Total and methyl mercury contents and distribution characteristics in cicada, Cryptotympana atrata (Fabricius).

Total and methyl mercury concentrations of cicada bodies, wings, and exuviae were investigated to study the mercury distribution characteristics. Results indicated that total and methyl mercury concentrations of cicada bodies were 2.64 mg/kg and 123.93 ng/g on average, respectively. In cicada tissues, total mercury concentrations were found to increase in the order of exuviae (0.50 mg/kg on average) < wings (0.98 mg/kg on average) < cicada bodies (2.64 mg/kg on average) and methyl mercury concentrations of cicada bodies were 123.93 ng/g on average and were the highest. Methyl mercury concentrations accounted for about 4.69% of total mercury in cicada bodies and most mercury was in inorganic forms in cicada. Sex differences of total mercury concentrations were significantly great (F = 8.433, p < 0.01) and total mercury concentrations of the males, which were 3.38 mg/kg on average, were much higher. Correlation analysis showed that neither total nor methyl mercury concentrations of cicada bodies was significantly related to the corresponding contents of soil (r = 0.0598, p > 0.05).

Mercury is recognized as a very toxic metal in the environment and can result in poisoning of wild animals and humans due to the fact that it can be biomagnified along the food chains (Mason et al. 1995; Boening 2000). Previous mercury researches have focused primarily on aquatic organisms, including fishes (Baeyens et al. 2003; Campbell et al. 2008) and invertebrates (Martin and Wang 2004). It is reported that most mercury in fish muscles was in methylated form (Baeyens et al. 2003). In recent years, total and methyl mercury pollution in terrestrial animals are recognized as significant problem, such as mammals (Horai et al. 2006), birds (Longcore et al. 2007), invertebrates (Heikens et al. 2001), insects (Devkota and Schmidt 2000), and reptiles (Jones and Holladay 2006). But still there is little research on the long-lived insects, such as cicada.

Field studies indicated that mercury can be taken up by insects and transferred to organisms occupying higher trophic level (Zhang et al. 2009). Some insects could accumulate large amounts of mercury and are regarded as the bio-indicator of mercury pollution in soil (Hsu et al. 2006). Cicada come out from the soil in late spring and are foods of many birds and entomophagous insects. Mercury can be absorbed efficiently by cicada (Magicicada cassini) and the mercury concentrations in males are significantly higher than that in females of the same species (Heckel and Keener 2007). Cicada with high mercury contents might threat people’ s health because cicada and their exuivae are important materials of Chinese traditional medicine.

Cicada is the representative long-lived insect species with special living habits, but little has been known about the mercury distribution characteristics in cicada, and the routes of cicada exposed to mercury are complex and still not determined. The primary objective of this study is to investigate total and methyl mercury accumulation in their bodies, hymenopterous wings and exuviae, and then mercury distribution characteristics in cicada are discussed in mercury-contaminated area. It is hoped to reveal the mercury pollution in the long-lived insects and help assess the health of terrestrial ecosystem throughly.

Materials and Methods

Huludao City is an important non-ferrous smelting and chemical industry area in northeast China. Mercury pollution is serious due to one chlor-alkali plant and two zinc smelteries there. Wuli River and Cishan River are two main rivers in the city. In the present study, cicada are collected from 10 sites by hand, of which most are close to the two Rivers: Huafei Bridge (S1), Huagong Bridge (S2), Huaji Bridge (S3), Wuli bridge (S4), the North bridge of Cishan(S5), Daochi village (S6), the South bridge of Cishan (S7), Cishan village (S8), Longwan Park(S9), and the new residential area (S10) (Fig. 1).

Fig. 1

Sample sites

Cicada (n = 67) and their exuviae (n = 235) were collected, sealed in polythene bags and preserved in portable refrigerator at 4°C in field. In laboratory, samples were washed with deionised water to remove mercury attached on the surface, distinguished the female and male, cut off their wings, dried them at 60°C to constant weights (Hsu et al. 2006), ground the samples to homogenous powders in a quartz bowl, and preserved in polythene bags in refrigerator at −4°C before used.

Soil (n = 62) was collected at the same places where cicada were trapped, sealed in polythene bags, then brought back to laboratory, dried at room temperature, ground to pass an 80-mesh nylon sieve, and preserved in polythene bags before use.

Total mercury of soil, cicada bodies, wings and exuviae were extracted following the method of H2SO4–HNO3–V2O5. All forms of Hg in samples were converted to Hg2+, and then Hg2+ was reduced to elemental Hg by addition of 20% SnCl2 solution. Cold atomic absorption technique was used to determine the total Hg with F732-V Hg detector whose detection limit is 5 × 10−2 ng/g.

MeHg in soil, cicada bodies and cicada exuviae were extracted firstly and then separated using the method described by Sun et al. (2007). 0.500 g of soil and biologic samples were weighed into a 50 mL polyethylene centrifuge tube. About 5 mL 6 mol/L HCl was added to extract all forms of mercury. The tube was placed overnight and then was ultrasonicly cleaned for 2 h. After that, tube was centrifugated at 3,000 rpm for 15 min. The supernatant fluid was transferred into a 10 mL polyethylene centrifuge tube; 2 mL of CH2Cl2 was added and shaken for 1 h to extract organomercury compounds into the CH2Cl2 phase. After centrifuging at 3,000 rpm for 15 min, the CH2Cl2 phase was transferred into a 50 mL glass tube; an additional 2 mL of CH2Cl2 was added into the 10 mL polyethylene centrifuge tube again to remove any remaining MeHg. The same steps repeated on the same sediment sample. Finally, 5 mL deionized water was added into the 50 mL glass tube, which had contained the 4 mL CH2Cl2 phase. The 50 mL glass tube was placed in a 60°C water bath and was aerated by N2. The CH2Cl2 was blown off and the organomercury compounds were left in the water phase. Finally, 1 mL 1:1 18 mol/L H2SO4 and 1 mL bromide agent were added into the 50 mL glass tube, which played the role of oxidation and indicator, respectively. After 1 h, a drop of hydroxylamine hydrochloride was added into the tube to deoxidize the residual bromide agent. The MeHg was determined by Tekran Model 2600 with a detection limit of 0.005 ng/L.

Precision and accuracy of the analytical methods were evaluated by comparing the mercury concentrations in certified reference materials to the measured values. The expected and measured concentrations in soil reference (GBW0-70405) were 0.290 ± 0.003 and 0.290 ± 0.0025 mg/kg, respectively; in the hair reference (GBW-07601) were 0.36 ± 0.05 and 0.40 ± 0.01 mg/kg, respectively. Methyl mercury expected and measured concentrations in reference (IAEA-443) were 0.17 ± 0.07 and 0.15 ± 0.03 mg/kg, respectively.

SPSS10.0 for windows and Excel 2003 were used for data analysis and Arcgis9.0 was used to draw the sample map.

Results and Discussion

Total and methyl mercury concentrations of soil varied from 0.16 to 20.37 mg/kg (mean, 4.08 mg/kg) and from 0.34 to 33.49 ng/g (mean, 9.17 ng/g), respectively (Fig. 2), and varied largely with the sample site (Table 1). No significant correlation was found between total and methyl mercury in soil (r = 0.147, p > 0.05).

Fig. 2

Sex differences of total and methyl mercury between female and male cicadas

Table 1

Total and methyl mercury of soil, cicada bodies, wings and exuviae

Site	THgs (mg/kg)	MeHgs (ng/g)	THgc (mg/kg)	THgw (mg/kg)	THge (mg/kg)	MeHge (ng/g)	MeHgc (ng/g)
S1	0.81	3.56	3.43	0.48			82.24
S2	2.54	6.93	0.51	1.01			79.02
S3	8.72	22.89	2.87	1.10			171.59
S4	2.54	5.50	1.50	1.33	1.46	6.39	157.56
S5	5.39	7.40	0.93	0.59			192.17
S6	10.96	12.01	5.25	1.19			134.88
S7	3.36	5.71	2.51	0.48			172.09
S8	0.49	5.56	8.19	0.88	0.23	13.15	27.41
S9	0.39	0.34	1.00	1.31	0.12		104.43
S10	0.27	15.41	3.27	0.27	0.17	3.61	82.95

THgs, THgc, THgw and THge were the total mercury concentrations in soil, cicada bodies, wings and exuviae; MeHgs, MeHge, and MeHgc were the methyl mercury concentrations in soil, cicada bodies and cicada exuviae

Total mercury concentrations of cicada bodies, wings, and exuviae varied from 0.21 to 9.99 mg/kg (mean, 2.64 mg/kg) in cicada bodies, from 0.20 to 3.72 mg/kg (mean, 0.98 mg/kg) in wings, from 0.08 to 1.95 mg/kg (mean, 0.50 mg/kg) in exuviae, respectively. Methyl mercury concentrations varied from 21.36 to 318.81 ng/g (mean, 123.93 ng/g) in cicada bodies, and varied from 3.61 to 13.15 ng/g (mean, 7.72 ng/g) in exuviae, respectively.

Total mercury concentrations of cicada bodies, wings, and exuviae were found to increase in the order of exuviae < wings < cicada bodies and vary with no significant differences. Methyl mercury concentrations of cicada bodies were about 2.54%–25.93% of total mercury (mean, 4.69%). For exuviae, the ratios were close to cicada bodies and varied from 0.44% to 5.72% (mean, 2.77%). The results showed that mercury was almost in inorganic form in cicada bodies.

No significant relationship was found between the total and methyl mercury in cicada (r = −0.442; p > 0.086). It is unknown that whether the cicada directly absorbed methyl mercury from soil or food or methyl mercury was formed in cicada bodies.

Total mercury concentrations of male cicada were significantly higher than those of female (F = 8.433, p < 0.01), which were much heavier (F = 33.10, p < 0.01). It was consistent with conclusions past reported (Heckel and Keener 2007) (Table 2).

Table 2

Sex difference of cicada body weights, THgc, THgw and MeHgc

Sex	n	Weight (g)	THgc (mg/kg)	THgw (mg/kg)	MeHgc (ng/g)
Female	27	0.94–1.31 (1.11)	0.21–2.72 (1.34)	0.29–3.72 (1.15)	31.26–192.17 (110.27)
Male	40	0.35–0.69 (0.54)	0.37–9.99 (3.38)	0.20–1.50 (0.87)	31.38–318.81 (132.12)

THgc and THgw were the total mercury concentrations in cicada bodies and wings; MeHgc were the methyl mercury concentrations in cicada bodies

Correlation analysis showed that neither total nor methyl mercury of cicada was significantly related with the corresponding mercury of soils (p > 0.05).

Both the highest total and methyl mercury concentrations of soil were found in Huagong Bridge (S3), where the chlor-alkali plant dumped its effluent in the past. From 1952 to 1980, the chlor-alkali plant produced NaOH, Cl2 and H2 using mercury electrodes as one of the main technologies and about 1,500 × 104t waste water were discharged into the Wuli River resulting in about 265t mercury precipitation in the surface sediment and soil (Zhao and Yan 1997). Although the chlor-alkali plant ceased operations using mercury as electrode in 1998, the concentrations of mercury in soil and sediments remains high around site S3. In Daochi village (S6), total and methyl mercury concentrations of soil were slightly lower than those in S3. Daochi village are heavily affected by the mercury atmospheric deposition due to the two zinc smelteries around here. Soil analyzed from site S10, a new residential neighborhood, contained below average total mercury but above average methyl mercury.

In the present work, both the average total and methyl mercury concentrations of cicada bodies were higher than those reported by Heckel and Keener (2007) Compared with the Locusta migratoria manilensis and Acrida chinensis in Huludao City, cicada could accumulate more mercury from the ambient (Table 3). Mercury concentrations of cicada were about 60 and 70 times for total mercury, 10 and 26 times for methyl mercury, of Locusta migratoria manilensis and Acrida chinensis, respectively (Zheng et al. 2008). Cicada are the representative long-lived insect species and suffer more mercury exposure than these annual insects. Cicada larvas live underground for about 4–5 years before the last metamorphosis. Food might be another important reason for high mercury level of cicada. Both Locusta migratoria manilensis and Acrida chinensis feed on plant leaves, but cicada larvas sucks the juice from plant roots of which part the highest mercury concentrations of plant are in Boening (2000).

Table 3

Total and methyl mercury concentrations comparison with other reports

Insect	THg (mg/kg)	MeHg (ng/g)	References
Locusta migratoria manilensis	0.013–0.154 (mean, 0.043)	1–12 (mean, 7)	Zheng et al. (2008)
Acrida chinensis	0.009–0.138 (mean, 0.037)	1– (mean, 3)
Paraten-odera sinensis	0.057–0.117
Insect	0.01–0.26 (mean, 0.10)		Hsu et al. (2006)
Magicicada cassini	0.01–0.05		Heckel and Keener (2007)
Cryptotympana atrata	0.21–9.99 (mean, 2.64)	21.6–318.81 (123.93)	This paper

THg was the total mercury concentration and MeHg was the methyl mercury concentration

It is reported that to excrete heavy metals onto the furs, surface skins, and wings might be the mechanisms for animals to endure the heavy metals contaminations (Heliövaara and Väisänen 1990). For example, feathers of birds often contain high mercury concentrations Longcore et al. (2007) and the highest mercury concentrations of grasshoppers are in the wings (Zhang et al. 2009). But total mercury concentrations of cicada wings were not high and this might due to their special living habits. Cicada infuses their body fluids to protend wings out after the last metamorphosis and this results total mercury concentrations of wings closed to those of cicada bodies. After their wings generation, cicada could only lived for about 60–70 days above ground which are much shorter than Locusta migratoria manilensis and Acrida chinensis, there might no enough time for cicada to transfer mercury to their wings.

Exuviae is also thought to excrete mercury out from animal bodies. Mercury concentrations of snake exuviae would be 0.4 mg/kg if snakes received 2.0 mg/kg mercury exposure per month (Jones and Holladay 2006). Though cicada will experience 5 ecdysis processes during their growth, mercury concentrations and weights of exuviae are low and no appreciable amounts of mercury would be excreted out from cicada bodies. It concludes that exuviae would not effectively reduce mercury poison to cicada.

Results showed mercury concentrations are different with different sex. There might be two possible reasons to explain the sex differences. The female cicada often are heavier than the males and biomass dilutions might reduce mercury concentrations of females. Heckel and Keener (2007) reported that the lower body weights of males resulted in the higher mercury concentrations than females. Another potential reason is that the female lay eggs for generation resulting in possible mercury excretion out from their bodies. No significant sex differences were found on methyl mercury or total mercury concentrations of wings, but methyl mercury concentrations of females were lower than those of males while the total mercury concentrations of wings are just contrary (Fig. 2).

The routes of cicada exposed to mercury were not determined in this paper. Heikens has reported that heavy metals in terrestrial invertebrates are related to metal contents in soil (2001). Correlation analysis showed that neither total nor methyl mercury of cicada was related with the corresponding mercury of soils significantly. Heckel and Keener (2007) had assumed the cicada was exposed to mercury through dermal contact, but the hypothesis was not proofed in this paper. We conjecture that cicada ingested mercury from their special food, the fluid of plant root, which part the highest mercury concentrations were found in plants. But it need more detail study to substantiate the guess.

This study showed that mercury pollution in soil and cicada in Huludao City was serious. Cicada could accumulate mercury greatly to high levels. Total and methyl mercury concentrations of soil were not significantly related with each other. In cicada tissues, total mercury were found to increase in the order of exuviae < wing < cicada bodies and methyl mercury in cicada bodies were the highest among them. Methyl mercury concentrations were about 4.69% of total mercury of cicada bodies and this indicated that most mercury was in inorganic forms in cicada bodies. Sex differences of total mercury concentration were significantly great, total and methyl mercury concentrations of the males were higher. Correlation analysis showed that neither total nor methyl mercury concentrations in cicada bodies were significantly related to the corresponding contents of soil.