Coding sequences (5,334 nt total) from elongation factor-la, elongation factor-2, and the largest subunit of RNA polymerase I1 were determined for 6 species of Tardigrada, 2 of Arthropoda, and 2 of Onychophora. Parsimony and likelihood analyses of nucleotides and amino acids yielded strong support for Tardigrada and all internal nodes (i.e., 100% bootstrap support for Tardigrada, Eutardigrada, Parachela, Hypsibiidae, and Macrobiotidae). Results are in agreement with morphology and an earlier molecular study based on analysis of 18s ribosomal sequences. Divergence times have been estimated from amino acid sequence data using an empirical Bayesian statistical approach, which does not assume a strict molecular clock. Divergence time estimates are pre-Vendian for Tardigrada/Arthropoda, Vendian or earlier for Eutardigrada/Heterotardigrada, Silurian to Ordovician for ParacheldApochela, Permian to Carboniferous for Hypsibiidae and Macrobiotidae, and Mesozoic for Isohypsibius/Thulinia (both within Hypsibiidae) and Macrobiotus/Richtersius (both within Macrobiotidae).

The eyes of aquatic pulmonates differ from those of terrestrial pulmonates; the latter, in species such as Cepaea nemoralis and Trichia hispidu, possess conventional, cup-shaped retinas, but the aquatic species Lymnaeu stugnalis, Radix peregra, Plzysa jontinalis, and Planorharius corizeus have retinas that are partitioned into dorsal and ventral depressions (“pits”). The pits are separated by an internal ridge, called the “crest”, and on account of their pigmentation can be seen in vivo. The dominant cellular components of the retinae of terrestrial as well as aquatic snails are pigmented cells and microvillar photoreceptors, the latter occurring in two morphologically distinct types (I and II). Aquatic snails with preferences for shallow water possess eyes with both type I and type I1 photoreceptive cells, but PI. corneus, an inhabitant of deeper water, only has type-I receptors, supporting an earlier finding that type I cells represent dim- and type IT cells bright-light receptors. On the basis of histological and optical comparisons, we conclude that the eyes of L. stngizutis and R.peregra, species that are known to escape and seek temporary refuge above the water surface, are well adapted to function in water as well as air, but that the eyes of P. fontinalis and Pl. corneus are less modified from those of their terrestrial ancestors.

Our results suggest that freshwater pulmonates like Lymnaea stagnalis, Radix peregra, Physa,fhntinalis, and Planorbarius corneus have inherited froin their terrestrial ancestors eyes with a spherical, immobile lens with fixed focal–length optics. Unable to change the dioptric apparatus to form an image under water, modifications to the retina had to occur if sharp vision was required. Computer–assisted calculations and 3–D eye reconstructions demonstrate that the photoreceptors in the deeper, ventral pit are in a position to perceive focused images under water. Vision in air, however, would favour photoreceptive cells located in the shallower, dorsal pit. On the basis of histological, ethological, and optical comparisons, we conclude that the eyes in L. stagnalis and R. peregra, species that are known to escape and seek temporary refuge above the water surface, are well adapted to function in water as well as air, but that the eyes in P. fontinalis and PI. corneus are less modified from those of their terrestrial ancestors. We also conclude that good resolving power may be of greater importance in the aquatic pulmonates than the terrestrial species, since the former have to locate thin, vertical stems of reeds and sedges to ascend in order to reach the surface to breathe.

In this work we investigated the involvement of putative nitric oxide (NO)-forming neurons in enteric plexuses of stylommatophoran gastropods. The nitric oxide synthase (NOS)containing cells were detected by NADPH diaphorase (NADPHd) histochemistry in the entreral nervous systems of several stylommatophoran species (Achatinacea: Achatina,fulica, Helicacea: Cepaea hortensis, Cepaea nemoralis, Discus rotundatus, Helicella obvia, Helix lucorurn, Helix lutescens, Monachoides umbrosa, Trichia hispida, Zebrina detrita, Succineacea: Succinea putris, Vertiliginacea: Clausilia dubia, Zonitacea: Arion ater, Arion subfuscus, L i m a maximus). We detected the NO synthesis of isolated midintestinal segments by Griess's quantification of nitrite, one end product of NO. Effects of the NOS substrate L-arginine and the NOS inhibitor Nw-nitro-L-arginine (NOARG) were also tested on nitrite production. We found NADPHd-reactive neurons and extrinsic nerves with NADPHd-stained fibers within the myenteric and submucosal networks of the midintestine of investigated members of Helicacea, Succineacea, and Vertiliginacea families. These networks innervated the midintestinal musculature and several nerve cells of the myenteric and submucosal plexi. In investigated members of Achatinacea and Zonitacea, NADPHd-stained networks were not detectable within the digestive tract. Administration of 1 mM L-arginine elevated, whereas 2 mM of NOARG diminished, the nitrite levels of the NADPHd-stained networks containing midintestine in C. nemoralis and H. lucarum. Enteral NADPHd staining was not detected in A. ater and L. maximus, and the nitrite production was not affected by L-arginine. Our results indicate a possible, but evolutionarily not conserved, NO-mediated enteral transmission in stylommatophoran gastropods.

The polychaete Boccardia proboscidea has poecilogonous development that includes the production of both planktotrophic and adelphophagic young. In this study, we use scanning electron microscopy to analyse external morphogenesis of planktotrophic offspring with emphasis on early embryos, morphogenesis during metamorphosis, and the dynamic nature of larval structures during early ontogeny. Larval growth involves addition of terminal chaetigers and formation of segment-specific structures such as cilia and chaetae. Our observations reveal that most ciliary bands are reduced or incomplete relative to those found in larvae of other polychaete families. We describe a small metatroch (consisting of only a few trochoblasts) in early embryos, which has not previously been reported in the Spionidae. The presence of the metatroch does not imply a function in opposed-band feeding, as a food groove intermediate between the prototroch and metatroch is lacking. A neurotroch, inconsistently reported in the Spionidae, is also present and terminates in a ciliated pit. Many larval structures (e.g., presumptive sensory organs) are short-lived, implying a shift towards early functionality of adult traits in larvae. Metamorphosis is gradual and occurs over the latter half of the larval life. The reduction of larval structures, and early development of adult traits, suggests an overall shift in morphology facilitating settlement and juvenile development.

The expected proportion of males in androdioecious populations (those comprised of males and hermaphrodites) largely depends on the fertilization opportunities of males. If male mating opportunities are low due to restricted access to hermaphroditic eggs, then populations will be hermaphrodite-biased. Hermaphrodites have two mechanisms available to limit male mating success: (1) pre-mating barriers to outcrossing, in which hermaphrodites choose not to pair with males and (2) post-mating barriers to outcrossing, in which hermaphrodite sperm has greater access to eggs than male sperm. In this study, we measured male mating success in the androdioecious clam shrimp Eulimnadia texana when pre-mating barriers to outcrossing were removed. These branchiopod crustaceans are small (5-8 mm), filter feeders that live in ephemeral pools in the deserts of the southwestern United States. Using genetic markers, we measured male mating success in laboratory experiments in two populations of these shrimp. We correlated mating success with clasping time, clasping during egg transfer, and male thrusting during egg transfer. Males fertilized an average of 24-40% of the hermaphrodites' eggs. Outcrossing success was positively correlated with clasping duration, and was nearly an order of magnitude higher for males thrusting during egg transfer relative to thrusting at other times during pairing. Because these estimates of mating success were similar to previously reported estimates (in which both pre- and post-mating barriers to outcrossing were potentially important), we deduced that pre-mating barriers to outcrossing do not greatly decrease male outcrossing success in E. texana; the low fertilization (25-50% of available eggs) by males is thus due to post-mating barrier(s) to outcrossing.

In contrast to marine bryozoans, the lophophore structure and the ciliary filter-feeding mechanism in freshwater bryozoans have so far been only poorly described. Specimens of the phylactolaemate bryozoan Plumatella repens were studied to clarify the tentacular ciliary structures and the particle capture mechanism. Scanning electron microscopy revealed that the tentacles of the lophophore have a frontal band of densely packed cilia, and on each side a zigzag row of laterofrontal cilia and a band of lateral cilia. Phalloidin-linked fluorescent dye showed no sign of muscular tissue within the tentacles. Video microscopy was used to describe basic characteristics of particle capture. Suspended particles in the incoming water flow, set up by the lateral ‘pump’ cilia on the tentacles, approach the tentacles with a velocity of 1-2 mm s^-1.Near the tentacles, the particles are stopped by the stiff sensory laterofrontal cilia acting as a mechanical sieve, as previously seen in marine bryozoans. The particle capture mechanism suggested is based on the assumed ability of the sensory stiff laterofrontal cilia to be triggered by the deflection caused by the drag force of the through-flowing water on a captured food particle. Thus, when a particle is stopped by the laterofrontal cilia, the otherwise stiff cilia are presumably triggered to make an inward flick which brings the restrained particle back into the downward directed main current, possibly to be captured again further down in the lophophore before being carried to the mouth via the food groove. No tentacle flicks and no transport of captured particles on the frontal side of the tentacles were observed. The velocity of the metachronal wave of the water-pumping lateral cilia was measured to be ˜0.2 mm s^-1, the wavelength was ˜7 μm, and hence the ciliary beat frequency estimated to be ˜30 Hz (˜20 “C). The filter feeding process in P. repens reported here resembles the ciliary sieving process described for marine bryozoans in recent years, although no tentacle flicks were observed in P. repens. The phylogenetic position of the phylactolaemates is discussed in the light of these findings.

To determine patterns of resource allocation among ascidians, we studied 16 colonial and solitary species. We measured investment in reproductive vs. structural material (tunic) both in terms of weight and caloric content, as well as fecundity and degree of larval complexity in the colonial species. Measurements in weight and caloric content were highly correlated in the species studied. A wide range of investment in reproduction was found. Tunic production was related to the growth form of the species, stolonic and solitary species investing less in tunic than massive species, but no significant relationship was found between investment in tunic production vs. reproduction. In colonial species we found that in species with small zooid size, the reproductive investment per zooid was significantly higher. There was a significant negative relationship between investment in reproduction and fecundity. We also found a significant relationship between reproductive investment and larval complexity. The overall trend was that species with low fecundity had large complex larvae and invested the most energy in reproduction.