Ultrastructure of the water-movement-sensitive sensilla in the medicinal leech

Behavioral and physiological experiments have shown that medicinal leeches are able to detect low amplitude surface waves, and further, that the transduction of this stimulus modality occurs primarily, if not exclusively, at the annular sensilla (Young, Dedwylder, and Friesen, 1981; Friesen, 1981). Here we examine the morphology of these specialized sensory structures using light, scanning electron, and transmission electron microscopes. We found that three types of ciliated sensory cells occur at the sensilla: (1) a uniciliate cell, with an axial cilium that projects at least 12 μm beyond the cuticle; (2) a multiciliate cell with from two to four grouped cilia that extend 1–3 μm beyond the cuticle; and (3) a second multiciliate cell, whose cilia project parallel to the body surface but remain within the cuticle. The cilia of all three cell types arise from the cuplike depressions which form the apices of slender, elongated cells (approximately 2 μm diameter × 50 μm length). A complexly interconnected ring of microvilli surrounds the cilium of the uniciliate cells. The morphology of the uniciliate cells closely resembles the structure of vibration-sensitive sensory neurons found in other species. We propose, based on previous results and our new findings, that the uniciliate receptor cells are the sensillar movement receptors which mediate leech sensitivity to water movements.     

Morphological and biochemical characterization of mineralizing primary cultures of avian growth plate chondrocytes: Evidence for cellular processing of Ca2+ and Pi prior to matrix mineralization

Advances in the culture of mineralizing growth plate chondrocytes provided an opportunity to study endochondral calcification under controlled conditions. Here we report that these cultures synthesize large amounts of proteins characteristically associated with mineralization: type II and X collagens, sulfated proteoglycans, alkaline phosphatase, and the bone-related proteins, osteonectin and osteopontin. Certain chondrocytes appeared to accumulate large amounts of Ca²⁺ and Pi during the mineralization process: laser confocal imaging revealed high levels of intracellular Ca²⁺ in their periphery and X-ray microanalytical mapping revealed the presence of many Ca²⁺- and Pi-rich cell surface structures ranging from filamentous processes 0.14 ± 0.02 μm by 0.5–2.0 μm, to spherical globules 0.70 ± 0.27 μm in diameter. Removal of organic matter with alkaline sodium hypochlorite revealed numerous deposits of globular (0.77 ± 0.19 μm) mineral (calcospherites) in the lacunae around these cells. The size and spatial distribution of these mineral deposits closely corresponded to the Ca²⁺-rich cell surface blebs. The globular mineral progressively transformed into clusters of crystallites. Taken with earlier studies, these findings indicate that cellular uptake of Ca²⁺ and Pi leads to formation of complexes of amorphous calcium phosphate, membrane lipids, and proteins that are released as cell surface blebs analogous to matrix vesicles. These structures initiate development of crystalline mineral. Thus, the current findings support the concept that the peripheral intracellular accumulation of Ca²⁺ and Pi is directly involved in endochondral calcification.     

Cytostructural dynamics of spreading and translocating cells

Cytostructural changes during fibroblast spreading and translocation and during the transition between the two states have been studied in living cells and in the same cells after fixation and immunofluorescent staining. In time-lapse sequences we observe that birefringent arcs, sometimes circles, concentric with the cell perimeter, form near the periphery of a spreading cell, or that arcs form near the leading edge of a locomoting cell. The arcs move toward the nucleus, where they disappear. In spreading cells, radial stress fibers extend from the region of the cell nucleus to the periphery. The arcs or circles and the stress fibers are visualized in the same cells after fixation and staining with fluorescein-conjugated antiactin antibodies. Stained images of spreading cells show the arcs and stress fibers in the same plane of focus. At points of intersection with arcs, stress fibers are bent toward the substrate on which the cell is moving. During a transitional stage between spreading and translocation the cytostructure undergoes reproducible changes. Arcs and circle cease to form. The radial stress fibers elongate, spiral around the nucleus, and move to the periphery as a band of filaments. We interpret the moving arcs as condensations of a microfilament network that move toward the nucleus as compression waves. As elements of the net are brought close together by the compression wave, contraction may occur and facilitate the condensations.     

Displacement and Return Movement of Chloroplasts in the Marine Dinophyte Pyrocystis noctiluca. Experiments with Optical Tweezers

Infrared laser traps (optical tweezers) were used to study laser-induced organelle movements in the marine alga Pyrocystis noctiluca (Dinophyta). These cells are highly suitable for optical micromanipulation due to their large size and extensive vacuole. Experiments were done with plastids held by optical tweezers and moved from the nuclear area into the vacuole. The subsequent retraction movement was analysed for speed. The displaced organelles remained connected to their original position by a thin cytoplasmic strand, often less than 1 μm in diameter. When the organelles were released they rapidly returned at an initial rate of 81.7 ± 7.8 μm . s^?1 (overall displacement 50 μm, measured distance 20 μm, 25 °C ± 1 °C, number of cells 22), slowing down with progressive retraction of the connecting strand. The return movement was reduced to 4.2 ± 0.2 μ .s^?1 (n = 10) when the organelles were displaced and held for 1 min. Displacement to a longer distance increased the rate of return movement. A change from a high to a low environmental temperature significantly reduced movement from 94.5 ± 9.0 . s^?1 (30 °C ± 1 °C, n = 22) to 34.5 ± 2.7 μm .s^?1 (5°C ± 1 °C, n = 22). Nocodazole and N-ethylmaleimide (NEM), inhibitors of microtubules and acto-myosin, respectively, did not affect the retraction of the connecting strand, but at high concentrations of NEM it became increasingly difficult to move organelles away from the nuclear area. We suggest that the return movement of organelles within laser-induced artificial strands mainly depends on the viscoelastic properties of the tonoplast. The quantification of these properties by optical tweezers allows determination of reactions of plant cells to temperature changes.     

Movement of a non-flagellate spermatozoon: A study of the male gamete of Nematospiroides dubius (Nematoda)

The spermatozoa of Nematospiroides dubius were studied using the scanning electron microscope and time-lapse cinematography. Spermatozoa undergo a profound change in morphology after insemination: they change from an elongate structure, 16–18 μm long, to a more rounded form about 5–10 μm in diameter. Spermatozoa from female worms stuck to, and migrated across a glass surface by the production of pseudopodia, but they adhered more readily to a glass surface coated with egg albumin. The average speed of a sample of six differentiated spermatozoa was 7·3 μm/min. Their locomotion is not considered to be amoeboid but resembles the movement of monopodial neutrophils. A hypothesis for the mechanism of movement is presented, and other possible functions of the pseudopodial region are discussed.     

Protein Arcs May Form Stable Pores in Lipid Membranes

Electron microscopy and atomic force microscopy images of cholesterol-dependent cytolysins and related proteins that form large pores in lipid membranes have revealed the presence of incomplete rings, or arcs. Some evidence indicates that these arcs are inserted into the membrane and induce membrane leakage, but other experiments seem to refute that. Could such pores, only partially lined by protein, be kinetically and thermodynamically stable? How would the lipids be structured in such a pore? Using the antimicrobial peptide protegrin-1 as a model, we test the stability of pores only partially lined by peptide using all-atom molecular dynamics simulations in POPC and POPE/POPG membranes. The data show that, whereas pure lipid pores close rapidly, pores partially lined by protegrin arcs are stable for at least 300 ns. Estimates of the thermodynamic stability of these arcs using line tension data and implicit solvent calculations show that these arcs can be marginally stable in both zwitterionic and anionic membranes. Arcs provide an explanation for the observed ion selectivity in protegrin electrophysiology experiments and could possibly be involved in other membrane permeabilization processes where lipids are thought to participate, such as those induced by antimicrobial peptides and colicins, as well as the Bax apoptotic pore.     

Protein Arcs May Form Stable Pores in Lipid Membranes

Electron microscopy and atomic force microscopy images of cholesterol-dependent cytolysins and related proteins that form large pores in lipid membranes have revealed the presence of incomplete rings, or arcs. Some evidence indicates that these arcs are inserted into the membrane and induce membrane leakage, but other experiments seem to refute that. Could such pores, only partially lined by protein, be kinetically and thermodynamically stable? How would the lipids be structured in such a pore? Using the antimicrobial peptide protegrin-1 as a model, we test the stability of pores only partially lined by peptide using all-atom molecular dynamics simulations in POPC and POPE/POPG membranes. The data show that, whereas pure lipid pores close rapidly, pores partially lined by protegrin arcs are stable for at least 300 ns. Estimates of the thermodynamic stability of these arcs using line tension data and implicit solvent calculations show that these arcs can be marginally stable in both zwitterionic and anionic membranes. Arcs provide an explanation for the observed ion selectivity in protegrin electrophysiology experiments and could possibly be involved in other membrane permeabilization processes where lipids are thought to participate, such as those induced by antimicrobial peptides and colicins, as well as the Bax apoptotic pore.     

Effect of cell movement by random mixing between the surface and bottom of photobioreactors on algal productivity

Effect of algae movement, as a result of random mixing, between the surface and bottom zones of shallow, moderately deep and deep photobioreactors (incident light intensities per unit volume were 8125, 4062 and 2031 μmol·m⁻³·s⁻¹, respectively) on the reactor productivity was investigated. The results showed that at low cell concentrations, movement of cells between the surface and bottom zones of shallow and moderately deep reactors had no significant effect on Chlorella pyrenoidosa C-212 growth and productivity. However, as the cell concentration in the reactors increased, cell movement between the two zones resulted in increased productivity of the shallow reactor but decreased productivity of the moderately deep reactor. On the other hand, in the deep reactor, random movement of cells between the two zones resulted in decreased Chlorella growth rate regardless of the cell concentration. This may be attributed to the fact that at high cell concentration or in a deep reactor, if the cells move between the surface and bottom of the reactor, they spend too long a time in the dark part of the reactor where there is no cell growth, and endogenous respiration as well as cell death may lead to a decrease in cell concentration. When Spirulina platensis M-135 cells were cultivated in the deep reactor, even at high cell concentration, movement of cells between the surface and bottom zones of the reactor led to an increase in the reactor productivity. The reasons for the difference in the results obtained with these two strains of algae could be attributed to the difference in their light requirements since it was found that the saturation light intensity and specific decrease in cell concentration when incubated in the dark were lower for Spirulina than for Chlorella cells.     

Wound healing in the cornea of the chick embryo: III. The influence of pore size of millipore filters on the migration of isolated epithelial sheets in culture

The migratory activity of epithelia isolated from the cornea and the dorsal skin of chick embryos of different ages was examined in vitro. Five types of Millipore filters differing in pore size served as models to represent degrees of unevenness of the substrate instead of the natural wound beds of the corneal stroma and the dorsal dermis. Migration of the epithelium was rapid and extensive when the pore size was below 0.8 μm, but was inhibited or stopped when the pore size reached or exceeded 0.8 μm. The effect of surface properties of the substratum on the motility of the cell membrane and thus on the movement of the cells is discussed.     

BIOGEOGRAPHY OF INDO-PACIFIC CICADOIDEA: A TENTATIVE RECOGNITION OF AREAS OF ENDEMISM

Abstract— The biogeography of the cicadas of the Indo-Pacific is discussed in relation to paleogeography and compared with distribution patterns found in other groups of organisms. The cicadas show a low degree of endemism in the mainland of southeast Asia and the Greater Sunda Islands, and a high degree of endemism in Sulawesi, New Guinea, and the islands of the west Pacific. The biogeography of the cicadas of these regions with high endemism is analyzed for four groups: the subtribe Cosmopsaltriaria, the tribe Prasiini, the genus Baeturia , and the Pacific Cryptotympanini. A review of the paleogeography of the Indo-Pacific, specifying the relevant barriers, island arcs, and land connections, is provided. The recognized areas of endemism are tentatively related to the geological history of the Indo-Pacific. Areas of endemism are the Sulawesi Arcs and the Outer and Inner Melanesian Arcs. New Guinea appears to be a composite of areas of different origin: the central mountains of the Inner Melanesian Arc, the north-coast mountains of the Outer Melanesian Arc, and the Vogelkop area, which is of uncertain origin. The Papuan Peninsula of New Guinea seems to be a zone of overlap between the Outer and the Inner Melanesian Arcs. The Pacific archipelagos of the Outer Melanesian Arcs (viz., the Bismarck Archipelago, Solomon Islands, Vanuatu, and the Fiji, Tonga, and Samoa Islands) represent distinct areas of endemism. The taxon-area cladogram of the Cosmopsaltriaria gives some indication of the relationships among the areas of endemism. The discussion is extended to groups of bats, frogs, psocids, butterflies, and moths of the Melanesian Arcs, as their patterns of distribution seem equally relevant for the recognition of the biogeographic interrelationships in the Indo-Pacific.     

Demiarcs,creaons and genons

Useful insights into the representation of natural systems can be gained by decomposing directed graphs (digraphs) into elementary components. Arcs of digraphs can be split into male demiarcs (outarcs) which leave vertices and female demiarcs (inarcs) which enter demiarcs. Likewise, a vertex can be split into an input perceiving side called the creaon and an output generating side called the genon. Digraphs can be regarded as being hierarchically organized because each vertex in a level-1 digraph can be expanded into a level-2 digraph. In general, each vertex of a level-i digraph can be expanded into a level-(i+1) digraph. Arcs of a level-i digraph can be regarded as bundles of level-(i + 1) arcs which are split at the vertex boundary. These elementary graphical components are shown to be useful for depicting input-output systems such as organisms, ecosystems and societies.     

Studies of excitable membrane formed on the surface of protoplasmic drops isolated from Nitella III. Impedance of the surface membrane

A protoplasmic drop isolated from an internodal cell of Nitella in an initial solution composed of 70 mM KNO₃, 50 mM NaNO₃ and 5 mM CaCl₂ became electrically excitable when the drop was placed in the final solution containing 0.5 mM KNO₃, 0.5 mM NaCl, 1 mM Ca(NO₃)₂ and 2 mM Mg(NO₃)₂. The electrical impedance of the surface membrane of the drop was measured both in the initial and final solutions at frequencies between 60 Hz and 100 kHz.The impedance and admittance loci of the surface membrane fell on circular arcs. The d.c. resistance R_m°, and the d.c. capacitance C_m° were determined by extrapolating the circular arcs to the low frequency limit. R_m° thus determined was in the range of 50–200 Ω·cm² in the initial solution, and increased to a steady value of 0.4–4.0 kΩ·cm² when the external solution was replaced by the final solution. After the protoplasmic drop was isolated from the internodal cell of Nitella, C_m° decreased monotonically from about 1.5 μF/cm² within 20 min and approached $\text{1.25±0.1 μ}\text{F/cm}{}^2$ both in the initial and final solutions. No appreciable difference was observed for C_m° in these two solutions.The impedance data were discussed in relation to the process of formation of the membrane at the surface of the protoplasmic drop. After the excitable stage was reached, the drop membrane impedance was found to decrease by a factor of 10 during excitation.     

Laser method for recording displacement of the heart and chest wall

Several non-invasive methods are in use for recording mechanocardiograms. In this paper a new laser technique will be presented to measure heart motion, chest wall displacement and other displacement curves of cardiovascular structures. Principles of the laser displacement technique are described. The measurement range within which displacement is sensed, is 32 mm with a detector to object distance of 25 cm and a resolution of 8 μm (digital output) or 16 μm (analogue output). The specific surface of which motion is sensed is 1 mm². The sensitivity of the system is 156 mV/mm at a frequency bandwidth of 0–2 kHz. Assessment of the laser displacement technique was carried out during 6 dog experiments on the closed chest, on the exposed heart, on blood vessels and also on the chest wall of 5 normal subjects. Displacement of the chest wall at the apical site ranges between 0.3–0.8 mm and of the exposed heart between 3–10 mm.     

Influence of oil shale on intertidal organisms: Effect of oil shale extract on settlement of the barnacle Balanus balanoides (L.)

As part of a study to investigate the effect of oil seeps on intertidal organisms, oil extracts of Blackstone oil shale from Kimmeridge on the Dorset coast were used in laboratory experiments to test their effect on the settlement of the barnacle Balanus balanoides (L.). Thin films of oil extract painted on the surface of pits in slate panels had no effect on cyprid settlement when applied up to a surface density of 2.8 g · m^?2, representing a thickness of 3.3 μm. Larger surface densities of oil stimulated cyprids to settle in far greater numbers than on unoiled panels. The maximum effect was obtained at a surface density of between 14.0 and 56.0 g · m ^?2, representing a thickness of 16.5 μm and 66.0 μm. With higher concentration of oil in the pits, stimulation to settle was reduced although cyprid settlement was still encouraged at a surface density of oil of 112g · m^?2 or 132 μm thickness.The unfractionated crude oil shale extract was a less powerful stimulus for barnacle settlement than a partially purified solution of the integumental protein arthropodin, another strong settlement inducer for barnacle cyprids.     

Colour and colour change in the grasshopper, Kosciuscola tristis

The males of the small grasshopper (Kosciuscola tristis), with a restricted range above 1830 m in the Australian Alps, exhibit a remarkable colour change. They are dark, almost black, when cold and change to a bright sky blue colour within minutes of exposure to warmth.Sections of cuticle fixed in the two conditions confirm that the cells underlying the cuticle contain two kinds of granules: large (diameter 1·0 μm) spherical, brown granules, and smaller (0·17 μm) less dense granules. In the blue (warm) condition the small granules are closely packed in the distal part of the cells, whereas the ‘black’ granules are found predominantly in the deeper proximal zones. Evidence is presented to suggest that the blue colour arises from Tyndall scattering of light by the suspension of small granules and is intensified by being seen against a dark background.In the black condition the black granules are found to have moved towards the surface, mingling with the smaller granules and ‘quenching’ the light scattering.The smaller granules are white in the isolated state. They consist of a mixture of uric acid and a pteridine, probably leucopterin.The epidermal cells contain numerous microtubules, which are directed towards the cell surface, that is, parallel to the direction of movement of the granules. It is possible that the microtubules are associated with the movement.     

Confocal measurement of the three-dimensional size and shape of plant parenchyma cells in a developing fruit tissue

Parenchyma cells from the inner mesocarp of a grape berry (Vitis vinifera L. cv. Chardonnay) were visualised in three-dimensions within a whole mount of cleared, stained tissue using confocal laser scanning microscopy and digital image reconstruction. The whole berry was fixed, bisected longitudinally, cleared in methyl salicylate, stained with safranin O and mounted in methyl salicylate. Optical slices were collected at 1.0 μm intervals to a depth of 150 μm. Neighbouring z-series were joined post-collection to double the field-of-view. Attenuation at depth of the fluorescent signal from cell walls was quantified and corrected. Axial distortion due to refractive index mismatch between the immersion and mounting media was calibrated using yellow-green fluorescent microspheres and corrected. Transmission electron microscopy was used to correct fluorescent measurements of cell wall thickness. Digital image reconstructions of wall-enclosed spaces enabled cells to be rendered as geometric solids of measurable surface area and volume. Cell volumes within the inner mesocarp tissue of a single grape berry exhibited a 14-fold range, with polysigmoidal distribution and groupings around specific size classes. Cell shape was irregular and the planes of contact were rarely flat or simple. Variability in cell shape was indicated by the range in surface area to volume ratios, from 0.080 to 0.198 μm^–1. Structural detail at the internal surface of the cell wall was apparent. The technique is applicable to a wide range of morphometric analyses in plant cell biology, particularly developmental studies, and reveals details of cell size and shape that were previously unattainable.     

Isolation of membrane vesicles with inverted topology by osmotic lysis of azotobacter vinelandii spheroplasts

Membrane vesicles were prepared from Azotobacter vinelandii spheroplasts by lysis in either potassium phosphate (pH 7.0) or Tris¹-acetate (pH 7.8) buffers. These 2 types of preparations differ considerably in their properties: (1) Examination by scanning electron microscopy reveals that the Pi vesicles consist primarily of closed structures 0.6–0.8 μm in diameter with a rough or particulate surface similar to that of spheroplasts. The Tris vesicles are significantly smaller, 0.1–0.3 μm in diameter, and have a much smoother surface structure. (2) Antisera from rabbits immunized with A. vinelandii lipopolysaccharide antigen will agglutinate Pi vesicles but not Tris vesicles. (3) Tris vesicles have a fourfold higher specific activity of latent H⁺-ATPase than Pi vesicles. After exposure to Triton X-100 similar ATPase activities are observed for both types of vesicles. (4) Pi vesicles transport calcium in the presence of ATP or lactate at less than 30% of the rates observed for Tris vesicles. (5) Tris vesicles have less than 22% of the transport capacity of Pi vesicles for accumulation of labeled sucrose and less than 3% of the capacity for valinomycin-induced uptake of rubidium observed during respiration. (6) Quinacrine fluorescence intensity is reduced by 30% during lactate oxidation and 20% during ATP hydrolysis by Tris vesicles. Under similar conditions, fluorescence in Pi vesicles is quenched by only 7% and less than 2%, respectively. These findings suggest that Pi vesicles have the normal orientation of the intact cell whereas Tris vesicles have an inverted topology.     

Effects of Light and Wind Speed on the Vertical Distribution of Microcystis aeruginosa Colonies of Different Sizes during a Summer Bloom

Different dynamics, of the vertical distribution of Microcystis aeruginosa colonies of different sizes, were examined in a large shallow lake (Taihu Lake) during a summer bloom. During the observation the Microcystis colonies, larger than 120 μm, were mainly concentrated in the upper layer both under calm and windy conditions. Colonies from 36 μm to 120 μm showed a clear relationship to wind conditions whereas colonies less than 36 μm showed a nearly uniform vertical distribution at the different depths. There was no clear relationship between the vertical distribution of colonies larger than 36 μm and light intensity. However, at solar noon, colonies less than 36 μm were mainly distributed in the middle layers of the water column. The results indicate that small colonies are easily affected by the wind‐induced mixing, and they show an ability for active movement in response to light intensity under calm conditions. In contrast, large colonies tend to show little diurnal repositioning to light intensity and thereby are mainly concentrated in the surface layer. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

The Effect of Temperature on the Light-Induced Pigment Movement in Fish Corneal Chromatophores

Corneal chromatophores of unusual morphology were used for studies on the influence of temperature on the intracellular pigment movement in two species of marine fish from different temperature zones: the tropical puffer, Canthigaster cinctus, and boreal whitespotted greenling, Hexagrammos stelleri. It was shown that both dispersion under bright illumination and aggregation at darkening are slower or decrease at lower temperatures when examined in the range of 12–27°C. The mean speed of the pigment translocations in the individual cell process was 0.38 μm/s at the highest temperature examined, with a range of 0.17–1.0 μm/s. Near the middle of the temperature range, the dynamic characteristics of cell pigment movement in tropical and boreal species were rather close, suggesting that there would be little divergent adaptations with respect to the mechanisms of the pigment transport. Corneal chromatophores are considered as a new promising model for cell motility studies.