Behavioral determinations of thresholds for n-butyl acetate and nbutyl alcohol in the tiger salamander (Ambystoma tigrinum)

Two groups of tiger salamanders (Ambystoma tigrinum) were conditionedto respond to odorant-air mixtures of n-butyl acetate (8.9 x10^–5M) or n-butyl alcohol (6.7 x l0^–5M). They werethen given tests with various concentrations of the trainingodorants presented using a temporal forced-choice method ofascending limits. Results showed that reliable responses toodorant-air presentations were obtained with concentrationsof n-butyl acetate above 2.4 x l0^–7M and with concentrationsof n-butyl alcohol above 8.5 x 10^–8M. These results arein substantial agreement with previous dectrophysiological findings.     

INHIBITION OF OLFACTION IN THE MOTH HELIOTHIS VIRESCENS BY THE SULFHYDRYL REAGENT FLUORESCEIN MERCURIC ACETATE

A combined electrophysiological, behavioral, and biochemicalstudy was initiated to determine the effects of the sulfhydryl-specificreagent fluorescein mercuric acetate (FMA) on olfaction in thetobacco budworm moth Heliothis virescens. The electroantennogram(EAG) response to the standard odorant n-pentyl acetate showedboth a time and concentration dependent inhibition by FMA. Treatmentof insect antennae with 2.52 x 10^–5 M FMA for 2 min reducedthe EAG by 50%, while treatment for 17 min reduced the EAG by80%. Incubation of antennae for 7 min with 2.52 x 10^–6M FMA resulted in 30% inhibition, while incubation with 2.52x 10^–6 M FMA for 7 min resulted in 65% inhibition. Antennalgrooming behavior was inhibited by FMA in a similar time andconcentration dependent manner as the EAG. Regeneration of previouslyinhibited behavioral and EAG responses has been observed withina 24-hr period. The interaction of protein, obtained by sonicatingintact antennae in phosphate buffer, with FMA was monitoredfluorometrically. Successive additions of antennal sonicateto FMA resulted in stepwise decreases in fluorescence. Partialrecovery of fluorescence was obtained by addition of cysteineto the FMA-antennal sonicate solution. The polarization of theFMA-antennal sonicate fluorescence decreased upon addition ofcysteine. These data indicate that FMA is reacting with a relativelylarge antennal protein (s) by mercaptide linkage and blockingthe olfactory transduction process.     

Effect of complete protein 4.1R deficiency on ion transport properties of murine erythrocytes

Moderate hemolytic anemia, abnormal erythrocyte morphology (spherocytosis), and decreased membrane stability are observed in mice with complete deficiency of all erythroid protein 4.1 protein isoforms (4.1^–/–; Shi TS et al. J Clin Invest 103: 331, 1999). We have examined the effects of erythroid protein 4.1 (4.1R) deficiency on erythrocyte cation transport and volume regulation. 4.1^–/– mice exhibited erythrocyte dehydration that was associated with reduced cellular K and increased Na content. Increased Na permeability was observed in these mice, mostly mediated by Na/H exchange with normal Na-K pump and Na-K-2Cl cotransport activities. The Na/H exchange of 4.1^–/– erythrocytes was markedly activated by exposure to hypertonic conditions (18.2 ± 3.2 in 4.1^–/– vs. 9.8 ± 1.3 mmol/10¹³ cell x h in control mice), with an abnormal dependence on osmolality (EC₅₀ = 417 ± 42 in 4.1^–/– vs. 460 ± 35 mosmol/kgH₂O in control mice), suggestive of an upregulated functional state. While the affinity for internal protons was not altered (K_0.5 = 489.7 ± 0.7 vs. 537.0 ± 0.56 nM in control mice), the V_max of the H-induced Na/H exchange activity was markedly elevated in 4.1^–/– erythrocytes (V_max 91.47 ± 7.2 compared with 46.52 ± 5.4 mmol/10¹³ cell x h in control mice). Na/H exchange activation by okadaic acid was absent in 4.1^–/– erythrocytes. Altogether, these results suggest that erythroid protein 4.1 plays a major role in volume regulation and physiologically downregulates Na/H exchange in mouse erythrocytes. Upregulation of the Na/H exchange is an important contributor to the elevated cell Na content of 4.1^–/– erythrocytes. spherocytosis; cell Na; Na/H exchange     

PSYCHOPHYSICAL CHARACTERIZATION OF MUSK CHEMICALS

The odor intensities of six commercial musks: celestolide, muskolactone,galaxolide, musk 36A^®, tonalid^®, and musk ambrette^*were matched by the method of equal odor intensity. Galaxolidewas arbitrarily used as the reference odorant in order to generatea scale for the determination of relative odor intensities.The odor intensities are expressed in terms of Stevens' psychophysicalpower function with the exponent value, b, ranging from 0.43to 0.73.     

Interstrain differences in bitter taste responses in mice

Interstrain differences in bitter taste responses were examinedusing inbred strains of mice. Taste responses were recordedfrom the glossopharyngeal and chorda tympani nerves of SWR/J,LP/J, BDP/J and DBA/2J mice. There were large differences inthe magnitude of responses to sucrose octaacetate (SOA) in boththe glossopharyngeal and chorda tympaninerves of SWR/J miceas compared with the other strains of mice. SOA thresholds ofSWR/J mice were 10^–7–^–6 M, whereas they were– 10^–4 M in LP/J mice. On the other hand, no appreciabledifferences were observed in the responses to quinine hydrochlorideand pnenyl-thio-carbamide. The results obtained in the presentexperiments fully explain the findings in behavioral studiesshowing that only SWR/J mice avoid SOA solutions whereas otherstrains do not. ^*Present address: Department of Physiology, Niigata UniversitySchool of Dentistry, Niigata 951, Japan     

Amiloride does not block taste transduction in the mudpuppy, Necturus maculosus

Activity of the glossopharyngeal nerve was recorded with bipolarsilver wire electrodes while taste stimuli were applied to thelingual surface in anesthetized mudpuppies. Taste stimuli wereinjected into a continuous stream of distilled water which wasrunning over the tongue, KCl, CaCl₂ and LiCl₂ at 0.4 M elicitedbrisk responses, as did HCl at 0.2 M and quinine at 6 x 10^–4M. Sucrose, glucose and saccharin did not elicit responses.Twenty amino acids were surveyed for their ability to evokea response at 0.04 M: 1-arginine, 1-valine, 1-phenylalanine,1-tryptophan, 1-tyrosine, 1-glutamic acid, 1-lysine and histidinealways evoked responses, whereas other amino acids either didnot evoke responses or only occasionally evoked responses. Thesupernatants from solutions of minced worms and minnows andPurina Trout Chow were effective taste stimuli. Pre-adaptingthe tongue to Ringer's solution by running a continuous streamof Ringer's solution over it eliminated responses to quinineand decreased responses to NaCl. Pre-adapting the tongue to10^–4 to 10^–3 M amiloride, a potent sodium channelblocker, did not alter the responses to NaCl, LiCl, or othertaste stimuli.     

The Effect of Morphactin (Methyl 2-Chloro-9-hydroxyfluorene-9-carboxylate) on Basipetal Transport of Indol-3-ylacetic Acid in Hypocotyl Sections of Phaseolus vulgaris L.

The effect of morphactin (methyl 2-chloro-9-hydroxyfluorene-9-carboxylate)on basipetal transport of auxin (Indol-3-ylacetic acid-2-¹⁴C)was studied in bean (Phaseolus vulgaris) hypocotyl with thedonor-receiver block method. Morphactin (5 x 10^–6m) reduced IAA (5 x 10^–6m) transportintensity by an average of 83 per cent and auxin transport capacityby 90 per cent, but transport velocity was not affected. Morphactin did not inhibit uptake of IAA into hypocotyl tissue,but it did prevent transfer of IAA from the tissue into receiverblocks. Chromatographic analysis of the tissue after 4 h IAA-2-¹⁴Ctransport showed that 54 per cent of the total activity wasin the form of IAA in the control and 42 per cent in the morphactintreated tissue. No difference was found in the rate of decarboxylationof IAA-1-¹⁴C between control and morphactin treated tissue sections.Nor could any difference between control and morphactin be shownin the radioactivity associated with a TCA ppt fraction. Ina study of the transportable auxin pool, morphactin decreasedthe size of the pool and increased the half-life of decay ofauxin transport from 1•22 h to 3•85 h. In a kineticanalysis of the reversal of morphactin (5 x 10^–6m) inhibitionby increasing concentration of IAA-2-14C (5 x 10^–6m to2 x 10^–5m), it was shown that IAA transport resemblesMichaelis-Menten enzyme reaction kinetics, and that inhibitionby morphactin fitted a ‘mixed type’ model. IAA hada dissociation constant of 8•5 x 10^–6m and morphactinthat of 4•3 x 10^–7m with a K_m for the transport processof 8•5 x 10^–6m.     

A simple and flexible device to odorize large stimulation areas

This paper describes a flow dilution olfactometer which allowsthe odorization of large stimulation areas and the easy manipulationof several odorants and/or concentrations. Generation of theodorized air is performed by mixing in two steps the odor vaporcontained in Tedlar bags with a pure air stream flowing continuouslyout of a nozzle. Discrete concentration values are obtainedby using pre-adjusted needle valves to change the vapor flowsampled in the bags. This kind of olfactometer was utilizedto study odor coding in the olfactory bulbs of rats and rabbits.Five Odorants were delivered at concentrations ranging from2 x 10^-4 to 1.5 x 10^-2 of the saturated vapor pressure. Measurementsshowed that lower concentrations can be obtained by fillingthe bags with a more diluted odor vapor. Furthermore, the numberof test odorants can be increased at low cost by increasingthe number of Tedlar bags.     

Microbial dynamics during the summer ice-loss phase in maritime Antarctic lakes

The dynamics of bacterioplankton and protozooplankton in twomaritime Antarctic lakes (Heywood Lake and Sombre Lake, SignyIsland, South Orkneys) were studied during the phase of icebreak-out (December and early January 1994/95). The lakes aresuffering animal-induced (fur seal) eutrophication, though HeywoodLake is most severely affected. Both lakes had morphologicallydiverse bacterial communities which increased during the studyperiod, reaching maxima of 80 x 10⁸ l^–1 in Heywood Lakeand 31.8 x 10⁸ l^–1 in Sombre Lake. Heterotrophic nanoflagellates(HNAN) reached a peak in late December with maxima of 40.6 x10⁸ l^–1 in Sombre Lake and 174 x 10⁵ l^–1 in HeywoodLake. Phototrophic nanoflagellates (PNAN) peaked in late Decemberafter ice loss in Heywood Lake (63 x 10⁵ l^–1), which coincidedwith a peak in a bloom of Chroomonas acuta which reached abundancesof 1.0 x 10⁸ l^–1. In Sombre Lake, ice persisted for alonger period and here PNAN reached their highest density atthe end of the study period (around 70.0 x 10⁵ l^–1). Ciliateabundance reached high levels in Heywood Lake (>60001^–1),while in Sombre Lake maximum abundance was 568l^–1. Protozooplanktondiversity was greater in the less-enriched Sombre Lake. Grazingrates of ciliates averaged 70.6 bacteria indiv.^–1 h^–1in Heywood Lake and 119.3 bacteria indiv.^–1 h^–1in Sombre Lake. The difference was a reflection of the differenttaxonomic make-up of the community in the lakes. HNAN grazingrates varied between 0.51 and 0.83 bacteria indiv.^–1 h^–1in Sombre and Heywood Lakes, respectively. Specific growth rates(r) h^–1 in Sombre Lake were 0.028 for ciliates and 0.013for HNAN, and in Heywood Lake 0.010 for ciliates and HNAN 0.012.These growth rates result in doubling times ranging between38 and 69 h for ciliates and around 55 h for HNAN.HNAN grazingon bacteria was curtailed in Heywood Lake in early January asa result of predation by microcrustacean larvae feeding on theplankton. Thus, for a short phase top-down control was apparentin the dynamics of Heywood Lake, a feature uncommon in Antarcticlake ecosystems. The impact of natural eutrophication on thesesystems is discussed in relation to other unaffected Antarcticlakes.     

A Study of the Exudation of Excised Maize Roots after Removal of the Epidermis and Outer Cortex

The fluid exudation rates and the ionic composition of the exudatesof isolated maize roots were compared with those of similarroots from which the epidermal and outer cortical cells hadbeen removed. The results indicate that in low ionic strengthmedia the salt fluxes into the exudation stream are severaltimes larger in the control than in the treated roots. As theionic strength of the bathing medium increases to 10 mM KClor greater, the salt fluxes become equal. A mechanism to accountfor this behaviour is discussed. The values of L_p, the hydraulic conductivity of the roots toradial water flow, are 0.26 x 10^–6 cm sec^–1 atm^–1for treated and 0.14 x 10^–6 cm sec^–1 atm^–1for control roots, but a statistical technicality precludeda significance test on this apparent difference. The kinetics of tritiated water exchange from external mediumto the exudation fluid in both control and treated roots werenot significantly different. The entry of labelled water seemsto be achieved by the fluid exudation rate in both cases; thusthe barrier to water movement to the exudate compartment remainsintact after removal of the epidermis.     

Laboratory-measured grazing and ingestion rates of the salp, Thalia democratica Forskal, and the doliolid, Dolioletta gegenbauri Uljanin (Tunicata, Thaliacea)

Grazing and ingestion rates of laboratory-born Thalia democraticaaggregates and Dolioletta gegenbauri gonozooids, phorozooidsand oozooids were determined while fed Isochrysis galbana (4–5µm diameter) alone or in combination with Peridinium trochoideum(16–18 µm diameter) at concentrations of 0.15–0.70mm³ x 1^–1. Grazing rates (ml x zooid^–1 x 24 h ^–1)ranged from 10 to 355, and at zooid weights greater than 5 µgcarbon were in order oozooid > gonozooid > aggregate.Grazing rates increased exponentially with increasing zooidweight. Weight-specific grazing rates (ml x µgC^–1x 24 h^–1) were independent of the four-fold initial foodconcentration. Mean weight-specific grazing rates increasedlinearly with increasing zooid weight for the aggregates andoozooids, but gonozooid mean rates were independent of zooidweight. Aggregate and gonozooid ingestion rates (10⁶ µm³x zooid^–1 x 24 h^–1) ranged from 4 to 134 while oozooidrates ranged from 3 to 67. All ingestion rates were independentof the initial food concentration but increased linearly withincreasing zooid weight at similar rates. All mean weight-specificingestion rates (ml x µgC^–1 x 24 h^–1) wereindependent of zooid weight. The mean aggregate daily ration(µgC ingested x µg body C^–1) was 59% and themean doliolid ration was 132%. Field studies indicate that normalconcentrations of D. gegenbauri in the Georgia Bight clear theirresident water volume (1 m³) in about 4 months, but that highlyconcentrated, swarm populations which occur along thermohalinefronts clear their resident water volume in less than 1 day. ¹Current address: MacLaren Plansearch Ltd., P.O.Box 13250, sta.A.,St.John's, Nfld. A1B 4A5     

UPTAKE OF ACETATE BY NEOTRICULA APERTA (GASTROPODA: POMATIOPSIDAE), THE SNAIL HOST OF SCHISTOSOMA MEKONGI IN THE LOWER MEKONG BASIN

All three races of Neotricula aperta, an epilithic, schistosometransmitting, snail of the Mekong and Mul rivers of NortheastThailand and southern Laos, were found to take up acetate froma dilute solution. After 48 h incubation the mean specific netuptake rates (µmol^–1 g^–1 h^–1), from750 µM acetate, were: 1.86, -race; 1.39, ß-raceand 3.25, y-race. Over 48 h the snails were able to achievereductions in the ambient acetate concentration of up to 60%.Incubations under bacteriostatis suggested that bacteria arenot involved in the uptake of acetate by N. aperta. The uptakecharacteristics conform to the Michaelis-Menten model. The transportconstants, J_max (µmol^–1 g^–1 h^–1) andK_t (µM) were 1.10 and 102 respectively (-race). Racialdifferences in uptake characteristics are discussed in relationto micro-habitat differences. HPLC indicated concentrations of acetate in y-N. aperta microhabitatsof around 325 µM. This suggests a pool size sufficientto satisfy only 6% of the snail's basal metabolic rate (BMR).Levels within the epilithic aufwuchs, however, are probablyhigh enough to provide for more than 50% of the BMR. The possible role of acetate in the energy metabolism of N.aperta is discussed. Short-chain carboxylic acids (such as acetate),arising from the decomposition of the aufwuchs, could representsources of fermentable organics that may be taken up by N. apertasnails and used to supplement their nutrition during times offood shortage. However, further investigations involving ¹⁴C-labellingtechniques are required. The findings of this investigationhave implications for the chemical ecology and life-cycle ofN. aperta. (Received 16 June 1994; accepted 28 July 1994)     

Short-term Products of 14C-acetate Assimilation by Chlorella pyrenoidosa in the Light

The kinetics of ¹⁴C-2-acetate assimilation by Chlorella pyrenoidosain the light were examined. Under aerobic conditions the primaryproduct of acetate assimilation was succinic acid which, afterten seconds, contained over 60 per cent of the ¹⁴C incorporatedby the cells. The percentage of the total ¹⁴C in succinate fellwith time, while that in citrate and glutamate increased. After1800 sec over 60 per cent of ¹⁴C was present in two compounds,glutamic acid and an unknown compound (X). Glucose-6-phosphate,fructose-6-phosphate, phosphoglyceric acid and phosphoenolpyruvicacid became labelled after 60 sec but together never containedmore than one per cent of the total ¹⁴C incorporated. Underanaerobic conditions succinate was still the primary productof acetate assimilation, and the absence of carbon dioxide resultedin a decrease in ¹⁴C incorporation into compound X. The patternof acetate assimilation in acetate grown and acetate adaptedChlorella was very similar to that in photo-autotrophicallygrown Chlorella. In the presence of 10^–6M DCMU, succinicacid was the primary product of acetate assimilation, but therewas an early Incorporation of ¹⁴C into glutamate, aspartate,and malate. 4 x10^–3M MFA did not effect the early incorporationof ¹⁴C into succinic acid, but resulted in accumulation of ¹⁴Cin citrate and a decreased amount in glutamate and in compound X.     

Effect of environmental factors on water utilization and boron accumulation and translocation in sugarcane

Rates of boron (B) accumulation and/or water utilization of3 month-old sugarcane plants were altered by changes in temperature,relative humidity, light intensity and duration of exposureto light. The effects of the environment on boron accumulationwere not directly dependent upon effects on water utilization.Boron accumulation was affected more than water uptake by increasingroot and air temperatures from 8°C to 37°C, and by raisingthe pH of the external solution from 5.7 to 7.0. Contrarily,water utilization decreased more than B accumulation when therelative humidity was increased from 30±5% to 95±5%,when light intensity was decreased or daily exposure to lightwas shortened and when the plants were pretreated with 5x10^–5M phenyl mercuric acetate, an anti-transpirant. The absorption of B by roots was experimentally separated fromits subsequent translocation to the shoots. Absorption of Bby roots was at least partially under metabolic control, sinceuptake from a 2 mg/liter B solution could occur against a concentrationgradient. Translocation of B from the roots to the shoot occurredpassively in the transpiration stream. ¹ Journal Series No. 1427 of the Hawaii Agricultural ExperimentStation. (Received March 2, 1972; )     

Vertical and temporal heterogeneity of planktonic ciliated protozoa in a humic lake

Seasonal population dynamics and the vertical distribution ofciliates were studied in relation to the particular food resourcesoccurring in a humic and moderately acidic lake (Lake Vassivière).The abundance (1.4 x 10³–20.4 x 10³ cells l^–1 mean= 4.8 x 10³ cells l^–1) and biomass (0.5–34.6 µgC l^–1, mean = 6.0 µg C l^–1) of ciliated protozoawere low and close to values reported for oligotrophic environments.The species composition of the population varied greatly withdepth. Whereas large-sized species of oligotrichs, some of whichwere mixotrophic, dominated at the surface, haptorids were bestrepresented in deep waters. The spatial distribution of thevarious groups of ciliates was largely determined by light andthe vertical distribution of microbial food resources (detritus,bacteria, algae) within the water column of this brown-coloredlake.     

Detection of infrasonic water oscillations by copepodids of Lepeophtheirus salmonis (Copepoda Caligida)

The cues that trigger infection of fish by parasitic copepodsare largely unknown. We show that copepodids of the parasiticcopepod Lepeophtheirus salmonus respond to uniform, linear accelerations,which are similar to those found in front of a swimming fish.Copepodid responses to vibrations at 1, 3, 5 and 10 Hz frequencywere filmed and analysed. The animals were stimulated in a completelywater-filled, clear perspex chamber, which was suspended likea swing in four wires from a steel frame. The chamber was movedby a vibrator which was fed amplified signals from a sine waveoscillator. On stimulation, copepodids responded by executingswimming bursts of 1–3 s duration. There was no apparentpreferred swimming direction. Sensitivity was highest at 3 Hz,with a threshold value of 5 x 10^–3 m s^–2 (rms).At 1 Hz the threshold was <6 dB higher, and sensitivity wasmarkedly reduced at 10 Hz, where the threshold was 1.8 x 10^–1m s^–2 rms. These results indicate that the copepodidsmay react to the near-field accelerations produced within centimetresof a swimming fish. Acceleration sensitivity may therefore bea cue that triggers high-speed swimming and subsequent infestationof the host. If this ability is present in holoplanktonic copepods,it may facilitate detection and escape from predatory fish.     

Bacterial biomass and production in a shallow bay

Bacterial biomass (BB, acridine orange) and bacterial secondaryproduction (BSP, [³H]thymidine incubations) were measured forthe first time in Concepción Bay (37°35'S, 73°01'W).BB ranged from 1.8x10⁶ to 22.5x10⁶ cells ml^–1 (the lattervalue observed near to an industrial effluent), BSP from 0.27x10⁶to 2.5x10⁶ cell ml^–1 day^–1 and heterotrophic turnoverrates between 0.15 and 1.0 doublings day^–1.     

Density and distribution of bacterioplankton and planktonic ciliates in the Bering Sea and North Pacific

The total number of planktonic bacteria in the upper mixed layerof the Bering Sea during the late spring-early summer periodranged between 1 and {small tilde}4 x 10⁶ ml^–1 (biomass10–40mg C m^–3). In the northern Pacific, along 47–52⁶N,the corresponding characteristics of the bacterioplankton densityin the upper mixed water layer were: total number 1–2x 10⁶ cells ml^–1 and biomass 15–46mg C m^–3Below the thermocline at 50–100 m, the density of bacterioplanktonrapidly decreased. At 300 m depth, it stabilized at 0.1–0.2x 106 cells ml^–1. The integrated biomass of bacterioplanktonin the open Bering Sea ranged between 1.2 and 3.6 g C m^–2(wet biomass 6–18 g m^–2) Its production per dayvaried from 2 to 23 mg C m^–3 days^–1 in the upper0–100 m. The numerical abundance of planktonic ciliatesin this layer was estimated to be from 3 to l0 x 10³ cells l^–1,and in the northern Pacific from 0.4 to 4.5 x 10³ l^–2.Their populations were dominated by naked forms of Strombidium,Strombilidium and Tontonia. In some shelf areas, up to 40% ofthe total ciliate population was represented by the symbioticciliate Mesodinium rubrum. The data on the integrated biomassof basic groups of planktonic microheterotrophs are also presented,and their importance in the trophic relationships in pelagiccommunities of subarctic seas is discussed.     

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.     

Temporal concentrations of sunscreen compounds (Mycosporine-like Amino Acids) in phytoplankton and in the New Zealand krill, Nyctiphanes australis G.O. Sars

This study investigated the relationship between seasonal changesin ambient UV-R, and sunscreen concentrations in phytoplanktonand krill. Concentrations of mycosprine-like amino acid (MAA)sunscreens were quantified in phytoplankton communities andin the krill Nyctiphanes australis over a 1-year period offthe Otago Coast, New Zealand. Ambient UV-B and UV-A ranged froma minimum mean daily dose of 2.19 x 10⁴ kJ day^–1 and 0.73x 10⁶ kJ day^–1 in June, to a maximum in January of 20.19x 10⁴ kJ day^–1 and 4.88 x 10⁶ kJ day^–1, respectively.Concentrations of MAAs (consisting almost entirely of Mycosporine-glycine)in the phytoplankton community were lowest in August (5.6 nmolµg^–1 Chl) when UV-R irradiances were minimal andhighest in January (41.4 nmol µg^–1 Chl) when UV-Rirradiances were maximal. Nyctiphanes australis was found tocontain five identified MAAs (mycosporine-glycine, shinorine,Porphyra-334, palythine and palythinol) and several unknownUV-R absorbing compounds. Concentrations ranged from 4.73 to15.51 nmol mg^–1 dw, with little indication of a seasonalcycle that could be correlated with changes in either phytoplanktonMAA concentrations or ambient UV-R irradiances. The findingssuggest that krill are neither accumulating MAAs in responseto changes in MAA concentrations in their phytoplankton food,or that MAA concentrations in krill are increased in responseto higher ambient UV-R irradiances. Concentrations of MAAs inkrill body parts (carapace, legs, eyes, antennae, muscle) weresimilar (4.89–5.98 nmol mg^–1 dw), with the exceptionof the carapace (2.03 nmol mg^–1 dw).