The effects of ants on herbivory and herbivore numbers on foliage of the mallee eucalypt,Eucalyptus incrassata Labill.*

Although there has been much recent interest in ant-plant mutualisms, few data are available on the effects of foraging ants on herbivore numbers and levels of herbivory on plants that do not offer specific inducements to attract ant visitation. In forestry plantations and tropical crops, ants have erratic but sometimes dramatic effects on the numbers of insect herbivores but, in more natural habitats, their effects on levels of herbivory appear to be largely unknown. In Australia, where ants and Eucalyptus woodlands are ubiquitous and abundant and where considerable debate has occurred regarding levels of herbivory in Eucalyptus forests, very little work has been done to examine the effects of ants on densities of insect herbivores on eucalypts. In this study, ants were experimentally excluded from mature and immature foliage of saplings of the mallee Eucalyptus incrassata in South Australia, and herbivore numbers and levels of leaf herbivory were assessed during the next 6 months. No significant differences in herbivory were found between ant-access and ant-exclusion treatments. In spring and early summer, ants were found in associations with aggregations of eurymelid bugs on young foliage, and the effects of ants on bug densities were experimentally investigated. Bug densities decreased rapidly in ant-exclusion treatments compared with ant-access controls. Ants also quickly removed seeds of E. incrassata from experimental caches. The potential of ants to limit the numbers of insect herbivores on eucalypts seems limited given their tendency to form mutualistic associations with sap-feeding Homopterans and because of a lack of other herbivores that are particularly vulnerable to ant predation.     

结核分枝杆菌可视化抗体检测蛋白芯片的制备

目的：利用克隆表达的7种结核分枝杆菌优势表位抗原,建立可视化抗体检测蛋白芯片,用于结核病辅助诊断。方法：将7种结核分枝杆菌优势表位抗原,即38kD、ESAT-6、CFP10、MPT64、Mtb8、Mtb8.4和Mtb16.3点于修饰的基片上,制备可检测7种结核抗体的多靶点蛋白微阵列,建立免疫金银染色检测系统;使用该芯片对48例临床结核病患者血液样品进行检测,并与“金标准”痰涂片（48例）和痰培养（其中的29例）检测结果进行比较,分析其敏感性;对30名献血员血液样品进行检测,分析其特异性。结果：可视化抗体检测蛋白芯片的敏感性分别为98.5％和96.6％,而痰涂片和痰培养检测方法的敏感性分别为35.4％和48.3％;可视化抗体检测蛋白芯片的特异性为93.3％。结论：建立的结核分枝杆菌可视化抗体检测蛋白芯片检测敏感性显著高于痰涂片和痰培养方法,可用于结核病的临床辅助诊断,提高痰涂片和痰培养假阴性的检出率。     

A 17‐element conodont apparatus from the Soom Shale Lagerstätte (Upper Ordovician), South Africa

Abstract:  Natural assemblages of a new conodont taxon, Notiodella keblon, from the Upper Ordovician Soom Shale Lagerstätte of South Africa contain 17 elements. This is the first time that a 17‐element apparatus plan has been unequivocally demonstrated in conodonts. The apparatus comprises paired P₁, P₂, P₃, M, S₁, S₂, S₃ and S₄ elements and an unpaired, axial S₀ element and provides a new template for use in the reconstruction of apparatuses from the collections of dispersed elements, particularly for those with icrion‐bearing P₁ elements and perhaps for other balognathids.     

Coordination between water transport capacity,biomass growth,metabolic scaling and species stature in co‐occurring shrub and tree species

The significance of xylem function and metabolic scaling theory begins from the idea that water transport is strongly coupled to growth rate. At the same time, coordination of water transport and growth seemingly should differ between plant functional types. We evaluated the relationships between water transport, growth and species stature in six species of co‐occurring trees and shrubs. Within species, a strong proportionality between plant hydraulic conductance (K), sap flow (Q) and shoot biomass growth (G) was generally supported. Across species, however, trees grew more for a given K or Q than shrubs, indicating greater growth‐based water‐use efficiency (WUE) in trees. Trees also showed slower decline in relative growth rate (RGR) than shrubs, equivalent to a steeper G by mass (M) scaling exponent in trees (0.77–0.98). The K and Q by M scaling exponents were common across all species (0.80, 0.82), suggesting that the steeper G scaling in trees reflects a size‐dependent increase in their growth‐based WUE. The common K and Q by M exponents were statistically consistent with the 0.75 of ideal scaling theory. A model based upon xylem anatomy and branching architecture consistently predicted the observed K by M scaling exponents but only when deviations from ideal symmetric branching were incorporated.     

Nonglutamate pore residues in ion selection and conduction in voltage-gated Ca(2+) channels

High-affinity, intrapore binding of Ca(2+) over competing ions is the essential feature in the ion selectivity mechanism of voltage-gated Ca(2+) channels. At the same time, several million Ca(2+) ions can travel each second through the pore of a single open Ca(2+) channel. How such high Ca(2+) flux is achieved in the face of tight Ca(2+) binding is a current area of inquiry, particularly from a structural point of view. The ion selectivity locus comprises four glutamate residues within the channel's pore. These glutamates make unequal contributions to Ca(2+) binding, underscoring a role for neighboring residues in pore function. By comparing two Ca(2+) channels (the L-type alpha(1C), and the non-L-type alpha(1A)) that differ in their pore properties but only differ at a single amino acid position near the selectivity locus, we have identified the amino-terminal neighbor of the glutamate residue in motif III as a determinant of pore function. This position is more important in the function of alpha(1C) channels than in alpha(1A) channels. For a systematic series of mutations at this pore position in alpha(1C), both unitary Ba(2+) conductance and Cd(2+) block of Ba(2+) current varied with residue volume. Pore mutations designed to make alpha(1C) more like alpha(1A) and vice versa revealed that relative selectivity for Ba(2+) over K(+) depended almost solely on pore sequence and not channel type. Analysis of thermodynamic mutant cycles indicates that the motif III neighbor normally interacts in a cooperative fashion with the locus, molding the functional behavior of the pore.     

Body Temperature and Physical Activity Correlates of the Menstrual Cycle in Chacma Baboons (Papio hamadryas ursinus)

We investigated the temporal relationship between abdominal temperature, physical activity, perineal swelling, and urinary progesterone and estradiol concentrations over the menstrual cycle in unrestrained captive baboons. Using a miniature temperature‐sensitive data logger surgically implanted in the abdominal cavity and an activity data logger implanted subcutaneously on the trunk, we measured, continuously over 6 months at 10‐min intervals, abdominal temperature and physical activity patterns in four female adult baboons Papio hamadryas ursinus (12.9–19.9 kg), in cages in an indoor animal facility (22–25°C). We monitored menstrual bleeding and perineal swelling changes, and measured urinary progesterone and estradiol concentrations, daily for up to 6 months, to ascertain the stage and length of the menstrual cycle. The menstrual cycle was 36 ± 2 days (mean ± SD) long and the baboons exhibited cyclic changes in perineal swellings, abdominal temperature, physical activity, urinary progesterone, and estradiol concentrations over the cycle. Mean 24‐hr abdominal temperature during the luteal phase was significantly higher than during the periovulatory phase (ANOVA, F_{(2, 9)} = 4.7; P = 0.04), but not different to that during the proliferative phase. Physical activity followed a similar pattern, with mean 24‐hr physical activity almost twice as high in the luteal than in the periovulatory phase (ANOVA, P = 0.58; F_{(2, 12)} = 5.8). We have characterized correlates of the menstrual cycle in baboons and shown, for the first time, a rhythm of physical activity and abdominal temperature over the menstrual cycle, with a nadir of temperature and activity at ovulation. Am. J. Primatol. 74:1143‐1153, 2012. © 2012 Wiley Periodicals, Inc.     

拼接信号序列单碱基变异提高马传染性贫血病毒mRNA拼接效率

分别以马传染性贫血(马传贫)驴强毒(D—A EIAV)RNA和马传贫驴白细胞弱毒疫苗(DLA EIAV)RNA为模板,利用RT—PCR的方法,克隆到马传贫强、弱毒株基因组外显子2及其下游的核苷酸序列。然后将报告基因CAT插入到EIAV内含子2env阅读框架中,构成CAT拼接报告系统。同时在强毒株重组表达质粒的基础上,将其外显子-3上游拼接受体位点的核苷酸序列CAG突变为弱毒株相应位置的核苷酸序列TAG,得到强毒单核苷酸突变株重组表达质粒。用构建的3个重组表达质粒DNA转染驴血白细胞,ELISA检测转染细胞CAT浓度。结果表明：EIAV强毒株重组表达质粒中CAT蛋白表达量最高,EIAV强毒株重组表达质粒次之,EIAV强毒突变株重组表达质粒最低。由于CAT基因被插入于各重组质粒中的EIAV内含子-2里,EIAV外显子-2、3之间的拼接可导致该基因的删除,因而其拼接效率低于EIAVmRNA外显子-2、3之间的拼接效率。实验数据表明,EIAV SA2拼接信号序列单碱基变异提高了SD2-SA2拼接效率;D—AEIAV SA2-SD2拼接效率比DLA EIAV相应位点拼接效率高。     

Narcissus late season yellows potyvirus: symptoms, properties and serological detection

Narcissus late season yellows virus (NLSYV) was obtained, apparently unmixed with other viruses, in selected naturally infected narcissus plants. The virus was not transmitted by manual inoculation to any of the 12 herbaceous species tested but was transmitted by Myzus persicae to virus-tested narcissus plants, which then developed symptoms characteristic of late season yellows. Typically, symptoms develop late in the growing season but their expression is unreliable. NLSYV particles, which measured c. 750 ± 12 nm, were purified from fresh leaf extracts of narcissus in 0·3 m sodium citrate containing 10 mm sodium EDTA and 10 mm sodium DIECA by differential centrifugation followed by clarification with diethyl ether, gel filtration and isopycnic banding in caesium sulphate. Using antibodies from antisera prepared to virus particles, NLSYV was detected by ELISA in 14 of the 18 cultivars examined and nine seemed totally infected. Detection of the virus by immunosorbent electron microscopy was as sensitive as by ELISA but neither test detected all infections. The virus was detected by ELISA only in samples collected after flowering and capsid antigen concentration was greatest in the distal region of leaves. The reliability of detection depended on the cultivar. Immuno-electron microscopy tests confirmed the occurrence of a distinct potyvirus, presumably narcissus degeneration, in narcissus cv. Grand Soleil d'Or, failed to detect any virus other than NLSYV in narcissus plants affected by white streak disease, and showed that NLSYV is related to three of five other potyviruses tested.