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Climate-induced changes in the vegetation pattern of China in the 21st century

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  • National Climate Center, CMA

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Quantifying climate-induced changes in vegetation patterns is essential to understanding land–climate interactions and ecosystem changes. In the present study, we estimated various distributional changes of vegetation under different climate-change scenarios in the 21st century. Both hypothetical scenarios and Hedley RCM scenarios show that the transitional vegetation types, such as shrubland and grassland, have higher sensitivity to climatic change compared to vegetation under extreme climatic conditions, such as the evergreen broadleaf forest or desert, barren lands. Mainly, the sensitive areas in China lie in the Tibetan Plateau, Yunnan-Guizhou Plateau, northeastern plain of China and eco-zones between different vegetations. As the temperature increases, mixed forests and deciduous broadleaf forests will shift towards northern China. Grassland, shrubland and wooded grassland will extend to southeastern China. The RCM-project climate changes generally have caused positive vegetation changes; vegetation cover will probably improve 19% relative to baseline, and the forest will expand to 8% relative to baseline, while the desert and bare ground will reduce by about 13%.
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SPECIAL ISSUE
Li Yu ÆMingkui Cao ÆKerang Li
Climate-induced changes in the vegetation pattern of China
in the 21st century
Received: 4 February 2006 / Accepted: 10 August 2006 / Published online: 3 November 2006
ÓThe Ecological Society of Japan 2006
Abstract Quantifying climate-induced changes in vege-
tation patterns is essential to understanding land–cli-
mate interactions and ecosystem changes. In the present
study, we estimated various distributional changes of
vegetation under different climate-change scenarios in
the 21st century. Both hypothetical scenarios and Hed-
ley RCM scenarios show that the transitional vegetation
types, such as shrubland and grassland, have higher
sensitivity to climatic change compared to vegetation
under extreme climatic conditions, such as the evergreen
broadleaf forest or desert, barren lands. Mainly, the
sensitive areas in China lie in the Tibetan Plateau,
Yunnan-Guizhou Plateau, northeastern plain of China
and eco-zones between different vegetations. As the
temperature increases, mixed forests and deciduous
broadleaf forests will shift towards northern China.
Grassland, shrubland and wooded grassland will extend
to southeastern China. The RCM-project climate
changes generally have caused positive vegetation
changes; vegetation cover will probably improve 19%
relative to baseline, and the forest will expand to 8%
relative to baseline, while the desert and bare ground will
reduce by about 13%.
Keywords Climate change ÆVegetation pattern Æ
China Æ21st century
Introduction
Vegetation cover is an important factor in ecosystem
processes, such as water balance, energy exchanges,
nutrients and carbon cycles, and reacts strongly to cli-
mate change (Betts et al. 1997). The vegetation–climate
interaction in the changing global climate is one of the
most important issues in global change studies.
Compared to other counties, terrestrial ecosystems in
China will probably confront more risks to climate
change in the future because of its unique climatic
character and topography. Several models have assessed
the responses of vegetation and functions of ecosystems
based on bioclimatic classifications and processed-based
equilibrium terrestrial biosphere models (Alex and Pre-
ntice 1996; Bachelet et al. 2001; Neilson 1995; Smith
et al. 1992; Woodward 1995). Zhang used the Holdrige’s
life-zone scheme, which simulated the potential vegeta-
tion distribution and NPP pattern in China, as well as
analyzed the responses to climate change (Zhang et al.
1993). However, the Holdrige scheme as a statistical
approach has not been appreciated on the global scale
(Prentice et al. 1993; Chen et al. 2003; Yue et al. 2005).
Ni and Zhao used the BIOME3 and MAPSS models to
simulate the potential vegetation distribution and re-
sponses to climate change in China, respectively (Ni
et al. 2000; Zhao et al. 2002). They both simulated the
regime of the potential vegetation under baseline climate
and analyzed the responses of potential vegetation to
climate change; however, the two models were con-
nected with functions of ecosystems such as the NPP
or water useful efficient (WUE), so analyses for the
responses of potential vegetation were not the emphases
in their research. Gao and Yu based their work on a
regional dynamic vegetation model that simulated the
effects of climate change on potential vegetation distri-
bution (Gao et al. 2000). Vegetation distribution was
determined by spatiotemporal patterns of radiation
energy and available water resources in their model. As a
dynamic vegetation model, it considered the vegetation
Global changes in terrestrial ecosystems
L. Yu ÆM. Cao ÆK. Li
Institute of Geographic Sciences
and Natural Resources Research,
Chinese Academy of Sciences, Beijing,
People’s Republic of China
L. Yu (&)
National Climate Centre,
China Meteorological Administration,
Zhongguancun Nandajie 46#, Haidian,
Beijing 100081, People’s Republic of China
E-mail: yul@igsnrr.ac.cn
Tel.: +86-10-68408506
Fax: +86-10-68408758
Ecol Res (2006) 21: 912–919
DOI 10.1007/s11284-006-0042-8
migration rates, which were assumed to be proportional
to the gradient of green biomass. The dynamic vegeta-
tion model is an efficient tool that has reduced some of
the uncertainty about the responses of vegetation to
climate change. But in the early stages of development,
validating and capturing disturbance-related effects be-
come major challenges for the dynamic vegetation
models (Peng 2000). Different methods of climate–veg-
etation classifications and different sources of data, such
as plant function types, climatic data and soil data,
prevented the results from being comparable with each
other (Hurtt et al. 1998; Kittel et al. 1995). Table 1
compares several other studies. In general, based on the
existing research in China, the most explicit results are
that the transitional vegetation classes, like shrubs and
grasslands, are more sensitive to climate change than
other types of vegetation under extreme climatic condi-
tions. As for the general pole-ward shift of some forest
belts for specific vegetation types, each study had its own
views.
The present study was conducted to give a quantita-
tive analysis of the changing directions of the vegetation
pattern in China due to climate change. We used a
process-based ecosystem model to estimate the vegeta-
tion distribution and its response to climate change in
the 21st century.
Methods
Description of the model
To quantify climate-induced changes in vegetation dis-
tribution, we used the carbon exchange between vege-
tation, soil and the atmosphere (CEVSA) model that has
a vegetation module to describe vegetation distribution
and the corresponding primary productivity, carbon
stocks in biomass and litter production (Cao and
Woodward 1998a,b). In the model, mean temperatures
of the coldest and warmest month, growing degree days
above 0 and 5°C, and the annual soil moisture index (h)
are used to determine the vegetation types. The cold
tolerance of plant types determined by the minimum
mean temperature of the coldest month, the heat
requirement of plant types determined by annual accu-
mulated temperature over 0 or 5°C, and the wet index
indicated the water condition of the environment, which
determined the phenology of vegetation. A soil moisture
index (h), accounting for the extent of drought, is de-
fined as (Prentice et al. 1993):
h¼AET
D:
According to the concept of equilibrium evapo-
transpiration (Jarvis et al. 1986), evaporative demand D
is thus determined by the energy supply, i.e., the surface
net radiation.
The parameters determining distribution for different
vegetation types in our model are shown in Table 2as
follows. The other parameters in the CEVSA model are
detailed by Cao and Woodward (1998a,b). In China, for
the effects of monsoon and terrain, the character of
climate and vegetation differed from any other areas in
the world; it induced the unique distribution of vegeta-
tion. Consequently, the thresholds of climatic factors are
different from other regions (Ni et al. 2000; Zhao et al.
2002).
Data
The set of independent environmental variables needed
to run the CEVSA model consists of: temperature,
precipitation, cloudiness, relative humidity, soil texture
and atmospheric CO
2
concentration. The climatic and
soil data sets grid at a resolution of 0.1°latitude and 0.1°
Table 1 Comparison to the three main research studies of potential vegetation responses to climate change in China
Ni (2000) Zhao et al. (2002) Gao et al. (2000)
Model BIOME3 MAPSS Regional vegetation dynamic model
Scenarios Hadley GCM Had CM2 Hypothetic scenarios
a
Vegetation type classes 18 11 20
b
Functions NPP WUE NPP
Vegetation change
Expanded vegetation type Tropical deciduous forest
Grasslands
Shrubland
Steppe and savannas
Subtropical needleleaf/broadleaf mixed
forest
Tropical broadleaf evergreen forest
Shrubland
Evergreen needleleaf forest
Gramineal grass and short shrubs
Evergreen broadleaf forests
Temperate evergreen conifer forests
Deciduous broadleaf forest
Shrunk vegetation type Desert alpine tundra
Ice/polar desert
Boreal deciduous forest
Boreal forest
Tundra
Grassland
Desert
Savannas
Subtropical conifer forests
Deciduous shrubs
Deciduous conifer forests
Gramineal steppes
a
CO
2
concentration 100%, 2°C in monthly mean temperature, and 20% in monthly precipitation
b
Including three agricultural types
913
longitude. The data on the contemporary climate are
derived from the data of about 730 weather stations of
the Chinese Meteorological Administration. The atmo-
spheric CO
2
concentration used for the contemporary
climate was downloaded from the website of Manualoa
Observation. Soil data including soil types and soil
texture came from a digital map of soil texture in China.
The vegetation classification in our model used the
method from Hansen (2000). Under the classification
system, we simplified the natural vegetation into 12
types, which are: evergreen needleleaf forest, evergreen
broadleaf forest, deciduous needleleaf forest, deciduous
broadleaf forest, mixed forest, woodland, wooded
grassland, closed shrubland, open shrubland, grassland,
desert and barren. To distinguish the conversion of
vegetation due to climate change, we reclassified the 12
vegetation types into 4 general vegetations, which are
forest (including woodland), shrubland (including open
shrubland and closed shrubland), grassland and desert
(including barren land). In our prediction, we assumed
that the C:N ratio of the vegetation biomass does not
vary with the change in climate.
Climate change scenarios
To simulate the response of vegetation to climate change
in the 21st century, we used two approaches to drive the
CEVSA model, hypothetical scenarios and RCM sce-
narios. Based on most GCMs’ results in China, we de-
signed the probable climate change scenarios to simulate
the response of natural vegetation. We ran the model
with four combinatorial scenarios of temperature and
precipitation change that denoted the probable change
of the future climate. In detail, the four scenarios of
climatic change were ±20% precipitation, 2 and 4°C
temperature increase by the baseline, expressed with
-P20T2,-P20T4,P20T2 and P20T4, respectively. We
also used Hadley RCM A2 scenario data of the Hadley
Climate Centre to drive the CEVSA model. It gave
equilibrium climate scenarios with a resolution of 50 km
by 50 km, interpolated to a 0.1°latitude/longitude data
grid by Anusplin software. Relative to the baseline
(1961–1990) climate, the annual mean temperature rose
about 4.4°C, and annual precipitation changed between
330 and 780 mm.
Results
Simulation potential vegetation distribution
The model was integrated for 1961–1990 average cli-
matic factors as the baseline for simulating the potential
vegetation distribution under the contemporary climate.
The results showed that evergreen broadleaf forests were
mainly distributed in areas throughout southern China,
and then converted to mixed forest. In our vegetation
classification, mixed forest included deciduous/evergreen
mixed forest and broadleaf/needleleaf forest. Besides the
southeast of China, there was also a distribution of
mixed forest in northeast China. Moreover, deciduous
needleleaf forests were also distributed in areas
throughout northernmost China. In central China, from
east to west, vegetation covers were deciduous broadleaf
forest, woodland, wooded grassland, shrubland and
grassland, respectively, all pfs that are vegetation tran-
sition zones in China. In southwest China, the vegeta-
tion cover mainly consists of evergreen needleleaf forest.
However, in the south edge of the Tibetan Plateau, the
vegetation cover was complex. The vegetation cover
included evergreen broadleaf forests and grasslands. In
the northwest of China, most areas are desert and barren
with patches of grasslands or shrublands. Mixed forest
has the highest percentage of all vegetation types, about
23%, while other forest types totaled 23%. Desert and
barren land totaled 14 and 17%, respectively. The per-
cent of grassland was 11%. Savanna and shrubland were
recorded at around 6 and 3%, respectively.
The preliminary validation of our results compared
well with the result of BIOME3 by Ni et al. (2000) and
the map of Chinese vegetation by Hou (1982). The
regime of natural vegetation simulated by our model was
mostly consistent with their results; all the vegetation
types were roughly captured by the model. But it should
be explained that these comparisons were not qualitative
or site-specific comparisons. In this paper, our objectives
were to show the relationship between the main climatic
factors and potential vegetation in China. Therefore, it
could be used to simulate the potential response of
vegetation induced by climate change (Fig. 1).
Vegetation changes under the hypothetic scenarios
of climate change by the end of the 21st century
Figure 2and Table 3show the potential vegetation
distributions and the type percents of vegetation under
the four scenarios. The general regimes of vegetation
have comparability to the baseline, but the areas of each
vegetation type are very different under different climate
conditions. In general, evergreen broadleaf forests will
expend in the south of China, but deciduous needleleaf
Table 2 Climatic parameters for potential vegetation types in the
CEVSA model
Vegetation definition T
min
(°C) GD5 (°C) Wet
index
Evergreen/deciduous 18 3,200–4,500/1,100 0.65
Needleaf/broadleaf 2.5 – 0.55
Forest 25.0 1,100 0.50
Shrub – 850 0.30
Grass – 650 0.08
Desert – 550
Barran – –
Note T
min
indicates minimum coldest month temperature; GD5
means accumulated temperature over 5°C
914
Fig. 1 The distribution of the
potential natural vegetation in
China simulated by the CEVSA
model
Fig. 2 Simulated distribution of vegetation in China under different hypothetic climatic scenarios
Table 3 The changed percent of vegetation types relative to baseline under the hypothetic scenarios
Vegetation types -P20T2 -P20T4 P20T2 P20T4
Evergreen needleleaf forest 10.3 1.3 30.3 50.9
Evergreen broadleaf forest 104.5 202.0 105.8 209.5
Deciduous needleleaf forest 55.4 67.3 38.5 48.2
Deciduous broadleaf forest 68.1 70.3 4.7 7.8
Mixed forest 42.0 71.3 15.2 45.2
Woodland 31.6 53.8 8.2 19.8
Wooded grassland 13.0 20.5 28.5 13.9
Closed shrubland 173.9 326.1 33.9 128.4
Open shrubland 155.4 176.3 116.0 124.0
Grassland 39.4 13.1 0.8 17.2
Desert 7.4 2.1 18.5 13.7
Barren 20.1 44.8 20.1 44.8
915
forest will shrink in the northeast of China due to tem-
perature increases. Shrubland will increase greatly and
barren land will decrease under the four climate change
scenarios.
The main shifts of vegetation due to precipitation
change take place between shrub and forest, grass and
shrub regardless of whether precipitation increases or
decreases. When precipitation increased, the shifts were
from shrubland to forest and from grassland to shrub-
land, which correlated with temperature increases. In
contrast, if precipitation decreased, the shifts were
mainly from forest to shrubland and from shrubland to
grassland.
Although the response of potential vegetation to
precipitation change and the shifts between vegetation
types were different than the response to temperature
change, the special regimes of sensitive areas to precip-
itation change resembled the temperature changes. Most
sensitive areas appeared in eco-transitions from forest to
grassland and occurred within the south brim of the
Tibetan Plateau. Correspondingly, precipitation de-
crease changed the regime of potential vegetation more
greatly than the effects of precipitation increase in Chi-
na.
The spatial changes of the four scenarios indicated
vegetation patterns that were high relative to precipita-
tion change (Figs. 3,4). Total areas affected were 40%
and almost 60% under two precipitation decrease sce-
narios. Moreover, the changed areas were 25 and 50%
under two precipitation increase scenarios, respectively.
In detail, under -P20T2 and -P20T4 scenarios, the most
change of vegetation occurred in forest shift to shrub-
land, shrubland to grassland and grassland to shrub-
land. In the north and northeast of China, most forest
will shift to shrubland. Original shrubland will shift
mostly to grassland. Vegetation cover on the Tibetan
Plateau will change dramatically. As a result, about 20%
of the precipitation will decrease and the temperature
will increase beyond 2°C of baseline, and forest areas
will decrease at least 16% under the baseline climate in
China. On the contrary, precipitation increase made a
more positive shift on vegetation, far more than the
negative shift. Forest areas will increase 43 and 52%
under the scenarios of P20T2 and P20T4 relative to the
forest areas of baseline. Besides some original shrubland
shift to forest, forest will be converted in the Tibetan
Plateau due to climate change. Profound changes in
grassland will also occur; most grassland will shift to
shrubland. From the four hypothetical scenarios, the
plains of north and northeast China were highly sensi-
tivity to precipitation change; the Tibetan Plateau and
eco-transition zones like shrubland were sensitive to
precipitation change and temperature change.
However, precipitation increase or decrease induced a
distinctness of vegetation regime, but the greatly chan-
ged areas were almost invariably to different climate
change scenarios. They mainly occured in the northeast
of China, the Tibetan Plateau, Yunnan-Guizhou Pla-
teau, transition areas of shrubland to grassland and
forest to shrubland. It indicated that the transitional
vegetation types, such as shrub and grassland, were
more sensitive to climate change than those under ex-
treme climate conditions, such as the evergreen broad-
leaf forest in the south of China and the deserts in the
northwest of China.
Fig. 3 The percent of vegetation under different hypothetic climatic
scenarios
Fig. 4 The shifts of vegetation relative to baseline under the
hypothetic scenarios
916
Vegetation changes under the Hadley RCM A2
scenarios by the end of the 21st century
Under the Hadley RCM A2 scenarios, evergreen
broadleaf forest became the dominant vegetation type
throughout most of southern China (Figs. 5,6). Ever-
green needleleaf forest increased in the southwest of
China, and most of the mixed forests and deciduous
broadleaf forests will spread throughout the northern
plain of China under the scenarios by the end of 21st
century. Relative to contemporary climate conditions,
evergreen forest will increase, especially evergreen
broadleaf forests. Deciduous forests and mixed forests
will also reduce, and deciduous needleleaf forests will
almost whither away completely in China. Shurbland
will increase, but grassland and desert will shrink to
some degree in the west of China, and barren land will
be reduced greatly. Vegetation cover will increase in the
Tibetan Plateau.
Under the climate of Hadley RCM A2 scenarios,
most vegetation types will change dramatically, but most
the change will be beneficial for vegetation cover. Most
shifts from grassland to shrubland will take place by the
end of 21st century; shrubland will shift to forest. The
negative shifts, i.e., shrublands to grasslands and forest
shift to shrubland, consisted of a small proportion of the
total vegetation change. The climate under Hadley
RCM A2 scenarios will enhance the cover of vegetation
in China. Forest areas will increase 58%, and the areas
of desert and bare ground will be reduced by about 32%
of their present areas (Table 4).
The main spatial change of vegetation occurred in the
Tibetan Plateau, Yun-Gui Plateau and the north and
northeastern plain of China under the Hadley RCM A2
Fig. 5 The spatial change of the vegetation regime relative to baseline under the hypothetical scenarios
Fig. 6 The distribution of
potential vegetation under
Hadley RCM A2 scenarios by
the end of the 21st century
917
scenarios, especially in the Tibetan Plateau. The results
indicated that these areas will have profound changes
according to the climate change and that current eco-
systems will be highly sensitive to climate change in the
future (Figs. 7,8,9). In some western areas of China,
climate change will improve the environmental condi-
tion, especially moist conditions, and vegetation cover
will increase in those areas. As a whole, climate condi-
tions will probably yield positive effects on the natural
vegetation in China without other disturbances. Total
vegetation cover increased about 19% under Hadley
RCM A2 scenarios relative to baseline.
Conclusions
We used the CEVSA model to quantify climate-induced
changes in vegetation distribution. Both the hypothetical
scenarios and the Hedley RCM scenarios showed that
the transitional vegetation ecosystems, such as shrub-
land and grassland, were more sensitive to climate
changes than other vegetation types under extreme cli-
matic conditions, such as the evergreen broadleaf forest
in the south of China and the desert and barren land in
the northwest of China. Main sensitive areas in China
are the Tibetan Plateau, Yunnan-Guizhou Plateau, the
northeastern plain of China, and those eco-zones be-
tween different ecosystems. Based on Hadley RCM
scenarios, by the end of the 21st century, vegetation
cover will probably improve in China, especially in the
Tibetan Plateau and some western areas of China, not
including other unforeseen disturbances. Forest areas
will increase by 8%, and desert and bare ground will
reduce by 13% of baseline. The total vegetation cover
will increase by 19% relative to the baseline climate. For
temperature increases, mixed forest and deciduous
broadleaf forest will shift towards northern China.
Grassland, shrubland and wooded grassland will extend
in the southeast of China.
Discussion
Our object for this paper is to analyze the effects induced
by climate change on the vegetation pattern. In fact,
different vegetation types have different time lags in
Table 4 The changed percent of vegetation types relative to base-
line under Hadley RCM A2 scenarios
Vegetation type Baseline Hadley RCM A2 Changed
Evergreen needleleaf forest 5.99 9.422 57.30
Evergreen broadleaf forest 8.288 25.371 206.12
Deciduous needleleaf forest 2.969 0.94 68.34
Deciduous broadleaf forest 4.612 5.569 20.75
Mixed forest 23.093 12.421 46.21
Woodland 1.282 1.511 17.86
Wooded grassland 6.463 5.815 10.03
Closed shrubland 2.839 10.603 273.48
Open shrubland 0.624 0.827 32.53
Grassland 11.971 8.756 26.86
Desert 14.084 9.184 34.79
Barren 17.783 9.583 46.11
0102030
1
2
3
4
5
6
7
10
9
8
11
12
Vegetation types
%
HadleyRCM
Baseline
Fig. 7 The percent of vegetation relative to baseline under Hadley
RCM A2 scenarios
Fig. 8 The shifts of vegetation relative to baseline under Hadley
RCM A2 scenarios
918
response to climate change and face varied kinds of
disturbances. The relationship between vegetation and
climate was not in equilibrium most of the time, so this
approach must include some uncertainties. However,
our analysis should still connect with the mechanics of
ecosystems and vegetation dynamics. Our work is a
primarily tentative approach to simulate the responses
of vegetation to climate change based on the relationship
between climate and vegetation, as well as to gain a
general comprehension of responses of potential vege-
tation to climate change in China.
Acknowledgments This research was supported by the Chinese
National Science Foundation.
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Fig. 9 The spatial change of
vegetation pattern under
Hadley RCM A2 scenarios
919
... Similarly, the largest overall changes were also observed within these two ecoregions with a few exceptions. These exceptions were located within the Manchu-Japanese Mixed Forest and the Tibetan Cold-winter deserts which are not only located within highly disturbed biomes, but are also in some of the most vulnerable regions in China's Northeast and on the Tibetan Plateau [36,49,50]. ...
... The largest overall changes observed were losses in tree cover (338.4 km 2 ) and grasslands (290.2 km 2 ), and an overall gain for flooded shrub or herbaceous cover (317.0 km 2 ). Of all the changes observed, many were concentrated in some of the most disturbed biomes and vulnerable regions within China [42,49,50]. The biomed with some of the largest changes include the Mongolian-Manchurian Steppe (temperate grasslands) and the Oriental Deciduous Forest (temperate broad-leaf forests). ...
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... The expansion ratio of suitable areas ranges between 13.79% to 32.13% and 15.11% to 34.44% according to the SSPs 245 and SSPs 585 scenario, respectively. Many studies predict that suitable distribution regions for different species will be created due to the global climate change effect (Yu et al. 2006;Varol et al. 2021Varol et al. , 2022b. This change actually means that the distribution regions suitable for some tree species will turn into suitable distribution regions for other plant species (Dyderski et al. 2018;Cantürk and Kulaç 2021;Fyllas et al. 2022). ...
... This change actually means that the distribution regions suitable for some tree species will turn into suitable distribution regions for other plant species (Dyderski et al. 2018;Cantürk and Kulaç 2021;Fyllas et al. 2022). For example, broad-leaved deciduous and mixed forests are predicted to expand towards the north of China (Yu et al. 2006). Dyderski et al. (2018) state that while the distribution ranges of Fraxinus excelsior, Fagus sylvatica, Quercus petraea, Abies alba, and Quercus robur are expanding, there will be a narrowing in the distribution regions of Pinus sylvestris, Larix decidua, Betula pendula, and Picea abies. ...
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Global climate change poses significant threats to ecosystems worldwide, particularly impacting long-lived forest tree species such as Pinus nigra. This study assessed the potential shifts in distribution areas for Pinus nigra, an important tree species, one highly vulnerable to global climate change, given its prevalence in continental climates, in Türkiye under different climate scenarios (SSPs 585 and 245). In this study, suitable distribution regions of Pinus nigra were evaluated based on SSPs 585 and SSPs 245 using nine different models. Results indicated potential losses in Pinus nigra distribution areas ranging from 15.0% to 43.5% (SSPs 245) and 19.7% to 48.9% (SSPs 585) by 2100. However, in 2100, new suitable distribution areas are expected to be formed at rates ranging from 13.8% to 32.1% and 15.1% to 34.4% according to the above scenarios. Because most of the newly formed suitable distribution regions are quite far from the areas where the species currently spreads, it seems necessary to provide the migration mechanism needed by the species by humans to prevent population losses in this process.
... The growth and spatial distribution pattern of the vegetation are affected by climatic conditions (temperature, radiation, precipitation, carbon dioxide and so on) [31][32][33][34][35][36], geographical environment (mountains and plains) [37][38][39][40][41] and human activities (grazing, fire, etc) [42][43][44][45][46]. It is reasonable to infer that climatic conditions have great influence on the vegetation pattern, which is verified as early as 2006 by Yu et al. [32]. ...
... The growth and spatial distribution pattern of the vegetation are affected by climatic conditions (temperature, radiation, precipitation, carbon dioxide and so on) [31][32][33][34][35][36], geographical environment (mountains and plains) [37][38][39][40][41] and human activities (grazing, fire, etc) [42][43][44][45][46]. It is reasonable to infer that climatic conditions have great influence on the vegetation pattern, which is verified as early as 2006 by Yu et al. [32]. Specifically, transitional vegetation types (such as shrubs and grasslands) are more vulnerable to climate change under the Hedley RCM climate situation, and similar distribution patterns can spread to other regions. ...
Article
Climate change has become increasingly severe, threatening ecosystem stability and, in particular, biodiversity. As a typical indicator of ecosystem evolution, vegetation growth is inevitably affected by climate change, and therefore has a great potential to provide valuable information for addressing such ecosystem problems. However, the impacts of climate change on vegetation growth, especially the spatial and temporal distribution of vegetation, are still lacking of comprehensive exposition. To this end, this review systematically reveals the influences of climate change on vegetation dynamics in both time and space by dynamical modelling the interactions of meteorological elements and vegetation growth. Moreover, we characterize the long-term evolution trend of vegetation growth under climate change in some typical regions based on data analysis. This work is expected to lay a necessary foundation for systematically revealing the coupling effect of climate change on the ecosystem.
... Several studies have suggested that climate change directly impacts vegetation and conversely, changes in vegetation can significantly affect climate change (Simeng, Qihang, and Chang 2021). Vegetation dynamics are sensitive to climate change, making them an important aspect of global change studies (Li et al. 2006;Wu et al. 2021). Moreover, nutrient cycles and microbial and physiological activities of vegetation can be affected by the changing patterns of climate and weather variables. ...
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Saudi Arabia has one of the greatest water shortages and the least vegetation in the world, which is potentially exacerbating the issue of environmental impacts. Therefore, it is crucial to understand the interaction between climate change, vegetation dynamics and land surface temperature (LST). The present study investigates the spatio‐temporal distributions, variations, change detection and trends of vegetation dynamics and surface temperature over eight agricultural sites in Saudi Arabia using the Normalised Difference Vegetation Index (NDVI) and LST from Landsat 7 (Enhance Thematic Mapper Plus: ETM⁺) and Landsat 8 (operational land imager: OLI) measurements for the period 2010–2023. The study also examined the relationship between NDVI, LST and climate variables such as air temperature, rainfall, relative humidity and soil moisture. Results showed that an NDVI > 0.20 represents vegetation in Saudi Arabia. Higher values of NDVI were found in Baysh, Jazan province, compared to other agricultural sites. Significant annual and seasonal variations in NDVI were also observed across eight major agricultural sites in Saudi Arabia, attributable to the region's varying climate conditions. Vegetation expansion in 2023 exceeded that in 2014 in Buraydah (304.34 km²), Tabarjal (63.81 km²), Hail (33.20 km²), Al Qirw (22.53 km²) and Baysh (3.07 km²), while reductions were noted in Wadi Al Dawasir (274.58 km²), Tabuk (88.56 km²) and Al Ahsa (27.30 km²). The LST over soil and vegetated surfaces showed that vegetation notably reduced LST at Hail (3.14°C), Al Ahsa and Wadi Al Dawasir (5.43°C), Buraydah (4.53°C), Baysh (2.71°C), Al Qirw (5.17°C), Tabuk (6.24°C) and Tabarjal (3.13°C). The study found that NDVI, LST and climate variables are positively and negatively correlated, which indicates a significant impact of climate change on vegetation patterns. The findings of this study are highly relevant for informing agricultural and environmental policy development in Saudi Arabia, with a focus on enhancing vegetation cover, mitigating the impacts of rising temperatures and advancing sustainable agricultural practices to address the challenges posed by climate change.
... Overall, the distribution pattern suggests a nuanced relationship between Ipomoea species and rainfall, moisture, and temperature levels. These climatic factors are known to influence the growth and spatial distribution patterns of the species [87][88][89][90][91][92]. The prevalence of Ipomoea individuals in humid zones particularly underscores their affinity toward moisture-rich habitats. ...
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The wild relatives of crops play a critical role in enhancing agricultural resilience and sustainability by contributing valuable traits for crop improvement. Shifts in climatic conditions and human activities threaten plant genetic resources for food and agriculture (PGRFA), jeopardizing contributions to future food production and security. Studies and inventories of the extant agrobiodiversity, in terms of numbers and distribution patterns of species and their genetic diversity, are primordial for developing effective and comprehensive conservation strategies. We conducted an ecogeographic study on Ipomoea species and assessed their diversity, distribution, and ecological preferences across different topographic, altitudinal, geographical, and climatic gradients, at a total of 450 sites across Mauritius. Species distribution maps overlaid with climatic data highlighted specific ecological distribution. Principal Component Analysis (PCA) revealed species distribution was influenced by geographical factors. Regional richness analyses indicated varying densities, with some species exhibiting localized distributions and specific ecological preferences while the other species showed diverse distribution patterns. Field surveys identified 14 species and 2 subspecies out of 21 species and 2 subspecies of Ipomoea reported in Mauritius. A gap in ex situ germplasm collections was observed and several species were identified as threatened. Further investigations and a more long-term monitoring effort to better guide conservation decisions are proposed.
... The distribution pattern of vegetation on the Tibetan Plateau is changing due to global climate change. Several studies indicate that the climate of the Tibetan Plateau will experience significant warming during the periods of 2041-2060 and 2061-2080, and that a considerable amount of vegetation on the plateau will exhibit an inclination towards expansion [37,48,49]. The study reveals that C. gigantea possesses a broad ecological niche width and, consequently, exhibits a strong capacity to adapt to changes in climate conditions. ...
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Cupressus gigantea (C. gigantea) is an endemic endangered species on the Tibetan Plateau; its potential suitable areas and priority protection in the context of global climate change remain poorly predicted. This study utilized Biomod2 and Marxan to assess the potential suitable areas and priority protection for C. gigantea. Our study revealed that the suitable areas of C. gigantea were concentrated in the southeastern Tibetan Plateau, with the center in Lang County. Temperature was identified as a crucial environmental factor influencing the distribution of C. gigantea. Over the coming decades, the suitable range of C. gigantea expanded modestly, while its overall distribution remained relatively stable. Moreover, the center of the highly suitable areas tended to migrate towards Milin County in the northeast. Presently, significant areas for improvement are needed to establish protected areas for C. gigantea. The most feasible priority protected areas were located between the Lang and Milin counties in Tibet, which have more concentrated and undisturbed habitats. These results provide scientific guidance for the conservation and planning of C. gigantea, contributing to the stability and sustainability of ecosystems.
... By studying the internal mechanism of vegetation pattern formation, which can help us protect vegetation and prevent land desertification to a certain extent. We all know that there are many factors affecting the pattern structure of vegetation, including natural factors (such as rainfall, temperature, light and other climatic factors) and human factors (such as deforestation, grazing and so on) (Yu et al. 2006;Wang et al. 2017;Baldi et al. 2013;Giesecke et al. 2017;Dumont et al. 2012;Raharimalala et al. 2010). At present, most of our models are based on the influence of rainfall on vegetation pattern. ...
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Vegetation patterns with a variety of structures is amazing phenomena in arid or semi-arid areas, which can identify the evolution law of vegetation and are typical signals of ecosystem functions. Many achievements have been made in this respect, yet the mechanisms of uptake–diffusion feedback on the pattern structures of vegetation is not fully understood. To well reveal the influences of parameters perturbation on the pattern formation of vegetation, we give a comprehensive analysis on a vegetation–water model in the forms of reaction–diffusion equation which is posed by Zelnik et al. (Proc Natl Acad Sci 112:12,327–12,331, 2015). We obtain the exact parameters range for stationary patterns and show the dynamical behaviors near the bifurcation point based on nonlinear analysis. It is found that the model has the properties of spot, labyrinth and gap patterns. Moreover, water diffusion rate prohibits the growth of vegetation while shading parameter promotes the increase of vegetation biomass. Our results show that gradual transitions from uniform state to gap pattern can occur for suitable value of parameters which may induce the emergence of desertification.
... It was reported that the population losses might go beyond 25% for Carpinus betulus at the altitudes lower than 1600 m and 30% for Carpinus orientalis at the altitudes lower than 1000 m, that there would be increases in suitable distribution areas at high altitudes and this increase may exceed 100% for Carpinus orientalis at the altitudes of 1000-2000 m (Varol et al., 2022). In China, it is projected that mixed and broad-leaved non-evergreen forests might expand towards the north (Yu et al., 2006). ...
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Global climate change is considered an irreversible problem, which might directly or indirectly affect all the organisms and ecosystems on the earth and the world has to struggle with. Plants having no effective movement mechanism are the group that global climate change will affect the most. In order to minimize the species and population losses, it is important to estimate the changes in the available distribution areas of species and to ensure the migration mechanism, which the species will need, by the hand of humans. The present study aims to reveal how potential distribution areas of fir, which is among the significant tree species of Turkey and significant portion of global distribution of which is in Turkey, will change from an altitudinal aspect because of the climate change. The results achieved showed that, because of the effects of global climate change, the suitable distribution areas of Abies nordmanniana subsp. nordmanniana will significantly decrease especially at high altitudes and that suitable distribution areas of Abies nordmanniana subsp. equi-trojani will reduce at altitudes higher than 1400 m but increase generally at the altitudes between 200 and 600 m. Moreover, suitable distribution areas of Abies cilicica will shift towards higher altitudes.
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Vegetation cover is essential to the ecologic and biogeochemical functioning of drylands. These systems are marked by spatiotemporal variation in vegetation cover and biomass. Regular monitoring of vegetation cover in drylands is critical for their conservation and management. This study examines the effectiveness of photo-based grid point intercept field survey for quantifying vegetation characteristics in drylands. The field data provides ground truth data for space borne remote sensing to analyze changes in vegetation cover. The study integrates rapid field photo sampling, GPS, and GIS to maximize raw data collection in the field and allow for subsequent sampling in the laboratory setting. Paired T-tests and simple linear regression were employed to assess sample size. Quantification of vegetation cover using minimum distance (MD), spectral angle mapper (SAM), and support vector machine (SVM) automated classification were assessed using visual sampling as a reference. Fifty sampling points are sufficient for quantifying vegetation cover of steppe, but are less adequate for desert steppe. The assessment of automated classifications of photo plots revealed that SAM outperformed both MD and SVM. Photo-based Grid-point Intercept provides a cost- and time-effective technique for data collection to support satellite and air platform remote sensing analysis of vegetation dynamics.
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This paper on reports the production of a 1 km spatial resolution land cover classification using data for 1992-1993 from the Advanced Very High Resolution Radiometer (AVHRR). This map will be included as an at-launch product of the Moderate Resolution Imaging Spectroradiometer (MODIS) to serve as an input for several algorithms requiring knowledge of land cover type. The methodology was derived from a similar effort to create a product at 8 km spatial resolution, where high resolution data sets were interpreted in order to derive a coarse-resolution training data set. A set of 37 294 x 1 km pixels was used within a hierarchical tree structure to classify the AVHRR data into 12 classes. The approach taken involved a hierarchy of pair-wise class trees where a logic based on vegetation form was applied until all classes were depicted. Multitemporal AVHRR metrics were used to predict class memberships. Minimum annual red reflectance, peak annual Normalized Difference Vegetation Index (NDVI), and minimum channel three brightness temperature were among the most used metrics. Depictions of forests and woodlands, and areas of mechanized agriculture are in general agreement with other sources of information, while classes such as low biomass agriculture and high-latitude broadleaf forest are not. Comparisons of the final product with regional digital land cover maps derived from high-resolution remotely sensed data reveal general agreement, except for apparently poor depictions of temperate pastures within areas of agriculture. Distinguishing between forest and non-forest was achieved with agreements ranging from 81 to 92% for these regional subsets. The agreements for all classes varied from an average of 65% when viewing all pixels to an average of 82% when viewing only those 1 km pixels consisting of greater than 90% one class within the high-resolution data sets.
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This chapter is a review on the modeling of the potential response of vegetation to global climate change.. Models provide a means of formalizing a set of assumptions/hypotheses linking pattern and process, allowing for extrapolation beyond the range of observed phenomena. The purpose of this chapter is not to provide an exhaustive review of models relating climate and plant pattern; rather it is to examine a specific set of models which are currently being used to investigate the question of plant response to climate change at a global scale. The focus is on developing a methodology for predicting changes in the large-scale distribution of vegetation (that is, global distribution of biomes or ecosystem complexes) under changing global climate patterns. This chapter starts with a discussion on climate–vegetation classification. The chapter focuses on the application of holdridge life-zone classification to climate change at a global scale, followed by the application of a plant energy balance model to predicting changes in leaf area under changing climate conditions. This is followed by the description of modeling temporal dynamics. Furthermore, this chapter introduces individual-based forest gap models. The chapter ends with the discussion of application of gap models to predict forest response to climate change.
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The Mapped Atmosphere-Plant-Soil System (MAPSS) model has been improved for simulating the potential vegetation distribution over China. Unlike North America, the environment in East China is largely controlled by the monsoon system, which affects the vegetation distribution differently than in North America. Furthermore, in MAPSS, the boreal forest is evergreen conifer, whereas in China it is largely deciduous conifer. To make the MAPSS results more suitable over China, we modified the lowest monthly temperature, which determines the northward boundary of temperate deciduous forest from -16° to -28°C. In addition, the minimum monthly rainfall during the growing season, which is used to judge broad-leaved-deciduous from evergreen need-leleaved forest, was changed from 40mm to 20mm. Other parameters related to rainfall patterns were also changed. The results were greatly improved, when compared to the map of Chinese vegetation zonation and more than 12 years of satellite data (NDVI). Using output from the General Circulation Model, Had-CM2, for simulating possible future climate changes induced by enriched greenhouse gases (GHG) and sulfate aerosols (SUL), we simulated the possible future (2020s, 2050s) potential vegetation distribution modeled by MAPSS with and without consideration of CO2-induced water-use-efficiency (WUE) changes. The results show that in East China, forest boundaries could shift northward, especially the boreal deciduous conifer forest, which may disappear from China. In the North China, and Liaohe river drainage area, forests and savannas could be replaced by grasslands.
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A Mapped Atmosphere-Plant-Soil System (MAPSS) has been constructed for simulating the potential biosphere impacts and biosphere-atmosphere feedbacks from climatic change. The system calculates the potential vegetation type and leaf area that could be supported at a site, within the constraints of the abiotic climate. Both woody vegetation and grass are supported and compete for light and water. The woody vegetation can be either trees or shrubs, evergreen or deciduous, and needleleaved or broadleaved. A complete site water balance is calculated and integrates the vegetation leaf area and stomatal conductance in canopy transpiration and soil hydrology. The MAPSS model accurately simulates the distributions of forests, grasslands, and deserts and reproduces observed monthly runoff. The model can be used for predictions of new vegetation distribution patterns, soil moisture, and runoff patterns in alternative climates.
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Publisher Summary The study of leaf anatomy and of the mechanisms of the opening and closing of stomatal guard cells leads one to suppose that the stomata constitute the main or even the sole regulating system in leaf transpiration. Meteorologists have developed a wide variety of formulae for estimating evaporation from vegetation that are based entirely on weather variables and take no account at all of the species composition or stomatal properties of the transpiring vegetation. These “potential evaporation” formulae are widely and, to a large degree, successfully used for estimating evaporation from vegetation that is not water-stressed. Transpiration depends on stomatal conductance, net radiation receipt and upon air saturation deficit, temperature, and wind speed. Saturation deficit and wind speed vary through leaf boundary layers, through canopies, and through the atmosphere above the canopies. The sensitivity of saturation deficit to changes in stomatal conductance depends on where the saturation deficit is measured. If all of the stomata on a single leaf change aperture in unison, there may be a substantial change in saturation deficit measured at the leaf surface but a negligible change in saturation deficit measured a centimetre or two away, outside the leaf boundary layer.
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A global primary productivity and phytogeography model is described. The model represents the biochemical processes of photosynthesis and the dependence of gas exchange on stomatal conductance, which in turn depends on temperature and soil moisture. Canopy conductance controls soil water loss by evapotranspiration. The assignment of nitrogen uptake to leaf layers is proportional to irradiance, and respiration and maximum assimilation rates depend on nitrogen uptake and temperature. Total nitrogen uptake is derived from soil carbon and nitrogen and depends on temperature. The long-term average annual carbon and hydrological budgets dictate canopy leaf area. Although observations constrain soil carbon and nitrogen, the distribution of vegetation types is not specified by an underlying map. Variables simulated by the model are compared to experimental results. These comparisons extend from biochemical processes to the whole canopy, and the comparisons are favorable for both current and elevated CO{sub 2} atmospheres. The model is used to simulate the global distributions of leaf area index and annual net primary productivity. These distributions are sufficiently realistic to demonstrate that the model is useful for analyzing vegetation responses to global environmental change. 116 refs., 11 figs.
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The equilibrium terrestrial biosphere model BIOME3 simulates vegetation distribution and biogeochemistry, and couples vegetation distribution directly to biogeochemistry. Model inputs consist of latitude, soil texture class, and monthly climate (temperature, precipitation, and sunshine) data on a 0.5° grid. Ecophysiological constraints determine which plant functional types (PFTs) may potentially occur. A coupled carbon and water flux model is then used to calculate, for each PFT, the leaf area index (LAI) that maximizes net primary production (NPP), subject to the constraint that NPP must be sufficient to maintain this LAI. Competition between PFTs is simulated by using the optimal NPP of each PFT as an index of competitiveness, with additional rules to approximate the dynamic equilibrium between natural disturbance and succession driven by light competition. Model output consists of a quantitative vegetation state description in terms of the dominant PFT, secondary PFTs present, and the total LAI and NPP for the ecosystem. Canopy conductance is treated as a function of the calculated optimal photosynthetic rate and water stress. Regional evapotranspiration is calculated as a function of canopy conductance, equilibrium evapotranspiration rate, and soil moisture using a simple planetary boundary layer parameterization. This scheme results in a two-way coupling of the carbon and water fluxes through canopy conductance, allowing simulation of the response of photosynthesis, stomatal conductance, and leaf area to environmental factors including atmospheric CO2. Comparison with the mapped distribution of global vegetation shows that the model successfully reproduces the broad-scale patterns in potential natural vegetation distribution. Comparison with NPP measurements, and with an FPAR (fractional absorbed photosynthetically active radiation) climatology based on remotely sensed greenness measurements, provides further checks on the model's internal logic. The model is envisaged as a tool for integrated analysis of the impacts of changes in climate and CO2 on ecosystem structure and function.
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A model to predict global patterns in vegetation physiognomy was developed from physiological considerations influencing the distributions of different functional types of plant. Primary driving variables are mean coldest-month temperature, annual accumulated temperature over 5-degrees-C, and a drought index incorporating the seasonality of precipitation and the available water capacity of the soil. The model predicts which plant types can occur in a given environment, and selects the potentially dominant types from among them. Biomes arise as combinations of dominant types. Global environmental data were supplied as monthly means of temperature, precipitation and sunshine (interpolated to a global 0.5-degrees grid, with a lapse-rate correction) and soil texture class. The resulting predictions of global vegetation patterns were in good agreement with the mapped distribution of actual ecosystem complexes (Olson, J.S., Watts, J.A. & Allison, L.J. (1983) ORNL-5862, Oak Ridge Nat. Lab., 164 pp.), except where intensive agriculture has obliterated the natural patterns. The model will help in assessing impacts of future climate changes on potential natural vegetation patterns, land-surface characteristics and terrestrial carbon storage, and in analysis of the effects of past climate change on these variables.