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IMPACT OF THE SALINITY GRADIENT
ON THE MOLLUSC FAUNA IN FLOODED MINE SUBSIDENCES
(KARVINA, CZECH REPUBLIC)
KAMILA KAŠOVSKÁ1
, ŁUKASZ PIERZCHAŁA2
*, EDYTA SIERKA3
,
BARBARA STALMACHOVÁ1
1  
Institute of Environmental Engineering, Faculty of Mining and Geology,
VŠB-Technical University of Ostrava,
Czech Republic, 17.listopadu 15, 708 00, Ostrava
2  
Central Mining Institute, Department of Water Protection,
Poland, Plac Gwarków 1, 40-166, Katowice
3  
Department of Geobotany and Nature Protection, Faculty of Biology and Environmental Protection, Silesian University
Poland, Jagiellońska 28, 40-032 Katowice
* Corresponding authors e-mail: lpierzchala@gig.eu
Keywords: Molluscs, water salinity, mine subsidence, Karvina, Czech Republic.
Abstract: This paper presents the impact of salinisation on the aquatic mollusc fauna in flooded mine
subsidences in the Karvina region (Czech Republic). The results of the previous research on salinity in flooded
mine subsidences show that some of them contain a high content of dissolved inorganic substances (above
1000 mg·l-1
). These substances can affect the vegetation and animals occurring in the water and the surrounding
area. The phylum of Mollusca was selected as a model group for the fieldwork as it includes species with the
proven bioindication potential.
The occurrence of aquatic mollusc species was studied at 10 sites. The sites were selected based on
the content of dissolved substances (the salinity gradient from <500 to >1000 mg·l-1
. A total of 12 aquatic
mollusc species were found, including one species identified as a potential bioindicator of the negative effect
of salinisation on aquatic biota.
The analysis showed statistically significant positive correlations between the content of dissolved
inorganic substances and the presence of alien species Potamopyrgus antipodarum (J.E. Gray, 1843).
The gradient of salinity significantly affects the species composition of the mollusc fauna in flooded mine
subsidences and may affect the biodiversity of this group.
INTRODUCTION
The increasing salinity (as a concentration of dissolved inorganic ions, further referred to
as TDS) in surface freshwater ecosystems is becoming a serious problem worldwide [38,
52, 21, 22], including the Czech Republic, especially in post-industrial structures, such as
flooded mine subsidences [25, 43]. Salinity is also regarded as one of the most important
environmental contamination types occurring in freshwater. Although dissolved salts are
ARCHIVES OF ENVIRONMENTAL PROTECTION
vol. 40 no. 1 pp. 87 - 99 2014
PL ISSN 2083-4772
DOI: 10.2478/aep-2014-0007
© Copyright by Polish Academy of Sciences and Institute of Environmental Engineering of the Polish Academy of Sciences,
Zabrze, Poland 2014
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88 KAMILA KAŠOVSKÁ, ŁUKASZ PIERZCHAŁA, EDYTA SIERKA, BARBARA STALMACHOVÁ
natural components of freshwater and some aquatic systems have naturally high salinity
levels the impact of excessive concentrations of dissolved salts derived from the human
activity may have profound and measurable effects on freshwater aquatic ecosystems
[15, 50, 19, 21, 31, 13, 14, 27]. Human activities, such as removal of vegetation [51, 40],
irrigation, mining [45] and industrial discharges [36, 37, 38, 39] may lead to a salinity
increase.
As evidenced by the previous research, the impact exerted by the increased salinity
on freshwater organisms [7, 10, 23, 31] is currently a worldwide environmental issue,
including in particular the protection of biodiversity of freshwater organisms. Although
the study by Kefford et al. [22] also proved that the tolerance of freshwater organisms to
salinity does not differ significantly, it is necessary to verify this statement and compare
it on a global scale. The comparison should account for different measurement methods
(and hence different units), as well as different approaches to this concept in different
parts of the world.
Several studies have been recently conducted in the field of lethal effects of different
salinity levels on molluscs and other macroinvertebrate species [21, 23, 52, 53], as well
as field research performed in wetlands, riverine ecosystems and marine biotopes [13, 14,
15, 31]. Macroinvertebrates (also molluscs) are able to respond to changes in the water
conditions and thus they may act as indicators of the biotope health. Their presence or
absence can indicate the extent of pollution. From a logistic perspective, they are good
research objects, because they are abundant, easily surveyed and taxonomically rich [11].
The diversity and abundance of molluscs can provide accurate information about the overall
health of the freshwater biotope. The present research focused on several physico-chemical
properties of water and the composition of the aquatic malacocoenosis [48].
The available data indicate that salinity above 1000 mg·l-1
[34, 33] may have an
adverse effect on aquatic biota. According to the aforementioned studies and the study
by Stalmachová et al. [46], water in the flooded mine subsidences is characterised by an
increased content of chlorides and sulphates (caused by leaching of tailings – mining
waste rock) and consequently the water salinity is above 1000 mg·l-1
.
There have been no prior field research, neither on mollusc communities in flooded
mine subsidences in the Czech Republic, nor on their response to salinity. The required
data from Central Europe (Czech Republic, Poland) is missing and it is necessary to fill
this gap.
This study evaluates whether the increasing salinity affected the aquatic mollusc
fauna in the flooded mine subsidences and compares the results with field studies from
Poland [48] and laboratory studies (ecotoxicity) from Australia and Africa. The second
objectives of this study was to identify species that are potentially useful for bioindication
of the increasing salinity in the flooded mine subsidences.
MATERIALS AND METHODS
Study area
The study area is located in Northeastern Moravia, the Czech Republic, the Karvina
region (Fig. 1). The entire region is strongly affected by underground coal mining. The
coal mining influences the vertical movement of the geological beds above the working
area. The character and strength of this movement depend on the thickness of the coal
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IMPACT OF THE SALINITY GRADIENT ON THE MOLLUSC FAUNA... 89
strata, the depth of their dipping and the hydrology [41]. This results in the ground sinking
above the coal excavation [44]. After a certain period of time, subsidence hollows are
filled with surface and ground water. Consequently, mining subsidence reservoirs are
created and eventually colonised by macrophytes, invertebrates (insects, molluscs etc.),
amphibians and waterfowl.
Fig. 1. Location of the study area: I – reservoirs: 1 – U cesty, 2 – Barbora,3 – U Obalovny,
4 – František skládka, 5 – U Kostela, 6 – Louky, 7 – Darkov, 8 – Bartošůvka, 9 – Pod lessem,
10 – Solecká; II – towns; III – border; IV – roads; V – railways; VI – location of study area
This type of reservoirs is characterised by a relatively shallow, regular shape, gentle
slopes of the shores, a flat bottom and, in most cases, a depth of 6.5 m [20]. Waters in these
reservoirs are stirred several times throughout the year (polymictic reservoirs). Intensive
mixing of the water column causes the transfer of bottom sediments, which reduces the
water transparency [9]. This flow results in oxygenated water and consequently in rapid
aerobic decomposition of suspended organic matter, and hence an increase in available
nutrients [35].
The vegetation is very similar to wetlands and consists of emergent species such
as Phragmites australis (Cav.) Trin. Ex Steud), Typha angustifolia (L.) T. latifolia (L.),
aquatic flora such as Batrachium aquatile (L.) Dumort., Myriophyllum verticillatum
(L.) and woody species from the genera Betula sp., Populus sp. or Salix sp. along the
shores, and in reclaimed parts − mostly Fagus sylvatica (L.), Carpinus betulus (L.), Alnus
glutinosa (L.) Gaertn. Flooded mine subsidences are also good refugia for amphibians,
reptiles and bird species.
The research on water salinity in the flooded mine subsidences was conducted at
10 sites located in the Karvina region. The sites were selected based on the previous
research performed by VŠB-Technical University of Ostrava. The detailed description of
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90 KAMILA KAŠOVSKÁ, ŁUKASZ PIERZCHAŁA, EDYTA SIERKA, BARBARA STALMACHOVÁ
the sites is presented in Table 1. The sites were divided into two groups according to their
size and depth: sink lakes (100 m2
in area and 2 m deep) and slide pools [42].
Table 1. Description of the research objects
Number Name
Dissolved
components
(mg·l-1
)
Location
Effect of soil
overburden,
tailings presence
Characteristics
1 U cesty > 1000
Horní Suchá
49°48'40''
18°28'49''
tailings remediation
from the shore
Primary subsidence
lake
2 Barbora > 1000
Horní Suchá
49°48'57''
18°28'41''
N, E and partly S made
of PT, in the E part
– reclaimed soil
Primary subsidence
lake
3 U Obalovny > 1000
Karviná – Doly
49°50'26''
18°27'05''
NE tailings material
Primary subsidence
lake
4
František
skládka
500–1000
Horní Suchá
49°48'50''
18°27'32''
S part with tailings
Primary subsidence
lake
5 U Kostela 500–1000
Karviná – Doly
49°50'04''
18°29'26''
reclamation since 1999
Primary subsidence
lake
6 Louky 500–1000
Karviná – Louky
49°48'37''
18°34'17''
reclamation 1996–
2008
Secondary large
subsidence lake
7 Darkov 500–1000
Karviná – Darkov
49°50'06''
18°33'03''
N and NE part with
tailings, reclamation
1997−2014
Primary subsidence
lake, reclaimed banks
8 Bartošůvka < 500
Havířov – Suchá
49°48'43''
18°26'04''
NE part with tailings
Primary subsidence
lake, reclaimed banks
9 Pod lesem < 500
Havířov – Suchá
49°49'01''
18°25'44''
reclaimed 2003–2010
Primary subsidence
lake
10 Solecká < 500
Horní Suchá
49°49'21''
18°29'02''
NW part with tailings,
penetrating to the
bottom
Primary subsidence
lake
Description of mollusc communities in flooded mine subsidences
Aquatic species were obtained using a metal sieve with a diameter of 20 cm (mesh size
0.8 × 0.8 mm) by washing out the aquatic vegetation and bottom substrate; in addition,
some direct collection from objects submerged in water (fallen logs, litter) was performed.
Harvesting was carried out for 1 hour (in the research sites) around the selected water
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IMPACT OF THE SALINITY GRADIENT ON THE MOLLUSC FAUNA... 91
reservoir. A more detailed description of the methodology can be found in the following
papers [3, 4, 5, 6]. This methodology is commonly used by the staff of the Agency for
Nature Conservation and Landscape to map the occurrence of aquatic mollusc species.
The nomenclature follows Horsák et al. [16]. The material is deposited in Kašovská
collection (Ostrava – Poruba). Some individuals were returned to their original habitat
immediately after the identification.
Ecoelements are presented according to [30, 26]. The tenth group consists of aquatic
molluscs, which are further divided into several basic and intermediate groups. The basic
type, i.e. the group PD (PALUDICOLAE), is known as overgrown swamps and marshes,
a group of associated PDT (periodic, overgrown marshy grounds) recurring types of
wetlands. Other ecoelements occurring at the site are SG (STAGNICOLAE – species of
larger and permanent lentic water bodies) and transient groups SG (RV) (RIVICOLAE
− types of lotic water), SGRV, SG – PD, RV (SG), which are intermediate between the
two above-mentioned groups (the abbreviations listed by priority).
Threat:NT− nearthreatened,LC−leastconcerned,VU−vulnerable,EN− endangered
according to IUCN [17].
The determination was performed by Beran [4], Horsák et al. [16], Ložek [29]. The
nomenclature follows the work by Horsák et al. [16].
Water parameters
Water sampling was carried out in 2010, once a month during the growing season
(May−October). At each site, permanent sampling stations were selected. Sampling
stations were located in the open water areas at a distance greater than 50 m from any
inflow or outflow. Samples were collected 2.5 m from the shore at a depth of 0–20 cm
into the sampling bottles (Bürkle). Temperature and oxygen saturation were measured (by
oxygen sensor Hach sension 6) in the collected samples. Before the analysis, the samples
were stored at a temperature of 10°C. The determined hydrochemical parameters are
presented in Table 2. To compare the salinity expressed in different units, the conversion
procedure of Pawlowicz [28] was applied.
Statistical analysis
Basic statistics were applied to describe the differences in the species richness and their
relationship to abiotic factors (dissolved inorganic ions, pH), ecological groups and sites.
Table 2. Standards of physico-chemical analysis of water parameters
Parameter Standard Name
pH ČSN ISO 10523 Determination of pH in the waters by potentiometry
total dissolved
substances
ČSN EN 872
Determination of dissolved solids by gravimetric
analysis
chlorides ČSN EN ISO 10304-1
Water quality – Determination of dissolved anions.
Part 1: Determination of bromide, chloride, fluoride,
nitrates, nitrites and phosphates
calcium ČSN ISO 6058
Water quality. Determination of calcium. Titrimetric
method with EDTA
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92 KAMILA KAŠOVSKÁ, ŁUKASZ PIERZCHAŁA, EDYTA SIERKA, BARBARA STALMACHOVÁ
Cluster analysis produced hierarchical clusters of items based on the Euclidean distance
measures. Cluster analysis was performed by the UPGMA methods from the software
MVSP 3.12. The statistics were used to assess the similarity between the sites in terms of
all analysed physico-chemical parameters of water.
Since the Shapiro-Wilk test indicated that the data have a normal distribution, we used
a parametric test in statistical analysis. For the correlation test between the malacocoenosis
characteristics and the environmental variables, we used Pearson’s Correlation Coefficient.
To investigate whether the largest portion of mollusc fauna variation is correlated with
environmental factors, the PCA method [32] was applied (from the software Canoco for
Windows 4.5) [49]. The number of environmental variables in the multivariate analysis
was reduced to parameters that were most strongly correlated with the main directions of
quantitative and qualitative variation in the analysed group (Pearson’s coefficient).
RESULTS
Cluster analysis of hydrochemical similarities between the sites split the analysed
locations into 2 groups. The most significant difference defines the group with locations
U Obalovny, Barbora and U cesty. These are flooded mine subsidences characterised
by the values of salinity above 1000 mg·l-1
(Fig. 2).
The group of flooded mine subsidences with salinity higher than 1000 mg·l-1
(mentioned above) is characterised by significantly different abundance of Potamopyrgus
antipodarum (J.E. Gray, 1843) (Fig. 3). There was no significant difference between
the abundance of ecoelements, the number of species, the number of individuals and
the Shannon and Evenness indices. The smallest number of species was found at the site
with the highest and the lowest salinity (Solecká, Barbora, U Obalovny) (Table 3).
Fig. 2. Results of the cluster analysis of 10 research objects in respect all analysed physico-chemical
parameters of water
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IMPACT OF THE SALINITY GRADIENT ON THE MOLLUSC FAUNA... 93
The correlation test between the hydrochemical parameters and the characteristics
of the analysed malacocoenosis shows a strong relationship between the water salinity
and the concentration of chlorides and the abundance of Potamopyrgus antipodarum
(J.E. Gray, 1843). A significant correlation was found between salinity, concentration of
chlorides and alien species (Table 4).
Fig. 3. Average abundance of species in the group of study plots with salinity higher than 1000 mg·l-1
(RL>1000 mg·l-1
) and in the group where salinity is lower (RL<1000 mg·l-1
). Species: Hip_com
– Hippeutis complanatus (Linnaeus, 1758), Ana_ana – Anodonta anatina (Linnaeus, 1758), Ani_vor – Anisus
vortex (Linnaeus, 1758), Sph_cor – Sphaerium corneum (Linnaeus, 1758), Apl_hyp – Aplexa hypnorum
(Linnaeus, 1758), Pla_cor – Planorbarius corneus (Linnaeus, 1758), Lym_sta – Lymnea stagnalis (Linnaeues,
1758), Rad_per – Radix peregra (Linnaeus, 1758), Sta_cor – Stagnicola corvus (Gmelin, 1778),
Phy_acu – Physella cf. acuta (Draparnaud, 1805), Gyr_alb – Gyraulus albus (O.F. Müller, 1774),
Pot_ant – Potamopyrgus antipodarum (Gray, 1843).
* denotes species with significantly different abundance between these two groups of study objects (p <0.05)
0
10
20
30
40
50
60
70
80
90
100
average
abundance
species
TDS>1000mg.l-1
TDS<1000mg.l-1
Table 3. Relationship between TDS (mg·l-1
), Shannon diversity index (Index and Evenness), the number
of species (Num. Spec) and the number of individuals (Num. Ind) at each search objects
TDS (mg·I-1
) Index Evenness Num. Spec. Num. Ind
Solecká 127 0.739 0.673 3 33
U lesa nad Bartošůvkou 237 1.381 0.771 6 363
Louky 432 1.456 0.748 7 81
Bartošůvka 684 0.457 0.255 6 523
Darkov 728 1.419 0.792 6 141
František skládka 731 0.537 0.488 3 23
U Kostela 911 0.379 0.273 4 207
U cesty 1068 1.29 0.663 7 88
Barbora 1701 1.19 0.858 4 197
U Obalovny 1982 0.623 0.899 2 273
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94 KAMILA KAŠOVSKÁ, ŁUKASZ PIERZCHAŁA, EDYTA SIERKA, BARBARA STALMACHOVÁ
Table 4. The result of correlation between environmental factors and malacocoenosis characteristics (*p <0.05)
TDS chlorides Pot_ant alien
TDS 1 0.69* 0.9* 0.65*
chlorides 0.89* 1 0.85* 0.58*
Pot_ant 0.85* 0.90* 1 0.72*
alien 0.58* 0.65* 0.72* 1
The results of PCA analysis (Fig. 4) indicated that the salinity and concentration of
chloride are positively correlated with the second and third ordination axes, which together
explain 22% of the variance (Table 5). There was no significant correlation with the first
ordination axis, which explains 65.3% of the variance. The abundance of Potamopyrgus
antipodarum (J.E. Gray, 1843) had the strongest correlation with these water parameters.
The number of species was negatively correlated with environmental factors.
Fig. 4. PCA ordination graph − the correlation between patterns of malacocoenosis variation and concentration
of chloride and water salinity (TDS). Species: Hip_com – Hippeutis complanatus (Linnæus, 1758), Ana_ana
– Anodonta anatina (Linnaeus, 1758), Ani_vor – Anisus vortex (Linnaeus, 1758), Sph_cor – Sphaerium
corneum (Linnaeus, 1758), Apl_hyp – Aplexa hypnorum (Linnaeus, 1758), Pla_cor – Planorbarius corneus
(Linnaeus, 1758), Lym_sta – Lymnea stagnalis (Linnaeues, 1758), Rad_per – Radix peregra (Linnaeus, 1758),
Sta_cor – Stagnicola corvus (Gmelin, 1778), Phy_acu – Physella cf. acuta (Draparnaud, 1805), Gyr_alb
– Gyraulus albus (O.F.Müller, 1774), Pot_ant – Potamopyrgus antipodarum (Gray, 1843).
Ecoelement groups: SGPD, PDt, RV (SG), SGRV, SG (for explanations see Methods).
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IMPACT OF THE SALINITY GRADIENT ON THE MOLLUSC FAUNA... 95
Table 5. Result of multivariate PCA analysis
Correlation Axis 1 Axis 2 Axis 3 Axis 4
chloride -0.0186 0.5063 0.7387 -0.0954
TDS -0.0288 0.4465 0.7043 -0.1383
Total variance
Eigenvalues 0.653 0.22 0.098 0.022 1
Species-environment correlations 0.029 0.523 0.785 0.138
Cumulative percentage variance
of species data 65.3 87.3 97.1 99.3
of species-environment relation 0.4 50 99.3 99.7
Sum of all eigenvalues 1
Sum of all canonical eigenvalues 0.122
DISCUSSION
The fauna of aquatic molluscs in flooded mine subsidences is generally considered to
be impoverished [2, 48]. Only 6 species were confirmed in England [1], 18 species in
Upper Silesia (Poland) [47], although in the reservoirs located near the heaps − only
6 species were found (in Upper Silesia, Poland). Compared to natural, “species rich”
aquatic reservoirs, more species were found for instance in the Bystřice – 26 [3].
As evidenced by the correlation analysis, the increasing salinity induced by the
chloride concentration was responsible for the increasing abundance of alien species,
including mostly Potamopyrgus antipodarum (J.E. Gray, 1843). This species has also
significantly higher abundance in the group of flooded mine subsidences with the salinity
above 1000 mg·l-1
. The results of PCA analysis indicated that the salinity affected by
chlorides is not the main environmental factor affecting the variability of the mollusc
community but has a considerable impact on the malacocoenosis. The multivariate
analysis revealed that the concentration of chloride could also affect the biodiversity
(a decreasing number of species and the Shannon index).
The latest findings about the effect of salinity on the biodiversity is summarised
in the study by Kefford et al. [24]. The maximum number of mollusc species was found
in the water with salinity 640–998 mg·l-1
and it declined in a statistically significant way
in the waters with higher and lower salinity. Kefford and Nugegoda [22] suggest that
salinity of 337–670 mg·l-1
is conducive to species richness. Our study produced very
similar results in terms of species abundance. Table 3 shows that there are different
responses on the species level. There were no statistically significant differences between
the range of salinity and the number of species, but a decreasing number of species was
observed with the lowest and the highest value of salinity. According to these results, the
optimum salinity for the species-rich malacocoenosis development is within the range
of 200–1100 mg·l-1
. Piscart et al. [38] suggested that the intermediate salinity levels
may be conducive to both salt sensitive and salt tolerant species in accordance with the
intermediate disturbance hypothesis of Connell [8]. This hypothesis assumes that in
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96 KAMILA KAŠOVSKÁ, ŁUKASZ PIERZCHAŁA, EDYTA SIERKA, BARBARA STALMACHOVÁ
habitats with low salinity, salt tolerant species tend to be excluded from the competition.
At a high salinity level, salt sensitive species would be excluded by salinity stress. While
at the intermediate salinity levels, both salt sensitive and salt tolerant species can coexist.
The minimum number of species was found at the site with the highest salinity (2 species
in the U obalovny reservoir, cca 1900 mg·l-1
). They were alien species (Potamopyrgus
antipodarum (J.E. Gray, 1843), Physella cf. acuta (Draparnaud, 1805) spreading to
newly created reservoirs in central Europe (such as former sandpits, mine subsidences
etc.) These species have a wide ecological amplitude and presumably tend to be good
competitors in higher salinity and they are inhibiting the development of other aquatic
mollusc species. The absence of native species in this reservoir could also be caused by
salinity stress.
Sublethal laboratory experiments [12, 16, 22] have demonstrated that freshwater
gastropods have their physiological optimum at the intermediate salinity that reduced
the growth both at lower and higher salinity, and which is reflected in the decreasing
numbers of individuals. Our study has proved, however, that this also depends on mollusc
species, because some of them, e.g. Potamopyrgus antipodarum (J.E. Gray, 1843) and
Physella cf. acuta (Draparnaud, 1805) are able to adapt to these conditions and even
prefer waters with a very high content of dissolved inorganic components (TDS). The
presence of these species could explain why we did not observe a decreasing number
of individuals with the increasing salinity. These species can be considered as potential
bioindicators of the increasing salinisation and its negative effects on fresh water biota.
The usefulness of Potamopyrgus antipodarum (J.E. Gray, 1843) as a bioindicator is
confirmed by a significant correlation with the salinity and significantly higher abundance
in the group of flooded mine subsidences with a broader salinity range.
We partly agree with the statements of Kefford et al. [21, 23, 24], but it is also
important to allow for the fact that we cannot evaluate molluscs only as a group, but also
as individuals.
CONCLUSIONS
This study shows that the increasing salinity affects the species composition of molluscs
and may affect the biodiversity of this group. We conclude that the number of individuals
per species with a wide ecological amplitude is increasing with the increasing salinity,
and the abundance of Potamopyrgus antipodarum (J.E. Gray, 1843) can be considered as
a potential bioindicator of the negative effect of salinisation on aquatic biota.
The data obtained during this study are, however, only the first step in recognising
this problem in the Czech Republic.
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IMPACT OF THE SALINITY GRADIENT ON THE MOLLUSC FAUNA... 97
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The definition of species richness used by species sensitivity distributions approximates observed effects
of salinity on stream macroinvertebrates. Environmental Pollution, 159, 302–310.
Unauthenticated
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98 KAMILA KAŠOVSKÁ, ŁUKASZ PIERZCHAŁA, EDYTA SIERKA, BARBARA STALMACHOVÁ
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Unauthenticated
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IMPACT OF THE SALINITY GRADIENT ON THE MOLLUSC FAUNA... 99
[50] Williams, W.D., Taaffe, R.G. & Boulton, A.J. (1991). Longitudinal distribution of macroinvertebrates in
two rivers subjekt to salinization, Hydrobiologia, 210, 151–160.
[51] Wood, W.E., (1924). Increase of salt in soil and stress following the destruction of the native vegetation,
Journal of Royal Society of Western Australia, 10, 35–47.
[52] Zalizniak, L., Kefford, B.J., Nugegoda, D. (2009a). Effects of different ionic composition on surfoval and
growth of Physa acuta, Aquatic Ecology, 43, 145–156.
[53] Zalizniak, L., Kefford, B.J. & Nugegoda, D. (2009b). Effects of pH on salinity tolerance of selected
freshwater invertebrates, Aquatic Ecology, 43, 135–144.
WPŁYW ZRÓŻNICOWANIA ZASOLENIA WÓD ZBIORNIKÓW W NIECKACH OSIADANIA
NA FAUNĘ MIĘCZAKÓW (KARWINA, CZECHY)
W artykule przedstawiono reakcję wodnych gatunków mięczaków (Mollusca), jako grupy modelowej, na za-
solenie wód zbiorników powstałych w nieckach osiadania rejonu Karwiny (Czechy). Analizę występowania
wodnych gatunków mięczaków przeprowadzono w obrębie 10 obiektów. Wody badanych zbiorników tworzyły
gradient zasolenia w zakresie od <500 do >1000 mg·l-1
. W ich obrębie stwierdzono występowanie łącznie
12 gatunków wodnych mięczaków, w tym jednego gatunku, który uznano za potencjalny indykator znacznego
zasolenia zbiorników. Wyniki analizy statystycznej wykazały istotną pozytywną zależność między zawartością
rozpuszczonych substancji nieorganicznych i występowaniem gatunku Potamopyrgus antipodarum (J.E. Gray,
1843). Wykazano, że gradient zasolenia w istotny sposób wpływa na skład gatunkowy fauny mięczaków, kształ-
tujących się w zbiornikach w nieckach osiadania oraz mieć wpływa na bioróżnorodność tej grupy.
Unauthenticated
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Impact of the salinity gradient on the mollusc fauna in flooded mine subsidences (Karvina, Czech Republic)

  • 1. IMPACT OF THE SALINITY GRADIENT ON THE MOLLUSC FAUNA IN FLOODED MINE SUBSIDENCES (KARVINA, CZECH REPUBLIC) KAMILA KAŠOVSKÁ1 , ŁUKASZ PIERZCHAŁA2 *, EDYTA SIERKA3 , BARBARA STALMACHOVÁ1 1   Institute of Environmental Engineering, Faculty of Mining and Geology, VŠB-Technical University of Ostrava, Czech Republic, 17.listopadu 15, 708 00, Ostrava 2   Central Mining Institute, Department of Water Protection, Poland, Plac Gwarków 1, 40-166, Katowice 3   Department of Geobotany and Nature Protection, Faculty of Biology and Environmental Protection, Silesian University Poland, Jagiellońska 28, 40-032 Katowice * Corresponding authors e-mail: lpierzchala@gig.eu Keywords: Molluscs, water salinity, mine subsidence, Karvina, Czech Republic. Abstract: This paper presents the impact of salinisation on the aquatic mollusc fauna in flooded mine subsidences in the Karvina region (Czech Republic). The results of the previous research on salinity in flooded mine subsidences show that some of them contain a high content of dissolved inorganic substances (above 1000 mg·l-1 ). These substances can affect the vegetation and animals occurring in the water and the surrounding area. The phylum of Mollusca was selected as a model group for the fieldwork as it includes species with the proven bioindication potential. The occurrence of aquatic mollusc species was studied at 10 sites. The sites were selected based on the content of dissolved substances (the salinity gradient from <500 to >1000 mg·l-1 . A total of 12 aquatic mollusc species were found, including one species identified as a potential bioindicator of the negative effect of salinisation on aquatic biota. The analysis showed statistically significant positive correlations between the content of dissolved inorganic substances and the presence of alien species Potamopyrgus antipodarum (J.E. Gray, 1843). The gradient of salinity significantly affects the species composition of the mollusc fauna in flooded mine subsidences and may affect the biodiversity of this group. INTRODUCTION The increasing salinity (as a concentration of dissolved inorganic ions, further referred to as TDS) in surface freshwater ecosystems is becoming a serious problem worldwide [38, 52, 21, 22], including the Czech Republic, especially in post-industrial structures, such as flooded mine subsidences [25, 43]. Salinity is also regarded as one of the most important environmental contamination types occurring in freshwater. Although dissolved salts are ARCHIVES OF ENVIRONMENTAL PROTECTION vol. 40 no. 1 pp. 87 - 99 2014 PL ISSN 2083-4772 DOI: 10.2478/aep-2014-0007 © Copyright by Polish Academy of Sciences and Institute of Environmental Engineering of the Polish Academy of Sciences, Zabrze, Poland 2014 Unauthenticated Download Date | 10/20/14 11:46 PM
  • 2. 88 KAMILA KAŠOVSKÁ, ŁUKASZ PIERZCHAŁA, EDYTA SIERKA, BARBARA STALMACHOVÁ natural components of freshwater and some aquatic systems have naturally high salinity levels the impact of excessive concentrations of dissolved salts derived from the human activity may have profound and measurable effects on freshwater aquatic ecosystems [15, 50, 19, 21, 31, 13, 14, 27]. Human activities, such as removal of vegetation [51, 40], irrigation, mining [45] and industrial discharges [36, 37, 38, 39] may lead to a salinity increase. As evidenced by the previous research, the impact exerted by the increased salinity on freshwater organisms [7, 10, 23, 31] is currently a worldwide environmental issue, including in particular the protection of biodiversity of freshwater organisms. Although the study by Kefford et al. [22] also proved that the tolerance of freshwater organisms to salinity does not differ significantly, it is necessary to verify this statement and compare it on a global scale. The comparison should account for different measurement methods (and hence different units), as well as different approaches to this concept in different parts of the world. Several studies have been recently conducted in the field of lethal effects of different salinity levels on molluscs and other macroinvertebrate species [21, 23, 52, 53], as well as field research performed in wetlands, riverine ecosystems and marine biotopes [13, 14, 15, 31]. Macroinvertebrates (also molluscs) are able to respond to changes in the water conditions and thus they may act as indicators of the biotope health. Their presence or absence can indicate the extent of pollution. From a logistic perspective, they are good research objects, because they are abundant, easily surveyed and taxonomically rich [11]. The diversity and abundance of molluscs can provide accurate information about the overall health of the freshwater biotope. The present research focused on several physico-chemical properties of water and the composition of the aquatic malacocoenosis [48]. The available data indicate that salinity above 1000 mg·l-1 [34, 33] may have an adverse effect on aquatic biota. According to the aforementioned studies and the study by Stalmachová et al. [46], water in the flooded mine subsidences is characterised by an increased content of chlorides and sulphates (caused by leaching of tailings – mining waste rock) and consequently the water salinity is above 1000 mg·l-1 . There have been no prior field research, neither on mollusc communities in flooded mine subsidences in the Czech Republic, nor on their response to salinity. The required data from Central Europe (Czech Republic, Poland) is missing and it is necessary to fill this gap. This study evaluates whether the increasing salinity affected the aquatic mollusc fauna in the flooded mine subsidences and compares the results with field studies from Poland [48] and laboratory studies (ecotoxicity) from Australia and Africa. The second objectives of this study was to identify species that are potentially useful for bioindication of the increasing salinity in the flooded mine subsidences. MATERIALS AND METHODS Study area The study area is located in Northeastern Moravia, the Czech Republic, the Karvina region (Fig. 1). The entire region is strongly affected by underground coal mining. The coal mining influences the vertical movement of the geological beds above the working area. The character and strength of this movement depend on the thickness of the coal Unauthenticated Download Date | 10/20/14 11:46 PM
  • 3. IMPACT OF THE SALINITY GRADIENT ON THE MOLLUSC FAUNA... 89 strata, the depth of their dipping and the hydrology [41]. This results in the ground sinking above the coal excavation [44]. After a certain period of time, subsidence hollows are filled with surface and ground water. Consequently, mining subsidence reservoirs are created and eventually colonised by macrophytes, invertebrates (insects, molluscs etc.), amphibians and waterfowl. Fig. 1. Location of the study area: I – reservoirs: 1 – U cesty, 2 – Barbora,3 – U Obalovny, 4 – František skládka, 5 – U Kostela, 6 – Louky, 7 – Darkov, 8 – Bartošůvka, 9 – Pod lessem, 10 – Solecká; II – towns; III – border; IV – roads; V – railways; VI – location of study area This type of reservoirs is characterised by a relatively shallow, regular shape, gentle slopes of the shores, a flat bottom and, in most cases, a depth of 6.5 m [20]. Waters in these reservoirs are stirred several times throughout the year (polymictic reservoirs). Intensive mixing of the water column causes the transfer of bottom sediments, which reduces the water transparency [9]. This flow results in oxygenated water and consequently in rapid aerobic decomposition of suspended organic matter, and hence an increase in available nutrients [35]. The vegetation is very similar to wetlands and consists of emergent species such as Phragmites australis (Cav.) Trin. Ex Steud), Typha angustifolia (L.) T. latifolia (L.), aquatic flora such as Batrachium aquatile (L.) Dumort., Myriophyllum verticillatum (L.) and woody species from the genera Betula sp., Populus sp. or Salix sp. along the shores, and in reclaimed parts − mostly Fagus sylvatica (L.), Carpinus betulus (L.), Alnus glutinosa (L.) Gaertn. Flooded mine subsidences are also good refugia for amphibians, reptiles and bird species. The research on water salinity in the flooded mine subsidences was conducted at 10 sites located in the Karvina region. The sites were selected based on the previous research performed by VŠB-Technical University of Ostrava. The detailed description of Unauthenticated Download Date | 10/20/14 11:46 PM
  • 4. 90 KAMILA KAŠOVSKÁ, ŁUKASZ PIERZCHAŁA, EDYTA SIERKA, BARBARA STALMACHOVÁ the sites is presented in Table 1. The sites were divided into two groups according to their size and depth: sink lakes (100 m2 in area and 2 m deep) and slide pools [42]. Table 1. Description of the research objects Number Name Dissolved components (mg·l-1 ) Location Effect of soil overburden, tailings presence Characteristics 1 U cesty > 1000 Horní Suchá 49°48'40'' 18°28'49'' tailings remediation from the shore Primary subsidence lake 2 Barbora > 1000 Horní Suchá 49°48'57'' 18°28'41'' N, E and partly S made of PT, in the E part – reclaimed soil Primary subsidence lake 3 U Obalovny > 1000 Karviná – Doly 49°50'26'' 18°27'05'' NE tailings material Primary subsidence lake 4 František skládka 500–1000 Horní Suchá 49°48'50'' 18°27'32'' S part with tailings Primary subsidence lake 5 U Kostela 500–1000 Karviná – Doly 49°50'04'' 18°29'26'' reclamation since 1999 Primary subsidence lake 6 Louky 500–1000 Karviná – Louky 49°48'37'' 18°34'17'' reclamation 1996– 2008 Secondary large subsidence lake 7 Darkov 500–1000 Karviná – Darkov 49°50'06'' 18°33'03'' N and NE part with tailings, reclamation 1997−2014 Primary subsidence lake, reclaimed banks 8 Bartošůvka < 500 Havířov – Suchá 49°48'43'' 18°26'04'' NE part with tailings Primary subsidence lake, reclaimed banks 9 Pod lesem < 500 Havířov – Suchá 49°49'01'' 18°25'44'' reclaimed 2003–2010 Primary subsidence lake 10 Solecká < 500 Horní Suchá 49°49'21'' 18°29'02'' NW part with tailings, penetrating to the bottom Primary subsidence lake Description of mollusc communities in flooded mine subsidences Aquatic species were obtained using a metal sieve with a diameter of 20 cm (mesh size 0.8 × 0.8 mm) by washing out the aquatic vegetation and bottom substrate; in addition, some direct collection from objects submerged in water (fallen logs, litter) was performed. Harvesting was carried out for 1 hour (in the research sites) around the selected water Unauthenticated Download Date | 10/20/14 11:46 PM
  • 5. IMPACT OF THE SALINITY GRADIENT ON THE MOLLUSC FAUNA... 91 reservoir. A more detailed description of the methodology can be found in the following papers [3, 4, 5, 6]. This methodology is commonly used by the staff of the Agency for Nature Conservation and Landscape to map the occurrence of aquatic mollusc species. The nomenclature follows Horsák et al. [16]. The material is deposited in Kašovská collection (Ostrava – Poruba). Some individuals were returned to their original habitat immediately after the identification. Ecoelements are presented according to [30, 26]. The tenth group consists of aquatic molluscs, which are further divided into several basic and intermediate groups. The basic type, i.e. the group PD (PALUDICOLAE), is known as overgrown swamps and marshes, a group of associated PDT (periodic, overgrown marshy grounds) recurring types of wetlands. Other ecoelements occurring at the site are SG (STAGNICOLAE – species of larger and permanent lentic water bodies) and transient groups SG (RV) (RIVICOLAE − types of lotic water), SGRV, SG – PD, RV (SG), which are intermediate between the two above-mentioned groups (the abbreviations listed by priority). Threat:NT− nearthreatened,LC−leastconcerned,VU−vulnerable,EN− endangered according to IUCN [17]. The determination was performed by Beran [4], Horsák et al. [16], Ložek [29]. The nomenclature follows the work by Horsák et al. [16]. Water parameters Water sampling was carried out in 2010, once a month during the growing season (May−October). At each site, permanent sampling stations were selected. Sampling stations were located in the open water areas at a distance greater than 50 m from any inflow or outflow. Samples were collected 2.5 m from the shore at a depth of 0–20 cm into the sampling bottles (Bürkle). Temperature and oxygen saturation were measured (by oxygen sensor Hach sension 6) in the collected samples. Before the analysis, the samples were stored at a temperature of 10°C. The determined hydrochemical parameters are presented in Table 2. To compare the salinity expressed in different units, the conversion procedure of Pawlowicz [28] was applied. Statistical analysis Basic statistics were applied to describe the differences in the species richness and their relationship to abiotic factors (dissolved inorganic ions, pH), ecological groups and sites. Table 2. Standards of physico-chemical analysis of water parameters Parameter Standard Name pH ČSN ISO 10523 Determination of pH in the waters by potentiometry total dissolved substances ČSN EN 872 Determination of dissolved solids by gravimetric analysis chlorides ČSN EN ISO 10304-1 Water quality – Determination of dissolved anions. Part 1: Determination of bromide, chloride, fluoride, nitrates, nitrites and phosphates calcium ČSN ISO 6058 Water quality. Determination of calcium. Titrimetric method with EDTA Unauthenticated Download Date | 10/20/14 11:46 PM
  • 6. 92 KAMILA KAŠOVSKÁ, ŁUKASZ PIERZCHAŁA, EDYTA SIERKA, BARBARA STALMACHOVÁ Cluster analysis produced hierarchical clusters of items based on the Euclidean distance measures. Cluster analysis was performed by the UPGMA methods from the software MVSP 3.12. The statistics were used to assess the similarity between the sites in terms of all analysed physico-chemical parameters of water. Since the Shapiro-Wilk test indicated that the data have a normal distribution, we used a parametric test in statistical analysis. For the correlation test between the malacocoenosis characteristics and the environmental variables, we used Pearson’s Correlation Coefficient. To investigate whether the largest portion of mollusc fauna variation is correlated with environmental factors, the PCA method [32] was applied (from the software Canoco for Windows 4.5) [49]. The number of environmental variables in the multivariate analysis was reduced to parameters that were most strongly correlated with the main directions of quantitative and qualitative variation in the analysed group (Pearson’s coefficient). RESULTS Cluster analysis of hydrochemical similarities between the sites split the analysed locations into 2 groups. The most significant difference defines the group with locations U Obalovny, Barbora and U cesty. These are flooded mine subsidences characterised by the values of salinity above 1000 mg·l-1 (Fig. 2). The group of flooded mine subsidences with salinity higher than 1000 mg·l-1 (mentioned above) is characterised by significantly different abundance of Potamopyrgus antipodarum (J.E. Gray, 1843) (Fig. 3). There was no significant difference between the abundance of ecoelements, the number of species, the number of individuals and the Shannon and Evenness indices. The smallest number of species was found at the site with the highest and the lowest salinity (Solecká, Barbora, U Obalovny) (Table 3). Fig. 2. Results of the cluster analysis of 10 research objects in respect all analysed physico-chemical parameters of water Unauthenticated Download Date | 10/20/14 11:46 PM
  • 7. IMPACT OF THE SALINITY GRADIENT ON THE MOLLUSC FAUNA... 93 The correlation test between the hydrochemical parameters and the characteristics of the analysed malacocoenosis shows a strong relationship between the water salinity and the concentration of chlorides and the abundance of Potamopyrgus antipodarum (J.E. Gray, 1843). A significant correlation was found between salinity, concentration of chlorides and alien species (Table 4). Fig. 3. Average abundance of species in the group of study plots with salinity higher than 1000 mg·l-1 (RL>1000 mg·l-1 ) and in the group where salinity is lower (RL<1000 mg·l-1 ). Species: Hip_com – Hippeutis complanatus (Linnaeus, 1758), Ana_ana – Anodonta anatina (Linnaeus, 1758), Ani_vor – Anisus vortex (Linnaeus, 1758), Sph_cor – Sphaerium corneum (Linnaeus, 1758), Apl_hyp – Aplexa hypnorum (Linnaeus, 1758), Pla_cor – Planorbarius corneus (Linnaeus, 1758), Lym_sta – Lymnea stagnalis (Linnaeues, 1758), Rad_per – Radix peregra (Linnaeus, 1758), Sta_cor – Stagnicola corvus (Gmelin, 1778), Phy_acu – Physella cf. acuta (Draparnaud, 1805), Gyr_alb – Gyraulus albus (O.F. Müller, 1774), Pot_ant – Potamopyrgus antipodarum (Gray, 1843). * denotes species with significantly different abundance between these two groups of study objects (p <0.05) 0 10 20 30 40 50 60 70 80 90 100 average abundance species TDS>1000mg.l-1 TDS<1000mg.l-1 Table 3. Relationship between TDS (mg·l-1 ), Shannon diversity index (Index and Evenness), the number of species (Num. Spec) and the number of individuals (Num. Ind) at each search objects TDS (mg·I-1 ) Index Evenness Num. Spec. Num. Ind Solecká 127 0.739 0.673 3 33 U lesa nad Bartošůvkou 237 1.381 0.771 6 363 Louky 432 1.456 0.748 7 81 Bartošůvka 684 0.457 0.255 6 523 Darkov 728 1.419 0.792 6 141 František skládka 731 0.537 0.488 3 23 U Kostela 911 0.379 0.273 4 207 U cesty 1068 1.29 0.663 7 88 Barbora 1701 1.19 0.858 4 197 U Obalovny 1982 0.623 0.899 2 273 Unauthenticated Download Date | 10/20/14 11:46 PM
  • 8. 94 KAMILA KAŠOVSKÁ, ŁUKASZ PIERZCHAŁA, EDYTA SIERKA, BARBARA STALMACHOVÁ Table 4. The result of correlation between environmental factors and malacocoenosis characteristics (*p <0.05) TDS chlorides Pot_ant alien TDS 1 0.69* 0.9* 0.65* chlorides 0.89* 1 0.85* 0.58* Pot_ant 0.85* 0.90* 1 0.72* alien 0.58* 0.65* 0.72* 1 The results of PCA analysis (Fig. 4) indicated that the salinity and concentration of chloride are positively correlated with the second and third ordination axes, which together explain 22% of the variance (Table 5). There was no significant correlation with the first ordination axis, which explains 65.3% of the variance. The abundance of Potamopyrgus antipodarum (J.E. Gray, 1843) had the strongest correlation with these water parameters. The number of species was negatively correlated with environmental factors. Fig. 4. PCA ordination graph − the correlation between patterns of malacocoenosis variation and concentration of chloride and water salinity (TDS). Species: Hip_com – Hippeutis complanatus (Linnæus, 1758), Ana_ana – Anodonta anatina (Linnaeus, 1758), Ani_vor – Anisus vortex (Linnaeus, 1758), Sph_cor – Sphaerium corneum (Linnaeus, 1758), Apl_hyp – Aplexa hypnorum (Linnaeus, 1758), Pla_cor – Planorbarius corneus (Linnaeus, 1758), Lym_sta – Lymnea stagnalis (Linnaeues, 1758), Rad_per – Radix peregra (Linnaeus, 1758), Sta_cor – Stagnicola corvus (Gmelin, 1778), Phy_acu – Physella cf. acuta (Draparnaud, 1805), Gyr_alb – Gyraulus albus (O.F.Müller, 1774), Pot_ant – Potamopyrgus antipodarum (Gray, 1843). Ecoelement groups: SGPD, PDt, RV (SG), SGRV, SG (for explanations see Methods). Unauthenticated Download Date | 10/20/14 11:46 PM
  • 9. IMPACT OF THE SALINITY GRADIENT ON THE MOLLUSC FAUNA... 95 Table 5. Result of multivariate PCA analysis Correlation Axis 1 Axis 2 Axis 3 Axis 4 chloride -0.0186 0.5063 0.7387 -0.0954 TDS -0.0288 0.4465 0.7043 -0.1383 Total variance Eigenvalues 0.653 0.22 0.098 0.022 1 Species-environment correlations 0.029 0.523 0.785 0.138 Cumulative percentage variance of species data 65.3 87.3 97.1 99.3 of species-environment relation 0.4 50 99.3 99.7 Sum of all eigenvalues 1 Sum of all canonical eigenvalues 0.122 DISCUSSION The fauna of aquatic molluscs in flooded mine subsidences is generally considered to be impoverished [2, 48]. Only 6 species were confirmed in England [1], 18 species in Upper Silesia (Poland) [47], although in the reservoirs located near the heaps − only 6 species were found (in Upper Silesia, Poland). Compared to natural, “species rich” aquatic reservoirs, more species were found for instance in the Bystřice – 26 [3]. As evidenced by the correlation analysis, the increasing salinity induced by the chloride concentration was responsible for the increasing abundance of alien species, including mostly Potamopyrgus antipodarum (J.E. Gray, 1843). This species has also significantly higher abundance in the group of flooded mine subsidences with the salinity above 1000 mg·l-1 . The results of PCA analysis indicated that the salinity affected by chlorides is not the main environmental factor affecting the variability of the mollusc community but has a considerable impact on the malacocoenosis. The multivariate analysis revealed that the concentration of chloride could also affect the biodiversity (a decreasing number of species and the Shannon index). The latest findings about the effect of salinity on the biodiversity is summarised in the study by Kefford et al. [24]. The maximum number of mollusc species was found in the water with salinity 640–998 mg·l-1 and it declined in a statistically significant way in the waters with higher and lower salinity. Kefford and Nugegoda [22] suggest that salinity of 337–670 mg·l-1 is conducive to species richness. Our study produced very similar results in terms of species abundance. Table 3 shows that there are different responses on the species level. There were no statistically significant differences between the range of salinity and the number of species, but a decreasing number of species was observed with the lowest and the highest value of salinity. According to these results, the optimum salinity for the species-rich malacocoenosis development is within the range of 200–1100 mg·l-1 . Piscart et al. [38] suggested that the intermediate salinity levels may be conducive to both salt sensitive and salt tolerant species in accordance with the intermediate disturbance hypothesis of Connell [8]. This hypothesis assumes that in Unauthenticated Download Date | 10/20/14 11:46 PM
  • 10. 96 KAMILA KAŠOVSKÁ, ŁUKASZ PIERZCHAŁA, EDYTA SIERKA, BARBARA STALMACHOVÁ habitats with low salinity, salt tolerant species tend to be excluded from the competition. At a high salinity level, salt sensitive species would be excluded by salinity stress. While at the intermediate salinity levels, both salt sensitive and salt tolerant species can coexist. The minimum number of species was found at the site with the highest salinity (2 species in the U obalovny reservoir, cca 1900 mg·l-1 ). They were alien species (Potamopyrgus antipodarum (J.E. Gray, 1843), Physella cf. acuta (Draparnaud, 1805) spreading to newly created reservoirs in central Europe (such as former sandpits, mine subsidences etc.) These species have a wide ecological amplitude and presumably tend to be good competitors in higher salinity and they are inhibiting the development of other aquatic mollusc species. The absence of native species in this reservoir could also be caused by salinity stress. Sublethal laboratory experiments [12, 16, 22] have demonstrated that freshwater gastropods have their physiological optimum at the intermediate salinity that reduced the growth both at lower and higher salinity, and which is reflected in the decreasing numbers of individuals. Our study has proved, however, that this also depends on mollusc species, because some of them, e.g. Potamopyrgus antipodarum (J.E. Gray, 1843) and Physella cf. acuta (Draparnaud, 1805) are able to adapt to these conditions and even prefer waters with a very high content of dissolved inorganic components (TDS). The presence of these species could explain why we did not observe a decreasing number of individuals with the increasing salinity. These species can be considered as potential bioindicators of the increasing salinisation and its negative effects on fresh water biota. The usefulness of Potamopyrgus antipodarum (J.E. Gray, 1843) as a bioindicator is confirmed by a significant correlation with the salinity and significantly higher abundance in the group of flooded mine subsidences with a broader salinity range. We partly agree with the statements of Kefford et al. [21, 23, 24], but it is also important to allow for the fact that we cannot evaluate molluscs only as a group, but also as individuals. CONCLUSIONS This study shows that the increasing salinity affects the species composition of molluscs and may affect the biodiversity of this group. We conclude that the number of individuals per species with a wide ecological amplitude is increasing with the increasing salinity, and the abundance of Potamopyrgus antipodarum (J.E. Gray, 1843) can be considered as a potential bioindicator of the negative effect of salinisation on aquatic biota. The data obtained during this study are, however, only the first step in recognising this problem in the Czech Republic. REFERENCES [1] Adams, J. & Robin, H., (1988). The fauna of mining subsidence pools in Northumberland, Transactions of the Natural History Society of Northumberland, Durham, and Newcastle-upon-Tyne, 55, 28–38. [2] Australian and New Zealand Environmental and Conservation Council (ANZECC) and Agricultural and Resource Management Council of Australia and New Zealand (ARMCANZ), (2000). National Water Quality Management Strategy, The Australian and New Zealand Guidelines for Fresh and Marine Water Quality, Paper No. 4 – Volume 1 Chapter 3, 3.5–4. Canberra, Australia: Department of the Environment and Heritage. Unauthenticated Download Date | 10/20/14 11:46 PM
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  • 12. 98 KAMILA KAŠOVSKÁ, ŁUKASZ PIERZCHAŁA, EDYTA SIERKA, BARBARA STALMACHOVÁ [25] Konečná, E. (2007). Eutrofizace poklesových kotlin. VŠB-Technická univerzita Ostrava. Disertační práce. Ostrava. [26] Lisický, J.M. (1991). Mollusca Slovenska. Bratislava: Veda, 199 (pp. 1340). [27] Lewin, I. & Smoliński, A. (2006). Rare and vulnerable species in the mollusc communities in the mining subsidence reservoirs of an industrial area (The Katowicka Upland, Upper Silesia, Southern Poland). Limnologica, 36, 181–191. [28] Pawlowicz, R. (2008). Calculating the conductivity of natural waters, Limnology and Oceanography: Methods, 6, 489–501. [29] Ložek, V. (1956). Klíč k určování československých měkkýšů – SAV. Bratislava (pp. 437). [30] Ložek, V. (2005). Suchozemští měkkýši jako ukazatele biodiverzity. In Vačkář, D. (Ed.), Ukazatele změn biodiverzity. Praha: Academia (pp. 262–273). [31] Marshall, N.A. & Bailey, P.C.E. (2004). Impact of secondary salinization on freshwater ecosystems: effect of constraining, experimental, short-term releases of saline wastewater on macroinvertebrates in lowland stream, Marine & Freshwater Research, 55, 509–523. [32] Meglen, R.R. (1992). Examining large databases: A chemometric approach using principal component analysis. Marine Chemistry, 39, 217–237. [33] Muschal, M. (2006). Assessment of risk to aquatic biota from elevated salinity – A case study from the Hunter River, Australia Journal of Environmental Management, 79, 266–278. [34] Nielsen, D.L, Brock, M.A., Rees, G.N. & Baldwin, D.S. (2003). Effects of increasing salinity on freshwater ecosystems in Australia, Australian Journal of Botany, 51, 6, 655–665. [35] Pertile, E. (2007). Hydrochemie zvodnělých poklesových kotlin ve vymezeném území Karvinska. Vysoká škola báňská – Technická univerzita Ostrava. Hornicko-geologická fakulta. Disertační práce. Ostrava. [36] Piscart, C., Moreteau, J.-C. & Beisel, J.-N. (2005). Biodiversity and Structure of macroinvertebrate communities along a small permanent salinity gradient, Muerthe River, France, Hydrobiologia, 551, 227–236. [37] Piscart, C., Moreteau, J.-C. & Beisel, J.-N. (2006a). Salinization consequence in running waters: use of a sentinel substráte as a bioassessment method. Journal of the North American Benthological Society, 25, 477–486. [38] Piscart, C., Moreteau, J.-C. & Beisel, J.-N. (2006b). Monitoring ganges in freshwater macroinvertebrate communities along a salinity gradient using artificial substrates. Environmental Monitoring and Assessment, 116, 529–542. [39] Piscart, C., Kefford, B.J. & Beisel, J.N. (2011). Are tolerance of non-native macroinvertebrates in France an indicator of potential for their translocation in a new area? Limnologica, 41, 107–112. [40] Peck, A.J. (1978). Salinization of non-irrigated soils and associated stress: a review. Australian Journal of Soil Research, 16, 157–168. [41] Quitte, E. (1971). Klimatické oblasti Československa. Climatic regions of Czechoslovakia. Studia geographica, 16, 1–47. [42] Stalmachová, B. (2001). Iniciace přírodních ekosystémů poddolované krajiny pro process obnovy území Karvinska. MŽP VaV/640/1/01. MS VŠB-TU, Ostrava. [43] Raclavská, H. & Škrobánková, H. (2007). Salinita vod poklesových kotlin v oblasti OKR. In Recyklace odpadů XI. ISBN 978-80-248-1597-8 (pp. 151–155). [44] Rzętała, M. (1998). Zróżnicowanie występowania sztucznych zbiorników wodnych na obszarze Wyżyny Katowickiej, Geographia. Studia et dissertationes, 22, 53–67. Prace Naukowe Uniwersytetu Śląskiego w Katowicach Nr 1723. Uniwersytet Śląski 1998. [45] Schulz, C.-J. (1998). Desalinization of running waters. I. Effects of desalinization on the bacterio-and viroplankton on the running waters of a creek in Northern Thuringia (Germany), Limnologica, 28, 367–376. [46] Stalmachová, B. et al. (2003). Strategie obnovy hornické krajiny. Technická univerzita Ostrava, Hornicko- -geologická fakulta. Ostrava. [47] Strzelec, M. (1993). Ślimaki (Gastropoda) antropogenicznych środowisk wodnych Wyżyny Śląskiej. Prace naukowe Uniwersytetu Śląskiego Nr 1358, Katowice (pp. 104). [48] Strzelec, M. & Serafiński, W. (2004). Biologia i ekologia ślimaków w zbiornikach antropogenicznych. Centrum dziedzictwa przyrody Górnego Śląska (pp. 90). [49] Ter Braak, C.J.F. & Šmilauer, P. (2002). CANOCO Reference Manual and CanoDraw for Windows User´s Guide. Software for Canonical Community Ordination (vision 4.5). Biometris, Wageningen and České Budějovice. Unauthenticated Download Date | 10/20/14 11:46 PM
  • 13. IMPACT OF THE SALINITY GRADIENT ON THE MOLLUSC FAUNA... 99 [50] Williams, W.D., Taaffe, R.G. & Boulton, A.J. (1991). Longitudinal distribution of macroinvertebrates in two rivers subjekt to salinization, Hydrobiologia, 210, 151–160. [51] Wood, W.E., (1924). Increase of salt in soil and stress following the destruction of the native vegetation, Journal of Royal Society of Western Australia, 10, 35–47. [52] Zalizniak, L., Kefford, B.J., Nugegoda, D. (2009a). Effects of different ionic composition on surfoval and growth of Physa acuta, Aquatic Ecology, 43, 145–156. [53] Zalizniak, L., Kefford, B.J. & Nugegoda, D. (2009b). Effects of pH on salinity tolerance of selected freshwater invertebrates, Aquatic Ecology, 43, 135–144. WPŁYW ZRÓŻNICOWANIA ZASOLENIA WÓD ZBIORNIKÓW W NIECKACH OSIADANIA NA FAUNĘ MIĘCZAKÓW (KARWINA, CZECHY) W artykule przedstawiono reakcję wodnych gatunków mięczaków (Mollusca), jako grupy modelowej, na za- solenie wód zbiorników powstałych w nieckach osiadania rejonu Karwiny (Czechy). Analizę występowania wodnych gatunków mięczaków przeprowadzono w obrębie 10 obiektów. Wody badanych zbiorników tworzyły gradient zasolenia w zakresie od <500 do >1000 mg·l-1 . W ich obrębie stwierdzono występowanie łącznie 12 gatunków wodnych mięczaków, w tym jednego gatunku, który uznano za potencjalny indykator znacznego zasolenia zbiorników. Wyniki analizy statystycznej wykazały istotną pozytywną zależność między zawartością rozpuszczonych substancji nieorganicznych i występowaniem gatunku Potamopyrgus antipodarum (J.E. Gray, 1843). Wykazano, że gradient zasolenia w istotny sposób wpływa na skład gatunkowy fauny mięczaków, kształ- tujących się w zbiornikach w nieckach osiadania oraz mieć wpływa na bioróżnorodność tej grupy. Unauthenticated Download Date | 10/20/14 11:46 PM