Effect of Aeolosoma sp. (Aphanoneura: Aeolosomatidae) on the Population Dynamics of Selected Cladoceran Species

Although oligochaete worms naturally coexist with cladocerans in many shallow freshwater ponds and lakes, their influence on the latter is not well established. In this work we studied the effect of Aeolosoma sp. on the population growth of Alona rectangula, Ceriodaphnia dubia, Daphnia pulex, Macrothrix triserialis and Moina macrocopa. Population growth studies were conducted at one algal food density (1 × 10⁶cells ml^–1 of Chlorella vulgaris). The experimental design was similar for all five cladoceran species, where we used 100 ml capacity transparent jars containing 50 ml of EPA medium with the desired algal density and three replicates for each treatment. The test medium was changed daily and fresh algal food was added. The initial density of each of the cladoceran species in the population growth studies was 0.4 ind ml^–1 while that of the worms 1.0 ind ml^–1. Following inoculation, we estimated daily the number of cladocerans and the worms for duration of 21 days. Regardless of the presence of worms, Moina macrocopa and Macrothrix triserialis showed rapid population growth while A. rectangula took more than 2 weeks to reach peak abundances. With the exception of M. triserialis, all the other our cladoceran species declined in the presence of Aeolosoma sp. The lowest peak population density (about 1 ind ml^–1) was observed for M. triserialisin controls. The remaining species had peak densities of about 3–5 ind ml^–1. The rates of population increase per day varied from 0.03 to 0.19 depending on the cladoceran taxa and the treatment. In general we found that pelagic taxa were more adversely affected by the presence of the worms than were the littoral cladocerans.     

Competition between Moina macrocopa and Ceriodaphnia dubia: a Life Table Demography Study

We analyzed the effect of competition on survival‐ and reproduction‐related parameters under two (0.5 · 10⁶ and 1.5 · 10⁶ cells ml^—1 of Chlorella) food densities between Moina macrocopa and Ceriodaphnia dubia using the life table demography approach. In general, regardless of the presence of Moina, the average lifespan and generation time were higher for C. dubia. However, rate of population increase (r) and values of reproductive effort were higher for M. macrocopa. The net reproductive values of C. dubia grown alone varied from 7.6 to 36.6 offspring female^—1 lifetime^—1, depending on Chlorella density. Corresponding values for Moina varied little (16.4 and 17.4 offspring female^—1 lifetime^—1). Values of gross reproductive rate, net reproductive rate and the generation time of both cladoceran species were higher in mixed cultures than when grown alone. The negative effect of competition was evident for both the cladoceran species, not in their reproductive rates, but in their generation times, and thus population growth rates. The role of competition and facilitation occurring between the two species was discussed in relation to different algal food levels.     

Functional responses during the early larval stages of the charal fish Chirostoma riojai (Pisces: Atherinidae) fed rotifers and cladocerans

Survival during early fish larval stages depends largely upon the availability of appropriate prey. Studied were the functional responses from hatching to 6 weeks of age of whitefish (Charal) (Chirostoma riojai) larvae that were offered selected rotifers (Brachionus rotundiformis and B. rubens) and cladocerans (Moina macrocopa and Ceriodaphnia dubia). The experiments were conducted in a 50 ml medium at a salinity of 2 g L^?1. Each treatment used four replicates. Rotifers were introduced at densities of 0.5, 1, 2, 4, 8 and 16 individuals ml^?1 and cladocerans at 0.1, 0.2, 0.4, 0.8, 1.6, 3.2, 4.8 and 6.4 individuals ml^?1. Two larvae, previously starved for 2 h, were introduced into each test jar and allowed to feed for 45 min. The difference between the initial and final zooplankton density represented prey consumption. C. riojai larvae showed Type II functional response curves, i.e. they consumed more zooplankton with increasing prey availability; above a certain prey density (8–16 individuals ml^?1 in rotifers and 3.2–6.4 individuals ml^?1 in cladocerans) the consumption rate tended to stabilize in most trials. Results are discussed in relation to aquaculture.     

Studies on functional response and prey selection using zooplankton in the anostracan Chirocephalus diaphanus Prevost, 1803

Freshwater cladocerans and rotifers were used as prey to study functional response and prey selection by adult females of Chirocephalus diaphanus under laboratory conditions. For functional response studies, we offered three rotifer species (Brachionus calyciflorus, B. patulus and Euchlanis dilatata) and three cladoceran species (Alona rectangula, Ceriodaphnia dubia and Moina macrocopa) at various densities ranging from 0.5 to 16 ind. ml^–1. We found increased zooplankton consumption with increasing prey density but beyond 4 ind ml^–1 cladocerans and 8 ind. ml^–1 rotifers, the number of animals eaten plateaued. In general, C. diaphanus consumed fewer large prey (cladocerans) and many more smaller zooplankton (rotifers). For prey selection experiments, we used B. calyciflrous, B. patulus, C. dubia and M. macrocopa, offered at the ratio of two rotifers: one cladoceran and at three prey densities (total zooplankton numbers: 3, 6 and 12 ind. ml^–1). Prey selectivity patterns followed the functional response trends. In general, regardless of prey types, with an increase in the available zooplankton, there was an increase in the number of prey consumed. At any given prey density, C. diaphanus consumed higher numbers of rotifers than cladocerans. Among the prey offered, B. patulus and M. macrocopa were positively selected. Results are discussed in light of possible control of zooplankton by anostracans in temporary ponds.     

Effect of mixed diets (cyanobacteria and green algae) on the population growth of the cladocerans <Emphasis Type="Italic">Ceriodaphnia dubia</Emphasis> and <Emphasis Type="Italic">Moina macrocopa</Emphasis>

Microcystis aeruginosa, a cosmopolitan form, is a colonial cyanobacterium, which is also common in many freshwater bodies in Mexico. In eutrophic water bodies cyanobacteria are often the main phytoplankton that co-exist with cladocerans. We evaluated the effect of mixed diets, comprising 0, 25, 50, 75, and 100% on dry weight basis of M. aeruginosa, and the rest of one of two green algal species (Chlorella vulgaris and Scenedesmus acutus), on the population growth of the cladocerans Ceriodaphnia dubia and Moina macrocopa. Regardless of the share of M. aeruginosa in the mixed diet, C. dubia fed Chlorella had a longer initial lag phase. However, in mixed diet with S. acutus, the lag phase of C. dubia increased with increasing proportion of M. aeruginosa. When raised on 100% M. aeruginosa, the population growth of C. dubia was lowered compared with 100% S. acutus or 100% C. vulgaris. Increased proportion of M. aeruginosa in the mixed diet also resulted in decreased abundance of M. macrocopa. Irrespective of diet type, M. macrocopa had a shorter lag phase than C. dubia. Depending on the diet type, the rate of population increase (r) of C. dubia varied from 0.07 to 0.26 d⁻¹ while that of M. macrocopa was higher (0.14–0.61 d⁻¹). For both cladoceran species, the lower r values were obtained when fed Microcystis. Our study showed that the strain of M. aeruginosa was not highly toxic to cause total elimination of either C. dubia or M. macrocopa. Addition of a green algal component to the diet improved the population growth rates of both cladoceran species.     

Responses of rotifers and cladocerans to Microcystis aeruginosa (Cyanophyceae): A demographic study

The response of selected rotifers and cladocerans to Microcystis aeruginosa, offered as colonies and single cells, was compared to that on a diet of Chlorella vulgaris using the life table demography approach. The test zooplankton species were Simocephalus vetulus, Daphnia carinata, Moina macrocopa, Scapholeberis kingi, Ceriodaphnia cornuta, Brachionus calyciflorus and Hexarthra mira. To detect the development of resistance to toxins from Microcystis in zooplankton, in addition to the laboratory cultured strain of Ceriodaphnia cornuta, another strain of the same species was also used (designated as C. cornuta 2, this was collected from a pond containing Microcystis and cultured in the laboratory on Chlorella for a few weeks prior to experimentation). Experiments were conducted at 20°C and 30°C. Survivorship was high on Chlorella in most species but low on diets of Microcystis. Except for C. cornuta 2, S. kingi and S. vetulus, all other test species were adversely affected by Microcystis. The ability to utilise Microcystis improved at 30°C in M. macrocopa, D. carinata and H. mira. The longest mean lifespan was recorded for C. cornuta 2 (25.3 ± 4.86 d) and the lowest for B. calyciflorus (0.58 ± 0.05 d). The highest net reproductive rate was observed for C. cornuta 1 (44.9 ± 4.88) and the longest generation time of 26.6 ± 2.13 d for S. vetulus. Among the cladocerans that showed positive values of population growth rate (r), M. macrocopa had the highest of 0.96 ± 0.04 per day.     

Lifetable demography of four cladoceran species in relation to algal food (Chlorella vulgaris) density

Algal food density is known to influence life history variables of cladoceran species. It is not, however, well established whether both littoral and planktonic cladocerans show similar trends when exposed to increasing food concentrations. In the present work, we studied the life table demography of four cladoceran species (Ceriodaphnia cornuta, Moina macrocopa, Pleuroxus aduncus and Simocephalus vetulus) in relation to three algal food concentrations (low: 0.5 × 10⁶, medium: 1.5 × 10⁶ and high: 4.5 × 10⁶ cells ml^–1 of Chlorella vulgaris) (in terms of carbon content, these were equivalent to 0.15, 0.45 and 1.35 g ml^–1, respectively) at 25 °C. In general, for all the tested cladoceran species, values of average lifespan, gross reproductive rate, net reproductive rate, generation time and the rate of population growth were higher at lower food concentrations. Furthermore, high food concentration resulted in a negative population growth rate (mean ± standard error: –0.091 ± 0.026) for P. aduncus. The highest population growth rate (0.602 ± 0.014) was recorded for M. macrocopa at low food density. S. vetulus had the longest average lifespan (40 ± 1 d) while M. macrocopa had the lowest (5 ± 1 d). C. cornuta showed better performance at medium food concentration. We conclude that among the algal concentrations used here, 0.5 × 10⁶ – 1.5 × 10⁶ was beneficial not only to the planktonic species but also to the littoral P. aduncus and S. vetulus while 4.5 × 10⁶ cells ml^–1 was unsuitable for all the cladocerans tested.     

Combined effects of food level and inoculation density on competition between Brachionus patulus (Rotifera) and the cladocerans Ceriodaphnia dubia and Moina macrocopa

Competition among cladocerans and rotifers is of considerable interest not only due to their close similarity in life history strategies, but also due to the considerable overlap they exhibit in their feeding habits. In tropical waterbodies, several genera of cladocerans, including Ceriodaphnia and Moina occur, simultaneously with rotifers. We tested over a period of 3 weeks the combined effects of food (0.5×10⁶ and 1.5×10⁶ cells ml^–1 of Chlorella) level and rotifer density on the competition between B. patulus and C. dubia and M. macrocopa using population growth experiments. For each cladoceran species we used 30 test jars of 50 ml capacity. The initial density of cladocerans was 0.2 ind ml^–1, while for B. patulus it was either 1 ind ml^–1 or 5 ind ml^–1. Neither the maximal population density nor the rate of population increase (r) of C. dubia was significantly affected by B. patulus. However, for M. macrocopa, both these variables were negatively affected by the rotifers. The combined effects of low food level and high initial density of B. patulus resulted in a 50% reduction in the peak population density of M. macrocopa. The population growth of B. patulus was negatively influenced by the presence of C. dubia and M. macrocopa. The results of the competition experiments conducted in the present study between cladocerans and rotifers suggest the existence of a more complex and delicate interaction than is generally thought.     

Predatory and toxic effects of the turbellarian (Stenostomum cf leucops) on the population dynamics of Euchlanis dilatata,Plationus patulus (Rotifera) and Moina macrocopa (Cladocera)

Catenulid turbellarians, common in shallow, tropical ponds, affect their rotifer prey via the production of toxins. There is, however, no quantitative information on their effect on the demography of their prey. Here, we test the impact of Stenostomum cf leucops on the population dynamics of the rotifers Euchlanis dilatata and Plationus patulus, and the cladoceran Moina macrocopa. Experiments were initiated with rotifers at 0.5 ind. ml⁻¹ and the cladoceran at 0.2 ind. ml⁻¹; growth patterns were compared in the absence and presence of worms (2 Stenostomum ind. per 50 ml). Results revealed that brachionids were most adversely affected: there was a lower growth rate of the rotifers in the presence of worms (P < 0.01, repeated measures ANOVA), although at the densities applied, the predator did not wipe out its prey. These littoral predators may therefore regulate rotifer prey in natural conditions. In Moina, the population evolved differently; initially, we found no difference between control and treatment, but after about 10 days, the population collapsed, irrespective of a direct or indirect contact with the predator. This delayed effect deserves more study, as it could represent flatworm toxin accumulation by the cladoceran.     

Cyanobacteria consumption by cladocerans: a case study on facilitation

Eutrophic systems are stressful for zooplankton species, especially for small organisms (<?1000 μm) that are inefficient in consuming large colonies or filaments of cyanobacteria. Certain mechanisms, however, enable organisms to coexist in spite of the stress related to poor food quality or manageability of the diet. The present work suggests that coprophagy is recurrent behavior in cladocerans that may facilitate the survival and growth of some species in eutrophic systems. We chose three clones of Moina macrocopa that inhabit eutrophic systems. The species selected as possible facilitators were the cladocerans Simocephalus vetulus and Daphnia similis, and the ostracod Heterocypris incongruens, because they are cosmopolitan, have high rates of cyanobacterial filtration and in some cases coexist with Moina. The design used for the demographic experiments of the three clones of M. macrocopa was based on the source of nutrition and consisted of a control diet of Scenedesmus acutus (1?×?10⁶ cells ml), a diet of undigested cyanobacteria (10?×?10⁶ cells ml), and this same diet after digestion by D. similis, S. vetulus or H. incongruens. The excreta of the cladocerans was a deficient diet for Moina, whose populations decreased by more than 1 individual per day. On the contrary, fecal pellets of the ostracod were a diet that allowed Moina to have positive population growth (0.3 day^?1). Our results help to explain the high densities achieved by cladocerans in eutrophic tropical water bodies where cyanobacterial blooms are normal.     

Ontogenetic Shifts in the Ability of the Cladoceran,Moina macrocopa Straus and Ceriodaphnia cornuta Sars to Utilize Ciliated Protists as Food Source

The ontogenetic diet shifts and age specific ability of the two cladoceran species Moina macrocopa and Ceriodaphnia cornuta to derive energy from ciliated protists have been investigated in laboratory. The postembryonic developmental rates and life table demography (longevity, age and size at first reproduction, fecundity and intrinsic rate of natural increase) of the cladocerans have been elucidated on algae (Chlorella vulgaris) and the ciliated protists (Tetrahymena pyriformis, Colpoda (c.f.) steini) as food. For either of the cladoceran, the somatic growth rate and average body size at first reproduction were higher with algal diet. During initial stages of development (0–5 days), either cladoceran realized higher rate of somatic growth on algal diet, subsequently ciliated protists supported significantly higher growth rate than the alga. Algal and ciliate diets did not differ in maximum body size (C. cornuta: 539–554 μm; M. macrocopa: 1274.8–1309 μm) reached by either of the cladocerans. The maximum body sizes were larger than size at first reproduction with either of the ciliated protists, however, with algal diet the maximum body sizes did not differ from the size at first reproduction in each case. In case of C. cornuta the generation time (20.5 ± 0.3 days on ciliate; 15.6 ± 0.17 days on algal diet), reproductive rates (net reproductive rate: 20.05 ± 3.2 on ciliate; 15.5 ± 1.2 on algal diet), and average life expectancy at hatching (27 ± 0.8 days on ciliate; 22.7 ± 0.71 days on alga) were higher, whereas the size at first reproduction (482 μm on ciliate; 521 μm on alga) was smaller with the ciliate than with an algal diet. The algal and the ciliate diets did not differ in survival (life expectancy at hatching: 9.2 ± 0.7 days) and fecundity (NRR: 23.6 ± 2.4) for M. macrocopa. The two ciliates used in the experiment did not differ in their performance as food source for either cladoceran species. Our results suggest that both the cladoceran species are able to utilize smaller ciliate (e.g., T. pyriformis, C. (c.f.) steini) as food; however with differential ability to derive energy from the ciliate diet and this ability is size and age structured in both cases. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

The efficacy of Scenedesmus morphology as a defense mechanism against grazing by selected species of rotifers and cladocerans

Phytoplankton often develop various defense mechanisms in response to zooplankton grazing, such as spines and colonies. While it is now known that increased spine length and cells in a colony of members of the genus Scenedesmus, when zooplankton grazing is intense, helps in reducing zooplankton filtering rates, the effect of these defense mechanisms at the population level has been observed in few studies. Here we present data on the growth rates of four zooplankton species, Brachionus calyciflorus, B. patulus, Ceriodaphnia dubia and Daphnia pulex at two food levels using two species of colony-forming Scenedesmus spp.: S. acutus (cell length = 18.2 ± 0.4 µm; width = 4.2 ± 0.1 µm; average colony length = 90 µm; width: 21 µm) and S. quadricauda (cell length: 21 ± 0.5 width 7.5 ± 0.3 µm; average colony length: 84 µm; width: 30 µm). Whereas S. acutus had no spines, S. quadricauda had spines of 6–10 µm. Population growth experiments of the test rotifers and cladocerans were conducted in 100 ml containers with 50 ml of the medium with test algae. Algae concentrations used were: 13 and 52 mg dw l^–1 of each of the two algal species offered in colonial forms. We used an initial inoculation zooplankter density of 1 ind. ml^–1 for either of the rotifer species and 0.2 ind. ml^–1 for either of the cladoceran species. In all, we had 64 test containers (4 test species of zooplankton × 2 test species of algae × 2 algal densities × 4 replicates). We found a significant effect of algal size on the growth rates of all the four tested species of zooplankton. The population growth rates of zooplankton ranged from ?0.58 to 0.66 and were significantly higher on diet of S. acutus than of S. quadricauda. Thus, our study confirms that the larger colony size and the formation of spines in S. quadricauda were effective defenses against grazing by both rotifers and smaller sized cladoceran Ceriodaphnia dubia but that larger-bodied Daphnia pulex could exploit both the algal populations equally.     

Grazing impact on the cyanobacterium Microcystis aeruginosa by the heterotrophic flagellate Collodictyon triciliatum in an experimental pond

We estimated the grazing impact of the heterotrophic flagellate Collodictyon triciliatum on the harmful, bloom-forming cyanobacterium Microcystis aeruginosa in an experimental pond during a Microcystis bloom from summer to winter in 2010. For these experiments, we calculated the grazing rates from the digestion rate of C. triciliatum and its food vacuole contents. During the study period, M. aeruginosa exhibited one bloom event with a maximum density of 1.1 × 10⁵ cells ml^?1. The cell density of C. triciliatum fluctuated from below the detection limit to 291 cells ml^?1. The number of M. aeruginosa cells ingested by C. triciliatum food vacuoles ranged between 0.4 and 10.8 cells flagellate^?1, and the digestion rate of C. triciliatum at 25 °C was 0.73 % cell contents min^?1. The grazing rate of C. triciliatum on the M. aeruginosa prey was 0.2–6.9 cells flagellate^?1 h^?1, and its grazing impact was 0.0–25.3 % standing stock day^?1. The functional response of C. triciliatum to the M. aeruginosa prey followed the Michaelis–Menten model of significance (r ² = 0.873, p < 0.001) in our experimental systems, in which the prey concentration varied from 1.0 × 10⁴ to 2.1 × 10⁶ cells ml^?1. The maximum grazing rate was 6.2 prey cells grazer^?1 h^?1, and the half-saturation constant was 1.2 × 10⁵ cells ml^?1. We present evidence that C. triciliatum grazing explained the remarkable decrease in M. aeruginosa cell density in the pond. The present study is the first demonstration of the high potential of protistan grazing on M. aeruginosa to reduce cyanobacterial blooms.     

Interactions between the Anomopod Cladocerans Ceriodaphnia Dubia,C. Cornuta,Simocephalus Vetulus and S. Serrulatus,the Aphanoneurid Worm Aeolosoma sp., and the Fish Skiffia Lermae: Predation or Competition,or Both?

We tested the reciprocal effects of water conditioned by exudates of Aeolosoma sp. (Aphanoneura, Oligochaeta) and fish (Skiffia lermae: Goodeidae) and by the presence of Aeolosoma sp. on the population dynamics of four species of anomopod cladocerans (C. cornuta, C. dubia, S. serrulatus and S. vetulus) at 25 °C for 26 days using Chlorella vulgaris(1 × 10⁶ cells ml^–1) as a basic food for all. We found that, regardless of treatment, C. cornuta and C. dubia had a long initial phase of slow growth, followed by a rapid increase after the second week and that, regardless of treatment, C. dubia had a higher rate of population increase per day than C. cornuta. S. vetulus had a longer lag phase than S. serrulatus. Fish-conditioned water resulted in growth inhibition in S. serrulatus, but had no effect on S. vetulus, while Aeolosoma-conditioned water inhibited growth of S. vetulus but not that of S. serrulatus. Our results suggest a scale of responses of cladocerans to exposure to fish- and worm-conditioned water and to the presence of worms, ranging from a mild stimulation to no effects to inhibited growth. Kairomone-effects on body size of C. cornuta were not significant, but beak length was strongly influenced, and more by fish than by worm kairomones. In S. vetulus, differences in size were not significant. However, individuals grown in the presence of worms had higher biomass while those grown in the presence of fish and worm kairomones showed a decreased weight. Effects of worm exudates and of their live biomass on cladocerans were thus opposite in Simocephalus. In Ceriodaphnia dubia, in contrast, they were additive. Aeolosoma was depressed by all four cladocerans, although worms tried to penetrate the valves of the cladocerans to feed on the tissue inside. In doing so, they suffered significant casualties, especially from blows of the powerful post-abdomen of Simocephalus. The nature of the cladoceran-worm interaction is therefore far from simple: in addition to the 'chemical communication' that is present, it has a predatory component (worms trying to feed on cladocerans) but the reverse might also be true (cladocerans filtering out tissues of disrupted Aeolosoma). Since both worms and cladocerans feed on algae, exploitative competition also seems to be involved. In this, the worms appear to be the inferior partner, although none of the experiments lasted long enough to drive any of the competing partners to extinction.     

Effects of Microcystis blooms on the crustacean plankton community: enclosure experiments in a subtropical lake

An enclosure experiment was conducted in July–September 2001 in subtropical eutrophic Lake Donghu (China) to test a hypothesis that a moderate cyanobacterial biomass would have a positive effect on small-sized cladocerans. Eight enclosures (12.5 m³) were arranged with different nutrient concentrations using the lake water, tap water, and sediment from Lake Donghu. Microcystis blooms appeared in enclosures with higher nutrient concentrations and the average fresh weight biomass of Microcystis spp. ranged from 4.6 to 30.4 mg l^?1 during the bloom period. Three cladocerans (Moina micrura, Diaphanosoma brachyurum, and Ceriodaphnia cornuta) and two cyclopoids (Mesocyclops dissimilis and Thermocyclops taihokuensis) dominated the crustacean plankton community during the experimental period. The C. cornuta biomass constituted the greatest percentage (55.9–90.0%) of cladoceran biomass in the Microcystis bloom treatments. When the Microcystis biomass increased, the average biomass of C. cornuta increased and the biomass of M. micrura and D. brachyurum decreased, whereas the cyclopoid biomass did not change significantly. The total biomass of cladoceran and crustacean plankton were significantly positively correlated with the Microcystis biomass. Our results indicate that a moderate biomass of Microcystis spp. can favor crustacean plankton to some extent and, furthermore, may impact food web structures in a eutrophic lake.     

Effect of the epizoic rotifer Brachionus rubens on the population growth of three cladoceran species

Using population densities and growth rates as criteria, we studied interactions between the epizoic rotifer Brachionus rubens and each of three cladoceran species differing in size and reproductive rates — Daphnia carinata, Moina macrocopa and Ceriodaphnia rigaudi. In all mixed — species experiments, B. rubens existed in both the epizoic mode, attached to the cladoceran host, and in the free-swimming mode. Rotifer population growth rates were significantly depressed in the presence of M. macrocopa, presumably as a consequence of exploitative and interference competition. The largest cladoceran, D. carinata probably did not suppress B. rubens, because the epizoic component of the rotifer population escaped from the deleterious effects of mechanical interference. Peak population numbers and initial population growth rates reached by all three cladocerans were lower in the presence of B. rubens, probably because of the adverse effects of the epizoic infestation, which was maximal on D. carinata and least on C. rigaudi. In mixed-species cultures of D. carinata and M. macrocopa, the presence of B. rubens helped D. carinata coexist with M. macrocopa, which otherwise would have suppressed the Daphnia.     

A rapid knockdown effect of Penicillium citrinum for control of the mosquito Culex quinquefasciatus in Thailand

Twenty local isolates of entomopathogenic fungi were determined for control of the larvae and adults of Culex quinquefasciatus. In a laboratory experiment, a Penicillium sp. CM-010 caused 100 % mortality of third-instar larvae within 2 h using a conidial suspension of 1 × 10⁶ conidia ml^?1. Its LC₅₀ was 3 × 10⁵ conidia ml^?1, and the lethal time (LT₅₀) was 1.06 h. Cloning and sequencing of its internal transcribed spacer region indicated that this Penicillium species is Penicillium citrinum (100 % identity in 434 bp). Mortality of the adult was highest with Aspergillus flavus CM-011 followed with Metarhizium anisopliae CKM-048 from 1 × 10⁹ conidia ml^?1. P. citrinum CM-010 at 1 × 10⁶ conidia ml^?1 killed 100 % larvae within 2 h while Bacillus thuringiensis var. israelensis at 5 ITU ml^?1 required 24 h. This P. citrinum CM-010 also greatly reduced survival of C. quinquefasciatus larvae in an unreplicated field test. Light and transmission electron micrographs showed that the fungal conidia were ingested by the larvae and deposited in the gut. The metabolite patulin was produced by P. citrinum CM-010 instead of citrinin.     

Population growth of some genera of cladocerans (Cladocera) in relation to algal food (Chlorella vulgaris) levels

We studied the patterns of population growth of 7 cladoceran species (Alona rectangula, Ceriodaphnia dubia, Daphnia laevis, Diaphanosoma brachyurum, Moina macrocopa, Scapholeberis kingi and Simocephalus vetulus) using 6 algal densities, viz. 0.05×10⁶, 0.1×10⁶, 0.2×10⁶, 0.4×10⁶, 0.8×10⁶ and 1.6×10⁶ cells ml^–1, of Chlorella vulgaris for 18 – 30 days. In terms of carbon content these algal concentrations corresponded to 0.29, 0.58, 1.16, 2.33, 4.65 and 9.31 g ml^–1, respectively. Cladocerans in the tested range of algal levels responded similarly, in that increasing the food concentrations resulted in higher numerical abundance and population growth rates (r). The peak population densities were (mean±standard error) 71±5; 17.1±0.4, 3.6±0.3, 12.7±1.1, 18.2±2.7, 15.8±1.0 and 10.9±0.02 ind. ml^–1, respectively for A. rectangula, C. dubia, D. laevis, D. brachyurum, M. macrocopa, S. kingi and S. vetulus. In general, the lowest r values were obtained for D. laevis (0.01±0.001) at 0.05×10⁶ cells ml^–1 food level while the highest was 0.283±0.004 for A. rectangula at 1.6×10⁶ cells ml^–1 of Chlorella. When the data of peak population density for each cladoceran species were plotted against the body length, we found an inverse relation, broadly curvilinear in shape. From regression equations between the food level and rate of population increase, we calculated the theoretical food quantity (the threshold level) required to maintain a zero population growth (r = 0) for each cladoceran species, which varied from 0.107 to 0.289 g ml^–1 d^–1 depending on the body size. When we plotted the cladoceran body size against the corresponding threshold food levels, we obtained a normal distribution curve. From this it became evident that for up to 1300 m body size, the threshold food level increased with increasing body size; however, beyond this, the threshold level decreased supporting earlier observations on rotifers and large cladocerans.     

A re-evaluation of the Macrothrix rosea-triserialis group, with the description of two new species (Crustacea Anomopoda: Macrothricidae)

We redescribe Macrothrix rosea (females and males) based on material collected in Belgium. We also compare seven populations of Macrothrix `triserialis' from different parts of the world, including a topotypical population of M. triserialis s. str. from Sri Lanka, and males from South India (here first described), relying heavily on the structure of the trunk limbs, beside classical features of morphology. M. rosea and M. triserialis are extremely closely related: males are easily separated, but the identification of females requires micro-characters such as the relative length of the apical segment of the setae natatoriae and the adornment of the first antenna and of the longest swimming seta of the antenna. M. rosea and triserialis together constitute a sub-group of the rosea-group. Macrothrix triserialis-like animals occur in the tropical–subtropical belts of four continents. We compare populations from Asia, South America and Africa, and find differences in microcharacters of the trunk limbs, but cannot decide whether these represent random variation or sound taxonomical differences. One of the basic characters of the Macrothrix rosea-triserialis subgroup is that the setae natatoriae of the postabdomen are implanted on a prominence, the `heel'. Other characters include the fact that the Fryer' forks are adorned with one or two big teeth only, and that the scrapers of trunk limb two form a row of eight without any doublings. Possibly, scraper five, and scraper four to a lesser degree has an enlarged subapical tooth. The exopodite of trunk limb three has four plumose setae, the back and front row of the endopodite six setae and/or receptors, the exopodite of trunk limb four has two setae, and the back row of the endopodite six setae, plus one on the gnathobase. The pre-epipodite of trunk limb five consists of three lobes, the `endopodite' is small, and the `exopodite' is reduced to a single seta. The male postabdomen has a tubular ending, without true end-claws, although a rudiment of an end-claw is seen in M. triserialis. Two new species are described: M. tabrizensis and M. agsensis. A comparison, including the males of Macrothrix triserialis, M. rosea, M. smirnovi and M. tabrizensis confirms the relationship of all these taxa, but also reveals a morphological series in the shape of the postabdomen, from a complete absence of end-claws, over rudiments of a pair of end-claws, to complete endclaws. Absence of end-claws is here considered to represent an evolved character state. Macrothrix smirnovi Ciros & Elías (1987) is less closely related to the rosea-triserialis group, and is considered to form a sub-group in its own right. It shows a short `heel' on the postabdomen, but carries a supplementary seta behind scraper 4 of the endopodite of trunk limb two, and has a male with a postabdomen that closely resembles that of the female. These are primitive characters, which are also found in Wlassicsia, Bunops and Onchobunops and provide a possible phylogenetic link between Macrothrix and these three genera, although the genetic distance between them is considered to be quite large.     

Production of aglycone protopanaxatriol from ginseng root extract using Dictyoglomus turgidum β-glycosidase that specifically hydrolyzes the xylose at the C-6 position and the glucose in protopanaxatriol-type ginsenosides

The hydrolytic activity of a recombinant β-glycosidase from Dictyoglomus turgidum that specifically hydrolyzed the xylose at the C-6 position and the glucose in protopanaxatriol (PPT)-type ginsenosides followed the order Rf > Rg₁ > Re > R₁ > Rh₁ > R₂. The production of aglycone protopanaxatriol (APPT) from ginsenoside Rf was optimal at pH 6.0, 80 °C, 1 mg ml^?1 Rf, and 10.6 U ml^?1 enzyme. Under these conditions, D. turgidum β-glycosidase converted ginsenoside R₁ to APPT with a molar conversion yield of 75.6 % and a productivity of 15 mg l^?1 h^?1 after 24 h by the transformation pathway of R₁ → R₂ → Rh₁ → APPT, whereas the complete conversion of ginsenosides Rf and Rg₁ to APPT was achieved with a productivity of 1,515 mg l^?1 h^?1 after 6.6 h by the pathways of Rf → Rh₁ → APPT and Rg₁ → Rh₁ → APPT, respectively. In addition, D. turgidum β-glycosidase produced 0.54 mg ml^?1 APPT from 2.29 mg ml^?1 PPT-type ginsenosides of Panax ginseng root extract after 24 h, with a molar conversion yield of 43.2 % and a productivity of 23 mg l^?1 h^?1, and 0.62 mg ml^?1 APPT from 1.35 mg ml^?1 PPT-type ginsenosides of Panax notoginseng root extract after 20 h, with a molar conversion yield of 81.2 % and a productivity of 31 mg l^?1 h^?1. This is the first report on the APPT production from ginseng root extract. Moreover, the concentrations, yields, and productivities of APPT achieved in the present study are the highest reported to date.