Isolation and Characterization of the Cytoplasmic Membranes from the Blue-Green Alga (Cyanobacterium) Anacystis nidulans

Cells of the blue-green alga (cyanobacterium) Anacyslis nidulanswere disintegrated, and their thylakoid membranes and cytoplasmicmembranes were isolated by floatation centrifugation on a sucrosedensity gradient. Electron micrographs revealed that the cytoplasmicmembranes formed single closed vesicles having diameters of200–400 nm. These membranes contained xanthophylls asthe major constituent pigments and rß-carotene andchlorophyll a as very minor ones. The major peaks in their absorptionspectra were due to carotenoids at 435, 455 and 487 nm, witha minor one due to chlorophyll a at 673 nm. These findings areconsistent with the yellow color of the cytoplasmic membranes.The absorption spectrum of the membranes in the carotenoid regionwas markedly affected by temperature: with a decrease in temperature,the peaks at 455 and 487 nm diminished and a new peak appearedat 390 nm. (Received February 12, 1983; Accepted June 20, 1983)     

Immunological identification of pigment component of a photochemically active chromoprotein (AGP) isolated from the blue-green alga Anabaena cylindrica

Pigment constitution of a photochemically active chromoprotein(ACP) isolated from the blue-green alga Anabaena cylindrica,was immunologically studied. Results confirmed our previousview that ACP is a complex of c-phycocyanin and a pigment havingabsorption peaks at 480 and 695 nm. Antisera of both ACP andphycocyanin did not significantly affect the photochemical activityof ACP. (Received August 15, 1972; )     

COPULATORY ACTIVITY AND SPERM PRODUCTION IN BULINUS (PHYSOPSIS) GLOBOSUS (GASTROPODA: PLANORBIDAE)

Young Bulinus (Physopsis) globosus performed male copulatoryactivity and cross-fertilized other snails before their femalereproductive tracts were mature. The two most immature snailsshowed preputial eversion when secretion was present only inthe muciparous gland and at the carrefour region of the oviduct.Sixteen snails showed preputial eversion and four snails cross-fertilizedother snails when their oothecal glands and/or major portionof the oviducts contained either no secretion or only scantyamounts. When paired with a partner snail for 12 or 20 consecutive days,adult snails copulated as males on approximately 60% of thedays paired and up to 8 consecutive days. Virgin snails raisedin isolation copulated as male at the same rate as non-virgin,community-raised snails. Ability to copulate as male was notdependent upon previous experience as male or female. Aftera single copulation as male after 7 days isolation, the hermaphroditicducts of maleacting snails contained 87 000 sperm. Sperm productionoccurred at approximately 50 000 sperm.d-¹, until at 10 dayspost-copulation, snails contained 639 000 sperm. (Received 25 May 1982;     

A Virus Infection in the Brown Alga Sorocarpus uvaeformis (Lyngbye) Pringsheim (Phaeophyta, Ectocarpales)

Virus-like particles were obsemed in zoospores and less frequentlyin vegetative cells of the filaments of mature plants of thebrown alga Sorocarpus uvaeformls. The particles, measuring approximately170 nm in diameter, are isometric in profile and show threedistinct zones. An electron dense rim (coat), 10 nm in thickness,is separated from a dense core, 110 nm in diameter, by an electronlight space 20 nm in width. When closely packed the particlesare usually separated from each other by a regular halo-likespace. Besides the isometric particles long flexuous structuresof variable length and measuring 75 nm in width were also found.The infection could be induced experimentally in healthy cellsby using either medium prevenient from infected cultures orcrude extracts obtained from infected plants.     

Cytosolic Ascorbate Peroxidase in Seedlings and Leaves of Maize (Zea mays)

Ascorbate peroxidase (APX) was purified to homogeneity frommaize (Zea mays L. cv.) coleoptiles. APX was a monomer witha molecular mass of 28 kDa, as determined by gel nitration andSDS-polyacrylamide gel electrophoresis. It contained one protohememoiety per molecule, with the oxidized form giving a Soret peakat 403 nm with small peaks at 502 and 638 nm, and the reducedform giving peaks at 435 and 556 nm. The enzyme was not inactivatedby depletion of ascorbate. Cell fractionation and immunohistochemicalstudies using polyclonal antibodies raised against maize APXrevealed that the enzyme was not located in the chloroplastsof green leaves. It was abundant in the cytoplasm but not inthe vacuoles of cells in the coleoptile, mesocotyl and youngleaves of seedlings. In mature green leaves, small amounts ofthe enzyme were distributed in vascular systems, in particularin the companion cells. The N-terminal amino acid sequence ofmaize APX exhibited high homology to pea cytosolic APX, spinachAPX and Arabidopsis APX, but not to APX from tea chloroplasts. (Received February 15, 1993; Accepted May 6, 1993)     

Developmental Ultrastructure of Cells and Plastids in the Petals of Wallflower (Erysimum cheiri)

An ultrastructural study of petal cells of wallflower (Erysimumcheirii) of the family Brassicaceae shows that the adaxial epidermalcells are of the conical papillate type whereas the cells ofthe abaxial epidermis are lenticular in shape. The abaxial epidermiscontains stomata, which are solitary and lack any obvious subsidiarycells. Pigmentation is apparent in both epidermal and internalmesophyll cells and results from the presence of both chromoplastsand large cytoplasmic vesicles containing pigment. These pigmentedvesicles are very obvious in preparations of fixed isolatedpetal cells. Chromoplasts are of the globular type and are presentin significant numbers in both epidermal and mesophyll cells.Division of chloroplasts in young petals prior to bud breakappears to give rise to the populations of chromoplasts observedin mature petals since there was no evidence of chromoplastdivision itself. The development of wallflower petals and theirchromoplasts is discussed in relation to development of petalsin the related species Arabidopsis thaliana. Copyright 1999Annals of Botany Company Wallflower, Erysimum cheiri, Chieranthus, petal development, chromoplasts, chloroplast differentiation.     

Fluorescence characteristics of cyanobacteria (blue-green algae)

The fluorescence characteristics of the cyanobacteria Synechocystisaquatilis Sauv., Microcystis firma (Breb. et Lenorm.) Schmidleand Synechococcus leopoliensis (Racib.) Kom. and the green algaScenedesmus quadricauda (Turp.) Breb. were examined. In thethree cyanobacteria, phycocyanin is the main accessory pigment.Phycoerythrin is not present in our investigated strains ofcyanobacteria. The highest excitation of the chlorophyll a (Chla) fluorescence of cyanobacteria resulted from light with wavelengthsof 620–630 nm. A definite ‘Kautsky’ effectis also evident at this wavelength. However, excitation withblue light (420–520 nm) produced only very slight fluorescence.The Kautsky effect is not evident at these wavelengths, evenat high photon flux densities. For Scenedesmus, fluorescencecharacteristics typical of green algae were found. The fluorescenceexcitation of cyanobacteria at 620 nm corresponds to a photosynthesispeak in the action spectrum measured in terms of O₂ production.The results underline the necessity of fluorescence measurementsat several wavelengths whenever mixed populations are involved.Such measurements also present possibilities for more accurateestimation of biomass and potential photosynthetic productionin mixed populations.     

THE CILIATED RIM OF THE VELUM OF LARVAE OF PECTEN MAXIMUS (BIVALVIA: PECTINIDAE)

During the early development of Pecten maximus, the prototrochof the trochophore becomes the rim of the velum of the veliger.The prototroch consists of a tract of randomly-distributed cilia,but in the veliger an ordered pattern of ciliation with somecompound cilia develops. The thin epithelium connecting thevelum to the body of the larva bears no cilia, nor does theupper surface of the velum (except for an apical tuft); themuch thicker epithelium of the velum rim, however, is profuselyciliated. The cilia are arranged in five bands or rings eachextending round the rim of the velum. The ring closest to theupper (i.e. ventral) surface of the velum is the inner preoralring of single cilia. Below this are two rings of much longercilia grouped to form blade-shaped cirri, which each consistof 2 or 3 rows of 10-15 cilia. The cilia substructures indicatethat the direction of active beat of the cirrus is along theaxis of the rows. This beating generates the main swimming current.The energy demands of beating are reflected in the numerouslarge mitochondria in the cells bearing the cirri. Nerve processesin the velum may control beating. Below the cirri are an adoraltract of shorter cilia and then a ring of postoral cilia. Thevelum anatomy is that of a typical bivalve veliger, but somefeatures distinguish Pecten maximus from other bivalves. Theonfiguration of the bands of cilia and the orientation of theirbeating suggest that the veliger captures food particles bythe ‘opposed band’ method. This configuration islikely to be homologous with those of other spiralian larvae. ^*Present address: School of Biological Scrences, PortsmouthPolytechnic, King Henry I Street, Portsmouth, PO1 2DY, U.K. (Received 30 September 1988; accepted 1 December 1988)     

Action Spectra for Step-Up Photophobic Response in Blepharisma

ABSTRACT The cells of Blepharisma which possess red pigment (blepharismin) show step-up photophobic response (temporal ciliary reversal induced by a sudden increase in light intensity). Bleaching of the cells by cold shock raised a threshold light intensity for the response, Oxidation of red pigment that produced blue pigment did not raise the threshold for the response. The action spectrum for the step-up photophobic response of the cells which possess normal red pigment had peaks at about 580, 540 and 490 nm, a value which coincided with peaks of an absorption spectrum of the red pigment. The absorption spectrum of oxidized pigment (blue pigment) shifted 20 nm toward infrared light. The action spectrum for the response of the cells which possess blue pigment also shifted 20 nm toward infrared light. Results suggest that red pigment might be involved in the step-up photophobic response. Key words. Blepharismin, ciliary reversal, photoreceptors, photoresponse.     

Purification and partial characterization of two biologically active compounds from the inflorescence of Sauromatum guttatum Schott (Araceae)

The active principle triggering the metabolic outburst of theappendices of certain arum lily species has been purified andpartially characterized. Although in the past it has been thoughtof as a single factor ("calorigen"), both paper chromatographyand DEAE-Sephadex ion exchange chromatography reveal that thereare two compounds (calorigen I and II) with calorigen activity.These can act alone or together, but show no synergism. Theyare low-molecular compounds which appear to be common constituentsof the inflorescence of Sauromatum guttatum Schott. CalorigenII is also present in the spadix of Arum maculatum L., Arumdioscoridis Sibth. & Sm., and Dracunculus vulgaris Schott.Calorigen I absorbs UV at 242, 267 and 278 nm, calorigen IIat 229 and 295 nm. No spectral changes are noted in alkalineenvironment, whereas at low pH-values there is a shift of theabsorption peaks of both compounds towards longer wavelengths.Calorigen II displays a strong blue fluorescence and has a maximalemission at 410 nm when activated at 295 nm. The possible mechanismof calorigen action is discussed. ¹ Present address: Department of Biochemistry, University ofWashington, Seattle, Washington 98195, U.S.A. (Received August 26, 1974; )     

Photoresponses of Matteuccia struthiopteris (L. ) Todaro

The germination of Malleucciu struthiopteris spores is lightdependent. All wavelengths between 400 and 750 nm promote germination,but two major peaks of promotion occur at 550 and 625 nm, anda minor peak of 450nm. A small number of spores germinato whom incubated in the darkwith IAA, kinetin, or gibberollie acid, but they do not undergofurther development. In red or white light no promotion of germinationover the control level is induced by the growth substances,only an inhibition at the higher concentrations.     

Larval development and metamorphosis in the marine pulmonate Amphibola crenata (Mollusca: Pulmonata)

The development of the free-swimming veliger of Amphibola is followed from hatching to settlement, and the larval structures compared with those of post-metamorphic juveniles and adult snails. Observations of living specimens and light-microscope sections were combined with scanning electron microscopy to build up a composite picture of veliger structure.
Four stages in the development of veligers are recognized, each being characterized by the appearance of organ systems such as the mantle cavity, larval heart, adult heart and kidney, and larval pallial gland. At or after metamorphosis, the larval systems (heart, kidney and pallial gland) disappear, and the developing adult organs move to the positions characteristic of adult snails.
Organogenesis in Amphibola veligers is compared with that of prosobranch and opisthobranch larvae, and with that of pulmonate larvae with direct development. The closest similarity is seen to be with opisthobranch veligers.     

The Spectral Sensitivities of Single Receptor Cells in the Lateral, Median, and Ventral Eyes of Normal and White-Eyed Limulus

Spectral sensitivity curves can be distorted by screening pigments. We have determined whether this is true for Limulus polyphemus by determining, from receptor potentials recorded using intracellular microelectrodes, spectral sensitivity curves for normal animals and for white-eyed animals (which lack screening pigment). Our results show: (a) In median ocelli, the curve for UV-sensitive receptor cells peaks at 360 nm and does not depend on the presence of screening pigment, (b) The curve for ventral eye photoreceptors is identical to that for retinular cells from the lateral eyes of white-eyed animals and peaks at 520–525 nm. (c) In normal lateral eyes, when the stimulating light passes through screening pigment, the curve indicates relatively more sensitivity in the red region of the spectrum than does the curve for white-eyed animals. Therefore, the screening pigment is probably red-transmitting, (d) In median ocelli, the curve for visible-sensitive cells peaks at 525 nm and is approximately the same whether the ocelli are from normal or white-eyed animals. However, the curve is significantly broader than that for ventral eyes and for lateral eyes from white-eyed animals.     

FOOD SELECTION IN THE LAND SNAIL LIMICOLARIA FLAMMEA MULLER (PULMONATA: ACHATINIDAE)

Food consumption by juvenile and adult specimens Limicolariaflammea was measured as dry weight of food eaten. The snailwas fed weekly for 15 months on four types of food (lettuce,potato, apple and carrot) and chalk provided, hence an opportunityto select for food. Juvenile snails showed greater selectivitydepending on whether the food was needed for somatic growthor reproduction. On the other hand, when fed exclusively onone each of the same food items and given no opportunity tochoose, the snails grew better on the same food items they selectedin the choice experiment. The absorption efficiencies (AD) werehigh, the utilisation efficiency (ECI) was 1–13% and showeddistinct peaks corresponding to egg production. Values for ECDwere 1.25–15.5%. Variation in growth rates was due mainlyto utilisation efficiencies of the four foods tested. Largeamounts of chalk were eaten during the period of somatic growthand greatly reduced during the reproductive phase of L. flammea.The significance of these findings to the snails ecology isdiscussed. (Received 9 April 1991; accepted 11 June 1991)     

THE ADDUCTOR AND RETRACTOR MUSCLES OF THE VELIGER OF PECTEN MAXIMUS (L.) (BIVALVIA)

In Pecten maximus (L.), retractor and adductor muscles becomefunctional in the early veliger larva. The twelve-day-old veligerhas four pairs of velar retractors, three pairs of retractorsattached to the posterior body wall and an anterior adductor.The pediveliger has in addition, pedal retractor muscles anda posterior adductor. The retractors consist of striated muscle:the adductors have both smooth and striated portions. The retractorsattach near the hinge, branch to a greater or lesser extent,then attach to specific areas of the velum, posterior body walland foot. Some features of the branching and of the dispositionof points of attachment form a pattern which exhibits mirrorsymmetry about the plane between the two shell valves. Thispattern is characteristic of the species. It is deduced thatretraction and protraction of the velum result from co-ordinatedsequences of muscle contractions. ^*Present address: Forest Products Research Centre, P.O. Box1358, Boroko, Papua New Guinea. (Received 15 June 1984;     

ULTRASTRUCTURAL LOCALIZATION OF COMPLEX CARBOHYDRATES AND PHOSPHATASES IN DIGESTIVE GLAND CELLS OF FEEDING AND HIBERNATING SNAILS, HELIX LUCORUM (GASTROPODA: HELICIDAE)

The digestive gland of normally-fed snails Helix lucorum, aswell as that of snails which had hibernated for 4 months wereexamined by the use of cytochemical techniques for detectionof acid and alkaline phos-phatase, as well as of periodate-reactive(PA-TCH-SP technique), sulfated (HID-TCH-SP technique) and carboxylatedcarbohydrates (LID-TCH-SP technique). The cytochemical resultssupport the hypothesis of intracellular digestion via lysosomalactivity of material taken up by endocytotic processes by thecells of the digestive gland. Four months hibernation did notaffect the intracellular distribution of polysac-charides andphosphatases in the cells of the digestive gland of H. lucorumcompared to that in the control snails. In addition, hibernationaffected the percentage of the calcium cells which significantlyincreased compared to the non-hibernating snails, whiie thepercentages of the digestive and excretory cells remained almoststable. However, the periodate-reactive sulfated and carboxylatedpolysaccharides of the digestive gland cells decreased in thehibernated snails compared to the controls. The results suggestthat the cytochemistry of periodate-reactive, sulfated and carboxylatedpolysaccharides used in the present study could, also, be appliedto the study of lysosomal activities. (Received 1 October 1991; accepted 4 December 1991)     

Opaline gland ultrastructure in Aplysia californica (Gastropoda: Anaspidea)

Secretions released from the ink and opaline glands of Aplysiacalifornica protect this shell-less mollusc from predators inseveral ways; the most recently discovered, phagomimicry, stimulatesthe feeding behaviours of the predator, distracting it fromthe sea hare. The structure of the ink gland has been reported,but little is known about the opaline gland. This paper comparesthe structure of the opaline gland of A. californica with thatof its ink gland, as well as two additional vesicle types foundin the epidermis. The opaline gland consists of single largecells, the vesicle cells, each with an enlarged nucleus, themaximum size of both exceeding that of respective structuresin the ink gland. Opaline vesicles, like ink vesicles, are enclosedby an external layer of muscle. Opaline vesicles, unlike inkvesicles, are not immersed in additional cells, but are freewithin the haemolymph and are, therefore, the probable sitefor the synthesis of their protein contents. The necks of individualopaline vesicles are fused into a central canal, but short necksconnecting each vesicle to the central canal remain; these arefilled with epithelial cells, but lack a muscular release valvelike that in the long necks of ink vesicles. Mucous cells containcircular arrays and are structurally distinct from opaline vesicles;mucous cells, though enlarged, are smaller than opaline or inkvesicle cells; they lack an external layer of muscle and a multicellularneck and, therefore, more closely match another vesicle typein the skin of A. californica, the white vesicle, which is involvedwith excess calcium excretion. (Received 22 September 2006; accepted 20 March 2007)     

RELATIONSHIPS BETWEEN SHELL SHAPE, WATER RESERVES, SURVIVAL AND GROWTH OF HIGHSHORE LITTORINIDS UNDER EXPERIMENTAL CONDITIONS IN NEW SOUTH WALES, AUSTRALIA

The shell morphologies of the highshore littorinids, Littorinaunifasciata Gray and Nodilittorina pyramidalis (Quoy & Gaimard)have previously been shown to vary at a variety of spatial scales,including among replicate sites at the same height, from heightto height and from shore to shore. In this study, the relationshipsbetween morphology of the shell, the reserves of water heldwithin the shell, the size of the foot and survival on differentshores and rates of growth in different habitats were examinedfor L. unifasciata and, to a lesser extent, N. pyramidalis.Reserves of water were not consistently related to size or shapeof the shell, but did increase as relative weight of shell increased.This may be due to the relatively smaller body providing moreinternal volume for extra-corporeal water. Water reserves andthe amount of free water held in the shell were also not relatedto loss of water or survival during extended periods of emersion.Although the shape of the shell on sheltered and exposed shoreswas correlated with size of the foot, with the snails on anexposed shore having larger apertures and feet than those ona sheltered shore, transplant experiments did not show differentialmortality between morphs from the different shores. All translocatedand transplanted snails disappeared from the exposed shore ata greater rate than from the sheltered shore, but this was probablydue to the snails dispersing out of the experimental areas ratherthan due to mortality. Therefore, many of the large-scale modelsthat have previously been used to describe patterns of shellshape in intertidal gastropods do not appear to be importantin these highshore littorinids. Finally, field experiments ongrowth of juvenile L. unifasciata indicated that rate of growth,largely governed by opportunity to feed rather than type andquantity of food, is the most likely explanation for the small-and large-scale patterns of shell shape that have been previouslydescribed in this species. (Received 22 October 1996; accepted 19 February 1997)     

THE PHYSIOLOGICAL EFFECTS OF AQUEOUS SUSPENSIONS OF PLANT MOLLUSCICIDES ON HELISOMA DURYI (GASTROPODA: PLANORBIDAE)

The behavioural and physiological responses of Heltsoma duryito solutions of three South African medicinal, mollusricidalplants (Warburgia salutans, Gardenia thunbergia and Apodytesdimidiata subsp dimidiata) were investigated. Clinical signsof toxic-lty, oxygen consumption, heart rate and water uptakewere used to assess response to these mollus-cicides. All plantsproduced symptoms characteristic of the distress syndrome describedby Harry & Aldrich (1963). Haemolysis, however, occurredonly in response to extracts of G. thunbergia. Respiratory failurein snails exposed to the W. salutans and G. thunbergia did notappear to be the primary cause of mortality. All plants produceda significant lowering of heart rate at lethal concentrations.Water unbalance, which is a commonly suggested effect, did notoccur. The difficulty of inferring mode of action from observedeffects is emphasized. Although some responses are common tothe three plant mollusci-cides under investigation, the differencesclearly indicate the potential for alternative modes of action. (Received 14 November 1995; accepted 17 April 1996)     

COPULATION AS FEMALES AND USE OF ALLOSPERM IN THE FRESHWATER SNAIL GENUS BULINUS (GASTROPODA:PLANORBIDAE)

Each of 8 snails in 2 groups of Bulinus (Physopsis) globosus,1 group raised in isolation and 1 group raised in community,were paired for 14 consecutive days with a male-acting partnersnail. In each group, the experimental snails, which were notallowed to act as males, were able to copulate as females onapproximately 94% of the days paired. Two copulations as female,with the same male partner, occurred on 50% of the days thatthe snails were paired, in the 2 groups combined. Non-receptivefemale behaviour by the experimental snails occurred frequently,and copulation was prevented by such behaviour during 6 pairings,3 in each group. Young B. (P.) africanus first copulated as females when theywere 31–33 days old. The accessory sex glands of the femalereproductive tracts of these young female-acting snails containedmoderate to large amounts of secretion. B. (P.) africanus, which were raised in pairs, laidcross-fertilizedeggs in isolation for an average of 76 days, and 1559 eggs/snailwere deposited before cross-fertilization ceased. Cross-fertilizedeggs were produced for as long as 120 days. After 1 copulation as female, virgin B. (P.) africanus laidcross-fertilized eggs for an average of 78 days and deposited3654 eggs/snail before crossfertilization ceased. Cross-fertilizedeggs were produced for as long as 113 days. After 2 copulationsas female, 1 copulation on each of 2 consecutive days, virginB. (P.) africanus laid cross-fertilized eggs for an averageof 102 days and produced 4397 eggs/snail before cross-fertilizationceased. Cross-fertilized eggs were produced for as long as 123days. Snails which were homozygous for an allele governing mantlepigment pattern were raised with a partner which was homozygousfor a different pigment pattern. Young produced in a 4-day periodafter the snails were isolated were 100% heterozygous. The snailswere then rearranged into pairs with a partner of the same genotypefor 4 days, during which time 26% of the young produced werehomozygous. The snails were again isolated for 4 days, and 49%of the young produced during this 4-day period were homozygous.The results of this experiment strongly suggest that multipleoutcrossing occurred. In B. (P.) africanus, stored allosperm were used to fertilizeeggs after 1, 4 and 7 weeks of starvation; after 1 and 4 weeksof 15°C low temperature and 4 weeks of 15°C + 4 weeksof 10°C low temperature; and after 1 and 4 weeks of desiccation.After 8 weeks of desiccation, 2 of 3 surviving snails reproducedby self-fertilization and 1 snail did not reproduce. Too fewsnails survived 8 weeks of desiccation for a conclusion to bereached on the ability of allosperm to survive. (Received 1 June 1984;