环境因子对海月水母螅状体存活与繁殖的影响

以我国黄渤海主要致灾大型水母海月水母的螅状体为实验材料,采用实验生态学方法研究了温度、盐度、光照强度、饵料量对其存活与繁殖的影响。结果表明,在0—25℃范围内,螅状体40 d的成活率均为100%,螅状体相对繁殖速度随温度的升高而增加;盐度在15—40范围内,螅状体40 d的成活率均为100%,盐度22.5组的螅状体相对繁殖速度最高,但盐度对螅状体种群数量影响不显著;螅状体相对繁殖速度随光照强度的增加而下降,黑暗条件有利于海月水母螅状体个体数量增加;螅状体相对繁殖速度随饵料量的增加而增加。研究结果说明海月水母螅状体对环境具有较强的适应性,水温升高、饵料量增加可导致海月水母螅状体种群数量快速增加。     

洱海蓝藻爆发的时空特征及影响因子

湖泊生态环境对区域气候变化和流域人类活动十分敏感。随着流域的持续开发,洱海作为云贵高原第二大淡水湖泊面临着严重的生态与环境问题,主要包括水质恶化和生态功能的衰退,其中蓝藻水华问题尤为突出。针对湖泊现代监测数据存在时间序列较短、连续监测记录缺乏、监测位点不完全一致等问题,应用沉积物记录开展色素等多指标分析和环境变化重建研究,并对洱海湖区南、中、北3个湖盆的沉积物记录进行对比分析,从而探讨洱海富营养化与蓝藻爆发的历史与变化特征,并识别藻类响应模式的空间异同。沉积物色素记录结果表明,洱海蓝藻生物量变化具有明显的时空差异性,呈现由南至北,先后增加、最后呈现蓝藻水华全湖性持续爆发的模式。进一步的简约模型方差分解结果表明气候变暖和营养盐富集是洱海蓝藻生物量变化的主要驱动因子,此外相对较浅的南部湖盆还受到水位波动、水动力减弱、水生植物演化的综合影响。因此,在气候变暖的背景下,控制水体营养盐输入、合理调控湖泊水位、提高水体透明度并恢复水生植物是控制洱海蓝藻水华爆发和进行生态恢复的重要措施。     

大型水母声学观测与评估技术研究进展

20世纪末以来,世界多个海域频繁出现大型水母暴发现象,对海洋生态系统、海洋渔业、沿海工业和滨海旅游业带来了巨大的灾难。为了研究大型水母生态习性,进而揭示其暴发机理并进行灾害的预警防治,近些年来国内外学者开展了大量的采用网具、目视、水下摄像、声学技术、航空影像等多种手段的大型水母监测调查工作,其中使用声学技术对大型水母进行资源评估和行为跟踪目前在欧美、日本、韩国等渔业发达国家已经开展了相关应用,在资源评估、运动学规律等研究中展现出较好的观测效果和应用潜力。目前我国在大型水母声学观测研究应用领域鲜有文献报道,通过介绍国际上利用声学技术对大型水母进行资源调查与评估、空间分布监测、运动规律等研究成果,为今后我国开展大型水母声学调查研究提供理论基础和科学依据。通过本文的分析,建议可以借鉴国际上采用科学鱼探仪、高分辨率成像声呐、声学信标等方法对大型水母进行监测调查和资源评估的研究成果,结合实际情况将声学技术逐步研究并应用到我国大型水母资源调查与评估、自然生态习性研究、重点水域大型水母动态监测预警中去,完善我国大型水母监测调查体系。     

Differences in the photoacclimation and photoprotection exhibited by two species of the ciguatera causing dinoflagellate genus,Gambierdiscus

In culture, Gambierdiscus spp. have been shown to prefer irradiances that are relatively low (≤250 μmol photons m⁻² s⁻¹) versus those to which they are frequently exposed to in their natural environment (>500 μmol photons m⁻² s⁻¹). Although several behavioral strategies for coping with such irradiances have been suggested, it is unclear as to how these dinoflagellates do so on a physiological level. More specifically, how do long term exposures (30 days) affect cell size and cellular chlorophyll content, and what is the photosynthetic response to short term, high irradiance exposures (up to 1464 μmol photons m⁻² s⁻¹)? The results of this study reveal that cell size and chlorophyll content exhibited by G. carolinianus increased with acclimation to increasing photon flux density. Additionally, both G. carolinianus and G. silvae exhibited reduced photosynthetic efficiency when acclimated to increased photon flux density. Photosynthetic yield exhibited by G. silvae was greater than that for G. carolinianus across all acclimation irradiances. Although such differences were evident, both G. carolinianus and G. silvae appear to have adequate biochemical mechanisms to withstand exposure to irradiances exceeding 250 μmol photons m⁻² s⁻¹ for at least short periods of time following acclimation to irradiances of up to 150 μmol photons m⁻² s⁻¹.     

Effect of CO2 on growth and toxicity of Alexandrium tamarense from the East China Sea,a major producer of paralytic shellfish toxins

In recent decades, the frequency and intensity of harmful algal blooms (HABs), as well as a profusion of toxic phytoplankton species, have significantly increased in coastal regions of China. Researchers attribute this to environmental changes such as rising atmospheric CO₂ levels. Such addition of carbon into the ocean ecosystem can lead to increased growth, enhanced metabolism, and altered toxicity of toxic phytoplankton communities resulting in serious human health concerns. In this study, the effects of elevated partial pressure of CO₂ (pCO₂) on the growth and toxicity of a strain of Alexandrium tamarense (ATDH) widespread in the East and South China Seas were investigated. Results of these studies showed a higher specific growth rate (0.31 ± 0.05 day⁻¹) when exposed to 1000 μatm CO₂, (experimental), with a corresponding density of (2.02 ± 0.19) × 10⁷ cells L⁻¹, that was significantly larger than cells under 395 μatm CO₂₍control). These data also revealed that elevated pCO₂ primarily affected the photosynthetic properties of cells in the exponential growth phase. Interestingly, measurement of the total toxin content per cell was reduced by half under elevated CO₂ conditions. The following individual toxins were measured in this study: C1, C2, GTX1, GTX2, GTX3, GTX4, GTX5, STX, dcGTX2, dcGTX3, and dcSTX. Cells grown in 1000 μatm CO₂ showed an overall decrease in the cellular concentrations of C1, C2, GTX2, GTX3, GTX5, STX, dcGTX2, dcGTX3, and dcSTX, but an increase in GTX1 and GTX4. Total cellular toxicity per cell was measured revealing an increase of nearly 60% toxicity in the presence of elevated CO₂ compared to controls. This unusual result was attributed to a significant increase in the cellular concentrations of the more toxic derivatives, GTX1 and GTX4.Taken together; these findings indicate that the A. tamarense strain ATDH isolated from the East China Sea significantly increased in growth and cellular toxicity under elevated pCO₂ levels. These data may provide vital information regarding future HABs and the corresponding harmful effects as a result of increasing atmospheric CO₂.     

Loop-mediated isothermal amplification method for rapid detection of the toxic dinoflagellate Alexandrium, which causes algal blooms and poisoning of shellfish

The marine dinoflagellate genus Alexandrium includes a number of species that produce potent neurotoxins responsible for paralytic shellfish poisoning, which in humans may cause muscular paralysis, neurological symptoms and, in extreme cases, death. Because of the genetic diversity of different genera and species, molecular tools may help to detect the presence of target microorganisms in marine field samples. Here we employed a loop-mediated isothermal amplification (LAMP) method for the rapid and simple detection of toxic Alexandrium species. A set of four primers were designed based upon the conserved region of the 5.8S rRNA gene of members of the genus Alexandrium . Using this detection system, toxic Alexandrium genes were amplified and visualized as a ladder-like pattern of bands on agarose gels under isothermal condition within 60 min. The LAMP amplicons were also directly visualized by eye in the reaction tube by the addition of SYBR Green I. This LAMP assay was 10-fold more sensitive than a conventional PCR method with a detection limit of 5 cells per tube when targeting DNA from Alexandrium minutum . The LAMP assay reported here indicates the potential usefulness of the technique as a valuable simple, rapid alternative procedure for the detection of target toxic Alexandrium species during coastal water monitoring.     

Long-term changes in amphipod population dynamics in a temperate estuary following ecosystem restoration

The Mondego estuary (Portugal) has suffered severe ecological stress over the last two decades, as manifested in the replacement of seagrasses by opportunistic macroalgae, degradation of water quality and increased turbidity. A restoration plan was implemented in 1998, which aimed to reverse the eutrophication effects, and especially to restore the original natural seagrass (Zostera noltii) community. This article explores the long-term changes in Ampithoe valida and Melita palmata (Amphipoda) populations in response to eutrophication (with consequent seagrass loss and macroalgal proliferation) and to the subsequent restoration plan (with progressive seagrass recovery and macroalgal biomass decline). Until the early 1990s, high densities of A. valida and M. palmata were recorded in the Mondego estuary, especially during the occurrence of the macroalgal bloom and during all the periods in which green macroalgae were available. After the implementation of the restoration plan, species abundance, biomass and production levels decreased considerably due to the progressive decline of green macroalgae. This implied the virtual disappearance of the amphipod population, mainly A. valida. Distinct behaviours displayed by the two species could be related to different food strategies and habitat preferences. Ampithoe valida showed feeding preferences for ephemeral softer, filamentous or bladed algae (e.g. Ulva sp.) due to its high caloric content, using the Z. noltii bed only as a habitat for protection against predators or shelter from wave action. On the other hand, M. palmata did not suffer a strong decline in its population density, biomass and production, which may indicate that this species is probably not a primary consumer of green macroalgae and may readily shift to alternative ecological niches. Handling editor: P. Viaroli     

ENVIRONMENTAL MODULATION OF KARLOTOXIN LEVELS IN STRAINS OF THE COSMOPOLITAN DINOFLAGELLATE,KARLODINIUM VENEFICUM (DINOPHYCEAE)1

We examined the influence of N or P depletion, alternate N‐ or P‐sources, salinity, and temperature on karlotoxin (KmTx) production in strains of Karlodinium veneficum (D. Ballant.) J. Larsen, an ichthyotoxic dinoflagellate that shows a high degree of variability of toxicity in situ. The six strains examined represented KmTx 1 (CCMP 1974, MD 2) and KmTx 2 (CCMP 2064, CCMP 2283, MBM1) producers, and one strain that did not produce detectable karlotoxin under nutrient‐replete growth conditions (MD 5). We hypothesized that growth‐limiting conditions would result in higher cell quotas of karlotoxin. KmTx was present in toxic strains during all growth phases and increased in stationary and senescent phase cultures under low N or P, generally 2‐ to 5‐fold but with some observations in the 10‐ to 15‐fold range. No karlotoxin was observed under low‐N or low‐P conditions in the nontoxic strain MD 5. Nutrient‐quality (NO₃, NH₄, urea, and glycerophosphate) did not affect growth rate, but growth on NH₄ produced 2‐ to 3‐fold higher cellular toxicity and a 50% higher ratio of KmTx 1‐1:KmTx 1‐3 in CCMP 1974. CCMP 1974 showed higher cellular toxicity at low salinity (≤5 ppt) and high temperature (25°C). Our results suggested that given the presence of a toxic strain of K. veneficum in situ, the existence of environmental conditions that favor cellular accumulation of karlotoxin is likely a significant factor underlying K. veneficum–related fish kills that require both high cell densities (10⁴ · mL^?1) and high cellular toxin quotas relative to those generally observed in nutrient‐replete cultures.     

ECTOCELLULAR GLUCOSIDASE AND PEPTIDASE ACTIVITY OF THE MIXOTROPHIC DINOFLAGELLATE PROROCENTRUM MINIMUM (DINOPHYCEAE)1

The activities of the enzymes α‐ and β‐glucosidase, and leucine aminopeptidase were measured in cultures of the dinoflagellate Prorocentrum minimum (Pavill.) J. Schiller and in field samples collected during dinoflagellate blooms occurring in tributaries of the Chesapeake Bay, Maryland, USA. Activities were measured using fluorogenic artificial substrates and partitioned among the >5 μm size fraction, small microbes fraction (0.1–5 μm), and dissolved phase (<0.1 μm). P. minimum and most other photosynthetic dinoflagellates are >5 μm in size and thus can be separated from the small microbes fraction, which contains most bacteria. Little to no glucosidase activity was detected associated with the >5 μm size fraction in cultures or in field samples, with most of the activity (67% to 93% in cultures, 54% to 100% in field samples) in the small microbes size fraction for both α and β glucosidase. In contrast, 67% to 90% of the total leucine aminopeptidase (LAP) activity in cultures was measured in the >5 μm fraction. Within a culture, LAP activity in the size fraction containing P. minimum decreased in response to ammonium and urea additions, but not in response to nitrate. In field samples, LAP activity was positively correlated with dinoflagellate abundance and chl a, and negatively correlated with ammonium concentration. During blooms, up to 34% of LAP activity was associated with the >5 μm fraction, indicating that when abundant, dinoflagellates may make a substantial contribution to ectocellular LAP activity in the water column.