海南三亚后海海域珊瑚礁生态系统的健康状况及其影响因素

分别采用鹞式调查法和断面监测法调查了海南三亚后海海域珊瑚的物种多样性、覆盖率、病害和补充量等指标,利用健康指数(CI)评估了后海珊瑚礁生态系统的健康状况,并初步分析了影响该区域珊瑚礁健康状况的主要因素。调查发现:后海海域造礁石珊瑚54种,覆盖率达到50%以上,珊瑚病害及死亡率低,珊瑚补充量高达4.5个·m-2,CI值介于1.87~2.27,表明后海海域的珊瑚礁生态系统非常健康。分析认为:后海海域浅水区域存在的海草床和大型藻类,以及珊瑚礁区高密度的植食性动物和夏季上升流的存在是该区域珊瑚礁生态系统健康的主要原因。海草和海藻将陆源污染物过滤吸收,确保进入珊瑚礁生态系统的水质良好;数量众多的植食性动物(如魔鬼海胆Diadema setosum等)调控了大型藻类和珊瑚之间的竞争关系,保证大型海藻不会威胁到珊瑚的健康生长;而后海海域夏季上升流的出现使得该海域珊瑚礁生态系统不会受到高温的影响,不会产生热白化现象。这样,多个因素的共同作用保证了后海珊瑚礁生态系统的健康。     

西沙东岛珊瑚礁鱼类种类组成特征与演变

为更好保护和管理东岛珊瑚礁鱼类资源, 2021和2022年通过水下摄影和水下潜水捕捞对东岛珊瑚礁鱼类进行现场调查,并结合历史研究探讨了东岛珊瑚礁鱼类种类组成及历史演变特征,结果如下:东岛共发现珊瑚礁鱼类235种,隶属于辐鳍鱼纲(Actinopterygii; 222种)和软骨鱼纲(Chondrichthyes; 13种),由16目、55科组成,其中鲈形目(Perciformes)鱼类最多,为181种,科层面,蝴蝶鱼科(Chaetodontidae)和鹦嘴鱼科(Scaridae)最多,均22种。东岛珊瑚礁鱼类物种数与其对应的最大全长成指数相关,随其增加而显著减少。东岛以小型鱼类最多,占总种类数的38.72%;其次是中型鱼类,为34.47%;大型鱼类为26.81%。从食性类型来看,东岛肉食性鱼类最多,占物种数的56.60%。各时间段之间鱼类的相似性指数均较低,证实了鱼类发生了显著的演替变化。研究较历史共有103种鱼类未发现,其中,肉食性鱼类占未发现鱼类的74.76%,同时未发现大型鱼类几乎全部分布在肉食性鱼类中; 14种位列于IUCN红色名录的鱼类,除一种外,其他均在此研究中未发现并均为大...     

捕捞对北部湾海洋生态系统的影响

利用Ecopath with Ecosim (EwE) 5.1软件构建了北部湾海洋生态系统1959—1960年的Ecosim模型,包含渔业、海洋哺乳动物、海鸟、中上层鱼类、底层鱼类、底栖无脊椎动物等20个功能组,通过与1997—1999年调查数据对比,分析了捕捞活动对北部湾生态系统的结构和功能的影响.结果表明：近40年来在捕捞强度不断增加的压力下,生态系统的结构和功能发生显著变化,长寿命、高营养级的肉食性鱼类生物量下降明显,系统以短寿命、小型鱼类和无脊椎动物占优势.1999年的大中型鱼类的生物量仅为1960年的6%,而小型鱼类和无脊椎动物则明显上升,尤其是头足类生物量上升了2.7倍,渔获物的营养级则从1960年的3.2降低到1999年的298,体现了“捕捞降低海洋食物网”的特点,目前的开发模式是不可持续的.利用20世纪90年代数据预测了降低捕捞压力后生态系统的变化.本研究证实了可以使用Ecosim模型预测捕捞压力对生态系统的影响.     

香溪河鱼类群落组成及资源评价

采用定置刺网的捕捞方法,于2005年3—4月在香溪河官庄坪库湾连续捕捞20次,共调查到21种鱼类。对采集的渔获物数据,分析了多样性和种群优势度。确定上层、中上层、中下层和底层的优势类群分别是贝氏、蒙古、翘嘴、鲫、鲤、蛇、鲇。三峡水库蓄水对官庄坪鱼类群落构成影响显著:鲤科鱼类种类组成比例占总种数76.2%,其中亚科有7种,占鲤科总数的43.8%。静水性生活的鱼类所占比重较大,已经形成优势种群。经济鱼类在生物量上占有举足轻重地位,上层肉食性鱼类以蒙古、翘嘴为主。鳅科鱼类基本绝迹。     

西沙群岛礁栖鱼类物种多样性及其食性特征

通过新的方法(即潜水调查法)调查了西沙群岛浅水区的礁栖鱼类, 并从食性角度分析鱼类群落特征及其对水质环境变化的响应。2006年5-6月, 对西沙群岛6个岛礁(东岛、永兴岛、羚羊礁、金银岛、华光礁和中建岛)共10个站位的礁栖鱼类种类、数量和长度进行了调查, 结合公开资料(FishBase等)确定鱼类食性。共记录到29科71属119种鱼, 其中50种是新记录。至此, 西沙群岛的鱼类总记录已达到717种。从不同站位来看, 永兴岛西的种类数量和Shannon-Wiener多样性指数均最高。多数鱼种分布范围狭小。摄食浮游动物和底栖无脊椎动物的鱼类是优势类群, 而草食性、杂食性和食物链顶端食性的鱼类数量和生物量较低, 反映出西沙群岛珊瑚礁生态系统整体上健康稳定。永兴岛的杂食性鱼类的数量比例和生物量比例均高于其他岛礁, 反映出鱼类群落已对水体富营养化产生响应。     

中国海域海洋生物的营养级指数变化特征

利用联合国粮农组织(FAO)1950-2011年渔获物捕捞量资料, 分析了我国海域(包括大陆海域、台湾海域、香港海域和澳门海域)129种渔获物的营养级指数变化特征。研究表明, 1950-1974年我国海洋营养级指数在3.45左右波动, 1975-1978年下降至3.35左右, 1982-1987年急剧下降到3.25并维持到1996年, 1997-2011年平稳回升至3.34。与全球海洋营养级指数相比, 1984年之前我国高于全球水平, 而1984年之后则低于全球水平。就生物类群而言, 鱼类对我国海洋营养级指数的贡献最大, 达73.1-85.8%; 甲壳动物次之, 为9.2-15.5%; 软体动物较小, 为3.3-11.6%; 其他无脊椎动物的贡献最小, 不超过1.8%。过度捕捞使我国部分渔获物由原来的长寿命、高营养级的底层鱼类变为现在的短寿命、低营养级的无脊椎动物和中上层鱼类。渔业捕捞许可管理制度、禁渔期和禁渔区制度、海洋捕捞产量“零增长”和“负增长”计划、增殖放流、扩大海洋保护区面积等措施的实施可能是我国海洋营养级指数回升的主要原因。     

亚龙湾珊瑚礁大型礁栖生物的群落结构及生态警示

鱼类和大型底栖生物等礁栖生物是珊瑚礁生态系统的重要组成部分,其群落信息是全面评价珊瑚礁生态系统健康状况的必要基础数据。基于录像样带法,分析了2018年12月底海南省三亚市亚龙湾珊瑚礁区17个站位礁栖鱼类和大型底栖生物的群落结构、数量分布及相似性,揭示了其中的生态警示,并提出相应的监管建议,旨在保护和恢复亚龙湾的珊瑚礁。结果表明:亚龙湾西岸及东排、西排共发现鱼类8科21属35种,以雀鲷科、隆头鱼科为主,平均密度为0.20尾·m^-2,金尾雀鲷、斑棘眶锯雀鲷和细鳞光鳃鱼为优势种;最近15年来,亚龙湾的鱼类资源持续衰退,目前已近于枯竭。另一方面,调查区的大型底栖生物以软珊瑚、大型底栖藻类、海百合和海胆为主,各类群的数量分布有所不同;造礁珊瑚的敌害生物小核果螺和长棘海星密度皆很低,目前尚不会对珊瑚礁构成威胁;整体而言,大型礁栖生物群落在亚龙湾西岸与东排、西排有较大的差异,间接反映出岛礁与岸礁环境存在差别,不过亚龙湾西岸湾口段的环境条件可能更接近岛礁;由于部分海区大型底栖藻类较多及可能存在的富营养化趋势,维持金尾雀鲷或其他植食性鱼类与藻类规模两者间的平衡,对恢复和保持亚龙湾珊瑚礁生态系统的健康尤为重要;同时,管控来自青梅河等的陆源污染,也是控制亚龙湾大型海藻增殖的关键;相比于海参,海百合对大型底栖藻类的依赖程度较低。调查区造礁珊瑚覆盖率与礁栖生物数量之间没有显著相关,可能与亚龙湾珊瑚礁退化严重及现存的种类以团块状造礁珊瑚为主,其构建的珊瑚礁生境空间异质性相对较低有关。为更好地保护亚龙湾的珊瑚礁,建议关注亚龙湾的水质,加强对捕鱼、潜水观光等旅游活动的监督管理,特别是应该立即实施长时间的渔业禁捕来恢复亚龙湾的渔业资源,并定期监控关键种群的数量变动。     

西沙珊瑚礁生态系统完整性评价与动态仿真模拟研究

以中国西沙珊瑚礁生态监控区为例,从生态系统完整性视角出发,结合珊瑚礁功能群组与环境变化的多重反馈效应,运用系统动力学方法构建了西沙珊瑚礁生态系统动态诊断模型,并通过基础情景和典型干扰情景（捕捞活动、陆源沉积、长棘海星（Acanthaster planci）暴发）的模拟过程,分析该生态监控区2010-2050年生态系统完整性的发展趋势及演变机理。结果显示：（1）系统动力学与生态系统完整性评价方法的整合,为珊瑚礁生态系统完整性的定量研究提供了一种可行性的方法;（2）珊瑚礁生态系统各效应指数中累积效应的变化最为明显,2010-2050年指数最大增长17.2,年均增长率约为1.2%,综合完整性指数在波动变化中稳步上升,珊瑚礁受损程度由中受损向中、低受损转变;（3）不同状态的珊瑚礁生态系统完整性,在其演化的不同阶段各有差异性,并且这种差异通常随时间推移才逐渐放大;（4）无论何种情景下,珊瑚礁生态系统都具有一定的恢复能力,尤其处于系统演化的释放重组阶段（2035-2040年）,生态系统的不稳定将创造了一定的可恢复性。研究结果对于分析西沙珊瑚礁生态系统的整体演化过程提供了理论借鉴,也为我国后续的珊瑚礁生态系统适应性修复理论模式研究提供了重要的基础。     

基于营养通道模型的渤海生态系统结构十年变化比较

根据1982年和1992年渤海渔业资源和生态环境调查数据,应用EwE建模软件,构建了两个时期的营养通道模型,并比较分析了10a间渤海生态系统结构以及渔业资源的变化.模型包含鳀、黄鲫、蓝点马鲛、其它中上层鱼类、小黄鱼、花鲈、其它底层鱼类、底栖鱼类、浮游动物、浮游植物、碎屑等17个功能群, 基本覆盖了渤海生态系统能量流动的途径.分析结果表明,1992年渤海生态系统的总生物量比1982年有所下降;小型中上层鱼类成为渔业资源的主要成分,其生物量较1982年明显增加;由于低营养级层次渔获物数量的增加,渔获物平均营养级有所下降.从系统规模看1982年大于1992年.1982年到1992年的十年间, 引起渤海生态系统结构变化的主要原因是初级生产力的变化以及捕捞因素.1982年与1992年渤海生态系统均处于不成熟的发育期,仍有较高的剩余生产量有待利用,因此渔业资源恢复的物质基础是有保证的.     

捕捞对长山群岛海域渔业生态系统的影响

为了评价捕捞对渔业生态系统的综合影响程度,建立渔业生态系统保护管理决策支持系统,本文基于状态、压力和生物群落响应PSR模型、利用层次分析法构建了捕捞对渔业生态系统的影响评价模型,包含渔船数量、捕捞压力指数、渔获量、底层鱼类比重、营养级、优势种单体重量、经济鱼类渔获量、多样性指数、均匀度指数3个层次9个指标,并选择1987—1988年和2006—2007年长山群岛游泳生物调查数据对其进行了定量评价。结果表明:近20年来,在捕捞强度不断增加的压力下,渔业生态系统的结构和功能发生显著变化,长寿命、高营养级的肉食性鱼类生物量下降明显,系统以短寿命、小型鱼类占优势;鱼类资源量、底层鱼类比重、营养级、优势种单体重量、经济鱼类渔获量、多样性指数、均匀度指数年退化率分别为4.75%、3.64%、0.31%、4.28%、2.32%、0.39%、1.14%;通过模型评价,渔业生态系统健康指数为0.34,低于评价等级Ⅲ级,说明近20年捕捞导致长山群岛渔业生态系统处于不健康状态。     

Does Herbivorous Fish Protection Really Improve Coral Reef Resilience? A Case Study from New Caledonia (South Pacific)

Parts of coral reefs from New Caledonia (South Pacific) were registered at the UNESCO World Heritage list in 2008. Management strategies aiming at preserving the exceptional ecological value of these reefs in the context of climate change are currently being considered. This study evaluates the appropriateness of an exclusive fishing ban of herbivorous fish as a strategy to enhance coral reef resilience to hurricanes and bleaching in the UNESCO-registered areas of New Caledonia. A two-phase approach was developed: 1) coral, macroalgal, and herbivorous fish communities were examined in four biotopes from 14 reefs submitted to different fishing pressures in New Caledonia, and 2) results from these analyses were challenged in the context of a global synthesis of the relationship between herbivorous fish protection, coral recovery and relative macroalgal development after hurricanes and bleaching. Analyses of New Caledonia data indicated that 1) current fishing pressure only slightly affected herbivorous fish communities in the country, and 2) coral and macroalgal covers remained unrelated, and macroalgal cover was not related to the biomass, density or diversity of macroalgae feeders, whatever the biotope or level of fishing pressure considered. At a global scale, we found no relationship between reef protection status, coral recovery and relative macroalgal development after major climatic events. These results suggest that an exclusive protection of herbivorous fish in New Caledonia is unlikely to improve coral reef resilience to large-scale climatic disturbances, especially in the lightly fished UNESCO-registered areas. More efforts towards the survey and regulation of major chronic stress factors such as mining are rather recommended. In the most heavily fished areas of the country, carnivorous fish and large targeted herbivores may however be monitored as part of a precautionary approach.     

Fishing degrades size structure of coral reef fish communities

Fishing pressure on coral reef ecosystems has been frequently linked to reductions of large fishes and reef fish biomass. Associated impacts on overall community structure are, however, less clear. In size‐structured aquatic ecosystems, fishing impacts are commonly quantified using size spectra, which describe the distribution of individual body sizes within a community. We examined the size spectra and biomass of coral reef fish communities at 38 US‐affiliated Pacific islands that ranged in human presence from near pristine to human population centers. Size spectra ‘steepened’ steadily with increasing human population and proximity to market due to a reduction in the relative biomass of large fishes and an increase in the dominance of small fishes. Reef fish biomass was substantially lower on inhabited islands than uninhabited ones, even at inhabited islands with the lowest levels of human presence. We found that on populated islands size spectra exponents decreased (analogous to size spectra steepening) linearly with declining biomass, whereas on uninhabited islands there was no relationship. Size spectra were steeper in regions of low sea surface temperature but were insensitive to variation in other environmental and geomorphic covariates. In contrast, reef fish biomass was highly sensitive to oceanographic conditions, being influenced by both oceanic productivity and sea surface temperature. Our results suggest that community size structure may be a more robust indicator than fish biomass to increasing human presence and that size spectra are reliable indicators of exploitation impacts across regions of different fish community compositions, environmental drivers, and fisheries types. Size‐based approaches that link directly to functional properties of fish communities, and are relatively insensitive to abiotic variation across biogeographic regions, offer great potential for developing our understanding of fishing impacts in coral reef ecosystems.     

Extinction vulnerability of coral reef fishes

With rapidly increasing rates of contemporary extinction, predicting extinction vulnerability and identifying how multiple stressors drive non-random species loss have become key challenges in ecology. These assessments are crucial for avoiding the loss of key functional groups that sustain ecosystem processes and services. We developed a novel predictive framework of species extinction vulnerability and applied it to coral reef fishes. Although relatively few coral reef fishes are at risk of global extinction from climate disturbances, a negative convex relationship between fish species locally vulnerable to climate change vs. fisheries exploitation indicates that the entire community is vulnerable on the many reefs where both stressors co-occur. Fishes involved in maintaining key ecosystem functions are more at risk from fishing than climate disturbances. This finding is encouraging as local and regional commitment to fisheries management action can maintain reef ecosystem functions pending progress towards the more complex global problem of stabilizing the climate.     

Phase shifts and the role of herbivory in the resilience of coral reefs

Cousin Island marine reserve (Seychelles) has been an effectively protected no-take marine protected area (MPA) since 1968 and was shown in 1994 to support a healthy herbivorous fish assemblage. In 1998 Cousin Island reefs suffered extensive coral mortality following a coral bleaching event, and a phase shift from coral to algal dominance ensued. By 2005 mean coral cover was <1%, structural complexity had fallen and there had been a substantial increase in macroalgal cover, up to 40% in some areas. No clear trends were apparent in the overall numerical abundance and biomass of herbivorous fishes between 1994 and 2005, although smaller individuals became relatively scarce, most likely due to the loss of reef structure. Analysis of the feeding habits of six abundant and representative herbivorous fish species around Cousin Island in 2006 demonstrated that epilithic algae were the preferred food resource of all species and that macroalgae were avoided. Given the current dominance of macroalgae and the apparent absence of macroalgal consumers, it is suggested that the increasing abundance of macroalgae is reducing the probability of the system reverting to a coral dominated state.     

Size-structural shifts reveal intensity of exploitation in coral reef fisheries

Fisheries exploitation represents a considerable threat to coral reef fish resources because even modest levels of extraction can alter ecological dynamics via shifts of stock size, species composition, and size-structure of the fish assemblage. Although species occupying higher trophic groups are known to suffer the majority of exploitative effects, changes in composition among lower trophic groups may be major, though are not frequently explored. Using size-based biomass spectrum analysis, we investigate the effects of fishing on the size-structure of coral reef fish assemblages spanning four geopolitical regions and determine if patterns of exploitation vary across trophic groups. Our analyses reveal striking evidence for the variety of effects fisheries exploitation can have on coral reef fish assemblages. When examining biomass spectra across the entire fish assemblage we found consistent evidence of size-specific exploitation, in which large-bodied individuals experience disproportionate reductions. The pattern was paralleled by and likely driven by, strongly size-specific reductions among top predators. In contrast, evidence of exploitation patterns was variable among lower trophic groups, in many cases including evidence of reductions across all size classes. The breadth of size classes and trophic groups that showed evidence of exploitation related positively to local human population density and diversity of fishing methods employed. Our findings highlight the complexity of coral reef fisheries and that the effects of exploitation on coral reefs can be realized throughout the entire fish assemblage, across multiple trophic groups and not solely restricted to large-bodied top-predators. Size-specific changes among fishes of lower trophic groups likely lead to altered ecological functioning of heavily exploited coral reefs. Together these findings reinforce the value of taking a multi-trophic group approach to monitoring and managing coral reef fisheries.     

Evaluation of indicators of nitrogen limitation in deep prairie lakes with laboratory bioassays and limnocorrals

A comparison of Kenyan reefs of different historical and observed levels of fishing exploitation showed that more exploited reef lagoons had greater sea urchin densities and sizes, fewer and smaller fish and less coral cover. In the most exploited lagoon the biomass of the burrowing sea urchin Echinometra mathaei increased five fold during the previous 15 years. An ecological study of the three most common omnivorous sea urchin species inhabiting hard substrate within these reef lagoons (E. mathaei, Diadema savignyi and D. setosum) suggests that they are ecologically separated by predation and avoid predators and competitors by occupying different size burrows or crevices within the lagoon. Predator removal through fishing activities may result in ecological release of the sea urchins and result in competitive exclusion of weaker competitors. The most exploited reef had a nearly monospecific barren of E. mathaei living outside burrows suggesting that E. mathaei may be the top competitor. Its ecological release appears to lead to a decrease in live coral cover, increased substrate bioerosion and eventually a loss of topographic complexity, species diversity, fish biomass and utilizable fisheries productivity. Data from the outer reef edge were more difficult to interpret but may indicate similar patterns. Within this area, physical stresses such as waves and currents may be a greater controlling force in regulating fishing activities and coral reef community structure.     

Impacts of predator depletion by fishing on the biomass and diversity of non-target reef fish communities

 An understanding of the indirect effects of fishing on predator-prey relationships is required for the development of valid multispecies yield models for reef fisheries and for determining the factors governing fish community structure at larger scales. We used an underwater visual census technique to examine the indirect effects of fishing on the biomass and diversity (species richness) of reef fishes in a series of ten traditional Fijian fishing grounds (qoliqoli) subject to a range of fishing intensities. All members of the families Chaetodontidae (butterflyfishes), Labridae (wrasses), Lutjanidae (snappers), Mullidae (goatfishes), Scaridae (parrotfishes) and the sub-family Epinephelinae (groupers and coral trout) which could be reliably identified were censused. Each species censused was assigned to one of three trophic groups: herbivore, invertebrate feeder or piscivore. The biomass of all piscivorous fishes and of large (>30 cm) piscivorous fishes differed significantly between qoliqoli and was significantly correlated with fishing intensity. However, the biomass of piscivorous fishes was not correlated with the biomass or diversity of their potential prey (which were not targeted by the fishery). This suggested that the indirect effects of fishing did not have an important bearing on fish diversity or biomass and that predation by the target species did not play an important role in structuring these Fijian reef fish communities. The results contrast with those from a number of studies at smaller scales and provided further indications that the structure of reef fish communities is not governed by a single dominant process, but by a range of processes which operate on different scales in different circumstances. Accepted: 29 July 1996     

Global assessment of the status of coral reef herbivorous fishes: evidence for fishing effects

On coral reefs, herbivorous fishes consume benthic primary producers and regulate competition between fleshy algae and reef-building corals. Many of these species are also important fishery targets, yet little is known about their global status. Using a large-scale synthesis of peer-reviewed and unpublished data, we examine variability in abundance and biomass of herbivorous reef fishes and explore evidence for fishing impacts globally and within regions. We show that biomass is more than twice as high in locations not accessible to fisheries relative to fisheries-accessible locations. Although there are large biogeographic differences in total biomass, the effects of fishing are consistent in nearly all regions. We also show that exposure to fishing alters the structure of the herbivore community by disproportionately reducing biomass of large-bodied functional groups (scraper/excavators, browsers, grazer/detritivores), while increasing biomass and abundance of territorial algal-farming damselfishes (Pomacentridae). The browser functional group that consumes macroalgae and can help to prevent coral–macroalgal phase shifts appears to be most susceptible to fishing. This fishing down the herbivore guild probably alters the effectiveness of these fishes in regulating algal abundance on reefs. Finally, data from remote and unfished locations provide important baselines for setting management and conservation targets for this important group of fishes.