Growth and grazing responses of Chrysochromulina ericina (Prymnesiophyceae): the role of irradiance, prey concentration and pH

The effect of irradiance, prey concentration and pH on the growth and grazing responses of the mixotrophic prymnesiophyte Chrysochromulina ericina under N-and P-replete conditions was studied using the pedinophyte Marsupiomonas pelliculata as prey. The two organisms were inoculated in monocultures and in mixed cultures at different predator: prey ratios at three irradiances and allowed to grow for 4–7 days. All cultures were non-axenic. Algal densities and pH were monitored throughout the experiments and growth and grazing rates were measured. An increase in growth of C. ericina cultures at irradiances of 25 and 70 μmol photons m⁻² s⁻¹ was observed after the addition of prey, while growth of C. ericina cultures at the high irradiance (150 μmol photons m⁻² s⁻¹) was unaffected by the addition of prey. However, although the growth of C. ericina increased at low irradiance (25 μmol photons m⁻² s⁻¹), it did not reach the same level as monocultures at the high irradiance (150 μmol photons m⁻² s⁻¹), suggesting that phagotrophy can only partly replace photosynthesis in C. ericina. Maximum growth rates of C. ericina at irradiances of 25 and 70 μmol photons m⁻² s⁻¹ were obtained at concentrations of > 0.15–0.3×10⁵ M. pelliculata ml⁻¹, corresponding to 50–100 μg C 1⁻¹. Ingestion of M. pelliculata cells by C. ericina did not generally follow Michaelis—Menten kinetics. Deviation from the expected saturation kinetics was especially pronounced at irradiances of 70 and 150 μmol photons m⁻² s⁻¹. At these irradiances ingestion of M. pelliculata cells by C. ericina decreased at high concentrations of M. pelliculata, indicating an increased uptake of bacterial prey in these cultures. The growth rate of C. ericina was affected in both monocultures and in mixed cultures when pH increased above 8.6, and growth stopped around pH 9. The prey alga M. pelliculata tolerated high pH better and, consequently, took over in the mixed cultures when pH exceeded 9. The ecological significance of mixotrophy in the genus Chrysochromulina is discussed. Published online: 4 July 2002     

Phytoplankton growth and microzooplankton grazing rates in a restricted Mediterranean lagoon (Bizerte Lagoon,Tunisia)

Phytoplankton growth and microzooplankton grazing were investigated in the restricted Bizerte Lagoon in 2002 and 2004. The 2002 study, carried out at one station from January to October, showed significant seasonal variations in phytoplankton dynamics. High growth rates (0.9–1.04 day⁻¹), chlorophyll a (Chl a) concentrations (6.6–6.8 μg l⁻¹) and carbon biomass (392–398 μg C l⁻¹) were recorded in summer (July), when several chain-forming diatoms had intensively proliferated and dominated the carbon biomass (74%). In 2004, four stations were studied during July, a period also characterized by the high proliferation of several diatoms that made up 70% of the algal carbon biomass. In 2004, growth rates (0.34–0.45 day⁻¹) and biomass of algae (2.9–5.4 μg Chl a l⁻¹ and 209–260 μg C l⁻¹) were low, which may be related to the lower nutrient concentrations recorded in 2004. Microzooplankton >5 μm were mainly composed of heterotrophic dinoflagellates and ciliates. Microzooplankton biomass peaked during summer (2002 320–329, 2004 246–361 μg C l⁻¹), in response to the enhanced phytoplankton biomass and production. The grazer biomass was dominated by ciliates (71–76%) in July 2002 and by heterotrophic dinoflagellates (52–67%) in July 2004. Throughout the year and at different stations, microzooplankton grazed actively on phytoplankton, removing 26–58% of the Chl a and 57-84% of the primary production. In 2002, the highest grazing impact was observed on the large algae (>10 μm) during the period of diatom dominance. These results have a significant implication for carbon export to depth. Indeed, the recycling of most of the diatom production by the microbial food web in the upper water column would reduce the flux of material to the seafloor. This should be considered when modeling the carbon cycling in coastal environments and under conditions of diatom dominance. During both studies, ciliates had higher growth rates (0.5–1.5 day⁻¹) and a higher carbon demand (165–470 μg C l⁻¹ day⁻¹) than dinoflagellates (0.1–0.5 day⁻¹, 33–290 μg C l⁻¹ day⁻¹). Moreover, when grazer biomass was dominated by ciliates (in July 2002), herbivory accounted for 71–80% of the C ingested by microzooplankton while it accounted only for 14–23% when dinoflagellates dominated the grazer biomass (in July 2004). These results suggest that, in contrast to findings from open coastal waters, ciliate species of the restricted Bizerte Lagoon were more vigorous grazers of the large algae (diatoms) than were dinoflagellates.     

Growth and grazing rates of bacteria groups with different apparent DNA content in the Gulf of Mexico

Growth rates and grazing losses of bacterioplankton were assessed by serial dilution experiments in surface waters in the Mississippi River plume, the northern Gulf of Mexico, a Texas coastal lagoon (Laguna Madre), southeast Gulf of Mexico surface water, and the chlorophyll subsurface maximum layer in the southeast Gulf of Mexico. Bacteria were quantified by flow cytometry after DNA staining with SYBR Green, which allowed for discrimination of growth and grazing rates of four bacteria subpopulations distinguished by their apparent DNA content and cell size (light scatter signal). Total bacteria growth rates (0.2–0.9 day^–1) were mostly balanced by grazing losses, resulting in net growth rates of –0.18 to 0.45 day^–1. Growth rates of DNA subpopulations varied within experiments, sometimes substantially. In most, but not all, experiments, the largest bacteria with highest DNA content exhibited the highest growth rates, but a relationship between DNA content and growth rates or grazing losses was absent. Small bacteria with the lowest DNA content showed positive growth rates in most experiments, sometimes higher than growth rates of bacteria containing more DNA, and were grazed upon actively. Low-DNA bacteria were not inactive and were an integral part of the microbial food web.Communicated by O. Kinne, Oldendorf/Luhe     

Growth rates of Corallina officinalis (Rhodophyta) at different temperatures

Specimens of Corallina officinalis L. were grown in the laboratory for 6 and 8 weeks at temperatures of 6°, 12°, 18°, and 25°C. After 6 weeks, the mean growth rates of main axes were 2.8 mm at 18°C, 2.9 mm at 12°C, and 0.2 mm at 5°C; no growth occurred at 25°C. At 6°C, growth increased with lower light intensities. The mean total increase in length of branchlets present when the plants were collected did not vary significantly at 12° and 18°C. At 12°C, axial intergenicula formed in culture produced more new branchlets than did field-grown intergenicula. Also, the production of these branchlets on cultured intergenicula was higher at 12°C than at 18°C.Based on a dissertation completed at Clark University in partial fulfillment of the requirements for a Master of Arts degree by B. J. Colthart.     

Fluorescence induction in the macroalgae Chondrus crispus (Rhodophyceae) and Ulva sp. (Chlorophyceae)

The induction of in vivo chlorophyll a (chl a) fluorescence (change in fluorescence intensity during a time-scale of ms to s) was measured to determine the potential of this technique for assessing the physiological condition of the macroalgae Chondrus crispus and Ulva sp. A gradient in variable fluorescence (P-F ₀ =peak minus initial fluorescence, a measure of Photosystem II activity) was found along the frond of C. crispus, the values increasing with distance from the thallus apex. No gradient was observed for Ulva sp. thalli. Nitrogen- or phosphorus-depleted Ulva sp. required a longer dark-conditioning period and had lower values of P-F ₀ than did controls. In contrast, no differences were found in P-F ₀ of N- or P-depleted C. crispus unless values were normalized to chl a. The irradiance history of C. crispus strongly influenced P-F ₀ , even after dark-conditioning: P-F ₀ declined by about 70% as the mean daily natural irradiance increased between 2 February and 14 March 1986; a negative correlation was observed between P-F ₀ and the photon flux density 1 d prior to the measurement; P-F ₀ remained elevated when C. crispus was grown under a low photon flux density; and P-F ₀ decreased in thalli within 5 d of transfer from growth under natural irradiance to an incubator with artificial irradiance. Changes in variable fluorescence at different growth irradiances of C. crispus may be due to adaptive changes in the relative absorption cross-section of this alga. The influence of irradiance history on Ulva sp. was minimal in comparison.Issued as NRCC No. 28730Part of this study was carried out while employed by Focal Marine Ltd., Bedford, Nova Scotia, Canada     

Estimation of Arctic copepod grazing rates in vivo and comparison with in-vitro methods

Gut evacuation rates were measured in Calanus hyperboreus and C. glacialis from two stations in Jones Sound, Northwest Territory (NWT) and one station in an Ellesmere Island Fjord during late summer of 1984. Gut content decreased exponentially with a rate constant, that, for Stage V C. glacialis at least, was independent of food type and time of day. Gut filling rates were measured in Stage V C. glacialis in the light and in the dark, at noon and midnight. Nighttime gut filling rates were very similar for both light intensities, and also similar to the daytime rate in the dark, whereas the daytime rate in the light was much lower. Ingestion rates were calculated for these latter experiments, including a rate term for defecation, and these results were compared to the values obtained from the observations of gut filling rates in vivo as reported in Head et al. (1985) and from long-term (2–3 d) bottle incubations as reported in Head et al. (in press). The following points were made: (1) in-vivo and in-vitro ingestion rates were very close if appropriate in-vitro experimental conditions were used with respect to light intensity and time of day; (2) copepods could fill their guts at a rate apparently higher than their normal nocturnal ingestion rate; and (3) the calculated rations were dependent on the shape of the observed diurnal feeding patterns.     

Nutritional value of Phaeocystis pouchetii (Prymnesiophyceae) and other phytoplankton for Acartia spp. (Copepoda): ingestion,egg production,and growth of nauplii

Ingestion and egg production by Acartia hudsonica (5°C) and A. tonsa (10°C) from Narragansett Bay, Rhode Island, USA, was measured in the laboratory over a range of concentrations of the prymnesiophyte Phaeocystis pouchetii and the diatom Skeletonema costatum. Both Acartia species reproduced well when fed unialgal diets of S. costatum. Egg production by females fed P. pouchetii, either as gelatioous colonies (primarily >200 m in diameter) or solitary cells (3 to 5 m), was not significantly different than that of starved females. Acartia spp. fed selectively on S. costatum in multialgal treatments. The presence of P. pouchetii did not reduce ingestion of S. costatum; the availability of S. costatum did not increase ingestion of P. pouchetii. Nauplii of A. hudsonica grew equally well on separate diets of P. pouchetii and Isochrysis galbana, two flagellates of similar size. Adult Acartia spp. reproduced poorly when fed these phytoplankton, suggesting that particle size may be more important than food quality in describing the responses. Grazing by Acartia spp. does not directly impact the dynamics of P. pouchetii, but may indirectly contribute to blooms of this prymnesiophyte by removal of competing phytoplankton.     

菌株Rhodococcus sp.Chr-9和Exiguobacterium sp.Chr-43的除铬(VI)特性

为了解环境因素对生物除铬(VI)的影响,并为铬(VI)污染环境的生物强化治理提供高效菌株,采用选择培养的方法从制革废水污泥样品中分离到2株革兰氏阳性铬(VI)去除菌——Rhodococcus sp.Chr-9和Exiguobacterium sp.Chr-43.菌株Chr-9和Chr-43在25~40℃内均能够较好生长,并高效去除铬(VI),菌株Chr-9和Chr-43的最适生长pH均为7.0~9.0,菌株在pH 7.0的培养基中去除铬(VI)的效率最高.加入0.2~0.5 mol/L的NO3-、SO42-和Cl-能够促进Chr-9和Chr-43的生长以及去除铬(VI)的效率.在含铬(VI)培养基中同时接种Chr-9和Chr-43时,Chr-9促进菌株Chr-43的生长,并提高菌株去除铬(VI)的效率.研究表明,pH、温度、阴离子和环境中的其它生物对铬(VI)的去除有明显影响.     

A method to determine in situ zooplankton grazing rates on natural particle assemblages

In situ zooplankton grazing rates on natural particle assemblages were stimated by measuring zooplankton uptake of labelled autotrophic (with Na¹⁴CO₃) and heterotrophic (with [methyl-³H]-thymidine) particulate matter in 1-h incubations in clear, Plexiglas, Haney chambers. The in situ grazing rates are in the same range as those measured for zooplankton in the laboratory using standard particle counting techniques. A negative selection coefficient for ³H-labelled particles indicated a lower filtration efficiency or avoidance of these particles by zooplankton.     

悬沙对小球藻生长的影响

在实验生态条件下研究了不同浓度和粒径大小的悬沙对小球藻(Chlorella sp.)生长的影响.结果发现:在泥沙与小球藻直接混合培养体系中,小球藻的种群增长可用Logistic增长模型拟合,拟合后的生长参数表明,随着悬沙浓度的增加,小球藻的环境负载能力a和种群瞬时增长率K显著减小,但到达拐点时间Tp的变化趋势在不同悬沙粒径组中存在差异.结果对于利用泥沙条件抑制水华爆发有着重要的意义.     

Fuel loss and flexible fuel deposition rates in a long-distance migrant

Most migrating birds alternate flight bouts with stopovers, during which they rest and replenish the fuel used during flight (refueling). The rate of refueling (fuel deposition rate, FDR) affects stopover duration, and hence is an important determinant of the overall time required for migration. Although environmental and endogenous factors affect FDR, the urge to refuel depends on the anticipated distance to be travelled and possibly also on the amount of fuel used during the flight preceding stopover. Combining a field study with a fasting–refueling experiment on long-term captive songbirds, we tested whether the extent of fuel loss prior to refueling indeed affects FDR. In the field study, we took a comparative approach and determined FDR in two subspecies of northern wheatear (Oenanthe oenanthe) that differ greatly in the distance flown, and thus the extent of fuel used to reach our study (stopover) site. As both winter in western sub-Sahelian Africa, they face the same remaining migration distance. We found that FDR was higher in the subspecies that uses more fuel to get to our study site. Solidifying this result, in the experiment on captive northern wheatears, we found that the extent of fuel loss as a consequence of fasting explained most of the variation in subsequent FDR. The observation that experimental birds losing little fuel did not maximize their FDR suggests there are costs to rapid refueling. Our study shows that FDR is shaped not just by current environmental and endogenous conditions but also by fuel loss prior to refueling.     

In situ feeding rates and grazing impact of zooplankton in a South African temporarily open estuary

Recent studies in temporarily open estuaries of South Africa have shown that phytoplankton biomass is at times low, when compared to the high standing stock of the grazers. In situ grazing rates of the dominant zooplankton species were estimated at the Mpenjati Estuary once during the winter closed phase, in August 1999, and once during the summer open phase, in February 2000. The study aimed at determining what proportion of the energetic demands of the dominant grazers of the estuary is met by the available phytoplankton. Results show that the gut of all species exhibited higher pigment concentrations during the night than during the day, both in winter and summer. Gut pigment contents ranged from 0.27 to 5.38 ng pigm individual^-1 in the mysid Gastrosaccus brevifissura, from 0.16 to 1.63 ng pigm individual^-1 in the copepod Pseudodiaptomus hessei, from 0.12 to 0.45 ng pigm individual^-1 in the copepod Acartia natalensis, and from 0.8 to 5.44 ng pigm individual^-1 in the caridean Palaemon sp. [where pigm is the sum of chlorophyll-a (chl-a) and phaeopigments]. During the winter closed phase, gut evacuation rates for G. brevifissura, P. hessei, and A. natalensis were 0.62, 0.42, and 0.46 h^-1, respectively. In summer, gut evacuation rates were 0.68, 0.48, and 0.46 h^-1 for G. brevifissura, P. hessei, and Palaemon sp., respectively. The rate of gut pigment destruction for G. brevifissura was 99.6% of the total ingested, one of the highest values ever recorded for any crustacean. A gut pigment destruction of 79.0% was measured for Palaemon sp., 95.7% for P. hessei, and 93.8% for A. natalensis. During winter the total grazing impact of the dominant zooplankton species ranged from 5.05 to 22.7 mg chl-a m^-2 day^-1 and accounted for 34-69% of the available chl-a in the water column. During summer, the grazing impact ranged between 0.45 and 0.65 mg chl-a m^-2 day^-1, accounting for 17-41% of the available chl-a in the water column. This shows that the dominant zooplankton species of the Mpenjati have a very high grazing impact on algal cells. At times this may exceed 100% of the available phytoplankton production, suggesting that the zooplankton community may often resort to other food sources to meet all its energetic demands.     

Ammonia excretion of Artemia sp. (crustacea: Branchiopoda) under axenic conditions)

Ammonia excretion of the Utah strain of Artemia sp. grown in axenic culture media was followed throughout the different stages of larval development. The ammonia accumulated in the culture medium does not affect ammonia excretion rates under our laboratory conditions. Growth rate, density and starvation all affect ammonia excretion. Ammonia excretion is directly related to the numerical growth index and inversely related to Artemia sp. density. Starved adult Artemia sp. excrete considerably lower amounts of ammonia than brine shrimp grown in nutritive medium. In view of the difficulties often encountered in estimating the excretion rates of small crustaceans, our culture conditions would appear advantageous for further studies on the purine metabolism of Artemia sp.     

Description and use of an improved method for determining estuarine zooplankton grazing rates on phytoplankton

A method of rapidly determining zooplankton grazing rates on natural mixed phytoplankton populations using ¹⁴C is described. The method simplifies the design of grazing experiments as the grazing time can be kept short enough to prevent recycling of the isotope, and growth of the phytoplankton substrate. Very high specific activity, ¹⁴C-labelled phytoplankton concentrated either by centrifugation or sieving, may be used either as the sole grazing substrate, or as a tracer in natural mixed phytoplankton. Zooplankton, confined in glass jars at either ambient, or higher than ambient concentrations, are permitted to feed on the phytoplankton for periods of 30 min and 2 h, and are then separated by sieving. The zooplankton community grazing rate, or, if the samples are sorted into species, the individual species grazing rates, can be determined after scintillation counting of the zooplankton. The rate of appearance of ¹⁴C-labelled phytoplankton in the zooplankton is an estimate of the grazing rate, and the slope of the line joining the grazing rates at various phytoplankton concentrations gives an estimate of the grazing rate constant for the zooplankton population. The method provides a quick way of obtaining both zooplankton population, and individual species grazing rates on natural mixed phytoplankton. In two experiments, labelled phytoplankton was used as the sole grazing substrate in concentrations ranging between 0.4 and 5 times ambient levels. Grazing rate constants, for net-caught zooplankton concentrated to 46 times (Experiment 1) and 28 times (Experiment, 2) ambient estuarine levels were-0.14and-0.12 of the phytoplankton standing stock per day, respectively. There was a linear increase in the amount of phytoplankton grazed with an increase in phytoplankton concentration up to four times ambient phytoplankton levels. When tracer amounts of labelled phytoplankton were added to samples containing both phytoplankton and zooplankton at ambient concentrations the grazing rate constants were-0.28 and-0.42 of the phytoplankton standing stock per day. We conclude that zooplankton grazing was the major control factor of phytoplankton population size during October–November 1975 in South West Arm, Port Hacking, near Sydney, Australia.     

Carbon-nitrogen relations at whole-cell and free-amino-acid levels during batch growth of Isochrysis galbana (Prymnesiophyceae) under conditions of alternating light and dark

Isochrysis galbana Parke, Strain CCAP 927/1, was grown in ammonium-limited batch culture under a 12 h light: 12 h dark illumination cycle. Samples were taken every 12 h over the 26 d period from lag phase through exponential into stationary phase (no net carbon fixation), with more frequent sampling at points of interest. Exponential cell-specific growth rate was 0.3 to 0.4d^-1. Cell division occurred during the dark phase, while cell volume increase, ammonium uptake, and pigment synthesis occurred during the light. Stationary phase cells were small, and the lag phase was long (5 d) even though the C:N ratio had returned from 18 to 6.5 within 2 d, followed by synthesis of chlorophyll a. Net chlorophyll synthesis ceased within 4 d of exhaustion of the nitrogen source. The chlorophyll c: chlorophyll a ratio remained constant during increasing nitrogen deprivation. Biovolume and carotenoids correlated with carbon biomass. Levels of chlorophyll a correlated poorly with carbon fixation and carbon biomass once the nitrogen source had been exhausted. Except after the addition of ammonium to nitrogen-deprived cells (refeeding), the content of intracellular glutamine and the glutamine: glutamate ratio were low during the dark phase, rising to a plateau within the first 1 h of illumination. Refeeding of cells which had only just exhausted the extracellular nitrogen source resulted in a much smaller increase in glutamine than refeeding of nitrogen-starved (stationary-phase) cells. Nitrogen biomass correlated with the presence of an unidentified intracellular amine.     

微囊藻毒素对束丝藻细胞生长和抗氧化系统的影响

为从活性氧(ROS)角度探讨微囊藻毒素(MC)导致藻类细胞死亡的机理及揭示藻细胞对MC诱发的氧化胁迫的响应机制,采用50和500μg·L-1的微囊藻毒素LR(MC-LR)处理束丝藻(Aphanizomenon sp. DC01)细胞,测定了细胞生长、细胞内活性氧(ROS)含量及抗氧化系统的变化.结果表明,50μg·L-1的MC-LR处理对藻细胞的生长无显著影响,而500μg·L-1的MC-LR处理可诱导藻细胞死亡.50μg·L-1的MC-LR处理的藻细胞ROS含量在处理第2d显著高于对照;但藻细胞能通过还原型谷胱甘肽(GSH)含量,超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPX)活性改变修复氧化损伤,使ROS水平在处理第3d恢复到对照水平.500μg·L-1的MC-LR处理可显著降低藻细胞GSH含量和SOD与GPX活性,刺激藻细胞生成过量的ROS;ROS在毒素处理4d后突然暴发,过量的ROS引起膜质过氧化,并最终导致藻细胞死亡。     

Ecological growth strategies in the seaweeds Gracilaria foliifera (Rhodophyceae) and Ulva sp. (Chlorophyceae): Soluble nitrogen and reserve carbohydrates

The seaweeds Gracilaria foliifera (Rhodophyceae) and Ulva sp. (Chlorophyceae) were grown in an outdoor continuous-flow system at both ambient incident light (I₀) and 0.13 I₀. During the winter, both species accumulated substantial soluble nitrogen reserves (up to 1020 g-at N·g dry wt^-1 in G. foliifera and 630 g-at N·g dry wt^-1 in Ulva sp.). The rate at which these N reserves were depleted was proportional to the growth rate. Seaweeds grown at 0.13 I₀ had lower growth rates and higher levels of soluble tissue N than plants grown at I₀. During the spring-summer growing season, peaks in tissue N followed nutrient peaks in the ambient seawater. Ulva sp. had higher nutrient uptake and growth rates than G. foliifera and showed greater fluctuations in soluble tissue N. This may characterize opportunistic seaweed species with high biomass turnover rates. At I₀, the levels of starch (up to 340 mg·g dry wt^-1 in G. foliifera and 170 mg·g dry wt^-1 in Ulva sp.) were highest during the spring and summer. During this period, fluctuations in starch content were inversely related to growth rate and soluble tissue N. Seaweeds grown at 0.13 I₀ did not accumulate starch. Neither species was found to overwinter with starch reserves.     

Role of Acinetobacter sp. in arsenite As(III) oxidation and reducing its mobility in soil

Microbial arsenite oxidation was observed by Acinetobacter sp. XS21, this strain oxidised arsenite As(III) up to 80?mM within 48–72?h of incubation. The present strain XS21 oxidised As(III) at a very high concentration in a shorter interval of time than any of the previous reported microbes. Further, XS21 was applied to the soil to observe its ability in reducing the mobility of As(III), and we found that Acinetobacter sp. XS21 efficiently removed arsenite from soluble-exchangeable fraction and removed 70% of the arsenite as compared to control. This feature makes it a potential candidate for bioremediation. Arsenic-resistant bacteria with strong As(III)-oxidising ability may have potential to improve bioremediation of As(III)-contaminated sites. To understand their basis of resistance and transformation we found the As(III) oxidase gene using degenerate primer and amplified ～550?bp of aioA gene. Amplified aioA gene sequence exhibiting 52% identity in terms of gene and deduced protein sequence to Uncultured bacterium, and Achromobacter sp. arsenite oxidase of larger subunit. Arsenite oxidase, an enzyme, was also observed in this isolate, which may provide a resistance and transforming ability. This bacterium was identified as Acinetobacter sp., by sequencing 16s rRNA gene sequence analysis.     

Role of ovarian follicle cells in vitellogenesis and oocyte resorption inCapitella sp. I (Polychaeta)

Capitella sp. I has a short generation time, is polytelic and produces broods of relatively large, yolky eggs at intervals of as short as 5–7 d at 20°C. The follicle cells surrounding vitellogenic oocytes in the medial portion of the ovary contain large nuclei, extensive arrays of rough endoplasmic reticulum and Golgi complexes. The coelomic surfaces of follicle cells in the outer layer are covered by blade-like microvilli, which project into the coelom. In the dorsal and lateral portions of the ovary, where mature oocytes are found, the follicle cells are covered by flat, stellate-shaped, peritoneal cells that resemble the podocytes of many invertebrate excretory organs and of the mammalian glomerulus. Changes occurring in the ovary during resorption of oocytes in the middle to advanced stages of vitellogenesis are described. Oogonia and previtellogenic oocytes are not resorbed and perhaps subsequently undergo vitellogenesis. The ovary in this highly opportunistic polychaete species may play a significant regulatory role in the control of reproduction by producing yolk precursors, regulating their uptake from the coelomic fluid via the activity of the follicle cells and by resorbing mature oocytes in response to stress.