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Original Research ARTICLE

Front. Plant Sci., 08 May 2018 | https://doi.org/10.3389/fpls.2018.00568

Thalli Growth, Propagule Survival, and Integrated Physiological Response to Nitrogen Stress of Ramalina calicaris var. japonica in Shennongjia Mountain (China)

Chuan-Hua Wang1,2*, Ming Wang1,2, Rao-Zhen Jia1,2 and Hua Guo1,2
  • 1Hubei International Scientific and Technological Cooperation Center of Ecological Protection and Management in the Three Gorges Area, China Three Gorges University, Yichang, China
  • 2Engineering Research Center of Eco-environment in the Three Gorges Reservoir Region, Ministry of Education, China Three Gorges University, Yichang, China

In this study, effects of nitrogen (N) availability on growth, survival of Ramalina calicaris var. japonica, and whether it respond nitrogen stress in an integrated physiological way was evaluated. Thalli growth and propagule survival, thalli N and phosphorus (P) content, and activity of phosphomonoesterase (PME) of R. calicaris var. japonica were determined in a field experiment. Its differentiate adsorption in ammonia and nitrate, the activity of glutamine synthetase (GSA) and nitrate reductase (NRA) also were investigated in a series of indoor experiments. The results showed that N deposition significantly decreased the growth and survival of this lichen, and the N sensitivity threshold was suggested at 6.0 kg N⋅ha-1⋅y-1. When the N deposition increased from 8.59 kg N⋅ha-1⋅y-1 to 14.24, 20.49, 32.99 and 57.99 kg N⋅ha-1⋅y-1, the growth rates of lichen thalli decreased by 26.47, 39.01, 52.18 and 60.3%, respectively; Whereas the survival rate of the lichen propagules decreased from 92.8% of control (0.0 kg N⋅ha-1⋅y-1) to 10.7% of 50.0 kg N⋅ha-1⋅y-1, when they were treated with 0.00, 6.25, 12.5, 25.0, and 50.0 kg N⋅ha-1⋅y-1 deposition. Compared with an adequate adsorption of ammonium N, no nitrate adsorption occurred when thalli was submerged in solution lower than 0.4 mM. Our results also suggested that thalli total nitrogen, N:P ratio increased with N availability, and the activity of PME was significantly correlated with thalli total nitrogen. These all indicated that phosphorus limitation occurred when R. calicaris var. japonica treated with higher nitrogen deposition. Compared with slightly effects of NRA, GSA of R. calicaris var. japonica responded nitrogen availability significantly; In addition, GSA and NRA negatively correlated with thalli growth rate and propagule survival significantly. These results indicated that nitrogen stress do decrease growth and survival of R. calicaris var. japonica, and lichen would be impacted by excess nitrogen in a integrated, not a fragmentary way, including nitrogen uptake, assimilation, even nutrient balance of nitrogen and phosphorous.

Introduction

Lichens mainly acquire mineral nutrients, including nitrogen (N) and phosphorus (P), directly from the atmosphere and rainfall via thalli surface, so they have evolved into a class of organisms sensitive to environmental pollution (Pearson and Skye, 1965; Galloway et al., 2004). Since 1840’s, the active N deposition in the global terrestrial ecosystem has increased 3.6 times (Galloway et al., 2004), which has led to a significant reduction in the plant diversity, especially in lichens (Geiser and Neitlich, 2007; Clark and Tilman, 2008).

The Shennongjia region is one of the main habitats for golden snub-nosed monkeys (Rhinopithecus roxellana), an endangered species on the Chinese red list of endangered animal species (Wang, 1998). Some epiphytic lichens are important fallback food for golden snub-nosed monkeys, accounting for approximately 40–60%, and even as high as 90%, of the diets of this monkey (Li, 2001, 2006; Guo et al., 2007). Among the lichens, Usnea luridorufa, Usnea longissima, Ramalina sinensis have been identified as food for golden snub-nosed monkeys (Li, 2006; Guo et al., 2007). A randomized sampling demonstrated absence of significant eutrophication in the area, but provided, along one of the main roads crossing the area, records of species like Xanthomendoza ulophyllodes and Phaeophyscia ciliata, that are characteristic for dust deposition and nutrient rich bark (Munzi et al., 2015). In this region, the wet N deposition in 2015 was 7.99 kg⋅ha-1⋅y-1 (Yang et al., 2018), which greatly exceeded the nitrogen deposition threshold of N-sensitive lichens of 3.2 kg⋅ha-1⋅y-1 (Fenn et al., 2008).

Ramalina calicaris var. japonica, a green algae lichen (Wu, 1987), is a dominant species among the epiphytic lichens in Shennongjia Mountain, China (Yang et al., 2017). It also exhibits quite strong N sensitivity in a previous research (Wang et al., 2015). Therefore, N deposition might have a significant impact on growth and survival of R. calicaris var. japonica in the Shennongjia region. Up to now, besides some preliminary researches on lichen taxonomy in this region, in-depth studies on the growth and survival response of these lichens to increasing N deposition is still scarce.

Lichenologist and ecologist have made many but fragmentary progresses to understand the nature of lichen sensitivity/tolerance to excess nitrogen. It is reported that less nitrogen tolerant lichens can uptake more ammonium nitrogen than nitrophytic lichens (Miller and Brown, 1999; Gaio-Oliveira et al., 2004; Hauck, 2010), and toxicity of ammonium on membrane integrity, photosynthetic performance, chlorophyll chemistry of sensitive lichens also were recognized as factors leading to species specific nitrogen tolerance (Munzi et al., 2009a,b, 2012, 2014). In addition, P-limitation, indicated by an activity elevation of phosphomonoesterase (PME), occurs when nitrogen addition is performed in some sensitive lichens (Hogan et al., 2010a,b). Hauck (2010) further suggests that carbon skeletons supplied by phytobiont are relevant to lichen’s ammonium tolerance, as the ability to provide sufficient carbon skeleton is correlated with ammonium tolerance in vascular plants (Schortemeyer et al., 1997). In summary, present theories to understand lichen nitrogen sensitivity/tolerance were diverse and fragmented, as the experiments are performed on different lichen species. Above all, species specific ability to assimilate ammonium and nitrate nitrogen were ignored at all in lichen nitrogen sensitivity studies, although high activities of glutamine synthetase (GS) and nitrate reductase (NR) have been proved crucial in producing tolerance to high ammonium concentrations in vascular plants (Cruz et al., 2006; Stevens et al., 2011).

We hypothesized that nitrogen stress would decrease growth and survival of physiologically sensitive lichens, and lichens would respond the stress in an integrated way from nitrogen uptake to metabolism. R. calicaris var. Japonica, an indigenous and N-sensitive dominant epiphytic lichen of Shennongjia Mountain, provided a perfect material to clarify whether N deposition will impact lichens growth and survival, and whether lichen will respond nitrogen stress in a integrated way, including a higher ammonium adsorption than nitrate, increased N, P content of thalli and their unbalance between them, elevation of the activity of PME, GS, and NR. Answering to these questions will contribute to understand the mechanisms underlying N sensitivity of lichens, also will be helpful in the management of winter food of golden snub-nosed monkeys in the Shennongjia Region.

Materials and Methods

Study Sites

The sampling site, mainly covered with mixed broadleaf-conifer forest (Tie et al., 2010), locates in a valley of Hongping Town of Shennongjia Region (31°34′N, 110°23′E, 1700 m altitude). The annual average temperature of this region is about 12°C, with an annual precipitation ranging from 1000 to 1800 mm (Tie et al., 2010). Background wet N load of the site is about 7.99 Kg ha-1 y-1, and nitrate and ammonia accounted for 40.75 and 44.08% of the total nitrogen of rainfall, respectively (Yang, et al., 2018).

Impacts of Nitrogen Addition on Thalli Growth, N, P Content, and PME

Nitrogen Treatment

Following methods of Johansson et al. (2011), five 1.2 m × 2.0 m experimental plots were established in a relatively open canopy gap in the study site. Each plot was equipped with a 1.5 m height wooden rack, on which an irrigation tube with 18 small sprinklers was fixed at 1.2 m height. A timer (ZYT02-M, Shanghai Zhuoyi Electronic Co., Ltd., China) precise to second level was used to control the spray schedule and duration of N addition.

In March 2015, healthy R. calicaris var. Japonica thalli with similar size were collected and numbered, and initial air dry weight (m1R) of each individual was measured using the reference sample method of McCune et al. (1996). Among the samples, ten individuals were randomly selected as reference samples, and stored at -18°C to determine the final dry mass of test samples.

To test the effects of N addition on lichen growth, N and P content, five deposition levels were designed to simulate future nitrogen loads, from no pollution to values largely above the suggested critical loads for forest ecosystems (Air Pollution Information System [APIS], 2013). The five plots were randomly assigned to the five N treatments. In each plot, 20 thalli were glued with clear silicone sealant to nylon monofilament loops, then were fixed on the wooden racks and irrigated for 18 s per day, with either natural rain water (nitrogen concentration is ∼0.097 mM, which was equal to a load of 0.5–0.6 Kg N ha-1 y-1), or NH4NO3 solutions 0.41, 0.81, 1.63, and 3.2 mM (which were prepared with deionized water). These solutions and spraying time can simulate 0.6, 6.25, 12.5, 25.0, and 50.0 Kg N ha-1 y-1 N addition precisely. Treatments lasted from April 1 to October 31, 2015. During the irrigation time, the precipitation amount was 1519 mm, and about 226 L water was used on each spraying unit, which was equal to a precipitation of 94.5 mm, and only accounted for 6.45% of total precipitation per year.

Determination Final Biomass of Test Samples

The Reference Method of McCune et al. (1996) was used to determine the final biomass of test samples. Upon finishing the N treatment, the test samples, together with reference samples, were air-dried at room temperature for 48 h, then their air dry weight (m2) were measured with a balance (CPJ303, OHAUS Corporation, United States). For subsequent analysis, test samples were transported to China Three Gorges University and stored in a -18°C refrigerator. The reference samples were oven-dried at 65°C, then dry weight of each individual was determined, after which initial and final water content of reference samples were calculated, then were used to calibrate the initial and final dry mass of the test samples (m1’ and m2’). Growth rate of each individual was calculated as: (m2’-m1’)/m1’ × 100%. In total, 20 replicates (thalli) were performed for each nitrogen treatment.

Determination of Ammonium N, Nitrate N, and Phosphorous Contents of Lichen Thalli

After finishing test 1.2.2, three lichen individuals were collected from one treatment, oven-dried and milled into powder, respectively, then three replicates were conducted for each nitrogen treatment. For each sample, about 500 mg of lichen material was digested with H2O2-H2SO4. Then phosphorus concentration (PC) was determined by phosphorus molybdenum heteropoly acid (PMA)-Malachite green spectrophotometry methods at 650 nm (Yang et al., 2018), nitrate, ammonium, and total N concentration (NC) in the digestion was determined with a San+++ auto analyzer (Skalar, Breda, Netherlands).

Assay of PME Activity

Phosphomonoesterase activity of lichen thalli was determined as the method of Turner et al. (2001). Briefly, in each nitrogen treatment, three lichen individuals were randomly selected from test 1.2.2, a piece of thallus of 2 cm length was cut from each thalli, then was added to 2.9 mL of 0.02 M citric acid–trisodium citrate solution. Then, 0.1 ml para-nitrophenylphosphate (pNPP) was added to the solution to reach a final concentration of 3 mM. Samples were subsequently incubated for 20 min at 15°C in a shaking water-bath in the dark. The reaction was terminated by transferring 2.5 ml of the essay solution into 0.25 ml terminator solution (1.1 M NaOH, 27.5 mM EDTA and 0.55 M K2HPO4). The absorbance was measured at a wavelength of 405 nm using a spectrophotometer (UV-5500PC, Metash instruments Co., Ltd., China). Thalli were then oven dried for 24 h at 65°C and weighed. Enzyme activity was expressed as μmol substrate hydrolysed g-1 dry mass h-1 using p-nitrophenol to calibrate the assay. Three replicates were performed for each nitrogen treatment.

Adsorption of Ammonium and Nitrate

A single factor experiment was designed in this study. The factors were KNO3 and (NH4)2SO4. Considered the total N concentration of precipitation in Shennongjia, 0.02, 0.05, 0.1, 0.2, 0.4, 0.8, 1.6, and 2.0 mM of KNO3 and (NH4)2SO4 solutions were prepared with CaSO4 solution (0.2 mM) to study adsorption of ammonium and nitrate of R. calicaris var. japonica.

Forty lichens were activated in a climatic chamber for 7 days under conditions of 15°C, 40∼60 μmol⋅m-2⋅s-1 and RH 95% (Johansson et al., 2012), then they were randomly divided into eight groups. One branch of each thalli (approximately 50 mg) was rinsed with deionized water, and immersed into a calcium sulfate solution (CaSO4, 0.2 mM) for 24 h to remove the residual N in free space. Upon draining the surface water, the sample was immersed and shaked in a tube with 10 mL of N solution for 30 min (Dahlman et al., 2004). In total, each nitrogen solution had five replicates. Ammonium and nitrate concentration of the post-treated solution were determined as the methods of Yang et al. (2016). Finally, sample branches were oven-dried at 65°C, and their dry masses were measured.

The N adsorption rate (A) was calculated as following: A = (Nt-N0)/m, where Nt is the ammonium or nitrate concentration of the post-N-treated solution, and N0 is the ammonium or nitrate concentration of the pre-treated solution, m was the mass of lichen branche.

Effects of N Deposition on Propagule Survival

Following methods of Armstrong (1990) and Sillett et al. (2000), Salix fargesii chips (5 cm × 8 cm) with bark were prepared to host lichen fragments. To that, epiphytes were removed carefully, then the chips were oven dried 24 h at 120°C to kill the organisms on the surface. Samples of R. calicaris var. japonica were manually crushed, and passed through a 2 mm and 5 mm mesh screen to ensure 2∼5 mm semi-natural size. Sixty lichen fragments were evenly sowed on each chips, then 20 chips were randomly divided into five groups (corresponding to five nitrogen treatments), each with four replicates. Each group was placed in a transparent plastics box and sprayed with artificial rainwater. The rainwater was prepared as in Johansson et al. (2010), which obtained 0.0, 0.05, 0.1, 0.2, and 0.4 mM NH4NO3. Considered the actual nitrogen concentration of our study site is about 0.097 mM (Yang et al., 2018), then above solutions could cover the actual and future nitrogen concentrations. Nitrogen deposition (0.0, 6.0, 12.5, 25.0, and 50.0 Kg N ha-1 y-1) was simulated through control the volume of the sprayed solution. The chips were sprayed every 2 days. All the boxes were placed in a climatic-chamber at 15 ± 2°C, RH 60 ± 5% and photoperiod of 12 h at 60∼80 μmol m-2 s-1 photons PAR. After 6 months, the survival of the lichen fragments was surveyed with microscope, fragments with normal color similar to reference lichens were considered healthy.

Effects of Nitrogen Deposition on GSA and NRA

Assay of GSA

Six groups of lichens were incubated 2 months under a condition, same to the steps described in Section “Adsorption of Ammonium and Nitrate.” We sprayed lichens every 3 days with one of 0.1, 0.2, 0.4, 0.8, 1.6, and 2.0 mM NH4NO3 solution. Glutamine synthetase activity (GSA) was measured as Zhao et al. (2002). In detail, 50 mg air dried lichen was manually grounded with 2 ml 5 mM phosphoric acid buffer (containing 0.5 mM EDTA, 50 mM K2SO4, pH 7.2), then the buffer was centrifuged 20 min (18000 rpm, 4°C). Subsequently, 1.2 ml crude enzyme liquid, 0.6 ml imidazole-HCl buffer (0.25 M), 0.4 ml glutamic sodium (0.30 M),0.4 ml ATP-Na (30 mM), 0.2 ml MgSO4 (0.5 M) were added into a tube. The tube was incubated in a 25°C water bath for 5 min, then 0.2 ml hydroxylamine (0.5 M) was added in. Fifteen minutes later, 0.8 ml ferric trichloride solution was added to terminate the reaction. We centrifuged the reaction solution 15 min (4500 rpm, 4°C), and absorption value (A) of the supernate was measured at 540 nm with spectrophotometer (UV-5500PC, Metash instruments Co., Ltd., China). Relative GSA was presented as A⋅h-1⋅g-1⋅DW, in which A was the absorption value of supernate. Three replicates were performed for each nitrogen treatment.

Assay of NRA

Nitrate reductase activity (NRA) was determined as the methods of Zhao et al. (2002). About 50 mg lichen apex was submerged in to a tube containing 10 ml solution of 0.10 mol⋅L-1 KNO3. Then the tube was vacuumized 30 min, subsequently N2 was supplied into the tubes. Thereafter, tube was incubated in a dark, 25°C chamber for 30 min. Then enzyme reaction was terminated by taking the lichen apex out of the tube. Absorption of reaction solution was measured with spectrophotometer at 540 nm (UV-5500PC, Metash instruments Co., Ltd., China), as well dry mass of the lichen apex was measured. NRA was expressed as mg NO2-⋅h-1⋅g-1⋅DW. Each nitrogen treatment was replicated three times.

Statistics

The effects of nitrogen availability on thalli growth, propagule survival, thalli nitrogen and phosphorous content, activity of GS, NR, and PME were analyzed with one-way ANOVA using the SPSS (IBM Corp. Released 2016. IBM SPSS Statistics Version 24.0). Differences were considered significant when P < 0.05. Comparisons of means were performed using a Tukey’s (HSD) test. Lichen adsorption response to nitrogen availability was plotted with Origin 7.5, and then its Km and Vmax were fitted with Michaelis–Menten model (V = VmaxC/(Km + C)) (Turner et al., 2001). Finally, correlations of above data, in addition with nitrogen availability, were analyzed with SPSS (IBM Corp. Released 2016. IBM SPSS Statistics Version 24.0).

Results

Effects of N Deposition on Thalli Growth and Propagule Survival

The results showed that the growth of R. calicaris var. japonica decreased when N deposition increased. Under N deposition of 8.59∼57.99 kg N ha-1.y-1, the growth rate of R. calicaris var. japonica declined from 52.8% (control, 8.59 kg N ha-1.y-1) to 20.97% (57.99 kg N ha-1.y-1). Accordingly, the extent of decrease under these N depositions relative to the control were 26.47, 39.01, 52.18, and 60.3%, respectively (see Figure 1A). At the same time, the survival of lichen propagules decreased from 92.8% (0.0 kg N ha-1.y-1) to 10.7% (50 kg N ha-1.y-1), indicating that a huge decrease (88.5%) of propagule survival occurred actually (Figure 1B). In general, except the treatments between 6.0 and 12.5 kg N ha-1.y-1, significant effects of other nitrogen depositions on survival were observed, then 6.0 kg N ha-1.y-1 could be deduced as the N-sensitive threshold for this lichen.

FIGURE 1
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FIGURE 1. Effects of nitrogen addition on growth (A, n = 20) and propagule survival (B, n = 4) of Ramalina calicaris var. japonica. (A) code of horizontal axis represented 8.59, 14.24, 20.49, 32.99, and 57.99 kg N ha-1. y-1, respectively; (B) code of horizontal axis represented 0.0, 6.25, 12.5, 25.0, and 50.0 kg N ha-1 y-1, respectively. Vertical bars indicate standard deviation. Different lowercases indicate significant differences using the Tukey test (significance level at p < 0.05).

Effects of N Deposition on N, P Content of Lichen Thalli

The results showed that N addition had significant effects on ammonium N (NH4+-N), total N (TN), total P (TP) and the N:P ratio (p < 0.05), but no effects on the nitrate content (p = 0.34) (see Table 1). In particular, except treatment of 14.24 kg N-1 ha-1 y-1, the NH4+-N, nitrate, TN, and TP of lichen all increased along the 8.59∼57.99 kg N-1 ha-1 y-1 treatments. Meanwhile, the N:P ratio always were greater than 10 (varied between 12.27 and 26.96 under the five nitrogen treatments), indicating that the lichen was in a constant state of N-induced P deficiency (see Table 1).

TABLE 1
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TABLE 1. ANOVA analysis of nitrogen addition on thalli nitrogen and phosphorous accumulation of Ramalina calicaris var. japonica (Mean ± SD, n = 3).

Response of PME to Nitrogen Deposition

An elevation of PME of R. calicaris var. japonica thalli occurred when they were treated with increasing nitrogen availability. In detail, when lichens were treated with the 14.24 kg N a-1 ha y-1, the PME was 35.65 μmol h-1 g-1 (Figure 2). Then, PME increased to 55.62 μmol h-1 g-1 when treated with the 57.99 Kg N ha-1 y-1 N solution.

FIGURE 2
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FIGURE 2. Response of phosphomonoesterase (PME) of R. calicaris var. japonica to nitrogen deposition (Mean ± SD, n = 3).

Adsorption of Ammonium N and Nitrate N

The results showed that the capacity of R. calicaris var. japonica to adsorpt nitrate N was much lower than that of ammonium N (see Figure 3). The NO3--N adsorption rate was negative at the concentration of 0.1–0.4 mM, suggesting that there are no nitrate N adsorption occurred under the present nitrogen environment of precipitation in Shennongjia Mountain. The adsorption of nitrate N increased as its concentration increased, but it cannot be fitted by the model of Michaelis–Menten equation. When the concentration of the solution was greater than 0.4 mM, the NO3--N adsorption rate changed from negative to positive, finally reached a maximum value of approximately 0.1 mg.g-1. In contrast, the adsorption of ammonium N by R. calicaris var. japonica fitted the Michaelis–Menten equation well (R2 = 0.9836, p < 0.01). The turning point occurred at an ammonium concentration of 0.2 mM, where the maximum adsorption rate (Vmax) was 0.436 mg.g-1. So its Vmax was four times of that of nitrate N. In addition, the Michaelis–Menten constant (Km) of ammonium was 0.082 mM, which indicated that R. calicaris var. japonica could utilize ammonium N at a very low concentration.

FIGURE 3
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FIGURE 3. Response of nitrate (A) and ammonium (B) uptake of R. calicaris var. japonica to nitrogen availability (Mean ± SD, n = 5).

Response of GSA and NRA to Nitrogen Deposition

Our results suggested that GSA of R. calicaris var. Japonica was significantly impacted by nitrogen deposition. In general, response of GSA to increasing nitrogen dose showed an initial increase, then decrease curve (See Figure 4A), it demonstrated the highest activity (35.85 A h-1 g-1 DW) at 0.8 mM, which was 2.46 times of the controls. GSA decreased when nitrogen solution were over 0.8 mM, suggesting that lichen was damaged under such nitrogen deposition strength. In contrast, our results proved that NRA was not impacted by increased nitrogen deposition (Figure 4B).

FIGURE 4
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FIGURE 4. (A) Response of glutamine synthetase activity (GSA) of R. calicaris var. japonica to nitrogen addition (Mean ± SD, n = 3). Code of horizontal axis represented 0.1, 0.2, 0.4, 0.8, 1.6, and 2.0 mM NH4NO3 solution, respectively. Vertical bars indicate standard deviation. Different lowercases indicate significant differences using the Tukey test (significance level at p < 0.05). (B) Response of nitrate reductase activity (NRA) of R. calicaris var. japonica to nitrogen addition (Mean ± SD, n = 3). Code of horizontal axis represented 0.1, 0.2, 0.4, 0.8, 1.6, and 2.0 mM NH4NO3 solution, respectively. Vertical bars indicate standard deviation. Different lowercases indicate significant differences using the Tukey test (significance level at p < 0.05).

Correlations

Table 2 showed the significant correlation coefficients (Pearson) among lichen variables. Lichen growth had strong correlations with the N provided, GSA, and NRA. Survival of propagules had a strong correlation with the N provided, the total nitrogen of thalli, the activity of PME and GSA. Activity of PME strongly correlated with the ammonium content, the total nitrogen content, GSA and NRA of thalli. In addition, GSA correlated with the nitrogen provided and NRA. Except above correlations, NRA, N:P ratio, nitrate content of thalli also strongly correlated with N provided.

TABLE 2
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TABLE 2. Correlations (Pearson) of R calicaris var. japonica.

Discussion

The results showed that the growth and survival rates of R. calicaris var. japonica all decreased as nitrogen availability increased. Unlike lichens as already observed on other Usnea species (Carreras et al., 1998; Munzi et al., 2013), we didn’t find any fertilization effects on both survival and growth of R. calicaris var. japonica. The lichen growth rate under the 57.99 kg N ha-1.y-1 treatment was only 39.72% of that under the 8.59 kg N ha-1.y-1P treatment (taking the background nitrogen load into accounted), and this difference was significant (p < 0.05). The propagule survival rate was 76.35% under the 6.0 kg N ha-1.y-1 treatment, which was significantly lower than the 92.84% survival rate under the 0.0 kg N ha-1.y-1 (control). We suggested that this toxic effect was reasonable, and similar effect on non-vasculated epiphytes of South west part of China had been reported by Song et al. (2012). This effect can be attributed to a higher background of 16.7 kg ha-1.y-1 N load of China forest, which is about four times of the safe threshold of boreal forest system.

According to the survival response, we suggested that the N deposition threshold of R. calicaris var. japonica was 6.0 kg N ha-1.y-1. This was consistent with the results of thalli growth, because even the least nitrogen addition also led to a growth decrease when nitrogen load higher than control (8.59 kg N ha-1.y-1), which suggested that its threshold based on growth was lower than 8.59 kg N ha-1.y-1. Furthermore, in the ecology of high plants, seedlings usually are vulnerable than mature individual, then it was reasonable to infer 6.0 kg N ha-1y-1 as the threshold for R. calicaris var. japonica. In fact, to date, there are no reports on the use of lichen thalli growth and propagule mortality to determine N deposition threshold. We creatively introduced “survival” from population ecology of high plants into lichens, through which we were able to observe the difference among nitrogen treatments conveniently. Compared with our research, previous researches concerning lichen nitrogen sensitivity mostly exist on their physiological response (Munzi et al., 2009a,b, 2012), which cannot evaluate lichens’ N deposition threshold quantitively at all; in addition, N deposition thresholds of many ecosystems were derived from empirical methods and model simulation (Geiser and Neitlich, 2007; Fenn et al., 2008; Geiser et al., 2010), which are quite labor and time consuming. Our results showed that not only propagule survival rate of R. calicaris var. japonica was sensitive to nitrogen stress, but also demonstrated convenience in determination the concentration and deposition of N load, lichen biomass and survival, so our method might be reliable and applicable to future studies.

Our results indicated that R. calicaris var. japonica responded nitrogen stress in an integrated way. Previous research suggested that photosynthesis system (indicated by Fv/Fm, which is the maximum quantum efficiency of photosystem II, and OD435/OD415 of chlorophyll) and cell membrane of this lichen were damaged by nitrogen stress (Wang et al., 2015). Our results indicated that it had a strong capacity to adsorb ammonium N, which is consistent with many studies that lichens adsorb ammonium N more readily than nitrate N (Miller and Brown, 1999; Dahlman et al., 2004; Gaio-Oliveira et al., 2004; Toze et al., 2005). The results showed that R. calicaris var. japonica could adsorb ammonium N in NH4+ solution at a relatively lower concentration (0.04 mM), and the Vmax was 0.43 mg.g-1. In contrast, NO3-N adsorption could not occur in R. calicaris var. japonica when the concentration of the NO3- solution was lower than 0.4 mM and the corresponding Vmax was only approximately 0.1 mg.g-1. Ammonium N adsorption in lichens is a passive process of ion exchange adsorption (Dahlman et al., 2004), then ammonium ions in solution can be rapidly bound to the extracellular space of the lichen thalli (Miller and Brown, 1999), so lichen species with more ion exchange sites would have stronger ammonium N adsorption capacity and thus be more susceptible to ammonium, which is thought to be one of the important mechanisms underlying N sensitivity in lichens (Gaio-Oliveira et al., 2005). In contrast, the adsorption of nitrate is an active process concerning oxygen and energy consumption (Crittenden, 1996), since nitrate, upon entering into cells, must be reduced to ammonium N before it can be utilized. Thus the cost of nitrate N utilization is rather higher than ammonium. Therefore, lichens tend to use ammonium N can be considered a consequence of long-term evolutionary adaptation. It should be noted that adsorption of both forms of N can occur in some lichen species (Johansson et al., 2010), so the ammonium N and nitrate N adsorption characteristics of lichens may be species specific.

The results showed that excessive application of N significantly damaged the balance between nitrogen and phosphorous of lichen thalli. We found an accumulation of NH4+-N, TN, TP but not that of NO3--N. Specifically, NH4+-N and TN exhibited an overall increasing trend as N deposition increased. When the intensity of N deposition reached 57.99 kg N ha-1.y-1, the growth rate of the lichen was inhibited, and the content of ammonium N decreased. However, there were no significant differences in the nitrate N content among the treatments. Studies have shown that as N deposition increases, the N-sensitive lichen Evernia prunastri accumulates more ammonium N than the N-tolerant lichen Xanthoria parietina, while X. parietina accumulates more nitrate N than E. prunastri (Gaio-Oliveira et al., 2005). Thus, our results are consistent with that of N-sensitive lichens. The results also showed that when N deposition was lower than 32.99 kg N ha-1.y-1, the lichen P content exhibited an increasing trend, but when N deposition was greater than 50.0 kg N ha-1.y-1, the P content significantly decreased, which also resulted in a sharply increasing of N:P(>10.0). Our results agreed with the response of Cladonia portentosa, which showed that N deposition led to an increase in the N content and the N:P ratio (Hogan et al., 2010b). Furthermore, we found that activity of PME was elevated with an increasing nitrogen supply, which meant that P limitation occurred as it was well known that elevation of PME is a response of P deficiency. In addition, external P addition could double the growth of Lobaria pulmonaria, which was a species of cyanolichens could fix atmospheric nitrogen (McCune and Caldwell, 2009). Therefore, it was of high possibility that the R. calicaris var. japonica would experience a P deficiency under present nitrogen conditions.

Our results suggested that GSA elevated significantly with increased nitrogen availability, then decreased when nitrogen stress reached 1.6 mM. This GSA elevation was consistent to the results from high plants, which proved that external nitrogen supply can stimulate the expression of GS gene (Chen et al., 2010). The decrease of GSA implied a damage occurred when lichen were treated with higher nitrogen solution. In contrast, NRA was faintly influenced by external nitrogen supply, though it also could be stimulated by external nitrogen (Wang et al., 2003). The differentiated appearance of GSA and NRA could be owing to the difference in thalli adsorption and accumulation between ammonium and nitrate. This also demonstrated that lichen respond nitrogen stress in an integrated way.

Conclusion

Nitrogen stress did impact growth and survival of R. calicaris var. Japonica in forest of Shennongjia Mountain, and its sensitive threshold indicated by the propagule survival rate was 6.0 kg N ha-1⋅y-1. R. calicaris var. japonica demonstrated an integrated physiological response to nitrogen stress, including selective adsorption between nitrate N and ammonium N, increased thalli N and P content, and P limitation, in addition with an activity elevation of PME and GSA.

Author Contributions

C-HW designed the whole experiment, determined the study sites, analyzed the data, and wrote the manuscript. MW conducted the field experiment and participated in measuring the N and P content of lichen thalli. R-ZJ conducted the experiment of propagule survival. HG finished the assay of activity of PME, GS, and NR, and conducted the experiments of adsorption of ammonium and nitrate.

Funding

This research was supported by the National Natural Science Foundation of China (NSFC31370536).

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.

Acknowledgments

We would like to thank Yang Lin for his work in lichen N and P determination. We would also like to thank Dr. Tianhua He for revising the manuscript.

References

Air Pollution Information System [APIS] (2013). Indicative values within nutrient nitrogen critical load ranges for use in air pollution impact assessments. Available at: http://www.apis.ac.uk/indicative-critical-load-values

Armstrong, R. A. (1990). Dispersal, establishment and survival of soredia and fragments of the lichen Hypogymnia physodes (L.) Nyl. New Phytol. 114, 239–245. doi: 10.1111/j.1469-8137.1990.tb00396.x

CrossRef Full Text | Google Scholar

Carreras, H. A., Gudiño, G. L., and Pignata, M. L. (1998). Comparative biomonitoring of atmospheric quality in five zones of Córdoba city (Argentina) employing the transplanted lichen Usnea sp. Environ. Pollut. 103, 317–325. doi: 10.1016/S0269-7491(98)00116-X

CrossRef Full Text | Google Scholar

Chen, S. Y., Li, G. K., Wang, Y., He, A. R., Chen, A., and Yu, X. L. (2010). The research progress of glutamine synthetase. Chin. Agric. Sci. Bull. 26, 45–49.

Google Scholar

Clark, C. M., and Tilman, D. (2008). Loss of plant species after chronic low-level nitrogen deposition to prairie grasslands. Nature 451, 712–715. doi: 10.1038/nature06503

PubMed Abstract | CrossRef Full Text | Google Scholar

Crittenden, P. D. (1996). The effect of oxygen deprivation on inorganic nitrogen uptake in an antarctic macrolichen. Lichenologist 28, 347–354. doi: 10.1006/lich.1996.0032

CrossRef Full Text | Google Scholar

Cruz, C., Bio, A. F., Domínguez-Valdivia, M. D., Aparicio-Tejo, P. M., Lamsfus, C., and Martins-Loução, M. A. (2006). How does glutamine synthetase activity determine plant tolerance to ammonium? Planta 223, 1068–1080.

PubMed Abstract | Google Scholar

Dahlman, L., Persson, J., Palmqvist, K., and Näsholm, T. (2004). Organic and inorganic nitrogen uptake in lichens. Planta 219, 459–467. doi: 10.1007/s00425-004-1247-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Fenn, M. E., Jovan, S., Yuan, F., Geiser, L., Meixner, T., and Gimeno, B. S. (2008). Empirical and simulated critical loads for nitrogen deposition in California mixed conifer forests. Environ. Pollut. 155, 492–511. doi: 10.1016/j.envpol.2008.03.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Gaio-Oliveira, G., Dahlman, L., Palmqvist, K., and Máguas, C. (2004). Ammonium uptake in the nitrophytic lichen Xanthoria parietina and its effects on vitality and balance between symbionts. Lichenologist 36, 75–86. doi: 10.1017/S0024282904014124

CrossRef Full Text | Google Scholar

Gaio-Oliveira, G., Dahlman, L., Palmqvist, K., Martins-Loução, M. A., and Máguas, C. (2005). Nitrogen uptake in relation to excess supply and its effects on the lichens Evernia prunastri (L.) Ach and Xanthoria parietina (L.) Th. Fr. Planta 220, 794–803. doi: 10.1007/s00425-004-1396-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Galloway, J. N., Dentener, F. J., Capon, E. D. G., Boyer, E. W., Howarth, R. W., Seitzinger, S. P., et al. (2004). Nitrogen cycles: past, present, and future. Biogeochemistry 70, 153–226. doi: 10.1007/s10533-004-0370-0

CrossRef Full Text | Google Scholar

Geiser, L. H., Jovan, S. E., Glavich, D. A., and Porter, M. K. (2010). Lichen-based critical loads for atmospheric nitrogen deposition in Western Oregon and Washington Forests, USA. Environ. Pollut. 158, 2412–2421. doi: 10.1016/j.envpol.2010.04.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Geiser, L. H., and Neitlich, P. N. (2007). Air pollution and climate gradients in western Oregon and Washington indicated by epiphytic macrolichens. Environ. Pollut. 145, 203–218. doi: 10.1016/j.envpol.2006.03.024

PubMed Abstract | CrossRef Full Text | Google Scholar

Guo, S. T., Li, B. G., and Watanabe, K. (2007). Diet and activity budget of Rhinopithecus roxellana in the Qinling Mountains, China. Primates 48, 268–276. doi: 10.1007/s10329-007-0048-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Hauck, M. (2010). Ammonium and nitrate tolerance in lichens. Environ. Pollut. 158, 1127–1133. doi: 10.1016/j.envpol.2009.12.036

PubMed Abstract | CrossRef Full Text | Google Scholar

Hogan, E. J., Minnullina, G., Sheppard, L. J., Leith, I. D., and Crittenden, P. D. (2010a). Response of phosphomonoesterase activity in the lichen Cladonia portentosa to nitrogen and phosphorus enrichment in a field manipulation experiment. New Phytol. 186, 926–933. doi: 10.1111/j.1469-8137.2010.03221.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Hogan, E. J., Minnullina, G., Smith, R. I., and Crittenden, P. D. (2010b). Effects of nitrogen enrichment on phosphatase activity and nitrogen: phosphorus relationships in Cladonia portentosa. New Phytol. 186, 911–925. doi: 10.1111/j.1469-8137.2010.03222.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Johansson, O., Nordin, A., Olofsson, J., and Palmqvist, K. (2010). Responses of epiphytic lichens to an experimental whole-tree nitrogen-deposition gradient. New Phytol. 188, 1075–1084. doi: 10.1111/j.1469-8137.2010.03426.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Johansson, O., Olofsson, J., Giesler, R., and Palmqvist, K. (2011). Lichen responses to nitrogen and phosphorus additions can be explained by the different symbiont responses. New Phytol. 191, 795–805. doi: 10.1111/j.1469-8137.2011.03739.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Johansson, O., Palmqvist, K., and Olofsson, J. (2012). Nitrogen deposition drives lichen community changes through differential species responses. Glob. Change Biol. 18, 2626–2635. doi: 10.1111/j.1365-2486.2012.02723.x

CrossRef Full Text | Google Scholar

Li, Y. (2001). The seasonal diet of the sichuan snub-nosed monkey (Pygathrix roxellana) in Shennongjia Nature Reserve, China. Folia Primatol. 72, 40–43. doi: 10.1159/000049919

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, Y. (2006). Seasonal variation of diet and food availability in a group of sichuan snub-nosed monkeys in Shennongjia Nature Reserve, China. Am. J. Primatol. 68, 217–233. doi: 10.1002/ajp.20220

PubMed Abstract | CrossRef Full Text | Google Scholar

McCune, B., and Caldwell, B. A. (2009). A single phosphorus treatment doubles growth of cyanobacterial lichen transplants. Ecology 90, 567–570. doi: 10.1890/08-0344.1

PubMed Abstract | CrossRef Full Text | Google Scholar

McCune, B., Derr, C. C., Muir, P. S., Shirazi, A., Silletts, C., and Dalyw, J. (1996). Lichen pendants for transplant and growth experiments. Lichenologist 28, 161–169. doi: 10.1006/lich.1996.0014

CrossRef Full Text | Google Scholar

Miller, J. E., and Brown, D. H. (1999). Studies of ammonia uptake and loss by lichens. Lichenologist 31, 85–93.

Google Scholar

Munzi, S., Branquinho, C., Cruz, C., and Loppi, S. (2013). Nitrogen tolerance in the lichen Xanthoria parietina: the sensitive side of a resistant species. Funct. Plant Biol. 40, 237–243. doi: 10.1071/FP12127

CrossRef Full Text | Google Scholar

Munzi, S., Cruz, C., Branquinho, C., Pinho, P., Leith, I. D., and Sheppard, L. J. (2014). Can ammonia tolerance amongst lichen functional groups be explained by physiological responses. Environ. Pollut. 187, 206–209. doi: 10.1016/j.envpol.2014.01.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Munzi, S., Paoli, L., Fiorini, E., and Loppi, S. (2012). Physiological response of the epiphytic lichen Evernia prunastri (L.) Ach. to ecologically relevant nitrogen concentrations. Environ. Pollut. 171, 25–29. doi: 10.1016/j.envpol.2012.07.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Munzi, S., Pirintsos, S. A., and Loppi, S. (2009a). Chlorophyll degradation and inhibition of polyamine biosynthesis in the lichen Xanthoria parietina under nitrogen stress. Ecotoxicol. Environ. Saf. 72, 281–285. doi: 10.1016/j.ecoenv.2008.04.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Munzi, S., Pisani, T., and Loppi, S. (2009b). The integrity of lichen cell membrane as a suitable parameter for monitoring biological effects of acute nitrogen pollution. Ecotoxicol. Environ. Saf. 72, 2009–2012. doi: 10.1016/j.ecoenv.2009.05.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Munzi, S., Thüs, H., Wolseley, P., and Wang, C. (2015). Monitoring environmental changes in the habitat of Rhinopithecus roxellana in Shennongjia Forestry District (China). Not. Della Soc. Lichenol. Ital. 28:47.

Pearson, L., and Skye, E. (1965). Air pollution affects pattern of photosynthesis in parmelia sulcata, a corticolous lichen. Science 148, 1600–1602. doi: 10.1126/science.148.3677.1600

PubMed Abstract | CrossRef Full Text | Google Scholar

Schortemeyer, M., Stamp, P., and Feil, B. (1997). Ammonium tolerance and carbohydrate status in maize cultivars. Ann. Bot. 79, 25–30. doi: 10.1006/anbo.1996.0298

CrossRef Full Text | Google Scholar

Sillett, S. C., McCune, B., Peck, J. E., Rambo, T. R., and Ruchty, A. (2000). Dispersal limitations of epiphytic lichens result in species dependent on old-growth forests. Ecol. Appl. 10, 789–799. doi: 10.1890/1051-0761(2000)010[0789:DLOELR]2.0.CO;2

CrossRef Full Text | Google Scholar

Song, L., Liu, W., Ma, W., and Qi, J. (2012). Response of epiphytic bryophytes to simulated N deposition in a subtropical montane cloud forest in southwestern China. Oecologia 170, 847–856. doi: 10.1007/s00442-012-2341-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Stevens, C. J., Smart, S. M., Henrys, P. A., Maskell, L. C., Crowe, A., Simkin, J., et al. (2011). Terricolous lichens as indicators of nitrogen deposition: evidence from national records. Ecol. Indic. 20, 196–202. doi: 10.1016/j.ecolind.2012.02.027

CrossRef Full Text | Google Scholar

Tie, J., Zhang, J., Peng, L. P., Wang, D. X., Hu, D. F., and Zhang, Z. X. (2010). Feeding habits of Rhinopithecus roxellana in Shennongjia Nature Reserve of china in winter and spring. Chin. J. Ecol. 29, 62–68.

Google Scholar

Toze, W. C., Hackell, D. D., and Silvester, W. B. (2005). Extreme isotopic depletion of nitrogen in New Zealand lithophytes and epiphytes; the result of diffusive uptake of atmospheric ammonia? Oecologia 144, 628–635.

PubMed Abstract | Google Scholar

Turner, B. L., Baxter, R., Ellwood, N. T. W., and Whitton, B. A. (2001). Characterization of the phosphatase activities of mosses in relation to their environment. Plant Cell Environ. 24, 1165–1176. doi: 10.1046/j.1365-3040.2001.00767.x

CrossRef Full Text | Google Scholar

Wang, C.-h., Yang, L., Yuan, Q.-l., Silvana, M., and Liu, M.-j. (2015). Nitrogen sensitivity of four epiphyte lichens from habitats of Rhinopithecus roxellana in Shennongjia Nature Reserve. Chin. J. Ecol. 34, 626–633.

Wang, L. Q., Wang, Y., Dong, Y., and Wang, W. B. (2003). Induced activity of nitrate reductase by nitrate and cloning of nitrate reductase gene. Chin. J. Biotechnol. 5, 632–635.

Google Scholar

Wang, S. (1998). Chinese Red List of Endangered Animal Species. Beijing: Science Press.

Wu, J. L. (1987). Iconography of Chinese Lichens. Beijing: China Outlook Press, 165–168.

Yang, L., Guo, H., Deng, J. J., Xu, T., and Wang, C. H. (2017). Diversity variation of epiphytic lichens between native tree species and introduced tree species in Shennongjia secondary forest. Sci. Silvae Sin. 53, 149–158.

Yang, L., Wang, C. H., and Li, T. (2016). A method for the determination of nitrogen chemical characteristics in trunk stem flow based on ultraviolet spectrophotometry. Sci. Silvae Sin. 52, 133–140.

Yang, L., Wang, M., and Wang, C.-h., (2018). Nitrogen and phosphorous characteristics of canopy water of eight dominant tree species in secondary forests of Shennongjia Mountain. Chinese J. Ecol. 37, 1018–1025.

Zhao, S. J., Shi, G. A., and Dong, X. C. (eds) (2002). Techniques of Plant Physiological Experiment. Beijing: China Agricultural Science and Technology Press, 96.

Google Scholar

Keywords: nitrogen deposition, nitrogen metabolism, epiphytic lichens, growth and survival, Shennongjia nature reserve

Citation: Wang C-H, Wang M, Jia R-Z and Guo H (2018) Thalli Growth, Propagule Survival, and Integrated Physiological Response to Nitrogen Stress of Ramalina calicaris var. japonica in Shennongjia Mountain (China). Front. Plant Sci. 9:568. doi: 10.3389/fpls.2018.00568

Received: 14 December 2017; Accepted: 11 April 2018;
Published: 08 May 2018.

Edited by:

Erik T. Nilsen, Virginia Tech, United States

Reviewed by:

Giacomo Cocetta, Università degli Studi di Milano, Italy
Ya-jun Gao, Northwest A&F University, China
Kansri-Boonpragob, Ramkhamhaeng University, Thailand

Copyright © 2018 Wang, Wang, Jia and Guo. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Chuan-Hua Wang, wang740301@ctgu.edu.cn