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Could we observe exomoons around β Pictoris b?

IntroductionThe discovery of the first extrasolar planets demonstrated that planets can form around other stars and be detected with current instrumentation. Since more than 200 moons exist in the Solar System, it is expected that they orbit exoplanets as well. Detecting an exomoon could set the next milestone in observations of exoplanetary systems.   Tidal interactions between planets and their satellites can heat a satellite’s interior. The most evident example is Io, which is the most tidally active body in the Solar System. Since tidal dissipation depends on the orbital and physical properties of the system, if tidal heating is vigorous enough in exoplanetary systems, there is a chance that Tidally Heated Exomoons (THEMs; Peters and Turner 2015) are detectable with current instrumentation and/or the JWST in infrared (IR) wavelengths. As a direct result of tidal heating, spectral signatures of volcanic activity could also be a method of detecting THEMs (Oza et al. 2019). Two of the gas giant planet moon systems are in long-lived mean motion resonances (MMR) and it is expected that the latter would prevail in extrasolar systems as well. Taking the Jovian satellites as an archetype for an exomoon system around β Pictoris b, this would mean that an MMR between two or more exomoons would make them detectable for larger timescales, maintaining tidal activity over the lifetime of the system.β Pictoris is a 23 Myr old star with a distance of 19.44 pc. A ≃10 Mj directly imaged planet is orbiting the star at 9.8 AU (Lagrange et al. 2020). The system is almost edge-on to our line of sight, making β Pictoris b a plausible candidate for the search of THEMs in the IR, through photocenter astrometry of the combined planet and moon (Agol 2015) or by looking for primary and secondary transits of the exomoon. MethodsWe scale up a Galilean satellite system around β Pictoris b in order to investigate which properties make a putative exomoon detectable. We use orbital-thermal coupled models that assume a layered, radially symmetric moon, consisting of a silicate mantle and a liquid core. We assume that heat is transferred via melt advection (Moore 2003) and mantle convection from the interior to the surface and we obtain equilibrium temperatures. We explore the parameter space of orbital and physical properties of an exomoon around β Pictoris b by using different rheological models (Maxwell, Andrade). ResultsGiven a semi-major axis and eccentricity for an 8MIo mass exomoon, we obtain the corresponding interior structure and heat flow through the moon, resulting in a calculated effective temperature at the surface. We present our results for our Andrade rheology model and heat transfer mechanisms (Figure 1) and place constraints on the feasible interior models and orbital parameters for a putative surface heat flux of an exomoon around β Pictoris b. At Io’s orbital eccentricity a 2RIo exomoon would need to be close to the Roche radius of β Pictoris b to reach 600 K and be observed with the JWST (Figure 2), however this limit relaxes for higher eccentricities and bigger moons. We find that the Andrade rheology results in higher surface temperatures when compared to the basic Maxwell viscoelastic model.Figure 1: Equilibrium surface temperatures of a 2RIo exomoon (Super-Io) around β Pictoris b using Andrade rheology and melt advection. The horizontal line shows Io’s orbital eccentricity. Figure 2: Fluxes at the β Pictoris system. The grey continuous line shows the modeled spectrum of a planet with similar parameters as β Pictoris b (Morley et al. 2015), the dashed black line the blackbody curve of the star and the purple line the one of a Super-Io (2RIo). The horizontal lines are the 5σ and 10,000s integration time detection limits of MIRI/JWST for various bands (Glasse 2010)). ReferencesAgol et al. (2015) The Astrophysical Journal, 812(1), p.5.Glasse (2010) SPIE, 7731, 77310K.Lagrange et al. (2020) Astronomy & Astrophysics, 642, p.A18.Moore  (2003) Journal of Geophysical Research, 108(E8).Morley et al. (2015) The Astrophysical Journal, 815(2), p.110.Oza et al. (2019) The Astrophysical Journal, 885(2), p.168.Peters and Turner (2013) The Astrophysical Journal, 769(2), p.98. 

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Biophysical Modeling of Mangrove Seedling Establishment and Survival Across an Elevation Gradient With Forest Zones

AbstractMangrove forest development critically depends on the establishment and survival of seedlings. Mechanistic insights into how water levels, waves and bed level dynamics influence the establishment process of individual mangrove seedlings are increasing. However, little is known about how spatial and temporal changes in water levels, waves and bed level dynamics across elevation gradients in mangrove forests facilitate/limit seedling dynamics. For this study, a new seedling establishment and growth model was integrated into a process‐based hydrodynamic and morphodynamic numerical model. This biophysical model was applied to a fringing mangrove forest located in the southern Firth of Thames, Aotearoa, New Zealand. This study quantifies the increasing establishment density and survival probability of mangrove seedlings from the lower‐elevated unvegetated intertidal flat toward the higher‐elevated mature mangrove forest. Three cross‐shore zones with distinctive seedling dynamics were identified: (a) a zone with daily tidal inundation where seedling dynamics are episodic and limited by the dispersal of individual propagules that rapidly anchor to the substrate by root growth, (b) a zone with daily to bi‐weekly tidal inundation where seedling dynamics respond to variations in spring‐neap tidal cycles and, (c) a zone with less than bi‐weekly inundation where seedling dynamics are governed by high propagule supply and seedling survival probability. The seedling establishment density and survival probability are dominated by annual extremes in tidal hydroperiod and bed shear stresses, respectively. The obtained parameterizations can be used to incorporate seedling dynamics in decadal‐timescale mangrove forest development models that are instrumental for mangrove management and restoration.

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Projecting Changes in the Drivers of Compound Flooding in Europe Using CMIP6 Models

AbstractWhen different flooding drivers co‐occur, they can cause compound floods. Despite the potential impact of compound flooding, few studies have projected how the joint probability of flooding drivers may change. Furthermore, existing projections may not be very robust, as they are based on only 5 to 6 climate model simulations. Here, we use a large ensemble of simulations from the Coupled Model Intercomparison Project 6 (CMIP6) to project changes in the joint probability of extreme storm surges and precipitation at European tide gauges under a medium and high emissions scenario, enabled by data‐proximate cloud computing and statistical storm surge modeling. We find that the joint probability will increase in the northwest and decrease in most of the southwest of Europe. Averaged over Europe, the absolute magnitude of these changes is 36%–49% by 2080, depending on the scenario. The large‐scale changes in the joint probability of extreme storm surges and precipitation are similar to those in the joint probability of extreme wind speeds and precipitation, but locally, differences can exceed the changes themselves. Due to internal climate variability and inter‐model differences, projections based on simulations of only 5 to 6 randomly chosen CMIP6 models have a probability of higher than 10% to differ qualitatively from projections based on all CMIP6 simulations in multiple regions, especially under the medium emissions scenario and earlier in the twenty‐first century. Therefore, our results provide a more robust and less uncertain representation of changes in the potential for compound flooding in Europe than previous projections.

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Abiotic origins of self‐organized ridge‐runnel patterns on tidal flats

AbstractStriking large‐scale spatial patterns in ecosystems, generated by self‐organization through biotic and abiotic feedback processes, influence ecosystem functioning and response to global environmental change. A remarkable example of this are the regular ridge‐runnel patterns found on tidal flats, which play an important role in mudflat‐marsh transitions. Yet the mechanisms driving their formation, and whether they are abiotic or biotic in origin, have not been elucidated. The underlying mechanisms are unraveled in this study through a combination of field measurements and targeted laboratory experiments. In the field, we find that on the ridges of the pattern, the sediment bed level is less dynamic and more resistant to erosion than in the runnels. In laboratory flume experiments, we find that erosion‐resistant surfaces, like those found on the ridges, can arise on time scales of hours to days due to the drying of the cohesive sediment bed, while this is prevented in waterlogged sediments in runnels. A disturbance‐recovery experiment on benthic algae then confirms that biological processes require a longer developmental period than the time scale at which we have observed drying‐induced erosion resistance to develop. Together, these results demonstrate that ridge‐runnel patterns begin from an abiotic initiation point that can subsequently provide a template for further biological establishment and self‐organization. Recognition of abiotic processes as catalysts of self‐organization can improve our understanding of ecosystem responses to environmental changes.

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Landscapes of fear can determine the dynamics of entire ecosystems. In response to perceived predation risk, prey can show physiological, behavioral, or morphological trait changes to avoid predation. This in turn can indirectly affect other species by modifying species interactions (e.g., altered feeding), with knock-on effects, such as trophic cascades, on the wider ecosystem. While such indirect effects stemming from the fear of predation have received extensive attention for herbivore-plant and predator-prey interactions, much less is known about how they alter parasite-host interactions and wildlife diseases. In this synthesis, we present a conceptual framework for how predation risk-as perceived by organisms that serve as hosts-can affect parasite-host interactions, with implications for infectious disease dynamics. By basing our approach on recent conceptual advances with respect to predation risk effects, we aim to expand this general framework to include parasite-host interactions and diseases. We further identify pathways through which parasite-host interactions can be affected, for example, through altered parasite avoidance behavior or tolerance of hosts to infections, and discuss the wider relevance of predation risk for parasite and host populations, including heuristic projections to population-level dynamics. Finally, we highlight the current unknowns, specifically the quantitative links from individual-level processes to population dynamics and community structure, and emphasize approaches to address these knowledge gaps.

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Co‐occurring intertidal ecosystem engineers with opposing growth strategies show opposite responses to environmental gradients during establishment

Coastal vegetated ecosystems including mangroves, seagrasses, and salt marshes are often shaped by positive plant–environment feedbacks. Plants improve their own living conditions with increasing patch size and density by attenuating hydrodynamics and stabilizing sediments. As these habitat modifications are critical for survival and growth, the positive density‐dependent nature of these feedbacks can lead to establishment thresholds for young plants in absence of mature conspecifics. Although feedback strength is known to depend on hydrodynamic exposure and plant traits (e.g. stiff versus flexible stems), it remains unclear how 1) opposing morphological plant traits affect establishment in contrasting environments, and 2) whether trait plasticity influences establishment success. Here, we investigate this by transplanting two tidal species with opposing growing strategies – Spartina anglica forms tussocks of stiff stems while Zostera noltii forms patches of stress‐avoiding flexible shoots – from two different donor sites in eight experimental locations. Results show that the survival and growth of both species was most successful at field locations with diverging environmental characteristics, while overall survival was highest for Z. noltii. Mainly, S. anglica survival was highest at locations with high organic matter and silt content and higher elevation relative to the tidal amplitude. In contrast, Z. noltii survival was highest at locations with larger grainsize and lower relative elevations. Furthermore, despite initial differences in plant traits between the two donor sites of Z. noltii, we found no effects of donor origin. Contrastingly, we found a significant effect of donor origin on S. anglica growth, even though transplants from the two donor sites showed no initial trait differences. Collectively, these results suggest that the stress‐tolerance strategy of S. anglica hampers establishment in exposed conditions, whereas the stress‐avoiding Z. noltii appears to be more susceptible to stress from desiccation and silty sediments.

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