ALBERT

Description: The proportion of body mass devoted to skeleton in marine invertebrates decreases along latitudinal gradients from large proportions in the tropics to small proportions in polar regions. A historical hypothesis—that latitudinal differences in shell production costs explain these trends—remains untested. Using field-collected specimens spanning a 79°N to 68°S latitudinal gradient (16,300 km), we conducted a taxonomically controlled evaluation of energetic costs of shell production as a proportion of the total energy budget in mollusks. Shell production cost was fairly low across latitudes at 〈10% of the energy budget and predominately 〈5% in gastropods and 〈4% in bivalves. Throughout life, shell cost tended to be lower in tropical species and increased slightly toward the poles. However, shell cost also varied with life stage, with the greatest costs found in young tropical gastropods. Low shell production costs on the energy budget suggest that shell cost may play only a small role in influencing proportional skeleton size gradients across latitudes relative to other ecological factors, such as predation in present-day oceans. However, any increase in the cost of calcium carbonate (CaCO 3 ) deposition, including from ocean acidification, may lead to a projected ~50 to 70% increase in the proportion of the total energy budget required for shell production for a doubling of the CaCO 3 deposition cost. Changes in energy budget allocation to shell cost would likely alter ecological trade-offs between calcification and other drivers, such as predation, in marine ecosystems.

Description: 〈p〉Antarctica and the surrounding Southern Ocean are facing complex environmental change. Their native biota has adapted to the region’s extreme conditions over many millions of years. This unique biota is now challenged by environmental change and the direct impacts of human activity. The terrestrial biota is characterized by considerable physiological and ecological flexibility and is expected to show increases in productivity, population sizes and ranges of individual species, and community complexity. However, the establishment of non-native organisms in both terrestrial and marine ecosystems may present an even greater threat than climate change itself. In the marine environment, much more limited response flexibility means that even small levels of warming are threatening. Changing sea ice has large impacts on ecosystem processes, while ocean acidification and coastal freshening are expected to have major impacts.〈/p〉

Description: Ash-free-dry-weight determinations for a representative range of living brachiopod genera have revealed that a consistently high proportion of total organic mass is contained within the shell, partly as the organic matrix for biomineralisation and partly as minute extensions of the mantle tissues (caeca) housed within hollow endopunctae permeating the shell. On average 40% to 50% of the total organic mass of both articulate and inarticulate brachiopods is situated within the shell. This is true even for a rhynchonellid brachiopod which does not possess endopunctae, but which has a more dense protein matrix in its shell. The effectively hidden constituent of brachiopod tissue mass which is included in this component has often been overlooked, and as a result total metabolic tissue mass has been underestimated. This throws into question some previous interpretations of brachiopod respiratory and metabolic data.The oxygen consumption rates of several living brachiopods have been measured, and when respiring tissue in caeca in the shell is taken into consideration, it is clear that brachiopod metabolic rates are low when compared with other marine invertebrates (e.g. between 10% and 50% of the oxygen uptake of comparable gastropods and bivalve molluscs held in similar conditions). This low rate cannot be attributed to a slower pumping rate by the brachiopod lophophore, as has been suggested, because the rate of water movement is comparable to that across the bivalve gill.Nitrogen excretion rates have also been measured for a few living brachiopods, allowing a comparison with rates of oxygen consumption and providing an indication of the metabolic substrates used. These data on oxygen: nitrogen ratios suggest that one Antarctic brachiopod utilises exclusively protein as a metabolic substrate, while a temperate latitude species uses mainly protein during winter but lipids and carbohydrates during summer months. Histological observations, particularly of Terebratulina retusa from temperate waters, show that a specialised tissue layer in the brachiopod outer mantle epithelium proximal to the shell may be the site of storage of the protein that is metabolised during winter, and of carbohydrate mobilised during gonadal development in summer. The caeca have also been suggested as sites of storage of metabolites, and the possible relationships between these areas of mantle are discussed. It seems that the ability to store nutrients in the mantle, combined with flexibility of substrate utilisation and an inherently low metabolic rate, have been important factors in brachiopod evolution.