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Blue Dinosaur Royal Ontario Museum

Blue Dinosaur Royal Ontario Museum

Blue Dinosaur Royal Ontario Museum

Blue Dinosaur Royal Ontario Museum

Banded fine-grained pyrite in shale from the Precambrian of Australia. (public display, Leadville Mining Museum, Leadville, Colorado, USA) A mineral is a naturally-occurring, solid, inorganic, crystalline substance having a fairly definite chemical composition and having fairly definite physical properties. At its simplest, a mineral is a naturally-occurring solid chemical. Currently, there are over 4900 named and described minerals - about 200 of them are common and about 20 of them are very common. Mineral classification is based on anion chemistry. Major categories of minerals are: elements, sulfides, oxides, halides, carbonates, sulfates, phosphates, and silicates. The sulfide minerals contain one or more sulfide anions (S-2). The sulfides are usually considered together with the arsenide minerals, the sulfarsenide minerals, and the telluride minerals. Many sulfides are economically significant, as they occur commonly in ores. The metals that combine with S-2 are mainly Fe, Cu, Ni, Ag, etc. Most sulfides have a metallic luster, are moderately soft, and are noticeably heavy for their size. These minerals will not form in the presence of free oxygen. Under an oxygen-rich atmosphere, sulfide minerals tend to chemically weather to various oxide and hydroxide minerals. Pyrite is a common iron sulfide mineral (FeS2). It’s nickname is “fool's gold”. Pyrite has a metallic luster, brassy gold color (in contrast to the deep rich yellow gold color of true gold - www.flickr.com/photos/jsjgeology/sets/72157651325153769/), dark gray to black streak, is hard (H=6 to 6.5), has no cleavage, and is moderately heavy for its size. It often forms cubic crystals or pyritohedrons (crystals having pentagonal faces). Pyrite is common in many hydrothermal veins, shales, coals, various metamorphic rocks, and massive sulfide deposits. The rock shown above consists of numerous bands of fine-grained pyrite interbedded with dark shale. Published research has shown that the pyrite is diagenetic, formed by sulfate reduction from sulfate-bearing groundwater that moved along bedding planes of the Urquhart Shale host rocks (see Painter et al., 1999). The sulfate source was evaporitic gypsum-anhydrite-barite in the same stratigraphic unit. Stratigraphy: Urquhart Shale, Mount Isa Group, Mesoproterozoic, ~1655 Ma Age of metamorphism: peak greenschist-facies metamorphism at ~1505 Ma during the Isan Orogeny Locality: Mount Isa Mines, northwestern Queensland, northeastern Australia Some info. from: Kawasaki & Symons (2010) - Dating of Mesoproterozoic metamorphism in the Mount Isa and George Fisher Zn-Pb-Cu-Ag deposits, Australia, by paleomagnetism. American Geophysical Union, Fall Meeting 2010, Abstract GP33C-0953. Painter et al. (1999) - Sedimentologic, petrographic, and sulfur isotope constraints on fine-grained pyrite formation at Mount Isa Mine and environs, northwest Queensland, Australia. Economic Geology 94: 883-912. Photo gallery of pyrite: www.mindat.org/gallery.php?min=3314

Banded iron formation from the Precambrian of Wyoming, USA. (~10.9 cm across at its widest) Banded iron formations, or BIFs, are unusual, dense sedimentary rocks consisting of alternating layers of iron-rich oxides and iron-rich silicates. Most BIFs are Proterozoic in age (although some are Late Archean), and do not form today - they're “extinct”! Many specific varieties of iron formation are known, and some are given special rock names. For example, jaspilite is an attractive reddish & silvery gray banded rock consisting of hematite, red chert (“jasper”), and specular hematite or magnetite. Because of their age, most BIFs have been around long enough to have been subjected to one or more orogenic (mountain-building) events. As such, most BIFs are folded and/or metamorphosed to varying degrees. BIFs are known from around the world, but some of the most famous & extensive BIF deposits are found in the vicinity of North America’s Lake Superior Basin. Many BIFs have economic concentrations of iron and are mined. BIFs are the most important variety of iron ore on Earth. Some iron mines in west-central Wyoming exploit BIFs in the Goldman Meadows Formation, a Mesoarchean unit exposed in the Wind River Range. These rocks have been multiply metamorphosed during the Precambrian. The result of this metamorphism is highly contorted folding and fracturing. The rock shown above is a folded quartz-hematite-limonite meta-BIF. Stratigraphy: iron formation member (probably the upper iron formation member) of the Goldman Meadows Formation, upper Mesoarchean, 2.87 Ga (metamorphosed in the Archean at 2.8 Ga and in the Mesoproterozoic at 1.4 Ga) Geologic context: northwestern flank of the South Pass Greenstone Belt, southern Wind River Range Locality: Atlantic City Iron Mine (open-pit mine; sample possibly collected from tailings piles around the now-flooded pit) (E1/2 of section 26, T30N, R100W, Miners Delight 7.5' USGS topographic quadrangle), South Pass-Atlantic City Mining District, along Rt. 28, southwestern side of South Pass, north of Atlantic City, southwestern Fremont County, west-central Wyoming, USA (mine is at 42° 32' 45" North latitude, 108° 44' 33" West longitude)

Palaeogeographic distribution of late Early and early Late Cretaceous pterosaur assemblages. Taxonomic composition of assemblages shown on Fig. 1. Palaeogeography based on Smith et al. 1994. Abbreviations: 1. Cambridge Greensand, England: 2. Lower Chalk, England: 3. Züümbayan Svita, Khuren-Dukh, Mongolia: 4. Lysaya Gora, Saratov, Russia: 5. Kem Kem red beds, Morocco: 6. Paw Paw Formation, Texas, USA: 7. Lagarcito Formation, San Luis, Argentina: 8. Santana and Crato Formations, Ceara, Brazil: 9. Toolebuc Formation, Queensland, Australia.

Precious opal from Australia. (public display, Denver Museum of Nature & Science, Denver, Colorado, USA) A mineral is a naturally-occurring, solid, inorganic, crystalline substance having a fairly definite chemical composition and having fairly definite physical properties. At its simplest, a mineral is a naturally-occurring solid chemical. Currently, there are over 4900 named and described minerals - about 200 of them are common and about 20 of them are very common. Mineral classification is based on anion chemistry. Major categories of minerals are: elements, sulfides, oxides, halides, carbonates, sulfates, phosphates, and silicates. The silicates are the most abundant and chemically complex group of minerals. All silicates have silica as the basis for their chemistry. "Silica" refers to SiO2 chemistry. The fundamental molecular unit of silica is one small silicon atom surrounded by four large oxygen atoms in the shape of a triangular pyramid - this is the silica tetrahedron - SiO4. Each oxygen atom is shared by two silicon atoms, so only half of the four oxygens "belong" to each silicon. The resulting formula for silica is thus SiO2, not SiO4. Opal is hydrous silica (SiO2·nH2O). Technically, opal is not a mineral because it lacks a crystalline structure. Opal is supposed to be called a mineraloid. Opal is made up of extremely tiny spheres (colloids - <a href="https://www.uwgb.edu/dutchs/acstalks/acscolor/OPALSPHR.jpg" rel="nofollow">www.uwgb.edu/dutchs/acstalks/acscolor/OPALSPHR.jpg</a>) that can be seen with a scanning electron microscope (SEM). Gem-quality opal, or precious opal, has a wonderful rainbow play of colors (opalescence). This play of color is the result of light being diffracted by planes of voids between large areas of regularly packed, same-sized opal colloids. Different opalescent colors are produced by colloids of differing sizes. If individual colloids are larger than 140 x 10-6 mm in size, purple & blue & green colors are produced. Once colloids get as large as about 240 x 10-6 mm, red color is seen (Carr et al., 1979). Not all opals have the famous play of colors, however. Common opal has a wax-like luster & is often milky whitish with no visible color play at all. Opal is moderately hard (H = 5 to 6), has a white streak, and has conchoidal fracture. Several groups of organisms make skeletons of opaline silica, for example hexactinellid sponges, diatoms, radiolarians, silicoflagellates, and ebridians. Some organisms incorporate opal into their tissues, for example horsetails/scouring rushes and sawgrass. Sometimes, fossils are preserved in opal or precious opal. The precious opal shown above is surrounded by silicified claystone. The rock is from the Griman Creek Formation, a Cretaceous-aged succession of nonmarine, fine-grained and coarse-grained siliciclastic sedimentary rocks. Stratigraphy: Griman Creek Formation, Albian Stage, upper Lower Cretaceous Locality: Coocoran Opal Field, west-southwest of Coocoran Lake, northern New South Wales, eastern Australia Photo gallery of opal: <a href="http://www.mindat.org/gallery.php?min=3004" rel="nofollow">www.mindat.org/gallery.php?min=3004</a> References cited: Carr et al. (1979) - Andamooka opal fields: the geology of the precious stones field and the results of the subsidised mining program. Geological Survey of South Australia Department of Mines and Energy Report of Investigations 51. 68 pp.

Precious opal from Australia. (public display, Denver Museum of Nature & Science, Denver, Colorado, USA) A mineral is a naturally-occurring, solid, inorganic, crystalline substance having a fairly definite chemical composition and having fairly definite physical properties. At its simplest, a mineral is a naturally-occurring solid chemical. Currently, there are over 4900 named and described minerals - about 200 of them are common and about 20 of them are very common. Mineral classification is based on anion chemistry. Major categories of minerals are: elements, sulfides, oxides, halides, carbonates, sulfates, phosphates, and silicates. The silicates are the most abundant and chemically complex group of minerals. All silicates have silica as the basis for their chemistry. "Silica" refers to SiO2 chemistry. The fundamental molecular unit of silica is one small silicon atom surrounded by four large oxygen atoms in the shape of a triangular pyramid - this is the silica tetrahedron - SiO4. Each oxygen atom is shared by two silicon atoms, so only half of the four oxygens "belong" to each silicon. The resulting formula for silica is thus SiO2, not SiO4. Opal is hydrous silica (SiO2·nH2O). Technically, opal is not a mineral because it lacks a crystalline structure. Opal is supposed to be called a mineraloid. Opal is made up of extremely tiny spheres (colloids - <a href="https://www.uwgb.edu/dutchs/acstalks/acscolor/OPALSPHR.jpg" rel="nofollow">www.uwgb.edu/dutchs/acstalks/acscolor/OPALSPHR.jpg</a>) that can be seen with a scanning electron microscope (SEM). Gem-quality opal, or precious opal, has a wonderful rainbow play of colors (opalescence). This play of color is the result of light being diffracted by planes of voids between large areas of regularly packed, same-sized opal colloids. Different opalescent colors are produced by colloids of differing sizes. If individual colloids are larger than 140 x 10-6 mm in size, purple & blue & green colors are produced. Once colloids get as large as about 240 x 10-6 mm, red color is seen (Carr et al., 1979). Not all opals have the famous play of colors, however. Common opal has a wax-like luster & is often milky whitish with no visible color play at all. Opal is moderately hard (H = 5 to 6), has a white streak, and has conchoidal fracture. Several groups of organisms make skeletons of opaline silica, for example hexactinellid sponges, diatoms, radiolarians, silicoflagellates, and ebridians. Some organisms incorporate opal into their tissues, for example horsetails/scouring rushes and sawgrass. Sometimes, fossils are preserved in opal or precious opal. The precious opal shown above is surrounded by silicified claystone. The rock is from the Griman Creek Formation, a Cretaceous-aged succession of nonmarine, fine-grained and coarse-grained siliciclastic sedimentary rocks. Stratigraphy: Griman Creek Formation, Albian Stage, upper Lower Cretaceous Locality: Coocoran Opal Field, west-southwest of Coocoran Lake, northern New South Wales, eastern Australia Photo gallery of opal: <a href="http://www.mindat.org/gallery.php?min=3004" rel="nofollow">www.mindat.org/gallery.php?min=3004</a> References cited: Carr et al. (1979) - Andamooka opal fields: the geology of the precious stones field and the results of the subsidised mining program. Geological Survey of South Australia Department of Mines and Energy Report of Investigations 51. 68 pp.

Eubrontes dinosaur track from the Jurassic of Connecticut, USA. Trace fossils are any indirect evidence of ancient life. They refer to features in rocks that do not represent parts of the body of a once-living organism. Traces include footprints, tracks, trails, burrows, borings, and bitemarks. Body fossils provide information about the morphology of ancient organisms, while trace fossils provide information about the behavior of ancient life forms. Interpreting trace fossils and determination of the identity of a trace maker can be straightforward (for example, a dinosaur footprint represents walking behavior) or not. Sediments that have trace fossils are said to be bioturbated. Burrowed textures in sedimentary rocks are referred to as bioturbation. Trace fossils have scientific names assigned to them, in the same style & manner as living organisms or body fossils. This track was made by a theropod, a group of small to large, carnivorous, bipedal dinosaurs. The specimen comes from a Triassic to Jurassic terrestrial sedimentary succession that filled up a half graben, many of which occur along America's eastern seaboard. Such half-graben basins formed during the Triassic as the Pangaea supercontinent tried to rift apart, but failed. Pangaea successfully broke apart during the Jurassic. Stratigraphy: East Berlin Formation, Newark Supergroup, Lower Jurassic Locality: unrecorded / undisclosed site at or near the town of Rocky Hill, central Connecticut, USA Info. at: mrdata.usgs.gov/geology/state/sgmc-unit.php?unit=CTJeb%3B0 and en.wikipedia.org/wiki/Eubrontes

Paleogeography and paleoclimate of the Late Jurassic - 150 Ma with dinosaur fossil localities: A = Tendaguru Formation, Tanzania C1 = Shishugou & Kalazha Formations, China C2 = Shangshaximiao (Upper Shaximiao) Formation, China E1 = Sables de Glos, Argiles d’Octeville, Marnes de Bléville, Kimmeridge Clay, Calcareous Grit, Corallian Oolite, Oxford Clay, Portland Stone, England & France E2 = Villar del Arzobispo, Alcobaça, Guimarota, Sobral, Amoreira-Porto Novo, Bombarral, Freixial, Lourinhã Formations, Spain & Portugal M1-6 = Morrison Formation, United States S1 = Toquí & Cañadón Calcáreo Formations, Chile & Argentina

Restored skeleton of Anzu wyliei (previously labelled as a specimen of Chirostenotes)

Restored skeleton of Anzu wyliei (previously labelled as a specimen of Chirostenotes)

Plotosaurus skeletal mount in Natural History Museum of Los Angeles County, California, United States.

Mounted skeleton of Plotosaurus from the Los Angeles County Natural History Museum; see the original image

Images documenting the 1947 Bikini Resurvey Project. Caption in scrapbook: Arlis McCartner from Canfield, Ohio, is shown with a seven foot shark, caught off the fantail of the CHILTON. ABCR 5032-1 Bikini Atoll Radiological Survey Scrapbook, p. 38. Subjects (LCTGM): Sharks--Marshall Islands Subjects (LCSH): McCartner, Arlis