815 research outputs found
Mammy\u27s Little Kinky Headed Boy
Sheet music contains anti-Black, racist language, stereotypes, and/or imagry. With Ukulele arrangement. Contains advertisements and/or short musical examples of pieces being sold by publisher.https://digitalcommons.library.umaine.edu/mmb-vp/7182/thumbnail.jp
A Wand\u27ring Minstrel
https://digitalcommons.library.umaine.edu/mmb-vp/2620/thumbnail.jp
Shuffle along: selection
https://digitalcommons.ithaca.edu/sheetmusic/1186/thumbnail.jp
Recent origin of low trabecular bone density in modern humans
Humans are unique, compared with our closest living relatives (chimpanzees) and early fossil hominins, in having an enlarged body size and lower limb joint surfaces in combination with a relatively gracile skeleton (i.e., lower bone mass for our body size). Some analyses have observed that in at least a few anatomical regions modern humans today appear to have relatively low trabecular density, but little is known about how that density varies throughout the human skeleton and across species or how and when the present trabecular patterns emerged over the course of human evolution. Here, we test the hypotheses that (i) recent modern humans have low trabecular density throughout the upper and lower limbs compared with other primate taxa and (ii) the reduction in trabecular density first occurred in early Homo erectus, consistent with the shift toward a modern human locomotor anatomy, or more recently in concert with diaphyseal gracilization in Holocene humans. We used peripheral quantitative CT and microtomography to measure trabecular bone of limb epiphyses (long bone articular ends) in modern humans and chimpanzees and in fossil hominins attributed to Australopithecus africanus, Paranthropus robustus/early Homo from Swartkrans, Homo neanderthalensis, and early Homo sapiens. Results show that only recent modern humans have low trabecular density throughout the limb joints. Extinct hominins, including pre-Holocene Homo sapiens, retain the high levels seen in nonhuman primates. Thus, the low trabecular density of the recent modern human skeleton evolved late in our evolutionary history, potentially resulting from increased sedentism and reliance on technological and cultural innovations
Point defect dynamics in bcc metals
We present an analysis of the time evolution of self-interstitial atom and
vacancy (point defect) populations in pure bcc metals under constant
irradiation flux conditions. Mean-field rate equations are developed in
parallel to a kinetic Monte Carlo (kMC) model. When only considering the
elementary processes of defect production, defect migration, recombination and
absorption at sinks, the kMC model and rate equations are shown to be
equivalent and the time evolution of the point defect populations is analyzed
using simple scaling arguments. We show that the typically large mismatch of
the rates of interstitial and vacancy migration in bcc metals can lead to a
vacancy population that grows as the square root of time. The vacancy cluster
size distribution under both irreversible and reversible attachment can be
described by a simple exponential function. We also consider the effect of
highly mobile interstitial clusters and apply the model with parameters
appropriate for vanadium and iron.Comment: to appear in Phys. Rev.
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In vitro model suggests oxidative stress involved in keratoconus disease
Keratoconus (KC) affects 1:2000 people and is a disorder where cornea thins and assumes a conical shape. Advanced KC requires surgery to maintain vision. The role of oxidative stress in KC remains unclear. We aimed to identify oxidative stress levels between human corneal keratocytes (HCKs), fibroblasts (HCFs) and keratoconus cells (HKCs). Cells were cultured in 2D and 3D systems. Vitamin C (VitC) and TGF-β3 (T3) were used for 4 weeks to stimulate self-assembled extracellular matrix (ECM). No T3 used as controls. Samples were analyzed using qRT-PCR and metabolomics. qRT-PCR data showed low levels of collagen I and V, as well as keratocan for HKCs, indicating differentiation to a myofibroblast phenotype. Collagen type III, a marker for fibrosis, was up regulated in HKCs. We robustly detected more than 150 metabolites of the targeted 250 by LC-MS/MS per condition and among those metabolites several were related to oxidative stress. Lactate levels, lactate/malate and lactate/pyruvate ratios were elevated in HKCs, while arginine and glutathione/oxidized glutathione ratio were reduced. Similar patterns found in both 2D and 3D. Our data shows that fibroblasts exhibit enhanced oxidative stress compared to keratocytes. Furthermore the HKC cells exhibit the greatest level suggesting they may have a myofibroblast phenotype
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