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Article

The Spatiotemporal Response of Vegetation Changes to Precipitation and Soil Moisture in Drylands in the North Temperate Mid-Latitudes

by
Zongxu Yu
1,2,†,
Tianye Wang
3,†,
Ping Wang
1,2,* and
Jingjie Yu
1,2
1
Key Laboratory of Water Cycle and Related Land Surface Processes, Institute of Geographic Sciences and Natural Resources Research, Chinese Academy of Sciences, Beijing 100101, China
2
University of Chinese Academy of Sciences, Beijing 100049, China
3
Yellow River Laboratory, Zhengzhou University, Zhengzhou 450001, China
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Remote Sens. 2022, 14(15), 3511; https://doi.org/10.3390/rs14153511
Submission received: 15 June 2022 / Revised: 17 July 2022 / Accepted: 19 July 2022 / Published: 22 July 2022
(This article belongs to the Special Issue Remote Sensing for Drought Monitoring and Forecasting)
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Abstract

:
Vegetation growth in drylands is highly constrained by water availability. How dryland vegetation responds to changes in precipitation and soil moisture in the context of a warming climate is not well understood. In this study, warm drylands in the temperate zone between 30 and 50° N, including North America (NA), the Mediterranean region (MD), Central Asia (CA), and East Asia (EA), were selected as the study area. After verifying the trends and anomalies of three kinds of leaf area index (LAI) datasets (GLASS LAI, GLEAM LAI, and GLOBAMAP LAI) in the study area, we mainly used the climate (GPCC precipitation and ERA5 temperature), GLEAM soil moisture, and GLASS LAI datasets from 1981 to 2018 to analyze the response of vegetation growth to changes in precipitation and soil moisture. The results of the three mutually validated LAI datasets show an overall greening of dryland vegetation with the same increasing trend of 0.002 per year in LAI over the past 38 years. LAI and precipitation exhibited a strong correlation in the eastern part of the NA drylands and the northeastern part of the EA drylands. LAI and soil moisture exhibited a strong correlation in the eastern part of the NA drylands, the eastern part of the MD drylands, the southern part of the CA drylands, and the northeastern part of the EA drylands. The results of this study will contribute to the understanding of vegetation dynamics and their response to changing water conditions in the Northern Hemisphere midlatitude drylands.

Graphical Abstract

1. Introduction

Drylands cover approximately 45% of the global land surface [1], and semiarid lands in particular have expanded over the last several decades [2,3]. Drylands support approximately 40% of the human population and host 20% of the major global plant [4]. Dryland ecosystems are fragile [5], and approximately 10–20% of global drylands are already degraded [6,7].
The global land surface temperature has increased by approximately 1.1 °C compared with the average in 1850–1900, and the current global warming rate will likely continue or accelerate due to increasing anthropogenic greenhouse gases [8]. Due to climate warming and atmospheric circulation anomalies, the global hydrological cycle is intensifying, and drylands are expected to become drier [9]. Recent studies indicated that evaporation increased by 1.1 mm·year−1, while precipitation and runoff decreased by −2.32 mm·year−1 and −0.8 mm·year−1, respectively, in global drylands from 1980 to 2015 [10]. Global coupled atmosphere–ocean general circulation models [2,11] have predicted that warm trends over drylands were twice as much as those over humid regions, and the area of global drylands is projected to expand by ∼10% by 2100.
Climate warming is applying a major strain on fragile dryland ecosystems and is likely to worsen in the future [12,13]. Nevertheless, greening of vegetation in some parts of drylands has been detected since the 1980s. Generally, water-restricted vegetation is widely distributed in drylands, especially in warm drylands south of 50°N [14]. The growth of vegetation in drylands is constrained primarily by water availability [15]. Precipitation provides a direct source of water for plants in drylands and plays a significant role in aridity index (AI) changes [11,16,17,18]. In addition, soil moisture, which is strongly dependent on precipitation and groundwater [19], plays an important role in vegetative growth, especially in arid and water-scarce areas [20]. Soil moisture has also been indicated to control evapotranspiration in the processes of energy and water exchange in dryland ecosystems [21,22,23].
Meanwhile, precipitation and soil moisture vary largely across spatial and temporal scales in drylands [24], such that changes in precipitation and soil moisture are anticipated to have direct effects on vegetation growth. Therefore, in this study, we investigated vegetation and its water source controls (mainly precipitation and soil moisture) across midlatitude (30–50°N) drylands of the Northern Hemisphere and selected four typical regions (i.e., western North America, Mediterranean region, Central Asia, and East Asia) for further analysis. The objectives of this study are to (1) characterize the temporal change trends and spatial patterns of dryland climate variables and vegetation growth in the mid-latitudes of the Northern Hemisphere from 1981 to 2018; (2) distinguish differences in vegetation growth, precipitation, and soil moisture among four selected typical regions; and (3) carry out attribution analyses of the response mechanism of dryland vegetation to precipitation and soil water under drought stress.

2. Materials and Methods

2.1. Study Area

In this research, we selected warm drylands in the temperate zone between 30 and 50°N as the study area where vegetation is severely limited by water resources [14,15]. The degree of drought in the study area can be divided into four categories based on the drought index (AI) [2,25]: hyperarid (AI < 0.05), arid (0.05 ≤ AI < 0.2), semiarid (0.2 ≤ AI < 0.5), and dry subhumid (0.5 ≤ AI < 0.65). Each of the four categories occupies a total area of 12%, 38%, 40%, and 10%, respectively, from hyperarid to dry subhumid. The four categories occupy 12%, 38%, 40%, and 10% of the total dryland area of 8.4 million km2 dryland area, and the dryland areas include western North America, the Mediterranean region and surrounding areas, Central Asia, and much of East Asia (Figure 1 and Figure 2). There are four climate types in the study area: temperate continental climate, Mediterranean climate, plateau mountain climate, and temperate monsoon climate, among which temperate continental climate is mainly and most widely distributed.
To better represent the changes in regional vegetation, four typical dryland regions were selected in the study area, including North America (NA, which includes United States and Mexico), the Mediterranean region (MD, which includes eleven European countries including Spain and Italy, six Asian countries including Turkey and Israel, and five African countries including Egypt and Libya), Central Asia (CA, which includes Kazakhstan, Uzbekistan, Kyrgyzstan, Tajikistan, and Turkmenistan), and East Asia (EA, which includes Mongolia, northwest China, and the Inner Mongolia Autonomous Region) [26,27,28,29].

2.2. Data Sources

2.2.1. Climate Data

Global Precipitation Climatology Centre (GPCC) monthly precipitation data (Version 2020) during the period from 1981 to 2018 at a spatial resolution of 0.5° (http://gpcc.dwd.de/ accessed on 7 March 2022) [30,31] were used in the study. Gridded datasets were based on the ~85,000 stations worldwide that had records lasting 10 years or longer. GPCC data have been widely applied in global water cycle and drought studies [32,33,34], and the GPCC precipitation data (PRE) were resampled and averaged annually.
ERA5-land monthly 2 m temperature averaged data during the period from the 1981 to 2018 period at a spatial resolution of 0.1° (https://www.copernicus.eu/ accessed on 7 March 2022) [35,36] were used. ERA5-Land is a replay of the land component of the ERA5 climate reanalysis, forced by meteorological fields from ERA5. ERA5 is the fifth generation ECMWF atmospheric reanalysis of the global climate. ERA5-land data have been widely applied in hydrological cycles and global climate change [37,38,39]. The ERA5-land temperature data (TMP) were resampled to average annually and 0.5° resolution with the nearest neighborhood method to match the spatial resolution of the precipitation dataset.

2.2.2. Soil Moisture Data

Global Land Evaporation Amsterdam Model (GLEAM) yearly soil moisture data (version 3.5a) during the period from 1981 to 2018 at a spatial resolution of 0.25° (https://www.gleam.eu/ accessed on 7 March 2022) [40,41,42] were used, including surface soil moisture (SMsurf) and deeper soil moisture (SMdeeper). GLEAM is a set of algorithms that separately estimate the different components of terrestrial evaporation based on satellite observations. GLEAM soil moisture data have been widely applied in terrestrial evapotranspiration and soil desiccation studies [43,44,45]. The GLEAM soil moisture data (SMsurf and SMdeeper) were resampled to a 0.5° resolution to match the spatial resolution of the climate datasets.

2.2.3. Potential Evapotranspiration and Evapotranspiration

Climatic Research Unit gridded Time Series (CRU TS) is a climate dataset (version TS4.00) on a 0.5° × 0.5° grid over all land domains of the world except Antarctica, which is derived by the interpolation of monthly climate anomalies from extensive networks of weather station observations (https://www.uea.ac.uk/ accessed on 7 March 2022) [46,47]. In this dataset, potential evapotranspiration (PET) is calculated using the Penman–Monteith formula [48]. The CRU TS data have been widely applied in water balance and the evolution of drought studies [49,50,51]. The dataset of potential evapotranspiration was selected from 1981 to 2018 and resampled to average annually and 0.5° resolution to match the spatial resolution of the climate datasets.
GLEAM yearly actual evaporation data (version 3.5a) during the period from 1981 to 2018 at a spatial resolution of 0.25° were used. The GLEAM actual evapotranspiration data (ET) were resampled to a 0.5° resolution to match the spatial resolution of the climate datasets.

2.2.4. Leaf Area Index (LAI) Data

The Global Land Surface Satellite (GLASS) product is primarily based on NASA’s Advanced Very High Resolution Radiometer (AVHRR) long-term data record (LTDR) and Moderate Resolution Imaging Spectroradiometer (MODIS) data, in conjunction with other satellite data and ancillary information using general regression neural networks (http://www.glass.umd.edu/ accessed on 7 March 2022) [52,53,54]. Currently, these products (version 50) are officially released leaf area index (LAI) images of 8 days from 1981 to 2018 based on NASA’s AVHRR. The GLASS LAI dataset is appropriate for the study of long-term global vegetation dynamics and has been widely used for various research purposes [55,56,57,58,59].
To verify the quality and availability of GLASS LAI data, GIMMS LAI and GLOBAMAP LAI datasets were adopted. The Global Inventory Modelling and Mapping Study (GIMMS) LAI3 g (version 4.0) dataset provides the longest global LAI time series from July 1981 to December 2016, with a resolution of 1/12° and a temporal resolution of 15 days. It was generated from AVHRR GIMMS NDVI3 g using an Artificial Neural Network-derived model [60]. The globmap leaf area index product (version 3) provides highly consistent long time-series leaf area index (LAI) data worldwide [61]. The GLOBMAP LAI is a combination of the AVHRR and MODIS LAI, with global coverage at a 15-day temporal resolution and an 8 km spatial resolution for the period from 1981 to 2018 [57]. The datasets of LAI were nearest resampled to 0.5° resolution and averaged annually [58].

2.2.5. Land Cover Data

The MODIS Land Cover Type Product (MCD12Q1) (http://modis-land.gsfc.nasa.gov/ accessed on 7 March 2022) [62,63] supplies global maps of land cover at annual time steps and 0.05° spatial resolution for 2001–present. The product contains the International Geosphere-Biosphere Programme (IGBP) legacy classification scheme in each 0.05° pixel, which was classified using the C4.5 decision tree algorithm that ingested a full year of 8-day MODIS nadir BRDF-adjusted reflectance [64,65,66]. A total of 450 MODIS Land Cover Type Product images of 8 days from 2004 to 2013 were selected to composite the annual average image and classify the type of vegetation in drylands between 30 and 50° N. Congener vegetations were combined and divided into habitats of trees, shrubs, and grasses. The images were resampled to 0.5° resolution with the nearest neighborhood method to match the spatial resolution of the climate datasets.
Before the actual research analysis was undertaken, considerable work was carried out to classify vegetation. According to MCD12Q1 land cover data and the IGBP classification scheme, the vegetation in the study area was divided into forest, shrublands, and grasslands. Forests and shrublands were “woody vegetation”, while grasslands and savannas were “herbaceous vegetation” (Table A1 and Figure A1 and Figure A2). Among them, woody vegetation and herbaceous vegetation accounted for 18% and 72%, respectively.

2.3. Method

2.3.1. Principal Component Analysis (PCA)

Many spatial datasets are highly dimensional and, as such, can be difficult to visualize and interpret. Therefore, it is often of interest to reduce the dimensionality of the data [67]. To screen and reconfirm the indices affecting vegetation LAI, principal component analysis (PCA) is established to explain the correlation degree between the mean value of water factor indices and LAI in the study area from 1981 to 2018 [68]. It is used to reduce the dimensionality of the multivariate dataset by extracting the information in the form of a small number of principal components, and the main principal factors can be extracted containing all the required information [69]. In the PCA, each principal component (PC) represents the direction of one eigenvector. The score on each PC represents the projection of each variable onto it, which is the weight of the variable. Loading represents the degree of correlation between each variable and PC. The cumulative variance contribution rate is often used as an index to judge the number of PCs. In general, the cumulative contribution rate is greater than 0.8. Before PCA, all variables are normalized.

2.3.2. Linear Regression Analysis

To analyze the trends in meteorological data, soil moisture data, and vegetation LAI from 1981 to 2018, a linear regression analysis method was established [70]. One-dimensional linear regression analysis of the trends is a method that can reflect the long-term dynamics of long time-series data. It is used to calculate spatiotemporal variations in variates [71,72,73]. The significance of these changes was determined using a T test at three significance levels of 0.05, 0.01, and 0.001.

2.3.3. Pearson Correlation Coefficient

The Pearson correlation coefficient (Pearson’s r) is a measure of linear correlation between two sets of data [74]. It is essentially a normalized measurement of the covariance, such that the result always has a value between −1 and 1. We performed Pearson’s correlations to analyze the linear relationships between vegetation growth influencing factors and LAI from 1981 to 2018 [75]. The significance of these changes was determined at a significance level of 0.05.

2.3.4. Partial Correlation Analysis

The partial correlation coefficient is used to study the correlation between an independent variable and the dependent variable by excluding the impact of the other independent variables [76]. For this research, we used the partial correlation coefficient to explore the relationship between climate variables and LAI, soil moisture, and LAI in areas where the LAI growth trend is higher than the average trend and LAI decline [77]. The significances of the calculated partial correlations at three significance levels were 0.05, 0.01 and 0.001.

2.3.5. Space Weighted Average

The spatial mean of the dataset was calculated, but the spatial variability of the pixel area cannot be solved due to the ordinary arithmetic mean. To solve the problem that the mean value of raster data varies with latitude area, Equation (1) was adopted. It was used to calculate the weighted average of the raster dataset over the entire study area [78].
X = ∑ i = 1 n X i × c o s ( l a t i ) ∑ i = 1 n c o s ( l a t i )
where X is the total mean of the regional variable, X i is the value of the variable at each raster data point, and l a t i is the latitude of the raster data point.

3. Results

3.1. Meteorological Characteristics

3.1.1. Spatial Patterns of Temperature (TMP), Potential Evapotranspiration (PET), and Precipitation (PRE)

As shown in Figure 3, TMP, PET, and PRE are highly spatially heterogeneous in the drylands between 30 and 50° N. The multiyear mean TMP in most areas of the study area was over 0 °C and varied from −13.89 °C to 26.72 °C, except that the multiyear mean TMPs in the mountainous areas of eastern Central Asia, the Qinghai–Tibet Plateau, and the northern Mongolia Plateau were less than 0 °C. The high TMPs with multiyear mean temperatures exceeding 20 °C were mainly concentrated in the drylands in the south-western United States, southern Central Asia, northern Africa, and southern Mediterra-nean, where the highest multiyear mean TMP reached 26.7 °C. The low TMP was mainly concentrated in the northern part of the study area, and the spatial distribution of temper-ature was affected by latitude and elevation. The temperature tended to decrease as the altitude and latitude changed from low to high.
The multiyear mean PET in the study area ranged from 596 mm to 2438 mm and decreased from south to north as a whole. High PET values exceeding 1200 mm per year were widely distributed in most areas of the study area, including the drylands of the southwestern United States, southern Mediterranean region, southern Central Asia, and arid and semiarid areas in China. As shown in Figure 3b, the multiyear mean PET was generally higher in hyperarid regions but lower in arid and semiarid regions. PET was affected by radiation and hydrothermal conditions, and the distribution of PET in drylands did not completely follow the distribution of the AI index. At the same time, the multiyear mean PET showed an increase in stratification from north to south in North America and Central Asia.
However, the multiyear mean PRE ranged from 22 mm to 1124 mm in the study area. In addition to the southwestern drylands of the United States, southern Mediterranean, and most of the drylands of Asia, many of the areas showed low annual PREs, with some regions far below 350 mm per year. The distribution of the multiyear mean PRE was similar to that of the AI in the study area. The low multiyear mean PRE below 500 mm occupied most of the study area and showed large to small change trends from humid to arid regions.
Although high PET was associated with radiation, wind speed, and vapor pressure differences, PET and PRE with long-term uneven spatial distributions were affected by differences in geography.

3.1.2. Temporal Variations in Temperature (TMP), Potential Evapotranspiration (PET), and Precipitation (PRE)

Figure 4 shows the temporal trends of the average annual TMP, PET, and PRE of the entire study area from 1981 to 2018. The average annual TMP (slope = 0.04, p < 0.001) and PET (slope = 1.53, p < 0.001) showed significant interannual increasing trends, but the average annual PRE showed an insignificant trend (slope = 1.53, p > 0.05). However, there were substantial differences in the changes in TMP, PET, and PRE in different regions reflecting different vegetation types (Figure 5). While the TMP in most regions showed an increasing trend, the TMP variation ranges of vegetation points varied between 0 °C and 0.12 °C per year, with most in the range of 0.3 °C to 0.06 °C per year. The PET variation ranges of vegetation points varied between −1.73 mm and 0.12 mm per year. The grid points with greater PET increases were mainly distributed in the central drylands of North America, the drylands in western Central Asia, and the drylands in northeast East Asia. Even though PRE had no significant trend overall (Figure 4c) and had no significant trends in European and Asian areas, PRE had significant decreasing trends in North American drylands.

3.2. Vegetation Conditions and Changes

3.2.1. Vegetation Leaf Area Index (LAI) Conditions

To represent the spatial variation in vegetation across the study area, GLASS LAI annual average data from 1981 to 2018 were applied (Figure A4). With the GIMMS LAI dataset and the GLOBAMAP LAI dataset [56], the temporal variation trends and anomalies of LAI in the whole study area were verified (Figure 6 and Figure A3).
All three LAI datasets in the study area showed significant increasing trends at a similar rate of 0.002 per year. Although LAI trends differ in spatial distribution, the LAI trend indicates the possibility of overall greening of vegetation in the study area (Figure A3). Compared with the LAI datasets of GLASS and GLOBAMAP, the LAI of GIMMS had larger anomalies in the study area, and the fitted trend line was significantly lower. Even though the fitting trend lines of GLASS and GLOBAMAP passed the significance test (p < 0.001), according to relevant literature [56,79], the global change in GLASS LAI is significant and more sensitive to drought than GLOBAMAP LAI. Therefore, the GLASS LAI dataset was chosen for further analysis.

3.2.2. Regional LAI Change

As shown in Figure 7, the vegetation LAI of EA, CA, and MD showed significant increasing trends over a 38-year period from 1981 to 2018 (MD: slope = 0.006, p < 0.001; CA: slope = 0.001, p < 0.001; EA: slope = 0.001, p < 0.01). However, there was no obvious trend of vegetation LAI increase in drylands of NA in terms of the region as a whole. The regional average LAI of drylands in the MD was at a high level, and the growth rate was the largest among the four regions. Compared to those of NA and MD, the regional average LAI changes of EA and CA were in a state of low fluctuation.
Given that the spatial distribution of vegetation variation trends was not uniform, the spatial variation trends of the annual average vegetation LAI in the four regions were analyzed (Figure 8).
In the drylands of NA, vegetation LAI increased significantly (> 0.006 per year) in the eastern parts of the drylands (0.2 ≤ AI < 0.5), where the terrain was flat and the altitude was low, while it decreased significantly in the central mountains and southwestern plains of the drylands (< −0.006 per year). In the Mediterranean surrounding area, most of the vegetation LAI showed significant increasing trends at higher elevations, where increasing trends exceeded 0.002 per year. For the vegetation LAI in the drylands of CA, grid points where vegetation LAI showed significant increases were scattered throughout the region, but most were concentrated in the southeastern part of drylands. In addition, the significant increasing trends of EA vegetation LAI were concentrated in the southeastern part of drylands in East Asia, while the significant decreasing trends were concentrated in the northwestern part of East Asia. It is worth noting that in the borderlands of southeast CA and northwest EA, AI shows a transition from semiarid to dry subhumid, and the elevations here were higher than the average elevations of the two regions. In the drylands of four typical regions, in general, the vegetation in the high-altitude area showed significant increasing trends, while the vegetation in the more arid area showed trends of browning and significant decrease. The overall situation of vegetation change trends in the four regions is shown in Table 1.

3.3. Relationship between the LAI and Effect Variables

3.3.1. Main Influencing Variables of LAI Based on PCA

The PCA method was applied to analyze and screen the main variables influencing vegetation LAI changes in the study area. Among them, the LAI, SMsurf, SMdeeper, PET, PRE, TMP, and ET were averaged over 38 years from 1981 to 2018.
As shown in Figure 9, we conducted a principal component analysis on the datasets in drylands between 30 and 50°N. The results showed that the first two principal components (PC1 and PC2) explained 79% of the variance: 53% by PC1 and 26% by PC2. PC3 explained 10% of the total variance. The correlation coefficients between the first principal component (PC1) and LAI, SMsurf, SMdeeper, PRE, and ET were large. The first principal component was a linear combination of LAI, SMsurf, SMdeeper, PRE, and ET, and the original variables all had positive effects on vegetation growth. From the loading figure of PC1, vegetation LAI may be related to precipitation and soil moisture (SMsurf and SMdeeper) from the perspective of vegetation growth water. The correlation coefficients between the second principal component (PC2) and PET and TMP were large, so the second principal component is a linear combination of PET and temperature, both of which have a positive effect on vegetation growth. From the loading figure of PC2, PET and TMP were positively correlated, indicating that the vegetation greening caused by the rise in PET may be related to the rise in TMP in the drylands of the study area. However, it is worth noting that the correlation coefficients between the first principal component (PC1) and SMsurf and SMdeeper were positive and that between PC1 and LAI was negative. Therefore, it is worth exploring the effect of precipitation soil moisture on dryland vegetation changes.

3.3.2. Relationship between the LAI and Precipitation and Soil Moisture

The Pearson correlation coefficient was calculated to evaluate the responses of the vegetation LAI to precipitation and soil moisture from 1981 to 2018. As shown in Figure 10, the relationship between LAI and precipitation showed strong correlations in the eastern part of NA drylands and the northeastern part of EA drylands. However, in CA and MD drylands, the spatial distribution of correlation coefficients between LAI and precipitation showed fragmentation and discontinuity, and some of these properties at a few sites passed the significance test. The correlation coefficients between LAI and surface soil moisture and deeper soil mois-ture also had a similar spatial distribution pattern as those between LAI and precipitation, which are shown in Figure A5 and Figure A6. However, as shown in Table 2, the Pearson coefficients for the relationships between the LAI and PRE and SMsurf and SMdeeper in the four regions were different in terms of proportions. In the long time series of 38 years, compared with MD and CA vegetation, NA and EA vegetation had stronger responses to PRE, SMsurf, and SMdeeper.
However, due to the influence of precipitation lag, the annual average vegetation LAI has no significant responses to precipitation in some regions within a year [80,81,82,83]. Based on this lack of response, the 12-month LAI and monthly mean values of precipitation were analyzed in the four study regions (NA, MD, CA, and EA). Monthly LAI data were obtained by the maximum value synthesis method compositing the 8-day time step of the GLASS LAI dataset. The maximum value synthesis method has reduced directional reflectance and off-nadir viewing effects, minimizes sun-angle and shadow effects, and minimizes aerosol and water-vapor effects [84]. The correlation coefficients between them with monthly variation were used to characterize the lag responses of LAI to precipitation.
As shown in Figure 11, there were vegetation LAI lag responses of 2–4 months and 4–6 months to precipitation in the drylands of CA and MD. These results also explained why there were many fragmented white grid points distributed on the map of LAI in response to precipitation and soil moisture based on annual mean value data in the two regions. Compared with CA, the lag response of vegetation in MD to precipitation was more serious. However, there were no obvious vegetation LAI lag responses in the drylands of NA and EA.

3.3.3. Long-Term Vegetation LAI Changes under the Influence of Precipitation and Soil Moisture

To identify the main factors affecting regional vegetation LAI, the variation trends of precipitation, surface soil moisture, and deeper soil moisture in the four regions from 1981 to 2018 are shown in Figure 12. In the trends of regional precipitation, no significant trends were evident in the four regions. The regional surface soil moisture and deeper soil moisture in the drylands of CA (slope = −0.002, p < 0.05) and NA (slope = −0.006, p < 0.01; slope = −0.004, p < 0.05) showed significant downwards trends.
Meanwhile, a partial correlation analysis was performed to evaluate the relationship between the 38-year average LAI and precipitation, surface soil moisture, and deeper soil moisture in the places where LAI increasing trends were greater than the regional average and LAI decreased significantly (Figure 7). As shown in Table 3, drylands where LAI decreased significantly (slope < 0 per year) exhibited positive correlations (p < 0.001) between LAI and SMsurf and negative correlations (p < 0.001) between LAI and SMdeeper in NA, MD, and EA. The correlations between LAI and PRE exhibited positive correlations (p < 0.001) in NA, CA, and EA. However, drylands where LAI increasing trends were greater than the regional average (slope > 0.001 and 0.006 per year) exhibited positive correlations (p < 0.001) between LAI and SMsurf in all four regions and negative correlations (p < 0.001) between LAI and SMdeeper in NA, MD, and EA. The correlations between LAI and PRE were positive (p < 0.001) in all four regions.

4. Discussion

4.1. Validation and Spatial Differentiation of Dryland Vegetation Greening

Global vegetation greening has become a widely recognized scientific phenomenon, and previous studies have indicated that increases in vegetation growth are due to the ease of climatic constraints and fertilization effects of elevated CO2 concentrations [85,86,87]. Related studies on global vegetation greening trend tests based on sensed data estimated that vegetation in the middle latitudes of the Northern Hemisphere showed a significant increasing trend overall, but there were certain differences in space, and the areas with more vegetation increases were mainly concentrated in the southeastern US, northern India, Mediterranean Northern regions and southeastern China [88,89,90,91,92]. At the same time, in high-altitude areas such as the Qinghai–Tibet Plateau, energy restriction is obvious for vegetation, and water conditions are not the only condition limiting vegetation growth [77,93,94].
However, this study found that due to water stress exacerbated by serious drought, vegetation decreased significantly in the drylands of Eurasia, Inner Asia, and the southwestern United States, which was shown by previous findings [95,96,97]. The greening of dryland vegetation may need further validation.
In this paper, a linear regression method was used to verify the greening of dryland vegetation in the north temperate mid-latitudes from 1981 to 2018 and to describe the interregional and intraregional variation characteristics of LAI changes. The slope of the linear regression equation represented the vegetation change at the grid point. This study found that there was a significant increase at a rate of 0.002 per year in the northern temperate midlatitude drylands and significant trends of vegetation greening in the drylands of the Mediterranean, Central Asia, and East Asia. These results are consistent with previous findings of vegetation greening in dryland areas of the Mediterranean, the Middle East, Northern China, and Mongolia [98,99,100,101]. Compared to previous studies, this study shows the following novel results: (1) Under the same water constraint conditions, the greening tendency and degree of vegetation at high altitudes were greater than those at low altitudes in drylands in the north temperate mid-latitudes, and (2) the greening rate of dryland vegetation does not completely follow the gradient distribution of the aridity index.

4.2. Vegetation Changes Response to Precipitation and Soil Moisture with Evapotranspiration Involved

Evapotranspiration (ET) represents the change state of dryland vegetation to a certain extent. ET is one of the biggest data gaps in water management [102]; it plays an important role in dryland water and energy cycles with large spatial heterogeneity and accounts for 88% of precipitation [29,103,104]. In areas where grassland is widely distributed, especially in our study area (herbaceous vegetation mainly), intense drought limits the supply level of water resources, and vegetation is more sensitive to precipitation than other influencing factors, such as temperature. According to the PCA results in our study (Figure 9), LAI, PRE, and ET are closely correlated on PC1. The transpiration/evapotranspiration (T/ET) values of natural ecosystems could be up to 0.85 in drylands. In long time-series statistics, evaporation and transpiration in dryland ecosystems were equivalents [105]. The mean transpiration rate is directly linked to the productivity of ecosystems from the vegetation point of view [106].
Evapotranspiration is an important part of heat flux and water exchange between the soil and atmosphere, and it is also one of the processes in which vegetation participates in the carbon budget of the global ecosystem. Shallow soil moisture (0–20 cm) can be rapidly lost by evaporation during dry periods [107]; however, it is an important water source for shallow-rooted herbaceous plants [108,109]. Deep soil moisture (20–60 cm) is primarily used for transpiration [110,111,112] for deeper-rooted woody plants. In our study, vegetation LAI’s strong responses to surface soil moisture content were closely related to years of rain, but the negative correlation between long-term vegetation LAI changes and deeper soil moisture showed that in drylands, in addition to the evaporation of surface soil moisture dissipation, deeper soil water in shallow roots is not used by vegetation. Deeper soil water drainage to deeper soil results in soil water drought [113,114]. Because of the hydraulic uplift of vegetation roots, the moisture of deeper soil moisture is reduced by some deep roots absorbing water from deeper soil layers and then releasing soil water into shallower soil by shallower vegetation roots in arid habitats [115,116,117,118]. The greening of dryland vegetation has resulted in excessive consumption of soil water resources and the formation of dry soil layers [119].
It is worth noting that increased TMP and PET, coupled with no significant change in precipitation, may increase the severity of dryland drought in the mid-latitudes of the North temperate zone as a manifestation of dryland expansion. Even if there were declines in individual years, the continuous rises of the multiyear mean temperature in the study area were the concentrated embodiment of global warming in local regional temperature changes.

4.3. Implications and Limitations

In this study, the trend of vegetation greening and its response to precipitation and soil water in the north temperate mid-latitudes were analyzed. The work is conducted without considering surface runoff and groundwater recharge [120,121,122,123].
Meanwhile, vegetation greening is a combination of a warming climate and human activities. Anthropogenic activities, such as fire [75,124,125], grazing and afforestation [92,126,127], also influence vegetation changes in the regions. Under the influence of climate change and human activities, we will continue to explore the effects of vegetation dryland vegetation greening on the hydrological cycle with groundwater and surface water participation in the future.

5. Conclusions

This study reveals the trends of dryland vegetation growth and its response to precipitation and soil moisture in the north temperate mid-latitudes from 1981 to 2018 under global warming. The average TMP, PET, and LAI increased at 0.04 °C, 1.53 mm and 0.002 per year from 1981 to 2018 in the study area, respectively. Dryland vegetation in the study area has a certain spatial heterogeneity in spatial distribution and variation trend and has a high response to precipitation and soil moisture. LAI grew faster in the eastern dryland of NA, dryland along the Mediterranean Sea, southeastern dryland of CA, and southeastern dryland of EA. There is a strong relationship between vegetation growth and regional water supply patterns. The regions with strong correlations between LAI and PRE, SMsurf and SMdeeper were located in the eastern and southwestern drylands of NA, the western dryland of MD, the southern drylands of CA, and the eastern drylands of EA. Our results are helpful for understanding vegetation dynamics in the drylands of northern temperate mid-latitudes and may play an important guiding role in vegetation protection against the background of global warming.

Author Contributions

Formal analysis, Z.Y.; investigation, Z.Y.; writing—original draft, Z.Y. and P.W.; conceptualization, T.W. and P.W.; data curation, Z.Y.; writing—review and editing, T.W. and J.Y.; funding acquisition, P.W. and J.Y.; methodology, T.W.; validation, T.W.; supervision, P.W. and J.Y.; software, T.W. All authors have read and agreed to the published version of the manuscript.

Funding

This study was funded by grants from the National Natural Science Foundation of China (NSFC) (Nos. 42071042 and 41877165), the Natural Science Foundation of Henan (No. 222300420327) and the Key Research Projects of Henan Higher Education Institutions (No. 22A170020).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.

Acknowledgments

The authors are grateful to our colleagues Shangyu Shi, Shiqi Liu, and Qiwei Huang for their advice. The authors gratefully acknowledge Dragana Panic, the anonymous associate editor, and two anonymous reviewers for their valuable comments and suggestions, which have led to substantial improvements over an earlier version of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A

Table
Table A1. Vegetation classification in the study area.
Table A1. Vegetation classification in the study area.
Vegetation BiomesFeatures (Vegetation Cover)Vegetation DistributionReclassified Vegetation Types
WoodyHerbaceous
Evergreen Needleleaf Forests>60%-forestlandWoody vegetation
Evergreen Broadleaf Forests>60%-
Deciduous Needleleaf Forests>60%-
Deciduous Broadleaf Forests>60%-
Mixed Forests>60%-
Closed Shrublands>60%-shrubland
Open Shrublands10–60%-
Woody Savannas30–60%-
Savannas10–30%DominatedgrasslandHerbaceous vegetation
Grasslands-Dominated
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Figure A1. Distributions of herbaceous and woody vegetation.
Figure A1. Distributions of herbaceous and woody vegetation.
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Figure A2. Distributions of the sampling points.
Figure A2. Distributions of the sampling points.
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Figure A3. Spatial variation in vegetation LAI across the study area.
Figure A3. Spatial variation in vegetation LAI across the study area.
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Figure A4. Temporal variation trends and anomalies of GLASS, GIMMS and GLOBAMAP LAI (**, p < 0.01; ***, p < 0.001).
Figure A4. Temporal variation trends and anomalies of GLASS, GIMMS and GLOBAMAP LAI (**, p < 0.01; ***, p < 0.001).
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Figure A5. Relationship between the LAI and surface soil moisture from 1981 to 2018 (p < 0.05) in (a) North America, (b) Mediterranean region, (c) Central Asia, and (d) East Asia.
Figure A5. Relationship between the LAI and surface soil moisture from 1981 to 2018 (p < 0.05) in (a) North America, (b) Mediterranean region, (c) Central Asia, and (d) East Asia.
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Figure A6. Relationship between the LAI and deeper soil moisture from 1981 to 2018 (p < 0.05) in (a) North America, (b) Mediterranean region, (c) Central Asia, and (d) East Asia.
Figure A6. Relationship between the LAI and deeper soil moisture from 1981 to 2018 (p < 0.05) in (a) North America, (b) Mediterranean region, (c) Central Asia, and (d) East Asia.
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Figure 1. Distribution map of the drylands between 30 and 50°N.
Figure 1. Distribution map of the drylands between 30 and 50°N.
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Figure 2. Elevation in the drylands between 30 and 50°N.
Figure 2. Elevation in the drylands between 30 and 50°N.
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Figure 3. Spatial distribution of the average annual temperature (TMP) (a), potential evapotranspiration (PET) (b), and precipitation (PRE) (c) over the study area from 1981 to 2018.
Figure 3. Spatial distribution of the average annual temperature (TMP) (a), potential evapotranspiration (PET) (b), and precipitation (PRE) (c) over the study area from 1981 to 2018.
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Figure 4. Temporal variations in the average annual temperature (TMP) (a), potential evapotranspiration (PET) (b), and precipitation (PRE) (c) over the entire study area from 1981 to 2018 (*** p < 0.001).
Figure 4. Temporal variations in the average annual temperature (TMP) (a), potential evapotranspiration (PET) (b), and precipitation (PRE) (c) over the entire study area from 1981 to 2018 (*** p < 0.001).
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Figure 5. Temporal trends of the average annual temperature (TMP) (a), potential evapotranspiration (PET) (b), and precipitation (PRE) (c) at vegetation distribution grid points from 1981 to 2018.
Figure 5. Temporal trends of the average annual temperature (TMP) (a), potential evapotranspiration (PET) (b), and precipitation (PRE) (c) at vegetation distribution grid points from 1981 to 2018.
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Figure 6. Temporal variation trends of the leaf area index (LAI) over the entire study area from 1981 to 2018 (** p < 0.01; *** p < 0.001).
Figure 6. Temporal variation trends of the leaf area index (LAI) over the entire study area from 1981 to 2018 (** p < 0.01; *** p < 0.001).
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Figure 7. Temporal variation trends of LAI in four regions from 1981 to 2018 (** p < 0.01; *** p < 0.001).
Figure 7. Temporal variation trends of LAI in four regions from 1981 to 2018 (** p < 0.01; *** p < 0.001).
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Figure 8. Spatial distribution of the change trends (p < 0.05) of vegetation LAI over four regions (a) North America, (b) Mediterranean region, (c) Central Asia, and (d) East Asia from 1981 to 2018.
Figure 8. Spatial distribution of the change trends (p < 0.05) of vegetation LAI over four regions (a) North America, (b) Mediterranean region, (c) Central Asia, and (d) East Asia from 1981 to 2018.
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Figure 9. Relationship between the LAI and effect variables based on PCA.
Figure 9. Relationship between the LAI and effect variables based on PCA.
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Figure 10. Relationship between the LAI and PRE from 1981 to 2018 (p < 0.05) (a) North America, (b) Mediterranean region, (c) Central Asia, and (d) East Asia.
Figure 10. Relationship between the LAI and PRE from 1981 to 2018 (p < 0.05) (a) North America, (b) Mediterranean region, (c) Central Asia, and (d) East Asia.
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Figure 11. Temporal variation lag effect of precipitation on vegetation LAI in four study regions: (a) North America, (b) Mediterranean region, (c) Central Asia, and (d) East Asia.
Figure 11. Temporal variation lag effect of precipitation on vegetation LAI in four study regions: (a) North America, (b) Mediterranean region, (c) Central Asia, and (d) East Asia.
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Figure 12. Temporal variation trends of precipitation, surface soil moisture and deeper soil moisture over four regions from 1981 to 2018 (* p < 0.05; ** p < 0.01).
Figure 12. Temporal variation trends of precipitation, surface soil moisture and deeper soil moisture over four regions from 1981 to 2018 (* p < 0.05; ** p < 0.01).
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Table
Table 1. Statistical results of the LAI change trend in the four regions.
Table 1. Statistical results of the LAI change trend in the four regions.
RegionTrend Ratio (%)
SignificantInsignificant
IncreasingDecreasing
NA27.5710.1962.24
MD56.232.3741.40
CA27.964.6467.40
EA23.9411.7064.36
ALL31.547.9660.51
Table
Table 2. Pearson coefficients for the relationships between the LAI and PRE, SMsurf, and SMdeeper in the four regions.
Table 2. Pearson coefficients for the relationships between the LAI and PRE, SMsurf, and SMdeeper in the four regions.
RelationshipRegionsCorrelation Ratio (%)
SignificantInsignificant
PositiveNegative
LAI and PRENA33.501.4465.06
MD12.950.2586.80
CA21.380.2678.35
EA34.490.4465.07
ALL27.510.7471.75
LAI and SMsurfNA38.131.9959.88
MD19.552.3778.08
CA22.790.3576.86
EA33.331.1565.51
ALL30.381.4868.15
LAI and SMdeeperNA38.242.0559.71
MD18.432.6278.95
CA24.980.4474.58
EA31.830.8967.29
ALL30.401.5068.11
Table
Table 3. Partial correlation coefficient between LAI and precipitation, surface soil moisture, and deeper soil moisture (*, p < 0.05; ***, p < 0.001).
Table 3. Partial correlation coefficient between LAI and precipitation, surface soil moisture, and deeper soil moisture (*, p < 0.05; ***, p < 0.001).
RegionsLAI TrendsSMsurfSMdeeperPRE
NA<0 yr−10.49 ***−0.44 ***0.57 ***
>0.001 yr−10.35 ***−0.35 ***0.71 ***
MD<0 yr−10.61 ***−0.61 ***0.43
>0.006 yr−10.48 ***−0.47 ***0.38 ***
CA<0 yr−1−0.180.230.77 ***
>0.001 yr−10.13 *−0.100.55 ***
EA<0 yr−10.50 ***−0.51 ***0.65 ***
>0.001 yr−10.35 ***−0.29 ***0.26 ***
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Yu, Z.; Wang, T.; Wang, P.; Yu, J. The Spatiotemporal Response of Vegetation Changes to Precipitation and Soil Moisture in Drylands in the North Temperate Mid-Latitudes. Remote Sens. 2022, 14, 3511. https://doi.org/10.3390/rs14153511

AMA Style

Yu Z, Wang T, Wang P, Yu J. The Spatiotemporal Response of Vegetation Changes to Precipitation and Soil Moisture in Drylands in the North Temperate Mid-Latitudes. Remote Sensing. 2022; 14(15):3511. https://doi.org/10.3390/rs14153511

Chicago/Turabian Style

Yu, Zongxu, Tianye Wang, Ping Wang, and Jingjie Yu. 2022. "The Spatiotemporal Response of Vegetation Changes to Precipitation and Soil Moisture in Drylands in the North Temperate Mid-Latitudes" Remote Sensing 14, no. 15: 3511. https://doi.org/10.3390/rs14153511

APA Style

Yu, Z., Wang, T., Wang, P., & Yu, J. (2022). The Spatiotemporal Response of Vegetation Changes to Precipitation and Soil Moisture in Drylands in the North Temperate Mid-Latitudes. Remote Sensing, 14(15), 3511. https://doi.org/10.3390/rs14153511

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