A Connection between Colony Biomass and Death in Caribbean Reef-Building Corals

Increased sea-surface temperatures linked to warming climate threaten coral reef ecosystems globally. To better understand how corals and their endosymbiotic dinoflagellates (Symbiodinium spp.) respond to environmental change, tissue biomass and Symbiodinium density of seven coral species were measured on various reefs approximately every four months for up to thirteen years in the Upper Florida Keys, United States (1994–2007), eleven years in the Exuma Cays, Bahamas (1995–2006), and four years in Puerto Morelos, Mexico (2003–2007). For six out of seven coral species, tissue biomass correlated with Symbiodinium density. Within a particular coral species, tissue biomasses and Symbiodinium densities varied regionally according to the following trends: Mexico≥Florida Keys≥Bahamas. Average tissue biomasses and symbiont cell densities were generally higher in shallow habitats (1–4 m) compared to deeper-dwelling conspecifics (12–15 m). Most colonies that were sampled displayed seasonal fluctuations in biomass and endosymbiont density related to annual temperature variations. During the bleaching episodes of 1998 and 2005, five out of seven species that were exposed to unusually high temperatures exhibited significant decreases in symbiotic algae that, in certain cases, preceded further decreases in tissue biomass. Following bleaching, Montastraea spp. colonies with low relative biomass levels died, whereas colonies with higher biomass levels survived. Bleaching- or disease-associated mortality was also observed in Acropora cervicornis colonies; compared to A. palmata, all A. cervicornis colonies experienced low biomass values. Such patterns suggest that Montastraea spp. and possibly other coral species with relatively low biomass experience increased susceptibility to death following bleaching or other stressors than do conspecifics with higher tissue biomass levels

BioTIME: A database of biodiversity time series for the Anthropocene.

MotivationThe BioTIME database contains raw data on species identities and abundances in ecological assemblages through time. These data enable users to calculate temporal trends in biodiversity within and amongst assemblages using a broad range of metrics. BioTIME is being developed as a community-led open-source database of biodiversity time series. Our goal is to accelerate and facilitate quantitative analysis of temporal patterns of biodiversity in the Anthropocene.Main types of variables includedThe database contains 8,777,413 species abundance records, from assemblages consistently sampled for a minimum of 2 years, which need not necessarily be consecutive. In addition, the database contains metadata relating to sampling methodology and contextual information about each record.Spatial location and grainBioTIME is a global database of 547,161 unique sampling locations spanning the marine, freshwater and terrestrial realms. Grain size varies across datasets from 0.0000000158 km2 (158 cm2) to 100 km2 (1,000,000,000,000 cm2).Time period and grainBioTIME records span from 1874 to 2016. The minimal temporal grain across all datasets in BioTIME is a year.Major taxa and level of measurementBioTIME includes data from 44,440 species across the plant and animal kingdoms, ranging from plants, plankton and terrestrial invertebrates to small and large vertebrates.Software format.csv and .SQL

The Effects of the UV-Blocker Oxybenzone (Benzophenone-3) on Planulae Swimming and Metamorphosis of the Scyphozoans Cassiopea xamachana and Cassiopea frondosa

Benzophenones are UV-blockers found in most common sunscreens. The ability of Scyphozoan planula larvae of Cassiopea xamachana and C. frondosa to swim and complete metamorphosis in concentrations 0–228 µg/L benzophenone-3 (oxybenzone) was tested. Planulae of both species swam in erratic patterns, 25–30% slower, and experienced significant death (p < 0.05) in the highest concentrations of oxybenzone tested, whereas the larvae exhibited normal swimming patterns and no death in ≤2.28 µg/L oxybenzone. In addition, metamorphosis decreased 10–30% over 3 days for both species maintained in 228 µg/L oxybenzone. These effects do not involve symbiotic dinoflagellates, as planulae larvae of Cassiopea sp. are aposymbiotic. It is concluded that oxybenzone can have a detrimental impact on these jellyfish

SPAWNING, DEVELOPMENT, AND ACQUISITION OF ZOOXANTHELLAE BY TRIDACNA SQUAMOSA (MOLLUSCA, BIVALVIA)

Volume: 161Start Page: 213End Page: 23

Preface

[Extract] Millions of people in the tropics are reliant, directly or indirectly, on coral reefs for their livelihoods. Whether their income is derived from tourism, fishing or ancillary activities, healthy coral reefs are essential to their welfare. However this is increasingly threatened by anthropogenic influences especially in developing countries where most of the world's reefs are found. Many scientists think that coral reefs may be changing, with a decrease in biodiversity and in extreme cases a phase change to an algal dominated ecosystem. Today's reefs are highly vulnerable to the frequency and scale of human impacts, especially changes in global climate resulting in higher sea temperatures and a lower pH. An estimated 30% of coral reefs are already severely damaged, and as many as 60% may be lost by 2030

Morphology of the Symbiosis Between Corculum cardissa (Mollusca: Bivalvia) and Symbiodinium corculorum (Dinophyceae)

Volume: 200Start Page: 336End Page: 34

PHOTOSYNTHESIS AND RESPIRATION IN TRIDACNA GIGAS AS A FUNCTION OF IRRADIANCE AND SIZE

Volume: 169Start Page: 230End Page: 24

Different Physiology in the Jellyfish Cassiopea xamachana and C. frondosa in Florida Bay

The jellyfish Cassiopea xamachana and C. frondosa co-occur within some habitats in the Florida Keys, but the frequency with which this occurs is low. It is hypothesized that the symbiosis with different dinoflagellates in the Symbiodiniaceae is the reason: the medusae of C. xamachana contain heat-resistant Symbiodinium microadriaticum (ITS-type A1), whereas C. frondosa has heat-sensitive Breviolum sp. (ITS-type B19). Cohabitation occurs at depths of about 3–4 m in Florida Bay, where the water is on average 0.36 °C cooler, or up to 1.1 °C cooler per day. C. frondosa tends not to be found in the warmer and shallower (<2 m) depths of Florida Bay. While the density of symbionts is about equal in the small jellyfish of the two species, large C. frondosa medusae have a greater density of symbionts and appear darker in color compared to large C. xamachana. However, the number of symbionts per amebocyte are about the same, which implies that the large C. frondosa has more amebocytes than the large C. xamachana. The photosynthetic rate is similar in small medusae, but a greater reduction in photosynthesis is observed in the larger medusae of C. xamachana compared to those of C. frondosa. Medusae of C. xamachana have greater pulse rates than medusae of C. frondosa, suggestive of a greater metabolic demand. The differences in life history traits of the two species were also investigated to understand the factors that contribute to observed differences in habitat selection. The larvae of C. xamachana require lower concentrations of inducer to settle/metamorphose, and they readily settle on mangrove leaves, submerged rock, and sand compared to the larvae of C. frondosa. The asexual buds of C. xamachana are of a uniform and similar shape as compared to the variably sized and shaped buds of C. frondosa. The larger polyps of C. frondosa can have more than one attachment site compared to the single holdfast of C. xamachana. This appears to be an example of niche diversification that is likely influenced by the symbiont, with the ecological generalist and heat-resistant S. microadriaticum thriving in C. xamachana in a wider range of habitats as compared to the heat-sensitive symbiont Breviolum sp., which is only found in C. frondosa in the cooler and deeper waters

Dynamic modeling and control strategies for Organic Rankine Cycle systems

Control and optimization are major issues in ORC systems applied to waste heat sources. This talk provides an overview of the current state of the art and of the main areas of R&D in that topic, including: - Steady-state and dynamic modeling of ORC cycles (simulation platforms, modeling paradigms, numerical issues) - Optimization of the working conditions for a given heat source and heat sink, and in particular of the evaporating temperature - Optimal start-up and shut-down strategies (grid synchronization, pressure overshoot, ...) - Control of the cycle under transient heat source conditions - Traditional and advanced controllers (PID, Model predictive control) The different adjustable working conditions (condensing/evaporating temperature, superheating, subcooling, working fluid flow rate) are listed with regard to the available degrees of freedom (pump/expander speed, secondary fluid flow rates and temperatures) and their optimal values are derived, depending on the target application