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The cutting-edge work done by ´ó·¢²ÊƱ Earth & Environmental Geoscience students and faculty is made possible by state-of-the-art facilities for both classroom instruction and scientific research.

Analytical Instrumentation

Broadband Seismometers

´ó·¢²ÊƱ owns and operates six broadband seismometers, designed to record ground motion from local earthquakes as well as earthquakes across the globe.  The seismometers include five Nanometrics Meridian Compact Posthole Seismometers and one Streckeisen STS-2.5 seismometer paired with Quanterra Q330S+ digitizer.

Broadband seismometers measure ground motion across a broad range of frequencies, detecting not only earthquakes, but also storms, footsteps, loud noises, and even passing vehicles!  These instruments measure ground motion (as movement velocity) as small as micrometers per second, and in three dimensions.  Motion is recorded electronically as a suspended weight moves independently from the casing, passing a magnet through coiled wires, inducing an electrical current.  To collect meaningful information on ground motion, these broadband seismometers are buried in locations of geologic interest for periods of time ranging from months to several years.

Geometrics 24-channel Geode Seismic Acquisition System

This seismic acquisition system measures ground motion to image the upper 10s to 100s of meters of the subsurface.  

Students us Geode seismic system in class
Students us Geode seismic system during a geophysics lab

The Geode seismic acquisition system includes 24 sensitive geophones that measure ground motion at very high frequencies at evenly-spaced distances.  Signals recorded by this system are typically from a man-made source, such as a weight-drop or the impact of a sledgehammer on a metal plate.  Timing of this signal is precisely synchronized with all 24 geophones to create records of how energy is transmitted through the ground, and how it reflects off of subsurface interfaces.

Geometrics G-857 Magnetometer

This instrument measures tiny deviations in the strength of the magnetic field, which are induced by changes in geology or by remnants of human activities.

The G-857 is a proton procession magnetometer, which measures magnetic fields to a sensitivity of tenths of a nanoTesla.  The sensor is filled with a fluid containing hydrogen atoms.  A strong magnetic field is created around the fluid, causing the protons of the hydrogen atoms to align within the field.  When the artificial magnetic field is released, the protons realign with the natural ambient magnetic field, creating an electrical current that is recorded by the instrument and converted to magnetic field strength.  By making measurements like this in many locations, we can create a map showing how the magnetic field varies spatially.  This can reveal changes in subsurface geology, buried objects containing small amounts of ferrous material, or even disturbed soils.

Inductively coupled plasma — mass spectrometer

Varian/Bruker 820-MS and Agilent HP4500

Inductively coupled plasma mass spectrometers (ICP-MS) measure the concentrations of trace and major elements in liquid or solid samples. The Varian 820-MS ICP-MS is set up to process data from solutions using the Cetac ASX-520 autosampler or solids using the New Wave UP 213nm laser ablation system. This laser ablation system allows researchers to get pinpoint, in situ data from solid samples like rocks, glass, and crystals. Both the Varian and Argilent instruments housed in this lab are quadrupole ICP-MS systems, so researchers can measure the majority of the periodic table in just seconds.

Instrument statistics

Download the Bruker 820-MS brochure.

Ion chromatography system

Metrohm 930 Compact single-channel ion chromatograph with cation and anion separation columns for water major ion analysis.

Scanning electron microscope

JEOL JSM-IT710HRLV Scanning Electron Microscope with Oxford 65 Ultim Max EDS Detector, Oxford C Swift EBSD Detector, and Deben Centaurus CL Detector
Purchased with a grant from the National Science Foundation

This instrument is used for detailed, high-magnification, 3-D imaging and qualitative/semi-quantitative chemical analysis of materials, along with phase identification and lattice orientation of crystalline solids.

Student using electron microscope in lab.
Student using electron microscope in lab.

How it works

A beam of high-energy electrons is produced by a field emission gun at the top of the column.  This focused beam continuously rasters back and forth across the sample. Interactions between the electron beam and the sample result in different types of emissions that are measured by a series of detectors located within the sample chamber. 

The SEM is equipped with two basic detectors that produce images from secondary electrons and backscattered electrons. Secondary electron imaging provides good three-dimensional topographic views of the sample. Backscattered electron images show less-defined topography but clearly display differences in elemental compositions because higher-atomic-number elements appear brighter. 
 

Three auxiliary detectors greatly enhance the analytical capabilities of this system. Imaging using the Centaurus cathode luminescence (CL) detector reveals chemical variations within individual grains containing elements that release some of the energy imparted by the electron beam back as visible light. For chemical analyses, characteristic X-ray energies emitted by each element within the sample are collected by the Oxford EDS detector and translated into elemental percentages and plots by Aztec software. This software also interfaces with the Oxford EBSD detector to determine phase and lattice orientations of crystalline substances by collecting back-scattered electrons diffracted in phase off a tilted sample.  

Instrument statistics

Quantitative analyses are performed at 20 kV using a 10 mm working distance, and are collected for 200 seconds of live time.
 

Stable isotope mass spectrometry

Delta Plus Advantage Stable Isotope Mass Spectrometer and Costech Elemental Analyzer
Funded by grant EAR-0216179 from the National Science Foundation

This system measures isotope ratios of C, O, and N from geological and biological samples.

Student using stable isotope mass spectrometer in lab.
Student using stable isotope mass spectrometer in lab.

How it works

Oxygen, carbon, or nitrogen must be separated from samples by some chemical method (such as combustion, dissolution in acids, or fusing with a laser in the presence of an oxidizer). Gases are then purified in a vacuum line (glass trellis-work in picture) or within the elemental analyzer. The purified gases are then introduced into the mass spectrometer, either by using the dual-inlet system or continuous flow mode, where they are bombarded by electrons and ionized. The ions travel down a flight tube and are separated according to mass by an electromagnet. The ions are then detected in Faraday cups at the end of the flight tube. The isotope ratio is calculated from the charge of the ions at the end of the flight tube. See Finnigan's brochure for instrument and analytical statistics.

 Image of stable isotope mass spectrometry lab.
Image of stable isotope mass spectrometry lab.

Although the differences in mass between the isotopes of the light gases are small (~11 percent between 16O and 18O), the isotope ratio is very sensitive to geological processes. Stable isotopes are commonly used in studies to determine paleoclimate, water-rock interaction, and metamorphic temperatures in rocks, and trophic level and paleodiet in fossils.

Research projects

The lab is used for class projects in geology and other departments (e.g., ENST 100 Earth and Environmental Processes, FSEM 124 Forensic Geology, GEOL 310 Economic Geology, GEOL 415 Marine Geology, GEOL 411 Isotope Geology, BIOL 476 Biodiversity and Ecosystem Ecology). Class projects have investigated plant physiology, lake sediments near Hamilton, N.Y., the origin of Pb-Zn ore deposits, and adulteration of maple syrup. Many students have used the lab for independent study projects and senior theses, and several have presented their projects at regional and national meetings.

 Glass tubing in ´ó·¢²ÊƱ’s stable isotope mass spectrometry lab.
Carbonate dissolution vessels in ´ó·¢²ÊƱ’s stable isotope mass spectrometry lab.

Papers from the isotope lab

* indicates collaborative research with students

Peck, WH, and *Eppich, GR, 2019, The Kilmar magnesite deposits: Evaporitic metasediments in the Grenville supergroup, Morin terrane, Quebec): Minerals, v. 9, 554. 

Peck, W.H., *Cummings, E.E., *Van Slyke, E. (2018). Carbon isotope composition of birch syrup. Journal of Food Composition and Analysis, v. 71, p. 25-27.

Peck, W.H., *Shramko, M.F., and Verbeek, E.R. (2016). Carbon and oxygen isotopes of secondary carbonates at Franklin and Sterling Hill. The Picking Table, v. 57, p. 29-38.

Peck, W.H. (2016). Protolith carbon isotope ratios in cordierite from metamorphic and igneous rocks. American Mineralogist, v. 101, p. 2279-2287.

Peck, W.H., and *Tubman, S.C. (2010). Changing carbon isotope ratio of atmospheric carbon dioxide: Implications for food authentication. Journal of Agricultural and Food Chemistry, v. 58(4), p. 2364–2367

Peck, W.H., Volkert, R.A., *Mansur, A., *Doverspike, B.A. (2009). Stable isotope and petrologic evidence for the origin of regional marble-hosted magnetite deposits and the zinc deposits at Franklin and Sterling Hill, New Jersey Highlands. Economic Geology, v. 104, p. 1037-1054.

Peck, W.H., and *Tumpane, K.P. (2007). Low carbon isotope ratios in apatite: An unreliable biomarker in igneous and metamorphic rocks. Chemical Geology, v. 245, p. 305-314.

Peck, W.H., Volkert, R.A., *Meredith, M.T., and *Rader, E.L. (2006). Calcite-graphite carbon isotope thermometry of the Franklin Marble, New Jersey Highlands. Journal of Geology, v. 114, p. 485-499.

Peck, W.H., *DeAngelis, M.T., *Meredith, M.T., *Morin, E. (2005). Polymetamorphism of marbles in the Morin terrane (Grenville Province, Quebec). Canadian Journal of Earth Sciences, v. 42, p. 1949-1965.

Abstracts from the isotope lab

* indicates collaborative research with students

Dunn, S.R., *Kotikian, M., *Achenbach, K., *Nesbit, J., *Montanye, B., Peck, W., and Markley, M. (2017). Calcite-graphite isotope thermometry in the Western Central Metasedimentary Belt, Grenville Province, Ontario. Geological Association of Canada/Mineralogical Association of Canada 2017 Meeting Abstracts with Programs, Abstract #295.

*Katz, S., and Peck, W.H. (2016). Mineralogy and stable isotopes of Dutchess and Litchfield county metasedimentary rocks. Geological Society of America Abstracts with Programs, v. 48(2), doi: 10.1130/abs/2016NE-272777.

Peck, W.H., and *Dawson, T.L. (2015). Carbon isotope investigation of channel carbon dioxide in ring silicates: Cordierite and beryl. Geological Society of America Abstracts with Programs, v. 47(7), p. 762.

*Montanye, B.R., and Peck, W.H. (2012). Carbon isotope thermometry in the Central Metasedimentary Belt Boundary Thrust Zone, Grenville Province, Ontario. Geological Society of America Abstracts with Programs, v. 44(2), p. 115.

*Rathkopf, C.A., Peck, W.H. (2010). Stable isotope geochemistry of marble-hosted Zn deposits, Central Metasedimentary Belt, Grenville Province, Ontario. Geological Society of America Abstracts with Programs, v. 42(1), p. 110.

*Halfhide, T.M., Peck, W.H. (20100. Calcite-graphite thermometry of marbles in the Sharbot Lake domain (Grenville Province, Ontario). Geological Society of America Abstracts with Programs, v. 42(1), p. 160.

*Tortorello, R.D., Peck, W.H. (2010). Calcite-graphite thermometry of marbles in the Frontenac terrane (Grenville Province, Ontario). Geological Society of America Abstracts with Programs, v. 42(1), p. 160.

April, R.H., *Coplin, A.L. (2008). The isotopic composition of organic carbon in Adirondack Spodosols. Geochimica et Cosmochimica Acta, v. 72, Issue 12, p. A30.

*Eppich, G.R., and Peck, W.H. (2006). Stable isotope geochemistry of the Kilmar magnesite deposits, Grenville Province, Quebec. Geological Society of America Abstracts with Programs, v.38, n. 2, p. 26.

Goldstein, A.G., Peck, W.H., and Selleck, B.W., *King, M., *Coliacomo, E., Kita, N.T., Valley, J.W. (2006). High-resolution stable isotope thermometry of Taconic strain fringes. Geological Society of America Abstracts with Programs, v. 38, n. 7, p. 18.

*Kinsman, N., Goldstein, A., Peck, W., and Selleck, B. (2006). Stable isotopes of strain fringes in Aptian slates near Lourdes, France. Geological Society of America Abstracts with Programs, v.38, n. 2, p. 26.

*King, M., *Coliacomo, E., Goldstein, A., Peck, W., and Selleck, B. (2006). Stable isotopes in strain fringes from the Taconic Mountains, Vermont. Geological Society of America Abstracts with Programs, v.38, n. 2, p. 26.

*Meredith, M.T., *Doverspike, B.A., Peck, W.H. (2003). Stable isotope geochemistry of the Franklin Marble (Grenville Province, New Jersey). Geological Society of America Abstracts with Programs, v.35, n. 3, p. 96.

*Nowak, R. (rnowak09@wooster.edu), Peck, W.H., Pollock, M. (2009). Protolith determination of the Hyde School garnet-sillimanite marginal gneisses, Adirondack Lowlands, NY. Geological Society of America Abstracts with Programs, v. 41(4), p. 52.

Peck, W.H., *DeAngelis, M.T., *Meredith, M.T., *Morin, E. (2004). Metamorphism of marbles in the Morin terrane (Grenville Province, Quebec). Geological Society of America Abstracts with Programs, v.36, n. 5, p. 460.

Peck, W.H., and *Tumpane, K.P. (2006). Low carbon isotope ratios in high-temperature apatite: Implications for use as a biomarker. Geological Society of America Abstracts with Programs, v. 38, n. 7, p. 46.

Peck, W.H., Volkert, R.A., *Mansur, A.T., Doverspike, B.A. (2008). Stable isotope constraints on the origin of Mesoproterozoic marble-hosted zinc and iron deposits, New Jersey Highlands. Geological Society of America Abstracts with Programs, v. 40(2), p. 61.

Peck, W.H., Volkert, R.A., *Mansur, A.T., *Eppich, G.R. (2008). A Stable Isotope Perspective on Sedimentation, Ore Genesis, and Metamorphism in the Southern Grenville Province. Geological Society of America Abstracts with Programs, v. 40(6), p. 234.

Selleck, B.W., Peck, W.H., McLelland, J.M., *Bergman, M., *Ellis, A., *Conti, C. (2008). Late Ottawan (ca. 1035 Ma) hydrothermal signatures in the southeastern Adirondack Lowlands: New geochronological, stable isotope and fluid inclusion results. Geological Society of America Abstracts with Programs, v. 40(2), p. 61.

*Tubman, S.C., Peck, W.H. (2008). Carbon isotopes of maple syrup: A record of atmospheric and environmental change. Geological Society of America Abstracts with Programs, v. 40(2), p. 18.

*Tumpane, K.P., and Peck, W.H, (2006). Large carbon isotope fractionations in apatite. Geological Society of America Abstracts with Programs, v.38, n. 2, p. 26.

X-ray diffractometer

Philips PW3040 X-ray Diffractometer with X'Pert Software
Purchased with a grant from the National Science Foundation 

X-ray diffraction is used to determine the identity of crystalline solids based on their atomic structure.

Student using x-ray diffractometer in lab
Student using x-ray diffractometer in lab.

´ó·¢²ÊƱ’s system uses Cu Kα radiation that has a wavelength of 1.54Ã…. Analyses are commonly run using a 40kV 45mA x-ray tube voltage, a 0.04° soller slit, 1° divergence and antiscatter slits, and a 1/2° (for powder) or 1/4° (for clays) receiving slit.

How it works

During x-ray diffraction analysis, x-ray beams are reflected off the parallel atomic layers within a mineral over a range of diffraction angles. Because the x-ray beam has a specific wavelength, for any given 'd-spacing' (distance between adjacent atomic planes) there are only specific angles at which the exiting rays will be 'in phase' and therefore rays will be picked up by the detector producing a peak on the 'diffractogram.' Like a human fingerprint, every mineral has its own distinct set of diffraction peaks that can be used to identify it.

Related research

This system has been used extensively to collect data for a wide variety of research. Some of the major projects include:

NSF/CRUI — Study on acid deposition and calcium depletion in Adirondack soils
ILWAS — Integrated Lake Watershed Acidification Study — study of the effects of acid deposition on three Adirondack lakes
RILWAS — Regional Integrated Lake Watershed Acidification Study: a study of the effects of acid deposition on lakes in the Adirondacks and various other locations across the United States, Canada, and Europe
ALBIOS — Aluminum Biogeochemistry Study: a study of the effects of aluminum on forested ecosystems
IFS — Integrated Forest Study, an international effort to study the effects of acid deposition on forest ecosystems throughout the United States, Canada, and Europe
DOE — study of the distribution of Cesium-137 in lake-bottom sediments

Hand-held x-ray fluorescence spectrometer

Thermo Fisher Niton XL3t ULTRA X-ray Fluorescence Spectrometer (XRF)

This instrument is used to determine the chemical composition of rocks, sediments, and soils in the field or in the lab. It can be used for both reconnaissance analysis of most elements, and it can also be standardized for quantitative analysis of specific elements in particular materials.

Using the same principle of ´ó·¢²ÊƱ’s laboratory x-ray fluorescence spectrometer, this hand-held unit uses high-energy x-ray photons to analyze geologic samples. The energy of secondary x-rays emitted by the sample during analysis is specific to each particular element, which can be used to determine its chemical composition.

Sample Preparation and Analytical Labs

Geochemistry lab

The "Geochem lab" accommodates a variety of soil, sediment, rock, and water sample preparations and analyses. It is fully equipped with centrifuges, balances, spectrometers, pH meters, titration apparatus, hoods, sieves, settling tubes, desiccators, field equipment, sonifiers, a convection oven, muffle furnace, waterbath, shaker table, and nutator, as well as all the necessary labware. This lab is used for student and faculty research throughout the summer and academic year.

This lab has been used extensively to collect data for a wide variety of research projects including:

Students preparing samples in the geochemistry lab
Students preparing samples for analysis in the Geochem Lab


NSF/CRUI — Study on Acid Deposition and Calcium Depletion in Adirondack Soils
DOE study of the distribution of Cesium-137 in lake bottom sediments
IFS — Integrated Forest Study: an international effort to study the effects of acid deposition on forest ecosystems throughout the United States, Canada, and Europe
ALBIOS — Aluminum Biogeochemistry Study - a study of the effects of aluminum on forested ecosystems
RILWAS — Regional Integrated Lake Watershed Acidification Study - a study of the effects of acid deposition on lakes in the Adirondacks and various other locations across the United States, Canada, and Europe
ILWAS — Integrated Lake Watershed Acidification Study - a study of the effects of acid deposition on three Adirondack lakes

Seismology & geophysics lab

The Geophysics lab at ´ó·¢²ÊƱ specializes in using passive source seismology to characterize and image the Earth’s crust and mantle.  The lab is equipped with desktop computers as well as a powerful Linux server for remote computations.  Seismic data collection is conducted using broadband seismometers.  Six seismometers are owned and maintained by ´ó·¢²ÊƱ, and the lab includes equipment to build and maintain solar power systems for the seismometers. For larger projects, these instruments are supplemented by instruments from a national pool and partner institutions.  The broadband seismometers have been deployed in the Adirondack Mountains, southern Alaska, Tanzania, and on ´ó·¢²ÊƱ’s campus to measure ground motions in those locations.  In addition to solid earth seismic equipment, the geophysics lab is equipped with equipment for studying the shallow subsurface, including a 24-channel seismic acquisition system and a portable magnetometer.

  • Seismicity of Upstate New York

Micropaleontological and microscopy labs