Did ciguatera prompt the late Holocene Polynesian voyages of discovery?

The famous Polynesian voyages characterized an intensive network of cultural exchange and colonization that was particularly active from ad 1000 to 1450. But, why would large groups of people leave their homelands to voyage into the unknown? Oceanic voyages are risky, albeit less so today than in the past. Landfalls were not guaranteed improvements over ports of departure. Taking the Cook Islands as an example, we ask whether harmful algal blooms that result in ciguatera fish poisoning in humans prompted past and present emigration pulses of peoples from within Polynesia. We take a multipronged approach to examine our hypothesis, involving: (1) archaeological evidence, (2) ciguatera fish poisoning reports since the 1940s, and (3) climate and temperature oscillations using palaeodatasets. The archaeological records of fish bones and hooks show abrupt changes in fishing practices in post‐ad 1450 records. Sudden dietary shifts are not linked to overfishing, but may be a sign of ciguatera fish poisoning and adjustment of fishing preference. While fishes form the staple diet of Polynesians, such poisoning renders fishes unusable. We show that ciguatera fish poisoning events coincide with Pacific Decadal Oscillations and suggest that the celebrated Polynesian voyages across the Pacific Ocean may not have been random episodes of discovery to colonize new lands, but rather voyages of necessity. A modern analogue (in the 1990s) was the shift towards processed foods in the Cook Islands during ciguatera fish poisoning events, and mass emigration of islanders to New Zealand and Australia.     

Colony self-shading facilitates Symbiodiniaceae cohabitation in a South Pacific coral community

The ecological success of tropical corals is regulated by symbiotic dinoflagellate algae (Symbiodiniaceae). Corals can associate with multiple Symbiodiniaceae species simultaneously, yet the conditions that permit Symbiodiniaceae cohabitation are not understood. We examined how corals self-shade their own tissues causing within-colony light gradients that drive Symbiodiniaceae photoacclimatory processes and positional genetic disparity. Paired light ‘exposed’ and ‘shaded’ samples from 20 coral species were collected from a shallow coral reef (Rarotonga, Cook Islands). Through active chlorophyll fluorometry, rapid light curves revealed that exposed Symbiodiniaceae exhibited 50% higher values in minimum saturating irradiances and demonstrated a shift towards preferential nonphotochemical quenching [1 – Q], consistent with higher overall light exposure. High-throughput or targeted DNA sequencing of ITS2 and psbA^ncr markers demonstrated that corals harboured distinct and/or differentially abundant Symbiodiniaceae ITS2 sequences (typically rare in relative abundance) or multiple ITS2 intragenomic variant profiles across shaded vs exposed regions. In Hydnophora cf. microconos, within-colony symbiont genetic disparity was positively correlated with the magnitude of difference in [1 – Q] utilisation. Together, these results suggest that within-colony light gradients produce distinct optical niches that enable symbiont cohabitation via photoadaptation, a phenomenon that is expected to increase the adaptive capacity of corals under future climates.

     

Protoplast Preparation from <Emphasis Type="Italic">Laminaria japonica</Emphasis> with Recombinant Alginate Lyase and Cellulase

Functional recombinant abalone alginate lyase (rHdAly) and β-1,4-endoglucanase (rHdEG66) were expressed as secreted proteins with baculoviral expression systems. The specific activity of each recombinant enzyme, 2,490 and 18.2 U/mg for rHdAly and rHdEG66, respectively, was comparable to its native form at 30°C. Purified rHdAly and rHdEG66 showed the highest specific activity both at 35°C and optimum pH 8.7 and 5.9, respectively. These properties were also comparable to those of the native enzymes. Protoplast isolation was attempted from Laminaria japonica using both rHdAly and rHdEG66. When L. japonica blades were incubated in artificial seawater containing rHdAly and rHdEG66, very low numbers of protoplasts (<1 × 10³ protoplasts/g fresh weight) resulted. However, using blades pretreated with proteinase K, the protoplast was increased up to 5 × 10⁶ protoplasts/g fresh weight. Since the average diameter of isolated protoplasts was 11.6 μm, these cells were mostly derived from the epidermal layer rather than the cortical layer. Our results suggest that at least three enzymes, alginate lyase, cellulase, and protease, are essential for effective protoplast isolation from L. japonica. The protoplast isolation method in this study is more useful than earlier methods because it preferentially yielded protoplasts of the epidermal layer, which are known to be able to be regenerated.