Defecation of Dimethylsulfoniopropionate (DMSP) by the Copepod Acartia tonsa as Functions of Ambient Food Concentration and Body DMSP Content

The dimethylsulfoniopropionate (DMSP) defecation rate of Acartiatonsa (calanoid copepod) feeding on Tetraselmis impellucida(prasinophyte) was correlated with food concentration and copepodbody DMSP content. Copepod fecal pellets represent a highlyconcentrated source of DMSP, and thus play an important rolein DMSP flux and microbial processes in the ocean.     

Zooplankton feeding ecology: does a diet of Phaeocystis support good copepod grazing, survival, egg production and egg hatching success?

The bloom-forming alga Phaeocystis is ingested by a varietyof zooplankton grazers, but is thought to be a poor source offood. We examined copepod grazing on solitary Phaeocystis cellsby adult females of Temora stylifera, and survival, fecal pelletproduction, egg production and egg hatching success in Calanushelgolandicus and T. stylifera over periods of 15 consecutivedays. Phaeocystis cell concentrations were high (1.2–3.6x 10⁴ cells ml^–1 for C. helgolandicus and 2.5–7.9x 10⁴ cells ml^–1 for T. stylifera), but within the rangeof maxima recorded for natural blooms. Both copepods survivedwell and continuously produced fecal pellets (indicating continuousgrazing) on a diet of Phaeocystis. However, egg production ratesfor both copepods were low, even though hatching success ofthe few eggs produced was high. Clearance rates for T. styliferawere higher than for most previous measurements of other copepodsfeeding on Phaeocystis solitary cells at lower cell concentrations.We conclude that even though copepods feed well upon Phaeocystis,resulting poor fecundity on this diet may inhibit copepod populationincreases during blooms, thereby contributing to the perpetuationof blooms. However, the high egg hatching success on this dietargues against Phaeocystis containing chemical compounds thatact as mitotic inhibitors reducing copepod egg viability, suchas those found in some other phytoplankters.     

Bacteria associated with a marine planktonic copepod in culture. I. Bacterial genera in seawater, body surface, intestines and fecal pellets and succession during fecal pellet degradation

In laboratory experiments, the bacterial flora of the zooplanktonmicrobial environments seawater, fecal pellets and associatedwith the external and internal surfaces of the copepod Acartiatonsa(Dana) were examined. The bacteria associated with fecal pelletswere dominated by Bacillus spp., Cytophaga/Flavobacterium spp.,Vibrio spp. and Pseudomonas spp. The same genera were foundin the seawater (0.22 7mu;m filtered) in which the pellets wereincubated. The bacteria showed a characteristic growth succession,and the abundance increased several orders of magnitude in theseawater during incubation of the pellets, indicating growthand proliferation based on the disintegrating/degrading fecalpellets. A carbon budget calculation revealed that organic matterfrom degrading fecal pellets could cover the carbon demand forthe growing bacterioplankton. The composition of the bacterialcommunity in the seawater and the fecal pellets also indicateda colonization of the pellets from bacterioplankton. The compositionof the bacteria associated with the copepods showed that bacterialgenera characterized as surface associated were preferentiallyassociated with fecal pellets, animal surfaces and intestines.This suggests a specific intestinal flora in the cultivatedcopepods composed of 10³ culturable bacteria per intestine (colony-formingunits, c.f.u.) or 10⁵ bacteria per intestine (acridine orangedirect counts, AODC), possibly colonizing the intestine passivelyduring filtration of algae. The activity of the bacterial communitieswas examined by the numencal ratio c.f.u.:AODC, where 1–19%of the bacteria were found active, with no significant differencebetween microbial environments.     

Sticholonche zanclea (Protozoa, Actinopoda) in fecal pellets of copepods and Euphausia sp. in Brazilian coastal waters.

Fecal pellets produced by mesozooplanktonic copepods (Centropages velificatus and Paracalanus parvus) and macrozooplanktonic Euphausiacea (Euphausia sp.) were examined using scanning electron microscopy. Fragments of the protozoan Sticholonche zanclea were found in both copepod and in Euphausia sp. fecal pellets, even when the abundance of the protozoan in the water was low. The results suggest that S. zanclea is an important food resource for different trophic levels, including meso- and macrozooplankton, in Brazilian coastal waters.     

Comparison of the metabolism of Acartia clausi and A. tonsa: influence of temperature and salinity

In the Marseilles region (French Mediterranean coast), A. clausi is one of the most abundant copepod species of the Gulf of Fos while A. tonsa constitutes the almost exclusive copepod species of the Berre lagoon, a neighbouring semi-closed brackish area communicating with the gulf. As different ecophysiological capabilities to stand the various temperature, salinity and food conditions could explain why these two species do not coexist in the same environment, comparative experiments were performed on metabolism and feeding. The respiration and ammonia excretion of the two species were measured in different combinations of temperature (10, 15 and 20 degrees C) and salinity (15, 25 and 35 per thousand). For each temperature, at the salinity of 35 per thousand, respiration rates were less in A. clausi than in A. tonsa, the contrary being observed at the lowest salinity. At any temperature ammonia excretion was greater at the intermediate salinity in A. tonsa and least in A. clausi. In Acartia tonsa, Q(10) of respiration and excretion were minimum at the lowest salinity, while in A. clausi they were unaffected by salinity variation. The O:N atomic ratio (from respiration and ammonia excretion rates) was significantly more elevated in A. clausi (mean 21.2; range 13.6-28.7) than in A. tonsa (mean 11.3; range 4.2-25) suggesting a more proteinic oriented metabolism in the later. Feeding experiments where Dunaliella tertiolecta30 per thousand) or lagoon (<16 per thousand) salinity. The relationships between ingestion and food concentration in the two species were not significantly different. These different results are compared to other ecophysiological information concerning these Acartia species (survival tolerances, osmotic regulation, feeding behaviour) and are discussed in relation with the characteristics of their niches in the studied region.     

Is Size of Fecal Pellets a Reliable Indicator of Species of Leporids in the Southern Rocky Mountains?

Abstract: In the southern Rocky Mountains, USA, snowshoe hares (Lepus americanus) and mountain cottontails (Sylvilagus nuttallii) are syntopic. Previous researchers used size of fecal pellets to identify leporid species in the Southern Rockies, a common criterion for identifying species of cervids. We measured 655 fecal pellets from 10 mountain cottontails and 2,374 fecal pellets from 23 snowshoe hares. We found no relationship between the body weight of mountain cottontails and the size of their fecal pellets (r = 0.04, F = 0.01, P = 0.91) but found one for snowshoe hares (r = 0.48, F = 9.3, P = 0.005). Although the 2 species differed in the size of their fecal pellets, the difference between means (1.2 mm) was sufficiently small to require measuring individual pellets and is only applicable to individuals of adult size. Although fecal pellet counts may be used to estimate presence and relative abundance of snowshoe hares in the absence of syntopic leporids, where multiple species of leporids are syntopic this method may yield misleading results.     

Mesozooplankton beneath the summer sea ice in McMurdo Sound,Antarctica: abundance,species composition,and DMSP content

The summer Phaeocystis antarctica bloom increases under-ice phytoplankton biomass in McMurdo Sound, Antarctica. The magnitude of mesozooplankton grazing on this bloom is unknown, and determines whether this production is available to the pelagic food web. We measured mesozooplankton abundance and body content of dimethylsulfoniopropionate (DMSP) during the McMurdo Sound austral summer (2006 and 2006–2007). Abundance varied from 20 to 4,500 ind. m⁻³ (biomass 0.02–274.0 mg C m⁻³), with peaks in mid-December and late-January/February. Abundance was higher but total zooplankton biomass lower in our study compared to previous reports. Copepods and the pteropod Limacina helicina dominated the zooplankton in both abundance and biomass. DMSP was detected in all zooplankton groups, with highest concentrations in copepod nauplii and L. helicina (95 and 54 nmol mg⁻¹ body C, respectively). Experiments suggested that L. helicina obtains DMSP by directly grazing on P. antarctica, which often accumulates to high biomass under the summer sea ice in McMurdo Sound.     

Estimating abundance of Sitka black-tailed deer using DNA from fecal pellets

Densely vegetated environments have hindered collection of basic population parameters on forest-dwelling ungulates. Our objective was to develop a mark–recapture technique that used DNA from fecal pellets to overcome constraints associated with estimating abundance of ungulates in landscapes where direct observation is difficult. We tested our technique on Sitka black-tailed deer (Odocoileus hemionus sitkensis) in the temperate coastal rainforest of Southeast Alaska. During 2006–2008, we sampled fecal pellets of deer along trail transects in 3 intensively logged watersheds on Prince of Wales Island, Alaska. We extracted DNA from the surface of fecal pellets and used microsatellite markers to identify individual deer. With genotypes of individual deer, we estimated abundance of deer with moderate precision (±20%) using mark–recapture models. Combining all study sites, we identified a 30% (SE = 5.1%) decline in abundance during our 3-year study, which we attributed to 3 consecutive severe winters. We determined that deer densities in managed land logged >30 years ago (7 deer/km², SE = 1.3) supported fewer deer compared to both managed land logged <30 years ago (10 deer/km², SE = 1.5) and unmanaged land (12 deer/km², SE = 1.4). Our study provides the first estimates of abundance (based on individually identified deer) for Sitka black-tailed deer and the first estimates of abundance of an unenclosed ungulate population using DNA from fecal pellets. Our tool enables managers to accurately and precisely estimate the abundance of deer in densely vegetated habitats using a non-invasive approach. © 2011 The Wildlife Society.     

Community structures of heterotrophic bacteria of copepod fecal pellets

The total and heterotrophic bacterial microflora of gut andfecal pellets of the copepod Temora stylifera was studied inthe coastal zone of the northwestern Mediterranean basin. Digestivetracts and feces were always found to contain bacteria. Withmean values close to 10¹¹ cells ml^–1and 10¹⁰ colony-formingunits (CFU) ml^–1, both total and heterotrophic communitiesfound in fecal pellets largely exceeded the corresponding bacterialmicroflora observed in surrounding seawater (10⁵ cells ml¹ and10³ CFU ml^–). In the same way, the frequency of dividingcells and mean cell volumes increased, respectively, from 3%and 0.12µm³ in seawater to >6% and 0.24 µm³ infecal pellets. The bacterial community structure was investigatedby carrying out 29 morphological and biochemical tests on 147isolated strains. Although Pseudomonas was always the most frequentlyencountered genus, the bacterial communities found in copepodfecal pellets clearly differ from those inhabiting seawater.Vibrio species, which were not detected in seawater microflora,were always present in fecal pellet communities. The close correspondenceobserved between the potential metabolic characteristics ofthe fecal bacterial communities isolated from a subantarcticdeposit feeder (Mytilus edulis) and from zooplankton in thisMediterranean study suggests that the fecal community differentiationis an even more general feature.     

Artspezifische Merkmale der Faeces von vier dominierenden Copepodenarten der Kieler Bucht

Zusammenfassung 1. Die Kotballen der planktischen CopepodenartenAcartia bifilosa, Centropages hamatus, Oithona similis undPseudocalanus elongatus werden in ihrer Form, Länge und Breite beschrieben.2. Die aus Länge, Breite und Grundform der Faeces berechneten durchschnittlichen Volumina liegen zwischen 13 × 10³ µm³ für beide Geschlechter der ArtOithona similis und 348 × 10³ µm³ für die Kotballen der Weibchen der ArtAcartia bifilosa.3. Die Dimensionen der Faeces der vier untersuchten Arten zeigen in mindestens einem der untersuchten Parameter signifikante Unterschiede. Im Falle der ArtenAcartia bifilosa undCentropages hamatus sind auch die Größen der Kotballen beider Geschlechter signifikant verschieden.4. Ein Vergleich von Labor- und Freilanduntersuchungen zeigt, daß die in sedimentiertem Seston gefundenen Faeces planktischer Copepoden sich mit Hilfe der experimentell gefundenen Charakteristika den dominierenden Arten zuordnen lassen.

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Species-characteristics of the fecal pellets of four dominating copepod species of Kiel bight

Mean length, width and shape of the fecal pellets of the four planktonic copepod species,Acartia bifilosa, Centropages hamatus, Oithona similis andPseudocalanus elongatus, were studied. Mean volumes of the fecal pellets of the different species vary between 13 × 10³ µm³ (males and females ofOithona similis) and 348 × 10³ µm³ (females ofAcartia bifilosa). The dimensions of the fecal pellets of the four species examined reveal significant differences in at least one of the criteria studied. InAcartia bifilosa andCentropages hamatus even the length and width of the fecal pellets of the two sexes are different. With respect to the characteristics described, a comparison made between fecal pellets found in cultures with those obtained from sediment of the Baltic Sea (Kiel Bight) has shown that the latter may be attributed to the copepod species under consideration.

     

High-speed video analysis of the escape responses of the copepod Acartia tonsa to shadows

The copepod Acartia tonsa exhibits a vigorous escape jump in response to rapid decreases in light intensity, such as those produced by the shadow of an object passing above it. In the laboratory, decreases in light intensity were produced using a fiber optic lamp and an electronic shutter to abruptly either nearly eliminate visible light or reduce light intensity to a constant proportion of its original intensity. The escape responses of A. tonsa to these rapid decreases in visible light were recorded on high-speed video using infrared illumination. The speed, acceleration, and direction of movement of the escape response were quantified from videotape by using automated motion analysis techniques. A. tonsa typically responds to decreases in light intensity with an escape jump comprising an initial reorientation followed by multiple power strokes of the swimming legs. These escape jumps can result in maximum speeds of over 800 mm s(-1) and maximum accelerations of over 200 m s(-2). In A. tonsa, photically stimulated escape responses differ from hydrodynamically stimulated responses mainly in the longer latencies of photically stimulated responses and in the increased number of power strokes, even when the stimulus is near threshold; these factors result in longer escape jumps covering greater distances. The latency of responses of A. tonsa to this photic stimulus ranged from a minimum of about 30 ms to a maximum of more than 150 ms, compared to about 4 ms for hydrodynamically stimulated escape jumps. Average response latency decreased with increasing light intensity or increasing proportion of light eliminated. Little change was observed in the vigor of the escape response to rapid decreases in visible light over a wide range of adaptation intensities.     

Importance of copepod faecal pellets to the fate of the DSP toxins produced by Dinophysis spp.

An ingestion experiment was carried out in Rı́a de Pontevedra (Spain) with the copepod Temora longicornis in order to determine ingestion rates of the DSP toxin-producers, Dinophysis spp. (Dinophyceae), and the excretion rate of Dinophysis spp. cells within the faecal pellets. Ingestion rate was a function of dinoflagellate abundance and did not vary with either the amount, or the composition of the co-occurring phytoplankton species in the food suspension. Faecal pellet production increased at higher food concentrations. Intact Dinophysis spp. cells representing 34.4% of the total Dinophysis cells ingested by the copepods were found within the pellets. T. longicornis was the only dominant copepod species in the area that fed on Dinophysis spp., thus the pellets produced by T. longicornis were the main source of copepod “toxic” pellets in the media during blooms of Dinophysis spp. These “toxic” pellets might contribute to the maintenance of the toxic algal blooms, if the cells inside the pellets remain viable, can spread the potential toxicity of the toxic dinoflagellates throughout the pelagic food web due to coprophagy, and/or be an important toxic vector into the benthic food web. However, during a Dinophysis spp. bloom, the percentage of cells excreted daily within the pellets was lower than 1% of the total dinoflagellate population and, moreover, copepod faecal pellets represent a small fraction of the sinking material in this area. Although it was not possible to measure the amount of toxins in the pellets, we concluded that copepod faecal pellets do not have an important role in the transport of DSP toxins through the food web in this area.     

Composition, abundance and distribution of macrozooplankton in Culebra Bay, Gulf of Papagayo, Pacific coast of Costa Rica and its value as bioindicator of pollution

The abundance, distribution and composition of the macrozooplankton of Culebra Bay, Costa Rica (10 degrees 38' N - 85 degrees 40' W) were studied at four stations throughout the dry (February-May) and rainy (September-November) seasons of 2000. The samples were collected at two-week intervals using a 500 microm mesh net with a 0.5 m diameter opening. Copepods (23-31%) and ostracods (20-34%) were predominant throughout the year, followed by cladocerans (2.5-14%), zoea (6.6-9.5%), and siphonophores (2.5-7.2%). High densities of zooplankton were obtained in February and March with peak abundance on March 18. The lowest densities were observed on September 3 and November 5. Significant differences in abundances at each station were observed for the groups Acartia tonsa (Copepoda), Ctenophora, Medusae, Ostracoda, Zoea, and Amphipoda. Comparison of the dry and rainy seasons revealed significantly higher zooplankton abundance in the dry season and copepod domination of all stations; during the rainy season ostracods dominated the off-shore areas. Zooplankton abundance and distribution are influenced by upwelling, which occurs during the dry season in Culebra Bay.     

Denaturing gradient gel electrophoresis analysis of 16S ribosomal DNA amplicons to monitor changes in fecal bacterial populations of weaning pigs after introduction of Lactobacillus reuteri strain MM53

The diversity and stability of the fecal bacterial microbiota in weaning pigs was studied after introduction of an exogenous Lactobacillus reuteri strain, MM53, using a combination of cultivation and techniques based on genes encoding 16S rRNA (16S rDNA). Piglets (n = 9) were assigned to three treatment groups (control, daily dosed, and 4th-day dosed), and fresh fecal samples were collected daily. Dosed animals received 2.5 x 10(10) CFU of antibiotic-resistant L. reuteri MM53 daily or every 4th day. Mean Lactobacillus counts for the three groups ranged from 1 x 10(9) to 4 x 10(9) CFU/g of feces. Enumeration of strain L. reuteri MM53 on MRS agar (Difco) plates containing streptomycin and rifampin showed that the introduced strain fluctuated between 8 x 10(3) and 5 x 10(6) CFU/g of feces in the two dosed groups. Denaturing gradient gel electrophoresis (DGGE) of PCR-amplified 16S rDNA fragments, with primers specific for variable regions 1 and 3 (V1 and V3), was used to profile complexity of fecal bacterial populations. Analysis of DGGE banding profiles indicated that each individual maintained a unique fecal bacterial population that was stable over time, suggesting a strong host influence. In addition, individual DGGE patterns could be separated into distinct time-dependent clusters. Primers designed specifically to restrict DGGE analysis to a select group of lactobacilli allowed examination of interspecies relationships and abundance. Based on relative band migration distance and sequence determination, L. reuteri was distinguishable within the V1 region 16S rDNA gene patterns. Daily fluctuations in specific bands within these profiles were observed, which revealed an antagonistic relationship between L. reuteri MM53 (band V1-3) and another indigenous Lactobacillus assemblage (band V1-6).     

使用粪堆数量估计日本奄美群岛上琉球兔的种群数量

为了测量奄美岛上濒危物种琉球兔 (Pentalagusfurnessi)的丰盛度 ,我们计数了森林中道路、溪流和森林地被物中的粪堆数量。计算用的模型包括新粪堆的数量及其年龄、总粪堆数量、每天产生的平均粪堆数 ,以及在森林地被物和溪边的粪堆数量的回归方程。估计在 1 993- 1 994年期间该岛上有 2 5 0 0 - 6 1 0 0只琉球兔 ,在 2 0 0 2 - 2 0 0 3年间有 2 0 0 0 - 4 80 0只。通过比较粪便丰盛度和在森林道路旁观察到的琉球兔数量 ,我们考察了该模型的有效性 ,最后将以前调查的数据应用于该模型以确定种群下降的程度     

Development and application of different methods for the detection of Toxoplasma gondii in water

Two methods, centrifugation and flocculation, were evaluated to determine their efficiencies of recovery of Toxoplasma gondii oocysts from contaminated water samples. Demineralized and tap water replicates were inoculated with high numbers of sporulated or unsporulated T. gondii oocysts (1 x 10(5) and 1 x 10(4) oocysts). The strain, age, and concentration of the seeded oocysts were recorded. Oocysts were recovered either by centrifugation of the contaminated samples at various g values or by flocculation with two coagulants, Fe(2)(SO(4))(3) and Al(2)(SO(4))(3). The recovery rates were determined with the final pellets by phase-contrast microscopy. Sporulated oocysts were recovered more effectively by flocculation with Al(2)(SO(4))(3) (96.5% +/- 21.7%) than by flocculation with Fe(2)(SO(4))(3) (93.1% +/- 8.1%) or by centrifugation at 2,073 x g (82.5% +/- 6.8%). For the unsporulated oocysts, flocculation with Fe(2)(SO(4))(3) was more successful (100.3% +/- 26.9%) than flocculation with Al(2)(SO(4))(3) (90.4% +/- 19.1%) or centrifugation at 2,565 x g (97.2% +/- 12.5%). The infectivity of the sporulated oocysts recovered by centrifugation was confirmed by seroconversion of all inoculated mice 77 days postinfection. These data suggest that sporulated Toxoplasma oocysts purified by methods commonly used for waterborne pathogens retain their infectivity after mechanical treatment and are able to induce infections in mammals. This is the first step in developing a systematic approach for the detection of Toxoplasma oocysts in water.     

Phycotoxin accumulation in zooplankton feeding on Alexandrium fundyense--vector or sink?

Zooplankton can consume toxic Alexandrium spp. dinoflagellatesin the Gulf of Maine and retain paralytic shellfish poisoning(PSP) toxins, potentially acting as toxin vectors. We performedexperiments to determine toxin budgets for common species ofcopepods (Acartia hudsonica, Eurytemora herdmani, Centropageshamatus) feeding on toxic Alexandrium fundyense, offered asmonocultures or in mixtures of algal prey, by comparing calculatedtoxin ingestion rates and toxin content of copepod body tissueand fecal pellets. When fed monocultures, both copepod tissueand fecal pellet fractions accounted for 5% each of the calculatedingested toxin, and thus by difference 90% was lost as a dissolvedfraction into the seawater medium. The presence of alternativefood did not significantly alter the efficiency of toxin retention.Sloppy feeding or regurgitation are probable mechanisms forrelease of toxin to sea water. Experiments using varying concentrationsof A. fundyense and alternativenon-toxic species did not showsignificant effects of cell concentration on toxin retentionefficiency. Total toxin retained and efficiency of retentionvaried among copepod species. Toxin profiles (% molar composition)of dinoflagellates, copepod tissues and fecal pellets differedslightly, suggesting some metabolic transformation. Becauseof their low retention efficiency, copepod grazers can effectivelydisperse PSP toxins produced by Alexandrium spp. into the environment,where they are much less likely to be harmful—zooplanktonact as a sink for PSP toxins. Nevertheless, sufficient toxinbody burdens are attained to contribute to propagation of PSPtoxins to other trophic levels.     

Relationship between specific dynamic action and protein deposition in calanoid copepods

The link between specific dynamic action (SDA) and protein deposition was investigated in copepodites stage V of two calanoid copepod species, the neritic Acartia tonsa and the oceanic Calanus finmarchicus. This was done by measuring respiration before, during, and after a specific feeding period and measuring the incorporation of carbon into proteins. These were also measured on individuals incubated with cycloheximide, an antibiotic that inhibits protein synthesis. The cycloheximide treatment significantly diminished the magnitude of SDA in both A. tonsa and C. finmarchicus, and inhibited carbon incorporation into protein in both species. This provides evidence that the rate at which protein deposition takes place greatly affects the magnitude of SDA. The specific respiration rates of both starving and feeding copepods were generally higher in A. tonsa than in C. finmarchicus. This influenced SDA, the magnitude of SDA normalised to an 8 h feeding period being threefold higher in A. tonsa (78.7+/-25.7 nlO(2) μgC(-1)) than in C. finmarchicus (27.5+/-11.6 nlO(2) μgC(-1)). This difference may arise due to differences in energy allocation in the organisms of the copepodite V stage of the two species. In this stage C. finmarchicus deposits large quantities of storage lipids, predominately wax esters, whereas A. tonsa deposits proteins during somatic growth.     

Modelling viral impact on bacterioplankton in the North Sea using artificial neural networks

The temporal variability of the viral impact on bacterioplankton during the summer-winter transition in the North Sea was determined and artificial neural networks (ANNs) were developed to predict viral production and the frequency of infected bacterial cells (FIC). Viral production and FIC were estimated using a virus-dilution approach during four cruises in the southern North Sea between July and December 2000 and an additional cruise in June 2001. Supplementary data such as bacterial production, and bacterial and viral abundance were collected to relate changes in FIC and viral production to the dynamics of other biotic parameters. Average viral abundance varied between 4.4 x 10(6) ml(-1) in December and 29.8 x 10(6) ml(-1) in July. Over the seasonal cycle, viral abundance correlated best with bacterial production. Average bacterial abundance varied between 0.5 x 10(6) ml(-1) in December and 1.3 x 10(6) ml(-1) in July. Monthly average values of FIC ranged from 9% in September to 39% in June and the average viral production from 11 x 10(4) ml(-1) h(-1) in December to 35 x 10(4) ml(-1) h(-1) in July. The data set was used to develop ANN-based models of viral production and FIC. Viral production was modelled best using sampling time, and bacterial and viral abundance as input parameters to an ANN with two hidden neurons. Modelling of FIC was performed using bacterial production as an additional input parameter for an ANN with three hidden neurons. The models can be used to simulate viral production and FIC based on regularly recorded and easily obtainable parameters such as bacterial production, bacterial and viral abundance.     

Bacterial Colonization on Fecal Pellets of Harpacticoid Copepods and on Their Diatom Food

Fecal pellets make up a significant fraction of the global flux of organic matter in oceans, and the associated bacterial communities in particular are a potential food source for marine organisms. However, these communities remain largely unknown. In the present study, the bacterial communities on fecal pellets of the benthic copepod Paramphiascella fulvofasciata feeding on the diatoms Navicula phyllepta and Seminavis robusta were analyzed. The aim of this study was to characterize the bacterial communities associated with the diatoms and the fecal pellets by means of DGGE profiling. Furthermore, isolated bacteria were characterized by means of partial 16S rRNA gene sequencing. The composition of the bacterial microflora on fecal pellets was studied in terms of the effect of the original food source, the age of the fecal pellets and the copepod’s identity. Alphaproteobacteria, Flavobacteria, and Bacilli were found on the fecal pellets; whereas on diatoms, exclusively Gammaproteobacteria were identified. Especially after eating N. phyllepta, there was an important increase in bacterial diversity, although the diatom N. phyllepta harbored a less diverse bacterial community than S. robusta. Our data suggest that the additional bacteria originate from the copepod’s digestive tract and largely depends on the initial food source.