Rhythms of locomotion expressed by Limulus polyphemus, the American horseshoe crab: I. Synchronization by artificial tides

Limulus polyphemus, the American horseshoe crab, has an endogenous clock that drives circatidal rhythms of locomotor activity. In this study, we examined the ability of artificial tides to entrain the locomotor rhythms of Limulus in the laboratory. In experiments one and two, the activity of 16 individuals of L. polyphemus was monitored with activity boxes and "running wheels." When the crabs were exposed to artificial tides created by changes in water depth, circatidal rhythms were observed in animals exposed to 12.4-h "tidal" cycles of either water depth changes (8 of 8 animals) or inundation (7 of 8 animals). In experiment three, an additional 8 animals were exposed to water depth changes under cyclic conditions of light and dark and then monitored for 10 days with no imposed artificial tides. Most animals (5) clearly synchronized their activity to the imposed artificial tidal cycles, and 3 of these animals showed clear evidence of entrainment after the artificial tides were terminated. Overall, these results demonstrate that the endogenous tidal clock that influences locomotion in Limulus can be entrained by imposed artificial tides. In the laboratory, these tidal cues override the influence of light/dark cycles. In their natural habitat, where both tidal and photoperiod inputs are typically always present, their activity rhythms are likely to be much more complex.     

Circalunidian clocks control tidal rhythms of locomotion in the American horseshoe crab,Limulus polyphemus

While many intertidal animals exhibit circatidal rhythms, the nature of the underlying endogenous clocks that control these rhythms has been controversial. In this study American horseshoe crabs, Limulus polyphemus, were used to test the circalunidian hypothesis by exposing them to four different tidal regimes. Overall, the results obtained support the circalunidian hypothesis: each of the twice-daily rhythms of activity appears to be controlled by a separate clock, each with an endogenous period of approximately 24.8 h. First, spontaneous “skipping” of one of the daily bouts was observed under several different conditions. Second, the presence of two bouts of activity/day, with different periods, was observed. Lastly, we were able to separately synchronize bouts of activity to two artificial tidal regimes with different periods. These results, taken together, argue in favor of two separate circalunidian clocks in Limulus, each of which controls one of the two bouts of their daily tidal activity rhythms.     

Circatidal rhythms of locomotion in the American horseshoe crab Limulus polyphemus: Underlying mechanisms and cues that influence them

<正> While eye sensitivity in the American horseshoe crab Limulus polyphemus has long been known to be under the controlof an endogenous circadian clock, only recently has horseshoe crab locomotion been shown to be controlled by a separateclock system. In the laboratory, this system drives clear activity rhythms throughout much of the year, not just during the matingseason when horseshoe crabs express clear tidal rhythms in the field. Water temperature is a key factor influencing the expressionof these rhythms: at 17℃ tidal rhythms are expressed by most animals, while at 11℃ expression of circatidal rhythms is rarelyseen, and at 4℃ rhythms are suppressed. Neither long (16:8 Light:Dark) nor short (8:16) photoperiods modify this behavior atany of these temperatures. Synchronization of these circatidal rhythms can be most readily effected by water pressure cycles bothin situ and in the lab, while temperature and current cycles play lesser, but possibly contributory, roles. Interestingly, Light:Darkcycles appear to have synchronizing as well as masking effects in some individuals. Evidence that each of two daily bouts ofactivity are independent suggests that the Limulus circatidal rhythm of locomotion is driven by two (circalunidian) clocks, eachwith a period of 24.8h. While the anatomical locations of either the circadian clock, that drives fluctuations in visual sensitivity, orthe circatidal clock, that controls tidal rhythms of locomotion, are currently unknown, preliminary molecular analyses have shownthat a 71 kD protein that reacts with antibodies directed against the Drosophila PERIOD (PER) protein is found in both the protocerebrumand the subesophageal ganglion     

The chemorepellent semaphorin is expressed in the horseshoe crab, Limulus polyphemus.

Semaphorins are a family of soluble and membrane-bound proteins that play a critical role in axonal guidance and other processes of neuronal development. Currently, more than twenty semaphorins have been identified, all of which share a conserved 500 amino acid domain near the amino terminus. Semaphorins are divided into eight classes according to species of origin and structural similarities. Classes 1 and 2 are found in invertebrates, classes 3 through 7 are present in vertebrates and viruses encode class V semaphorin. Microarray analysis of Limulus CNS RNA revealed the presence of a semaphorin-like gene in Limulus polyphemus. Based on these data, we aligned 31 different sequences and designed degenerate primers for the consensus domains (WTT/SFLKA) and (DPY/VCA/GW). RT-PCR products were generated using 6 forward primers and 4 reverse primers. The expected size PCR products (750 bp) was obtained and then ligated with pCR II TOPO vector and transferred into E. coli Top 10. Five partial semaphorin cDNAs were found in Limulus: semaphorins 1a, 1b, 2a, 2b and F (now known as 5) were partially cloned. Subsequent Northern blot analyses using these Limulus specific-probes revealed hybridization with total RNAs purified from six different tissues.     

Spermiogenesis in the horseshoe crab,Limulus polyphemus

Groups of spermatids of Limulus polyphemus undergo differentiation in thin-walled cysts within the seminiferous tubules. The nucleus compacts to a spherical shape, but retains a much less condensed nuclear appendage, whose unique pores are each surrounded by a microtubule. The appendage, unmodified mitochondria, glycogen, and coated vesicles, all present in the mature spermatozoon, suggest an unusual degree of metabolic self-sufficiency of the cell. The acrosome is associated with a 50 μ-long acrosomal filament that penetrates the nucleus during spermiogenesis and coils up in the cytoplasm, enveloped by two outer nuclear membranes. The filament, which eventually comes to lie in the circumnuclear cisterna, retains a covering of one membrane during its discharge at the time of the acrosome reaction. The posterior region of the head forms a thin-walled collar with peculiar internal supports around the base of the flagellum. Serverance of intercellular bridges between spermatids, cytoplasm elimination, and rupture of the cyst precede liberation of the immature spermatozoa into the lumen of the seminiferous tubules. Notwithstanding its peculiarities, the Limulus spermatozoon, with its simple shape closely resembling that of annelids and molluscs, represents the most primitive arthropod spermatozoon congruent with the evolutionary stability of the xiphosurans.     

Primary structure of anti-lipopolysaccharide factor from American horseshoe crab, Limulus polyphemus

The complete amino acid sequence of anti-lipopolysaccharide (LPS) factor purified from the hemocytes lysate of the American horseshoe crab, Limulus polyphemus, was determined by characterization of the NH2-terminal sequence and the peptides generated after digestion of the protein with lysyl endopeptidase, clostripain, and Staphylococcus aureus V8 protease. Upon sequencing the peptides by the automated Edman method, the following primary structure was obtained: (Sequence: in text). During the sequence analysis, two species of the protein, which differed from each other at one locus, were found and characterized. L. polyphemus anti-LPS factor was a basic protein consisting of a single polypeptide chain of 101 residues and a calculated molecular weight of 11,786 or 11,800. The hydrophobic NH2-terminal sequence and the clustering of positive charges found in the disulfide loop yielded a typical amphipathic character of this protein. Moreover, L. polyphemus anti-LPS factor showed 83% sequence identity with the Tachypleus tridentatus protein, and the sequence similar to that observed in the EF-hand structure was found to contain in the COOH terminal portions of these proteins, although its function is unknown.     

Histamine metabolism in the visual system of the horseshoe crab Limulus polyphemus

There is now strong evidence that arthropod photoreceptors use histamine as a neurotransmitter. The synthesis, storage and release of histamine from arthropod photoreceptors have been demonstrated, and the postsynaptic effects of histamine and the endogenous neurotransmitter are similar. However, a full understanding of these photoreceptor synapses also requires knowledge of histamine inactivation and metabolism. Relatively little is known about histamine metabolism in the nervous system of arthropods, and mechanisms appear to differ with the species. This study focuses on histamine metabolism in visual tissues of the horseshoe crab Limulus polyphemus, a chelicerate. We present two major findings: (1) histamine is metabolized to imidazole acetic acid and to gamma-glutamyl histamine. (2) relatively low levels of histamine metabolites accumulate in Limulus visual tissues.     

Cuticular proteins from the horseshoe crab,Limulus polyphemus

Proteins were purified from the carapace cuticle of a juvenile horseshoe crab, Limulus polyphemus, and several of them were characterized by amino acid sequence determination. The proteins are small (7-16 kDa) and their isoelectric points range from 6.5 to 9.2. They have high contents of tyrosine, ranging from 13.5 to 35.4%. Some of the proteins show sequence similarity to cuticular proteins from other arthropod groups, with the most pronounced similarity to proteins from the cuticle of the spider Araneus diadematus. Two proteins show sequence similarity to a hexamerin storage protein from Blaberus discoidalis.     

The morphology of the horseshoe crab (Limulus polyphemus) visual system

Summary Efferent fibers to the compound eye of the horseshoe crab, Limulus polyphemus, not only innervate the various pigment cells, but also invade the eccentric cell dendrite and the retinula cells. This finding provides a structural basis for the coupling of circadian rhythm between the efferents and the receptor cells.This short communication is Publication No. 1130 of the Oregon Regional Primate Research Center. The research was supported by Grants RR-00163 and EY-00392 from the National Institutes of Health     

Lipids from nerve tissues of the horseshoe crab, Limulus polyphemus.

1. The predominant lipids of nerve cords, ganglion and brain from horseshoe crabs were cholesterol (11% of lipid) and phospholipid (81% of lipid). 2. Major phospholipids were phosphatidyl ethanolamine and phosphatidyl choline with lesser amounts of phosphatidyl serine and phosphatidyl inositol and sphingomyelin. 3. The phospholipid fraction was characterized by a high content of plasmalogen, i.e. alk-1-enyl acyl phosphatides, so that 42% of the ethanolamine phosphatides were the plasmalogen, phosphatidal ethanolamine. 4. Phosphatidyl choline and phosphatidyl ethanolamine were high in polyunsaturation with 20:4 and 20:5 major fatty acids. Sphingomyelin had predominantly long chain saturated fatty acids. 5. Cerebrosides and gangliosides, which are associated with vertebrate nerve tissues, were absent from nerves of horseshoe crabs.     

Green algal infection of American horseshoe crab (Limulus polyphemus) exoskeletal structures

Degenerative lesions in the dorsum of the horseshoe crab (Limulus polyphemus) exoskeleton, eyes, arthrodial membrane, and base of the telson were documented in a population of wild caught laboratory animals. The disease can lead to loss of tissue structure and function, deformed shells, abnormal molting, loss of ocular structures, erosion of interskeletal membranes, and cardiac hemorrhage. Microscopy, histopathology, and in vitro culture confirmed the causative agent to be a green algae of the family Ulvaceae. Further research may explain how green algae overcome horseshoe crab innate immunity leading to external and internal damage.     

Presence of microorganisms in hemolymph of the horseshoe crab Limulus polyphemus.

Hemolymph samples obtained from Limulus polyphemus at the time of collection and after a 1-week holding period exhibited a significant increase in bacterial levels. No differences were observed in the ability of amoebocyte lysate, prepared from these same samples, to gel in the presence of lipopolysaccharide.     

An atlas of the brain of the horseshoe crab Limulus polyphemus

An atlas of the brain of the horseshoe crab Limulus polyphemus is developed. All of the neuronal groups are identified and named, and regions of neuropil are segregated and named where possible. The nomenclature incorporates functionally neutral earlier names and assigns geographical names to newly distinguished structures. The atlas provides a basis for correlating the results of neuroanatomical, neurophysiological, and neurochemical studies, which yield information about individual neurons or groups of neurons in this species.     

Spatial control of photomechanical movements in the lateral eye of the American horseshoe crab, Limulus polyphemus

This study asks whether photomechanical movements in the retinal cells of the lateral eye of the American horseshoe crab, Limulus polyphemus, are controlled locally within each ommatidium, or whether they are a retinal array property involving lateral communication between ommatidia. Three experiments were performed. A small spot, a vertical slit down the center, or the anterior third of an otherwise masked eye was illuminated. The contralateral eye was fully illuminated in each experiment and served as a light-adapted control. Morphometric analyses of aperture length and rhabdom dimensions were made from serial 1-microm plastic sections. The results suggest there is a different spatial threshold for photomechanical movement for aperture lengthening than for rhabdom lengthening. When only a few ommatidia are illuminated, the aperture does not change. When about 10% are illuminated, they lengthen, but the masked ommatidia do not. When about a third are illuminated, all the ommatidia in the eye lengthen together, including the two thirds that were masked. When either only a few ommatidia or about 10% of the ommatidia are illuminated, rhabdom shape is unchanged. When a third of the eye is illuminated, the illuminated rhabdoms lengthen, but the masked rhabdoms do not.