Ac. Roberts et al., DEANESMITHITE, HG21+HG32+CR6+O5S2, A NEW MINERAL SPECIES FROM THE CLEAR CREEK CLAIM, SAN BENITO COUNTY, CALIFORNIA, Canadian Mineralogist, 31, 1993, pp. 787-793
Deanesraithite, idealized as Hg21+Hg32+Cr6+O5S2, is triclinic, space g
roup P1BAR, with unit-cell parameters refined from powder data: a 8.11
6 (6), b 9.501 (8), c 6.891 (9) angstrom, alpha 100.43 (8)-degrees, be
ta 110.24 (8)-degrees, gamma 82.80 (8)-degrees, V 489 (2) angstrom3, a
:b:c = 0.8542:1: 0.7253, Z = 2. The strongest eight lines in the X-ray
powder pattern [d in angstrom(I)(hkl)] are: 5.72(90)(110BAR), 3.373(6
0)(112BAR,102BAR,121BAR), 8(100)(122BAR,212BAR,131BAR,112BAR,202BAR,03
1BAR), 2.864(50b)(012,201,220BAR,022BAR), 2.774(50)(221BAR), 2.536(50)
(132BAR), 2.486(50)(310), and 2.425(60)(221,032BAR,302BAR). The minera
l is a rare constituent in a small prospect pit near the long-abandone
d Clear Creek mercury mine, New Idria district, San Benito County, Cal
ifornia. It is most closely associated with cinnabar and edoylerite in
a host rock principally composed of quartz and magnesite. Deanesmithi
te typically occurs as fan-shaped aggregates of elongate crystals and,
less commonly, as isolated clusters of bladed to acicular radiating c
rystals. Tabular crystals also are present but rare. The largest known
crystal is 0.5 mm in length, but the average crystal length is approx
imately 0.1 mm. Individual crystals are subhedral to euhedral, with bo
th a bladed and a tabular habit. Crystals are flattened on {100}; blad
ed crystals are elongate [001]; tabular crystals are elongate [010]; s
triations on {100} are parallel to [001]; cleavage {110BAR} well-devel
oped, {001} fair. Forms observed are: {100}, {320}, (001), {510BAR}, {
011BAR}, {010}, {210}, (310), {410}, (510), {610}, {11O0BAR}, {320BAR}
, {210BAR}, (023), {032BAR}, and {101BAR}. The mineral is orange-red w
ith a less intense orange-red streak. Physical properties include: ada
mantine luster; transparent; nonfluorescent; brittle to friable; irreg
ular to subconchoidal fracture; hardness less than 5; calculated densi
ty 8.06 (for empirical formula), 8.14 g/cm3 (for idealized formula). I
n polished section, deanesmithite is weakly bireflectant and weakly pl
eochroic. In reflected plane-polarized light, it is dark bluish grey t
o light grey with bright yellow-orange to orange-red internal reflecti
ons. Measured reflectance values are tabulated, in air and in oil, for
two crystals. Electron-micro-probe analyses yielded Hg2O 34.9, HgO 54
.4, CrO3 8.6, S 5.3, sum 103.2, less O=S 2.6, total 100.6 wt.%, corres
ponding to Hg1.981+Hg2.972+Cr1.026+O5.05S1.95 based on O+S=7. The orig
inal value for HgO, 90.7 wt.%, was partitioned in a ratio of 2 Hg2O :
3 HgO after the crystal structure was determined. The crystal structur
e was solved by direct methods and refined to R = 2.92% from 1748 obse
rved X-ray reflections [I > 2.5 sigma(I)] out of a total of 2808 uniqu
e reflections obtained from measuring and averaging the whole sphere o
f data to a 2theta of 60-degrees collected with MoKalpha radiation. Im
portant features of the crystal structure are summarized. The name is
for Professor Deane K. Smith, Pennsylvania State University, for his m
any contributions to structural and experimental mineralogy, and for h
is long time service to the International Centre for Diffraction Data.