城镇化背景下深圳典型流域鱼类群落特征及驱动因子

理解城镇的快速发展对河流鱼类群落结构的影响,是城镇河流科学管理和生物多样性保护的关键基础。本研究于2019年丰水期（8月）和枯水期（11月）,选取我国城镇化典型城市-深圳域内两个处于不同城镇化程度的代表性流域,应用多重统计方法比较分析了流域间鱼类群落结构的差异,并探讨了驱动鱼类群落变异的关键环境要素。结果发现,城镇化程度高的观澜河流域其鱼类种类组成、优势类群、生物多样性指数与城镇化程度低的坪山河流域有明显差别。 具体表现为：城镇化程度高的流域土著敏感种类如异鱲、吸鳅等几近消失,优势类群为外来入侵耐受种类,其物种多样性显著低于城镇化程度低的流域（P<0.05）。同时,外来鱼类在城镇河段其数量占比平均达92.5%,广泛分布于深圳城镇河流中。在环境因素方面,城镇化程度高的观澜河流域水体理化指标总氮、总磷、氨氮、化学需氧量、生化需氧量、高锰酸盐指数均显著性高于城镇化程度低的坪山河流域（P<0.05）。基于Bray-Curtis距离的冗余分析显示：城镇用地占比和总氮是影响观澜河和坪山河流域鱼类群落差异的主要因素。城镇化进程中河流生境的改变已影响到土著鱼类的生物多样性。因此,推动以恢复土著鱼类生物多样性的河流生态治理与保护是今后水生态目标管理的重要方向。     

刘家峡水库网箱养鱼场纤毛虫群落特征

2006年3月至2007年2月, 用活体观察法和直接计数法对刘家峡水库网箱养鱼场纤毛虫群落进行了研究.共鉴定到77种纤毛虫, 其中包括4个未定名种, 隶属于3纲11目34科43属.下毛目为优势类群, 前口目为次优势类群, 异毛目为偶见类群.善变膜袋虫、长圆膜袋虫、珍珠映毛虫、钩刺斜管虫和大口瞬目虫为春季群落优势种; 善变膜袋虫、颗粒膜袋虫和珍珠映毛虫为夏季群落优势种; 颗粒膜袋虫和善变膜袋虫为秋季群落优势种; 冬季无明显优势种.纤毛虫物种数的周年动态呈单峰型, 8、9月份物种数最多, 有52种, 3月份最少, 只有18种; 物种数的季节动态为: 夏季＞秋季＞春季＞冬季.纤毛虫丰度的周年动态呈三峰型, 高峰分别出现在4月、6月和9月份, 5月份采样前夕水库调水导致丰度骤降是造成三峰型的主要原因; 纤毛虫丰度的季节动态为: 夏季＞秋季＞春季＞冬季.纤毛虫物种多样性指数的周年动态为: 8月份最大, 3月份最小.相关性分析结果表明, 对网箱养鱼场纤毛虫物种数影响最大的因子是水温, 其次是透明度和pH值, 投放饲料量的影响最小; 对网箱养鱼场纤毛虫丰度影响最大的是投放饲料量, 其次是水温和pH值, 透明度的影响最小.     

Differences in root architecture influence attraction of fishes to mangroves: A field experiment mimicking roots of different length, orientation, and complexity

Benthic structure plays an important role as shelter and feeding habitat for demersal fauna. While many studies have investigated the relationship between structural complexity of aquatic vegetation and the number of species or abundance of motile organisms, little is known of the attractiveness of submerged mangrove roots. We tested the importance of various root attributes in attracting fish species in a field experiment using different artificial mangrove units (AMUs) with PVC pipes mimicking roots to exclude interaction with other environmental and biotic factors. We manipulated length, vertical orientation, and three-dimensional structural complexity of root mimics in the AMUs to explore their effects on the fish community variables: fish abundance, number of species and community composition. Pipe length and three-dimensional structure did not have an effect on fish community variables. Vertical pipe orientation had a significant effect and AMUs with standing pipes showed higher total fish abundances and number of species than AMUs with hanging pipes. Also community composition differed greatly between AMUs with standing versus hanging pipes. At species level, demersal fish species mainly occupied AMUs with standing pipes and occurred only at very low abundances when hanging pipes dominated in the AMUs; in contrast, the semi-pelagic swimmer Sphyraena barracuda showed a trend of higher abundance in AMUs with mainly hanging pipes. When analyzed across all AMUs, fish abundances of demersal as well as semi-pelagic species decreased significantly with increasing interspatial pipe distance among AMUs, suggesting that distance to refuge may be the underlying mechanism for the observed patterns. The above findings are important in the context of the worldwide degradation of mangroves, because human alteration to mangrove vegetation affects its structure and thus composition and size of fish communities.     

云南雨石得电站工程建设对巴江渔业资源及生态环境的影响

综述了巴江渔业资源状况和雨石得电站建设对资源和环境的影响。巴江共有鱼类60种,其中土著鱼类47种。有16个水生动物新种(其中鱼类新种14个),和国家二级保护动物红瘰疣螈。屯站建成后将对巴江急流鱼种及洄游鱼种的生存造成不利影响。当前应采取切实可行的生态措施,以保护巴江特有的生物资源。     

Timing and size of blooms of the ctenophore Mnemiopsis leidyi in relation to temperature in Narragansett Bay, RI

The ctenophore Mnemiopsis leidyi is at the northern extreme of its geographic range in Narragansett Bay, an estuary on the northeast coast of the United States. Blooms have typically been observed in late summer and fall according to records from 1950 to 1979. We document an expansion of the seasonal range of this important planktonic predator to include springtime blooms during the 1980s and 1990s. This shift to an earlier seasonal maximum is associated with increasing water temperature in Narragansett Bay. Temperatures in spring have risen, on average, 2 °C from 1950 to 1999 with warm years being associated with the positive phase of the North Atlantic Oscillation. During 1999, M. leidyi appeared earlier in spring and was more abundant than during any previous year for which records are available. Changes in the seasonal pattern and abundance of this predator are likely to have important effects on planktonic ecosystem dynamics of Narragansett Bay. These include reduction of zooplankton abundance in spring followed by increases in size and frequency of summer phytoplankton blooms. Earlier blooms of M. leidyi may also reduce survival of eggs and larvae of fish because, as in 1999, they coincide with the period of peak spawning.     

Distribution of ichthyoplankton in the eastern Peter the Great Bay,Sea of Japan,in June and July of 2007

Comparison of the results of ichthyoplankton surveys conducted at 97 stations in the eastern part of the Peter the Great Bay of the Sea of Japan, in June–July 2007 with the similar research data of the 1950s shows that at present, as was the case 50 years ago, flatfish eggs belonging mainly to the yellowfin sole Limanda aspera and brown sole Pleuronectes herzensteini prevail in the local ichthyoplankton (up to 86%). The highest concentrations of these species’ eggs were recorded in the Vostok Bay and Strelok Bay. The spawning activity of flatfish in 2007 is found to be lower than in the mid 1900s, but the significance of the eastern part of the Peter the Great Bay for flatfish reproduction remains large. The importance of long-term monitoring in this area, which is being subjected to steadily growing anthropogenic impacts, is also proven.     

Evolutionary ecology of opsin gene sequence,expression and repertoire

Linking molecular evolution to biological function is a long‐standing challenge in evolutionary biology. Some of the best examples of this involve opsins, the genes that encode the molecular basis of light reception. In this issue of Molecular Ecology, three studies examine opsin gene sequence, expression and repertoire to determine how natural selection has shaped the visual system. First, Escobar‐Camacho et al. ( 2017 ) use opsin repertoire and expression in three Amazonian cichlid species to show that a shift in sensitivity towards longer wavelengths is coincident with the long‐wavelength‐dominated Amazon basin. Second, Stieb et al. ( 2017 ) explore opsin sequence and expression in reef‐dwelling damselfish and find that UV‐ and long‐wavelength vision are both important, but likely for different ecological functions. Lastly, Suvorov et al. ( 2017 ) study an expansive opsin repertoire in the insect order Odonata and find evidence that copy number expansion is consistent with the permanent heterozygote model of gene duplication. Together these studies emphasize the utility of opsin genes for studying both the local adaptation of sensory systems and, more generally, gene family evolution.     

Morphology and Phylogeny of Calyptospora paranaidji n. sp. (Eimeriorina: Calyptosporidae), an Apicomplexan Parasite of the Hepatic Tissue of Cichla piquiti Kullander & Ferreira, 2006, From a Reservoir in the Brazilian Amazon Region

The coccidians of the family Calyptosporidae are parasites of the tissue and organs of fish and aquatic invertebrates, in particular in the tropical region. In contrast with other apicomplexans of the suborder Eimeriorina, the diversity and ecology of the species of the genus Calyptospora have been poorly investigated, resulting in a lacuna that restricts the understanding of the distribution and prevalence of this group of eukaryote microparasites in the Amazon region. In the present study, the integrated comparative analysis of morphological characteristics, histological and structural traits, and the sequences of a fragment of the 18S rRNA gene, provides support for the identification of a new species of Calyptospora, found parasitizing the hepatic tissue of the piscivorous blue peacock bass, Cichla piquiti, captured in the reservoir of the Estreito hydroelectric dam on the middle Tocantins River in northern Brazil. This new species was named Calyptospora paranaidji n. sp.