Forty years ago, Leander Keck criticised the ‘tyranny of titles’ in the study of New Testament Christology. While Keck rightly criticised early- to mid-twentieth approaches to titles for Jesus, there is no denying the importance of titles in New Testament texts. This article summarises classic twentieth-century approaches to christological titles and discusses the most important criticisms. The root issue of such approaches is the conflation of titles and concepts. A constructive proposal is offered for reading christological titles as literary strategies of characterisation. This approach begins by carefully defining what is meant by a title and how titles might be distinguished from common nouns and names. Six principles for the productive interpretation of titles are then discussed: 1) titles must be distinguished from other christological material like motifs, typologies, and references to biblical texts; 2) titles must be distinguished from each other; 3) titles are meaningful not because they refer to particular ideas but because of their relationship with biblical texts, religious life, and culture; 4) what a title does is more important than what a title means; 5) titles are flexible, polyvalent, and ambiguous; 6) titles must be read alongside other titles and non-titular material. Finally, it is demonstrated how this literary approach to titles will be fruitful for contemporary discussions in New Testament Christology and contribute to the renewal of New Testament Christology that Keck called for several decades ago.1

The formation of hematite from amorphous Fe(III)hydroxide in aqueous systems at pH 6 and 70°C, both with and without oxalate, was followed by kinetic measurements, electron microscopy, i.r. spectroscopy and thermal analysis.

In the absence of oxalate, small amorphous particles coalesce into aggregates which eventually become single crystals of hematite. When oxalate is present, crystal growth is much faster and does not proceed through the intermediate stage of aggregation. Aggregates, when formed, consist of groups of single crystals. It is suggested that oxalate accelerates the nucleation of hematite crystals by acting as a template, the Fe-Fe distance in Fe-oxalate ions being similar to that in hematite.

Surface properties of reduced charge montmorillonites (RCM) whose exchange capacities were saturated with tetra-alkylammonium cations, were studied with X-ray diffraction, nitrogen, and water adsorption. Methods were utilized for preparing montmorillonite of varying charge and of swelling reduced-charge clay with ethanol. As charge reduction proceeds, all layers retain some exchangeable cations until about half the original charge is reached at which point collapsed layers begin to appear and increase to about 60 per cent at maximum charge reduction. Charge reduction thus appears to proceed in a non-homogeneous fashion. When saturating exchange sites with tetra-alkylammonium ions in ethanol solvent, intercalation of salt in uncharged layers was noted if the samples were not completely washed. Nitrogen adsorption isotherms at liquid nitrogen temperatures showed considerable interlamellar penetration of tetramethylammonium (TMA+) clays, resulting in high calculated surface areas. Much less adsorption on the tetra-n-propylammonium (TPA+) clays was observed. Surface areas were increased upon reduction of charge up to the point where collapsed layers began to be appreciable, whereupon measured areas decreased. Water adsorption isotherms reflected the hydration properties of the exchangeable cation as well as the surface available for adsorption.

Within southern US newspapers, the Indian Uprising of 1857 was reported and read across a global colour line, which posited the superiority of whiteness against the “darker races,” thereby developing a framework through which white Southerners could amplify their own internal fears about the possibility of slave rebellion. News printed in southern newspapers about the events in India can be seen through a lens of the South's racial hierarchy and can also be analysed as part of a wider global system of nineteenth-century white supremacy. Despite Anglophobia and fear of abolitionists, southern enslavers could also find it within themselves to support the British when it came to the maintenance of a global hierarchy of whiteness. The news from India could be read as a form of contextual substitution, in which southern slaveholders could see perceived racial parallels between themselves and the British in India, and between the “darker races” of the world, whether that was the enslaved African American or the Indian Sepoy.

The results of X-ray diffraction, DTA, i.r. spectroscopy, and chemical tests are presented for some chlorites typical of the Flagstaff Hill area. The area is notable for the large variety of chlorite types occurring in considerable quantities. Chlorite, in this area, is found as veins, as pseudomorphs, and as individual crystals. Textures vary from massive, fine-grained aggregates to books which are more than 20 mm in width. Crystals more than 5 mm in size occur in parallel groupings at rock interfaces. Judging from 45 chlorite samples studied, sheridanite is most abundant; clinochlore and ripidolite are common. Penninite and its Cr-chlorite equivalent are less abundant. The parent rock is an irregularly shaped ultramafic body surrounded by low-grade schists and located very close to a granodiorite stock. The original ultramafic rocks have been highly altered by metamorphism and metosomatism into assemblages comprised mainly of serpentine, talc, hornblende, and chlorite with relics of olivine, pyroxene, and other less abundant original minerals. Much of the exposed rock is essentially monomineralic, mostly consisting of various polytypes of serpentine. Preliminary investigation indicates that the area merits much more study because of the opportunity for readily observing the various chlorite types and determining their genesis, alteration sequences and weathering characteristics. The area, being easily accessible, could also serve as an adequate source for samples to be used as reference standards.

The clay minerals formed in a deeply weathered boulder conglomerate of Middle Old Red Sandstone (Devonian) age in north-east Scotland have been studied by a variety of physical and chemical techniques. The granite and granulite boulders in this deposit are completely weathered. With the exception of microcline, all the feldspars in these rocks—orthoclase feldspar, orthoclase-microperthite, albite, and oligoclase—weather to a Cheto-type montmorillonite, poor in iron. Electron and optical microscopy indicate that the weathering transformation is a direct one, without the intervention of any intermediate crystalline or well-defined amorphous phase. Structural control of the primary mineral over the formation of the montmorillonite seems to have been a minimal factor and the evidence suggests that the clay mineral crystallized from the soluble or colloidal products arising from the decomposed feldspars. Smaller amounts of kaolinite also formed during weathering but largely from the weathering of muscovite. The environment in which these changes occurred seems to have been alkaline in a relatively closed system. Chemical analyses of related cores and weathered shells of granite and granulite bounders show only a slight decrease of silica and an increase in magnesia. Judging from the extent of alteration to secondary clay minerals, the order of resistance towards weathering of the primary minerals in these rocks is plagioclase = orthoclase < muscovite < biotite < microcline < quartz.

Three sepiolite clays studied showed evidence for the presence of structural hydroxyl groups in three to five different environments depending on the composition of the clay. A 3720 cm−1 i.r. frequency is shown to be characteristic of SiOH at crystal edges which are very abundant in sepiolites. This band has not been seen by most workers because the Nujol, fluorolube or KBr used in sample preparation perturb it sufficiently to obscure it under other OH stretching bands. The 3680 cm−1 band is confirmed as being from the (Mg)3OH and evidence of a very small band near 3640 cm−1 is suggested to arise from limited trioctahedral substitution. The very crystalline Ampandrandava sepiolite shows only the above three bands. The intermediately crystalline Vallecas shows a 3620 cm−1 band in addition which is characteristic of dioctahedral systems and is due to either some vacancy sites or to the presence of attapulgite. This dioctahedral band is greater in the less crystalline Salinelles sepiolite; in addition, it has a smaller 3585 cm−1 band. Mg-Al-vacancy and Mg-Fe‴-vacancy are suggested as the source of the 3620 cm−1 and 3585 cm−1 bands.

Artificial alteration of thirty-five trioctahedral and one dioctahedral micas by solutions varying in strength from 0·001 to 1·00 molal magnesium sulfate was found to approximate a normal exchange reaction after surface effects are eliminated. The equilibrium constants for the reaction:

$1/2M{g}^{2+}+K-mica=M{g}_{1/2}-mica+K^{+}\left(vermiculite\right)$$1/2 {Mg^{2+}}+K-mica=Mg_{1/2}-mica+K^+(vermiculite)$

range from 0·0001 to 0·0028 and average 0·0010 in value. X-ray diffraction study reveals that iron-rich micas tend to develop a 1:1 mixed-layer biotite-vermiculite structure in weak magnesium sulfate solutions whereas magnesium-rich biotite and phlogopite alter to vermiculite. Mica composition also influences the degree of alteration of mica to vermiculite. High fluorine and octahedral multivalent cation contents tend to retard the reaction whereas high magnesium content and perhaps high calcium contents tend to favor the alteration. The equilibrium constant data indicate that vermiculite and hydrobiotite are more stable than trioctahedral micas in most weathering environments.

X-ray diffraction patterns obtained from montmorillonite-dextran complexes prepared with either B-512F or Polytran dextran showed maximum oven-dry crystal expansions of about 5·3 Å. X-ray diffraction patterns of individual complex preparations containing < 20 per cent dextran showed evidence of both expanded and collapsed crystals. The observation of expanded and collapsed crystals in individual preparations has not been previously reported and was apparently related to clay preparation. An estimate of the quantity of dextran which could be interacting with the silicate surface was obtained using polymer adsorption weights and volumes. At maximum adsorption almost all adsorbed B-512F could be in contact with the mineral surface, but only two thirds of the adsorbed Polytran could be in contact with the mineral surface.

The combined use of electron microscopy and of selected area diffraction (SAD) has been applied to the study of montmorillonites from Wyoming and from Camp-Berteaux, of nontronite, and of hectorite. The study shows that only the elementary layers of the Wyoming montmorillonite and of the nontronite are single two-dimensional crystals. The elementary layers of the montmorillonite from Camp-Berteaux are formed by edge-to-edge associations of very small elements with mutual orientations of about 60° or multiples of 60°. The layers of hectorite are formed by edge-to-edge association of laths with fluctuations of orientation of the order of 10° rotation around adjoining edges. The SAD patterns of Wyoming montmorillonite show that the single layer plane symmetry group of this mineral is c1m1; nontronite layers belong to the symmetry group c2mm. The study of thick particles shows that in turbostratic smectites the layers are stacked with mutual rotations around the perpendicular to their plane. This mode of stacking explains the absence of hkl reflections. High resolution diffraction (HRD) patterns obtained with sample inclined to the electron beam show that only the structure of hectorite approaches the ideal model; nontronite and montmorillonite exhibit appreciable distortions with respect to the ideal model. HRD diagrams provide precise information for the refinement of the crystal structures of smectites