111 research outputs found
Seasonal variation of zooplankton community structure and trophic position in the Celtic Sea: A stable isotope and biovolume spectrum approach
Zooplankton on continental shelves represent an important intermediary in the transfer of energy and matter from phytoplankton to the wider ecosystem. Their taxonomic composition and trophic interactions with phytoplanktonvaryinspaceandtime, andinterpreting theimplicationsofthis constantlyevolvinglandscaperemainsamajorchallenge.Herewecombineplanktontaxonomicdatawiththeanalysisofbiovolumespectraand stableisotopestoprovideinsightsintothetrophicinteractionsthatoccurinashelfseaecosystem(CelticSea) across the spring-summer-autumn transition. Biovolume spectra captured the seasonal development of the zooplankton community well, both in terms of total biomass and trophic positioning, and matched trophic positionsestimatedbystableisotopeanalysis.InearlyApril,largemicroplankton(63–200µm)occupiedhigher trophic positions than mesozooplankton (>200µm), likely reflecting the predominance of nanoplankton (2–20µm) that were not readily available to mesozooplanktongrazers. Biomass and number of trophic levels increasedduringthespringbloomaselevatedprimaryproductionallowedforahigherabundanceofpredatory species.DuringJuly,theplanktonassemblageoccupiedrelativelyhightrophicpositions,indicatingimportant links to the microbial loop and the recycling of organic matter. The strong correlation between biomass and communitytrophiclevelacrossthestudysuggeststhattheCelticSeaisarelativelyenclosedandpredominantly energy-limited ecosystem. The progression of the zooplankton biomass and community structure within the centralshelfregionwasdifferenttothatattheshelf-break,potentiallyreflectingincreasedpredatorycontrolof copepodsby macrozooplanktonandpelagicfishesattheshelfbreak.Wesuggestthatthecombinationofsize spectra and stable isotope techniques are highly complementary and useful for interpreting the seasonal progressionoftrophicinteractionsintheplankton
Mass variance from archival X-ray properties of dark energy survey year-1 galaxy clusters
For abstract see published article
Pre-surgical mapping of eloquent cortex for paediatric epilepsy surgery candidates: Evidence from a review of advanced functional neuroimaging
Purpose: A review of all published evidence for mapping eloquent (motor, language and memory) cortex using advanced functional neuroimaging (functional magnetic resonance imaging [fMRI] and magnetoencephalography [MEG]) for paediatric epilepsy surgery candidates has not been conducted previously. Research in this area has predominantly been in adult populations and applicability of these techniques to paediatric populations is less established. Methods: A review was performed using an advanced systematic search and retrieval of all published papers examining the use of functional neuroimaging for paediatric epilepsy surgery candidates. Results: Of the 2,724 papers retrieved, 34 met the inclusion criteria. Total paediatric participants identified were 353 with an age range of 5 months-19 years. Sample sizes and comparisons with alternative investigations to validate techniques are small and variable paradigms are used. Sensitivity 0.72 (95% CI 0.52-0.86) and specificity 0.60 (95% CI 0.35-0.92) values with a Positive Predictive Value of 74% (95% CI 61-87) and a Negative Predictive Value of 65% (95% CI 52-78) for fMRI language lateralisation with validation, were obtained. Retrieved studies indicate evidence that both fMRI and MEG are able to provide information lateralising and localising motor and language functions. Conclusions: A striking finding of the review is the paucity of studies (n = 34) focusing on the paediatric epilepsy surgery population. For children, it remains unclear which language and memory paradigms produce optimal activation and how these should be quantified in a statistically robust manner. Consensus needs to be achieved for statistical analyses and the uniformity and yield of language, motor and memory paradigms. Larger scale studies are required to produce patient series data which clinicians may refer to interpret results objectively. If functional imaging techniques are to be the viable alternative for pre-surgical mapping of eloquent cortex for children, paradigms and analyses demonstrating concordance with independent measures must be developed
Coccolithophore calcification fails to deter microzooplankton grazers.
Phytoplankton play a central role in the regulation of global carbon and nutrient cycles,
forming the basis of the marine food webs. A group of biogeochemically important
phytoplankton, the coccolithophores, produce calcium carbonate scales that have been
hypothesized to deter or reduce grazing by microzooplankton. Here, a meta-analysis
of mesocosm-based experiments demonstrates that calcification of the cosmopolitan
coccolithophore, Emiliania huxleyi, fails to deter microzooplankton grazing. The median
grazing to growth ratio for E. huxleyi (0.56 � 0.40) was not significantly different among
non-calcified nano- or picoeukaryotes (0.71 � 0.31 and 0.55 � 0.34, respectively).
Additionally, the environmental concentration of E. huxleyi did not drive preferential
grazing of non-calcified groups. These results strongly suggest that the possession
of coccoliths does not provide E. huxleyi effective protection from microzooplankton
grazing. Such indiscriminate consumption has implications for the dissolution and fate
of CaCO3 in the ocean, and the evolution of coccoliths
Stellar mass as a galaxy cluster mass proxy: application to the Dark Energy Survey redMaPPer clusters
We introduce a galaxy cluster mass observable, μ⋆, based on the stellar masses of cluster members, and we present results for the Dark Energy Survey (DES) Year 1 (Y1) observations. Stellar masses are computed using a Bayesian model averaging method, and are validated for DES data using simulations and COSMOS data. We show that μ⋆ works as a promising mass proxy by comparing our predictions to X-ray measurements. We measure the X-ray temperature–μ_{⋆} relation for a total of 129 clusters matched between the wide-field DES Y1 redMaPPer catalogue and Chandra and XMM archival observations, spanning the redshift range 0.1 < z < 0.7. For a scaling relation that is linear in logarithmic space, we find a slope of α = 0.488 ± 0.043 and a scatter in the X-ray temperature at fixed μ_{*} of σ1nT_{x}|μ_{*} = 0.266_{-0.020}^{+0.019} for the joint sample. By using the halo mass scaling relations of the X-ray temperature from the Weighing the Giants program, we further derive the μ⋆-conditioned scatter in mass, finding σ1nM|μ_{*} = 0.26_{-0.10}^{+0.15}. These results are competitive with well-established cluster mass proxies used for cosmological analyses, showing that μ_{⋆} can be used as a reliable and physically motivated mass proxy to derive cosmological constraints
The XMM Cluster Survey analysis of the SDSS DR8 redMaPPer catalogue: implications for scatter, selection bias, and isotropy in cluster scaling relations
In this paper, we present the X-ray analysis of Sloan Digital Sky Survey DR8 redMaPPer (SDSSRM) clusters using data products from the XMM Cluster Survey (XCS). In total, 1189 SDSSRM clusters fall within the XMM-Newton footprint. This has yielded 456 confirmed detections accompanied by X-ray luminosity (LX) measurements. Of these clusters, 381 have an associated X-ray temperature measurement (TX). This represents one of the largest samples of coherently derived cluster TX values to date. Our analysis of the X-ray observable to richness scaling relations has demonstrated that scatter in the TX-λ relation is roughly a third of that in the LX-λ relation, and that the LX-λ scatter is intrinsic, i.e. will not be significantly reduced with larger sample sizes. Analysis of the scaling relation between LX and TX has shown that the fits are sensitive to the selection method of the sample, i.e. whether the sample is made up of clusters detected 'serendipitously' compared to those deliberately targeted by XMM. These differences are also seen in the LX-λ relation and, to a lesser extent, in the TX-λ relation. Exclusion of the emission from the cluster core does not make a significant impact on the findings. A combination of selection biases is a likely, but yet unproven, reason for these differences. Finally, we have also used our data to probe recent claims of anisotropy in the LX-TX relation across the sky. We find no evidence of anistropy, but stress this may be masked in our analysis by the incomplete declination coverage of the SDSS
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Dark Energy Survey year 1 results: cosmological constraints from cluster abundances and weak lensing
We perform a joint analysis of the counts and weak lensing signal of redMaPPer clusters selected from the Dark Energy Survey (DES) Year 1 dataset. Our analysis uses the same shear and source photometric redshifts estimates as were used in the DES combined probes analysis. Our analysis results in surprisingly low values for S8=σ8(Ωm/0.3)0.5=0.65±0.04, driven by a low matter density parameter, Ωm=0.179+0.031−0.038, with σ8−Ωm posteriors in 2.4σ tension with the DES Y1 3x2pt results, and in 5.6σ with the Planck CMB analysis. These results include the impact of post-unblinding changes to the analysis, which did not improve the level of consistency with other data sets compared to the results obtained at the unblinding. The fact that multiple cosmological probes (supernovae, baryon acoustic oscillations, cosmic shear, galaxy clustering and CMB anisotropies), and other galaxy cluster analyses all favor significantly higher matter densities suggests the presence of systematic errors in the data or an incomplete modeling of the relevant physics. Cross checks with x-ray and microwave data, as well as independent constraints on the observable-mass relation from Sunyaev-Zeldovich selected clusters, suggest that the discrepancy resides in our modeling of the weak lensing signal rather than the cluster abundance. Repeating our analysis using a higher richness threshold (λ≥30) significantly reduces the tension with other probes, and points to one or more richness-dependent effects not captured by our model
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