Living it up: Super-rich enclave and transnational elite urbanism in Singapore

Notwithstanding the burgeoning scholarship on enclave urbanism, urban gating has often been pigeonholed as an intra-urban development that is somewhat ‘epiphenomenal’ to wider global processes. Overlooked in the literature is how gated communities as globally-oriented spaces are intertwined with the transnational lifeworlds of its elite inhabitants. As key sites where transnational super-rich elites organize their consumption and reproduce their purportedly global lifestyle, gated communities are now emerging as a new ‘meta-geographical form’ that circulates in and around rapidly globalizing cities. Drawing on the case study of Sentosa Cove, an exclusive waterfront gated community in Singapore catering to ‘high net-worth’ residents, this paper critically examines how elite localities and transnationalism are being socially and spatially reproduced in the city-state. To this end, the paper makes a distinct contribution by bringing to bear critical transnationalism perspectives in the understanding of urban gating and the privileged geographies of the global super-rich.     

Exsolution and coarsening in iron-free clinopyroxene during isothermal annealing

Exsolution and coarsening in Fe-free clinopyroxene of composition En_45.1Di_54.9 was studied at temperatures of 1300, 1200, and 1100°C, and annealing times between 10 min and 4320 h. Based on the wavelength of the exsolution lamellae, the exsolution process can be divided into exsolution sensu stricto and coarsening. During exsolution sensu stricto, the average wavelength of the “001” and “100” lamellae remains constant in contrast to the subsequent coarsening process. A progressive development of the microstructure is observed before coarsening which includes formation of island-like regions of dark contrast without phase separation, occurrence of pigeonite and diopside domains predominantly elongated along (100), formation of “100” exsolution lamellae, dissolution of the “100” lamellae, and predominant occurrence of “001” exsolution lamellae. All observations are in accordance with the exsolution mechanism of spinodal decomposition. After termination of the exsolution process, coarsening of the exsolution lamellae is observed. The “001” lamellae coarsen according to the rate law

     

Surface properties, solubility and dissolution kinetics of bamboo phytoliths

Although phytoliths, constituted mainly by micrometric opal, exhibit an important control on silicon cycle in superficial continental environments, their thermodynamic properties and reactivity in aqueous solution are still poorly known. In this work, we determined the solubility and dissolution rates of bamboo phytoliths collected in the Réunion Island and characterized their surface properties via electrophoretic measurements and potentiometric titrations in a wide range of pH. The solubility product of “soil” phytoliths ( at 25 °C) is equal to that of vitreous silica and is 17 times higher than that of quartz. Similarly, the enthalpy of phytoliths dissolution reaction is close to that of amorphous silica but is significantly lower than the enthalpy of quartz dissolution. Electrophoretic measurements yield isoelectric point pH_IEP = 1.2 ± 0.1 and 2.5 ± 0.2 for “soil” (native) and “heated” (450 °C heating to remove organic matter) phytoliths, respectively. Surface acid-base titrations allowed generation of a 2-pK surface complexation model. Phytoliths dissolution rates, measured in mixed-flow reactors at far from equilibrium conditions at 2 ? pH ? 12, were found to be intermediate between those of quartz and vitreous silica. The dissolution rate dependence on pH was modeled within the concept of surface coordination theory using the equation:

     

Development in Nepal: Investment in the status quo

Despite billions of dollars provided by donors, Nepal's quest for development remains unfulfilled. Nepal's rugged topography is a serious obstacle, but this development failure has social roots. The first root is Nepal's power structure. A feudal elite, supported by British India, controlled Nepal until 1951, extracted and wasted the agricultural surplus, and excluded all modern influences. The post-1951 government adopted development as its goal and justification, but was still controlled by the same elite. Rivalries between the superpowers and between India and China produced a flow of foreign aid which has tripled each decade. Through its control of the state, Nepal's elite has directed and diverted foreign aid into channels which consolidate its power. This is manifested in the pervasive corruption, which is essential, not accidental, to the system. The second root of Nepal's development failure is inappropriate development theories, which have emphasized investment in infrastructure, but have ignored most of the 90% of the population who are subsistence farmers. The third root is the consistently dismal implementation of development projects by indigenous and expatriate development workers. The institutional ignoring of corruption amounts to collusion between foreign aid donors and indigenous elite.     

The community morphology of skilled migration: the changing role of voluntary and community organisations (VCOs) in the grounding of British migrant identities in Paris (France)

Research into skilled migrant communities tends to emphasize the grounding of identities through transnationalism and mobility. Less research has been conducted into how skilled migrants actually ground their identities within the city through everyday social networks. The paper addresses this imbalance by examining the changing significance of British voluntary and community organisations (VCOs) in Paris, France. Combining qualitative and quantitative data, findings show local migrant networks to be important focal points for the British even though migrants’ lives may increasingly be transnational in orientation. The research also shows that in situ social networks are evolving. Specifically, traditional forms of elite expatriate communality are not as omnipotent as they once were, with the popularity of some high-profile British VCOs in Paris declining over recent decades. The paper argues that the link between social dynamism and communal morphology helps explain this shift: as British middle-class lifestyles have fragmented, and as the British migrant population in Paris has grown in scale and scope, so the range of VCOs and associated informal networks has grown. Whilst some skilled migrants still embed within traditional expatriate organisations, Britishness is increasingly grounded elsewhere; both within the city through alternative social networks, and located beyond the city through transnational ties.     

Inhibition of calcite precipitation by orthophosphate: Speciation and thermodynamic considerations

The inhibition of heterogeneous calcite precipitation by orthophosphate was investigated under four different solution compositions using a pH-stat system. The system composition was designed to maintain a constant degree of supersaturation with respect to calcite, but with different carbonate/calcium ratios and pH values during precipitation. Inhibition in the presence of orthophosphate was found to be more effective at lower carbonate/calcium ratios and lower pH values. With the assumption that the calcite precipitation rate is proportional to the surface concentration of active crystal-growth sites, the reduction in the rate of calcite precipitation by phosphate can be explained by a Langmuir adsorption model using a conditional equilibrium constant and total phosphate concentration. Through a detailed analysis of chemical speciation in the solution phase and calcite surface speciation using chemical equilibrium computer modeling, the “conditional” equilibrium constants obtained at different solution compositions were found to converge to a single “non-conditional” value if only was considered in the adsorption reaction. This suggests that is the responsible species for inhibition of calcite precipitation because it adsorbs to the surface and blocks the active crystal-growth sites. The standard enthalpy change (ΔH⁰) and standard entropy change (TΔS⁰) of the adsorption reaction, determined by experiments performed from 15 to 45 °C, were 58.5 and 98.3 kJ/mol, respectively. The high positive values of the standard enthalpy change and the standard entropy change suggest that the adsorption reaction is an endothermic reaction, chemisorptive in nature, and driven by the entropy change, most likely resulting from the dehydration process that accompanies the adsorption of onto the calcite surface.     

Pb diffusion in monazite: a combined RBS/SIMS study

We report measurements of Pb diffusion in both synthetic (CePO₄) and natural monazites run under dry, 1-atm conditions. Powdered mixtures of prereacted CePO₄ and PbZrO₃ were used as the source of Pb diffusant for “in-diffusion” experiments conducted in sealed Pt capsules for durations ranging from a few hours to several weeks. Following the diffusion anneals, Pb concentration profiles were measured with Rutherford Backscattering Spectroscopy (RBS) and supplemented by measurements with secondary ion mass spectrometry (SIMS). In order to evaluate potential compositional effects upon Pb diffusivity and simulate diffusional Pb loss that might occur in natural systems, we also conducted “out-diffusion” experiments on Pb-bearing natural monazites. In these experiments, monazite grains were surrounded by a synthetic zircon powder to act as a “sink.” Monazites from these experiments were analyzed with SIMS. Over the temperature range 1100 to 1350°C, the Arrhenius relation determined for in-diffusion experiments on synthetic monazite is given by:

     

Oxygen self-diffusion “fast-paths” in titanite single crystals and a general method for deconvolving self-diffusion profiles with “tails”

Like most other minerals, titanite rarely if ever forms perfect crystals. In addition to the point defects that might affect lattice diffusion, there may be extended line- or planar defects along which fast diffusion could occur. During the course of an experimental study of oxygen lattice diffusion in titanite, we found that almost all of the ¹⁸O uptake profiles produced in natural titanite crystals departed from the complementary error function solution expected for simple lattice diffusion with a constant surface concentration. Instead, they exhibited “tails” extending deeper into the samples than expected for simple lattice diffusion. The purpose of this contribution is to report on these features—described as “fast-paths” for oxygen diffusion—and outline a method for coping with them in extracting information from diffusion profiles.For both dry and hydrothermal experiments in which the “fast paths” are observed, ¹⁸O was used as the diffusant. In dry experiments, the source material was ¹⁸O-enriched SiO₂ powder, while ¹⁸O-enriched water was used for the hydrothermal experiments. Diffusive uptake profiles of ¹⁸O were measured in all cases by nuclear reaction analysis (NRA) using the ¹⁸O (p,α)¹⁵N reaction [see Zhang X. Y., Cherniak D. J., and Watson E. B. (2006) Oxygen diffusion in titanite: lattice and fast-path diffusion in single crystals. Chem. Geol.235 105-123].In our experiments, different sizes of “tails” (with varying ¹⁸O concentrations) were observed. Theoretically, under the same temperature and pressure conditions, the sizes of tails should be affected by two factors: the diffusion duration and the defect density. For the same experiment duration, the higher the defect density, the larger the “tail”; for the same defect densities, the longer the diffusion duration, the larger the “tail.”The diffusion “tails” could be a result of either planar defects or one-dimensional “pipe” diffusion. AFM imaging of HF etched titanite surfaces confirmed that the etched features might be caused by either parallel planar defects or parallel pipe defects, but could not differentiate between these possibilities. Through theoretical calculations simulating the tailed diffusion profiles using reasonable assumptions of lattice diffusivities and fast-path diffusivities, and comparing these with tail features measured in our samples, it can be concluded that the “tails” observed in our experiments are caused by planar defects rather than pipe defects.A new method was developed for separating the “fast-path” contribution from the overall composite diffusion profile consisting of both “fast-path” and lattice diffusion. Through this process, the lattice diffusion coefficient could be determined, which is required to analyze the tail. The oxygen diffusion rates in the fast-paths were obtained by traditional graphical analysis methods, using the Whipple-Le Claire equation (for 2-D defects) assuming that the width of the fast-path is 1 nm. Two Arrhenius relations were obtained for the fast-path diffusion phenomenon, one for experiments under dry conditions, and the other for hydrothermal conditions:

     

Reading representations of women’s war experiences in the Changi Chapel and Museum, Singapore

In this paper, we highlight the way Singapore commemorates its involvement during the Second World War. After briefly tracing the genesis of war commemoration within the nation, we turn to one specific problematic--the gendered portrayals of the war within a particular war memorial in Singapore, the Changi Chapel and Museum. Through a reading of landscape texts, interviews with key figures, visitors and other ethnographic data, we explore the specific ways in which women have either been omitted or stereotypically represented within the site. We proceed to provide possible reasons for this, arguing how the male-centric focus of the site may be due to the perpetuation of hegemonic ideals of war as being a traditionally “male” terrain, and the fact that “silence” is often part of women’s approach to their war experiences. We also argue that gendered portrayals of the war within the site is also an unconscious product of the patriarchal nature of the Singapore state and nation-building endeavours that have placed limits on a more substantial inclusion of women’s stories vis-à-vis the men’s.     

Effects of magnesium ions on near-equilibrium calcite dissolution: Step kinetics and morphology

Dissolution kinetics at the aqueous solution-calcite interface at 50 °C were investigated using in situ atomic force microscopy (AFM) to reveal the influence of magnesium concentration and solution saturation state on calcite dissolution kinetics and surface morphology. Under near-equilibrium conditions, dissolved Mg²⁺ displayed negligible inhibitory effects on calcite dissolution even at concentrations of . Upon the introduction of , the solution saturation state with respect to calcite, , acted as a “switch” for magnesium inhibition whereby no significant changes in step kinetics were observed at Ω_calcite<0.2, whereas a sudden inhibition from Mg²⁺ was activated at Ω_calcite?0.2. The presence of the Ω-switch in dissolution kinetics indicates the presence of critical undersaturation in accordance with thermodynamic principles. The etch pits formed in solutions with exhibited a unique distorted rhombic profile, different from those formed in Mg-free solutions and in de-ionized water. Such unique etch pit morphology may be associated with the anisotropy in net detachment rates of counter-propagating kink sites upon the addition of Mg²⁺.     

Solid solutions of trace Eu(III) in calcite: Thermodynamic evaluation of experimental data over a wide range of pH and pCO2

The thermodynamics of dilute Eu-calcite solid solutions formed under widely different pH-pCO₂ conditions at T = 25°C and p = 1 bar were investigated using three sets of Eu(III) uptake experiments, two of which were taken from the literature: (a) recrystallization in synthetic cement pore water at pH ∼ 13 and pCO₂ ∼ 10⁻¹³ bar (this work); (b) coprecipitation in 0.1 M NaClO₄ at pH ∼ 6 and pCO₂ ∼ 1 bar; (c) coprecipitation in synthetic seawater at pH ∼ 8 and pCO₂ ranging from 3 × 10⁻⁴ to 0.3 bar.Solid solution formation was modeled using the Gibbs energy minimization (GEM) method. In a first step (“forward” modeling), we tested ideal binary solid solution models between calcite and the Eu end-members Eu₂(CO₃)_3, EuNa(CO₃)₂, Eu(OH)CO₃ or Eu(OH)₃, for which solids with independently measured solubility products exist. None of these four binary solid solutions was capable of reproducing all three experimental datasets simultaneously. In a second step (“inverse” modeling), ideal binary solid solutions were constructed between calcite and the candidate Eu end-members EuO(OH), EuH(CO₃)₂ and EuO(CO₃)_0.5, for which no independent solubility products are available. For each single data point and each of these end-members, a free energy of formation with inherent activity coefficient term ( = G_α^o + RT lnγ_α) was estimated from “dual thermodynamic” GEM calculations. The statistical mean of was then calculated for each of the three datasets. A specific end-member was considered to be acceptable if a standard deviation of ± 2 kJ mol⁻¹ or less resulted for each single dataset, and if the mean -values calculated for the three datasets coincided. No binary solid solution with any of the seven above mentioned end-members proved to satisfy these criteria.The third step in our analysis involved consideration of ternary solid solutions with CaCO₃ as the major end-member and any two of the seven considered Eu trace end-members. It was found that the three datasets can only be reproduced simultaneously with the ternary ideal solid solution EuH(CO₃)₂ - EuO(OH) - CaCO₃, setting = −1773 kJ mol⁻¹ and = −955 kJ mol⁻¹, whereas all other end-member combinations failed. Our results are consistent with time-resolved laser fluorescence data for Cm(III) and Eu(III) indicating that two distinct species are incorporated in calcite: one partially hydrated, the other completely dehydrated. In conclusion, our study shows that substitution of trivalent for divalent cations in carbonate crystal structures is a more complex process than the classical isomorphic divalent-divalent substitution and may need consideration of multicomponent solid solution models.     

“Racism in a Melting Pot…?” Trinidadian mid-life transnational migrants’ views on race and colour-class on return to their homes of descent

This paper deals with second-generation, one-and-a-half generation and “prolonged sojourner” Trinidadian transnational migrants, who have decided to ‘return’ to the birthplace of their parents. Based on 40 in-depth interviews, the paper considers both the positive and critical things that these youthful transnational migrants report about returning to, and living in, this multi-ethnic plural society and the salience of racial and colour-class stratification as part of their return migration experiences. Our qualitative analysis is based on the narratives provided by these youthful returnees, as relayed “in their own words”, presenting critical reflections on racism, racial identities and experiences as transnational Trinidadians. It is clear that it is contexts such as contemporary working environments, family and community that act as the reference points for the adaptation “back home” of this strongly middle-class cohort. We accordingly encounter a diverse, sometimes contesting set of racial issues that emerge as salient concerns for these returnees. The consensus is that matters racial remain as formidable legacies in the hierarchical stratification of Trinidadian society for a sizeable number. Many of our respondents reported the positive aspects of racial affirmation on return. But for another sub-set, the fact that multi-ethnic and multi-cultural mixing are proudly embraced in Trinidad meant that it was felt that return experiences were not overly hindered, or blighted by obstacles of race and colour-class. For these returnees, Trinidad and Tobago is seen as representing a 21st century “Melting Pot”. But for others the continued existence of racial divisions within society - between ethnic groups and among those of different skin shades - was lamented. In the views of these respondents, too much racial power is still ascribed to ‘near-whiteness’. But for the most part, the returnees felt that where race played a part in their new lives, this generally served to advantage them. However, although the situation in Trinidad appears to have been moderated by assumptions that it remains a racial ‘Melting Pot’, the analysis strongly suggests that the colour-class system of stratification is still playing an essential role, along with racial stereotyping in society at large.     

Equilibrium mass-dependent fractionation relationships for triple oxygen isotopes

With a growing interest in small ¹⁷O-anomaly, there is a pressing need for the precise ratio, ln¹⁷α/ln¹⁸α, for a particular mass-dependent fractionation process (MDFP) (e.g., for an equilibrium isotope exchange reaction). This ratio (also denoted as “θ”) can be determined experimentally, however, such efforts suffer from the demand of well-defined process or a set of processes in addition to high precision analytical capabilities. Here, we present a theoretical approach from which high-precision ratios for MDFPs can be obtained. This approach will complement and serve as a benchmark for experimental studies. We use oxygen isotope exchanges in equilibrium processes as an example.We propose that the ratio at equilibrium, θ^E ≡ ln¹⁷α/ln¹⁸α, can be calculated through the equation below:

     

In situ Atomic Force Microscopy study of dissolution of the barite (0 0 1) surface in water at 30 °C

The dissolution behavior of the barite (0 0 1) surface in pure water at 30 °C was investigated using in situ Atomic Force Microscopy (AFM), to better understand the dissolution mechanism and the microtopographical changes that occur during the dissolution, such as steps and etch pits. The dissolution of the barite (0 0 1) surface started with the slow retreat of steps, after which, about 60 min later, the <hk0> steps of one unit cell layer or multi-layers became two-step fronts (fast “f” and slow “s” steps) with a half-unit cell layer showing different retreat rates. The “f” step had a fast retreat rate (≈(14 ± 1) × 10⁻² nm/s) and tended to have a jagged step edge, whereas the “s” step (≈(1.8 ± 0.1) × 10⁻² nm/s) had a relatively straight front. The formation of the “f” steps led to the formation of a new one-layer step, where the front of the “s” step was overtaken by that of the immediate underlying “f” step. The “f” steps also led to the decrease of the <hk0> steps and the increase in the percentage of stable steps parallel to the [0 1 0] direction during the dissolution.Etch pits, which could be observed after about 90 min, were of three types: triangular etch pits with a depth of a half-unit cell, shallow etch pits, and deep etch pits. The triangular etch pits were bounded by the step edges parallel to [0 1 0], [1 2 0], and [] and had opposite orientations in the upper half and lower half layers. Shallow etch pits that had a depth of two or more half-unit cell layers had any two consecutive pits pointing in the opposite direction of each other. The triangular etch pit appeared to grow by simultaneously removal of a row of ions parallel to each direction from the three step edges. At first, deep etch pits were elongated in the [0 1 0] direction with a curved outline and then gradually developed to an angular form bounded by the {1 0 0}, {3 1 0}, and (0 0 1) faces. The retreat rate of the (0 0 1) face was much slower than those of the {1 0 0} and {3 1 0} and tended to separate into two rates ((0.13 ± 0.01) × 10⁻² nm/s for the deep etch pits derived from a screw dislocation and (0.07 ± 0.01) × 10⁻² nm/s for those from other line defects).The changes in the dissolution rate of a barite (0 0 1) surface during the dissolution were estimated using the retreat rates and densities of the various steps as well as the growth rates, density, and areas of the lateral faces of the deep etch pits that were obtained from this AFM analysis. Our results showed that the dissolution rate of the barite (0 0 1) surface gradually increased and approached the bulk dissolution rate because of the change in the main factor determining the dissolution rate from the density of the steps to the growth and the density of the deep etch pits on the surface.     

Oxygen fugacity dependence of Os solubility in haplobasaltic melt

Os equilibrium solubilities were determined at 1350 °C over a wide range of oxygen fugacities (−12 < log fO₂ < −7) applying the mechanically assisted equilibration technique (MAE) at 10⁵ Pa (= 1 bar). Os concentrations in the glass samples were analysed using ID-NTIMS. Additional LA-ICP-MS and SEM analyses were performed to detect, visualize and analyse the nature and chemistry of “nanonuggets.” Os solubilities determined range at a constant temperature of 1350 °C from 0.63 ± 0.04 to 37.4 ± 1.16 ppb depending on oxygen fugacity. At the highest oxygen fugacities, Os³⁺ can be confirmed as the main oxidation state of Os. At low oxygen fugacities (below log fO₂ = −8), samples are contaminated by nanonuggets which, despite the MAE technique, were still not removed entirely from the melt. However, the present results indicate that applying MAE technology does reduce the amount of nanonuggets present significantly, resulting in the lowest Os solubility results reported to date under these experimental conditions, and extending the experimentally accessible range of fO₂ for these studies to lower values. Calculated metal/silicate melt partition coefficients are therefore higher compared to previous studies, making Os more siderophile. Neglecting the as yet unknown temperature dependence of the Os metal/silicate melt partition coefficient, extrapolation of the obtained Os solubilities to conditions for core-mantle equilibrium, results in a , while metallic alloy/silicate melt partition coefficients range from 1.4 × 10⁶ to 8.6 × 10⁷, in agreement with earlier findings. Therefore remains too high by 2-4 orders of magnitude to explain the Os abundance in the Earth’s mantle as result of core-mantle equilibrium during core formation.     

Navigating the terrains of transnational education: Children of Chinese ‘study mothers’ in Singapore

This paper demonstrates the value of child-centred migration studies which highlight children’s role in shaping the migration journeys of their families, as well as their own projected journeyings. It examines the case of children from China who move to Singapore, an aspiring global education hub, expressly for the purpose of an overseas education that will facilitate longer-term migration and life goals. Focus is given specifically to the children of ‘study mothers’ or peidu mama (literally: ‘mothers accompanying their children who are studying’). Through interviews with the teenagers and the conceptual optic of ‘social navigation’, our paper demonstrates that children are resilient and creative beings able to navigate the twists and turns of their immediate trajectories, as well as develop their own goals and projected destinations for their futures. The paper calls for a refinement in the way we understand children’s mobilities. First, in arguing that their spatial journeying across the terrains of transnational education cannot be decoupled from their process of social becoming and emotional development from passive followers to active negotiators, we wish to disrupt hegemonic discourses and dominant representations of children in migration as simply ‘migrant’s children’ and restore them to the status of ‘migrant children’. Second, adopting the concept of social navigation as an analytical lens allows us to highlight the fluid ways that young people think about their futures and the different pathways by which they can get there. This leads us to conceive of social and cultural capital accumulation through transnational education as a process with many more degrees of provisionality than what is often presented in the literature as a ‘strategic project’ with a fixed and abstract goal.     

Gendering transnational communities: a comparison of Singaporean and British migrants in China

Studies of transnational communities and transnational labour migration have focused almost exclusively on the movement of low-skilled and unskilled workers across international boundaries. While these groups may be numerically dominant, it must be recognised that there are increasing numbers of managers and professionals engaged in work-related migration in association with the intensification of economic globalisation processes. Work which has been conducted on highly skilled migrants has largely been limited to examinations of intra-firm mobility and the workspace. This approach fails to consider the ways in which the migrants' experiences are embedded in the social, economic and political practices of the host country, but also in a specific household context. It is unsurprising, therefore, that the gendered dimensions of the life of these migrants and their accompanying family members has been somewhat under-researched.Flows of expatriates can lead to the constitution of both ‘communities of transnationals', as particular cities become foci of the activities of the ‘transnational capitalist class', as well as ‘transnational communities' which involve regular and sustained contact between individuals across national boundaries. In this paper we examine these social formations using two groups of migrants––British and Singaporean migrants to China (both mainland China and the Hong Kong SAR). We focus on the gender characteristics of these groupings, but also the gender division of labour in the creation and maintenance of these ‘communities'. The paper is based on qualitative research carried out in China, Singapore and the UK 1997–2001.     

Complexation of Cu in Hydrothermal NaCl Brines: Ab initio molecular dynamics and energetics

Chloride complexation of Cu⁺ controls the solubility of copper(I) oxide and sulfide ore minerals in hydrothermal and diagenetic fluids. Solubility measurements and optical spectra of high temperature CuCl solutions have been interpreted as indicating the formation of CuCl, , and complexes. However, no other monovalent cation forms tri- and tetrachloro complexes. EXAFS spectra of high temperature Cu-Cl solutions, moreover, appear to show only CuCl and complexes at T > 100 °C. To reconcile these results, I investigated the nature and stability of Cu-Cl complexes using ab initio cluster calculations and ab initio (Car-Parrinello) molecular dynamics simulations for CuCl-NaCl-H₂O systems at 25 to 450 °C. Ab initio molecular dynamic simulations of 1 m CuCl in a 4 m Cl solution give a stable complex at 25 °C over 4 ps but show that the third Cl⁻ is weakly bound. When the temperature is increased along the liquid-vapour saturation curve to 125 °C, the complex dissociates into and Cl⁻; only forms at 325 °C and 1 kbar. Even in a 15.6 m Cl brine at 450 °C, only the complex forms over a 4 ps simulation run.Cluster calculations with a static dielectric continuum solvation field (COSMO) were used in an attempt directly estimate free energies of complex formation in aqueous solution. Consistent with the MD simulations, the complex is slightly stable at 25 °C but decreases in stability with decreasing dielectric constant (ε). The complex is predicted to be unstable at 25 °C and becomes increasingly unstable with decreasing dielectric constant. In hydrothermal fluids (ε < 30) both the and complexes are unstable to dissociation into and Cl⁻.The results obtained here are at odds with recent equations of state that predict and complexes are the predominant species in hydrothermal brines. In contrast, I predict that only complexes will be significant at T > 125 °C, even in NaCl-saturated brines. The high-temperature (T > 125 °C) optical spectra of CuCl solutions and solubility measurements of Cu minerals in Cl-brines need to be reinterpreted in terms of only the CuCl and complexes.