The Biological Bulletin

In the ophioplutei of brittle stars, the posterior coeloms are commonly assumed to be produced by a transverse fission of the initially formed coeloms; but in ophioplutei of Ophiopholis aculeata, the posterior coeloms first appear separately as aggregations of mesenchyme-like cells near the base of the posterolateral arms. Initiation of posterior coeloms was similar in ophioplutei of another family and may be similar in diverse ophiuroids. Initiation is easily missed without frequent observations. Early interpretations that diagrammed a fission of the first-formed coeloms appear to have influenced later authors for more than a century. Growth of posterior coeloms from a small initial size facilitated observations of developmental plasticity in growth of coeloms relative to that of larval arms. This plasticity, as observed in echinoplutei of echinoids, is relatively greater growth of a ciliary band for food capture when food is scarce and relatively greater growth of juvenile structures that will function after metamorphosis when food is abundant; however, juvenile structures develop extensively as a rudiment within the echinopluteus prior to settlement and metamorphosis, whereas in ophioplutei there is little development of juvenile structures until metamorphosis. In ophioplutei there is, therefore, less scope for shifting growth to structures that gain function after metamorphosis. Nevertheless, we found that when ophioplutei were at higher concentrations of food, the growth of the posterior coeloms was greater relative to the growth of the larval arms. Developmental plasticity in allocation of growth to larval and postlarval equipment can occur despite disparate patterns of development.

The trophic ecology of the invasive apple snail Pomacea canaliculata was intensely investigated because of the impacts of its grazing on aquatic vegetation, including crops. However, this freshwater snail also gathers food from the water surface by using a pedal funnel, a distinctive trophic behavior called pedal surface collecting. We investigated the diel fluctuations of this trophic behavior through four whole-day field observations in a stream. We recorded the lowest pedal funnel frequencies during light hours and the highest after sunset, a pattern similar to that of general activity. We evaluated through laboratory experiments the influence of water temperature and velocity, photoperiod, and a possible endogenous rhythm on this behavior. Pedal funnels are formed within the whole temperature range in which this snail is active. The highest pedal funnel formation rates were recorded at 30 °C, but the food captured was the same regardless of temperature. Pedal funnels were not observed at water velocities above 0.12 m·s⁻¹, but below this limit the rate and time spent in funnels remained constant with velocity. Despite the time of day, pedal funnels were scarce under constant artificial light, ruling out an endogenous rhythm. Both in the laboratory and in the stream, the highest levels of pedal funnels were observed during dark periods, probably as a strategy to avoid detection by visual predators. Pedal surface collecting on floating matter could represent an additional impact of invasive apple snails on freshwater ecosystems, but it could also be used for the specific delivery of molluscicides against them.

Following traumatic spinal cord injury, most mammalian species are unable to achieve substantial neuronal regeneration and often experience loss of locomotor function. In contrast, larval sea lampreys (Petromyzon marinus) spontaneously recover normal swimming behaviors by 10–12 weeks post-injury, which is supported by robust regeneration of spinal axons. While recovery of swimming behavior is well established, the lamprey’s ability to recover more complex behaviors, such as burrowing, is unknown. Here we evaluated the lamprey’s ability to burrow into a sand substrate over the typical time course of functional recovery (1–11 weeks post-injury). Compared to uninjured control lampreys, which burrow rapidly and completely, spinal-transected animals did not attempt burrowing until 2 weeks post-injury; and they often did not succeed in fully covering their entire body in the sand. Burrowing behavior gradually improved over post-injury time, with most animals burrowing partially or completely by 9–11 weeks post-injury. Burrowing behavior has two components: the initial component that resembles swimming with propagated body undulations and the final component that pulls the tail under the sand. While the duration of the initial component did not differ between control and spinal-transected animals across the entire recovery period, the duration of the final component in spinal-transected animals was significantly longer at all time points measured. These data indicate that, after spinal cord injury, lampreys are able to recover burrowing behaviors, though some deficits persist.

For many historical and contemporary experimental studies in marine biology, seawater carbonate chemistry remains a ghost factor, an uncontrolled, unmeasured, and often dynamic variable affecting experimental organisms or the treatments to which investigators subject them. We highlight how environmental variability, such as seasonal upwelling and biological respiration, drive variation in seawater carbonate chemistry that can influence laboratory experiments in unintended ways and introduce a signal consistent with ocean acidification. As the impacts of carbonate chemistry on biochemical pathways that underlie growth, development, reproduction, and behavior become better understood, the hidden effects of this previously overlooked variable need to be acknowledged. Here we bring this emerging challenge to the attention of the wider community of experimental biologists who rely on access to organisms and water from marine and estuarine laboratories and who may benefit from explicit considerations of a growing literature on the pervasive effects of aquatic carbonate chemistry changes.

The catecholamine 3,4-dihydroxyphenethylamine, or dopamine, acts as a neurotransmitter across a broad phylogenetic spectrum. Functions attributed to dopamine in the mammalian brain include regulation of motor circuits, valuation of sensory stimuli, and mediation of reward or reinforcement signals. Considerable evidence also supports a neurotransmitter role for dopamine in gastropod molluscs, and there is growing appreciation for its potential common functions across phylogeny. This article reviews evidence for dopamine’s transmitter role in the nervous systems of gastropods. The functional properties of identified dopaminergic neurons in well-characterized neural circuits suggest a hypothetical incremental sequence by which dopamine accumulated its diverse roles. The successive acquisition of dopamine functions is proposed in the context of gastropod feeding behavior: (1) sensation of potential nutrients, (2) activation of motor circuits, (3) selection of motor patterns from multifunctional circuits, (4) valuation of sensory stimuli with reference to internal state, (5) association of motor programs with their outcomes, and (6) coincidence detection between sensory stimuli and their consequences. At each stage of this sequence, it is proposed that existing functions of dopaminergic neurons favored their recruitment to fulfill additional information processing demands. Common functions of dopamine in other intensively studied groups, ranging from mammals and insects to nematodes, suggest an ancient origin for this progression.

Many shell-bearing gastropods exhibit pre-capture behaviors when encountering predatory asteroid sea stars. As shown in this meta-analysis of 48 studies on 24 sea star and 100 gastropod and chiton species, almost three-quarters of prey escape by moving or tumbling away, whereas the remaining species clamp tightly to the substratum or otherwise resist. The aim of the present paper is to correlate these behaviors with predicted shell traits, including those with gravitational stability for species that escape on the substratum and those that clamp, and those with a strongly sculptured shell in species that resist sea star attacks. Escaping species and those that clamp have gravitationally stable shells, with the center of gravity located above the broad aperture and large foot. Species that resist have significantly more sculptured shells. All of these traits would also work well in encounters with other slow-moving predators, such as gastropods and planarians. Although the sea stars are generalist predators, and the gastropods have many enemies besides sea stars, cool-water gastropods are well adapted to predatory sea stars on temperate and polar coasts, where most hard-bottom sea stars with molluscan diets occur. The prominence of escape among cool-water gastropods seems contradictory, given that locomotor speed rises with increasing temperature; but tropical gastropods rely more on armor than on escape, because of the prevalence of faster, more powerful predators in warm water. The black pigment of shells of many temperate prey species of sea stars might confer crypsis against these predators.