Will We Do If We Can? Habitual Qualitative and Quantitative Physical Activity in Multi-Morbid, Older Persons with Cognitive Impairment

This study aimed to identify determinants of quantitative dimensions of physical activity (PA; duration, frequency, and intensity) in community-dwelling, multi-morbid, older persons with cognitive impairment (CI). In addition, qualitative and quantitative aspects of habitual PA have been described. Quantitative PA and qualitative gait characteristics while walking straight and while walking turns were documented by a validated, sensor-based activity monitor. Univariate and multiple linear regression analyses were performed to delineate associations of quantitative PA dimensions with qualitative characteristics of gait performance and further potential influencing factors (motor capacity measures, demographic, and health-related parameters). In 94 multi-morbid, older adults (82.3 ± 5.9 years) with CI (Mini-Mental State Examination score: 23.3 ± 2.4), analyses of quantitative and qualitative PA documented highly inactive behavior (89.6% inactivity) and a high incidence of gait deficits, respectively. The multiple regression models (adjusted R$^{2}$ = 0.395–0.679, all p < 0.001) identified specific qualitative gait characteristics as independent determinants for all quantitative PA dimensions, whereas motor capacity was an independent determinant only for the PA dimension duration. Demographic and health-related parameters were not identified as independent determinants. High associations between innovative, qualitative, and established, quantitative PA performances may suggest gait quality as a potential target to increase quantity of PA in multi-morbid, older persons

The First Billion Years project - III: The impact of stellar radiation on the coevolution of Populations II and III

With the first metal enrichment by Population (Pop) III supernovae (SNe), the formation of the first metal-enriched, Pop II stars becomes possible. In turn, Pop III star formation and early metal enrichment are slowed by the high energy radiation emitted by Pop II stars. Thus, through the SNe and radiation they produce, Populations II and III coevolve in the early Universe, one regulated by the other. We present large (4 Mpc)^3, high resolution cosmological simulations in which we self-consistently model early metal enrichment and the stellar radiation responsible for the destruction of the coolants (H2 and HD) required for Pop III star formation. We find that the molecule-dissociating stellar radiation produced both locally and over cosmological distances reduces the Pop III star formation rate at z > 10 by up to an order of magnitude compared to the case in which this radiation is not included. However, we find that the effect of LW feedback is to enhance the amount of Pop II star formation. We attribute this to the reduced rate at which gas is blown out of dark matter haloes by SNe in the simulation with LW feedback, which results in larger reservoirs for metal-enriched star formation. Even accounting for metal enrichment, molecule-dissociating radiation and the strong suppression of low-mass galaxy formation due to reionization at z < 10, we find that Pop III stars are still formed at a rate of ~ 10^-5 M_sun yr^-1 Mpc^-3 down to z ~ 6. This suggests that the majority of primordial pair-instability SNe that may be uncovered in future surveys will be found at z < 10. We also find that the molecule-dissociating radiation emitted from Pop II stars may destroy H2 molecules at a high enough rate to suppress gas cooling and allow for the formation of supermassive primordial stars which collapse to form ~ 100,000 solar mass black holes.Comment: 17 pages, 11 figures; accepted for publication in MNRAS; some figures downgraded, high resolution version available at http://www.as.utexas.edu/~jljohnson/FiBY_III.pd

The first low-mass stars: critical metallicity or dust-to-gas ratio?

We explore the minimal conditions which enable the formation of metal-enriched solar and sub-solar mass stars. We find that in the absence of dust grains, gas fragmentation occurs at densities nH ~ [10^4-10^5]cm^{-3} when the metallicity exceeds Z ~ 10^{-4} Zsun. The resulting fragmentation masses are > 10 Msun. The inclusion of Fe and Si cooling does not affect the thermal evolution as this is dominated by molecular cooling even for metallicities as large as Z = 10^{-2} Zsun. The presence of dust is the key driver for the formation of low-mass stars. We focus on three representative core-collapse supernova (SN) progenitors, and consider the effects of reverse shocks of increasing strength: these reduce the depletion factors, fdep = Mdust/(Mdust+Mmet), alter the shape of the grain size distribution function and modify the relative abundances of grain species and of metal species in the gas phase. We find that the lowest metallicity at which fragmentation occurs is Z=10^{-6} Zsun for gas pre-enriched by the explosion of a 20 Msun primordial SN (fdep > 0.22) and/or by a 35 Msun, Z=10^{-4} Zsun SN (fdep > 0.26); it is ~ 1 dex larger, when the gas is pre-enriched by a Z = 10^{-4} Zsun, 20 Msun SN (fdep > 0.04). Cloud fragmentation depends on the depletion factor and it is suppressed when the reverse shock leads to a too large destruction of dust grains. These features are all consistent with the existence of a minimum dust-to-gas ratio, Dcr, above which fragmentation is activated. We derive a simple analytic expression for Dcr which, for grain composition and properties explored in the present study, reads Dcr = [2.6 - 6.3] x 10^{-9}. When the dust-to-gas ratio of star forming clouds exceeds this value, the fragmentation masses range between 0.01 Msun and 1 Msun, thus enabling the formation of the first low-mass stars.Comment: accepted by MNRAS, 12 pages, 8 figure

Star Formation in Molecular Clouds

Star formation is one of the least understood processes in cosmic evolution. It is difficult to formulate a general theory for star formation in part because of the wide range of physical processes involved. The interstellar gas out of which stars form is a supersonically turbulent plasma governed by magnetohydrodynamics. This is hard enough by itself, since we do not understand even subsonic hydrodynamic turbulence very well, let alone supersonic non-ideal MHD turbulence. However, the behavior of star-forming clouds in the ISM is also obviously influenced by gravity, which adds complexity, and by both continuum and line radiative processes. Finally, the behavior of star-forming clouds is influenced by a wide variety of chemical processes, including formation and destruction of molecules and dust grains (which changes the thermodynamic behavior of the gas) and changes in ionization state (which alter how strongly the gas couples to magnetic fields). As a result of these complexities, there is nothing like a generally agreed-upon theory of star formation, as there is for stellar structure. Instead, we are forced to take a much more phenomenological approach. These notes provide an introduction to our current thinking about how star formation works.Comment: To appear in the XVth Special Courses of the National Observatory of Rio de Janeiro, 49 pages, 11 figures, AIP conference format. This is a pedagogic introduction to star formation science, intended for beginning grad students or advanced undergraduate

The number of tree species on Earth

One of the most fundamental questions in ecology is how many species inhabit the Earth. However, due to massive logistical and financial challenges and taxonomic difficulties connected to the species concept definition, the global numbers of species, including those of important and well-studied life forms such as trees, still remain largely unknown. Here, based on global groundsourced data, we estimate the total tree species richness at global, continental, and biome levels. Our results indicate that there are 73,000 tree species globally, among which ∼9,000 tree species are yet to be discovered. Roughly 40% of undiscovered tree species are in South America. Moreover, almost one-third of all tree species to be discovered may be rare, with very low populations and limited spatial distribution (likely in remote tropical lowlands and mountains). These findings highlight the vulnerability of global forest biodiversity to anthropogenic changes in land use and climate, which disproportionately threaten rare species and thus, global tree richness

The number of tree species on Earth.

One of the most fundamental questions in ecology is how many species inhabit the Earth. However, due to massive logistical and financial challenges and taxonomic difficulties connected to the species concept definition, the global numbers of species, including those of important and well-studied life forms such as trees, still remain largely unknown. Here, based on global ground-sourced data, we estimate the total tree species richness at global, continental, and biome levels. Our results indicate that there are ∼73,000 tree species globally, among which ∼9,000 tree species are yet to be discovered. Roughly 40% of undiscovered tree species are in South America. Moreover, almost one-third of all tree species to be discovered may be rare, with very low populations and limited spatial distribution (likely in remote tropical lowlands and mountains). These findings highlight the vulnerability of global forest biodiversity to anthropogenic changes in land use and climate, which disproportionately threaten rare species and thus, global tree richness

The number of tree species on Earth.

One of the most fundamental questions in ecology is how many species inhabit the Earth. However, due to massive logistical and financial challenges and taxonomic difficulties connected to the species concept definition, the global numbers of species, including those of important and well-studied life forms such as trees, still remain largely unknown. Here, based on global ground-sourced data, we estimate the total tree species richness at global, continental, and biome levels. Our results indicate that there are ∼73,000 tree species globally, among which ∼9,000 tree species are yet to be discovered. Roughly 40% of undiscovered tree species are in South America. Moreover, almost one-third of all tree species to be discovered may be rare, with very low populations and limited spatial distribution (likely in remote tropical lowlands and mountains). These findings highlight the vulnerability of global forest biodiversity to anthropogenic changes in land use and climate, which disproportionately threaten rare species and thus, global tree richness

Evenness mediates the global relationship between forest productivity and richness

1. Biodiversity is an important component of natural ecosystems, with higher species richness often correlating with an increase in ecosystem productivity. Yet, this relationship varies substantially across environments, typically becoming less pronounced at high levels of species richness. However, species richness alone cannot reflect all important properties of a community, including community evenness, which may mediate the relationship between biodiversity and productivity. If the evenness of a community correlates negatively with richness across forests globally, then a greater number of species may not always increase overall diversity and productivity of the system. Theoretical work and local empirical studies have shown that the effect of evenness on ecosystem functioning may be especially strong at high richness levels, yet the consistency of this remains untested at a global scale. 2. Here, we used a dataset of forests from across the globe, which includes composition, biomass accumulation and net primary productivity, to explore whether productivity correlates with community evenness and richness in a way that evenness appears to buffer the effect of richness. Specifically, we evaluated whether low levels of evenness in speciose communities correlate with the attenuation of the richness–productivity relationship. 3. We found that tree species richness and evenness are negatively correlated across forests globally, with highly speciose forests typically comprising a few dominant and many rare species. Furthermore, we found that the correlation between diversity and productivity changes with evenness: at low richness, uneven communities are more productive, while at high richness, even communities are more productive. 4. Synthesis. Collectively, these results demonstrate that evenness is an integral component of the relationship between biodiversity and productivity, and that the attenuating effect of richness on forest productivity might be partly explained by low evenness in speciose communities. Productivity generally increases with species richness, until reduced evenness limits the overall increases in community diversity. Our research suggests that evenness is a fundamental component of biodiversity–ecosystem function relationships, and is of critical importance for guiding conservation and sustainable ecosystem management decisions

Native diversity buffers against severity of non-native tree invasions

Determining the drivers of non-native plant invasions is critical for managing native ecosystems and limiting the spread of invasive species$^{1,2}$. Tree invasions in particular have been relatively overlooked, even though they have the potential to transform ecosystems and economies$^{3,4}$. Here, leveraging global tree databases$^{5,6,7}$, we explore how the phylogenetic and functional diversity of native tree communities, human pressure and the environment influence the establishment of non-native tree species and the subsequent invasion severity. We find that anthropogenic factors are key to predicting whether a location is invaded, but that invasion severity is underpinned by native diversity, with higher diversity predicting lower invasion severity. Temperature and precipitation emerge as strong predictors of invasion strategy, with non-native species invading successfully when they are similar to the native community in cold or dry extremes. Yet, despite the influence of these ecological forces in determining invasion strategy, we find evidence that these patterns can be obscured by human activity, with lower ecological signal in areas with higher proximity to shipping ports. Our global perspective of non-native tree invasion highlights that human drivers influence non-native tree presence, and that native phylogenetic and functional diversity have a critical role in the establishment and spread of subsequent invasions