Stopover Ecology of Autumn Landbird Migrants in the Boise Foothills of Southwestern Idaho

The topography of western North America provides a complex landscape for landbird migrants, and stopover patterns in this region are poorly understood. We examined seven years of stopover data (1997–2003) from a montane area in southwestern Idaho to determine whether this area provides suitable stopover habitat. We compared the proportion of birds recaptured, stopover duration, and changes in energetic condition within and among species and between two mist-netting sites located in different habitats. The proportion of birds recaptured ranged from zero to over 20%, and fewer than 5% of individuals were recaptured in most species. Mean minimum stopover durations from recapture data ranged from 1 to 10 days; most species averaged less than 6 days. Stopover duration estimates from open-population models were comparable but generally greater than estimates from recapture data. As found in stopover studies from other regions, stopover metrics varied within and among species in Idaho. However, most migrants in this study exhibited an ability to gain mass, evidenced both by recapture data and by regression of energetic condition against time since sunrise. These data imply that montane habitats in Idaho are suitable stopover sites. It follows that these habitats might serve an important role for many landbird migrants during the period of late summer molt and autumn migration, a time when many lowland areas of the West, including some riparian systems, are especially arid. We suggest that including montane nonriparian habitats in future stopover ecology studies will allow for a more complete understanding of migrant habitat needs in the West

Effects of Regional Cold Fronts and Localized Weather Phenomena on Autumn Migration of Raptors and Landbirds in Southwest Idaho

Weather has a significant effect on avian migration, but whether the influence is similar across diverse geographic regions and across all species remains to be determined. We evaluated the effect of regional cold fronts and localized weather phenomena on the timing of autumn migration of multiple species of landbirds and raptors in southwest Idaho. The focus of the analysis was on total landbirds and the ten most common landbird species, along with total raptors and the eight most common raptor species. Using 13 years of data from the Idaho Bird Observatory in southwest Idaho (1997–2009), including standardized mist-net captures of landbirds and counts of raptors during autumn migration, we determined significant patterns that advance our understanding of the variables influencing avian migration in the West. Our data show a depression of numbers of most migratory species on the days immediately before, during, and after the passage of a cold front, with peak flights of most species occurring several days prior to or after cold fronts. This pattern was further substantiated by a detailed analysis of many weather variables illustrating that the majority of species choose to migrate during calmer winds, high pressure, and between cold fronts when the opportunity presents itself. In the Intermountain West, cold fronts are fewer in fall than in much of the rest of North America, so migrants may have greater choice of conditions under which to migrate and this behavior may be more common

Molt Strategies and Age Differences in Migration Timing Among Autumn Landbird Migrants in Southwestern Idaho

Intraspecific patterns of autumn migration timing are not well known, particularly in the western United States. Here, we (1) describe autumn migration timing and age ratios of landbird migrants in southwestern Idaho, (2) examine differences in timing among age and sex classes, and (3) demonstrate how prebasic molt strategies affect migration timing differences between age classes. As a group, Neotropical migrants were most common from late July through early September, whereas temperate migrants were most common from mid-September into early October. Proportion of hatch-year birds was 74.5% for all migrants combined and ranged from 33.3% to 100% for individual species. Timing differences between sex classes were detected in only a few species and no general patterns emerged. In 22 of 31 Neotropical and temperate migrants examined, there were significant differences in timing between adults and hatch-year birds. In species in which adults begin fall migration before replacing flight feathers, adults migrated earlier than hatch-year birds. Conversely, in species in which adults molt flight feathers on or near the breeding grounds before departing on fall migration, hatch-year birds migrated earlier than adults in all but one case. Therefore, it appears that molt strategy is a powerful determinant of intraspecific migration timing differences and, to our knowledge, this is the first study to document this pattern among migrant passerines of North America

Diagnostic Laparoscopy and Adhesiolysis: Does It Help with Complex Abdominal and Pelvic Pain Syndrome (CAPPS) in General Surgery?

This study was conducted to determine if lysis of bowel adhesions has a role in the surgical management of adhesions for treating complex abdominal and pelvic pain syndrome

Proteoglycan 4 (PRG4)/Lubricin and the Extracellular Matrix in Gout

Proteoglycan 4 (PRG4) is a mucinous glycoprotein secreted by synovial fibroblasts and superficial zone chondrocytes, released into synovial fluid, and adsorbed on cartilage and synovial surfaces. PRG4′s roles include cartilage boundary lubrication, synovial homeostasis, immunomodulation, and suppression of inflammation. Gouty arthritis is mediated by monosodium urate (MSU) crystal phagocytosis by synovial macrophages, with NLRP3 inflammasome activation and IL-1β release. The phagocytic receptor CD44 mediates MSU crystal uptake by macrophages. By binding CD44, PRG4 limits MSU crystal uptake and downstream inflammation. PRG4/CD44 signaling is transduced by protein phosphatase 2A, which inhibits NF-κB, decreases xanthine oxidoreductase (XOR), urate production, and ROS-mediated IL-1β secretion. PRG4 also suppresses MSU crystal deposition in vitro. In contrast to PRG4, collagen type II (CII) alters MSU crystal morphology and promotes the macrophage uptake of MSU crystals. PRG4 deficiency, mediated by imbalance in PRG4-degrading phagocyte proteases and their inhibitors, was recently implicated in erosive gout, independent of hyperuricemia. Thus, dysregulated extracellular matrix homeostasis, including deficient PRG4 and increased CII release, may promote incident gout and progression to erosive tophaceous joint disease. PRG4 supplementation may offer a new therapeutic option for gout

cAMP Attenuates TGF-β\u27s Profibrotic Responses in Osteoarthritic Synoviocytes: Involvement of Hyaluronan and PRG4

Osteoarthritis (OA) is characterized by synovitis and synovial fibrosis. Synoviocytes are fibroblast-like resident cells of the synovium that are activated by transforming growth factor (TGF)-β to proliferate, migrate, and produce extracellular matrix. Synoviocytes secrete hyaluronan (HA) and proteoglycan-4 (PRG4). HA reduces synovial fibrosis in vivo, and the Prg4−/− mouse exhibits synovial hyperplasia. We investigated the antifibrotic effects of increased intracellular cAMP in TGF-β-stimulated human OA synoviocytes. TGF-β1 stimulated collagen I (COL1A1), α-smooth muscle actin (α-SMA), tissue inhibitor of metalloproteinase (TIMP)-1, and procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2 (PLOD2) expression, and procollagen I, α-SMA, HA, and PRG4 production, migration, and proliferation of OA synoviocytes were measured. Treatment of OA synoviocytes with forskolin (10 μM) increased intracellular cAMP levels and reduced TGF-β1-stimulated COL1A1, α-SMA, and TIMP-1 expression, with no change in PLOD2 expression. Forskolin also reduced TGF-β1-stimulated procollagen I and α-SMA content as well as synoviocyte migration and proliferation. Forskolin (10 μM) increased HA secretion and PRG4 expression and production. A cell-permeant cAMP analog reduced COL1A1 and α-SMA expression and enhanced HA and PRG4 secretion by OA synoviocytes. HA and PRG4 reduced α-SMA expression and content, and PRG4 reduced COL1A1 expression and procollagen I content in OA synoviocytes. Prg4−/− synovium exhibited increased α-SMA, COL1A1, and TIMP-1 expression compared with Prg4+/+ synovium. Prg4−/− synoviocytes demonstrated strong α-SMA and collagen type I staining, whereas these were undetected in Prg4+/+ synoviocytes and were reduced with PRG4 treatment. We conclude that increasing intracellular cAMP levels in synoviocytes mitigates synovial fibrosis through enhanced production of HA and PRG4, possibly representing a novel approach for treatment of OA synovial fibrosis

The Autocrine Role of Proteoglycan-4 (PRG4) in Modulating Osteoarthritic Synoviocyte Proliferation and Expression of Matrix Degrading Enzymes

Background: Lubricin/proteoglycan 4 (PRG4) is a mucinous glycoprotein secreted by synovial fibroblasts and superficial zone chondrocytes. Recently, we showed that recombinant human PRG4 (rhPRG4) is a putative ligand for CD44 receptor. rhPRG4-CD44 interaction inhibits cytokine-induced rheumatoid arthritis synoviocyte proliferation. The objective of this study is to decipher the autocrine function of PRG4 in regulating osteoarthritic synoviocyte proliferation and expression of catabolic and pro-inflammatory mediators under basal and interleukin-1 beta (IL-1β)- stimulated conditions. Methods: Cytosolic and nuclear levels of nuclear factor kappa B (NFκB) p50 and p65 subunits in Prg4+/+ and Prg4-/- synoviocytes were studied using western blot. Nuclear translocation of p50 and p65 proteins in osteoarthritis (OA) fibroblast-like synoviocytes (FLS) in response to IL-1β stimulation in the absence or presence of rhPRG4 was studied using DNA binding assays. OA synoviocyte (5000 cells per well) proliferation following IL-1β (20 ng/ml) treatment in the absence or presence of rhPRG4 (50–200 μg/ml) over 48 hours was determined using a colorimetric assay. Gene expression of matrix metalloproteinases (MMPs), tissue inhibitor of metallproteinases-1 (TIMP-1), TIMP-2, IL-1β, IL-6, IL- 8, TNF-α, cycloxygenae-2 (COX2) and PRG4 in unstimulated and IL-1β (1 ng/ml)-stimulated OA synoviocytes, in the presence or absence of rhPRG4 (100 and 200 μg/ml), was studied following incubation for 24 hours. Results: Prg4-/- synoviocytes contained higher nuclear p50 and p65 levels compared to Prg4+/+ synoviocytes (p \u3c 0. 05). rhPRG4 (100 μg/ml) reduced p50 and p65 nuclear levels in Prg4+/+ and Prg4-/- synoviocytes (p \u3c 0.001). Similarly, rhPRG4 (200 μg/ml) inhibited NFκB translocation and cell proliferation in OA synoviocytes in a CD44-dependent manner (p \u3c 0.001) via inhibition of IκBα phosphorylation. IL-1β reduced PRG4 expression in OA synoviocytes and rhPRG4 (100 μg/ml) treatment reversed this effect (p \u3c 0.001). rhPRG4 (200 μg/ml) reduced basal gene expression of MMP-1, MMP-3, MMP-13, IL-6, IL-8, and PRG4 in OA synoviocytes, while increasing TIMP-2 and cycloxygenase-2 (COX2) expression (p \u3c 0.001). rhPRG4 (200 μg/ml) reduced IL-1β induction of MMP-1, MMP-3, MMP-9, MMP-13, IL-6, IL-8, and COX2 expression in a CD44-dependent manner (p \u3c 0.001). Conclusion: PRG4 plays an important anti-inflammatory role in regulating OA synoviocyte proliferation and reduces basal and IL-1β-stimulated expression of catabolic mediators. Exogenous rhPRG4 autoregulates native PRG4 expression in OA synoviocytes

Fiber-Based Measurement of Bow-Shock Spectra for Reentry Flight Testing

We demonstrated a fiber-based approach for obtaining optical spectra of a glowing bow shock in a high-enthalpy air flow. The work was performed in a ground test with the NASA Ames Aerodynamic Heating Facility (AHF) that is used for atmospheric reentry simulation. The method uses a commercial fiber optic that is embedded in the nose of an ablating bluntbody model and provides a line-of-sight view in the streamwise direction - directly upstream into the hot post-shock gas flow. Both phenolic impregnated carbon ablator (PICA) and phenolic carbon (PhenCarb 28) materials were used as thermal protection systems. Results show that the fibers survive the intense heat and operate sufficiently well during the first several seconds of a typical AHF run (20 MJ/kg). This approach allowed the acquisition of optical spectra, enabling a Boltzmann-based electronic excitation temperature measurement from Cu atom impurities (averaged over a line-of-sight through the gas cap, with a 0.04 sec integration time)