On the Initial Mass Function of Population III Stars

The collapse and fragmentation of filamentary primordial gas clouds are explored using 1D and 2D hydrodynamical simulations coupled with the nonequilibrium processes of H2 formation. The simulations show that depending upon the initial density,there are two occasions for the fragmentation of primordial filaments. If a filament has relatively low initial density, the radial contraction is slow due to less effective H2 cooling. This filament tends to fragment into dense clumps before the central density reaches $10^{8-9}$ cm$^{-3}$, where H2 cooling by three-body reactions is effective and the fragment mass is more massive than some tens $M_\odot$. In contrast, if a filament is initially dense, the more effective H2 cooling with the help of three-body reactions allows the filament to contract up to $n\sim 10^{12}$ cm$^{-3}$. After the density reaches $n\sim 10^{12}$ cm$^{-3}$, the filament becomes optically thick to H2 lines and the radial contraction subsequently almost stops. At this final hydrostatic stage, the fragment mass is lowered down to $\approx 1M_\odot$ because of the high density of the filament. The dependence of the fragment mass upon the initial density could be translated into the dependence on the local amplitude of random Gaussian density fields or the epoch of the collapse of a parent cloud. Hence, it is predicted that the initial mass function of Population III stars is likely to be bimodal with peaks of $\approx 10^2 M_\odot$ and $\approx 1M_\odot$, where the relative heights could be a function of the collapse epoch.Comment: Accepted by Ap

Fire Suppression Impacts on Fuels and Fire Intensity in the Western U.S.: Insights from Archaeological Luminescence Dating in Northern New Mexico

Here, we show that the last century of fire suppression in the western U.S. has resulted in fire intensities that are unique over more than 900 years of record in ponderosa pine forests (Pinus ponderosa). Specifically, we use the heat-sensitive luminescence signal of archaeological ceramics and tree-ring fire histories to show that a recent fire during mild weather conditions was more intense than anything experienced in centuries of frequent wildfires. We support this with a particularly robust set of optically stimulated luminescence measurements on pottery from an archaeological site in northern New Mexico. The heating effects of an October 2012 CE prescribed fire reset the luminescence signal in all 12 surface samples of archaeological ceramics, whereas none of the 10 samples exposed to at least 14 previous fires (1696–1893 CE) revealed any evidence of past thermal impact. This was true regardless of the fire behavior contexts of the 2012 CE samples (crown, surface, and smoldering fires). It suggests that the fuel characteristics from fire suppression at this site have no analog during the 550 years since the depopulation of this site or the 350 years of preceding occupation of the forested landscape of this region

Lysophosphatidic Acid Acyltransferase β (LPAATβ) Promotes the Tumor Growth of Human Osteosarcoma

Osteosarcoma is the most common primary malignancy of bone with poorly characterized molecular pathways important in its pathogenesis. Increasing evidence indicates that elevated lipid biosynthesis is a characteristic feature of cancer. We sought to investigate the role of lysophosphatidic acid acyltransferase β (LPAATβ, aka, AGPAT2) in regulating the proliferation and growth of human osteosarcoma cells. LPAATβ can generate phosphatidic acid, which plays a key role in lipid biosynthesis as well as in cell proliferation and survival. Although elevated expression of LPAATβ has been reported in several types of human tumors, the role of LPAATβ in osteosarcoma progression has yet to be elucidated.Endogenous expression of LPAATβ in osteosarcoma cell lines is analyzed by using semi-quantitative PCR and immunohistochemical staining. Adenovirus-mediated overexpression of LPAATβ and silencing LPAATβ expression is employed to determine the effect of LPAATβ on osteosarcoma cell proliferation and migration in vitro and osteosarcoma tumor growth in vivo. We have found that expression of LPAATβ is readily detected in 8 of the 10 analyzed human osteosarcoma lines. Exogenous expression of LPAATβ promotes osteosarcoma cell proliferation and migration, while silencing LPAATβ expression inhibits these cellular characteristics. We further demonstrate that exogenous expression of LPAATβ effectively promotes tumor growth, while knockdown of LPAATβ expression inhibits tumor growth in an orthotopic xenograft model of human osteosarcoma.Our results strongly suggest that LPAATβ expression may be associated with the aggressive phenotypes of human osteosarcoma and that LPAATβ may play an important role in regulating osteosarcoma cell proliferation and tumor growth. Thus, targeting LPAATβ may be exploited as a novel therapeutic strategy for the clinical management of osteosarcoma. This is especially attractive given the availability of selective pharmacological inhibitors