Ultrastructure of the integument during moulting of the quiescent tritonymphal instar of trombiculid mite Hirsutiella zachvatkini (Acariformes: Trombiculidae)

The ultrastructure of the integument of the quiescent reduced tritonymph of the trombiculid mite Hirsutiella zachvatkini (Schluger) was investigated by means of transmission electron microscopy. Mites were investigated daily during the 14–16 day tritonymphal period (imagochrysalis). This period includes the deutonymphal moult (1–3 days), the quiescent tritonymph period (2–4 days), and the tritonymphal moult into the adult mite (6–10 days). A distinct recognizable feature of the tritonymphal moulting cycle is a sequence of events independent of precise time intervals. This process involves partial destruction and reorganization of the hypodermis of the previous instar, and formation of a new hypodermis of the subsequent instar from islands of rudimentary hypodermal cells. The integument of the reduced tritonymph differs greatly from that of both larva and active deutonymph and adult. It consists of a simply organized hypodermal layer of varying thickness and a thick clear poorly lamellate cuticle with curved pore canals, and lacking setae. The epicuticle is very thin and without a clear protein layer. The tritonymphal instar as such with its own cuticle situated near the hypodermis is encased within the detached covering of the previous active deutonymph, and may be considered a calyptostasic and entirely pharate instar. There is a tendency for reduced tritonymphal stage to be eliminated from ontogenesis and this stage is not homologous to the pupa of insects.     

Ultrastructural localization of monoamines in the epidermis of Lumbricus terrestris (L.)

Summary Receptor cells in the epithelium and the basiepithelial nerve net of the prostomium of Lumbricus terrestris were investigated with electron microscope with special regard to the presence of monoamines. The receptor cells are found in groups of about 40 intermingled with supportive cells. After pretreatment with -methyl-noradrenaline and fixation with potassium permanganate a few receptor cells in each group and some nerve fibres in the basiepithelial nerve net contain small granular vesicles (about400 Å) characteristic for monoaminergic neurons. The distribution and relative number of these receptor cells and nerve fibres coincide well with previous reports on fluorescent receptor cells and varicose fibres. That the monoamine-storing small granular vesicles not are visualized until pretreatment with -methyl-noradrenaline is in accordance with recent microspectrofluorometric analysis, which shows that dopamine is the only primary monoamine present in the epithelium.In the epithelium there are occasional receptor cells and nerve fibres containing large vesicles (1000–1800 Å) which resemble the neurosecretory vesicles in the central nervous system. Photoreceptor cells having an intracellular cavity with microvilli and cilia have infrequently been observed at the base of the epithelium.No synapses on the mucous cells have been noticed. Nor have any synaptic specializations been observed in the basiepithelial nerve net. The morphological conditions necessary for the existence of possible axo-axonal synapses are briefly discussed.This work was supported by grants from the Helge Ax: son Johnson Foundation and the Magn. Bergvall Foundation.     

Effect of osmotic gradient on ADH-induced intramembranous particle aggregates in toad bladder

Summary Paired toad urinary bladders were prepared without or with an osmotic gradient (175 mosm) across them, stimulated for 2.5 (n=6), 5 (n=6), 30 (n=6) or 60 (n=6) min with ADH (20 mU/ml), and studied by freeze-fracture electron microscopy. Water permeability at these times was assessed in additional bladders (n=6 for each case) after tissue fixation according to the technique of Eggena. After both 60 and 30 min of ADH stimulation, the presence of a gradient compared with the absence of one was associated with fewer aggregates (242±35vs. 382±14 ×235 m^–2 at 60 min,P<0.01; 279±36vs. 470±51 ×235 m^–2 at 30 min,P<0.01) and lower water permeability (8.4±1.1vs. 18.8±1.8g×min^–1×cm^–1 ×mosm ^–1 at60min,P<0.005; 9.2±1.0vs. 22.0±2.1 g ×min^–1×cm^–2×mosm ^–1 at 30 min,P<0.001). In addition, with a gradient both maximum water permeability and maximum aggregate frequency were reached nearly together; a similar correspondence occurred without a gradient. We conclude that in the presence of an osmotic gradient both the ADH-associated aggregates and the water permeability response to ADH are prevented from reaching the higher levels observed in bladders not exposed to a gradient.     

Adaptations for reproduction and development in the skin-brooding ghost pipefishes,Solenostomus

Synopsis Ghost pipefishes comprise a small family (Solenostomidae) of skin-brooding fishes related to true pipefishes and seahorses (Syngnathidae).Solenostomus embryos develop within the fused pelvic fins of the female, unlike syngnathids in which males brood the eggs. Embryos, enclosed in egg envelopes, are attached to epidermal stalks, termed cotylephores, that occur only in brooding females. Cotylephores are cellular outgrowths of the epithelium on the inside surface of the pelvic fins. They attain a mean length of 687 ± 3.89 m and diameter of 105 ± 3.38 m. Cotylephores originate on the epithelial surface that lies over the lepidotrichia and they develop into multi-headed cylindrical branches approximately 125 ± 3.65 m in length and 78 ± 2.19 m in diameter. A mean of 26 ± 0.63 lateral branches are found on fully developed cotylephores. Each branch terminates in a wide apical calyx, approximately 112 ± 4.16 m in diameter, to which the egg envelope adheres. Adjacent calyces of the same cotylephore establish attachments with the envelope of a single egg. Cotylephores are composed of a surface epithelium that is continuous with the skin and a fibrous connective tissue core that contains blood vessels that ramify into an apical capillary plexus. The plexus may function in maternal-embryonic metabolic exchange. The cotylephores ofSolenostomus closely resemble the epidermal stalks (cotylephores) that are the sites of egg attachment in the skin-brooding South American catfish,Platystacus cotylephorus. Based on similarity in structure and probable function, cotylephores in the two groups of fishes are an example of evolutionary convergence.     

Adenosine transport and nitrobenzylthioinosine binding in human placental membrane vesicles from brush-border and basal sides of the trophoblast

Summary The nucleoside transport activity of human placental syncytiotrophoblast brush-border and basal membrane vesicles was compared. Adenosine and uridine were taken up into an osmotically active space. Adenosine was rapidly metabolized to inosine, metabolism was blocked by preincubating vesicles with 2-deoxycoformycin, and subsequent adenosine uptake studies were performed in the presence of 2-deoxycoformycin. Adenosine influx by brush-border membrane vesicles was fitted to a two-component system consisting of a saturable system with apparent Michaelis-Menten kinetics (apparentK _m approx. 150 m) and a linear component. Adenosine uptake by the saturable system was blocked by nitrobenzylthioinosine (NBMPR), dilazep, dipyridamole and other nucleosides. Inhibition by NBMPR was associated with high-affinity binding of NBMPR to the brush-border membrane vesicles (apparentK _d 0.98±0.21nm). Binding of NBMPR to these sites was blocked by adenosine, inosine, uridine, thymidine, dilazep and dipyridamole, and the respective apparentK _i values were 0.23±0.012, 0.36±0.035, 0.78±0.1, 0.70±0.12 (mm), and 0.12 and 4.2±1.4 (nm). In contrast, adenosine influx by basal membrane vesicles was low (less than 10% of the rate observed with brush-border membrane vesicles under similar conditions), and hence no quantitative studies of adenosine uptake could be performed with these vesicles. Nevertheless, high-affinity NBMPR binding sites were demonstrated in basal membrane vesicles with similar properties to those in brushborder membrane vesicles (apparentK _d 1.05±0.13nM and apparentK _i values for adenosine, inosine, uridine, thymidine, dilazep and dipyridamole of 0.14±0.045, 0.54±0.046, 1.26±0.20, 1.09±0.18mm and 0.14 and 3.7±0.5nm, respectively). Exposure of both membrane vesicles to UV light in the presence of [³H]NBMPR resulted in covalent labeling of a membrane protein(s) with a broad apparentM _r on SDS gel electropherograms of 77,000–45,000, similar to that previously reported for many other tissues, including human erythrocytes. We conclude that the maternal (brush-border) and fetal (basal) surface of the human placental syncytiotrophoblast posses broad-specificity, facilitated-diffusion, NBMPR-sensitive nucleoside transporters.     

An ultrastructural study of the larval integument of the midge,Chironomus riparius meigen (Diptera: Chironomidae)

Summary The larval integument of the midge, Chironomus riparius Mg., is unusually thin although it conforms with the normal insect pattern. The cuticle of the post-cephalic segments is about 3 m thick and overlies an epidermis which has an irregular basal plasma membrane resulting in spaces occurring between it and the basement membrane. The ventral tubuli have a similar epidermis but the cuticle is somewhat thinner. The anal papillae have the thinnest cuticular covering with a uniquely folded epicuticle of variable thickness, and their epidermis has the characteristics of a transporting epithelium. No evidence of pore canals could be found in the cuticle of any part except the head capsule which has a remarkably smooth epicuticle and a distinct layer which may represent the exocuticle. There are no spaces between the basement membrane and basal plasma membrane of the epidermis in the head. Ultrastructural evidence would suggest that gaseous exchange can occur across most of the post-cephalic integument.The author is indebted to Mrs. L. Rolph and Mr. R.L. Jones for their technical assistance     

Differences in L-alanine uptake by livers of Wistar and lean Zucker rats

The L-alanine uptake by livers of Wistar and lean Zucker rats has been studied. The hepatic uptake and fractional extraction rates of alanine were estimated in 50–55 day old rats. No significant differences in amino acid concentrations and blood flows in afferent and efferent liver vessels were seen in lean Zucker rats when compared with Wistar rats. However, the hepatic uptake (1.6±0.1 and 0.7±0.1 mol/min/100 g bw, p<0.01) and the fractional extraction (26.8±2.1 and 15.2±3.1%, p<0.05) were much lower in Zucker than in Wistar rats. The hepatic active transport of L-alanine was determinedin vitro using isolated plasma membrane vesicles. Vesicles isolated from livers of lean Zucker rats showed similar values of Km (2.5±0.7 vs 2.0±0.5 mM for Wistar and Zucker respectively, N.S.), but lower values of Vmax when compared with Wistar rats (1.1±0.1 vs 0.6±0.005 nmol/mg prot 5 s, p<0.01, for Wistar and lean Zucker rats respectively). These results indicate that, the liver of lean Zucker rats concentrates alanine less efficiently than the liver of Wistar rats. This fact correlates well with a lower capacity of the Na⁺-dependent L-alanine trasport in liver plasma membrane vesicles from lean Zucker rats.     

Isoforms of Na,K-ATPase inArtemia salina: II. Tissue distribution and kinetic characterization

Summary To characterize the molecular properties conveyed by the isoforms of the subunit of Na,K-ATPase, the two major transepithelial transporting organs in the brine shrimp (Artemia salina), the salt glands and intestines, were isolated in pure form. The isoforms were quantified by ATP-sensitive fluorescein isothiocyanate (FITC) labeling. The salt gland enzyme exhibits only the 1 isoform, whereas the intestinal enzyme exhibits both the 1 and the 2 isoforms. After 32 hours of development, Na,K-ATPase activity [in mol P_i/mg protein/hr (1u)] in whole homogenates was 32±6 in the salt glands and 12±3 in the intestinal preparations (mean±sem). The apparent half-maximal activation constants (K _1/2) of the salt gland enzyme as compared to the intestinal enzyme were 3.7±0.6mm vs. 23.5±4mm (P<0.01) for Na⁺, 16.6±2.2mm vs. 8.29±1.5mm for K⁺ (P<0.01), and 0.87±0.8mm vs. 0.79±1.1mm for ATP (NS). The apparentK _i's for ouabain inhibition were 1.1×10^–4 m vs. 2×10^–5 m, respectively. Treatment of whole homogenates with deoxycholic acid (DOC) produced a maximal Na,K-ATPase activation of 46% in the salt gland as compared to 23% in the intestinal enzyme. Similar differences were found with sodium dodecyl sulfate (SDS). The two distinct forms of Na,K-ATPase isolated from the brine shrimp differed markedly in three kinetic parameters as well as in detergent sensitivity. The differences inK _1/2 for Na⁺ and K⁺ are more marked than those reported for the mammalian Na,K-ATPase isoforms. These differences may be attributed to the relative abundances of the subunit isoforms; other potential determinants (e.g. differences in membrane lipids), however, have not been investigated.During the tenure of an Educational Commission For Foreign Medical Graduates Visiting Associate Professorship.     

Studies on the ultrastructure of the integument of the rotifer Habrotrocha rosa Donner (Aschelminthes)

Summary The integument of the rotifer Habrotrocha rosa Donner is provided with pores and formed by an extrasyncytial cuticle and a syncytial hypodermis. The hypodermis peripherally contains 3 layers of dense cytoplasm and borders the cuticle by an asymmetric cell membrane. The wall of the pores is stiffened proximally like an annulus. The pores lead into cytoplasmic invaginations which are surrounded by vesicles. Close to and also beneath the condensed cytoplasmic layers microbodies are found, which are interpreted as microperoxisomes. Subhypodermal layers of muscles are connected with the cytoplasm of the hypodermis by desmosome-like structures.I am indebted to Dr. H. Breucker, Anatomisches Institut Hamburg, and Prof. Dr. W. Becker, Zoologisches Institut Hamburg, under whose direction this work was carried out. Supported by the Deutsche Forschungsgemeinschaft (Be 464/10)     

Mercuric(II) chloride modulates single-channel properties of carbachol-activated Cl− channels in cultured neurons ofAplysia californica

Summary 1. The effect of mercuric(II) chloride on kinetic parameters of carbacholactivated single chloride channels were studied in cultured neurons of the marinemollusk, Aplysia californica.2. Single neurons ofAplysia were cultured in L-15 medium containing 1 mM -d-xyloside, which improved the success rate for gigaseal formation by 46%. Carbachol-activated single chloride channels were recorded in the cell-attached patch clamp configuration. Recordings with control solution (1 µM carbachol) and with test solution (1 µM carbachol +1 µM HgCl₂) were performed successively on the same neuron.3. In both the control and the test solution the open and closed time distributions were fitted with a double-exponential function. However, kinetic analysis revealed that Hg²⁺ caused a significant reduction of the mean closed time (10.37±1.08 vs. 3.32±0.02 msec) and of the second time constant ₂ of the closed time distribution (2.09±0.05 vs. 0.66±0.5 msec). The reduction of ₂, i.e., fewer events in the longer closed state under the action of Hg²⁺, may be the physical cause for the reduction of the mean closed time and thus underlies the increased open probabilityp ₀ (0.13±0.01 vs. 0.29±0.01 msec) of carbachol-activated chloride channels.4. Inorganic Hg²⁺ affects the acetylcholine receptor at lower concentrations than previously reported.     

Über die Ultrastruktur des Komplexauges von Daphnia pulex

Zusammenfassung Die Komplexaugen von erwachsenen Daphnien (Daphnia pulex) und deren Verankerung wurden elektronenmikroskopisch untersucht. Das Auge enthält 4 Bau-Elemente: 1. Deckzellen, 2. Interzellularsubstanz, 3. Linsenzellen und 4. pigmenthaltige Receptorzellen. Ihre Ultrastruktur wird beschrieben.Da die lichtbrechende Substanz als kompakter Körper innerhalb der Linsenzellen liegt, gehört der Linsenkörper zum euconen Typ. Er wird von aufgereihten Mitochondrion umgeben, ist nicht durch eine Membran vom Cytoplasma getrennt und zeigt eine nach innen zunehmende Elektronendichte.Die zentral gelegene, sehr dichte Zone grenzt basal an das Rhabdomer, nur durch die Zellmembran von ihm getrennt. Das Rhabdomer besteht aus Mikrovilli, die durch close contacts miteinander verbunden sind. Desmosomen-ähnliche Haftstrukturen zwischen Linsen- und Receptorzellen kommen in der Nähe der Rhabdomere vor. Aus den jeweils 8 Receptorzellen eines Ommatidiums entspringen basal 8 Neuriten, die zunächst durch eine Basalmembran, im Bereich des Hilus außerdem durch einen Gliafortsatz aus dem Ganglion opticum gebündelt werden. Das ganze Auge ist an der Körperoberfläche (Cuticularzellen und Cuticula) durch einen Halteapparat aufgehängt, der aus spezialisierten Zellen und Basalmembran-artigem Material besteht.

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On the ultrastructure of the compound eye of daphnia pulex

Summary Compound eyes of adult Daphnia pulex and their connection with the integument have been examined electron microscopically. The eye contains four elements: 1. covering cells, 2. intercellular substance, 3. lense cells and 4. receptor cells containing pigment. Their ultrastructure is described. Since the light refracting medium forms a compact lense body within the cytoplasm of lense cells it belongs to the eucone type. Though being surrounded by threaded mitochondria the lense body is not separated from the cytoplasm by a membrane. Electron density increases towards its center. At its basal part the central zone being covered only by a plasma membrane borders on the rhabdomer, the microvilli of which show close contacts between each other. There are desmosome-like contacts between lense and receptor cells at the periphery of the rhabdomer. 8 receptor cells each giving off 1 neurite build up the ommatidium. The 8 neurites of one ommatidium are bundled by a basement membrane and a glial process originating from the optic ganglion. The eye in toto is tied to the integument (cuticular cells, cuticula) by a complicated supporting apparatus, which consists of specialized cells and basement membrane-like material.

     

Effect of spring flooding on endophyte differentiation,nitrogenase activity,root growth and shoot growth inMyrica gale

Summary Spring flooding was investigated as a possible limiting factor in the development of nitrogenase activity, root growth, and shoot growth inMyrica gale. Dormant, one year oldMyrica gale plants were placed in a greenhouse in early April and given three treatments: control (not flooded), flooded-water (flooded with water to 2.5 cm above the soil level) and flooded-peat (flooded with water-saturated peat to 4.0 cm above the soil level). Nitrogenase activity was absent at budbreak but appeared concurrently with the differentiation of vesicles by theFrankia sp. endophyte. Flooding delayed the onset of nitrogenase activity, substantially reduced the specific nitrogenase activity of the nodules, and also severely limited the production of the new nodule biomass. Consequently by 67 days past budbreak nitrogenase activity was much greater in the control plants (5.55±0.42 mol C₂H₄/plant.h; ± SE; N=9) than in the flooded-water (1.18±0.29) and flooded-peat (0.15±0.05) plants. Production of new secondary roots was substantially reduced in the flooded plants but adventitious roots were rapidly produced along the flooded portion of the stem in the better aerated zone near the surface. New nodules formed on several adventitious roots by 67 days indicating that the plants are able to replace their largely nonfunctional deeply flooded nodules with new nodules in the aerobic zone. Initially shoot growth was unaffected by flooding but by 67 days the flooded plants had substantially less leaf biomass, lower leaf and stem nitrogen concentrations, and less total shoot nitrogen content than the control plants.     

Ultrastructure of the main excretory duct epithelium of the female mouse submandibular gland with special reference to sexual dimorphism

The fine structure of the main excretory duct epithelium (MEDE) of female mouse submandibular gland was investigated by scanning and transmission electron microscopy and the results compared with the previously established structure of male mouse MEDE. A comparative analysis of the subepithelial capillaries of both sexes was also performed. In this pseudostratified epithelium, principal cell-types were observed: types-I,-II,-III and basal cells. This differed significantly from male MEDE, where type-II and-III are absent and type-I cells are the most numerous. The latter cell-type had abundant mitochondria, a few lipid-containing granules, lysosomes in the infra-nuclear cytoplasm and well-developed basal infoldings. These cells were also characterized by abundant glycogen granules throughout the cytoplasm, many profiles of strands of smooth endoplasmic reticulum in the apical region, and lysosomes in the infra-nuclear region. Type-II cells were the second most numerous. Their most characteristic features were the presence of tubular vesicles which appeared to be invaginated from the plasma membrane, RER, SER, free ribosomes, a few peroxisomes with nucleoids, and primary lysosomes in extremely light cytoplasm. They had many mitochondria throughout the cytoplasm, except in the apical region, a few lipid-containing granules and no basal infoldings. Type-III cells were very few and were characterized by well developed basal infoldings, abundant free ribosomes, RER, SER, vesicles containing moderately dense material, and many lipid-containing granules. They also had many mitochondria throughout the cytoplasm, except apically. Basal cells had a large nucleus and the cytoplasm had few organelles. In the male continuous capillaries predominated in the subepithelial network, and capillary density per 200 m of epithelium (3.76±1.54) was lower than in the female, as was the number of fenestrae per 10 m of available endothelium (4.46±1.71). In the female, fenestrated capillaries predominated, and the capillary density per 200 m of epithelium was 6.76 (±1.54), and the number of fenestrae per 10 m of available endothelium was 4.91 (±1.77).     

Observations of the pattern of secondary wall development in the hypodermis of onion (Allium cepa) roots

Summary This brief communication reports the appearance, under certain circumstances, of root hypodermal cells with transfer cell labyrinths. These cells lie at regular intervals around the hypodermis at the bases of onion bulb roots. They are narrower (smaller tangential dimension) than unmodified cells but have the same radial dimension. These narrow cells contain small vacuoles, their main volume being composed of a cytoplasm rich in organelles, especially mitochondria. When treated with a low concentration of lanthanum nitrate solution, the tracer accumulates in the outer tangential wall and in small vacuoles and vesicles.     

Ultrastructural observations of the testicular epithelium and spermatozoa of <Emphasis Type="Italic">Pseudochordodes bedriagae</Emphasis> (Gordiida,Nematomorpha)

Two questions are of interest concerning the male reproductive system in Gordiida: (1) is the epithelium surrounding the testis continuous or discontinuous and (2) is the type of spermatozoon as described at the transmission electron-microscopical level for the two species of Gordius typical for all Gordiida? An examination of the South American species Pseudochordodes bedriagae has allowed us to add new information to this poorly studied phylum. Testicular tubes are large, filled with spermatozoa, and surrounded by a continuous epithelium. The epithelial cells that line the posterior testes occasionally overlap, and their cytoplasm is narrow and contains dense granules, abundant endoplasmic reticulum, and vesicles. The plasma membrane possesses microvilli with many filaments. This epithelium rests on a basement membrane. The spermatozoa in P. bedriagae resemble the known spermatozoa of two Gordius species but differ in presenting a uniform halo layer of less dense chromatin that surrounds the dense chromatin in the nucleus. The finding that a similar type of spermatozoa occurs in both genera (Pseudochordodes and Gordius) makes it likely that it is present in all other Gordiida and is therefore an autapomorphy of the Gordiida.     

Fast vesicle transport in PC12 neurites: velocities and forces

Although the mechanical behavior of single-motor protein molecules such as kinesin has been carefully studied in buffer, the mechanical behavior of motor-driven vesicles in cells is much less understood. We have tracked single vesicles in neurites of PC12 cells with a spatial precision of ±30 nm and a time resolution of 120 ms. Because the neurites are thin, long, straight, and attached to the surface of planar cover glasses, the velocity of individual vesicles could be measured for times as long as 15 s and distances as long as 15 m. The velocity of anterograde vesicles was in most cases constant for periods of 1–2 s, then changed in a step-like fashion to a new constant velocity. The viscoelastic modulus felt by the vesicles within live PC12 cells was determined from the Brownian motion, using Masons generalization of the Stokes–Einstein equation. From Stokes law, the drag force at the smallest sustained velocity was 4.2±0.6 pN for vesicles of radius 0.30–0.40 m, about half the maximum force which conventional kinesin can develop during bead assays in buffer. We interpret the observed velocity steps as changes of ±1 or occasionally ±2 in the number of active motor proteins dragging that vesicle along a microtubule. Assuming that the motor is conventional kinesin, which hydrolyzes one ATP per 8 nm step along the microtubule, the motor protein efficiency in PC12 neurites is approximately 35%.     

Studies on the embryology and gynoecium structures inDrimys winteri (Winteraceae) and someAnnonaceae

Drimys winteri (Winteraceae) and 11 species ofAnnonaceae, namelyAnnona montana, Artabotrys hexapetalus, Bocagea sp.,Papualthia sp.,Polyalthia nitidissima, Tetrameranthus umbellatus, T. duckei, Uvaria sp.,Xylopia malayana, X. aromatica, andX. emarginata, were investigated embryologically with special reference to development of ovule and embryo sac. The ovules are anatropous, crassinucellate and in most taxa bitegmic. The inner integument is of epidermal origin. TheAnnonaceae investigated have a multi-layered, later vascularized outer integument with most probably subepidermal initiation. In contrast,Drimys winteri has a three-layered, non-vascularized outer integument of epidermal origin. The annonaceous genusTetrameranthus (T. umbellatus andT. duckei) possesses a middle integument between the inner and the outer one, stated here for the first time in a neotropic representative ofAnnonaceae. Within the angiosperms this feature occurs inAnnonaceae only. The embryological characters are rather homogeneous. Differences between the species investigated are found in, e.g. the number of cell layers in the inner integument, which is commonly two inAnnonaceae as compared to three inDrimys winteri, the presence or absence of a hypostase, the number of layers in the nucellar epidermis, great differences in size of ovules, and the species-specific pattern of tannin deposition in the ovules. In the species so far investigated the embryo sacs develop according to thePolygonum-type. InXylopia malayana andBocagea sp. in addition the carpels were investigated. They are conduplicate. InXylopia malayana the free carpels are united by an extragynoecial compitum, inBocagea sp. each stigma produces its isolated mucilage cap. The results obtained from the investigated taxa are discussed and compared with published data on embryology and gynoecium structure in other annonaceous and winteraceous taxa.     

Ultrastructure of the osphradium of Aplysia californica

Summary The osphradium of Aplysia californica, a sensory organ, is a small yellow-brown epithelial patch located in the mantle cavity immediately anterior to the rostral attachment of the gill. Scanning electron microscopy reveals a round ellipsoid structure of 0.6–1 mm in diameter with a central, occasionally folded, sensory epithelium. The central area is covered with microvilli and surrounded by a densely ciliated epithelium. Transmission electron micrographs show that the columnar supporting cells in the sensory epithelium contain an abundance of apical pigment granules and microvilli. Between the epithelial-supporting cells, the putative sensory elements consist of thin neurites (0.4–1.5 m in diameter) that reach the sea-water side of the osphradium. The neurites contain many neurotubules, mitochondria, vesicles and cilia in their apices. The nerve endings originate from cell bodies up to 40 m below the epithelium or in the osphradial ganglion itself, as revealed by electron microscopy and retrograde labeling with Lucifer yellow. There appear to be two populations of putative sensory cells, a large population of heavily stained cell bodies 4–10 m in diameter and a few scattered cells of large diameter (25–60 m). Following lanthanum impregnation, septate junctions can be seen between all types of cells in the epithelium, 3–5 m below the sea-water surface. This study provides new information for further investigation of osmo- and mechanosensation in Aplysia californica.     

Pulse NMR studies of water permeability in phosphatidylcholine vesicles containing general anesthetics

Summary Phosphatidylcholine was extracted from egg yolks and sonicated withn-alkyl alcohols to give vesicles. The magnetic environment of the external compartment was then modified by the addition of shift reagent (Co²⁺). This allowed determination of the average lifetime for exchange of water molecule protons by observing the relaxation rate dependence on the interval between pulses in a Carr-Purcell sequence. For vesicles containingn-hexanol as 33% of lipid, the average water molecule lifetime in the internal compartment was found to be substantially less than that for a vesicle without hexanol. The lifetime, 11.3±4 msec, is equivalent to a permeability coefficient of 60 /sec at 34°C.     

Purification and characterization of homodimeric methylmalonyl-CoA mutase from<Emphasis Type="Italic"> Sinorhizobium meliloti</Emphasis>

High activity (>60 munit/mg protein) of 5-deoxyadenosylcobalamin-dependent methylmalonyl-CoA mutase (EC 5.4.99.2) was constantly found during growth of a strain of the root-nodule-forming bacterium Sinorhizobium meliloti harboring an extra plasmid-encoded copy of the methylmalonyl-CoA-mutase-encoding bhbA gene. The enzyme was purified to homogeneity and characterized. The purified enzyme was found to be a colorless apo-form. The apparent molecular weight of the enzyme was calculated to be 165,000±5,000 by Superdex 200 HR gel filtration. SDS-PAGE of the purified enzyme resolved one protein band with an apparent molecular mass of 80.0±2.0 kDa, indicating that the S. meliloti enzyme is composed of two identical subunits. The NH₂-terminal sequence was identical to that predicted from the bhbA nucleotide sequence. Monovalent cations were required for enzyme activity.Abbreviations AdoCbl 5-Deoxyadenosylcobalamin - KPB Potassium phosphate buffer - MCM Methylmalonyl-CoA mutase - PVDF Polyvinylidene difluoride