Investigations of subsurface flow constructed wetlands and associated geomaterial resources in the Akumal and Reforma regions,Quintana Roo,Mexico

Subsurface flow constructed wetlands in the village of Akumal, Quintana Roo, Mexico were surveyed to determine the general status of the wetland systems and provide baseline information for long term monitoring and further study. Twenty subsurface flow wetlands were surveyed and common problems observed in the systems were overloading, poor plant cover, odor, and no secondary containment. Bulk mineral composition of aggregate from two subsurface flow constructed wetlands was determined to consist solely of calcite using bulk powder X-ray diffraction. Some soil structure is developed in the aggregate and aggregate levels in wetlands drop at an estimated rate between 3 and 10 cm/year for overloaded wetlands owing to dissolution. Mineral composition from fresh aggregate samples commonly is a mixture of calcite and aragonite. Trace amounts of Pb, Zn, Co, and Cr were observed in fresh aggregate. Coefficients of permeability (k) varied from 0.006 to 0.027 cm/s with an average values being 0.016 cm/s. Grain size analysis of fresh aggregate samples indicates there are unimodal and multimodal size distributions in the samples with modes in the coarse and fine sand being common. Investigations of other geologic media from the Reforma region indicate that a dolomite with minor amounts of Fe-oxide and palygorskite is abundant and may be a better aggregate source that the current materials used. A Ca-montmorillonite bed was identified in the Reforma region as well and this unit is suitable to serve as a clay liner to prevent leaks for new and existing wetland systems. These newly discovered geologic resources should aid in the improvement of subsurface flow constructed wetlands in the region. Although problems do exist in these wetlands with respect to design, these systems represent a successful implementation of constructed wetlands at a community level in developing regions.     

Ca-Mg inter-diffusion in synthetic polycrystalline dolomite-calcite aggregate at elevated temperatures and pressure

This study measures the reaction rate of dolomite and aragonite (calcite) into Mg-calcite at 800, 850, and 900°C and 1.6 GPa. The dry synthetic dolomite-aragonite aggregate transformed very rapidly into dolomite-calcite polycrystalline aggregate while Mg-calcites formed at a relatively slow rate, becoming progressively richer in Mg with run time. We modeled the reaction progress semi-empirically by the first-order rate law. The temperature dependence of the overall transport rate of MgCO₃ into calcite can be described by the kinetic parameters (E?=?231.7 kJ/mol and A _o ?=?22.69 h^?1). Extrapolation using the Arrhenius equation to the conditions during exhumation of UHPM rocks indicates that the reaction of dolomite with aragonite into Mg-saturated calcite can be completed as the P-T path enters the Mg-calcite stability field in a geologically short time period (<1 Ky). On the other hand, the extrapolation of the rate to prograde metamorphic conditions reveals that the Mg-calcite formed from dolomitic marble in the absence of metamorphic fluid may not reach Mg-saturation until temperatures corresponding to high-grade metamorphism (e.g., >340°C and >10 My). SEM-EDS analysis of individual calcite grains shows compositional gradients of Mg in the calcite grains. The Mg-Ca inter-diffusion coefficient at 850°C is around 1.68?×?10^?14 m²/sec if diffusion is the major control of the reaction. The calculated closure temperatures for Ca-Mg inter-diffusion as a function of cooling rate and grain size reveal that Ca/Mg resetting in calcite in a dry polycrystalline carbonate aggregate (with grain size around 1 mm) may not occur at temperatures below 480°C at a geological cooling rate around 10°C/My, unless other processes, such as short-circuit interdiffusion along grain boundaries and dislocations, are involved.     

Variation in production,input and preservation of metastable calcium carbonate off Somalia during the last 90,000 years

To improve our understanding of the Late Pleistocene and Holocene carbonate system of the western Arabian Sea a high-resolution sedimentary record off Somalia has been analysed. The 15.26-m-long piston core 905 comprises a complete record of the last 90,000 years. We have measured concentrations of carbonate minerals, i.e., aragonite, calcite, Mg-calcite, and element ratios (Sr/Ca) together with pteropod counts and an estimation of the preservation state of pteropod shells to trace temporal changes in carbonate production and preservation.The Sr/Ca ratio shows strong similarities to the aragonite percentage and the δ¹⁸O record of the planktic foraminifer Neogloboquadrina dutertrei. High Sr/Ca ratios together with fragments of corals found in the coarse fraction indicate that most of the aragonite is of shallow water origin (high-Sr aragonite) and pteropods contribute much less than expected. High resuspensional input of shallow-marine aragonite occurs during sea-level highstands (interglacials) and low input during lowstands (glacials).The Mg-calcite concentration record resembles the whole pteropod abundance and pteropod shell preservation records confirming the use of Mg-calcite in combination with pteropod preservation proxies to reconstruct past fluctuations in carbonate dissolution. Preservation of aragonite and Mg-calcite increases during stadials, H-equivalents, YD and late Marine Isotope Stage (MIS) 3. During late MIS 5/early MIS 4 and in the Late Holocene absence of few pteropods as well as low Mg-calcite weight percentages point to strong dissolution of aragonite and Mg-calcite.     

Polycrystalline calcite to aragonite transformation kinetics: experiments in synthetic systems

The kinetics of the calcite to aragonite transformation have been investigated using synthetic polycrystalline calcite aggregates, with and without additional minerals present. The reaction progresses as a function of time were measured at four temperature/pressure conditions: (1) 550 °C/1.86 GPa; (2) 600 °C/2.11 GPa; (3) 650 °C/2.11 GPa, and (4) 700 °C/2.29 GPa. Experiments reveal that Mg-calcite and Fe-calcite transforms to aragonite at considerably slower rates than pure calcite, and that Sr-bearing calcite and calcite + quartz aggregates transform at significantly higher rates than pure calcite. The reaction progresses vs. time data for pure calcite were fitted to Cahns grain-boundary nucleation and interface-controlled growth model. Evidence for interface-controlled growth is provided by petrographic observations of grain boundaries. The activation energy for aragonite growth from the synthetic polycrystalline calcite determined in this study is significantly lower than that previously determined from a natural marble. The discrepancy in rates and activation energy may be attributed to the nature of grain boundaries, to deformational strain or the presence of impurities in the studied samples, and likely to uncertainties in experimental conditions. The results of this study imply that the variation of local petrologic conditions, in addition to temperature, pressure and grain size, may play an important role in determining the rates for the calcite to aragonite transformation in nature.Editorial responsibility: W. Schreyer     

Carbonate cementation of some Pleistocene temperate marine sediments

Carbonate cementation of some carbonate and quartz sands in three raised beaches of temperate origins was investigated. The carbonate of the cements was found to have been derived from the dissolution of skeletal debris. The sandstones, so produced, now possess only low-magnesium calcite, but the original sediments, like adjacent modern beach and blown sands, probably contained low-magnesium calcite, aragonite and some high-magnesium calcite, all of skeletal origin. In meteoric water the dissolution has occurred of all carbonate within minute, tubulelike, volumes of sand. Concurrent deposition in adjacent volumes of sand of low-magnesium calcite formed cements that are irregularly nodular or uneven on a small scale. Aragonite within the minute nodules has been replaced paramorphically by low-magnesium calcite. Additional local carbonate cements were formed at later dates, around and within solution pipes.     

Hydrochemistry of waters from five cenotes and evaluation of their suitability for drinking-water supplies, northeastern Yucatan, Mexico

 Waters from five cenotes that are currently being used for aquatic recreational activities and that lie along the Cancun–Tulum touristic corridor, Mexico, were evaluated hydrochemically to determine whether the cenotes may be considered as potential drinking-water sources. Several parameters exceed the Mexican Drinking Water Standards (MDWS), but since they do not pose a significant health threat, four of the five cenotes may be used as drinking-water sources. The common contaminants in the Yucatan Peninsula, fecal coliforms and nitrate, are in most cases below the MDWS (0–460 MPN/100 ml and 0.31–1.18 mg/L, respectively). Although these four cenotes meet the MDWS, a careful groundwater management policy needs to be developed to avoid contamination (fecal and nitrates) and salt-water intrusion. Received, October 1996 Revised, June 1997; March 1998 Accepted, July 1997     

海南岛全新世海滩岩

在海南岛及邻近小岛沿岸,往往可以发现现代潮间带海滩上的砂砾石沉积物已被胶结成岩的现象。同样,全新世中、晚期形成的各种类型的滨海相沉积物,也经常程度不同地胶结起来了。     

Aragonitische Lumachellen im bituminösen Wealden des Emslandes

In the Wealden beds of the Dalum oil pool (NW-Germany), cycles of the following composition have been deposited especially on synsedimentary uplifts: Bituminous shales (at the base) — shales with cyrena layers — cyrena coquinas (at the top). The cyrena and gastropod shells are preserved in aragonite, if they are embedded in shale or surrounded by oil, which stopped the diagenesis. Water saturated coquinae, poor in clay, are always calcitisated. As a consequence, the transformation aragonite → calcite should have been performed by solution and recrystallisation. Only in aragonitic shells, organic structures are visible by fluorescence microscopy. In the bituminous shales, admixtures of Mg-calcite have been preserved sporadically.     

Aragonite laminae in hot water travertine crusts, Rapolano Terme, Italy

Small (5–30 μm) aggregates of aragonite needles occur in calcite crystal crusts of present day hot water slope travertines at Rapolano Terme in Tuscany, Italy. The aggregates are mainly concentrated in irregular, wispy and dark laminae which cross-cut calcite crystal feathers to create a pervasive millimetre scale banded appearance in the deposit; they also occur less commonly scattered irregularly through the calcite layers. The aragonite needle aggregates are in the form of crosses, fascicles (sheaf shaped bundles, or dumbbell shaped), rosettes and spherulites. Locally, irregular masses of needles also occur. The fascicles, rosettes and spherulites have hollow centres which resemble microbial components (?fungal spores, bacterial colonies and pollen), suggesting that the aragonite crystals are biotically nucleated. The lamination is interpreted to reflect diurnal control. Stimulation of microbial activity during daylight concentrates cells in laminae and promotes aragonite calcification. Calcite feather crystals, although traversed by the aragonite aggregate laminae, have a clear appearance under the light microscope. They form more or less continuously through the diurnal cycle by abiotic precipitation. The constant association of aragonite with organic nuclei, irrespective of whether the latter are in laminae or scattered through the calcite layers, supports a biotic control on aragonite formation. Lamination in Pleistocene travertines is superficially similar to that in the present day deposits, but is diagenetically altered. In the Pleistocene deposits, the calcite feathers appear dark under the light microscope and the aragonite aggregates, where they are not altered to dark calcite, are dissolved, together with parts of the adjacent spar calcite, and therefore appear light coloured.     

A method for the stochastic modeling of karstic systems accounting for geophysical data: an example of application in the region of Tulum, Yucatan Peninsula (Mexico)

The eastern coast of the Yucatan Peninsula, Mexico, contains one of the most developed karst systems in the world. This natural wonder is undergoing increasing pollution threat due to rapid economic development in the region of Tulum, together with a lack of wastewater treatment facilities. A preliminary numerical model has been developed to assess the vulnerability of the resource. Maps of explored caves have been completed using data from two airborne geophysical campaigns. These electromagnetic measurements allow for the mapping of unexplored karstic conduits. The completion of the network map is achieved through a stochastic pseudo-genetic karst simulator, previously developed but adapted as part of this study to account for the geophysical data. Together with the cave mapping by speleologists, the simulated networks are integrated into the finite-element flow-model mesh as pipe networks where turbulent flow is modeled. The calibration of the karstic network parameters (density, radius of the conduits) is conducted through a comparison with measured piezometric levels. Although the proposed model shows great uncertainty, it reproduces realistically the heterogeneous flow of the aquifer. Simulated velocities in conduits are greater than 1 cm?s^?1, suggesting that the reinjection of Tulum wastewater constitutes a pollution risk for the nearby ecosystems.     

An interatomic potential model for carbonates allowing for polarization effects

An empirical model for investigating the behaviour of CaCO₃ polymorphs incorporating a shell model for oxygen has been created. The model was constructed by fitting to: the structure of aragonite and calcite; their elastic, static and high-frequency dielectric constants; phonon frequencies at the wave vectors [&frac; 0 2] and [0 0 0] of calcite; and vibrational frequencies of the carbonate deformation modes of calcite. The high-pressure phase transition between calcite I and II is observed. The potentials for the CO₃ group were transferred to other carbonates, by refitting the interaction between CO₃ and the cation to both the experimental structures and their bulk modulus, creating a set of potentials for calculating the properties of a wide range of carbonate materials. Defect energies of substitutional cation defects were analyzed for calcite and aragonite phases. The results were rationalized by studying the structure of calcite and aragonite in greater detail.     

Formation of low‐magnesium calcite at cold seeps in an aragonite sea

This study investigates the conditions of occurrence and petrographic characteristics of low‐Mg calcite (LMC) from cold seeps of the Gulf of Mexico at a water depth of 2340 m. Such LMC mineral phases should precipitate in calcite seas rather than today's aragonite sea. The ¹³C‐depleted carbonates formed as a consequence of anaerobic oxidation of hydrocarbons in shallow subsurface cold seep environments. The occurrence of LMC may result from brine fluid flows. Brines are relatively Ca²⁺‐enriched and Mg²⁺‐depleted (Mg/Ca mole ratio <0.7) relative to seawater, where the Mg/Ca mole ratio is ~5, which drives high‐Mg calcite and aragonite precipitation. The dissolution of aragonitic mollusk shells, grains and cements was observed. Aerobic oxidation of hydrocarbons and H₂S is the most likely mechanism to explain carbonate dissolution. These findings have important implications for understanding the occurrence of LMC in deep water marine settings and consequently their counterparts in the geological record.     

Geochemical processes,evidence and thermodynamic behavior of dissolved and precipitated carbonate minerals in a modern seawater/freshwater mixing zone of a small tropical island

The geochemical processes and thermodynamic behavior of dissolved and precipitated carbonate minerals controlling the hydrochemistry of an aquifer in the seawater/freshwater mixing zone of a small island are identified. Field and laboratory analyses, geochemical modeling (PHREEQC) and multivariate statistical analysis (MSA) provide a quantitative interpretation for the geochemistry of the carbonate-dominated aquifer. Geochemical analyses and modeling results show that dissolution and re-precipitation of CaCO₃ are the prevalent processes governing geochemical reactions in the mixing zone. Furthermore, this was confirmed by coherent statistical output that incorporates Principle Component Analysis (PCA) and k-means Cluster Analysis (k-CA). Generally, the composition of the lowland sandy soil was rather homogeneous and was primarily composed of quartz, aragonite, calcite and Mg-calcite. Thermodynamic model calculations indicate that the carbonate minerals calcite, aragonite and dolomite are supersaturated in the mixing zone. Nevertheless, Powder X-ray Diffraction (PXRD) and Scanning Electron Microscope (SEM) examination verified the occurrence of low-Mg-calcite (LMC) and the absence of dolomite, attributed to thermodynamic/kinetic hindrance, cation disorder and the presence of dolomite crystal growth rate inhibitors (such as SO₄). The results suggest that dissolution of aragonite and precipitation of LMC drives the solid phase geochemistry in the small tropical island aquifer.     

Aragonite crystallization from strained calcite at reduced pressures and its bearing on aragonite in low-grade metamorphism

Aragonite, the dense form of CaCO₃, grew hydrothermally at 100–300° C and dry at 300–400° C at very low pressures from calcite strained by grinding. Nearly complete inversion to aragonite occurred in some runs with Ca-Mg chloride solutions at 0–2.4 kb and 100–200° C on strained calcite having a (10¯14) reflection with a half-width of 0.48° 2 Cu K. A little aragonite grew dry at one atm. from the ground calcite at 300–400° C in a few hrs. Simultaneous shear during recrystallization of calcite in a rotating squeezer resulted in significant aragonite at 300–400° C several kb. below the stability field. No inversion occurred in any ground calcite when previously annealed in CO₂ at 500° C for a few hrs. Thermochemical data show that at least 200 cal/mole of strain energy can be produced in calcite by mild deformation. This much stored energy would lower the pressure requirements of aragonite, relative to the strained calcite by more than 3 kb, and our observation that aragonite growth was faster than strain recovery of calcite indicates that aragonite can grow in nature at reduced pressures from strained calcite.Some experiments were also carried out on highly magnesian calcites with the thought that aragonite might also form at the expense of this metastable material. No aragonite was produced, but the possibility that this mechanism could be operative in nature cannot be discounted.The microtexture of aragonitic deformed marbles from NW Washington (prehnite-pumpellyite facies rocks, courtesy of J. A. Vance) as well as electron probe microanalysis of these rocks indicates that aragonite selectively replaced highly strained calcite. The calcite-aragonite transition is thus a questionable indicator of high-pressure in certain metamorphic rocks.     

Holocene meteoric dolomitization of Pleistocene limestones, North Jamaica

Wholesale removal of the unstable carbonate phases aragonite and Mg-calcite, and precipitation of calcite and dolomite is currently taking place where phreatic waters (the modern water table) invade 120,000-year-old Pleistocene biolithites (Falmouth Formation), North Jamaica. Pleistocene rocks presently in the vadose zone are relatively unaltered, and consist of mineralogically unstable scleractinian biolithites. At the water table, a narrow zone of solution, a ‘water table cave’ is commonly encountered. Below the water table the rocks are invariably more highly altered than those above. Mg-calcites are very rare, and considerable dissolution of aragonite has commonly occurred. Dolomite occurs as 8–25 μm, subhedral to euhedral crystals replacing micrite, or precipitated as void linings. The isotopic composition of the dolomite (δO¹⁸=-1·0 %0, δC¹³=-8·4 %0), and its high strontium content (3000 p.p.m.) suggest precipitation as CO₂-oversaturated meteoric groundwaters invade the mineralogically unstable biolithites, dissolve Mg-calcites and Sr-rich aragonites, and de-gas. Because some dolomitized rocks are enriched in magnesium relative to unaltered biolithites, addition of magnesium to the system is necessitated, and is probably derived from sea water in the mixing zone. Phreatic meteoric diagenesis is thus demonstrated to be a rapid process, and to be capable of dolomitization.     

Quantitative analysis of calcite and Mg-calcite by X-ray diffraction: effect of grinding on peak height and peak area

Mineralogical analysis of calcite and Mg-calcite by X-ray diffraction requires that the samples be ground to a powder. Such grinding determines the particle size of the powder and the structural damage of the minerals. Both of these in turn affect the peak intensities recorded by the X-ray machine. Most carbonate sediments are inhomogeneous; they contain both calcite and Mg-calcite which are affected differently by grinding. Such differences cause quantitative analytical results to be inconsistent with the true mineralogical abundance. The two acceptable methods of analysis—(1) measurement of peak height from the base and (2) measurement of the area under the peak—were compared to determine if sample preparation affects the quantitative results. In samples with variable and relatively small amounts of calcite and Mg-calcite the measurement of peak height yields more reproducible results than does the measurement of peak areas. Different proportions of particle size of the mineralogical components in a sample powder, affect proportionally more the peak areas than the peak heights. Extensive grinding causes structural damage of the component minerals which affects much more the peak areas than the peak heights. Thus for quantitative analyses of calcite and Mg-calcite in inhomogeneous carbonate samples which require differing grinding times and have greatly variable amounts of calcite and Mg-calcite, the peak height measurement seems to be a better method than peak area measurement.     

Microtextures of detrital sand grains from the Tecolutla,Nautla, and Veracruz beaches,western Gulf of Mexico,Mexico: implications for depositional environment and paleoclimate

Detrital sand grains from three beaches (Tecolutla, Nautla, and Veracruz) along the western Gulf of Mexico were studied by a scanning electron microscope, to investigate the depositional environment and paleoclimate. Totally, 24 microtextures are identified; among them, 13 are grouped as mechanical origin, 5 as mechanical and/or chemical origin, and 6 as chemical origin. These microtextures are nonuniformly distributed among the three beach areas. Concoidal fractures, straight and arcuate steps at Tecolutla and Veracruz beaches indicate that the sand grains were derived from the crystalline rocks. The abundance of angular outline grains at the Nautla beach supports for short transportation probably close to the source area. The domination of rounded sand grains in the Veracruz beach reveals that the sediments were derived by the aeolian mechanism. Chattermark trials at the Veracruz beach sands are indicating a wet tropical climate. Chemical features like silica globules, silica pellicle, and trapped diatoms in the Tecolutla and Veracruz beach sands suggest a silica saturated environment. Similarly, chemical etching and solution pits are common in the Veracruz beach sands, which are probably linked to the contaminated sea water. Desiccation crack at Veracruz beach sands is an indicator of temperature changes in the beach environment. Broken benthonic foraminifera Elphidium discoidale sp. present in the Veracruz beach indicates a high-energy littoral environment.     

巴布亚新几内亚合恩半岛晚第四纪上升珊瑚礁造礁珊瑚的成岩历史

更新世以来,剧烈的构造运动已将巴布亚新几内亚合恩半岛东北海岸的晚第四纪珊瑚礁阶地抬升上千米.阶地中造礁珊瑚的成岩变化和成岩产物的组构特征反映了该礁的成岩历史,充分体现该区快速构造上升的影响.海水潜流带和淡水渗流带为上升礁的主要成岩环境.生物钻孔、生物碎屑填隙、珊瑚文石针粗化、珊瑚骨骼的溶解和新生变形转化,以及其不同矿物成分和组构的种种胶结物的胶结作用是造礁珊瑚经历的主要成岩作用.地球化学资料表明其成岩变化发生于开放的化学体系之中.     

Effect of orthophosphate on the dissolution kinetics of biogenic magnesian calcites

The dissolution behavior of two biogenic Mg-calcites, the echinoid, Tripneustes (12 mol% MgCO₃), and the red alga, Neogoniolithon (18 mol% MgCO₃ plus brucite), was studied using free-drift methods in distilled water and phosphate-spiked solutions at 25°C and P_CO2 = 1 atm. Small concentrations of phosphate strongly inhibit dissolution rates. Inhibition increases with increased phosphate levels and with approach toward saturation. Near saturation, dissolution rates are reduced by 10³ by the presence of 0.6 μmol adsorbed-P/m². The magnitude of phosphate inhibition is similar to that observed for low-Mg calcite, and like calcite, the mechanism of inhibition is probably by adsorption of P at surface kink sites. Phosphate appears to inhibit removal of Mg and Ca equally during Mg-calcite dissolution. Rates of brucite dissolution are unaffected by phosphate.Mg-calcites containing >8.5 mol% MgCO₃ should be thermodynamically unstable relative to aragonite in most natural waters. Recent work, however, shows that in contrast to its effect on the behavior of Mg-calcites. phosphate does not inhibit aragonite dissolution. The presence of phosphate might thus reverse the relative stability of these two minerals during diagenesis of shallow marine carbonate sediments.     

Diagenesis and geochemistry of porites corals from Papua New Guinea: Implications for paleoclimate reconstruction

Coral proxy records of sea surface temperature (SST) and hydrological balance have become important tools in the field of tropical paleoclimatology. However, coral aragonite is subject to post-depositional diagenetic alteration in both the marine and vadose environments. To understand the impact of diagenesis on coral climate proxies, two mid-Holocene Porites corals from raised reefs on Muschu Island, Papua New Guinea, were analysed for Sr/Ca, δ¹⁸O, and δ¹³C along transects from 100% aragonite to 100% calcite. Thin-section analysis showed a characteristic vadose zone diagenetic sequence, beginning with leaching of primary aragonite and fine calcite overgrowths, transitional to calcite void filling and neomorphic, fabric selective replacement of the coral skeleton. Average calcite Sr/Ca and δ¹⁸O values were lower than those for coral aragonite, decreasing from 0.0088 to 0.0021 and −5.2 to −8.1‰, respectively. The relatively low Sr/Ca of the secondary calcite reflects the Sr/Ca of dissolving phases and the large difference between aragonite and calcite Sr/Ca partition coefficients. The decrease in δ¹⁸O of calcite relative to coral aragonite is a function of the δ¹⁸O of precipitation. Carbon-isotope ratios in secondary calcite are variable, though generally lower relative to aragonite, ranging from −2.5 to −10.4%. The variability of δ¹³C in secondary calcite reflects the amount of soil CO₂ contributing ¹³C-depleted carbon to the precipitating fluids. Diagenesis has a greater impact on Sr/Ca than on δ¹⁸O; the calcite compositions reported here convert to SST anomalies of 115°C and 14°C, respectively. Based on calcite Sr/Ca compositions in this study and in the literature, the sensitivity of coral Sr/Ca-SST to vadose-zone calcite diagenesis is 1.1 to 1.5°C per percent calcite. In contrast, the rate of change in coral δ¹⁸O-SST is relatively small (−0.2 to 0.2°C per percent calcite). We show that large shifts in δ¹⁸O, reported for mid-Holocene and Last Interglacial corals with warmer than present Sr/Ca-SSTs, cannot be caused by calcite diagenesis. Low-level calcite diagenesis can be detected through X-ray diffraction techniques, thin section analysis, and high spatial resolution sampling of the coral skeleton and thus should not impede the production of accurate coral paleoclimate reconstructions.