Mantis shrimp

Abstract: Interactive effects of three alternating normoxia-hypoxia cycles on benthic prey exploitation by mobile fish (spot, Leiostomus xanthurus; and hogchoker, Trinectes maculatus) and a burrowing crustacean (Squilla empusa) were investigated in the York River, Chesapeake Bay, Virginia, USA, in 1989. Predators collected in four depth strata (A: 5 to 10 m; B: 10 to 14 m; C: 14 to 20 m; D:>20 m) variously affected by hypoxia were separated into size classes (three for spot and two each for hogchoker and mantis shrimp) to examine potential ontogenetic influences in prey selection. The most severe effects of hypoxia on the benthos occurred in the two deepest strata (C and D) and decreased in shallower strata (B>A), with Stratum A never affected by low oxygen. Predators investigated exhibited dietary evidence of optimal prey exploitation during or immediately after hypoxic events. In most instances gut contents contained significantly larger, deeper-burrowing prey during periods of low oxygen than during alternating peroids of normal oxygen levels. Spot consumed a greater biomass (45 to 73%) of polychaetes than other prey, with crustaceans initially also constituting a main dietary component but decreasing in importance later in the study period. The deep-burrowing anemone, Edwardsia elegans, was an important prey species for spot, particularly in the lower depth strata affected by hypoxia. Prey consumed by 10-to 15-cm-long spot increased significantly in size during some hypoxic events, suggesting a sublethal effect of hypoxia on large benthic species. Polychaetes (primarily Glycera americana, Notomastis latericeus and Loimia medusa) were dominant dietary components in hogchoker, making up between 85 and 98% of the diet. Bivalve siphons became important prey for hogchoker in the three deepest strata and were only consumed after the August hypoxia. Stomach contents of mantis shrimp were difficult to identify in most instances due to the near complete mastication of consumed prey. Crustaceans were important prey initially but became less conspicuous in the diet subsequent to the July hypoxia event, when hydroids became more dominant. Overall, predator species exhibited optimal exploitation of moribund or slowly recovering benthos affected by hypoxia. The sublethal effects of hypoxia through increased availability of benthos to resident predators can have important consequences for energy flow in areas such as the York River which experience periodic low-oxygen cycles.

Abstract: SUMMARY Mantis shrimp are renowned for their unusual method of breaking shells with brief, powerful strikes of their raptorial appendages. Due to the extreme speeds of these strikes underwater, cavitation occurs between their appendages and hard-shelled prey. Here we examine the magnitude and relative contribution of the impact and cavitation forces generated by the peacock mantis shrimp Odontodactylus scyllarus . We present the surprising finding that each strike generates two brief, high-amplitude force peaks, typically 390–480 μs apart. Based on high-speed imaging, force measurements and acoustic analyses, it is evident that the first force peak is caused by the limb9s impact and the second force peak is due to the collapse of cavitation bubbles. Peak limb impact forces range from 400 to 1501 N and peak cavitation forces reach 504 N. Despite their small size, O. scyllarus can generate impact forces thousands of times their body weight. Furthermore, on average, cavitation peak forces are 50% of the limb9s impact force, although cavitation forces may exceed the limb impact forces by up to 280%. The rapid succession of high peak forces used by mantis shrimp suggests that mantis shrimp use a potent combination of cavitation forces and extraordinarily high impact forces to fracture shells. The stomatopod9s hammer is fundamentally different from typical shell-crushing mechanisms such as fish jaws and lobster claws, and may have played an important and as yet unexamined role in the evolution of shell form.

Abstract: One of the most complex eyes in the animal kingdom can be found in species of stomatopod crustaceans (mantis shrimp), some of which have 12 different photoreceptor types, each sampling a narrow set of wavelengths ranging from deep ultraviolet to far red (300 to 720 nanometers) (1–3). Functionally, this chromatic complexity has presented a mystery (3–5). Why use 12 color channels when three or four are sufficient for fine color discrimination? Behavioral wavelength discrimination tests (Δλ functions) in stomatopods revealed a surprisingly poor performance, ruling out color vision that makes use of the conventional color-opponent coding system (6–8). Instead, our experiments suggest that stomatopods use a previously unknown color vision system based on temporal signaling combined with scanning eye movements, enabling a type of color recognition rather than discrimination.

Abstract: STOMATOPOD crustaceans, commonly named mantis shrimps, have compound eyes of unique design. A central band composed of six parallel rows of ommatidia separates two peripheral ommatidial groups, and all three regions view the same area of visual space1–3. In the central bands of members of the stomatopod superfamily Gonodactyloidea, four of the ommatidial rows are built of tiers of photoreceptors; in two of these rows, the photoreceptors themselves contain coloured filters4. Such a design could in principle produce many spectral classes of photoreceptors using only a single visual pigment4,5. We measured the absorption spectra of the coloured filters and the visual pigments in frozen sections of retinae of a typical species, Pseudosquilla ciliata, using end-on microspectrophotometry. The retina contains not one, but as many as ten visual pigments, each in a distinct photoreceptor class, having maximum absorbances at wavelengths from 400 to 539 nm. Because of the unique anatomy of stomatopod eyes, ten or more spectral types of photoreceptors exist in this species.