The colloidal fraction of dissolved organic carbon in seawater is one
of the largest reservoirs of organic carbon on the planet, outweighing
phytoplankton or the bacteria by a considerable margin. Even though t
his colloid-sized material is a carbon reservoir of global significanc
e, it is not easily accessible to the bacteria and may escape extensiv
e biological degradation by virtue of its particle size characteristic
s. However, when larger colloids (between 0.2 and 2.0 mum in diameter)
are incorporated into microaggregates (that are tens of mum to mm acr
oss), colloidal organic carbon (COC) is broken down as the aggregates
become bioreactors for organic material. For example, the aggregation
of colloids and bacteria by surface coagulation triggers a brief (2 to
4 h) episode of bacterial respiration. The bioreactive nature of aggr
egates is confirmed in their development as sites of intense bacterial
exoenzyme activity, even though the organic material released by this
activity remains largely uncoupled from bacterial growth. The degrada
tion of COC in aggregates is a process that is missing from current mo
dels of carbon transport and ocean productivity. In addition, while th
e COC caught up into aggregates may be more bioreactive than previousl
y suspected, respiration of the aggregated material persists for only
a few hours. Realistic measurements of respiration should take this sh
ort-lived, but intense, response to aggregation into account.