We present here the DECam Ecliptic Exploration Project (DEEP), a 3 yr NOAO/NOIRLab Survey that was allocated 46.5 nights to discover and measure the properties of thousands of trans-Neptunian objects (TNOs) to magnitudes as faint as VR similar to 27 mag, corresponding to sizes as small as 20 km diameter. In this paper we present the science goals of this project, the experimental design of our survey, and a technical demonstration of our approach. The core of our project is "digital tracking," in which all collected images are combined at a range of motion vectors to detect unknown TNOs that are fainter than the single exposure depth of VR similar to 23 mag. Through this approach, we reach a depth that is approximately 2.5 mag fainter than the standard LSST "wide fast deep" nominal survey depth of 24.5 mag. DEEP will more than double the number of known TNOs with observational arcs of 24 hr or more, and increase by a factor of 10 or more the number of known small (<50 km) TNOs. We also describe our ancillary science goals, including measuring the mean shape distribution of very small main-belt asteroids, and briefly outline a set of forthcoming papers that present further aspects of and preliminary results from the DEEP program.

We present a detailed study of the observational biases of the DECam Ecliptic Exploration Project's B1 data release and survey simulation software that enables direct statistical comparisons between models and our data. We inject a synthetic population of objects into the images, and then subsequently recover them in the same processing as our real detections. This enables us to characterize the survey's completeness as a function of apparent magnitudes and on-sky rates of motion. We study the statistically optimal functional form for the magnitude, and develop a methodology that can estimate the magnitude and rate efficiencies for all survey's pointing groups simultaneously. We have determined that our peak completeness is on average 80% in each pointing group, and our magnitude drops to 25% of this value at m(25) = 26.22. We describe the freely available survey simulation software and its methodology. We conclude by using it to infer that our effective search area for objects at 40 au is 14.8 deg(2), and that our lack of dynamically cold distant objects means that there at most 8 x 10(3) objects with 60 < a < 80 au and absolute magnitudes H <= 8.

The search for habitable environments and biomarkers in exoplanetary atmospheres is the holy grail of exoplanet science. The detection of atmospheric signatures of habitable Earth-like exoplanets is challenging owing to their small planet-star size contrast and thin atmospheres with high mean molecular weight. Recently, a new class of habitable exoplanets, called Hycean worlds, has been proposed, defined as temperate ocean-covered worlds with H2-rich atmospheres. Their large sizes and extended atmospheres, compared to rocky planets of the same mass, make Hycean worlds significantly more accessible to atmospheric spectroscopy with JWST. Here we report a transmission spectrum of the candidate Hycean world K2-18 b, observed with the JWST NIRISS and NIRSpec instruments in the 0.9-5.2 mu m range. The spectrum reveals strong detections of methane (CH4) and carbon dioxide (CO2) at 5 sigma and 3 sigma confidence, respectively, with high volume mixing ratios of similar to 1% each in a H2-rich atmosphere. The abundant CH4 and CO2, along with the nondetection of ammonia (NH3), are consistent with chemical predictions for an ocean under a temperate H2-rich atmosphere on K2-18 b. The spectrum also suggests potential signs of dimethyl sulfide (DMS), which has been predicted to be an observable biomarker in Hycean worlds, motivating considerations of possible biological activity on the planet. The detection of CH4 resolves the long-standing missing methane problem for temperate exoplanets and the degeneracy in the atmospheric composition of K2-18 b from previous observations. We discuss possible implications of the findings, open questions, and future observations to explore this new regime in the search for life elsewhere.

As basaltic rocks formed at the base of the oceanic floor are transported back to the Earth's mantle along sub-duction zones, they undergo transitions and introduce compositional and thermal heterogeneities in the deeper parts of the mantle. Studying the melting phase relations of basaltic lithologies at elevated pressures and tem-peratures provides insights into what potentially happens at different depths in the lower mantle now and throughout the past billion years of active plate tectonics. Using laser heated - diamond anvil cell experiments combined with in situ X-Ray Diffraction measurements at synchrotron sources, we revisit the crystallization and melting properties of natural basaltic samples at 60-100 GPa and up to 4000 K. Diffraction patterns highlight the major phases: bridgmanite and Ca-perovskite, followed by crystallization of Si-rich phases (mainly stishovite) and Calcium Ferrite (CF-type) Na and Al-rich phase. Recovered samples were prepared using focused ion beam techniques for detailed chemical analyses of the extracted thin sections by electron microscopies in order to resolve sub-micron features and understand the chemical partitioning of elements induced by melting at high pressure and temperature conditions. We confirm that the liquidus phase is Ca-perovskite, which segregates during melting and is recovered as rings that encapsulate a melt pool throughout the studied pressure range. The melt pocket shows a concentric structure consisting of an alumino-silicate envelope surrounding an Fe-rich silicate part. At the center of samples, an Fe-O-S metal pond is often observed. We associate the observation of segregation of liquid phases to capillary forces. The differentiation of melt pockets into three melts is tenta-tively attributed to Marangoni effects, i.e. temperature-induced surface tension gradients in the samples. Central metal ponds are indirectly best interpreted as related to the disproportionation reaction of Fe2+ into Fe3+ and Fe(0) in bridgmanite whereas the two silicate-melt pools could be associated to the formation of two immiscible liquids upon melting of basalts. On the basis of these observations, we propose that melting of basaltic lithologies at lower mantle pressures could lead to important chemical differentiation mostly characterized by Fe enrich-ment at increasing depth.

In this study, we investigated phase transformations of CaTiO3 perovskite using x-ray diffraction at high pressure and high temperature up to 170 GPa and 4500 K in a laser-heated diamond-anvil cell. We report a high-pressure dissociation of CaTiO3 into CaO-B2 and CaTi2O5 with a monoclinic P2/m structure, instead of the expected transformation of the orthorhombic distorted perovskite structure into a post-perovskite phase. We propose that this transition may be favored by the B1 to B2 phase change of CaO at around 60 GPa. In order to provide additional information on the high pressure properties of CaTiO3 perovskite, we measured its melting temper-ature using CO2 laser heated diamond anvil cell up to 55 GPa yielding a fit of the melting curve to a Kraut-Kennedy empirical law according to: Tm (K) = 2188 * [1 + 4.23 * (Delta V/V0)]. To provide some further insight into the thermodynamic properties of CaTiO3, we determined the P-V-T equation of state of the orthorhombic mineral perovskite, fitted by using a third order Birch-Murnaghan equation of state and a Berman thermal expansion model. The fit of the data yields to K0 = 180.6(4) GPa, K ' 0 = 4 (fixed), partial differential K/ partial differential T =-0.022(1) GPa K-1, alpha 1 = 3.25(5) x 10-5 K-1, alpha 2 = 1.3(1) x 10-8 K-2

FeO represents an important end-member for planetary interiors mineralogy. However, its properties in the liquid state under high pressure are poorly constrained. Here, in situ high-pressure and high-temperature X-ray diffraction experiments, ab initio simulations, and thermodynamic calculations are combined to study the local structure and density evolution of liquid FeO under extreme conditions. Our results highlight a strong shortening of the Fe-Fe distance, particularly pronounced between ambient pressure and similar to 40 GPa, possibly related with the insulator to metal transition occurring in solid FeO over a similar pressure range. Liquid density is smoothly evolving between 60 and 150 GPa from values calculated for magnetic liquid to those calculated for non-magnetic liquid, compatibly with a continuous spin crossover in liquid FeO. The present findings support the potential decorrelation between insulator/metal transition and the high-spin to low-spin continuous transition, and relate the changes in the microscopic structure with macroscopic properties, such as the closure of the Fe-FeO miscibility gap. Finally, these results are used to construct a parameterized thermal equation of state for liquid FeO providing densities up to pressure and temperature conditions expected at the Earth's core-mantle boundary.

Accurate and precise measurements of spectroradiometric temperature are crucial for many high pressure experiments that use diamond anvil cells or shock waves. In experiments with sub-millisecond timescales, specialized detectors such as streak cameras or photomultiplier tubes are required to measure temperature. High accuracy and precision are difficult to attain, especially at temperatures below 3000 K. Here, we present a new spectroradiometry system based on multianode photomultiplier tube technology and passive readout circuitry that yields a 0.24 mu s rise-time for each channel. Temperature is measured using five color spectroradiometry. During high pressure pulsed Joule heating experiments in a diamond anvil cell, we document measurement precision to be +/- 30 K at temperatures as low as 2000 K during single-shot heating experiments with 0.6 mu s time-resolution. Ambient pressure melting tests using pulsed Joule heating indicate that the accuracy is +/- 80 K in the temperature range 1800-2700 K.

Solid iron-silicon alloys play an important role in planetary cores, especially for planets that formed under reducing conditions, such as Mercury. The CsCl (B2) structure occupies a considerable portion of the Fe-Si binary phase diagram at pressure and temperature conditions relevant for the core of Mercury, yet its thermodynamic and thermoelastic properties are poorly known. Here, we report in situ X-ray difraction measurements on iron-silicon alloys with 7-30 wt% Si performed in laser-heated diamond-anvil cells up to similar to 120 GPa and similar to 3000 K. Unit-cell volumes of the B2 phase at high pressures and high temperatures have been used to obtain a composition-dependent thermal equation of state of this phase. In turn, the thermal equation of state is exploited to determine the composition of the B2 phase in hcp+B2 mixtures at 30-100 GPa and to place constraints on the hcp+B2/B2 phase boundary, determined to vary between similar to 13-18 wt% Si in the considered pressure and temperature range. The hcp+B2/B2 boundary of Fe-Si alloys is observed to be dependent on pressure but weakly dependent on temperature. Our results, coupled with literature data on liquid equations of state, yield an estimation of the density contrast between B2 solid and liquid under Mercury's core conditions, which directly relates to the buoyancy of the crystallizing material. While the density contrast may be large enough to form a solid inner core by the gravitational sinking of B2 alloys in a Si-rich core, the density of the B2 solid is close to that of the liquid at solidus conditions for Si concentration approaching similar to 10 wt% Si.