栖息地质量对黑叶猴活动时间分配的影响

2005 年9 月至2006 年8 月,在广西弄岗国家级自然保护区和扶绥珍贵动物保护区各选择一群黑叶猴作为研究对象,采用瞬时扫描取样法收集相关的行为数据。通过比较两个地理种群活动时间分配的数据来探讨栖息地质量对黑叶猴活动时间分配的影响。结果表明:生活在低质量栖息生境的黑叶猴猴群较生活在高质量栖息生境的猴群花费更多的时间休息和觅食,而用于移动和社会活动的时间相应减少。分析表明,栖息地质量的差异所造成的食物可获得性以及食物组成的差异可能是影响黑叶猴群活动时间分配差异的重要因素。虽然不同活动的峰值在日活动节律中出现的时间存在差异,但总的日活动节律在不同地理种群中表现出相同的趋势,即早晨和下午出现两个明显的觅食高峰,而中午则是长时间的休息;移动的高峰通常发生在觅食高峰之前。     

喀斯特石山生境中熊猴的雨季食物组成

开展食物组成研究为人们了解灵长类对栖息地的反应提供了很好的途径,对深刻理解动物的行为可塑性及适应性具有重要意义。猕猴属(Macaca)为果食性灵长类,但是不同种类的食性差异很大;即使便同一物种,其不同地理种群也因其栖息环境不同,食物组成存在差异。一般说来,热带地区的种类比生活在较高纬度的种类采食更多的果实。于2012年7—9月,采用瞬时扫描法对广西弄岗自然保护区石山中的两群熊猴(Macaca assamensis)进行了跟踪和观察,对猴群的雨季食物组成及其日时段变化规律进行了研究。结果表明:研究期间熊猴共采食45种植物,其中乔木30种,灌木3种,藤本11种,草本1种。平均每月采食植物22.3种。嫩叶和果实是熊猴的主要食物,分别占食物组成的52.4%和46.1%(其中未成熟果实占21.3%,成熟果实占24.8%)。另外,花占食物组成的0.9%,成熟叶和其它部位分别占0.3%。石山特有植物芸香竹(Bonia saxatilis)的嫩叶提供了43.8%的食物。9种主要植物分别占食物组成的2%,共为猴群提供了85.5%的食物。分析还发现熊猴并不是严格按照环境中的植物生物量来选择食物。嫩叶在弄岗熊猴的食物中的比例高于其他地理种群,而果实低于其他地理种群,这可能与喀斯特石山中果实的丰富度和可利用性较低有关。熊猴一天中不同时间段的食物组成并不相同,主要表现在:熊猴上午时间段对成熟果实和总果实的采食比例高于下午时间段,而嫩叶的采食比例低于下午时间段。另外,不同时间段的食物组成受外界温度的影响,表现为温度与嫩叶的觅食比例成正比,与成熟果实和总果实的觅食比例成反比。这可能与猴群采取的能量平衡策略有关。对熊猴的食物组成的日时段变化规律进行首次报道,研究结果将有助于深入理解熊猴对喀斯特石山生境的适应策略。     

黑叶猴食物组成及其季节性变化

对灵长类来说,喀斯特石山生境是一种比较独特的生活环境。喀斯特森林具有生物量低,物种多样性高的特点,生活于其中的灵长类的食物资源受环境的影响强烈,有明显的季节性变化。黑叶猴(Trachypithecus francoisi)是生活在喀斯特石山的特有灵长类动物。在食物资源波动较大的石山生境中,黑叶猴如何在食物匮乏时期获得食物?是否采取了大多数灵长类的应对策略,还是采用适应喀斯特环境的特殊对策?为了回答这些问题,2005年9月至2006年8月,在广西弄岗国家级自然保护区选择一群黑叶猴作为观察对象,采用瞬时扫描取样法收集相关的食性数据。通过比较不同季节食物组成的差异来探讨黑叶猴如何应对喜食食物(嫩叶、果实)的季节性缺乏的问题。结果表明:黑叶猴共采食92种植物,其中乔木和灌木38种,藤本植物52种,草本植物1种,寄生植物1种。猴群平均每月采食食物22.8种(6-34种),月平均食物多样性指数为2.5(1.6-3)。在弄岗黑叶猴的食物组成中,树叶占总觅食记录的71%,其中嫩叶46.9%,成熟叶24.1%的;果实、花和种子分别占13.2%、6.3%和4.3%;其他食物类型占5.4%,分别包括茎1.8%,叶柄1.1%,未知部位2.5%。黑叶猴的食物组成具有明显的季节性差异。在旱季,平均月食物种类和食物多样性指数分别为29.3和2.8,明显高于雨季的16.2和2.1。在雨季,嫩叶在食物中的比例明显高于旱季(61.5%相对32.3%);在旱季,猴群对成熟叶的采食比例明显高于雨季(39.4%相对8.9%),且在该季节才利用种子作为食物,占食物组成的8.6%。黑叶猴的食物组成受食物可获得性的影响。主要表现为嫩叶在食物中所占的比例与其可获得性有显著的正相关关系(r=0.865,n=12,P=0.000)。另外,当成熟叶和果实的可利用性降低时,黑叶猴的食物多样性指数提高(成熟叶:r=-0.602,n=12,P=0.039;果实:r=-0.716,n=12,P=0.009)。黑叶猴在嫩叶丰富的雨季,它们采食更多的嫩叶;而在喜食性食物短缺的旱季,它们采取选择更多种类的成熟叶和种子为食,同时它们采食的种类和食物多样性也相应地增加。这与大多数叶食性灵长类的适应策略相似。     

黑叶猴在喀斯特石山生境的觅食活动

2002 年 8 月至2003 年 7 月,对一群生活在广西扶绥珍稀动物保护区内孤立石山中的黑叶猴进行观察,通过收集有关栖息地利用的数据,从中探讨栖息地的破碎化对其生态习性的影响.研究结果表明：猴群的觅食活动在石山各个部位的分布存在着显著差异,它们更偏好在山腰觅食（66.1%）,而较少利用山脚（18.6%）和山顶（15.3%）.从横向水平来看,猴群的觅食活动主要集中在6个觅食斑块,总面积为7.94 hm^2,约占栖息地面积的18.9%.觅食斑快中黑叶猴喜食食物的植株密度明显高于非觅食斑块.虽然树叶在黑叶猴食物组成中占绝大部分,但其食物组成具有明显的季节性变化.与之相对应,猴群对觅食斑块的利用也表现出明显的季节性差异.     

黑叶猴在旱季对喀斯特石山生境的利用

2005年12月～2006年2月,对广西弄岗国家级自然保护区喀斯特森林中的黑叶猴行为进行观察。用瞬时扫描法收集黑叶猴的栖息地利用数据,以分析该物种在旱季对喀斯特石山的利用策略。研究结果表明,黑叶猴对不同坡向的选择有明显差异,其中东向比例最高,达到64.95%;其次是北向,占20.22%;南向和西向最少,分别占9.08%和5.74%。黑叶猴在旱季对坡向的选择可能与温度调节有关。黑叶猴对不同的山体部位的利用不尽相同,猴群对崖壁的利用比例(40.27%)明显高于山脚(29.52%)、山坡(22.18%)和山顶(8.04%)。黑叶猴主要选择崖壁作为休息场所,占总记录的55.92%;主要选择山脚作为觅食场所,占总记录的59.71%。还发现黑叶猴对乔木的利用率最高,占总记录的68.04%;其次为裸岩,占27.27%;灌木最少,仅为4.69%。黑叶猴对不同山体部位的利用差异可能与猴群对觅食利益和捕食风险的权衡有关。本研究为深入了解黑叶猴的石山适应策略提供了基础,也为该濒危物种的栖息地保护提供了依据。     

广西黑叶猴栖息地景观格局破碎化分析及其对种群的影响

黑叶猴(Trachypithecus francoisi)是仅分布于喀斯特石山生境的珍稀濒危灵长类动物。由于非法捕杀和人类活动干扰,其种群数量正在急剧减少。同时,随着森林砍伐和土地开垦的加速,其栖息地严重破碎化。因此,了解栖息地破碎化对黑叶猴种群的影响对于保护这一珍稀濒危物种具有重要意义。基于遥感影像、土地利用数据以及黑叶猴种群调查数据,通过Fragstats软件开展广西黑叶猴栖息地景观破碎化分析,并通过相关性和多元逐步回归分析,探讨了景观格局对广西黑叶猴种群数量的影响。结果表明：(1)广西黑叶猴栖息地呈现破碎化严峻、斑块形状复杂化、斑块团聚程度较弱且分散化的现象;栖息地以林地景观占据重要优势,但人为景观的干扰十分强烈;在不同地区中,生境破碎化程度、人为干扰强度以及景观配置均呈现不同的特征,其中扶绥地区人为干扰最为强烈,德保地区的景观块数破碎化程度较为严重,而龙州地区的人为干扰程度最小,其森林景观最为聚集。(2)蔓延度指数、平均斑块分维指数、林地面积、林地斑块大小、裸岩面积和裸岩面积比重等景观指数与黑叶猴种群数量有显著正向关系,Shannon多样性指数则是显著负向关系;而耕地面积、耕地...     

广西弄岗黑叶猴栖息地选择与利用

2005年9月至2006年8月对广西弄岗国家自然保护区内一群黑叶猴进行行为观察,采用瞬时扫描法观察并收集猴群的栖息地利用数据,分析黑叶猴对喀斯特石山栖息地的选择与利用规律。结果表明,黑叶猴对不同山体部位的利用有显著性差异(χ~2=43.063,df=4,P0.001)。黑叶猴对崖壁的利用频率最高(占总记录的36.67%±9.44%),其次是山坡(32.30%±9.57%),对山脚(14.15%±5.01%)、山顶(11.24%±8.42%)和平地(5.63%±2.92%)的利用较少。分析发现,黑叶猴对山体部位的利用没有显著的季节性差异(山顶:Z=-0.160,P=0.837;崖壁:Z=-0.320,P=0.749;山坡:Z=-0.480,P=0.631;山脚:Z=-1.601,P=0.109;平地:Z=0,P=1)。黑叶猴将崖壁作为主要的休息场所,山坡和山脚为主要的移动和觅食场所。黑叶猴对栖息地的利用受食物可获得性的影响。当食物中花的可获得性降低时,猴群增加对山脚的利用;当嫩叶可获得性降低时,猴群增加在崖壁移动的频率;当果实的可获得性升高时,猴群增加在平地觅食的频率。食物组成与黑叶猴栖息地利用也有关系。总体来看,黑叶猴对山顶的利用频率与花的觅食比例呈显著正相关;对山脚的利用频率与果实+种子的觅食比例呈显著正相关。猴群在山顶休息的频率随花和成熟叶的觅食比例的上升而上升;在山脚休息的频率随果实+种子的觅食比例的上升而上升。猴群在山坡觅食的频率随果实+种子的觅食比例的下降而上升;在山脚觅食的频率随嫩叶的觅食比例的下降而上升。另外,平均最低温度与猴群在平地觅食的频率呈负相关关系。分析表明食物的分布和数量对黑叶猴栖息地利用有重要影响,黑叶猴对栖息地的选择是在觅食利益与风险之间进行权衡的结果。     

广西扶绥黑叶猴活动节律和日活动时间分配

2002 年8 月至2003 年7 月,对生活在完全被周围农田隔离的石山中的一群黑叶猴的昼夜活动节律和日活动时间分配进行研究。采用以群为单位的焦点动物观察法和连续记录法,每月对猴群连续10 d 跟踪观察。结果表明:3 月至10 月,黑叶猴的昼夜活动节律由8 个环节组成,11 月至2 月由9 个环节组成,移动、觅食和休息在活动节律中重复出现,晒太阳仅出现在11 月至翌年2 月。休息占黑叶猴日活动时间的比例最大,其次是觅食、移动、晒太阳和理毛。黑叶猴的日活动时间分配具有明显的月变化规律,相关性分析表明,环境温度、栖息地的食物丰富度和光照强度是影响黑叶猴日活动时间分配的主要因素。进一步分析认为,黑叶猴的活动时间分配体现了叶食性灵长类的特点,更体现了黑叶猴对北热带喀斯特石山环境的适应特点。     

贵州麻阳河地区野生黑叶猴与同域放养山羊冬季食物重叠的初步分析

于2009年12月～2010年2月采用瞬时扫描取样法对贵州麻阳河自然保护区的5个黑叶猴Trachypithecus francoisi猴群以及同域放养的山羊羊群的取食行为进行观察记录,并对两者的取食数据进行比较分析,以期了解该地区黑叶猴与放养山羊在食物资源最为匮乏的冬季的资源竞争关系,为黑叶猴的保护管理提供科学依据.研究结果表明:黑叶猴冬季取食植物67种,放养山羊同期取食植物44种,两者食物重叠26种;对26种重叠食物的采食分别占黑叶猴与放养山羊冬季取食时间的76.2％与22.0％;黑叶猴冬季采食的19种主要食物(＞1％冬季采食时间)中,有14种为放养山羊所采食,占黑叶猴与山羊冬季采食时间的71.7％与17.8％;黑叶猴与山羊冬季食物生态位宽度分别为0.68与0.39,两者的冬季食物生态位重叠指数C=0.74.表明贵州麻阳河地区黑叶猴与同域放养山羊在食物最为匮乏的冬季存在较为激烈的食物资源竞争关系.     

广西扶绥黑叶猴的主要食源植物及其粗蛋白含量

食物的营养物质是影响动物食物选择的生态因子。研究动物食物的营养组成及其对野生动物取食的影响对野生动物的保护具有重要的参考意义。为了研究喀斯特环境中食物粗蛋白对黑叶猴食物选择的影响,2006年1月-12月在广西扶绥自然保护区, 采用焦点动物取样法和连续记录法研究了片断化栖息地中黑叶猴的觅食行为,同时采集黑叶猴取食部位样本共40种190份,用凯氏定氮法测量其粗蛋白含量。结果表明,黑叶猴取食的食物包括嫩叶、成熟叶、花、果和种子等部位;食源植物的生活型包括了乔木、灌木、藤本和草本。食物的平均粗蛋白含量为12.7%,有明显的季节性变化。4月份样品的月平均粗蛋白含量全年最高,高达19.1%,而最低在6月份,仅为5.4%。食物的粗蛋白含量在前半年和后半年之间没有显著的差异（z= -1.28,p= 0.20）,在雨季和旱季之间亦无差异（z= -1.22,p= 0.22）;不同食源植物部位的平均粗蛋白含量不同,嫩叶的年平均粗蛋白含量最高,为13.7%,其次是成熟叶和花,分别是13.0%和12.1%,果实最低,仅为9.6%;不同生活型的食源植物粗蛋白含量不同,藤本的粗蛋白含量最高,为 14.1%,草本的最低,仅为10.1%,乔木和灌木分别是11.3%。不同食源植物的取食时间与其粗蛋白含量没有显著的相关关系（p>0.05）,粗蛋白含量不是影响黑叶猴取食的主要因素。     

Synthesis and luminescence properties of a blue-emitting Sr(3.5) Y(6.5) O(2) (PO(4) )(1.5) (SiO(4) )(4.5) :Eu(2+) phosphor

A novel blue‐emitting Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:Eu²⁺ phosphor was synthesized via a solid‐state reaction. Powder X‐ray diffraction (XRD) analysis demonstrated that the Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5 host had a hexagonal crystal structure in the space group P6₃/m and unit cell parameters a = 9.418 Å, c = 6.900 Å. The as‐prepared phosphor showed a blue emission and all the main emission peaks were located at around 466 nm for different excitation wavelengths of 297, 333 and 391 nm. The temperature dependence of the photoluminescence property was investigated in the range 20–250 °C, and the emission intensity decreased to 71% of the initial value at room temperature on increasing the temperature to 150 °C. According to the classical theory of fluorescent thermal quenching, the activation energy (ΔE) for the thermal quenching luminescence of the as‐prepared Sr_3.45Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:0.05Eu²⁺ phosphor was determined to be 0.20 eV. Copyright © 2011 John Wiley & Sons, Ltd.     

Collagen-like triple helix formation of synthetic (Pro-Pro-Gly)10 analogues: (4(S)-hydroxyprolyl-4(R)-hydroxyprolyl-Gly)10, (4(R)-hydroxyprolyl-4(R)-hydroxyprolyl-Gly)10 and (4(S)-fluoroprolyl-4(R)-fluoroprolyl-Gly)10.

For the rational design of a stable collagen triple helix according to the conventional rule that the pyrrolidine puckerings of Pro, 4-hydroxyproline (Hyp) and 4-fluoroproline (fPro) should be down at the X-position and up at the Y-position in the X-Y-Gly repeated sequence for enhancing the triple helix propensities of collagen model peptides, a series of peptides were prepared in which X- and Y-positions were altogether occupied by Hyp(R), Hyp(S), fPro(R) or fPro(S). Contrary to our presumption that inducing the X-Y residues to adopt a down-up conformation would result in an increase in the thermal stability of peptides, the triple helices of (Hyp(S)-Hyp(R)-Gly)(10) and (fPro(S)-fPro(R)-Gly)(10) were less stable than those of (Pro-Hyp(R)-Gly)(10) and (Pro-fPro(R)-Gly)(10), respectively. As reported by B?chinger's and Zagari's groups, (Hyp(R)-Hyp(R)-Gly)(10) which could have an up-up conformation unfavorable for the triple helix, formed a triple helix that has a high thermal stability close to that of (Pro-Hyp(R)-Gly)(10). These results clearly show that the empirical rule based on the conformational preference of pyrrolidine ring at each of X and Y residues should not be regarded as still valid, at least for predicting the stability of collagen models in which both X and Y residues have electronegative groups at the 4-position.     

Role of tfdC(I)D(I)E(I)F(I) and tfdD(II)C(II)E(II)F(II) gene modules in catabolism of 3-chlorobenzoate by Ralstonia eutropha JMP134(pJP4)

The enzymes chlorocatechol-1,2-dioxygenase, chloromuconate cycloisomerase, dienelactone hydrolase, and maleylacetate reductase allow Ralstonia eutropha JMP134(pJP4) to degrade chlorocatechols formed during growth in 2,4-dichlorophenoxyacetate or 3-chlorobenzoate (3-CB). There are two gene modules located in plasmid pJP4, tfdC(I)D(I)E(I)F(I) (module I) and tfdD(II)C(II)E(II)F(II) (module II), putatively encoding these enzymes. To assess the role of both tfd modules in the degradation of chloroaromatics, each module was cloned into the medium-copy-number plasmid vector pBBR1MCS-2 under the control of the tfdR regulatory gene. These constructs were introduced into R. eutropha JMP222 (a JMP134 derivative lacking pJP4) and Pseudomonas putida KT2442, two strains able to transform 3-CB into chlorocatechols. Specific activities in cell extracts of chlorocatechol-1,2-dioxygenase (tfdC), chloromuconate cycloisomerase (tfdD), and dienelactone hydrolase (tfdE) were 2 to 50 times higher for microorganisms containing module I compared to those containing module II. In contrast, a significantly (50-fold) higher activity of maleylacetate reductase (tfdF) was observed in cell extracts of microorganisms containing module II compared to module I. The R. eutropha JMP222 derivative containing tfdR-tfdC(I)D(I)E(I)F(I) grew four times faster in liquid cultures with 3-CB as a sole carbon and energy source than in cultures containing tfdR-tfdD(II)C(II)E(II)F(II). In the case of P. putida KT2442, only the derivative containing module I was able to grow in liquid cultures of 3-CB. These results indicate that efficient degradation of 3-CB by R. eutropha JMP134(pJP4) requires the two tfd modules such that TfdCDE is likely supplied primarily by module I, while TfdF is likely supplied by module II.     

Induction of in vitro flowering in Dendrobium Madame Thong-In (Orchidaceae) seedlings is associated with increase in endogenous N(6)-(Delta (2)-isopentenyl)-adenine (iP) and N (6)-(Delta (2)-isopentenyl)-adenosine (iPA) levels

We analysed the endogenous cytokinin levels of Dendrobium Madame Thong-In seedlings grown in vitro during vegetative and flowering-inductive periods. HPLC was used to fractionate the extracts and radioimmunoassay (RIA) was used for assay of zeatin (Z), dihydrozeatin (DZ), N(6)-(Delta(2)-isopentenyl)-adenine (iP) and their derivatives. Coconut water used in experiments was found to contain high level (>136 pmol ml(-1)) of zeatin riboside (ZR). Protocorms and seedlings cultured in medium with coconut water were found to contain 0.5-3.9 pmol g(-1) FW of the cytokinins analysed. Seedlings (1.0-1.5 cm) cultured in flowering-inductive liquid medium containing 6-benzyladenine (BA, 4.4 muM) and coconut water (CW, 15%) contained up to 200 and 133 pmol g(-1) FW of iP and iPA, respectively. These levels were significantly higher than all other cytokinins analysed in seedlings of the same stage and were about 80- to 150-folds higher than seedlings cultured in non-inductive medium. During the transitional (vegetative to reproductive) stage, the endogenous levels of iP (178 pmol g(-1) FW) and iPA (63 pmol g(-1) FW) were also significantly higher than cytokinins in the zeatine (Z) and dihydrozeatin (DZ) families in the same seedlings. Seedlings that grew on inductive medium but remained vegetative contained lower levels of iPA. The importance of the profiles of iP and its derivatives in induction of in vitro flowering of D. Madame Thong-In is discussed.     

Biology of Bactrocera (Zeugodacus) tau (Walker) (Diptera: Tephritidae)

The biology of the fruit fly Bactrocera tau, an important horticultural pest, was studied under laboratory conditions at 25°C and 60–70% relative humidity on Cucurbita maxima. The duration of mating averaged 408.03 ± 235.93 min. After mating, the female fly had a preoviposition period of 11.7 ± 4.49 days. The oviposition rate was 9.9 ± 8.50 eggs and fecundity was 464.6 ± 67.98 eggs/female. Eggs were elliptical, smooth and shiny white, turning darker as hatching approached, and measured 1.30 ± 0.07 mm × 0.24 ± 0.04 mm. The chorion has polygonal microsculpturing and is species-specific with polygonal walls. The egg period lasts for 1.3 ± 0.41 days. The duration of the larval period is 1.2 ± 0.42, 1.7 ± 0.48 and 4.0 ± 0.94 days for first, second and third instars, respectively. Pupation occurs in the sand or soil and pupal periods are 7.0 ± 0.47 days. The life cycle from egg to adult was completed in 14.2 ± 1.69 days; the longevity of mated females and males was 130.33 ± 14.18 and 104.66 ± 31.21 days, respectively. At least two to three generations were observed from June 2008 to June 2009.     

The helix-coil transitions of poly (dA)-poly (dT) and poly (dA-dT)-poly (dA-dT)

Helix–coil transition curves are calculated for poly (dA) poly(dT) and poly (dA-dT) poly (dA-dT) using the integral equation approach of Goel and Montroll.⁵ The transitions are described by the loop entropy model with the exponent of the loop entropy factor, k, remaining an arbitrary constant. The theoretical calculations are compared with experimental transition curves of the two polymers. Results indicate that the stacking energies for these two polymers differ by about 1 kcal/mole of base pairs. Also, a fit between theory and experiment was not possible for k > 1.70.     

Spectroscopic investigations of Er(3+) :CdO-Bi(2) O(3) -B(2) O(3) glasses

This article reports on the optical properties of Er³⁺ ions doped CdO–Bi₂O₃–B₂O₃ (CdBiB) glasses. The materials were characterized by optical absorption and emission spectra. By using Judd–Ofelt theory, the intensity parameters Ω_λ (λ = 2, 4, 6) and also oscillatory strengths were calculated from the absorption spectra. The results were used to compute the radiative properties of Er³⁺:CdBiB glasses. The concentration quenching and energy transfer from Yb³⁺–Er³⁺ were explained. The stimulated emission cross‐section, full width at half maximum (FWHM) and FWHM × values are also calculated for all the Er³⁺:CdBiB glasses. Copyright © 2011 John Wiley & Sons, Ltd.