Seasonality buffers carbon budget variability across heterogeneous landscapes in Alaskan Arctic tundra

Arctic tundra exhibits large landscape heterogeneity in microtopography, hydrology, and active layer depth. While many carbon flux measurements and experiments are done at or below the mesoscale (≤1 km), modern ecosystem carbon modeling is often done at scales of 0.25°–1.0° latitude, creating a mismatch between processes, process input data, and verification data. Here we arrange the naturally complex terrain into mesoscale landscape types of varying microtopography and moisture status to evaluate how landscape types differ in terms of CO2 and CH4 balances and their combined warming potential, expressed as CO2 equivalents (CO2-eq). Using a continuous 4 year dataset of CO2 and CH4 fluxes obtained from three eddy covariance (EC) towers, we investigate the integrated dynamics of landscape type, vegetation community, moisture regime, and season on net CO2 and CH4 fluxes. EC towers were situated across a moisture gradient including a moist upland tundra, a heterogeneous polygon tundra, and an inundated drained lake basin. We show that seasonal shifts in carbon emissions buffer annual carbon budget differences caused by site variability. Of note, high growing season gross primary productivity leads to higher fall zero-curtain CO2 emissions, reducing both variability in annual budgets and carbon sink strength of more productive sites. Alternatively, fall zero-curtain CH4 emissions are equal across landscape types, indicating site variation has little effect on CH4 emissions during the fall despite large differences during the growing season. We find that the polygon site has the largest mean warming potential (107 ± 8.63 g C–CO2-eq m−2 yr−1) followed by the drained lake basin site (82.12 ± 9.85 g C–CO2-eq m−2 yr−1) and the upland site (77.19 ± 21.8 g C–CO2-eq m−2 yr−1), albeit differences were not significant. The highest temperature sensitivities are also at the polygon site with mixed results between CO2 and CH4 at the other sites. Results show a similar mean annual net warming effect across dominant landscape types but that these landscape types vary significantly in the amounts and timing of CO2 and CH4 fluxes

Proton-proton scattering above 3 GeV/c

A large set of data on proton-proton differential cross sections, analyzing powers and the double polarization parameter A_NN is analyzed employing the Regge formalism. We find that the data available at proton beam momenta from 3 GeV/c to 50 GeV/c exhibit features that are very well in line with the general characteristics of Regge phenomenology and can be described with a model that includes the rho, omega, f_2, and a_2 trajectories and single Pomeron exchange. Additional data, specifically for spin-dependent observables at forward angles, would be very helpful for testing and refining our Regge model.Comment: 16 pages, 19 figures; revised version accepted for publication in EPJ

Determination of pi-N scattering lengths from pionic hydrogen and pionic deuterium data

The pi-N s-wave scattering lengths have been inferred from a joint analysis of the pionic hydrogen and the pionic deuterium x-ray data using a non-relativistic approach in which the pi-N interaction is simulated by a short-ranged potential. The pi-d scattering length has been calculated exactly by solving the Faddeev equations and also by using a static approximation. It has been shown that the same very accurate static formula for pi-d scattering length can be derived (i) from a set of boundary conditions; (ii) by a reduction of Faddeev equations; and (iii) through a summation of Feynman diagrams. By imposing the requirement that the pi-d scattering length, resulting from Faddeev-type calculation, be in agreement with pionic deuterium data, we obtain bounds on the pi-N scattering lengths. The dominant source of uncertainty on the deduced values of the pi-N scattering lengths are the experimental errors in the pionic hydrogen data.Comment: RevTeX, 20 pages,4 PostScript figure

Thermokarst landscape exhibits large nitrous oxide emissions in Alaska’s coastal polygonal tundra

Global atmospheric concentrations of nitrous oxide have been increasing over previous decades with emerging research suggesting the Arctic as a notable contributor. Thermokarst processes, increasing temperature, and changes in drainage can cause degradation of polygonal tundra landscape features resulting in elevated, well-drained, unvegetated soil surfaces that exhibit large nitrous oxide emissions. Here, we outline the magnitude and some of the dominant factors controlling variability in emissions for these thermokarst landscape features in the North Slope of Alaska. We measured strong nitrous oxide emissions during the growing season from unvegetated high centered polygons (median (mean) = 104.7 (187.7) µg N2O-N m−2 h−1), substantially higher than mean rates associated with Arctic tundra wetlands and of similar magnitude to unvegetated hotspots in peat plateaus and palsa mires. In the absence of vegetation, isotopic enrichment of 15N in these thermokarst features indicates a greater influence of microbial processes, (denitrification and nitrification) from barren soil. Findings reveal that the thermokarst features discussed here (~1.5% of the study area) are likely a notable source of nitrous oxide emissions, as inferred from chamber-based estimates. Growing season emissions, estimated at 16 (28) mg N2O-N ha−1 h−1, may be large enough to affect landscape-level greenhouse gas budgets

The Two-Nucleon Potential from Chiral Lagrangians

Chiral symmetry is consistently implemented in the two-nucleon problem at low-energy through the general effective chiral lagrangian. The potential is obtained up to a certain order in chiral perturbation theory both in momentum and coordinate space. Results of a fit to scattering phase shifts and bound state data are presented, where satisfactory agreement is found for laboratory energies up to about 100 Mev.Comment: Postscript file; figures available by reques

Replacement of grass and maize silages with lucerne silage: effects on performance, milk fatty acid profile and digestibility in Holstein-Friesian dairy cows

In total, 20 multiparous Holstein-Friesian dairy cows received one of four diets in each of four periods of 28-day duration in a Latin square design to test the hypothesis that the inclusion of lucerne in the ration of high-yielding dairy cows would improve animal performance and milk fatty acid (FA) composition. All dietary treatments contained 0.55 : 0.45 forage to concentrates (dry matter (DM) basis), and within the forage component the proportion of lucerne (Medicago sativa), grass (Lolium perenne) and maize silage (Zea mays) was varied (DM basis): control (C)=0.4 : 0.6 grass : maize silage; L20=0.2 : 0.2 : 0.6 lucerne : grass : maize silage; L40=0.4 : 0.6 lucerne : maize silage; and L60=0.6 : 0.4 lucerne : maize silage. Diets were formulated to contain a similar CP and metabolisable protein content, with the reduction of soya bean meal and feed grade urea with increasing content of lucerne. Intake averaged 24.3 kg DM/day and was lowest in cows when fed L60 (P0.05) by dietary treatment. Digestibility of DM, organic matter, CP and fibre decreased (P<0.01) with increasing content of lucerne in the diet, although fibre digestibility was similar in L40 and L60. It is concluded that first cut grass silage can be replaced with first cut lucerne silage without any detrimental effect on performance and an improvement in the milk FA profile, although intake and digestibility was lowest and plasma urea concentrations highest in cows when fed the highest level of inclusion of lucerne

Reviews and syntheses: A framework to observe, understand, and project ecosystem response to environmental change in the East Antarctic Southern Ocean

Systematic long-term studies on ecosystem dynamics are largely lacking for the East Antarctic Southern Ocean, although it is well recognized that such investigations are indispensable to identify the ecological impacts and risks of environmental change. Therefore, here we develop a framework for establishing a long-term cross-disciplinary study and argue why the eastern Weddell Sea and the easterly adjacent sea off Dronning Maud Land (WSoDML) is a well suited area for such an initiative. As in the Eastern Antarctic in general, climate and environmental change have so far been comparatively muted in this area. A systematic long-term study of its environmental and ecological state can thus provide a baseline of the current situation, an assessment of future changes, and sound data can act as a model to develop and calibrate projections. Establishing a long-term observation (LTO) and long-term ecological research (LTER) programme now would allow the study of climate-driven ecosystem changes and interactions with impacts arising from other anthropogenic activities, from their very onset. Through regular autonomous and ship-based LTO activities, changes in ocean dynamics, geochemistry, biodiversity and ecosystem functions and services can be systematically explored and mapped. This observational work should be accompanied by targeted LTER efforts, including experimental and modelling studies. This approach will provide a level of long-term data availability and ecosystem understanding that are imperative to determine, understand, and project the consequences of climate change and support a sound science-informed management of future conservation efforts in the Southern Ocean

Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry.

Purpose: Type 2 diabetes (T2D) has been reported to be associated with an elevated risk of breast cancer. It is unclear, however, whether this association is due to shared genetic factors. Methods: We constructed a genetic risk score (GRS) using risk variants from 33 known independent T2D susceptibility loci and evaluated its relation to breast cancer risk using the data from two consortia, including 62,328 breast cancer patients and 83,817 controls of European ancestry. Unconditional logistic regression models were used to derive adjusted odds ratios (ORs) and 95 % confidence intervals (CIs) to measure the association of breast cancer risk with T2D GRS or T2D-associated genetic risk variants. Meta-analyses were conducted to obtain summary ORs across all studies. Results: The T2D GRS was not found to be associated with breast cancer risk, overall, by menopausal status, or for estrogen receptor positive or negative breast cancer. Three T2D associated risk variants were individually associated with breast cancer risk after adjustment for multiple comparisons using the Bonferroni method (at p < 0.001), rs9939609 (FTO) (OR 0.94, 95 % CI = 0.92–0.95, p = 4.13E−13), rs7903146 (TCF7L2) (OR 1.04, 95 % CI = 1.02–1.06, p = 1.26E−05), and rs8042680 (PRC1) (OR 0.97, 95 % CI = 0.95–0.99, p = 8.05E−04). Conclusions: We have shown that several genetic risk variants were associated with the risk of both T2D and breast cancer. However, overall genetic susceptibility to T2D may not be related to breast cancer risk

Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1

Peer reviewe

No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.

BACKGROUND: BRCA1 interacting protein C-terminal helicase 1 (BRIP1) is one of the Fanconi Anaemia Complementation (FANC) group family of DNA repair proteins. Biallelic mutations in BRIP1 are responsible for FANC group J, and previous studies have also suggested that rare protein truncating variants in BRIP1 are associated with an increased risk of breast cancer. These studies have led to inclusion of BRIP1 on targeted sequencing panels for breast cancer risk prediction. METHODS: We evaluated a truncating variant, p.Arg798Ter (rs137852986), and 10 missense variants of BRIP1, in 48 144 cases and 43 607 controls of European origin, drawn from 41 studies participating in the Breast Cancer Association Consortium (BCAC). Additionally, we sequenced the coding regions of BRIP1 in 13 213 cases and 5242 controls from the UK, 1313 cases and 1123 controls from three population-based studies as part of the Breast Cancer Family Registry, and 1853 familial cases and 2001 controls from Australia. RESULTS: The rare truncating allele of rs137852986 was observed in 23 cases and 18 controls in Europeans in BCAC (OR 1.09, 95% CI 0.58 to 2.03, p=0.79). Truncating variants were found in the sequencing studies in 34 cases (0.21%) and 19 controls (0.23%) (combined OR 0.90, 95% CI 0.48 to 1.70, p=0.75). CONCLUSIONS: These results suggest that truncating variants in BRIP1, and in particular p.Arg798Ter, are not associated with a substantial increase in breast cancer risk. Such observations have important implications for the reporting of results from breast cancer screening panels.The COGS project is funded through a European Commission's Seventh Framework Programme grant (agreement number 223175 - HEALTH-F2-2009-223175). BCAC is funded by Cancer Research UK [C1287/A10118, C1287/A12014] and by the European Community´s Seventh Framework Programme under grant agreement number 223175 (grant number HEALTH-F2-2009-223175) (COGS). Funding for the iCOGS infrastructure came from: the European Community's Seventh Framework Programme under grant agreement n° 223175 (HEALTH-F2-2009-223175) (COGS), Cancer Research UK (C1287/A10118, C1287/A 10710, C12292/A11174, C1281/A12014, C5047/A8384, C5047/A15007, C5047/A10692, C8197/A16565), the National Institutes of Health (CA128978) and Post-Cancer GWAS initiative (1U19 CA148537, 1U19 16 CA148065 and 1U19 CA148112 - the GAME-ON initiative), the Department of Defense (W81XWH-10-1- 0341), the Canadian Institutes of Health Research (CIHR) for the CIHR Team in Familial Risks of Breast Cancer, Komen Foundation for the Cure, the Breast Cancer Research Foundation, and the Ovarian Cancer Research Fund. This study made use of data generated by the Wellcome Trust Case Control consortium. Funding for the project was provided by the Wellcome Trust under award 076113. The results published here are in part based upon data generated by The Cancer Genome Atlas Project established by the National Cancer Institute and National Human Genome Research Institute.This is the author accepted manuscript. The final version is available from BMJ Group at http://dx.doi.org/10.1136/jmedgenet-2015-103529