海洋真菌抗污损活性天然产物研究

黏附于海洋船舶或人工设施表面的污损生物给人类海洋生产活动与生态环境带来诸多不利影响.将具有抗污损活性的化合物开发成防污涂料是目前防治海洋生物污损的最常用手段之一.而大量传统有机金属防污剂因其严重毒副作用被禁用,亟须开发高效、环境友好型抗污损涂料.海洋真菌能够产生大量结构新颖、作用机制独特的高效、低毒/无毒抗污损活性次级...     

海洋生物防污作用机制及应用前景

海洋污损生物的附着会对人类活动产生不利影响。栖息于海洋环境中的动植物在长期的进化过程中针对污损生物的附着形成了忍耐、躲避与物理、化学等自我保护和防御机制以保持自身体表的洁净。本文从以上方面综述了海洋生物的天然防污作用机制,并对其应用前景进行了展望。了解和掌握海洋生物天然防污作用机制,有利于新型环保防污技术的研制和开发,进而从根本上解决海洋污损生物的危害难题。     

化学生态学在海洋污损生物防除中的应用

在海洋环境中,许多海洋生物都能产生对环境无危害的、具有防污活性的次生代谢产物以保护自身的洁净,利于自身的生存.用化学生态学的方法从海洋生物中提取天然防除物质成为近年来解决海洋污损生物问题的新思路,其目标是寻找高效无毒的防污材料取代原有的对海洋环境有严重危害的化学合成防污材料.虽然目前对提取生物的次生代谢产物的防污机理还所知甚少,但不少从海洋生物中获得的天然产物已显示出良好的防污活性.要解决污损生物防污问题,还需对天然产物的作用机制、生态学效应、天然产物与涂料的结合、控制和释放及野外实验进行更加深入的研究与探讨.     

藤壶附着：从基底探测到胶的固化

藤壶在水下设施上的牢固黏附一方面造成极大的污损和危害,另一方面为水下的牢固粘接提供了灵感.相关的防污和水下超粘接等技术的解决强烈依赖于对其附着过程及分子机制的理解.目前,对藤壶黏附的宏观过程已有了较为深入的了解,主要包括基底探测、信号传导、胶液分泌以及胶的固化,但对该过程中作用的分子机制如受体蛋白的识别、基因表达的调控以及胶蛋白的交联固化的研究依然有限,而上述任何阶段的干扰都可为防污或水下粘接提供重要的理论指导.因此,深入理解各阶段的相关分子机制对防污和水下粘接至关重要.本文综述了近年来对藤壶附着的相关进展,介绍附着过程中的内部信号分子响应以及胶液分泌过程中的固化交联机制,指出了存在的问题,并提出进一步可能的研究要点.     

海洋硅藻附着研究进展

随着人类对海洋资源的进一步开发和利用,越来越多的人工设备用于水下操作,而海洋生物污损在很大程度上制约了这些设备的应用,给人类带来重大的经济损失。因此,海洋生物污损的形成机制与防治成为当前研究的一个热点。海洋硅藻是海洋生物污损过程中形成生物膜的主要物种,其在水下固相表面的附着可诱导大型污损生物的附着,从而影响生物污损群落的形成。本文综述了硅藻在固相表面的附着机理、固相表面性质对硅藻附着的影响及具有应用前景的广谱抗污损高分子材料的研究进展,并展望海洋硅藻附着研究前景。     

近海设施双壳类污损特点及应对措施概述

双壳类软体动物是引发海洋生物污损现象的重要生物类群。污损近海设施的该类型生物主要为紫贻贝(Mytilusedulis)、齿缘牡蛎(Dendostrea folium)、褶牡蛎(Alectryonella plicatula)、长牡蛎(Crassostrea gigas)和日本巨牡蛎(C.nippona)等种类; 在纬度较低的热带、亚热带近海海域, 污损性双壳类以牡蛎为优势种, 而温带近海海区则是紫贻贝;至于深度方面, 牡蛎污损的范围大于紫贻贝。近海设施污损生物的防除主要通过水下人工清除作业、安装波浪驱动海生物防除装置、涂装防污漆、电解海水、添加杀生剂和生物控制等途径, 加强近海污损性双壳类研究不仅有助于促进海洋生态学研究的发展, 而且可为研发新型高效环保防污技术奠定基础。     

抗污损海洋天然产物的开发及其作用机理研究进展

首先对近年发表在学术期刊Biofouling上的一篇关于抗污损化合物的综述做一简短总结。其次,突出介绍了对无脊椎污损生物附着和变态分子水平的调控机制的研究近来的进展。旨在给那些从事生物污损和抗污损技术研究的科研人员提供一定的帮助。     

厚壳贻贝低分子量足丝蛋白的初步鉴定(英文)

足丝蛋白是贻贝科(Mytilidae)所特有一种在水环境中也能表现出强黏附功能的蛋白,也是目前开发新型生物黏附剂的主要候选分子。厚壳贻贝(Mytilus coruscus)广泛分布于我国东部沿海,是我国具有重要经济价值的贻贝,其足丝粗硬,黏附力强,关于厚壳贻贝的足丝蛋白的研究目前尚未见报道。通过醋酸抽提结合反相高效液相色谱分离,从厚壳贻贝足丝盘中分离纯化到数种低分子量足丝蛋白,经质谱鉴定和氨基酸序列测定,其中三种足丝蛋白(分子量6 kD左右)属于贻贝足丝蛋白-3(mytilus foot protein-3,mfp-3)家族,且序列中富含DOPA,另有三种足丝蛋白为未知新型足丝蛋白。石英晶体微天平分析表明,厚壳贻贝低分子量足丝蛋白在金表面有较强的吸附能力,这与其黏附功能是直接相关的。以上工作为深入了解厚壳贻贝低分子量足丝蛋白的分子多样性以及黏附机制奠定了基础。     

海洋污损的微生物学过程与机制研究进展

海洋生物污损主要由微生物腐蚀(MIC)与生物淤积(MBF)造成。细菌的附着及生物被膜的形成在微观尺度为微生物腐蚀提供了环境条件,而生物淤积则从宏观层面加速了污损的进程。近年来,海洋生物污损在全球范围内造成了巨大的经济损失,各类抗污损的方法也相继开发。微生物行为在污损的形成中扮演着重要角色,包括细菌在基质上的定殖,微生物被膜的产生,微生物结构的组装以及氧化还原性质的改变等。本文中,笔者聚焦海洋污损的微生物学机制,对生物污损的发生条件、影响因素、形成机制、群体感应调节特征进行了总结,并对防控方法进行了归纳,以期从生态学层面深入认识海洋污损的动力学过程,并为开发新型环保型防污材料提供借鉴思路。     

污损性海鞘的生态特点研究展望

海鞘生长快,繁殖迅速,能产生大量在短时间内附着的幼虫,是海洋污损生物群落中的重要成员,对海上人工设施会产生严重危害。污损性海鞘主要由悉尼海鞘(Ascidia sydneiensis)、史氏菊海鞘(Botryllus schlosseri)、米氏小叶鞘(Diplosoma listerianum)、柄瘤海鞘(Styela clava)、红贺海鞘(Herdmania momus)等9科29属103种组成,其中在太平洋海域64种、印度洋23种、大西洋44种,而北冰洋海域仅3种;另外,其附着污损具有明显的地域性和季节特点,并与深度有关。今后应加强污损性海鞘的生态调查和分类研究,阐明深海及两极海域附着污损特点,揭示幼虫附着变态过程的分子调控机理,完善幼虫采集培养技术,以期更好地掌握海鞘生物学特性与生态特点,丰富和发展海洋生态学内容,并为海洋污损生物的防除奠定基础,促进海洋经济产业的发展。     

The impact of the sea anemone Actinothoe sphyrodeta on Mytilus galloprovincialis mussel cultivation (Galicia,Spain)

Abstract

Marine mussel aggregations act as a substratum and refuge for many fouling species. Mussel cultivation in Galicia, Spain, is carried out on hanging ropes in subtidal systems. The fauna associated with this cultivation includes a large number of invertebrates that compete for space or food with the mussels, or use their clusters as a refuge from predators or water turbulence. Outbreaks of the epibiont anemone Actinothoe sphyrodeta have been reported in cultivated Galician mussels since 2013, but their impact has not been investigated rigorously. Here, the temporal and spatial variability of Actinothoe sphyrodeta on mussel shells throughout one year is presented. Sampling of mussel size, weight and byssus attachment strength allowed mussel tenacity (attachment strength relative to size) to be calculated. A higher presence of Actinothoe sphyrodeta correlated with lower mussel tenacity and greater biomass losses, suggesting that this species could be an economically important biofouling component.     

Potential Impact of Filter-feeding Invaders on Temperate Inland Freshwater Environments

Since the 1990s, biological invasions have captured the attention of the scientific community as an important element of global change and a major threat to biodiversity. The inland waters of South America provide two examples of biological invasions. This review examines bivalve invasions in South America, summarizes the research results for two species, the Asian clam (Corbicula fluminea) and the golden mussel (Limnoperna fortunei), and suggests further studies. The rapid expansion of invasive bivalves into these environments involves significant changes. Until now, C. fluminea, the Asian clam, did not produce generalized macrofouling in the Neotropical region, as is common in the Holarctic region. However, the first specific cases of macrofouling by C. fluminea were recently detected in heat interchangers of power stations in Brazil. On the other hand, L. fortunei is provoking new economic impacts in South American freshwaters through macrofouling. Before the invasion by the golden mussel, macrofouling was recorded only in the marine and estuarine environments of the Neotropical region. The impact caused by invasive bivalves in this region is not only economic, however. Rapid changes in the benthic community, favoring the presence of Oligochaeta and Hirudinea, as well as the displacement of native species of mollusks, are among the problems related to the presence of the golden mussel. Another issue is the settlement of golden mussels on native bivalves. This bivalve is now a new element in the diet of some native fish species, being the main food item in some cases.     

Effects of artificial epibionts on byssogenesis,attachment strength,and movement in two size classes of the blue mussel,Mytilus edulis

Blue mussels (Mytilus edulis) can alter the strength of byssal attachment and move between and within mussel aggregations on wave‐swept shores, but this movement ability may be limited by epibiont fouling. We quantified the effects of artificial epibiont fouling on the production of byssal threads, attachment strength, and movement in two size classes of blue mussels. In a factorial experiment, large epibiont‐covered mussels produced more functional byssal threads (i.e., those continuous from animal to substrate) after 24 h than large unfouled and small fouled mussels, but not more than small unfouled mussels. Small unfouled mussels formed and released more byssus bundles compared to any other treatment group, which indicates increased movement. Conversely, epibiont fouling resulted in decreased numbers of byssus bundles shed, and therefore reduced movement in small mussels. Epibiont‐covered mussels started producing byssal threads sooner than unfouled mussels, while small mussels began producing byssal threads earlier compared to large mussels. Mean attachment strength from both size classes increased by 9.5% when mussels were artificially fouled, and large mussels had a 34% stronger attachment compared to small mussels. On the other hand, a 2.3% decrease in attachment strength was found with increasing byssus bundles shed. Our results suggest that fouling by artificial epibionts influences byssal thread production and attachment strength in large mussels, whereas epibionts on small mussels impact their ability to move. Mussels are able to respond rapidly to fouling, which carries implications for the dynamics of mussel beds in their intertidal and subtidal habitats, especially in relation to movement of mussels within and among aggregations.     

Zebra mussel adhesion: structure of the byssal adhesive apparatus in the freshwater mussel, Dreissena polymorpha

The freshwater zebra mussel (Dreissena polymorpha) owes a large part of its success as an invasive species to its ability to attach to a wide variety of substrates. As in marine mussels, this attachment is achieved by a proteinaceous byssus, a series of threads joined at a stem that connect the mussel to adhesive plaques secreted onto the substrate. Although the zebra mussel byssus is superficially similar to marine mussels, significant structural and compositional differences suggest that further investigation of the adhesion mechanisms in this freshwater species is warranted. Here we present an ultrastructural examination of the zebra mussel byssus, with emphasis on interfaces that are critical to its adhesive function. By examining the attached plaques, we show that adhesion is mediated by a uniform electron dense layer on the underside of the plaque. This layer is only 10-20 nm thick and makes direct and continuous contact with the substrate. The plaque itself is fibrous, and curiously can exhibit either a dense or porous morphology. In zebra mussels, a graded interface between the animal and the substrate mussels is achieved by interdigitation of uniform threads with the stem, in contrast to marine mussels, where the threads themselves are non-uniform. Our observations of several novel aspects of zebra mussel byssal ultrastructure may have important implications not only for preventing biofouling by the zebra mussel, but for the development of new bioadhesives as well.     

环境DNA技术在贻贝入侵监测中的应用挑战

沼蛤(Limnoperna fortunei)和斑马贻贝(Dreissena polymorpha)是淡水系统中常见的入侵贻贝物种,对其种群规模的持续监测是入侵贻贝防治管控中的关键环节。随着分子生物学技术的发展,入侵物种监测中逐渐尝试利用环境DNA(eDNA)技术实现快速、灵敏检测。然而,在入侵物种引入-定植-扩散过程的监测中,eDNA技术的灵敏度及定量效果受到诸多因素的影响,给实际应用带来挑战。系统梳理了国内外学者利用eDNA技术监测沼蛤、斑马贻贝等入侵物种的研究进展;分析了eDNA技术的采样方案、引物设计、定量分析、质量保证、原位便携仪器设计等影响监测效率与准确率的关键环节;进一步探讨了eDNA技术在贻贝入侵监测中的优势和局限性,以及未来的改进方向。     

Overland transport of recreational boats as a spreading vector of zebra mussel <Emphasis Type="Italic">Dreissena polymorpha</Emphasis>

In aquatic ecosystems invasive species are among the most important threats to biodiversity worldwide. Understanding the dispersal mechanisms of aquatic invaders is very important for protection and management of vulnerable water bodies. Here we ask how recreational boats that are transported overland could contribute to the dispersal of invasive zebra mussels among lakes in Switzerland. Using a questionnaire sent to registered boat owners, we surveyed properties of transported boats and collected information on self-reported mussel fouling and transport activities of boat owners. We also sampled boat hulls at launching ramps and harbors for biofouling invertebrates. Boats that were kept seasonally or year-round in water were found to have high vector potential with mussel fouling rates of more than 40 %. However, only about 6 % of boats belonging to these groups were transported overland to other water bodies. Considering that approximately 100,000 recreational boats are registered in Switzerland, we estimated that every year around 1400 boats fouled with mussels are transported overland. Such boats pose a high risk of distributing zebra mussels between water bodies. Our results suggest that there is a considerable risk that recreational boats may spread new fouling species to all navigable water bodies within the study area. We speculate that one such species could be the quagga mussel, which has not yet invaded lakes in Switzerland. On a more positive note, our study has identified the group of high-risk boats so that possible control measures would only affect a relatively small number of boat owners.     

Byssal proteins of the freshwater zebra mussel,Dreissena polymorpha

The freshwater zebra mussel (Dreissena polymorpha) is a notorious biofouling organism. It adheres to a variety of substrata underwater by means of a proteinaceous structure called the byssus, which consists of a number of threads with adhesive plaques at the tips. The byssal proteins are difficult to characterize due to extensive cross-linking of 3,4-dihydroxyphenylalanine (DOPA), which renders the mature structure largely resistant to protein extraction and immunolocalization. By inducing secretion of fresh threads and plaques in which cross-linking is minimized, three novel zebra mussel byssal proteins were identified following extraction and separation by gel electrophoresis. Peptide fragment fingerprinting was used to match tryptic digests of several gel bands against a cDNA library of genes expressed uniquely in the mussel foot, the organ which secretes the byssus. This allowed identification of a more complete sequence of Dpfp2 (D. polymorpha foot protein 2), a known DOPA-containing byssal protein, and a partial sequence of Dpfp5, a novel protein with several typical characteristics of mussel adhesive proteins.     

Induction of settlement in mussel (Perna canaliculus) larvae by vessel noise

Underwater sound plays an important role in the settlement behaviour of many coastal organisms. Large steel-hulled vessels are known to be a major source of underwater sound in the marine environment. The possibility that underwater sound from vessels may promote biofouling of hulls through triggering natural larval settlement cues was investigated for the mussel, Perna canaliculus. The mussel larvae showed significantly faster settlement when exposed to the underwater noise produced by a 125-m long steel-hulled passenger and freight ferry. Median time to attachment on the substrata (ie settlement) was reduced by 22% and the time taken for all experimental larvae to settle was reduced by 40% relative to a silent control. There was no difference in the survival of the mussel larvae among the various noise treatments. The decrease in settlement time of the mussel larvae appeared to correlate with the intensity of the vessel sound, suggesting that underwater sound emanating from vessels may be an important factor in exacerbating hull fouling by mussels.     

Detachment,displacement and reattachment activity in a freshwater byssate mussel (Limnoperna fortunei): the effects of light,temperature and substratum orientation

The ability of the freshwater bivalve Limnoperna fortunei to voluntarily detach from the substratum, crawl and reattach as a function of illumination, temperature, substratum orientation, and mussel size was investigated. Thirty-two per cent of the 879 experimental animals detached and reattached elsewhere at least once during five- to eight-day experiments. The proportions of mobile mussels were significantly higher in permanent darkness than under permanent illumination. Displacement distances were also higher in darkness, but statistical differences with illuminated individuals were inconclusive. No evidence of circadian rhythms was detected. Mobile mussels were often significantly smaller than non-mobile individuals. It was not possible to detect the effect of water temperature (22°C and 31°C), or substratum orientation (topside and underside) on mussel mobility, but because the power of the statistical tests was low, future experiments are needed to confirm this result. The ability of mussels to voluntarily detach and reattach elsewhere has important implications for biofouling control.