The role of social capital in fishing community sustainability: case of Shelter Cove, CA

Community development scholars have consistently highlighted the importance of social capital – the glue that keeps a community together – for the development and long-term sustainability of rural communities. There has been less discussion about the role of social capital in fishing communities. This thesis explores the historical trajectory of social capital in Shelter Cove, CA, a small, remote fishing community with an attempt to understand how the type and level of social capital have and may continue to affect the progress and sustainability of the community. Data for this thesis were collected as part of a strategic planning effort in the Shelter Cove fishing community that documented community members’ perceptions of the current state of this fishing community and recommendations of how things could be improved. Interview data from the Shelter Cove Fishing Community Sustainability Plan (FCSP) were analyzed to provide the 2017 to 2018 context of participants’ perceptions of the fishing community. Research methods included semi-structured interviews with 50 individuals, three public workshops, and document review and archival research. These data were paired with additional document review and historical analysis of the path that led the community to its current state of social capital. Both of these data streams were qualitatively coded to find emergent themes. Social capital emerged as an area for capital asset development that had been strong historically, but that has eroded over time as a result of a multitude of events that left the fishing community less resilient to unforeseen changes. This thesis provides general pathways and recommendations for rural fishing communities to invest further in their social capital assets through both bonding and bridging social networks to prepare them to be more sustainable fishing communities in the future

A Near-Infrared Stellar Census of the Blue Compact Dwarf Galaxy VII~Zw~403

We present near-infrared single-star photometry for the low-metallicity Blue Compact Dwarf galaxy VII~Zw~403. We achieve limiting magnitudes of F110W~$\approx$~25.5 and F160W~$\approx$~24.5 using one of the NICMOS cameras with the HST equivalents of the ground-based J and H filters. The data have a high photometric precision (0.1 mag) and are $>95$% complete down to magnitudes of about 23, far deeper than previous ground-based studies in the near-IR. The color-magnitude diagram contains about 1000 point sources. We provide a preliminary transformation of the near-IR photometry into the ground system...Comment: Accepted for publication by the AJ, preprint has 49 pages, 2 tables, and 16 figure

Validation of techniques to mitigate copper surface contamination in CUORE

In this article we describe the background challenges for the CUORE experiment posed by surface contamination of inert detector materials such as copper, and present three techniques explored to mitigate these backgrounds. Using data from a dedicated test apparatus constructed to validate and compare these techniques we demonstrate that copper surface contamination levels better than 10E-07 - 10E-08 Bq/cm2 are achieved for 238U and 232Th. If these levels are reproduced in the final CUORE apparatus the projected 90% C.L. upper limit on the number of background counts in the region of interest is 0.02-0.03 counts/keV/kg/y depending on the adopted mitigation technique.Comment: 10 pages, 6 figures, 6 table

Search for 14.4 keV solar axions from M1 transition of Fe-57 with CUORE crystals

We report the results of a search for axions from the 14.4 keV M1 transition from Fe-57 in the core of the sun using the axio-electric effect in TeO2 bolometers. The detectors are 5x5x5 cm3 crystals operated at about 10 mK in a facility used to test bolometers for the CUORE experiment at the Laboratori Nazionali del Gran Sasso in Italy. An analysis of 43.65 kg d of data was made using a newly developed low energy trigger which was optimized to reduce the detectors energy threshold. An upper limit of 0.63 c kg-1 d-1 was established at 95% C.L.. From this value, a lower bound at 95% C.L. was placed on the Peccei-Quinn energy scale of fa >= 0.76 10**6 GeV for a value of S=0.55 for the flavor-singlet axial vector matrix element. Bounds are given for the interval 0.15 < S < 0.55.Comment: 14 pages, 6 figures, submitted to JCA

Stellar Population Astrophysics (SPA) with the TNG. Stock 2, a little-studied open cluster with an eMSTO

Stock 2 is a little-studied open cluster that shows an extended main-sequence turnoff (eMSTO). In order to investigate this phenomenon and characterise the cluster itself, we performed high-resolution spectroscopy in the framework of the Stellar Population Astrophysics project. We employed the High Accuracy Radial velocity Planet Searcher in the Northern hemisphere spectrograph at the Telescopio Nazionale Galileo (TNG). We completed our observations with additional spectra taken with the Catania Astrophysical Observatory Spectropolarimeter. We observed 46 stars (dwarfs and giants). They represent by far the largest sample collected for this cluster to date. We provide the stellar parameters, the extinction, and the radial and projected rotational velocities for most of the stars. Chemical abundances for 21 species with atomic numbers up to 56 have also been derived. We note a differential reddening in the cluster field with an average value of 0.27 mag. This appears the main cause for the observed eMSTO because it cannot be explained as the result of different rotational velocities, as found in other clusters. We estimate an age for Stock 2 of 450 ± 150 Ma, which corresponds to a MSTO stellar mass of ≈2.8 M⊙. The cluster mean radial velocity is about 8.0 km s−1. We find a solar-like metallicity for the cluster, [Fe/H] = −0.07 ± 0.06, compatible with its galactocentric distance. The chemical abundances of main-sequence stars and giants are compatible within the errors. The exceptions are barium and strontium, which are clearly overabundant in giants, and cobalt, which is only marginally overabundant. Finally, the chemical composition of Stock 2 is fully compatible with the composition observed in other open clusters of the Galactic thin-disc population. Based on observations made with the Italian Telescopio Nazionale Galileo (TNG) operated on the island of La Palma by the Fundación Galileo Galilei of the INAF (Istituto Nazionale di Astrofisica) at the Observatorio del Roque de los Muchachos. This study is part of the Large Program titled SPA - Stellar Population Astrophysics: the detailed, age-resolved chemistry of the Milky Way disk (PI: L. Origlia), granted observing time with HARPS-N and GIANO-B echelle spectrographs at the TNG

Three cases of bone metastases in patients with gastrointestinal stromal tumors

Gastrointestinal stromal tumors (GISTs) are rare, but represent the most common mesenchymal neoplasms of the gastrointestinal tract. Tumor resection is the treatment of choice for localized disease. Tyrosine kinase inhibitors (imatinib, sunitinib) are the standard therapy for metastatic or unresectable GISTs. GISTs usually metastasize to the liver and peritoneum. Bone metastases are uncommon. We describe three cases of bone metastases in patients with advanced GISTs: two women (82 and 54 years of age), and one man (62 years of age). Bones metastases involved the spine, pelvis and ribs in one patient, multiple vertebral bodies and pelvis in one, and the spine and iliac wings in the third case. The lesions presented a lytic pattern in all cases. Two patients presented with multiple bone metastases at the time of initial diagnosis and one patient after seven years during the follow-up period. This report describes the diagnosis and treatment of the lesions and may help clinicians to manage bones metastases in GIST patients

Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish

Autosomal recessive hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) maps to the SPG11 locus in the majority of cases. Mutations in the KIAA1840 gene, encoding spatacsin, have been shown to underlie SPG11-linked HSP-TCC. The aim of this study was to perform candidate gene analysis in HSP-TCC subjects from Asian families and to characterize disruption of spatacsin function during zebrafish development. Homozygosity mapping and direct sequencing were used to assess the ACCPN, SPG11, and SPG21 loci in four inbred kindreds originating from the Indian subcontinent. Four novel homozygous SPG11 mutations (c.442+1G>A, c.2146C>T, c.3602_3603delAT, and c.4846C>T) were identified, predicting a loss of spatacsin function in each case. To investigate the role of spatacsin during development, we additionally ascertained the complete zebrafish spg11 ortholog by reverse transcriptase PCR and 5′ RACE. Analysis of transcript expression through whole-mount in situ hybridization demonstrated ubiquitous distribution, with highest levels detected in the brain. Morpholino antisense oligonucleotide injection was used to knock down spatacsin function in zebrafish embryos. Examination of spg11 morphant embryos revealed a range of developmental defects and CNS abnormalities, and analysis of axon pathway formation demonstrated an overall perturbation of neuronal differentiation. These data confirm loss of spatacsin as the cause of SPG11-linked HSP-TCC in Asian kindreds, expanding the mutation spectrum recognized in this disorder. This study represents the first investigation in zebrafish addressing the function of a causative gene in autosomal recessive HSP and identifies a critical role for spatacsin during early neural development in vivo

Whole Genome Deep Sequencing of HIV-1 Reveals the Impact of Early Minor Variants Upon Immune Recognition During Acute Infection

Deep sequencing technologies have the potential to transform the study of highly variable viral pathogens by providing a rapid and cost-effective approach to sensitively characterize rapidly evolving viral quasispecies. Here, we report on a high-throughput whole HIV-1 genome deep sequencing platform that combines 454 pyrosequencing with novel assembly and variant detection algorithms. In one subject we combined these genetic data with detailed immunological analyses to comprehensively evaluate viral evolution and immune escape during the acute phase of HIV-1 infection. The majority of early, low frequency mutations represented viral adaptation to host CD8+ T cell responses, evidence of strong immune selection pressure occurring during the early decline from peak viremia. CD8+ T cell responses capable of recognizing these low frequency escape variants coincided with the selection and evolution of more effective secondary HLA-anchor escape mutations. Frequent, and in some cases rapid, reversion of transmitted mutations was also observed across the viral genome. When located within restricted CD8 epitopes these low frequency reverting mutations were sufficient to prime de novo responses to these epitopes, again illustrating the capacity of the immune response to recognize and respond to low frequency variants. More importantly, rapid viral escape from the most immunodominant CD8+ T cell responses coincided with plateauing of the initial viral load decline in this subject, suggestive of a potential link between maintenance of effective, dominant CD8 responses and the degree of early viremia reduction. We conclude that the early control of HIV-1 replication by immunodominant CD8+ T cell responses may be substantially influenced by rapid, low frequency viral adaptations not detected by conventional sequencing approaches, which warrants further investigation. These data support the critical need for vaccine-induced CD8+ T cell responses to target more highly constrained regions of the virus in order to ensure the maintenance of immunodominant CD8 responses and the sustained decline of early viremia

EXD2 governs germ stem cell homeostasis and lifespan by promoting mitoribosome integrity and translation

Mitochondria are subcellular organelles critical for meeting the bioenergetic and biosynthetic needs of the cell. Mitochondrial function relies on genes and RNA species encoded both in the nucleus and mitochondria, as well as their coordinated translation, import and respiratory complex assembly. Here we describe the characterization of exonuclease domain like 2 (EXD2), a nuclear encoded gene that we show is targeted to the mitochondria and prevents the aberrant association of mRNAs with the mitochondrial ribosome. The loss of EXD2 resulted in defective mitochondrial translation, impaired respiration, reduced ATP production, increased reactive oxygen species and widespread metabolic abnormalities. Depletion of EXD2/CG6744 in D.melanogaster caused developmental delays and premature female germline stem cell attrition, reduced fecundity and a dramatic extension of lifespan that could be reversed with an anti-oxidant diet. Our results define a conserved role for EXD2 in mitochondrial translation that influences development and aging