Ultrastructure of spermiogenesis and spermatozoa in Prorhynchus sp. (Platyhelminthes,Lecithoepitheliata, Prorhynchidae)

Summary

Mature sperm of Prorhynchus sp. have an elongated nucleus, multiple mitochondria and dense bodies, and two free axonemes which are located in grooves of the main shaft for much of their length. The axonemes are subterminally inserted and have the typical 9+ ‘1’ arrangement unique to Platyhelminthes and synapomorphic for taxa of Trepaxonemata. The testis follicles examined had small numbers of developing spermatids and very few mature sperm were present. During spermiogenesis, spermatids remain joined in clusters by distinctive bridges. In each spermatid two centrioles (with an intercentriolar body between them) give rise to free axonemes which grow out in opposite directions from each other. Indistinct ciliary rootlets are present. The axonemes are carried distally from the main spermatid mass on an elongating process and turn back towards the main spermatid mass. Nucleus, mitochondria and dense bodies move into the shaft, and the spermatid elongates before detaching from others in the cluster. This is the first detailed study of sperm and spermiogenesis in Lecithoepitheliata. Mature sperm are distinctly different from those of prolecithophorans, to which they are reputedly related, the latter having aflagellate sperm without dense bodies.     

Ultrastructure of the flame bulbs and protonephridial capillaries of Prorhynchus (Lecithoepitheliata, Prorhynchidae, Turbellaria)

The flame bulb of Prorhynchus is formed by a single cell. Its nucleus is not located in the cytoplasm at the base of the flame. Cilia of the flame have cross-striated hollow ciliary rootlets converging towards their tips. The maximum number of cilia counted was 13. The weir consists of a single row of longitudinal ribs that contain longitudinal filaments and possess regularly arranged protrusions along their surface appearing as transverse bands in horizontal section. A 'membrane' of extracellular material extends between the ribs. and loose material fills the places between the ribs, with a denser layer midway between adjacent ribs. Distally, the ribs fuse to form a continuous tube without a junction. Small protonephridial capillaries lack junctions, larger ducts have lateral flames and patches of long microvilli. Large excretory ducts open into a ciliated and lamellated cavity which is connected by a narrow canal to the excretory pore. The terminal part of the canal close to the pore possesses many cilia and microvilli. Phylogenetic implications of the findings are discussed.     

Resource competition between genetically varied and genetically uniform populations of Daphnia pulex (Leydig): does sexual reproduction confer a short‐term ecological advantage?

Small competitive advantages may suffice to compensate for a large disadvantage in intrinsic growth capacity. This well‐known principle from ecology has recently been applied to the enduring question of how sexual reproduction can persist in the face of invasion by female‐only parthenogens. Small competitive advantages resulting directly from sexual reproduction are predicted to cancel a two‐fold disadvantage in intrinsic growth capacity caused by males (which do not themselves produce offspring) comprising half the sexual population. In this paper we test the principal assumption of this theory, that the genetic variation produced by sexual reproduction confers a competitive advantage over self‐identical asexual invaders. We set up competition between a diverse clonal assembly of Daphnia pulex and genetically uniform populations from single clones. At young ages, the population comprising genetically varied Daphnia had significantly higher birth rates in competition with populations of genetically uniform Daphnia than in competition with itself, indicating competitive release and a Lotka–Volterra competition coefficient α₁₂ < 1. No such difference was apparent under conditions of greater food stress, possibly due to individuals channelling more energy into survival, or for old‐aged populations, possibly as a result of reduced selective pressures for high reproduction in old females. Mean birth rates differed between the clones at all ages in the presence of competition, providing evidence of variation in life history traits between clones. A Lotka–Volterra model predicted empirical estimates of α₁₂ = 0.896 (genetically uniform on varied) and α₂₁ = 1.010 (varied on uniform), which permits immediate coexistence of a sexual population of D. pulex even with an asexual lineage having twice the intrinsic growth capacity. © 2005 The Linnean Society of London, Biological Journal of the Linnean Society, 2005, 85 , 111–123.     

Value of long‐term ecological studies

Long‐term ecological studies are critical for providing key insights in ecology, environmental change, natural resource management and biodiversity conservation. In this paper, we briefly discuss five key values of such studies. These are: (1) quantifying ecological responses to drivers of ecosystem change; (2) understanding complex ecosystem processes that occur over prolonged periods; (3) providing core ecological data that may be used to develop theoretical ecological models and to parameterize and validate simulation models; (4) acting as platforms for collaborative studies, thus promoting multidisciplinary research; and (5) providing data and understanding at scales relevant to management, and hence critically supporting evidence‐based policy, decision making and the management of ecosystems. We suggest that the ecological research community needs to put higher priority on communicating the benefits of long‐term ecological studies to resource managers, policy makers and the general public. Long‐term research will be especially important for tackling large‐scale emerging problems confronting humanity such as resource management for a rapidly increasing human population, mass species extinction, and climate change detection, mitigation and adaptation. While some ecologically relevant, long‐term data sets are now becoming more generally available, these are exceptions. This deficiency occurs because ecological studies can be difficult to maintain for long periods as they exceed the length of government administrations and funding cycles. We argue that the ecological research community will need to coordinate ongoing efforts in an open and collaborative way, to ensure that discoverable long‐term ecological studies do not become a long‐term deficiency. It is important to maintain publishing outlets for empirical field‐based ecology, while simultaneously developing new systems of recognition that reward ecologists for the use and collaborative sharing of their long‐term data sets. Funding schemes must be re‐crafted to emphasize collaborative partnerships between field‐based ecologists, theoreticians and modellers, and to provide financial support that is committed over commensurate time frames.     

Role of Bacteriocin During Plaque Formation by Streptococcus salivarius and Streptococcus sanguis on a Tooth in an Artificial Mouth

Bacteriocinogenic strains of Streptococcus salivarius antagonized Strep. sanguis on blood agar and in Todd-Hewitt broth with, but not without, sucrose. Each organism produced plaque in vitro but, after a mixed inoculum with both organisms, the numbers of Strep. sanguis rapidly fell to <0.01% plaque organisms. A non-bacterio-cinogenic mutant of Strep. salivarius was itself inhibited by Strep. sanguis in the plaque-producing system; derivatives of Strep. sanguis partially resistant to bacteriocin in the plate test nevertheless failed to co-habit plaque with bacteriocinogenic Strep. salivarius. The latter could suppress Strep. sanguis in established monoculture plaque but only if sucrose were continuously supplied. It was concluded that the effect of bacteriocin in plaque formation by these streptococci is linked to other as yet unknown properties which may account for the absence of Strep. salivarius from plaque in vivo .     

The characterization of trypsin-positive black-pigmented Bacteroides isolated from sheep periodontal disease

Twenty trypsin-positive black-pigmented Bacteroides strains independently isolated from periodontal lesions in sheep were characterized by Gram stain, biochemical tests, haemagglutination, gas liquid chromatography, API ZYM system profiles and catalase activity. All strains reacted uniformly in these tests, the reactions closely resembling those reported for human strains of Bacteroides gingivalis .     

Ultrastructure of the pharynx of Prorhynchus (Platyhelminthes, Lecithoepitheliata)

The pharynx variabilis of Prorhynchus is strongly muscular, with a small pharyngeal fold and a thin surrounding sheath. There is one row of inner longitudinal musclcs, up to six rows of inner circular muscles, many radial muscles, one row of outer circular and one row of outer longitudinal muscles, with no sphincter muscle groups. Three kinds of secretion, produced in a cluster of gland cell bodies posterior to the pharynx, enter the pharynx wall. They travel anteriorly in ducts and two kinds unite in a common duct just prior to discharging into the anterior region of the pharynx lumen. The perikarya of lumen epithelial cells lie within the pharynx musculature and, at the anterior and posterior margins of the pharynx, external to the pharynx. Bundles of ciliated receptors are numerous at the anterior and posterior constrictions. Similarities in the ultrastructure of flame bulbs of Rhabdocoela and Lecithoepitheliata suggest a relationship between these groups. However, the usefulness of pharynx ultrastructure for platyhelminth phylogeny cannot be assessed until complete ultrastructural studies of various groups of Rhabdocoela have been made.     

The ultrastructure of the protonephridial system of Götte's larva of Stylochus mediterraneus (Polycladida, Platyhelminthes)

The protonephridial system of Götte's larva of Stylochus mediterraneus was studied by electron microscopy. There is one protonephridium on each side of the body, formed by one terminal and one canal cell. The terminal filtration apparatus is formed by a single cell (the terminal cell) with several globular processes, the largest of which includes the nucleus. Fingers of cytoplasm (leptotriches) from each process penetrate the lumen surrounding the bundle of cilia and fingers from adjacent processes interdigitate to form a pattern of convoluted slits which constitute the weir. The single canal cell is inserted internally to the terminal cell at the top of the weir and encloses the lumen without a junction. Septate junctions are present between the terminal and canal cells. The lumen of the canal cell is smooth-walled for most of its length and cilia arise and terminate at all levels of the terminal and canal cells. Posterior to the larval mouth opening, the canal cell crosses the epithelium and the lumen ramifies to form the excretory opening. The terminal apparatus closely resembles that found in the freshwater planarian Bdellocephala brunnea .     

Spermiogenesis and sperm ultrastructure in Cylindrostoma fingalianum (Platyhelminthes,Prolecithophora) with notes on a protozoan (kinetoplastid) symbiont closely associated with allosperm

Summary

The only positive synapomorphy uniting members of the platyhelminth turbellarian taxon, Prolecithophora, is a peculiar membranous system present in much of the shaft of the sperm. This investigation followed the development of this membrane system during spermiogenesis in Cylindrostoma fingalianum and its appearance in the mature sperm. Formation begins with invaginations of the early spermatid shaft outer cell membrane. The invaginations enlarge and the membrane becomes increasingly folded. They appear to be subsequently supplemented with membranous material supplied by an extensive vacuolar system originating from the Golgi apparatus in the main cytoplasmic mass of the spermatid. Throughout development, and in mature sperm, the membranous system forms a part of the outer cell membrane and is also intimately associated with the elongate mitochondrion that lies between the membranous column and the nucleus. The nucleus is highly lobed and the sperm cell lacks flagella or axonemes or the dense bodies found in most other turbellarian taxonomic divisions. A kinetoplastid protozoon present in considerable numbers amongst allosperm is also described.