N、P营养盐对塔玛亚历山大藻(Alexandrium tamarense)生长的影响

模拟自然海水营养盐浓度状况,在N、P浓度分别为10-500μg L-1 N和0.74-74μg L-1 P时,研究N、P双因子限制(N、P浓度同时降低,N:P固定为15:1)及单因子限制(保持N或P为最高浓度,只降低一种营养盐浓度)对有毒赤潮藻塔玛亚历山大藻(Alexandrium tamarense)生长的影响。结果表明,塔玛亚历山大藻细胞能较快进入对数生长期,但N、P双因子限制能明显影响其生长,在N、P浓度分别低于100μg L-1 N和15μg L-1 P时,细胞密度无明显增长;而N或P分别受限时,生长态势明显优于N、P同时受到限制的试验组,而且N、P单因子中度限制对生长影响较小。结果说明塔玛亚历山大藻对单因子营养元素限制较强的适应能力,可使其在常常出现单营养因子限制的自然水体中维持一定生长速率和细胞密度,并有助于滤食该藻的贝类体内麻痹性贝类毒素的积累。     

陕西黄龙山林区褐马鸡春季夜栖地选择

2006年4～6月,在陕西黄龙山林区,对褐马鸡(Crossoptilon mantchuricum)春季夜栖地的选择进行了研究.共记录到22个夜栖地,以夜栖树为中心做一个10 m×10 m样方,测定夜栖地海拔、坡向、坡度、坡位、地貌特征、夜栖树高度和胸径、乔木层盖度、乔木的数量、灌木层盖度、草本盖度、水源距离、人为干扰距离、林缘距离、栖枝高度和栖位上盖度等参数;通过9条样带测定54个随机样方,除栖枝高度和栖位上盖度外,指标相同.结果表明,褐马鸡春季夜栖地多偏向以坡度较大、山坡和山脊、接近水源、远离林边、人为干扰距离较远、乔木盖度和密度较大、栖树胸径较大、灌木层盖度和草本层盖度较小为主要特征的地方.主成分分析表明,前5个特征值的累积贡献率达到72.746%,可以较好地反映褐马鸡春季夜栖地生境特征.根据载荷系数绝对值大小,将褐马鸡春季夜栖地生境选择影响因子分别命名为地形和林下植被因子、气象因子、稳定性因子和水因子.影响褐马鸡夜栖地选择的关键因素是安全、舒适和栖息地转换的方便程度.     

红树植物淹水胁迫响应研究进展

潮汐淹水是红树植物面临的主要环境胁迫之一,也是导致目前红树林造林成活率低的一个关键因子。由于长期适应于水淹生境,红树植物发育出一套适应于潮间带生长的抗淹水机制。综述了与红树植物相关的抗淹水胁迫响应机制,包括了形态结构、生长、水分和光合作用、膜脂过氧化系统和根系脱氢酶系统、内源激素和胁迫多胺等5个方面。提出应用人工潮汐系统研究红树植物的淹水抗性机理是确定不同种类红树植物的耐淹水能力的有效手段。并指出生长的研究是淹水胁迫响应研究的基础,而与分子手段相结合的激素水平的研究将在红树植物抗性胁迫研究中得到重视。     

Dephosphorylation of skeletal muscle phosphorylase,glycogen synthase,and phosphorylase kinase β-subunit by a Mn2+-activated protein phosphatase

An Mn²⁺-activated phosphoprotein phosphatase of M_r = 80,000 from rabbit muscle catalyzes the dephosphorylation of skeletal muscle proteins that are phosphorylated by either phosphorylase kinase or cAMP-dependent protein kinase. Phosphorylase or glycogen synthase labeled by phosphorylase kinase at seryl residues 14 or 7, respectively, are both dephosphorylated by the phosphatase. Phosphorylase a and glycogen synthase compete with one another for the phosphatase. The phosphatase discriminates between different sites labeled by the cAMP-dependent protein kinase: glycogen synthase phosphorylated either to 1.0 or 1.8 mol phosphate/mol, or phosphorylase kinase phosphorylated on its β-subunit serve as substrates for the phosphatase, but the phosphorylase kinase α-subunit, the phosphorylated phosphatase inhibitor 1, or casein do not. Histone fraction IIA, phosphorylated by the catalytic subunit, was a poor substrate even at a concentration of 100 μm. Phosphorylation of the α-subunit of phosphorylase kinase had no influence on the kinetics of dephosphorylation of the β-subunit. Thus, the M_r = 80,000 phosphatase meets the functional definition of a protein phosphatase 1 [Cohen, P. (1978) Curr. Top. Cell. Regul.14, 117–196]. Furthermore, from a comparison of the known phosphorylated sites of these proteins, it appears that the phosphatase discriminates between different sites present in the phosphoproteins tested on the basis of the K_m values for the reactions. It displays a preferential activity toward proteins with a primary structure wherein basic residues are two positions amino-terminal from the phosphoserine, AgrLysX-YSer(P) or LysArgX-YSer(P), rather and one residue away, ArgArgX-Ser(P).     

Lysine biosynthesis and the evolution-of pennate marine diatoms

The classification of lysine biosynthetic pathways in various organisms have been used to investigate their descent in evolution. We have attempted these determinations in the diatoms Amphora coffeaeformis var:perpusilla (Grunow Cleve.) and Phaeodactylum tricornutum (Bohlin). Additionally, we have verified earlier results of Vogel in a green alga, Chlorella pyrenoidosa strain Tx 71105 (Texas Culture Collection). Our research indicates that the diaminopimelic acid route is involved in all three organisms. While these studies do not exclude the possible co-existence of the α-aminoadipic acid route, the results imply a closer evolutionary relationship of pennate diatoms to bacteria and “classical” photosynthetic plants rather than to heterotrophic or mixotrophic fungi and atypical algal strains such as the Euglenophyta.     

Liquid seaweed extracts identified using <Superscript>1</Superscript>H NMR profiles

Aqueous extracts of Ascophyllum nodosum and several other brown seaweeds are manufactured commercially and widely distributed for use on agricultural crops. The increasingly regulated international trade in such products requires that they be standardized and defined to a degree not previously required. We examined commercially available extracts using quantitative ¹H NMR and principal components analysis (PCA) techniques. Extracts manufactured over a 4-year period using the same process exhibited characteristic profiles that, on PCA, clustered as a discrete group distinct from the other commercial products examined. In addition to recognizing extracts made from different seaweeds, analysis of the ¹H spectra in the 0.35–4.70 ppm region allowed us to distinguish amongst extracts produced from the same algal species by different manufacturers. This result established that the process used to make an extract is an important variable in defining its composition. A comparison of the ¹H NMR integrals for the regions 1.0–3.0 ppm and 3.0–4.38 ppm revealed small but significant changes in the A. nodosum spectra that we attribute to seasonal variation in gross composition of the harvested seaweed. Such changes are reflected in the PCA scores plots and contribute to the scatter observed within the data point cluster observed for Acadian soluble extracts when all data are pooled. Quantitative analysis using ¹H NMR (qNMR) with a certified external standard (caffeine) showed a linear relationship with extract concentration over at least an order of magnitude (2.5–33 mg/mL; R ² > 0.97) for both spectral regions integrated. We conclude that qNMR can be used to profile (or “fingerprint”) commercial seaweed extracts and to quantify the amount of extract present relative to a suitably chosen standard. Issued as NRCC no. 42,652.     

象山港春、夏季大中型浮游动物空间异质性

为探明象山港大中型浮游动物空间分布特征及主要影响因素,分别于2010年4月、7月大、小潮期对浮游动物群落和相关环境因子进行调查。四个航次共检出浮游动物成体14大类64种、浮游幼体10大类14种,春、夏季群落结构差异极显著(P=0.001),物种更替率为66.7%,优势种差异明显,共同优势种仅有短尾类溞状幼虫(Brachyura zoea)和仔鱼(Fish larvae)两类幼体;同一季节大、小潮物种相似度约为60%,群落结构差异较小(P=0.031);春季生物量和丰度高于夏季,但物种多样性低于夏季。温度是浮游动物群落季节变化的主导因素。方差分析、聚类和多维尺度分析显示:浮游动物群落空间异质性分布方式受潮流影响,群落结构在大潮期梯度分布特征明显,小潮期通常呈斑块性分布;生物量、丰度和多样性等参数的空间分布取决于群落的分布特征,并受影响于该参数在狭湾口内外的差异。典范对应分析及环境参数统计分析表明:梯度分布主要由盐度、悬浮物的梯度性特征决定;主导斑块性分布的因素多样,不同情况下可能为水深、叶绿素a、营养盐和内外水团相互作用;梯度性和斑块性分布均受到潮流影响。总体来看,象山港浮游动物空间分布主要受水文因素控制,受化学和生物因素影响较弱,其中叶绿素a浓度仅在春季与浮游动物丰度有一定相关性,溶解氧、酸碱度和营养盐等水质参数对浮游动物空间分布几乎无直接影响。     

Postnatal changes in fatty acids composition of brown adipose tissue

It has been demonstrated that thermogenic activity of brown adipose tissue (BAT) is higher during the early postnatal period, decreasing towards a low adult level. The present study examined postnatal changes in the lipid composition of BAT. BAT from pre-weaning rats at 4 and 14 days old showed the following differences in lipid composition compared to that from adults of 12 weeks old. (i) Relative weight of interscapular BAT to body weight was markedly greater. (ii) BAT-triglyceride (TG) level was lower, while BAT-phospholipid (PL)level was higher. (iii) In TG fatty acids (FA) polyunsaturated fatty acids (PU; mol %), arachidonate index (AI), unsaturation index (UI) and PU/saturated FA (SA) were higher; rare FA such as eicosadienoate, bishomo--linolenic acid and lignoceric acid in mol % were also higher. (iv) In PL-FA monounsaturated FA (MU) in mol % was lower; PU mol %, AI and UI were higher. These features in BAT of pre-weaning rats resembled those in the cold-acclimated adults, suggesting a close relationship of the PL-FA profile to high activity of BAT.     

Tolerance of brown bear spermatozoa to conditions of pre-freezing cooling rate and equilibration time

Specific protocols for the cryopreservation of endangered Cantabrian brown bear spermatozoa are critical to create a genetic resource bank. The aim of this study was to assess the effect of cooling rates and equilibration time before freezing on post-thawed brown bear spermatozoa quality. Electroejaculates from 11 mature bears were extended to 100 × 10⁶ spermatozoa/mL in a TES–Tris–Fructose–based extender, cryopreserved following performance of the respective cooling/equilibration protocol each sample was assigned to, and stored at −196 °C for further assessment. Before freezing, after thawing, and after 1 hour's incubation post-thawing at 37 °C (thermal stress test), the quality of the samples was assessed for motility by computer-assisted semen analysis, and for viability (SYBR-14/propidium iodide), acrosomal status (peanut agglutinin–fluorescein isothiocyanate /propidium iodide), and sperm chromatin stability (SCSA) by flow cytometry. In experiment 1, three cooling rates (0.25 °C/min, 1 °C/min, and 4 °C/min) to 5 °C were assessed. After thawing, total motility (%TM) was higher and percentage of damaged acrosomes (%dACR) was lower (P < 0.05) for 0.25 °C/min than for 4 °C/min. The thermal stress test data indicated equally poor quality (P < 0.05) for the 4 °C/min cooled samples in viability (%VIAB), %dACR, %TM, and progressive motility (%PM). In experiment 2, the effect of a pre-freezing equilibration period at 5 °C for 1 hour (cooling at 0.25 °C/min) was evaluated. Samples kept at 5 °C for 1 hour showed higher (P < 0.05) values than the nonequilibrated ones for both thawing (%dACR) and thermal stress test (%VIAB, %TM, and %PM). In experiment 3, samples stored without cooling and equilibration (direct freezing) were compared with the samples cooled at 0.25 °C/min and equilibrated for 1 hour (control freezing). Using thermal stress test, we observed that direct freezing causes damage in viability, acrosomal status, and motility of spermatozoa compared with the control group (P < 0.05). In conclusion, our results suggest that slow cooling rates to 5 °C and at least 1 hour equilibration time are necessary for the effective cryopreservation of brown bear sperm.     

Differential Regulation of Ca<Superscript><Emphasis Type="Bold">2+</Emphasis></Superscript> Signaling and Membrane Trafficking by Multiple P2 Receptors in Brown Adipocytes

Extracellular ATP triggers changes in intracellular Ca²⁺, ion channel function, and membrane trafficking in adipocytes. The aim of the present study was to determine which P2 receptors might mediate the Ca²⁺ signaling and membrane trafficking responses to ATP in brown fat cells. RT-PCR was used to determine which P2 receptors are expressed in brown fat cells. Responses to nucleotide agonists and antagonists were characterized using fura-2 fluorescence imaging of Ca²⁺ responses, and FM 1-43 fluorescence imaging and membrane capacitance measurements to assess membrane trafficking. The pharmacology of the Ca²⁺ responses fits the properties of the P2Y receptors for which mRNA is expressed, but the agonist and antagonist sensitivity of the membrane-trafficking response was not consistent with any P2 receptor described to date. Brown adipocytes expressed mRNA for P2Y₂, P2Y₆, and P2Y₁₂ metabotropic receptors and P2X₁, P2X₂, P2X₃, P2X₄, P2X₅, and P2X₇ ionotropic receptors. The agonists ATP, ADP, UTP, UDP and 2′, 3′-(benzoylbenzoyl) ATP (BzATP) increased intracellular Ca²⁺, while 100 μM suramin, pyridoxal-phosphate-6-azophenyl-2′ 4′-disulfonic acid (PPADS), or Reactive Blue 2 partially blocked Ca²⁺ responses. ATP, but not ADP, UTP, UDP or BzATP activated membrane trafficking. The membrane response could be blocked completely with 1 μM PPADS but not by the antagonist MRS2179. We conclude that multiple P2 receptors mediate the ATP responses of brown fat cells, and that membrane trafficking is regulated by a P2 receptor showing unusual properties.