Walstromite, BaCa₂Si₃O₉, known only from metamorphic rocks of North America, was found in small veins of unusual rankinite paralava within gehlenite hornfelses of the Hatrurim Complex, Israel. It was detected at two localities—Gurim Anticline and Zuk Tamrur, Hatrurim Basin, Negev Desert. The structure of Israeli walstromite [with P $\overline{1}$ space group and cell parameters a = 6.74874(10) Å, b = 9.62922(11) Å, c = 6.69994(12) Å, α = 69.6585(13)°, β = 102.3446(14)°, γ = 96.8782(11)°, Z = 2, V = 398.314(11) ų] is analogous to the structure of walstromite from type locality—Rush Creek, eastern Fresno County, California, USA. The Raman spectra of all tree minerals exhibit bands related to stretching symmetric vibrations of Si-O-Si at 650–660 cm⁻¹ and Si-O at 960–990 cm⁻¹ in three-membered rings (Si₃O₉)⁶⁻. This new genetic pyrometamorphic type of walstromite forms out of the differentiated melt portions enriched in Ba, V, S, P, U, K, Na, Ti and F, a residuum after crystallization of rock-forming minerals of the paralava (rankinite, gehlenite-åkermanite-alumoåkermanite, schorlomite-andradite series and wollastonite). Walstromite associates with other Ba-minerals, also products of the residual melt crystallization as zadovite, BaCa₆[(SiO₄)(PO₄)](PO₄)₂F and gurimite, Ba₃(VO₄)₂. The genesis of unusual barium mineralization in rankinite paralava is discussed. Walstromite is isostructural with minerals—margarosanite, BaCa₂Si₃O₉ and breyite, CaCa₂(Si₃O₉), discovered in 2018.

Ariegilatite, BaCa₁₂(SiO₄)₄(PO₄)₂F₂O (R $\overline{3}$ m, a = 7.1551(6) Å, c = 41.303(3) Å, V = 1831.2(3) ų, Z = 3), is a new member of the nabimusaite group exhibiting a modular intercalated antiperovskite structure derived from hatrurite. It was found in a few outcrops of pyrometamorphic rocks of the Hatrurim Complex located in the territories of Israel, Palestine and Jordan. The holotype specimen is an altered spurrite marble from the Negev Desert near Arad city, Israel. Ariegilatite is associated with spurrite, calcite, brownmillerite, shulamitite, CO₃-bearing fluorapatite, fluormayenite-fluorkyuygenite and a potentially new mineral, Ba₂Ca₁₈(SiO₄)₆(PO₄)₃(CO₃)F₃O. Ariegilatite is overgrown and partially replaced by stracherite, BaCa₆(SiO₄)₂[(PO₄)(CO₃)]F. The mineral forms flat disc-shaped crystals up to 0.5 mm in size. It is colorless, transparent, with white steaks and vitreous luster. Optically, ariegilatite is uniaxial, negative: ω = 1.650(2), ε = 1.647(2) (λ = 589 nm). The mean composition of the holotype ariegilatite, (Ba_0.98K_0.01Na_0.01)_Σ1(Ca_11.77Na_0.08Fe²⁺_0.06Mn²⁺_0.05Mg_0.04)_Σ12(Si_3.95Al_0.03Ti_0.02)_Σ4(P_1.70C_0.16Si_0.10S⁶⁺_0.03V_0.01)_Σ2F_2.04O_0.96, is close to the end-member formula. The structure of ariegilatite is described as a stacking of the two modules {F₂OCa₁₂(SiO₄)₄}⁴⁺ and {Ba(PO₄)₂}⁴⁻ along (001). Ariegilatite, as well as associated stracherite, are high-temperature alteration products of minerals of an early clinker-like association. These alterations took place under the influence of pyrometamorphism by-products, such as gases and fluids generated by closely-spaced combustion foci.

The Hatrurim Basin, Israel, is located on the western border of the Dead Sea Transform. This is one of the localities of a unique pyrometamorphic complex whose genesis remains problematic. This paper deals with zeolite-bearing rock that is known in the Hatrurim Basin only. The strata subjected to zeolitization is called the “olive unit” and consists of anorthite–pyroxene (diopside–esseneite) hornfels. Zeolitization occurred in an alkaline environment provided by the interaction of meteoric water with Portland-cement-like rocks of the Hatrurim Complex. The resulting zeolite-bearing rocks contain 20–30% zeolitic material. The main zeolitic minerals are calcic: thomsonite-Ca ± Sr, phillipsite-Ca, gismondine-Ca, and clinoptilolite-Ca. The remainder is calcite, diopsidic pyroxene, garnets (either Ti-andradite and/or hydrogrossular), and less frequently, fluorapatite, opal, and others. Their major mineralogical and chemical compositions resemble carbonated zeolite-blended Portland mortar. Rocks show different values of porosity. Their mechanical characteristics are much better for samples with porosity values below 24%. The related parameters are like those of blended concretes. The minimal age of zeolitization is 5 Ka. The natural zeolite-bearing rocks are resistant to weathering in the Levant desert climate.

In the last 15 years, zeolite-like mayenite, Ca₁₂Al₁₄O₃₃, has attracted significant attention in material science for its variety of potential applications and for its simple composition. Hydrogen plays a key role in processes of electride material synthesis from pristine mayenite: {Ca₁₂Al₁₄O₃₂}²⁺(O²) → {Ca₁₂Al₁₄O₃₂}²⁺(e⁻)₂. A presence of molecular hydrogen in synthetic mayenite was not confirmed by the direct methods. Spectroscopy investigations of mayenite group mineral fluorkyuygenite, with empirical formula (Ca_12.09Na_0.03)_∑12.12(Al_13.67Si_0.12Fe³⁺_0.07Ti⁴⁺_0.01)_∑12.87O_31.96 [F_2.02Cl_0.02(H₂O)_3.22(H₂S)_0.15□_0.59]_∑6.00, show the presence of an unusual band at 4038 cm⁻¹, registered for the first time and related to molecular hydrogen, apart from usual bands responding to vibrations of mayenite framework. The band at 4038 cm⁻¹ corresponding to stretching vibrations of H₂ is at lower frequencies in comparison with positions of analogous bands of gaseous H₂ (4156 cm⁻¹) and H₂ adsorbed at active cation sites of zeolites (4050–4100 cm⁻¹). This points out relatively strong linking of molecular hydrogen with the fluorkyuygenite framework. An appearance of H₂ in the fluorkyuyginite with ideal formula Ca₁₂Al₁₄O₃₂[(H₂O)₄F₂], which formed after fluormayenite, Ca₁₂Al₁₄O₃₂[□₄F₂], is connected with its genesis. Fluorkyuygenite was detected in gehlenite fragments within brecciaed pyrometamorphic rock (Hatrurim Basin, Negev Desert, Israel), which contains reduced mineral assemblage of the Fe-P-C system (native iron, schreibersite, barringerite, murashkoite, and cohenite). The origin of phosphide-bearing associations is connected with the effect of highly reduced gases on earlier formed pyrometamorphic rocks.

For the first time, chromium disulphides, known from meteorites, such as caswellsilverite, NaCrS₂; grokhovskyite, CuCrS₂; and a potentially new mineral, AgCrS₂, as well as the products of their alteration, such as schöllhornite, Na_0.3CrS₂∙H₂O, and a potentially new mineral with the formula {Fe_0.3(Ba,Ca)_0.2} CrS₂·0.5H₂O, have been found in terrestrial rock. Layered chromium disulphides were found in unusual phosphide-bearing breccia of the pyrometamorphic Hatrurim Complex in the Negev Desert, Israel. The chromium disulphides belong to the central fragment of porous gehlenite paralava cementing altered host rock clasts. The empirical formula of caswellsilverite is (Na_0.77Sr_0.03Ca_0.01)_Σ0.81(Cr³⁺_0.79Cr⁴⁺_0.18V³⁺_0.01 Fe³⁺_0.01)_Σ0.99S₂·0.1H₂O, and the end-member content of NaCrS₂ is 76%. It forms single crystals in altered pyrrhotite aggregates. Grokhovskyite has the empirical formula {Cu⁺_0.84Fe³⁺_0.10Ca_0.06 Na_0.01 Sr_0.01Ba_0.01}_Σ1.03(Cr³⁺_0.94 Fe³⁺_0.05 V³⁺_0.05)_Σ1.00S₂·0.35H₂O, and the CuCrS₂ end-member content is 75–80%. A potentially new Ag-bearing chromium disulphide is characterised by the composition (Ag_0.89Cu_0.07)_Σ0.96(Cr_0.98 Fe_0.03V_0.01Ni_0.01)_Σ1.04S₂. Caswellsilverite, grokhovskyite and AgCrS₂ form in gehlenite paralava at high temperatures (near 1000 °C) and low pressure under reducing conditions. The structure of the layered chromium disulphides, MCrS₂, is characterised by the presence of hexagonal octahedral layers (CrS₂)¹⁻, between which M-sites of the monovalent cations Ag, Cu and Na set. A low-temperature alteration of the layered chromium disulphides, when schöllhornite and {Fe_0.3(Ba,Ca)_0.2}CrS₂·0.5H₂O form, is reflected in the composition and structural modification of the layer with monovalent cations, whereas the octahedral layer (CrS₂)¹⁻ remains unchanged.