Changes in abundance and distribution of marine top predators can indicate environmental change or anthropogenic pressure requiring management response. Here, we used an extensive dataset (21 years) to conduct a spatial and temporal analysis of grey seal strandings in Cornwall and the Isles of Scilly, close to the southern edge of the breeding range of the species. A total of 2007 strandings were reported from 2000 to 2020, increasing by 474% from 35 to 201 individuals per year during this period. The continued rise in strandings was consistent across all life stages and timeframes (5, 10 and 20 years), underpinning the suggestion of increasing abundance in the region. The observed seasonality differed by life stage, coinciding with the increased presence of animals near the coast for key life phases such as breeding, moulting and pupping. Strandings are widely distributed across the coast of Cornwall and the Isles of Scilly; however, most strandings were recorded on the north coast of Cornwall (70%) where major pupping and haul out sites are found. Despite hosting several pupping and haul out sites, a small proportion was recorded on the Isles of Scilly (5%) where it is thought that strandings are particularly underreported. Describing baselines in magnitude of strandings and life-stage compositions across space and time allows future deviations in frequency, demographic composition or spatial distribution to be detected and investigated. We demonstrate the utility of long-term citizen science data to provide valuable and cost-effective information on the distribution and abundance of a highly mobile marine mammal.

The appearance of Beaker pottery in Britain and Ireland during the twenty-fifth century bc marks a significant archaeological horizon, being synchronous with the first metal artefacts. The adoption of arsenical copper, mostly from Ireland, was followed by that of tin-bronze around 2200 bc. However, whilst the copper mine of Ross Island in Ireland is securely dated to the Early Bronze Age, and further such mines in the UK have been dated to the Early and Middle Bronze Age, the evidence for the exploitation of tin ores, the other key ingredient to make bronze, has remained circumstantial. This article contains the detailed analyses of seven stone artefacts from securely dated contexts, using a combination of surface pXRF and microwear analysis. The results provide strong evidence that the tools were used in cassiterite processing. The combined analysis of these artefacts documents in detail the exploitation of Cornish tin during this early phase of metal use in Britain and Ireland.

The new mineral ferroberaunite, Fe2+Fe3+5(PO4)4(OH)5⋅6H2O (IMA2021-36; symbol: Fbru), occurs in cavities of ‘limonite’ iron ore from the Gravel Hill mine, Perranzabuloe, Cornwall, England. Its flattened prismatic crystals up to 400 μm long are dark green to olive green, transparent to translucent, with a vitreous lustre, pearly on cleavages. The Mohs hardness is ~3–4. The density measured by the flotation method is 2.94(2) g⋅cm–3, the calculated density is 2.907 g⋅cm–3. Ferroberaunite is biaxial (–), with α = 1.736(2), β = 1.765(3), γ = 1.786(5) at 589 nm, 2Vmeas. = 68(3)°, 2Vcalc. = 79°; dispersion of optical axes is strong, r > v; orientation is Y = b; X ≈ a, Z ≈ c. Pleochroism is strong: X = bluish-green >> Z = green > Y = yellow. Electron-microprobe analyses gave the empirical formula (Fe2+0.75Ca0.01Mn0.02Fe3+0.22)Σ1.00(Fe3+4.88Al0.04)Σ4.92(PO4)4O0.11(OH)4.76⋅6H2O. Ferroberaunite is monoclinic, C2/c, with a = 20.8708(3), b = 5.1590(8), c = 19.2263(3) Å, β = 93.3186(17)°, V = 2066.7(3) Å3 and Z = 4. The eight strongest lines in the powder X-ray diffraction pattern are [dmeas, Å (Irel., %) (hkl)]: 10.410 (100) (200), 9.606 (14) (002), 7.271 (11) (20$\bar{2}$), 5.203 (4) (400), 3.467 (12) (600), 3.325 (6) (60$\bar{2}$), 3.201 (6) (006), 2.600 (4) (800). The mineral is isostructural with beraunite, redefined recently as Fe3+6(PO4)4O(OH)4⋅6H2O.

The occurrence, chemical composition and structural characterisation of the new mineral kernowite, ideally Cu2Fe(AsO4)(OH)4⋅4H2O, the Fe3+-analogue of liroconite, Cu2Al(AsO4)(OH)4⋅4H2O, are described. Kernowite (IMA2020-053) occurs on specimens probably sourced from the Wheal Gorland mine, St Day, Cornwall, UK, in the cavities of a quartz-gossan rich in undifferentiated micro-crystalline grey sulfides and poorly crystalline arsenic phases including both pharmacosiderite and olivenite-group minerals. The average composition of kernowite determined from several holotype fragments by electron microprobe analysis is Cu1.88(Fe0.79Al0.09)Σ0.88(As1.12O4)(OH)4⋅3.65H2O. The structure of kernowite has been determined in monoclinic space group I2/a (a non-standard setting of C2/c) by single-crystal X-ray diffraction (SCXRD) to R1 = 0.025, wR2 = 0.051 and Goodness-of-fit = 1.112. Unit-cell parameters from SCXRD are a = 12.9243(4) Å, b = 7.5401(3) Å, c = 10.0271(3) Å, β = 91.267(3)°, V = 976.91(6) Å3 and Z = 4. The chemical formula of this crystal indicated by SCXRD from refined site-scattering is Cu2(Fe3+0.84(1)Al0.16)AsO4(OH)4⋅4H2O. The network of hydrogen bonding has been determined and is similar to that reported for liroconite from Wheal Gorland by Plumhoff et al. (2020).

Accurately dating the creation and development of earthwork features is a long-standing problem for archaeologists. This article presents results from Bosigran (Cornwall, UK), where boundary banks believed to be prehistoric in origin are assessed using optically stimulated luminescence profiling and dating (OSL-PD). The results provide secure construction dates for different boundaries in the Bronze and Iron Ages, as well as chronologies for their early medieval and later development. The research demonstrates not only the prehistoric origins of these distinctive Cornish field systems, but also a practical and cost-effective methodology suitable for dating earthworks around the world.

Quartz-hematite veins in the St. Austell pluton feature an assemblage of authigenic kaolin, illite, chlorite and hematite. Similar assemblages occur in altered granites adjacent to the veins. Complex textures in the veins and altered granites show that kaolin was an initial precipitate from hydrothermal fluids that was subsequently replaced by illite, hematite and chlorite. The sequence of mineral precipitation reflects a kinetic control on crystal growth, with early nonequilibrium precipitation of kaolin from fluids with compositions appropriate for the equilibrium formation of illite. Hematite formed under relatively oxidizing conditions that subsequently became more reducing to permit the late precipitation of chlorite. Illite associated with the quartz-hematite veins differs texturally, mineralogically and chemically from the coarsely crystalline hydrothermal muscovite (sericite or gilbertite) associated with quartz-tourmaline veins and greisen. Quartzhematite veins are thus considered to record a distinct mineralization event that is not related to the early greisenization or the economic kaolinization.

The type specimen of liskeardite, (Al, Fe)3AsO4(OH)6·5H2O, from the Marke Valley Mine, Liskeard District, Cornwall, has been reinvestigated. The revised composition from electron microprobe analyses and structure refinement is [Al29.2Fe2.8(AsO4)18(OH)42(H2O)22]·52H2O. The crystal structure was determined using synchrotron data collected on a 2 μm diameter fibre at 100 K. Liskeardite has monoclinic symmetry, space group I2, with the unit-cell parameters a = 24.576(5), b = 7.754(2) Å, c = 24.641(5) Å, and β = 90.19(1)º. The structure was refined to R = 0.059 for 9769 reflections with I > 3σ(I). It is of an open framework type in which intersecting polyhedral slabs parallel to (101) and (10) form 17.4 Å × 17.4 Å channels along [010], with water molecules occupying the channels. Small amounts (<1 wt.%) of Na, K and Cu are probably adsorbed at the channel walls The framework comprises columns of pharmacoalumite-type, intergrown with chiral chains of six cis edge-shared octahedra. It can be described in terms of cubic close packing, with vacancies at both the anion and cation sites. The compositional and structural relationships between liskeardite and pharmacoalumite are discussed and a possible mechanism for liskeardite formation is presented.

The cathodoluminescence (CL) of cassiterite (SnO2) from the paragenetic sequence in the lodes at South Crofty Mines has been used in the interpretation of the processes which govern mineral deposition. Luminescence is controlled by the substitution of Ti, Fe and W for Sn in the cassiterite lattice. Ti and W behave as luminescence activators whereas Fe quenches luminescence. The observed colours and intensity of the luminescence are believed to result from the interplay between these effects. Successive generations of cassiterite formed during the separate stages of paragenetic evolution show different luminescence colours. These are believed to reflect changes in bulk composition of the fluid, which is indicated by the systematic variation in the composition of tourmaline in the associated gangue.

CL also reveals details of growth and deformation in individual crystals. Growth textures observed in CL are broad concentric growth banding, oscillatory zoning and sector zoning. Sector boundaries often show a zig-zag form which is indicative of competitive growth of adjacent crystal faces. Interpretation of CL textures is used to support the hypothesis that cassiterite growth took place under two main regimes. These are, firstly, conditions in which fluid pressure decreased abruptly when tectonic reactivation caused dilation of parts of the lode fracture system and secondly, conditions of sustained hydraulic pressure within fractured vein fill. In tectonically induced fractures the crystals are stubby, have non-equivalent growth faces and are commonly tetragonal bipyramidal forms in which sector zoning is invariably present. In hydraulic fractures crystals take a predominantly tetragonal prismatic form. Thus, it is believed that growth under these contrasting conditions leads to distinctive morphology and zoning in cassiterite, providing a basis for typomorphic characterisation.

Vochtenite, a new mineral from the Basset Mine, southeast of Camborne in Cornwall, England, is a ferrous-ferric magnesium-bearing hydroxy uranyl phosphate mineral. It is monoclinic with a = 12.606, b = 19.990, c = 9.990 Å, β = 102.31° Z = 3; the ideal formula is:

The strongest lines in the X-ray powder diffraction pattern are: 9.998(100)(020), 4.999(30)(040), 4.892(45)(002), 3.475(70)(311), 3.333(50)(060), 3.087(40)(232), and . Vochtenite is brown in colour with a bronzy lustre and is non-fluorescent. Mohs hardness is 2.5 and the density (calc.) = 3.663 g/cm3. There is a prominent (010) cleavage. Vochtenite is optical biaxial negative, 2V (calc.) = 89(3)° its dispersion is indiscernible. Refractive indices are α = 1.575(2), β = 1.589(2), γ = 1.603(2), and the pleochroism is very weak. Orientation X(α)∥b is perpendicular to (010) and Z(γ)∧c is small. The mineral occurs as subparallel (0.5–1.0 mm) crystal aggregates with a pseudo-quadratic outline. The mineral is named vochtenite after Prof. Dr. Ing. R. F. C. Vochten of the State University of Antwerpen, Belgium.

The Carnmenellis pluton is a post-orogenic granite of Hercynian age, comprised largely of porphyritic biotite granites which possess LREE enriched patterns with slight negative Eu anomalies. Electron microprobe and ICP spectrometry data are presented for monazite, which occurs as an accessory mineral in all granite types, and it is demonstrated that this mineral is the principal host for LREE in the biotite granites. HREE are strongly partitioned into the accessory minerals xenotime, apatite, and zircon; only Eu substitutes significantly into the essential minerals. The behaviour of the REE during granite differentiation is controlled by the behaviour of the radioactive accessory minerals, which limits the usefulness of these elements in the petrogenetic modelling of granitic rocks.

Multi-packer hydraulic tests and radioactive tracer experiments carried out in boreholes in the Carnmenellis granite have shown that the flow of water through the rock is largely confined to narrow zones separated by zones of very low permeability. Correlation of the hydraulic data with geological data from oriented cores has shown that most of the flow is associated with discrete geological features, including pegmatitic and other veins, and elvan (quartz-feldspar porphyry) dykes, characteristic features of the granite of the area. Joints have also been found to conduct water, particularly in the upper 250 m of the granite. The permeability of the granite has been found not to be simply a function of fracture frequency, long sections of highly fractured rock having no associated flow under test conditions. While flow paths have been found to become less frequent with depth, flow rates do not vary over the depths studied, the highest flow rate recorded at the site being associated with a vein at 637 m. Water-conducting fractures have been found to have certain preferred orientations which vary with depth. A set striking 155°C is particularly well developed in the upper 250 m of the granite. This orientation is significant in that it is parallel to the cross-courses in the nearby mineralized belt with which the younger (Tertiary) mineralization tends to be associated and from which thermal brines issue into several local mines. These fractures are also approximately parallel to the maximum horizontal stress which affects the granite and which appears to be responsible for the selective opening of joints of certain orientations.

Gyrolite containing no detectable Al (<0.04 wt.%) has been found as aggregates of platey crystals to 6 mm at Dean Quarry, the Lizard, Cornwall. The gyrolite occurs embedded in calcite which fills a fracture vein in gabbro. Paragenetic evidence is inconclusive, but suggests that gyrolite formed relatively early, after prehnite, and possibly around the same time as analcime and natrolite.

Infrared spectroscopy is a rapid method of distinguishing between pseudomalachite and its polymorphs reichenbachite and ludjibaite. This technique, backed by X-ray diffraction has shown that a number of specimens labelled ‘pseudomalachite’ from Cornwall, in particular from Old Gunnislake mine, are of reichenbachite, thus identified for the first time from the British Isles. Reichenbachite has also been identified with pseudomalachite from Miguel Vacas mine, Vila Viçosa, Evora, Portugal. Identification of pseudomalachite from a number of other localities world-wide has been confirmed, and some specimens have been shown to be arsenatian.