The rapid production of H₂S has become a common response of plants to various HM stress, among HMs, Cd is the most severe stress due to its toxicity and stability (Ahmad, 2016). In rice seedlings, 0.5 mM Cd stress resulted in an increment of H₂S content from approximately 5 μmol g^-1 fresh weight (FW) to approximately 6 μmol g^-1 FW. The addition of 0.1 mM NaHS caused an even further increase in the level of H₂S (approximately 8 μmol g^-1 FW) as compared with Cd treatment alone. Exposure to 0.2 mM hypotaurine (HT, H₂S scavenger) with NaHS decreased H₂S level compared with NaHS alone, indicating that this elevated level of H₂S is correlated with the enhanced Cd tolerance (Mostofa et al., 2015). Zhang et al. (2015) found that the endogenous H₂S emission was stimulated by Cd stress in Chinese cabbage. The relative expression of DCD1 and DES1 (cysteine desulfhydrase, OAS-TL homogenous family) genes (responsible for H₂S synthesis) was up-regulated after treatment with Cd with a range of concentrations (0, 5, 10, and 20 mM) for 24 h. Expression of DES1 at 5 mM Cd already showed a significant increase, and at 20 mM Cd was 4.7 times of the control. Following a similar pattern, the endogenous H₂S concentrations also significantly rose from 0.38 to 0.58 nmol mg^-1 protein min^-1 at 20 mM. Chromium (Cr), existing in the form of Cr³⁺ and Cr⁶⁺, is regarded as the second most common HM, both forms have become major environmental pollution sources. In foxtail millet seedlings, Fang H. et al. (2014) also reported that the expressions of H₂S-emission related genes LCD, DCD2, and DES markedly increased during the first 12 h of Cr⁶⁺ exposure following decline at 24 h, while the expression of DCD1 was consistently increased from 0 to 24 h under 10 mM Cr⁶⁺ stress. Additionally, the H₂S production rate is induced by Cr⁶⁺ stress in dose- and time-dependent manner, and this induction was the most significant with 24 h of 10 mM Cr⁶⁺ treatment (from 0.6 to 1.6 nmol mg^-1 protein min^-1). These results imply that endogenous H₂S synthesis was activated by Cr⁶⁺ stress by activating its emission system in foxtail millet. Inconceivably, in compared with to other plant species, the both species Chinese cabbage and foxtail millet show a remarkable tolerance to HM (Cd and Cr⁶⁺). At 20 mM Cd for Chinese cabbage and 10 mM Cr⁶⁺ for foxtail millet, these treatment concentrations are far beyond the physiological level (generally micromolar concentrations) for many plant species, the precise physiological, biochemical, and molecular mechanisms are waiting for being uncovered.

Salt stress commonly leads to an osmotic stress response, similar to drought stress, which triggers rapid generation of second messengers like H₂S. In alfalfa seedlings, the increasing concentration of NaCl (from 50 to 300 mM) progressively caused the induction of total LCD activity and the increase of endogenous H₂S production (from 30 to 70 nmol g^-1 FW) (Lai et al., 2014). Exposure of strawberry seedlings to salinity (100 mM NaCl) and non-ionic osmotic stress (10% PEG-6000) greatly enhanced H₂S concentration (48 and 50 nmol g^-1 FW) in leaves, while 0.1 mM NaHS-pretreated plants subsequently exposed for 7 days to both stress factors were found to accumulate significantly higher amounts of H₂S (55 nmol g^-1 FW) in their leaves compared with NaCl-stressed plants (Christou et al., 2013).

One of the most severe abiotic stresses being experienced world-wide is drought. In Arabidopsis seedlings, the results of Shen et al. (2013) showed that treating wild type with polyethylene glycol (PEG) 8000, to simulate drought stress, caused an increase in production rate of endogenous H₂S (0.8 nmol mg^-1 protein min^-1). At early stage of osmotic exposure (PEG 6000 for 2 days), the endogenous H₂S in wheat seeds rapidly increased from 1.5 to 3.5 μmol g^-1 dry weight (DW) (Zhang et al., 2010a).

Low temperature is a major environmental stress factors that limit plant growth, development and distribution. In grape (Vitis vinifera L.) seedlings, chilling stress at 4°C induced the expression of L/DCD genes and increased the activities of L/DCD, which in turn enhanced endogenous H₂S accumulation (from 7 to 15 μmol g^-1 FW) (Fu et al., 2013). Similarly, Shi et al. (2013) also found that cold stress treatment at 4°C could induce the accumulation of endogenous H₂S level (14 nmol g^-1 FW) in bermudagrass [Cynodon dactylon (L). Pers.] seedlings. To uncover the adaptive strategies of alpine plants to the extremely cold conditions prevailing at high altitudes, Ma et al. (2015), using a comparative proteomics, investigated the dynamic patterns of protein expression in Lamiophlomis rotata plants grown at three different altitudes (4350, 4,800, and 5,200 m), and the results showed that the levels and enzyme activities of proteins (OAS-TL, CAS, L/DCD) involved in H₂S biosynthesis markedly increased at higher altitudes (4,800 and 5,200 m), and that H₂S accumulation increased to 12, 22, and 24 nmol g^-1 FW, respectively, demonstrating that H₂S plays a central role during the adaptation of L. rotata to environmental stress at higher altitudes.

Similar to other stresses, high temperature also can induce endogenous H₂S generation in many species of plant. In 3-week-old seedlings of tobacco, Chen et al. (2016) found that treatment with high temperature at 35°C increased the activity of LCD, which in turn induced the production of endogenous H₂S (8 nmol g^-1 FW) in tobacco seedlings, and that H₂S production remained elevated level after 3 days of high temperature exposure. More interestingly, H₂S production by high temperature can induce the accumulation of jasmonic acid, followed by promoting nicotine synthesis. These data suggest that H₂S and nicotine biosynthesis is linked in tobacco plants subjected to high temperature stress. Additionally, heat stress caused a marked modulation in H₂S content in strawberry seedlings, as indicated in a significant increase after 1, 4, and 8 h of exposure to 42°C compared with control plants. A significant increase in H₂S content was also observed in 0.1 mM NaHS-pretreated plants after 1 h exposure to heat stress, gradually lowering to control levels thereafter (Christou et al., 2014).

Recently, Li et al. (2016) found that UV-B radiation could induce H₂S production in leaves of barley seedlings, reaching a peak of approximately 230 nmol g^-1 FW after 12 h of exposure, which in turn promoted the accumulation of UV-absorbing compounds flavonoids and anthocyanins. H₂S began to decline with time, but it is overall significantly higher than that of the control (approximately 125 nmol g^-1 FW) at 48 h of exposure. A similar trend was observed for LCD activity, which was corroborated by the application of DL-propargylglycine (PAG, an inhibitor of LCD) that resulted in complete inhibition of the H₂S production and the accumulation of UV-absorbing compounds induced by UV-B radiation (Li et al., 2016).

Flooding often leads to hypoxia in plant roots, which significantly limits agriculture production. In pea (Pisum sativum L.) seedlings, Cheng et al. (2013) found that hypoxia could activate H₂S biosynthesis system (LCD, DCD, OAS-TL, and CS), which in turn induced the accumulation of endogenous H₂S from approximately 0.9 (control) to 5.1 μmol g^-1 FW (hypoxia for 24 h), indicating that H₂S might be a hypoxia signaling that triggers the tolerance of the pea seedlings to hypoxic stress, this hypothesis was further supported by exogenously applied NaHS.

Pathogen infection is a common biotic stress in plants. In oilseed rape (Brassica napus L.) seedlings, fungal infection with Sclerotinia sclerotiorum led to an even stronger increase in H₂S, reaching a maximum of 3.25 nmol g^-1 DW min^-1 2 days after infection, suggesting that the release of H₂S seems to be part of the response to fungal infection (Bloem et al., 2012).

In addition to above-described abiotic and biotic stressors, H₂S signaling in plant cells also can be triggered by exogenously applying NaHS (H₂S donor) or up-regulating the expression of genes involved in H₂S biosynthesis like L/DCD under normal growth conditions. In strawberry seedlings, treatment of root with 0.1 mM NaHS resulted in significantly elevated H₂S concentration (35 nmol g^-1 FW) in leaves compared with control plants (25 nmol g^-1 FW) (Christou et al., 2013). In wheat seeds, the endogenous H₂S level [4.5 μmol g^-1 dry weight (DW)] in NaHS-treated seed was slightly higher than that of control (1.7 mol g^-1 DW) (Zhang et al., 2010a). These results indicated that H₂S is easy to enter into plant cells and follow on being transported to other tissues or organs due to its highly lipophilic property, which in turn exert its physiological role in plants.

Additionally, Jin et al. (2011) found that the Arabidopsis seedlings expressing L/DCD showed higher endogenous H₂S content under both normal (6 nmol mg^-1 protein min^-1) and drought stress conditions (14 nmol mg^-1 protein min^-1) compared with the control (3 nmol mg^-1 protein min^-1), and the expression pattern of L/DCD was similar to the drought associated genes dehydration-responsive element-binding proteins (DREB2A, DREB2B, CBF4, and RD29A) induced by dehydration, while exogenous application of H₂S (80 μM) was also found to stimulate further the expression of drought associated genes. In addition, drought stress significantly induced endogenous H₂S production in both transgenetic plant and wild type, a process that was reversed by re-watering (Jin et al., 2011). Interestingly, Arabidopsis seedlings overexpressing LCD or pre-treated with NaHS exhibited higher endogenous H₂S level (from 2 to 10 nmol g^-1 FW), followed by improving abiotic stress (drought, salt, and chilling) tolerance and biotic stress (bacteria) resistance, while LCD knockdown plants or HT (H₂S scavenger) pre-treated plants displayed lower endogenous H₂S level and decreased stress resistance (Shi et al., 2015).

In conclusion, above-mentioned researches in this section display that: (1) under normal growth conditions, the content of endogenous H₂S or production rate in various plant species are different, ranging from 2 nmol g^-1 FW to 7 μmol g^-1 FW or 0.38 to 6 nmol mg^-1 protein min^-1. These differences may be relative to measurement methods, plant species and development stage, and experiment system. (2) Under abiotic stress conditions, the level of endogenous H₂S in various plant species is averagely increased by 2∼2.5-fold, indicating that different environment stresses can trigger the H₂S signaling, which may be a trigger that induces the acquisition of cross-adaptation in plants.

Heavy metals refer to a group of metal elements with a density greater than 6 g/cm³, including Cr, Cu, Zn, and so forth (Gupta et al., 2013; Ahmad, 2016). Due to their toxicity and stablility, HM has become the major abiotic stress in plants, and even threatens human health by way of the food chain. HM stress commonly results in oxidative stress, that is, the excessive accumulation of ROS, which leads to lipid peroxidation, protein oxidation, enzyme inactivation, and DNA damage (Yadav, 2010; Gupta et al., 2013; Ahmad, 2016). However, higher plants have evolved a sophisticated antioxidant defense system to scavenge excessive ROS and maintain its homeostasis in plants (Foyer and Noctor, 2009, 2011).

Arsenic (As) is a highly toxic metalloid, it is major pollutant in the soil. In pea seedlings, As treatment increased the accumulation of ROS, which in turn damage to lipids, proteins and biomembranes. Meanwhile, higher cysteine level was observed in As-stress seedlings in comparison to all other treatments (As-free; NaHS; As + NaHS), while these effects were alleviated by the addition of NaHS (Singh et al., 2015). Further experiments showed that As treatment inhibited the activity of the enzymes involved in the ascorbic acid (AsA)–glutathione (GSH) cycle, whereas their activities were enhanced by application of NaHS (Singh et al., 2015). In addition, the redox status of AsA and GSH was disturbed, as indicated by a steep decline in their reduced/oxidized ratios. However, exogenously applied NaHS restored the redox status of the AsA and GSH pools under As stress (Singh et al., 2015). Furthermore, NaHS treatment ameliorated As toxicity, which was coincided with the increased accumulation of H₂S. The results demonstrated that H₂S might counterbalance ROS-mediated damage to macromolecules by reducing the accumulation of As and triggering up-regulation of the AsA–GSH cycle, further suggesting that H₂S plays a crucial role in plant priming, and in particular for pea seedlings in mitigating As stress.

Under Cr stress, exogenous application of NaHS could improve the germination rate of wheat seeds in a dose-dependent manner and the activities of amylase, esterase as well as antioxidant enzymes superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX) and glutathione peroxidase (GPX), whereas reduced the activity of lipoxygenase and over-production of malondialdehyde (MDA) as well as H₂O₂ induced by Cr, and sustained higher endogenous H₂S level (Zhang et al., 2010b). Additionally, NaHS pretreatment increased the activities of SOD and CAT, but decreased that of lipoxygenase in wheat under Cu stress (Zhang et al., 2008), these results were consisted with the response of wheat to Cr stress (Zhang et al., 2010b).

Also, NaHS could alleviate the inhibitory effect of Cu stress in wheat in a dose-dependent manner, and H₂S or HS^- derived from NaHS rather than other sulfur-containing components (S^2-, SO₄^2-, SO3^2-, HSO₄^-, and HSO₃^-) attribute to the potential role in promoting seed germination under Cu stress (Zhang et al., 2008). Further experiments showed that NaHS could increase amylase and esterase activities, reduced the disturbance of plasma membrane integrity induced by Cu in the radicle tips, and sustain lower MDA and H₂O₂ levels in germinating seeds (Zhang et al., 2008), similar to the reports by (Zhang et al., 2010b).

Aluminium (Al), a non-essential element for plants, adversely affects plant growth, development and survival, especially in acid soil. In barley (Hordeum vulgare L.) seedlings, Al stress inhibited the elongation of roots, while pretreatment with NaHS partially rescued the inhibition of root elongation induced by Al, and this rescue was closely correlated with the decrease of Al accumulation in seedlings (Chen et al., 2013). Additionally, application of NaHS significantly alleviated citrate secretion and oxidative stress (as indicated in lipid peroxidation as well as ROS burst) induced by Al by activating the antioxidant system (Chen et al., 2013). Similar results were reported by Zhang et al. (2010c) in wheat (Triticum aestivum L.).

Though zinc (Zn) is an essential element for plants, its toxic effects can be observed when being excessive accumulation in plants. In Solanum nigrum L. seedlings, H₂S ameliorated the inhibition of growth by excess Zn, especially in roots, and an increase in free cytosolic Zn²⁺ content in roots, which was correlated well with the down-regulation of Zn uptake and homeostasis related genes expression like zinc-regulated transporter (ZRT), iron-regulated transporter (IRT)-like protein (ZIP) and natural resistance associated macrophage protein (NRAMP) (Liu et al., 2016). In addition, H₂S further enhanced the expression of the metallothioneins to chelate excessive Zn and alleviated Zn-oxidative stress by regulating the genes expression of antioxidant enzymes (Liu et al., 2016).

Salts stress is negative effects of excessive salt on seed germination, plant growth and development, and even survival, which is a major abiotic stress in agriculture production world-wide. Salt stress commonly leads to direct and indirect injury, namely ion toxicity, osmotic stress, nutrient imbalance, and oxidative stress (Ahmad et al., 2013a,b). To combat with salt injury, plants have evolved many protective strategies, including osmotic adjustment by synthesizing osmolytes such as proline (Pro), glycine betaine (GB), trehalose (Tre), and total soluble sugar (TSS); ion and nutrient balance by regulating transporter; and enhancement of antioxidant capacity by activating the activity of antioxidant enzymes SOD, CAT, APX, GPX and glutathione reductase (GR), as well as by synthesizing antioxidants like AsA and GSH (Ahmad et al., 2013a,b). In salt-sensitive wheat cultivar LM15, the results of Bao et al. (2011) showed that wheat seed priming with different concentrations of NaHS (0.01, 0.05, 0.09, 0.13 mM) for 12 h could significantly alleviate the inhibition of seed germination and seedling growth induced by 100 mM NaCl in a concentration-dependent manner, as indicated in germination rate, germination index, vigor index and growth of seedlings of wheat. In alfalfa (Medicago sativa), NaHS pretreatment differentially activate total and isoenzymatic activities as well as corresponding transcripts of antioxidant enzymes (SOD, CAT, POD, and APX) under 100 mM NaCl stress, thus resulting in the alleviation of oxidative damage induced by NaCl (Wang et al., 2012). In addition, NaCl stress inhibited seed germination and seedling growth, but pretreatment with NaHS could significantly attenuate this inhibitive effect and increase the ratio of potassium (K) to sodium (Na) in the root parts (Wang et al., 2012). Also, under 100 mM NaCl stress, Arabidopsis roots displayed a great increase in electrolyte leakage and Na⁺/K⁺ ratio, indicating that Arabidopsis was sensitive to salt stress, while treatment with NaHS enhanced the salt tolerance by maintaining a higher K⁺/Na⁺ ratio (Li J. et al., 2014). In addition, the level of gene expression and the phosphorylation of plasma membrane H⁺-ATPase and Na⁺/H⁺ antiporter protein was promoted by H₂S, while the effect of H₂S on the plasma membrane Na⁺/H⁺ antiporter system was removed by diphenylene iodonium (DPI, a PM NADPH oxidase inhibitor) or dimethylthiourea (DMTU, an ROS scavenger) (Li J. et al., 2014), suggesting that H₂S can maintain ion homeostasis in salt-stress Arabidopsis root in the H₂O₂-dependent manner.

Similar to other stressors, drought stress, namely water deficiency, usually leads to osmotic stress and oxidative stress, which adversely affects plant growth, development and production (Iqbal et al., 2016). Plants can maintain water balance and ROS homeostasis by osmotic adjustment and antioxidant system (Foyer and Noctor, 2009, 2011; Iqbal et al., 2016). Zhang et al. (2010d) found that the germination rate reduced gradually with the increasing concentrations of PEG-6000, which mimicked osmotic stress, while NaHS treatment could promote wheat seed germination under osmotic stress in a dose-dependent manner, Na⁺ and other sulfur-containing components (S^2-, SO₄^2-, SO3^2-, HSO₄^-, and HSO₃^-) were not able to replace NaHS, confirming H₂S or HS^- derived from NaHS contribute to the protective roles (Zhang et al., 2010d). Further experiments showed that NaHS treatment significantly increased CAT and APX activities, reduced that of lipoxygenase as well as the accumulation of MDA and H₂O₂ in seeds (Zhang et al., 2010d). Additionally, exogenously applied NaHS increased the activities of APX, GR, dehydroascorbate reductase (DHAR) and gamma-glutamylcysteine synthetase in wheat seedlings, as well as the contents of AsA, GSH, total ascorbate and total glutathione under water stress compared to the control without NaHS treatment, which in turn decreased the MDA content and electrolyte leakage induced by water deficiency in wheat seedlings (Shan et al., 2011). In Arabidopsis seedlings, under drought stress, the expression pattern of L/DCD was similar to the drought associated genes, whose express was stimulated further by H₂S (Jin et al., 2011). Also, seedlings treated with NaHS exhibited a higher survival rate and a significant reduction in the size of the stomatal aperture compared to the control (Jin et al., 2011). In addition to these, García-Mata and Lamattina (2010) also found that, in Vicia faba (L.) var. major and Impatiens walleriana Hook. f., H₂S treatment could increase relative water content (RWC) and protect plants against drought stress.

Low temperature stress includes chilling stress (>0°C) and freezing stress (<0°C). Low temperature usually leads to osmotic stress and oxidative stress, plants can reduce the low temperature injury by osmotic adjustment and activating antioxidant system (Foyer and Noctor, 2009, 2011; Iqbal et al., 2016). Shi et al. (2013) found that exogenous application of NaHS conferred multiple stress tolerance including freezing tolerances in bermudagrass, in reflected in decreased electrolyte leakage and increased survival rate under freezing conditions. Additionally, NaHS treatment mitigated the ROS burst and cell damage induced by freezing stress via modulating the activities of antioxidant enzymes CAT, GPX and GR, as well as non-enzymatic GSH pool and redox state (Shi et al., 2013). In grape (Vitis vinifera L) seedlings, Fu et al. (2013) reported that treatment with NaHS showed the high activity of SOD and gene expression of VvICE1 and VvCBF3, lowed superoxide radical and MDA levels as well as cell membrane permeability under chilling stress at 4°C, while HT treatment displayed contrary effect under the chilling stress. Also, Arabidopsis seedlings overexpressing LCD or pretreating with NaHS exhibited higher endogenous H₂S level and stronger chilling stress tolerance, while LCD knockdown or HT pre-treated plants displayed lower endogenous H₂S level and weaker stress resistance. Moreover, H₂S could up-regulate the expression of genes involved in multiple abiotic and biotic stress and inhibited ROS accumulation (Shi et al., 2015). Ma et al. (2015) found that the levels and enzyme activities of proteins involved in H₂S biosynthesis (L/DCD, CAS, OAS-TL) markedly increased at higher altitudes at 4800 and 5200 m, which in turn maintained higher H₂S level. Exogenous H₂S application reduced ROS and RNS (reactive nitrogen species) damage by increasing antioxidant enzyme and GSNOR (S-nitrosoglutathione reductase) activities, activated the downstream defense response, resulting in protein degradation as well as Pro and SS accumulation. However, such defense responses could be reversed by HT and PAG, respectively. These results illustrated that H₂S plays a central role in L. rotata uses multiple strategies to adapt to the alpine stress environment. Also, H₂S fumigation maintained higher values of lightness and peel firmness of banana fruit and reduced the accumulation of MDA under chilling stress (Luo et al., 2015). In addition, H₂S could increase the activities of GPX, SOD, CAT, APX, GR and the phenylalanine ammonia lyase and total phenolics content, which in turn improved antioxidant capacity of banana fruits, reducing H₂O₂ and superoxide anion accumulation (Luo et al., 2015). Further experiments also found that H₂S fumigation elevated Pro content by activating P5CS activity and decreasing that of ProDH, which might be related to chilling injury tolerance improvement (Luo et al., 2015), similar to the report by Li and Gong (2013). These data indicate that H₂S alleviated the chilling injury may be achieved through the enhancement of antioxidant system and Pro accumulation in banana fruit.

Along with global warming, high temperature has already become a noticeable abiotic stress worldwide, and the mechanisms of high temperature injury and heat tolerance have attracted much attention (Wahid et al., 2007; Asthir, 2015; Hemmati et al., 2015). Christou et al. (2011) found that pre-treatment of roots with NaHS effectively alleviated the decrease in leaf chlorophyll fluorescence, stomatal conductance and relative leaf water content in strawberry (Fragaria x ananassa cv. Camarosa) under heat stress at 42°C, as well as an increase in ion leakage and MDA accumulation in comparison with plants directly subjected to heat stress. In addition, NaHS pretreatment preserved AsA/GSH homeostasis, as evidenced by lower AsA and GSH pool redox disturbances and enhanced transcription of AsA and GSH biosynthetic enzymes, 8 h after heat stress exposure. Furthermore, NaHS root pretreatment increased the gene expression of antioxidant enzymes (cAPX, CAT, MnSOD, GR), heat shock proteins (HSP70, HSP80, HSP90), and aquaporins (PIP) (Christou et al., 2014). These results suggest that H₂S root pretreatment activates a coordinated network of heat shock defense-related pathways at a transcriptional level and systemically protects strawberry plants from heat stress-induced damage. Our previous study also showed that 0.7 mM NaHS treatment increased the activities of CAT, GPX, SOD and GR, and the contents of GSH and AsA, as well as the ratio of reduced antioxidants to total antioxidants [AsA/(AsA+DHA) and GSH/(GSH +GSSG)] in maize seedlings under normal culture conditions compared with the control (Li Z.G. et al., 2014). Under heat stress, antioxidant enzymes activities, antioxidants contents and the ratio of the reduced antioxidants to total antioxidants in control and treated seedlings all decreased, but NaHS-treated seedlings maintained higher antioxidant enzymes activities and antioxidants levels as well as reduced antioxidants/total antioxidants ratio (Li Z.G. et al., 2014), similar results also were found in tobacco cells (Li et al., 2015). In addition, NaHS pretreatment significantly increased the survival percentage of tobacco cells under heat stress and regrowth ability after heat stress, alleviated a decrease in vitality of cells and an increase in electrolyte leakage and MDA accumulation (Li et al., 2012b). Meanwhile, the heat tolerance induced by NaHS was markedly enhanced by exogenous application of Ca²⁺ and its ionophore A23187, respectively, while was weakened by addition of Ca²⁺ chelator ethylene glycol-bis(b-aminoethylether)- N,N,N′,N′-tetraacetic acid, plasma membrane channel blocker La³⁺, as well as calmodulin antagonists chlorpromazine and trifluoperazine, respectively (Li et al., 2012b). Similarly, in maize, pretreatment with NaHS markedly improved the germination percentage of seeds and the survival percentage of seedlings under heat stress, alleviated an increase in electrolyte leakage of roots and a decrease in tissue vitality and accumulation of MDA in coleoptiles of maize seedlings (Li et al., 2013a). Furthermore, NaHS pretreatment could improve the activity of Δ¹-pyrroline-5-carboxylate synthetase (P5CS) and lowered that of Pro dehydrogenase (ProDH), which in turn induced the accumulation of endogenous Pro in maize seedlings (Li et al., 2013a). Also, exogenously applied Pro could increase endogenous Pro content, followed by increase in the survival percentage of maize seedlings under heat stress (Li et al., 2013a). These results suggest that NaHS pretreatment can improve the heat tolerance in plants and the acquisition of heat tolerance induced by NaHS may require the synergistic effect of antioxidant system, calcium messenger system, HSPs and Pro.

Flooding stress usually causes hypoxia, and even anoxia in plant roots, plants can improve hypoxia tolerance by reducing oxidative damage (van Dongen and Licausi, 2014). Cheng et al. (2013) found that hypoxia could induce root tip death of pea seedlings, while pretreatment with exogenous H₂S dramatically alleviated cell death by protecting root tip cell membranes from ROS damage induced by hypoxia and by inhibiting ethylene production. Conversely, root tip death induced by hypoxia was strongly enhanced by inhibiting the key enzymes responsible for endogenous H₂S biosynthesis (adding hydroxylamine to inhibit LCD activity). These results demonstrated that H₂S can enhance the tolerance of the plant to hypoxic stress by alleviating hypoxia-induced root tip death in pea seedlings.

More interestingly, H₂S also could transcriptionally regulate MIR393-mediate auxin signaling, including MIR393a/b and their target genes (TIR1, AFB1, AFB2, and AFB3), and this regulation was related with H₂S-induced antibacterial resistance (Shi et al., 2015).

All of the above studies in this section show exogenous application of NaHS (a H₂S donor) can induce cross-adaptation to HM, salt, osmosis, drought, cold, heat and hypoxia stresses in different plant species, and the optimal NaHS concentration range from 0.05 to 1.5 mM (Table 2), while higher NaHS concentration (>1.5 mM) exhibits negative effect on plant growth, development, survival, and even the acquisition of stress tolerance. Therefore, the optimal concentration of NaHS should be carefully selected according to plant species and experimental system.