Snapping behaviour in intraspecific agonistic encounters in the snapping shrimp (Alpheus heterochaelis)

During intraspecific agonistic encounters in snapping shrimp (Alpheus heterochaelis) the behaviour of the snapper, emitting a fast water jet by very rapid closure of the large modified snapper claw, and the receiver was analysed by single frame video analysis before, during, and after the snap. During snapping the opponents usually face each other. Snapping is most frequently preceded by touch of frontal appendages. The snapping animal keeps its snapper claw slightly across the midline, shielding frontal body parts, and its tailfan bent downwards. The mean claw cocking duration (generating muscle tension) before snapping amounts to about 500 ms. In 58% of the snaps, the snapper claw pointed at the opponent, its claws, densely covered with sensory hairs, representing the main target of the water jet. The mean distance for these directed snaps was 0.9 cm, while undirected snaps were emitted from larger distances of on average 3.4 cm. The snapper usually withdraws immediately after snapping, the receiver approaches. Initial snaps are often answered by return snaps and both are emitted from smaller distances and hit more often than subsequent snaps.     

Variable microsatellite markers for a snapping shrimp (Alpheus armillatus) species complex

Snapping shrimp (Alpheus) are an important ecological component of tropical marine systems and are excellent models for studies of phylogeography and behavioural ecology. Here, I describe 10 variable microsatellite loci for the Alpheus armillatus species complex of snapping shrimp. The primers were tested on 60 individuals representing three evolutionary lineages within the complex, and yielded three to 21 alleles. These loci will be effective tools in future studies on population genetics and mating behaviour in this complex.     

Deception with honest signals: signal residuals and signal function in snapping shrimp

Animals in competitive interactions often assess the competitiveability of opponents using signals. Signals used in competitiveinteractions are generally predicted to be honest, but opento low levels of deceit. Such "incomplete honesty" in signalscan be studied by using signal residuals, the residuals fromthe regression of a measure of signal structure on competitiveability. Specifically, individuals with positive signal residualsproduce signals that exaggerate their competitive ability; deceptive use of these signals may occur if signalers for whom the signalexaggerates their apparent competitive ability use the signalmore frequently. I used this framework to examine the use ofthe open chela display by big-clawed snapping shrimp (Alpheusheterochaelis). Competitive interactions between snapping shrimpare resolved primarily on the basis of body size, and the open chela display is used by males to assess body size. I foundthat the production of the open chela display by males respondingto superior competitors depends on chela residuals, such thatindividuals for whom the display exaggerates their apparentsize produce the display more often. This effect can be seenboth in response to isolated chelae and in staged competitiveinteractions. Interactions involving shrimp with larger chela residuals are long and highly escalated, suggesting that chelaresiduals affect assessment of competitive ability. Thus, theincreased use of the open chela display by males for whichthe display exaggerates apparent body size is an example ofdeceptive use of an otherwise honest signal.     

Two new decapod (Crustacea,Malacostraca) complete mitochondrial genomes: bearings on the phylogenetic relationships within the Decapoda

Recent advances in molecular phylogenetics are continuously changing our perception of decapod phylogeny. Although the two suborders Dendrobranchiata and Pleocyemata within the Decapoda are widely accepted, this taxonomic view is now challenged when using mitochondrial protein‐coding genes to investigate the decapod phylogeny, especially for the basal pleocyematan groups. Here, we enhanced taxonomic coverage by sequencing the genomes of two basal decapod taxa Alpheus distinguendus and Panulirus ornatus, representing two infraorders, Caridea and Achelata, respectively. Based on these two and other available mitochondrial genomes, we evaluated the usefulness of protein‐coding genes in resolving deep phylogenetic relationships of the Decapoda using maximum likelihood and Bayesian analyses. The mt genomic results revealed a novel gene order because of the reverse transposition of trnE (transfer, trn for Glutamate) and a pseudogene‐like trnS (AGN) [trn for Serine (S₁, AGN)] in the mitochondrial genome of A. distinguendus, and a duplicate of 89 bp sequences in the putative noncoding region of P. ornatus. Our phylogenetic inferences suggest monophyly of the Decapoda and its two suborders, and that several lineages within the Reptantia are consistently recovered with high nodal supports. Our findings suggest that the best mitochondrial genome phylogeny can be found on the premise that systematic errors should be minimized as much as possible. © 2011 The Linnean Society of London, Zoological Journal of the Linnean Society, 2011, 162 , 471–481.     

Post-autotomy claw regrowth and functional recovery in the snapping shrimp Alpheus angulosus

The ability to regenerate lost tissues, organs or whole body parts is widespread across animal taxa; in some animals, regeneration includes transforming a remaining structure to replace the one that was lost. The transformation of one limb into another involves considerable plasticity in morphology, physiology and behavior, and snapping shrimp offer excellent opportunities for studying this process. We examined the changes required for the transformation of the small pincer to a mature snapping claw in Alpheus angulosus. First molt claws differ from mature claws in overall shape as well as in morphology related to snapping function; nonetheless, shrimp with first molt claws do produce snaps. While most shape variables of second molt claws do not differ significantly from mature claws, the plunger (structure required for snap production) does not reach mature size until the third molt for females, or later for males. Thus, the pincer claw can be transformed into a functional snapping claw in one molt, although both the underlying morphology and superficial shape are not fully regenerated at this stage. The rapid production of a functional snapping claw that we observe in this study suggests that this particular function is of significant importance to snapping shrimp behavior and survival.     

Individual discrimination in the big-clawed snapping shrimp,Alpheus heterochelis

Rahman et al. (Rahman, N., Dunham, D.W. and Govind, C.K. (). Mate recognition and pairing in the big-clawed snapping shrimp, Alpheus herterochelis. Mar. Fresh. Behav. Physiol., 34, 213–226.) demonstrated discrimination by snapping shrimp between former mates and unfamiliar conspecifics, but did not test individual discrimination. In the present study, snapping shrimp showed discrimination between familiar and unfamiliar same-sex conspecifics by preferentially entering that arm of a Y-maze leading to familiar individuals. Furthermore, after being exposed to water from the home tanks of unknown individuals, they later showed an elevated response to this water, if the direction from which the water came into their tank was changed to be novel. This indicates that test subjects associated a familiar chemical stimulus with its location in the environment. This discrimination could only have been made if that chemical signature were recognised as different from that of another chemically familiar individual. This result also demonstrates that the water surrounding an individual contains sufficient (chemical) information to allow discrimination of one individual from another.     

Mate recognition and pairing in the big‐clawed snapping shrimp,Alpheus heterochelis

Most studied snapping shrimp are found in male‐female pairs, cohabiting a common shelter. Studying Alpheus heterochelis in the laboratory, we determined that both sexes discriminate a former mate, from which they have been separated for 24 h, from a stranger. Strangers are more aggressive towards each other and show significantly lower frequencies of non‐agonistic (stroking and touching) behaviours than do former mates. We also established that the probability of re‐pairing between former mates and the pairing latency are strongly dependent on which sex remained in the home tank. If the female remains resident, she is equally likely to pair with a stranger and with her former mate (when tested separately), and there is no difference in pairing latency. If the male remains resident, the frequency of pairing between former mates is significantly higher than between strangers, and the pairing latency is significantly shorter. From these differences, we infer that the social bond may be adapted to absence from the shelter by the female, but not by the male.     

Evidence for three major clades within the snapping shrimp genus Alpheus inferred from nuclear and mitochondrial gene sequence data

The snapping shrimp genus Alpheus is among the most diverse of caridean shrimps, and analyses of taxa separated by the Isthmus of Panama have been used to estimate rates of molecular evolution. Although seven morphological groups have been informally suggested, no formal phylogenetic analysis of the genus has been previously attempted. Here we infer the phylogenetic relationships within Alpheus using sequence data from two nuclear genes, glucose-6-phosphate isomerase and elongation factor-1alpha, and from the mitochondrial gene cytochrome oxidase I. Three major clades corresponding to previously noted morphological features were identified. Discrepancies between earlier informal morphological groupings and molecular analyses largely consisted of species whose morphologies were not entirely typical of the group to which they had been assigned. The traditional placements of shrimp with highly sessile lifestyles and consequently simplified morphologies were also not supported by molecular analyses. Phylogenies for Alpheus suggest that specialized ecological requirements (e.g., symbiotic associations and estuarine habitats) and modified claw morphologies have evolved independently several times. These new analyses also support the sister species status of transisthmian pairs analyzed previously, although very similar pairs were not always resolved with the more slowly evolving nuclear loci. In addition, six new cryptic species were identified in the course of these studies plus a seventh whose status remains to be determined.     

Muscle remodeling in adult snapping shrimps via fast-fiber degeneration and slow-fiber genesis and transformation

Bilateral asymmetry of the paired snapper/pincer claws may be reversed in adult snapping shrimps (Alpheus heterochelis). Removal of the snapper claw triggers transformation of the contralateral pincer claw into a snapper and the regeneration of a new pincer claw at the old snapper site. During this process the pincer closer muscle is remodeled to a snapper-type, and these alterations have been examined with the electron microscope. There is selective death of the central band of fast fibers, accompanied by an accumulation of electron-dense crysttaline bodies in the degenerating fibers. Two principal types of hemocytes (amebocytes and coagulocytes) invade the area and the degenerating muscle fibers. New myotubes also appear in this central site. The myotubes are characterized by a prolific network of presumptive sarcoplasmic reticulum and transverse tubules, nascent myofibrils, and crystalline bodies. The myotubes are innervated by many motor nerve terminals, and they subsequently differentiate into long-sarcomere (8–12 m), slow muscle fibers. Remodeling of the central band, therefore, occurs by degeneration of the fast fibers and their replacement by new slow fibers. Remnants of the degenerating fast fibers act as scaffolding for the myotubes which originate from adjacent satellite cells. The crystalline bodies may represent protein stores from the degeneration of the fast fibers, recycled for use in the genesis of new fibers. The invading hemocytes appear to play several roles, initially phagocytosing the fast muscle fibers, transporting the crystalline bodies into the new myotubes, and acting as stem cells for the new muscle fibers. Apart from the central band of fibers, the remaining pincer-type slow fibers with sarcomere lengths of 5–7 m are transformed via sarcomere lengthening into snapper-type slow fibers with sarcomere lengths of 7–12 m. Thus, during claw transformation in adult snapping shrimps, the pincer closer muscle is remodeled into a snapper closer muscle by selective death of the fast-fiber band, replacement of the fast-fiber band by new slow fibers, and transformation of the existing slow fibers to an even-slower variety. Note. This paper is dedicated to the fond memory of Professor M.S. Laverack whose enjoyment of biological research and gentle encouragement of such endeavours touched all those who knew him.     

Genetic,ecological, and behavioural divergence between two sibling snapping shrimp species (Crustacea: Decapoda: Alpheus)

Examination of genetic and ecological relationships within sibling species complexes can provide insights into species diversity and speciation processes. Alpheus angulatus and A. armillatus, two snapping shrimp species with overlapping ranges in the north-western Atlantic, are similar in morphology, exploit similar ecological niches and appear to represent recently diverged sibling species. We examined phylogenetic and ecological relationships between these two species with: (i) sequence data from two mitochondrial genes (16S rRNA and COI); (ii) data on potential differences in microhabitat distribution for A. armillatus and A. angulatus; and (iii) data from laboratory experiments on the level of reproductive isolation between the two species. DNA sequence data suggest A. armillatus and A. angulatus are sister species that diverged subsequent to the close of the Isthmus of Panama, and that haplotype diversity is lower in A. armillatus than in A. angulatus. Both species are distantly related to A. heterochaelis and A. estuariensis, two species with which A. angulatus shares some similarities in coloration. Ecological data on the distribution of A. angulatus and A. armillatus from two locations revealed differences in distribution of the two species between habitat patches, with each patch dominated by one or the other species. However, there was no apparent difference in distribution of the two species within habitat patches with respect to microhabitat location. Ecological data also revealed that heterospecific individuals often occur in close proximity (i.e. within metres or centimetres) where sympatric. Behavioural data indicated that these species are reproductively isolated, which is consistent with speciation in transient allopatry followed by post-divergence secondary contact. Our data further resolve taxonomic confusion between the sibling species, A. armillatus and A. angulatus, and suggest that sympatry in areas of range overlap and exploitation of similar ecological niches by these two recently diverged species have selected for high levels of behavioural incompatibility.