滇金丝猴雌性个体间的理毛行为

相互理毛行为广泛存在于社会性群居灵长类动物中,通常具有清洁卫生和社会交往功能。2012年10月至2013年6月,我们在云南白马雪山国家级自然保护区对一人工辅助投食滇金丝猴群,采用全事件取样法和焦点动物取样法收集了雌性个体间相互理毛的行为数据,包括理毛的部位、理毛的姿势、理毛的时间和回合数。研究结果表明:滇金丝猴雌性个体之间每次相互理毛的平均时间为5.7 min。相互理毛部位较多的发生在自我理毛不能进行(达到)的部位(61.1%);在不能自我理毛部位的相互理毛行为持续时间长,平均9.7 min;在个体能够进行自我理毛部位的相互理毛持续时间短,平均为3.2 min。相互理毛的姿势以对坐为主(48.4%),不同理毛姿势的理毛时间差异显著。新迁入家庭单元的雌性个体为理毛的首先发起者,但其获得被理毛的时间却并不多。滇金丝猴雌性个体相互理毛部位、理毛姿势和理毛时间的差异表明,它们之间的相互理毛行为符合卫生功能假说和社会功能假说。     

川金丝猴的相互理毛行为是否具有卫生功能

应用目标动物取样法,在113天的跟踪观察（有效观察时间351小时）的基础上,收集了293个相互理毛回合（bout)的数据,对秦岭川金丝猴（Rhinopithecus roxellana）玉皇庙西梁群个体间的相互理毛进行了分析,检验相互理毛是否符合卫生功能假说（Hygienic functional hypothesis)。在分析数据前我们将标本的体表分为17部分,并定义了各部分的界限和其所占全身表面积百分比。根据自我理毛行为在身体表面各部位可进行的难易程度,将其分为不可进行,难以进行和易于进行部位的三种类型。为了了解相互理毛是否集中在自我理毛不容易进行的部位,我们做了三个相应的分析：自我理毛在全身的分配,各部位得到相互理毛的情况,不同年龄性别组得到相互理毛的情况。结果表明限法进行自我理毛的部位得到相对多的相互理毛,难以进行自我理毛的部位得到相互理毛百分比与其占总表面百分比相一致,易于进行部位得到相对少的相互理毛。这种自我理毛与相互理毛之间的补偿关系符合卫生假说。但是并非所有难以或无法进行自我理毛的部位得到均匀的相互理毛,相互理毛主要集中在背部和肛门繁殖区,不同年龄性别组的相互理毛受到社会等级的影响,相互理毛的这种选择性分配,说明除了有卫生功能外还应该有其它的功能含义。     

黄山野生短尾猴理毛发生部位的差异

理毛行为是指动物个体用双手或单手从自身或其他个体的毛发中检出颗粒物并放入嘴里咀嚼或直接用嘴进行清理的过程,在灵长类动物社会中普遍存在且频繁发生。本研究以栖息于安徽黄山的野生短尾猴（Macaca thibetana）为研究对象,于2019年7-12月采用目标动物取样法采集行为数据,通过比较自我理毛和社会理毛的发生部位和发生过程,期望揭示该物种理毛行为发生部位的差异性。结果显示,短尾猴的社会理毛发生频率及平均持续时间均显著高于自我理毛。自我理毛多采用双手或单手的方式,而社会理毛则更倾向于使用双手。自我理毛大多分布于后肢前部、后肢后部以及手臂前部等部位,而社会理毛则更多的分布于背部、脸部、躯干侧部、手臂后部等部位。就理毛过程而言,自我理毛选择身体部位的随机性较强,而社会理毛则呈现明显的差异性,短尾猴社会理毛行为开始偏好在背部和脸部,结束部位则更多集中于背部。结果表明,野生短尾猴自我理毛和社会理毛在行为方式、发生过程以及部位选择上均呈现显著差异,很大程度上取决于动物个体自身所能接触的部位。同时,结果提示,两个个体参与的社会理毛行为发生过程中可能体现出参与理毛个体的社会关系的变化特征,为认识和理解理毛行为的社会功能提供更多的基础依据。     

灵长类相互理毛的影响因素、功能及其利益分析

理毛行为是动物行为学研究的主要内容之一,根据理毛的对象可分为自我理毛(Autogrooming)和相互理毛(Allogrooming),其中相互理毛是灵长类重要的社会行为。现在认为相互理毛可能与社会参量(亲缘关系、性别、年龄、等级制度、繁殖状况等)有联系,并且有一定的社会功能。本文论述了理毛行为的分类、影响相互理毛的因素、相互理毛功能假说及其相互理毛的投入-收益分析,以便人们对相互理毛的行为进行更深入的研究。     

社会关系和性关系中的自我理毛行为

有很多观点解释了动物自我理毛的作用。例如,动物通过自我理毛可以清除在与附近的同种异性接触期间传播来的寄生虫,当嗅出同种异性的气味时也可能自我理毛,因为自我理毛是一种动物在逃避还是战斗之间所面临的进退两难选择时表现出来的改向行为。动物可以通过自我理毛缓解紧张,因而是一种缓解冲动的方式。在其它情况下,动物自我理毛可能表示对同种个体的反应,它们在不同场合下普遍存在自我理毛行为,表明这种行为有多种功能。因此,在这篇综述中,作者尽量避免自我理毛具有其它功能的争议,我们无意把自我理毛看成一种仅仅是对焦虑和紧张的反应、降低体温的机制,或者是一种护理体表的行为,我们也感到这种观点没有新意,这种有局限性的观点不支持自我理毛行为具有多种功能。我们在本文中更多关注的是自我理毛的特定背景,即当一个个体遇到同种个体的气味而出现的自我理毛行为[动物学报5l（5）：772-779,2005]。     

笼养黑叶猴拟母亲行为的观察

2002年3～12月,采用焦点动物观察法和全事件行为记录法对南宁动物园人工饲养的5群黑叶猴的拟母亲行为进行了观察。5群黑叶猴中,有幼体9只,成年个体19只。观察发现非母雌性黑叶猴的拟母亲行为有怀抱、携带、接近、理毛、吻婴5种类型;各种行为类型发生的频次从高到低分别为接近（46．19％）、怀抱和携带（24．14％）、吻婴（20．36％）和理毛（9．31％）。通过比较还发现：1）幼体出生几个月内（4～8月龄）,黑叶猴拟母亲行为经常发生。2）拟母亲行为的强度与幼体的年龄具有较大的关联性,与非母雌性的育婴经验有关,育婴经验缺乏的非母雌性对幼体表现出比有育婴经验的个体更强烈的兴趣。3）拟母亲行为发生受幼猴母亲的默认程度的影响,有些母亲不允许其它雌猴接触幼体。4）拟母亲行为有助于缓解群内雌性个体间的冲突,调节群内个体间的关系。     

笼养雌性黑叶猴尿中性腺激素水平变化与性行为、等级序位的关系

2003年10月30日至2004年11月21日,采集了3只笼养雌性黑叶猴妊娠期和1只笼养雌性黑叶猴发情期的晨尿,并用放射免疫分析法检测尿液中孕酮和雌二醇浓度,同时用全事件观察法观察黑叶猴的行为,分析雌性黑叶猴的行为与其尿中的性腺激素的关系。研究结果发现:1)进入妊娠期,雌性黑叶猴尿中的雌二醇浓度逐渐上升,中后期达高峰;而尿中孕酮浓度在妊娠初期仍维持在放免法的灵敏度以下,妊娠约1个月后才升高至灵敏度以上(13.39ng/mgCr);2)在妊娠中期,雌性黑叶猴仍维持着较高频率的邀配行为,但与雌激素的变化无明显的相关关系;3)发情期,雌猴尿中的雌二醇浓度与其邀配行为呈正相关;4)雌性黑叶猴的性激素高低与其等级序位无关,但序位高的雌猴繁殖较早。     

迁地保育林麝的侵犯性、等级序位及相互关系

侵犯性是动物个性的重要维度之一,体现了其主动挑衅和攻击其他个体的倾向。动物的侵犯性与其社会结构及等级序位存在紧密关系。本研究于2018年6月1日至7月31日对四川马尔康林麝繁育场的圈养林麝(Moschus berezovskii)进行了行为取样,计算林麝个体的侵犯性个性(侵犯性指数)和等级序位指数,分析圈养林麝的侵犯性和等级序位格局、影响因素及相互关系。结果表明,圈养林麝的侵犯性在性别间存在显著差异,雄性林麝的侵犯性(0.45±0.09,n=22)显著高于雌性(0.22±0.06,n=30)(P 0.05),年龄和驯养密度对其侵犯性的效应均不显著(P 0.05),说明林麝侵犯性的刚性较强;圈养林麝等级序位的性别间差异不显著(P 0.05),亚成体麝与成体麝的等级序位差异也未达显著水平(P 0.05),原因在于麝场的建群未区分年龄组;圈养林麝个体的侵犯性与其等级序位显著正相关,林麝个体的侵犯性越大,其等级序位越高(r=0.73,P 0.05),推测这与社群的序位等级构建和资源竞争有关。     

笼养川金丝猴理毛行为功能

<正>理毛行为(Grooming behavior)的定义是动物个体对自身或其同类个体体表(皮肤、毛发或羽毛等)进行的多种形式护理,包括对体表进行有规律的梳理,以及用舌头或嘴唇舔皮肤和毛发等(Veà et al., 1999)。在灵长类动物中,理毛行为大多表现为个体接触和探查自身或另一个体体表被毛,将毛发分开后从中拣出盐粒或皮肤寄生物放入口中咀嚼或直接用嘴咬食被毛下的盐粒或皮肤寄生物(李银华和李保国, 2002)。依据理毛接收对象的不同,可将     

藏酋猴社群雌体的性行为模式

猕猴属中大部分种类的繁殖类型可划分为季节性繁殖和非季节性繁殖两大类型。但是藏酋猴全年均有交配行为发生,而产仔仅在１～８月间,其类型属特殊的非季节性交配－季节性产仔繁殖类型。藏酋猴雌性在妊娠后选择的交配对象主要是高序位的雄性,但非妊娠雌性则主要选择低序位雄性。妊娠后的雌性交配频率低于非妊娠雌性,同时它们与成年雄性间理毛行为的发生频率亦低,反之受到成年雄性攻击的频率却高。     

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.     

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.     

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.     

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.     

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.     

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.     

Cationic (tripyrrinato)palladium(II) complexes

The formation of cationic palladium(II)complexes [TrpyPd^II]⁺X⁻ by salt metathesis of the respective trifluoroacetates with different salts of weakly coordinating anions X⁻ was investigated. With non-hydrolizable counterions, cationic mono- and dinuclear complexes are observed depending on the nature of the anion X⁻ and the solvent. The mononuclear cations, which are only formed with X = BAr^F, most probably carry a weakly bound molecule of dichloromethane at the fourth coordination site of Pd^II. When treated with diazoalkanes, only these are sufficiently reactive to form carbene complexes. Four- and five coordinate Lewis base adducts [TrpyPd^IIL]⁺ with L = CH₃NC, tBuNH₂, PMe₃, PEt₃ and PiPr₃ and [TrpyPd^IIL₂]⁺ with L = PMe₃ were prepared from the mononuclear cations [TrpyPd^II]⁺BAr^F−. From structural studies it becomes apparent, that the formation of stable five coordinate Pd^II species is restricted to medium size ligands and depends on the delicate balance between the steric influence of L and the strain, which is induced on the TrpyPd^II unit.