登录注册
Quick Links : Mindat手册The Rock H. Currier Digital LibraryMindat Newsletter [Free Download]
主页关于 MindatMindat手册Mindat的历史版权Who We Are联系我们于 Mindat.org刊登广告
捐赠给 MindatCorporate Sponsorship赞助板页已赞助的板页在 Mindat刊登 广告的广告商于 Mindat.org刊登广告
Learning CenterWhat is a mineral?The most common minerals on earthInformation for EducatorsMindat ArticlesThe ElementsThe Rock H. Currier Digital LibraryGeologic Time
搜索矿物的性质搜索矿物的化学Advanced Locality Search随意显示任何一 种矿物Random Locality使用minID搜索邻近产地Search Articles搜索词汇表更多搜索选项
搜索:
矿物名称:
地区产地名称:
关键字:
 
Mindat手册添加新照片Rate Photos产区编辑报告Coordinate Completion Report添加词汇表项目
Mining Companies统计会员列表Mineral MuseumsClubs & Organizations矿物展及活动The Mindat目录表设备设置The Mineral Quiz
照片搜索Photo GalleriesSearch by Color今天最新的照片昨天最新的照片用户照片相集过去每日精选照片相集Photography

Salisbury Mining District, USAi
Regional Level Types
Salisbury Mining DistrictMining District (Abandoned)
USACountry

This page is currently not sponsored. Click here to sponsor this page.
PhotosSearch
Latitude & Longitude (WGS84):
42° North , 73° West (est.)
Estimate based on other nearby localities or region boundaries.
Margin of Error:
~22km
Type:
Mining District (Abandoned)
Mindat Locality ID:
24267
Long-form identifier:
mindat:1:2:24267:2
GUID (UUID V4):
d7ff68e0-a911-4bab-bb51-b92ff7898aa2


A group of goethite mines around the tri-state (CT-MA-NY) border junction that worked what is probably a metamorphosed, lateritic soil horizon formed on the unconformity between the Cambro-Ordovician Stockbridge Marble and the overlying Ordovician Walloomsac Schist. These mines were an important industry for the region and the country during the late 18th until the very early 20th century and fed many iron furnaces in the tri-state area. A map can be found here: https://www.mindat.org/photo-879814.html

Most of the literature calls the ore limonite, brown hematite, turgite, etc. because the term goethite was not in prevalent use in North America at that time and because Shepard's 1837 Report on the Geologic Survey of Connecticut used those terms - although the chemical analysis he gives is clearly goethite. All modern references acknowledge the goethite character of the ore.

The Salisbury Mine (Ore Hill Mine) in Connecticut was the largest and most important of these mines, and as it is pretty much centrally located in the district, its coordinates are used below for the entire district as well.

Shepard's (1837) description:

Limonite.—This species includes all the ores which have heretofore afforded iron to commerce in this State, if we except the unimportant quantity derived from the magnetic iron-sand above mentioned. It presents a number of mineralogical varieties, depending on diversities in mechanical composition, the intermixture of foreign species, and rarely of organic impurities. Among these varieties the following may be enumerated as the most important: fibrous brown hematite, compact hematite, ochrey brown iron ore, and bog iron-ore.

Fibrous brown hematite consists of 82 peroxide of iron, 14 water, 2 oxide of manganese and 1 silica, in the hundred parts, while bog iron-ore contains from 40 to 50 p. c. of peroxide of iron, the other ingredients being silica, alumina, water and oxide of manganese, with frequent traces of phosphoric acid.

The fibrous brown hematite, compact hematite, and the ochrey mixtures of the two, are generally confined to primitive rocks, as gneiss and mica-slate. They afford materials for very large iron-works in many countries, and are universally regarded as the best ores for yielding a malleable iron, and for being easily converted into steel. Although these ores (which may be referred to, under the general name of hematite) are confined to a limited district of the State, they nevertheless appear to constitute its richest metallic resource.


Some basic details from Hobbs (1907):

The iron which comes into the market under the name of “Salisbury iron” is smelted from limonite ores mined in northwestern Litchfield County, Connecticut; Berkshire Co., Mass.; and portions of Dutchess and Columbia counties in the State of New York. The ore was first mined, and much the largest amount of ore has now for a long time been obtained at mines situated within the town of Salisbury, Connecticut. No geological report seems to have been made upon this ore district as a whole, though many widely scattered papers have made reference to it, and together constitute a considerable body of scientific information.

In spite of the rather low grade of the ores (40 to 50 and exceptionally 55 to 57 per cent. of metallic iron) and the recent vast development of iron mining within the Lake Superior region, the Salisbury mines continue to be worked. This is largely due to the peculiar properties of the ore; particularly its high content of manganese and its low percentage of phosphorus, and to the methods of smelting and founding which are employed; the furnaces of the Salisbury and Richmond regions being among the few still left in America which use charcoal as fuel. The pig iron produced from these ores is especially adapted to the manufacture of car wheels, since it is of sufficient strength to resist the strains and shocks to which the wheel body is subjected, and has further the property of taking a deep chill, so that the tread and flange of the wheel can be made to withstand the wear upon them. That the fame of the Salisbury iron for this purpose is well founded has been amply demonstrated by tests carried out by Thurston and others.

HISTORY.

Iron was mined in Salisbury at least as early as 1734, the pioneer forge, with a capacity of one hundred and fifty pounds of iron for each charge, having been erected in that year in the village of Lime Rock. The ore for it was furnished from the “Davis” or “Forbes” pit at Lakeville, then known as the “Hendricks.”

In 1781 a forge had been erected at Mount Riga on the summit plain of the Mount Washington mass, nearly one thousand feet above the mines in the valley.

In 1830 the first foundry for remelting pig iron was built at Lime Rock and soon came into the possession of Mr. Milo Barnum, the founder of the Barnum Richardson Company. This company now controls all of the ore that is mined within the Salisbury district proper, and has also an interest in the Richmond Iron Company, which operates the “Cone” mine in the Richmond district.

The mines at Salisbury, which are known as the “Old Hill,” the “Chatfield” and the “Davis,” were acquired by the Barnum Richardson Company, and have now been worked for periods of about one hundred, seventy-five and one hundred and seventy years respectively. Other mines of the region were soon purchased by the company, the greater number being near the eastern, southern or western margins of the great elevated mass situated near the common boundaries of Connecticut, Massachusetts and New York, and generally known as Mount Washington. As time went on the Barnum Richardson Company acquired many other properties in the vicinity, though most of them have now been abandoned and are so flooded with water as to afford few facilities for inspection.

Charcoal blast furnaces for the smelting of the Salisbury ores have been situated at Lime Rock, Falls Village, East Canaan, Chapinville, Cornwall Bridge, Huntsville, Amenia, Sharon Valley, Millerton, Mount Riga and Copake, all in or near the mining district....Only the furnaces at Lime Rock, Canaan, Richmond and Van Deusenville are now in use.

DISTRIBUTION OF THE MINES.

The greater number of the iron mines of the Salisbury district are located either at or near the boundary of the areas of Hudson schist with those of the Stockbridge dolomite. In this regard they have the same position as most of the other limonite deposits which have been opened along the base of the Appalachian Mountain system from Vermont to Alabama. A further fact of distribution which is of much significance is the arrangement of the mines of the Salisbury group about the base of the elevated area of Mount Washington. This mountain mass rises abruptly to heights of sixteen hundred to eighteen hundred feet above the level of the valley surrounding it. Its greatest length is seventeen miles, and its maximum breadth about six miles (see Fig. 11). The more important of the exploited ore beds form a nearly continuous series encircling the mountain mass at its base.

As properly included with the group of mines bordering on the Mount Washington mass should be mentioned those which extend southward along the line of the Ten Mile River and the Harlem River Railroad; which mines, with the last nine of the above, form a linear series which may be conveniently termed the Ten Mile series...

COMPOSITION OF THE ORES.

General Statement. - The ores of the Salisbury district have been described as largely limonite, with which is associated a small amount of turgite, and in variable quantity ores of manganese. From certain of the mines, notably the “Ore Hill,” “Amenia,” and “Copake” mines, the so-called “dead-head” or “white horse” has also been mined. This latter material, generally described as iron carbonate, is usually but an impure variety of that mineral, since it generally contains considerable silica and a sericitic or talcose mineral.

The superiority of the Salisbury ores is largely to be ascribed to the low content of phosphorus and the high content of manganese; and these qualities are enhanced by the method of smelting in charcoal furnaces.
...individual mines have their peculiarities of composition. The “Davis” ore is particularly valuable because of its high content of manganese, this is to a less extent true of that from the “Ore Hill” mine. Richest of all, in this constituent, however, was the black ore of the “Chatfield” mine, and the genuine manganese ore from the “Scoville” pit. It thus appears that the ores richest in manganese are distributed in the bodies which occur along the eastern and southeastern base of the Mt. Washington mass. The mine at South Kent was abandoned on account of the high content of phosphorus.

The fact that zinc is associated in minute quantities with manganese in nature has been illustrated by the operation of the Salisbury smelters, even though it has not been indicated by the chemical analyses. The tendency of this element to sublime results in its collection in the throats of furnaces, from which it is recovered when the furnaces are “blown out.”

Select Mineral List Type

Standard Detailed Gallery Strunz Chemical Elements

Mineral List

Mineral list contains entries from the region specified including sub-localities

18 valid minerals. 2 (TL) - type locality of valid minerals. 1 erroneous literature entry.

Detailed Mineral List:

Aurichalcite
Formula: (Zn,Cu)5(CO3)2(OH)6
Bementite ?
Formula: Mn7Si6O15(OH)8
Description: Listed as associated with rhabdophane but no site-specific details given.
Churchite-(Y)
Formula: Y(PO4) · 2H2O
Habit: colloform with concentric layers
Colour: pale yellow-white
Description: Thin colloform crust on goethite with an associated opal-AN-like layer. In Januzzi (1994) the discoverer states, "Recent examination, by way of x-ray and semi-quantitative analysis uncovered a new species for the Scoville Ore Bed in Salisbury, Connecticut; the mineral churchite, a relatively inconspicuous species and confused (no doubt often) with rhabdophane and probably more common than realized. Florencite should be looked for when churchite occurs in a deposit of this type. A hyalite-like mineral evidently forming before churchite lies just beneath it (the specimen is in the author’s collection)-this species is very possibly evansite."
Cryptomelane
Formula: K(Mn4+7Mn3+)O16
Habit: botryoidal
Colour: black with blue tint
Dolomite
Formula: CaMg(CO3)2
Galena
Formula: PbS
Gibbsite
Formula: Al(OH)3
Habit: radially fibrous masses, stalactitic and spherical concretions, and as incrustations
Goethite
Formula: α-Fe3+O(OH)
Localities: Reported from at least 23 localities in this region.
Habit: mostly earthy and massive, rarely radially fibrous masses, stalactitic, botryoidal, spherical
Colour: brown to dark brown nearly black, some botryoidal and lustrous specimens are iridescent
Description: Often misclassified as limonite, or "brown hematite" in older literature. Most material is massive dull earthy ore, best specimens have stalactitic to botryoidal forms with a highly lustrous, black surface.
Halloysite ?
Formula: Al2(Si2O5)(OH)4
Description: Listed as associated with rhabdophane but no site-specific details given.
Hematite
Formula: Fe2O3
Description: The ore is goethite, but most old literature calls it "hematite", "brown hematite", "turgite", etc., yet all specimens have a brown streak not a red streak.
Hemimorphite
Formula: Zn4Si2O7(OH)2 · H2O
'Limonite'
Localities: Reported from at least 16 localities in this region.
Lithiophorite ?
Formula: (Al,Li)MnO2(OH)2
Description: Listed as associated with rhabdophane but no site-specific details given.
Pyrolusite
Formula: Mn4+O2
Habit: massive, botryoidal or as lustrous tabular crystals to 3mm in pockets in goethite.
Colour: black
Description: According to Schairer (1931): "Occurs crystallized (probably pseudomorphous) at Salisbury and Kent, also as aggregates of coarse columnar grains or needles or as coatings on limonite. The quality of the iron produced at the iron mines of northwestern Connecticut was due to the presence of this mineral in the ore."
Rhabdophane-(La) (TL)
Formula: La(PO4) · H2O
Type Locality:
Habit: botryoidal to stalagtitic
Colour: brownish to pale yellow-white, pinkish
Rhabdophane-(Nd) (TL)
Formula: Nd(PO4) · H2O
Type Locality:
Habit: botryoidal to stalagtitic
Colour: brownish to pale yellow-white, pinkish
Siderite
Formula: FeCO3
Smithsonite
Formula: ZnCO3
Sphalerite
Formula: ZnS
Talc
Formula: Mg3Si4O10(OH)2
Description: According to Hobbs (1901): "...irregular block-like masses of so-called 'white horse.' The 'white horse' somewhat resembles the dolomite, but has soapy feel and contains 50 per cent or more of ferric oxide. It appears to be a mixture of iron carbonate and talc, and elsewhere in the Salisbury district it has been mined for the iron which it contains. At the surface it weathers to a brown color owing to the hydration of the iron oxide."
'Tennantite Subgroup'
Formula: Cu6(Cu4C2+2)As4S12S

List of minerals arranged by Strunz 10th Edition classification

Group 2 - Sulphides and Sulfosalts
Sphalerite2.CB.05aZnS
Galena2.CD.10PbS
'Tennantite Subgroup'2.GB.05Cu6(Cu4C2+2)As4S12S
Group 4 - Oxides and Hydroxides
Goethite4.00.α-Fe3+O(OH)
Hematite ?4.CB.05Fe2O3
Pyrolusite4.DB.05Mn4+O2
Cryptomelane4.DK.05aK(Mn4+7Mn3+)O16
Gibbsite4.FE.10Al(OH)3
Lithiophorite ?4.FE.25(Al,Li)MnO2(OH)2
Group 5 - Nitrates and Carbonates
Smithsonite5.AB.05ZnCO3
Siderite5.AB.05FeCO3
Dolomite5.AB.10CaMg(CO3)2
Aurichalcite5.BA.15(Zn,Cu)5(CO3)2(OH)6
Group 8 - Phosphates, Arsenates and Vanadates
Rhabdophane-(La) (TL)8.CJ.45La(PO4) · H2O
Rhabdophane-(Nd) (TL)8.CJ.45Nd(PO4) · H2O
Churchite-(Y)8.CJ.50Y(PO4) · 2H2O
Group 9 - Silicates
Hemimorphite9.BD.10Zn4Si2O7(OH)2 · H2O
Talc9.EC.05Mg3Si4O10(OH)2
Halloysite ?9.ED.10Al2(Si2O5)(OH)4
Bementite ?9.EE.05Mn7Si6O15(OH)8
Unclassified
'Limonite'-

List of minerals for each chemical element

HHydrogen
H Aurichalcite(Zn,Cu)5(CO3)2(OH)6
H BementiteMn7Si6O15(OH)8
H Churchite-(Y)Y(PO4) · 2H2O
H GibbsiteAl(OH)3
H Goethiteα-Fe3+O(OH)
H HalloysiteAl2(Si2O5)(OH)4
H HemimorphiteZn4Si2O7(OH)2 · H2O
H Lithiophorite(Al,Li)MnO2(OH)2
H Rhabdophane-(La)La(PO4) · H2O
H Rhabdophane-(Nd)Nd(PO4) · H2O
H TalcMg3Si4O10(OH)2
LiLithium
Li Lithiophorite(Al,Li)MnO2(OH)2
CCarbon
C Aurichalcite(Zn,Cu)5(CO3)2(OH)6
C DolomiteCaMg(CO3)2
C SideriteFeCO3
C SmithsoniteZnCO3
OOxygen
O Aurichalcite(Zn,Cu)5(CO3)2(OH)6
O BementiteMn7Si6O15(OH)8
O Churchite-(Y)Y(PO4) · 2H2O
O CryptomelaneK(Mn74+Mn3+)O16
O DolomiteCaMg(CO3)2
O GibbsiteAl(OH)3
O Goethiteα-Fe3+O(OH)
O HalloysiteAl2(Si2O5)(OH)4
O HematiteFe2O3
O HemimorphiteZn4Si2O7(OH)2 · H2O
O Lithiophorite(Al,Li)MnO2(OH)2
O PyrolusiteMn4+O2
O Rhabdophane-(La)La(PO4) · H2O
O Rhabdophane-(Nd)Nd(PO4) · H2O
O SideriteFeCO3
O SmithsoniteZnCO3
O TalcMg3Si4O10(OH)2
MgMagnesium
Mg DolomiteCaMg(CO3)2
Mg TalcMg3Si4O10(OH)2
AlAluminium
Al GibbsiteAl(OH)3
Al HalloysiteAl2(Si2O5)(OH)4
Al Lithiophorite(Al,Li)MnO2(OH)2
SiSilicon
Si BementiteMn7Si6O15(OH)8
Si HalloysiteAl2(Si2O5)(OH)4
Si HemimorphiteZn4Si2O7(OH)2 · H2O
Si TalcMg3Si4O10(OH)2
PPhosphorus
P Churchite-(Y)Y(PO4) · 2H2O
P Rhabdophane-(La)La(PO4) · H2O
P Rhabdophane-(Nd)Nd(PO4) · H2O
SSulfur
S GalenaPbS
S SphaleriteZnS
S Tennantite SubgroupCu6(Cu4C22+)As4S12S
KPotassium
K CryptomelaneK(Mn74+Mn3+)O16
CaCalcium
Ca DolomiteCaMg(CO3)2
MnManganese
Mn BementiteMn7Si6O15(OH)8
Mn CryptomelaneK(Mn74+Mn3+)O16
Mn Lithiophorite(Al,Li)MnO2(OH)2
Mn PyrolusiteMn4+O2
FeIron
Fe Goethiteα-Fe3+O(OH)
Fe HematiteFe2O3
Fe SideriteFeCO3
CuCopper
Cu Aurichalcite(Zn,Cu)5(CO3)2(OH)6
Cu Tennantite SubgroupCu6(Cu4C22+)As4S12S
ZnZinc
Zn Aurichalcite(Zn,Cu)5(CO3)2(OH)6
Zn HemimorphiteZn4Si2O7(OH)2 · H2O
Zn SmithsoniteZnCO3
Zn SphaleriteZnS
AsArsenic
As Tennantite SubgroupCu6(Cu4C22+)As4S12S
YYttrium
Y Churchite-(Y)Y(PO4) · 2H2O
LaLanthanum
La Rhabdophane-(La)La(PO4) · H2O
NdNeodymium
Nd Rhabdophane-(Nd)Nd(PO4) · H2O
PbLead
Pb GalenaPbS

Localities in this Region

Other Regions, Features and Areas that Intersect


This page contains all mineral locality references listed on mindat.org. This does not claim to be a complete list. If you know of more minerals from this site, please register so you can add to our database. This locality information is for reference purposes only. You should never attempt to visit any sites listed in mindat.org without first ensuring that you have the permission of the land and/or mineral rights holders for access and that you are aware of all safety precautions necessary.

References

 
矿物 and/or 产地  
Mindat Discussions Facebook Logo Instagram Logo Discord Logo
版权所有© mindat.org1993年至2024年,除了规定的地方。 Mindat.org全赖于全球数千个以上成员和支持者们的参与。
隐私政策 - 条款和条款细则 - 联络我们 - Report a bug/vulnerability Current server date and time: 2024.4.26 14:43:59 Page updated: 2023.9.30 16:19:08
Go to top of page