| 1. |
- Jones, M. I., et al.
(författare)
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A hot Saturn on an eccentric orbit around the giant star K2-132
- 2018
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Ingår i: Astronomy and Astrophysics. - : EDP Sciences. - 0004-6361 .- 1432-0746. ; 613
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Tidskriftsartikel (refereegranskat)abstract
- Although the majority of radial velocity detected planets have been found orbiting solar-type stars, a fraction of them have been discovered around giant stars. These planetary systems have revealed different orbital properties when compared to solar-type star companions. In particular, radial velocity surveys have shown that there is a lack of giant planets in close-in orbits around giant stars, in contrast to the known population of hot Jupiters orbiting solar-type stars. It has been theorized that the reason for this distinctive feature in the semimajor axis distribution is the result of the stellar evolution and/or that it is due to the effect of a different formation/evolution scenario for planets around intermediate-mass stars. However, in the past few years a handful of transiting short-period planets (P less than or similar to 10 days) have been found around giant stars, thanks to the high-precision photometric data obtained initially by the Kepler mission, and later by its two-wheel extension K2. These new discoveries have allowed us for the first time to study the orbital properties and physical parameters of these intriguing and elusive substellar companions. In this paper we report on an independent discovery of a transiting planet in field 10 of the K2 mission, also reported recently by Grunblatt et al. (2017, AJ, 154, 254). The host star has recently evolved to the giant phase, and has the following atmospheric parameters: T-eff = 4878 +/- 70 K, log g = 3.289 +/- 0.004, and [Fe/H] = 0.11 +/- 0.05 dex. The main orbital parameters of K2-132 b, obtained with all the available data for the system are: P = 9.1708 +/- 0.0025 d, e = 0.290 +/- 0.049, M-p = 0.495 +/- 0.007 M-J and R-p = 1.089 +/- 0.006 R-J. This is the fifth known planet orbiting any giant star with a < 0 : 1, and the most eccentric one among them, making K2-132 b a very interesting object.
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| 2. |
- Jayasekara, Harindra, et al.
(författare)
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Associations of alcohol intake, smoking, physical activity and obesity with survival following colorectal cancer diagnosis by stage, anatomic site and tumor molecular subtype
- 2018
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Ingår i: International Journal of Cancer. - : Wiley. - 0020-7136 .- 1097-0215. ; 142:2, s. 238-250
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Tidskriftsartikel (refereegranskat)abstract
- The influence of lifestyle factors on survival following a diagnosis of colorectal cancer (CRC) is not well established. We examined associations between lifestyle factors measured before diagnosis and CRC survival. The Melbourne Collaborative Cohort Study collected data on alcohol intake, cigarette smoking and physical activity, and body measurements at baseline (1990-1994) and wave 2 (2003-2007). We included participants diagnosed to 31 August 2015 with incident stages I-III CRC within 10-years post exposure assessment. Information on tumor characteristics and vital status was obtained. Tumor DNA was tested for microsatellite instability (MSI) and somatic mutations in oncogenes BRAF (V600E) and KRAS. We estimated hazard ratios (HRs) for associations between lifestyle factors and overall and CRC-specific mortality using Cox regression. Of 724 eligible CRC cases, 339 died (170 from CRC) during follow-up (average 9.0 years). Exercise (non-occupational/leisure-time) was associated with higher CRC-specific survival for stage II (HR=0.25, 95% CI: 0.10-0.60) but not stages I/III disease (p for interaction=0.01), and possibly for colon and KRAS wild-type tumors. Waist circumference was inversely associated with CRC-specific survival (HR=1.25 per 10 cm increment, 95% CI: 1.08-1.44), independent of stage, anatomic site and tumor molecular status. Cigarette smoking was associated with lower overall survival, with suggestive evidence of worse survival for BRAF mutated CRC, but not with CRC-specific survival. Alcohol intake was not associated with survival. Survival did not differ by MSI status. We have identified pre-diagnostic predictors of survival following CRC that may have clinical and public health relevance.
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| 3. |
- Aaberge, Rolf, et al.
(författare)
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Tony Atkinson and his Legacy
- 2017
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Ingår i: The Review of Income and Wealth. - : Wiley. - 0034-6586 .- 1475-4991. ; 63:3, s. 411-444
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Tidskriftsartikel (refereegranskat)abstract
- Tony Atkinson is universally celebrated for his outstanding contributions to the measurement and analysis of inequality, but he never saw the study of inequality as a separate branch of economics. He was an economist in the classical sense, rejecting any sub-field labelling of his interests and expertise, and he made contributions right across economics. His death on 1 January 2017 deprived the world of both an intellectual giant and a deeply committed public servant in the broadest sense of the term. This collective tribute highlights the range, depth and importance of Tony's enormous legacy, the product of almost fifty years’ work.
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| 4. |
- Jayasekara, Harindra, et al.
(författare)
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Lifetime alcohol intake is associated with an increased risk of KRAS plus and BRAF-/KRAS- but not BRAF plus colorectal cancer
- 2017
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Ingår i: International Journal of Cancer. - : Wiley. - 0020-7136 .- 1097-0215. ; 140:7, s. 1485-1493
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Tidskriftsartikel (refereegranskat)abstract
- Ethanol in alcoholic beverages is a causative agent for colorectal cancer. Colorectal cancer is a biologically heterogeneous disease, and molecular subtypes defined by the presence of somatic mutations in BRAF and KRAS are known to exist. We examined associations between lifetime alcohol intake and molecular and anatomic subtypes of colorectal cancer. We calculated usual alcohol intake for 10-year periods from age 20 using recalled frequency and quantity of beverage-specific consumption for 38,149 participants aged 40-69 years from the Melbourne Collaborative Cohort Study. Cox regression was performed to derive hazard ratios (HRs) and 95% confidence intervals (CIs) for the association between lifetime alcohol intake and colorectal cancer risk. Heterogeneity in the HRs across subtypes of colorectal cancer was assessed. A positive dose-dependent association between lifetime alcohol intake and overall colorectal cancer risk (mean follow-up=14.6 years; n=596 colon and n=326 rectal cancer) was observed (HR=1.08, 95% CI: 1.04-1.12 per 10 g/day increment). The risk was greater for rectal than colon cancer (p(homogeneity)=0.02). Alcohol intake was associated with increased risks of KRAS+ (HR=1.07, 95% CI: 1.00-1.15) and BRAF-/KRAS- (HR=1.05, 95% CI: 1.00-1.11) but not BRAF+ tumors (HR=0.89, 95% CI: 0.78-1.01; p(homogeneity)=0.01). Alcohol intake is associated with an increased risk of KRAS+ and BRAF-/KRAS- tumors originating via specific molecular pathways including the traditional adenoma-carcinoma pathway but not with BRAF+ tumors originating via the serrated pathway. Therefore, limiting alcohol intake from a young age might reduce colorectal cancer originating via the traditional adenoma-carcinoma pathway.
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| 5. |
- Verheyen, Kris, et al.
(författare)
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201 Combining Biodiversity Resurveys across Regions to Advance Global Change Research
- 2017
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Ingår i: BioScience. - : Oxford University Press (OUP). - 0006-3568 .- 1525-3244. ; 67:1, s. 73-83
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Tidskriftsartikel (refereegranskat)abstract
- More and more ecologists have started to resurvey communities sampled in earlier decades to determine long-term shifts in community composition and infer the likely drivers of the ecological changes observed. However, to assess the relative importance of and interactions among multiple drivers, joint analyses of resurvey data from many regions spanning large environmental gradients are needed. In this article, we illustrate how combining resurvey data from multiple regions can increase the likelihood of driver orthogonality within the design and show that repeatedly surveying across multiple regions provides higher representativeness and comprehensiveness, allowing us to answer more completely a broader range of questions. We provide general guidelines to aid the implementation of multiregion resurvey databases. In so doing, we aim to encourage resurvey database development across other community types and biomes to advance global environmental change research.
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