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Article

First Observation of Unicellular Organisms Concentrating Arsenic in ACC Intracellular Inclusions in Lake Waters

by
Agathe Martignier
1,
Montserrat Filella
2,*,
Jean-Michel Jaquet
1,
Mathieu Coster
3 and
Daniel Ariztegui
1
1
Department of Earth Sciences, University of Geneva, 1205 Geneva, Switzerland
2
Department F.-A. Forel for Environmental and Aquatic Sciences, Institute for Environmental Sciences, University of Geneva, 1205 Geneva, Switzerland
3
Service de l’écologie de l’Eau, 1219 Geneva, Switzerland
*
Author to whom correspondence should be addressed.
Geosciences 2022, 12(1), 32; https://doi.org/10.3390/geosciences12010032
Submission received: 9 November 2021 / Revised: 5 January 2022 / Accepted: 6 January 2022 / Published: 8 January 2022
(This article belongs to the Special Issue Current and Future Perspectives in Microbial Carbonate Precipitation)
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Abstract

:
In unicellular organisms, intracellular inclusions of amorphous calcium carbonate (ACC) were initially described in cyanobacteria and, later, in unicellular eukaryotes from Lake Geneva (Switzerland/France). Inclusions in unicellular eukaryotes, named micropearls, consist of hydrated ACCs, frequently enriched in Sr or Ba, and displaying internal oscillatory zonations, due to variations in the Ba:Ca or Sr:Ca ratios. An analysis of our database, consisting of 1597 micropearl analyses from Lake Geneva and 34 from Lake Titicaca (Bolivia/Peru), showed that a certain number of Sr- and Ba-enriched micropearls from these lakes contain As in amounts measurable by EDXS. A Q-mode statistical analysis confirmed the existence of five chemically distinct morpho-chemical groups of As-bearing micropearls, among which was a new category identified in Lake Geneva, where As is often associated with Mg. This new type of micropearl is possibly produced in a small (7–12 μm size) bi-flagellated organism. Micropearls from Lake Titicaca, which contain Sr, were found in an organism very similar to Tetraselmis cordiformis, which was observed earlier in Lake Geneva. Lake Titicaca micropearls contain larger As amounts, which can be explained by the high As concentration in the water of this lake. The ubiquity of this observed biomineralization process points to the need for a better understanding of the role of amorphous or crystalline calcium carbonates in As cycling in surface waters.

1. Introduction

Amorphous calcium carbonate (ACC) is the least stable polymorph of calcium carbonate. Even if chemically unstable, ACC is found naturally in taxa as wide-ranging as sea urchins, corals, molluscs, and foraminifera [1]. Recently, the presence of intracellular inclusions of ACC has been described in cyanobacteria [2,3] and in unicellular eukaryote organisms [4]. The intracellular inclusions of near-amorphous calcium carbonates produced by unicellular eukaryote organisms, and often enriched with other elements such as Sr and Ba, were named ‘micropearls’ [4]. Strontium-enriched micropearls were initially found to be produced by an extensively studied phytoplanktonic organism (Tetraselmis cordiformis) in the waters of Lake Geneva [4] and were soon observed to be common among many Tetraselmis species, and potentially in the whole class of Chlorodendrophyceae [5]. The cells of these green algae can contain more than 200 micropearls, of approximately 1 μm each. Present in multiple regions around the world, such species have been well described by biologists, but the micropearls have been overlooked due to their easy dissolution during most biological sample preparation procedures. Micropearls appear translucent in light microscopy but can be observed using Nomarski differential interference contrast [6]. The function of these mineral inclusions in the organism remains to be understood. Barium-enriched micropearls (Ba/Ca up to 90) have also been described in Lake Geneva [4]. They are produced by at least one organism, but its identification has remained elusive, even when scanning electron microscopy (SEM) observation of fixed samples, optical and epifluorescence microscopy, flow cytometry, and metagenomics were applied for identification purposes in more than 25 sampling campaigns over five years. A common characteristic of this biomineralization process in unicellular eukaryotes is the organisms’ capacity to strongly concentrate chemical elements from the surrounding water, even if they are present at low or very low concentration levels. Organisms also seem to be element-specific, i.e., a given species mainly concentrates a given element (e.g., Sr or Ba) [4,5].
All the cations biomineralized in the two previously described micropearl types are alkaline-earth elements (Ca, Sr, Ba, with some Mg often present). The exploration of our extensive collection of filtered water samples from Lake Geneva, containing monthly collected samples since June 2012, has now led to the energy-dispersive X-ray spectroscopy (EDXS) based detection of another element, As, in some specimens of the previously described micropearls and in a new type, never described before. From a chemical point of view, the presence of As in micropearls is not surprising, since the affinity of AsV for calcium carbonate is well known [7]. However, it is remarkable that this biomineralization process has never been described, considering that the toxicity of the element [8,9,10] has caused it to be widely studied. Numerous As chemical species, such as inorganic (mainly arsenate), methylated (mainly dimethylarsenate), arsenoribosides, and metabolites have been described in unicellular algae [11,12], but, to our knowledge, until Keren et al. [13] described the biomineralization of calcium arsenate by Entotheonella sp., the only other As biogenic mineral described had been orpiment [14].
The treatment of EDXS data for classification purposes, as in this study, is far from straightforward and requires a sound understanding of the analytical signals, as well as a rigorous statistical treatment. For this reason, we have paid particular attention to both aspects and discuss them in detail. The procedure developed here could guide further studies, where the treatment of similar data is needed.

2. Methods

2.1. Study Area

A water sampling program has been carried out at the GE3 station (46.2994° N/6.2197° E, depth: 70 m) in Lake Geneva (Switzerland/France) (Figure S1) by the SECOE (Service de l’écologie de l’Eau) of Canton Geneva since 1995, for water quality monitoring purposes. From June 2012, additional samples have been collected at depths ranging from 0 to 72 m, depending on the situation of the Chl a maximum, to study the particulate matter composition (Table S1). A few samples taken at station SHL2 (46.452° N/6.589° E, depth: 309 m) (Figure S1), at the deepest part of Lake Geneva, and in Lake Titicaca (Bolivia, Chua 16.19991° S/68.78534° W, depth: ~40 m) (Figure S2) in February 2017, were also included in this study. Altogether, the database consists of 1597 micropearl analyses from Lake Geneva and 34 from Lake Titicaca.

2.2. Sample Preparation

The sample preparation method consists of a pre-sieving of 250–400 mL of water (depending on the concentration of organisms present in the water) through a 64 µm mesh to eliminate larger grains or organisms, followed by rapid filtration through polycarbonate filters (pore size: 0.2, 1, 2, or 5 µm) under less than 10 mb vacuum, making sure that water is completely drained from the filter. The filter is then kept at room temperature in the dark. This method does not preserve the integrity of the cell morphology, because the organic matter is altered by drying, but it nevertheless retains some of its characteristics (size and approximate shape of the cell) and allows preserving perfectly the micropearls for several years. In order to better understand the morphology of the cells producing micropearls (e.g., presence of flagella), some additional samples were fixed with glutaraldehyde (2%) or alkaline lugol before filtration.

2.3. SEM-EDSX

Gold-coated samples (~10 nm layer) were imaged by a JEOL 7001 FA FEG scanning electron microscope (SEM) equipped with an integrated EDXS detector (JEOL model EX-94300S4L1Q), which provided semiquantitative compositional analyses (accelerating voltage: 15 kV, beam current: 7 nA, acquisition time: 30 s). The whole energy range (0–20 keV) was acquired and used for element detection.
The following elements were analyzed: Al, As, Ba, Ca, Cl, K, Mg, Na, P, S, Si, and Sr. The detection level for all the elements measured was estimated at 1%. Analytical results are gathered in an Excel database (SI_excel_1). Results are expressed in mol% and closed to 100%. This means that the percentages given in this study do not refer to the real composition, but are relative to the total concentration of the elements reliably measured in the samples. Caveats involved and choices made concerning EDXS measurements are discussed in detail in Section 4.1.

2.4. FIB-TEM

Focused ion beam (FIB) preparation of some electron-transparent lamellae (25 μm size) of micropearls and subsequent analyses by transmission electron microscopy (TEM) were performed at the Interdisciplinary Centre for Electron Microscopy of the EPFL (Lausanne, Switzerland) using a Zeiss NVision 40 CrossBeam instrument (Ga LMIS; 10 keV; 700 pA). A FEI Tecnai Osiris TEM with a high brightness XFEG gun and 4 windowless Super-X SDD detectors allowed the EDXS mapping of As, Ba, C, Ca, and Sr.

2.5. Arsenic Concentrations in Lake Water

Arsenic concentrations in Lake Geneva, determined by ICP-MS, are in the range 1.0–1.2 μg L−1. Concentrations were measured by ICP-MS on a Fisons PQ2+ before 2006 and on a Thermo-Fisher X7 II from 2006 to 2018, both in their standard configurations by the SECOE (Service de l’écologie de l’Eau) of Canton Geneva, Switzerland. The analytical accuracy was followed by analyzing certified reference materials SLRS-4 (before 2010) and SLRS-5 (after 2010) (National Research Council Canada). The analytical laboratory is accredited for the analysis of the trace elements in freshwaters (accreditation number: STS245; ISO norm 17025). Profiles show non-conservative behavior. Reported concentrations of As in Lake Titicaca are higher: 8–15 μg L−1 [15,16]. Arsenic in Lake Titicaca is mostly of geogenic origin and weakly affected by mining sources.

2.6. Morpho-Chemical Classification

A tentative typology of As-containing micropearls was established based on the presence of the most characteristic chemical elements, the origin of the samples and the visual SEM morphology of the micropearl-bearing cells (observed as clearly defined organic patches, Figure 1, Figure 2 and Figure S3). The procedure followed is detailed on the flowchart in Figure 3.

2.7. Data Processing

The statistical treatment of the typology, preliminarily established in 2.6, requires considering the possible presence of element concentration values below their detection limit, as well as the existence of non-normal or polymodal distributions. As can be observed in our analytical results database (SI_excel_1, sheet no 1), several elements display a large number of values below the detection level of 1.0 mol%. Following the strategy proposed by Antweiler [17], we computed summary statistics and inter-group comparisons on two versions of our data set: the instrument-generated data set, called lab following the terminology in Antweiler and Taylor [18]), and a left-censored data set where all readings below 1.0 mol% (hereafter called nondetects, ND) have been replaced by the value 1.0 mol%.
The statistical analysis of the data in Q-mode proceeded as follows:
  • Application of criteria for the conservation of descriptors. Some of the elements analyzed have a large proportion either of zeros (lab) or ND (left-censored), which must be eliminated to avoid meaningless statistics. Based on [18,19,20], the criteria for elimination were for lab data: proportion of zero values >0.6, and for left-censored data: proportion of ND >0.7 (Table S2 and SI_Excel_1, sheet no 1). This procedure led to different sets of descriptors among the various morpho-chemical groups (Table 1 and Table 2).
  • Examination of the descriptor distribution. Descriptors were tested for normality using the Shapiro–Wilks W criterion at a significance level of p ≥ 0.05, implemented in the ‘Univariate/Normality Test’ module of the PAST software, v. 4.02 [21] (SI_Excel_1, sheet no 15). To test for log normality, the W criterion was applied after a log transformation of the descriptors. Bimodality was estimated by visual inspection of the histograms, after an unsuccessful attempt to use the ‘Model/Mixture analysis’ module of PAST (see Table S3).
  • For the left-censored data, treatment of nondetects according to Helsel [22]. This robust estimation method, between parametric and non-parametric, is based on regression on order statistics (ROS), implemented in the R environment package called NADA [19]. It is generally preferred to maximum likelihood methods [23] or simple substitution methods [18]. An example of the ROS treatment for MC2/Cl and Sr descriptors is detailed in SI-excel_2.xlsx.
  • Test of the significance (at the 0.05 significance level) of the differences between the descriptor median values among morpho-chemical groups. Performed with the PAST module ‘Univariate/Several-Sample tests’ using Mann–Witney pairwise U criterion. The 2 × 2 comparisons are labelled ‘D’ when the difference is significant, and ‘S’ otherwise (see Table 3 and SI_Excel_1, sheet no 4).
  • Exploratory graphic display of samples in the ternary systems Mg-Ca-As, As-Sr-Ba, and Mg-As-Ba (Figure 4 and SI_Excel_1, sheet no 26).

3. Results

3.1. Tentative Morpho-Chemical Classification of Arsenic-Containing Micropearls

  • Application of the working scheme in Figure 3 gave a total dataset consisting of 267 micropearl analyses containing As >1 mol%, observed in samples from 28 different campaigns in Lake Geneva between July 2012 and July 2018 (SI_Excel_1, Table S1), plus 34 micropearls analyzed from Lake Titicaca (see database in SI_excel_1). Five morphological groups were identified:
  • The presence of Ba (n = 66) yielded two possibly distinct morpho-chemical groups, MC1 (Big Ba) and MC2 (Small Ba). The distinction between MC1 and MC2 is based on cell diameter and Ba concentration (20 µm, Ba < 55 mol% for MC1; 7–10 µm, Ba > 55 mol% for MC2).
  • The presence of Sr yielded MC3 (Lake Geneva) (n = 70) and MC4 (Lake Titicaca) (n = 34) groups. MC3 corresponds to well-defined, globular cells of ~15 µm diameter, which were attributed to Tetraselmis cordiformis in [4] and, thus, will be called Sr-Tetraselmis micropearls here (Figure 4). As-containing micropearls from Lake Titicaca (Sr-Titicaca) show a strong morphological similarity with the MC3 type (Figure 4).
  • The remaining As-containing micropearls (n = 97) (MC5) often contain Mg and seem to be produced by a single type unicellular organism with cells of approximately ~9 µm diameter. These micropearls, named MgAs (Figure 4, bottom), are small (~0.7 µm diameter) and rather difficult to detect in backscattered SEM images, due to the relatively low atomic mass of the elements involved.

3.2. Lab or Left-Censored Data?

The descriptors retained for analysis are shown in the data matrices of Table 1 (lab data) and Table 2 (left-censored data), after the elimination of those with a number of ND exceeding the criteria given in Table S2. The type of data to be used for further interpretation was chosen following two criteria:
  • Level of differences between median values in Table 1 and Table 2, shown in Table S3. Differences are small: left-censored data are slightly lower because they have not been closed to 100% (SI_excel_1 and Table 3), with the exception of unreliable values in [MC2/Cl] due to poor ROS fit (see SI_excel_2.xlsx).
  • Contrasts in the matrices of difference/similarity between morpho-chemical groups (Table 3 and their differences in Table S4). Some discrepancies exist between both datasets for Na, Cl, K, and, especially, Mg: globally speaking, significant differences (in pink in Table S4) or similarities (in green) are more numerous in the lab dataset, suggesting that the ROS transform attenuates the comparison between the groups. This is in accordance with Antweiler’s results [17] for group comparisons. For these reasons, further discussion will be restricted to the lab dataset.

3.3. Statistical Confirmation of the Typology

Statistical distributions are heterogeneous across descriptors and groups (Table S5). They are rarely normal, more often lognormal, and sometimes polymodal. This is why non-parametric methods were used to test for differences between morpho-chemical groups. Table 3a shows the significant differences (D) or similarity (S) in the descriptor median values between morpho-chemical groups, based on the Mann–Witney U criterion. For a given group and all the descriptors, the index propDg (bottom line of the table) gives the proportion of significant differences or statistical separability between a group and all other groups. Separability is excellent for MC1, MC2, and MC5. It is a little lower for MC3 and MC4, because of the similarity between these Sr-containing groups. The role of the various descriptors in the groups’ separability can be illustrated by the index propDv (rightmost column in the table). Apart from K, all the descriptors have a high discriminating power. The maximum values (1.0) for Ba justifies its role in the initial dichotomy applied in the definition of the morpho-chemical groups. There are also significant differences in As and Ca concentration between all groups. Finally, Mg (present in all groups; Table 1) has a weak separating power (propDv = 0.7) because it presents similar concentrations in MC3 and MC4.
It is interesting to compare the composition of MC3 and MC4 (Figure S5). There are no significant differences in Mg, K, and Sr content. In contrast, the As concentration is much higher in Sr-Titicaca (MC4) (median 11.4 mol%; Table 1) than in Sr-Tetraselmis (1.9 mol%), with a reverse contrast in Ca (90.8 vs. 69.3 mol%). Na and Cl are present only in Lake Titicaca.
The global chemical composition of the As micropearls can be summarized in ternary diagrams encompassing their main constituents (Mg, Ca, As, Sr, and Ba) and showing the degree of separability between the morpho-chemical groups (Figure 4). These diagrams are 2-D representations of a five-member space, with the following features confirming the results of Table 1 and Table 2: (i) The Big Ba (MC1) and Small Ba (MC2) types are optimally separated by their Ca and Mg content (Table 1; Figure 4 top and bottom). (ii) The Sr-Tetraselmis (MC3) group is separated from the others on the Sr–As axis (Figure 4 middle); this group also has more P, K, and Ca. (iii) The MgAs (MC5) group is also distinct on the Sr–As axis. (iv) The Small Ba, Big Ba, and Sr-Tetraselmis groups match those previously established in [4,5], whereas the MgAs group had not been identified previously. Thus, the statistical analysis of the chemical composition of the As-bearing micropearls confirmed the initial subdivision into five morpho-chemical groups, with significant differences in their chemical composition.

3.4. Description of the Confirmed Categories of As-Containing Micropearls

3.4.1. Ba Micropearls (MC1 and MC2)

The Big Ba group (MC1) is characterized by organic patches of 20–25 µm in diameter, with well-defined limits when the sample was fixed (Figure 1a and Figure 2). Barium content in the micropearls varies between 24 and 52 mol% and As between 1 and 2.6 mol%. The organic patches of the Small Ba group (MC2) are smaller (~7 µm) and their Ba and As content higher (53–74 mol% and 1–19 mol %, respectively (Figure 1(a2)). The mean Ba and As concentrations are significantly different in both groups, and Mg reaches a maximum concentration in MC2 (14.2 mol%). Most of the Ba micropearls previously studied [4,5] did not contain As; the present study includes only those containing more than 1 mol% of As, which represent 13% of all the Ba-micropearls measured in Lake Geneva (66/515).

3.4.2. Sr Micropearls (MC3 and MC4)

The globular shape of the cells producing MC3 micropearls is very characteristic (Figure 1b and Figure 2d). Cells (size: 15–20 µm) were attributed to Tetraselmis cf. cordiformis, a Chlorodendrophycea microalga, following the results of a study on cultured strains of this genus [5]. Sr-micropearls contain high amounts of Ca (79–96 mol%), and varying amounts of Sr (0–17 mol%), with traces of Mg, P, and K. Arsenic reaches up to 14 mol% (mean 2.6 mol%). Most of the micropearls of this type do not contain As: the present statistical analysis includes only those containing more than 1 mol% of As, which represent only 16% of the Sr-micropearls measured in Lake Geneva (138/881). Micropearls containing As may coexist with micropearls containing only Ca and Sr within the same cell. MC4 micropearls from Lake Titicaca, and the cell producing them, present a morphology very similar to MC3 micropearls (Figure 2). Compared to MC3, Lake Titicaca micropearls have similar Mg and Sr content but are much higher in As and lower in Ca (As mean 11.1 vs 2.6 mol%; Figure S5).

3.4.3. MgAs Micropearls (MC5)

The organic patches containing these micropearls measure approximately 9 µm (Figure 2a) and have ill-defined boundaries. In total, 97 micropearls were analyzed by EDXS in 44 different cells (Figure 5). Unlike the other groups, the composition of the micropearls produced by these cells nearly always contains As, in concentrations above the technique detection limit: 97% contain As, while only three micropearls in all these unicellular organisms were observed to be composed of Mg and Ca only. While the Ca content (mean 85 mol%, Table 1) varies very little in this group, micropearls within the same cell may have very different As concentrations. In general, the largest micropearls show higher As levels than the smaller ones. Images of a sample fixed with alkaline lugol showed that the organic matter surrounding the MgAs micropearls in the dried samples was a cell probably with two flagella (Figure 5b1,b2).

3.5. Localization of As in the Sr-Micropearls of Lake Geneva (MC3)

Thin sections of Sr-rich micropearls (MC3) produced by Tetraselmis and containing As were prepared by FIB, from a sample from Lake Geneva (10 July 2012 at 6 m) and mapped by TEM-EDXS (Figure 6). Cross-sections show that As, albeit in low concentrations, is concentrated in the outer parts of the micropearls with a thin outermost layer, seeming to exclusively contain Ca. Such a difference is visible by comparing the As and the Ca EDXS maps of Figure 6. The micropearl on the right-hand side of the mapping in Figure 6 presents a homogeneous content in As, because this cross-section is only superficial: it does not approach the center of the micropearl, and only the outer layer is mapped. TEM-EDXS analysis performed in the area containing As of the first sample (EDXS arrow in Figure 6) gave 91 mol% Ca, 6 mol% Sr, 2 mol% As, and 1 mol% P.

3.6. The Monthly Abundance of the MgAs Micropearls in Lake Geneva

Combined with earlier data, samples issued from 20 different campaigns in Lake Geneva, between June 2013 and August 2017 (Table S1) indicate that the organisms forming these micropearls are most abundant between March and May and are absent from August to January in Lake Geneva (Figure 7). The abundance estimate presented in this figure was achieved by spending the same amount of observation time on each sample previously selected for that specific part of the study. Samples were then classified depending on the number of MgAs micropearls encountered during that limited time (0 = none, 1 = rare, 2–3 = present, >4 = frequent).

4. Discussion

4.1. Analytical Procedure

EDXS provides a suitable tool for the analysis of our samples; the use of alternative techniques, such as electron probe microanalysis, being excluded because of the requirements of sample preparation (i.e., polished, smooth surface). However, the use of EDXS is not without drawbacks, in particular, the complexity of the phenomena involved in any spectroscopic technique triggered by electron beams makes an accurate quantitative analysis difficult. Indeed, the use of standards is severely limited by proper sets of standards being unavailable, while the so-called standard-less quantification methods require accessing fundamental and instrumental parameters [24], which makes their application difficult in practice. We used EDXS in a semi-quantitative mode, because it largely fit our purpose (i.e., spotting the presence of some chemical elements in micropearls and the classification of the organisms producing them). Employing semiquantitative EDXS is common practice in similar samples [25]. Since all measurements have been performed by the same operator, using the same apparatus in the same conditions on similar samples (i.e., similar matrix), instrumental parameters, such as the incident angle of the primary beam, are expected to have a similar effect on all chemical elements measured. Matrix effects have been accounted for by ZAF corrections performed with the ZAF-correction software provided by JEOL.
Light elements (atomic number Z < 11) are not well quantified by EDXS. It is, however, common practice to estimate the percentage composition of light elements from EDXS measurements on the basis of hypotheses made about the chemical identity of the compounds present. Even if this can be done quite confidently for minerals with a known stoichiometry, the method is not trivial for several reasons, namely: (i) the low energy X-rays produced by elements with Z between 4 and 10 (which includes C, N, and O) are prone to strong absorption by the specimen; (ii) electrons involved in producing the characteristic X-rays of these elements are also involved in their chemical bonding and, thus, different compounds may influence the shape or position of peaks; (iii) water and natural organic matter bound in mineral structures are not identified by EDXS and will be included in the analysis without distinction; (iv) C often accumulates as a contaminant on the sample surface in an electron microscope; and (v) k-factors of C are usually not very reliable. When this method is applied to the study of simple, well-defined crystalline carbonates, it is generally more accurate to calculate the quantity of O (and sometimes C) on the base of stoichiometric considerations, rather than to measure it, even if this requires knowledge of the valence of the cations, information which is not provided by EDXS. However, in the case of our samples, it was not even possible to apply such a method because: (i) ACC are amorphous and do not have a constant, well-known stoichiometry; (ii) the identity of the As compounds present in the samples is unknown and, possibly, variable; (iii) ACC are covered by, and may even include, organic matter of unknown composition, but rich in C and O; (iv) the size of the micropearls is often smaller than the surface area covered by the beam, implying that an undefined and variable amount of organic matter (surrounding the micropearl) is simultaneously ‘measured’. For all these reasons, we did not take light elements (C, N, and O) into account for the elemental quantification of the micropearl composition.
During the EDXS measurements, care was taken to avoid the inclusion of parasitic elements whose presence derives from possible adjacency effects linked to the probe collecting counts in a volume (~2 μm3) sometimes larger than micropearls. For instance, the MgAs micropearls (MC5) were often surrounded by diatom debris, which would disqualify Si as a true constituent of the micropearls. Sodium (in MC2) and Al (in MC1) are probably parasitic as well, whereas Na in MC4, given the simultaneous presence of Cl, expresses the saline nature of Lake Titicaca (salinity: 0.8 mg L−1, [26]).
Since the position of the Kα line of Mg (1.253 keV) is very close to the Lα line of As (1.282 keV), the presence of the Kα line of As (10.530 keV) was always verified (see Figure S3 as an example). The total absence of correlation between the measured values of Mg and As was also verified.

4.2. Statistical Methodology

The nature of the dataset used in this study require paying special attention to the applied statistical treatment. In particular, our data are characterized by the presence of rather numerous non-detects or left-censored readings, a common situation in geochemical surveys [20]. Such data should not be merely eliminated, but treated following one of the numerous treatments hitherto applied to left-censored data [17,22,27,28,29]. The various strategies to deal with left-censored or below-detection data have been discussed by Antweiler and Taylor [18], in the perspective of computing summary statistics, which is one of the purposes of the present work. Based on their dataset, these authors found that the nonparametric Kaplan–Meier (NP-KM) was the overall best technique for summary statistics, with regression on order statistics (ROS) being an adequate alternative. In our own dataset, having the same cut-off level (1 mol%) for all the descriptors, NP-KM reduces to a simple substitution by the cut-off value, which would yield strongly biased estimates for all summary statistics (Table 3 in [18]). For comparisons between groups, Antweiler [17] found that instrument-derived data (i.e., our lab data) performed very well relative to other more sophisticated techniques. This is why, essentially, we based our analysis on lab data.
The application of such an approach led to the matrix of descriptors shown in Table 1. Median values, allowing for the non-normal distribution and occasional polymodality of the descriptors, were chosen for the statistical comparison between the morpho-chemical groups. Based on the non-parametric Mann–Whitney U criterion, differences or similarities per descriptor (Table 3) confirmed the initial subdivision of As micropearls into distinct morpho-chemical groups. In particular, all the groups differed significantly in terms of the main constituents, Ca and As.
No R-mode analysis was undertaken. The nature of our data (closure at 100%) would imply the application of compositional data analysis concepts [30,31]. These involve, among others, the imputation of non-detects, a delicate and controversial operation [27,32].

4.3. Arsenic in Micropearls

According to the FIB-SEM-EDXS results for Sr-enriched micropearls, As seems to be present, at least in quantities high enough to be detected by EDXS, in the external part of the micropearls. Arsenic presence, either by sorption or precipitation, on ACC is easy to understand, based on many studies of As interactions with calcite, both in the laboratory [33,34,35,36], geological [37,38], and environmental settings [39,40]. It is, however, not yet possible to explain the difference in As distribution (in external layer) compared with Sr –zoning. It would be tempting to make the hypothesis that As does not form a solid solution with Ca, unlike what was suggested for Ca-Sr and Ca-Ba [41], but this mechanism is controversial for amorphous solids in general [42]. Our observations are, unfortunately, still too limited to allow any sound mechanistic insight in the physico-chemical mechanisms explaining the presence of As in the micropearls.
Low As concentrations and its external-only presence point to As being an incidental addition to the micropearls formed by the previously described organisms (MC1, MC2, and MC3) and by the Lake Titicaca organisms (MC4). Despite the extensive literature on As in algae, only two old studies mention Tetraselmis algae (Tetraselmis chuii, a marine alga) growing in the presence of As [43,44]. These authors found that the algae incorporated As rather efficiently and formed a lipid-soluble organic As compound.
The present study allowed the discovery of a new category of micropearls, where As is often associated with Mg, possibly in a small unicellular bi-flagellated eukaryote. These micropearls had not been described before, probably because they are much less abundant in Lake Geneva than the previously described types. Moreover, they are challenging to detect, due to their small size and the fuzzy limits of the organic envelope, and due to the fact that, unlike Ba- or Sr-micropearls, the relatively low atomic mass of As does not easily allow their location in backscattered SEM images. Even with fixation, the shape and features of the organism are ill preserved. No clear limit is seen in the dried organic patches, which are the remains of the cells after sample desiccation. We can only state that the cells producing such MgAs-micropearls measure between 7–12 µm and are thus part of the nanoplankton in Lake Geneva, following the size-based classification elaborated by Dussart [45]. In addition, these eukaryotic organisms appear to be biflagellates (Figure 5) and are present in the lake water between February and June (Figure 7). Unfortunately, despite our efforts, the data obtained until now do not allow us to confirm the exact nature of this organism. Indeed, although nanoplankton includes phytoplankton, some of the smaller ciliates and heterotrophic flagellates, as well as prokaryotes [46], can also enter this size category.
It is not yet possible to predict the importance of this type of biomineralization at the ecosystem level. In the case of groundwaters, the most studied environmental systems in relation to geogenic As contamination (and a serious environmental health threat), the most widely accepted mechanism of As release to groundwater is the reduction of iron oxyhydroxides containing a large amount of As, under anoxic conditions [47]. However, a poor correlation between the concentrations of As and Fe in As-contaminated groundwater has sometimes been observed [48]. This has led to the study of other mechanisms at play, depending on the biogeochemical conditions of the environment (e.g., As desorption, dissolution of sulfide-As bearing compounds, etc.). In particular, the role of calcite and the formation of solid calcium arsenates [40] have received increasing attention as effective scavengers of As. Arsenic behavior in eutrophic lakes has also mostly been linked to Fe oxyhydroxides cycling [49,50,51], but much less studied. The biomineralization process observed here might draw further attention to the role of Ca in As cycling in surface waters.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/geosciences12010032/s1, Table S1: Sampling campaigns at location GE3 (6.2197° E/ 46.2994° N) in Lake Geneva (Switzerland/France); Table S2: Proportion of non-detects in descriptors and morpho-chemical groups; Table S3: Summary statistics differences between lab and left-censored data (Values of Table 1a minus values of Table 1b); Table S4: Discrepancies between Table 3A (lab) and Table 3B (left-censored); Table S5: Tests on descriptors distribution shape per morpho-chemical group (lab data); Figure S1: Location of the two sampling points in Lake Geneva (Switzerland/France): GE3 and SHL2: Figure S2: Location of the sampling point in Lake Titicaca (Bolivia/Peru); Figure S3: Image of three different types of micropearls present in Lake Geneva; Figure S4: Raw EDXS data for some samples shown in Figure 3 showing the whole energy range measured; Figure S5: Comparison of the composition of Sr-Tetraselmis (MC3) in Lake Geneva and Sr-Titicaca (MC4); Figure S6: Relationship between the size of micropearls and their arsenic concentration; SI_excel_1.xlsx: Databases and statistical results for As-bearing micropearls from Lakes Geneva and Titicaca; SI_excel_2.xlsx: Example of computation of summary statistics with a regression equation on probability scale (ROS technique).

Author Contributions

Conceptualization, A.M., M.F., J.-M.J. and D.A.; methodology, A.M. and J.-M.J.; software, J.-M.J.; validation, A.M., M.F. and J.-M.J.; formal analysis, J.-M.J.; investigation, A.M., M.F., J.-M.J. and M.C.; resources, M.C.; data curation, J.-M.J.; writing---original draft preparation, A.M., M.F. and J.-M.J.; writing---review and editing, M.F., J.-M.J., M.C. and D.A.; visualization, A.M.; supervision, M.F. and D.A.; project administration, M.F. and D.A.; funding acquisition, M.F. and D.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Gerbert Rüf Stiftung (Basel, Switzerland), Project Microbials GRS-071/17 as well as the University of Geneva.

Data Availability Statement

All data are provided in the Supporting Information files.

Acknowledgments

We deeply thank Dario Acha and Stephane Guedron for providing the infrastructure and help needed for sampling in Lake Titicaca, the data and maps of the sampling location, and carefully reading of the manuscript. We thank Pascale Nirel for her help and for insightful discussions. The efficient contribution of the University of Geneva BELS librarians in providing literature references is gratefully acknowledged.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Specimens of the four types of micropearls incorporating As in Lake Geneva. All are secondary-electron SEM images of dried filters except (a1): backscattered SEM image of a dried sample fixed with glutaraldehyde. Micropearls appear white or light grey against the darker organic matter. Elements linked to sample coating were not taken into account in the calculations: Au (a,c) and Pt/Pd (b). Whole spectra of samples are shown in Figure S4. Pores of the filters appear as small black dots. Water samples were taken from Lake Geneva at GE3 location on (a1) 10.07.2018, cumulative sample between 0 and 50 m, (a2) 14.06.2016, 10 m, (b) 06.08.2013, 10 m depth, (c) 19.05.2015, 18 m. d: diatom frustule fragments. OM and yellow dotted lines: unrelated organic matter. Scale bars: 5 µm.
Figure 1. Specimens of the four types of micropearls incorporating As in Lake Geneva. All are secondary-electron SEM images of dried filters except (a1): backscattered SEM image of a dried sample fixed with glutaraldehyde. Micropearls appear white or light grey against the darker organic matter. Elements linked to sample coating were not taken into account in the calculations: Au (a,c) and Pt/Pd (b). Whole spectra of samples are shown in Figure S4. Pores of the filters appear as small black dots. Water samples were taken from Lake Geneva at GE3 location on (a1) 10.07.2018, cumulative sample between 0 and 50 m, (a2) 14.06.2016, 10 m, (b) 06.08.2013, 10 m depth, (c) 19.05.2015, 18 m. d: diatom frustule fragments. OM and yellow dotted lines: unrelated organic matter. Scale bars: 5 µm.
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Figure 2. Micropearls observed in Lake Titicaca (Sr-Titicaca/MC4), compared to Sr-Tetraselmis micropearls of Lake Geneva (MC3). SEM images of dried filters. (a,b,d): Backscattered electron images. (c): Secondary electron image. (a–c): Water sample taken in Lake Titicaca in February 2017, (a,b) Sr-Titicaca micropearls, clustered inside the organic cell which produced them. The SEM-EDXS spectrum illustrates the typical composition of these micropearls. Presence of gold is due to sample coating. (c): Zoom on Sr-Titicaca micropearls, expelled from a cell during filtration. (d): For comparison, Tetraselmis cordiformis cell, from Lake Geneva, with its Sr-rich micropearls (MC3). Sampled at the GE3 location (6.08.2013, 20 m depth). The larger and slightly darker inclusions are polyphosphate inclusions (p), which are sometimes present in these unicellular algae. The small black dots in the background are the pores of the filter. d: diatom. s: silica. Thick scale bar: 1 µm. Thin scale bar: 5 µm.
Figure 2. Micropearls observed in Lake Titicaca (Sr-Titicaca/MC4), compared to Sr-Tetraselmis micropearls of Lake Geneva (MC3). SEM images of dried filters. (a,b,d): Backscattered electron images. (c): Secondary electron image. (a–c): Water sample taken in Lake Titicaca in February 2017, (a,b) Sr-Titicaca micropearls, clustered inside the organic cell which produced them. The SEM-EDXS spectrum illustrates the typical composition of these micropearls. Presence of gold is due to sample coating. (c): Zoom on Sr-Titicaca micropearls, expelled from a cell during filtration. (d): For comparison, Tetraselmis cordiformis cell, from Lake Geneva, with its Sr-rich micropearls (MC3). Sampled at the GE3 location (6.08.2013, 20 m depth). The larger and slightly darker inclusions are polyphosphate inclusions (p), which are sometimes present in these unicellular algae. The small black dots in the background are the pores of the filter. d: diatom. s: silica. Thick scale bar: 1 µm. Thin scale bar: 5 µm.
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Figure 3. Procedure for the definition of five morpho-chemical groups among the As-bearing micropearls in Lakes Geneva and Titicaca.
Figure 3. Procedure for the definition of five morpho-chemical groups among the As-bearing micropearls in Lakes Geneva and Titicaca.
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Figure 4. Mg-Ca-As, Mg-Ba-As, and Sr-Ba-As ternary representation of micropearls containing As and their morpho-chemical groups.
Figure 4. Mg-Ca-As, Mg-Ba-As, and Sr-Ba-As ternary representation of micropearls containing As and their morpho-chemical groups.
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Figure 5. Morphology of the organic matter surrounding the MgAs micropearls (MC5). Secondary-electron SEM image of a dried filter. Sample (a) was filtered and dried, while sample (a1) shows the raw image and (a2) shows an approximate delimitation of the dried cell in which the micropearls were formed; (b) was fixed with alkaline lugol before filtration; therefore, the organism is better preserved, allowing the observation of two flagella (detail shown on image (b2)). Pores of the filter (0.2 µm) appear as small black dots. Water samples taken in Lake Geneva at (a) SHL2 location, 10 m depth, 11.05.2015, (b) GE3 location, 10 m depth, 21.04.2016. d: diatom. Scale bar: 5 µm.
Figure 5. Morphology of the organic matter surrounding the MgAs micropearls (MC5). Secondary-electron SEM image of a dried filter. Sample (a) was filtered and dried, while sample (a1) shows the raw image and (a2) shows an approximate delimitation of the dried cell in which the micropearls were formed; (b) was fixed with alkaline lugol before filtration; therefore, the organism is better preserved, allowing the observation of two flagella (detail shown on image (b2)). Pores of the filter (0.2 µm) appear as small black dots. Water samples taken in Lake Geneva at (a) SHL2 location, 10 m depth, 11.05.2015, (b) GE3 location, 10 m depth, 21.04.2016. d: diatom. Scale bar: 5 µm.
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Figure 6. STEM-HAADF images and EDXS maps from FIB-cuts of a Sr-Tetraselmis micropearl (MC3) sample showing the location of As. The water sample was taken on 10.07.2012, at 6-m depth. Arsenic is concentrated in the external layers of the micropearls. Note that the Pt protection layer on top of the samples (from FIB preparation) also produces an X-ray line at the energy window used for As, causing it to be included in the As mapping. The position of the FIB-cut is marked by a red line in the inset SEM image.
Figure 6. STEM-HAADF images and EDXS maps from FIB-cuts of a Sr-Tetraselmis micropearl (MC3) sample showing the location of As. The water sample was taken on 10.07.2012, at 6-m depth. Arsenic is concentrated in the external layers of the micropearls. Note that the Pt protection layer on top of the samples (from FIB preparation) also produces an X-ray line at the energy window used for As, causing it to be included in the As mapping. The position of the FIB-cut is marked by a red line in the inset SEM image.
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Figure 7. Estimation of the monthly abundance of MgAs micropearls (MC5) in Lake Geneva. Organisms forming this type of micropearls are observed between February and July.
Figure 7. Estimation of the monthly abundance of MgAs micropearls (MC5) in Lake Geneva. Organisms forming this type of micropearls are observed between February and July.
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Table
Table 1. Lab data: descriptive statistics of characteristic elements in the five morpho-chemical groups of As-containing micropearls in Lake Geneva (MC1, MC2, MC3 and MC5) and Lake Titicaca (MC4). Ns: number of samples. Nv: number of descriptors. SD: standard deviation. Grey: not taken into consideration because of a proportion of zero values >0.6. P and S eliminated because they exceed this criterion in all groups.
Table 1. Lab data: descriptive statistics of characteristic elements in the five morpho-chemical groups of As-containing micropearls in Lake Geneva (MC1, MC2, MC3 and MC5) and Lake Titicaca (MC4). Ns: number of samples. Nv: number of descriptors. SD: standard deviation. Grey: not taken into consideration because of a proportion of zero values >0.6. P and S eliminated because they exceed this criterion in all groups.
Morpho GrNsNvStatNaMgAlSiPSClKCaAsSrBa
MC1166Mean 0.60.9 58.31.51.837.0
Big Ba SD 0.71.2 7.00.41.26.6
Median 0.30.6 58.51.31.837.4
MC2506Mean0.710.1 3.0 16.05.41.163.8
Small Ba SD1.01.5 3.6 3.63.91.04.9
Median0.19.9 0.0 15.94.61.264.5
MC3705Mean 0.5 1.290.32.65.4
Sr-Tetraselmis SD 0.6 0.93.52.33.3
Median 0.3 1.290.81.95.1
MC4347Mean5.91.3 8.51.366.111.15.8
Sr-Titicaca SD6.81.9 6.71.313.83.93.8
Median4.10.4 6.41.269.311.45.9
MC5974Mean 4.8 2.1 84.78.4
MgAs SD 3.7 3.9 6.15.8
Median 5.3 0.4 85.27.4
Table
Table 2. Left-censored data: descriptive statistics of characteristic elements in the five morpho-chemical groups of As-containing micropearls in Lake Geneva (MC1, MC2, MC3, and MC5) and Lake Titicaca (MC4). Ns: number of samples. Nv: number of descriptors. SD: standard deviation. Green: ROS-treated. White: lab values (always above detection limit). Grey: not taken into consideration because of a proportion of zero values exceeding 0.7. P and S eliminated because they exceed this criterion in all groups.
Table 2. Left-censored data: descriptive statistics of characteristic elements in the five morpho-chemical groups of As-containing micropearls in Lake Geneva (MC1, MC2, MC3, and MC5) and Lake Titicaca (MC4). Ns: number of samples. Nv: number of descriptors. SD: standard deviation. Green: ROS-treated. White: lab values (always above detection limit). Grey: not taken into consideration because of a proportion of zero values exceeding 0.7. P and S eliminated because they exceed this criterion in all groups.
Morpho GrNsNvStatNaMgAlSiPSClKCaAsSrBa
MC1165Mean 0.8 57.41.41.936.3
Big Ba SD 1.2 7.50.41.16.4
Median 0.3 57.31.31.736.4
MC2506Mean 9.9 4.1 15.75.31.362.6
Small Ba SD 1.5 2.8 3.73.90.84.6
Median 9.8 3.0 15.04.41.263.6
MC3704Mean 1.386.72.55.3
Sr-Tetraselmis SD 0.65.62.33.1
Median 1.288.31.84.9
MC4347Mean5.91.7 8.51.465.811.15.7
Sr-Titicaca SD6.71.6 6.61.113.83.93.6
Median4.11.2 6.41.269.311.45.9
MC5974Mean 5.3 2.3 82.58.2
MgAs SD 2.8 3.7 6.45.7
Median 5.1 0.9 82.87.3
Table
Table 3. Differences (D, pink) or similarity (S, green) in the descriptors medians between morpho-chemical groups, based on Mann–Witney U criterion (p ≥ 0.05). propDv: proportion of differences per descriptor. propDg: proportion of differences per morpho-chemical group. (a): Lab data. (b): left-censored data. Grey: not taken into consideration.
Table 3. Differences (D, pink) or similarity (S, green) in the descriptors medians between morpho-chemical groups, based on Mann–Witney U criterion (p ≥ 0.05). propDv: proportion of differences per descriptor. propDg: proportion of differences per morpho-chemical group. (a): Lab data. (b): left-censored data. Grey: not taken into consideration.
(a) Lab Data(b) Left-Censored Data
MC1MC2MC3MC4MC5PropDv MC1MC2MC3MC4MC5PropDv
NaMC1 1NaMC1
MC2 D MC2
MC3 MC3
MC4 D MC4 X
MC5 MC5
MgMC1 DSSD0.7MgMC1 1
MC2D DDD MC2 DD
MC3SD SD MC3
MC4SDS D MC4 D D
MC5DDDD MC5 D D
AlMC1X AlMC1
MC2 MC2
MC3 MC3
MC4 MC4
MC5 MC5
SiMC1 SiMC1
MC2 MC2
MC3 MC3
MC4 MC4
MC5 X MC5 X
ClMC1 1ClMC1 1
MC2 D MC2 D
MC3 MC3
MC4 D MC4 D
MC5 MC5
KMC1 0KMC1 1
MC2 MC2
MC3 S MC3 S
MC4 S MC4 S
MC5 MC5
CaMC1 DDDD1CaMC1 DDDD1
MC2D DDD MC2D DDD
MC3DD DD MC3DD DD
MC4DDD D MC4DDD D
MC5DDDD MC5DDDD
AsMC1 DDDD1AsMC1 DDDD1
MC2D DDD MC2D DDD
MC3DD DD MC3DD DD
MC4DDD D MC4DDD D
MC5DDDD MC5DDDD
SrMC1 DDD 0.8SrMC1 DDD 0.8
MC2D DD MC2D DD
MC3DD S MC3DD S
MC4DDS MC4DDS
MC5 MC5
BaMC1 D 1BaMC1 D 1
MC2D MC2D
MC3 MC3
MC4 MC4
MC5 MC5
PropDg0.910.80.81 PropDg110.80.91
nD1418121412 nD1215101310
nS20440 nS00220
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Martignier, A.; Filella, M.; Jaquet, J.-M.; Coster, M.; Ariztegui, D. First Observation of Unicellular Organisms Concentrating Arsenic in ACC Intracellular Inclusions in Lake Waters. Geosciences 2022, 12, 32. https://doi.org/10.3390/geosciences12010032

AMA Style

Martignier A, Filella M, Jaquet J-M, Coster M, Ariztegui D. First Observation of Unicellular Organisms Concentrating Arsenic in ACC Intracellular Inclusions in Lake Waters. Geosciences. 2022; 12(1):32. https://doi.org/10.3390/geosciences12010032

Chicago/Turabian Style

Martignier, Agathe, Montserrat Filella, Jean-Michel Jaquet, Mathieu Coster, and Daniel Ariztegui. 2022. "First Observation of Unicellular Organisms Concentrating Arsenic in ACC Intracellular Inclusions in Lake Waters" Geosciences 12, no. 1: 32. https://doi.org/10.3390/geosciences12010032

APA Style

Martignier, A., Filella, M., Jaquet, J. -M., Coster, M., & Ariztegui, D. (2022). First Observation of Unicellular Organisms Concentrating Arsenic in ACC Intracellular Inclusions in Lake Waters. Geosciences, 12(1), 32. https://doi.org/10.3390/geosciences12010032

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