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Journal ArticleDOI

Greenhouse gas emissions (CO2, CH4, and N2O) from several perialpine and alpine hydropower reservoirs by diffusion and loss in turbines

11 Apr 2012-Aquatic Sciences (SP Birkhäuser Verlag Basel)-Vol. 74, Iss: 3, pp 619-635
TL;DR: In this paper, the first results of greenhouse gas emissions from reservoirs at high elevations in the Alps were investigated, and the results indicate reservoirs from subalpine/alpine regions to be only minor contributors of greenhouse gases to the atmosphere compared to other reservoirs.
Abstract: We investigated greenhouse gas emissions (CO2, CH4, and N2O) from reservoirs located across an altitude gradient in Switzerland. These are the first results of greenhouse gas emissions from reservoirs at high elevations in the Alps. Depth profiles were taken in 11 reservoirs located at different altitudes between the years 2003 and 2006. Diffusive trace gas emissions were calculated using surface gas concentrations, wind speeds and transfer velocities. Additionally, methane entering with the inflowing water and methane loss at the turbine was assessed for a subset of the reservoirs. All reservoirs were emitters of carbon dioxide and methane with an average of 970 ± 340 mg m−2 day−1 (results only from four lowland and one subalpine reservoir) and 0.20 ± 0.15 mg m−2 day−1, respectively. One reservoir (Lake Wohlen) emitted methane at a much higher rate (1.8 ± 0.9 mg m−2 day−1) than the other investigated reservoirs. There was no significant difference in methane emissions across the altitude gradient, but average dissolved methane concentrations decreased with increasing elevation. Only lowland reservoirs were sources for N2O (72 ± 22 μg m−2 day−1), while the subalpine and alpine reservoirs were in equilibrium with atmospheric concentrations. These results indicate reservoirs from subalpine/alpine regions to be only minor contributors of greenhouse gases to the atmosphere compared to other reservoirs.

Summary (3 min read)

Introduction

  • In the early 1990s artificial lakes and reservoirs were discovered as potential greenhouse gas emitters (Rudd et al. 1993; Kelly et al. 1994).
  • The question was put forward whether hydroelectric reservoirs, especially in the tropics, could still be considered cleaner energy sources compared to fossil alternatives (Fearnside 1997, 2002; Delmas et al.
  • In total, Swiss reservoirs cover an area of nearly 120 km2 (approximately 0.01 % of the area Electronic supplementary material.

Present Address:

  • The main emission pathways for greenhouse gases from reservoir surfaces are the diffusive flux across the air–water interface and bubble flux resulting from supersaturation in the sediment.
  • Changes in isotopic signature caused by methane emission are small (Knox et al. 1992), while turbulent diffusion has no effect.
  • Furthermore, the authors examined the importance of river inflows for the methane content of reservoirs at different altitudes and the contribution of methane loss to total methane emissions.

Study sites

  • Between September 2003 and August 2006, 11 Swiss reservoirs from different regions and elevations were sampled for greenhouse gases (Table 1; Fig. 1 for reservoir properties and locations, Table 3 for sampling dates).
  • A drop of reservoir water of several hundred meters through pipes and tunnels before it reaches the turbines is the result.
  • Two of the reservoirs investigated (Lakes Oberaar, alpine and Sihl, lowland) are pump-storage reservoirs, which receive water from a reservoir or lake located at lower altitude (Lake Grimsel for Lake Oberaar and Lake Zurich for Lake Sihl).
  • Sampling time was restricted to late spring until autumn, as access to the high altitude reservoirs was limited due to weather conditions and water content was low after ice-melt.

Methods

  • Sampling A SBE 19 CTD probe (Sea Bird Electronics) equipped with an oxygen and pH sensor was used to collect hydrographic data (conductivity, temperature, depth, light transmission, pH and dissolved oxygen).
  • Winkler samples were used to correct the offset in the oxygen sensor.
  • Samples for dissolved gas analysis were flushed with 2–3 times the bottle volume before the samples were preserved with NaOH (pH [ 12) or Cu(I)Cl, then closed with a butyl septa while carefully avoiding air bubbles in the bottles.
  • Inflows, outflows Methane concentrations were measured in the in- and outflowing water of six reservoirs.
  • If possible the CTD probe was used, but if depth of the river was not sufficient, temperature and conductivity were measured with a WTW LF 330 conductivity meter, pH with a Metrohm 704 pH-meter and oxygen with a WTW Multi 340i multi probe.

CO2

  • Dissolved CO2 (DIC) was calculated using the measured alkalinity, temperature, pH, and the dissociation constants of H2CO3 and HCO3 - (Plummer and Busenberg 1982).
  • Samples for alkalinity were taken at the surface and at the bottom of the water column.

CH4 and N2O

  • Concentrations of dissolved methane and nitrous oxide were measured by the headspace technique similar to McAuliffe (1971).
  • The oven temperature was kept constant at 70 C and the detector temperature was 340 C.
  • The carbon isotopic signature of methane was determined similar to the method described by Sansone et al. (1997).
  • The model estimates the air–water flux F [mg m-2 day-1] using the water saturation concentration Ceq [M], the measured water concentration Cw [M] of the greenhousegas, the transfer velocity k [cm h-1] and a unit conversion factor f.

Results

  • CO2 concentrations and emissions Surface concentrations of CO2 were supersaturated in all five reservoirs for which data are available (Table 2) with concentrations ranging from 40–280 lmol L-1.
  • In nearly all lakes, alkalinity measured above at the bottom of the lake was nearly 0.5 units higher than at the lake surface, except for Lake Luzzone and Lake Wohlen , where values were similar (data not shown).
  • Figure 2a, b show a typical profile for an alpine reservoir (Lake Grimsel) and for a lowland reservoir (Lake Lungern).
  • Methane concentrations, d13C isotopic composition and emissions.

Concentrations and isotopic composition

  • In the 11 reservoirs sampled, three characteristic types of methane profiles were identified.
  • In the following, one example for each profile type will be illustrated.
  • In Lake Santa Maria , methane concentrations on all three sampling dates (June, July, and August) increased towards the bottom (Fig. 3b).
  • These profiles showed a local maximum of methane concentrations in intermediate water layers.
  • Concentrations increase again towards the sediment and reach the highest concentrations above the sediment at 100 nmol L-1 in August.

Emissions

  • Concentrations in Lake Bianco were at saturation (*3 nmol L-1), therefore the methane emissions were negligible (Table 2; Fig. 4).
  • Right Temperature (black line), light transmission (yellow line), conductivity (green line) and dissolved oxygen concentration (red) profiles of Lake Bianco.
  • B Left Methane concentrations (open symbols) and isotopic composition (full symbols) in Lake Santa Maria on 7 June , 6 July and 23 August 2005 .
  • Concentrations tend do decrease later in the year, but this is not a common trend for all reservoirs.

Discussion

  • One reason the CH4 emissions the authors measured are low compared to diffusive fluxes from other reservoirs in general could be that they have been measured at deep sites of the reservoirs where emissions are lower compared to shallow, littoral areas (Duchemin et al.
  • This increase causes a shift away from DIC and H2CO3 towards CO3 2- causing lower concentration differences between water and the atmosphere and thus smaller fluxes.
  • When looking at the methane profiles of reservoirs (Fig. 3; supplementary material 1–3), there is an obvious difference between alpine reservoirs which have dissolved methane concentrations below 60 nmol L-1 and subalpine/lowland reservoirs which have maximum concentrations above 100 nmol L-1 and up to 6,500 nmol L-1.
  • A third reason is that ebullition, a potential pathway for methane emission, is not included in their calculations.
  • Lower concentrations of DIC (only Lake Luzzone, subalpine) and CH4 in reservoirs of higher elevations (Table 2; Fig. 3 and supplementary material 1) reflect the less favourable conditions for internal productivity and respiration (lower temperatures, shorter ice-free periods, less nutrients) compared to lower elevations.

Methane sources

  • Generally, the carbon cycle in oxic lakes and reservoirs assumes methane production in the sediments followed by methane oxidation during the diffusion into the water column (e.g. Kuivila et al. 1988).
  • An exception is Lake Oberaar , which is a pumpstorage reservoir and receives substantial amounts of water from Lake Grimsel , and thus is more likely controlled by the methane inflow from Lake Grimsel than by the inflow of glacial melt water.
  • This implies that methane loss from water passing the turbine could be equally important as methane loss via the reservoir surface in alpine and subalpine reservoirs, while being of less importance for lowland reservoirs.

Conclusions

  • The most important greenhouse gas emitted from the perialpine and alpine reservoirs the authors sampled in Switzerland is CO2.
  • Temperature and organic matter input are presumably the most important factors for the decrease the authors found, while reservoir morphology of the predominantly steep and deep subalpine/alpine reservoirs could be an important factor as well.
  • The amount of external methane entering via inflows is sufficient to explain the emission rates found in some reservoirs in spring and early summer, while contributions from other sources (e.g. sediments) increase towards autumn for two lowland reservoirs.
  • The authors would like to thank MeteoSchweiz for supplying wind speed data.
  • Additionally the authors would like to thank Markus Fette, Michael Schurter, Michael Meyer, Ilia Ostrovsky, David Finger and Lorenz Jaun for their assistance during sampling.

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ETH Library
Greenhouse gas emissions (CO2,
CH4, and N2O) from several
perialpine and alpine hydropower
reservoirs by diffusion and loss in
turbines
Journal Article
Author(s):
Diem, T.; Koch, S.; Schwarzenbach, S.; Wehrli, B.; Schubert, C.J.
Publication date:
2012-07
Permanent link:
https://doi.org/10.3929/ethz-b-000059528
Rights / license:
In Copyright - Non-Commercial Use Permitted
Originally published in:
Aquatic Sciences 74(3), https://doi.org/10.1007/s00027-012-0256-5
This page was generated automatically upon download from the ETH Zurich Research Collection.
For more information, please consult the Terms of use.

RESEARCH ARTICLE
Greenhouse gas emissions (CO
2
,CH
4
, and N
2
O) from several
perialpine and alpine hydropower reservoirs by diffusion
and loss in turbines
T. Diem
S. Koch
S. Schwarzenbach
B. Wehrli
C. J. Schubert
Received: 18 April 2011 / Accepted: 2 March 2012 / Published online: 11 April 2012
Ó Springer Basel AG 2012
Abstract We investigated greenhouse gas emissions
(CO
2
,CH
4
, and N
2
O) from reservoirs located across an
altitude gradient in Switzerland. These are the first results
of greenhouse gas emissions from reservoirs at high
elevations in the Alps. Depth profiles were taken in 11
reservoirs located at different altitudes between the years
2003 and 2006. Diffusive trace gas emissions were calcu-
lated using surface gas concentrations, wind speeds and
transfer velocities. Additionally, methane entering with the
inflowing water and methane loss at the turbine was
assessed for a subset of the reservoirs. All reservoirs were
emitters of carbon dioxide and methane with an average of
970 ± 340 mg m
-2
day
-1
(results only from four lowland
and one subalpine reservoir) and 0.20 ± 0.15 mg m
-2
day
-1
, respectively. One reservoir (Lake Wohlen) emitted
methane at a much higher rate (1.8 ± 0.9 mg m
-2
day
-1
)
than the other investigated reservoirs. There was no sig-
nificant difference in methane emissions across the altitude
gradient, but average dissolved methane concentrations
decreased with increasing elevation. Only lowland reser-
voirs were sources for N
2
O (72 ± 22 lgm
-2
day
-1
),
while the subalpine and alpine reservoirs were in equilib-
rium with atmospheric concentrations. These results
indicate reservoirs from subalpine/alpine regions to be only
minor contributors of greenhouse gases to the atmosphere
compared to other reservoirs.
Keywords Greenhouse gases Emissions Reservoirs
Methane Alpine
Introduction
In the early 1990s artificial lakes and reservoirs were dis-
covered as potential greenhouse gas emitters (Rudd et al.
1993; Kelly et al. 1994). The question was put forward
whether hydroelectric reservoirs, especially in the tropics,
could still be considered cleaner energy sources compared
to fossil alternatives (Fearnside 1997, 2002; Delmas et al.
2001; Pacca and Horvath 2002). Estimates suggest total
emissions from reservoirs of about 70 Tg CH
4
year
-1
and
1,000 Tg CO
2
year
-1
, accounting for 7 % of the anthro-
pogenic emissions of these gases (St. Louis et al. 2000).
Based on a much larger dataset, Barros et al. (2011)
recently estimated reservoirs to emit only 176 Tg CO
2
year
-1
and 4 Tg CH
4
year
-1
. There is, however, a high
variability of trace gas emissions between different reser-
voirs, which leads to large uncertainties in quantification of
global emissions and the available amount of data is still
small compared to the number of reservoirs. So far there is
limited information about emissions from reservoirs in the
temperate climate zone (e.g. Soumis et al. 2004; DelSontro
et al. 2010), which account for approximately 40 % of all
reservoirs (Barros et al. 2011), and to our knowledge none
from alpine reservoirs. In total, Swiss reservoirs cover an
area of nearly 120 km
2
(approximately 0.01 % of the area
Electronic supplementary material The online version of this
article (doi:10.1007/s00027-012-0256-5) contains supplementary
material, which is available to authorized users.
T. Diem (&) S. Koch S. Schwarzenbach B. Wehrli
C. J. Schubert
Department of Surface Waters-Research and Management,
EAWAG, Seestrasse 79, 6047 Kastanienbaum, Switzerland
e-mail: ttd2@st-andrews.ac.uk
Present Address:
T. Diem
School of Geography and Geosciences,
University of St. Andrews, Irvine Building,
North Street, St. Andrews KY16 9AL, Scotland, UK
Aquat Sci (2012) 74:619–635
DOI 10.1007/s00027-012-0256-5
Aquatic Sciences
123

of temperate hydroelectric reservoirs), 60 % of which are
situated at an elevation above 1,000 m a.s.l. (http://www.
bfe.admin.ch/php/modules/publikationen/stream.php?extla
ng=de&name=de_242311927.pdf).
The main emission pathways for greenhouse gases from
reservoir surfaces are the diffusive flux across the air–water
interface and bubble flux (ebullition) resulting from
supersaturation in the sediment. Bubbles mainly transport
methane and only small amounts of carbon dioxide. The
strong temperature dependence of methane production (e.g.
Zeikus and Winfrey 1976; Kelly and Chynoweth 1981;
Nguyen et al. 2010) suggests a decrease of methane
emissions with decreasing temperatures at higher eleva-
tions. Besides emissions from the reservoir surface, other
emission pathways that can significantly contribute to total
gas emissions have recently drawn attention, i.e. gas
release immediately below the turbine and emissions fur-
ther downstream (Abril et al. 2006; Roehm and Tremblay
2006; Kemenes et al. 2007). Emissions from these two
pathways contribute methane amounts similar to reservoir
surface loss (Gue
´
rin et al. 2006; Kemenes et al. 2007) and
are thus highly relevant for greenhouse gas (especially
methane) emissions from reservoirs.
Besides sediments, other relevant sources of surface
water greenhouse gases in lakes or estuaries are rivers and
inflows (de Angelis and Lilley 1987; Upstill-Goddard et al.
2000; Murase et al. 2005). Thus reservoir inflows could
contribute a considerable amount of dissolved greenhouse
gases to the epilimnion of the reservoir and therewith the
water layer is significant for diffusive surface flux.
Inflowing water that has not yet completely mixed in a
reservoir can be identified by hydrographic data (for
example temperature and conductivity) or by the isotopic
composition of methane, which can also be used to dis-
tinguish between different sources (for example inflows
and sediment flux) of methane. However, when using the
isotopic composition of methane, one has to keep in mind
that methane oxidation can significantly alter d
13
C values
(Barker and Fritz 1981; Whiticar 1999). In stratified oxic
waters, methane oxidation is limited to a narrow zone at the
oxic–anoxic interface (Rudd et al. 1976). Changes in iso-
topic signature caused by methane emission are small
(Knox et al. 1992), while turbulent diffusion has no effect.
With this study, we provide the first data on greenhouse
gas emissions from hydropower reservoirs across an alti-
tude gradient in the Swiss Alps (Central Europe). We
calculated diffusive fluxes of CO
2
,CH
4
and N
2
O from the
surface concentrations of several Swiss reservoirs at dif-
ferent times of the year. Eleven reservoirs at different
altitudes were sampled and compared for diffusive green-
house gas emissions over an altitude gradient, assuming
conditions for greenhouse gas production and emission to
decrease with altitude. Furthermore, we examined the
importance of river inflows for the methane content of
reservoirs at different altitudes and the contribution of
methane loss to total methane emissions.
Study sites
Between September 2003 and August 2006, 11 Swiss
reservoirs from different regions and elevations were
sampled for greenhouse gases (Table 1; Fig. 1 for reservoir
properties and locations, Table 3 for sampling dates). The
reservoirs are distributed along an elevation gradient from
481 to 2,368 m a.s.l. and climate varies accordingly
between the different reservoirs. For example, average
yearly air temperatures range from *8 °C at Lake Wohlen
(lowland) to nearly 0 °C at Lake Oberaar (alpine). Average
precipitation differs by a factor of 3 between the reservoirs
and is listed in Table 1 together with the geology of the
watershed and other reservoir characteristics. Unfortu-
nately, nutrient data was only available for some reservoirs
(supplementary Table A).
There are several specific features concerning reservoirs
in alpine Switzerland. Reservoirs set in alpine valleys with
steep slopes are rather deep (up to 230 m) with small
littoral zones, due to the rapid increase of water depth. This
is especially important and distinguishes those reservoirs
from lowland reservoirs and lakes where littoral zones are
very important for overall greenhouse gas emissions of
oligotrophic lakes (Thebrath et al. 1993; Casper 1996).
Another feature is that water is pumped from neighbouring
valleys into the reservoirs, enlarging the reservoir catch-
ment area in some cases quite substantially. Electricity
production uses the elevation difference between mountain
reservoirs and power stations in the valley. A drop of
reservoir water of several hundred meters through pipes
and tunnels before it reaches the turbines is the result. A
second water outflow (called residual water) is a legally
established amount of water that has to be released from
the reservoirs to provide the river ecosystem downstream
with a minimum amount of water. A last characteristic of
these reservoirs is that the majority of the water filling the
reservoirs is available from spring to autumn when the snow
stored in winter melts. Thus, water level declines in winter and
reaches its minimum in early spring with, in some cases, less
than 10 % of the maximum water volume left.
Two of the reservoirs investigated (Lakes Oberaar,
alpine and Sihl, lowland) are pump-storage reservoirs,
which receive water from a reservoir or lake located at
lower altitude (Lake Grimsel for Lake Oberaar and Lake
Zurich for Lake Sihl). While the water volume of Lake
Oberaar is replaced up to ten times every year by pumping,
it only contributes a minor part to Lake Sihl. Lake Wohlen
(lowland) on the other hand is a run-of-the-river reservoir,
620 T. Diem et al.
123

Table 1 Properties of the sampled reservoirs
Lake Location
(latitude/
longitude)
Elevation
(m)
Classification Year of
construction
Volume
(Mio m
3
)
Surface
(km
2
)
Greatest
depth (m)
Average
depth (m)
Retention
time (days)
Geology of watershed Average yearly
precipitaion (mm)
1. Lake Wohlen 46°58
0
N/7°19
0
E 481 Lowland
a
1920 25 3.65 20 7 2–3 Sedimentary rocks
(marl, sandstone,
limestone, clay)
1,000–1,200
2. Lake Gruye
`
re 46°39
0
N/7°06
0
E 677 Lowland
a
1947 200 9.6 75 21 75 Fluvial deposits, limestone 1,200–1,600
3. Lake Lungern 46 48
0
N/8°10
0
E 689 Lowland
a
1920 65 2.01 68 32 100–200 Sedimentary rocks
(lime, marl)
1,400–2,000
4. Lake Sihl 47°08
0
N/8°48
0
E 889 Lowland
a
1936 96.5 10.85 23 9 140
d
Sedimentary rocks
(limestone, marl)
1,200–1,600
5. Lake Luzzone 46°34
0
N/8°58
0
E 1,591 Subalpine
b
1963 88 1.44 181 61 230 Deformed sedimentary,
metamorphic and
igneous rocks
1,600–2,000
6. Lake Zeuzier 46°21
0
N/7°26
0
E 1,777 Subalpine
b
1957 51 0.85 140 60 120 Sedimentary rocks 2,000–2,400
7. Lake Santa Maria 46°34
0
N/8°48
0
E 1,908 Subalpine
b
1968 67 1.17 86 57 100–200
e
Granite, gneiss and
paragneiss
2,000–2,400
8. Lake Grimsel 46°34
0
N/8°20
0
E 1,908 Alpine
c
1932 101 2.72 100 37 20–50
f
Igneous rocks (granite) 2,400–3,000
9. Lago Bianco 46°24
0
N/10°01
0
E 2,234 Alpine
c
1912 21 1.5 53 14 100–200
g
Igneous rocks (granite) 2,000–2,400
10. Lake Oberaar 46°33
0
N/8°16
0
E 2,303 Alpine
c
1953 61 1.46 90 42 30–60
f
Igneous rocks (granite) 2,400–3,000
11. Lake Dix 46°04
0
N/7°24
0
E 2,368 Alpine
c
1961 401 4.3 227 93 30–50 Igneous rocks (granite) 1,600–2,400
a
Lowland reservoirs is used for reservoirs below 1,000 m a.s.l
b
Subalpine reservoirs is used for reservoirs between 1,000 and approximately 1,900 m a.s.l., which do not have a whitish water color due to a high amount of particles from glacial melt water
c
Alpine reservoirs are is used for reservoirs above 1,900 m a.s.l., which do have a whitish water color due to a high amount particles from glacial melt water
d
About 10 % of the water in the lake are pumped from Lake Zurich
e
Is connected with two other reservoirs to one power station
f
Water from Lake Grimsel is pumped into Lake Oberaar at night and released back to Lake Grimsel during the day for energy production; this way the volume of Lake Oberaar gets replaced
about ten times every year
g
Is a storage reservoir for Lake Palu
¨
, no direct energy production
Greenhouse gas emission from alpine reservoirs 621
123

which has a steady inflow from a river, a small capacity (as
well as a small water retention time) and has water flowing
through it all the time. All other reservoirs are conventional
reservoirs, which use the dam to create a large water
storage capacity, produce electricity during times of
demand or store the water in the meantime.
Reservoirs were selected to roughly include the whole
extent of reservoir depths (4–227 m), sizes (0.1–10.9 km
2
),
volume (0.4–401 Mio m
3
) and altitude distributions
(459–2,446 m a.s.l.) of the reservoirs. Sampling time was
restricted to late spring until autumn, as access to the high
altitude reservoirs was limited due to weather conditions
and water content was low after ice-melt.
Methods
Sampling
A SBE 19 CTD probe (Sea Bird Electronics) equipped with
an oxygen and pH sensor was used to collect hydrographic
data (conductivity, temperature, depth, light transmission,
pH and dissolved oxygen). The water column was sampled
with a 5 L Niskin bottle and aliquots were immediately
transferred into bottles with a tube, avoiding bubbles
(Winkler bottles for oxygen, 200 mL plastic bottles for
alkalinity and 600 mL glass bottles for methane and nitrous
oxide concentration). Samples were taken at different
depths for each reservoir, usually below the surface, above
the sediment and every 10 or 20 m in between. Sample
sites are at the deepest point of the dam basin and for some
reservoirs a second site was examined closer to the inlet.
Replicates were taken for dissolved gas concentrations.
Winkler samples were used to correct the offset in the
oxygen sensor. Unfiltered water was titrated with 0.1 M HCl
for alkalinity. Samples for dissolved gas analysis were flushed
with 2–3 times the bottle volume before the samples were
preserved with NaOH (pH [ 12) or Cu(I)Cl, then closed with
a butyl septa while carefully avoiding air bubbles in the bot-
tles. To calibrate the pH sensor (SBE 18 pH sensor, SeaBird,
measurement range 0–14, accuracy 0.1 pH units), solutions of
known pH (pH = 4, 7 and 9) were used before each sampling
date. The accuracy of the pH sensor was not sufficient for low
conductivity lakes, thus CO
2
concentrations and fluxes for
reservoirs with conductivities below 100 lScm
-1
were not
calculated.
Fig. 1 Locations of the sampled reservoirs (for numbers see Table 1)
622 T. Diem et al.
123

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References
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Journal ArticleDOI
TL;DR: In this paper, the authors measured the open water conditions in two hydroelectric reservoirs, Lokka and Porttipahta, in the northern boreal zone in Finland, and concluded that if there is a good long-term availability of phosphorus and nitrogen, the intensive internal C cycle associated with the primary production could maintain high CH4 and CO2 production for decades.
Abstract: [1] Concentrations and fluxes of greenhouse gases methane (CH4), carbon dioxide (CO2), and nitrous oxide (N2O) were measured during open water conditions in two hydroelectric reservoirs, Lokka and Porttipahta, in the northern boreal zone in Finland. These reservoirs were located on peat and forest soils and were built in 1967 and 1970, respectively. Over 20 years after their flooding, the reservoirs were still largely supersaturated with dissolved CH4 and CO2. Measured with floating static chambers, the stations in Lokka released more CH4 (means of 5.3–119 mg m−2 d−1) during the open water periods in 1994 and 1995 than the stations in Porttipahta (means of 2.5–4.8 mg m−2 d−1), measured in 1995. The mean CO2 emission rates in Lokka (21–133 mg m−2 h−1) and Porttipahta (36–95 mg CO2 m−2 h−1) were more similar. The chamber measurements could not detect episodic CH4 ebullition in Lokka Reservoir, indicated by generally higher CH4 fluxes (means of 2.6–660 mg m−2 d−1) obtained with bubble gas collectors than with the chambers. The seasonal mean N2O fluxes were generally low, ranging from −89 to 270 μg m−2 d−1. There was no clear association between the CH4 emissions and the bottom type, including mineral soils and old peat deposits. The flooded vegetation, higher nutrient content, and primary production in the water column rather than old peat could account for the higher CH4 emissions from the stations in Lokka. This conclusion is supported by the high content of modern carbon (C) in methane (percent modern C of 92–104%) that was extracted from the sediment of Lokka. The results suggested that if there is a good long-term availability of phosphorus and nitrogen, the intensive internal C cycle associated with the primary production could maintain high CH4 and CO2 production for decades, similar to the situation in eutrophied natural lakes.

171 citations


"Greenhouse gas emissions (CO2, CH4,..." refers background in this paper

  • ...Nitrous oxide emissions Similar to previous findings, fluxes of N2O in lakes and reservoirs are small in open water areas (Huttunen et al. 2002)....

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Journal ArticleDOI
TL;DR: Application of physical and chemical concepts, complemented by studies of prokaryotes in ice cores and permafrost, has led to the present understanding of how microorganisms can metabolize at subfreezing temperatures on Earth and possibly on Mars and other cold planetary bodies.

162 citations


"Greenhouse gas emissions (CO2, CH4,..." refers background in this paper

  • ...Other potential sources for methane in alpine reservoirs could be glacial meltwater (Tung et al. 2005; Price 2007; Wadham et al. 2008) and glacial forefields (Bárcena et al. 2010)....

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  • ...Other potential sources for methane in alpine reservoirs could be glacial meltwater (Tung et al. 2005; Price 2007; Wadham et al. 2008) and glacial forefields (Bárcena et al....

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Journal ArticleDOI
TL;DR: In terms of the total carbon budget of the lake, the upward flux of methane is insignificant with only about 2% of the carbon fixed by primary production being returned as methane as mentioned in this paper.
Abstract: Aerobic oxidation is important in the cycling of methane in the sediments of Lake Washington. About half of the methane flux from depth is oxidized to CO, in the upper 0.7 cm of the sediments and the remainder escapes into the water column. In terms of the total carbon budget of the lake, the upward flux of methane is insignificant with only about 2% of the carbon fixed by primary production being returned as methane. The upward flux of methane, however, does represent about 20% of the organic carbon decomposed within the sediments. In addition, methane oxidation consumes 7-10% of the total oxygen

155 citations


"Greenhouse gas emissions (CO2, CH4,..." refers background in this paper

  • ...Generally, the carbon cycle in oxic lakes and reservoirs assumes methane production in the sediments followed by methane oxidation during the diffusion into the water column (e.g. Kuivila et al. 1988)....

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Journal ArticleDOI
TL;DR: In this paper, the authors measured in coastal waters of the southern North Sea, in two adjacent U.K. estuaries with well-defined turbidity maxima (Humber and Tyne) and in their associated river catchments, during a series of campaigns covering the period 1993-1999.
Abstract: Dissolved CH4was measured in coastal waters of the southern North Sea, in two adjacent U.K. estuaries with well-defined turbidity maxima (Humber and Tyne) and in their associated river catchments, during a series of campaigns covering the period 1993–1999. In general, samples from all three environments were significantly to highly CH4 enriched relative to atmospheric air. Observed river water concentrations, ∼ 33–152 nmol L−1 (940–4305% saturation) for the Humber river catchment and ∼ 3–62 nmol L−1 (86–1754% saturation) in the river Tyne, were within but toward the low end of the range of CH4 concentrations in river waters world wide. In sea waters from the outer Wash estuary (U.K. coast) and adjacent to the Dutch coast, CH4 was highly but nonlinearly correlated with salinity, consistent with strong CH4 removal from river and/or estuarine CH4 sources influencing these locations. In transects along the Humber and Tyne estuaries, CH4 was highly negatively nonconservative, confirming the estuarine removal hypothesis. For both estuaries, highest CH4 concentrations, ∼190–670 nmol L−1 (6000–21,000% saturation) in the Humber and ∼650 nmol L−1(21,800% saturation) in the Tyne, were observed at very low salinity in the vicinity of the turbidity maximum. Importantly, these concentrations greatly exceeded measured river water values, implying for both situations the existence of a large in situ CH4 supply associated with high turbidity. Time series measurements at two locations in the upper Tyne subsequently confirmed the strong correspondence of dissolved CH4 and turbidity in the vicinity of the turbidity maximum. CH4removal estimated for the Humber, Tyne, Wash, and Rhine-Scheldt estuaries was ∼ 90% of the low-salinity CH4 input. On the basis of this and river discharge data, −7.I×108 mol CH4 may be removed annually in estuaries bordering the southern North Sea. Of this, ∼6.6×108mol may be lost by air-sea exchange. This represents an additional atmospheric CH4 flux from the North Sea unaccounted for in previous work, which may have, consequently, underestimated this source by ∼50%. Upward scaling of this estimate based on the mean of reported river water CH4 concentrations implies a previously unaccounted for ∼6.3–24×109 mol (i.e., ∼ 0.1–0.4 × 1012 g) CH4 yr−1 which may be lost globally to gas exchange in estuaries, increasing previous such estimates by ∼8–50%. However, as it is based on data that exclude the possibility of elevated CH4 levels at estuarine turbidity maxima, even this revision is likely to be conservative. Detailed studies of CH4 distributions in major world estuaries would now be required in order to successfully reevaluate the CH4 budget of the coastal marine atmosphere.

153 citations


"Greenhouse gas emissions (CO2, CH4,..." refers background in this paper

  • ...Besides sediments, other relevant sources of surface water greenhouse gases in lakes or estuaries are rivers and inflows (de Angelis and Lilley 1987; Upstill-Goddard et al. 2000; Murase et al. 2005)....

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Journal ArticleDOI
TL;DR: In this paper, it was shown that the isotopic fractionation during gas transfer for these gases is not equal to the square root of their reduced mass in water, as would be predicted by an extension of the kinetic theory of ideal gases to dissolved gases.
Abstract: The authors present experimental results that show that the kinetic isotopic fractionation during gas exchange is 0.9972 [plus minus] 0.0002 for oxygen, 0.9992 [plus minus] 0.0002 for methane, 0.9987 [plus minus] 0.0001 for nitrogen and 0.982 [plus minus] 0.002 for hydrogen, and that the equilibrium fractionation between water and gas phases is 1.037 for hydrogen. They show that the isotopic fractionation during gas transfer for these gases is not equal to the square root of their reduced mass in water, as would be predicted by an extension of the kinetic theory of ideal gases to dissolved gases. The use of isotopes as tracers of biogeochemical gases requires knowledge of the fractionation factor for air-water gas transfer; there have been few direct measurements of these factors. 31 refs., 11 figs., 1 tab.

152 citations


"Greenhouse gas emissions (CO2, CH4,..." refers background in this paper

  • ...Changes in isotopic signature caused by methane emission are small (Knox et al. 1992), while turbulent diffusion has no effect....

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Frequently Asked Questions (2)
Q1. What contributions have the authors mentioned in the paper "Greenhouse gas emissions (co2, ch4, and n2o) from several perialpine and alpine hydropower reservoirs by diffusion and loss in turbines" ?

The authors investigated greenhouse gas emissions ( CO2, CH4, and N2O ) from reservoirs located across an altitude gradient in Switzerland. 

Further studies are needed to support this and determine up to which altitude bubble flux plays a role in reservoirs of the Alps. As a result the reservoir stores methane from rivers, which otherwise would probably emit on the way down the mountain, and exposes it to potential methane oxidation inside the reservoir. And finally two anonymous reviewers for their helpful comments and suggestions.