Thermal Alteration of Labile Elements in Carbonaceous Chondrites

Carbonaceous chondrite meteorites are some of the oldest Solar System planetary materials available for study. The CI group has bulk abundances of elements similar to those of the solar photosphere. Of particular interest in carbonaceous chondrite compositions are labile elements, which vaporize and mobilize efficiently during post-accretionary parent-body heating events. Thus, they can record low-temperature alteration events throughout asteroid evolution. However, the precise nature of labile-element mobilization in planetary materials is unknown. Here we characterize the thermally induced movements of the labile elements S, As, Se, Te, Cd, Sb, and Hg in carbonaceous chondrites by conducting experimental simulations of volatile-element mobilization during thermal metamorphism. This process results in appreciable loss of some elements at temperatures as low as 500 K. This work builds on previous laboratory heating experiments on primitive meteorites and shows the sensitivity of chondrite compositions to excursions in temperature. Elements such as S and Hg have the most active response to temperature across different meteorite groups. Labile element mobilization in primitive meteorites is essential for quantifying elemental fractionation that occurred on asteroids early in Solar System history. This work is relevant to maintaining a pristine sample from asteroid (101955) Bennu from the OSIRIS-REx mission and constraining the past orbital history of Bennu. Additionally, we discuss thermal effects on surface processes of near-Earth asteroids, including the thermal history of "rock comets" such as (3200) Phaethon. This work is also critical for constraining the concentrations of contaminants in vaporized water extracted from asteroid regolith as part of future in situ resource utilization for sustained robotic and human space exploration.Comment: 12 pages of text, 3 tables, 7 figures, accepted by Icaru

Accumulation of heavy metals in food web components across a gradient of lakes

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/109770/1/lno20004571525.pd

Diaryltriazolium Photoswitch: Reaching a Millisecond Cycloreversion with High Stability and NIR Absorption

The exceptional thermal stability of diarylethene closed isomers enabled many applications but also prevented utilization in photochromic systems that require rapid thermal reversibility. Herein, we report the diaryltriazolium (DAT+) photoswitch undergoing thermal cycloreversion within a few milliseconds and absorption of the closed form in the near-infrared region above 900 nm. Click chemistry followed by alkylation offers modular and fast access to the electron-deficient DAT+ scaffold. In addition to excellent fatigue resistance, the introduced charge increases water solubility, rendering this photoswitch an ideal candidate for exploring biological applications

Design of an epidemiologic study of drinking water arsenic exposure and skin and bladder cancer risk in a U.S. population

Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/155818/1/Karagas_et_al_1998_Design_of_an_epidemiologic.pd

Design of an epidemiologic study of drinking water arsenic exposure and skin and bladder cancer risk in a U.S. population.

Ingestion of arsenic-contaminated drinking water is associated with an increased risk of several cancers, including skin and bladder malignancies; but it is not yet clear whether such adverse effects are present at levels to which the U.S. population is exposed. In New Hampshire, detectable levels of arsenic have been reported in drinking water supplies throughout the state. Therefore, we have begun a population-based epidemiologic case-control study in which residents of New Hampshire diagnosed with primary squamous cell (n = 900) and basal cell (n = 1200) skin cancers are being selected from a special statewide skin cancer incidence survey; patients diagnosed with primary bladder cancers (n = 450) are being identified through the New Hampshire State Cancer Registry. Exposure histories of these patients will be compared to a control group of individuals randomly selected from population lists (n = 1200). Along with a detailed personal interview, arsenic and other trace elements are being measured in toenail clipping samples using instrumental neutron activation analysis. Household water samples are being tested on selected participants using a hydride generation technique with high-resolution inductively coupled plasma mass spectrometry. In the first 793 households tested arsenic concentrations ranged from undetectable (0.01 microgram/l) to 180 microgram/l. Over 10% of the private wells contained levels above 10 microgram/l and 2.5% were above 50 microgram/l. Based on our projected sample size, we expect at least 80% power to detect a 2-fold risk of basal cell or squamous cell skin cancer or bladder cancer among individuals with the highest 5% toenail concentrations of arsenic

Design of an Epidemiologic Study of Drinking Water Arsenic Exposure and Skin and Bladder Cancer Risk in a U.S. Population

Ingestion of arsenic-contaminated drinking water is associated with an increased risk of several cancers, including skin and bladder malignancies; but it is not yet clear whether such adverse effects are present at levels to which the U.S. population is exposed. In New Hampshire, detectable levels of arsenic have been reported in drinking water supplies throughout the state. Therefore, we have begun a population-based epidemiologic case-control study in which residents of New Hampshire diagnosed with primary squamous cell (n = 900) and basal cell (n = 1200) skin cancers are being selected from a special statewide skin cancer incidence survey; patients diagnosed with primary bladder cancers (n = 450) are being identified through the New Hampshire State Cancer Registry. Exposure histories of these patients will be compared to a control group of individuals randomly selected from population lists (n = 1200). Along with a detailed personal interview, arsenic and other trace elements are being measured in toenail clipping samples using instrumental neutron activation analysis. Household water samples are being tested on selected participants using a hydride generation technique with high-resolution inductively coupled plasma mass spectrometry. In the first 793 households tested arsenic concentrations ranged from undetectable (0.01 microgram/l) to 180 microgram/l. Over 10% of the private wells contained levels above 10 microgram/l and 2.5% were above 50 microgram/l. Based on our projected sample size, we expect at least 80% power to detect a 2-fold risk of basal cell or squamous cell skin cancer or bladder cancer among individuals with the highest 5% toenail concentrations of arsenic

Markers of low level arsenic exposure for evaluating human cancer risks in a US population

Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/155831/1/Karagas_et_al_2001_Markers_of_low_level.pd

Efficient preparation of internally modified single-molecule constructs using nicking enzymes

Investigations of enzymes involved in DNA metabolism have strongly benefited from the establishment of single molecule techniques. These experiments frequently require elaborate DNA substrates, which carry chemical labels or nucleic acid tertiary structures. Preparing such constructs often represents a technical challenge: long modified DNA molecules are usually produced via multi-step processes, involving low efficiency intermolecular ligations of several fragments. Here, we show how long stretches of DNA (>50 bp) can be modified using nicking enzymes to produce complex DNA constructs. Multiple different chemical and structural modifications can be placed internally along DNA, in a specific and precise manner. Furthermore, the nicks created can be resealed efficiently yielding intact molecules, whose mechanical properties are preserved. Additionally, the same strategy is applied to obtain long single-strand overhangs subsequently used for efficient ligation of ss- to dsDNA molecules. This technique offers promise for a wide range of applications, in particular single-molecule experiments, where frequently multiple internal DNA modifications are required