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1 rhythm in the stomatogastric ganglion of the spiny lobster.
3 es compared to federally managed areas, with spiny lobsters and horn sharks completely absent from no
4 These results imply that true navigation in spiny lobsters, and perhaps in other animals, is based o
5 dies of hermit crabs, crayfish and lobsters, spiny lobsters, and shrimps are homologous to insect mus
6 ggest the olfactory L-glutamate receptors of spiny lobsters are novel types of L-glutamate receptors
7 , and biomass of three key predator species (spiny lobster, California sheephead, and horn shark) bet
8 we undertake the first analysis of Caribbean spiny lobster diet using a stable isotope approach (carb
9 improving yield regionally for a sustainable spiny lobster fishery, apparently through the spillover
11 postlarvae in the Florida Keys and adults of spiny lobster from the Florida Keys and throughout the C
12 rons of the stomatogastric ganglion (STG) of spiny lobsters, Ih can be endogenously upregulated to co
13 ne stimulates the feeding pathway to deceive spiny lobsters into attending to a false food stimulus,
14 ges on the survival, growth, and movement of spiny lobsters is growing, the effect on their chemosens
16 of the sounds from various sizes of European spiny lobsters (Palinurus elephas), recorded between 0.5
17 he lateral flagellum of the antennule of the spiny lobster Panulirus argus houses more than 1,000 mor
19 olfactory receptor neurons of the Caribbean spiny lobster Panulirus argus possesses receptors for L-
20 tal types on the antennules of the Caribbean spiny lobster Panulirus argus revealed three types of no
21 anulirin, isolated from the hemocytes of the spiny lobster Panulirus argus with regulatory functions
26 of the functional response of the California spiny lobster Panulirus interruptus, foraging on a key e
30 s with two gastropod predators-the Caribbean spiny lobster (Panulirus argus) and the grunt black marg
32 nd macroalgal abundance with fishery data of spiny lobster (Panulirus interruptus) landings to evalua
33 w how healthy, normally gregarious Caribbean spiny lobsters (Panulirus argus) avoid conspecifics that
34 atogastric nervous system of male and female spiny lobsters (Panulirus interruptus), focused on dynam
35 plysia californica), which, when attacked by spiny lobsters (Panulirus interruptus), release defensiv
38 r (PD) neurons of the pyloric network in the spiny lobster, Panulirus interruptus, and its modulation
39 ethal attack by a co-occurring predator, the spiny lobster, Panulirus interruptus, might be a natural
40 ircuit in the stomatogastric ganglion of the spiny lobster, Panulirus interruptus, results not only f
46 rchitecture of neurogenic complexes in adult spiny lobsters, Panulirus argus, based on transmission e
48 ed significantly with body size, the largest spiny lobsters producing SL up to 167 dB re 1 uPa(2).
49 duced-pH seawater altered the orientation of spiny lobster pueruli toward chemical cues produced by L
51 l pathway was previously unrecognized in the spiny lobster's diet, and these results are the first em
53 different realistic propagation conditions, spiny lobster sounds can be detectable up to several kil
55 to act on peripheral chemosensory neurons of spiny lobsters, stimulating feeding-related behaviours a
56 e rhythmically active pyloric circuit of the spiny lobster, the pyloric dilator (PD) neurons are memb
57 e rhythmically active pyloric circuit of the spiny lobster, the synapse between the lateral pyloric (
59 chemical cues from conspecifics are used by spiny lobsters to identify suitable shelter and cues fro