Colony growth and evidence for colony multiplication in Phaeocystis pouchetii (Prymnesiophyceae) isolated from mesocosm blooms

Using well plates of Phaeocystis pouchetii colonies isolatedfrom experimental mesocosms in western Norway, increases incolony size and division were documented. Median longest lineardimensions increased 0–7 µm h^–1; literaturePhaeocystis globosa values are 0.9–4.7 µm h^–1.Ten to twelve percent of colonies divided at rates of 0.21–0.28divisions day^–1. Daughter colonies were 100 µm smallerthan mother colonies. Colonies delayed 3.5–4.9 days tofirst division, compared with literature values of 4–5days for P. globosa. This study provides the first experimentalevidence for colony division of wild P. pouchetii.     

Cladoceran filtration rate-body length relations: model improvements developed for a Microcystis-dominated hypertrophic reservoir

Filtering rates were measured for zooplankton species in Situon single-celled Chlorella and on four Microcystis colony sizefractions (5–20, 20–40, 40–60 and 60–100µm) in a hypertrophic reservoir. Natural-log-transformedfiltration rates of five cladoceran species, one copepod andone rotifer were included in an all-food-particle, all-speciesmultiple regression model which explained 43% of the variancein filtration rate as a function of animal body length. An additional14% and 7.6% of the variance was attributable to food type andzooplankton species respectively, with temperature accountingfor <4% of the variance. Restricting the filtration ratemodel to cladocerans alone explained 51% of the variance asa function of animal length, 16% as a function of food type,7.5% as a function of species and only 0.2% as a function oftemperature. In linear filtration rate models for each foodtype, cladoceran body length explained 70% of the variance whenfeeding on Chlorella and between 57 and 67% of the varianceon the four Microcystis colony fractions. Models describingcladoceran filtration rates on Chlorella and the 5–20µm Microcystis colony fraction were significantly differentfrom the three models on larger colonies due to cladoceran responsesto increasing food particle size. Accordingly, a combined modelfor Microcystis colonies >20 µm was developed. Inclusionof food quality factors such as cyanophyte colony size seemsjustified in models aimed at estimating clearance rates, resourceutilization and phytoplankton grazing losses in plankton orecosystem studies when applied to eutrophic or hypertrophiclakes where large cyanophyte particles are abundant.     

Daily irradiance governs growth rate and colony formation of Phaeocystis (Prymnesiophyceae)

Phaeocystis was cultured at a range of ecologically significantdaily irradiances under nutrient-replete conditions. Below athreshold of 100 W h m^–1 day^–1, the cells were smalland flagellated, and remained solitary. Above this threshold,the cells were larger and able to form colonies. Growth rateand colony formation were maximum at sea surface irradiances(>700 W h m^–2 day^–2). Presumably, colonial growthis a strategy to maintain optimum growth rates in the watercolumn. Sinking, nutrient-stressed colonies reach low irradiancesand colonial cells can transform into small solitary flagellatedcells. These observations are important in understanding theecology and life cycle of Phaeocystis.     

Interrelation Between Growth Rate of Individual Potato (Solanum tuberosum L.) Tubers and Their Cell Number

In potato plants fast and slow growing tubers develop on thesame plant. A hypothetical causality between tuber growth rateand tuber cell number was investigated by determining the tubercell number with the aid of an automatic counting procedure.Our data show a close correlation between tuber size and cellnumber over the whole range of tuber volumes considered (3–28cm³). If the influence of tuber size on cell number is eliminatedby means of a partial correlation analysis, the cell numberof the entire tuber is not significantly correlated with itsgrowth rate. An exclusive consideration of the smaller cells(10–30 µm) in the apical tuber region, where thecell division rate in potato tubers is highest, reveals a loosebut significant partial correlation to tuber growth rate (r= 0.383, P < 0.05). The growth rate of the slow growing tubers of any potato plantmay be enhanced by removing the fast growing tubers. In thefirst few days this enhanced growth rate is not due to a stimulationof cell division rate, but rather due to cell expansion. Potato, Solanum tuberosum L., tuber growth rate, tuber cell number     

The initiation of Phaeocystis colonies

This study was designed to elucidate the sequence of eventsthat leads to the formation of new colonies of Phaeocystis sp.(strain PCC 540) starting from single cells released from maturecolonies. Colonies were first isolated by filtration onto a10 µm mesh. Colonial cells were then liberated by shakingand inoculated into individual culture wells containing mediumwith a PO₄^2– concentration of {small tilde}1 µM.Cell size and shape were determined daily by image analysis,while chlorophyll and DNA distributions were estimated by flowcytometry. Released cells were non-flagellated and mostly locatedin the G₁ phase of the cell cycle. They developed flagella andup to 90% became motile within 24 h. Swarmers lost motilityrapidly, became elongated, began to cycle again, excreted amucilaginous compound and divided leading to new colonies withina few days. During this reproducible process, no change of ploidycould be observed. Colonies initially adhered to the bottomof culture wells. Frequent mixing drastically reduced the fractionof colonies produced and their volume. High initial PO₄^2–concentrations (5 µM) delayed colony appearance, whereaslow concentrations (0.3 µM) prevented colony formation.The two main conclusions of this study are: (i) under favorableconditions ({small tilde}1 µM PO₄^2– no mixing),a large percentage of released colonial cells give back coloniesafter going through a flagellated stage; (ii) sexuality doesnot appear to be involved in this process. ¹Present address: CREMA BP 5, F-17137 L'Houmeau, France     

Control of daughter centriole formation by the pericentriolar material

Controlling the number of its centrioles is vital for the cell, as supernumerary centrioles cause multipolar mitosis and genomic instability. Normally, one daughter centriole forms on each mature (mother) centriole; however, a mother centriole can produce multiple daughters within a single cell cycle. The mechanisms that prevent centriole 'overduplication' are poorly understood. Here we use laser microsurgery to test the hypothesis that attachment of the daughter centriole to the wall of the mother inhibits formation of additional daughters. We show that physical removal of the daughter induces reduplication of the mother in S-phase-arrested cells. Under conditions when multiple daughters form simultaneously on a single mother, all of these daughters must be removed to induce reduplication. The number of daughter centrioles that form during reduplication does not always match the number of ablated daughter centrioles. We also find that exaggeration of the pericentriolar material (PCM) by overexpression of the PCM protein pericentrin in S-phase-arrested CHO cells induces formation of numerous daughter centrioles. We propose that that the size of the PCM cloud associated with the mother centriole restricts the number of daughters that can form simultaneously.     

Isolation, Culture, and Plant Regeneration of Protoplasts of Two Shrubby Oxalis Species from South America

Protoplasts were successfully isolated from internodal callustissues of both Oxalis glaucifolia and O. rhombeo-ovata whenthey were digested in a solution containing 0.1% (w/v) MacerozymeR-10, 0.5% (w/v) cellulase Onozuka R-10 and 0.3 mmol m^–3sucrose. Protoplasts proliferated to give cell colonies on Gamborget al.'s B5 medium supplemented with 0.3 mmol m^–3 mannitol,0.5 mg dm^–32, 4-D, and 2.0 mg dm^–3 kinetin. Calluswas produced upon transfer of cell colonies to Murashige andSkoog medium containing 2.0 mg dm^–3 l-naphthaleneaceticacid (NAA) and 0.1 mg dm^–3 kinetin for O. glaucifolia,or with 5.0 mg dm^–3 NAA and 0.5 mg dm^–3 6-benzylaminopurine,for O. rhombeo-ovata. Plants were regenerated from O. glaucifoliaprotoplasts on a medium containing 0.1 mg dm–3 NAA, 1.0mg dm^–3 kinetin and 1.0 mg dm^–3 gibberellic acid,but only vascular nodules were differentiated by O. rhombeo-ovataprotoplast-derived calli. Key words: Tissue culture, protoplasts, plant regeneration, Oxalis spp     

Pyrosoma atlanticum (Tunicata, Thaliacea): diel migration and vertical distribution as a function of colony size

A large population of the colonial pelagic tunicate Pyrosomaatlanticum occurred in April 1991 in offshore waters of theLigurian Sea (Northwestern Mediterranean). The high numbersof colonies caught allowed their vertical distribution and dielmigration in the 0–965 m water column to be describedas a function of their size. Daytime depths and amplitudes ofthe migration were correlated with colony size. The amplitudeof the migration ranged from 90 m for 3-mm-length colonies to760 m for 51-mm-length colonies, with a mean amplitude of 410m for the whole population, all sizes pooled. The results ofhorizontal hauls at a given depth around sunrise and sunsetshowed a marked diurnal symmetry of the migratory cycle relativeto noon, and that migration of the population was not cohesive.For example, the larger the colonies, the later after sunsetthey reached the upper layers during their upward migration.     

Persistence of cell cycle times over many generations as determined by heritability of colony sizes of ras oncogene-transformed and non-transformed cells

Abstract. The persistence of cell lifetimes during about 10 successive cell generations was investigated by comparing the number of cells in primary colonies and in secondary colonies derived from primary colonies. Primary colonies were grown from single cells for 3 or 4 days (a time equivalent to an average of five cell generations) and the number of cells in each primary colony determined. Cells in each primary colony were dispersed to initiate secondary colonies, grown for the same time, and the number of cells in secondary colonies determined. Several criteria were used to compare primary and related secondary colonies, the most informative was found to be regression and correlation coefficients between number of cells in primary colonies and mean numbers of cells in related secondary colonies. For two non-transformed mouse fibroblast cell lines, NIH 3T3 and BALB 3T3, the regression and correlation coefficients of cell number in primary and secondary colonies were positive. This suggests inheritance of cell lifetimes over many cell generations. After the addition of an activated ras oncogene (human cellular Harvey ras , or viral Kirsten ras ) some regression and correlation coefficients changed in magnitude but all remained positive. Comparison of experimental data and the results of computer simulations suggest that several models of inheritance of cell lifetimes are not adequate to explain the results, including a model of independence between lifetimes of mother and daughter cells and the common model that describes daughter cells as inheriting the lifetime of their mother with deviation. Simulations do suggest that cell lifetimes are inherited within clones as deviation from the lifetime of the initial cell, and that the ras oncogene does not destroy persistence within clones but does increase heterogeneity of cell lifetimes.     

On the trophic fate of Phaeocystis pouchetii (Harlot). III. Functional responses in grazing demonstrated on juvenile stages of Calanus finmarchicus (Copepoda) fed diatoms and Phaeocystis

The objective of this study was to quantify the functional responsein feeding rate in the various developmental stages of Calanusfinmarchicus to different concentrations of the diatoms Thalassiosiranordenskioeldii and Porosira glacialis, and the haptophyseanPhaeocystis pouchetii. Grazing of copepodite stage I–VC.finmarchicus was measured using two different approaches.Feeding rates were obtained from either incubation experiments,estimating the rate of removal of particles from suspension,or by quantifying the turnover rate of the plant pigments inthe gut. Clearance as a function of algal concentration (1–30µg plant pigment 1^–1) was described in juvenilestages of C.finmarchicus fed the diatoms T.nordenskioeldii [20µm equivalent spherical diameter (ESD)], P.glacialis (40µm ESD), and two size categories (30–100 µmand >100 µm ESD) of the gelatinous alga P.pouchetii.When the copepodite stages were fed T.nordenskioeldii, the gutcontent of plant pigments was in general higher than when fedP.glacialis. Rates obtained were variable when the same copepoditestages were offered the two size categories of P.pouchetii,but within the same order of magnitude as those obtained forthe larger diatom. At unialgal diets, diatoms were more readilyconsumed than the larger size fraction among colonies of P.pouchetiiby copepodite stage I–III C.finmarchicus. But given anappropriate prey size, C.finmarchicus grazed both diatoms andcolonies of gelatinous algae at equal rates. A linear relationshipbetween gut content and food concentrations <10 µgchlorophyll 1^–1 was found. This indicates that the ingestionrate in C.finmarchicus is directly proportional to the ambientfood concentration during the most productive period in Mayand June in high latitudes irrespective of algal species present. ¹Present address: Marine Biological Laboratory, University ofCopenhagen, Strandpromenaden 5, DK-3000 Helsingør, Denmark ²Present address: Greater Copenhagen Council, Gl. KøgeLandevej 1–3, DK-2550 Valby, Denmark     

Lemna paucicostata Hegelm. 6746: LIFE CYCLE AND CHARACTERIZATION OF THE COLONY TYPES IN A POPULATION

The sequence of frond emergence and the intervals required for daughter colony separation have been determined for Lemna paucicostata Hegelm. 6746 growing under standardized conditions. After separation of a new mother colony, the first daughter colony is produced from the left meristematic pocket and separates after approximately 60 hours, the second daughter, produced from the right pocket, separates after a further 30 hours, and the third daughter, again from the left, after a further 40 hours. The pattern of alternating longer and shorter intervals for separation of daughters continues throughout the life of the mother colony.     

Ecological investigations of blooms of colonial Phaeocystis pouchetti--I. Abundance, biochemical composition, and metabolic rates

A winter bloom of the colonial stage of the prymnesiophyte Phaeocystispouchetit was studied in the 13-m³ mesocosms of the Marine EcosystemResearch Laboratory on Narragansett Bay, Rhode Island The tankswere temperature regulated at 4±2°C but differedin their nutrient concentrations and in situ irradiances. Oneof the tanks was a control without added nutrients, one receiveda temporary nutrient spike and two others received daily N/P/Siinputs. Photosynthesis and growth rates of colonies exposedto a range of natural light levels were measured at weekly intervals.Particulate carbon production and release of dissolved organiccarbon (DOC) by the entire plankton community was determinedconcurrently. Photosynthesis and growth rates of Phaeocystisin tanks receiving daily nutrient additions were asymptoticfunctions of irradiance. Light-saturated rates exhibited asymptoticrelationships with dissolved inorganic nitrogen (N) levels.N-Limited populations showed more variable responses. Althoughirradiance and N availability regulated the population dynamicsof Phaeocystis, the presence or absence of silicate (S₁) influencedits relative importance in each tank. Phaeocystis dominatedcommunity metabolism in the absence of Si, but co-occurred withextensive stands of diatoms when Si was available. A significantpositive correlation was found between the contribution by Phaeocystisto community production and the proportion of photosynthatereleased as DOC In all tanks, Phaeocystis populations exhibitedcycles of abundance in which division of cells within coloniespreceded the multiplication of colonies. The production of newcolonies apparently occurred via two mechanisms: the formationof colonies from solitary cells, and the cleavage of largercolonies into smaller daughter colonies. Phaeocystis in tankswith near undetectable nutrient levels contained C:N, C:Chla, and C:ATP ratios several times higher than colonies in nutnent-repletetanks. Phaeocystis C:Chl a and C:ATP ratios were substantiallygreater than those of non-gelatinous phytoplankton due to carbohydratestorage in colony gelatin In contrast, C:N ratios in Phaeocystisand non-gelatinous phytoplankton were similar, suggesting astorage depot of organic N outside of the cells. The resultssupport the notion that Phaeocystis colonies function as biologicalentities rather than as passive aggregations of cells.     

Egg capsules, eggs and embryos of the southwestern Atlantic gastropod Coronium coronatum (Gastropoda: Muricidae)

The egg capsules, eggs and embryos of the muricid gastropodCoronium coronatum are described for the first time. Capsulesare sessile, bulliform, semi-circular, with a plug in the dorsalcenter. Sutures split the capsule into two asymmetrical halves.Recently laid capsules showed the presence of 3639 (n = 2) uncleavednurse eggs with a diameter of 180–210 µm (mean= 197.4 ± 8.9). The number of early embryos was 9–11.The size of the embryos was 320 x 320 to 820–880 µm.Nine pre-hatching embryos of 3.94 mm (n = 8, SD = 0.32)were found inside the older capsule. SEM illustrations of embryosand radulae are provided. Comparison of shell and radula ofembryos with the protoconch and radulae of adults of C. coronatumrevealed that the capsule belongs to this species. (Received 18 March 2006; accepted 10 October 2006)     

Overwintering of Microcystis aeruginosa Kutz. in a shallow lake

The standing crop and photosynthetic activity of Microcystisaeruginosa Kütz. in both the plankton and sediment wereinvestigated from November 1979 to May 1982 in Lake Kasumigaura,Japan. The number of planktonic colonies of this species decreasedfrom early autumn to early spring, but increased in the sedimentduring late summer and autumn. The overwintering colonies inthe sediment were –100–1000 times greater per unitarea than those in lake water. No photoinhibition of photosynthesiscould be observed in overwintering Microcystis. The values ofthe initial slopes of photosynthesis-light (P-I) curves weresimilar to those of the summer population, although the maximumphotosynthetic rate (P_max) measured at 20°C was lower thanthat of the summer planktonic population. In winter the valuesof initial slope of the P-I curve, and the ratio of phycobilinto chlorophyll a sorted from sediment were higher than in coloniesfrom the plankton.     

Effect of Calcium Chloride Concentration on Growth and Sporulation of Saprolegnia terrestris Cookson ex Seymour

As CaCl₂ concentration in the growth medium was reduced from27.4 to 0.107 µM the range of oospore number per oogoniumin Saprolegnia terrestris increased from 1 to 8 to 1 to 25 ormore, oospore size decreased and the precision of correlationbetween oospore number per oogonium and oogonial diameter decreased,but colony d. wt was not affected. The threshold CaCl₂concentrationrequired to give the lower range of oospore number per oogoniumwas independent of the concentration of other mineral nutrientsin the growth medium. The number of oogonia formed per unitarea of colony was affected by the concentration both of CaCl₂and of other mineral nutrients. Oospores formed in 0.107 µMCaCl₂ medium were often multinucleate but otherwise of normalappearance. The oospore abortion rate was increased from 3.09per cent at 27.4 µM CaCl₂ to 8.2 per cent at 0.107 µMCaCl₂. calcium, oogonia, oospores, Saprolegnia terrestris Cookson ex Seymour     

Effects of Chloroplast DNA Content on the Cell Proliferation and Aging in Chlamydomonas reinhardtii

Chlamydomonas is an unicellular green alga that contains one cup-shaped chloroplast with about 60 copies of cpDNA. Chloroplasts (cp) multiply in the cytoplasm of the plant cell by binary division, with multiple copies of cpDNA transmitted and maintained in successive generations. The effect of cpDNA copy number on cell proliferation and aging was investigated using a C. reinhardtii moc mutant, which has an undispersed cp-nucleoid and unequal segregation of cpDNA during cell division. When the mother cell divided into four daughters, one moc daughter cell chloroplast contained about 60 copies of cpDNA, and the chloroplasts in the three other daughter cells contained the 4–7 copies of cpDNA. In liquid medium, the number of moc cells at the period of stationary phase was about one-third that of the wild type. To observe the process of proliferation and aging in the mother cell, we used solid medium. Three out of four moc cell spores were preferentially degenerated 60 days after cell transfer. To confirm this, wild-type and moc mother cells containing four daughter cells were treated with novobiocin to inhibit cpDNA replication. Cell degeneration increased only in the moc strain following novobiocin introduction. In total, our results suggest that cells possessing smaller amounts of cpDNA degenerate and age more rapidly. Received 7 September 2000/ Accepted in revised form 14 February 2001     

The Demography of Colony Fission from 1878–1970 Among the Hutterites of North America

Periodic colony fision has been characteristic ofHutterite society for more than 100 years. From 1878–1970 fission occurred an average of every 14–15 years when colonies attained a size of 166 persons. Emigrating groups were comprised of35%–55% of the mother colony's population. Between founding and fission, daughter populations grew at an average rate of 4.3% per year. Over time, fissioning size and length of fission cycles decreased, but the size of new daughter colonies and rate of population growth remained constant through 1960. Demographic analysis suggested that the model of fission followed by the Hutterites has not always focused on even division of the mother colony into two equal-sized groups, but rather that they have had a fairly constant conceptual model of the size that new colonies should be. As fissioning size decreased over time the proportionate size of new colonies increased, maintaining the absolute size nearly constant since 1900. These findings suggest a number of questions for further investigation.     

A Comparative Study of Early Seed Development in Genotypes of Barley and Rye

Early seed development was studied in 17 genotypes of barley,Hordeum vulgare L., and 11 genotypes of rye, Secale cerealeL. The numbers of cells and nuclei in the embryos and endospermsof developing seeds were scored daily for 5 days after selfpollination. For embryos, the mean cell doubling times variedfrom 9.2–12.9 h for barley and 15.7–22.7 h for rye.Endosperm mitotic cycle times of both species were shortestover the first 24 h after pollination but then became longer.A non-linear correlation was found between the number of embryocells and the number of endosperm nuclei in barely and rye andis similar to that for other members of the Triticeae. Hordeum vulgare L., Secale cereale L., barley, rye, embryo, endosperm, mean cell doubling time     

Cellular Levels of Ribulose 1,5 Bisphosphate Carboxylase and Chloroplast Compartment Size in Wheat Mesophyll Cells

Pyke, K. A. and Leech, R. M. 1987. Cellular levels of ribulose1,5 bisphosphate carboxylase and chloroplast compartment sizein wheat mesophyll cells.—J. exp. Bot. 38: 1949–1956. The amount of the photosynthetic enzyme ribulose 1,5 bisphosphatecarboxylase (RUBISCO),as determined in mesophyll cells in primarywheat leaves was related to the size of the chloroplast compartmentwithin the cell for wheat species of three ploidy levels. Asimilar comparison was made for several genotypes of the hexaploidbreadwheat Triticum aestivum. Estimation of total chloroplastvolume per mesophyll cell was made assuming chloroplasts tobe oblate spheroid in shape. A significant correlation was found between the amount of RUBISCOper cell and the total chloroplast volume per cell for diploid,tetraploid and hexaploid wheat species. A significant correlationbetween cellular RUBISCO level and total chloroplast volumeper cell was also observed for a range of genotypes of the hexaploidT. aestivum but these genotypes of T. aestivutn accumulate agreater amount of RUBISCO per unit chloroplast volume than doany other wheat species. For these genotypes of T. aestivumthe stromal concentration of RUBISCO was estimated at 0·5mol m^–3 with a ribulose Msphosphate binding site concentrationof 4·0 mol m^–3. These results are discussed with respect to a gene dosage hypothesisto explain the accumulation of RUBISCO in leaf mesophyll cells. Key words: Ribulose, bisphosphate carboxylase, wheat chloroplasts, mesophyll cells