福建沿海湿地鸻鹬类资源调查

1997年1月～2003年4月,采用直接计数法与航线调查法相结合的方法对福建省海岸湿地的涉禽进行了调查,共发现鸻鹬类43种及亚种计56386只。结合以往的调查记录,得知福建沿海鸻鹬类共53种及亚种,占全国该类群总种数的62％。冬候鸟和旅鸟是本地鸻鹬类中占优势的生态类群。目前沿海滩涂的围垦和鸟类食物的减少,是鸻鹬类所面临的主要威胁。尽快制定湿地保护与合理利用的规划,对福建沿海湿地鸟类的保护至关重要。闽江口湿地不仅是鸻鹬类集中分布的区域,同时也是世界珍禽黑脸琵鹭(Platalea minor)重要的停歇地,应尽快建立闽江口湿地自然保护区。     

青海湖鸻鹬类群落特征和时空分布

于2006年至2009年间对环青海湖鸻鹬类的群落特征和时空分布进行了资源调查,以期对青海湖保护管理提供科学依据。根据青海湖的地形、植被和水系分布以及水鸟聚集特点,环青海湖选择了15个调查地点,采用直接计数法进行了14次调查,并应用Shannon-wiener指数进行了多样性分析。共记录到鸻鹬类4科28种。数量上红脚鹬(Tringa totanus)、环颈鸻(Charadrius alexandrinus)和黑尾塍鹬(Limosa limosa)是当地的主要物种,分别占鸻鹬类调查总数的33.3%、22.0%和16.2%。分布上环颈鸻最为广泛,在各调查地点均有发现,其次为红脚鹬、黑尾塍鹬和青脚滨鹬(Calidris temminckii),分布地点达10处以上。黑马河和布哈河口多样性较高,这与其适宜的河漫滩和沼泽等栖息环境以及丰富的食物有关。季节上8~10月多样性较高,其次是4~5月。青海湖鸻鹬类的数量高峰依次为10月、8月和5月,物种数高峰为8月和4月,并且秋季物种数高于春季。主要物种红脚鹬和环颈鸻的迁徙动态较为一致,均是8月份达到全年数量最高值,次高峰为5月和10月;黑尾塍鹬的数量在10月份达到全年最高峰。青海湖鸻鹬类迁徙时间与渤海湾较为一致,这可能与历史上长期形成的迁徙模式有关。鄱阳湖和洞庭湖的鸻鹬类主要物种与青海湖比较接近,但数量远远多于青海湖。近年来,游客和游船等人为活动的增加导致青海湖产生局部污染,因此应重视环青海湖生态环境的保护管理,减少对鸻鹬类等水鸟栖息地的人为干扰。     

盐地碱蓬盐沼与相邻泥质滩涂湿地迁徙期鸻鹬类的群落组成及行为差异

盐地碱蓬(Suaeda salsa)盐沼湿地是黄渤海地区河口区域的重要湿地类型, 是水鸟迁徙停歇期的重要栖息地。本研究以辽河口国家级自然保护区为研究地点, 通过对盐地碱蓬盐沼湿地和相邻泥质滩涂两个固定样区连续三年的水鸟组成调查和行为观察, 分析盐地碱蓬盐沼湿地在鸻鹬类多样性维持和栖息地利用中的作用。共记录到鸻鹬类水鸟28种6,348只次, 其中盐地碱蓬湿地记录到4科13种, 泥质滩涂记录到4科27种, 泥质滩涂的物种多样性显著高于盐地碱蓬盐沼湿地。此外, 盐地碱蓬盐沼湿地与相邻的泥质滩涂的鸻鹬类鸟类群落组成存在较大差异, 盐地碱蓬盐沼湿地的鸟类群落组成以体型较大的大杓鹬(Numenius madagascariensis)、白腰杓鹬(N. arquata)、灰鸻(Pluvialis squatarola)等为主, 而泥质滩涂以环颈鸻(Charadrius alexandrinus)、黑腹滨鹬(Calidris alpina)等小型鸻鹬类为主, 这说明两种生境在鸟类多样性维持中具有不同的功能。行为分析发现, 泥质滩涂中栖息鸟类的主要行为为取食(58.71%-93.26%), 而盐地碱蓬盐沼湿地鸟类的行为既包括较大比例的取食, 也包括休息, 特别是在春季迁徙期。这进一步说明, 两种生境在水鸟的栖息地利用中具有一定的生态功能差异。尽管盐地碱蓬盐沼湿地记录到的鸟类物种数和数量均低于泥质滩涂, 但是, 两种生境中存在较大比例的共同分布物种, 这说明其生态功能具有较强的生态互补性, 二者作为一种独特的湿地景观组合, 在鸻鹬类迁徙停歇期的栖息地利用和物种多样性维持中发挥着不可替代的作用。     

钦州湾越冬鸻鹬类对不同生境利用分析

2008年12月至2009年1月及2011年12月至2012年1月先后两次对钦州湾的越冬鸻鹬类进行了调查,对越冬鸻鹬类退潮后在各类型生境的分布情况和原因进行了分析,以期为制定有效保护越冬鸟类及其生境的措施提供科学依据。结果表明,在不同的天气情况下退潮后各生境内记录到的鸻鹬类物种数和种群数量均不同,钦州湾不同生境鸻鹬类结构特征随天气变化改变。相似性比较显示,晴天各生境中鸻鹬类相似性指数最高的是盐田-养殖塘生境和农田生境,相似性指数为0.96;鸻鹬类相似性指数最低的是红树林滩涂生境和光滩生境,相似性指数为0.49。阴冷天气各生境中鸻鹬类相似性指数最高的是光滩生境和盐田-养殖塘生境,相似性指数为0.79;最低是红树林滩涂生境和光滩生境,相似性指数为0.52。分析表明人类活动的干扰对越冬鸻鹬类生境选择的影响较大。     

洪泽湖冬春季鱼塘生境中鸻鹬类群落特征与栖息模式

2005年冬季和2006年春季及冬季对洪泽湖东部湿地自然保护区内淮河入洪泽湖河口处(33°06'～33°07'N,118°29'～118°30'E)人工鱼塘生境中鸻鹬类群落进行了研究.设置了4个样地,总面积157 hm2.共记录到鸻鹬类19种,其中冬季10种,春季15种.从数量上看,冬季鱼塘中的鸟类总数量远大于春季.在冬春季滞留期间,鸻鹬类种群数量变动比较剧烈,反映了其迁徙集中的特点.鸻鹬类主要在鱼塘生境中休息和觅食,对鱼塘内泥滩和浅水区小生境利用率最高.洪泽湖地区的鱼塘生境和渔业方式使鱼塘成为鸻鹬类冬、春季的重要栖息地.     

崇明东滩鸻鹬类迁徙路线的环志分析

崇明东滩为东亚-澳大利西亚鸻鹬类迁徙路线上的重要迁徙停歇地.本文通过分析崇明东滩回收的异地环志鸻鹬类记录及异地回收的崇明东滩环志的鸻鹬类记录,研究崇明东滩鸻鹬类的迁徙路线.1979～2008年间,崇明东滩共回收到来自澳大利亚西北部、澳大利亚维多利亚、美国阿拉斯加及新西兰北岛等17个国家与地区环志的鸻鹬类265只,包括大滨鹬(Calidris tenuirostris)、斑尾塍鹬(Limosa lapponica)、红腹滨鹬(C.canutus)等16种鸟类,其中春季北迁期间的记录占总数的93%;2003～2008年间,澳大利亚西北部、新西兰南岛、中国大陆及新西兰北岛等10个国家与地区回收到崇明东滩环志的大滨鹬、斑尾塍鹬、红腹滨鹬等12种鸟类,共计164只.在所有与崇明东滩鸻鹬类存在迁徙连接的20个国家和地区中,澳大利亚西北部的回收记录占全部回收记录的55%.根据斑尾塍鹬和红腹滨鹬不同亚种的越冬地分布,崇明东滩回收的斑尾塍鹬有L.l.menzbieri与L.l.baueri两个亚种,红腹滨鹬有C.a.piersmai和C.a.rogersi两个亚种.     

鸭绿江口湿地鸻鹬类停歇地的生物生态研究

鸭绿江口湿地是鸻鹬类在东亚一澳大利亚北迁路线上的最重要停歇地,潮间带上的双壳类、腹足类、多毛类等底栖动物为鸻鹬类提供了能量保障.2010年3月-2011年6月对鸭绿江口潮间带的生物生态进行了调查研究.研究结果表明,生物群落结构相对简单,主要以双壳类、腹足类和多毛类为主,优势种演替明显,系统具有低多样性低密度的特点.鸻鹬类能量补充来源相对匮乏,饵料生物量的更新速度较慢,所提供的能值也相对较低,江户明樱蛤、青蛤(幼体)和长吻沙蚕是鸻鹬类的主要食物来源.鸻鹬类主要集中在低潮带下区觅食,在北迁高峰期对低潮带下区饵料生物影响较显著,尤其对江户明樱蛤丰度影响最明显.泥螺作为优势种,生态位最宽,分布于整个调查断面和潮带,但因体表分泌一种毒性粘液而不被鸻鹬类取食.饵料生物的种群补充能力较强,在鸻鹬类迁徙高峰期之后,饵料丰度和生物量又会恢复到正常水平.虽然目前人类对鸻鹬类的威胁显现较小,但使人类一生态系统一滨鸟之间持续和谐统一,必须综合考量鸭绿江口湿地包括人类在内的生态系统各关键组分之间的生态关联,兼顾生态系统的完整性和人类社会经济发展的可持续性.     

环渤海滨海湿地鸻鹬类水鸟多样性及其环境影响因子

环渤海湿地是水鸟南北迁徙的重要驿站,尤其对于该线路上的鸻鹬鸟类具有非常重要的意义。以环渤海地区12处典型滨海湿地为研究对象,于2016-2020年每年春季开展水鸟调查,明确了鸻鹬类水鸟群落组成及其时空变化,采用结构方程模型 （Structural Equation Modeling,SEM）分析了鸻鹬类水鸟多样性与环境因子的响应关系,评估了各环境因子的影响强度。结果表明：（1）共记录到鸻鹬类水鸟7科51种,几乎全部为旅鸟。全球极危物种1种,濒危物种3种,近危物种9种。国家一级保护鸟类2种,国家二级保护鸟类8种。黑腹滨鹬（Calidris alpina）、大滨鹬（Calidris tenuirostris）、黑尾塍鹬（Limosa limosa）、灰鸻（Pluvialis squatarola）、斑尾塍鹬（Limosa lapponica）个体数量最多。（2）山东黄河三角洲、辽宁辽河口、天津北大港等河口湿地,水鸟种类多,单位面积水鸟数量较少。（3）河北沧州沿海、山东滨州贝壳堤岛及其周边区域为环渤海地区湿地集中区,水鸟种类较多。（4）综合影响强度为保护强度>食物>气候,建立自然保护地是保护水鸟多样性的最有效措施。（5）建议将河北南大港湿地和鸟类省级自然保护区提升至国家级,扩大滨州贝壳堤岛与湿地国家级自然保护区面积,对山东黄河三角洲、辽宁辽河口覆盖的各级各类自然保护地进行优化整合。研究结果能为环渤海地区鸻鹬类水鸟保护策略的制定提供相关依据。     

江苏省鸟类新纪录——剑鸻

正2016年4月4日,作者在江苏省张家港市长江沿岸(120°48'20. 57″E,31°54'3. 16″N,海拔0 m)进行鸟类调查时,于沿江滩涂发现1只鸻鹬类水鸟并拍到照片(图1),该鸟腿和嘴基为橘黄色(嘴端黑色),腹部至尾下白色,喉部为白色,且具完整白色颈圈和黑色胸带,前额具白黑相间的斑,后额、翅膀及背部为灰褐色。经查阅《中国鸟类野外手册》(约翰·马敬能等,2000),确定其为剑鸻Charadrius hiaticula,结合《中国鸟类分类与分布名录(第三版)》(郑光美,2017),确定剑鸻为江苏省分布新纪录。剑鸻隶属于鸻形目Charadriiformes鸻科Charadriidae     

长江口杭州湾鸻形目鸟类群落季节变化和生境选择

在长江口南岸杭州湾北岸滨海滩涂进行了鸻形目鸟类的资源调查,以及鸟类栖息地选择模式分析,2004年3月至2005年1月共统计到鸟类25种,春季优势种为大缤鹬(Calidris tenuirostris)、尖尾缤鹬(Calidris alpine)和红颈滨鹬(Calidris ruficollis);夏季为环颈(Charadrius alexandrinus)、青脚鹬(Tringa nebularia)和蒙古沙(Charadrius mongolus),秋季为环颈、红颈滨鹬和青脚鹬,冬季为黑腹滨鹬(Calidris alpina)、环颈和泽鹬(Tringa stagnatilis),鸟类总体数量呈春季>秋季>冬季>夏季,海堤外(自然滩涂)和堤内(人工湿地)鸟类种数四季大致相等,但鸟类平均密度季节差异显著。通过对样点内鸟类与环境因子进行多元分析,初步总结出堤外滩宽和光滩宽是影响鸟类栖息的最关键因子,海三棱草(Scirpus× mariquete)覆盖比例和潮上坪宽度的影响程度次之。堤内浅水塘比例和裸地比例是影响形目鸟类分布的关键因子,海三棱草覆盖比例也起正向作用。而人类干扰大、芦苇(Phragmites communis)/互花米草(Spartina alternifloral)密植和高水位的区域不利于鸟类利用。     

Degradation and conversion of somatostatin in normal and diabetic rats in vivo and in vitro

Plasma somatostatin-like immunoreactivity in the portal and jugular veins of streptozotocin diabetic rats was compared with that in normal control rats. In the diabetic group, somatostatin levels in the portal (p less than 0.05) and jugular (p less than 0.01) veins were both elevated compared with those in the control group. Moreover, the degree of elevation was greater in the jugular vein than in the portal vein. To further investigate the role of the liver in the clearance of somatostatin-28 in vivo, 2 micrograms of somatostatin-28 was administered as a bolus into the external jugular vein of intact and functionally hepatectomized rats. The mean half-time of somatostatin-28 was significantly longer in intact diabetic rats than in controls (p less than 0.05). The functional hepatectomy did not cause a significant difference in the half-time in diabetic rats but made it longer in control rats. These results suggest that the longer half-time of somatostatin-28 in diabetic rats in vivo is due to its slower hepatic clearance. The hepatic clearance of somatostatin-28 and somatostatin-14 was further studied in vitro using a recirculating liver perfusion method. The hepatic clearance of 1.2 nM of either somatostatin-28 or somatostatin-14 was significantly lower in diabetic rats than in controls (p less than 0.01). This indicates that elevated plasma somatostatin levels in diabetic rats are caused at least in part by decreased hepatic clearance of somatostatin.(ABSTRACT TRUNCATED AT 250 WORDS)     

Production of arsine and methylarsines in soil and in culture

Arsenate, arsenite, monomethylarsonate, and dimethylarsinate were added to different soils, and evolution of gaseous arsenical products was determined over 3 weeks. Arsine was produced in all three soils from all substrates, whereas methylarsine and dimethylarsine were produced only from methylarsonate and dimethylarsinate, respectively. At least three times more arsine than dimethylarsine was produced in soil incubated with dimethylarsinate. Resting cell suspensions of Pseudomonas and Alcaligenes produced arsine as the sole product when incubated anaerobically in the presence of arsenate or arsenite. In all instances, no trimethylarsine was observed, nor could any evidence be shown for the methylation of any arsenical substrate in soil or in culture. It was concluded that reduction to arsine, not methylation to trimethylarsine, was the primary mechanism for gaseous loss of arsenicals from soil.     

Importance of guanine nitration and hydroxylation in DNA in vitro and in vivo

Guanine (Gua) modification by nitrating and hydroxylating systems was investigated in DNA. In isolated calf thymus DNA, 8-NO(2)-Gua and 8-oxo-Gua were dose-dependently formed with peroxynitrite, and 8-NO(2)-Gua was released in substantial amounts. Myeloperoxidase (MPO) with H(2)O(2) and NO(2)(-) reacted with calf thymus DNA to form 8-NO(2)-Gua dose dependently without release of 8-NO(2)-Gua. The frequency of strand breaks was higher than the sum of 8-NO(2)-Gua and 8-oxo-Gua, particularly in the MPO-treated DNA, indicating the importance of other types of damage. The activation of human neutrophils and lymphocytes with phorbol ester did not induce 8-NO(2)-Gua and 8-oxo-Gua in their nuclear DNA. However, 8-NO(2)-Gua was found in calf thymus DNA co-incubated with activated neutrophils in the presence of NO(2)(-). No significant formation of 8-NO(2)-Gua was found in liver DNA from mice treated with Escherichia coli lipopolysaccharide. The incubation of peroxynitrite or MPO-H(2)O(2)-NO(2)(-)-treated DNA with formamidopyrimidine glycosylase (Fpg) released 8-oxo-Gua, but not 8-NO(2)-Gua, indicating that 8-NO(2)-Gua is not a substrate for Fpg. Although 8-NO(2)-Gua was generated in isolated DNA by different nitrating systems, other types of damage were formed in abundance, and the lesion could not be found reliably in nuclear DNA, suggesting that the biological importance is limited.     

Development and comparison of in vivo and in vitro models for endometritis in cows and mares

In order to investigate pathogenic mechanisms of acute endometritis in cows and mares, we established an in vivo model in both species. Based on the results of an in vitro transmigration system, human recombinant interleukin-8 (rhIL-8; 1.25 microg per mare and 5 microg per cow in 50 ml phosphate-buffered saline) was used to attract polymorphonuclear neutrophil granulocytes (PMNs) into the uteri. Peak numbers of uterine neutrophils were attracted after 6h, in both cows and mares. On average, mares responded more sensitively than cows, with 15 times higher numbers of rhIL-8-attracted uterine neutrophils (72+/-8 x 10(7)cells). In contrast to in vitro studies, in vivo migrated neutrophils (uterine neutrophils) of both species displayed a significantly reduced MHC class I expression. Expression of the CD11a molecule was significantly enhanced on equine uterine neutrophils but downregulated on bovine cells. Compared with untreated autologous peripheral neutrophils, both uterine and in vitro migrated neutrophils showed no alteration of phagocytic capacity. The ability to generate reactive oxygen species (ROS) was significantly upregulated in bovine and equine uterine neutrophils. This was also observed after in vitro migration of equine neutrophils, whereas ROS generation by bovine neutrophils was significantly depressed. In summary, the concept of inducing endometritis directly by local application of human interleukin-8 has been reliably successful in cows and mares. The model permits the analysis of PMN migration into the uterus under defined and controlled conditions. The observed differences between cows and mares with respect to phenotypical and functional characteristics of in vivo attracted uterine cells point to species-related features of neutrophil migration. In vitro transmigrated bovine and equine cells partially differ in phenotype and function from uterine neutrophils. Therefore, the in vitro transmigration assay cannot completely represent the in vivo endometritis model described here.     

Activity of native and dextran-modified hyaluronidase in in vitro and in vivo systems

Modified hyaluronidase derivatives have been obtained. Covalent coupling of the enzyme with aldehyde dextran results in 65-85% protein binding to the carrier, residual catalytic activity accounting for 90-100% of the baseline. Modified hyaluronidase is more thermostable than the native enzyme. The data on intravenous drug distribution in the mouse organs are promising and ensure effective use of modified hyaluronidase for the treatment of pulmonary diseases.     

Interactions of cadmium and selenium in rat plasma in vivo and in vitro

⁷⁵Se and ¹⁰⁹Cd tracers were used to study the binding of Se and Cd to plasma proteins at various SeO₃^2? doses and times up to 24 h after the simultaneous subcutaneous administration of SeO₃^2? and CdCl₂ to adult male rats. The simultaneous injection of CdCl₂ and SeO₃^2? markedly increased both Se and Cd plasma levels over that in control animals. Gel permeation chromatography of plasma indicated that at all times up to 24 h Cd and Se were bound in an atomic ratio of approx. 1 : 1 in 330 000 and 130 000 dalton fractions. From 4 to 24 h, Cd and Se appeared in the 420 000 dalton fraction, also with an atomic ratio of approx. 1 : 1. The 330 000 dalton molecules appeared to have a maximal binding capacity for the Cd-Se complex at a concentration of approx. 30 μmol/ml of plasma, while the 130 000 and 420 000 dalton molecules show a higher binding capacity. Studies in vitro revealed that SeO₃^2? does not interact directly with Cd and plasma proteins. It is metabolized by erythrocytes to a form that interacts in an atomic ratio of 1 : 1 with Cd to form a protein-bound complex of 130 000 daltons.     

Biosynthesis of beta-glucuronides of retinol and of retinoic acid in vivo and in vitro

After the intraportal injection of retinol-6,7-(14)C to rats, the O-ether derivative of retinol, retinyl -glucosiduronate, appears in the bile. Both retinoyl -glucuronide and retinyl -glucosiduronate are also synthesized in vitro when washed rat liver microsomes are incubated with uridine diphosphoglucuronic acid (UDPGA) and either retinoic acid or retinol, respectively. The synthesis of retinoyl -glucuronide was also demonstrated in microsomes of the kidney and in particulate fractions of the intestinal mucosa. The glucuronides were characterized by their UV absorption spectra, by their quenching of UV light or fluorescence under it, by their thin-layer chromatographic behavior in two solvent systems, and by the identification of products released during their hydrolysis by -glucuronidase. With retinoic acid as the substrate, the UDP glucuronyl transferase of rat liver microsomes had a pH optimum of 7.0, a temperature optimum of 38 degrees C, and a marked dependence on the concentrations of both retinoic acid and UDPGA, but was unaffected by a number of possible inhibitors, protective agents, and competitive substrates. The conversion of retinal to retinoic acid and the synthesis of retinoyl -glucuronide from retinoic acid could not be detected in whole homogenates, cell fractions, or outer segments of the bovine retina.