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Stable carbon isotopes of woods during carbonization and their correlation with climatic factors

  • Fan Luo,

    Roles Conceptualization, Formal analysis, Investigation, Methodology, Writing – original draft, Writing – review & editing

    Affiliation School of Earth Science and Resources, Chang’an University, Xi’an, Shaanxi, China

  • Nan Sun ,

    Roles Conceptualization, Funding acquisition, Methodology, Writing – review & editing

    sunnan@chd.edu.cn

    Affiliations School of Earth Science and Resources, Chang’an University, Xi’an, Shaanxi, China, Shaanxi Key Laboratory of Early Life and Environments, Northwest University, Xi’an, Shaanxi, China

  • Xiabo Li,

    Roles Formal analysis

    Affiliation School of Earth Science and Resources, Chang’an University, Xi’an, Shaanxi, China

  • Junfeng Guo,

    Roles Methodology

    Affiliation School of Earth Science and Resources, Chang’an University, Xi’an, Shaanxi, China

  • Liang Xiao,

    Roles Methodology

    Affiliation School of Earth Science and Resources, Chang’an University, Xi’an, Shaanxi, China

  • Peng Lei

    Roles Methodology

    Affiliation Shaanxi Branch of China National Geological Exploration Center of Building Materials Industry, Xi’an, Shaanxi, China

Abstract

To explore the applicability of the carbon isotope composition (δ13C) of fossil charcoal for the quantitative reconstruction of paleoclimates, we selected five points in Shaanxi province, from north to south, to collect modern Pinus species and Quercus species to sample covering areas with obvious climatic differences. In order to reveal the relationships between δ13C of charcoal and climate variables on the basis of carbonization experiments, we evaluated the fractionation mechanism of δ13C of charcoal, and compared the differences between δ13C of charcoal in wildfire experiments and indoor experiments regarding genera and species. The results showed significant differences in δ13C between genera but no significant differences among species. Additionally, the δ13C of charcoal was significantly negatively correlated with precipitation and positively correlated with evaporation, which could be determined from δ13C values in the study area to reconstruct ancient precipitation and evaporation in the future.

1. Introduction

Climate has attracted wide attention from the international community and academic circles as an important factor affecting the human living environment [13]. The period 2010–2019 is the hottest decade since modern meteorological observations were recorded [4]. Global warming has become an indisputable fact, and the warming effect has become a hot topic of interest in the international community [5]. Understanding the laws governing climate change and its warming effect is a key problem to be solved. The high–resolution quantitative reconstruction of paleoclimate plays an important role in understanding the changes in climate systems.

In recent years, the quantitative study of plant indicators has produced many results, such as the hydrological and climatic trends of lakes in the southwestern part of the Loop Basin since 40 ka, which were quantitatively reconstructed by several organic matter geochemical indicators [6]. By establishing the magnetization rate of loess-paleosoil as a function of mean annual rainfall, we recovered the paleosoil rainfall during the warm interglacial period of the Loess Plateau [7]. By establishing the transfer function of diatom-climate factors, we provided a basis for paleoclimate reconstruction at different scales in southwestern China [8]. By the numerical conversion function of lake mesocosms and temperature, we quantitatively reconstructed the Late Pleistocene temperature peaks in central Italy by the numerical conversion function between lake mesocosms and temperature [9]. Using carbonate sediments in lakes, we quantitatively reconstructed the early to mid-Holocene hydrological climate change in eastern Washington [10], and the Late Holocene rainfall at Karwar, west coast of India, was quantitatively reconstructed by a conversion function of the sporulation diversity to climate factors [11]. Based on a phytolith-climate factor conversion function, the annual average temperature, rainfall, and relative humidity in the peat section of an elm tree in Northeast China was inferred for the past three thousand years [12]. Temperature and rainfall variations between 6200 yr. cal BP-5600 yr. cal BP in the Guanzhong Basin of the southern Loess Plateau were quantitatively reconstructed by charcoal [13,14]. However, in the past, paleoclimate reconstruction using plant indicators mainly used the coexistence approach or the transformation function method. The accuracy of the former depends on the number of sample species; the more species considered, the higher the accuracy [15]. If the number of species obtained at the sampling site is small, the error of the obtained results is large. The use of the latter is based on the premise that plant indicators are linearly related to climate, and the number of species is required to be sufficiently large, with limited in its application [16]. Therefore, more accurate and better reconstruction methods are needed.

In response, an isotopic analysis method has been proposed [1719], and the application of this method to pollen [2022], phytoliths [2325], and seeds [26] have revealed a new opportunity for high-precision quantitative reconstruction of paleoclimates. Tree annual rings with good temporal continuity and high accuracy have long been important indicators for paleoclimate studies, and recent studies on tree wheel isotopes have greatly improved the accuracy of paleoclimate reconstruction [2734]. The analysis of charcoal, as plant fossils, is an important indicator for paleoclimate reconstruction due to its easy accessibility and high identification accuracy [19,30,3537], especially in areas where sporulation is poorly preserved. Charcoal remains have become an important complement to sporulation studies, and thus, the paleoclimatic significance of charcoal isotopes has become a hot topic of interest for scholars.

Recent studies have shown a significant correlation between charcoal stable carbon isotopes and climate factors [38,39]. Accordingly, the results of studying carbon isotopes in charcoal at Neanderthal sites from the Paleolithic Age showed that the climate in the study area changed periodically from humid to arid [37]. The results of charcoal isotope studies at the Sibudu Cave site indicate that the study area underwent a warm-wet to cold-dry to warm-wet variation between 70 ka and 48 ka [35]. The above-mentioned studies qualitatively reconstructed the paleoclimate through charcoal stable isotopes with low precision; therefore, some scholars reconstructed the paleoclimate quantitatively by establishing isotope-climate factor relationship functions. For example, the analysis of charcoal carbon isotopes in the archaeological sites of the Segre and Cinca Valleys concluded that the climate of the Iberian Peninsula from 2000 B.C. to A.D. For example, the driest period in the Iberian Peninsula from 2000 B.C.E. to A.D. from 900 to 300 B.C.E. [19], and charcoal carbon isotope analysis of the archaeological site of Valencia Province showed that the climate changed throughout the Holocene in the study area, and the precipitation in the spring and summer of B.C.E. was always higher than the present [40]. The above findings provide new ideas for the quantitative reconstruction of paleoclimate, but the following questions remain to be explored:

  1. The climate-charcoal δ13C model in the previous study was based on the carbonization of the present species in a muffle furnace, while the charcoal at the site was formed by wildfire.
  2. The climate-charcoal δ13C models in previous studies were based on the species level, but since charcoal is often identified only at the genus level and a few species can be identified at the species level, is it possible to model δ13C at the genus level?
  3. Previous work has mainly focused on Europe, America and Africa, and the data from the above research cannot be directly applied to other regions due to differences in environment and species distribution in different regions.

To solve the above problems, improve the application of stable carbon isotopes in quantitative paleoclimate reconstruction, and obtain more accurate paleoclimate data, we selected areas sensitive to climate change and rich in charcoal remains for our research work. By collecting modern wood, conducting wildfire and laboratory carbonization experiments to compare their differences, determining the mechanism of stable carbon isotope fractionation in wood, comparing the variability of stable carbon isotope fractionation between genera and species, and exploring the correlation between charcoal stable carbon isotopes and climatic factors, we applied the method to archeological sites and obtained accurate paleoclimatic information in the study area.

2. Study area

Shaanxi Province, which has a continental monsoon climate overall, is composed of three geomorphologic units located on the northern Loess Plateau, in the central Guanzhong Basin and in the southern Shannan Mountains, corresponding to the middle temperate, warm temperate and subtropical climatic zones, respectively. The average annual rainfall and temperature gradually increase from north to south. The average annual temperature of northern Shaanxi is 7–12°C, where the average annual rainfall is 472 mm; the corresponding values for Guanzhong are 12–14°C and 504 mm, and those for southern Shaanxi are approximately 13–15°C and 1276 mm, respectively (http://data.cma.cn/). Rainfall is mainly concentrated in summer and autumn.

3. Materials and methods

3.1 Sampling.

Through the statistical analysis of the types of charcoal species at the existing archeological sites, it was found that Pinus sp. and Quercus sp. are the two most common wood types at these sites [4143]. Pinus sp. is distributed from the Northern Hemisphere in the Arctic through North Africa, Central America and South Asia to south of the equator. There are 22 Pinus species in China. Quercus sp. is distributed in the northern temperate zone and tropical mountains, and there are approximately 110 species in China, distributed in both northern and southern provinces. There Pinus species and five Quercus species were examined in this study, which is useful for investigating the differences in stable isotopes among species.

In this study, two plant samples of Pinus sp. and Quercus sp. were collected in five regions (Fig 1) of Zhidan County, Fengyukou, Jiwozi, Zhenba County and Caobazi (Table 1). A total of 12 trees were sampled, and uniform samples were selected from small tree branches with a diameter of 5 cm.

3.2 Experimental carbonization

After the collected samples were dried naturally, they were cut into cylinders of 1 cm. Samples were cut from each collected branch and divided into five groups. Each group was composed of two samples. One of them was used as a control group, in which no carbonization treatment was carried out, and the remaining four pieces were wrapped with aluminum foil. Three of these four pieces were used in indoor experiments, and the last was used in a wildfire experiment.

The three samples wrapped in aluminum foil were placed in a muffle furnace and carbonized at temperatures of 300°C, 400°C and 500°C for 30 min; this combustion was allowed to continue for 240 min [46,47].

The last sample wrapped in aluminum foil was placed next to a fire ignited in an open space so that it would be completely carbonized.

3.3 Stable isotope determination

All samples were ground into powder with a mortar to stabilize the determination of carbon isotopes. In this experiment, the classic closed bottle method of organic carbon isotope analysis was adopted. An appropriate amount of the sample was mixed with copper oxide, platinum wire and copper wire and placed in a quartz bottle. The bottle was first subjected to vacuum pumping with a vacuum line. Thereafter, the bottle was removed and placed in a muffle furnace, where oxidation was conducted at 850°C for 2.5 hours.

The CO2 gas was collected and purified with a liquid nitrogen cold trap and then sent to a mass spectrometer for carbon isotope analysis. The instrument used in the experiment was a MAT251 stable isotope mass spectrometer from the Institute of Earth Environment, Chinese Academy of Sciences. The analytical accuracy corresponded to the national standard furnace black (GBW04407) carbon isotope analysis accuracy, which was better than ±0.1‰.

3.4 Analysis methods

In this study, statistical analysis of the data was performed using Origin and SPSS software. Since the distribution type of the samples was unknown, the widely applied independent sample nonparametric test was used to compare the similarities and differences of charcoal δ13C between genera and species and the similarities and differences of fractionation results of different carbonization methods; then, principal component analysis and correlation analysis were performed on charcoal δ13C with rainfall, evaporation and temperature to reveal the correlation between δ13C and rainfall, evaporation and temperature; finally, the linear fitting method was used. Finally, a linear regression was performed on the climate factors significantly correlated with charcoal δ13C to establish the charcoal δ13C-climate factor relationship function.

4. Results

The samples were analyzed via stable carbon analysis, and the results are shown in Table 2. In Caobazi, without carbonization, the range of δ13C values in Pinus sp. was –27.33‰ to –27.49‰, and the range of δ13C values in Quercus sp. was –29.14‰ to –29.46‰. Under the conditions of carbonization at 300°C, the range of δ13C values in Pinus sp. was –28.23‰ to –28.38‰, and that in Quercus sp. was –29.49‰ to –29.86‰. Under the conditions of carbonization at 400°C, the range of δ13C values in Pinus sp. was –28.21‰ to –28.21‰, and that in Quercus sp. was –29.80‰ to –29.92‰. Under the conditions of carbonization at 500°C, the range of δ13C values in Pinus sp. was –28.35‰ to –28.45‰, and that in Quercus sp. was –29.20‰ to –29.20‰. Under the conditions of carbonization by wildfire, the range of δ13C values in Pinus sp. was –28.42‰ to –28.42‰, and that in Quercus sp. was –29.99‰ to –31.66‰.

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Table 2. δ13C (‰ VPDB) of wood samples heated at different temperatures.

https://doi.org/10.1371/journal.pone.0270133.t002

In Zhenba, without carbonization, the range of δ13C values in Pinus sp. was –26.74‰ to –26.92‰, and the range of δ13C values in Quercus sp. was –27.87‰ to –28.09‰. Under the conditions of carbonization at 300°C, the range of δ13C values in Pinus sp. was –27.46‰ to –27.57‰, and that in Quercus sp. was –27.91‰ to –28.35‰. Under the conditions of carbonization at 400°C, the range of δ13C values in Pinus sp. was –27.77‰ to –28.28‰, and that in Quercus sp. was –28.35‰ to –28.37‰. Under the conditions of carbonization at 500°C, the range of δ13C values in Pinus sp. was –27.33‰ to –28.21‰, and that in Quercus sp. was –28.19‰ to –28.33‰. Under the conditions of carbonization by wildfire, the range of δ13C values in Pinus sp. was –26.84‰ to –28.14‰, and that in Quercus sp. was –28.96‰ to –29.06‰.

In Jiwozi, without carbonization, the range of δ13C values in Pinus sp. was –28.49‰ to –28.66‰. Under the conditions of carbonization at 300°C, the range of δ13C values in Pinus sp. was –29.02‰ to –29.62‰. Under the conditions of carbonization at 400°C, the range of δ13C values in Pinus sp. was –29.36‰ to –29.46‰. Under the conditions of carbonization at 500°C, the range of δ13C values in Pinus sp. was –29.45‰ to –29.56‰. Under the conditions of carbonization by wildfire, the range of δ13C values in Pinus sp. was –29.71‰ to –29.82‰.

In Fengyukou without carbonization, the range of δ13C values in Pinus sp. was –25.37‰ to –25.83‰, and that in Quercus sp. was –27.24‰ to –28.10‰. Under the conditions of carbonization at 300°C, the range of δ13C values in Pinus sp. was –25.77‰ to –26.40‰, and that in Quercus sp. was –27.60‰ to –28.35‰. Under the conditions of carbonization at 400°C, the range of δ13C values in Pinus sp. was –26.35‰ to –26.58‰, and that in Quercus sp. was –26.79‰ to –28.47‰. Under the conditions of carbonization at 500°C, the range of δ13C values in Pinus sp. was –26.89‰ to –26.95‰, and that in Quercus sp. was –26.98‰ to –28.41‰. Under the conditions of carbonization by wildfire, the range of δ13C values in Pinus sp. was –25.88‰ to –26.82‰, and that in Quercus sp. was –27.66‰ to –28.30‰.

In Zhidan, without carbonization, the range of δ13C values in Pinus sp. was –25.58‰ to –26.07‰, and that in Quercus sp. was –26.48‰ to –26.49‰. Under the conditions of carbonization at 300°C, the range of δ13C values in Pinus sp. was –26.13‰ to –26.34‰ and that in Quercus sp. was –26.60‰ to –26.88‰. Under the conditions of carbonization at 400°C, the range of δ13C values in Pinus sp. was –26.14‰ to –26.49‰, and that in Quercus sp. was –26.83‰ to –26.87‰. Under the conditions of carbonization at 500°C, the range of δ13C values in Pinus sp. was –26.57‰ to –27.07‰, and that in Quercus sp. was –26.89‰ to –27.41‰. Under the conditions of carbonization by wildfire, the range of δ13C values in Pinus sp. was –26.18‰ to –28.07‰, and that in Quercus sp. was –27.62‰ to -27.69‰.

According to our experimental data (Table 2), the δ13C values of different genera differed, and the values for the same genus varied in diverse growth environments. Under various carbonization conditions, the δ13C is most positive at Jiwozi among five sites.

5. Discussion

5.1 Characteristics of stable carbon isotopes in different genera and species after wood carbonization

Previous studies have shown that the pyrolysis of wood hemicellulose, cellulose and lignin occurs at 170–240°C, 240–310°C, and 320–400°C, respectively, during the heating process [48]. At temperatures above 400°C, the carbon-containing organic matter of wood is basically completely pyrolyzed [2,46] and forms C = C bonds with a stable structure [49,50]. Hemicellulose shows the highest δ13C values in wood, cellulose shows the second highest, and lignin shows the lowest [17,18,51]. Therefore, with increasing carbonization temperature, the δ13C value of charcoal decreases gradually, and the δ13C values of charcoal decrease substantially from 25°C–300°C. At 300–400°C, the δ13C value of charcoal decreases slightly, and C = C bonds formed at 400–500°C. At this stage, the change of δ13C value depends on the redox reaction process. Oxidation reactions occur when C-H bonds are broken during the bonding process, and the δ13C of charcoal decreases; reduction reactions occur when C-O bonds are broken, and the δ13C of charcoal increases [46,52,53]. Thus, the δ13C values of Pinus armandii, Pinus massoniana, Quercus acutissima Carr, Quercus aliena Blume, and Quercus dentate Thunb increased with carbonization temperature, and the δ13C values of Pinus tabulaeformis, Quercus aliena Blume var., and Quercus mongolica Fischer decreased with temperature; the changes were related to the redox reaction processes during carbonization (Fig 2).

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Fig 2. δ13C (‰ VPDB) mean fractionation values of wood samples of Pinus sp. and Quercus sp. at different temperatures.

13C mean fractionation values of untreated wood is zero. 1- Pinus armandii; 2- Pinus massoniana; 3- Pinus tabulaeformis; 4- Quercus acutissima Carr; 5- Quercus aliena Blume; 6- Quercus aliena Blume var.; 7- Quercus dentata Thunb; 8- Quercus mongolica Fischer).

https://doi.org/10.1371/journal.pone.0270133.g002

The carbon isotopes of trees are derived from two sources, the plant itself and the fixation of atmospheric CO2 by plant photosynthesis [17,31,54,55]. Nonparametric tests for independent samples comparing Pinus and Quercus genera under the same climatic conditions showed significance(sig) < 0.05(Table 3) for Caobazi, Zhenba, Fengyukou, and Zhidan, which in summary shows that there is a significant difference between Pinus sp. and Quercus sp. samples in general. Comparing the Pinus and Quercus genera under the same carbonization conditions, it is obvious that the values of Pinus genera are higher than those of Quercus genera (Fig 3). The atmospheric CO2 was consistent between Pinus sp. and Quercus sp. under the same growth conditions, and the variability in δ13C between the two was caused by the physiological characteristics of the plants; the stomatal conductance of Pinus sp. was lower than that of Quercus sp., reducing the concentration of intercellular CO2 and thus increasing δ13C [56]; also, the nitrogen concentration on the leaf surface of Pinus sp. was lower than that of Quercus sp., leading to a lower efficiency of photosynthesis N concentration on the leaf surface of Pinus sp. was lower than that of Quercus sp., resulting in lower photosynthetic efficiency than Quercus sp. and thus decreasing 12C, increasing δ13C [57,58]. From the above analysis, there were significant differences in δ13C among charcoal genera.

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Fig 3. Comparison of δ13C (‰ VPDB) data for Pinus sp. and Quercus sp.

https://doi.org/10.1371/journal.pone.0270133.g003

The δ13C of different genera of charcoal was significantly different, and further comparison of the differences between different species of charcoal of the same genus was performed. Due to the limitations of vegetation distribution, the genus Pinus has only one species in Zhidan, Fengyukou, CaoBaZi and JiWoZi and two species in Zhenba; the genus Quercus has only one species in Zhidan, Zhenba and CaoBaZi and three species in Fengyukou. Therefore, we will apply the independent sample nonparametric test to analyze the interspecific differences between the genus Pinus in Zhenba and the genus Quercus in Fengyukou. The results showed a significant value of 0.404 (sig>0.05) between Pinus genera and a significant value of 0.298 (sig>0.05) for Quercus genera (Table 3), indicating that there were no significant differences between species of Pinus genera and between species of Quercus genera.

According to our results combined with previous research results [2,59], a significant difference in isotopic fractionation occurs at the genus level, but there is little difference in isotopic fractionation between different species of the same genus, so the isotopic analysis of charcoal can be performed based on the genus level.

5.2 Comparison of wildfire carbonization and indoor carbonization

Carbonization of extant wood to charcoal and determination of charcoal stable carbon isotopes is the first step in quantitative paleoclimate reconstruction, which currently uses isotopes to reconstruct paleoclimate by indoor carbonization to obtain δ13C of current species and establish a linear relationship [19,26,37], while reconstruction of paleoclimate The samples used are derived from wildfire carbonization, whether these two different carbonization methods affect charcoal stable carbon isotope fractionation and determine whether the relationship model established for extant species can be applied to paleoclimate reconstruction, and thus, both methods need to be further explored.

In this paper, wildfire carbonization and indoor carbonization experiments were conducted with Pinus sp. and Quercus sp. as test samples, and a nonparametric test was performed on two independent samples of the results obtained from wildfire carbonization and indoor carbonization, and we chose the mean of the carbonization results for the analysis due to the heterogeneity of the wildfire carbonization temperature, which showed sig >0.05 (Table 3). This shows that there is no difference between the δ13C obtained by the two carbonization methods. The differences between the two types of carbonization were mainly reflected in three aspects: heating method, carbonization environment and oxygen amount. The samples in this experiment were all wrapped with aluminum foil during carbonization, which acted as an oxygen barrier, so the differences in carbonization environment and oxygen amount were negligible. The heating method of wildfire carbonization is a low to high temperature ramp-up, while the heating method of indoor carbonization is a constant temperature ramp-up. The loss of hemicellulose, cellulose, and lignin components is faster during the ramp-up process, and fractionation is faster under wildfire carbonization than indoor carbonization, but the early fractionation of stable carbon isotopes does not have a major effect on the pyrolysis of the three components [19,35,47,55], it is the final temperature reached in both ways that determines the pyrolysis reaction, and since the three-component has a fixed pyrolysis temperature and content [48], the loss of pyrolytic components such as hemicellulose is the same at the same final temperature of carbonization, and the degree of stable carbon isotope fractionation is the same; therefore, with the same final temperature, the warming and constant temperature processes only affect the rate of pyrolysis reactions of components such as hemicellulose and do not affect the fractionation results of the pyrolysis reactions.

When the carbonization temperature reaches 400°C, the charcoal undergoes redox reactions, and the C-containing chemical bonds inside the wood, including C-O and C-H bonds, break and form C = C bonds. This bonding process affects the fractionation of charcoal δ13C. C = C bond formation is faster under constant temperature conditions, and thus, bond formation is faster under indoor carbonization conditions than under wildfire carbonization. Since the composition of chemical bonds is inherent to wood, when wood is completely carbonized, all C-containing bonds are converted to C = C bonds [49,50]. Therefore, for the same genus of wood, warming and constant temperature processes change the rate of redox reactions only during C = C bond formation and do not affect the final bond formation results. In summary, the difference in the carbonization method only changes the rate of fractionation and does not affect the final result of wood pyrolysis fractionation; thus, charcoal obtained by indoor carbonization can be used to simulate wildfire carbonization.

5.3 Correlation of the stable carbon isotopic composition of charcoal with climatic factors

The carbon isotope composition in plants is derived mainly from atmospheric CO2, Leaf stomata are the main avenue for atmospheric CO2 to enter the plant. The stomatal conductance is affected by climate factors such as precipitation (P), evaporation (E), and temperature (T), which affect the fixation of CO2 by plants [6062]. The δ13C values of both Pinus sp. and Quercus sp. wood were significantly negatively correlated with precipitation and positively correlated with evaporation. The relationship between temperature, an important climatic factor affecting plant growth, and plant δ13C is more complex. The experimental data also showed that the δ13C of Pinus sp. was correlated with the mean temperature, while Quercus sp. showed no correlation with the mean temperature (Table 4). Carboxylase is a catalyst in plants that uses free HCO3- to act as a catalyst during photosynthesis in the presence of biotin and ATP, and its activity affects the rate of photosynthesis and stomatal conductance, thus changing the plant CO2 concentration and affecting plant δ13C [60,63]. It was shown that temperature affects the activity of carboxylase, and at temperatures above the optimum temperature range of carboxylase, as the temperature increases, the activity of carboxylase decreases, causing an increase in plant δ13C; at temperatures below the optimum temperature range, as the temperature increases, the activity of carboxylase increases, causing a decrease in plant δ13C; at temperatures in the optimum temperature range, changes in temperature do not affect the activity of carboxylase, and thus, plant δ13C remains unchanged [6466], while different plants have different temperature adaptations of carboxylase [62,67]; thus, different genera of wood indicators for reconstructing rainfall and evapotranspiration in the study area.

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Table 4. Pearson correlation coefficients(r) between δ13C (‰ VPDB) and climatic parameters of wood.

https://doi.org/10.1371/journal.pone.0270133.t004

The previous study showed the stable carbon isotopic composition of wood undergoes fractionation during carbonization, so does the stable carbon isotopic composition of charcoal still have the above correlation with climate factors? As seen by the PCA weighting diagram (Figs 4 and 5), the δ13C of charcoal at different carbonization temperatures (δ13C3 (300°C carbonization condition), δ13C4 (400°C carbonization condition), δ13C5 (500°C carbonization condition), and δ13Cw (wildfire carbonization condition) are all distributed in the positive axis part of PC1 and distributed along the PC2 axis from the negative axis to the positive axis in the same order as the δ13C values from large to the positive axis. The order of distribution along the PC2 axis from the negative axis to the positive axis is generally consistent with the order of δ13C values from large to small. In Fig 4, the direction of δ13C is opposite to P and T, and the angle with T is greater than P, and it is in the same direction with E, indicating that Pinus sp. charcoal is negatively correlated with rainfall and temperature and positively correlated with evaporation; in Fig 5, the direction of δ13C is opposite to P, perpendicular to T, and in the same direction with E, indicating that Quercus sp. charcoal is negatively correlated with rainfall, positively correlated with evaporation, and has no obvious correlation with temperature relationship, which is consistent with the wood performance (Table 4). Thus, the fractionation of δ13C of charcoal during carbonization does not mask relevant climatic information, and in summary, charcoal δ13C is a potential indicator of rainfall and evaporation in the reconstructed study area.

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Fig 4. Component weights plot of the principal components analysis (Pinus).

(P is precipitation; T is temperature; E is evaporation; δ13Cun (without carbonization); δ13C3 (300°C carbonization condition), δ13C4 (400°C carbonization condition), δ13C5 (500°C carbonization condition), and δ13Cw (wildfire carbonization condition).

https://doi.org/10.1371/journal.pone.0270133.g004

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Fig 5. Component weights plot of the principal components analysis (Quercus).

(P is precipitation; T is temperature; E is evaporation; δ13Cun (without carbonization); δ13C3 (300°C carbonization condition), δ13C4 (400°C carbonization condition), δ13C5 (500°C carbonization condition), and δ13Cw (wildfire carbonization condition).

https://doi.org/10.1371/journal.pone.0270133.g005

Linear regression analysis of δ13C of charcoal of Pinus sp. and Quercus sp. with rainfall and evaporation at the sampling sites (Table 5) showed good linearity in the fit between charcoal and climatic factors at different temperatures (Fig 6). In the future, charcoal samples of Pinus sp. and Quercus sp. obtained from archaeological sites can have their δ13C values determined, and the carbonization temperature can be determined by Raman spectroscopy [31]. Then, substituting the charcoal δ13C into the above linear relationships for the corresponding temperatures can reconstruct the paleo-rainfall and paleo-evaporation in the study area. It is worth noting that the use of fossil fuels since the industrial revolution has led to a significant increase in atmospheric CO2 concentration, and when using the linear relationship, the sample δ13C needs to be corrected to remove the effect of changes in atmospheric CO2 concentration on carbon isotope fractionation.

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Fig 6. Relationship between the δ 13C (‰ VPDB) value and climate factor.

https://doi.org/10.1371/journal.pone.0270133.g006

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Table 5. Linear regression analysis of δ13C (‰ VPDB) of charcoal (P is precipitation; E is evaporation).

https://doi.org/10.1371/journal.pone.0270133.t005

6. Conclusions

Significant differences in isotopic fractionation existed at the genus level, while the differences in isotopic fractionation between species of the same genus were not significant, so the charcoal could be analyzed isotopically based on the genus level.

There is no significant difference between the δ13C of charcoal obtained by wildfire carbonization and indoor carbonization. The δ13C of charcoal of a certain genus can be obtained based on the simulation of indoor carbonization, and a linear relationship between δ13C and the climate factor of charcoal can be established.

After wood is carbonized to charcoal by burning, the original climate information is still preserved, and charcoal δ13C is a potential indicator for reconstructing rainfall and evaporation in the study area. The δ13C values of charcoal samples obtained from archaeological sites can be used to reconstruct paleorainfall and paleoevaporation after correcting for the effect of atmospheric CO2 changes on them.

Supporting information

Acknowledgments

We thank the reviewers and editors for their constructive suggestions and comments on this paper.

References

  1. 1. An CB, Feng ZD, Tang LY, Chen FH. Environmental changes and cultural transition at 4 cal. ka BP in central Gansu. Acta Geographic Sinica. 2003; 58:743–748(in Chinese).
  2. 2. Audiard B, Blasco T, Brossier B, Fiorentino G, Battipaglia G, Théry–Parisot I. δ13C referential in three Pinus species for a first archaeological application to paleolithic contexts: “Between intra and inter individual variation and carbonization effect.” Journal of Archaeological Science: Reports. 2018; 20 (December 2017): 775–783.
  3. 3. Berglund BE. Human impact and climate changes–Synchronous events and a causal link? Quaternary International. 2003; 104: 7–12.
  4. 4. WMO. The State of the Global Climate in 2019 Statement. 2019.
  5. 5. IPCC. An IPCC special report on the impacts of global warming of 1.5°C above preindustrial levels and related. 2018.
  6. 6. Xingchen Y, Maotang C, Jianmin H, et al. The paleolake hydrology and climate change since the~ 40 ka in the Hetao Basin, Inner Mongolia, China [J]. Quaternary International, 2020, 553: 73–82.
  7. 7. Gao X, Hao Q, Oldfield F, et al. New high‐temperature dependence of magnetic susceptibility‐based climofunction for quantifying paleoprecipitation from Chinese loess[J]. Geochemistry, Geophysics, Geosystems, 2019, 20(8): 4273–4291.
  8. 8. Zou Y, Wang L, He H, et al. Application of a Diatom Transfer Function to Quantitative Paleoclimatic Reconstruction—A Case Study of Yunlong Lake, Southwest China[J]. Frontiers in Earth Science, 2021, 9: 509.
  9. 9. Marchegiano M, Horne D J, Gliozzi E, et al. Rapid Late Pleistocene climate change reconstructed from a lacustrine ostracod record in central Italy (Lake Trasimeno, Umbria)[J]. Boreas, 2020, 49(4): 739–750.
  10. 10. Fernandez A, Steinman BA, Abbott MB. Application of a lacustrine carbonate sediment Proxy System Model to the quantitative reconstruction of past hydroclimatic change in Eastern Washington State[C]//AGU Fall Meeting Abstracts. 2020, 2020: PP048–08.
  11. 11. Srivastava J, Manjunatha B R, Balakrishna K, et al. Quantitative pollen-based reconstruction of the vegetation diversity in response to the late-Holocene climate change near Karwar, south-west coast of India[J]. Quaternary International, 2021.
  12. 12. Zhang XR, Hu K, Fang S, Wang DP, Zheng HB. Construction and application of phyolith–climate transfer function in peat surface deposits of Northeast China. Acta Sedimentologica Sinica. 2008; 26(4): 677–682(in Chinese).
  13. 13. Sun N, Li XQ, Dodson J, Zhou XY, Zhao KL, Yang Q. Plant diversity of the Tianshui Basin in the western Loess Plateau during the mid-Holocene charcoal records from archaeological sites. Quaternary International. 2013; 308–309: 27–35.
  14. 14. Sun N, Li X, Dodson J, et al. The quantitative reconstruction of temperature and precipitation in the Guanzhong Basin of the southern Loess Plateau between 6200 BP and 5600 BP[J]. The Holocene, 2016, 26(8): 1200–1207.
  15. 15. Mosbrugger V and Utescher T. The coexistence approach–a method for quantitative reconstructions of tertiary terrestrial palaeoclimate data using plant fossils. Palaeogeography, Palaeoclimatology, Palaeoecology. 1997; 134(1–4): 61–86.
  16. 16. Grimm EC and GL Jacobson JR. Late-Quaternary vegetation history of the eastern United States. Developments in Quaternary Sciences. 2003; 1: 381–402.
  17. 17. McCarroll D. and Loader NJ. Stable isotopes in tree rings. Quaternary Science Reviews. 2004; 23(7–8): 771–801.
  18. 18. Ferrio JP and Voltas J. Carbon and oxygen isotope ratios in wood constituents of Pinus halepensis as indicators of precipitation, temperature and vapour pressure deficit. Tellus B: Chemical and Physical Meteorology. 2005; 57(2): 164–173.
  19. 19. Ferrio JP, Alonso N, López JB, Araus JL, Voltas J. Carbon isotope composition of fossil charcoal reveals aridity changes in the NW Mediterranean Basin. Global Change Biology. 2006; 12(7): 1253–1266.
  20. 20. Loader NJ and Hemming DL. Spatial variation in pollen δ13C correlates with temperature and seasonal development timing. Holocene. 2001; 11(5): 587–592.
  21. 21. Loader NJ and Hemming DL. The stable isotope analysis of pollen as an indicator of terrestrial palaeoenvironmental change: A review of progress and recent developments. Quaternary Science Reviews. 2004; 23(7–8): 893–900.
  22. 22. Hope JA. The carbon stable isotope composition of pollen. Review of Palaeobotany and Palynology. 2004; 132(3–4): 291–313.
  23. 23. Smith FA and White JWC. Modern calibration of phytolith carbon isotope signatures for C3/C4 paleograssland reconstruction. Palaeogeography, Palaeoclimatology, Palaeoecology. 2004; 207(3–4): 277–304.
  24. 24. Lu HY, Wu NQ, Liu KB, Jiang H, Liu TS. Phytoliths as quantitative indicators for the reconstruction of past environmental conditions in China II: palaeoenvironmental reconstruction in the Loess Plateau. Quaternary Science Reviews. 2007; 26(5–6): 759–772.
  25. 25. Gao Y, Li Z, Zhu R, Wang N. Quantitative reconstruction of Holocene millennial–scale precipitation in the Asian monsoon margin of northwest China, revealed by phytolith assemblages from calcareous root tubes in the Tengger Desert. Climate Dynamics. 2020; 55(3–4): 755–770.
  26. 26. Yang Q, Li XQ, Zhou XY, Zhao KL, Sun N. Quantitative reconstruction of summer precipitation using a mid–Holocene δ13C common millet record from Guanzhong Basin, northern China. Climate of the Past. 2016; 12(12): 2229–2240.
  27. 27. Kress A, Saurer M, Siegwolf RTW, et al. A 350 year drought reconstruction from AlPinus tree ring stable isotopes[J]. Global Biogeochemical Cycles, 2010, 24(2).
  28. 28. Treydte K, Schleser GH, Schweingruber FH, et al. The climatic significance of δ13C in subalPinus spruces (Lötschental, Swiss Alps) a case study with respect to altitude, exposure and soil moisture[J]. Tellus B, 2001, 53(5): 593–611.
  29. 29. Evans MN, Reichert BK, Kaplan A, et al. A forward modeling approach to paleoclimatic interpretation of tree‐ring data[J]. Journal of Geophysical Research: Biogeosciences, 2006, 111(G3).
  30. 30. Voltas J, Chambel MR, Prada MA, Ferrio JP. Climate–related variability in carbon and oxygen stable isotopes among populations of Aleppo Pinus grown in common–garden tests. Trees–Structure and Function. 2008; 22(6): 759–769.
  31. 31. Baton F, Nguyen Tu TT, Derenne S, Delorme A, Delarue F, Dufraisse A. Tree–ring δ13C of archeological charcoals as indicator of past climatic seasonality. A case study from the Neolithic settlements of Lake Chalain (Jura, France). Quaternary International. 2017; 457: 50–59.
  32. 32. Monson R K, Szejner P, Belmecheri S, et al. Finding the seasons in tree ring stable isotope ratios[J]. American journal of botany, 2018, 105(5).
  33. 33. Xu C, Zhao Q, An W, et al. Tree-ring oxygen isotope across monsoon Asia: Common signal and local influence [J]. Quaternary Science Reviews, 2021, 269: 107156.
  34. 34. Zheng J, Liu Y, Hao Z, et al. State-of-art and perspective on global synthesis studies of climate change for the past 2000 years [J]. Quaternary Sciences, 2021, 41(2): 309–322.
  35. 35. Hall G, Woodborne S, Scholes M. Stable carbon isotope ratios from archaeological charcoal as palaeoenvironmental indicators. Chemical Geology. 2008; 247(3–4): 384–400.
  36. 36. Aguilera M, Espinar C, Ferrio JP, Pérez G, Voltas J. A map of autumn precipitation for the third millennium BP in the eastern Iberian Peninsula from charcoal carbon isotopes. Journal of Geochemical Exploration. 2009; 102(3): 157–165.
  37. 37. Audiard B, Thery–Parisot I, Blasco T, Mologni C, Texier PJ, Battipaglia G. Crossing taxonomic and isotopic approaches in charcoal analyses to reveal past climates. New perspectives in paleobotany from the paleolithic Neanderthal dwelling–site of La Combette (Vaucluse, France). Review of Palaeobotany and Palynology. 2019; 266: 52–60.
  38. 38. Dawson TE, Mambelli S, Plamboeck AH, Templer PH, Tu KP. Stable isotopes in plant ecology. Annual Review of Ecology and Systematics. 2002; 33: 507–559.
  39. 39. Seftigen K, Linderholm H W, Loader N J, et al. The influence of climate on 13C/12C and 18O/16O ratios in tree ring cellulose of Pinus sylvestris L. growing in the central Scandinavian Mountains [J]. Chemical Geology, 2011, 286(3–4): 84–93.
  40. 40. Aguilera M, Ferrio J P, Pérez G, et al. Holocene changes in precipitation seasonality in the western Mediterranean Basin: a multi‐species approach using δ13C of archaeobotanical remains[J]. Journal of Quaternary Science, 2012, 27(2): 192–202.
  41. 41. Wang SZ, Wang ZL, He N. Research on charcoal unearthed from Pottery Temple Site. Archaeology and Technology. 2011; (3): 91–97 (in Chinese).
  42. 42. Wang SZ, Fang YM, Zhao ZJ. Vegetation, paleoclimate and plant use during Longshan era: case study of anthracology of wandian Site in Henan Province. Quaternary Research. 2012; 32(2): 226–235 (in Chinese).
  43. 43. Li XQ, Sun N, Dodson J, Zhou XY. Human activity and its impact on the landscape at the Xishanping site in the western Loess Plateau during 4800–4300 cal yr BP based on the fossil charcoal record. Journal of Archaeological Science. 2012; 39(10): 3141–3147.
  44. 44. The data set is provided by Landsat (http://landsat.visibleearth.nasa.gov/).
  45. 45. National Earth System Science Data Center, National Science & Technology Infrastructure of China (http://www.geodata.cn).
  46. 46. Jones TP and Chaloner WG. Fossil charcoal, its recognition and palaeoatmospheric significance. Palaeogeography, Paleoclimatology, Paleoecology. 1991; 97(1–2): 39–50.
  47. 47. Turney CSM, Wheeler D, Chivas AR. Carbon isotope fractionation in wood during carbonization. Geochimica et Cosmochimica Acta. 2006; 70(4): 960–964.
  48. 48. Zeriouh A. and Belkbir L. Thermal decomposition of a Moroccan wood under a nitrogen atmosphere. Thermochimica Acta.1995; 258(C): 243–248.
  49. 49. Qian Y, Engel MH, Macko SA. Stable isotope fractionation of biomonomers during protokerogen formation. Chemical Geology. 1992; 101: 201–210.
  50. 50. Krull ES, Skjemstad JO, Graetz D, Grice K, Dunning W, Cook G, et al. 13C-depleted charcoal from C4 grasses and the role of occluded carbon in phytoliths. Organic Geochemistry. 2003; 34: 1337–1352.
  51. 51. Borella S, Leuenberger M, Saurer M, Siegwolf R. Reducing uncertainties in δ13C analysis of tree rings: pooling, milling, and cellulose extraction. Journal of Geophysical Research Atmospheres. 1998; 103(D16): 19519–19526.
  52. 52. Galimov EM. Isotope organic geochemistry, Organic Geochemistry. 2006; 37(10): 1200–1262.
  53. 53. Galimov EM, Kaminskiy FV, Kodina LA. New data on carbonado carbon isotope compositions. Geochem. 1985; Int 22: 18–21.
  54. 54. Farquhar GD, Caemmerer S, Berry JA. A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta. 1980; 149(1): 78–90.
  55. 55. Leavitt SW, Donahue DJ, Long A. Charcoal production from wood and cellulose: implications for radiocarbon dates and accelerator target production. Radiocarbon. 1982; 24: 27–35.
  56. 56. Carnicer J, Barbeta A, Sperlich D, et al. Contrasting trait syndromes in angiosperms and conifers are associated with different responses of tree growth to temperature on a large scale [J]. Frontiers in Plant Science, 2013, 4: 409.
  57. 57. Flexas J, Ribas‐Carbo M, DIAZ‐ESPEJO A, et al. Mesophyll conductance to CO2: current knowledge and future prospects [J]. Plant, cell & environment, 2008, 31(5): 602–621.
  58. 58. Guerrieri R, Belmecheri S, Ollinger S V, et al. Disentangling the role of photosynthesis and stomatal conductance on rising forest water-use efficiency[J]. Proceedings of the National Academy of Sciences, 2019, 116(34): 16909–16914.
  59. 59. Resco V, Ferrio JP, Carreira JA, Calvo L, Casals P, Ferrero–Serrano Á, et al. The stable isotope ecology of terrestrial plant succession. Plant Ecology and Diversity. 2011; 4(2–3): 117–130.
  60. 60. Zhang CJ, Chen FH, Jin M. Study on modern plant C–13 in western China and its significance. Chinese Journal of Geochemistry. 2003; 22(2): 97–106.
  61. 61. Sun B, Dilcher DL, Beerling DJ, Zhang C, Yan D, Kowalski E. Variation in Ginkgo biloba L. leaf characters across a climatic gradient in China. Proceedings of the National Academy of Sciences of the United States of America. 2003; 100(12): 7141–7146. pmid:12777617
  62. 62. Farquhar G and Wong S. An empirical model of stomatal conductance. Functional Plant Biology. 1984; 11(3): 191.
  63. 63. Farquhar GD, Ehleringer JR, Hubick KT. Carbon isotope discrimination and photosynthesis. Annual Review of Plant Physiology and Plant Molecular Biology. 1989; 40(1): 503–537.
  64. 64. Schleser GH, Frielingsdorf J, Blair A. Carbon isotope behaviour in wood and cellulose during artificial aging. Chemical Geology.1999; 158(1–2): 121–130.
  65. 65. Chen T, Qin DH, Li JF, Ren JW, Liu XH, Sun WZ. Study on climatic significance of fir tree-ring δ13C from Zhaosu county of Xinjiang region. China journal of glaciology and geocryology. 2000; 20(4): 347–352(in Chinese).
  66. 66. Zhang RB, Yuan YJ, Wei WS, Shanng HM, Yu SL, Zhang TW, et al. Response of Stable Carbon Isotope of Larix sibirica Ledeb. Tree-rings to Climate Change. Arid zone research. 2012; 2(29):328–334(in Chinese).
  67. 67. Hemming DI, Switsur VR, Waterhouse JS, Heaton THE, Carter AHC. Climate variation and the stable carbon isotope composition of tree ring cellulose: an intercomparison of Quercus robur, Fagus sylvatica and Pinus silvestris. Tellus B: Chemical and Physical Meteorology. 1998; 50(1): 25–33.