Bacterial dynamics and distribution during a spring diatom bloom in the Hudson River plume, USA

Bacterial abundance and [³H]thymidine incorporation rates wereused to characterize bacterial distributions and dynamics duringa spring diatom bloom in the coastal plume of the Hudson Riverduring March, 1981. Bacterial abundance did not decline significantlyaway from the plume or across the continental shelf. However,a pronounced gradient was observed for [³H]thymidine incorporation. Following a northeast gale, a bloom of Skeletonema costatumdeveloped in response to coastal upwelling. As the plume becamesaltier, warmer and larger, bacterial abundance averaged 1.3x 10⁹ cells 1^–1. Bacterial incorporation of [³H]thymidineinto cold 5% TCA insoluble materials, bacterial production andspecific growth rates averaged 80–120 pmol 1^–1 d^–1,1.4–2.0 x 10⁹ cells 1^–1 and 1.2–1.5 d^–1.respectively. The mean density of bacteria in the plume didnot change even though growth rates were higher than expectedlosses from sinking, mixing and export. The abundance and production levels of attached bacteria inthe plume were significantly higher than they were in coastalwater outside the plume. In contrast, free bacterial levelswere similar in all regions of the shelf and plume. Bacterialparameters in the plume were not correlated with phytoplanktonpigment concentrations, while significant positive correlationswere found in shelf waters >33 salinity. Thus bacteria werecoupled to phytoplankton in shelf waters but not in the plumewhere allochthonous dissolved matter was probably supportingthe bacteria. ^*Lamont-Doherty Geological Observatory Contribution No. 3459 ²Present address: Department of Microbiology, University ofGeorgia, Athens, GA 30602, USA.     

Growth and production of heterotrophic nanoflagellates in a meso-eutrophic lake

The growth of heterotrophic nanoflagellates (HNF) in mesotrophicLake Constance was measured in situ during a 13 month period.Experiments were conducted with 10 µm pre-filtered lakewater incubated in diffusion chambers at 3 m water depth atthe sampling location for 24 h. Growth rates were calculatedfrom changes in cell numbers occurring during the period ofincubation. Growth rates of all dominant taxa showed pronouncedseasonal variation (–0.13 to 1.76 day^–1 and weregenerally highest in summer at high water temperatures. In situgrowth rates were well below maximum growth rates known forthe respective and similar species from laboratory experiments.While water temperature was a key parameter positively relatedto the growth of all HNF species, the effect of various potentialfood items was taxon specific and less clear. Bacterial abundancewas equally important as temperature for growth in the smallbactenvorous Spumella sp., but was insignificant for growthrates of the larger omnivorous Kathablepharis sp. In Spuniellasp., 84% of the observed seasonal variation of its growth ratecould be explained by temperature and bacterial food supply.Based on these results, a multiple linear regression equationwith temperature and bacterial concentration as dependent variableswas calculated for the growth rate of Spumella. Taxon-specificproduction rates were derived from growth rates and averagebiomass of these two species, and compared to total HNF productionestimated from previously measured community growth rates andbiomass in Lake Constance. Production peaks of Spumella sp.and Kathablepharis sp. alternated seasonally. Total HINF productionranged from –0.01 to 10 mg C m^–3 day^–1. Theaverage seasonal production varied between 1.4 and 33 mg C m^–3day^–1 over 6 consecutive years. These small protozoa thuscontribute a substantial amount to total zooplankton productionin Lake Constance.     

The dynamics of heterotrophic nanoflagellates and bacterioplankton in a large ultra-oligotrophic Antarctic lake

The abundance of both heterotrophic nanoflagellates (HNAN) andbacterioplankton in a large (9km²) ultraoligotrophic Antarcticlake (Crooked Lake) were investigated from December 1992 untilNovember 1993. HNAN abundance peaked in spring, summer and autumn,falling to lowest numbers during the winter. Numbers rangedbetween 0 and 50.9x10⁴ l^–1. Bacterioplankton abundancewas highest during the late summer and then fell progressivelytowards winter and autumn (range 1.19–4.46x10⁶ l^–1)In contrast to numbers, mean cell volumes (MCV) of the bacteriareached their highest in spring, and consequently highest bacterialbiomass occurred at this time. MCV ranged between 0.052 and0.224µm³. Bacterial production measurements followingthe incorporation of [³H] thymidine into DNA and [¹⁴C] leucineinto protein using a doubling-labelling procedure were undertakenin January, June, August, October and November. Rates variedbetween 2.8 and 52 ng C l¹ h¹. On occasions, a significant differencein production rates based on the uptake of leucine and thymidinewas observed, suggesting unbalanced growth. Highest rates ofproduction coincided with times of high dissolved organic carbonlevels in the water column and lowest production with low levelsof DOC. HNAN grazing rates were measured by following the uptakeof fluorescently labelled bacteria and averaged 4.8 bacterialcells individual¹ day¹ at 2 and 4°C. Specific growth rates(h¹) ranged around 0.00070–0.00077 in both the field andlaboratory, giving doubling times of 37.3 and 41.0 days, respectively.These low rates of grazing and growth indicate that there isno adaptation to low temperatures in these freshwater protists.Based on these data, the gross production efficiency is 24%.HNAN removed between 0.1 and 9.7% of bacterial production perday.     

Photoadaptation in Antarctic phytopfankton: variations in growth rate, chemical composition and P versus I curves

The response of phytoplankton to variations in the light regimewas studied during the VULCAN and ACDA cruises in the Antarctic.Unenriched batch cultures of 12–19 days' duration reachedchl concentrations of 10–50 µg^–1 and exhibitedexponential growth rates, with the maximal rate being 0.41 doubl,day^–1. Ice edge algae exhibited maximum growth rates atphoton flux densities (PFD) of 30–100 µE m^–2S^–1and the growth rate was reduced by about 30% at 500–1000µE m^–2S^–1 The chl/C ratio ranged between 0.004and 0.018, with the lowest ratios at PFDs above 500 µEm^–2S^–1 chl/C ratios were also below maximum at PFDsbelow 40–50 µE m^–2S^–1 The C:N:P ratioswere close to the Redfield ratios; the Si/C ratio averaged 0.16(atoms), and the ATP/C ratio averaged from 0.0024 to 0.0050in different culture senes. When thawed after having been frozenfor 10 days, shade-adapted cultures were in a much better conditionthan sun-adapted ones. P versus I data showed that the maximumassimilation number varied from 0.75 to 4.4 µg C (µgchl)^–1h^–1. It varied inversely with the chl/C ratio;therefore the maximum carbon turnover rate varied little betweensamples (0.024/0.035 h^–1). Low biomass communities exhibitedrelatively high values for (the initial slope of P versus Icurves), low values for 1_sat (160–330 µE m^–2S^–1),and they were susceptible to photoinhibition. In contrast, communitiesdominated by Odontella weissflogii exhibited low values for, a high value for I_sat (560 µE m^–2S^–1 andthey tolerated high PFDs. The photo-adaptational status of thephytoplankton in natural water samples is discussed relativeto the profile of water column stability and mixing processes.     

Nutrient cycling through phytoplankton, bacteria and protozoa, in selectively filtered Lake Vechten water

The breakdown of organic carbon of dead Synechococcus cell walls,added to selectively filtered Lake Vechten water, was not acceleratedby protozoa. During 4 weeks of incubation at 15°C no significantdecrease of total organic carbon was observed. However, heterotrophicnanoflagel-lates (HNAN) and ciliates strongly increased theremineralization of N and especially P, from both cell wallsand cell extract. Bacterioplankton growth did not result innet P mineralization but in P uptake. P was remineralized onlyin the presence of protozoan grazers. Both HNAN and ciliatesgrazed on bacteria, with ingestion rates estimated at 27–96bad HNAN^–1 h^–1 and 129 bact ciliate^–1 h^–1respectively. Grazers increased N mineralization too, althoughN was also mineralized in the absence of protozoa. The phytoplanktoncell walls yielded less P but more N remineralization than thecell extract. Thus, protozoa can strongly accelerate cyclingof specific nutrients through plankton. Nuclepore filters werefound to cause artificial DOC release during selective filtration.     

Diurnal variations in the contributions of autotrophic picoalgae and heterotrophic bacteria to planktonic production in an upland lake

An investigation of the diurnal variation in contributions toproduction of the autotrophic and heterotrophic components ofthe picoplankton community was carried out during August andSeptember in Llyn Padarn, a mesotrophic upland lake in NorthWales. The picoplankton was separated using 1 µm pore-sizedfilters into the smaller cell sized fraction (<1 µm),the majority of the bacteria and the larger cell sized picoalgae(<3>1 µm), together with some bacteria. The distributionof bacterial heterotrophic activity between these two fractionsof picoplankton was assessed by uptake of [¹⁴C]glucose and differentialfiltration. Thus, the absolute autotrophic production by picoalgaeand the heterotrophic contribution by bacteria to picoplanktoncommunity production via uptake of extracellular organic carbon(EOC) were determined. Rates of picoplankton community productionexhibited diurnal variation with maximum rates of 19.1 mg Cm^–3 h^–1 recorded at 18.00 h at 4 m depth in September.The bacterial contribution to picoplankton community productionincreased markedly between 15.00 and 18.00 h. Rates of absoluteautotrophic production varied less over 24 h than rates of accumulationin bacteria of ¹⁴C-labelled EOC released from the entire phytoplanktoncommunity. Bacteria contributed up to 86–98% of the neworganic carbon within the picoplankton community at the endof the day. The maximum rate of absolute autotrophic productionin the picoplankton was 1.6 mg C m^–3 h^–1 at 18.00h at 1 m in August, and the maximum rate of bacterial accumulationof new organic carbon was 18.5 mg C m^–3 h^–1 at 18.00h in September at 4 m depth. The diurnal pattern of picoplanktoncommunity production involved increasing rates during the daywith a maximum at 18.00 h. Autotrophic processes were dominantin the first 3–6 h of the light cycle and heterotrophicuptake of ¹⁴C-labelled EOC was the major component from 15.00h onwards. Bacterial uptake of newly released EOC by phytoplanktonwas rapid, comprised the majority of picoplankton production,particularly later in the day, and contributed a maximum of60% of the total pariculate primary production in plankton between15.00 and 18.00 h at 4 m in September with a mean contributionof between 6 and 26% over 24 h in these investigations. Theimportance of autotrophic processes in picoplankton communityproduction has been overestimated in previous investigations.Bacteria play a major role in transferring newly produced EOCrapidly from phytoplankton to the picoplankton community. Atthe end of the day, the majority of newly produced organic carbonis in bacterial cells and this production is significant inthe dynamics of carbon production within the entire planktoniccommunity.     

Indirectly fluorescently labelled flagellates (IFLF): a tool to estimate the predation on free-living heterotrophic flagellates

A procedure was developed to estimate the direct grazing impacton free-living heterotrophic nanoflagellates (HNF). Culturedflagellates were labelled by feeding on brightly fluorescingbacteria (FLB) and then offered as indirectly fluorescentlylabelled flagellates (IFLF) to potential predators of HNF. Thenumber of FLB in the predators' food vacuoles could be convertedinto IFLF uptake and consumption of HNF. This new techniquewas used to study the HNF-ciliate relationship in the pelagiczone of Lake Constance. Three groups of ciliates were detectedas HNF grazers: small representatives of the genus Strobilidium.a small Haltena-like ciliate (probably Halteria grandinella)and a Codonella sp. Tintinnidium sp. group The ingestion ofHNF by these groups of ciliates ranged between 3 and 15, 3 and39, and 3 and 7 HNF ciliate^–1 h^–1; respectively.The IFLF method allows the direct determination of ingestedflagellate prey in the food vacuoles of their predators. Becauseindigenous living prey organisms were used, tracer discriminationcan be reduced.     

The influence of temperature and light on the upper limit of Microcystis aeruginosa production in a hypertrophic reservoir

Primary production was measured for 7 years, using the in situ¹⁴C-method in hypertrophic Hartbeespoort Dam, South Africa,to examine the influence of light and water temperature on theupper limit of Microcystis aeruginosa production. Water temperaturesvaried from 11 to >25°C and chlorophyll concentrationsreached 6500 mg m^–3. The maximum volumetric rate of production(A_max) was 12->8800 mg C m^–3 h^–1 with areal productions(A) of 69->3300 mg C m^–2 h^–1 for euphotic zonedepths of <0.5–8.4 m. The intrinsic parameters of phytoplanktonproduction (, A_max/B, I_k) indicated that the phytoplankton populationwas adapted to high light levels. Both A_max/B and I_k were correlatedwith temperature. Under optimal conditions, , the theoreticalupper limit of A, was calculated to be 2.8 g Cm^–2 h^–1,while the measured rate was 2.5 g Cm^–2 h^–1. Measuredareal rates exceeding were overestimated due to methodologicalproblems when working with Microcystis scums. Light and watertemperature interacted to yield high production rates: watertemperature through its direct effect on photosynthetic ratesand indirectly in the formation of diurnal mixed layers; lightindirectly through water temperature and directly through itsattenuation and induction of light-adapted physiology in Microcystis.     

Assessment of Calanus finmarchicus growth and dormancy using the aminoacyl-tRNA synthetases method

We obtained growth rates of the copepod Calanus finmarchicusat different locations across the North Atlantic between May1998 and June 2004. Animals were incubated for 2–9 daysand fed either with natural food assemblages or with culturedalgae. During this period, we measured both somatic weight-specificgrowth rates (measured as protein change) and aminoacyl-tRNAsynthetases (AARS) activity. We found a highly significant relationshipbetween AARS activity and growth in protein content (R² = 0.55,P < 0.001). Significant AARS activity also occurred whengrowth was negative, the relationship predicting an AARS activitylevel of 8.33 nmPPi·mg protein^–1·h^–1when somatic growth is zero. This is because AARS activity isexpected even when growth is negative, owing to the continuedprotein turnover in the cells. The AARS method allowed for thefirst time the study of protein metabolism in overwinteringC. finmarchicus. Our study results showed that overwinteringcopepods had significantly lower values of AARS activity thannon-diapausing animals (t = –3.51, P < 0.002). TheAARS method opens the possibility to better understand physiologydynamics of deep-water organisms (e.g. the beginning and endof diapause).     

Bacterioplankton growth, grazing mortality and quantitative relationship to primary production in a humic and a clearwater lake

Bacterial growth and grazing mortality were estimated from Mayto October in two south Swedish oligotrophic lakes, one beinga clearwater lake (water colour 5–10 mg Pt l^–1 DOC2.9–3.4 mg l^–1, Secchi disk depth 5.0–9.4m) and the other a humic, brownwater lake (water colour 105–165mg Pt l^–1, DOC 13.7–22.7mg l^–1, Secchi diskdepth 1.3–2.1 m). Specific rates of growth and grazingmortality were generally similar for both lakes. However, theabundance of bacteria was consistently 2–3 times higherin the water of the humic lake, suggesting that the total productionand consumption of bacterial cells were also higher than inthe dearwater lake. The ratio of bacterial secondary productionto primary production was higher in the humic lake than in theclearwater lake, indicating that the bacterioplankton of thehumic lake utilize allochthonous substrates, in addition tosubstrates originating from autochthonous primary production.Most of the bacterial loss in both lakes could be attributedto small protozoan grazers. This implies that allochthonousand autochthonous organic carbon fixed by bacterioplankton isless important in terms of carbon flow to higher trophic levelsthan would be expected if macrozooplankton were the dominantbacterivores, providing a more direct and efficient transferof carbon to larger organisms.     

Bacterivory in seawater samples estimated by a dual radioactive-labelling technique

A dual radioactive-labelled bacteria technique using Vibrio(DRLV), developed for laboratory studies on bacterivory, hasbeen refined for use at the concentrations of prey and predatorstypcially found at sea. Experiments with estuarine water collectedin spring and in autumn showed that bacterivorous nanoflagellates(HNF) (concentration 1.38±0.35x10³ HNF ml^–1) ingested2.7±0.96 DRLV flagellate1^–1 h^–1 at concentrationsof 0.8–2.2x10⁶ DRLV ml^–1 in the presence of 2.04±0.68x10⁶natural bacteria ml^–1. The method was also applied tosamples collected in October in the Celtic Sea, when on average1 ml of water from the surface layer contained 1.41±0.16x10⁶natural bacteria, 14.6x10³ cyanobacteria, 530±170 HNF,7.3±3.0x103 phototrophic nanoflagellates (1.5–4µm), 49.0±26.5 phototrophic dinoflagellates, 36.3±12.6heterotrophic dinoflagellates and 21.3±9.5 Leucocryptosmarina. Under these conditions the grazing rate in most samplesdid not exceed the coefficient of variation of the method (2%),although we estimate the grazing rate was -1.6 DRLV HNF^–1h^–1 and on one occasion a rate of 2.45 was recorded. Thegross growth efficiency for protein of -30% displayed by naturalHNF means that they could release about     

Viral lysis and grazing loss of bacteria in nutrient- and carbon-manipulated brackish water enclosures

A 3 week enclosure experiment was carried out at the Gulf of Finland, the Baltic Sea. After additions of inorganic nutrients [nitrogen (N) + phosphorus (P)] and a carbon source (sucrose), we followed bacterial, viral and heterotrophic nanoflagellate (HNF) abundances, as well as bacterial production and the frequency of bacteria visibly infected with viruses. Furthermore, the decay rate of virus particles was measured three times during the enclosure experiment from the KCN-treated water samples. Bacterial mortality caused by viral lysis was estimated using the decay rates and the fraction of bacteria infected. Nutrient (N + P) additions stimulated phytoplankton growth [the chlorophyll (Chl) a concentration increased from <5 g l^-1 up to 19 g l^-1], while sucrose additions increased bacterial production (from 4-6 x 10⁷ l^-1 h^-1). The phytoplankton blooms affected bacterial production only slightly. Bacterial mortality that was explained by viruses ranged from <2% to 13% when estimated from the visibly infected cells, and from 8% to 808% when the decay rates (range 0.052-0.765 h^-1) were used. Assuming a clearance rate of 5 nl flagellate^-1 h^-1, the HNF community could graze 16-135% of total bacterial loss.      

Nitrogenous nutrient uptake by phytoplankton and ammonium regeneration by microbial assemblage in Lake Biwa

In situ rates of nitrate, ammoniwn and urea uptake by the phytoplanktonassemblage, and the regeneration rate of ammonium by the microbialassemblage, in Lake Biwa were measured using the nitrogen 15tracer method from 1985 to 1987. The rate of total nitrogen(sum of ammonium, nitrate and urea) uptake was in the rangeof 62–594 ng N^–1 r^–1 h^–1. The percentagecontribution of ammonium uptake was 41–92%, that of urea4–58% and that of nitrate <1–28% of total uptake.The annual mean new production which was supported by nitrateuptake was 18% of the total production in 1986. The phytoplanktonassemblage in Lake Biwa preferentially utilized regeneratednitrogen, such as ammonium and urea, whose concentration wasmuch lower than that of nitrate throughout the observation penodwithout in summer. The in situ nitrogen uptake rate was almostsufficient to meet the nitrogen requirement of the phytoplanktonassemblage, except in midsummer when the nitrate concentrationwas below the detection limit of 0.3 µg N r^–1. Inthe trophogemc layer, the rate of ammonium regeneration was66–272 ng N 1^–1 h^–1 Although the ambient ammoniumconcentration in the trophogenic layer was maintained at aroundthe half-saturation constant for ammonium uptake kinetics, theammomum uptake rates were always highly correlated with ammoniumregeneration rates. From the size fractionation experimentsand estimates from the literature, it was suggested that themicrobial assemblage <1 µm may have been the most importantagent responsible for the ammonium regeneration processes inthe trophogenic layer.     

Ecological studies on the phytoplankton of Boknafjorden, western Norway. II. Environmental control of photosynthesis

Both predicted (incubator) and measured (in situ) ¹⁴C-assimilationrates were studied from February to November 1981 at three stationsin Boknafjorden, a deep silled fjord of western Norway. Sampleswere taken from different light depths within the euphotic zone.A high degree of conformity was found between the two approaches.Daily values of carbon assimilation integrated over the euphoticzone varied between 0.05 and 1.4 g C m^–2. Yearly primaryproduction varied between stations from 82 to 112 g C m^–2(120–148 g C m^–2 when based on average light conditions).The light-saturation curve parameters ^B and P^B_max ranged from0.0056 to 0.0537 mg C mg Chla^–1 h^–1 µE^–1m² and from 0.7 to 8.5 mg C mg Chla^–1 h^–2 (in situassimilation numbers ranged from 0.9 to 9.3 mg C mg Chla^–1h^–1) respectively, which compare well with those publishedfrom the northwestern side of the Atlantic. The overall importanceof light in controlling photosynthesis throughout the year wasrevealed by the light utilization index , estimated to be 0.43mg C mg Chla^–1 E^–1 m². The maximum quantum yieldwas encountered on August 17, with 0.089 mol CE^–1. Chla/Cratios above and below 0.010 were found to be typical for shade-and light-adapted cells respectively. Assimilation numbers andgrowth rates were linearly related only when considering light-adaptedcells. Consistent with the findings of this study, the applicabilityof I_K, ^B and P^B_max as indicators of light-shade adaptation propertiesshould be questioned. Maximum growth rates were encounteredduring an autumn bloom of the dinoflagellate Gyrodinium aureolum(1.0 doublings day^–1), while 0.7–0.8 doublings day^–1were found for a winter bloom (water temperature of 2°C)of the diatom Skeletonema costatum. No unambiguous temperatureeffect on assimilation number and growth of phytoplankton couldbe recognized in Boknafjorden. A tendency towards increasedassimilation numbers coinciding with increased water columnstability was revealed. The highest P^B_max values were oftenencountered at almost undetectable nutrient concentrations.At least during summer this could be attributed to recyclingof nutrients by macro- and/or microzooplankton, responsiblefor a greater part of the primary production now being grazeddown. This study supports the convention that the depth of theeuphotic zone may extend considerably below the 1% light depth.     

Carbon dynamics in the 'grazing food chain' of a subtropical lake

Studies were conducted over a 13 month period at four pelagicsites in eutrophic Lake Okeechobee, Florida (USA), in orderto quantify carbon (C) uptake rates by size-fractionated phytoplankton,and subsequent transfers of C to zooplankton. This was accomplishedusing laboratory ¹⁴C tracer methods and natural plankton assemblages.The annual biomass of picoplankton (<2 µm), nanoplankton(2–20 µm) and microplankton (<20 µm averaged60, 389 and 100 µg C 1^–1 respectively, while correspondingrates of C uptake averaged 7, 51 and 13 µg C1^–1h^–1. The biomass of microzooplankton (40–200 µm)and macrozooplankton (<200 µm averaged 18 and 60 µgC 1^–1, respectively, while C uptake rates by these herbivoregroups averaged 2 and 3 µg C 1^–1 h^–1. Therewere no strong seasonal patterns in any of the plankton metrics.The ratio of zooplankton to phytoplankton C uptake averaged7% over the course of the study. This low value is typical ofthat observed in eutrophic temperate lakes with small zooplanktonand large inedible phytoplankton, and indicates ineffectiveC transfer in the grazing food chain. On a single occasion,there was a high density (<40 1^–1) of Daphnia lumholrzii,a large-bodied exotic cladoceran. At that time, zooplanktoncommunity C uptake was <20 µg C 1^–1 h^–1and the ratio of zooplankton to phytoplankton C uptake was near30%. If D.lumholrzii proliferates in Lake Okeechobee and theother Florida lakes where it has recently been observed, itmay substantially alter planktonic C dynamics.     

Dissolved organic carbon released by zooplankton grazing activity-a high-quality substrate pool for bacteria

Experiments were designed to investigate whether processes relatedto zooplankton feeding have a positive effect on bacterial growth.Bacterial abundance and [³H]thymidine incorporation rates werefollowed in grazer-free batch cultures originally containingeither Scenedesmus quadricauda or Rhodomonas lacustris as foodsources, and Daphnia cucullata or Eudiaptomus graciloides asgrazers. Compared with controls lacking either animals or algae,a significantly higher bacterial abundance and productivityoccurred in cultures which contained both phyto- and zoo-plankton.The same experimental methodology was tested during the declineof a diatom spring bloom in a eutrophic, temperate lake. A significantincrease in bacterial biomass was observed due to the grazingactivity of in situ mesozooplankters during the clear-waterphase. Our results demonstrated that the dissolved carbon pathwayfrom mesozooplankton to bacteria averaged 57% (26–78%)of the algal carbon filtered from suspension.     

Nanoheterotroph grazing on bacteria and cyanobacteria in oxic and suboxic waters in coastal upwelling areas off northern Chile

The vertical distribution and abundance of microbial assemblagesand the grazing of nanoheterotrophs upon prokaryotes in oxicand suboxic waters were examined in two coastal upwelling areasoff northern Chile where a shallow Oxygen Minimum Zone (OMZ)is characteristic. Prokaryotic prey included bacterioplanktonand cyanobacteria (Synechococcus); both displayed a bimodaldistribution, with abundance maxima above and within the upperOMZ. Flagellates numerically dominated the nanoplankton andwere mostly concentrated in the oxic layer. Mean ingestion ratesof cyanobacteria by nanoflagellates (vacuole content method)ranged from 0.2 to 1.1 cells flagellate^–1 h^–1 andmean consumption rates (34–160 cells mL^–1 h^–1)were four times higher in the oxic layer. With the selectiveinhibitors technique, specific grazing rates on bacteria werelow (<0.1 h^–1) and consumption did not control bacterialproduction in the surface layer but did so in the suboxic layer(accounting for >100% of bacterial production). With thesame method, the specific grazing rate on cyanobacteria rangedbetween zero and 0.23 h^–1 with no clear differences betweenoxygen conditions; prey growth and production were always higherthan the grazing pressure (accounting for <17% of cyanobacterialproduction). The impact of grazing by nanoheterotrophs in regulatingthe production of prokaryotes in oxic and suboxic waters inthis region is discussed.     

Leaf Extension in Zea mays: III. FIELD MEASUREMENTS OF LEAF EXTENSION IN RESPONSE TO TEMPERATURE AND LEAF WATER POTENTIAL

Leaf extension rates of young maize plants were measured inthe field. Large diurnal fluctuations of air temperature fromabout 5—35°C caused extension rates to vary from 0·4mm h^–1– 3·6 mm h^–1. When the temperatureof the shoot apical meristem was kept at 30–34°C,extension rates remained constant, despite diurnal fluctuationsof air temperature. Leaf water potentials () above –8 or –9 bars hadlittle apparent effect on extension rate. It was concluded that gradients within leaves could account for this.     

Grazing rates for three life history stages of the doliolid Dolioletta gegenbauri Uljanin (Tunicata, Thaliacea)

Grazing rates for Dolioletta gegenbauri averaged 2.5 ml zooid^–1h^–1 for trophozooids, 2.7 for phorozooids and 5.8 forgonozooids. In situ and laboratory rates were comparable forboth trophozooids and phorozooids.     

Ethylene and Ethane Production in 2,4-D Treated and Salt Treated Tobacco Tissue Cultures

Gas chromatography was used to measure ethylene (ethene) andethane production by tobacco (Nicotiana tabacum cv. Wisconsinno. 38) callus tissues grown on media containing inorganic saltsaccording to Murashige and Skoog (1962), sucrose, myo-inositol,thiamine-HCl kinetic according to Linsmaier and Skoog (1965),and either 2,4-dichiorophenoxyacetic acid (2,4-D) in the range0–100 mgl^–1 or 2 mgl^–1 indoi-3-ylacetic acidplus NaCl in the range 0–200 Meq l^–1. Ethylene productionrates were high (> 500 nl h^–1 g^1– fresh weight)initially in all treatments. Subsequently, ethylene productiondeclined in rapidly growing cultures but remained high in moderatelyand severely 2,4-D (> 0·5 mgl^–1) stressed andin severely NaCl (150 Meql^–1) stressed cultures. Highinitial rates of ethane production (> 200 nl h^–1 g^–1fresh weight) were obtained under conditions of severe stresscaused by 2,4-D or NaCl but not in control or moderately inhibitedcultures. With further incubation ethane production declinedin the severely stressed cultures. It is concluded that ethyleneproduction can be used as an index of moderate 2,4-D stressand severe NaCl stress by virtue of the high persisting ratesof ethylene production in stressed cultures. Ethane productioncan be used as an early index of severe stress caused by either2,4-D or NaCl in vitro. Nicotiana tabacum L., tobacco, ethylene, ethenen, ethane, 2,4-dichlorophenoxyacetic acid, auxin, stress, callus tissue