Dacha Atienza

Is global ocean sprawl a cause of jellyfish blooms

Jellyfish (Cnidaria, Scyphozoa) blooms appear to be increasing in both intensity and frequency in many coastal areas worldwide, due to multiple hypothesized anthropogenic stressors. Here, we propose that the proliferation of artificial structures – associated with (1) the exponential growth in shipping, aquaculture, and other coastal industries, and (2) coastal protection (collectively, “ocean sprawl”) – provides habitat for jellyfish polyps and may be an important driver of the global increase in jellyfish blooms. However, the habitat of the benthic polyps that commonly result in coastal jellyfish blooms has remained elusive, limiting our understanding of the drivers of these blooms. Support for the hypothesized role of ocean sprawl in promoting jellyfish blooms is provided by observations and experimental evidence demonstrating that jellyfish larvae settle in large numbers on artificial structures in coastal waters and develop into dense concentrations of jellyfish-producing polyps.

Temperature effects on asexual reproduction rates of scyphozoan species from the northwest Mediterranean Sea

In recent decades, many areas worldwide have experienced mass occurrences of jellyfish. To determine how temperature may affect jellyfish populations in the northwest (NW) Mediterranean Sea, we maintained polyps of three scyphozoan species, Aurelia aurita, Rhizostoma pulmo, and Cotylorhiza tuberculata in the laboratory at three temperatures (14, 21, 28°C) to test effects on survival and production of new polyps and ephyrae. Temperature significantly affected survival of all species, with longest survival of A. aurita and R. pulmo at 14°C and of C. tuberculata at 21°C. More polyps were budded by all species at temperatures above 14°C. A. aurita produced the most buds polyp−1 (43.5) and R. pulmo the fewest (8.8). Strobilation occurred only at 14°C for A. aurita and at 21°C for C. tuberculata. For R. pulmo, fewer polyps strobilated and strobilated later at 14°C. These patterns of survival and asexual reproduction were seasonally appropriate for each species in the NW Mediterranean, where A. aurita medusae occur earliest (~April–May) in cool waters, followed by R. pulmo during May–June, and then by C. tuberculata in mid-summer. Comparisons among scyphozoan species suggested that many may be restricted by low temperatures, and that global warming may benefit temperate species, but not tropical or boreal species.

Trophic ecology of Calanoides acutus in Gerlache Strait and Bellingshausen Sea waters (Antarctica, December 2002)

We measured ingestion rates of Calanoides acutus on different microbial components of the Gerlache Strait (GE) and Bellingshausen Sea (BE) waters during December 2002. At the time of the study the abundance of both zooplankton (42–133 ind m−3) and phytoplankton (0.76–1.5 µg chlorophyll a l−1) were low, indicating that the spring phytoplankton bloom was still not fully developed. C. acutus showed high clearance rates along the study (up to 432 ml ind−1 day−1), selecting for large motile organisms such as ciliates and the dinoflagellate Gyrodinium spp., although their feeding impact was always <0.1% of the standing stock of any of their prey. The total daily rations were low (∼2% body carbon per day), mostly the result of phytoplankton consumption (except for station GE3 in which heterotrophic flagellates contributed to 73% of the diet), and barely enough to cover metabolic demands. Based on the relationship between oxygen (carbon) consumption and ammonia excretion (considered as indicative of the metabolic substrate) it seems that standard metabolic demands were supplied, apart from the diet, by the use of their own non-structural proteins, whereas the remaining reserve-lipids were used to produce eggs.