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Asia Chapter 24
24.4.2. Terrestrial and Inland Water Systems
24.4.2.1. Sub-regional Diversity
Boreal forests and grasslands dominate in North Asia, deserts and semi-
deserts in Central and West Asia, and alpine ecosystems on the Tibetan
Plateau. Human-dominated landscapes predominate in the other sub-
regions, but the major natural ecosystems are temperate deciduous and
subtropical evergreen forests in East Asia, with boreal forest in the
northeast and grasslands and deserts in the west, while Southeast Asia
was largely covered in tropical forests. South Asia also has tropical
forests, with semi-desert in the northwest and alpine ecosystems in the
north. Asia includes several of the world’s largest river systems, as well
as the world’s deepest freshwater lake, Lake Baikal, the semi-saline
Caspian Sea, and the saline Aral Sea.
24.4.2.2. Observed Impacts
Biological changes consistent with climate trends have been reported in
the north and at high altitudes, where rising temperatures have relaxed
constraints on plant growth and the distributions of organisms. Few
changes have been reported from tropical lowlands and none linked to
climate change with high confidence, although data are insufficient to
distinguish lack of observations from lack of impacts. Impacts on inland
water systems have been difficult to disentangle from natural variability
and other human impacts (Bates et al., 2008; Vörösmarty et al., 2010;
Zheng, 2011; see Section 4.3.3.3). For example, the shrinking of the Aral
Sea over the last 50 years has resulted largely from excessive water
extraction from rivers, but was probably exacerbated by decreasing
precipitation and increasing temperature (Lioubimtseva and Henebry,
2009; Kostianoy and Kosarev, 2010).
24.4.2.2.1. Phenology and growth rates
In humid temperate East Asia, plant observations and satellite
measurements of “greenness” (Normalized Difference Vegetation Index
(NDVI); see Section 4.3.2.2) show a trend to earlier leafing in spring
since the 1980s, averaging 2 days per decade, although details vary
between sites, species, and periods (Table SM24-6; detected with high
confidence and attributed to warming with medium confidence). Earlier
spring flowering and delayed autumn senescence have also been
recorded (Table SM24-6). Trends in semiarid temperate regions were
heterogeneous in space and time (Liu et al., 2013a; Yu, Z. et al., 2013a,b).
Earlier greening has been reported from boreal forests (Delbart et al.,
2008) and from the Hindu-Kush-Himalayan region (Panday and Ghimire,
2012; Shrestha et al., 2012), but with spatial and temporal heterogeneity.
Patterns were also heterogeneous in Central Asia (Kariyeva et al., 2012).
On the Tibetan Plateau, spring growth advanced until the mid-1990s,
but the trend subsequently differs between areas and NDVI data sets
(Yu et al., 2010, 2012; Dong et al., 2013; Jin et al., 2013; Shen et al.,
2013; Yu, Z. et al., 2013a; Zhang, G. et al., 2013; Zhang, L. et al., 2013).
Satellite NDVI for Asia for 1988–2010 shows a general greening trend
(i.e., increasing NDVI, a rough proxy for increasing plant growth), except
where water is limiting (Dorigo et al., 2012). Changes at high latitudes
(
>60°N) show considerable spatial and temporal variability, despite a
consistent warming trend, reflecting water availability and non-climatic
factors (Bi et al., 2013; Jeong et al., 2013). Arctic tundra generally showed
increased greening since 1982, while boreal forests were variable (Goetz
et al., 2011; de Jong et al., 2012; Epstein et al., 2012; Xu et al., 2013).
An overall greening trend for 2000–2011 north of the boreal forest
correlated with increasing summer warmth and ice retreat (Dutrieux et
al., 2012). In China, trends have varied in space and time, reflecting
positive impacts of warming and negative impacts of increasing drought
stress (Peng et al., 2011; Sun et al., 2012; Xu et al., 2012). The steppe
region of northern Kazakhstan showed an overall browning (decreasing
NDVI) trend for 1982–2008, linked to declining precipitation (de Jong et
al., 2012). In Central Asia, where NDVI is most sensitive to precipitation
(Gessner et al., 2013), there was a heterogeneous pattern for 1982–
2009, with an initial greening trend stalled or reversed in some areas
(Mohammat et al., 2013).
Tree-ring data for 800–1989 for temperate East Asia suggests recent
summer temperatures have exceeded those during past warm periods
of similar length, although this difference was not statistically significant
(Cook et al., 2012). Where temperature limits tree growth, growth rates
have increased with warming in recent decades (Duan et al., 2010; Sano
et al., 2010; Shishov and Vaganov, 2010; Borgaonkar et al., 2011; Xu et
al., 2011; Chen et al., 2012a,b,c,d, 2013; Li et al., 2012), while where
drought limits growth, there have been increases (Li et al., 2006; Davi
et al., 2009; Shao et al., 2010; Yang et al., 2010) or decreases (Li et al.,
2007; Dulamsuren et al., 2010a, 2011; Kang et al., 2012; Wu et al., 2012;
Kharuk et al., 2013; Liu et al., 2013b), reflecting decreasing or increasing
water stress (high confidence in detection, medium confidence in
attribution to climate change). In boreal forest, trends varied between
species and locations, despite consistent warming (Lloyd and Bunn,
2007; Goetz et al., 2011).
24.4.2.2.2. Distributions of species and biomes
Changes in species distributions consistent with a response to warming
have been widely reported: upwards in elevation (Soja et al., 2007;
Bickford et al., 2010; Kharuk et al., 2010a,b,e; Moiseev et al., 2010; Chen
et al., 2011; Jump et al., 2012; Grigor’ev et al., 2013; Telwala et al., 2013)
or polewards (Tougou et al., 2009; Ogawa-Onishi and Berry, 2013) (high
confidence in detection, medium confidence in attribution to climate
change). Changes in the distributions of major vegetation types (biomes)
have been reported from the north and high altitudes, where trees are
invading treeless vegetation, and forest understories are being invaded
from adjacent biomes (Kharuk et al., 2006; Soja et al., 2007; Bai et al.,
2011; Singh et al., 2012; Wang and Liu, 2012). In central Siberia, dark
needle conifers (DNCs) and birch have invaded larch-dominated forest
over the last 3 decades (Kharuk et al., 2010c,d; Osawa et al., 2010; Lloyd
et al., 2011). Meanwhile, warming has driven larch stand crown closure
and larch invasion into tundra at a rate of 3 to 10 m yr
–1
in the northern
forest-tundra ecotone (Kharuk et al., 2006). Shrub expansion in arctic
tundra has also been observed (Blok et al., 2011; Myers-Smith et al.,
2011; see Section 28.2.3.1). Soil moisture and light are the main factors
governing the forest-steppe ecotone (Soja et al., 2007; Zeng et al., 2008;
Eichler et al., 2011; Kukavskaya et al., 2013), and Mongolian taiga
forests have responded heterogeneously to recent climate changes, but