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Frontiers in Plant Science logoLink to Frontiers in Plant Science
. 2019 Aug 13;10:939. doi: 10.3389/fpls.2019.00939

Environmental Factors Variably Impact Tea Secondary Metabolites in the Context of Climate Change

Selena Ahmed 1,*, Timothy S Griffin 2, Debra Kraner 1, M Katherine Schaffner 2, Deepak Sharma 1, Matthew Hazel 2, Alicia R Leitch 1, Colin M Orians 3, Wenyan Han 4, John Richard Stepp 5, Albert Robbat 6, Corene Matyas 7, Chunlin Long 8, Dayuan Xue 9, Robert F Houser 2, Sean B Cash 2
PMCID: PMC6702324  PMID: 31475018

Abstract

Climate change is impacting food and beverage crops around the world with implications for environmental and human well-being. While numerous studies have examined climate change effects on crop yields, relatively few studies have examined effects on crop quality (concentrations of nutrients, minerals, and secondary metabolites). This review article employs a culturally relevant beverage crop, tea (Camelia sinensis), as a lens to examine environmental effects linked to climate change on the directionality of crop quality. Our systematic review identified 86 articles as relevant to the review question. Findings provide evidence that shifts in seasonality, water stress, geography, light factors, altitude, herbivory and microbes, temperature, and soil factors that are linked to climate change can result in both increases and decreases up to 50% in secondary metabolites. A gap was found regarding evidence on the direct effects of carbon dioxide on tea quality, highlighting a critical research area for future study. While this systematic review provides evidence that multiple environmental parameters are impacting tea quality, the directionality and magnitude of these impacts is not clear with contradictory evidence between studies likely due to confounding factors including variation in tea variety, cultivar, specific environmental and agricultural management conditions, and differences in research methods. The environmental factors with the most consistent evidence in this systematic review were seasonality and water stress with 14 out of 18 studies (78%) demonstrating a decrease in concentrations of phenolic compounds or their bioactivity with a seasonal shift from the spring and /or first tea harvest to other seasons and seven out of 10 studies (70%) showing an increase in levels of phenolic compounds or their bioactivity with drought stress. Herbivory and soil fertility were two of the variables that showed the greatest contradictory evidence on tea quality. Both herbivory and soil fertility are variables which farmers have the greatest control over, pointing to the importance of agricultural management for climate mitigation and adaptation. The development of evidence-based management strategies and crop breeding programs for resilient cultivars are called for to mitigate climate impacts on crop quality and overall risk in agricultural and food systems.

Keywords: climate change, crop quality, secondary metabolites, food systems, agriculture

Introduction

Climate Change and Crop Quality

Impacts of climate change on agricultural systems threaten crops with notable implications for farmer livelihoods and human health (Odada et al., 2008; Pachauri et al., 2014; Campbell et al., 2016). Since the 1950s, agricultural systems have experienced gradual systematic changes in average climate conditions including unprecedented multi-decadal warming, increased inter-annual variability of the Earth's surface temperatures, changes in average precipitation, greater weather variability, and more extreme weather conditions (Pachauri et al., 2014). These climatic changes have decreased agricultural productivity and shifted the geographic range of many crops (Lobell and Asner, 2003; Porter and Semenov, 2005). Concurrently, productivity of some crops has increased with a rise in temperatures (Ewert et al., 2005). Increasing atmospheric carbon dioxide (CO2) has decreases concentrations of micronutrients zinc (Zn) and iron (Fe) as well as protein for C3 grains and legumes (Myers et al., 2014). While the literature provides substantial evidence on the impact of climate change on crop yields (Lobell and Asner, 2003; Hertel et al., 2010; Lobell et al., 2011), fewer studies have focused on the effects of climate change on crop quality (Porter and Semenov, 2005; Ahmed and Stepp, 2016).

Crop quality is a multi-dimensional parameter that refers to the nutritional, health, and sensory attributes of crops as measured by the presence, absence, and/or concentrations of phytonutrients, minerals, and primary and secondary metabolites (i.e., bioactive food components or phytochemicals) as well as associated bioactivity, shelf life, and organoleptic properties (i.e., color, visual appeal, aroma, taste, and texture) (Mattos et al., 2014; Ahmed and Stepp, 2016). Secondary metabolites are non-nutrient plant constituents that impact crop quality through an influence on flavor, appearance, stability (Tomás-Barberán and Espin, 2001) and health-promoting attributes including mitigating micronutrient deficiencies (Johns and Sthapit, 2004) and the risk of diet-related chronic disease including cancer, heart disease, and diabetes (Liu, 2013). Over 100,000 secondary metabolites have been identified in five chemical classes including phenolics, terpenes, alkaloids, and other nitrogen-containing compounds, phytosterols, and organosulfur compounds (Goldberg, 2003; Swift et al., 2004).

Plants have evolved secondary metabolites to protect themselves from various abiotic and biotic stressors (Fraenkel, 1959; Coley et al., 1985). Since the synthesis of secondary metabolites represents a metabolic cost, plants tend to produce these compounds in notable concentrations if they have the ecological cue to do so based on interactions between environmental (Lower and Orians, 2003; Björkman et al., 2011; Kowalsick et al., 2014), agricultural (Ahmed et al., 2013), genetic (van-Dam and Vrieling, 1994), and physiological factors (Coley et al., 1985; Glynn et al., 2007). Each crop has specific secondary metabolites that characterize crop quality while the presence of other secondary metabolites is viewed as deleterious for crop quality due to off-flavors or toxicity attributes. Climate change factors have resulted in a decrease of multiple secondary metabolites in a range of food and beverage crops including coffee (Villarreal et al., 2009), tea (Ahmed et al., 2014a,b; Kowalsick et al., 2014), grapes (Xu et al., 2011), brown rice (Britz et al., 2007), kale (Zietz et al., 2010), tomatoes (Kacjan-Maršič et al., 2010), and peanuts (Casini et al., 2003).

Tea as a Model System for Examining Climate Effects on Crop Quality

This review article employs tea (Camelia sinensis; Theaceae) to understand how climate change impacts crop quality of a culturally-relevant beverage plant. Tea, the botanical source of all white, green, oolong, black and pu-erh tea beverages, was selected as a study system because of its prevalence in diets globally, its production in over 50 countries on five continents (FAOSTAT, 2016), and because it is a plant that is cultivated for its quality based on secondary metabolites (Ahmed et al., 2010). Polyphenolic catechin, methylxanthine (i.e., caffeine), and volatile secondary metabolites, coupled with carbohydrates and amino acids, contribute to tea quality through influencing the flavor and appearance of tea (Drewnowski and Gomez-Carneros, 2000; Scharbert et al., 2004) as well as its health claims including anti-oxidative, anti-inflammatory, neuro-protective, cardio-protective, anti-cancer, anti-microbial, and anti-atherosclerotic activities (Trevisanato and Kim, 2000; Lin et al., 2003; Clement, 2009). Tea is further suitable as a study system to examine the effects of climate change because it is a woody perennial that experiences multiple decadal effects of climate change. Successful tea cultivation tea is dependent on climatic conditions including temperature, rainfall, humidity, and solar radiation (Wijeratne, 1996).

Marx et al. (2017) identified 14 articles highlighting that shifts in rainfall and solar radiation influence tea yields and quality with implications for farmer livelihoods. For example, Biggs et al. (2018) demonstrate that climate change is impacting farmer livelihoods across four major tea-growing regions of Assam, India. Boehm et al. (2016) show that a decrease in solar radiation in the previous growing season is associated with lower tea yields. However, the literature is missing a systematic review that synthesizes the evidence of environmental effects on tea quality and, the directionality of changes in quality parameters.

This study addresses the aforementioned knowledge gap through a systematic literature review that examines the following question: What are effects of environmental variation related to climate change on tea quality? Given the lack of studies examining long-term effects of climate change on tea quality, we synthesize studies that examine the effects of environmental factors that are shifting with climate change. This review can inform future research by identifying literature gaps and new research questions while serving as a model for literature reviews on climate change effects on crop quality.

Systematic Review Methods

The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA; Moher et al., 2009) and the Guidelines for Systematic Review and Environmental Synthesis in Environmental Management (Collaboration for Environmental Evidence, 2013) were applied to design a systematic review protocol to collect evidence on the following closed-frame study question: What are effects of environmental variation related to climate change on tea quality? We used the PICO (Population, Intervention/Exposure, Comparator, Outcome) framework elements (Schardt et al., 2007) to structure our systematic review.

The biological population/study unit is tea (Camellia sinensis L.; Theaceae). The intervention/exposure that we examined is environmental variability linked to climate change, which includes variables including temperature, precipitation, elevation, seasonality, location, herbivory, soil, and solar radiation. As we found a lack of published studies directly examining climate effects on tea quality based on our preliminary review, we included environmental factors that vary with global change in systematic review search protocol. The comparator assessed in our review was variation in a specific environmental variable from a baseline evaluation or other comparison. The outcomes that we examined were impacts on the biochemical parameter of tea quality including secondary metabolite chemistry that consists of phenolic catechins, methylxanthines (including caffeine), amino acids (including theanine), and a range of volatile compounds.

A multidisciplinary team of subject experts and a review methodology expert collaboratively designed the systematic review protocol. Specifically, the multidisciplinary team of subject experts included scientists with expertise in the fields of plant biology, chemistry, soil science, herbivory, phytochemistry, biochemistry, agronomy, food science, tea science, and climate change. Establishment of the review protocol involved preliminary scoping of search terms to test the search strategy for indication of the volume of relevant literature. Search terms were identified and revised during an iterative process after examining relevant articles from the search and refining search terms to meet both evidence needs as well as feasibility for a systematic review. Following are the key components of the final search terms that included a combination of tea, environmental factor linked to climate change, and quality parameter: “tea OR camellia sinensis” AND “climate change OR global warming OR season OR solar radiation OR precipitation OR geographic area OR temperature OR soil OR wind OR annual bud burst OR carbon dioxide” AND “antioxidant OR caffeine OR phytochemical OR catechin OR theaflavin OR flavonol OR polyphenol OR secondary metabolite.” Supplementary Table 1 lists the final search terms used in this systematic review. The final search terms were tested with a set of known relevant articles.

A total of five publication databases were searched: PubMed, Web of Science, EBSCO GreenFILE, Scopus, and, Agricola. Databases were selected that are commonly used to search for articles in the areas of food systems, agriculture, climate change, secondary metabolite chemistry, and human health. Inclusion criteria were restricted to peer-review articles published in the English language from 2000 to 2015. The software program Covidence was used to manage articles identified within the publication databases and was further used for screening of articles. Following the search, the retrieved articles were screened by a review panel of three reviewers (KS, MH, and SA) to minimize reviewer bias in identifying articles for their relevance to the review question using a-priori inclusion criteria. Two reviewers from the review panel screened each article. Decision discrepancies (inclusion or exclusion) were discussed by the entire panel for resolution. The final set of articles was critically appraised for their design on focusing on environmental effects on tea quality.

The final set of articles in the study was read by a separate data extraction review panel (DK, DS, and AL). Appropriate data from each of these articles were extracted by one of three members of the data extraction panel and placed into a table highlighting specific study parameters including environmental factor, variety and cultivar of tea, quality indicator, method(s) of analysis, and outcomes. A second member on the data extraction panel reviewed extracted data in the table to verify that appropriate data was extracted.

The final search resulted in the retrieval of 9,750 articles including 1,754 duplicates for a total of 7,996 articles (Supplementary Figure 1). From this, 93 articles were identified by the review panel for inclusion in the review. These articles were relevant to the review question using our a priori inclusion criteria. Nine of these articles were removed from the search because it was not possible to retrieve the full text of these papers, resulting in a total of 84 articles that were included in the synthesis of our systematic review.

Each article included in the study was grouped on the basis of which environmental factor(s) were assessed in the study, and then placed in a corresponding table of the most prevalent environmental factors that emerged from the systematic review. Articles were placed in multiple tables if they examine multiple environmental variables. For each environmental factor table, we applied a coding framework to quantify the number of articles that demonstrated directional changes (increase, decrease, or no change) of specific tea quality parameters. Specifically, we quantified the following quality parameters: (1) increase, decrease, or no change in catechins and other phenolic compounds with an increase in [environmental factor, i.e., temperature], (2) increase, decrease, or no change in catechins and other phenolic compounds with a decrease in [environmental factor, i.e., temperature], (3) increase, decrease, or no change in caffeine with an increase in [environmental factor, i.e., temperature], (4) increase, decrease, or no change in caffeine with a decrease in [environmental factor, i.e., temperature], (5) increase, decrease, or no change in terpenoids and other volatiles with an increase in [environmental factor, i.e., temperature], (6) increase, decrease, or no change in terpenoids and other volatiles with a decrease in [environmental factor, i.e., temperature], (7) increase, decrease, or no change in amino acids with an increase in [environmental factor, i.e., temperature] and, (8) increase, decrease, or no change in amino acids with a decrease in [environmental factor, i.e., temperature]. Unfortunately, as the studies used different measures of crop quality and variable experimental designs, we were unable to quantitatively compare between studies. Three reviewers (DS, DK, and SA) coded the outcomes for each article to ensure there were no discrepancies. The resulting data were summarized into a narrative synthesis and a quantitative synthesis.

Some environmental factors were merged together due to their relatedness and presentation in the literature. Geographic area was separated from altitude as it was presented separately in the literature. While the systematic review did not identify a study on carbon dioxide effects on tea quality, we summarize a recent study outside of the time frame as this is a critical abiotic stressor associated with climate change. Those studies that included multiple variables were analyzed individually for all relevant environmental factors.

Results

Findings from the systematic review highlighted the following environmental factors as being prevalent in the literature as impacting tea quality:

  1. seasonality (including change of harvest season such as shifts between spring, summer, autumn, and winter harvest seasons or shifts between dry and wet seasons as well as bud burst; 18 studies; Supplementary Table 2);

  2. water stress (including precipitation; 10 studies; Supplementary Table 3);

  3. geography (8 studies; Supplementary Table 4);

  4. light factors (including solar radiation; 6 studies; Supplementary Table 5);

  5. altitude (5 studies; Supplementary Table 6);

  6. herbivory and microbes (5 studies; Supplementary Table 7);

  7. temperature (4 studies; Supplementary Table 8) and;

  8. soil and nutrient factors (27 studies; Supplementary Table 9).

The most prevalent crop quality parameters in the literature addressing the study question were total phenolic concentration, catechin content [including epigallocatechin gallate (EGCG), epicatechin gallate (ECG), epigallocatechin (EGC), and catechin gallate (CG)], and antioxidant activity. Other prevalent quality parameters include caffeine, theaflavin, thearubigin, tannins, carotenoids, terpene alcohols (i.e., linalool and geraniol) and other aromatic volatiles, fatty acid composition, chlorophyll, glycoside precursors, proanthocyanidin, and lipoxygenase and glycosidase enzymatic activities. Overall, increases in the aforementioned secondary metabolites is associated with increased crop quality until a specific threshold for human flavor preference when a further increase is no longer considered desirable. Total color, brightness, and flavor of brewed tea were measured as organoleptic quality parameters linked to secondary metabolite concentrations. High-performance liquid chromatography (HPLC) and colorimetric spectrophotometry assays were the most prevalent methods for analyzing tea quality.

The reviewed studies were carried out in a range of tea producing and consuming countries (Figure 1). In addition, the studies included a wide range of different tea cultivars of the assamica and sinensis varieties of Camellia sinensis including AC-259, T-78, B-157, B-777, S-449, UPASI-9, UP-2, UP-3, UP-8, BSS-2, TV-23, TV-25, TV-26, ZC108, ZC302, LJ 43, Derepazari 7, Fener, Yulan, and Fudingdaba. However, many of studies did not specify the variety, cultivar, or landrace of the tea examined. The lack of information on the variety of tea as well as the broad range of cultivars examined prevented analysis of the response of tea plants to environmental variables on the basis of tea variety and cultivar.

Figure 1.

Figure 1

Environmental factors assessed by location. Map depicting the range of tea producing and consuming countries where the studies identified in this systematic review were carried out along with the corresponding environmental factors assessed.

Seasonality

One-fifth (18 of 86) of the studies reviewed assessed the effects of seasonality factors on tea quality including change of harvest season between spring, summer, autumn, and winter harvest seasons or shifts between dry and wet seasons as well as bud burst (Figure 2; Supplementary Table 2). The main seasonality factor examined was comparing the spring harvest to either the summer, monsoon, autumn, and winter, with a comparison between the spring and monsoon season being the most prevalent seasonal comparator. The spring tea harvest season is generally the first harvest season that follows winter dormancy in direct response to increased temperatures (Ahmed and Stepp, 2012). The main quality parameters measured in reviewed studies on seasonality were phenolic secondary metabolites (including individual catechin compounds) and / or antioxidant activity (14 studies), followed by volatile metabolites (4 studies), and caffeine (a methylxanthine compound; 4 studies).

Figure 2.

Figure 2

Effects of seasonality on tea quality. The horizontal axis depicts the percentage of studies and the vertical axis depicts directional changes in key quality parameters corresponding to climate change related environmental shifts.

Fourteen seasonality studies demonstrated that concentrations of individual catechins, phenolic secondary metabolites, and / or antioxidant activity decreased with a seasonal shift from the spring and/or first tea harvest to other seasons, particularly the monsoon season (Sud and Baru, 2000; Saikia and Mahanta, 2002; Akhlas, 2003; Venkatesan et al., 2007; Chen et al., 2010, 2014; Kottur et al., 2010; Ansari et al., 2011; Jayasekera et al., 2011, 2014; Xu et al., 2012; Ahmed et al., 2014b; Baptista et al., 2014; Topuz et al., 2014). Phenolic catechin compounds are generally associated with high tea quality; however, relatively high concentrations of particular phenolics are linked to a bitter or astringent taste that is generally less desired by consumers (Ahmed et al., 2014b). Two seasonal studies showed that while some phenolic secondary metabolites, and/or antioxidant activity decreased with a seasonal shift from the spring and / or first tea harvest to other seasons, other secondary metabolites and / or antioxidant activity increased. Ahmed et al. (2014b) demonstrated that concentrations of desirable phenolic catechins were up to 50% lower during the beginning of the monsoon season compared to the spring, while total phenolic concentrations and antioxidant activity increased.

The four seasonality studies measuring tea volatiles demonstrated that some volatile compounds increased with the seasonal transition from the spring and/or first tea harvest and that other compounds decreased (Saikia and Mahanta, 2002; Rawat and Gulati, 2008; Tontul et al., 2013; Kowalsick et al., 2014). Kowalsick et al. (2014) demonstrated that the number and concentration of over 300 volatile compounds from 18 chemical families either increased, decreased, or stayed the same with the onset of the monsoon from the spring season. This study showed that in general the spring season has a greater number and higher concentration of volatiles associated with high tea quality (Kowalsick et al., 2014). Three studies showed that caffeine concentrations decreased with a transition from the spring season to the summer monsoon season (Akhlas, 2003; Ansari et al., 2011; Ahmed et al., 2014b) and one study found caffeine to increase during the summer (Saito et al., 2007). One study provided evidence of an increase in amino acids with the transition from the spring to the summer monsoon (Saikia and Mahanta, 2002).

Six of the 14 seasonality studies provided evidence that while some quality parameters decreased with a shift in season, other measures of quality increased (Saikia and Mahanta, 2002; Venkatesan et al., 2007; Rawat and Gulati, 2008; Tontul et al., 2013; Ahmed et al., 2014b; Kowalsick et al., 2014). Rawat and Gulati (2008) found that total content of glycosidic bound flavor compounds was highest during early growth flush (April—mid June), declined during rains (mid June—September), and exhibited recovery during the backend flush (mid September—November). The authors further found an increase in the terpene index and a decrease in terpenoid/non-terpenoid ratio during the rains due to a marked decrease in terpenoid compounds (mainly aromatic geraniol). Jayasekera et al. (2011) found that variation of tea quality on the basis of season was further dependent on geographic location with some plantations having higher quality during the dry season and others having higher quality during the monsoon.

Water Stress

A total of 10 studies examined responses of tea plants to low water availability, including drought stress and soil moisture content (Figure 3; Supplementary Table 3). Five of these studies showed an increase in phenolic compounds and/or antioxidant activity with drought stress (Hernández et al., 2006; Upadhyaya et al., 2011, 2013; Ahmed et al., 2013; Bhattacharya et al., 2014) while two studies showed a decrease in these compounds (Cheruiyot et al., 2007, 2008) and two other studies showed both an increase and decrease in these compounds with drought stress (Chakraborty et al., 2002; Upadhyaya and Panda, 2004). Hernández et al. (2006) found that phenolics (including epicatechin and epigallocatechin gallate) accumulated in drought-stressed tea plants. Cheruiyot et al. (2007) found that declining soil water content over a 12-week period significantly reduced growth and total polyphenolic concentrations in tea shoots depending on cultivar type. Chakraborty et al. (2002) highlight that while phenolic secondary metabolites initially increase with drought stress, they decrease during extended drought stress.

Figure 3.

Figure 3

Effects of water stress on tea quality. The horizontal axis depicts the percentage of studies and the vertical axis depicts directional changes in key quality parameters corresponding to climate change related environmental shifts.

One water stress study examined the effect of drought stress on levels of volatile compounds (Cao et al., 2007). Cao et al. (2007) showed that the number of aromatic constituents in fresh tea leaves was highest under a soil water content of 54% (relative to field capacity) and lowest under a soil relative water content of 100%. None of the water stress studies examined the effects of water stress on caffeine levels in tea.

Geography

While geography is not directly changing with climate change, areas that are suitable for agriculture are shifting with climate change. The eight studies examining the effects of geography on tea quality (Figure 4; Supplementary Table 4) focused on agroclimatic zones, location, and karst topography. Geography was found to notably impact catechins and other tea polyphenols in seven studies (Borse et al., 2002; Li et al., 2007; Bhuyan et al., 2009, 2013; Lee et al., 2015). Two studies showed that caffeine varied with geography (Borse et al., 2002; Lee et al., 2010), two studies showed that amino acids varied with geography (Lee et al., 2010, 2015), and no studies showed that volatiles varied with geography. One study found that location notably impacts sensory parameters of tea and that this directly corresponds to higher phenolic theaflavin and therubigin tea constituents (Bhuyan et al., 2009).

Figure 4.

Figure 4

Effects of geography on tea quality. The horizontal axis depicts the percentage of studies and the vertical axis depicts directional changes in key quality parameters corresponding to climate change related environmental shifts.

Light Factors

The six studies on the effects of light factors explored shading treatment, light intensity, and light quality (Figure 5; Supplementary Table 5). One of these studies found that polyphenols increased with an increase in light (Zhang et al., 2014) while one study found an inverse relationship of light and polyphenols (Zheng et al., 2008) and two studies showed that some polyphenols increase with an increase in light and others decrease (Ku et al., 2010; Song et al., 2012). Ku et al. (2010) found that shade cultured green tea (tencha) had lower levels of phenolic epigallocatechin and epicatechin compounds as well as higher levels of amino acids compared to unshaded green tea while having higher levels of gallocatechin. These difference in polyphenol profiles resulted in the shade cultured tea to have higher umami profile and less astringent taste than the unshaded tea.

Figure 5.

Figure 5

Effects of light factors on tea quality. The horizontal axis depicts the percentage of studies and the vertical axis depicts directional changes in key quality parameters corresponding to climate change related environmental shifts.

Three light studies found that caffeine levels decrease with an increase in light (Song et al., 2012; Lee et al., 2013; Zhang et al., 2014) while one of these studies found that caffeine levels increased at specific amounts of light (Song et al., 2012). Song et al. (2012) demonstrated a non-linear relationship between shade levels (10% shade to 60% shade) and tea quality based on six secondary metabolites (L-theanine, caffeine, -epicatechin, -epicatechin gallate, -epigallocatechin gallate, and –epigallocatechin). Three of the light studies indicate that some terpenoids and other volatiles increase while others decrease with a change in light levels (Ku et al., 2010; Song et al., 2012; Zhang et al., 2014). Overall, increased light results in decreased concentrations of amino acids (Ku et al., 2010; Song et al., 2012; Deng et al., 2013; Lee et al., 2013; Zhang et al., 2014).

Altitude

Studies demonstrate that higher elevation is generally associated with higher tea quality as measured by higher levels of catechins and other polyphenols as well as caffeine (Figure 6; Supplementary Table 6). Four studies found that tea catechins and other polyphenols increased with elevation (associated with cooler temperatures and higher oxidative stress) (Akhlas, 2003; Abeywickrama et al., 2010, 2011; Ohno et al., 2011) and one study found lower catechin levels with higher elevation (Chen et al., 2014). Three studies found that caffeine was higher in tea cultivated at higher elevation as compared to lower elevation (Akhlas, 2003; Abeywickrama et al., 2010; Ohno et al., 2011) and one study found lower caffeine levels with higher elevation (Abeywickrama et al., 2011). One study demonstrated that amino acid levels increase with higher elevation compared to lower elevation (Ohno et al., 2011) while one study found that amino acids were higher for lower elevation tea samples (Abeywickrama et al., 2011). One recent study (not included in this review) demonstrated an increase in favorable aromatic compounds that have sweet, floral, and honey-like notes with an increase in elevation while exhibiting a decrease in caffeine, epicatechin gallate, gallocatechin, and catechin (Kfoury et al., 2018).

Figure 6.

Figure 6

Effects of altitude on tea quality. The horizontal axis depicts the percentage of studies and the vertical axis depicts directional changes in key quality parameters corresponding to climate change related environmental shifts.

Herbivory and Microbes

Three studies on herbivory and two studies on microbes examined the effects of various insects (tea aphids, tea mosquito bug, and Kanzawa spider mites) and microbes (phomospsis and Arbusular mucro fungi from natural and cultivated tea rhizospheres) (Figure 7; Supplementary Table 7). Herbivory resulted in either a decrease in catechins (1 study; Chakraborty and Chakraborty, 2005), increase in catechins (1 study; Dong et al., 2011), increases in volatiles (1 study; Dong et al., 2011), and increase in some volatiles and decrease in other volatiles (1 study; Han and Chen, 2002). Han and Chen (2002) found that tea aphid-damaged tea shoots showed the presence of volatile compounds benzaldehyde and E-2-hexenoic acid which favorably contribute to aroma. Intact tea shoots on the other hand had butanoic acid-3-hexenyl ester and 1-octanol. None of the herbivory studies demonstrated that caffeine and amino acid levels were impacted.

Figure 7.

Figure 7

Effects of herbivory on tea quality. The horizontal axis depicts the percentage of studies and the vertical axis depicts directional changes in key quality parameters corresponding to climate change related environmental shifts.

One microbe study focused on the pathogen phomospsis (Ponmurugan and Baby, 2007) and the other focused on the healthy soil fungi Arbusular mucro (Singh et al., 2010). The presence of the pathogen reduced polyphenol and amino acid levels in Ponmurugan and Baby (2007). Inoculating tea plants with arbuscular mycorrhizal fungi increased catechin and other polyphenol levels in tea as well as amino acids and caffeine (Singh et al., 2010).

Temperature

Three of the four temperature studies (Figure 8; Supplementary Table 8) found an inverse relationship between temperature and tea quality on the basis of catechins, phenolic secondary metabolites, and antioxidant compounds/activity (Lee et al., 2010; Wang et al., 2011; Wei et al., 2011) while one study showed that increased temperature resulted in increased catechin compounds (Yao et al., 2005). Wei et al. (2011) showed that higher catechin content was related to lower temperatures (same as higher elevation). Yao et al. (2005) showed that tea quality as determined by key catechin compounds [(-)-epigallocatechin gallate, (-)-epicatechin gallate, and catechin gallate] was higher during warm months and lower during cool months. Wang et al. (2011) showed that increased temperatures were associated with an increase in (-)-epigallocatechin, (-)-epicatechin, (-)-epicatechin gallate, and (-)-epigallocatechin gallate while catechin (C) decreased. Only one temperature study examined caffeine levels in tea (Lee et al., 2010). Lee et al. (2010) showed that green tea samples grown at high temperature had lower levels of caffeine and catechin compounds compared to those at lower temperature.

Figure 8.

Figure 8

Effects of temperature on tea quality. The horizontal axis depicts the percentage of studies and the vertical axis depicts directional changes in key quality parameters corresponding to climate change related environmental shifts.

Soil and Nutrient Factors

The 26 soil studies examined a range of soil nutrients including aluminum, zinc, iron, nitrogen, phosphorus, magnesium, selenium, manganese, potassium, and boron (Al, Zn, Fe, N, P, Mg, Se, Mn, K, and B, respectively) as well as pH levels (Supplementary Table 9). Broadly, these studies have two (sometimes overlapping) foci: (1) micro-nutrient fertility, and (2) macro-nutrient fertility, with several of the micro-nutrient studies assessing toxicity. Several of the reviewed soil studies assessed the impacts of both deficiency and sufficiency on quality parameters. These studies highlight how soil and nutrient factors notably impact catechin and other phenolic compounds (Hu et al., 2003; Ruan et al., 2007a; 2010, 2013; Chen et al., 2011; Jayaganesh et al., 2011; Duan et al., 2012; Lin et al., 2012; Sae-Lee et al., 2012; Yang et al., 2014), antioxidant defense enzymes (Hajiboland et al., 2013), caffeine (Yang et al., 2014; Sedaghathoor et al., 2019), amino acids (Hu et al., 2003; Venkatesan et al., 2004, 2005; Ruan et al., 2007a; 2010, 2013; Jayaganesh and Venkatesan, 2010; Jayaganesh et al., 2011; Lin et al., 2012; Yang et al., 2014), vitamins (Hu et al., 2003), and flavor (Venkatesan et al., 2006). Each of these is summarized below (Supplementary Table 9).

Although many crop species are inhibited by high levels of soluble aluminum (Al) in the soil, most often found at low soil pH (e.g., pH < 5.0), we found multiple studies that demonstrated that Al stimulates tea growth (Mukhopadyay et al., 2012), phytochemical concentration associated with high-quality tea (Chen et al., 2011; Duan et al., 2012; Sae-Lee et al., 2012; Hajiboland et al., 2013), or both. Both Duan et al. (2012) and Sae-Lee et al. (2012)found that increasing Al resulted in higher polyphenol, caffeine, and amino acid content of tea leaves; Sae-Lee et al. (2012) also noted higher content of catechins with increasing Al, and also with increasing Se. Hajiboland et al. (2011) found that Al supplementation could compensate for B deficiency.

The stimulation of tea growth resulted in increased amino acid and vitamin C from application of Se (Hu et al., 2003). Deficiency and toxicity impacts from Zn (Mukhopadhyay et al., 2013) and Fe (Hemalatha and Venkatesan, 2011) were observed on growth and enzymatic activity in tea; Venkatesan et al. (2007) also observed that excess Mn resulted in lower amino acid and carotenoid content of tea leaves. Three papers evaluated the impacts of Mg fertilization on growth and composition of tea. The work of Ruan et al. (2012) focused on growth, which increased with Mg addition, but also Mg content and amino acid mobility in tea plants. Jayaganesh and Venkatesan, (2010) and Jayaganesh et al. (2011) also noted increased amino acid content with the addition of Mg, and Jayaganesh et al. (2011) observed that different forms of Mg had differential effects on catechin and carotenoid content of tea leaves. Increasing the supply of available N in soil was found to increased amino acid content of tea leaves (Venkatesan et al., 2005; Ruan et al., 2007b, 2010), although other studies (Han et al., 2008; Hamid et al., 2014) noted primarily increased growth with increasing N availability, rather than changes in plant composition.

Carbon Dioxide

While this review did not retrieve any studies on the effects of carbon dioxide on tea quality, we summarize one recent study outside of the time frame of our review. Li et al. (2017) found that there was a significant increase in concentrations of total catechins and other polyphenols along with theanine and free amino acids with elevated carbon dioxide. Concurrently, levels of caffeine decreased (Li et al., 2017). These chemical findings are in sync with expression levels of biosynthetic genes for catechins and theanine that were up-regulated in tea leaves under elevated carbon dioxide levels while levels of biosynthetic genes for caffeine were down-regulated.

Discussion and Conclusion

While the majority of research examining the effects of climate change on food systems has focused on crop yields (Lobell and Asner, 2003; Hertel et al., 2010; Lobell et al., 2011), this systematic literature review highlights that multiple environmental variables linked to climate change also significantly impact crop quality as measured by secondary metabolites associated with flavor attributes and health claims for human consumers (Wolfe et al., 2008; Liu, 2013). Specifically, findings provide evidence that shifts in seasonality, water stress, geography, light factors, altitude, herbivory and microbes, temperature, and soil factors that are linked to climate change can result in both increases and decreases up to 50% in secondary metabolites. A gap was found regarding evidence on the direct effects of carbon dioxide on tea quality, highlighting a critical research area for future study. The reviewed studies provides evidence that environmental factors linked to climate change can result in changes in the following biochemical measures of tea quality: phenolic catechins (i.e., epigallocatechin gallate, epicatechin gallate, epigallocatechin, and catechin gallate), total phenolic concentration, antioxidant activity, caffeine, theaflavin, thearubigin, tannins, carotenoids, terpene alcohols (i.e., linalool and geraniol) and other aromatic volatiles, fatty acids, chlorophyll, enzymes, and enzymatic activities. It is important to note that while an increase in many secondary metabolites represents an increase in crop quality, it may represent a decrease in crop quality for other secondary metabolites including those with off flavors or whose increased consumption by human consumers may result in toxicity (Kfoury et al., 2018). While this systematic review provides evidence that multiple environmental parameters are impacting tea quality, the directionality and magnitude of these impacts is not clear with contradictory evidence between studies. Findings build on a recent literature review highlighting the importance of understanding climate change effects on tea production (Marx et al., 2017) by providing evidence on the multi-directionality of changes in crop quality in response to shifts in environmental factors that are shifting with global change. As crop quality is a key determinant of health in the food system, findings have broader implications for other culturally-relevant crops managed and used by people for food, medicinal, and aesthetic purposes including fruits, vegetables, tree nuts, and beverage crops (Ahmed and Stepp, 2016).

The environmental factors with the most consistent evidence in this systematic review were seasonality and water stress. Specifically, a total of 14 out of 18 studies (78%) demonstrated a decrease in concentrations of phenolic compounds or their bioactivity with a seasonal shift from the spring and /or first tea harvest to other seasons. Seven out of ten studies (70%) showed an increase in levels of phenolic compounds or their bioactivity with drought stress. However, for both seasonality and water stress, multiple studies highlighted that while some secondary metabolite compounds increase, other compounds decrease, pointing to the complexity of understanding tea quality. Based on the evidence regarding seasonality and geographic variability highlighted in this study, tea quality is likely to increase during some parts of the year in some geographic areas with climate change (i.e., during periods of drought) while decreasing at other times of the year (i.e., during extended monsoon periods). However, if drought stress exceeds moisture thresholds of tea plants in a warming world, productivity will be jeopardized.

Herbivory and soil fertility were two of the variables that showed the greatest contradictory evidence with mixed impacts on tea quality. A surprising finding was that while many crop species are inhibited by high levels of soluble aluminum (Al) in the soil, we found multiple studies that demonstrated that Al not only stimulated tea growth (Mukhopadyay et al., 2012), but also phytochemical concentration associated with high-quality tea (Chen et al., 2011; Duan et al., 2012; Sae-Lee et al., 2012; Hajiboland et al., 2013). Both herbivory and soil fertility are variables which farmers have the greatest control over, pointing to the importance of agricultural management for climate mitigation and adaptation. Farmers can respond at some capacity to climate-driven shifts on crop quality at the level of individual fields or farms. However, beyond specific thresholds, adaptation would require geographic shifts in production, yet these thresholds are largely unknown for crop quality.

The contradictory evidence found in this systematic review likely results from multiple confounding factors associated with each study including variation in tea variety, cultivar, specific environmental and agricultural management conditions, and differences in methods that make comparisons across studies difficult. For example, previous research indicates that different varieties and cultivars of a specific species such as tea may respond variably to the same environmental factor such as seasonality (Owuor and Chavanji, 1986). Owuor and Chavanji (1986) found that seasonal fluctuations variably impacted the caffeine content of tea plants depending on the type of clone. Controlled experiments are called for that examine the impacts of specific environmental factors on multiple tea varieties and cultivars including climate resilient cultivars. In addition, future research efforts should focus on not just understanding the implications of individual factors on specific attributes of crops, but on modeling the system-wide impacts of simultaneous changes on crop biological systems to better understand the long-term implications of climate change. This includes understanding complex interactions of crops with the environment including dynamic feedback loops in which the presence and concentrations of secondary metabolites are impacted by a cascade of abiotic and biotic conditions such as changes in precipitation, temperature, and pests (Fields and Orians, 2006; Schepp, 2009). Research is further needed to analyze the quality of studies included in this systematic review and similar reviews regarding the effects of climate-related changes on crop quality.

The overall lack of consistency in evidence for climate-driven effects on tea quality, coupled with our inability to quantitatively compare study outcomes because of a lack of comparable measures and information on tea variety, points to the challenge of measuring crop quality and the multidimensional nature and complexity of this parameter. One way to overcome this challenge is to design more widely agreed upon international standards of crop quality for different culturally and economically relevant crops along with implementing global collaborative projects with shared experimental designs to allow for comparison of outcomes across multiple studies on crop quality through space and time.

In addition, the lack of studies examining the interplay of multiple environmental factors on tea quality highlights the need for an ecosystems approach in examining multi-trophic interactions in tea systems as well as implications for consumers and farmer livelihoods. Further research is needed to analyze the quality of studies included in this systematic review. While our synthesis contributes to elucidating the directionality of changes in tea quality in response to environmental change, we were unable to quantitatively compare study outcomes because of a lack of comparable measures. Future work to develop standardized protocols for measuring crop quality to enable monitoring of this parameter and comparisons between studies is also needed.

Multiple agricultural, physiological, and molecular innovations have been identified toward the development of climate resilient tea systems (Ahmed, 2018). At the agricultural level, climate mitigation strategies for tea farms include agricultural diversification, tree planting and maintaining vegetative cover, management of soil organic matter and carbon sequestration, water management, controlling pests and disease, and migration and relocating agroecosystems to more suitable locations (Ahmed and Stepp, 2016; Ahmed, 2018). Physiological and molecular innovations for enhancing climate resilience of tea farms include: (1) cultivation of tea from seed versus from clonal propagules, (2) micropropagation, (3) traditional breeding methods of climate-smart cultivars, (4) genetically modified crops and, (5) sustainable intensification (Ahmed, 2018). Traditional breeding methods of climate-smart tea cultivars including those with enhanced resistance to climate variability such as extreme drought, early- maturing varieties, and biofortified crops that accumulate more minerals and vitamins (Ahmed, 2018). Research is needed to measure the effectiveness of these strategies for enhancing the resilience of shifts in crop quality to climate change. While farmers can respond at some capacity to climate-driven shifts on crop quality at the level of individual fields or farms, changes beyond specific ecological and physiological thresholds would require geographic shifts in production. Future research is called for to elucidate what these thresholds are for crop quality for a range of staple and nutrient-dense crops that support food security and human health.

These findings have notable implications for the sustainability and resilience of agricultural systems in the context of global environmental change. Thus, it is essential to develop and implement evidence-based adaptation strategies for growing crops in ways that are resilient to climate change and support both environmental and human well-being. Based on our reflections on lessons learnt from this systematic review, we recommend the following next steps for advancing the understanding of climate change effects on crop quality as well as for responding to this challenge:

  1. Carry out farm-level research on the effectiveness of various agricultural practices for climate adaptation and mitigation for tea plants and other food and beverage crops including the cost-effectiveness, replicability, and adaptability for different geographic contexts as well as differing scales and models of production. Findings should be applied to design and disseminate climate resilient agricultural guidelines that should be supported by policy including providing economic and social incentives.

  2. Invest in breeding of climate-resilient crop cultivars that includes the evaluation of crop quality to multiple environmental factors and identification of crop quality thresholds.

  3. Design more widely agreed upon international standards of crop quality for multiple culturally and economically relevant crops

  4. Implement long-term global collaborative projects with shared experimental designs and “big data” sharing to allow for comparison of outcomes across multiple studies on crop quality through space and time. These studies should model system-wide impacts of simultaneous environmental changes on agricultural systems and implications for nutrition and human health to better understand the dynamic feedback loops in the food systems and associated social and ecological long-term implications of climate change.

  5. Foster cross-sector collaboration between researchers, practitioners, producers, and policy makers to develop evidence-based adaptation strategies that reduce vulnerability of food systems to shifts in crop quality toward supporting sustainability.

Data Availability

All datasets generated for this study are included in the manuscript and/or the Supplementary Files.

Author Contributions

SA and TG conceived of the study question for the systematic review and guided the systematic review team. SA, TG, and MS designed the systematic review protocol with guidance from RH. All authors contributed to search terms. MS, SA, and MH served on the review panel to identify articles to be included in the study. DK, SA, DS, and AL served on the data extraction panel. SA, CM, and DK created the Figures and Tables. SA and TG wrote the manuscript with contributions from all authors. All authors approved the final manuscript submitted. SA and SC led the submission of the manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Footnotes

Funding. The authors received funding support for the study presented here from the following agencies: (1) United States National Science Foundation - Award NSF CNH BCS-1313775 (SA, TG, CO, JS, AR, CM, and SC; https://www.nsf.gov), (2) United States National Science Foundation - Award NSF RII Track-2 FEC 1632810 (SA; https://www.nsf.gov), (3) United States National Institute of General Medical Sciences of the National Institutes of Health - Award P20GM103474 (SA; http://nih.gov), (4) United States National Institute of General Medical Sciences of the National Institutes of Health - Award 5P20GM104417 (SA; http://nih.gov), (5) National Natural Science Foundation of China - Award 31761143001 (CL; http://www.nsfc.gov.cn/english/site_1/index.html), (6) Ministry of Education of China Award B08044 (CL and DX; http://old.moe.gov.cn//publicfiles/business/htmlfiles/moe/moe_2792/index.html). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2019.00939/full#supplementary-material

References

  1. Abeywickrama K., Ratnasooriya W., Amarakoon A. (2010). Oral diuretic activity of hot water infusion of Sri Lankan black tea (Camellia sinensis L.) in rats. Pharmacogn. Mag. 6:271. 10.4103/0973-1296.71788 [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Abeywickrama K. R. W., Ratnasooriya W. D., Amarakoon A. M. T. (2011). Oral hypoglycaemic, antihyperglycaemic and antidiabetic activities of Sri Lankan broken orange pekoe fannings (BOPF) grade black tea (Camellia sinensis L.) in rats. J. Ethnopharmacol. 135, 278–286. 10.1016/j.jep.2011.02.035 [DOI] [PubMed] [Google Scholar]
  3. Ahmed S. (2018). Toward the development of climate resilient tea systems: agroecological, physiological, and molecular innovations, in Stress Physiology of Tea in the Face of Climate Change, ed Han W. (Missouri, TX: Springer Nature; ), 53–72. [Google Scholar]
  4. Ahmed S., Orians C. M., Griffin T. S., Buckley S., Unachukwu U., Stratton A. E., et al. (2014a). Effects of water availability and pest pressures on tea (Camellia sinensis) growth and functional quality. AoB Plants. 6:plt054. 10.1093/aobpla/plt054 [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Ahmed S., Peters C. M., Chunlin L., Meyer R., Unachukwu U., Litt A., et al. (2013). Biodiversity and phytochemical quality in indigenous and state-supported tea management systems of Yunnan, China. Conserv. Lett. 6, 28–36. 10.1111/j.1755-263X.2012.00269.x [DOI] [Google Scholar]
  6. Ahmed S., Stepp J. R. (2012). Pu-erh tea: botany, production, and chemistry, in Tea in Health and Disease Prevention, ed Preedy V. (London; Waltham, MA; San Diego, CA: Academic Press; Elsevier Science and Technology; ), 59–72. [Google Scholar]
  7. Ahmed S., Stepp J. R. (2016). Beyond yields: Climate change effects on specialty crop quality and agroecological management. Elem. Sci. Anth. 4:000092 10.12952/journal.elementa.000092 [DOI] [Google Scholar]
  8. Ahmed S., Stepp J. R., Orians C., Griffin T., Matyas C., Robbat A., et al. (2014b). Effects of extreme climate events on tea (Camellia sinensis) functional quality validate indigenous farmer knowledge and sensory preferences in tropical China. PLoS ONE. 9:e109126. 10.1371/journal.pone.0109126 [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Ahmed S., Unachukwu U., Stepp J. R., Peters C. M., Chunlin L., Kennelly E. (2010). Pu-erh Tea Tasting in Yunnan, China: correlation of drinkers' perceptions to phytochemistry. J. Ethnopharmacol. 132, 176–185. 10.1016/j.jep.2010.08.016 [DOI] [PubMed] [Google Scholar]
  10. Akhlas M. (2003). Qualitative assessment of fresh tea produced in Pakistan growing under different agro-ecological conditions and fertilizer treatments. Pak J Bot. [Google Scholar]
  11. Ansari H. R., Asil H. M., Rabiei B., Dadashpour A. (2011). Impacts of flushing and fermentation times on the quality of black tea. Genetika 43, 537–548. 10.2298/GENSR1103537A [DOI] [Google Scholar]
  12. Baptista J., Lima E., Paiva L., Castro A. R. (2014). Value of off-season fresh camellia sinensis leaves. antiradical activity, total phenolics content and catechin profiles. LWT Food Sci. Technol. 59(2, Part 1), 1152–1158. 10.1016/j.lwt.2014.06.004 [DOI] [Google Scholar]
  13. Bhattacharya A., Saini U., Joshi R., Kaur D., Pal A. K., Kumar N., et al. (2014). Osmotin-expressing transgenic tea plants have improved stress tolerance and are of higher quality. Transgenic Res. 23, 211–223. 10.1007/s11248-013-9740-5 [DOI] [PubMed] [Google Scholar]
  14. Bhuyan L. P., Hussain A., Tamuly P., Gogoi R. C., Bordoloi P. K., Hazarika M. (2009). Chemical characterization of CTC black tea of northeast India: correlation of quality parameters with tea tasters' evaluation. J. Sci. Food Agric. 89, 1498–1507. 10.1002/jsfa.3614 [DOI] [Google Scholar]
  15. Bhuyan L. P., Sabhapondit S., Baruah B. D., Bordoloi C., Gogoi R., Bhattacharyya P. (2013). Polyphenolic compounds and antioxidant activity of CTC black tea of north-east India. Food Chem. 141, 3744–3751. 10.1016/j.foodchem.2013.06.086 [DOI] [PubMed] [Google Scholar]
  16. Biggs E. M., Gupta N., Saikia S. D., Duncan J. M. A. (2018). The tea landscape of Assam: multi-stakeholder insights into sustainable livelihoods under a changing climate. Environ. Sci. Policy 82, 9–18. 10.1016/j.envsci.2018.01.003 [DOI] [Google Scholar]
  17. Björkman M., Klingen I., Birch A. N., Bones A. M., Bruce T. J., Johansen T. J., et al. (2011). Phytochemicals of Brassicaceae in plant protection and human health–Influences of climate, environment, and agronomic practice. Phytochemistry 72, 538–556. 10.1016/j.phytochem.2011.01.014 [DOI] [PubMed] [Google Scholar]
  18. Boehm R., Cash S. B., Anderson B. T., Ahmed S., Griffin T. S., Robbat A., et al. (2016). Association between empirically estimated monsoon dynamics and other weather factors and historical tea yields in China: results from a yield response model. Climate 4, 20 10.3390/cli4020020 [DOI] [Google Scholar]
  19. Borse B. B., Jagan Mohan Rao L., Nagalakshmi S., Krishnamurthy N. (2002). Fingerprint of black teas from India: identification of the regio-specific characteristics. Food Chem. 79, 419–424. 10.1016/S0308-8146(02)00191-7 [DOI] [Google Scholar]
  20. Britz S. J., Prasad P. V. V., Moreau R. A., Allen L. H. J., Kremer D. F., Boote K. J. (2007). Influence of growth temperature on the amounts of tocopherols, tocotrienols, and γ-oryzanol in brown rice. J. Agric. Food Chem. 55, 7559–7565. 10.1021/jf0637729 [DOI] [PubMed] [Google Scholar]
  21. Campbell B. M., Vermeulen S. J., Aggarwal P. K., Corner-Dolloff C., Girvetz E., Loboguerrero A. M., et al. (2016). Reducing risks to food security from climate change. Global Food Security. 11, 34–43. 10.1016/j.gfs.2016.06.002 [DOI] [Google Scholar]
  22. Cao P., Liu C., Liu K. (2007). Aromatic constituents in fresh leaves of lingtou dancong tea induced by drought stress. Front. Agric. China 1, 81–84. 10.1007/s11703-007-0015-x [DOI] [Google Scholar]
  23. Casini C., Dardanelli J. L., Martínez M. J., Balzarini M. N., Borgogno C. S., Nassetta M. (2003). Oil quality and sugar content of peanuts (Arachis hypogaea) grown in Argentina: their relationship with climatic variables and seed yield. J Agric Food Chem. 51, 6309–6313. 10.1021/jf030183j [DOI] [PubMed] [Google Scholar]
  24. Chakraborty U., Chakraborty N. (2005). Impact of environmental factors on infestation of tea leaves by helopeltis theivora, and associated changes in flavonoid flavor components and enzyme activities. Phytoparasitica 33, 88–96. 10.1007/BF02980930 [DOI] [Google Scholar]
  25. Chakraborty U., Dutta S., Chakraborty B. N. (2002). Response of tea plants to water stress. Biol Plant. 45, 557–562. 10.1023/A:1022377126056 [DOI] [Google Scholar]
  26. Chen G. H., Yang C. Y., Lee S. J., Wu C. C., Tzen J. T. C. (2014). Catechin content and the degree of its galloylation in oolong tea are inversely correlated with cultivation altitude. J. Food Drug Anal. 22, 303–309. 10.1016/j.jfda.2013.12.001 [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Chen Y., Jiang Y., Duan J., Shi J., Xue S., Kakuda Y. (2010). Variation in catechin contents in relation to quality of ‘Huang Zhi Xiang’ oolong tea (Camellia sinensis) at various growing altitudes and seasons. Food Chem. 119, 648–652. 10.1016/j.foodchem.2009.07.014 [DOI] [Google Scholar]
  28. Chen Y. M., Tsao T. M., Liu C. C., Lin K. C., Wang M. K. (2011). Aluminum and nutrients induce changes in the profiles of phenolic substances in tea plants (Camellia sinensis CV TTES, No. 12 (TTE)). J. Sci. Food Agric. 91, 1111–1117. 10.1002/jsfa.4291 [DOI] [PubMed] [Google Scholar]
  29. Cheruiyot E. K., Mumera L. M., Ng'etich W. K., Hassanali A., Wachira F. (2007). Polyphenols as potential indicators for drought tolerance in tea (Camellia sinensis L.). Biosci. Biotechnol. Biochem. 71, 2190–2197. 10.1271/bbb.70156 [DOI] [PubMed] [Google Scholar]
  30. Cheruiyot E. K., Mumera L. M., Ng'etich W. K., Hassanali A., Wachira F., Wanyoko J. K. (2008). Shoot epicatechin and epigallocatechin contents respond to water stress in tea [Camellia sinensis (L.) O. Kuntze]. Biosci. Biotechnol. Biochem. 72, 1219–1226. 10.1271/bbb.70698 [DOI] [PubMed] [Google Scholar]
  31. Clement Y. (2009). Can green tea do that? A literature review of the clinical evidence. J. Prev. Med. 49, 83–87. 10.1016/j.ypmed.2009.05.005 [DOI] [PubMed] [Google Scholar]
  32. Coley P. D., Bryant J. P., Chapin F. S. (1985). Resource availability and plant antiherbivore defense. Science 230, 895–899. 10.1126/science.230.4728.895 [DOI] [PubMed] [Google Scholar]
  33. Collaboration for Environmental Evidence (2013). Guidelines for Systematic Review and Evidence Synthesis in Environmental Management. Version 4.2. Environmental Evidence. Available online at: www.environmentalevidence.org/Documents/Guidelines/Guidelines4.2.pdf
  34. Deng W. W., Fei Y., Wang S., Wan X. C., Zhang Z. Z., Hu X. Y. (2013). Effect of shade treatment on theanine biosynthesis in Camellia sinensis seedlings. J. Plant Growth Regul. 71, 295–299. 10.1007/s10725-013-9828-1 [DOI] [Google Scholar]
  35. Dong F., Yang Z., Baldermann S., Sato Y., Asai T., Watanabe N. (2011). Herbivore-induced volatiles from tea (Camellia sinensis) plants and their involvement in intraplant communication and changes in endogenous nonvolatile metabolites. J. Agric. Food Chem. 59, 13131–13135. 10.1021/jf203396a [DOI] [PubMed] [Google Scholar]
  36. Drewnowski A., Gomez-Carneros C. (2000). Bitter taste, phytonutrients, and the consumer: a review. Am. J. Clin. Nutr. 72, 1424–1435. 10.1093/ajcn/72.6.1424 [DOI] [PubMed] [Google Scholar]
  37. Duan X., Hu X., Chen F., Deng Z. (2012). Bioactive ingredient levels of tea leaves are associated with leaf Al level interactively influenced by acid rain intensity and soil Al supply. J Food Agric Environ. 10, 1197–1204. [Google Scholar]
  38. Ewert F., Rounsevell M. D. A., Reginster I., Metzger M. J., Leemans R. (2005). Future scenarios of European agricultural land use: I. Estimating changes in crop productivity. Agric. Ecosyst. Environ. 107, 101–116. 10.1016/j.agee.2004.12.003 [DOI] [Google Scholar]
  39. FAOSTAT (2016). Available online at: http://www.fao.org/statistics/en/
  40. Fields M. J., Orians C. M. (2006). Specificity of phenolic glycoside induction in willow seedlings (Salix sericea) in response to herbivory. J. Chem. Ecol. 32, 2647–2656. 10.1007/s10886-006-9188-7 [DOI] [PubMed] [Google Scholar]
  41. Fraenkel G. S. (1959). The raison d'etre of secondary plant substances. Science 1466–70. 10.1126/science.129.3361.1466 [DOI] [PubMed] [Google Scholar]
  42. Glynn C., Herms D. A., Orians C. M., Hansen R. C., Larsson S. (2007). Testing the growth–differentiation balance hypothesis: dynamic responses of willows to nutrient availability. New Phytol. 176, 623–634. 10.1111/j.1469-8137.2007.02203.x [DOI] [PubMed] [Google Scholar]
  43. Goldberg G. (2003). Plants: Diet and health. The Report of a British Nutrition Foundation Task Force. Oxford: Blackwell Publishing; 10.1002/9780470774465 [DOI] [Google Scholar]
  44. Hajiboland R., Bahrami Rad S., Barceló J., Poschenrieder C. (2013). Mechanisms of aluminum-induced growth stimulation in tea (Camellia sinensis). J. Plant Nutr. Soil Sci. 176, 616–625. 10.1002/jpln.201200311 [DOI] [Google Scholar]
  45. Hajiboland R., Bastani S., Rad S. B. (2011). Effect of light intensity on photosynthesis and antioxidant defense in boron deficient tea plants. Acta Biol. 55, 265–272. Available online at: http://www.sci.u-szeged.hu/ABS [Google Scholar]
  46. Hamid F., Ahmad T., Waheed A., Ahmad N., Aslam S. (2014). Effect of different levels of nitrogen on the chemical composition of tea (C. sinensis L.) grown at higher altitude. J. Mater. Environ. Sci. 5, 73–80. [Google Scholar]
  47. Han B. Y., Chen Z. M. (2002). Composition of the volatiles from intact and tea aphid-damaged tea shoots and their allurement to several natural enemies of the tea aphid. J. Appl. Entomol. 126, 497–500. 10.1046/j.1439-0418.2002.00692.x [DOI] [Google Scholar]
  48. Han W. Y., Ma L. F., Shi Y. Z., Ruan J. Y., Kemmitt S. J. (2008). Nitrogen release dynamics and transformation of slow release fertiliser products and their effects on tea yield and quality. J. Sci. Food Agric. 88, 839–846. 10.1002/jsfa.3160 [DOI] [Google Scholar]
  49. Hemalatha K., Venkatesan S. (2011). Impact of iron toxicity on certain enzymes and biochemical parameters of tea. Asian J. Biochem. 6, 384–394. 10.3923/ajb.2011.384.394 [DOI] [Google Scholar]
  50. Hernández I., Alegre L., Munné-Bosch S. (2006). Enhanced oxidation of flavan-3-ols and proanthocyanidin accumulation in water-stressed tea plants. Phytochemistry 67, 1120–1126. 10.1016/j.phytochem.2006.04.002 [DOI] [PubMed] [Google Scholar]
  51. Hertel T. W., Burke M. B., Lobell D. B. (2010). The poverty implications of climate-induced crop yield changes by 2030. Global Environ. Change 20, 577–585. 10.1016/j.gloenvcha.2010.07.001 [DOI] [Google Scholar]
  52. Hu Q., Xu J., Pang G. (2003). Effect of selenium on the yield and quality of green tea leaves harvested in early spring. J. Agric. Food Chem. 51, 3379–3381. 10.1021/jf0341417 [DOI] [PubMed] [Google Scholar]
  53. Jayaganesh S., Venkatesan S. (2010). Impact of magnesium sulphate on biochemical and quality constituents of black tea. Am. J. Food Technol. 5, 31–39. 10.3923/ajft.2010.31.39 [DOI] [Google Scholar]
  54. Jayaganesh S., Venkatesan S., Senthurpandian V. (2011). Impact of different sources and doses of magnesium fertilizer on biochemical constituents and quality parameters of black tea. Asian J Biochem. 6, 273–281. 10.3923/ajb.2011.273.281 [DOI] [Google Scholar]
  55. Jayasekera S., Kaur L., Molan A. L., Garg M. L., Moughan P. J. (2014). Effects of season and plantation on phenolic content of unfermented and fermented Sri Lankan tea. Food Chem. 152, 546–551. 10.1016/j.foodchem.2013.12.005 [DOI] [PubMed] [Google Scholar]
  56. Jayasekera S., Molan A. L., Garg M., Moughan P. J. (2011). Variation in antioxidant potential and total polyphenol content of fresh and fully-fermented Sri Lankan tea. Food Chem. 125, 536–541. 10.1016/j.foodchem.2010.09.045 [DOI] [Google Scholar]
  57. Johns T., Sthapit B. R. (2004). Biocultural diversity in the sustainability of developing-country food systems. Food Nutr. Bull. 25, 143–155. 10.1177/156482650402500207 [DOI] [PubMed] [Google Scholar]
  58. Kacjan-Maršič N., Sircelj H., Kastelec D. (2010). Lipophilic antioxidants and some carpometric characteristics of fruits of ten processing tomato varieties, grown in different climatic conditions. J. Agric. Food Chem. 58, 390–397. 10.1021/jf902465e [DOI] [PubMed] [Google Scholar]
  59. Kfoury N., Morimoto J., Kern A., Scott E. R., Orians C. M., Ahmed S., et al. (2018). Striking changes in tea metabolites due to elevational effects. Food Chem. 264, 334–341. 10.1016/j.foodchem.2018.05.040 [DOI] [PubMed] [Google Scholar]
  60. Kottur G., Venkatesan S., Kumar S., Shanmugasundaram R., Murugesan S. (2010). Diversity among various forms of catechins and its synthesizing enzyme (phenylalanine ammonia lyase) in relation to quality of black tea (Camellia spp.). J. Sci. Food Agric. 90, 1533–1537. 10.1002/jsfa.3981 [DOI] [PubMed] [Google Scholar]
  61. Kowalsick A., Kfoury N., Robbat A., Ahmed S., Orians C., Griffin T., et al. (2014). Metabolite profiling of camellia sinensis by automated sequential, multidimensional gas chromatography/mass spectrometry reveals strong monsoon effects on tea constituents. J. Chromatogr A. 1370, 230–239. 10.1016/j.chroma.2014.10.058 [DOI] [PubMed] [Google Scholar]
  62. Ku K. M., Choi J. N., Kim J., Kim J. K., Yoo L. G., Lee S. J., et al. (2010). Metabolomics analysis reveals the compositional differences of shade grown tea (Camellia sinensis L.). J. Agric. Food Chem. 58, 418–426. 10.1021/jf902929h [DOI] [PubMed] [Google Scholar]
  63. Lee J. E., Lee B. J., Chung J. O., Hwang J. A., Lee S. J., Lee C. H., et al. (2010). Geographical and climatic dependencies of green tea (Camellia sinensis) metabolites: a 1H NMR-based metabolomics study. J. Agric. Food Chem. 58, 10582–10589. 10.1021/jf102415m [DOI] [PubMed] [Google Scholar]
  64. Lee J. E., Lee B. J., Chung J. O., Kim H. N., Kim E. H., Jung S., et al. (2015). Metabolomic unveiling of a diverse range of green tea (Camellia sinensis) metabolites dependent on geography. Food Chem. 174, 452–459. 10.1016/j.foodchem.2014.11.086 [DOI] [PubMed] [Google Scholar]
  65. Lee L. S., Choi J. H., Son N., Kim S. H., Park J. D., Jang D. J., et al. (2013). Metabolomic analysis of the effect of shade treatment on the nutritional and sensory qualities of green tea. J. Agric. Food Chem. 61, 332–338. 10.1021/jf304161y [DOI] [PubMed] [Google Scholar]
  66. Li T., Yu L. J., Li M. T., Li W. (2007). Comparative studies on the qualities of green teas in Karst and non-Karst areas of Yichang, Hubei Province, PR China. Food Chem. 103, 71–74. 10.1016/j.foodchem.2006.07.027 [DOI] [Google Scholar]
  67. Li X., Zhang L., Ahammed G. J., Li Z. X., Wei J. P., Shen C., et al. (2017). Stimulation in primary and secondary metabolism by elevated carbon dioxide alters green tea quality in Camellia sinensis L. Sci. Rep. 7:7937. 10.1038/s41598-017-08465-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Lin Y. S., Tsai Y. J., Tsay J. S., Lin J. K. (2003). Factors affecting the levels of tea polyphenols and caffeine in tea leaves. J. Agric. Food Chem. 51, 1864–1873. 10.1021/jf021066b [DOI] [PubMed] [Google Scholar]
  69. Lin Z. H., Qi Y. P., Chen R. B., Zhang F. Z., Chen L. S. (2012). Effects of phosphorus supply on the quality of green tea. Food Chem. 130, 908–914. 10.1016/j.foodchem.2011.08.008 [DOI] [Google Scholar]
  70. Liu R. H. (2013). Health-promoting components of fruits and vegetables in the diet. Adv. Nutr. Int. Rev. J. 4, 384S−392S. 10.3945/an.112.003517 [DOI] [PMC free article] [PubMed] [Google Scholar]
  71. Lobell D. B., Asner G. P. (2003). Climate and management contributions to recent trends in US agricultural yields. Science 299:1032 10.1126/science.1077838 [DOI] [PubMed] [Google Scholar]
  72. Lobell D. B., Schlenker W., Costa-Roberts J. (2011). Climate trends and global crop production since 1980. Science 333, 616–620. 10.1126/science.1204531 [DOI] [PubMed] [Google Scholar]
  73. Lower S. S., Orians C. M. (2003). Soil nutrients and water availability interact to influence willow growth and chemistry but not leaf beetle performance. Entomol. Exp. Appl. 107, 69–79. 10.1046/j.1570-7458.2003.00037.x [DOI] [Google Scholar]
  74. Marx W., Haunschild R., Bornmann L. (2017). Global warming and tea production—the bibliometric view on a newly emerging research topic. Climate 5:46 10.3390/cli5030046 [DOI] [Google Scholar]
  75. Mattos L. M., Moretti C. L., Jan S., Sargent S. A., Lima C. E. P., Fontenelle M. R. (2014). Chapter 19: Climate changes and potential impacts on quality of fruit and vegetable crops, in Emerging Technologies and Management of Crop Stress Tolerance (San Diego, CA: Academic Press; ), 467–486. 10.1016/B978-0-12-800876-8.00019-9 [DOI] [Google Scholar]
  76. Moher D., Liberati A., Tetzlaff J., Altman D. G. (2009). The PRISMA group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement. PLoS Med. 6:e1000097 10.1371/journal.pmed.1000097 [DOI] [PMC free article] [PubMed] [Google Scholar]
  77. Mukhopadhyay M., Das A., Subba P., Bantawa P., Sarkar B., Ghosh P., et al. (2013). Structural, physiological, and biochemical profiling of tea plants under zinc stress. Biol Plant. 57, 474–480. 10.1007/s10535-012-0300-2 [DOI] [Google Scholar]
  78. Mukhopadyay M., Bantawa P., Das A., Sarkar B., Bera B., Ghosh P., et al. (2012). Changes of growth, photosynthesis and alteration of leaf antioxidative defence system of tea [Camellia sinensis (L) O. Kuntze] seedlings under aluminum stress. Biometals 25, 1141–1154. 10.1007/s10534-012-9576-0 [DOI] [PubMed] [Google Scholar]
  79. Myers S. S., Zanobetti A., Kloog I., Huybers P., Leakey A. D., Bloom A. J., et al. (2014). Increasing CO2 threatens human nutrition. Nature 510:139. 10.1038/nature13179 [DOI] [PMC free article] [PubMed] [Google Scholar]
  80. Odada E. O., Scholes R. J., Noone K., Mbow C., Ochola W. O. (2008). A Strategy for Global Environmental Change Research in Africa. Stockholm, Science Plan and Implementation Strategy. IGBP Secretariat. [Google Scholar]
  81. Ohno A., Oka K., Sakuma C., Okuda H., Fukuhara K. (2011). Characterization of tea cultivated at four different altitudes using 1H NMR analysis coupled with multivariate statistics. J. Agric. Food Chem. 59, 5181–5187. 10.1021/jf200204y [DOI] [PubMed] [Google Scholar]
  82. Owuor P, Chavanji A. M. (1986). Caffeine contents of clonal tea: seasonal variations and effects of plucking standards under Kenyan conditions. Food Chem. 20, 225–233. 10.1016/0308-8146(86)90175-5 [DOI] [Google Scholar]
  83. Pachauri R. K., Allen M. R., Barros V. R., Broome J., Cramer W., Christ R., et al. (2014). CLIMATE Change 2014: Synthesis Report. Contribution of Working Groups, I., II and III to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change (IPCC). [Google Scholar]
  84. Ponmurugan P., Baby U. (2007). Morphological, physiological and biochemical changes in resistant and susceptible cultivars of tea in relation to phomopsis disease. Plant Pathol. J. 6, 91–94. 10.3923/ppj.2007.91.94 [DOI] [Google Scholar]
  85. Porter J. R., Semenov M. A. (2005). Crop responses to climatic variation. Philos. T R. Soc. B 360, 2021–2035. 10.1098/rstb.2005.1752 [DOI] [PMC free article] [PubMed] [Google Scholar]
  86. Rawat R., Gulati A. (2008). Seasonal and clonal variations in some major glycosidic bound volatiles in Kangra tea (Camellia sinensis (L.) O. Kuntze). Eur. Food Res. Technol. 226:1241 10.1007/s00217-007-0753-2 [DOI] [Google Scholar]
  87. Ruan J., Gerendás J., Haerdter R., Sattelmacher B. (2007a). Effect of alternative anions (Clvs SO42-) on concentrations of free amino acids in young tea plants. J. Plant Nutr. Soil Sci. 170, 49–58. 10.1002/jpln.200625142 [DOI] [Google Scholar]
  88. Ruan J., Gerendás J., Härdter R., Sattelmacher B. (2007b). Effect of root zone pH and form and concentration of nitrogen on accumulation of quality-related components in green tea. J. Sci. Food Agric. 87, 1505–1516. 10.1002/jsfa.2875 [DOI] [Google Scholar]
  89. Ruan J., Haerdter R., Gerendás J. (2010). Impact of nitrogen supply on carbon/nitrogen allocation: a case study on amino acids and catechins in green tea [Camellia sinensis (L) O. Kuntze] plants. Biol Plant. 12, 724–734. 10.1111/j.1438-8677.2009.00288.x [DOI] [PubMed] [Google Scholar]
  90. Ruan J., Ma L., Shi Y. (2013). Potassium management in tea plantations: its uptake by field plants, status in soils, and efficacy on yields and quality of teas in China. J. Plant Nutr. Soil Sci. 176, 450–459. 10.1002/jpln.201200175 [DOI] [Google Scholar]
  91. Ruan J., Ma L., Yang Y. (2012). Magnesium nutrition on accumulation and transport of amino acids in tea plants. J. Sci. Food Agric. 92, 1375–1383. 10.1002/jsfa.4709 [DOI] [PubMed] [Google Scholar]
  92. Sae-Lee N., Kerdchoechuen O., Laohakunjit N. (2012). Chemical qualities and phenolic compounds of Assam tea after soil drench application of selenium and aluminum. Plant Soil. 356, 381–393. 10.1007/s11104-012-1139-1 [DOI] [Google Scholar]
  93. Saikia P., Mahanta P. K. (2002). Specific fluctuations in the composition of lipoxygenase-and glycosidase-generated flavors in some cultivated teas of Assam. J. Agric. Food Chem. 50, 7691–7699. 10.1021/jf0257345 [DOI] [PubMed] [Google Scholar]
  94. Saito S. T., Gosmann G., Saffi J., Presser M., Richter M. F., Bergold A. M. (2007). Characterization of the constituents and antioxidant activity of Brazilian green tea (Camellia sinensis var. assamica IAC-259 cultivar) extracts. J Agric Food Chem. 55, 9409–9414. 10.1021/jf071796p [DOI] [PubMed] [Google Scholar]
  95. Scharbert S., Holzmann N., Hofmann T. (2004). Identification of the astringent taste compounds in black tea Infusions by combining instrumental analysis and human bioresponse. J. Agric. Food Chem. 52, 3498–3508. 10.1021/jf049802u [DOI] [PubMed] [Google Scholar]
  96. Schardt C., Adams M. B., Owens T., Keitz S., Fontelo P. (2007). Utilization of the PICO framework to improve searching PubMed for clinical questions. BMC Med. Inform. Decis. Mak. 7:16. 10.1186/1472-6947-7-16 [DOI] [PMC free article] [PubMed] [Google Scholar]
  97. Schepp K. (2009). Strategy to Adapt to Climate Change for Michimikuru Tea Farmers in Kenya. AdapCC Report. Deutsche Gesellschaft fur Technische Zusammenarbeit (GTZ) GmbH, Eschborn, Germany. Available online at: http://adapcc.org/en/kenya.htm
  98. Sedaghathoor S., Torkashv A. M., Hashemabadi D., Kaviani B. (2019). Yield and quality response of tea plant to fertilizers. Afr J Agric Res. 4, 568–570. 10.1631/jzus.2006.B0696 [DOI] [Google Scholar]
  99. Singh S., Pandey A., Kumar B., Palni L. M. S. (2010). Enhancement in growth and quality parameters of tea [Camellia sinensis (L) O. Kuntze] through inoculation with arbuscular mycorrhizal fungi in an acid soil. Biol. Fertil Soils 46, 427–433. 10.1007/s00374-010-0448-x [DOI] [Google Scholar]
  100. Song R., Kelman D., Johns K., Wright A. (2012). Correlation between leaf age, shade levels, and characteristic beneficial natural constituents of tea (Camellia sinensis) grown in Hawaii. Food Chem. 133, 707–714. 10.1016/j.foodchem.2012.01.078 [DOI] [Google Scholar]
  101. Sud R. G., Baru A. (2000). Seasonal variations in theaflavins, thearubigins, total colour and brightness of Kangra orthodox tea (Camellia sinensis (l) O. Kuntze) in Himachal Pradesh. J. Sci. Food Agric. 80, 1291–1299. [DOI] [Google Scholar]
  102. Swift M. J., Izac A. M., Van N. M. (2004). Biodiversity and ecosystem services in agricultural landscapes—are we asking the right questions? Agric. Ecosyst. Environ. 104, 113–134. 10.1016/j.agee.2004.01.013 [DOI] [Google Scholar]
  103. Tomás-Barberán F. A., Espin J. C. (2001). Phenolic compounds and related enzymes as determinants of quality in fruits and vegetables. J. Sci. Food Agric. 81, 853–876. 10.1002/jsfa.885 [DOI] [Google Scholar]
  104. Tontul I., Torun M., Dincer C., Sahin-Nadeem H., Topuz A., Turna T., et al. (2013). Comparative study on volatile compounds in Turkish green tea powder: impact of tea clone, shading level and shooting period. Food Res. Int. 53, 744–750. 10.1016/j.foodres.2012.12.026 [DOI] [Google Scholar]
  105. Topuz A., Dinçer C., Torun M., Tontul I., Nadeem H. S., Haznedar A., et al. (2014). Physicochemical properties of Turkish green tea powder: effects of shooting period, shading, and clone. Turk. J. Agric. For. 38, 233–241. 10.3906/tar-1307-17 [DOI] [Google Scholar]
  106. Trevisanato S. I., Kim Y. I. (2000). Tea and health. Nutr. Rev. 58, 1–10. 10.1111/j.1753-4887.2000.tb01818.x [DOI] [PubMed] [Google Scholar]
  107. Upadhyaya H., Dutta B. K., Panda S. K. (2013). Zinc Modulates Drought-Induced Biochemical Damages in Tea [Camellia sinensis (L) O Kuntze]. J. Agric. Food Chem. 61, 6660–6670. 10.1021/jf304254z [DOI] [PubMed] [Google Scholar]
  108. Upadhyaya H., Panda S. K. (2004). Responses of Camellia sinensis to drought and rehydration. Biol. Plant. 48, 597–600. 10.1023/B:BIOP.0000047158.53482.37 [DOI] [Google Scholar]
  109. Upadhyaya H., Panda S. K., Dutta B. K. (2011). CaCl2 improves post-drought recovery potential in Camellia sinensis (L) O. Kuntze. Plant Cell Rep. 30, 495–503. 10.1007/s00299-010-0958-x [DOI] [PubMed] [Google Scholar]
  110. van-Dam N. M., Vrieling K. (1994). Genetic variation in constitutive and inducible pyrrolizidine alkaloid levels in Cynoglossum officinale L. Oecologia 99, 374–378. 10.1007/BF00627751 [DOI] [PubMed] [Google Scholar]
  111. Venkatesan S., Hemalatha K., Jayaganesh S. (2007). Characterization of manganese toxicity and its influence on nutrient uptake, antioxidant enzymes and biochemical parameters in tea. Res. J. Phytochem. 1, 52–60. 10.3923/rjphyto.2007.52.60 [DOI] [Google Scholar]
  112. Venkatesan S., Murugesan S., Ganapathy M. N., Verma D. P. (2004). Long-term impact of nitrogen and potassium fertilizers on yield, soil nutrients and biochemical parameters of tea. J. Sci. Food Agric. 84, 1939–1944. 10.1002/jsfa.1897 [DOI] [Google Scholar]
  113. Venkatesan S., Murugesan S., Pandian V. S., Ganapathy M. (2005). Impact of sources and doses of potassium on biochemical and green leaf parameters of tea. Food Chem. 90, 535–539. 10.1016/j.foodchem.2004.05.014 [DOI] [Google Scholar]
  114. Venkatesan S., Senthurpandian V. K., Murugesan S., Maibuam W., Ganapathy M. N. (2006). Quality standards of CTC black teas as influenced by sources of potassium fertiliser. J. Sci. Food Agric. 86, 799–803. 10.1002/jsfa.2418 [DOI] [Google Scholar]
  115. Villarreal D., Laffargue A., Posada H., Bertrand B., Lashermes P., Dussert S. (2009). Genotypic and environmental effects on coffee (Coffea arabica L.) bean fatty acid profile: impact on variety and origin chemometric determination. J. Agric. Food Chem. 57, 11321–11327. 10.1021/jf902441n [DOI] [PubMed] [Google Scholar]
  116. Wang L., Wei K., Jiang Y., Cheng H., Zhou J., He W., et al. (2011). Seasonal climate effects on flavanols and purine alkaloids of tea (Camellia sinensis L.). Eur. Food Res. Technol. 233, 1049–1055. 10.1007/s00217-011-1588-4 [DOI] [Google Scholar]
  117. Wei K., Wang L., Zhou J., He W., Zeng J., Jiang Y., et al. (2011). Catechin contents in tea (Camellia sinensis) as affected by cultivar and environment and their relation to chlorophyll contents. Food Chem. 125, 44–48. 10.1016/j.foodchem.2010.08.029 [DOI] [Google Scholar]
  118. Wijeratne M. A. (1996). Vulnerability of Sri Lanka tea production to global climate change. Water Air Soil Pollut. 92, 87–94. 10.1007/978-94-017-1053-4_8 [DOI] [Google Scholar]
  119. Wolfe K. L., Kang X., He X., Dong M., Zhang Q., Liu R. H. (2008). Cellular antioxidant activity of common fruits. J. Agric. Food Chem. 56, 8418–8426. 10.1021/jf801381y [DOI] [PubMed] [Google Scholar]
  120. Xu C., Zhang Y., Zhu L., Huang Y., Lu J. (2011). Influence of growing season on phenolic compounds and antioxidant properties of grape berries from vines grown in subtropical climate. J Agric Food Chem. 59, 1078–1086. 10.1021/jf104157z [DOI] [PubMed] [Google Scholar]
  121. Xu W., Song Q., Li D., Wan X. (2012). Discrimination of the production season of Chinese green tea by chemical analysis in combination with supervised pattern recognition. J. Agric. Food Chem. 60, 7064–7070. 10.1021/jf301340z [DOI] [PubMed] [Google Scholar]
  122. Yang T., Li H., Hu X., Li J., Hu J., Liu R., et al. (2014). Effects of fertilizing with N, P, Se, and Zn on regulating the element and functional component contents and antioxidant activity of tea leaves planted in red soil. J. Agric. Food Chem. 62, 3823–3830. 10.1021/jf5004286 [DOI] [PubMed] [Google Scholar]
  123. Yao L., Caffin N., D'arcy B., Jiang Y., Shi J., Singanusong R., et al. (2005). Seasonal variations of phenolic compounds in Australia-grown tea (Camellia sinensis). J. Agric. Food Chem. 53, 6477–6483. 10.1021/jf050382y [DOI] [PubMed] [Google Scholar]
  124. Zhang Q., Shi Y., Ma L., Yi X., Ruan J. (2014). Metabolomic analysis using ultra-performance liquid chromatography-quadrupole-time of flight mass spectrometry (UPLC-Q-TOF MS) uncovers the effects of light intensity and temperature under shading treatments on the metabolites in tea. PLoS ONE 9:e112572. 10.1371/journal.pone.0112572 [DOI] [PMC free article] [PubMed] [Google Scholar]
  125. Zheng X., Jin J., Chen H., Du Y., Ye J., Lu J., et al. (2008). Effect of ultraviolet B irradiation on accumulation of catechins in tea (Camellia sinensis (L) O. Kuntze. Afr. J. Biotechnol. 7, 3283–3287. 10.5897/AJB08.509 [DOI] [Google Scholar]
  126. Zietz M., Weckmüller A., Schmidt S., Rohn S., Schreiner M., Krumbein A., et al. (2010). Genotypic and climatic influence on the antioxidant activity of flavonoids in kale (Brassica oleracea var. sabellica). J. Agric. Food Chem. 58, 2123–2130. 10.1021/jf9033909 [DOI] [PubMed] [Google Scholar]

Associated Data

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Supplementary Materials

Data Availability Statement

All datasets generated for this study are included in the manuscript and/or the Supplementary Files.


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