Next Article in Journal
Effect of Soaking Time and Salt Concentration on Mechanical Characteristics of Slip Zone Soil of Loess Landslides
Next Article in Special Issue
Pollen Geochronology from the Atlantic Coast of the United States during the Last 500 Years
Previous Article in Journal
Natural and Anthropogenic Groundwater Contamination in a Coastal Volcanic-Sedimentary Aquifer: The Case of the Archaeological Site of Cumae (Phlegraean Fields, Southern Italy)
Previous Article in Special Issue
Conservation Paleobiology as a Tool to Define Reference Conditions in Naturally Stressed Transitional Settings: Micropaleontological Insights from the Holocene of the Po Coastal Plain (Italy)
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Water
Volume 12
Issue 12
10.3390/w12123464
water-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Stable Oxygen and Carbon Isotope Composition of Holocene Mytilidae from the Camarones Coast (Chubut, Argentina): Palaeoceanographic Implications

by
Gabriella Boretto
1,
Giovanni Zanchetta
2,3,4,*,
Ilaria Consoloni
2,
Ilaria Baneschi
5,
Massimo Guidi
5,
Ilaria Isola
6,7,
Monica Bini
2,3,
Luca Ragaini
2,
Filippo Terrasi
8,
Eleonora Regattieri
5 and
Luigi Dallai
5,6,9
1
Centre for the Investigation of Earth Sciences (CICTERRA-CONICET), Universidad Nacional the Córdoba, Av. Velez Sarsfield 1611, X5016GCA Cordoba, Argentina
2
Dipartimento di Scienze della Terra, Università di Pisa, Via S. Maria 53, 56126 Pisa, Italy
3
CIRSEC Centre For Climatic Change Impact, University of Pisa, Via del Borghetto 80, 56124 Pisa, Italy
4
Istituto di Geologia Ambientale e Geoingegneria, IGAG-CNR, Via Salaria km 29,300, 00015 Montelibretti, Rome, Italy
5
Istituto di Geoscienze e Georisorse IGG-CNR, Via Moruzzi 1, 56100 Pisa, Italy
6
Istituto Nazione di geofisica e Vulcanologia, Via della Faggiola 32, 56100 Pisa, Italy
7
Istituto Nazione di geofisica e Vulcanologia, Via Vigna Murata 605, 00143 Roma, Italy
8
CIRCE, Department of Environmental Sciences, Second University of Naples, Viale Lincoln, 5, 81100 Caserta, Italy
9
Dipartimento di Scienze della Terra, Università di Roma “La Sapienza”, Ple A. Moro 5, 00185 Roma, Italy
*
Author to whom correspondence should be addressed.
Water 2020, 12(12), 3464; https://doi.org/10.3390/w12123464
Submission received: 27 October 2020 / Revised: 2 December 2020 / Accepted: 8 December 2020 / Published: 9 December 2020
(This article belongs to the Special Issue Climate Change and Anthropogenic Impact on Coastal Environments)
Browse Figures
Review Reports Versions Notes

Abstract

:
The stable isotope composition of living and of Holocene Mytilidae shells was measured in the area of Camarones (Chubut, Argentina). The most striking results were the high δ18O values measured in samples older than ca. 6.1 cal ka BP. In the younger samples, the δ18O values remained substantially stable and similar to those of living specimens. Analysis of the data revealed the possibility for this isotopic shift to be driven mainly by changes in temperature probably accompanied by minor changes in salinity, suggesting cooler seawater before 6.1 cal ka BP, with a maximum possible temperature shift of ca. 5 °C. A possible explanation of this change can be related to a northward position of the confluence zone of the Falkland and Brazilian currents. This is consistent with the data obtained in marine cores, which indicate a northerly position of the confluence in the first half of the Holocene. Our data are also in line with the changes in wind strength and position of the Southern Westerlies Wind, as reconstructed in terrestrial proxies from the Southernmost Patagonia region.

1. Introduction

The Brazilian Current flowing southward and the Falkland (Malvinas) Current flowing northward dominate the upper-level circulation of the Atlantic coast of Southern South-America (Figure 1a). The Falkland Current is a branch of the Circumpolar Current and flows along the continental shelf of Argentina until it reaches the Brazil Current offshore the Río de la Plata estuary at ca. 38° [1,2]. Proxy data show that the front position has changed at millennial and at glacial/interglacial scales [3,4], as a result of changes in the position of the South Westerly Winds and of the long-term variations in the sea-surface temperature (SST) anomaly in the Agulhas-Benguela current [4,5]. At the inter-hemispheric scale, the position of the confluence of the Brazilian and of the Falkland currents also seems to be related to variations in the Atlantic Meridional Overturning circulation (AMOC) strength [4]. The changes in the front position have probably affected the biogeographic distribution of marine mollusks in the southern coast of South America. For instance, during the Middle Holocene, the presence of abundant mollusc fauna of ‘Brazilian affinity’ along the coast of the Bonaerense region, in a southern position compared to their current habitat, has been interpreted as a further penetration southward of the Brazilian Current [6]. Similarly, coastal marine successions over the northern Patagonia contain some differences in the marine fossil association between interglacials, which may be linked to changes in the position and strength of the Falkland and Brazilian currents [7,8,9,10,11]. These have pronounced differences in terms of temperature, salinity and oxygen isotope composition, with the Falkland current characterised by colder and fresher conditions compared to the Brazilian one [12,13]. The changes in their relative position could be identified by using the oxygen isotope composition (δ18O) of biological carbonates. For instance, [14] found that there is currently a strong oxygen isotopic gradient at the confluence of the Brazilian and Falkland currents (>2‰) in the calcite of Globorotalia inflata and G. truncatulinoides, collected at the top of the marine cores. This gradient was used by [4] to characterise the shift in the position of the confluence zone during the Holocene. Attempts have also been made to obtain palaeoceanographic information from coastal deposits outcropping along the Atlantic coast of Argentina by means of stable isotopes. Such efforts have been strongly influenced by the local mixture between continental and marine waters, overprinting possible isotopic effects related to regional changes in the oceanic circulation [15,16,17,18,19,20,21]. Recent data from Patagonia have been focussed on isotopic sclerochronology [22,23], which gives information on annual variability, whereas no clear interpretation has emerged from the study of bulk samples [23].
In this paper, we discuss the stable oxygen and carbon isotope geochemistry of living and of Holocene shells of Mytilidae collected in sections situated near the Camarones village (Chubut, Argentina; Figure 1a–c). Our aim was to obtain information of possible palaeoceanographic changes on the coastal area of this sector of Patagonia since the Holocene transgression on land was recorded. The absence of significant river inflow reduced the possibility of water mixing effects and complications related to changes in local salinity.

2. Site Description

The study area is part of the Bahía Camarones, an approximately 40 km-wide gulf extending from ca. 44°54′ S to 44°34′ S (Figure 1b). Structurally speaking, the area is located on the southern edge of the so-called ‘North Patagonia Massif’. Mainly Jurassic volcanic rock forms the pre-Quaternary succession [24]. Inland morphology is dominated by flat surfaces covered with gravely fluvial deposits (‘Rodados Patagonicos’, [25]) of poorly constrained age. Close to the coast, alternations of Quaternary littoral and continental deposits are present [24]. Quaternary marine coastal deposits have been extensively studied and mapped by [26,27,28,29,30,31,32]. Most of the recent studies on the Holocene transgression are referred to the southern part of the Bahía Camarones thanks to the intensive field work of Schellmann and Radtke [28,29,30], which supplied robust chronological constraints for coastal aggradation during the Holocene by using the radiocarbon dating method. The stratigraphy and chronology of these successions have been recently implemented by the works of [31,32,33]. Aguirre [7] and Aguirre et al. [10] provided a detailed description of the paleontological associations for different littoral units, including the Holocene sections.
The meteorological station of the Camarones village records a mean annual precipitation of 287 mm/a with a mean annual temperature of 12.6 °C. Throughout the year, the strong activity of the southern westerlies causes elevated soil evapotranspiration, turning the area into a semiarid and poorly vegetated land [34]. The potential evapotranspiration, calculated by the Thornthwaite method, indicates an annual value of <700 mm, with a maximum of ≥100 mm in January (warm season) and a minimum of 15 mm in June (cold season). The annual evapotranspiration exceeds the rainfall, so the annual water deficit reaches approximately 450 mm, without considering the additional effect of the strong winds (http://www.ambiente.chubut.gov.ar).
Like most of coastal Patagonia, the area is dominated by high-energy, macro-tidal (>4 m) and stormy conditions [35], resulting in a coastal morphology dominated by cliffs, wave-cut platforms and coarse-clastic beach ridges (‘swash built ridges’ sensu [36]).
For this area, Falabella et al. [37] and the Argentine Naval Hydrography Service (http://www.hidro.gov.ar/ceado/Ef/Inventar.asp) reported an annual mean sea-surface temperature (SST) of around 12 °C; an average SST of 15.6 °C in the warm season; an average of 7.7 °C in the cold season; and a sea surface salinity (SSS) between ca. 33 and 33.5‰. This is in agreement with the satellite data, which indicate an average temperature of the sea off Camarones of 12 ± 3 °C for 2015 (http://seatemperature.org).

3. Materials and Methods

Several field campaigns were performed by the authors between 2009 and 2012. The samples were stored in the Laboratory of Paleoclimatology and Geoarchaeology of the University of Pisa. During the field campaigns, modern shells accumulated on the beach after sea storms were collected in several locations of S. Jorge’s Gulf (Figure 1b and Figure 2B).
Only shells with still-connected valves preserving the hinge ligament and with a fresh aspect, indicating that they had died recently, were selected. Whole shells were immersed for ca. 24 in a H2O2 solution in order to remove remains of organic matter. They were then washed in an ultrasonic bath and rinsed several times with deionised water. One shell of the pair was grounded in an agate mortar and was used for stable isotope analyses. A similar procedure was followed for fossil shells selected from Holocene deposits (Figure 1c). The powder obtained was not subject to further pre-treatments, to avoid undesirable isotopic effects.
The deposits in which the shells were collected are described in [30,31], which includes some radiocarbon dating (Table 1). Additional samples were collected and dated for this work (Table 1). Similarly to modern specimens, the fossil shells were collected in deposits interpreted as storm accumulations (Figure 2B [31]).
In one case, the shell samples were collected from a small shellmidden [31]. Whole shells for radiocarbon dating were cleaned in an ultrasonic bath with the addition of H2O2 and then gently etched with diluted HCl. The radiocarbon measurements were performed at the CIRCE laboratory in Caserta [38,39]. Calibration was performed using the Marine13 curve in CALIB 6 [40], even if we need to take into account that the marine reservoir effect for the Patagonia marine shallow waters is poorly constrained and likely to be highly variable [30,41]. Therefore, the calibration offered by CALIB may be locally underestimated.
Carbonate powders were reacted under vacuum with 105% phosphoric acid at 70 °C and the evolved CO2 gas was purified by using successions of cryogenic traps and then analysed with a MAT252 mass spectrometer available at IGG-CNR of Pisa. The isotopic results are reported by the conventional δ-notation in per mille (‰) values, namely percentage per thousand, and normalised to the Vienna Pee Dee Belemnite scale (V-PDB) using the internal working standards of Carrara Marble (MAB1), cross-checked against the NBS18 and NBS19 international reference materials. Mean analytical precision for both δ18O and δ13C is usually better than 0.15‰. The modern samples pertain to the Mytilidae family: Aulacomya atra and Mytilus edulis (Table 2).
One group of fossil samples belongs to Mytilidae Brachidontes purpuratus and two groups of samples belong to Nacella (Patinigera) deaurata (Table 3).
Few superficial marine waters were collected during the 2011 and 2010 fieldwork (Table 4). The δ18O values were determined after equilibration with CO2 [42] and measured with a Thermo Finnigan MAT-252 mass spectrometer. The data are reported in per mille values (‰) with respect to V-SMOW. Analytical reproducibility was usually 0.1‰.
Mytilus edulis (the ‘blue mussel’) is an epifaunal suspension feeder found in intertidal-up-to-subtidal environments (reported to be up to 25 m in depth) attached to rocks and to other hard substrates [43], or as loose beds on sandy substrata [44]. The mussel is eurythermal and well acclimated in a +5 to +20 °C temperature range, with an upper sustained thermal tolerance limit of about +29 °C for adults [45]. It does not thrive in salinities lower than 15‰. Aulacomya atra is an epifaunal suspension feeder species living in intertidal-up-to-subtidal environments generally as low as 30/40 m [46], and attached to rocks and to other hard substrates. It is euryhaline, able to withstand values higher or lower than those of typically marine species. It is, however, also reported to adapt to intertidal pools with low salinity (15–20‰).
Brachidontes purpuratus is an epibyssate and a filter feeder species living on hard bottoms in shallow littoral areas (supratidal to infralittoral zones). This species has been recorded in intertidal highly energetic marine waters among algae or in estuarine zones in low-salinity pools [10]. The species Nacella (Patinigera) deaurata is an epibenthic, sessile grazing feeder, found on the rocky shores of supralittoral, intertidal and sublittoral environments up to 30 m deep [47,48]. No data have been found on the salinity tolerance of this species. However, as it is also an intertidal form, it is certainly euryhaline with an ability to withstand values different from those that are typically marine.
Mytilidae shells are a mix of aragonite and calcite layers [49]. As aragonite can turn into calcite during the processes of alteration and diagenesis, a set of XRD analyses were performed on living and fossil shells to confirm the existence of the mixture.
Owing to the wide variability of isotopic composition resulting from the process of shell accumulation, we normalised the isotopic composition to 100% of calcite, without considering the ratio of calcite/aragonite, as performed for instance by [18]. Indeed, the identified isotopic variability is within the potential correction because of the different isotopic fractionation of the calcium carbonate polymorphs in both carbon and oxygen [50,51,52,53].

4. Results

Both modern and Holocene shells are well preserved (usually maintaining their original colour). XRD analyses show that the Holocene shells are a mixture of aragonite and calcite, just like the modern specimens, confirming that they have not experienced diagenetic transformation. Modern samples collected at different sites show a relatively narrow range of isotopic variability (<1‰) for both the carbon and the oxygen isotope ratio (Table 2). The isotopic variability of the modern populations can be accounted for the fact that Mytilidae usually live for only a few years, when they experience different environmental conditions (i.e., salinity and temperature) in different seasons and different years, also related to the local tidal conditions. This finding is consistent with the observation that in living populations, different individuals show small differences and they offset from the isotopic equilibrium condition [54]. Furthermore, the collected shells are the result of storm accumulation on the beach; shells of different ontogenetic ages (even if only adult individuals were selected) and living on different microenvironments (different depths, tidal conditions, etc.) are mixed together. This variability is usually replicated in the fossils, which were accumulated under the same processes (Figure 2B), even if the isotopic range is usually higher. The selection of shells with joined valves at the same level significantly reduces the possibility of having collected reworked individuals related to different accumulation events and/or, in the worst of cases, eroded from older layers. However, a wider variability can be expected in fossil accumulation than in living shells usually collected in a single storm berm. Fossil accumulation can be the result of the more complex accumulation of several storms and possible later stages of further shell dispersion.
All in all, modern shells of M. edulis and A. atra collected in the same storm accumulation show very small differences in isotopic composition, substantially overlapping in terms of oxygen and carbon isotope composition (Table 5). This indicates that the δ18O and δ13C values of M. edulis and A. atra in the area can be used interchangeably, with negligible error, for the reconstruction of past coastal conditions.
Shell isotopic data of the Holocene sections (Figure 3 and Figure 4) younger than ca. 6100 a cal BP, including living shells, overlap along a relatively narrow range of δ18O values (between ca. +1.50 and +1.00‰). Older samples show significantly higher δ18O values ranging from ca. +2 to +2.5‰, with no overlaps with the younger samples. Carbon isotope compositions show a more complex pattern of variability, with partial overlaps for samples of different ages ranging from ca. +1.1 to +2.8‰ (Figure 3 and Figure 4).

5. Discussion

The δ18O values of the mollusc shells are functions of both δ18O of seawater, temperature [51,55,56,57], and additional ‘vital effects’ [56,58,59]. Wanamaker et al. [60] proposed the following empirical relation (Equation (1)) between temperature and isotopic composition of water and of carbonate shells for M. edulis:
T°C = 16.28(±0.10) − 4.57(±0.15) [δ18Oc − δ18Ow] + 0.06 [δ18Oc − δ18Ow]2
where δ18Ow is the isotopic composition of water with respect to V-SMOW, while δ18Oc is the isotopic composition of carbonate with respect to V-PDB. This implies a Δδ18Oc/°C of ca. −0.2‰/°C between ca. 5 and 25 °C. This equation agrees with the experimental data [53] obtained in precipitated carbonate close to isotopic equilibrium (however, for isotopic equilibrium on marine carbonate, see [61]).
At glacial to interglacial scale, global seawater δ18Ow values are mostly related to changes in the amount of water stored in continental ice [62,63]. A change of ca. 0.009‰/m in the eustatic sea-level component is estimated globally [63,64], with lower sea-level characterised by higher δ18O seawater values. Surface seawater isotopic composition is also influenced by changes in the evaporation and/or dilution with freshwater, which is often marked by changes in salinity [65,66], characterising different oceanic currents.
According to [13], the δ18O seawater value in the study area today should be around −0.3–−0.2‰. This value is slightly higher than the few isotopic data obtained on the samples occasionally collected in the area (Table 4), which yielded a δ18O average value of −0.48 ± 0.36‰. We obtained an average calcification temperature of ca. 11.3 °C (Equation (1)) by using the average δ18O values of the modern shells collected in the Camarones area (1.03 ± 0.15‰ for M. edulis, Table 2) and the δ18O values of seawater of −0.2‰ (Equation (1)), close to local average temperature; instead, we obtained a value of ca. 9.5 °C by using the measured isotopic values of seawater in Table 4. The measured δ18Ow values underestimate the temperature probably as a result of the changes in seasonal and local salinity.
Colonese et al. [21] and Yan et al. [67] proposed to evaluate the regional δ18Ow by using a relation with sea surface salinity (SSS) (Equation (2)):
δ18Ow (‰) = 0.30 SSS − 10.52
The δ18Ow values of seawater will range from ca. –0.6 to –0.5‰ by introducing the average SSS values reported for the area by [37]. This suggests that Equation (2) is not an excellent predictor for the isotopic composition of seawater in the area, even if the obtained results are still reasonable. This brief discussion, however, seems to confirm that by using a correct value of δ18Ow seawater, Equation (1) correctly reconstructs the annual average temperature, so that all the M. edulis shells could be used locally for this purpose.
The carbon isotope composition of mollusc shells depends mostly on dissolved inorganic carbon (DIC) isotopic composition and the metabolic CO2 amount involved in shell calcification [59,68,69]. Significant offsets compared to isotopic equilibrium conditions are reported for different species, and these offsets are generally species-dependent [70,71,72]. The carbon isotope composition of M. edulis has been used in the past for tracking changes in DIC isotopic composition and salinity related to mixing processes between different water masses [60,73]. For M. edulis, Wanamaker et al. [60] found that δ13C values were substantially lower than predicted values at equilibrium [52] and that the differences between the δ13C measured and the δ13C at the isotopic equilibrium increased with increasing salinity. According to [74], the incorporation of different amounts of metabolic CO2 in M. edulis can reduce the use of δ13C as an indicator of DIC and salinity, but may be useful to assess metabolic differences between different populations. However, it can be used as an indicator of large δ13C changes in the isotopic composition of DIC and of salinity. In our case, the use of δ13C data was further complicated by the use of other Mytilidae species for which experimental data are not available (see Table 5). However, no great differences seem to be present in the whole set of data. Therefore, no dramatic changes seem to have occurred in the DIC of the area, which may also support relatively minor changes in seawater salinity, with no substantial mix with fresher or saltier waters.
However, the most relevant and interesting features of the isotopic data regard the high δ18O values shown by samples older than ca. 6100 cal yr BP (Figure 4). Before ca. 6100 cal a BP, the average δ18O value is +2.4 ± 0.2‰, whereas the average value for younger samples (including the modern ones) is +1.3 ± 0.2‰. According to Equation (1), this corresponds to a lower temperature (ca. 5 °C) for the samples older than 6100 a cal BP if no change has occurred in the isotopic composition of seawater. The eustatic sea-level component for the last ca. 7000 a shows no significant variations that could justify great changes in seawater isotopic composition [64]. However, an estimation of ca. 5 °C cooler water is probably a maximum value, without considering any changes in salinity. However, it is of particular interest to note that, associated with the larger changes in the δ18O values at ca. 6.1 cal ka BP, there are no equivalent changes in the δ13C of the mollusc shells, suggesting that the no particular changes in seawater condition (i.e., salinity and DIC) occurred.
This estimated temperature value may contrast with paleontological evidence, which suggest ca. 1–3 °C warmer waters for this part of Patagonia during the middle Holocene [75]. However, the period of warmer temperatures inferred from mollusc analyses is not chronologically well-constrained and it may have occurred in some unsampled periods because of the discontinuity in our chronological records. For instance, model simulations tend to place the Holocene thermal optimum at high latitudes in the Southern hemisphere between ca. 6000 and 3000 cal a BP [73]. However, our isotopic data do not support specific warmer intervals compared to the present conditions for the investigated record, if the data are simply interpreted in terms of temperature changes.
On the other hand, the higher isotopic composition recorded in the period before ca. 6.1 cal ka BP might have been due to changes in salinity (i.e., more evaporated waters). By assuming no significant changes in surface temperature compared to the present conditions, we can calculate seawater δ18O values of ca. +1.4‰ (Equation (1)), which appear unrealistic for the present-day distribution of isotopic seawater composition [13], and these values should be accompanied by more unrealistic changes in salinity (ca. 48‰, from Equation (2)). Therefore, a plausible explanation is that most of the changes in the measured δ18O values were driven by temperature, even if we cannot rule out a minor change in local salinity, which is not completely supported by carbon isotopic composition.
Considering that temperature could be the main component, the only reliable explanation for such great mutations in temperature is a change in the energy and influence of the Falkland Current in the area. According to [4], the shift in the position of the Brazilian and Malvinas currents confluence occurred several times during the Holocene, as indicated by stable isotopes in the G. inflata of the marine GeoB13862-1 core (Figure 5C).
In particular, before ca. 6 cal ka BP, there was a tendency toward a northward position of the confluence zone. This may have produced a major and stronger influence of the Falkland current in the Camarones area, which rendered the seawater cooler than in younger periods. Warmer sea conditions might have occurred later during a period of maximum southward shift in the confluence zone between 4.5 and 5.5 cal ka BP (Figure 5C), thus favouring the penetration and survival of warmer marine mollusc association, as indicated by paleontological studies [75]. The northward position of the confluence before ca. 6.1 cal ka BP might have decreased the temperature with no major changes in terms of isotopic sea-water composition compared to the present-day conditions. According to [13], local seawater oxygen isotopic composition does not show an important isotopic gradient over the influence of the Falkland current, as also observable in marine core data [4]. Voigt et al. [4] interpreted the change in the position of current confluence as a consequence of the change in the position and strength of the South Westerly Winds. In this perspective, it is worth considering the correlation with the oxygen isotope composition of carbonates from the Laguna Potrok Aike ([73], Figure 5B) in southern Patagonia. This proxy is interpreted as an indication of the strength and position of the southern westerlies. According to [73], progressive warming after the Last Glacial Maximum produced weak Westerlies during the Lateglacial and early Holocene, interrupted by an interval with strengthened Westerlies between ca. 13.4 and 11.3 cal ka BP. Wind strength increased at 9.2 cal ka BP and significantly intensified until 7.0 cal ka BP. Subsequently, wind intensity diminished and stabilised to conditions similar to those of the present day (Figure 5B).
If our interpretation is correct, the oxygen isotope data obtained for the Mytilidae shells collected from the Camarones area support the hypothesis according to which the intensity changes in the Falkland Current during the Holocene may have been driven by the changes in the position of the Westerlies (Figure 5). The continental and marine proxies selected and shown in Figure 5 [4,73] are consistent with this interpretation.
According to [76], several proxy records of southernmost Patagonia show an Early Holocene thermal maximum between ca. 11.5 and 8.5 ka and lower temperatures during the last 8 ka. For this sector of the Atlantic coast of Patagonia, our data show a warming after ca. 6 cal ka BP, suggesting that in this sector, the effect of the Falkland current delayed the occurrence of a ‘thermal maximum’ of some millennia.

6. Conclusions

The oxygen isotope composition of the Mytilidae collected near the Camarones village shows that important changes occurred between ca. 6800 and 6100 cal a BP. Analysis of the data seems to suggest that this condition may have been related to important changes in temperature, probably at a maximum of ca. 5 °C. This change is likely to have been caused by a northward shift in the position of the confluence of the Falkland and Brazilian currents, driven by a change in the strength and position of the Westerlies. According to the isotopic data presented in our paper, the presence of mollusc association, indicating warmer conditions (1–3 °C) during the middle Holocene, was probably younger than ca. 6800 cal a BP. However, the low resolution achieved in this pilot study and the poor chronological constraint for mollusk association do not allow us to be more precise. However, these data indicate that raised marine terraces over the Patagonian coast may contain valuable paleoceanographic information, which can be improved in resolution for the Holocene and extended back to the older Interglacial.

Author Contributions

Conceptualization, G.B., I.C. and G.Z.; methodology, I.C., I.B., G.B. and G.Z.; validation, I.B., M.G., I.I., F.T. and L.D.; formal analysis, I.C., I.B., M.G., E.R., F.T. and L.D.; investigation (including field work), I.C., G.B., G.Z., I.B., I.I., M.B. and L.R.; resources, G.Z., M.G. and L.D.; data management, I.C., I.I., M.B. and G.B.; original draft preparation, I.C., G.B. and G.Z.; supervision, G.Z.; project administration, G.Z.; funding acquisition, G.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This work was funded by the University of Pisa (Progetto Ateneo 2007, Leader G. Zanchetta; Progetto Ateneo PRA 2015 Leader G. Zanchetta) and MIUR (PRIN2008, Leader G. Zanchetta

Acknowledgments

We wish to thank J. Cause and the no-profit CADACE organization for the logistical support provided in the field campaign.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Peterson, R.G.; Stramma, L. Upper-level circulation in the South Atlantic Ocean. Prog. Oceanogr. 1991, 26, 1–73. [Google Scholar] [CrossRef] [Green Version]
  2. Stramma, L.; England, M. On the water masses and mean circulation of the South Atlantic Ocean. J. Geophys. Res. 1999, 104, 863–883. [Google Scholar] [CrossRef]
  3. Laprida, C.; Chapori, N.G.; Chiessi, C.M.; Violante, R.A.; Watanabe, S.; Totah, V. Middle Pleistocene sea surface temperature in the Brazil-Malvinas Confluence Zone: Paleoceanographic implications based on planktonic foraminifera. Micropaleontology 2011, 57, 183–194. [Google Scholar]
  4. Voigt, I.; Chiessi, M.C.; Prange, M.; Mulitza, S.; Groeneveld, J.; Varma, V.; Henrich, R. Holocene shifts of the westerlies across the South Atlantic. Paleoceanography 2015. [Google Scholar] [CrossRef] [Green Version]
  5. Lumpkin, R.; Garzoli, S. Interannual to decadal changes in the western South Atlantic’s surface circulation. J. Geophys. Res. 2011, 116, C01014. [Google Scholar] [CrossRef] [Green Version]
  6. Aguirre, M.L.; Whatley, R.C. Late Quaternary marginal marine deposits from north-eastern Buenos Aires Province, Argentina: A review. Quat. Sci. Rev. 1995, 14, 223–254. [Google Scholar] [CrossRef]
  7. Aguirre, M.L. Late Pleistocene and Holocene palaeoenvironments in Golfo San Jorge, Patagonia: Molluscan evidence. Mar. Geol. 2003, 194, 3–30. [Google Scholar] [CrossRef]
  8. Aguirre, M.L.; Sirch, Y.N.; Richiano, S. Late Quaternary molluscan assemblages from Bahía Bustamante coastal area (Patagonia, Argentina): Palaeoecology and palaeoenvironments. J. S. Am. Earth Sci. 2005, 20, 13–32. [Google Scholar] [CrossRef]
  9. Aguirre, M.L.; Perez, S.; Sirch, Y.N. Morphological variability of Brachidontes swainson (Bivalvia, Mytilidae) in the marine Quaternary of Argentina (SW Atlantic). Palaeogeogr. Palaeoclimatol. Palaeoecol. 2005, 239, 100–125. [Google Scholar] [CrossRef]
  10. Aguirre, M.L.; Richiano, S.; Sirch, Y.N. Palaeoenvironments and palaeoclimates of the Quaternary molluscan faunas from the coastal area of Bahía Vera- Camarones (Chubut, Patagonia). Palaeogeogr. Palaeoclimatol. Palaeoecol. 2006, 229, 251–286. [Google Scholar] [CrossRef]
  11. Aguirre, M.L.; Donato, M.; Richiano, S.; Farinati, E.A. Pleistocene and Holocene interglacial molluscan assemblages from Patagonian and Bonaerensian littoral (Argentina, SW Atlantic): Palaeobiodiversity and palaeobiogeography. Palaeogeogr. Palaeoclimatol. Palaeoecol. 2011, 308, 277–292. [Google Scholar] [CrossRef]
  12. Schmidt, G.-A.; Bigg, G.-R.; Rohling, E.J. Global Seawater Oxygen-18 Database. 1999. Available online: http://www.giss.nasa.gov/data/o18/data/ (accessed on 6 January 2019).
  13. LeGrande, A.N.; Schmidt, G.A. Global gridded data set of the oxygen isotopic composition in seawater. Geophys. Res. Lett. 2006, 33, L12604. [Google Scholar] [CrossRef] [Green Version]
  14. Chiessi, C.M.; Ulrich, S.; Mulitza, S.; Pätzold, J.; Wefer, G. Signature of the Brazil-Malvinas Confluence (Argentine Basin) in the isotopic composition of planktonic foraminifera from surface sediments. Mar. Micropaleontol. 2007, 64, 52–66. [Google Scholar] [CrossRef]
  15. Panarello, H. Oxygen-18 temperatures on present and fossil invertebrate shells from Tunel Site, Beagle Channel, Argentina. Quat. S. Am. Antarct. Penins. 1987, 5, 83–92. [Google Scholar]
  16. Aguirre, M.L.; Leng, M.; Spiro, B. Palaeoenvironmental interpretation of the isotopic composition (C, O, and Sr) of modern and Holocene Mactra isabelleana (Bivalvia) from the NE coastal area of Buenos Aires Province, Argentina. Holocene 1998, 8, 613–621. [Google Scholar] [CrossRef]
  17. Aguirre, M.L.; Zanchetta, G.; Fallick, A. Stable isotope composition of Littoridina australis from the coast of Buenos Aires Province, Argentina, during Holocene climatic fluctuations. Geobios 2002, 35, 79–80. [Google Scholar] [CrossRef]
  18. Obelic, B.; Àlvarez, A.; Argullós, I.; Piana, E.L. Determination of water palaeotemperature in the Beagle Channel (Argentina) during the last 6000 yr through stable isotope composition of Mytilus edulis shells. Quat. S. Am. Antarct. Penins. 1998, 11, 47–71. [Google Scholar]
  19. Bonadonna, F.P.; Leone, G.; Zanchetta, G. Stable isotope analysis on the last 30 ka molluscan fauna from pampa grassland, Bonaerense region, Argentina. Palaeogeogr. Palaeoclimatol. Palaeoecol. 1999, 153, 289–308. [Google Scholar] [CrossRef]
  20. Colonese, A.C.; Camaros, E.; Verdun, E.; Estèvez, J.; Giralt, S.; Rejas, M. Integrated archaeozoological research of shell middens: New insights into hunter-gatherer-fisher coastal exploitation in Tierra Del Fuego. J. Isl. Coast. Archaeol. 2011, 6, 235–254. [Google Scholar] [CrossRef]
  21. Colonese, A.C.; Verdún-Castelló, E.; Álvarez, M.; Godino, I.B.; Zurro, D.; Salvatelli, L. Oxygen isotopic composition of limpet shells from the Beagle Channel: Implications for seasonal studies in shell middens of Tierra del Fuego. J. Archaeol. Sci. 2012, 39, 1738–1748. [Google Scholar] [CrossRef]
  22. Boretto, G.; Consoloni, I.; Moran, G.A.; Regattieri, E.; Gordillo, S.; Fucks, E.; Zanchetta, G.; Dallai, L. Oxygen stable isotope analyses on Ameghinomya antiqua shells: A promising tool for palaeoenvironmental reconstruction along the Quaternary patagoinian Argentina coast? Alp. Mediterr. Quat. 2019, 32, 57–72. [Google Scholar]
  23. Aguirre, M.L.; Richiano, S.; Voelker, A.H.L.; Dettman, D.L.; Schone, B.R.; Panarello, H.O.; Donato, M.; Gomez Pera, L.; Castro, L.E.; Medina, R. Late Quaternary nearshore molluscan patterns from Patagonia: Windows to southern southwestern Atlantic-Southern Ocean. Glob. Planet. Chang. 2019, 181, 102990. [Google Scholar] [CrossRef]
  24. Lema, H.; Busteros, A.; Franchi, M. Hoja Geológica 4566-II y IV, Camarones (1:250.000); Programa Nacional de Cartas Geológicas de la República Argentina: Buenos Aires, Argentina, 2001; Volume 261, pp. 1–53. [Google Scholar]
  25. Martinez, O.A.; Coronato, A.M.J. The late Cenozoic fluvial deposits of Argentine Patagonia. Dev. Quat. Sci. 2008, 11, 205–226. [Google Scholar]
  26. Codignotto, J.O. Depósitos elevados y/o acrección Pleistoceno-Holoceno en la costa fueguino patagónia. In Proceedings of the Simp. Oscilaciones del Nivel del Mar el Ultima Hemiciclo Deglacial en la Argentina, Mar del Plata, Argentina, 6–7 April 1983; CIC; Universidad Nacional de Mar del Plata: Mar del Plata, Argentina, 1984; pp. 12–26. [Google Scholar]
  27. Codignotto, J.O.; Kokot, R.R.; Marcomini, S.C. Neotectonism and sea level changes in the coastal zone of Argentina. J. Coast. Res. 1992, 8, 125–133. [Google Scholar]
  28. Schellmann, G.; Radtke, U. ESR dating stratigraphically well-constrained marine terraces along the Patagonian Atlantic coast (Argentina). Quat. Int. 2000, 68/71, 261–273. [Google Scholar] [CrossRef]
  29. Schellmann, G.; Radtke, U. Coastal terraces and Holocene sea-level changes along the Patagonian Atlantic coast. J. Coast. Res. 2003, 19, 963–996. [Google Scholar]
  30. Schellmann, G.; Radtke, U. Timing and magnitude of Holocene sea-level changes along the middle and south Patagonian Atlantic coast derived from beach ridge systems, littoral terraces and valley-mouth terraces. Earth Sci. Rev. 2010, 103, 1–30. [Google Scholar] [CrossRef]
  31. Zanchetta, G.; Consoloni, I.; Isola, I.; Pappalardo, M.; Ribolini, A.; Aguirre, M.; Fucks, E.; Baneschi, I.; Bini, M.; Ragaini, L.; et al. New insights on the Holocene marine transgression in the Bahía Camarones (Chubut, Argentina). Ital. J. Geosci. 2012, 131, 19–31. [Google Scholar]
  32. Isola, I.; Bini, M.; Ribolini, A.; Pappalardo, M.; Consoloni, I.; Fucks, E.; Boretto, G.; Ragaini, L.; Zanchetta, G. Geomorphologic map of northeastern sector of San Jorge Gulf (Chubut, Argentina). J. Maps 2011, 7, 476–485. [Google Scholar] [CrossRef] [Green Version]
  33. Bini, M.; Isola, I.; Zanchetta, G.; Pappalardo, M.; Ribolini, A.; Ragaini, L.; Baroni, C.; Boretto, G.; Fuck, E.; Morigi, C.; et al. Middle Holocene relative sea-level along Atlantic Patagonia: New data from Camarones (Chubut, Argentina). Holocene 2018, 28, 56–64. [Google Scholar] [CrossRef] [Green Version]
  34. Coronato, M.J.; Coronato, F.; Mazzoni, E.; Vásquez, M. The physical geography of Patagonia and Tierra del Fuego. Dev. Quat. Sci. 2008, 11, 13–55. [Google Scholar]
  35. Isla, F.I.; Bujalesky, G.G. Coastal geology and geomorphology of Patagonia and Tierra del Fuego Archipelago. Dev. Quat. Sci. 2008, 11, 227–240. [Google Scholar]
  36. Tanner, W.F. Origin of beach ridges and swales. Mar. Geol. 1995, 129, 149–161. [Google Scholar] [CrossRef]
  37. Falabella, V.; Campagna, C.; Croxall, J. (Eds.) Atlas del Mar Patagónico. Especies y Espacios; Wildlife Conservation Society y BirdLife International: Buenos Aires, Argentina, 2009; Available online: http://www.atlas-marpatagonico.org (accessed on 15 January 2019).
  38. Terrasi, F.; De Cesare, N.; D’Onofrio, A.; Lubritto, C.; Marzaioli, F.; Passariello, I.; Rogalla, D.; Sabbarese, C.; Borriello, G.; Casa, G.; et al. High precision 14C AMS at CIRCE. Nucl. Instrum. Methods Phys. Res. Sect. B Beam Interact. Mater. At. 2008, 266, 2221–2224. [Google Scholar] [CrossRef]
  39. Terrasi, F.; Rogalla, D.; De Cesare, N.; D’Onofrio, A.; Lubritto, C.; Marzaioli, F.; Passariello, I.; Rubino, M.; Sabbarese, C.; Casa, G.; et al. A new AMS facility in Caserta/Italy. Nucl. Instrum. Methods Phys. Res. Sect. B Beam Interact. Mater. At. 2007, 259, 14–17. [Google Scholar] [CrossRef]
  40. Reimer, P.J.; Bard, E.; Bayliss, A.; Beck, J.W.; Blackwell, P.G.; Bronk Ramsey, C.; Buck, C.E.; Cheng, H.; Edwards, R.L.; Friedrich, M.; et al. INTCAL13 and MARINE13 radiocarbon age calibration curves 0–50,000 years cal BP. Radiocarbon 2013, 55, 1869–1887. [Google Scholar] [CrossRef] [Green Version]
  41. Cordero, R.R.; Panarello, H.; Lanzelotti, S.; Favier Dubois, C.M. Radiocarbon age offsets between living organisms from the marine and continental reservoir in coastal localities of Patagonia. Radiocarbon 2003, 45, 9–15. [Google Scholar] [CrossRef] [Green Version]
  42. Epstein, S.; Mayeda, T.K. Variations of oxygen-18 of waters from natural sources. Geochim. Cosmochima Acta 1953, 4, 213–224. [Google Scholar] [CrossRef]
  43. Seed, R.; Suchanek, T.H. Population and community ecology of Mytilus. In The Mussel Mytilus: Ecology, Physiology, Genetics and Culture; Gossling, E.M., Ed.; Elsevier: New York, NY, USA, 1992; pp. 87–170. [Google Scholar]
  44. Lozan, J.L.; Lampe, R.; Matthaus, W.; Rachor, E.; Rumhor, H.; Westernagen, H.V. (Eds.) Warnsignale aus der Ostsee: Wissenschaftliche Fakten; University of Hamburg, Institute of Hydrobiology: Hamburg, Germany, 1996; 385p. [Google Scholar]
  45. Almada-Villela, P.C.; Davenport, J.; Gruffydd, L.D. The effects of temperature on the shell growth of young Mytilus edulis L. J. Exp. Mar. Biol. Ecol. 1982, 59, 275–288. [Google Scholar] [CrossRef]
  46. Zaixso, H.E. Distribución submareal del mitílido Aulacomya atra atra (Molina) en el Golfo San José (Argentina) en relación a la profundidad, características del fondo y condiciones hidrográficas. Physis 1999, 57, 1–10. [Google Scholar]
  47. Morriconi, E. Reproductive biology of the limpet Nacella (P.) deaurata (Gmelin, 1791) in bahía Lapataia (Beagle Channel). Sci. Mar. 1999, 63, 417–426. [Google Scholar] [CrossRef]
  48. Gonzáles-Wevar, C.A.; Nakano, T.; Cañete, J.I.; Poulin, E. Concerted genetic, morphological and ecological diversification in Nacella limpets in the Magellanic Province. Mol. Ecol. 2011, 20, 1936–1951. [Google Scholar] [CrossRef] [PubMed]
  49. Carter, J.G. Skeletal Biomineralization Patterns and Evolutionary Trends; Van Nostrand Reinhold: New York, NY, USA, 1990; Volume 1, 832p. [Google Scholar]
  50. Tarutani, T.; Clayton, R.N.; Mayeda, T.K. The effect of polymorphism and magnesium substitution on oxygen isotope fractionation between calcium carbonate and water. Geochim. Cosmochim. Acta 1969, 33, 987–996. [Google Scholar] [CrossRef]
  51. Grossman, E.L.; Ku, T.-L. Oxygen and carbon isotope fractionation in biogenic aragonite: Temperature effect. Chem. Geol. 1986, 59, 59–74. [Google Scholar] [CrossRef]
  52. Romanek, C.S.; Grossman, E.L.; Morse, J.W. Carbon isotope fractionation in synthetic aragonite and calcite: Effects of temperature and precipitations rate. Geochim. Cosmochim. Acta 1992, 29, 1347–1353. [Google Scholar]
  53. Kim, S.-T.; O’Neil, J.R. Equilibrium and nonequilibrium oxygen isotope effect in synthetic carbonates. Geochim. Cosmochim. Acta 1997, 61, 3461–3475. [Google Scholar] [CrossRef]
  54. Shanahan, T.M.; Pigati, J.S.; Dettman, D.L.; Quade, J. Isotopic variability in the aragonite shells of freshwater gastropods living in springs with nearly constant temperature and isotopic composition. Geochim. Cosmochim. Acta 2005, 69, 3949–3966. [Google Scholar] [CrossRef]
  55. Craig, H. Measurement of oxygen isotope paleotemperatures. In Stable Isotopes in Oceanographic Studies and Paleotemperatures; Tongiorgi, E., Ed.; Consiglio Nazionale delle Ricerche: Spoleto, Italy, 1965; pp. 161–182. [Google Scholar]
  56. Wefer, G.; Berger, W.H. Isotope paleontology: Growth and composition of extant calcareous specie. Mar. Geol. 1991, 100, 207–248. [Google Scholar] [CrossRef]
  57. Schöne, B.R.; Oschmann, W.; Kröncke, I.; Dreyer, W.; Janssen, R.; Rumohr, H.; Houk, S.D.; Freyre Castro, A.D.; Dunca, E.; Rössler, J. North Atlantic Oscillation dynamics recorded in shells of a long-lived bivalve mollusk. Geology 2003, 31, 1037–1040. [Google Scholar] [CrossRef]
  58. McConnaughey, T. 13C and 18O isotopic disequilibrium in biological carbonates: II. In vitro simulation of kinetic isotope effects. Geochim. Cosmochim. Acta 1989, 53, 163–171. [Google Scholar] [CrossRef]
  59. McConnaughey, T.A.; Burdett, J.; Whelan, J.F.; Paull, C.K. Carbon isotopes in biological carbonates: Respiration and photosynthesis. Geochim. Cosmochim. Acta 1997, 61, 611–622. [Google Scholar] [CrossRef]
  60. Wanamaker, A.D.; Kreutz, K.J.; Borns, H.W.; Introne, D.S.; Feindel, S.; Funder, S.; Rawson, P.D.; Barber, B.J. Experimental determination of salinity, temperature, growth, and metabolic effects on shell isotope chemistry of Mytilus edulis collected from Maine and Greenland. Paleoceanography 2007, 22, PA2217. [Google Scholar] [CrossRef]
  61. Daëron, M.; Drysdale, R.N.; Peral, M.; Huyghe, D.; Blamart, D.; Coplen, T.B.; Lartaud, F.; Zanchetta, G. Most Earth-surface calcites precipitate out of isotopic equilibrium. Nat. Commun. 2019, 10, 429. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  62. Shackleton, N.J. Oxygen isotopes, ice volume and sea level. Quat. Sci. Rev. 1987, 6, 183–190. [Google Scholar] [CrossRef]
  63. Shakun, J.D.; Lea, D.W.; Lisiecki, L.E.; Raymo, M.E. An 800-kyr record of global surface ocean δ18O and implications for ice volume-temperature coupling. Earth Planet. Sci. Lett. 2015, 426, 58–68. [Google Scholar] [CrossRef] [Green Version]
  64. Lambeck, K.; Rouby, H.; Purcell, A.; Sun, Y.; Sambridge, M. Sea level and global ice volumes from the last glacial maximum to the Holocene. Proc. Natl. Acad. Sci. USA 2014, 111, 15296–15303. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Ingram, B.L.; Ingle, J.C.; Conrad, M.E. Stable isotope record of late Holocene salinity and river discharge in San Francisco Bay. California. Earth Planet. Sci. Lett. 1996, 141, 237–247. [Google Scholar] [CrossRef]
  66. Lécuyer, C.; Reynard, B.; Martineau, F. Stable isotope fractionation between mollusk shells and marine waters from Martinique Island. Chem. Geol. 2004, 213, 293–305. [Google Scholar] [CrossRef]
  67. Yan, L.; Schöne, B.R.; Arkhipkin, A. Eurhomalea exalbida (Bivalvia): A reliable recorder of climate in southern South America? Palaeogeogr. Palaeoclimatol. Palaeoecol. 2012, 250–252, 91–100. [Google Scholar] [CrossRef]
  68. McConnaughey, T.A.; Gillikin, D.P. Carbon isotopes in mollusk shell carbonates. Geo Mar. Lett. 2008, 28, 287–299. [Google Scholar] [CrossRef]
  69. Geist, J.; Auerswald, K.; Boom, A. Stable carbon isotopes in freshwater mussel shells: Environmental record or marker for metabolic activity? Geochim. Cosmochim. Acta 2005, 69, 3545–3554. [Google Scholar] [CrossRef]
  70. Baroni, C.; Zanchetta, G.; Fallick, A.E.; Longinelli, A. Molluscs stable isotope record of a core from Lake Frassino (northern Italy): Hydrological and climatic changes during the last 14 ka. Holocene 2006, 16, 827–837. [Google Scholar] [CrossRef]
  71. Dettman, D.L.; Reische, A.K.; Lohmann, K.C. Controls on the stable isotope composition of seasonal growth bands in aragonitic fresh-water bivalves (unionidae). Geochim. Cosmochim. Acta 1999, 63, 1049–1057. [Google Scholar] [CrossRef]
  72. Mook, W.G. Paleotemperatures and chlorinities from stable carbon and oxygen isotopes in shell carbonate. Palaeogeogr. Palaeoclimatol. Palaeoecol. 1971, 9, 245–263. [Google Scholar] [CrossRef]
  73. Oehlerich, M.; Mayr, C.; Griesshaber, E.; Lücke, A.; Oeckler, O.M.; Ohlendorf, C.; Wolfgang, W.; Schmahl, W.W.; Zolitschka, B. Ikaite precipitation in a lacustrine environment e implications for palaeoclimatic studies using carbonates from Laguna Potrok Aike (Patagonia, Argentina). Quat. Sci. Rev. 2013, 71, 46–53. [Google Scholar] [CrossRef]
  74. Gillikin, D.A.; Lorrain, A.; Bouillon, S.; Willenz, P.; Dehairs, F. Stable carbon isotopic composition of Mytilus edulis shells: Relation to metabolism, salinity, δ13CDIC and phytoplankton. Org. Geochem. 2006, 37, 1371–1382. [Google Scholar] [CrossRef] [Green Version]
  75. Aguirre, M.L.; Richiano, S.; Álvarez, M.F.; Eastoe, C. Malacofauna Cuaternaria del litoral norte de Santa Cruz (Patagonia, Argentina). Geobios 2009, 42, 411–434. [Google Scholar] [CrossRef]
  76. Kilian, R.; Lamy, F. A review of Glacial and Holocene paleoclimate records from southernmost Patagonia (49–55 degrees S). Quat. Sci. Rev. 2012, 53, 1–23. [Google Scholar] [CrossRef]
Water 12 03464 g001 550
Figure 1. (a) General location map, with the position of the Falkland and Brazilian currents; (b) position of living and fossil shells collected in the study area; (c) Holocene sections sampled along the Camarones coast projected on Quick bird image. Labels correspond to those in Table 1.
Figure 1. (a) General location map, with the position of the Falkland and Brazilian currents; (b) position of living and fossil shells collected in the study area; (c) Holocene sections sampled along the Camarones coast projected on Quick bird image. Labels correspond to those in Table 1.
Water 12 03464 g001
Water 12 03464 g002 550
Figure 2. (A) Examples of shell accumulation over the Patagonian beaches; (B) examples of fossil storm accumulation.
Figure 2. (A) Examples of shell accumulation over the Patagonian beaches; (B) examples of fossil storm accumulation.
Water 12 03464 g002
Water 12 03464 g003 550
Figure 3. Oxygen and carbon isotope composition for fossil shells. Median calibrated radiocarbon age is reported for each group.
Figure 3. Oxygen and carbon isotope composition for fossil shells. Median calibrated radiocarbon age is reported for each group.
Water 12 03464 g003
Water 12 03464 g004 550
Figure 4. Oxygen and carbon isotope composition for fossil shells. Median calibrated radiocarbon age for each group is reported.
Figure 4. Oxygen and carbon isotope composition for fossil shells. Median calibrated radiocarbon age for each group is reported.
Water 12 03464 g004
Water 12 03464 g005 550
Figure 5. (A) Oxygen isotope records from this work plotted against isotopic composition of G. inflata [4] in the Brazilian and Falkland confluence zone (C) and oxygen isotopic composition of carbonates from laguna Potro Aike (B) [73].
Figure 5. (A) Oxygen isotope records from this work plotted against isotopic composition of G. inflata [4] in the Brazilian and Falkland confluence zone (C) and oxygen isotopic composition of carbonates from laguna Potro Aike (B) [73].
Water 12 03464 g005
Table
Table 1. Radiocarbon dating.
Table 1. Radiocarbon dating.
SampleField Code14C a BP
(±2σ)		14C cal a BP
(±2σ)
(Median Probability)		Species
UCI65211WP60B *390 ± 50-Aulacomya atra
UCI65210WP60A **915 ± 20477–560
(518)		Aulacomya atra
DSH2167G002 ** 14070 ± 503948–4271
(4106)		Nacella (Patinigera) deaurata
DSH2738AO154D5132 ± 675313–5608
(5493)		Mytilus edulis
DSH2745WPi4365562 ± 435861–6092
(5949)		Mytilus edulis
DSH2734WP104B5675 ± 455947–6196
(6080)		Mytilus edulis
UCI65213WP63B **6365 ± 206750–6913
(6834)		Mytilus edulis
DSH4026AO1906486 ± 466867–7138
(6990)		Mytilus edulis
Calibration following Reimer et al. [40]. * Modern specimen; ** After Zanchetta et al. [31]; 1 Shellmidden.
Table
Table 2. Stable isotope composition (oxygen and carbon) of modern samples collected along the S. Jorge Gulf (see Figure 1b for position).
Table 2. Stable isotope composition (oxygen and carbon) of modern samples collected along the S. Jorge Gulf (see Figure 1b for position).
Localityδ13C‰ (V-PDB)δ18O‰ (V-PDB)
Camarones North
Aulacomya atra
1.81.4
1.91.0
2.01.3
1.41.3
2.01.2
1.31.4
Mean1.7 ± 0.31.3 ± 0.2
Camarones South
Aulacomya atra1.11.4
1.41.5
1.61.3
0.51.0
1.91.5
Mean1.3 ± 0.51.4 ± 0.2
Mytilus edulis
1.40.9
1.41.2
Mean1.4 ± 0.01.0 ± 0.1
Bahia Bustamante
Aulacomya atra
1.31.3
1.81.2
1.81.4
1.81.2
Mean1.7 ± 0.21.3 ± 0.1
Mytilus edulis
1.70.9
1.71.0
1.61.0
1.50.8
Mean 1.6 ± 0.10.9 ± 0.1
Bahia Bustamante South
Aulacomya atra
1.81.3
1.81.6
1.41.4
1.61.6
1.71.6
Mean1.7 ± 0.11.5 ± 0.2
Bahia Solano
Aulacomya atra
1.71.5
1.61.1
Mean1.7 ± 0.01.3 ± 0.2
Mytilus edulis
1.61.7
1.41.0
1.71.0
Mean1.6 ± 0.11.2 ± 0.4
Rada Tilly
Aulacomya atra
2.21.4
2.21.2
1.71.5
2.31.5
Mean2.1 ± 0.31.4 ± 0.1
Mytilus edulis
1.81.2
1.31.0
1.31.2
Mean1.5 ± 0.31.1 ± 0.1
Caleta Olivia
Aulacomya atra
1.51.5
1.71.5
1.91.7
1.91.7
1.51.5
1.61.4
Mean1.6 ± 0.21.6 ± 0.1
Table
Table 3. Isotopic composition (oxygen and carbon) from samples from Holocene sections along the Camarones coastal area. For location see Figure 1c.
Table 3. Isotopic composition (oxygen and carbon) from samples from Holocene sections along the Camarones coastal area. For location see Figure 1c.
Speciesδ13C‰ (V-PDB)δ18O‰ (V-PDB)Age (a BP)
Aulacomya atra2.21.4915 ± 20
2.71.6
2.31.2
2.31.3
2.11.0
1.71.4
2.31.4
1.51.4
2.01.6
Mean2.1 ± 0.41.4 ± 0.2
Brachidontes purpuratus2.51.3
Aulacomya atra1.81.14074 ± 50
1.61.1
1.61.2
1.21.1
Mean1.6 ± 0.31.2 ± 0.02
Patinigera deaurata1.11.4
1.21.2
Mean1.2 ± 0.01.3 ± 0.1
Mytilus edulis1.71.35132 ± 67
1.71.3
Mean1.7 ± 0.01.3 ± 0.15
Mytilus edulis1.91.25562 ± 43
1.91.22
Mean1.9 ± 0.01.2 ± 0.0
Mytilus edulis2.61.35675 ± 45
2.81.5
2.41.1
2.81.2
Mean2.6 ± 0.21.3 ± 0.2
Mytilus edulis2.12.56350 ± 20
2.12.4
2.72.5
2.22.2
1.82.2
2.22.5
2.02.2
2.52.7
Mean2.2 ± 0.32.4 ± 0.2
Mytilus edulis1.82.46486 ± 46
1.92.3
1.72.5
2.12.2
Mean1.9 ± 0.22.3 ± 0.2
Table
Table 4. Oxygen isotope composition, temperature, salinity and pH of seawater collected along the Camarones coast.
Table 4. Oxygen isotope composition, temperature, salinity and pH of seawater collected along the Camarones coast.
Lat.Long.Date of SamplingConductibility (25 °C mS)pHCl
(ppm)		T
(°C)		δ18O
V-SMOW (‰)
S44°42′51″O065°40′31.80″2/201144.448.04-18.5−1.07
S44°42′51″O065°40′31.80″2/2010--18,710-−0.66
S44°50′19.5″O065°43″05.1″2/201148.588.1018,92321.5−0.38
S44°52′54.7″O065°40′12.0″2/201145.518.0418,88718.50.03
S45°04″23.6″O066°26′46.8″2/201142.368.0219,03017.5−0.40
S44°59′12.1″O066°11′50.9″2/201143.458.0318,85215.6−0.41
Table
Table 5. Average isotopic differences between Mytilus edulis and Aulacomya atra in different localities of S. Jorge Gulf.
Table 5. Average isotopic differences between Mytilus edulis and Aulacomya atra in different localities of S. Jorge Gulf.
Localityδ18OMytilus-δ18OAulacomya (‰)δ13CMytilus-δ13CAulacomya (‰)
Camarones South−0.310.07
Bahia Bustamante−0.38−0.05
Bahia Solano0.030.35
Rada Tilly−0.27−0.65
Mean−0.23 ± 0.18−0.07 ± 0.42
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Boretto, G.; Zanchetta, G.; Consoloni, I.; Baneschi, I.; Guidi, M.; Isola, I.; Bini, M.; Ragaini, L.; Terrasi, F.; Regattieri, E.; et al. Stable Oxygen and Carbon Isotope Composition of Holocene Mytilidae from the Camarones Coast (Chubut, Argentina): Palaeoceanographic Implications. Water 2020, 12, 3464. https://doi.org/10.3390/w12123464

AMA Style

Boretto G, Zanchetta G, Consoloni I, Baneschi I, Guidi M, Isola I, Bini M, Ragaini L, Terrasi F, Regattieri E, et al. Stable Oxygen and Carbon Isotope Composition of Holocene Mytilidae from the Camarones Coast (Chubut, Argentina): Palaeoceanographic Implications. Water. 2020; 12(12):3464. https://doi.org/10.3390/w12123464

Chicago/Turabian Style

Boretto, Gabriella, Giovanni Zanchetta, Ilaria Consoloni, Ilaria Baneschi, Massimo Guidi, Ilaria Isola, Monica Bini, Luca Ragaini, Filippo Terrasi, Eleonora Regattieri, and et al. 2020. "Stable Oxygen and Carbon Isotope Composition of Holocene Mytilidae from the Camarones Coast (Chubut, Argentina): Palaeoceanographic Implications" Water 12, no. 12: 3464. https://doi.org/10.3390/w12123464

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop