Next Article in Journal
Evaluation of Three Chitin Metal Silicate Co-Precipitates as a Potential Multifunctional Single Excipient in Tablet Formulations
Next Article in Special Issue
Mycosporine-Like Amino Acids: Relevant Secondary Metabolites. Chemical and Ecological Aspects
Previous Article in Journal
On the Chemistry, Toxicology and Genetics of the Cyanobacterial Toxins, Microcystin, Nodularin, Saxitoxin and Cylindrospermopsin
Previous Article in Special Issue
Distribution and Abundance of MAAs in 33 Species of Microalgae across 13 Classes
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Combined Effects of UVR and Temperature on the Survival of Crab Larvae (Zoea I) from Patagonia: The Role of UV-Absorbing Compounds

Estación de Fotobiología Playa Unión and Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Casilla de Correos N° 15 (9103) Rawson, Chubut, Argentina
*
Author to whom correspondence should be addressed.
Mar. Drugs 2010, 8(5), 1681-1698; https://doi.org/10.3390/md8051681
Submission received: 22 April 2010 / Revised: 12 May 2010 / Accepted: 21 May 2010 / Published: 25 May 2010
(This article belongs to the Special Issue Marine Photoprotective Compounds)

Abstract

:
The aim of our study was to assess the combined impact of UVR (280–400 nm) and temperature on the first larval stage (Zoea I) of three crab species from the Patagonian coast: Cyrtograpsus altimanus, C. angulatus, and Leucippa pentagona. We determined the survival response of newly hatched Zoea I after being exposed for 8–10 h under a solar simulator (Hönle SOL 1200) at 15 and 20 °C. There was no mortality due to Photosynthetic Active Radiation (PAR, 400–700 nm) or ultraviolet-A radiation (UV-A, 315–400 nm), and all the observed mortality was due to ultraviolet-B radiation (UV-B, 280–315 nm). The data of larval mortality relative to exposure time was best fit using a sigmoid curve. Based on this curve, a threshold (Th) and the lethal dose for 50% mortality (LD50) were determined for each species. Based on the Th and LD50, C. altimanus was found to be the most resistant species, while L. pentagona was found to be the most sensitive to UV-B. For both species of Cyrtograpsus, mortality was significantly lower at 20 °C than at 15 °C; however, no significant differences between the two temperature treatments were found in L. pentagona. Bioaccumulation of UV-absorbing compounds in the gonads and larvae of C. altimanus, and to a lesser extent in C. angulatus, might have contributed for counteracting the impact of UV-B. However, most of the resilience to UV-B observed with the increase in temperature might be due to an increase in metabolic activity caused by a repair mechanism mediated by enzymes.

Graphical Abstract

1. Introduction

Climate change, due to anthropogenic activities, has two main outcomes i.e., the increase of ultraviolet radiation (UVR, 280–400 nm), especially of UV-B (280–315 nm), due to ozone depletion, and the increase in temperature due to the release of greenhouse gases. Both have important consequences for organisms and ecosystems [1,2]. On the one hand, solar radiation is the driving energy that makes possible the production of organic matter via photosynthesis by autotrophic organisms. Most photosynthetic processes use Photosynthetic Active Radiation (PAR, 400–700 nm). On the other hand, solar UVR, both at normal and enhanced levels, has been found to cause biological damage. The negative impact of UV-B radiation on various targets of aquatic organisms (e.g., DNA, photosystems, proteins, etc.) has been particularly well documented in the literature [35]. However, UV-A radiation (315–400 nm) has been found to be both beneficial by participating in photosynthesis and repair processes, as well as detrimental, by inducing reactive oxygen species [68] and also by adversely affecting the performance of photosystem II [9,10]. Previous studies have highlighted the importance of an increase in temperature, at least as seen in a higher growth rate—of almost five-fold—in the larvae of the crab Paralomis granulosa, when comparing the rates at 15 °C and at 3 °C [11]. Additionally, a temperature increase resulted in lower mortality of zooplankton due to the higher effectiveness of enzymatic activity, including the activities of those proteins involved in the photorepair mechanism [1214]. However, some stenotherm species may not be able to cope with a potential increase in temperature. For example, studies carried out with Asplanchna girodi [12] demonstrated that the UVR tolerance was significantly reduced with elevated temperatures.
While extensive literature on the separate effects of these two stressors (i.e., temperature and UVR) upon diverse aspects of performance within aquatic organisms is currently available, as of today, little is known about the combined effects of them. This is important as they can act synergistically or antagonistically [15]. An early study carried out with symbiotic algae reported significantly higher cellular concentrations of superoxide radicals and hydrogen peroxide when the cultures were exposed to elevated temperatures, both with and without exposure to UVR [16]. The overall responses seem to have a high degree of species-specificity [17]. The acclimation or repair capacities, of the organisms influences the observed impacts [14]. It is noteworthy to mention the role of UV-absorbing compounds (i.e., mycosporine like amino acids, MAAs) in protecting an important number of organisms against UVR stress (at least partially), ranging from phytoplankton, to macroalgae, zooplankton and invertebrates [18,19]. Besides, organisms may display one or more mechanisms to repair the damage caused by UVR [9], as some of them are temperature-dependent. Overall, responses to different abiotic variables are the result of highly complex interactions within the organism.
In an attempt to asses such responses to abiotic variables, the aim of this study was to evaluate the combined effects of both UVR and temperature on three crab larvae species that are characteristic of the Argentinean Sea: Cyrtograpsus altimanus, Cyrtograpsus angulatus and Leucippa pentagona (Crustacea, Decapoda). A number of reasons guarantee the importance of working with these species of Decapoda: Firstly, in the temperate—cold waters of the SW Atlantic Ocean, 39 species of decapod crustaceans were described [20,21]. Some of these species are important links in the food web, and constitute a large part of the diet for predators such as fish [22] and seabirds [23]. Furthermore, some decapod crustaceans are of commercial importance. They command high market prices [24,25]. Additionally, the life cycle of crabs, as well as that of many other marine invertebrates, has a planktonic larval phase, after which metamorphosis and settlement occur. During this larval phase, and especially during the Zoea, high mortality (>80%) has been reported [26]. This is mainly due to biotic factors, such as predation and lack of food and also because of abiotic factors, such as solar radiation and temperature [27]. Finally, particular species used in our experimentation account for a high proportion of the total larvae present in the water column: 35% of Cyrtograpsus spp. and 11% in L. pentagona [28].
To achieve our objective, we exposed newly hatched crab larvae to three ultraviolet radiation levels (i.e., using a solar simulator) while incubating them to two temperatures of 15 °C and 20 °C. Both sets of conditions are ecologically relevant as they are similar to the observed conditions on the sea surface during the study period. In addition, an increase in temperature during the early spawning season simulated an extreme change condition for future climate change scenarios [29]. After the incubation period, we evaluated the mortality and correlated our results with the presence of UV-absorbing compounds and carotenoids. The results of this work seem straightforward. On the one hand, we have gained knowledge on the effects of both UVR and temperature on these organisms (which have been poorly sampled within the context of both global change and Patagonian ecosystems). On the other hand, we can speculate on the potential implications of these stressors to local ecosystems.

2. Results and Discussion

2.1. General responses of crab larvae to radiation and temperature

No significant larval mortality was determined in samples exposed to Photosynthetic Active Radiation (PAR) + ultraviolet-A (UV-A) radiation (PA treatment) or to PAR alone—P treatment (<7%, P > 0.11). On the other hand, significant mortality was observed in all experiments in samples exposed to full simulated solar radiation (i.e., PAR + UV-A + UV-B, PAB treatment). Therefore, we will only present the results for all crab larvae that received full radiation under the different irradiance/temperature conditions (Figure 1). The fact that larval mortality was only due to UV-B radiation is consistent with previous findings obtained with shrimp larvae [30,31] and with other crab larvae species [32]. The mortality, as a function of the exposure time, varied according to the irradiance and temperature conditions at which the larvae were exposed and incubated. However, the general response was of a rather constant mortality prior to that of threshold value. After that, mortality increased significantly as time progressed, reaching 100% towards the end of the experiments. Sigmoid curves were the best fit to describe mortality as a function of exposure time. Three parameters were determined and used to compare the responses and sensitivity of species under the different experimental conditions: (a) A threshold value (Th) below which no mortality was detected. This threshold was set at the first maximum gradient of change in the curve, mortality vs. time/dose; (b) The lethal dose at which 50% of the larvae died (LD50); and (c) The mortality rate, as the slope of mortality vs. time.

2.2. Threshold

In order to compare data obtained between the irradiance and temperature treatments, we calculated the threshold (Th) values based both on time (Tht) and on the dose (Thd) associated with each irradiance level (Figure 2). For all species, Tht values were negatively correlated with the irradiance level at both temperatures (Figures 2A, 2C and 2E). Tht values were significantly lower (P < 0.01, F (2, 6) > 990) when the larvae were exposed to higher UV-B irradiances (i.e., Tht at 2.19 W m−2 < Tht at 1.22 W m−2 < Tht at 0.76 W m−2). In both species of Cyrtograpsus, Tht was significantly higher at 20 °C than at 15 °C (P < 0.01, F (1, 4) > 175), within each irradiance level (Figures 2A and 2C), suggesting a higher resistance at 20 °C. For L. pentagona, however, there were no significant differences in threshold values between temperatures within each irradiance level (Figure 2E). The Thd values (Figures 2B, 2D and 2F) were significantly different between temperatures for C. altimanus (P < 0.01, F (1, 16) = 29.39, Figure 2B) and for C. angulatus (P < 0.01, F (1, 16) = 460.42, Figure 2D), but not for L. pentagona (P = 0.42, F (1, 16) = 0.68, Figure 2F). On the other hand, there were no differences in Thd among two or more irradiance levels within each species, thus suggesting that the larvae started to die, in general, at approximately the same dose. However, for C. altimanus (Figure 2B), the Thd at 20 °C was significantly lower (P < 0.01, F (1, 7) = 303.51) at 0.76 W m−2 than at the other two irradiance levels. This indicates that the C. altimanus larvae started to die at a lower dose as compared to the other two irradiance levels, similarly to found in previous studies [33] carried out with the rotifer Asplanchna girodi and in the cladocera Daphnia pulicaria, where short incubations at high UVR irradiances were less lethal than long-term exposure to low UVR irradiances. These authors [33] speculated that photoenzymatic repair (PER) was not linear in animals, and that there was a clear link between PER and reciprocity (i.e., the effect of dosage is independent of the effects of irradiance or dose rate).
In most of our experiments, Thd values were similar within the same temperature. However, in the case of both Cyrtograpsus species, Thd values increased at high temperature. This behavior suggests that repair mechanisms counteracted the UV-B impact until attainment of Thd, and the increase of temperature resulted in a more effective repair, thus increasing the tolerance of the larvae towards short wavelengths. This increased survival of up to 50% at 20 °C, as compared to that at 15 °C, is consistent with results found within other studies. These experiments were carried out with Daphnia catawba and Leptodiaptomus minutus [12], Daphnia pulicaria [13], and Evechinus chloroticus and Diadema setosum [14]. The studies suggested a synergism between temperature and UV-B tolerance that is dependent on enzymatic repair to cope with UV-B’s harmful effects. It is suggested that this mechanism is mostly used in organisms that inhabit temperate and tropical waters, while photoprotection might be more effective in cold waters [13].

2.3. Rate of mortality and LD50

The rate of mortality (i.e., slope) increased significantly with increasing irradiance in C. altimanus (Figure 3A, R2 = 0.95 and P < 0.01, F (2, 15) = 11.01) and L. pentagona (Figure 3E, R2 = 0.96 and P < 0.01, F (2, 15) = 12.26). There were no significant differences in mortality (P = 0.056, F (1, 10) = 4.69) in C. angulatus at 0.76 and 1.22 W m−2 (Figure 3C). However, there was a significant difference between mortality at these two irradiances and mortality at the highest level of irradiance (i.e., 2.19 W m−2; P < 0.01, F (1, 16) = 28.27). In the case of C. altimanus (Figure 3A) and L. pentagona (Figure 3E), there were no significant differences between the 1.22 Wm−2 and 2.19 W m−2 irradiance levels. In the three species, there were no significant differences in the mortality rates between temperatures within each irradiance level. The LD50 also increased significantly in both species of Cyrtograpsus at 20 °C as compared to the values at 15 °C, for all irradiance levels (Figure 3B and 3D). However, no significant differences were observed between temperatures in the LD50 for L. pentagona (Figure 3F). In general, and for the three species, the LD50 was similar to Thd in terms of its response to irradiance and temperature.

2.4. UV-absorbing compounds and carotenoids

It has been widely documented in the literature that UV-absorbing compounds, as well as carotenoids, help organisms cope with excess radiation [19]. While UV-absorbing compounds (mainly mycosporine-like amino acids, MAAs) absorb in the UVR region and directly protect the organisms by absorbing and dissipating UVR energy, carotenoids are involved in antioxidant activities. They counteract the effects of free radical products generated by UV-B exposure [19,34]. In our study, we evaluated the concentrations of both UV-absorbing compounds and carotenoids within different tissues of both adults and larvae. The spawning season encompasses the austral spring-summer and early autumn. Thus, we tested for differences in the concentration of UV-absorbing compounds and carotenoids during these periods by taking samples (i.e., duplicate or triplicates) during the three seasons. No intra-seasonal differences in UV-absorbing compounds and/or carotenoids were found (data not shown). Therefore, we pooled all the data per tissue/larvae/species; the concentrations of UV-absorbing compounds and carotenoids are shown in Figure 4.
There was high variability in the concentration of these compounds among different tissues and species, but carotenoids were, in general, in significantly higher concentrations than the UV-absorbing compounds (Figure 4). Although there were significant amounts of UV-absorbing compounds in some tissues of the three species (P < 0.05, n = 7–9), only C. altimanus had them in significantly higher concentration in the gonads and larvae than in the rest of the tissues (P < 0.05, KW-H (1, 57) = 15.56, Figure 4A). In addition, both species of Cyrtograpsus had significant concentrations of UV-absorbing compounds in the larvae (Figures 4A and 4C). However, in C. altimanus, the concentration was significantly higher than the concentration in C. angulatus (P < 0.05, KW-H (1, 14) = 10.67). We did not find any significant differences in the UV-absorbing compounds found in the larvae obtained from adults that were kept at the two experimental temperatures. Similarly as mentioned above, we did not find significant differences in the UV-absorbing compounds found in the larvae/adults obtained at different moments during the spawning season, and consequently at different water temperatures. This would suggest that the concentration of UV-absorbing compounds in these three species was not dependent upon temperature, but rather upon the diet of the adults. Indeed, the dependence of UV-absorbing compound accumulation on diet has been determined in several species [3539]. On the other hand, in situ studies carried out with phytoplankton and krill [40] did not find a temporal relationship of MAA concentrations between these organisms: MAA concentrations in phytoplankton were generally low in the winter and high in the summer; however, their concentration in krill remained relatively constant during the year.
When looking at either the Thd (Figure 2) or at the LD50 (Figure 3) of the three studied species, our results suggest that C. altimanus larvae were the most resistant to UV-B radiation. The relatively high concentrations of UV-absorbing compounds present in the C. altimanus larvae (Figure 4), when compared to the other species, may partially contribute to the relatively higher resistance to UV-B. However, as mentioned above, the concentration of UV-absorbing compounds did not vary between the two temperatures tested. Therefore, the increased tolerance at 20 °C in this species, as well as that of C. angulatus, might be more related to efficient enzymatic repair.
Carotenoids were present in significant amounts within the gonads and larvae of the three species. They appeared in significantly higher concentrations (P < 0.05) than that of the other tissues (Figure 4B, 4D and 4F). The highest amount of carotenoids was found in L. pentagona and the lowest in C. angulatus. Carotenoids could have provided some protection to the larvae; however, no clear relationship between carotenoids and resistance/mortality was observed. Previous studies [39] determined that in Leptodiaptomus minutus (a calanoid copepod), the resistance to UVR increased 2.5-fold for UVR-acclimated, MAA-rich animals (i.e., with UV-absorbing compounds), but only 1.5-fold for UVR-acclimated, carotenoid-rich animals. The authors suggested that UVR-stressed animals switched from carotenoid to MAA accumulation when MAA was available through the diet. Furthermore, Persau et al. [41] compared the MAA and carotenoid accumulation on calanoid copepod populations from various lakes with different UVR transparencies. They observed a shift from high carotenoid/low MAA content in spring, to low carotenoid/high MAA content in summer in calanoids from the UVR-transparent lakes. This suggests a relatively higher MAA content and therefore, a more effective photoprotection, when organisms were present in high UVR-transparent lakes

2.5. Ecological implications

The spawning season for the three studied species encompass spring–summer and early autumn. Thus adults and larvae are exposed to relatively high temperatures and solar radiation conditions (Figure 5). The daily doses of solar UV-B reaching the sea surface varied from about 2 to 45 kJ m−2, while the surface water temperature changed from about 10 to 22 °C in the study area. The maximum UV-B irradiance in the area can be up to 1.8 W m−2 during noon time [42], which is much less than the irradiances received in tropical areas [43].
Sea surface temperature had significant variability throughout the year, being coldest in August and hottest in February (range of circa 10 to 22 °C). Our experimental conditions fall within the normal variability of both temperature and UVR in Patagonia. Indeed, two of the irradiance conditions used in our experiments were lower and one was higher than the highest irradiances reached in summer at noon time. Additionally, the temperatures used represent two extremes at which larvae are developing in situ. In our study, 100 % mortality of larvae was reached in all irradiance-temperature experiments, even at doses that were lower than the highest reached in the area.
In the Patagonia area, wind strength strongly conditions the depth of the upper mixing layer (UML) which in turn, modulates the mean irradiance received by plankton organisms [44]. Moreover, Patagonia is characterized by the presence of strong winds, predominantly from west, during the spring and summer [45]. Wind is also important in re-suspending particulate material (mainly in coastal areas), thus increasing the attenuation of solar radiation in the water column. As reported in an earlier study [46] carried out in Bahía Camarones (250 km from our study area), the UV-B penetration at 1% of the surface irradiance was 3.5 m depth (i.e., KUVB = 1.27 m−1), whereas UV-A and PAR penetrated deeper, down to 7 and 15 m, respectively. Based on these values of penetration of solar radiation, which are representative for our study area, we calculated the UV-B irradiance/dose in the water column and we compared them with the parameters obtained from the sigmoid fit (Figure 1). For example, the intermediate irradiance of 1.22 W m−2 would be encountered at <30 cm depth at noon when the maximum irradiance of 1.8 W m−2 is measured at the surface; in the case of the irradiance of 0.76 W m−2, it would be found at a depth <0.68 m. Based on these values, the Thd would be reached after at least for 5 hours in the case of L. pentagona, and after 6.5–10 hours for Cyrtograpsus spp., depending on the water temperature. However, larvae and plankton are moving in the water column, rather than staying still at a fixed depth. Thus, we also need to consider the depth distribution of the species, in order to infer the degree of stress caused by both solar radiation and temperature.
It should be noted that the adults of Cyrtograpsus (the two less UVR-sensitive species) are normally found at places receiving high solar radiation levels, such as the shallow sub-tidal and intertidal zones. On the other hand, adults of L. pentagona had a deeper distribution [20]. Still, the three species considered in this study have their spawning season during spring-summer-fall (mainly between September and April) and thus they are exposed to a wide range of irradiances as shown in Figure 5. In addition, the larvae have vertical migrations in the water column, as seen in most planktonic species [47,48]. They therefore receive irradiance that not only varies with the season, but also with their position in the water column. A recent study of vertical behavior within Patagonian larval crabs [28] demonstrated that most of L. pentagona larvae inhabit the upper layers of the water column at night and that they swim downwards during daytime. On the other hand, a lower percentage of larvae of the Cyrtograpsus spp. were observed in the upper water column near the surface in shallow places during daylight. However, the larvae of the Cyrtograpsus spp. seem to be advected far away from the coastal area where high grazing pressure occurs, and return to the coastal site when they are at the Megalopa phase, as only the first two stages of Zoea and the Megalopa were found in coastal samples, while the other three larval stages (ZIII, ZIV and ZV) were found far away from the coast [28]. We do not know however, if there is any change in sensitivity of the larvae as they develop through the different stages. However, larvae staying in coastal areas might be exposed to less radiation than in open waters as a result of differential turbidity (i.e., turbidity is higher in coastal areas). Despite the fact that the larvae in situ seem to be receiving a dose that is lower than the calculated UV-B Thd, (and thus little mortality would be expected), one cannot rule out that ambient UV-B levels may increase as result of climate change [5]. Furthermore, there are other indirect effects, such as changes in food-chain interactions, that can be more influential than direct effects on individual organisms at any single trophic level [49,50]. In addition, sub-lethal effects such as the lower growth rates observed in cod larvae [8], the increase in respiration rates in Daphnia catawba [51], or the high oxygen consumption and swimming activity occurring in juvenile rainbow trouts [52], might occur at low doses and thus are not considered in our survival experiments.

3. Experimental Section

3.1. Sampling/maintenance of specimens

Ovigerous females (i.e., near to spawning) of the crabs Cyrtograpsus altimanus (Rathbun, 1914), Cyrtograpsus angulatus (Dana, 1851), and Leucippa pentagona (Milne Edwards, 1833) were collected during spring, summer, and autumn of the years 2007 and 2008 to obtain newly hatched larvae. The specimens were collected from different places in the Patagonian coast (Chubut Province, Argentina) (Figure 6): C. altimanus were obtained during low tide from intertidal rock pools in Punta Cuevas, while L. pentagona were collected from Playa Paraná by scuba diving. C. angulatus females were obtained from the Chubut River estuary using traps. All specimens were immediately taken to the laboratory at the Estación de Fotobiología Playa Unión (EFPU, 15–60 min from the sampling site) where they were kept in aquaria under a 12:12 light: dark photoperiod in a controlled-temperature chamber (at 15 or 20 °C, depending on the experiment, see below) for at least two days, when the experiments were performed to determine the combined effects of UVR and temperature on survival (see below). Specimens were fed once a week with fish meat, after which the seawater was replaced. Prior to the hatch period, females were transferred to an individual aquarium to get a pool of larvae (Zoea I) from the same female, thus reducing the potential variability between organisms within any one experiment. The aquaria were checked twice a day and only larvae less than 16 h from hatching were used in the experiments. A lamp providing dim light was placed in one side of each aquarium to allow larvae to swim towards the illuminated corner, where they were collected using a pipette. In this way, we selected healthy and photoactive larvae that were then used in the experiments.

3.2. Experimental set up

For each survival experiment, 20 larvae (recently hatched Zoea I from the same female) were placed in 180-mL glass beakers (10 cm of diameter) with 100 mL of sterilized seawater and exposed for circa 12 hours under artificial UVR-PAR using a solar simulator (Hönle system, Sol 1200, Germany). Three quality radiation treatments, each one with three replicates, were implemented on each experiment as follows: (1) Treatment PAB, larvae receiving full radiation (PAR + UV-A + UVB, 290–700 nm), glass beakers covered with Ultraphan 290 or acetate film to screen out UV-C emitted by the solar simulator; (2) Treatment PA, larvae receiving radiation in the range 320–700 nm (UV-A + PAR), glass beakers covered with Folex UV cut-off filter (Montagefolie, No. 10155099) and (3) Treatment P (control), larvae receiving radiation in the range 400–700 nm (only PAR), glass beakers covered with Ultraphan UV Opak Digefra film. The transmission characteristics of filters and materials were previously reported [10]. The nine experimental units (i.e., the three radiation treatments and the three replicates) were randomly distributed on a black water bath container at 15 or 20 °C under the solar simulator. The irradiance level was fixed for each experiment by placing all beakers (n = 9) at the same distance from the solar simulator. Three different irradiance levels were used in different experiments (Table 1). At least one experiment was done with each species under any one radiation-temperature combination.

3.3. Mortality determinations

During the irradiation period, the beakers (three at a time) containing the larvae were taken out of the radiation source every 1–2 hours, and live and dead larvae were counted. Since larvae of the three species used in all the experiments had positive phototactic orientations, we considered ecologically dead those individuals that did not react towards a dim light source in one side of the receptacle. This counting procedure took less than 2 minutes, therefore the time away from the radiation source was considered negligible. Mortality was defined as the percentage of dead larvae, with respect to the total number (n = 20) of larvae in the beaker.

3.4. Analysis of UV absorbing compounds

UV-absorbing compounds were measured in the whole larvae as well as in the hepathopancreas (digestive gland), muscles, gonads, embryos and exoskeleton of female adult specimens and in hepathopancreas, muscles and exoskeleton of male adult specimens. Samples (duplicates or triplicates) were obtained at the beginning, middle, and at the end of the spawning season to assess for intra-seasonal differences. Fresh samples were placed in 15-mL centrifuge tubes with 5 mL of absolute methanol, sonicated for 20 minutes at 25 °C, and extracted for at least 1 hour. We are aware that UV-absorbing compounds are slightly underestimated by this procedure, as it was shown that 20% methanol is the best extraction solvent for these compounds [53]. However, since no significant differences were found previously in our laboratory between the two extraction methods, and because we were limited by the amount of sample, we considered this procedure to be appropriate for the purposes of our investigation. After the extraction period, the samples were centrifuged for 15 minutes at 1,500 rpm and the spectral characteristics of the supernatants were measured from 280 to 750 nm via a scanning spectrophotometer (Hewlett Packard model 8453E). The estimation of the amount of UV-absorbing compounds was obtained by peak analysis at 310–360 nm [54]. The amount of UV-absorbing compounds was normalized per gram of dry weight, which was determined by drying sub-samples in the oven at 35 °C for 24 hours until constant weight.

3.5. Analysis of carotenoids

The same spectra obtained to determine UV-absorbing compounds were also used to estimate total carotenoids concentration. This was calculated from the absorbance spectra, using the formula of Hairston [55] as: C = (D × V × 104)/(E × W), where C is the carotenoid concentration in the sample (in ug mg−1 dry weight); D, the absorbance at 472 nm; V, the volume of the extract (in mL); E, the extinction coefficient (2,500); and W, the dry weight (in mg) of the sample.

3.6. Radiation/temperature data

The irradiance levels under the solar simulator were measured using a broadband filter radiometer ELDONET (Real Time Computers, Inc.) that has channels for UV-B (280–315 nm), UV-A (315–400 nm), and Photosynthetic Active Radiation (PAR, 400–700 nm). Field radiation data was also obtained with an ELDONET radiometer (Real Time Computer Inc.) that is permanently installed on the roof of the Estación de Fotobiología Playa Unión (EFPU). Sea surface temperature data was obtained with a digital thermometer at 50 cm depth hanging in a buoy at a site near Punta Cuevas and Playa Paraná (data provided by F. Dellatorre). The thermometer registered data every 5 minutes and the data was stored in a datalogger. Temperature data was similar to that measured in the estuary of Chubut River [56].

3.7. Statistical Analysis

Mortality data vs. exposure time were plotted for each irradiance-temperature condition and for each of the species selected. Sigmoid curves were considered the best fit, and threshold (Th) and lethal dose 50 (LD50) were determined from these curves. One-way ANOVA tests were used to determine significant differences in Th, mortality rate, and LD50 among irradiances, temperatures and species. Two-ways ANOVA tests were used to determine interactions between factors (i.e., irradiance and temperature) [57]. Because the amount of UV-absorbing compounds and total carotenoids did not follow homocedasticity, intra-seasonal differences and differences among tissues were statistically analyzed using the non-parametric Kruskal Wallis test [57].

4. Conclusions

The results of this work seem straightforward: On the one hand, we have gained knowledge on the combined effects of UVR and temperature on three crab species of Patagonian waters (which have been poorly sampled in the context of global change). On the other hand, our data allowed us to speculate on the potential implications of these stressors on crab larvae characteristics within the area. Our data also suggests a great variability amongst species, not only in the acclimation capacity (i.e., amount and body distribution of protecting compounds) but also in their response to the combined effects of UVR and temperature. Some of these acclimations and responses could be partially related to their habitat location and to the amount of solar radiation received. The lack of intra-seasonal differences suggests that other mechanisms, rather than simple acclimation to low and high irradiances, seem to be acting. One such mechanism seems to be presence of UV-absorbing and carotenoids compounds, whose concentrations within tissues are more related to the diet than to the irradiance conditions. Another one, as suggested by the increased UV-B tolerance at increasing temperatures in some of the species, is the enzymatic repair activity that seems to be enhanced at higher temperature. Nevertheless, while this latter mechanism seems to be important in C. angulatus larvae, it seems to be weak and not stimulated (by an increase in temperature) in L. pentagona larvae. Overall, our results suggest that C. altimanus is the most UV-B-resistant species and that this seems to be the result of both well-developed repair mechanisms and the presence of protective compounds. Nevertheless, all the larvae tested had a UV-B LD50 that is significantly lower than the daily incident UV-B irradiance at the surface. This would not only affect the survival of these species but also would condition their distribution in the water column. Of the three species, only the Cyrtograpsus larvae had a significant increase in the LD50 with increasing temperature, suggesting that these species would be more suitable for success under the eventual temperature increase (due to climate change). The fate of the other species in the case of increasing temperature, or with respect to the potential changes in behavior of all species (i.e., swimming to depth, distribution towards more turbid waters, etc.), as well any potential sub-lethal effects, however, remains unknown.

Acknowledgements

We thank Pedro J. Barón and Fernando G. Dellatorre for their suggestions and support at the time of obtaining and maintaining crabs specimens used in this study. We also thank Virginia Villafañe for her comments and corrections to the Ms. We thank the comments and suggestions of two anonymous reviewers. This work was supported by Agencia Nacional de Promoción Científica y Tecnológica— ANPCyT (PICT No. 2007-01651) and Fundación Playa Unión. This work is in partial fulfillment for a Ph. D. degree of R. D. Hernandez Moresino. This is Contribution No. 116 of Estación de Fotobiología Playa Unión.
  • Samples Availability: Available from the authors.

References

  1. Harley, CDG; Hughes, AR; Hultgre, KM; Miner, BG; Sorte, CJB; Thornber, CS; Rodriguez, LF; Tomanek, L; Williams, SL. The impacts of climate change in coastal marine systems. Ecol Lett 2006, 9, 228–241. [Google Scholar]
  2. Nelson, GC; Bennet, E; Berhe, AA; Cassman, K; DeFries, R; Dietz, T; Dobermann, A; Dobson, A; Janetos, A; Levy, M; Marco, D; Nakicenovic, N; O’Neill, B; Norgaard, R; Petschel-Held, G; Ojima, D; Pingali, P; Watson, R; Zurek, M. Anthropogenic drivers of ecosystem change: An overview. Ecol Soc 2006, 11, 29. [Google Scholar]
  3. De Mora, SJ; Demers, S; Vernet, M. The Effects of UV Radiation on Marine Ecosystems; Cambridge University Press: Cambridge, UK, 2000; pp. 1–324. [Google Scholar]
  4. Helbling, EW; Zagarese, HE. UV Effects in Aquatic Organisms and Ecosystems; The Royal Society of Chemistry: Cambridge, UK, 2003; pp. 1–575. [Google Scholar]
  5. Häder, DP; Kumar, HD; Smith, RC; Worrest, RC. Effects of solar UV radiation on aquatic ecosystems and interactions with climate change. Photochem Photobiol Sci 2007, 6, 267–285. [Google Scholar]
  6. Setlow, RB; Grist, E; Thompson, K; Woodhead, AD. Wavelengths effective in induction of malignant melanoma. Proc Natl Acad Sci USA 1993, 90, 6666–6670. [Google Scholar]
  7. Vega, MP; Pizarro, RA. Oxidative stress and defence mechanisms of the freshwater cladoceran Daphnia longispina exposed to UV radiation. J Photochem Photobiol B Biol 2000, 54, 121–125. [Google Scholar]
  8. Lesser, MP; Farrell, JH; Walker, CW. Oxidative stress, DNA damage and p53 expression in the larvae of Atlantic cod (Gadus morhua) exposed to ultraviolet (290–400 nm) radiation. J Exp Biol 2001, 204, 157–164. [Google Scholar]
  9. Buma, AGJ; Boelen, P; Jeffrey, WH. Helbling, EW, Zagarese, HE, Eds.; UVR-induced DNA damage in aquatic organisms. In UV Effects in Aquatic Organisms and Ecosystems; The Royal Society of Chemistry: Cambridge, UK, 2003; pp. 291–327. [Google Scholar]
  10. Villafañe, VE; Sundbäck, K; Figueroa, FL; Helbling, EW. Helbling, EW, Zagarese, HE, Eds.; Photosynthesis in the aquatic environment as affected by UVR. In UV Effects in Aquatic Organisms and Ecosystems; Royal Society of Chemistry: Cambridge, UK, 2003; pp. 357–397. [Google Scholar]
  11. Anger, K; Thatje, S; Lovrich, G; Calcagno, J. Larval and early juvenile development of Paralomis granulosa reared at different temperatures: tolerance of cold and food limitation in a lithodid crab from high latitudes. Mar Ecol Prog Ser 2003, 253, 243–251. [Google Scholar]
  12. Williamson, CE; Grad, G; De Lange, HJ; Gilroy, S. Temperature-dependent ultraviolet responses in zooplankton: Implications of climate change. Limnol Oceanogr 2002, 47, 1844–1848. [Google Scholar]
  13. MacFadyen, EJ; Williamson, CE; Grad, G; Lowery, M; Jeffrey, WH; Mitchell, DL. Molecular response to climate change: Temperature dependence of UV-induced DNA damage and repair in the freshwater crustacean Daphnia pulicaria. Global Change Biol 2004, 10, 408–416. [Google Scholar]
  14. Lamare, MD; Barker, MF; Lesser, MP; Marshall, C. DNA photorepair in echinoid embryos: Effects of temperature on repair rate in Antarctic and non-Antarctic species. J Exp Biol 2006, 209, 5017–5028. [Google Scholar]
  15. Hoffman, JR; Hansen, LJ; Klinger, T. Interactions between UV radiation and temperature limit inferences from single-factor experiments. J Phycol 2003, 39, 268–272. [Google Scholar]
  16. Lesser, MP. Elevated temperatures and ultraviolet radiation cause oxidative stress and inhibit photosynthesis in symbiotic dinoflagellates. Limnol Oceanogr 1996, 41, 271–283. [Google Scholar]
  17. Persaud, AD; Williamson, CE. Ultraviolet and temperature effects on planktonic rotifers and crustaceans in northern temperate lakes. Freshwater Biol 2005, 50, 467–476. [Google Scholar]
  18. Dunlap, WC; Shick, JM. Ultraviolet radiation-absorbing mycosporine-like amino acids in coral reef organisms: A biochemical and environmental perspective. J Phycol 1998, 34, 418–430. [Google Scholar]
  19. Banaszak, AT. Helbling, EW, Zagarese, HE, Eds.; Photoprotective physiological and biochemical responses of aquatic organisms. In UV Effects in Aquatic Organisms and Ecosystems; The Royal Society of Chemistry: Cambridge, UK, 2003; pp. 329–356. [Google Scholar]
  20. Spivak, ED. Los crustáceos decápodos del Atlántico sudoccidental (25°–55°S): Distribución y ciclos de vida. Invest Mar 1997, 25, 69–91. [Google Scholar]
  21. Arntz, WE; Gorny, M; Soto, R; Lardies, M; Retamal, M; Wehrtmann, IS. Species composition and distribution of decapod crustaceans in the waters off Patagonia and Tierra del Fuego, South America. Sci Mar 1999, 63, 303–314. [Google Scholar]
  22. Moreno, CA; Jara, HF. Ecological studies on fish fauna associated with Macrocystis pyrifera belts in the south of Fueguian Islands, Chile. Mar Ecol Prog Ser 1984, 15, 99–107. [Google Scholar]
  23. Delhey, JKV; Carrete, M; Martínez, MM. Diet and feeding behaviour of Olrog’s Gull Larus atlanticus in Bahía Blanca, Argentina. Ardea 2001, 89, 319–329. [Google Scholar]
  24. Boschi, EE. Las pesquerías de crustáceos decápodos en el litoral de la República Argentina. Invest Mar 1997, 25, 19–40. [Google Scholar]
  25. Wyngaard, JG; Iorio, MI; Boschi, EE. ¿Es viable el desarrollo de pesquerías de cangrejos en la Argentina? INIDEP 2001, 101, 9. (In Spainish) [Google Scholar]
  26. Morgan, SG. Young, CM, Sewell, MA, Rice, ME, Eds.; Life and death in the plankton: Larval mortality and adaptation. In Ecology of Marine Invertebrate Larvae; CSC Press: Boca Raton, FL, USA, 1995; pp. 279–321. [Google Scholar]
  27. Pechenik, JA. Larval experience and latent effects—metamorphosis is not a new beginning. Int Comp Biol 2006, 46, 323–333. [Google Scholar]
  28. Dellatorre, FG. Influencia de factores ambientales sobre la distribución y el asentamiento de larvas de cangrejos braquiuros y anomuros con potencial pesquero en Golfo Nuevo. Ph D Thesis, Universidad Nacional del Comahue, Bariloche, Argentina, 2009. [Google Scholar]
  29. IPCC, Climate Change 2007: The Physical Science Basis. In Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change; Cambridge University Press: New York, NY, USA, 2007; p. 996.
  30. Damkaer, DM; Dey, DB; Heron, GA. Dose/dose rate responses of shrimp larvae to UV-B radiation. Oecologia 1981, 48, 178–182. [Google Scholar]
  31. Damkaer, DM; Dey, DB. UV damage and photoreactivation potentials of larval shrimp, Pandalus platyceros, and adult euphausiids, Thysanoessa raschii. Oecologia 1983, 60, 169–175. [Google Scholar]
  32. Hovel, KA; Morgan, SG. Susceptibility of estuarine crab larvae to ultraviolet radiation. J Exp Mar Biol Ecol 1999, 237, 107–125. [Google Scholar]
  33. Grad, G; Williamson, CE; Karapelou, DM. Zooplankton survival and reproduction responses to damaging UV radiation: A test of reciprocity and photoenzymatic repair. Limnol Oceanogr 2001, 46, 584–591. [Google Scholar]
  34. Roy, S. De Mora, SJ, Demers, S, Vernet, M, Eds.; Strategies for the minimization of UV-induced damage. In The Effects of UV Radiation in the Marine Environment; Cambridge University Press: Cambridge, UK, 2000; pp. 177–205. [Google Scholar]
  35. Carroll, AK; Shick, JM. Dietary accumulation of UV-absorbing mycosporine-like aminoacids (MAAs) by the gree sea urchin (Strongylocentrotus droebachiensis). Mar Biol 1996, 124, 561–569. [Google Scholar]
  36. Newman, SJ; Dunlap, WC; Nicol, S; Ritz, D. Antarctic krill (Euphausia superba) acquire a UV-absorbing mycosporine-like amino acid from dietary algae. J Exp Mar Biol Ecol 2000, 255, 93–110. [Google Scholar]
  37. Gonçalves, RJ; Villafañe, VE; Helbling, EW. Photorepair activity and protective compounds in two freshwater zooplankton species (Daphnia menucoensis and Metacyclops mendocinus) from Patagonia, Argentina. Photochem Photobiol Sci 2002, 1, 996–1000. [Google Scholar]
  38. Helbling, EW; Menchi, CF; Villafañe, VE. Bioaccumulation and role of UV-absorbing compounds in two marine crustacean species from Patagonia, Argentina. Photochem Photobiol Sci 2002, 1, 820–825. [Google Scholar]
  39. Moeller, RE; Gilroy, S; Williamson, CE; Grad, G; Sommaruga, R. Dietary acquisition of photoprotective compounds (mycosporine-like amino acids, carotenoids) and acclimation to ultraviolet radiation in a freshwater copepod. Limnol Oceanogr 2005, 50, 427–439. [Google Scholar]
  40. Riemer, U; Lamare, MD; Peake, BM. Temporal concentrations of sunscreen compounds (Mycosporine-like Amino Acids) in phytoplankton and in the New Zealand krill, Nyctiphanes australis G.O. Sars. J Plankton Res 2007, 29, 1077–1086. [Google Scholar]
  41. Persaud, AD; Moeller, RE; Williamson, CE; Burns, CW. Photoprotective compounds in weakly and strongly pigmented copepods and co-occurring cladocerans. Freshwater Biol 2007, 52, 2121–2133. [Google Scholar]
  42. Villafañe, VE; Marcoval, MA; Helbling, EW. Photosynthesis versus irradiance characteristics in phytoplankton assemblages off Patagonia (Argentina): Temporal variability and solar UVR effects. Mar Ecol Prog Ser 2004, 284, 23–34. [Google Scholar]
  43. Gao, K; Li, G; Helbling, EW; Villafañe, VE. Variability of UVR effects on photosynthesis of summer phytoplankton assemblages from a tropical coastal area of the South China Sea. Photochem Photobiol 2007, 83, 802–809. [Google Scholar]
  44. Helbling, EW; Villafañe, VE; Holm-Hansen, O. Weiler, CS, Penhale, PA, Eds.; Effects of ultraviolet radiation on Antarctic marine phytoplankton photosynthesis with particular attention to the influence of mixing. In Ultraviolet Radiation in Antarctica: Measurements and Biological Effects; American Geophysical Union: Washington, DC, USA, 1994; pp. 207–227. [Google Scholar]
  45. Villafañe, VE; Barbieri, ES; Helbling, EW. Annual patterns of ultraviolet radiation effects on temperate marine phytoplankton off Patagonia, Argentina. J Plankton Res 2004, 26, 167–174. [Google Scholar]
  46. Helbling, EW; Barbieri, ES; Marcoval, MA; Gonçalves, RJ; Villafañe, VE. Impact of solar ultraviolet radiation on marine phytoplankton of Patagonia, Argentina. Photochem Photobiol 2005, 81, 807–818. [Google Scholar]
  47. Alonso, C; Zagarese, HE; Rocco, V; Barriga, JP; Battini, MA. Surface avoidance by freshwater zooplankton: Field evidence on the role of ultraviolet radiation. Limnol Oceanogr 2004, 49, 225–232. [Google Scholar]
  48. Queiroga, H; Blanton, J. Interactions between behaviour and physical forcing in the control of horizontal transport of Decapod Crustacean larvae. Adv Mar Biol 2005, 47, 107–214. [Google Scholar]
  49. Hessen, D; De Lange, HJ; Van Donk, E. UV-induced changes in phytoplankton cells and its effects on grazers. Freshwater Biol 1997, 38, 513–524. [Google Scholar]
  50. Williamson, CE; Hargreaves, BR; Orr, PS; Lovera, PA. Does UV play a role in changes in predation and zooplankton community structure in acidified lakes? Limnol Oceanogr 1999, 44, 774–783. [Google Scholar]
  51. Fischer, JM; Fields, PA; Pryzbylkowski, PG; Nicolai, JL; Neale, PJ. Sublethal exposure to UV radiation affects respiration rates of the freshwater cladoceran Daphnia catawba. Photochem Photobiol 2006, 82, 547–550. [Google Scholar]
  52. Alemanni, ME; Lozada, M; Zagarese, HE. Assessing sublethal effects of ultraviolet radiation in juvenile rainbow trout (Oncorhynchus mykiss). Photochem Photobiol Sci 2003, 2, 867–870. [Google Scholar]
  53. Tartarotti, B; Sommaruga, R. The effect of different methanol concentrations and temperatures on the extraction of mycosporine-like amino acids (MAAs) in algae and zooplankton. Arch Hydrobiol 2002, 154, 691–703. [Google Scholar]
  54. Helbling, EW; Chalker, BE; Dunlap, WC; Holm-Hansen, O; Villafañe, VE. Photoacclimation of antarctic marine diatoms to solar ultraviolet radiation. J Exp Mar Biol Ecol 1996, 204, 85–101. [Google Scholar]
  55. Hairston, NG, Jr. The adaptive significance of color polymorphism in two species of Diaptomus (Copepoda). Limnol Oceanogr 1979, 24, 15–37. [Google Scholar]
  56. Helbling, EW; Pérez, DE; Medina, CD; Lagunas, MG; Villafañe, VE. Phytoplankton distribution and photosynthesis dynamics in the Chubut River estuary (Patagonia, Argentina) throughout tidal cycles. Limnol Oceanogr 2010, 55, 55–65. [Google Scholar]
  57. Zar, JH. Biostatistical Analysis, 4th ed; Prentice Hall: Englewood Cliffs, NJ, USA, 1999. [Google Scholar]
Figure 1. Larvae mortality (%), as a function of exposure time, for samples under the PAB treatment exposed to UV-B irradiances of 2.19, 1.22 and 0.76 W m−2, and temperatures of 15 and 20 °C. A, B, and C are experiments carried out with larvae exposed at 15 °C; D, E, and F are experiments carried out with larvae exposed at 20 °C. A total of 28 experiments were done, with at least one experiment (with triplicates) for each irradiance-temperature condition. Each symbol in the Figure represents the mean of the triplicates and the red curves are the best fit lines for each irradiance condition.
Figure 1. Larvae mortality (%), as a function of exposure time, for samples under the PAB treatment exposed to UV-B irradiances of 2.19, 1.22 and 0.76 W m−2, and temperatures of 15 and 20 °C. A, B, and C are experiments carried out with larvae exposed at 15 °C; D, E, and F are experiments carried out with larvae exposed at 20 °C. A total of 28 experiments were done, with at least one experiment (with triplicates) for each irradiance-temperature condition. Each symbol in the Figure represents the mean of the triplicates and the red curves are the best fit lines for each irradiance condition.
Marinedrugs 08 01681f1
Figure 2. Threshold values for the three larvae species as a function of the UV-B irradiance level. Panels A, C, and E are the thresholds expressed in minutes of exposure (Tht), while panels B, D, and F are the thresholds (Thd) expressed in kJ m−2. The values are the mean and standard deviation (n ≥ 3). The * on top of the bars indicates differences between temperatures for each irradiance level. Lower case and capital letters indicate differences among irradiances at 15 °C and 20 °C, respectively.
Figure 2. Threshold values for the three larvae species as a function of the UV-B irradiance level. Panels A, C, and E are the thresholds expressed in minutes of exposure (Tht), while panels B, D, and F are the thresholds (Thd) expressed in kJ m−2. The values are the mean and standard deviation (n ≥ 3). The * on top of the bars indicates differences between temperatures for each irradiance level. Lower case and capital letters indicate differences among irradiances at 15 °C and 20 °C, respectively.
Marinedrugs 08 01681f2
Figure 3. Rate of mortality (% mortality min−1) and LD50 (in kJ m−2) as a function of the UV-B irradiance levels for C. altimanus (A, B), C. angulatus (C, D), and L. pentagona (E, F). The values are the mean and standard deviation (SD) (n ≥ 3). * indicates significant differences between temperatures for each irradiance level. Lower case letters and capital letters indicate differences among irradiances at 15 °C and 20 °C, respectively.
Figure 3. Rate of mortality (% mortality min−1) and LD50 (in kJ m−2) as a function of the UV-B irradiance levels for C. altimanus (A, B), C. angulatus (C, D), and L. pentagona (E, F). The values are the mean and standard deviation (SD) (n ≥ 3). * indicates significant differences between temperatures for each irradiance level. Lower case letters and capital letters indicate differences among irradiances at 15 °C and 20 °C, respectively.
Marinedrugs 08 01681f3
Figure 4. UV-absorbing compounds (A, C, and E) and total carotenoids (B, D, and F) found in the three species used in the experiments. The values are the mean and standard error (SE) of samples (n = 7–9) collected at three different periods during the spawning season and pooled together (explanation in the text). The numbers in the x-axis 1 to 4 indicate female tissues; number 5 corresponds to the whole larvae, and numbers 6 to 8 are male tissues. The * on top of the bars indicates that the concentration is significantly different from zero. Lower case letters indicate significant differences among tissues.
Figure 4. UV-absorbing compounds (A, C, and E) and total carotenoids (B, D, and F) found in the three species used in the experiments. The values are the mean and standard error (SE) of samples (n = 7–9) collected at three different periods during the spawning season and pooled together (explanation in the text). The numbers in the x-axis 1 to 4 indicate female tissues; number 5 corresponds to the whole larvae, and numbers 6 to 8 are male tissues. The * on top of the bars indicates that the concentration is significantly different from zero. Lower case letters indicate significant differences among tissues.
Marinedrugs 08 01681f4
Figure 5. Surface UV-B daily doses (red line) and surface water temperature (blue line) throughout the year in the study area (see Figure 6). The horizontal lines indicate the spawning season for Cyrtograpsus spp. and L. pentagona.
Figure 5. Surface UV-B daily doses (red line) and surface water temperature (blue line) throughout the year in the study area (see Figure 6). The horizontal lines indicate the spawning season for Cyrtograpsus spp. and L. pentagona.
Marinedrugs 08 01681f5
Figure 6. Map showing the sampling sites and their relative position in South America.
Figure 6. Map showing the sampling sites and their relative position in South America.
Marinedrugs 08 01681f6
Table 1. Irradiance levels (in W m−2) used in the experiments.
Table 1. Irradiance levels (in W m−2) used in the experiments.
Distance to the solar simulator (m)PAR (W m−2)UV-A (W m−2)UV-B (W m−2)
0.56223.589.42.19
0.85125.849.11.22
1.0984.5300.76

Share and Cite

MDPI and ACS Style

Moresino, R.D.H.; Helbling, E.W. Combined Effects of UVR and Temperature on the Survival of Crab Larvae (Zoea I) from Patagonia: The Role of UV-Absorbing Compounds. Mar. Drugs 2010, 8, 1681-1698. https://doi.org/10.3390/md8051681

AMA Style

Moresino RDH, Helbling EW. Combined Effects of UVR and Temperature on the Survival of Crab Larvae (Zoea I) from Patagonia: The Role of UV-Absorbing Compounds. Marine Drugs. 2010; 8(5):1681-1698. https://doi.org/10.3390/md8051681

Chicago/Turabian Style

Moresino, Rodrigo D. Hernández, and E. Walter Helbling. 2010. "Combined Effects of UVR and Temperature on the Survival of Crab Larvae (Zoea I) from Patagonia: The Role of UV-Absorbing Compounds" Marine Drugs 8, no. 5: 1681-1698. https://doi.org/10.3390/md8051681

Article Metrics

Back to TopTop