Research Article  Open Access
M. A. Murado, M. A. Prieto, "Oversimplification and Overstandardization in Biological Methods: Sperm Bioassays in Ecotoxicology as a Case of Study and a Proposal for Their Reformulation", The Scientific World Journal, vol. 2014, Article ID 936202, 13 pages, 2014. https://doi.org/10.1155/2014/936202
Oversimplification and Overstandardization in Biological Methods: Sperm Bioassays in Ecotoxicology as a Case of Study and a Proposal for Their Reformulation
Abstract
An interesting toxicological bioassay (fertilization inhibition in sea urchin) uses as assessment criterion a variable (fertilization ratio) whose variation with time creates two types of difficulties. First, it fails to distinguish between the toxic effect and the spontaneous decline in the sperm activity, causing some inconsistencies. Second, the sensitivity of the fertilization ratio to many other variables of the system requires a complex standardization, constraining the achievement of the method without solving its main problem. Our proposal consists of using a parameter (sperm halflife) as the response of the assay, and describing explicitly the behavior of the system as a simultaneous function of dose and time. This new focus is able to solve the problematic character of the results based on the fertilization ratio and by using the same data set which is required by the conventional approach; it simplifies the protocol, economizes experimental effort, provides unambiguous and robust results, and contributes to the detection of an artefactual temperature effect, which is not very evident under the usual perspective. Potential application of this new approach to the improvement of other formally similar bioassays is finally suggested.
1. Introduction
In the study of biological systems, at times a defined gap exists between the recognition of the complexity, which should be accepted for describing certain phenomena in a reasonably realistic way, and the oversimplifications often applied to basic problems, frequently involving important practical consequences. Usually such gaps are not justified by differences between the levels of study, since a simpler approach from a factual point of view does not involve necessarily simpler formal tools. The more common reasons argued in this regard are related to the supposed usefulness of routines which can be solved in practically automatic ways to favour their reproducibility. However, this advantage disappears when—as it is very usual—the routine leads to the need of standardizing many variables or when—as it occurs occasionally as well—its original purpose is distorted.
Under this perspective, we will discuss and propose new focus for a useful bioassay which is based on the drop of the fertilizing success of free spawners in the presence of a toxic agent and is applied since years ago in the ecotoxicological field. This method, with interesting capabilities, was initially designed for sea urchin, in which the immediate formation of the fertilizing membrane around the egg makes the detection of the products of the process easy. Afterwards, the procedure has been applied to other organisms, such as the coral Acropora millepora [1] or the polychaete Hydroides elegans [2], and it is quite clear that the essence of the bioassay—and its problems as well—can be generalized to very different situations from the original one.
2. Theoretical Background and Methods
2.1. The Conventional Approach
The current procedure, with precedents since almost one century ago [3], is a synthesis of those that were developed by Dinnel et al. [4–6] and Pagano et al. [7–9], and it is recommended at present by environmental agencies [10]. The bioassay involves the exposure of a sperm suspension to increasing levels of a toxic agent, during increasing times, followed by the addition of an egg suspension to the treated sperm [11, 12]. After the time required to reach the asymptotic maximum of the fertilization ratio in the absence of the agent (control), the products of the process are fixed with formalin and counted. Subsequently, the toxic effect of the increasing doses of the agent over the fertilization ratio is assessed through any doseresponse (DR) model.
Thus, if and are the fertilization ratios in the absence of toxic (control) and at the toxic concentration (dose) , respectively, the response, quantified as , can be described with the Weibull doseresponse model, as an example, which is an especially versatile DR model [13–16]. Using this equation in a reparametrized form [17–19], which makes it appropriate in this context, we can write where is the asymptotic maximum of , the dose, the dose corresponding to halfmaximum response ( if ), and a shape parameter that defines (together with and ) the maximum slope of the function.
It should be underlined that this assay solves elegantly several key issues of the DR analysis: (a) it works with a large population, a condition that is difficult to satisfy if the target species is not a microorganism; (b) it deals with an ontogenically essential and physiologically sensitive process; (c) it is a fast test, avoiding the changes in the physicalchemical system [5] or in the biotic sensitivity [20] which are possible in longer assays, such as those that are focused on larval growth inhibitions. Short times are specially interesting in the assessment of lipophilic toxics, whose micelles can coalesce during the course of static assays lasting a number of hours, causing uncertainty regarding the real dose in the immediate environment of the organism.
However, the direct use of the drop in the fertilization ratio as response pays a steep price in practical complications and ambiguity of the results, both because of the characteristics of the system and the structure of its formal treatment.
2.1.1. Exigencies of the Biologic System
Some necessary cautions in this regard are of a common kind in many analytical methods. This is the case, for example, of the effects of state variables as temperature and composition (essentially pH and salinity) or the need to use glass material [5]. A fact that has also correlates in other methods is the requirement, for maximizing the sensitivity, of a fertilization ratio for the control close to 1, but less than 1, to avoid as much as possible hiding the toxic effect by a possible excess of sperm. However, in a more specific and obstructive way, the assay is affected by particular variables, such as: the absolute and relative gamete concentrations; the contact time; the sperm age; the dilution of the system accelerates the consumption of its limited energy reserve, probably due to an increase of respiration, and therefore shorts out its life span. The control of these last factors is difficult, because the existence of interactions among them [21] prevents the individualized selection of appropriate values. In fact, standardization is a customary claim in the bibliography regarding this method [22–24], and other authors [25] even have argued the need to use more than one gamete ratio to take into account the reproductive failure due to polyspermy.
2.1.2. Implications of the Descriptive Approach
Under this point of view, the method shows the following problematic aspects.(1)Although it is recognized that the exposure time to toxic agent affects the fertilization ratio [5], this variable is not formally included into univariate DR models as (1). Therefore, since each time leads to a different assessment, the decision about which is more representative is arbitrary.(2)The short life span of the gametes makes feasible a more realistic assay, in which the exposure time cover as their entire life period, as it occurs in natural conditions. The use of briefer exposure times can only contribute to increase the error and underestimate the toxic effect.(3)If the sum of the exposure and contact times does not exceed the sperm life span, it could happen (assuming that the toxic action reduces the sperm activity) that, at the end point, the fertilization processes are, under different doses, at different distances from their respective maxima, making any comparison questionable.(4)The values of the fertilization ratio contain information regarding the effects of the toxic action and the sperm age, but the formal treatment ignores the second one. Thus, the variability linked to both effects is accumulated only over the toxic action, causing two undesirable consequences: the inaccuracy of the result and the bias of the parametric estimates.(5)Finally, as we will see in the results section, temperature exerts an inevitable and purely artefactual effect—that is apart from the one ruled by the Arrhenius equation—in any assessment through the conventional method.
2.2. Factual Frame of the Assay: Fertilization Kinetics
In the reproductive phenomenology of the sea urchin, rich in studies, the most of its quantitative behavior, both in experimental [21] and observational [26] contexts, is explained by a fertilization kinetic model which Vogel et al. [27] called—a curious tribute to Mozart—Don Ottavio. This model assumes that the random encounter between gametes follows a second order kinetics, in which the egg retains a certain number of spermatozoa, irrespective of the fertilizing character of the event. Thus, the fertilization ratio , and being the initial concentrations of gametes, can be described as where the kinetic constants and (mm^{3}·s^{−1}: required volume for a fertilizing rate of one egg per second) are the product of the sperm speed by the total (in ) or effective (in ) egg section.
Several authors [25, 26, 28] have pointed out that this model does not take into account the fertility failures due to polyspermy induced by high ratios, which produce no asymptotic curves, but with a drop after a maximum. However, this problem is outside the strict kinetic process, and therefore (2) can provide a useful perspective for guiding the assay considered here.
If the idea is to base the evaluation on parametric variations, a first option (not very feasible, but that needs to be discussed) would be to use the parameters and of (2), both dependent on the sperm activity, which is the sensitive variable of the system. As illustrated in Figure 1, the fertilization rate and the asymptotic value of decrease if does it, and the asymptotic value decreases if increases. Thus, at a given ratio, the kinetic data at different doses of a toxic agent would able to assess the toxic effect on both parameters.
(a)
(b)
(c)
This approach could be simplified by taking into account that at the high ratios which are used in practice, the process can be considered as following a pseudofirst order kinetics. In fact, all profiles of Figure 1 could be adjusted with a high accuracy () to the model: where the parameters and , both potentially sensitive to the toxic effect, are the asymptotic maximum of and the maximum specific rate of fertilization, respectively.
However, the use of either of these parametric pairs (both , and , ) has several disadvantages. One is the sensitivity of the required data, measured in a relatively short time interval, to the experimental error. Another one is the dependence of the parametric values on the ratio (Figure 2, which also shows that the effect of the overall gamete population becomes less relevant as the contact time increases). Finally, the variations of each parametric pair are in general strongly correlated. Therefore, solving separately the kinetic and DR models would be a requirement, which would result in losing the advantages of a simultaneous solution as it will be proposed next, making use of another aspect of the work of Vogel et al. [27].
(a)
(b)
(c)
2.3. An Alternative Proposal
The main issue of the bioassay here studied is the fact that the sperm activity declines simultaneously with age and the toxic action, within the same timeframe and following in both cases a sigmoidal profile. Our proposal consists of accepting this dualism and submitting it to a model able to describe simultaneously, but in a distinctive way, both phenomena. It requires defining the response not as a function of the fertilization ratio , which varies with time, but as a function of a time parameter, such as the sperm halflife .
The sperm life span—and therefore its halflife—is determined through the drop of the fertilization ratio with time, which Vogel et al. [27] described with the normal mass function. As this function lacks in the explicit algebraic form that is required for our purpose, we will use the Weibull mass function, that is, (1), now in its decreasing form: where is the initial maximum of , is time, is the halflife, and is the shape parameter. It should be noted that varies between a maximum value at age zero (independent of the toxic agent, because it implies a null exposure time) and a null value when the sperm exhausts its life span (at a dosedependent time). Thus, it can be considered that , and then expression (4) is reduced to When this equation was applied to the data from [27], the resulting value of minutes was in good agreement (Figure 3(a)) with the result obtained by these authors using the normal distribution ( minutes).
(a) Data from Vogel et al. [27]
(b) Relationships between the maxima of and the spermatic lifespan
Now, if decreases from a value in the absence of toxic to a value in the presence of a given dose of the studied toxic, the response can be formulated as where is (1). Thus, the bivariate model should provide an unambiguous evaluation of the toxic effect on the sperm halflife.
Since is determined from the maximum value of at different sperm ages, from now on a distinction should be made between two maxima of with different meaning (Figure 3(b)). is the asymptotic maximum of , obtained after enough contact time () at any working conditions, for example, at different sperm ages. is the initial maximum value corresponding to at the age which is considered as zero.
2.4. Experimental Procedure and Standardization Needs
The experimental protocol should observe the same cautions as the conventional one regarding the manipulation of the gamete suspensions, and it differs very little from this last one regarding its execution. In the beginning of the test, the following materials—volumes are only indicative—should be prepared: (i) a suspension of sperm and another one of eggs at the appropriate concentrations (see below) for the assay; (ii) series of tubes each: doses of the toxic agent in 9.5 mL of seawater and one control. Under these conditions, the bioassay involves the following:(1)at time zero, to add 100 μL of the sperm suspension to all tubes;(2)at increasing times (including zero), covering the entire sperm life span estimated for control, to initiate fertilization in the corresponding series by adding 400 μL of the egg suspension;(3)after a sufficient contact time to reach, in each series, the asymptotic value in control to fix the products of the process by adding 100 μL of formalin solution.
The use of the parameter , instead of the variable , as the basis of the assessment offers here another important advantage. Indeed, is a sensitive value to the initial gamete ratio () and, in fact, in assays based on the variation of , Dinnel et al. [5] stated that the sensitivity to the toxic agent is inversely correlated with ratio. However, if, within a wide range of values (with constant ), at age zero (i.e., ) is coded as 1, in all cases the same value of is obtained, which makes this criterion very robust against variations of ratio.
In fact, the only particular variable of the system that affects the sperm halflife is the sperm dilution, due to its role in the oxygen availability, as described by Levitan et al. [21]. Thus, the only condition that determines the appropriate ratio is the need to avoid a sperm excess that could hide the toxic effect. This is achieved if , what does not prevent to code this value as 1. Dinnel et al. [5] used values in the reasonable range , but it should be noted that the closer is to 1, the clearer results are obtained.
Clarity makes equally advisable low working temperatures, which extend the sperm halflife and provide a “space” (see Figure 4(B2)) for life spans that are shortened by the toxic action. Later on, another important implication of the temperature will be discussed.
The test is also consistent against objections about the possible effects of polyspermy [25, 26, 28], because the sperm halflife is not related to subsequent fertilization failures or larval malformations (relevant in larval assays) which can derive from a multifertilized egg.
2.5. Numerical Methods for Comparing the Two Approaches
A comparison between the described alternatives through a reasonable experimental effort would lack statistical reliability. Another solution is to use simulation experiments with realistic values, including error. As we shall see later, such a solution is especially appropriate in the present case.
Simulations were carried out by assigning concrete parametric values to model (7) to generate, in a Microsoft Excel spreadsheet, virtual assays with 8 doses at 7 times, including zero in both cases. An ad hoc macro was written to execute series of 2,000 virtual assays, each of them involving the following operations: (1) addition of a normal homoscedastic error to the modelgenerated values of ; (2) fitting of the result to models (1) and (7) to estimate their parameters by nonlinear least squares (quasiNewton), through the Solver complement included into Microsoft Excel; (3) calculation of the parametric confidence intervals (Student’s test, with ) by applying Solver Aid macro [29].
To facilitate comparisons, doses, times, and fertilization ratios were coded into the interval [0; 1]. Since the response is sigmoidal both as a function of dose and time, the values of both variables were established according to a geometric progression with a ratio , where is the first nonnull term of the series and the number of terms, including zero. The experimental error was simulated with random normal numbers as described previously [30], by using the following expression: where and are two random uniform numbers as provided by the spreadsheet. The values routinely assigned to were 0.05(0.025)0.15 and, for some cases, was reached (i.e., from 5 to 25% of the maximum value of the dependent variable ). Also for clarity, we have used the notation CI for the confidence semiinterval as % of the parametric value. Thus, in the usual expression , estimate is statistically significant only when .
Since fittings were carried out with in the Student’s test, a virtual series is considered statistically significant (95%) when 100% of the 2,000 repetitions are significant. Now, the parametric CI can be calculated according to two criteria: (1) averaging the CI resulting from the 2,000 repetitions; (2) calculating them on the basis of the 2,000 parametric estimates. Although both criteria differ very little, the second one is slightly more concessive, and it was not applied. Skewness and kurtosis coefficients of the parametric distributions were calculated using all estimates, significant or not. Although they are informative values, it should be kept in mind that their basis on the moments of third and fourth order tends to exaggerate the effect of the more deviant estimates from mean.
3. Results and Discussion
Conventional (M0) and alternative (M1) methods use the same data sets: fertilization ratios at a toxic concentration and a time . However, the different formal frames in which they are processed make the nature of the respective results different.
In M0, DR model (1) is individually applied, at each time, to a response defined as , that is, as the decrease—increasing with the dose—of the fertilization ratio at a given time. In M1, model (7) is directly applied to the whole of the values, and the response, increasing with the dose as well, is the decrease of the sperm halflife. As far as here, we have used the same parametric notation in DR model (1) and in the DR part (second equation) of model (7). From now on, if necessary, we will distinguish between both meanings by using the subscripts and .
The fact that M0 and M1 use the same observational values within different conceptual frames has an important consequence for the validation (or refutation) of M1, since this approach is under the obligation to explain the results from M0, as well. If it is so, the abundant experimental results which have led to accept M0 become an experimental validation of M1. And in such a case, the selection of one or another approach is reduced to compare the logical consistence of their conclusions as well as the statistical reliability of results that are affected by the same error in the dependent variable ().
3.1. Relationships between the Conventional and Alternative Assays
Firstly, to clarify the ideal relationships between the two descriptions, both were applied to a set of simulations carried out by assigning the parametric values specified in Table 1 to model (7), supposing an assay without replicates with a negligible, but nonnull, error (), to allow the running of the statistical tests.

Results (Table 1 and Figure 4) showed that the assessments derived from the M0 approach are exactly as those described in bibliography. Dinnel et al. [5], for example, working with silver nitrate as a toxic agent, specified that the “fertilization success was inversely related to sperm exposure time” and, indeed, the decrease with time of the values of could be described with a hyperbolic equation (Figure 4(U2)). Such a description, however, is not very interesting, since the notion of is meaningless both at zero time and at times beyond the sperm life span, preventing the existence of useful reference points.
Since a simulation with model (7) produces, through model (1), the typical results of the M0 approach, the descriptive capability above required for accepting M1 is proven. Thus, it can be stated that a response which increases with time in terms of the drop in arises as a consequence of a toxic action which reduces the sperm halflife. But in such a case, the assessment should be based on the variation of the halflife parameter, because the use as response to the drop at a given time necessarily leads to a result in which the effects of the toxic action and the sperm age are confused.
This fact is illustrated in Figure 4(B3), which represents the response to the toxic agent defined as —that is, in the appropriate form for model (1)—in the bivariate frame of model (7). In these conditions, if intercept is subtracted to each curve, the fittings to model (1) produce the same values as those obtained using the responses defined with respect to the control at each time, according to the M0 approach. But this perspective makes evident that the fall of the fertilizing capability due to the toxic action begins, at each time, at a different level, determined by the remaining capability of the sperm at this age. Despite the low value of used, the CI of the parametric estimates obtained with (1) were 10–100 times higher than those produced by (7). The degrees of freedom involved in one and another model justify to a large extent this difference, which to a minor extent is due to the fact that none DR model by itself can explain satisfactorily the behavior of this system. Later, we will see other consequences of the M0 approach.
3.2. Effects of the Experimental Error
The same simulations were now performed using five different levels of experimental error [], under the four conditions resulting from combining single or duplicate observations with raw or smoothed (moving average, window = 3) data.
As expected in the light of the preceding results, model (1) was appreciably more error sensitive. In assays without replicates, the proportion of repetitions with all significant estimates did not reach 100% at any of the times considered, even with the lowest error (). With two replicates, or smoothing without replicates, 100% of significant estimates were reached at the times and . By combining two replicates with smoothing, also 100% was found at . With , the model was only significant at , , and—with pronounced skewness and kurtosis—, when, besides two replicates and smoothing, the concessive criterion described in the numerical methods section was applied to the CI calculation.
Model (7) produced, instead, satisfactory fittings in the twenty cases (Figure 5, top). The most errorsensitive parameters were those linked to slopes ( and ), , , and being remarkably robust. In the studied range of , the CI increase of the parametric estimates was only slightly deviated from linearity at the two higher errors in assays without replicates, where the frequency of statistically significant estimates decreased to 99.8 and 99.3%. Otherwise, all the estimates were significant at 100% of the 2,000 repetitions. The use of two replicates reduced markedly the CI (minimal reduction was 27% in and maximal 52% in ), increasing at 100% the frequency of the significant estimates of with the highest error. Smoothing along the variable produced equivalent results and, when it was applied with two replicates, the CI reductions varied between 31% and 66% , all the estimates being significant in 100% of repetitions even if .
Figure 6 and Table 2 illustrate the advantages of the M1 approach supposing a single assay with , two replicates, and no smoothing. Another comparison, using the same error and selecting for M0 the time with the best fit, is that referring to the distributions of the parametric estimates, supposing 2,000 repetitions, two replicates, and smoothing (Figure 7). Even so, M0 produced strongly biased and platykurtic distributions, very problematic in practice.

3.3. Smoothing
The moving average method is recommended by some authors [24] to determinate accurately the ED_{50} and, indeed, it reduces the effect of the experimental error, giving statistical significance to estimates which would not have it by using raw data. The drawback is the bias that this method produces in some parametric estimates. In a Weibull function without error, the usual smoothing (window = 3) causes bias only on the parameter , reducing slightly the slope (an effect that is accentuated by higher order windows). In the presence of error, the situation becomes more complex, since smoothing tends to correct the slope increase, statistically associated with the homoscedastic error, but it is easy to realize that it can also lead to overestimate the asymptote, if it is not properly defined by the experimental data (this problem is usually corrected by including the restriction in the fitting algorithm, although at the risk of biasing the parameters and ).
A bivariate model as (7) admits smoothing along either of its two variables, or even both. The above described results were obtained by smoothing along the dose and, as shows the top part of Figure 5, the drawback was an admissible underestimation of the parameters and . Smoothing along the time was less satisfactory for two reasons: the moving average method involved less values and a decreasing sigmoid—first equation of model (7)—proved to be more sensitive than an increasing one to the homoscedastic error (we ignore the cause of this fact, but it was repeatedly confirmed in series of 2,000 runs, with symmetrical curves or not). In any case, this treatment produced a strong bias in the parameter (1.98 instead of 2.50), and weaker in .
When smoothing was applied along both variables (Figure 5, down), the result showed a strong bias in (the least important parameter of the system), but in return it produced, even with , unbiased estimates for the rest of the parameters; all of them (including ) are significant in 100% of the repetitions. This means that all toxicological parameters, as well as the sperm halflife, can be estimated with a reasonable accuracy, even when the standard deviation of the observations reaches 25% of their maximum value.
3.4. Error and Experimental Effort
It is pertinent to note that the conditions imposed to the described simulations were stricter than the real ones. In practice, the fertilization ratio at time zero is a unique value of the system, independent of the dose and coded as 1. Thus, no initial value can be greater than 1 and, after a certain time, especially in the presence of toxic, values are in practice much less probable than those due to a random normal—with mean equal to 0–number generator. Moreover, although a value —producing a negative response —is possible, a value is not. In Figures 6(B1) and 6(B2), it can be seen that a part of the accepted error corresponds to such cases ( and ). If simulation includes a condition converting these values into 0 and 1, respectively, the CI produced by model (7), without replicates or smoothing, are reduced 16–20% (the gain is lower in model (1)). This condition, although may be more realistic, was not used.
On the other hand, experimental evidence suggests that the real error in this assay is rather heteroscedastic and stronger in middle than in extreme observational values. Irrespective of using ordinary or weighted least squares as regression method, this condition produces less drastic deviations than those derived from the homoscedastic error applied here.
In any case, to achieve the precision obtained with model (7) without replicates, using model (1)—now ignoring its problematic interpretation—would require at least 45 replicates. Thus, a usual assay in the M0 approach, with 8 doses and 4 times, would need at least 128 experimental units. In the M1 approach, units would produce at least an equivalent precision and more information, and even the use of two replicates (112 units) would be more economic, with a much higher precision. Moreover, one additional dose improves CI in both approaches, but one additional time only does it in the case of M1, since in M0 it means merely to obtain a new and different DR profile. Finally, the simpler protocol required by the M1 approach minimizes the operative inaccuracies potentially affecting the independent variables.
4. Discussion
As a consequence of the drift with time produced by the M0 approach in a toxicological assessment, the values underestimate the toxic potency (regarding in M1) at short times and overestimate it at longer times. The opposite occurs in the maximum response regarding . The statistically most acceptable fittings are found in general at central times, but even so, the variations in the toxicological parameters are too wide; the best fit is not necessarily the most representative one and there is not a criterion to define a priori the most appropriate time.
On the other hand, if the DR curves resulting from the two approaches are compared, it can be stated that M0 tends to underestimate the effects of low doses even when at high times (Figure 6(U and B)). Although extremely arguable, two indexes very cited in the ecolegal field [31] are NOEC and LOEC (no observed and lowest observed effect concentration, resp.). Both are obtained by variance analysis, define essentially the limitations of this analysis as a method of toxicological assessment, and are definitely tending to underestimate any toxic effect. This will be underestimated a fortiori, if NOEC and LOEC are based on the M0 approach.
Even more controversial is the fact that the results of the M0 approach depend on the sperm halflife in the assay conditions (in fact, halflife should be included among the standardization needs for M0). Since temperature shortens , its effect (canceled in M1 by using halflife variations) takes part in M0 through the effect of on the fertilization ratio, on which the assessment is based (Figure 8). This creates an inevitable and artifactual underestimation of the toxicity at low temperatures, beyond the result of a slower metabolism, and a complementary overestimation at high temperatures. Since bioassays are usually carried out at temperatures close to those characterizing the habitat of the wild animal, the application of M0 will involve a higher legislative tolerance in cold than in warm seas.
5. Conclusions
The bioassay studied here is of a special elegance and applicability, which are lost to a great extent because of the use of the fertilization ratio as evaluation criterion. The essence of this issue is the fact that, in a dynamic system, any perturbation cannot be properly characterized through isolate values of any nonlinearintime variable but through the variation of some parameter of a model including time in its structure. This conflict, not too rare in physiological contexts, is similar, for example, to that one that arises when a toxic effect on a microbial or cellular batch culture is assessed by using a variable as biomass or some primary metabolite, instead of some parameter of some growth equation.
When this characteristic of the target system is not taken into account, the difficulty to obtain reproducible results often leads to an accumulation of procedural restrictions which only overstandardize the protocol, obstructing its execution without solving the main problem. We believe that sperm bioassays are currently in this condition, despite the existence of very rigorous results about the fertilization kinetics and the factors affecting it, which provide the key to reformulate the toxicological focus in the form proposed here.
Focusing the bioassay on a parameter (the sperm half life) is necessary, first of all, if we want a toxicological assessment with a unique solution and a clear interpretation. It is also more realistic, since the exposure of the gametes to the toxic during only a fraction of their life span has little to do with what occurs in natural conditions. Finally, the procedure is conceptually more direct, experimentally simpler, and more robust against the observational error and variations in the particular variables of the system, and it removes the artifactual effect of temperature.
Using a bivariate model can seem a disadvantage regarding other apparent simpler routines. In this case, however, the current informative means make its application trivial, while the apparently simpler solution requires a more embarrassing protocol and produces more problematic results. DeLean et al. [32] underlined time ago, in a similar context to this, the advisability of “…analyzing all of the curves simultaneously, forcing them to share certain parameters in common.” In agreement with this opinion, we believe [33–36] that bivariate approaches of the type proposed here could improve any bioassay in which the inhibitory or stimulatory action of an effector is superposed on the variation with time of the target system or the particular time course of the response is a relevant aspect of that action. Some bioassays that are based on hemolytic processes could be examples on this matter.
Finally, from the ecotoxicological point of view, it could be pointed out that, in contrast to what seems an implicit assumption, the sperm bioassays are not an alternative to larval ones. In fact, the two types of results can be considered only as two components of the real impact of the toxic under study on the target species. Perhaps this type of assumptions is part of the reasons explaining why the state of many ecosystems is more critical than which is supposed by the parsimony of the respective environment protection policies.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
Acknowledgments
The authors express thanks to Ministerio de Ciencia e Innovación (CTM201018411, FEDER funds from European Union) for financial support. Miguel Angel Prieto Lage was awarded JAEpredoctoral contract by CSIC. They want to express their gratitude to Araceli Menduiña Santomé and Diego Rial Conde for their technical work.
References
 A. P. Negri and A. J. Heyward, “Inhibition of coral fertilisation and larval metamorphosis by tributyltin and copper,” Marine Environmental Research, vol. 51, no. 1, pp. 17–27, 2001. View at: Publisher Site  Google Scholar
 Z.C. Xie, C. W. Nga, P.Y. Qian, and J.W. Qiu, “Responses of polychaete Hydroides elegans life stages to copper stress,” Marine Ecology Progress Series, vol. 285, pp. 89–96, 2005. View at: Google Scholar
 L. Hoadley, “Certain effects of the salts of the heavy metals on the fertilization reaction in Arbacia punctulata,” Biological Bulletin, vol. 44, pp. 255–279, 1923. View at: Google Scholar
 P. A. Dinnel, Q. J. Stober, and D. H. DiJulio, “Sea urchin sperm bioassay for sewage and chlorinated seawater and its relation to fish bioassays,” Marine Environmental Research, vol. 5, no. 1, pp. 29–39, 1981. View at: Publisher Site  Google Scholar
 P. A. Dinnel, J. M. Link, and Q. J. Stober, “Improved methodology for a sea urchin sperm cell bioassay for marine waters,” Archives of Environmental Contamination and Toxicology, vol. 16, no. 1, pp. 23–32, 1987. View at: Publisher Site  Google Scholar
 P. A. Dinnel, J. M. Link, Q. J. Stober, M. W. Letourneau, and W. E. Roberts, “Comparative sensitivity of sea urchin sperm bioassays to metals and pesticides,” Archives of Environmental Contamination and Toxicology, vol. 18, no. 5, pp. 748–755, 1989. View at: Google Scholar
 G. Pagano, A. Esposito, and G. G. Giordano, “Fertilization and larval development in sea urchins following exposure of gametes and embryos to cadmium,” Archives of Environmental Contamination and Toxicology, vol. 11, no. 1, pp. 47–55, 1982. View at: Google Scholar
 G. Pagano, M. Cipollaro, G. Corsale et al., “Comparative toxicities of benzene, chlorobenzene, and dichlorobenzenes to sea urchin embryos and sperm,” Bulletin of Environmental Contamination and Toxicology, vol. 40, no. 4, pp. 481–488, 1988. View at: Google Scholar
 G. Pagano, B. Anselmi, P. A. Dinnel et al., “Effects on sea urchin fertilization and embryogenesis of water and sediment from two rivers in Campania, Italy,” Archives of Environmental Contamination and Toxicology, vol. 25, no. 1, pp. 20–26, 1993. View at: Google Scholar
 Environment Canada, “Biological test method: fertilization assay using echinoids (sea urchins and sand dollars), amended November 1997,” North Vancouver, BC, Canada, EPS 1/RM/27, 1992. View at: Google Scholar
 S. Lera and D. Pellegrini, “Evaluation of the fertilization capability of Paracentrotus lividus sea urchin storaged gametes by the exposure to different aqueous matrices,” Environmental Monitoring and Assessment, vol. 119, no. 1–3, pp. 1–13, 2006. View at: Publisher Site  Google Scholar
 A. Fabbrocini, M. Di Stasio, and R. D'Adamo, “Computerized sperm motility analysis in toxicity bioassays: a new approach to pore water quality assessment,” Ecotoxicology and Environmental Safety, vol. 73, no. 7, pp. 1588–1595, 2010. View at: Publisher Site  Google Scholar
 M. A. Murado, M. P. González, and J. A. Vázquez, “Doseresponse relationships: an overview, a generative model and its application to the verification of descriptive models,” Enzyme and Microbial Technology, vol. 31, no. 4, pp. 439–455, 2002. View at: Publisher Site  Google Scholar
 M. A. Murado, J. A. Vázquez, D. Rial, and R. Beiras, “Doseresponse modelling with two agents: application to the bioassay of oil and shoreline cleaning agents,” Journal of Hazardous Materials, vol. 185, no. 23, pp. 807–817, 2011. View at: Publisher Site  Google Scholar
 P. Riobó, B. Paz, J. M. Franco, J. A. Vázquez, and M. A. Murado, “Proposal for a simple and sensitive haemolytic assay for palytoxin. Toxicological dynamics, kinetics, ouabain inhibition and thermal stability,” Harmful Algae, vol. 7, no. 4, pp. 415–429, 2008. View at: Publisher Site  Google Scholar
 P. Riobó, B. Paz, J. M. Franco, J. A. Vázquez, M. A. Murado, and E. Cacho, “Mouse bioassay for palytoxin. Specific symptoms and doseresponse against dosedeath time relationships,” Food and Chemical Toxicology, vol. 46, no. 8, pp. 2639–2647, 2008. View at: Publisher Site  Google Scholar
 J. A. Vázquez, M. P. González, and M. A. Murado, “Effects of lactic acid bacteria cultures on pathogenic microbiota from fish,” Aquaculture, vol. 245, no. 1–4, pp. 149–161, 2005. View at: Publisher Site  Google Scholar
 M. A. Murado and J. A. Vázquez, “The notion of hormesis and the doseresponse theory: a unified approach,” Journal of Theoretical Biology, vol. 244, no. 3, pp. 489–499, 2007. View at: Publisher Site  Google Scholar
 M. A. Murado and J. A. Vázquez, “Biphasic toxicodynamic features of some antimicrobial agents on microbial growth: a dynamic mathematical model and its implications on hormesis,” BMC Microbiology, vol. 10, article 220, 2010. View at: Publisher Site  Google Scholar
 N. Kobayashi, “Comparative sensitivity of various developmental stages of sea urchins to some chemicals,” Marine Biology, vol. 58, no. 3, pp. 163–171, 1980. View at: Publisher Site  Google Scholar
 D. R. Levitan, M. A. Sewell, and F.S. C. FuShiang Chia, “Kinetics of fertilization in the sea urchin Strongylocentrotus franciscanus: interaction of gamete dilution, age, and contact time,” Biological Bulletin, vol. 181, no. 3, pp. 371–378, 1991. View at: Google Scholar
 A. A. Novelli, C. Losso, P. F. Ghetti, and A. V. Ghirardini, “Toxicity of heavy metals using sperm cell and embryo toxicity bioassays with Paracentrotus lividus (Echinodermata: Echinoidea): comparisons with exposure concentrations in the Lagoon of Venice, Italy,” Environmental Toxicology and Chemistry, vol. 22, pp. 1295–1301, 2003. View at: Google Scholar
 S. Lera, S. Macchia, and D. Pellegrini, “Standardizing the methodology of sperm cell test with Paracentrotus Lividus,” Environmental Monitoring and Assessment, vol. 122, no. 1–3, pp. 101–109, 2006. View at: Publisher Site  Google Scholar
 E. Jonczyk, K. G. Doe, P. C. Wells, and S. G. Yee, “Technical evaluation of the sea urchin fertilization test proceedings of a workshop in Dartmouth, Nova Scotia,” in Proceedings of the 17th Annual Aquatic Toxicity Workshop, P. Chapman, F. Bishay, E. Power et al., Eds., vol. 1 of Canadian Technical Report Of Fisheries & Aquatic Sciences no.1774, pp. 323–330, Vancouver, BC, Canada, 1991. View at: Google Scholar
 D. J. Marshall, “Reliably estimating the effect of toxicants on fertilization success in marine broadcast spawners,” Marine Pollution Bulletin, vol. 52, no. 7, pp. 734–738, 2006. View at: Publisher Site  Google Scholar
 P. R. Krause, “Effects of an oil production effluent on gametogenesis and gamete performance in the purple sea urchin (Strongylocentrotus purpuratus stimpson),” Environmental Toxicology and Chemistry, vol. 13, no. 7, pp. 1153–1161, 1994. View at: Google Scholar
 H. Vogel, G. Czihak, P. Chang, and W. Wolf, “Fertilization kinetics of sea urchin eggs,” Mathematical Biosciences, vol. 58, no. 2, pp. 189–216, 1982. View at: Google Scholar
 C. A. Styan and A. J. Butler, “Fitting fertilisation kinetics models for freespawning marine invertibrates,” Marine Biology, vol. 137, no. 56, pp. 943–951, 2000. View at: Publisher Site  Google Scholar
 S. Prikler, “Robert de Levie: advanced Excel for scientific data analysis, 2nd ed.,” Analytical and Bioanalytical Chemistry, vol. 395, pp. 1945–1964, 2009. View at: Google Scholar
 G. E. P. Box and M. E. Muller, “Note on the generation of random normal deviates,” The Annals of Mathematical Statistics, vol. 29, pp. 610–611, 1958. View at: Google Scholar
 M. A. Murado and M. A. Prieto, “NOEC and LOEC as merely concessive expedients: two unambiguous alternatives and some criteria to maximize the efficiency of doseresponse experimental designs,” Science of the Total Environment, vol. 461462, pp. 576–586, 2013. View at: Google Scholar
 A. DeLean, P. J. Munson, and D. Rodbard, “Simultaneous analysis of families of sigmoidal curves: application to bioassay, radioligand assay, and physiological doseresponse curves,” The American journal of physiology, vol. 235, no. 2, pp. E97–E102, 1978. View at: Google Scholar
 M. A. Murado Garcia and M. A. Prieto Lage, “Doseresponse analysis in the joint action of two effectors. A new approach to simulation, identification and modelling of some basic interactions,” PLoS ONE, vol. 8, Article ID e61391, 2013. View at: Google Scholar
 M. A. Prieto, M. A. Murado, J. A. Vázquez, Y. Anders, and T. P. Curran, “A new microplate procedure for simultaneous assessment of lipophilic and hydrophilic antioxidants and prooxidants, using crocin and βcarotene bleaching methods in a single combined assay: tea extracts as a case study,” Food Research International, vol. 53, pp. 836–846, 2013. View at: Google Scholar
 M. A. Prieto, J. A. Vázquez, and M. A. Murado, “Comparison of several mathematical models for describing the joint effect of temperature and ph on glucanex activity,” Biotechnology Progress, vol. 28, no. 2, pp. 372–381, 2012. View at: Publisher Site  Google Scholar
 M. A. Prieto, J. A. Vázquez, and M. A. Murado, “Hydrolysis optimization of mannan, curdlan and cell walls from Endomyces fibuliger grown in mussel processing wastewaters,” Process Biochemistry, vol. 46, no. 8, pp. 1579–1588, 2011. View at: Publisher Site  Google Scholar
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