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  1. ABSTRACT We present Atacama Large Millimetre/submillimetre Array observations of the brightest cluster galaxy Hydra-A, a nearby (z = 0.054) giant elliptical galaxy with powerful and extended radio jets. The observations reveal CO(1−0), CO(2–1), 13CO(2–1), CN(2–1), SiO(5–4), HCO+(1–0), HCO+(2–1), HCN(1–0), HCN(2–1), HNC(1–0), and H2CO(3–2) absorption lines against the galaxy’s bright and compact active galactic nucleus. These absorption features are due to at least 12 individual molecular clouds that lie close to the centre of the galaxy and have velocities of approximately −50 to +10 km s−1 relative to its recession velocity, where positive values correspond to inward motion. The absorption profiles are evidence of a clumpy interstellar medium within brightest cluster galaxies composed of clouds with similar column densities, velocity dispersions, and excitation temperatures to those found at radii of several kpc in the Milky Way. We also show potential variation in a ∼10 km s−1 wide section of the absorption profile over a 2 yr time-scale, most likely caused by relativistic motions in the hot spots of the continuum source that change the background illumination of the absorbing clouds. 
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  2. Multi-phase filamentary structures around brightest cluster galaxies (BCG) are likely a key step of AGN-feedback. We observed molecular gas in three cool cluster cores, namely Centaurus, Abell S1101, and RXJ1539.5, and gathered ALMA (Atacama Large Millimeter/submillimeter Array) and MUSE (Multi Unit Spectroscopic Explorer) data for 12 other clusters. Those observations show clumpy, massive, and long (3−25 kpc) molecular filaments, preferentially located around the radio bubbles inflated by the AGN. Two objects show nuclear molecular disks. The optical nebula is certainly tracing the warm envelopes of cold molecular filaments. Surprisingly, the radial profile of the H α /CO flux ratio is roughly constant for most of the objects, suggesting that (i) between 1.2 and 6 times more cold gas could be present and (ii) local processes must be responsible for the excitation. Projected velocities are between 100 and 400 km s −1 , with disturbed kinematics and sometimes coherent gradients. This is likely due to the mixing in projection of several thin (and as yet) unresolved filaments. The velocity fields may be stirred by turbulence induced by bubbles, jets, or merger-induced sloshing. Velocity and dispersions are low, below the escape velocity. Cold clouds should eventually fall back and fuel the AGN. We compare the radial extent of the filaments, r fil , with the region where the X-ray gas can become thermally unstable. The filaments are always inside the low-entropy and short-cooling-time region, where t cool / t ff  <  20 (9 of 13 sources). The range of t cool / t ff of 8−23 at r fil , is likely due to (i) a more complex gravitational potential affecting the free-fall time t ff (sloshing, mergers, etc.) and (ii) the presence of inhomogeneities or uplifted gas in the ICM, affecting the cooling time t cool . For some of the sources, r fil lies where the ratio of the cooling time to the eddy-turnover time, t cool / t eddy , is approximately unity. 
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  3. Abstract

    Coral bleaching is the single largest global threat to coral reefs worldwide. Integrating the diverse body of work on coral bleaching is critical to understanding and combating this global problem. Yet investigating the drivers, patterns, and processes of coral bleaching poses a major challenge. A recent review of published experiments revealed a wide range of experimental variables used across studies. Such a wide range of approaches enhances discovery, but without full transparency in the experimental and analytical methods used, can also make comparisons among studies challenging. To increase comparability but not stifle innovation, we propose a common framework for coral bleaching experiments that includes consideration of coral provenance, experimental conditions, and husbandry. For example, reporting the number of genets used, collection site conditions, the experimental temperature offset(s) from the maximum monthly mean (MMM) of the collection site, experimental light conditions, flow, and the feeding regime will greatly facilitate comparability across studies. Similarly, quantifying common response variables of endosymbiont (Symbiodiniaceae) and holobiont phenotypes (i.e., color, chlorophyll, endosymbiont cell density, mortality, and skeletal growth) could further facilitate cross‐study comparisons. While no single bleaching experiment can provide the data necessary to determine global coral responses of all corals to current and future ocean warming, linking studies through a common framework as outlined here, would help increase comparability among experiments, facilitate synthetic insights into the causes and underlying mechanisms of coral bleaching, and reveal unique bleaching responses among genets, species, and regions. Such a collaborative framework that fosters transparency in methods used would strengthen comparisons among studies that can help inform coral reef management and facilitate conservation strategies to mitigate coral bleaching worldwide.

     
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