Cultivating hybrid collectives: research methods for enacting community food economies in Australia and the Philippines

Across the globe, groups are experimenting with initiatives to create alternatives to the dominant food system. What role might research play in helping to strengthen and multiply these initiatives? In this paper we discuss two research projects in Australia and the Philippines in which we have cultivated hybrid collectives of academic researchers, lay researchers and various non-human others with the intention of enacting community food economies. We feature three critical interactions in the “hybrid collective research method”: gathering, which brings together those who share concerns about community food economies; reassembling, in which material gathered is deliberatively rebundled to amplify particular insights; and translating, by which reassembled ideas are taken up by other collectives so they may continue to “do work”. We argue that in a climate-changing world, the hybrid collective research method fosters opportunities for a range of human and non-human participants to act in concert to build community food economies.     

Symbiotic zooxanthellae enhance boring and growth rates of the tropical sponge Anthosigmella varians forma varians

Several species of boring sponges harbor symbiotic zooxanthellae, and it is believed that the symbiont enhances boring activity of host sponges. This hypothesis was tested using manipulative field experiments to assess the effect of intracellular zooxanthella populations on boring rates of the tropical sponge Anthosigmella varians forma varians. Portions of sponge were attached to 60 calcium carbonate blocks of known weight. Three sets of 10 blocks were grown at high light levels and three sets of 10 blocks were grown at low light levels for 105 d in the Florida Keys, Florida, USA. Boring rates, growth rates (lateral growth and within-substratum tissue penetration), and zooxanthella populations were measured at the end of the experiment. Absolute rates of boring and growth of A. varians forma varians were significantly greater when zooxanthella densities were higher. Boring rate and tissue penetration related to final surface area of sponge attachment was also enhanced when zooxanthella densities were higher, suggesting that the symbiont plays a physiological role in the decalcification process. This is in contrast to the role that zooxanthellae play in coral hosts. Based on the results of this study, it appears that the presence of zooxanthellar symbionts has important ecological and life-history consequences for host sponges. Ability to laterally overgrow competitors will be correlated with the size and activity of zooxanthella populations. In addition, the fitness of host sponges will be enhanced by algal symbionts, since greater penetration within substrata will result in an increase in production of tissue that can be converted into storage, feeding and reproductive functions.     

Jellyfish aggregations and leatherback turtle foraging patterns in a temperate coastal environment

Leatherback turtles (Dermochelys coriacea) are obligate predators of gelatinous zooplankton. However, the spatial relationship between predator and prey remains poorly understood beyond sporadic and localized reports. To examine how jellyfish (Phylum Cnidaria: Orders Semaeostomeae and Rhizostomeae) might drive the broad-scale distribution of this wide ranging species, we employed aerial surveys to map jellyfish throughout a temperate coastal shelf area bordering the northeast Atlantic. Previously unknown, consistent aggregations of Rhizostoma octopus extending over tens of square kilometers were identified in distinct coastal "hotspots" during consecutive years (2003-2005). Examination of retrospective sightings data (>50 yr) suggested that 22.5% of leatherback distribution could be explained by these hotspots, with the inference that these coastal features may be sufficiently consistent in space and time to drive long-term foraging associations.     

Natural food,foregut clearance-rate and activity of the crab Scylla serrata

The natural diet, rate of foregut clearance and diurnal activity of the crab Scylla serrata were determined. The gut volume is related to size of crab as gut volume (ml)=0.07e^0.033x , where x=carapace width in millimetres. Fifty per cent of crabs collected in Australia and South Africa contained molluscan remains and about 21% contained crustacean remains — chiefly grapsid crabs. Fish remains were rarely found, and it was concluded that S. serrata does not normally catch mobile forms such as fish and penaeid prawns. Gut clearance of organic tissue was rapid and almost complete after 12 h. Fish bone was retained for a mean time of 2 to 3 days, and shell for 5 to 6 days. Time-lapse photography, using infra-red light, was used to record activity. Visible light flashes reduced activity. S. serrata remained buried during the day, emerging at sunset to spend the night feeding, which occurred intermittently even when unlimited food was available. If no food was present the amount of time spent on the substrate surface was halved.     

Abundance,breeding and growth of the crab Scylla serrata in two South African estuaries

Populations of the crab Scylla serrata (Forskal) were studied in two South African estuaries from 1971 until 1974. One estuary was open to the sea, the other was closed by a sandbar. Population density in the closed estuary was estimated by means of mark-release-recapture data from tagged crabs. The population of S. serrata was estimated as 1 crab/124m² and the production at 3.4 g/m²/annum. Catch per unit effort data from the closed estuary indicated a natural mortality of 41% in the crabs' second year and 60% in the third. Growth was studied in both estuaries by means of size-frequency analysis and from tagging returns. Growth was rapid in the first 12 to 15 months, when the crabs attained a carapace width of 80 to 160 mm. Thereafter growth slowed, and after 3 years crabs were between 140 and 180 mm in carapace width. Females mated in summer at a carapace width of 103 to 148 mm, males at 141 to 166 mm. After mating, females migrated out of both estuaries into the sea.