Accepted Manuscript Methylmercury and total mercury content in soft tissues of two bird species wintering in the Baltic Sea near Gdansk, Poland
Małgorzata Rutkowska, Gabriela Bajger-Nowak, Diana Kowalewska, Szymon Bzoma, Elżbieta Kalisińska, Jacek Namieśnik, Piotr Konieczka PII:
S0045-6535(18)32270-7
DOI:
10.1016/j.chemosphere.2018.11.162
Reference:
CHEM 22646
To appear in:
Chemosphere
Received Date:
28 June 2018
Accepted Date:
25 November 2018
Please cite this article as: Małgorzata Rutkowska, Gabriela Bajger-Nowak, Diana Kowalewska, Szymon Bzoma, Elżbieta Kalisińska, Jacek Namieśnik, Piotr Konieczka, Methylmercury and total mercury content in soft tissues of two bird species wintering in the Baltic Sea near Gdansk, Poland, Chemosphere (2018), doi: 10.1016/j.chemosphere.2018.11.162
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ACCEPTED MANUSCRIPT 1
Methylmercury and total mercury content in soft
2
tissues of two bird species wintering in the Baltic Sea
3
near Gdansk, Poland
4
Małgorzata Rutkowska1*, Gabriela Bajger-Nowak1, Diana Kowalewska1, Szymon Bzoma2,
5
Elżbieta Kalisińska3, Jacek Namieśnik1, Piotr Konieczka1
6
1
7 8
Gdańsk, 11/12 G. Narutowicza Street, Poland; e-mail:
[email protected]; 2
9 10 11
Gdańsk University of Technology, Faculty of Chemistry, Department of Analytical Chemistry, 80-233
Waterbird Research Group KULING, 81-526 Gdynia, 34/7 Świerkowa Street, Poland; e-mail:
[email protected];
3
Pomeranian Medical University, Department of Biology and Medical Parasitology, 70-411 Szczecin, Poland, 72 Powstancow Wielkopolskich Street, Poland; e-mail:
[email protected];
12
* Corresponding author:
[email protected]; telephone number: +48 58 347 16 01
13
Abstract: Of the various forms of Hg occurring in nature, (mono) methylmercury (MeHg) is an
14
especially toxic form and practically all forms of Hg can be converted into MeHg as a result of
15
natural processes. Total mercury (THg) and MeHg were determined in tissues of two piscivorous
16
birds: razorbill Alca torda and black-throated loon Gavia arctica to provide baseline data on current
17
mercury concentrations for liver, kidneys and pectoral muscle mercury concentrations of birds
18
which winter on the south Baltic Sea coast. Intra and inter-specific comparisons were carried out.
19
The study is conducted between winter and autumn and the distributions of mercury in tissues
20
were compared with data in other studies. The following paper contains discussion of the results
21
based on the statistical analysis and ecology aspect. The highest average Hg content was in the liver
22
(loon ≈ 3.86 mg kg-1 dw; razorbill ≈ 1.57 mg kg-1 dw), then in the kidneys (loon ≈ 3.14 mg kg-1 dw;
23
razorbill ≈ 1.53 mg kg-1 dw) and the lowest concentrations were in pectoral muscles (loon ≈ 1.97 mg
24
kg-1 dw; razorbill ≈ 0.67 mg kg-1 dw).
25
Keywords: Mercury; methylmercury; birds; liver; kidney; pectoral muscle. 1
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27
1. Introduction
28
Mercury (Hg) is one of the priority hazardous contaminants in the world (Jackson, 1998;
29
Stenhouse et al., 2018) and it can enter the environment naturally and as a result of human activities.
30
Anthropogenic emissions of Hg include fossil fuels combustion, gold mining, the roasting of sulfide
31
ores, the production of paper and drugs, the chloralkali process, and agriculture whereas natural
32
releases are mainly due to volcanoes (Horowitz et al., 2014; Rutkowska et al., 2014; Valdersnes et al.,
33
2016). Mercury is mainly present in gaseous form in the atmosphere.
34
exclusively of the element Hg with a global residence time in the atmosphere of about 6-24 months.
35
As a result, this Hg species can be transported over long distances in the atmosphere, and the
36
atmosphere is the main route for its introduction into the marine environment (Lamborg et al., 2014;
37
Mason et al., 1994; Schroeder et al., 1998). When Hg is introduced in the environment, especially
38
aquatic ecosystems, it can be biologically transformed by various methylating microbes into
39
methylmercury (MeHg) (Camacho et al., 2015; Valdersnes et al., 2016). MeHg is a dangerous
40
neurotoxin; it can be absorbed by organisms and biomagnify up the food chain (Fox et al., 2017). Hg
41
and MeHg contaminations are not only a problem to aquatic ecosystems but also to land animals
42
occupying higher trophic levels (Fu et al., 2010). Semi-aquatic mammals and piscivorous birds
43
accumulate MeHg from their diet due to the consumption of fish and other aquatic biota (Ackerman
44
et al., 2016; Åkerblom et al., 2014; Depew et al., 2013; Eagles-Smith et al., 2016; Houserová et al., 2007;
45
Sullivan and Kopec, 2018; Whitney and Cristol, 2017). High levels of Hg compounds in avian tissues
46
can affect immune, cardiovascular and nervous systems, as well as reproductive capacity (Eagles-
47
Smith et al., 2018, 2016; Fu et al., 2010; Harada, 1995; Morel et al., 1998; Tan et al., 2009; Tartu et al.,
48
2013). Also MeHg is able to cross the blood–brain barrier and can be deposited in eggs (Boening, 2000;
49
Frederick and Jayasena, 2011). That is why marine and other aquatic birds are particularly valuable
50
and effective monitoring tools for assessing contamination of the marine environment (Hothem et
This state includes almost
2
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al., 1998; Kalisińska et al., 2010). Additional, studying marine bird ecology should serve as a proxy
52
and a harbinger of changes in marine ecosystems (Mallory et al., 2006).
53
At present, a number of different analytical methods are used to determine Hg and MeHg in
54
samples with a complex matrix composition. The determination of THg is carried out the vapour
55
generation technique coupled to atomic absorption spectrometry (CV-AAS) (Gonzalvez et al., 2010,
56
2009; Ruelas-Inzunza et al., 2009; Vieira et al., 2009), fluorescence spectrometry (CV-AFS) (Wang et
57
al., 2017). The speciation of mercury is usually carried out by high-performance liquid
58
chromatography (HPLC) (Jagtap et al., 2011; Zhu et al., 2017) and gas chromatography (GC) (Gorecki
59
et al., 2013) coupled with element selective (atomic fluorescence, atomic absorption, atomic emission)
60
and mass spectrometric
61
et al., 2007, 2006; Jagtap et al., 2011; Rodil et al., 2002; Zhu et al., 2017).
detection
technique (Ferreira et al., 2015; Gorecki et al., 2013; Houserová
62
This work reports the concentrations of THg and MeHg in three different tissues (pectoral
63
muscle, liver and kidney), in two seasons (winter and autumn) of two bird species: razorbill (Alca
64
torda) and black-throathed loon (Gavia arctica), both are predominantly fed with fish and both
65
wintering in the south part of the Baltic Sea (the Gulf of Gdansk). The razorbill is an Alcidae seabird
66
species that breeds in high latitudes and black-throated loon is a migratory aquatic bird living in the
67
northern hemisphere, mainly breeding in freshwater lakes in northern part of Europe and Asia. The
68
Baltic Sea is one of the most polluted seas.
69
sides by land (only a few shallow straits link to the North Sea), which poses a high risk to the marine
70
environment due to pollution by toxic compounds. Seabirds are often used as biomonitors of marine
71
ecosystem health and have frequently been used to monitor Hg in marine environments via internal
72
tissues (Espín et al., 2012; Monteiro and Furness, 1995). These species are considered as indicators of
73
marine ecosystem pollution because they are large, wide-ranging, abundant, long-lived, and easy to
74
observe and monitor. In addition, they are of public interest and often at the top of the food chain
75
(Burger and Gochfeld, 2004; Espín et al., 2012). As many seabird species return to the same nesting
It is an inland sea of northern Europe, surrounded on all
3
ACCEPTED MANUSCRIPT 76
and colony sites each year and travel long distances to feed, they accumulate contaminants over time
77
and space (Burger, 1993; Espín et al., 2012; ).
78
2. Materials and methods
79
2.1. Sampling site description
80
The Gulf of Gdansk (area - 4940 km2) lies in the southern part of the Baltic Sea. The Gulf is
81
partially enclosed, being bordered by the Hel Peninsula and by continental Poland. The three cities
82
of Gdynia, Sopot and Gdansk discharge wastewaters into the gulf and are the three main outlets of
83
the Vistula River, which drains most of Poland, including the major industrial regions and cities. Not
84
surprisingly, the Gulf is considered to be polluted by heavy metals including Hg and its compounds
85
(Glasby and Szefer, 1998; Szefer et al., 2002, 1998, 1990) .
86
2.2. Sample collection and pretreatment
87
The examined birds were found in the Baltic Sea water bodies: Gulf of Gdansk and Coastal Zone
88
(Fig. 1). Birds were drowned in fish-nets as a bycatch. There were two bird species: razorbill (n = 37),
89
and black-throated loon (n = 13), which in majority had drowned in fishing nets. Birds were examined
90
in terms Hg content and had been collected from year 2006 up to 2011. Every examined bird had
91
determined gender, age, place and date of finding, and species identification. Some birds were too
92
young to determine their gender, because the gonads were not fully developed. It is also extremely
93
difficult to define the exact bird age. For this study the age of the razorbills was determined by the
94
bow's characteristics and of loons by the characteristics of the feathers based on the available
95
identification keys. In case of the bird species which are objects of our interest, it is possible to divide
96
them into two age groups: juvenile and adult. Before reaching the laboratory, tissue parts were
97
separated through dissection using a stainless steel scalpel (which was disinfected with methanol
98
after each use), including the liver, pectoral muscle and kidney. Skeletal muscle sample was cut out
99
from the upper right part of the pectoral muscle. Kidney sample was cut out from the right kidney. 4
ACCEPTED MANUSCRIPT 100
All tissue samples were weighed (wet mass), placed in Zip-Lock bags and immediately frozen for
101
later analysis.
102
Figure 1. Area of the Baltic Sea where razorbill and black-throated loon were gathered (the size of
103
the dots are related to the number of samples taken in that specific point).
5
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After being transported to the laboratory, the bird tissues were freeze-dried at -51 °C/0.027
105
mbar/48 h (LABCONCO with a 6 L capacity, USA). Lyophilised samples were weighed (dry mass)
106
on the analytical balance and homogenised in the agate mortar. After preparation, the powdered
107
samples were sealed in polyethylene bags and stored in a -20 °C refrigerator for further analysis.
108
2.3. Reagents and standards
109
All the used reagents were of analytical-reagent grade unless otherwise stated. The solutions
110
were prepared using ultra-pure water Milli-Q. Hg standard-MSHG at a concentration 100.48 ± 0.22
111
µg mL-1 in 3.3% HCl was purchased from Inorganic Ventures, INC (USA). Certified reference material
112
BCR-463 -Tuna fish (MeHg - 3.04 ± 0.16 µg g-1; Hg -2.85 ± 0.16 µg g-1) was obtained from
113
IRMM (Geel, Belgium) and Certified reference material DOLT – 4 - Dogfish liver (MeHg as Hg - 1.33
114
± 0.12 mg kg-1; Hg - total element mass fraction -
115
National Research Council of Canada. L-Cysteine (98%), Buffer Solution Standard (Phosphate pH
116
Standard Equimolar Solution) pH 6.86 (25 °C) and additive B (activated alumina) were obtained from
117
Nacalai Tesque, Inc, Kyoto and Wako pure Chemical Industries, Ltd (Japan). Additive M (sodium
118
carbonate + calcium hydroxide) and buffer solution of pH 7.00 ± 0.05 were purchased from POCh
119
(Poland). Toluene and HBr were obtained from Sigma Aldrich, MO (USA).
120
2.4. Sample preparation for MeHg determination
121
2.58 ± 0.22 mg kg-1) was purchased from the
MeHg in bird tissues was extracted following the method described by Maggi et al. (Maggi et
122
al., 2009) with a few modifications. Approximately 250 mg of homogenized dried
123
samples were hydrolyzed with 5 mL of 48% hydrobromic acid (HBr) by shaking for 5 min. After the
124
hydrolysis process, 10 mL of toluene was added to the samples and organomercury species were
125
extracted by mixing vigorously for 20 min in a mechanical shaker. The extracts were then centrifuged
126
at 3000 rpm for 10 min. The supernatant with organomercury species was collected in a clean
127
centrifuge tube. The samples were double-extracted by repeating the previous toluene extraction
128
process with 5 mL of toluene. The combined organic extracts were double back-extracted using 3 mL
bird tissue
6
ACCEPTED MANUSCRIPT 129
of 1% (v/v) L-cysteine aqueous solution to draw out MeHg from the collected toluene. The L-cysteine
130
extracts were mixed vigorously for 20 min and centrifuged for 5 min. This process was repeated once
131
more using another 3 mL of L-cysteine. Approximately 200 µL the L-cysteine extracts was collected
132
for immediate analysis using Mercury Analyser (MA-2000) purchased from Nippon Instruments
133
Corporation (Japan).
134
2.5. Determination procedure
135
The analyses were carried out with a Mercury Analyser (MA 2000) using cold vapour atomic
136
absorption spectrometry technique (CV-AAS). The extracts and freeze-dried samples (liquid sample
137
for MeHg analysis and solid sample for THg determination, n=3) are thermally decomposed by
138
controlled heating (T=850˚C/4 min). Hg is further atomized and free Hg vapour is collected by a Hg
139
collection agent in the form of gold amalgam. Hg collection agent is heated to release atomic Hg
140
(T=600˚C/1 min). The released Hg is detected using cold atomic absorption method at a wavelength
141
of 253.7 nm in the detector’s absorption cell. As a method of removing part of substances that could
142
interfere with measurement, Nippon Instruments Corporation uses two kinds of additives: additive
143
B (activated alumina) and additive M sodium carbonate + calcium hydroxide). They have to be used
144
in accordance with special procedure which includes the appropriate preparation of the additives
145
(heating them at 750 °C for about an hour) and an appropriate scheme for the addition of additives
146
together with a sample for porcelain boats, depending on the type of sample. The rest of interferes is
147
removed in the scrubber filled with the KOH solution. The procedure for the determination of THg
148
and MeHg is schematically shown in Figure 2.
7
ACCEPTED MANUSCRIPT
149 150 151
Figure 2: Scheme of the procedure for the THg and MeHg determination.
2.6. Method validation
152
The numerical values of the calibration curves regression parameters were the basis for
153
estimating the value of the limit of detection and quantification of the analytical method. The limit of
154
detection (LOD) is defined as the lowest content of the analyte that can be detected (without
155
quantitative determination) by a measuring-apparatus with a certain probability. While the limit of
156
quantification (LOQ) is the minimum amount or minimum concentration for quantification possible
157
by the system with a predetermined accuracy and precision (Konieczka and Namieśnik, 2007).
158
The limit of detection (LOD) was calculated using the equation (1):
159
𝐿𝑂𝐷 =
3.3 𝑠𝑎 𝑏
(1)
160
Sa – the standard deviation of the intercept of calibration curve
161
b – the slope of the calibration line
162
When calculating the numerical value of the LOQ were assumed dependence, described by the
163
equation (2):
164 8
ACCEPTED MANUSCRIPT
165
𝐿𝑂𝑄 = 3 ∙ 𝐿𝑂𝐷 (2)
166 167
Obtained numerical values LOD and LOQ were converted to the corresponding value of MDL
168
and MQL - the limits of detection and quantification of the analytical method, assuming that the mass
169
of the sample is 100 mg.
170
The next validation parameters were repeatability and intermediate precision. Repeatability was
171
expressed as a coefficient of variation (CV) test samples results in a single analytical cycle. The
172
intermediate precision was calculated as the coefficient of variation for all the results obtained in all
173
the analyzed samples (Konieczka and Namieśnik, 2007).
174
The trueness of the measurements for T-Hg and MeHg were accompanied by the analysis of two
175
certified reference material BCR-463 (Tuna fish muscles) and DOLT-4 (Dogfish liver). The average
176
recovery of BCR-463 for THg and MeHg were 97.1 and 88.4% respectively and the average recovery
177
of DOLT – 4 for THg and MeHg were 97.0% and 95.0% respectively . Based on the results can be seen
178
that the recovery of the analytical procedure is at a satisfactory level. Acceptable recovery for this
179
type of analysis should be in the range of 80 to 120%. Individual standard uncertainties were
180
determined using a series of test results. For this purpose, a series of results were used to calculate
181
the standard deviation (s), then the relative standard deviation (RSD) and the value of the relative
182
standard uncertainty (u) and the expanded uncertainty (U) according to the following equations:
183
184
185
186
𝑠=
∑𝑛
𝑥𝑚𝑒𝑎𝑛)
𝑛‒1
𝑅𝑆𝐷 =
𝑢=
(𝑥 𝑖 ‒
𝑖=1
𝑅𝑆𝐷 𝑛
𝑠 𝑥𝑚𝑒𝑎𝑛
2
(3)
(4)
(5)
(6)
9
ACCEPTED MANUSCRIPT 187
where: k – coverage factor (usually 2), c – average concentration of the analyte, x - single result,
188
xmean -measurement average result obtained for a given series of measurements, n - number of
189
obtained results (replicates) for a given series of measurements for a given sample. All of the
190
validation parameters are presented in Table 1 (based on Konieczka & Namieśnik (Konieczka and
191
Namieśnik, 2008)).
192
Table 1. Calculated validation parameters for MeHg and THg in birds tissue samples.
Parameter
Value
Analyte
Hg
MeHg
10 measuring points (10. 20. 31. 41. 51. 62. 72. 82. 92. 103 [ng]),
Linearity
0.999
3 repetitions, f(m) = 1.0006m* – 0.15
6 measuring points (0.10. 0.31. 0.51. 0.71. 0.91. 1.02[ ng]),
1.000
3 repetitions, f(m) = 0.9987m* + 1.1 (LOD) [ng]
0.096
LOQ [ng]
0.29
MDL [ng/g]
0.96
1.0
MQL [ng/g]
2.9
3.1
Measuring range [ng/g]
2.9 ÷ 102.5
3.1 ÷ 110.0
Repetability CV [%]
2.8
1.4
Intermediate precision CV [%]
4.7
3.9
BCR-463 (n=3)
97.1 ± 2.4
88.4 ±1.1
DOLT-4 (n=3)
97.0 ± 1.9
95.0 ± 1.0
Recovery ± Uncertainty (k=2) [%]
193
*m
= mass of the total Hg [ng]
194 195
2.7. Statistical analysis 10
ACCEPTED MANUSCRIPT 196
Median (Med), arithmetic mean (AM), standard deviation (SD), THg and MeHg concentrations
197
and the percentage of MeHg in THg (%MeHg) in soft tissues of razorbill and black-throated loon
198
were calculated. Due to the fact that mercury tends to accumulate in the internal tissues of birds with
199
age, the division of birds into two age categories (Ad, adult - adults and Im, immature - young) was
200
taken into account in the calculations. Since the concentration distribution of mercury deviates from
201
the expected normal distribution, non-parametric
202
compare the two parameters, and the Kruskal-Wallis test to compare three parameters (K - kidney, L
203
- liver, M - muscle).
tests were used: U test and Mann-Whitney test to
204
Intraspecific comparisons were carried out which include:
205
• age categories (Ad, Im);
206
• types of biological material (K, L, M);
207
• seasons: A, autumn (October - December) and W, winter (January - March).
208
Interspecific comparisons were carried out which include:
209
both bird species and age categories.
210
3. Results and discussion
211
The aim of this study was to provide baseline data on current mercury concentrations for liver,
212
kidneys and pectoral muscle Hg concentrations of birds which winter on the south Baltic Sea coast,
213
which had drowned in fishing nets, in order to assess exposure to Hg, to determine the impact of age
214
and sex of the specimens analysed. Intra and inter-specific comparisons were carried out.
215
Bioaccumulation of Hg species in the in tissues of razorbills and black-throathed loons living in the
216
vicinity of the Baltic Sea ecosystem have also been investigated. To show statistically significant
217
differences and correlations between the contents of analytes in some of the analysed tissues and bird
218
age or season when the samples were acquired, xenobiotic content statistical analysis has been used.
219
3.1. Intraspecific comparisons
11
ACCEPTED MANUSCRIPT 220
Table 2 summarizes the concentrations of THg, MeHg and %MeHg in the biological samples for
221
both species of birds. The mean values were calculated for juveniles, adults, and for all birds collected
222
for analysis (for some birds it was impossible to determine the age category). Water content in
223
individual sample types was determined. Water content in the liver, kidneys and pectoral muscles
224
was about 70%.
225
3.2. Razorbill
226
Taking into consideration all the analyzed individuals (n = 37), it was found that both the
227
concentration of THg and MeHg was similar in the liver and kidney whereas significantly smaller in
228
pectoral muscle. Statistically significant differences in the concentration of THg and MeHg in liver vs
229
muscle and kidney vs muscle (K-W test: H=49.57, p<0.0001; H=42.91, p<0.0001, respectively) were
230
observed. Juveniles relative to adults had a significantly lower concentration of THg and MeHg in
231
kidneys and a significantly lower concentration of THg in the liver. Concentrations for both THg and
232
MeHg in muscles were similar in both age groups. Lower MeHg proportion in the liver of the adults
233
compared to younger birds can be result of demethylation of MeHg by selenium (Se) which occurs
234
over a long period of time in adults compared to young birds. These differences are influenced also
235
by variations in condition of the examined individuals, removal of a significant amount of MeHg
236
during moulting, and often different content and proportions of various forms of Hg and Se in food
237
intaken from water. Many waterbirds associated with the Se-rich environment use a different method
238
of Hg detoxification. In their tissues and organs, especially in the liver, various forms of Hg and Se
239
may form biologically inactive complexes at the end of the detoxification process (Kalisinska et al.,
240
2014). Se is considered to be a natural MeHg and inorganic Hg antagonist that potently counteracts
241
or eliminates symptoms of toxicity that would otherwise accompany high MeHg/Hg exposures
242
(Arcagni et al., 2017; Frederick and Jayasena, 2011; Ralston et al., 2007; Ralston and Raymond, 2010;
243
Yamashita et al., 2013). Interactions between Se and Hg have previously been observed in fish and
244
other aquatic biota (Arcagni et al., 2017; Ralston and Raymond, 2010).
12
ACCEPTED MANUSCRIPT 245
There were no significant differences in the values of %MeHg between age groups in any of the
246
tested tissues (Table 2). For the analysis in autumn, 24 individuals, and in winter 10 specimens, were
247
collected (for 3 birds the month of collection was not reported). The analyses showed that in all types
248
of samples median concentrations of THg and MeHg were significantly higher in winter than in
249
autumn (kidney: 1.444 vs 0.782 mg THg kg-1 and 1.171 vs 0.656 mg MeHg kg-1, M-W test Z=3.38,
250
p<0.001 and 3.80, p<0.0001, respectively; liver: 1.608 vs 0.852 mg THg kg-1, M-W test Z=3.55, p<0.0001
251
and Z=2.58, p<0.01 respectively; muscle: 1.608 and 0.852 mg THg kg-1, and 1.318 and 0.776 mg MeHg
252
kg-1, M-W test Z=3.86, p<0.0001 and Z=3.60, 0.0001, respectively).
13
253
Table 2. Concentrations (in mg kg-1 dw) of total mercury (THg), methylmercury (MeHg) and the percentage of MeHg in THg (%MeHg) in soft tissues of the razorbill Alca
254
torda and the black-throated loon Gavia arctica wintering on the Polish Baltic coast as well as and comparisons of THg, MeHg, %MeHg/THg between age groups (im
255
immature, ad adult, Med median, AM arithmetic mean, SD standard deviation, M-W Mann-Whitney test, NS difference non-significant) Kidney
Species
Liver
Muscle
THg
MeHg
%MeHg
THg
MeHg
%MeHg
THg
MeHg
%MeHg
n
12
12
12
12
12
12
12
12
12
Med
0.944
0.759
82.1
1.177
0.844
82.8
0.401
0.378
90.3
AM±SD
0.98±0.41
0.81±0.34
82.8±9.1
1.15±0.56
0.91±0.54
77±17
0.49±0.27
0.41±0.26
79±24
Range
0.376-1.750
0.328-1.482
70.8-99.5
0.484-2.424
0.330-2.123
28.4-96.4
0.191-1.057
0.036-0.965
16.4-97.6
n
7
7
7
7
7
7
7
7
7
Med
1.423
1.127
79.4
1.731
1.299
81.8
0.613
0.557
90.8
AM±SD
1.53±0.51
1.18±0.45
78±16
1.57±0.44
1.21±0.36
78±10
0.67±0.18
0.54±0.14
82±17
Alca torda Im
Ad
Range
0.730-2.299
0.527-2.011
49.0-99.3
0.660-1.953
0.540-1.652
57.0-85.0
0.430-0.970
0.311-0.769
51.4-98.0
Im vs Ad
M-W
Z=2.155
Z=1.986
NS
Z=1.986
NS
NS
NS
NS
NS
p<0.05
p<0.05
All specimens1
n
37
37
37
37
36
36
37
36
36
Med
0.873
0.667
82.1
1.109
0.822
84.3
0.454
0.393
90.8
AM±SD
1.05±0.43
0.81±0.36
78±13
1.18±0.47
0.93±0.40
79±13
0.52±0.21
0.42±0.19
80±19
Range
0.376-2.299
0.328-2.011
31.3-99.5
0.484-2.424
0.330-2.123
28.4-96.4
0.191-1.057
0.036-0.965
16.4-99.3
n
9
9
9
8
8
8
9
9
9
Med
1.439
1.073
70.7
2.047
1.110
63.1
1.119
0.673
74.8
AM±SD
2.5±1.8
1.27±0.56
62±19
3.0±2.4
1.31±0.54
57±21
2.0±2.3
0.89±0.57
65±23
Range
0.891-6.358
0.711-2.129
33.5-81.6
1.091-7.091
0.665-2.398
15.3-75.7
0.543-7.384
0.410-2.215
14.2-93.1
n
3
3
3
3
3
3
3
3
3
p<0.05
(p<0.09)
Gavia arctica Im
Ad
1
Im vs Ad All
256
specimens2
1unknown
Med
1.256
0.822
65.4
1.568
1.048
63.9
0.573
0.466
81.4
AM±SD
3.1±3.4
1.5±1.3
59±14
3.9±4.1
1.9±1.6
61 ±16
1.5±1.7
1.3±1.6
80±14
Range
1.154-7.007
0.798-3.027
43.2-69.2
1.412-8.597
1.002-3.734
43.4-74.3
0.494-3.516
0.336-3.155
68.0-89.7
M-W
NS
NS
NS
NS
NS
NS
NS
NS
NS
n
13
13
13
12
12
12
13
13
13
Med
1.352
1.015
69.2
2.002
1.110
63.1
0.774
0.665
74.8
AM±SD
2.6±2.1
1.31±0.71
62±17
3.2±2.6
1.47±0.84
58±18
1.2±2.0
0.96±0.83
69±20
Range
0.891-7.007
0.711-3.027
33.5-81.6
1.091-8.597
0.665-3.734
15.3-75.7
0.494-7.384
0.336-3.155
14.2-93.1
age category of 18 specimens.
2unknown
age category of one specimen
2
ACCEPTED MANUSCRIPT 257
3.3. Black-throated loon
258
In the total group (n = 13) some differences were detected between the concentrations of THg
259
and MeHg in the liver, kidneys and muscles (M-W test: H = 7.06, p <0.05, H = 7.63, p <0.05,
260
respectively). The lowest median concentrations of THg and MeHg were detected in muscles (Table
261
2) and they were only significantly different from corresponding concentrations found in the liver of
262
black-throated loon. The median values for MeHg and THg content in the three types of the analyzed
263
samples do not differ in a statistically significant way. Between percentage medians of MeHg in THg
264
set for the three types of samples studied, there were no statistically confirmed differences. In this
265
species, a small number of specimens (n = 13) were available, the age category was defined for 12
266
birds (Ad n = 3, Im n = 9). Comparative analysis between young and adult birds has shown no
267
differences in the concentrations of THg, MeHg and %MeHg. However, it has been shown that
268
individuals obtained in the autumn season had lower levels of hepatic THg than those collected in
269
the winter season: 1.508 vs 4.472 mg kg-1 (M-W test: Z = 1.95, p <0.05). The difference between seasons
270
could also be influenced by the use of the energetic reserves and for instance, a decrease of the size
271
of the liver leads to an increase of Hg concentration just because of its mass variation (Fort et al.,
272
2015).
273
3.4. Interspecific comparisons
274
In the pectoral muscle, kidney and liver of the examined birds of the razorbill species from
275
Poland, THg concentrations ranged from 0.191 to 1.057; 0.376 to 2.299; 0.484 to 2.424 mg kg-1 dw
276
respectively (Table 2). The mercury content in individual tissues is higher than the mercury content
277
in fish from the Baltic Sea (Table 3), as confirmed by the conclusion of mercury bioaccumulation
278
ability in food chain (Árvay et al., 2017). Also the most important factor governing the level of Hg
279
and organomercury compounds in the tissues of an animal appears to be the diet (Arcagni et al.,
280
2017).
281 1
ACCEPTED MANUSCRIPT 282
Table 3. Literature data on the content Hg in biological samples from different parts of the world. SPECIES
GEOGRAPHICAL REGION
TYPE OF
INDIVIDUALS
SAMPLE
Sprat -
(Sprattus sprattus)
Poland (coastal
Herring
zone of the
(Clupea harengus)
Baltic Sea)
Cod (Gadus morhua)
-
-
-
-
Razorbills (Alca torda)
(Mediterranean coastline, La Marina, Elche, Alicante)
USA (Minnesota)
-1]
(Polak-
0.022 ± 0.013[µg g
-
1]
0.031 ± 0.022 [µg g -1]
1.8 ± 0.65[µg g -1] juvenile
1.38 ± 0.49 [µg g -1]
Brain
1.22 ± 0.40 [µg g -1]
Vane
1.03 ± 0.59 [µg g -1]
Shaft
0.48 ± 0.15 [µg g -1]
(Espín et
Liver
3.00 ± 0.87 [µg g
-1]
al., 2012)
2.54 ± 0.82 [µg g
-1]
Kidney Muscle
adult
1.68 ± 0.51 [µg g -1] 1.67 ± 0.52 [µg g -1]
Vane
3.76 ± 0.97 [µg g -1]
Shaft
1.95 ± 0.44 [µg g -1]
Liver
8.0 ± 1.9 (3.6 - 23.1) [µg g -1] 39.3 ± 29.2
adult
(3.4 - 103.0) [µg g 1]
Common Loons
Canada (Quebec)
(Gavia immer) Goosander (Mergus merganser)
Goosander (Mergus merganse)
Finland (Lake Päijänne)
Feather
Muscle
males
17.6 [µg g -1]
females
8.9 [µg g -1]
-
18.1 [µg g -1]
Liver
14.7 [µg g -1]
Kidney
9.9 [µg g -1]
Poland (River Odra
Brain
estuary)
Breast
-
Bone
torda)
(Atlantic Ocean)
Kidney
albatrosses
Southern Pacific and Indian Oceans
Liver
Pichner, W. E. Braselt et al., 2002) (Champoux et al., 2006) (Sarkka et al., 1978)
(Kalisińska et al., 2010)
10.13 ± 4.71 [µg g 1] -
6.48 ± 2.14 [µg g -
(Fort et al.,
1]
2015)
3.99 ± 1.56 [µg g -
Muscle Wandering
(Bischoff, J.
0.08 [µg g -1]
Liver Bay of Biscay
1.3 [µg g -1] 2.3 [µg g -1]
muscle
Razorbills (Alca
Juszczak, 2009)
Kidney
juvenile (Gavia immer)
0.014 ± 0.005 [µg g
2.68 ± 0.86 [µg g -1]
Brain
Common Loons
REFERENCES
(RANGE) d/w *
Liver Muscle Spain
-
Hg MEAN
1] adult
920.0 ± 794.1
(Hindell et
[µg g -1]
al., 1999) 2
ACCEPTED MANUSCRIPT (Diomedea exulans) Shy albatrosses
36.3 ± 21.4
(Thalassarche
[µg g -1]
cauta)
283
∗The numerical values are given as originally stated in the cited literature.
284 285
These results were similar to northern gannet (Morus bassanus) from the Portuguese Atlantic
286
coast where THg concentrations were 0.473 – 0.851; 0.952 – 3.423; 1.291 – 2.603 µg g-1 dw for muscle,
287
kidney and liver respectively [40]. For these results, it can be observed that the THg concentration in
288
the liver is lower than in the kidney in comparison to the results obtained for the birds from Poland.
289
Comparable results were also obtained during the determination of Hg content in tissues of razorbills
290
living in Mediterranean coastline (Table 3) (Espín et al., 2012).
291
Higher THg concentrations were reported in razorbills species from the Portuguese Atlantic
292
coast where mean THg contents for muscle, kidney and liver were 2.669; 3.939; 6.094 µg g-1 dw
293
respectively (Ribeiro et al., 2009) and populations of the species from Scandinavia and North America
294
in the 1960– 1980 (concentration in the breast muscle was 6.094 µg g-1dw) when agricultural use of
295
MeHg-pesticides was on a large scale (Barr, 1986).
296
In our study THg concentration in the pectoral muscle kidney and liver of black-throated loon
297
were even higher and ranged from 1.091 to 8.597; 0.494 to 7.384 and 0.891 to 7.007mg kg-1 dw
298
respectively (Table 2). Total mercury concentrations in muscle, kidney and liver in populations of
299
loons (specifically Gavia immer) from eastern Canada was found to be 2.9; 15; 19 µg g-1 dw and in
300
mergansers (Mergus merganser) 3.0; 11; 15 µg g-1 dw respectively (Scheuhammer et al., 1998), which
301
does not go beyond the typical concentrations for species of predatory birds from different areas of
302
the world (Evers et al., 2005). Significant higher mercury concentrations in the tissues of birds of the
303
same species as birds described in this paper were observed in birds living in the Minnesota State
304
(USA) (Bischoff, J. Pichner, W. E. Braselt et al., 2002). For adults, the concentration of mercury in the
305
liver in the range 3.4 to 103.0 mg kg-1 dw (Table 3). However, these levels may related not only to the
306
diet of these animals, but also by the fact that the north-eastern part of North America is characterized 3
ACCEPTED MANUSCRIPT 307
by high Hg content in the geological surface and significant anthropogenic pollution of the
308
environment by this metal (Bischoff, J. Pichner, W. E. Braselt et al., 2002). Therefore, it can be
309
suggested that THg concentrations in birds depend on the Hg contamination in their habitats, but
310
also on their position in the food chain.
311
Recently, levels that may be indicative of adverse effects were suggested for THg concentrations
312
in the liver and kidneys of nonmarine birds (Shore et al., 2011). Bird death may be expected when
313
either hepatic or nephric concentrations were greater than 20 mg kg-1 or 40 mg kg-1 wet weight (more
314
than 67 mg kg-1 and 133 mg kg-1 dry wt), respectively. A conservative threshold for toxic effects of
315
Hg in waterbirds are 5 mg kg-1 wet weight or 16.7 mg g-1 dry weight in the liver (Bearhop et al., 2000;
316
Burger, 1993; Burger and Gochfeld, 2004; Pillatzki et al., 2011; Zillioux et al., 1993).
317
4. Conclusions
318
This study, having regard to the statistical analysis of all the collected individuals of razorbill
319
and black-throated loon, showed that in the compared similar tissues (kidney, liver and muscle)
320
median concentrations of THg and MeHg are significantly higher in the black-throated loon than in
321
razorbill. This may indicate that demethylation by Se in this species is effective.
322
On the other hand the percent MeHg in THg (%MeHg) it is significantly higher in the razorbill
323
than in black-throated loon. For example in razorbill, pectoral muscle MeHg accounted for about 91
324
% of total mercury and in black-throated loon for about 75% of total mercury (Table 2). Similar %
325
MeHg has been found in great cormorant and great crested grebe (Podiceps cristatus) from the Czech
326
Republic (Houserová et al., 2007), osprey (Pandion haliaetus) from Norway (Norheim and Froeslie, A.
327
(Veterinaerinstituttet, 1978), and brown pelican (Pelecanus occidentalis) from the Gulf of California
328
(Ruelas-Inzunza et al., 2009).
329
Muscle MeHg fraction of THg in freshwater and coastal piscivorous birds is generally higher
330
than 80% because demethylation process in the muscle tissue is very weak (Kalisinska et al., 2014).
331
This type of difference was not found when compared to adults belonging to the studied species.
4
ACCEPTED MANUSCRIPT 332
However, among young representatives of razorbill and black-throated loon some differences have
333
been shown. Nephric, hepatic and muscular THg and the concentration MeHg in muscle was
334
markedly higher in the black-throated loon compared to razorbill (MW test: Z = 2.31, p <0.05; Z = 2.43,
335
p <0.02; Z = 2.74 p <0.01; Z + 2.67, p <0.01, respectively).
336
In groups of analyzed common birds from Poland, the average hepatic THg concentration did
337
not exceed lethal concentration, compared to the Canadian population of this species where total
338
mercury content was higher than this specified value.
339
Consumption of fish is the main pathway to methylmercury exposure for birds. It can cause
340
adverse effects on reproductive success, behaviour and cell development. Methylmercury is able to
341
cross the blood – brain barrier and can be passed from the mother to the eggs. Our results help us to
342
better understand the accumulation of mercury in the selected tissues of two species of birds (Alca
343
torda and Gavia arctica), showing significant differences between the contents of MeHg in the selected
344
tissues and the close correlations between the contents of methylmercury and inorganic mercury in
345
some analysed tissues.
346 347
Acknowledgments: The authors would like to thank to Ewelina Kołodziejczak and Dominika Michalska for
348
their assistance in performing chemical analyses.
349
Conflicts of Interest: The authors declare no conflict of interest.
350 351
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ACCEPTED MANUSCRIPT Highlights
Concentrations of Hg and MeHg in Alca torda and Gavia arctica tissues were measured; The highest average content of Hg was in liver in comparison to the other tissues; The average hepatic THg concentration did not exceed lethal concentration. Intra and inter-specific comparisons were carried out.