Whole-cell recording coupled with biocytin injection revealed four types of interneurons intrinsic to the olfactory lobe (OL) of the spiny lobster Panulirus argus. Each type of neuron had a distinct pattern of arborization within the three anatomically defined regions of OL glomeruli (cap, subcap and base). Type I interneurons innervated all three regions, while types II, III and IV branched only in the cap, subcap and base, respectively. Type I interneurons responded to electrical stimulation of the antennular (olfactory) nerve with a burst of 1­20 action potentials and a 1­10 s depolarization. Type II (cap) interneurons responded to the same input with a burst of 1­3 action potentials followed by a shorter hyperpolarization. Type III (subcap) interneurons responded with a burst of 1­6 action potentials followed by a delayed, 0.5­4 s depolarization. Type IV (base) interneurons responded with a brief depolarization or a burst of 1­3 action potentials followed by a 1 s hyperpolarization. The regionalized arborization and the different response properties of the type II, III and IV interneurons strongly imply that lobster olfactory glomeruli contain functionally distinct regions, a feature that should be useful in understanding the multiple synaptic pathways involved in processing olfactory input.
Deep-sea isopods of the family Munnopsidae exhibit four modes of swimming: forward striding, slow backward pedalling, fast backward pedalling and escape, the first two of which use asymmetric phases of leg movement. Instead of moving the left and right limbs (pereopods, P2­P7) of a segment in-phase (e.g. RP2LP2, RP3LP3, RP4LP4), as do most aquatic insects, leg movement is more like that of fast-walking insects, where closest synchrony occurs between diagonal limbs (e.g. RP2LP3, RP3LP4, RP4LP2). This is similar to the alternating tripod gait used by many animals on land to prevent them from toppling over. It therefore seems likely that this group of isopods learned to walk before they could swim.