Population Synthesis in the Blue. II. The Spectroscopic Age of 47 Tucanae

We develop a new set of models for intermediate-metallicity single stellar populations in the blue/optical region and use those models to determine the spectroscopic age of 47 Tuc. The models are based on a moderately high resolution (1.8 Å, FWHM) empirical spectral library, state-of-the-art theoretical isochrones from M. Salaris and the most recent set from the Padova group, and new semiempirical calibrations between fundamental stellar parameters and observables. Model line strengths include all corrections for deficiencies of the stellar library that are described in Paper I. We highlight the importance of correctly modeling the luminosity function (LF) of the cluster at the level of the giant branch, in order to achieve a good reproduction of the integrated spectrum; agreement between the spectroscopic age and the age based on the cluster's color-magnitude diagram (CMD) is achieved only if the observed LF is used rather than the theoretical ones, which either do not include asymptotic giant branch stars (Salaris) or underpredict the total number counts of bright giants in the cluster by a factor of 2 (Padova). After all corrections are made, the CMD and the spectroscopic ages (from Hγ and Hβ) are in close agreement: ~11-12 Gyr for Salaris isochrones and ~13 Gyr for Padova. The difference between the model ages is due to the inclusion of atomic diffusion in the Salaris models. Previously older spectroscopic ages were due to the underestimate of the number of red giants and/or the use of isochrones that neglected the effects of He diffusion and α-enhancement. Uncertainties in spectroscopic age determinations of old stellar populations stem from a number of effects, the most important of which are the Teff and [Fe/H] scales of the giant stars used in the stellar library, the LF on the upper giant branch, and the assumed metallicity of the target stellar population itself. A ±1 Gyr uncertainty in age results from uncertainties of ±75 K in the Teff scale of the library giants, 0.1 dex in the level of the giant branch LF, and ±0.1 dex in the assumed [Fe/H] of either the target stellar population or the assumed zero point of the metallicity scale of the stellar library. A similar underestimate in the bright giant LF, if it exists in current supersolar metallicity models, would cause spectroscopic ages of elliptical galaxies inferred from such models to be too high by approximately 30%

Detailed Analysis of Nearby Bulgelike Dwarf Stars II. Lithium Abundances

Li abundances are derived for a sample of bulgelike stars with isochronal ages of 10-11 Gyr. These stars have orbits with pericentric distances, Rp, as small as 2-3 kpc and Zmax < 1 kpc. The sample comprises G and K dwarf stars in the metallicity range -0.80<[Fe/H]< +0.40. Few data of Li abundances in old turn-off stars (> 4.5 Gyr) within the present metallicity range are available. M67 (4.7 Gyr) and NGC 188 (6 Gyr) are the oldest studied metal-rich open clusters with late-type stars. Li abundances have also been studied for few samples of old metal-rich field stars. In the present work a high dispersion in Li abundances is found for bulgelike stars for all the metallicity range, comparable with values in M67. The role of metallicity and age on a Li depletion pattern is discussed. The possible connection between Li depletion and oxygen abundance due to atmospheric opacity effects is investigated.Comment: 9 pages, 7 figure

H-delta in the Integrated Light of Galaxies: What Are We Actually Measuring?

We present a cautionary study exploring the reliability of the H-delta line in the integrated spectra of galaxies for determining galaxy ages. Our database consists of the observed integrated spectra of ~120 early-type galaxies, of 7 metal-rich globular clusters in M31 and the Galactic globular cluster 47 Tuc, and of the open cluster M67. We have measured H-delta using index definitions designed to assess contamination from the CN molecule in and around H-delta by choosing combinations of bandpasses that both avoid and include a region of CN molecular lines redward of H-delta. We find systematic differences in the ages derived from H-delta measurements among the various definitions when extracting ages from H-delta in old stellar populations with enhanced CN bands due to non-solar abundance ratios. We propose that neighboring CN lines have a strong effect on pseudocontinuum and central bandpass levels. For stellar populations which have non-solar abundance ratios in C and/or N, population synthesis models that do not account for abundance ratio variations cannot reproduce accurately the CN 4216 \AA band, which leads to a corresponding inaccuracy in reproducing the various H-delta indices. Hence, caution must be used when extracting galaxy ages from the H-delta line in old stellar populations with significant non-solar abundance ratios.Comment: 8 figures, 2 table

Population Synthesis in the Blue I. Synthesis of the Integrated Spectrum of 47 Tucanae from its Color-Magnitude Diagram

We perform an empirical synthesis of the blue integrated spectrum of the metal-rich globular cluster 47 Tucanae, based directly on the color-magnitude diagram of the cluster coupled to a moderately high-resolution spectral library. Freed from any significant dependence on theory, we are able to perform a fundamental test of the adequacy of the spectral library and its associated stellar parameters. Excellent fits are achieved for almost all absorption-line indices studied, provided the computations are corrected for two limitations of the spectral library, namely, the lack of a representative set of metal-poor giants and the absence of CN-strong stars. The latter effect is corrected by means of spectrum synthesis from model photospheres, considering the abundance pattern of CN-strong and CN-normal stars. We also need to perform a slight correction of the metallicity of the cluster (by --0.05 dex in relation to the standard value [Fe/H]=-0.7) in order to match the metal-line index measurements in the cluster spectrum. After these relatively small adjustments, the overall spectral agreement is good. Good fits are achieved for Hbeta, Hgamma, Mgb, , Ca4227 and Fe4383, and only Hdelta_F is overpredicted. Thus, ages inferred from Hdelta_F are slightly older than the ages based on the other Balmer lines, by ~ 3 Gyrs. The success of this exercise suggests that previous failures to synthesize the spectrum of 47 Tuc must have arisen from inadequacies in the theoretical evolutionary isochrones and/or luminosity functions. Such a possibility is considered in a companion paper

Rarity of monodominance in hyperdiverse Amazonian forests.

Tropical forests are known for their high diversity. Yet, forest patches do occur in the tropics where a single tree species is dominant. Such "monodominant" forests are known from all of the main tropical regions. For Amazonia, we sampled the occurrence of monodominance in a massive, basin-wide database of forest-inventory plots from the Amazon Tree Diversity Network (ATDN). Utilizing a simple defining metric of at least half of the trees ≥ 10 cm diameter belonging to one species, we found only a few occurrences of monodominance in Amazonia, and the phenomenon was not significantly linked to previously hypothesized life history traits such wood density, seed mass, ectomycorrhizal associations, or Rhizobium nodulation. In our analysis, coppicing (the formation of sprouts at the base of the tree or on roots) was the only trait significantly linked to monodominance. While at specific locales coppicing or ectomycorrhizal associations may confer a considerable advantage to a tree species and lead to its monodominance, very few species have these traits. Mining of the ATDN dataset suggests that monodominance is quite rare in Amazonia, and may be linked primarily to edaphic factors

Fiber Optical Cable and Connector System (FOCCoS) for PFS/Subaru

FOCCoS, Fiber Optical Cable and Connector System, has the main function of capturing the direct light from the focal plane of Subaru Telescope using optical fibers, each one with a microlens in its tip, and conducting this light through a route containing connectors to a set of four spectrographs. The optical fiber cable is divided in 3 different segments called Cable A, Cable B and Cable C. Multi-fibers connectors assure precise connection among all optical fibers of the segments, providing flexibility for instrument changes. To assure strong and accurate connection, these sets are arranged inside two types of assemblies: the Tower Connector, for connection between Cable C and Cable B; and the Gang Connector, for connection between Cable B and Cable A. Throughput tests were made to evaluate the efficiency of the connections. A lifetime test connection is in progress. Cable C is installed inside the PFI, Prime Focus Instrument, where each fiber tip with a microlens is bonded to the end of the shaft of a 2-stage piezo-electric rotatory motor positioner; this assembly allows each fiber to be placed anywhere within its patrol region, which is 9.5mm diameter.. Each positioner uses a fiber arm to support the ferrule, the microlens, and the optical fiber. 2400 of these assemblies are arranged on a motor bench plate in a hexagonal-closed-packed disposition.Comment: 11 pages, 20 figure

Building a Portuguese Coalition for Biodiversity Genomics

The diverse physiography of the Portuguese land and marine territory, spanning from continental Europe to the Atlantic archipelagos, has made it an important repository of biodiversity throughout the Pleistocene glacial cycles, leading to a remarkable diversity of species and ecosystems. This rich biodiversity is under threat from anthropogenic drivers, such as climate change, invasive species, land use changes, overexploitation or pathogen (re)emergence. The inventory, characterization and study of biodiversity at inter- and intra-specific levels using genomics is crucial to promote its preservation and recovery by informing biodiversity conservation policies, management measures and research. The participation of researchers from Portuguese institutions in the European Reference Genome Atlas (ERGA) initiative, and its pilot effort to generate reference genomes for European biodiversity, has reinforced the establishment of Biogenome Portugal. This nascent institutional network will connect the national community of researchers in genomics. Here, we describe the Portuguese contribution to ERGA’s pilot effort, which will generate high-quality reference genomes of six species from Portugal that are endemic, iconic and/or endangered, and include plants, insects and vertebrates (fish, birds and mammals) from mainland Portugal or the Azores islands. In addition, we outline the objectives of Biogenome Portugal, which aims to (i) promote scientific collaboration, (ii) contribute to advanced training, (iii) stimulate the participation of institutions and researchers based in Portugal in international biodiversity genomics initiatives, and (iv) contribute to the transfer of knowledge to stakeholders and engaging the public to preserve biodiversity. This initiative will strengthen biodiversity genomics research in Portugal and fuel the genomic inventory of Portuguese eukaryotic species. Such efforts will be critical to the conservation of the country’s rich biodiversity and will contribute to ERGA’s goal of generating reference genomes for European species.info:eu-repo/semantics/publishedVersio

Geographic patterns of tree dispersal modes in Amazonia and their ecological correlates

Unidad de excelencia María de Maeztu CEX2019-000940-MAim: To investigate the geographic patterns and ecological correlates in the geographic distribution of the most common tree dispersal modes in Amazonia (endozoochory, synzoochory, anemochory and hydrochory). We examined if the proportional abundance of these dispersal modes could be explained by the availability of dispersal agents (disperser-availability hypothesis) and/or the availability of resources for constructing zoochorous fruits (resource-availability hypothesis). Time period: Tree-inventory plots established between 1934 and 2019. Major taxa studied: Trees with a diameter at breast height (DBH) ≥ 9.55 cm. Location: Amazonia, here defined as the lowland rain forests of the Amazon River basin and the Guiana Shield. Methods: We assigned dispersal modes to a total of 5433 species and morphospecies within 1877 tree-inventory plots across terra-firme, seasonally flooded, and permanently flooded forests. We investigated geographic patterns in the proportional abundance of dispersal modes. We performed an abundance-weighted mean pairwise distance (MPD) test and fit generalized linear models (GLMs) to explain the geographic distribution of dispersal modes. Results: Anemochory was significantly, positively associated with mean annual wind speed, and hydrochory was significantly higher in flooded forests. Dispersal modes did not consistently show significant associations with the availability of resources for constructing zoochorous fruits. A lower dissimilarity in dispersal modes, resulting from a higher dominance of endozoochory, occurred in terra-firme forests (excluding podzols) compared to flooded forests. Main conclusions: The disperser-availability hypothesis was well supported for abiotic dispersal modes (anemochory and hydrochory). The availability of resources for constructing zoochorous fruits seems an unlikely explanation for the distribution of dispersal modes in Amazonia. The association between frugivores and the proportional abundance of zoochory requires further research, as tree recruitment not only depends on dispersal vectors but also on conditions that favour or limit seedling recruitment across forest types