e-flow-ch4
TRANSCRIPT
![Page 1: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/1.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 1/32
![Page 2: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/2.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 2/32
82 | Environme ntal Flows
both surface runoff and subsurface ow (including return ows) of precipitation and
snowmelt which are related to the climate. Humans have no direct control over the
climate but their activities have started affecting the climate and the climate change is now
projected to have signicant effects on the river ow regimes all over the Earth (Arnell et
al. 2001, Döll and Schmied 2012, Schneider et al. 2012). The impacts of climate change onriver ow in India have been examined by Rao (1993, 1995), Jha and Sharma (2008) and
Gosain et al. (2011). The amounts of precipitation entering the rivers is affected by various
human activities in their catchment and the effects of deforestation, plantation, agriculture,
urbanisation, and other land use changes have been investigated through many eld studies
as well as modeling techniques (e.g.; Negi 2002, Bruinzeel 2004, Brauman et al. 2007, Wei
et al. 2008, Cui et al. 2012, Ellison et al. 2012, Liu et al. 2012).
However, the single most important human intervention impacting the ow regimes
of the rivers is the construction of a physical barrier across the river bed with the primary
objective of preventing the ow downstream, partly or fully, so that it can be diverted
or stored for various other uses. These physical barriers range from a low weir to gated
barrages and mighty dams. Weirs are constructed to divert ow into a canal, and are usually
low in height so that some water continues to ow over the crest to downstream reaches
except during the very low ow period. Weirs are also constructed on small coastal streams
to prevent tidal ingress (such as along the coast in Gujarat) but the streams are turned from
their estuarine character into shallow freshwater reservoirs. Barrages are similar structures
with adjustable gates are installed over the weir to regulate the water surface at different
levels at different times. All barrages have a considerably large pondage (storage) that may
extend to several hundred meters behind them depending upon the gradient and the height
of the gates. In Maharashtra (India) there are also Kolhapuri Type weirs (KT Bandharas) which are provided with sluice gates right over the leveled river bed and therefore, do not
store any water when the gates are opened. Large dams store water of which a signicant
amount is a dead storage. They are provided with sluice gates at a higher level, usually
nearer the top of the dam, for releasing water when required. Some dams are provided with
a bottom outlet for ushing the sediments and releasing water from deep below the surface.
Generally, the water is abstracted by diversion at higher levels into canals.
Far more numerous dams have been constructed for the hydropower generation than
for other purposes and the discussions on instream ows (environmental ows) have had
their beginning in the impacts of these projects (see chapter 6). In South Asia also, the
hydroelectric power project (HEPs) have been at the centre of the debate on environmentalows. The hydropower plants are of different types: the diversion or run-of-the-river (RoR)
hydropower plants (with low or high heads, storage (or impoundment) hydropower plants
and pumped storage hydropower plants. All along the Himalayan belt, hundreds of the so-
called run-of-river hydropower plants are actually based on large storages that block the
river completely. Chamera I HEP is based on a 140 m high concrete dam on River Ravi.
The river ow from the reservoirs is diverted into head-race tunnels (HRTs) which carry
it to penstocks for delivery to the turbines and the release through tail race tunnels (TRT)
back into the same river (sometimes into another river) many kilometers downstream. The
![Page 3: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/3.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 3/32
Environm ental Flows | 83
reservoirs usually extend upstream to several kilometers, depending upon the height of the
dam and the gradient. The HEPs have often been developed (or are in different stages of
development) in cascades on the same river and its tributaries so close to each other that the
TRT of the upstream project opens just above the tail reach of the reservoir of downstream
project, thereby leaving no space for the river water to ow (Figures 1 to 3).
IMPACTS OF DAMS
The impacts of dams, particularly large dams, have been debated globally for many decades in
the context of the submergence of forest and agricultural lands and settlements, displacement
of people and the issues related to their rehabilitation, and economic development benets
(Goldsmith and Hildyard 1984, McCully 2001, Rangachari 2006). Until recently, the
ecological and environmental aspects, however, have attracted relatively little attention
because these impacts were not felt, experienced or observed immediately or in the short
term. The dams impact areas both upstream and downstream of their siting, and throughall stages of their development – before and during construction as well as through their
operation. The impacts of dams and other diversion structures depend upon the type, size
(storage capacity relative to the river ow; but also area and depth), mode of operation and
geographic location of the reservoir behind them. They invariably alter the ow regime – its
magnitude, duration, frequency, timing and ow velocity. The ow regime in turn affects
the physico-chemical characteristics of the habitat, the dynamics of sediment transport,
the river morphology, the connectivity with the oodplains and the biota. The continuity
and longitudinal connectivity of the river is disrupted. Various ecological/environmental
impacts of the dams have been discussed in several recent publications (McCartney et al.
2001, Robson et al. 2011). Here we examine briey only the impacts related to the alterationof the ow regime. These are divided into upstream and downstream impacts though some
upstream impacts have their inuence on the downstream environment as well. It must also
be appreciated that where a dam is constructed upstream of an existing dam, the reach of
the river below it has already been impacted upon by the existing dam’s upstream impacts.
New dams are also created some distance downstream of the TRT outfalls to utilise the water
released from an existing HEP for further power generation. The river stretch between the
two dams is thus affected by both the upstream impacts and the downstream impacts, and
may sometimes lose its riverine character completely.
Upstream ImpactsThe construction of a dam converts a section of the owing stream into a stagnant water
body. Depending upon the geographic location and height of the dam, the reservoirs vary
in shape (from linear in mountainous areas to dendritic in low gradient areas where several
tributaries are affected), shoreline to surface area ratio, and maximum and mean depths.
Three zones can usually be identied: a riverine zone where the owing conditions still
prevail, a transitional zone in the middle section, and a lacustrine zone closer to the dam
(Figure 4; Rast and Straskraba 2000). The abstraction of water determines the amplitude
and frequency of uctuations in the water level that result in the exposure of the littoral
![Page 4: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/4.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 4/32
84 | Environme ntal Flows
F
i g u r e 1 .
E x i s t i n g a n d p r o p o s e d h
y d r o p o w e r p r o j e c t s i n u p p e r r e a c h e s o f R .
G a n g a
( c o u r t e s y S A N D R P ,
N e w D e l h i )
![Page 5: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/5.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 5/32
![Page 6: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/6.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 6/32
86 | Environme ntal Flows
F i g u r e 3 .
E x i s
t i n g a n d p r o p o s e d h y d r o p o w e r p r o j e c t s i n A r u n a c h a l P r a d e s h ( c o u r t e s y S A N D R P ,
N e w D e l h i )
![Page 7: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/7.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 7/32
Environm ental Flows | 87
and tail reach areas of the reservoir. These changes in the hydrological regimes are of an
extremely high order and magnitude in rivers with high seasonal variation in their ow. The
operation of ‘peaking’ power plants utilises the ow accumulated over a long period of one
or more days for power generation for a couple of hours only. Thus, the upstream habitats
experience a diurnal cycle of deep ooding and exposure (drawdown) instead of the small
ows that occurred in the river channel before the construction of the diversion structures.
Such frequent water level uctuations on a daily basis affect all kinds of organismsas well as their physico-chemical environment. The temperature of water in a reservoir is
usually higher in the winter and lower in the summer than it would be in the river before the
dam. These temperature changes directly affect the aquatic biota and also the microclimate
of the region around the reservoir. The lacustrine section of the reservoir usually becomes
thermally stratied with a deeper layer of water (hypolimnion) with low temperature (see
Uhlman 1982 for south Indian reservoirs) although the currents generated by large water
level uctuations can prevent thermal stratication in smaller and shallow reservoirs.
Another effect of the dam is on the ow velocity and turbulence which come to naught and
Figure 4. Characteristic of three zones in a reservoir(reproduced with permission, from Rast and Strakraba 2000)
![Page 8: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/8.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 8/32
88 | Environme ntal Flows
hence, most of the coarser sediments carried by the river are deposited in the reservoirs.
Since the Himalayan rivers are known to carry sediment loads that are highest in the world,
many reservoirs get lled much earlier than expected.
Further, signicant changes occur in the water quality of the reservoirs as a result
of release of nutrients from the sediments, and following death and decomposition of the
vegetation submerged during lling of the reservoir (e.g., Chang and Wen 1998). The increased
availability of nutrients and the still water conditions promote the growth of phytoplankton
(eutrophication). A recent study shows that frequent water level changes caused by the
withdrawal of water for hydropower generation caused replacement of macrophytes in the
littoral zone by green benthic algae which could support high macroinvertebrate biomass
(Thompson and Ryder 2008). The inputs of both allochthonous (brought by the river) and
autochthonous organic matter (by phytoplankton) gradually result in anoxic conditions
in the hypolimnion and consequently further changes in water quality. The altered ow
regimes and increased nutrient levels in the reservoirs are known to be responsible for their
rapid colonisation by exotic invasive plants (such as Salvinia, Pistia and water hyacinth in
many reservoirs of tropical Asia and Africa), sh, molluscs and insects (for references, see
McCartney et al. 2001, McCartnety 2009). The operationally induced water level uctuations
in the reservoirs, have signicant impacts on the littoral and riparian vegetation which may
be completely eliminated or develop with a different species composition (cf. Nilsson and
Jansson 1995).
Creation of the reservoirs has further consequences for the fauna in the affected area.
All terrestrial animals disappear from the submerged areas and their populations decline
with the loss of the habitat. Most impacted are the species dependent upon riverine forests,
and other riparian ecosystems, and those adapted to the fast-owing conditions of the mainriver course (McAllister et al. 1999). The riverine sh are unable to adapt to the lacustrine
conditions and may survive for some time close to the shores of the reservoirs. The overall sh
diversity and populations soon decline and are often replaced by exotic species. Hoeinghaus
et al. (2009) report that the shery of the Parana River (Brazil) changed drastically after
the formation of Itaipu Reservoir as the high-value migratory species were replaced by
reservoir-adapted introduced species. The migratory sh species are the most affected as
they are unable to reach their spawning, nursery and feeding habitats. Dams or barrages in
the downstream reaches prevent migration of the sh from the sea or estuary to freshwater
habitats upstream (Marmulla 2001). The inability of the migratory species to move upstream
does not affect them alone but has some serious consequences for other biota as well througha variety of species interactions. Greathouse et al. 2006) observed that the loss of migratory
freshwater shrimp and sh populations in Puerto Rico (USA) from high-gradient streams
above large dams dramatically increased the populations of epilithic algal biomass, ne
benthic organic matter, ne benthic inorganic matter and non-decapod invertebrate biomass
which constituted their basal food resources and invertebrate competitors and prey. The
effects were however much smaller in case of low gradient streams.
One of the consequences of deposition of sediments behind dams and barrages is
the development of shallow water or waterlogged habitats which are quickly colonised by
![Page 9: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/9.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 9/32
Environm ental Flows | 89
various macrophytes, support macroinvertebrates and turn into suitable habitats for a wide
range of avian fauna besides other wildlife. Some of these human-created biodiversity-
rich habitats are sometimes utilised by important fauna, particularly migratory waterfowl,
and are therefore, recognised for their conservation value. A few are even designated as
nature reserves, wildlife sanctuaries or internationally important wetlands. In India, Pongdam, Harike, Ropar and Kanjli are among the Ramsar sites. Even Loktak lake – another
Ramsar site is a former oxbow transformed into a reservoir for hydropower generation by
constructing a barrage. Asan Conservation Reserve near Dehradun, Jayakwadi and Ujni
wildlife sanctuaries in Maharashtra are also similar wetland habitats that developed with
time behind the dams or barrages. It is not readily realised, however, that these newly
developed habitats harbour also a variety of disease vectors such as bilharzia-carrying
snails, mosquitoes and intermediate hosts for ukes that do not survive in running waters.
Downstream Impacts
Downstream of the dams the ow regimes change drastically. Most of the large dams andhydropower projects do not release water other than the small amounts of seepage or leakage
from the diversion structure and gates. Depending upon their storage capacity relative to the
river’s discharge, excess ow is released through the sluices provided at different levels. Even
in case of barrages, the river downstream may receive no ow during the low ow season
because of high demand of water for irrigation and domestic uses during the dry period (also
hot in the monsoonal south Asian region). The ow can be expected to be near normal ow
in the rainy season if there is no storage upstream. Thus, in general, the downstream ow
regime is altered in magnitude (volume), frequency, duration, timing and the amplitude
(difference between low ows and peak ows). The ecosystem responses to the alterations in
ow characteristics and consequent changes in landscape interactions, along with suggestedmitigation measures, are reviewed by Renöfält (2010) and a summary is provided in Table 1.
Each upstream project affects the hydrological regime of the downstream area and thereby
the next project below it (Figure 5). The velocity of ow is also regulated by the process of
release from the diversion structures. The annual river ow downstream decline heavily
(Goes 2002) with large decrease in the peak ows though the dry season ows are increased
steeply (Beilfuss and dos Santos 2001). Flow regulation results in lower ood magnitudes
and but longer stream ow duration (Elliott and Hammack 2000).
The hydropower projects often claim that because the ows diverted through the
tunnels to the powerhouse is released back into the river, there is no change in the ow. A
fairly long stretch of the river between the dam and the TRT outfall either remains dry orexperiences a highly altered ow regime if any signicant tributary joins it. After the TRT
discharges water into the river, very signicant and important hydrological changes occur
in the downstream reaches, especially in case of projects with peaking power generation.
The rate and velocity of discharge from the TRT are governed by operational factors (Figure
6). The ow regime downstream of the TRT outfall is then altered to daily pulses of very
large volumes for a short duration followed by a long period of no additional ow. Under
natural conditions the river would experience continuous small ows with very only small
diurnal changes except when the ow is derived solely from the snow melt. Only smaller
![Page 10: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/10.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 10/32
90 | Environme ntal Flows
Table 1. Impacts of hydropower projects on ows, ecosystem responses to these impacts
and management options (modied from Renöfält et al. 2010)
Flow
attribute
Change in ow Ecosystem response Management option
Flow ⁄ Hydrology
Magnitude Increase in variability
Organisms and organic matterushed down
Reduce range of ow variation
Flow stabilised Competitive species becomedominant
Productivity and decompositionrate decrease
Exotics invade and increaseRiparian species fail to establish
Increase seasonal variationin ow
Periodically ush thechannels to remove exotics
Frequency Increase in variability Increased erosion and stress to biota
Reduced habitat availability
Reduce frequency of ow variation
Decrease in variability
Flushing of sediments decreases
Competitive species becomedominant
Increase seasonal variationin ow
Periodically ush thechannels to remove exotics
Timing Change ofseasonal ow
variables
Reduced habitat availability
Life cycles disrupted, growthdeclines and succession patternaltered
Exotics invade
Provide ow for seasonal owpeaks and higher minimum
ows
Remove exotics suitably
Duration Prolonged lowows
Changes in abundance anddiversity
Organisms experiencephysiological stress
Increase seasonal high ows
Prolongedinundation
Changes in riparian communities Reduce high ows
Shortened low
ows
Greater availability of aquatic
habitats
Increase seasonal low ows
Smaller oodpeaks
Terrestrial organisms startcolonising
Increase duration of seasonalood peaks
Rate ofChange
Rapid changein river level
Organisms washed out andstranded
River banks collapse byundercutting
Establishment of riparian biotaaffected
Reduce rates of change
![Page 11: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/11.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 11/32
Environm ental Flows | 91
snow-fed streams at high altitudes experience ash ood like ows for 2-4 hours in the
afternoon and no ow during the night. It should be pointed out that hydro-peaking can
have severe ecological effects on a river. Depending on the rate of discharge acceleration
benthic invertebrates and also juvenile and small sh can get washed away with the ush, which results in decimation of benthic fauna, reduction of sh biomass and also changes to
the structure of sh populations. During the down-surge benthic invertebrates and sh can
get trapped in pools that might dry out later on so the animals either die or become easy prey
for predators (ICPDR 2013).
Unusually high volumes of water may sometimes be released for navigational and
recreational purposes, thereby affecting the river stretch between the dam/barrage and the
point of interest. Similar changes in ow regimes occur also due to managed ow releases
for other desired benets downstream.
Landscape Interactions
Velocity Flowing waterhabitatsconverted into
standing waterhabitats
Declines of lotic species andincrease of lentic species
Remove dams
Longitudinal Longitudinalconnectivityinterrupted bydams, barrages,etc.
Communities fragmented due toreduced migration ⁄ dispersal
Sediment redistribution decreases
Nutrients and organic matterretained in reservoirs
Remove dams
Facilitate migration acrossdams
Restore riparian and aquatichabitats
Flush out the sediment fromreservoirs
Lateral Floodplainsdisconnected
Reduced colonisation andrecruitment of riparian organisms
Decline in number of species
Ecological functions such asprimary production decline
Facilitate connection betweenriparian/oodplain areas andthe river channel throughoverbank ooding
Suitably modify ripariantopography/slope to enhanceriparian vegetation
Vertical Ground waterdisconnectedfrom Surface
water
Decline in number of species
Reproductive failure in sh
Decline in river water quality(changes in dissolved oxygen andtemperature)
Improve exchange betweensurface and hyporheichabitats
Remove ne sediments fromthe gravel beds
Temporal ReducedHeterogeneity New habitats cannot be formed(e.g., by sediment redistribution)
Non-indigenous species increase inplace of native species
Declne in habitat diversity andhence, lower beta diversity
Enhance habitat diversity bymodifying the ow regime
![Page 12: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/12.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 12/32
92 | Environme ntal Flows
Figure 5. Effect of an upstream HEP on the ow regime (ow duration curve) of the downstreamproject in Himachal Pradesh. The data are for years 1986, 1994 and 2006
![Page 13: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/13.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 13/32
Environm ental Flows | 93
These changes in the ow regime have a direct impact upon the channel morphology,
water quality, composition of biotic communities and various ecosystem processes (see
Hildebrand 1980a,b, Loar and Sale 1981, Turbak et al. 1981). In general, the aquatic habitats
shrink to small area within the channel, the riparian areas remain and oodplain-channel
interactions are reduced signicantly with a change the extent, depth, duration and timing
of ooding. Various impacts of hydropower projects are shown in Figure 7. Cortes et al.
(2011) provide a comprehensive review of the impacts of hydropower dams on the rivers in
general and sh in particular.
Impacts on Sediments
The dams effectively reduce the sediments transported downstream and the impacts of the
reduced sediment loads extend far beyond those of the river channel morphology, oodplain
dynamics and fertility and river biota to the deltaic zone. The impacts of ow regulation on
the deltas of Rivers Nile, Ganga-Brahmaputra, Mekong and Yangtze are among the well
known examples (Biswas 1992, Bohannon 2010, Yang et al. 2005, Xu and Milliman 2009,
Xue et al. 2011, Gupta et al. 2012).
Figure 6. Daily discharge (m3 s-1) for an average year before (a) and after (b) regulation(reproduced with permission, from Cortes et al. 2002)
![Page 14: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/14.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 14/32
94 | Environme ntal Flows
The nature and amount of sediments received downstream changes drastically as
the coarser sediments are retained behind the diversion structures. However, if and when
the coarser sediments are ushed out periodically during maintenance or during the
ood season, their dispersion over the river bed and transport downstream creates manyproblems for the channel morphology and the biota. In the absence of volume or velocity of
ow, ner sediments settle down in the river bed, and smother the vegetation, periphyton,
benthicalgae and macroinvertebrates, and affect also the feeding and growth of other
organisms. Flushing by periodic high ows results in greater erosion. Downstream of a dam,
reduction in sediment load in rivers can also result in increased erosion of riverbanks and
beds, loss of oodplains (through erosion and lower accretion) and degradation of coastal
deltas. Aggradation of the river bed may however occur if the sediment are entrained into
the river from the oodplain and tributaries but are unable to move downstream. Further
changes in the stream bed occur due to gravel and sand mining facilitated by easy access to
the river channel. Increased agricultural activity on the oodplain, often extending right onto the dry river bed, durther disturbs the sediments, lls up small water bodies and pools,
and promotes meandering and shifting of the river channel in successive years (see Raman
and Gopal 2007, 2009).
Impacts on Water Temperature
The temperature regime of the river water downstream is altered in two ways. First, in the
absence of ow from upstream, the temperature of the remaining water in the channel rises
during the summer and drops down during the winter. The extent of these changes depends
Figure 7. Impact of hydropower dams on important habitat and biotic components of riversFew other impacts on upstream systems and oodplains are not shown.
(adapted from Vovk Korz 2008)
![Page 15: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/15.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 15/32
Environm ental Flows | 95
also upon the geographical location and the stream bed characteristics (rocky, gravelly,
sandy, etc.). Average water temperature below the Danjiangkou dam on the Hanjiang River
(China) are reported to have increased during winter and decreased during the summer
season by 4-6 C (Liu and Yu 1992). This altered temperature regime has an inuence also
on the areas adjacent to the rivers in the absence of its moderating inuence. Second, therelease of water from the reservoirs alters the temperature regime of the downstream areas
signicantly over long stretches, depending upon whether the water is released from the
surface or the deeper layers (for references, see McCartney et al. 2009).
Impacts on Water Quality
All human activities which modiy the river ow affect the water quality (Table 2). The lack of
ow has a direct signicant inuence on the water quality because of the absence of dilution,
reduced oxygen availability and consequently, large reduction in the assimilation capacity of
the organisms. The downstream areas may experience an increase in salinity caused by the
reduced freshwater ows or a decrease in salinity dure to ushing by freshwater releases.Such salinity changes occur especially in the estuarine reaches and coastal regions where
the regulation of freshwater ows alters the interaction with the tidal uxes. Under low ow
conditions water quality degradation is caused by many variables (Nilsson and Renöfält
2008; Table 3). The discharge of wastewater or organic wastes entering the river with the
storm runoff invariably creates complex situations of degraded water quality. The issue
of water quality is among the most intensely debated issues concerning rivers as people
abstract increasingly more water. This is best exemplied by River Yamuna in Delhi where
it has no natural ow but receives only the sewage which is partially treated. Many smaller
rivers throughout India have turned for their entire course into sewage drains. However, it
Table 2. Ecological impacts of direct or indirect modications of the river ow (from Chapman 1996)
Activity/modication Effects
Construction of locks Enhancement of eutrophicationPartial storage of ne sediments may result in anoxic interstitial waters
Damming Enhancement of eutrophication (bottom anoxia, high organic matterin surface waters, etc.)Complete storage of sediments resulting in potential sh kills duringsluice gate operation (high ammonia, BOD and TSS)
Dredging Continuous high levels of TSS, and resultant silting of gravelspawning areas in downstream reachesRegressive erosion upstream of dredging areas may prevent sh migration
Felling of riparian woodland Continuous high levels of TSS, and resultant silting of gravelspawning areas in downstream reachesIncreased nitrate input from contaminated groundwaters
Flood plain reclamation andriver bed channelisation
Loss of ecological diversity, including specic spawning areas Loss of biological habitats, especially for sh
BOD Biochemical oxygen demand; TSS Total suspended solids
![Page 16: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/16.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 16/32
96 | Environme ntal Flows
Table 3. Examples of situations when combinations of water quality variables and
extreme discharge conditions can produce environmental problems
(reproduced with permission, from Nilsson and Renofalt 2008).
Water quality variables Low ows High ows
Pollutants Concentrations can reach toxiclevels
Can be washed out from adjacent,otherwise unooded uplands;dilution reduces but does noteliminate risk for toxicity
Drugs PPCP:s (Pharmaceuticals andPersonal Care Products) can
become toxic; natural estrogenscan feminize sh
Nutrients Can lead to eutrophicationand acidication; N levels can become toxic
Removed from watercourse bydownstream transport, uptake by riparian vegetation anddenitrication
Salts Can lead to acidication,mobilization of toxic metals andinvasion of salttolerantspecies
Organic Matter &sediments
Considerable addition thatincreases turbidity, which reducesprimary productivity and may
increase acidity and threatensh production Organic mattercan reduce pH Sedimentationof transported inorganic matterrestructures channel
High temperature Lowers oxygen content, makescontaminants more toxic, lowersproductivity
Low temperature Surface ice cover leads toreduced oxygen Open water and
low air temperatures can fosterexcessive formation of frazilice and anchor ice that damageaquatic biota Open water andtemperatures rising from belowto above 0°C lead to meltinganchor ice that can jam up andproduce local oods and uplandice that damage riparian andupland biota
If high ows occur during periods with low temperatures and surface
ice, water can be forced on top ofthe ice, often leading to oods, orthe ice cover may break up and runthe risk of jamming
![Page 17: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/17.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 17/32
Environm ental Flows | 97
must be emphasised that the assimilation capacity of the rivers without any ow alteration
is also not unlimited, and ow alone cannot take care of the problem of pollution.
Impacts on Ground Water
Another major impact of the altered ow regimes is on the ground water aquifers along therivers and under their oodplains as the inltration is drastically reduced. Peak ows for short
periods and of a lower magnitude such as those experienced by the regulated rivers during
the rainy season restrict the time and land area under ooding for groundwater recharge.
Similar effects occur also in the hilly regions depending upon the geology, topography (river
bed slope) and substrate characteristics. A lowering of the groundwater table close the river
channels is experienced throughout the India and in neighbouring countries because of the
excessive abstraction and absence of groundwater recharge (CGWB 2011, Soni and Singh
2013; Figures 8a,b).
Impacts on Aquatic Biodiversity The biota of the river, its riparian zone and the oodplain are impacted by the combined
and interacting inuences of altered ow regimes, sediment characteristics and the physico-
chemical quality of water. The overall consequence is a decline of biological diversity, and
often the invasion by undesirable species. The changes in the macroinvertebrate communities
downstream of the reservoirs have been investigated in numerous cases. Physical variables
such as the water depth and current velocity, and sediment characteristics have been
observed to inuence their species composition, density and biomass (e.g., Xiaocheng et al.
2008, Rehn et al. 2008, Wu et al. 2010, Mantel et al. 2010, Maroneze et al. 2011, Carlisle et al.
2012). While a signicant reduction in the species richness of molluscs has been observed in
Figure 8a. Annual hydrograph of groundwater of the Yamuna oodplain near Palla Temple, Delhi(data from CGWB5). Monitoring well located 700 m from the river (from Soni and Singh 2013)
![Page 18: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/18.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 18/32
98 | Environme ntal Flows
many studies (Layzer et al. 1993, Seddon 2000), there are also reports of spread of pulmonate
snails which are vectors of schistosomiasis and other diseases (e.g., Brown 1994).
Assani et al. (2006) however observed that a signicant reduction in the frequency
and magnitude of the minimum discharges during the growing season (April–September)
and the formation of numerous new geomorphological features (islets, pebble bars and rock
outcrops) in the low ow channel downstream of a dam in Belgium, was accompanied witha large increase in the number of vascular plant species downstream from the dam. Changes
occur in the species composition and diversity of riparian and oodplain vegetation even
with relatively small changes in water levels (Chauhan and Gopal 2005). Cogels et al. (1997)
reported rapid expansion of aquatic macrophytes along River Senegal after stabilisation of
water levels whereas in the alluvial oodplain of Zambezi, Beilfuss et al. (2001) observed
an increase in density of woody species and drought tolerant grasses which displaced ood-
tolerant species. The riparian forests, grasses or other plants may even be eliminated by
larger changes in the ow regimes (e.g., Nilsson et al. 1997). Another recent study on the
impact of dams showed the importance of ow variability to the development of riparian
vegetation. Bejarano et al. (2011) observed that the annual ow uctuations had beenreduced below the dam and that this effect decreased further downstream with the entry of
tributaries. Reduced ow variability triggered establishment of trees and shrubs towards the
mid-channel along the entire study reach. Shrubs were most impacted by ow regulation in
terms of lateral movement, but the effect on trees extended furthest downstream. Species
richness after regulation increased for trees but decreased for shrubs though the species
composition was affected by other factors.
The impacts of altered ow regimes on sh diversity and sh populations have
received considerable attention throughout the world (Table 4). In the river channel,
Figure 8b. Annual hydrograph of groundwater of the Yamuna oodplain at Burari,Delhi (data from CGWB5). Monitoring well located 1700 m from the river
(reproduced with permission, from Soni and Singh 2013)
![Page 19: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/19.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 19/32
Environm ental Flows | 99
degradation of water quality favours algal blooms and/or lamentous algae whereas the loss
of food and feeding and breeding sites results in the loss of sheries. In contrast to a shift
in sh species composition from riverine to lacustrine one in the reservoirs, downstream
of dams, sh populations are affected by their inability to migrate to upstream habitats
and disconnection of the river and oodplain, in addition to the reduction in ow itself. Water temperature inuences many important ecological processes. It affects growth in
freshwater sh, both directly and indirectly, through feeding behaviour, food assimilation,
and the production of food organisms. Temperature has a direct relationship with the
availability of oxygen as its solubility changes more rapidly at lower temperatures (0.405
mg/L reduction from 0°C to 1°C) than at higher temperature (0.261 mg/L with temperature
Table 4. Signicance of alteration of different components of ood regimes to sh
Characteristics Biological signicance
Smoothness of oodcurve
• Loss of eggs and nests through stranding or exposure due to rapidchanges in level.
• Stranding of eggs and fry of some species
Increased rapidity ofchanges to level
• Submergence of nests to great depths• Rapid currents may sweep fry and larvae past suitable sites• Increases stranding mortalities of sh mortalities of sh in temporary
oodplain pools.
Acceleration of ows atinappropriate times
• Pelagic eggs and larvae in drift swept past suitable nursery sites
Slowing of ow atinappropriate time
•Pelagic eggs and larvae settle out of drift and fail to reach sites orkilled by anoxic conditions
Failure of ood peak toarrive at correct time
• Failure of migratory species to mature, migrate and spawn.
Decoupling of ood peakfrom temperature peak
• Failure of thermally sensitive sh to spawn• Reduced growth rate of fry and adult.
Extensive abstraction of water in dry season
• Fish killed by excessive de-oxygenation.• Fish gets more exposed to shing pressure and predation.• Failure in maintain dry season refuges.
Reduction in depth of
ooding
• Reduction in spawning success.
• Reduced food and shelter areas for fry and adult.• Overall drop in production. Failure in ooding may result in yearclass spawning of species.
Flooding period reduction • Reduction in growing season small sh falls to predators
Interruption to continuityof ooding.
• Loss of eggs and fry unable to sustain in drift to colonize.
Flow • E-ow requirement, timing of ow, speed of discharge, water level.
Habitat connectivity • Removal / mitigation obstruction to sh movement, maintain accessto inowing tributaries in lakes / impoundments
![Page 20: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/20.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 20/32
100 | Envi ronment al Flows
increase from 10 to 11 °C and 0.128 mg/L with rise in temperature from 30 to 31°C). Thus,
even a small increase in water temperature in the hilly regions has greater implications for
the coldwater shes such as trout. Lessard and Hayes (2003) examined the effects of release
of water with higher summer temperature from an impoundment on downstream sh and
macroinvertebrate communities in a cold-water stream. They observed that increasingtemperatures downstream coincided with lower densities of cold-water sh species such as
brown trout ( Salmo trutta), brook trout ( Salvelinus fontinalis) and slimy sculpin (Cottus
cognatus) while overall sh species richness increased downstream (Figure 9 a,b). Density
of Cottus bairdi, another cold-water species, was not affected by temperature changes below
the dams. Macroinvertebrates showed shifts in community composition below dams that
increased temperature. Changes in the physiochemical conditions, primary production and
channel morphology may however, benet some species but not without having an adverse
effect on most of the native species.
Figure 9 a. Relation between sh populationdensity (loge transformed) and mean summer
temperature ( °C) at upstream (open diamonds)and downstream (closed squares) samples.
(reproduced with permission, from Lessard and Hayes 2003)
Figure 9 b. Regression of differences in shspecies richness on differences in mean summertemperature between above dam and below dam
reaches (R2 = 0.79).
![Page 21: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/21.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 21/32
Environm ental Flows | 101
In India, the impacts of ow alteration on riverine sheries have been reported in
many publications (Vass et al. 2006, 2011, Das et al. 2007, Pathak and Tyagi 2010) though
the Ganga-Brahmaputra river systems have received most attention. However, it needs
to be pointed out that these studies do not provide any quantitative relationship between
changes in sheries and river ows because the ow data are classied (not accessible), andthe high levels of pollution from the domestic and industrial wastewaters mask the effects
of changes in ow regimes.
During the past fty years, the sh catch from River Ganga has been declining
regularly (Table 5; Figure 10). Though the extent of decline in the total catch and its species
composition varies in different sections of the river, the major carps and large sized catshes
( A. aor, A. seenghala, W. attu) declined sharply while the smaller species exhibited only
slight changes. During 2001-08, the sheries improved in general, mainly due to invasion
of exotic species, C. carpio and O. niloticus. These changes can be attributed to several
Table 5. Decline in sh catch in river Ganga (from Pathak et al. 2010)
Period MajorCarps
Largecatshes
Hilsa Exotics Others Total
1961-68 424.91 201.35 97.17 null 211.96 935.39
1972-80 135.17 98.55 9.66 null 197.86 441.25
1981-90 155.73 99.40 4.31 null 247.59 507.03
1991-00 28.91 62.74 4.51 null 178.20 274.36
2001-06 38.58 40.56 1.20 64.27 223.41 368.01
Figure 10. Changes in sh catch in River Ganga during 1955 to 2003 (from Pathak et al. 2010)
![Page 22: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/22.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 22/32
102 | Envi ronment al Flows
other factors besides the reduction in river ows caused by hundreds of diversion structures
on various tributaries (for details see Vass et al. 2011). It is noteworthy that in Murray
Darling basin also, exotic species like the introduced carp, Cyprinus carpio, expanded with
simultaneous decline of native sh (Gehrke et al. 1995). The oodplain habitats have also
decreased signicantly with the construction of embankments and the degradation and/orloss of oodplain water bodies.
Most of the Indian migratory shes are potamodromous. The big catsh, Pangasius
pangasius travels the longest distance upstream for reproduction. Fishes in the hill
streams migrate both up and downstream periodically in response to rising water levels or
temperatures to access food or to new habitats or spawning areas or for the post-spawning
movement (Table 6). Numerous dams and hydropower projects in the hills, particularly
the Himalayan belt, are now affecting the trout and mahaseer. Indian mottled eel,
Anguilla bengalensis is the only noteworthy catadromous migrant which descends the R.
Brahamaputra from its hill stream tributaries around November-December every year for
spawning in the Bay of Bengal.
Hilsa (Tenualosa ilisha) is the most popular anadromous species which used to
travel longest distance upstream for breeding in the rivers of all major rivers (Ganga,
Brahmaputra, Mahanadi, Godavari, Krishna, Cauvery and Narmada. For Hilsa, the post-
Table 6. Migration pattern of migratory sh species in India
Species Spawning time
J F M A M J J A S O N D
Tor putitora(Golden mahaseer)
U U U U U D DD
August-Sept.
Tor tor(Deep bodied mahseer)
U U U U D DD
May-August
Acrossocheilus hexagonolepis(Copper mahseer)
U U U U U D DD
May-June; August – Sept.
Schizothorax richardsonii(Snow trout)
U U U March-May
Schizothorax progastrus U U U March-May
Hilsa Tenualosa ilisha U U July-Augustanadromous
Pangasius pangasius U U U June-August
Catla catla U U U U May-August
Labeo rohita U U U U May-August
Cirrhinus mrigala U U U U May-august
Indian mottled eel, Anguillabengalensis
D D June-July (Catadromous)
![Page 23: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/23.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 23/32
Environm ental Flows | 103
monsoon and late winter run is the major run returning to the estuary for growth and
survival in brackish or low salinity waters. During the early monsoon or late summer hilsa
migrated upstream up to Allahabad in the Ganga, and Mettur in Cauvery (Ghosh 1965,
Sreenivasan 1976). This migration has been severely affected by the dams, barrages and
anicuts on Hanga, Cauvery and other rivers but the dramatic changes in hilsa have attractedgreater attention in the lower reaches of River Ganga because of the Farakka barrage which
was constructed for augmenting river ow to the Hooghly estuary of River Ganga to meet
the needs of the Kolkata Port. The barrage became operational in 1975. Soon thereafter the
catch composition of the sheries immediately above Farrakka changed considerably as
the hilsa declined sharply (Table 7). Hilsa now occurs only downstream of the lock gates of
the feeder canal at Farakka.
The diversion structures and altered ow regimes have impacted the mammal and
bird populations also (Nilsson and Dynesius 1994). Throughout south Asia dolphins have
disappeared from many rivers such as River Ganga upstream of Middle Ganga Barrage
at Bijnor, and most of its tributaries (Smith et al. 2000, Sinha and Sharma 2003). The
Farakka Barrage on River Ganga has also caused a decline in the dolphin population (Sinha
2000). In China, river dolphin, ( Lipotes vexillifer, has disappeared after construction of
the Xinjiang dam (Liu et al. 1999). On the other hand, beaver populations have increased
following reduced ow in some rivers (Hayeur 2001).
In the long term, reduced ooding alters vegetation communities that may be
important for a wide range of mammal and bird species (Table 8). In arid regions, riparian vegetation may be the only signicant vegetation, and many animals will have adapted
behavioural patterns to t with seasonal ooding. If the ooding regime is altered, changes
in vegetation may place the birds and animals that depend on it at risk. An example is the
decline of the wattled cranes ( Bugeranus carunculatus) on the Kafue Flats after the ow
was altered by the Itezhi-tezhi dam (Kamweneshe and Beilfuss 2002).
Impacts on Estuaries and Backwaters
The effect of changes in freshwater ows on salinity in estuarine and backwater areas was
Table 7. Catch composition (%) at Lalgola during pre- and post-Farakka periods
Group 1963-76 1980-90 1991-00
Major carps 0.33 4.47 9.76
Large catshes 0.12 9.34 13.58
Hilsa 92.02 29.68 16.80
Others 7.53 56.51 59.86
Total (Mg) 121.43 57.31 106.35
![Page 24: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/24.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 24/32
104 | Envi ronment al Flows
mentioned above in the context of water quality. The changes in the salinity regimes have
many major consequences for the estuarine biota and ecological processes as well as for
coastal sheries. Bunn et al. (1998) have discussed the inuence of river ows on coastal
sheries in some detail. In India and Bangladesh, the impacts have been investigated in
some detail for many years (since the construction of Farakka barrage) in respect of hilsa
and shrimp sheries and the changes in the vegetation of Sundarban mangroves. The major
changes have been summarised by Chauhan and Gopal (2013). The debate has however
been shadowed by importance of ow to the Kolkata Port, and the Indo-Bangladesh disputeon sharing of Ganga waters.
The Farakka barrage has resulted in steep decline in the hilsa catch both upstream
and downstream of the barrage. However, freshwater diversion through the feeder canal
has altered the hydrology and salinity gradient of the Hooghly estuary, and consequently
the extension of the freshwater tidal zone has occurred till further downstream in the Indian
Sundarban. With the habitats gradually turning favourable for Hilsa spawners, breeding
grounds have shifted downstream of the Farakka Barrage, showing species adaptation to
changing situations. These changes are also accompanied by signicant changes in the
Table 8. Reported effects of ow regulation on river biota (adapted from Bragg et al. 2005)
Biotic groups Effects of ow regulation
Macrophytes Large changes in species composition; may be greatly reduced or proliferate indifferent habitats depending upon depth, velocity, and other ow characteristics. Very high ows usually scour the vegetation, substrate and organic matter.
Invertebrates Generally resilient but taxonomic composition and abundance change greatly withow regime.Changes in the substrate characteristics (e.g., sediment texture) affect theinvertebrate assemblages.Flushing and catastrophic drift of Plecopteran larvae reported due to intermittent‘hydropeaking’ ows.
Fish Fish feeding habits change due to changes in invertebrate communities.Scouring, erosion and textural change of spawning habitats due to sudden high
discharge and largw uctuations; also river bank erosion results in greater turbidity(ne sediment load)Swimming affected by high ow velocity and often juveniles concentrate in shallow
water areas or get stranded when ow decreases abruptly.Changes in reproductive development and spawning behaviour of sh.Changes in sh assemblages – species composition and abundance
General Downstream plant and animal communities are affected adversely and drasticallySediment composition below dams is severely altered and affects sh and benthic
biota.Large variations in ow velocity destroy pool/rife relationships; render the stream
banks unstable.
Riparian vegetation altered due to changes in sediment dynamics
![Page 25: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/25.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 25/32
Environm ental Flows | 105
species composition and yields of estuarine sheries which are now being slowly but steadily
replaced by freshwater species.
Similar impacts hve occurred in other estuarine systems as well. Several dams and
barrages in the Damodar River basin have resulted in a decreased silt load and lower
deposition of detritus in the estuaries downstream, thereby affecting the sheries. Estuaries
of Krishna and Godavari rivers have become hypersaline, and sh species with low salinity
tolerance have been wiped out (Das et al. 2007). Among other estuarine systems impacted
by changes in river ows, the Vembanad lake (a backwater in Kerala) and the Lake Chilika (a
coastal lagoon on the east coast of India) – both Ramsar sites – have attracted many studies
(e.g., Das and Jena 2008, Dujovny 2009, .Mishra 2012, Abe and James 2013).
Socio-Cultural and Livelihood Impacts
As described in the previous chapter, rivers provide many social and cultural services which
are linked directly to the ow regimes besides their indirect relationship with the river’s
abiotic and biotic components. Alteration of the ow regimes, therefore, has also signicant
social, cultural, economic and health impacts on the human populations which live along
the rivers and depend upon them for livelihoods. As mentioned earlier also, while the socio-
economic impacts in areas upstream of the dam sites have received global attention, little
attention is paid to these impacts along the downstream reaches where usually a much
larger area and greater population are affected. Richter et al. (2010) point out that the
large dams can severely disrupt natural riverine production systems – especially sheries,
ood-recession agriculture and dry-season grazing (Table 9). Few examples given in the
foregoing account show that the capture sheries usually decline and the oodplain and
riparian vegetation changes greatly. Together with a reduction in the area of oodplains, theresource availability and quality fall sharply. It is common knowledge in South Asian region
and many other countries that the introduced exotic species of sh, such as tilapia, are not
preferred by the human consumers and hence have a lower market value. Hoeinghaus et
al. (2009) report that in the Parana River (Brazil), the replacement of migratory species by
introduced species resulted in higher energetic costs of sheries production whereas market
value decreased as a result of consumer preferences. Similar problems of availability, quality
and costs occur everywhere with plant resources, sediments and of course water itself. Large
number of people depends on the oodplains for reeds, cattails, grasses and also fuelwood,
for cultivating various crops, particularly vegetables, and aquatic plants like Trapa and lotus
in shallow water areas, and for extracting sand and gravel. Reduced sediment transport onlyleads to illegal and excessive exploitation. Some communities/social groups are engaged
in water transport, preparing materials to support shing, supporting cultural/religious
activities and various recreational activities for their livelihood. We are not aware of
published quantitative estimates of these activities and affected people. Richter et al. (2010)
estimate that globally 472 million river-dependent people live downstream of large dams
along impacted river reaches and call for “comprehensive assessments of dam costs and
benets, as well as to the social inequities between dam beneciaries and those potentially
disadvantaged by dam projects”.
![Page 26: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/26.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 26/32
106 | Envi ronment al Flows
At the end, we would like to draw attention to two important studies. Barbier and
Thompson (1991) compared the agricultural, shing and fuelwood benets lost through
reduced ooding downstream against the gains from increased irrigation production
upstream in the Hadejia-Jama’are River Basin in northern Nigeria. They observed that
the irrigation benets can only partially replace the benets lost due to reduced oodplain
inundation. In a recent study, Wang et al. (2009) determined the effects of hydropower
development on watershed level ecosystem services, using 21 indicators and various
methods of economic valuation such as the market value method, opportunity cost method,
Table 9. Fisheries status before and after dam construction. (modied from Richter et al. 2010)
River/Country Fish species Catch or # sh speciescaught
Kafue Gorge damand Itezhitezhi dam,Zambia
Oreochromis andersonii,a key ood-plain-dependent tilapia species
In 1968, 50% of thecatch consisted ofthe commerciallyimportant O.andersonii
By 1983, only 3% ofcatch was made of O.andersonii
Kafue Gorge damand Itezhitezhi dam,Zambia
Increase in predatorspecies: Clariusgariepinus,
Macuseniusmacrolepitus, Labeo maolybdinus, Hepsetus odeo
Families supported by shing: 2600(1977)
Families supported byshing: 1157 (1985)
Urra dam Colombia 6000 Ng/year 1700 Ng/year (early 1990s)
Salandi dam, India 350 Ng/year (1960-1965) 25 Ng/year (1995-2000)
Pak Mun dam,Thailand
265 sh species 50 species have disappeared and otherspecies show marked population declinesFish catch decreased by 60-80%
Kainji dam, Nigeria 30% decrease in catch, and reduction of Mormyridae species from 20% ofsh community to 5% (commercially important)
Aswan High dam,Egypt
Number of harvested shspecies: 47
Number declined to 25 at Assuit and to 14at Cairo; in Kafr el Zayer reach, number and
size increasedXinanjiang dam,China
Macrura reevesii Freshwatersh: 96 species
85 species
Manantali and Diamadams , Mali andSenegal
23,500 Ng/year Reduced by 50% (net loss of 11,250 Ng/ year)
Three Gorges dam,China
Four speciesof carp (silver,
bighead, grass, black)
Commercial harvest:3,360,000 Ng (2002)
1,010,000 Ng (2004),1,680,000 Ng (2005)
![Page 27: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/27.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 27/32
Environm ental Flows | 107
project restoration method, travel cost method, and contingent valuation method. Three
representative hydropower projects in the Jiulong River Watershed in southeast China were
considered. They concluded that biodiversity loss and water quality degradation accounted
for 80-94% of the major negative impacts, the value of negative impacts ranged from 64%
to 91% of the value of positive benets, and that the average environmental cost per unit ofelectricity was about 75% of its on-grid power tariff.
It can be safely concluded that the short-term gains from a reservoir or hydropower
project (over their average life span) may not compensate for the accumulated long-term
loss of river’s ecosystem services. There is a clear urgent need for proper valuation of all
quantitative and qualitative aspects of the water resource development projects.
REFERENCES
Abe, George and James, E.J. 2013. Impacts of anthropogenic regulation on streamow in the humid
tropics of Western Ghat regions of Kerala state. International Journal of Advances in Engineering& Technology 6: 1895-1905.
Arnell, N.; Liu, C.; Compagnucci, R.; da Cunha, L.; Hanaki, K.; Howe, C.; Mailu, G.; Shiklomanov,I.; Stakhiv. E. and Döll, P. 2001. Hydrology and water resources. Pages 192-232, In: McCarthy,J.J.; Canziani, O.F.; Leary, M.A.; Dokken, D.J. and White, K.S. (Editors) Climate Change2001: Impacts, Adaptation, and Vulnerability. Contribution of Working Group II to the Third
Assessment Report of the Intergovernmental Panel on Climate Change. Cambridge UniversityPress, Cambridge.
Assani, A.A.; Petit, F. and Leclercq, L, 2006. The relation between geomorphological features andspecies richness in the low ow channel of the Warche, downstream from the Bu¨tgenbach dam(Ardennes, Belgium). Aquatic Botany 85: 112-120.
Barbier, E.B. and Thompson, J.R. 1998. The value of water: Floodplain versus large-scale irrigation benets in Northern Nigeria. Ambio 27: 434-440.
Beilfuss, R. and dos Santos, D. 2001. Patterns of hydrological change in the Zambezi Delta,Mozambique. Working Paper No. 2, Zambezi Basin Crane and Wetland Conservation Program,Baraboo.
Beilfuss, R., Moore, D., Bento, C. and Dutton, P. 2001. Patterns of vegetation change in the ZambeziDelta, Mozambique. Working Paper No. 3, Zambezi Basin Crane and Wetland ConservationProgram, Baraboo.
Bejarano, M. Dolores, Nilsson, C., González Del Tánago, M. and Marchamalo, M. 2011, Responsesof riparian trees and shrubs to ow regulation along a boreal stream in northern Sweden.Freshwater Biology 56: 853–866.
Bergkamp, G.; McCartney, M.; Dugan, P.; McNeely, J. and Acreman, M. 2000. Dams, ecosystemfunctions and environmental restoration: Thematic Review II.1. World Commission on Dams,Cape Town. 199 pages.
Biswas, A.K. 1992. The Aswan High Dam revisited. Ecodecision, September: 67–69.
Bohannon, J. 2010. The Nile delta’s sinking future. Science 327: 1444-1447.
Brauman, K.A.; Daily, G.C.; Duarte, T.K. and Mooney, H.A. 2007. The nature and value of ecosystemservices: An overview highlighting hydrologic services. Annual Review of EnvironmentalResources 32: 67–98.
Brown, D.S. 1994. Freshwater Snails of Africa and Their Medical Importance. Taylor & Francis,
London.
![Page 28: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/28.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 28/32
108 | Envi ronment al Flows
Bruijnzeel, L.A. 2004. Hydrological functions of tropical forests: not seeing the soil for the trees? Agriculture, Ecosystems and Environment 104: 185–228.
Bunn, S.E.; Loneragan, N.R. and Yeates, M. 1998. The inuence of river ows on coastal sheries.Pages 106-114, In: Arthington, A.H. and Zalucki, J.M. (Editors), Comparative Evaluation ofEnvironmental Flow Assessment Techniques: Review of Methods. Land and Water ResourcesResearch and Development Corporation Occasional Paper No. 27/98, Canberra, ACT.
Carlisle, D. M.; Nelson, S.M. and Eng, K. 2012. Macroinvertebrate community condition associated with the severity of streamow alteration. River Research and Applications. doi: 10.1002/rra.2626
CGWB (Central Ground Water Board). 2011. Ground Water Year Book –India, 2010-11. CentralGround Water Board, Ministry of Water Resources, Faridabad.
Chang, S.P. and Wen, C.G. 1998. Nutrient release from inundated land of a tropical reservoir (Nanhuareservoir, Taiwan). Water Science and Technology 37(2): 325–332.
Chapman. D. (Editor). 1996. Water Quality Assessments - A Guide to Use of Biota, Sediments and Water in Environmental Monitoring. Second Edition. Publicsed for UNESCO/WHO/UNEP, by
E & FN Spon, London.Chauhan, Malavika, and Gopal, B. 2005. Vegetation structure and dynamics of a oodplain wetland
along a subtropical regulated river. River Research and Applications 21: 513-534.
Chauhan, Malavika and Gopal, B. 2013. Sundarban Mangroves: Impact of Water Management inthe Ganga River Basin. Pages 125-148, In: Sanghi, Rashmi (Editor) Our National River Ganga:Lifeline of Millions. Springer, Dordrecht.
Cogels, F.X.; Coly, A. and Niang, A. 1997. Impact of dam construction on the hydrological regime andquality of a Sahelian ake in the River Senegal Basin. Regulated Rivers: Research and Management13: 27–41.
Collier, M., Webb, R.H. and Schmidt, J.C. 1996. Dams and Rivers: A Primer on the DownstreamEffects of Dams. US Geological Survey Circular 1126. Tuscon.
Cortes, R.M.V.; Ferreira, M.T.; Oliveira, S.V. and Oliveira, D. 2002. Macroinvertebrate communitystructure in a regulated river segment with different ow conditions. River Research and
Applications 18: 367–382.
Cui, X.; Liu, S. and Wei, C. 2012. Impacts of forest changes on hydrology: a case study of large watersheds in the upper reaches of Minjiang River watershed in China. Hydrology and EarthSystem Sciences 16: 4279–4290.
Das, B.P. and Jena, J. 2008. Impact of Mahanadi basin development on ecohydrology of Chilika.pages 697-702, In: Sengupta, M. and Dalwani, R. (Editors) Proceedings of Taal 2007 - The 12th
World Lake Conference. Ministry of Environment and Forests, New Delhi.
Das, M.K.; Samanta, S. and Saha, P.K. 2007. Riverine Health and Impact on Fisheries in India. PolicyPaper No. 01, Central Inland Fisheries Research Institute, Barrackpore, Kolkata. 120.
Döll, P. and Schmied, H.M. 2012. How is the impact of climate change on river ow regimes relatedto the impact on mean annual runoff? A global-scale analysis. Environmental Research Letters7: 014037 doi:10.1088/1748-9326/7/1/014037
Dujovny, E. 2009. The Deepest Cut: Political ecology in the dredging of a new sea mouth in ChilikaLake, Orissa, India. Conservation and Society [online] 7: 192-204. Available from: http://www.conservationandsociety.org/text.asp?2009/7/3/192/64736
Elliott, J.G. and Hammack, L.A. 2000. Entrainment of riparian gravel and cobbles in an alluvialreach of a regulated canyon river. Regulated Rivers: Research and Management 16: 37–50.
Ellison, D.; Futter, M.N. and Bishop, K. 2012. On the forest cover–water yield debate: from demand-to supply-side thinking. Global Change Biology 18: 806–820.
![Page 29: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/29.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 29/32
Environm ental Flows | 109
Gehrke, P.C.; Brown, P.; Schiller, C.B.; Moffatt, D.B. and Bruce, A.M. 1995. River regulation and sh
communities in the Murray–Darling River system, Australia. Regulated Rivers: Research and
Management 11(3–4): 363–375.
Ghosh, A.N. 1965. Observations on the hilsa shery of the river Jamuna during the years 1955-62 at
Allahabad. Journal of the Zoological Society of India.17(1&2): 135-149.Goes, B.J.M. 2002. Effects of river regulation on aquatic macrophyte growth and oods in the
Hadejia-Nguru wetlands and ow in the Yobe river, Northern Nigeria: Implications for future
water management. River Research and Applications 18(1): 81–95.
Goldsmith, E. and Hildyard, N. 1984. The Social and Environmental Effects of Large Dams: Volume
1. Overview, Wadebridge Ecological Centre, Worthyvale Manor Camelford, Cornwall, U.K.
Gosain, A.K.; Rao, Sandhya and Arora, Anamika. 2011. Climate change impact assessment of water
resources of India. Current Science 101: 356-371.
Greathouse, E.A.; Pringle, C.M.; McDowell, W.H. and Holmquist, J.G. 2006. Indirect upstream
effects of dams: consequences of migratory consumer extirpation in Puerto Rico. Ecological
Applications 16: 339-52.
Gupta, H.; Kao, Shuh-Ji and Dai, Minhan. 2012.The role of mega dams in reducing sediment uxes:
A case study of large Asian rivers. Journal of Hydrology 464-465: 447-458.
Hayeur, G. 2001. Summary of knowledge Acquired in Northern Environments from 1970 to 2000.
Hydro-Quebec, Montreal.
Hildebrand, S.G. 1980a. Analysis of Environmental Issues Related to Small-Scale Hydroelectric
Development. II. Design Considerations for Passing Fish Upstream Around Dams.
ORNUTM-7396. Oak Ridge National Laboratory, Oak Ridge,Tennessee. 78 pages.
Hildebrand, S.G. 1980b. Analysis of Environmental Issues Related to Small-Scale Hydroelectric
Development. III. Water level uctuation. ORNL/TM-7453. Oak Ridge National Laboratory,
Oak Ridge, Tennessee. 78 pages + Appendix.
Hoeinghaus, D.J.; Agostinho, A.A.; Gomes, L.C.; Pelicice, F.M.; Okada, E.K.; Latini, J.D.; Kashiwaqui,E.A.L. and Winemiller, K.O. 2009. Effects of river impoundment on ecosystem services of large
tropical rivers: embodied energy and market value of artisanal sheries. Conservation Biology
23: 1222-1231.
ICPDR. 2013. Guiding Principles on Sustainable Hydropower Development in the Danube Basin.
International Commission for the Protection of the Danube River, Vienna.
Jha, R. and Sharma, K.D. 2008. Assessment of Climate Change Impacts on Low Flow in a
Representative River Basin in India. http://www.groundwater-conference.uci.edu/les/
Chapter1/2008_conf_Jha %20R%20and%20Sharma,%20KD.pdf
Kamweneshe, B. and Beilfuss, R. 2002. Population and Distribution of Wattle Crane and Other Large
Waterbirds on the Kafue Flats, Zambia. Working Paper No. 5, Zambezi Basin Crane and WetlandConservation Program, Baraboo.
Lessard, J.L. and Hayes, D.B. 2003. Effects of elevated water temperature on sh and macroinvertebrate
communities below small dams. River Research and Applications 19: 721–732.
Layzer, J.B.; Gordon, M.E. and Anderson, R.M. 1993. Mussels: the forgotten fauna of regulated
rivers—a case study of the Caney Fork River. Regulated Rivers: Research and Management,
8(1–2), 63–71.
Liu, J.K. and Yu, Z.T. 1992. Water quality changes and effects on sh populations in the Hanjiang
River, China, following hydroelectric dam construction. Regulated Rivers: Research and
Management 7: 359–368.
![Page 30: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/30.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 30/32
110 | Envi ronment al Flows
Liu, R.; Wang, D. and Zhou, K. 1999. Effects of water development on river cetaceans in China. Pages
40-42, In: Randall, R.R.; Smith, B.D. and Kasuya, T. (Editors). Biology and Conservation of
Freshwater Cetaceans in Asia. Occasional Paper No. 23, IUCN, Cambridge, UK.
Liu, Z.; Yao, Z.; Huang, H.; Wu, S. and Liu, G. 2012. Land use and climate changes and their impacts
on runoff in the Yarlung Zangbo River Basin, China. Land Degradation and Development DOI:10.1002/ldr.1159.
Loar, J.M. and Sale, M.J. 1981. Analysis of Environmental Issues Related to Small-Scale Hydroelectric
Development. V. Instream Flow Needs for Fishery Resources. ORNL/TM-7861. Oak Ridge
National Laboratory, Oak Ridge Tennessee, 139 pages
Mantel, S.K.; Muller, N.W.J. and Hughes, D.A. 2010. Ecological impacts of small dams on South
African rivers Part 2: biotic response - abundance and composition of macroinvertebrate
communities. Water SA (Online).36: 361-370.
Marmulla, G. (Editor). 2001. Dams, Fish and Fisheries. Opportunities, Challenges and Conict
Resolution. FAO Fisheries Technical Paper 419. FAO, Rome. 166 pages.
Maroneze, D.M.; Tupinambás, T.H.; França, J.S. and Callisto, M. 2011. Effects of ow reduction
and spillways on the composition and structure of benthic macroinvertebrate communities in aBrazilian river reach. Brazilian Journal of biology = Revista Brasileira de Biologia 71: 639-651.
McCartney, M.P.; Sullivan, C. and Acreman, M.C. 2001. Ecosystem Impaacts of Large Dams.
Background Paper Nr. 2, Prepared for IUCN / UNEP / WCD. IUCN and UNEP, Switzerland.
McCartney, M. 2009. Living with dams: managing the environmental impacts. Water Policy 11,
Supplement 1: 121–139.
McCully, P. 2001. Silenced Rivers: The Ecology and Politics of Large Dams. Zed Books, London.
Mishra, H.K. 2012. Post-construction effects of Naraj barrage on Chilika Lake and suggested measure.
Water and Energy International 69: 40-43.
Negi, G.C.S. 2002. Hydrological research in the Indian Himalayan mountains: Soil and water
conservation. Current Science 83: 974-980.Pathak, V. and Tyagi, R.K. 2010 Riverine Ecology and sheries vis-a-vis hydrodynamic alterations
Impacts and remedial measures. Bulletin 161. Central Inland Fisheries Research Institute,
Barrackpore.
Poff, N.L. and Zimmerman, J.K.H. 2010. Ecological responses to altered ow regimes: a literature
review to inform the science and management of environmental ows. Freshwater Biology 55:194–205
Raman, R. and Gopal, B. 2007. Effect of ow regulation on river morphology and land use in theoodplain of River Yamuna in Haryana and U.P. Pages 105-137, In: Martin, P.; Gopal, B.,
and Southey, C. (Editors) Restoring River Yamuna: Concepts, Strategies and Socio-EconomicConsiderations. National Institute of Ecology, New Delhi.
Rangachari, R. 2006. Bhakra-Nangal Project. Socio-Economic and Environmental Impacts. Third World Centre, Mexico. 256 pages.
Raman, R. and Gopal, B. 2009. Recent land use/land cover changes in the oodplain of the highlyregulated River Yamuna Upstream of Delhi. International Journal of Ecology and Environmental
Sciences 35: 237-254.
Rao, P.G. 1995. Effect of climate change on streamows in the Mahanadi River Basin, India. WaterInternational 20: 205-212.
Rao, P.G. 1993. Climatic changes and trends over a major river basin in India. Climate Research 2:215-223.
![Page 31: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/31.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 31/32
Environm ental Flows | 111
Rast, W. and Straskraba, M. 2000. Lakes and Reservoirs. Volune 1. Similarities, Differences andImportance. International Lake Environment Committee, Shiga, Japan.
Rehn, Andrew C.; von Ellenrieder, N. and Ode, Peter R. 2008. Assessment of Ecological Impacts ofHydropower Projects on Benthic Macroinvertebrate Assemblages: A Review of Existing Data
Collected for FERC Relicensing Studies. California Energy Commission, PIER Energy‐RelatedEnvironmental Research Program. CEC-500-2007-040.
Renöfält, B.M.; Jansson, R. and Nilsson, C. 2010. Effects of hydropower generation and opportunitiesfor environmental ow management in Swedish riverine ecosystems. Freshwater Biology 55: 49-
67.
Richter, B.D.; Baumgartner, J.V.; Powell, J. and Braun, D.P. 1996. A method for assessing hydrologicalteration within ecosystems. Conservation Biology 10: 1163-1174.
Richter, B.D.; Postel, S.; Revenga, C.; Scudder, T.; Lehner, B.; Churchill, A. and Chow, M. 2010. Lostin development’s shadow: The downstream human consequences of dams. Water Alternatives3(2): 14-42
Robson, A.; Cowx, I.G. and Harvey, J.P. 2011. Impact of run-of-river hydro-schemes upon sh
populations. Phase 1. Literature review. WFD114:Project Final Report. .Scotland and NorthernIreland Forum for Environmental Research (SNIFFER), Edinburgh, Scottland, UK.
Sarkar, U.K.; Pathak, A.K.; Sinha, R.K.; Sivakumar, K.; Pandian, A.K.; Pandey, A.; Dubey, V.K. andLakra, W.S. 2012. Freshwater sh biodiversity in the River Ganga (India): changing pattern,
threats and conservation perspectives. Reviews in Fish Biology and Fisheries 22: 251-272
Schneider, C.; Laizé, C.L.R.; Acreman, M.C. and Flörke, M. 2012. How will climate change modify
river ow regimes in Europe? Hydrology and Earth System Sciences Discussion 9: 9193–9238.
Scudder, Thayer T. 2005. The Future of Large Dams: Dealing with Social, Environmental, Institutionaland Political Costs. Earthscan, London. 408 pages. (Reprint 2012, CRC Press)
Seddon, M.B. 2000. Molluscan Biodiversity and the Impact of Large Dams. IUCN, Gland, Switzerland.
Sinha, R.K. 2000. Status of the Ganges River dolphin (Platanista gangetica) in the vicinity of Farakka
Barrage, India. Pages 42-48, In: Reeves, R.R.; Smith, B.D. and Kasuya, T. (Editors) Biology andConservation of Freshwater Cetaceans in Asia. IUCN Species Survival Commission Occasional
Paper 23, Gland, Switzerland and Cambridge, UK.
Sinha, R.K. and Sharma, G. 2003. Current status of the Ganges river dolphin in the rivers Kosi and
Son. Journal of the Bombay Natural History Society . 100(1): 27-37.
Smith, B.D.; Sinha, R.K.; Zhou, K.; Chaudhry, A.A.; Renjun, L.; Wang, D.; Ahmed, B.; Haque, A.K.M.and Sapkota, K. 2000. Register of water development projects affecting Asian river cetaceans.Pages 22-39, In: Reeves, R.R.; Smith, B.D. and Kasuya, T. (Editors) Biology and Conservationof Freshwater Cetaceans in Asia. IUCN/SSC Occasional Paper No. 23, Gland, Switzerland andCambridge, UK.
Soni, V. and Singh, D. 2013. Floodplains: self-recharging and self-sustaining aquifers for city water.Current Science 104: 420-422.
Sreenivasan, A. 1976. Fish production and sh population changes in some South Indian reservoirs.Indian Journal of Fisheries 23 (1 & 2): 133–152.
Thompson, R.M. and Ryder, G.R. 2008. Effects of hydroelectrically induced water level uctuationson benthic communities in Lake Hawea, New Zealand, New Zealand Journal of Marine andFreshwater Research 42: 197-206.
Turbak, S.C.; Reichle, D.R. and Shriner, C.R. 1981. Analysis of environmental issues related to small-scale hydroelectric development. IV. Mortality resulting from turbine passage.ORNL/TM-7521.Oak Ridge National Laboratory, Oak Ridge Tennessee, 112 pages.
![Page 32: E-Flow-ch4](https://reader034.vdocument.in/reader034/viewer/2022052313/577cc1271a28aba71192655f/html5/thumbnails/32.jpg)
8/10/2019 E-Flow-ch4
http://slidepdf.com/reader/full/e-flow-ch4 32/32
Vass, K.K.; Mitra, K.; Suresh, V.R.; Katiha, P.K. and Srivastava, N.P. (Editors). 2006. River Fisheriesin India: Issues and Current Status. Inland Fisheries Society of India, Barrackpore, Kolkata.
Vass, K.K.; Das, Manas K.; Tyagi, R.K.; Katiha, Pradeep K.; Samanta, S.; Shrivastava, N.P.;Bhattacharjya, B.K.; Suresh, V.R.; Pathak, V.; Chandra, G.; Debnath, D. and Gopal, B. 2011.
Strategies for Sustainable Fisheries in the Indian Part of the Ganga-Brahmaputra River Basins.International Journal of Ecology and Environmental Sciences 37 (4): 157-218.
Vovk-Korz. A.; Korze, D.; Goltara, A.; Conte, G.; Toniutti, N. and Smolar-Zvanut, N. 2008. Reviewof best practices/guidelines for compensation measures for hydropower generation facilities.Certication for Hydro: Improving Clean Energy. Intelligent Energy, Europe
Wang, G.; Fang, Q.; Zhang, L.; Chen, W.; Chen, Z. and Hong, H. 2010. Valuing the effects of hydropowerdevelopment on watershed ecosystem services: Case studies in the Jiulong RiverWatershed,Fujian Province, China. Estuarine, Coastal and Shelf Science 86: 363–368.
Wu, N.; Tang, T.; Fu, X.; Jiang, W.; Li, F.; Zgou, S.; Cai, Q. and Fohrer, N. 2010. Impacts of cascaderun-of-river dams on benthic diatoms in the Xiangxi River, China. Aquatic Sciences 72: 117-125
Xiaocheng, Fu; Tang, Tao; Jiang, Wanxiang; Li, Fengqing; Wu, Naicheng; Zhou, Shuchan and Cai,
Qinghua, 2008. Impacts of small hydropower plants on macroinvertebrate communities. ActaEcologica Sinica, 28(1): 45−52.
Xiaohua. Wei; Ge, Sun; Shirong Liu; Hong Jiang; Guoyi Zhou and Limin Dai. 2008. The forest-streamow relationship in China: a 40-year retrospect. Journal of the American Water Resources
Association 44: 1076-1085.
Xu, Kehui and Milliman, J.D. 2009. Seasonal variations of sediment discharge from the YangtzeRiver before and after impoundment of the Three Gorges Dam. Geomorphology 104: 276-283.
Xue, Z.; Liu, J.P. and Ge, Q.A. 2011. Changes in hydrology and sediment delivery of the Mekong Riverin the last 50 years: connection to damming, monsoon, and ENSO. Earth Surface Processes andLandforms 36: 296–308.
Yang, S.L.; Zhang, J.; Zhu, J.; Smith, J.P.; Dai, S.B.; Gao, A. and Li, P. 2005. Impact of dams on
Yangtze River sediment supply to the sea and delta intertidal wetland response. Journal ofGeophysical Research 110: F03006,