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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

Citations
More filters
Posted ContentDOI
TL;DR: In this paper, N2O and CH4 measurements were performed simultaneously or at different times, which is essential for the interpretation of the comparison, and the authors highlight the unique implications from this study and how it leads forward towards better understanding the complexity and reducing the future challenges.
Abstract: Line 7: Unclear what control site means here as stable control conditions may be difficult to maintain under fluctuating water. Please clarify in what way these two sites served as control. (This is explained in the later text so this comment is about clarity for those only reading the abstract. However I think the word control site signals something else than what is the case here and what is called control site here does not stand out as very different from the other sites with stable water moisture, e.g. the NF site, so I wonder if it would not be good to omit using the word “control” to reduce the risk of confusion.) L17: Were N2O and CH4 measurements performed simultaneously or at different times? This is essential for the interpretation of the comparison. L 18-20: The sentence “It showed that N2O flux and CH4 flux was influenced by distinct factors and in differing ways.” is a bit vague. Would it be possible to briefly explain how N2O and CH4 fluxes and regulation differed instead? L20-22: Instead of ending the abstract with emphasizing the complexity and challenges – please highlight the unique implications from this study and how it leads forward towards better understanding the complexity and reducing the future challenges.

4 citations

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01 Jan 2013
TL;DR: In this article, a grande echelle of the Gaz a Effet de Serre (GES) en relation avec the creation of a reservoir hydroelectrique, Nam Theun 2 (NT2) dans la region subtropicale de la Republique Democratique Populaire du Laos, Asie, is presented.
Abstract: L'augmentation de l'interet concernant la part des reservoirs hydroelectrique dans l'augmentation de la concentration atmospherique des Gaz a Effet de Serre (GES) a amene a mesurer les emissions nettes d'un reservoir hydroelectrique, Nam Theun 2 (NT2) dans la region subtropicale de la Republique Democratique Populaire du Laos, Asie. Ce travail est la premiere evaluation de l'empreinte carbone des GES (c'est a dire : les emissions apres ennoiement moins les emissions avant ennoiement) en relation avec la creation d'un reservoir hydroelectrique. C'est le resultat d'une etude a grande echelle qui s'est deroulee pendant cinq ans (2008-2012). Nous avons tout d'abord quantifie les sources et les puits majeurs des GES des composants terrestres et aquatiques du paysage avant ennoiement (Mai 2008). Ensuite, a partir d'Avril 2009, cette etude similaire a ete realisee au niveau du reservoir, sa zone de marnage et son aval. C'est en Octobre 2009 que le reservoir hydroelectrique NT2 a, pour la premiere fois, atteint son niveau maximal et c'est huit mois plus tard, en Mars 2010, que les turbines ont fonctionnees pour la premiere fois. En se basant sur un suivi bimensuel et sur cinq missions de terrain couvrant toutes les saisons, les emissions des principaux GES (c'est a dire l'oxyde nitreux (N2O), le methane (CH4) et le dioxyde de carbone (CO2)) ont ete mesurees d'Avril 2009 a Decembre 2011. Les emissions ont ete determinees a la surface du reservoir (flux diffusifs et ebullitifs) ainsi que dans les sols de la zone de marnage, qui peut atteindre 370 km2 pour une surface totale de reservoir de 450 km2.

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    [...]

  • ...…summer surface concentrations of 23.7 μM for lakes and 21.1 μM for reservoirs were lower than lakes and reservoirs in the Alpine region of Europe (Diem et al. 2012; Pighini et al. 2018) and non-arctic North American lakes (Cole et al. 1994), and more than an order of magnitude lower than…...

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  • ...Previous work has shown subalpine and alpine reservoir contribution to global CO2 emissions to be small (Diem et al. 2012), and this study confirms that high-elevation alpine reservoirs as well as natural alpine lakes are likely small overall contributors to global emissions....

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DissertationDOI
01 Jan 2014
TL;DR: It is demonstrated that anammox bacteria coexist with sulfide-dependent denitrifiers in the water column of the Lake Lugano north basin, and it is shown that denitrification was the major benthic NO3- reduction pathway in the southern basin.
Abstract: The consequences of detrimental alterations caused to the natural nitrogen (N) cycle are manifold To tackle problems, such as eutrophication of coastal marine and lacustrine environments, or increasing emissions of greenhouse gas nitrous oxide (N2O), requires a clear understanding of the microbial N cycle A promising tool to study N transformations is the measurement of the stable isotope composition of N compounds The overall goal of this project was to improve the understanding of N transformation pathways and associated isotope effects, using the meromictic northern and the monomictic southern basins of Lake Lugano as natural model systems Toward this goal, we collected samples from the water column of both basins for dissolved inorganic nitrogen (DIN) analyses (including N2:Ar, N2O), molecular microbiological phylogenetic analyses, 15N-labeling experiments (water column and sediments), and stable N and O isotope (and N2O isotopomer) measurements First, we identified the main processes responsible for fixed N elimination in the Lake Lugano north basin The stable redox transition zone (RTZ) in the mid-water column provides environmental conditions that are favorable for both, anaerobic ammonium oxidation (anammox), as well as sulfur-driven denitrification Previous marine studies suggested that sulfide (H2S) inhibits the anammox reaction In contrast to this we demonstrated that anammox bacteria coexist with sulfide-dependent denitrifiers in the water column of the Lake Lugano north basin The maximum potential rates of both processed were comparatively low, but consistent with nutrient fluxes calculated from concentration gradients Furthermore, we showed that organotrophic denitrification is a negligible nitrate-reducing pathway in the Lake Lugano north basin Based on these findings, we next interpreted the N and O isotope signatures in the Lake Lugano north basin Anammox and sulfide-dependent denitrification left clear N (in NO3- and NH4+) and O (in NO3-) isotope patterns in the water column However, the associated isotope effects were low compared to previous reports on isotope fractionation by organotrophic denitrification and aerobic ammonium oxidation We attribute this apparent under-expression to two possible explanations: 1) The biogeochemical conditions (ie, substrate limitation, low cell specific N transformation rates) that are particularly conducive in the Lake Lugano RTZ to an N isotope effect under-expression at the cellular-level, or 2) a low process-specific isotope fractionation at the enzyme-level Moreover, an 18O to 15N enrichment ratio of ~089 associated with NO3- reduction suggested that the periplasmic dissimilatory nitrate reductase Nap was more important than the membrane-bound dissimilatory Nar While in the meromictic north basin, most fixed N elimination took place within the water column RTZ, seasonal mixing and re-oxygenation of the water column in the south basin suggests N2 production within the sediments We showed that denitrification was the major benthic NO3- reduction pathway in the southern basin Benthic anammox and dissimilatory nitrate reduction to ammonium (DNRA) rates remained close to the detection limit A comparison between benthic N2 production rates and water column N2 fluxes revealed that during anoxic bottom water conditions, ~40% of total N2 production was associated with benthic and ~60% with pelagic processes This quantitative partitioning was confirmed by N isotope analysis of water column NO3- The N isotope enrichment factor associated with total NO3- reduction was ~14‰ This translates into a sedimentary N2 contribution of 36-51%, if canonical assumptions for N isotope fractionation associated with water column (15ewater = 20-25‰) and sedimentary (15esed = 15-3‰) denitrification are made Finally, we compared the N2O production and consumption pathways in the northern and southern basin and found contrasting N2O dynamics Maximum N2O concentrations in the south basin (>900 nmol L-1) greatly exceeded maximum concentrations in the north basin ( 32‰ in the south basin indicated nitrification via hydroxylamine (NH2OH) oxidation as the prime N2O source, whereas in the north basin N2O production was attributed to nitrifier denitrification In the north basin, N2O was completely reduced within the RTZ This chemolithotrophic N2O reduction occurred with an 18O to 15N enrichment ratio of ~25, which is consistent with previous reports for organotrophic N2O reduction In conclusion, our study highlights the importance of chemolithotrophic processes in aquatic ecosystems Moreover, the expression of N isotope fractionation can be variable in nature and depends on various factors such as the pathways of NO3- dissimilation (organotrophic vs chemolithotrophic), the main catalyzing enzymes, the pathways of NH4+ oxidation (nitrification vs anammox), and the controlling environmental conditions (eg, substrate limitation, cell specific N transformation rates) Hence, this study suggests to refrain from universal, canonical assumptions of N isotope fractionation in N budget calculations Additional stable isotope measurements such as O isotopes in NO3-, or the 15N site preference in N2O are powerful tools to identify and quantify microbial N transformation pathways occurring simultaneously or in close vicinity For a successful interpretation of such data, however, a mechanistic understanding of the processes leading to certain characteristic isotopic signatures in the environment is needed

4 citations

Journal Article
TL;DR: In this article, the main emission paths from aquatic environments are diffusivefluxes across the air-water interface, bubbleble( ebullition) fluxes resulting from supersaturation of sediment, and plantmediated fluxes.

4 citations

References
More filters
Journal ArticleDOI
TL;DR: In this paper, the influence of variability in wind speed on the calculated gas transfer velocities and the possibility of chemical enhancement of CO2 exchange at low wind speeds over the ocean is illustrated using a quadratic dependence of gas exchange on wind speed.
Abstract: Relationships between wind speed and gas transfer, combined with knowledge of the partial pressure difference of CO2 across the air-sea interface are frequently used to determine the CO2 flux between the ocean and the atmosphere. Little attention has been paid to the influence of variability in wind speed on the calculated gas transfer velocities and the possibility of chemical enhancement of CO2 exchange at low wind speeds over the ocean. The effect of these parameters is illustrated using a quadratic dependence of gas exchange on wind speed which is fit through gas transfer velocities over the ocean determined by the natural-14C disequilibrium and the bomb-14C inventory methods. Some of the variability between different data sets can be accounted for by the suggested mechanisms, but much of the variation appears due to other causes. Possible causes for the large difference between two frequently used relationships between gas transfer and wind speed are discussed. To determine fluxes of gases other than CO2 across the air-water interface, the relevant expressions for gas transfer, and the temperature and salinity dependence of the Schmidt number and solubility of several gases of environmental interest are included in an appendix.

4,187 citations


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

  • ...Schmidt numbers were calculated for the measured water temperatures according to Wanninkhof (1992) and the authors cited therein....

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Journal ArticleDOI
TL;DR: In this paper, the solubility coefficients for carbon dioxide in water and seawater are calculated for the data of Murray and Riley, and are fitted to equations in temperature and salinity of the form used previously to fit solubilities of other gases.

2,788 citations


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

  • ...Dissolved gas concentrations were calculated using solubility data from Wiesenburg and Guinasso (1979) for methane, from Weiss and Price (1980) for nitrous oxide, and from Weiss (1974) for carbon dioxide....

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Journal ArticleDOI
TL;DR: In this paper, the major dissolved carbon species in diagenetic settings are represented by the two carbon redox endmembers CH4 and CO2, and they can be tracked with the aid of carbon ( 13 C / 12 C ) and hydrogen ( D/H≡ 2 H/ 1 H ) isotopes.

2,589 citations


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

  • ...This oxidation is indicated by increasing d13C values of methane (Barker and Fritz 1981; Whiticar 1999)....

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  • ...However, when using the isotopic composition of methane, one has to keep in mind that methane oxidation can significantly alter d13C values (Barker and Fritz 1981; Whiticar 1999)....

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  • ...This oxidation is indicated by increasing d(13)C values of methane (Barker and Fritz 1981; Whiticar 1999)....

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01 Jan 1972
TL;DR: The variation in growth rate with temperature of unicellular algae suggests that an equation can be written to describe the maximum expected growth rate for temperatures less than 40°C, a logical starting point for modeling phytoplankton growth and photosynthesis in the sea.
Abstract: The variation in growth rate with temperature of unicellular algae suggests that an equation can be written to describe the maximum expected growth rate for temperatures less than 40°C. Measured rates of phytoplankton growth in the sea and in lakes are reviewed and compared with maximum expected rates. The assimilation number (i.e., rate of photosynthetic carbon assimilation per weight of chlorophyll a) for phytoplankton photosynthesis is related to the growth rate and the carbon/chlorophyll a ratio in the phytoplankton. Since maximum expected growth rate can be estimated from tempera­ ture, the maximum expected assimilation number can also be estimated if the carbon/ chlorophyll a ratio in the phytoplankton crop is known. Many investigations of phytoplankton photosynthesis in the ocean have included measures of the assimilation number, while fewer data are available on growth rate. Assimilation numbers for Antarctic seas are low as would be expected from the low ambient temperatures. Tropical seas and temperate waters in summer often show low assimilation numbers as a result of low ambient nutrient concentrations. However, coastal estuaries with rapid nutrient regeneration processes show seasonal variations in the assimilation number with temperature which agree well with expectation. The variation in maximum expected growth rate with temperature seems a logical starting point for modeling phytoplankton growth and photosynthesis in the sea.

2,264 citations


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

  • ...1999), as do low temperatures (Eppley 1972), having an effect on the overall amount of autochthonous carbon available....

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  • ...Additionally, increased UV-radiation at higher elevations reduces primary productivity (Sommaruga et al. 1999), as do low temperatures (Eppley 1972), having an effect on the overall amount of autochthonous carbon available....

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Journal ArticleDOI
TL;DR: In this paper, the authors compared the solubility of calcite, aragonite, and vaterite in CO2-H2O solutions between 0 and 90°C using the Debye-Huckel individual ion activity coefficients.

1,673 citations


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

  • ...Dissolved CO2 (DIC) was calculated using the measured alkalinity, temperature, pH, and the dissociation constants of H2CO3 and HCO3 - (Plummer and Busenberg 1982)....

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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.