation of 17.3 μmol CO2 m-1 s-1 at RCP 8.5 was observed while no significant difference was recorded at RCP 4.5 treatments compared to the normal climatic conditions (Table 2).

Table 2: Comparative changes in hot pepper in RCP 4.5 and RCP 8.5 at 171 days after transplanting.



The reduction of fruit yield by 89.2% compared to the normal climatic conditions. The number of harvesting days decreased from 49 to 37 days at RCP 8.5 treatment. Various RCP climate change scenarios showed a reduction in yield and growth, while negative effects were observed for photosynthesis, morphogenesis and fruit characteristics. However, more resilience was noted in the RCP 4.5 treatment of hot pepper (Lee et al., 2017) (Fig 3).

Fig 3: RCP treatments wise morphological stages of Capsicum annuum L. Image from Lee et al., (2017).


 
Cucumber
 
Sex expression of male and female flowers may get affected: low-temperature results in more female flower production and high temperature leads to more male flower production (Wien, 1997).
 
Cauliflower
 
High humidity with 15-25°C temperature is the ideal condition, excess temperature may delay the curd initiation. The crop duration decline was seen with increasing temperature. The curd weight had a very small negative effect on rising temperature. However, Increasing CO2 leads to an increase in curd weight and it also affects product quality (Olesen and Grevsen, 1993; Singh, 2010).
 
Tuber crops
 
Potato
 
The optimum temperature for the emergence of potatoes is 22-24°C and well-drained soil with a pH of 4.8-5.8. Since it is a heat-sensitive crop, less than the optimum temperature delays the growth of the sprouts.  A temperature increase beyond the optimum level results in lower sprout growth, it decreases the productivity and tuber numbers of the potatoes (Sale, 1979, Ghosh et al., 2000; Rykaczewska, 2015). The occurrence of frost may be infrequent due to the warming of winter, which will result in a longer growing period and more productivity in these regions (Singh et al., 2005; Singh, 2008). Leaf does not expand fully at a very high temperature, which results in comparatively less light interception. The tuber yield also gets affected drastically even at moderately high temperatures without much affecting total biomass production and photosynthesis (Peet and Wolfe, 2000). The late blight (Phytophthora infestans) pathogen is dependent on climatic factors for infection (Lehsten et al., 2017) (Fig 4).

Fig 4: Late blight caused by Phytophthora infestans. Image from Lehsten et al., (2017).



Soil-borne pathogens like Synchytrium endobioticum triggering warts and Spongospora subterranean results in a powdery scab are enhanced by high soil moisture and low temperature. Global warming is most likely to reduce wart infection, powdery scab infection, charcoal rot, Sclerotium wilt and bacterial wilt (Singh et al., 2013). A rise in the CO2 level also affects the quality of the potato, increasing the amount of dry matter and starch. The decrease in the level of nitrates and glycoalkaloids results in higher-quality tubers. However, almost all types of nutrients get reduced in the tuber under elevated CO2 conditions (Cao and Tibbitts, 1997; Schapendonk et al., 2000; Donnelly et al., 2001; Fangmeier et al., 2002).
  
Sweet potato, cassava, greater yam, elephant foot yam and taro
 
The yield reduction may result due to < 20% soil moisture availability in sweet potato while for cassava it was a 28-42% decrease in yield in drought-like situations (Ramanujam, 1990). Pushpalatha et al., (2021) carried out a detailed study on tuber crops by using the LARS weather generator to derive future climatic conditions for 2030, 2050 and 2070. The predicted results differ for different locations. The climate projection indicates the increase in minimum (3.4°C) and maximum (3.8°C) temperature; the rainfall prediction is from -721 to 448 mm. (Table 3).

Table 3: Prediction of tuber crop yield changes from 2030 to 2070.


 
Potential diseases and pests outbreaks
 
Lehmann et al., (2020) identify the severity of the threat insects pose as a pest and identify at least one response to warming, 41% of responses showed increased pest damage and 4% showed consistency with reduced effects. However, 55% of the insect pests exhibited mixed reactions. It shows that the severity depends on the circumstances and it may decrease or increase with ever-increasing climate change. Further research is needed to understand the complex responses of each species across the geographic range. Overall, insect pests negatively influence the productivity and profitability of forestry and agricultural operations (Lehmann et al., 2020). Crop yield may improve as a slight increase may benefit the crop yield to improve from the Tropic of Cancer and Tropic of Capricorn towards the north and South poles, respectively. A slight increase in temperature in higher latitudes will aid agricultural production, however, the impact will vary based on the varieties of the crop as well as the regional climate and topography (Malhotra, 2017). Warm conditions are suitable for blight and mildew diseases in addition to pests like bugs and beetles. Overall, the different growth stages turned in favour of pests viz. population growth, several generations, developmental seasons, crop pests phenology and invasion by migrant pests species (Haokip et al., 2020).
 
Carbon sequestration potential of horticulture
 
Horticulture can counter the adverse consequences of global warming by providing an additional carbon sink. biogas. The high-density cashew crop tremendously helps in carbon sequestration. Rubber, coffee and cocoa horticulture crops possess the significant potential for sequestration of carbon dioxide from the atmosphere. Mitigation of climate change is possible with the creation of agroforestry sinks (Albrecht and Kandji, 2003, Montagnini and Nair, 2004). In high-density plantations, it has been estimated that CO2 sequestration of 32.25-59.22 t CO2/ha up to seven years of crop growth is possible (Rupa et al., 2013). The coconut tree can sequester up to 0.3 to 2.3 Certified Emission Reduction (CER) of CO2 annually. However, carbon stocks may vary depending on the agro-climatic zones and the soil type (Hebbar et al., 2013). Perennial horticultural crops can sequester more carbon dioxide than annual horticultural crops. In a terrestrial ecosystem, the scope of carbon sequestration is more compared to the agriculture or agroforestry system. The different crops have different carbon sequestration potentials. The decreasing order of carbon sequestration is mango, cashew, rose, vegetable, medicinal and aromatic plants. This system also helps in earning carbon credits for the horticulture system for carbon sequestration. A scientific experiment was conducted by ICAR-CPCRI, Kerala, in May-July 2015. The CO2 sequestration was highest for the intercropping as compared to the monocrop (Bhagya and Maheswarappa, 2017; Ganeshamurthy et al., 2020) (Table 4).

Table 4: Carbon sequestration potential per hector.


 
Mitigation measures
 
The potential of horticulture as a global carbon sink like the natural forest is valuable and can be exploited for the sequestration of carbon. The major adaptation approaches based on research by various scholars recommended are delaying the sowing dates, changing a variety of seeds, developing heat-tolerant and climate-resilient varieties, modification of fertilizer use, conservation of soil moisture and irrigation at the critical stages of the plants. The efficient species of horticulture crops need to develop like water succulent crops, less use of chemical fertilisers and replace with organic green manure.

The use of some of the salinity tolerant varieties of different horticulture crops like mango (Bappakai, Nileshwar dwarf, Kurakkan), Citrus (Cleopatra mandarin), lime (Cleopatra mandarin) and fig (Ficus glomerata). The drought-tolerant varieties such as citrus (Rangpur Lime), ber fruit (Ziziphus rotundifolia Lam., Ziziphus nummularia, Z. mauritiana var. Shukhawani and Tikdi), pomegranate (Ruby variety of Punica granatum) and sapota (Khirani) are important for plantations (Singh et al., 2009; Singh, 2010).

For citriculture, variety breeding, rootstock breeding, change in cultivation techniques, resource optimisation and scientific knowledge have to develop. For fruit crops, the dormancy avoidance method can be employed to help in budburst without chilling temperature. It made it possible to grow temperate crops in tropical regions like India and Kenya. The artificial bud-breaking methods may help to desiccate the trees, manual defoliation, late pruning and delayed irrigation. The chilling requirement can be manipulated by planting the tree cultivars for a longer period so that it can help in adaptation. For litchi, certain mitigation measures like biotechnological interventions, breeding programmes and agro-technological advances may help to mitigate the negative impacts of climate change. To address biotic stresses, adaptation strategies like balanced nutrition, supply of plant growth regulators, bio-fertilisers, pruning and canopy management, deficit irrigation and fruit thinning may be considered for better litchi production (Kumar, 2016).  For cashew crops, conservation of soil and water, mulching, proper irrigation and green manuring are the best options to tackle climate change (Rupa et al., 2013). For coconut, the use of scientific technologies with drought-tolerant cultivars, soil conservation, water management and cultural practices are recommended (Hebbar et al., 2013).

Grafting of the vegetable can be helpful to resist drought, flooding, salinity, environmental stresses and water use efficiency (Kubota et al., 2008; Kumar et al., 2017). Land degradation problems can be mitigated by using certain management options like growing green manure crops, zero tillage, crop residue retention and ground cover maintenance. In addition to that, agroforestry and horticulture can reduce soil erosion and nutrient leaching. To enhance food security, increased food productivity, agroforestry, improved cropland management, agriculture diversification, integrated water management and improved livestock management have the potential to mitigate the negative impacts of climate change (IPCC, 2019).

The evaporative cooling approach to increase the number of chilling hours may help to induce the bud burst. The use of intermittent overhead sprinklers during the hottest hours is also useful to ensure chilling and bud burst. Certain chemical treatments like hydrogen cyanamide and DNOC oil lead to earlier bud break by three to four weeks (Haokip et al., 2020). Some of the mitigation strategies like land and plant management practices, canopy management, microclimate modification, microsite modification, weather forecasting system, effective water management, water harvesting, soil conservation, use of degraded and wasteland for fruit production, high-density planting and use of a net house or poly house are very effective for fruit crops (Nath et al., 2019). A reduction in animal-origin food, less consumption of livestock products and policy measures are needed to mitigate the negative impacts (Friel et al., 2009). The development of a healthy, diversified forest ecosystem that can tolerate more environmental stress. It may include disease control, pest management, forest fire management and limiting livestock grazing and logging will certainly result in a more resilient ecosystem. Suitable adaptation strategies should be supported through policies and institutions as well (FAO, 2015). A database of high-temperature risks associated with present and future climatic patterns is required to create. The spread of various diseases and pests under various climatic conditions and their impacts on horticulture crops are essential to document across the agroecological zones. The carbon sequestration and carbon release from horticulture crops need to quantify (Singh, 2013).

REFERENCES


  1. Albrecht, A. and S.T. Kandji (2003). Carbon sequestration in tropical agroforestry systems. Agriculture, Ecosystems and Environment. 99: 15-27.

  2. Bebber, D.P. (2019). Climate change effects on black sigatoka disease of banana. Philosophical Transactions of the Royal Society B 374: 20180269.

  3. Bhagya, H.P. and Maheswarappa, H.P. (2017). Carbon sequestration potential in coconut-based cropping systems. Indian Journal of Horticulture. 74: 1-5.

  4. Bindi, M., Fibbi, L., Lanini, M. and Miglietta, F. (2001). Free Air CO2 Enrichment (FACE) of grapevine (Vitis vinifera L.): I. Development and testing of the system for CO2 enrichment. European Journal of Agronomy. 14: 135-143.

  5. Campostrini, E., Schaffer, B., Ramalho, J.D.C., González, J.C., Rodrigues, W.P., da Silva, J.R.  and Lima, R.S. (2018). Environmental factors controlling carbon assimilation, growth and yield of papaya (Carica papaya L.) under water-scarcity scenarios. Water scarcity and sustainable agriculture in semiarid environment, Elsevier: 481-505.

  6. Cao, W. and Tibbitts, T.W. (1997). Starch concentration and impact on specific leaf weight and element concentrations in potato leaves under varied carbon dioxide and temperature.  Journal of Plant Nutrition. 20: 871-881.

  7. Das, S. and A.B. Sharangi (2018). Impact of climate change on spice crops. Indian Spices, Springer: 379-404.

  8. Donnelly, A., Lawson, T., Craigon, J., Black, C.R., Colls, J.J. and Landon, G. (2001). Effects of elevated CO2 and O3 on tuber quality in potato (Solanum tuberosum L.). Agriculture, Ecosystems and Environment. 87: 273-285.

  9. Erickson, A. and Markhart, A. (2002). Flower developmental stage and organ sensitivity of bell pepper (Capsicum annuum L.) to elevated temperature. Plant, Cell and Environment. 25: 123-130.

  10. Fangmeier, A., De Temmerman, L., Black, C., Persson, K. and Vorne, V. (2002). Effects of elevated CO2 and/or ozone on nutrient concentrations and nutrient uptake of potatoes. European Journal of Agronomy. 17: 353-368.

  11. FAO (2015). Climate Change and Food Security: Risks and Responses. Rome, Italy, Food and Agriculture Organization of the United Nations: 1-122.

  12. Fares, A., Bayabil, H.K., Zekri, M., Mattos-Jr, D. and Awal, R. (2017). Potential climate change impacts on citrus water requirement across major producing areas in the world. Journal of Water and Climate Change. 8: 576-592.

  13. Ferraz, T.M., Netto, A.T., Reis, F.D., Pecanha, A.L., De Sousa, E.F., Machado Filho, J.A., Rodrigues, W.P., Glenn, D.M. and Campostrini, E. (2015). Relationships between sap-flow measurements, whole-canopy transpiration and reference evapotranspiration in field-grown papaya (Carica papaya L.). Theoretical and Experimental Plant Physiology. 27: 251-262.

  14. Friel, S., Dangour, A.D., Garnett, T., Lock, K., Chalabi, Z., Roberts, I., Butler, A., Butler, C.D., Waage, J., McMichael, A.J. and Haines, A. (2009). Public health benefits of strategies to reduce greenhouse-gas emissions: Food and Agriculture. The Lancet. 374: 2016-2025.

  15. Ganeshamurthy, A.N., Kalaivanan, D. and Rajendiran, S. (2020). Carbon Sequestration Potential of Perennial Horticultural Crops in Indian Tropics. Carbon Management in Tropical and Sub-Tropical Terrestrial Systems, Springer: 333-348.

  16. Geisenberg, C. and Stewart, K. (1986). Field Crop Management. The Tomato Crop, Springer: 511-557.

  17. Ghosh, S.C., Asanuma, K.I., Kusutani, A. and Toyota, M. (2000). Effects of temperature at different growth stages on nonstructural carbohydrate, nitrate reductase activity and yield of potato. Environment Control in Biology. 38: 197-206.

  18. Gimenez-Benavides, L., García-Camacho, R., Iriondo, J.M. and Escudero, A. (2010). Selection on flowering time in Mediterranean high-mountain plants under global warming. Evolutionary Ecology. 25: 777-794.

  19. Gregory, P.J., Ingram, S.I. and Brklacich, M. (2005). Climate change and food security. Philosophical Transactions of the Royal Society B: Biological Sciences. 360(1463): 2139-2148.

  20. Gruda, N. (2005). Impact of environmental factors on product quality of greenhouse vegetables for fresh consumption. Critical Reviews in Plant Sciences: 24:227-247.

  21. Haokip, S.W., Shankar, K. and Lalrinngheta, J. (2020). Climate change and its impact on fruit crops. Journal of Pharmacognosy and Phytochemistry. 9: 435-438.

  22. Hazarika, T. (2013). Climate change and Indian horticulture: Opportunities, challenges and mitigation strategies. International Journal of Environmental Engineering Management. 4: 629-630.

  23. Hebbar, K.B., Balasimha, D. and Thomas, G.V. (2013). Plantation crops response to climate change: Coconut perspective. climate-resilient horticulture: Adaptation and Mitigation Strategies: 177-187.

  24. Hiwale, S. (2015). Sustainable Horticulture in Semiarid Dry Lands. New Delhi, Springer.

  25. IPCC (2001). Climate Change 2001: Synthesis Report. A Contribution of Working Groups I, II and III to the Third Assessment Report of the Integovernmental Panel on Climate Change. R.T. Watson and the Core Writing Team. Cambridge, United Kingdom and New York, NY, USA: 398.

  26. IPCC (2007). Climate Change 2007: Impacts, Adaptation and Vulnerability. Contribution of Working Group II to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. Parry, M.L., Canziani, O.F., Palutikof, J.P., Linden, P.J. and Hanson, C.E. Cambridge, UK: 976.

  27. IPCC (2013). Summary for policymakers Climate Change 2013: The Physical Science Basis. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change. Stocker, T., Qin, D., Plattner, G. et al., NY USA.

  28. IPCC (2019). Summary for Policymakers. Climate Change and Land: An IPCC special report on climate change, desertification, land degradation, sustainable land management, food security and greenhouse gas fluxes in terrestrial ecosystems. Shukla, P.R., Skea, J., Buendia, E.C. et al., 1-41.

  29. IPCC (2021). Climate Change 2021: The Physical Science Basis. Contribution of Working Group I to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change, IPCC.

  30. Kubota, C., Michael, A., McClure, N., Kokalis-Burelle, M.G.. Bausher and Rosskopf, E.N. (2008). Vegetable grafting: History, use and current technology status in North America. Horticultural Sciences. 43: 1664-1669.

  31. Kumar, P., Rouphael, Y., Cardarelli, M. and Colla, G. (2017). Vegetable grafting as a tool to improve drought resistance and water use efficiency. Frontiers in Plant Science. 8(1130).

  32. Kumar, R. (2016). Litchi. Abiotic Stress Physiology of Horticultural Crops, Springer: 235-266.

  33. Kumar, S.N. and Aggarwal, P.K. (2013). Climate change and coconut plantations in India: Impacts and potential adaptation gains. Agricultural Systems. 117: 45-54.

  34. Lawande, K., Singh, H.P., Singh, J.P. and Lal, S.S. (2010). Impact of Cimate Change on Onion and Garlic Production. Challenges of Climate Change-Indian Horticulture. New Delhi, Western Publishing House. 100-103.

  35. Lee, S.G., Kim, S.K., Lee, H.J., Lee, H.S. and Lee, J.H. (2017). Impact of moderate and extreme climate change scenarios on growth, morphological features, photosynthesis and fruit production of hot pepper. Ecology and Evolution. 8: 197-206.

  36. Leeuwen, V.C. and Darriet, P. (2016). The impact of climate change on viticulture and wine quality. Journal of Wine Economics. 11: 150-167.

  37. Lehmann, P., Ammunét, T., Barton, M., Battisti, A., Eigenbrode, S.D., Jepsen, J.U., Kalinkat, G., Neuvonen, S., Niemelä, P., Terblanche, J.S., Økland, B. and Björkman, C. (2020). Complex responses of global insect pests to climate warming. Frontiers in Ecology and the Environment. 18: 141-150.

  38. Lehsten, V., Wiik, L., Hannukkala, A. andreasson, E., Chen, D., Ou,  T., Liljeroth, E., Lankinen, Å. and Grenville-Briggs, L. (2017). Earlier occurrence and increased explanatory power of climate for the first incidence of potato late blight caused by Phytophthora infestans in Fennoscandia. PloS one 12: e0177580.

  39. Mahouachi, J., Socorro, A.R. and Talon, M. (2006). Responses of papaya seedlings (Carica papaya L.) to water stress and re-hydration: Growth, photosynthesis and mineral nutrient imbalance. Plant and Soil. 281: 137-146.

  40. Malhotra, S. (2017). Horticultural crops and climate change: A review. Indian Journal of Agricultural Sciences. 87: 12-22.

  41. Mechlia, N.B. and Carroll, J.J. (1989). Agroclimatic modeling for the simulation of phenology, yield and quality of crop production. International Journal of Biometeorology 33: 36-51.

  42. Menzel, C.M. (2005). Plant water relations and irrigation. Litchi and longan: Botany, Production and Uses: 183-207.

  43. Mira de Orduña, R. (2010). Climate change associated effects on grape and wine quality and production. Food Research International. 43: 1844-1855.

  44. Montagnini, F. and Nair, P. (2004). Carbon sequestration: An underexploited environmental benefit of agroforestry systems. New vistas in agroforestry, Springer: 281-295.

  45. Nath, V., Kumar, G., Pandey, S.D. and Pandey, S. (2019). Impact of climate change on tropical fruit production systems and its mitigation strategies. Climate Change and Agriculture in India: Impact and Adaptation: 129-146.

  46. Nawaz, R., Abbasi, N.A., Hafiz, I.A. and Khalid, A. (2020). Impact of climate variables on growth and development of Kinnow fruit (Citrus nobilis Lour x Citrus deliciosa Tenora) grown at different ecological zones under climate change scenario. Scientia Horticulturae. 260: 108868.

  47. Olesen, J.E. and Grevsen, K. (1993). Simulated effects of climate change on summer cauliflower production in Europe. European Journal of Agronomy. 2: 313-323.

  48. Peet, M.M. and Wolfe, D.W. (2000). Crop Ecosystem Responses to Climate Change: Vegetable Crops, CABI Publishing, New York and Wallingford, UK.

  49. Posthumus, H., Morris, J., Hess, T.M., Neville, D., Phillips, E. and Baylis, A. (2009). Impacts of the summer 2007 floods on agriculture in England. Journal Flood Risk Management. 2: 182-189.

  50. Pushpalatha, R., Santhosh Mithra, V.S., Sunitha, S., Goerge, J., Nedunchezhiyan, M., Mamatha, K., Ashok, P., Alam, S., Saud, B.K., Tarafdar, J., Mitra, S., Deo, C., Velmurugan, M., Suja, G., Ravi, V. and Gangadharan, B. (2021). Impact of climate change on the yield of tropical root and tuber crops vs. Rice and potato in India. Food Security: 1-14.

  51. Rajan, S., Ravishankar, H., Tiwari, D., Singh, V.K., Saxena, P., Singh, S., Reddy, Y.T.N., Upreti, K.K., Burondkar, M. M., Bhagwan, A. and Kennedy, R. (2013). Harmonious phenological data: A basic need for understanding the impact of climate change on mango. Climate-resilient horticulture: Adaptation and Mitigation Strategies: 53-65.

  52. Rajan, S., Tiwari, D., Singh, V., Saxena, P., Singh, S., Reddy, Y., Upreti, K., Burondkar, M., Bhagwan, A. and Kennedy, R. (2011). Application of extended BBCH scale for phenological studies in mango (Mangifera indica L.). Journal of Applied Horticulture. 13: 108-114.

  53. Rajatiya, J., Varu, D.K., Gohil, P., Solanki, M., Halepotara, F., Gohil, M., Mishra, P. and Solanki, R. (2018). Climate change: impact, mitigation and adaptation in fruit Crops. Int. J. Pure App. Biosci 6: 1161-1169.

  54. Ramanujam, T.J.P. (1990). Effect of moisture stress on photosynthesis and productivity of cassava. 24: 217-224.

  55. Rana, R.S., Bhagat, R.M. and Kalia, V. (2011). Impact of climate change on apple crop in Himachal Pradesh. Journal of Agrometeorology. 13: 97-103.

  56. Rao, N.K.S. (1995). Management of heat, moisture and other physical stress factors in tomato and chili in India. Collaborative vegetable research in South Asia, Tainan, Proceedings of the SAVERNET Midterm review workshop, AVRDC.

  57. Ravi, I. and Mustaffa, M.M. (2013). Impact, adaptation and mitigation strategies for climate resilient banana production. climate- resilient horticulture: Adaptation and Mitigation Strategies. 45-52.

  58. Repellin, A., Daniel, C. and Zuily Fodil, Y. (1994). Merits of physiological tests for characterizing the performance of different coconut varieties subjected to drought. Oleagineux (France).

  59. Repellin, A., Thi, A.T., Tashakorie, A., Sahsah, Y., Daniel, C. and Zuily-Fodil, Y. (1997). Leaf membrane lipids and drought tolerance in young coconut palms (Cocos nucifera L.). European Journal of Agronomy. 6: 25-33.

  60. Rosenzweig, C., Iglesius, A., Yang, X.B., Epstein, P.R. and Chivian, E. (2001). Climate change and extreme weather events- Implications for food production, plant diseases and pests. Global Change and Human Health. 2.

  61. Rupa, T.R., Rejani, R. and Bhat, M.G. (2013). Impact of climate change on cashew and adaptation strategies. Climate-resilient horticulture: Adaptation and Mitigation Strategies. 189-198.

  62. Rykaczewska, K. (2015). The effect of high temperature occurring in subsequent stages of plant development on potato yield and tuber physiological defects. American Journal of Potato Research. 92: 339-349.

  63. Sale, P.J. (1979). Growth of potatoes (Solanum tuberosum L.) to the small tuber stage as related to soil temperature. Australian Journal of Agricultural Research. 30: 667-675.

  64. Sato, S., Peet, M.M. and Thomas, J.F. (2002). Determining critical pre and post anthesis periods and physiological processes in Lycopersicon esculentum Mill. exposed to moderately elevated temperatures. Journal of Experimental Botany. 53: 1187-1195.

  65. Schapendonk, H.C., van Oijen, M., Dijkstra, P., Pot, C.S., Jordi, W.J.R. and Stoopen, G.M. (2000). Effects of elevated CO2 concentration on photosynthetic acclimation and productivity of two potato cultivars grown in open-top chambers. Functional Plant Biology. 27: 1119-1130.

  66. Singh, B.P., Dua, V.K., Govindakrishnan, P.M. and Sharma, S. (2013). Impact of climate change on potato. Climate-resilient horticulture: Adaptation and mitigation Strategies. H. Singh, N. Rao and K. Shivashankar. India, Springer: 125-135.

  67. Singh, H. (2013). Adaptation and mitigation strategies for climate- resilient horticulture, Adaptation and Mitigation Strategies. India, Springer: 1-12.

  68. Singh, H., Shukla, S. and Malhotra, S. (2009). Ensuring Quality Planting Material in Horticulture Crops. A Book of Lead Papers 9th Agricultural Science Congress, Kashmir, Srinagar.

  69. Singh, H.C.P., Singh, H.P., Singh, J.P. and Lal, S.S. (2010). Impact of climate change on horticultural crops. Challenges of Climate Change in Indian Horticulture. New Delhi, Westville Publishing House: 1-8.

  70. Singh, J. (2008). INFOCROP-POTATO a model for simulating growth and yield of potato in the sub-tropics. Shimla, India, Central Potato Research Institute.

  71. Singh, J., Govindakrishnan, P., Lal, S. and Aggarwal, P.J.P.R. (2005). Increasing the efficiency of agronomy experiments in potato using INFOCROP-POTATO model. 48: 131-152.

  72. Singh, R.N., Majumder, P.K. and Sharma, D.K. (1966). Sex Expression in Mango (Mangifera indica L.) with Reference to Prevailing Temperature. Proceedings of American Society Horticulture Science. (pp.71-96).

  73. Sivakumar, M. (2019). Natural disasters and their mitigation for sustainable agricultural development. International Journal of Social Science and Management Studies. 5: 1-10.

  74. Stover, R.H. (1972). Banana, Plantain and Abaca Diseases. London, Commonwealth Mycology Institute London: 316.

  75. Turner, D.W., Fortescue, J.A. and Thomas, D.S. (2007). Environmental physiology of the bananas (Musa spp.). Brazilian Journal of Plant Physiology. 19: 463-484.

  76. Varma, V. and Bebber, D.P. (2019). Climate change impacts on banana yields around the world. Nature Climate Change. 9: 752-757.

  77. Wien, H.C. (1997). The Cucurbits: Cucumber, Melon, Squash and Pumpkin. The Physiology of Vegetable Crops. Wallingford, UK, CAB International: 43-86.

  78. Wurr, D., Hand, D., Edmondson, R., Fellows, J., Hannah, M. and Cribb, D. (1998). Climate change: A response surface study of the effects of CO2 and temperature on the growth of beetroot, carrots and onions. The Journal of Agricultural Science. 131(2): 125-133.

  79. Yadukumar, N., Raviprasad, T. and Bhat, M. (2010). Effect of Climate Change on Yield and Insect Pests Incidence on Cashew. New Delhi, Westville Publishing House. 49-54.
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