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<article xmlns:xlink="http://www.w3.org/1999/xlink" xml:lang="en" article-type="review-article">
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Sensors</journal-id>
<journal-title>Sensors</journal-title>
<issn pub-type="epub">1424-8220</issn>
<publisher>
<publisher-name>Molecular Diversity Preservation International (MDPI)</publisher-name></publisher></journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3390/s111211157</article-id>
<article-id pub-id-type="publisher-id">sensors-11-11157</article-id>
<article-categories>
<subj-group>
<subject>Review</subject></subj-group></article-categories>
<title-group>
<article-title>Earthworms and Soil Pollutants</article-title></title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Hirano</surname><given-names>Takeshi</given-names></name><xref ref-type="aff" rid="af1-sensors-11-11157"><sup>1</sup></xref><xref ref-type="corresp" rid="c1-sensors-11-11157"><sup>*</sup></xref></contrib>
<contrib contrib-type="author">
<name><surname>Tamae</surname><given-names>Kazuyoshi</given-names></name><xref ref-type="aff" rid="af2-sensors-11-11157"><sup>2</sup></xref></contrib></contrib-group>
<aff id="af1-sensors-11-11157">
<label>1</label> Department of Life and Environment Engineering, Faculty of Environmental Engineering, University of Kitakyushu, Kitakyushu, Fukuoka, 808-0135, Japan</aff>
<aff id="af2-sensors-11-11157">
<label>2</label> Division of Teacher Training, Faculty of Education and Culture, University of Miyazaki, Miyazaki, 889-2192, Japan; E-Mail: <email>k-tamae@cc.miyazaki-u.ac.jp</email></aff>
<author-notes>
<corresp id="c1-sensors-11-11157">
<label>*</label> Author to whom correspondence should be addressed; E-Mail: <email>t-hirano@kitakyu-u.ac.jp</email>; Tel.: +81-93-695-3206; Fax: +81-93-695-3299.</corresp></author-notes>
<pub-date pub-type="collection">
<year>2011</year></pub-date>
<pub-date pub-type="epub">
<day>28</day>
<month>11</month>
<year>2011</year></pub-date>
<volume>11</volume>
<issue>12</issue>
<fpage>11157</fpage>
<lpage>11167</lpage>
<history>
<date date-type="received">
<day>12</day>
<month>10</month>
<year>2011</year></date>
<date date-type="rev-recd">
<day>1</day>
<month>11</month>
<year>2011</year></date>
<date date-type="accepted">
<day>18</day>
<month>11</month>
<year>2011</year></date></history>
<permissions>
<copyright-statement>© 2011 by the authors; licensee MDPI, Basel, Switzerland.</copyright-statement>
<copyright-year>2011</copyright-year>
<license>
<p>This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).</p></license></permissions>
<abstract>
<p>Although the toxicity of metal contaminated soils has been assessed with various bioassays, more information is needed about the biochemical responses, which may help to elucidate the mechanisms involved in metal toxicity. We previously reported that the earthworm, <italic>Eisenia fetida</italic>, accumulates cadmium in its seminal vesicles. The bio-accumulative ability of earthworms is well known, and thus the earthworm could be a useful living organism for the bio-monitoring of soil pollution. In this short review, we describe recent studies concerning the relationship between earthworms and soil pollutants, and discuss the possibility of using the earthworm as a bio-monitoring organism for soil pollution.</p></abstract>
<kwd-group>
<kwd>earthworm</kwd>
<kwd>metal</kwd>
<kwd>oxidative DNA damage</kwd></kwd-group></article-meta></front>
<body>
<sec sec-type="intro">
<label>1.</label>
<title>Introduction</title>
<p>It is well known that earthworms play an important role in the soil macrofauna biomass. They are extremely important in soil formation, principally by consuming organic matter, fragmenting it, and mixing it intimately with soil mineral particles to form water-stable aggregates [<xref ref-type="bibr" rid="b1-sensors-11-11157">1</xref>]. In particular, the bioaccumulation ability of earthworms is essential for a bio-monitoring organism [<xref ref-type="bibr" rid="b2-sensors-11-11157">2</xref>]. Therefore, the earthworm is likely to be an excellent organism for this purpose.</p>
<p>A bio-monitoring method would be appropriate to evaluate metal toxicity, because of its sensitivity and availability for unknown metabolites. Organisms such as fish, snails, and plants have been employed as bio-monitors [<xref ref-type="bibr" rid="b3-sensors-11-11157">3</xref>–<xref ref-type="bibr" rid="b5-sensors-11-11157">5</xref>]. Although this approach is useful and promising, it is also somewhat limited, because it could be available only for a specific combination of a living organism with certain substances. Hence, it is important to find appropriate living organisms as bio-monitors for each type of assessment.</p>
<p>Recent research has indicated that the earthworm is a candidate bio-monitor organism for soil pollutants, because it plays an important role in the soil macrofauna biomass. The species <italic>Eisenia fetida</italic> (Savigny, 1826, <italic>E. fetida</italic>) is most commonly used in ecotoxicology, and is recognized as a useful bio-monitor for testing the chemical toxicity of soil [<xref ref-type="bibr" rid="b6-sensors-11-11157">6</xref>]. In particular, this species’ proximity to the soil contaminants is a merit for the analysis [<xref ref-type="bibr" rid="b7-sensors-11-11157">7</xref>,<xref ref-type="bibr" rid="b8-sensors-11-11157">8</xref>].</p>
<p>In this short review, we describe the possible use of the earthworm as a bio-monitoring organism for soil pollutants, by summarizing our previous work [<xref ref-type="bibr" rid="b9-sensors-11-11157">9</xref>] and that of other researchers.</p></sec>
<sec>
<label>2.</label>
<title>Effects of Metals on Earthworms</title>
<p>Earthworms have been indicated as a candidate bio-monitoring organism for soil pollutants. To establish a bio-monitoring system using earthworms, the effects of various chemical pollutants on earthworms have been studied. The accumulation of both natural and depleted uranium in earthworms was analyzed to evaluate the corresponding biological effects [<xref ref-type="bibr" rid="b10-sensors-11-11157">10</xref>]. The study showed that no effects were observed in terms of mortality or weight reduction, but cytotoxic and genetic effects were identified at quite low natural uranium concentrations. Among metals, methyl mercury might be more easily absorbed by and accumulated in earthworms [<xref ref-type="bibr" rid="b2-sensors-11-11157">2</xref>], suggesting that the earthworm is an ideal candidate for monitoring methyl mercury. Lee <italic>et al</italic>. also mentioned that metal bioaccumulation by earthworms could be used as an ecological indicator of metal availability [<xref ref-type="bibr" rid="b11-sensors-11-11157">11</xref>]. On the other hand, metal pollution reportedly had no effect on earthworm communities [<xref ref-type="bibr" rid="b12-sensors-11-11157">12</xref>].</p>
<p>Chemicals and ecological risk assessments should be based on the effects of the mixture, rather than those of a single compound. In this context, Natal-de-Luz <italic>et al</italic>. investigated the effects of sludge contaminated with chromium, copper, nickel, and zinc, and soils freshly spiked with the same mixture of metals, on <italic>Eisenia andrei</italic> [<xref ref-type="bibr" rid="b13-sensors-11-11157">13</xref>]. They detected a decrease in the metal bioavailability for earthworms, promoted by the high organic matter content of the sludge. The binary mixture effects of cadmium and zinc on the mortality of <italic>Aporrectodea caliginosa</italic> were also investigated by Qiu <italic>et al</italic>. [<xref ref-type="bibr" rid="b14-sensors-11-11157">14</xref>]. They reported that the effects of the cadmium and zinc mixtures on the mortality of <italic>Aporrectodea caliginosa</italic> were mainly antagonistic, and the magnitude of the antagonism was dependent upon both the relative concentrations of cadmium and zinc and their concentration magnitudes. The effects of combinations of metals and other chemical agents, such as pesticides, on earthworms were also investigated. Lister <italic>et al.</italic> studied the effects of a binary mixture of nickel and chlorpyrifos, an organophosphate insecticide, on Lumbricid earthworms, and found that both chemicals were rapidly accumulated to equilibrium [<xref ref-type="bibr" rid="b15-sensors-11-11157">15</xref>]. Although the nickel uptake followed the same pattern as the single chemicals, the rates of chlorpyrifos uptake and elimination were faster, suggesting that a mixture of chemicals in soil might enhance the toxicity to organisms.</p>
<p>Taken together, an analysis using a single chemical compound does not necessarily reflect its toxicity for organisms in the environment. Therefore, when using earthworms as a bio-monitoring organism, careful attention should be paid to the target chemicals’ characteristics. A summary of the recently reported data about the effects of chemical agents in soil on earthworms is provided in <xref ref-type="table" rid="t1-sensors-11-11157">Table 1</xref>.</p>
<p>In terms of the relationship between metals and earthworms, cadmium has been extensively studied and is known to affect the earthworm’s physiological state, in terms of bioaccumulation [<xref ref-type="bibr" rid="b16-sensors-11-11157">16</xref>], a slight decrease in weight [<xref ref-type="bibr" rid="b17-sensors-11-11157">17</xref>], and oxidative DNA damage generation [<xref ref-type="bibr" rid="b9-sensors-11-11157">9</xref>]. However, the earthworm is not useful for all chemical substances in soil. For example, nickel is not accumulated in the earthworm, and thus had no effects on growth, as shown in <xref ref-type="fig" rid="f1-sensors-11-11157">Figure 1</xref> [<xref ref-type="bibr" rid="b9-sensors-11-11157">9</xref>].</p>
<p>Among the factors that define the toxicological effects of metals on organisms are metal binding proteins, such as metallothioneins (MTs). MTs, cysteine-rich cationic proteins, play a critical role in preventing metal toxicity. Two MT isoforms (MT1 and MT2) were identified in the earthworm [<xref ref-type="bibr" rid="b24-sensors-11-11157">24</xref>], and MT2 was increased in cadmium-exposed earthworms [<xref ref-type="bibr" rid="b25-sensors-11-11157">25</xref>]. Stürzenbaum <italic>et al</italic>. demonstrated that the earthworm had the intrinsic capacity to efficiency sequester and compartmentalize cadmium via a metallothionein-mediated trafficking pathway, by using X-ray microanalysis, quantitative polymerase chain reaction, and immunohistochemical techniques [<xref ref-type="bibr" rid="b16-sensors-11-11157">16</xref>]. Therefore, MT1/MT2 should be considered in the establishment of a bio-monitoring system using earthworms. These findings prompted us to assess the usefulness of earthworms as a bio-monitor. However, there are no established methods for using earthworms for this function.</p></sec>
<sec sec-type="methods">
<label>3.</label>
<title>Methods for the Detection of Metal Toxicity by Using Earthworms</title>
<p>In soil pollution, metal contamination is a critical event. To prevent metal toxicity, we must first understand the metal’s features and assess its toxicity. However, the methods used for the assessment of metal toxicity are often not sensitive enough, because metals can be toxic below the technical detection limits. To overcome this limitation, many research efforts have been made to develop detection techniques or assessment methods for metal contamination of soil. Furthermore, the toxic actions of metals sometimes depend on their metabolites generated in living organisms. Thus, adequate methods to assess metal toxicity are difficult to develop.</p>
<p>As we stated above, the earthworm is a candidate organism for the assessment of pollutants, but is not useful for all chemical substances in soil. Therefore, when using the earthworm as a bio-monitoring organism for soil pollutants, it is important to select the appropriate target substances. We have presented several methods using earthworms.</p>
<p>The analysis of earthworm reproduction is a useful method for the evaluation of chemical substances in the environment. The effects of cadmium and zinc on the reproduction of <italic>Enchytraeus albidus</italic> were investigated. Both metals reportedly affected the enchytraeids’ reproduction [<xref ref-type="bibr" rid="b26-sensors-11-11157">26</xref>].</p>
<p>Nahmani <italic>et al</italic>. suggested that life cycle parameters, such as cocoon production and hatching rate, of <italic>Eisenia fetida</italic> were more sensitive to metal pollution than survival or weight change [<xref ref-type="bibr" rid="b27-sensors-11-11157">27</xref>]. These studies revealed that the earthworm should be useful for the detection of the cytotoxic effects of certain types of chemical agents in soil, by selecting adequate parameters.</p></sec>
<sec>
<label>4.</label>
<title>8-Oxoguanine Generation in Metal-Treated Earthworm DNA</title>
<p>Quantitative and qualitative analyses of the oxidative DNA damage generated in living organisms are useful for the evaluation of the genotoxic effects of soil pollutants, because all aerobic organisms are constantly exposed to oxygen molecules. In particular, 7,8-dihydro-8-oxoguanine (8-oxoguanine, 8-oxo-Gua, <xref ref-type="fig" rid="f2-sensors-11-11157">Figure 2</xref>), a major form of oxidative DNA damage, may have an important role in carcinogenesis, because it causes the GC-to-TA transversion type point mutation [<xref ref-type="bibr" rid="b28-sensors-11-11157">28</xref>–<xref ref-type="bibr" rid="b30-sensors-11-11157">30</xref>]. 8-oxo-Gua is constantly generated in DNA and the nucleotide pool by reactive oxygen species (ROS), due to exposure to endogenous or exogenous factors.</p>
<p>We recently analyzed the accumulation of 8-oxo-Gua in the DNA of <italic>E. fetida</italic> exposed to heavy metals, to determine if a method using earthworms as a bio-monitor would be useful for the assessment of soil mutagenicity [<xref ref-type="bibr" rid="b9-sensors-11-11157">9</xref>]. We employed cadmium and nickel as test metals, because the carcinogenic potentials of cadmium and nickel have been established for humans and animals [<xref ref-type="bibr" rid="b31-sensors-11-11157">31</xref>,<xref ref-type="bibr" rid="b32-sensors-11-11157">32</xref>], and these metals are known to generate 8-oxo-Gua in DNA [<xref ref-type="bibr" rid="b33-sensors-11-11157">33</xref>–<xref ref-type="bibr" rid="b36-sensors-11-11157">36</xref>]. In the study, <italic>E. fetida</italic> were kept in a 20 liter stainless steel tank at an ambient temperature of 24 °C, using mold with skim milk as a food source until metal exposure [<xref ref-type="fig" rid="f3-sensors-11-11157">Figures 3(A,B)</xref>]. Three to six individuals were kept in a 600 mL glass container [<xref ref-type="fig" rid="f3-sensors-11-11157">Figure 3(C)</xref>] containing 50 g of soil with/without metals (CdCl<sub>2</sub> or NiCl<sub>2</sub>). They were exposed to 10 or 200 μg metal/g soil for 1, 2, and 3 weeks or 10 μg metal/g soil for 3 months. As a result, we detected a high level of cadmium accumulation in <italic>E. fetida</italic> [<xref ref-type="fig" rid="f4-sensors-11-11157">Figures 4(A,C)</xref>]. On the other hand, no Ni accumulation was observed [<xref ref-type="fig" rid="f4-sensors-11-11157">Figures 4(B,C)</xref>].</p>
<p>In addition, we observed positive 8-oxo-Gua staining in the gut epithelial layers in almost all samples [<xref ref-type="fig" rid="f5-sensors-11-11157">Figure 5(A)</xref>]. The metal absorption routes include the digestive system and the surface wall [<xref ref-type="bibr" rid="b37-sensors-11-11157">37</xref>,<xref ref-type="bibr" rid="b38-sensors-11-11157">38</xref>], but the main route is the digestive system. Since gut epithelial layers are frequently exposed to ROS, 8-oxo-Gua accumulation was constantly detected. Although the 200 μg cadmium-exposed <italic>E. fetida</italic> showed relatively stronger signals at 2 weeks in comparison to the others, almost all of the specimens showed positive signals in the gut epithelial layers, and the differences in the signal strength were too small to conclude that cadmium exposure increased 8-oxo-Gua accumulation in the organs. On the other hand, the positive signals in the seminal vesicles were clearly detected only in <italic>E. fetida</italic> treated with 10 μg of cadmium at 3 months [<xref ref-type="fig" rid="f5-sensors-11-11157">Figure 5(B)</xref>]. The seminal vesicles are considered as metallothionein (MT)-poor organs. Therefore, it seems reasonable to speculate that a lower level of MT expression is involved in the accumulation of cadmium-induced DNA damage.</p>
<p>Therefore, we would like to propose the merit of analyzing DNA damage generated in earthworms for the assessment of soil pollution. Besides analysis of 8-oxo-Gua generation, single-cell gel electrophoresis (comet) assay may be a useful tool for evaluation of genotoxic effects of pollutants on earthworms. Bonnard <italic>et al</italic>. indicated genotoxic effects of an industrially contaminated soil on <italic>E. fetida</italic> by using comet assay [<xref ref-type="bibr" rid="b39-sensors-11-11157">39</xref>]. Although these studies suggested the utility of measuring DNA damage for evaluation, there are presently only a few reports about DNA damage in the earthworm [<xref ref-type="bibr" rid="b9-sensors-11-11157">9</xref>,<xref ref-type="bibr" rid="b40-sensors-11-11157">40</xref>].</p></sec>
<sec sec-type="conclusions">
<label>5.</label>
<title>Conclusions</title>
<p>Our previous data demonstrated the possible utility of using earthworms as a bio-monitoring organism, by measuring the oxidative DNA damage generated in the earthworms as a bio-monitoring method for assessing soil mutagenicity. However, many points remain unresolved. For example, this method would only be reliable for bio-accumulated metals, such as cadmium, but not for non-bio-accumulated metals, such as nickel, even if they generate 8-oxo-Gua. Furthermore, it is not clear how the pollution level of soil should be evaluated, based on the data from earthworms. Although several studies have been performed, no standardized method has been established, according to our knowledge. Further studies will be required to establish a broader bio-monitoring method using earthworms to assess soil pollution.</p></sec></body>
<back>
<ack>
<p>The authors thank Ki-Hyun Kim, Guest Editor of “Sensing of Toxic and Hazardous Metals in Various Environmental Media”, a special issue of <italic>Sensors</italic>, for inviting us to write this review article, and Elsevier LTD for permission to reproduce the material in reference [<xref ref-type="bibr" rid="b9-sensors-11-11157">9</xref>] as <xref ref-type="fig" rid="f1-sensors-11-11157">Figures 1</xref>, <xref ref-type="fig" rid="f4-sensors-11-11157">4</xref> and <xref ref-type="fig" rid="f5-sensors-11-11157">5</xref> in this article. This work was supported by a grant from The Foundation for Earth Environment.</p></ack>
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<sec sec-type="display-objects">
<title>Figures and Table</title>
<fig id="f1-sensors-11-11157" position="float">
<label>Figure 1.</label>
<caption>
<p>All <italic>E. fetida</italic> were weighed under wet conditions in the short-term <bold>(A)</bold> and the long-term <bold>(B)</bold> experiments. Each data point represents the mean of six <italic>E. fetida</italic>. The treatment of <italic>E. fetida</italic> with 200 μg Cd/g soil resulted in body weight loss, suggesting Cd-induced growth inhibition. In the long-term experiment, each data point represents the mean of 16 <italic>E. fetida</italic>, and no significant differences between any groups were observed. (Nakashima <italic>et al</italic>. [<xref ref-type="bibr" rid="b9-sensors-11-11157">9</xref>], Copyright Elsevier.)</p></caption>
<graphic xlink:href="sensors-11-11157f1.gif"/></fig>
<fig id="f2-sensors-11-11157" position="float">
<label>Figure 2.</label>
<caption>
<p>Structure of 7,8-dihydro-8-oxoguanine (8-oxo-Gua). 8-oxo-Gua is formed by hydroxylation of guanine at the C-8 position.</p></caption>
<graphic xlink:href="sensors-11-11157f2.gif"/></fig>
<fig id="f3-sensors-11-11157" position="float">
<label>Figure 3.</label>
<caption>
<p>(<bold>A</bold>) <italic>Eisenia fetida</italic>; (<bold>B</bold>) <italic>E. fetida</italic> were kept in a 20 liter stainless steel tank; (<bold>C</bold>) <italic>E. fetida</italic> were maintained in a 600 mL glass container when they were exposed to heavy metals.</p></caption>
<graphic xlink:href="sensors-11-11157f3.gif"/></fig>
<fig id="f4-sensors-11-11157" position="float">
<label>Figure 4.</label>
<caption>
<p>Heavy metal accumulation in <italic>E. fetida</italic>. Each data point represents the mean of three individuals. Heavy metal concentrations were measured by atomic absorption spectrometry, and are expressed as μg per body weight (data are modified from Nakashima <italic>et al.</italic> [<xref ref-type="bibr" rid="b9-sensors-11-11157">9</xref>], Copyright Elsevier).</p></caption>
<graphic xlink:href="sensors-11-11157f4.gif"/></fig>
<fig id="f5-sensors-11-11157" position="float">
<label>Figure 5.</label>
<caption>
<p>Immunohistochemical analyses of 8-oxo-dG accumulation in alimentary canal (AC) <bold>(A)</bold> and seminal vesicles (SV) <bold>(B)</bold> of <italic>E. fetida</italic> (S1) [data of (B) are modified from Nakashima <italic>et al.</italic> [<xref ref-type="bibr" rid="b9-sensors-11-11157">9</xref>], Copyright Elsevier].</p></caption>
<graphic xlink:href="sensors-11-11157f5.gif"/></fig>
<table-wrap id="t1-sensors-11-11157" position="float">
<label>Table 1.</label>
<caption>
<p>Recent reports on the effects of chemical agents in earthworms.</p></caption>
<table frame="hsides" rules="rows">
<thead>
<tr>
<th align="center" valign="middle"><bold>Species</bold></th>
<th align="center" valign="middle"><bold>Chemical agents</bold></th>
<th align="center" valign="middle"><bold>Effects</bold></th>
<th align="center" valign="middle"><bold>References</bold></th></tr></thead>
<tbody>
<tr>
<td align="left" valign="middle"><italic>Lumbricus rubellus</italic></td>
<td align="left" valign="middle">Cd</td>
<td align="left" valign="middle">Bioaccumulation</td>
<td align="left" valign="middle">Stürzenbaum <italic>et al</italic>. (2004) [<xref ref-type="bibr" rid="b16-sensors-11-11157">16</xref>]</td></tr>
<tr>
<td align="left" valign="middle"><italic>Lumbricus rubellus</italic></td>
<td align="left" valign="middle">Cd and Cu</td>
<td align="left" valign="middle">A slight decrease in weight.</td>
<td align="left" valign="middle">Burgos <italic>et al</italic>. (2005) [<xref ref-type="bibr" rid="b17-sensors-11-11157">17</xref>]</td></tr>
<tr>
<td align="left" valign="middle"><italic>Eisenia fetida</italic></td>
<td align="left" valign="middle">Cd and Ni</td>
<td align="left" valign="middle">Cd, but not Ni, accumulated and generated 8-oxoguanine in earthworm.</td>
<td align="left" valign="middle">Nakashima <italic>et al</italic>. (2008) [<xref ref-type="bibr" rid="b9-sensors-11-11157">9</xref>]</td></tr>
<tr>
<td align="left" valign="middle"><italic>Eisenia fetida</italic></td>
<td align="left" valign="middle">Cu and ciprofloxacin (CIP)</td>
<td align="left" valign="middle">Cu may be partly assimilated as Cu-CIP complexes I by earthworms, changing the bioavailability, subcellular distribution, and toxicity of Cu to earthworms.</td>
<td align="left" valign="middle">Huang <italic>et al</italic>. (2009) [<xref ref-type="bibr" rid="b18-sensors-11-11157">18</xref>]</td></tr>
<tr>
<td align="left" valign="middle"><italic>Lumbricus rubellus</italic></td>
<td align="left" valign="middle">Pb and Zn</td>
<td align="left" valign="middle">Accumulated in the posterior alimentary canal.</td>
<td align="left" valign="middle">Andre <italic>et al</italic>. (2009) [<xref ref-type="bibr" rid="b19-sensors-11-11157">19</xref>]</td></tr>
<tr>
<td align="left" valign="middle"><italic>Drawida</italic> sp., <italic>Allolobophora</italic> sp., <italic>Limnodrilus</italic> sp.</td>
<td align="left" valign="middle">Mercury</td>
<td align="left" valign="middle">Mercury was mostly present in inorganic forms in earthworms. The bioaccumulation factors of methyl mercury from soil in earthworms were much higher than those of total mercury.</td>
<td align="left" valign="middle">Zhang <italic>et al</italic>. (2009) [<xref ref-type="bibr" rid="b2-sensors-11-11157">2</xref>]</td></tr>
<tr>
<td align="left" valign="middle"><italic>Lumbricus terrestris</italic></td>
<td align="left" valign="middle">TiO<sub>2</sub></td>
<td align="left" valign="middle">An enhanced apoptotic frequency, which was higher in the cuticle, intestinal epithelium and chloragogenous tissue than in the longitudinal and circular musculature.</td>
<td align="left" valign="middle">Lapied <italic>et al</italic>. (2011) [<xref ref-type="bibr" rid="b20-sensors-11-11157">20</xref>]</td></tr>
<tr>
<td align="left" valign="middle"><italic>Eisenia fetida</italic></td>
<td align="left" valign="middle">azodrin</td>
<td align="left" valign="middle">Concentration-dependent changes in the morphology and the AChE activity.</td>
<td align="left" valign="middle">Rao and Kavitha (2004) [<xref ref-type="bibr" rid="b21-sensors-11-11157">21</xref>]</td></tr>
<tr>
<td align="left" valign="middle">No description</td>
<td align="left" valign="middle">polybrominated diphenyl ethers</td>
<td align="left" valign="middle">Bioaccumulation</td>
<td align="left" valign="middle">Sellström <italic>et al</italic>. (2005) [<xref ref-type="bibr" rid="b22-sensors-11-11157">22</xref>]</td></tr>
<tr>
<td align="left" valign="middle"><italic>Eisenia fetida</italic></td>
<td align="left" valign="middle">metalaxyl</td>
<td align="left" valign="middle">Metalaxyl was rapidly assimilated by earthworms, and the bioaccumulation of metalaxyl was enantioselective, with preferential accumulation of the S-enantiomer.</td>
<td align="left" valign="middle">Xu <italic>et al</italic>. (2011) [<xref ref-type="bibr" rid="b23-sensors-11-11157">23</xref>]</td></tr></tbody></table></table-wrap></sec></back></article>
