Crustacean zooplankton communities in 13 lakes of Yunnan-Guizhou plateau: Relationship between crustacean zooplankton biomass or size structure and trophic indicators after invasion by exotic fish

We investigated crustacean zooplankton communities and their relationships to environmental factors in 13 lakes of Yunnan-Guizhou plateau to determine whether there is a consistent relationship between trophic indicators and crustacean zooplankton biomass or size structure. The lakes showed a wide range of trophic status, with total phosphorus (TP) ranging from 0.013 to 0.268 mg.L−1, and chlorophyll a from 0.9 to 76.26 μg.L−1. Continuous stocking with exotic planktivorous fish had taken place on a wide scale in these plateau lakes. About 36 species of Crustacea were found, of which Cladocera were represented by 20 taxa (12 genera), and Copepoda by 16 taxa (13 genera). Canonical correspondence analysis partitioned these species into two clusters. Physicochemical features and food-webs of different lakes seemed to be the key factors determining zooplankton species composition and distribution patterns. Between the 13 lakes, there was no significant relationship between cladocerans and chlorophyll a suggesting phytoplankton biomass was little controlled by macrozooplankton. The positive correlation between chlorophyll a and copepods suggested the high copepods biomass or size structure caused by the invasion of exotic planktivorous fish had a negative effect on water quality

Analysis of Impact of Well-Facilitated Farmland Construction—Engineering Measures on Farmland Quality

We studied the influence and correlation of soil improvement, farmland ecological protection, soil fertilization, and field infrastructure construction on the quality grade of well-fertilized farmland in the engineering measures of well-fertilized farmland construction. Taking Xiao County of the Anhui Province as the study area, based on the software platforms of SPSS, ArcGIS10.6, and the county farmland resource management information system, we investigated the farmland quality changes of well-facilitated farmland before and after construction using the fuzzy evaluation method and analytic hierarchy process. We used principal component analysis and the gray relational method to analyze the impact and correlation of various engineering measures on farmland quality. The farmland quality grade in the study area was improved by a 0.59 grade after the construction of the well-facilitated farmland. Well-facilitated farmland construction engineering measures mainly affected the farmland quality through 12 factors, such as the soil bulk density, tillage layer texture, irrigation and drainage guarantee rates, forest network density, and field road accessibility. There is a strong correlation between these factors and the characteristics of farmland quality; the degrees of correlation were 0.865–0.610, respectively. The highest correlation degree was 0.939 between the deep plowing and deep loosening soil improvement project and the improvement of the well-facilitated basic farmland quality; this was followed by soil fertilization with an increased application of organic fertilizer, farmland ecological protection, and the field infrastructure project with correlations of 0.936, 0.857, and 0.563, respectively. Represented by the improvement of farmland fertility, the soil improvement project had the strongest impact on well-facilitated farmland quality. The soil fertility project, farmland ecological protection project, and the field infrastructure project were the second most important, with very close degrees of correlation

Contrasting energy pathways at the community level as a consequence of regime shifts

Ecological regime shifts typically result in abrupt changes in ecosystem structure through several trophic levels, which leads to rapid ecosystem reconfiguration between regimes. An interesting aspect of the impact of regime shift is that alternative regimes may induce distinct shifts in energy pathways; these have been less tested than structural changes. This paper addresses this by using stable isotopes to establish the energy pathways in fish communities. We specifically focus on the impact of regime shift on changes of the energy pathways, and how the magnitude and direction of these changes affect the local community. We found that energy pathways significantly varied among the planktivorous, benthivorous, and piscivorous trophic guilds as a result of the alternative regimes. The regime shift from a clear to a turbid state altered the food web towards planktonic energy pathways and truncated food chain length, which is indicative of less ecological efficiency. This was confirmed by the adaptive foraging strategies of prevalent omnivores in the current communities. These structural and functional characteristics of trophic interactions might not facilitate classic trophic cascading effects in such a turbid regime and suppress the system’s response to environmental changes, e.g., nutrient loading, and restoration efforts in turbid to clear water regime shifts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00442-013-2878-2) contains supplementary material, which is available to authorized users

Effects of nonylphenol on the growth and microcystin production of Microcystis strains

Both organic pollution and eutrophication are prominent environmental issues concerning water pollution in the world. It is important to reveal the effects of organic pollutants on algal growth and toxin production for assessing ecological risk of organic pollution. Since nonylphenol (NP) is a kind of persistent organic pollutant with endocrine disruptive effect which exists ubiquitously in environments, NP was selected as test compound in our study to study the relationship between NP stress and Microcystis growth and microcystin production. Our study showed that responses of toxic and nontoxic Microcystis aeruginosa to NP stress were obviously different. The growth inhibition test with NP on M. aeruginosa yielded effect concentrations EbC50 values within this range of 0.67-2.96 mg/L. The nontoxic M. aeruginosa strains were more resistant to NP than toxic strains at concentration above 1 mg/L. Cell growth was enhanced by 0.02-0.2 mg/L NP for both toxic and nontoxic strains, suggesting a hormesis effect of NP on M. aeruginosa. Both toxic and nontoxic strains tended to be smaller with increasing NP. But with the increased duration of the experiment, both the cell size and the growth rate began to resume, suggesting a quick adaptation of M. aeruginosa to adverse stress. NP of 0.05-0.5 mg/L significantly promoted microcystin production of toxic strain PCC7820, suggesting that NP might affect microcystin production of some toxic M. aeruginosa in the field. Our study showed that microcystin excretion was species specific that up to 75% of microcystins in PCC7820 were released into solution, whereas > 99% of microcystins in 562 remained in algal cells after 12 days' incubation. NP also significantly influenced microcystin release into cultural media. The fact that NP enhanced growth and toxin production of M. aeruginosa at low concentrations of 0.02-0.5 mg/L that might be possibly found in natural freshwaters implies that low concentration of NP may favor survival of M. aeruginosa in the field and may play a subtle role in affecting cyanobacterial blooms and microcystin production in natural waters. (c) 2006 Elsevier Inc. All rights reserved.Both organic pollution and eutrophication are prominent environmental issues concerning water pollution in the world. It is important to reveal the effects of organic pollutants on algal growth and toxin production for assessing ecological risk of organic pollution. Since nonylphenol (NP) is a kind of persistent organic pollutant with endocrine disruptive effect which exists ubiquitously in environments, NP was selected as test compound in our study to study the relationship between NP stress and Microcystis growth and microcystin production. Our study showed that responses of toxic and nontoxic Microcystis aeruginosa to NP stress were obviously different. The growth inhibition test with NP on M. aeruginosa yielded effect concentrations EbC50 values within this range of 0.67-2.96 mg/L. The nontoxic M. aeruginosa strains were more resistant to NP than toxic strains at concentration above 1 mg/L. Cell growth was enhanced by 0.02-0.2 mg/L NP for both toxic and nontoxic strains, suggesting a hormesis effect of NP on M. aeruginosa. Both toxic and nontoxic strains tended to be smaller with increasing NP. But with the increased duration of the experiment, both the cell size and the growth rate began to resume, suggesting a quick adaptation of M. aeruginosa to adverse stress. NP of 0.05-0.5 mg/L significantly promoted microcystin production of toxic strain PCC7820, suggesting that NP might affect microcystin production of some toxic M. aeruginosa in the field. Our study showed that microcystin excretion was species specific that up to 75% of microcystins in PCC7820 were released into solution, whereas > 99% of microcystins in 562 remained in algal cells after 12 days' incubation. NP also significantly influenced microcystin release into cultural media. The fact that NP enhanced growth and toxin production of M. aeruginosa at low concentrations of 0.02-0.5 mg/L that might be possibly found in natural freshwaters implies that low concentration of NP may favor survival of M. aeruginosa in the field and may play a subtle role in affecting cyanobacterial blooms and microcystin production in natural waters. (c) 2006 Elsevier Inc. All rights reserved

Crustacean zooplankton communities in 13 lakes of Yunnan-Guizhou plateau: Relationship between crustacean zooplankton biomass or size structure and trophic indicators after invasion by exotic fish

We investigated crustacean zooplankton communities and their relationships to environmental factors in 13 lakes of Yunnan-Guizhou plateau to determine whether there is a consistent relationship between trophic indicators and crustacean zooplankton biomass or size structure. The lakes showed a wide range of trophic status, with total phosphorus (TP) ranging from 0.013 to 0.268 mg.L−1, and chlorophyll a from 0.9 to 76.26 μg.L−1. Continuous stocking with exotic planktivorous fish had taken place on a wide scale in these plateau lakes. About 36 species of Crustacea were found, of which Cladocera were represented by 20 taxa (12 genera), and Copepoda by 16 taxa (13 genera). Canonical correspondence analysis partitioned these species into two clusters. Physicochemical features and food-webs of different lakes seemed to be the key factors determining zooplankton species composition and distribution patterns. Between the 13 lakes, there was no significant relationship between cladocerans and chlorophyll a suggesting phytoplankton biomass was little controlled by macrozooplankton. The positive correlation between chlorophyll a and copepods suggested the high copepods biomass or size structure caused by the invasion of exotic planktivorous fish had a negative effect on water quality

Development of tolerance against toxic Microcystis aeruginosa in three cladocerans and the ecological implications

This is the first experimental study to compare difference in the development of tolerance against toxic Microcystis among multi-species of cladocerans (Daphnia, Moina and Ceriodaphnia) pre-exposed to two M. aeruginosa PCC7820 strains (MC-containing and MC-free). Zooplankton were divided into S population (fed Scenedesmus), M-F population (fed Scenedesmus + MC-free Microcystis), and M-C population (fed Scenedesmus + MC-containing Microcystis). M-F and M-C populations were pre-exposed to Microcystis strains for 4 weeks, and their newborns were collected for experiments. A pre-exposure to MC-containing or MC-free Microcystis increased tolerance against toxic Microcystis. The marked increases in survival rate and median lethal time (LT50, 100-194% increase) in the M-C population of Ceriodaphnia suggest that small-sized cladocerans may develop stronger tolerance against Microcystis than large-sized ones when both groups are exposed to toxic Microcystis. This may explain why dominant Daphnia is usually replaced by small-sized cladocerans when cyanobacteria bloomed in summer in eutrophic lakes. (c) 2005 Elsevier Ltd. All rights reserved.This is the first experimental study to compare difference in the development of tolerance against toxic Microcystis among multi-species of cladocerans (Daphnia, Moina and Ceriodaphnia) pre-exposed to two M. aeruginosa PCC7820 strains (MC-containing and MC-free). Zooplankton were divided into S population (fed Scenedesmus), M-F population (fed Scenedesmus + MC-free Microcystis), and M-C population (fed Scenedesmus + MC-containing Microcystis). M-F and M-C populations were pre-exposed to Microcystis strains for 4 weeks, and their newborns were collected for experiments. A pre-exposure to MC-containing or MC-free Microcystis increased tolerance against toxic Microcystis. The marked increases in survival rate and median lethal time (LT50, 100-194% increase) in the M-C population of Ceriodaphnia suggest that small-sized cladocerans may develop stronger tolerance against Microcystis than large-sized ones when both groups are exposed to toxic Microcystis. This may explain why dominant Daphnia is usually replaced by small-sized cladocerans when cyanobacteria bloomed in summer in eutrophic lakes. (c) 2005 Elsevier Ltd. All rights reserved

Contrasting energy pathways at the community level as a consequence of regime shifts

Ecological regime shifts typically result in abrupt changes in ecosystem structure through several trophic levels, which leads to rapid ecosystem reconfiguration between regimes. An interesting aspect of the impact of regime shift is that alternative regimes may induce distinct shifts in energy pathways; these have been less tested than structural changes. This paper addresses this by using stable isotopes to establish the energy pathways in fish communities. We specifically focus on the impact of regime shift on changes of the energy pathways, and how the magnitude and direction of these changes affect the local community. We found that energy pathways significantly varied among the planktivorous, benthivorous, and piscivorous trophic guilds as a result of the alternative regimes. The regime shift from a clear to a turbid state altered the food web towards planktonic energy pathways and truncated food chain length, which is indicative of less ecological efficiency. This was confirmed by the adaptive foraging strategies of prevalent omnivores in the current communities. These structural and functional characteristics of trophic interactions might not facilitate classic trophic cascading effects in such a turbid regime and suppress the system's response to environmental changes, e.g., nutrient loading, and restoration efforts in turbid to clear water regime shifts.Ecological regime shifts typically result in abrupt changes in ecosystem structure through several trophic levels, which leads to rapid ecosystem reconfiguration between regimes. An interesting aspect of the impact of regime shift is that alternative regimes may induce distinct shifts in energy pathways; these have been less tested than structural changes. This paper addresses this by using stable isotopes to establish the energy pathways in fish communities. We specifically focus on the impact of regime shift on changes of the energy pathways, and how the magnitude and direction of these changes affect the local community. We found that energy pathways significantly varied among the planktivorous, benthivorous, and piscivorous trophic guilds as a result of the alternative regimes. The regime shift from a clear to a turbid state altered the food web towards planktonic energy pathways and truncated food chain length, which is indicative of less ecological efficiency. This was confirmed by the adaptive foraging strategies of prevalent omnivores in the current communities. These structural and functional characteristics of trophic interactions might not facilitate classic trophic cascading effects in such a turbid regime and suppress the system's response to environmental changes, e.g., nutrient loading, and restoration efforts in turbid to clear water regime shifts