179 research outputs found
A Cladistic Analysis of \u3cem\u3endh\u3c/em\u3eF Sequences from Representative Species of \u3cem\u3eSaintpaulia\u3c/em\u3e and \u3cem\u3eStreptocarpus\u3c/em\u3e Subgenera and \u3cem\u3eStreptocarpella\u3c/em\u3e (Gesneriaceae)
Two African genera of the Gesneriaceae, Saintpaulia and Streptocarpus, are similar in many respects. Both genera have blue to purple flowers, pollen of similar shape and exine sculpting, embryos with one-celled uninucleate chalazal haustoria, shared vegetative structures among some species, and are among the few genera in the Gesneriaceae which include species with chromosome count of n=15. Similarity of these features has indicated that the two genera are likely to be closely related. This study examines the sequences of the chloroplast gene ndhF among several representative Saintpaulia and representatives of Streptocarpus subgenera Streptocarpella and Streptocarpus. The results of this analysis are congruent with those of previous analysis based on the nuclear ribosomal region, ITS. Saintpaulia was found to be nested within Streptocarpus and Streptocarpella. The results raise the possibility of the taxonomic revision of these genera, and this is discussed. Comparisons between the data sets are made regarding utility of the two regions, sample size and outgroup
Wholeâgenome sequencing and genome regions of special interest : lessons from major histocompatibility complex, sex determination, and plant selfâincompatibility
Whole-genome sequencing of non-model organisms is now widely accessible and has allowed a range of questions in the field of molecular ecology to be investigated with greater power. However, some genomic regions that are of high biological interest remain problematic for assembly and data-handling. Three such regions are the major histocompatibility complex (MHC), sex-determining regions (SDRs) and the plant self-incompatibility locus (S-locus). Using these as examples, we illustrate the challenges of both assembling and resequencing these highly polymorphic regions and how bioinformatic and technological developments are enabling new approaches to their study. Mapping short-read sequences against multiple alternative references improves genotyping comprehensiveness at the S-locus thereby contributing to more accurate assessments of allelic frequencies. Long-read sequencing, producing reads of several tens to hundreds of kilobase pairs in length, facilitates the assembly of such regions as single sequences can span the multiple duplicated gene copies of the MHC region, and sequence through repetitive stretches and translocations in SDRs and S-locus haplotypes. These advances are adding value to short-read genome resequencing approaches by allowing, for example, more accurate haplotype phasing across longer regions. Finally, we assessed further technical improvements, such as nanopore adaptive sequencing and bioinformatic tools using pangenomes, which have the potential to further expand our knowledge of a number of genomic regions that remain challenging to study with classical resequencing approaches
Marine liquid cloud geometric thickness retrieved from OCO-2's oxygen A-band spectrometer
This paper introduces the OCO2CLD-LIDAR-AUX product, which uses the Cloud-Aerosol Lidar and Infrared
Pathfinder Satellite Observation (CALIPSO) lidar and the Orbiting Carbon
Observatory-2 (OCO-2) hyperspectral A-band spectrometer. CALIPSO provides a
prior cloud top pressure (Ptop) for an OCO-2-based retrieval of
cloud optical depth, Ptop and cloud geometric thickness expressed
in hPa. Measurements are of single-layer liquid clouds over oceans from
September 2014 to December 2016 when collocated data are available. Retrieval
performance is best for solar zenith angles <45â and when
the cloud phase classification, which also uses OCO-2's weak CO2
band, is more confident. The highest quality optical depth retrievals agree
with those from the Moderate Resolution Imaging Spectroradiometer (MODIS)
with discrepancies smaller than the MODIS-reported uncertainty. Retrieved
thicknesses are consistent with a substantially subadiabatic structure over
marine stratocumulus regions, in which extinction is weighted towards the
cloud top. Cloud top pressure in these clouds shows a 4 hPa bias compared
with CALIPSO which we attribute mainly to the assumed vertical structure of
cloud extinction after showing little sensitivity to the presence of
CALIPSO-identified aerosol layers or assumed cloud droplet effective radius.
This is the first case of success in obtaining internal cloud structure from
hyperspectral A-band measurements and exploits otherwise unused OCO-2 data.
This retrieval approach should provide additional constraints on
satellite-based estimates of cloud droplet number concentration from visible
imagery, which rely on parameterization of the cloud thickness.</p
Orbiting Carbon Observatory-2 (OCO-2) cloud screening algorithms: validation against collocated MODIS and CALIOP data
The objective of the National Aeronautics and Space Administration's (NASA) Orbiting Carbon Observatory-2 (OCO-2) mission is to retrieve the column-averaged carbon dioxide (COâ) dry air mole fraction (XCO2) from satellite measurements of reflected sunlight in the near-infrared. These estimates can be biased by clouds and aerosols, i.e., contamination, within the instrument's field of view. Screening of the most contaminated soundings minimizes unnecessary calls to the computationally expensive Level 2 (L2) X_(COâ) retrieval algorithm. Hence, robust cloud screening methods have been an important focus of the OCO-2 algorithm development team. Two distinct, computationally inexpensive cloud screening algorithms have been developed for this application. The A-Band Preprocessor (ABP) retrieves the surface pressure using measurements in the 0.76 ”m Oâ A band, neglecting scattering by clouds and aerosols, which introduce photon path-length differences that can cause large deviations between the expected and retrieved surface pressure. The Iterative Maximum A Posteriori (IMAP) Differential Optical Absorption Spectroscopy (DOAS) Preprocessor (IDP) retrieves independent estimates of the COâ and HâO column abundances using observations taken at 1.61 ”m (weak COâ band) and 2.06 ”m (strong COâ band), while neglecting atmospheric scattering. The COâ and HâO column abundances retrieved in these two spectral regions differ significantly in the presence of cloud and scattering aerosols. The combination of these two algorithms, which are sensitive to different features in the spectra, provides the basis for cloud screening of the OCO-2 data set.
To validate the OCO-2 cloud screening approach, collocated measurements from NASA's Moderate Resolution Imaging Spectrometer (MODIS), aboard the Aqua platform, were compared to results from the two OCO-2 cloud screening algorithms. With tuning of algorithmic threshold parameters that allows for processing of ââ 20â25 % of all OCO-2 soundings, agreement between the OCO-2 and MODIS cloud screening methods is found to be ââ 85 % over four 16-day orbit repeat cycles in both the winter (December) and spring (AprilâMay) for OCO-2 nadir-land, glint-land and glint-water observations.
No major, systematic, spatial or temporal dependencies were found, although slight differences in the seasonal data sets do exist and validation is more problematic with increasing solar zenith angle and when surfaces are covered in snow and ice and have complex topography. To further analyze the performance of the cloud screening algorithms, an initial comparison of OCO-2 observations was made to collocated measurements from the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) aboard the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO). These comparisons highlight the strength of the OCO-2 cloud screening algorithms in identifying high, thin clouds but suggest some difficulty in identifying some clouds near the surface, even when the optical thicknesses are greater than 1
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Cross-cultural invariances in the architecture of shame
This set of experiments shows that in 15 traditional small-scale societies there is an extraordinarily close correspondence between (i) the intensity of shame felt if one exhibited specific acts or traits and (ii) the magnitude of devaluation expressed in response to those acts or traits by local audiences, and even foreign audiences. Three important and widely acknowledged sources of cultural variation between communitiesâ}geographic proximity, linguistic similarity, and religious similarity{â}all failed to account for the strength of between-community correlations in the shame{â}devaluation link. This supplies a parallel line of evidence that shame is a universal system, part of our species{â} cooperative biology, rather than a product of cultural evolution.Human foragers are obligately group-living, and their high dependence on mutual aid is believed to have characterized our species{â} social evolution. It was therefore a central adaptive problem for our ancestors to avoid damaging the willingness of other group members to render them assistance. Cognitively, this requires a predictive map of the degree to which others would devalue the individual based on each of various possible acts. With such a map, an individual can avoid socially costly behaviors by anticipating how much audience devaluation a potential action (e.g., stealing) would cause and weigh this against the action{â}s direct payoff (e.g., acquiring). The shame system manifests all of the functional properties required to solve this adaptive problem, with the aversive intensity of shame encoding the social cost. Previous data from three Western(ized) societies indicated that the shame evoked when the individual anticipates committing various acts closely tracks the magnitude of devaluation expressed by audiences in response to those acts. Here we report data supporting the broader claim that shame is a basic part of human biology. We conducted an experiment among 899 participants in 15 small-scale communities scattered around the world. Despite widely varying languages, cultures, and subsistence modes, shame in each community closely tracked the devaluation of local audiences (mean r = +0.84). The fact that the same pattern is encountered in such mutually remote communities suggests that shame{âs match to audience devaluation is a design feature crafted by selection and not a product of cultural contact or convergent cultural evolution
Taxonomic surrogacy in biodiversity assessments, and the meaning of Linnaean ranks
Copyright © 2006 The Natural History MuseumThe majority of biodiversity assessments use species as the base unit. Recently, a series of studies have suggested replacing numbers of species with higher ranked taxa (genera, families, etc.); a method known as taxonomic surrogacy that has an important potential to save time and resources in assesments of biological diversity. We examine the relationships between taxa and ranks, and suggest that species/higher taxon exchanges are founded on misconceptions about the properties of Linnaean classification. Rank allocations in current classifications constitute a heterogeneous mixture of various historical and contemporary views. Even if all taxa were monophyletic, those referred to the same rank would simply denote separate clades without further equivalence. We conclude that they are no more comparable than any other, non-nested taxa, such as, for example, the genus Rattus and the phylum Arthropoda, and that taxonomic surrogacy lacks justification. These problems are also illustrated with data of polychaetous annelid worms from a broad-scale study of benthic biodiversity and species distributions in the Irish Sea. A recent consensus phylogeny for polychaetes is used to provide three different family-level classifications of polychaetes. We use families as a surrogate for species, and present ShannonâWiener diversity indices for the different sites and the three different classifications, showing how the diversity measures rely on subjective rank allocations.Y. Bertrand, F. Pleijel and G. W. Rous
The role of immigrants in the assembly of the South American rainforest tree flora
The Amazon lowland rainforest flora is conventionally viewed as comprising lineages that evolved in biogeographic isolation after the split of west Gondwana (ca. 100 Myr ago). Recent molecular phylogenies, however, identify immigrant lineages that arrived in South America during its period of oceanic isolation (ca. 100â3 Myr ago). Long-distance sweepstakes dispersal across oceans played an important and possibly predominant role. Stepping-stone migration from Africa and North America through hypothesized Late Cretaceous and Tertiary island chains may have facilitated immigration. An analysis of inventory plot data suggests that immigrant lineages comprise ca. 20% of both the species and individuals of an Amazon tree community in Ecuador. This is more than an order of magnitude higher than previous estimates. We also present data on the community-level similarity between South American and palaeotropical rainforests, and suggest that most taxonomic similarity derives from trans-oceanic dispersal, rather than a shared Gondwanan history.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/83303/1/Pennington2004.pd
Soil seed bank of the invasive Robinia pseudoacacia in planted Pinus nigra stands
Pinus nigra and Robinia pseudoacacia are exotic trees used for afforestation in Hungary. Pinus nigra was non-invasive, however R. pseudoacacia escaped from cultivation and invaded several vegetation types including pine plantations. It has recently been planned to cut P. nigra plantations and replace them by native tree stands, especially in nature reserves. The scattered presence of R. pseudoacacia specimens in pine stands might place constraints on planned tree replacement because of their vegetative resprouting
and recolonization from an established seed bank. The aim of this study was to investigate the soil seed bank under the canopy of solitary R. pseudoacacia specimens found in P. nigra plantations. Altogether 250 soil samples were collected from the 0â6 and 6â12 cm
soil layers under solitary Robinia trees of varying ages (with basal areas between 62.4 and 1089.3 cm2). Seeds were separated by sieving then scarified and germinated. Seed bank density ranged between 640 and 2285 seedsmâ2 with an average distribution of 82.7% and 17.3% in the upper and lower soil layer, respectively. Total density of the seed bank and also the seed bank ratio of the lower soil layer increased with tree age. The accumulated seed bank of R. pseudoacacia should be considered in the careful planning of tree replacement operations in Pinus nigra stands
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