Airborne differences in odors emitted byRattus norvegicus in response to reward and nonreward

To test the hypothesis that rats (Rattus norvegicus) emit airborne, differential odors in response to reward and nonreward, donor rats received random sequences of rewarded and nonrewarded placements in small compartments and an airstream transported odors from these compartments to test rats in a separate chamber. When donors remained in the compartments during, or were removed just prior to, air transport, test rats utilized transported odors as discriminative cues signaling their own reward and nonreward for a lever-press response. When the airstream was passed through a clean compartment containing paper flooring extracted from donor compartments, test rats were not able to discriminate. Test trials to assess for control by food odors suggest that donor-produced odors, rather than food odors per se, provided the discriminative signals for test rats. Results confirm the existence of somewhat volatile, although apparently stable, odors emitted in response to reward and nonreward, and implicate a differential in amount and/or type of odor produced by donors to these two events as the source of discriminative control.     

褐家鼠的声行为研究

研究鼠类声行为，对探索鼠害控制的新方法有重要意义。在实验室条件下通过对11只褐家鼠（Rattusnor—vegicus）行为的观察和对860个叫声的分析，初步得知褐家鼠4种明显不同的声行为。单个体见到人时的惊恐叫声呈多谐变频的声谱结构，叫声的持续时间较长，平均在（473土271）ms，通常有3个主要的谐音，MPF为（2820土258）Hz。当两个体一起发生追打时，势弱个体表现出与其行为相应的3种明显不同的叫声：打斗时的惊叫声频率最高，MPF为（5091土1365）Hz，频率范围宽达（9225土3292）Hz，大多是多谐结构；面对势强个体的叫声的振幅低，为（O．44土0．25）V，几呈多谐恒频结构，MPF和频宽分别为（2917土1463）Hz和（4360土3421）Hz；堵挡在通道口的叫声的持续时间长，叫声的频率最低，MPF为（1384土878）Hz。     

Taxon-specific differences in responsiveness to capsaicin and several analogues: Correlates between chemical structure and behavioral aversiveness

The present set of experiments was designed to explore avian insensitivity to capsaicin. Based upon a molecular model of avian chemosensory repellency, we hypothesized that structural modifications of the basic capsaicin molecule, which is itself not aversive to birds, might produce aversive analogues. To this end, European starlings (Sturnus vulgaris) and Norway rats (Rattus norvegicus) were given varied concentrations of synthetic capsaicin and four analogues (methyl capsaicin, veratryl amine, veratryl acetamide, vanillyl acetamide) in feeding and drinking tests. The results agreed with a model that we are developing to describe the chemical nature of avian repellents. Synthetic capsaicin and vanillyl acetamide were not repellent to birds, owing to the presence of an acidic phenolic OH group. Conversely, veratryl acetamide was aversive, due to the basic nature of this compound. For rats, repellent effectiveness among compounds was reversed: synthetic capsaicin was the best repellent while veratryl acetamide was the worst. We speculate that this taxonomic reversal may reflect basic differences in trigeminal chemoreception. In any case, it is clear that chemical correlates of mammalian repellents are opposite to those that predict avian repellency.     

Exposure to Urine of Canids and Felids, but not of Herbivores, Induces Defensive Behavior in Laboratory Rats

Predator odors induce defensive behavior in many prey species. For various reasons, studies carried out up to now have been unable to establish whether predator odor recognition is innate or not. Mostly, only particular odors or wild-living (i.e., experienced) test animals have been used in these studies, restricting the conclusiveness of the observations. In the present study, the behavioral effects of exposure to different predator odors on predator odor-naive laboratory male rats were compared with the effects of different nonpredator odors and of a no-odor control stimulus. Results show that exposure to urine of canids and felids, but not of herbivores or conspecifics, induce defensive behaviors. Taken together, the study provides support for the hypothesis that there is an innate recognition of predator odors in laboratory rats.     

Responses of Wild Norway Rats (Rattus norvegicus) to Predator Odors

If rats could be shown to avoid the odors of predators, then conservation managers could manipulate this behavior to exclude rats from important conservation sites. We evaluated the ability of six predator odors to elicit avoidance responses by wild-caught Norway rats (Rattus norvegicus) from two New Zealand populations (Kapiti Island and North Island). Kapiti Island is free of mammalian predators, while the North Island has established populations of felids, canids, and mustelids. Three of the predator odors were real and three were synthesized volatile ingredients of real animal feces or urine. We compared the rats' responses to predator odors with their responses to three natural herbivore odors. We used a Y maze, and rats were offered the choice of an odor in one arm of the maze and distilled water in the other arm. Each choice arm was ducted at the entrance to remove air and the odor. We recorded: (1) the time until the rat left the first arm of the maze, (2) the time until the rat visited each arm, (3) the number of visits to each arm, (4) the amount of time spent in each arm, and (5) a total activity score for each rat. Kapiti rats showed an aversion to five of the six predator odors, despite never having encountered them before. Kapiti rats visited herbivore odors more often than carnivore odors and were less active in the presence of carnivore odors than they were when tested with herbivore odors. In addition, Kapiti rats approached some herbivore odors more quickly than they approached carnivore odors. North Island rats appeared to avoid cat urine, but despite being predator experienced, did not show a consistent aversion to the carnivore odors we tested. Both samples of rats, but particularly the North Island group, showed high individual variation. We conclude that predator odors are unlikely to be an effective management tool for all populations of this species of rat because of this high individual variability and the likelihood that each island population will differ in its responses to a given odor.     

Kinase CDK2 in Mammalian Meiotic Prophase I: Screening for Hetero- and Homomorphic Sex Chromosomes

Cyclin-dependent kinases (CDKs) are crucial regulators of the eukaryotic cell cycle. The critical role of CDK2 in the progression of meiosis was demonstrated in a single mammalian species, the mouse. We used immunocytochemistry to study the localization of CDK2 during meiosis in seven rodent species that possess hetero- and homomorphic male sex chromosomes. To compare the distribution of CDK2 in XY and XX male sex chromosomes, we performed multi-round immunostaining of a number of marker proteins in meiotic chromosomes of the rat and subterranean mole voles. Antibodies to the following proteins were used: RAD51, a member of the double-stranded DNA break repair machinery; MLH1, a component of the DNA mismatch repair system; and SUN1, which is involved in the connection between the meiotic telomeres and nuclear envelope, alongside the synaptic protein SYCP3 and kinetochore marker CREST. Using an enhanced protocol, we were able to assess the distribution of as many as four separate proteins in the same meiotic cell. We showed that during prophase I, CDK2 localizes to telomeric and interstitial regions of autosomes in all species investigated (rat, vole, hamster, subterranean mole voles, and mole rats). In sex bivalents following synaptic specificity, the CDK2 signals were distributed in three different modes. In the XY bivalent in the rat and mole rat, we detected numerous CDK2 signals in asynaptic regions and a single CDK2 focus on synaptic segments, similar to the mouse sex chromosomes. In the mole voles, which have unique XX sex chromosomes in males, CDK2 signals were nevertheless distributed similarly to the rat XY sex chromosomes. In the vole, sex chromosomes did not synapse, but demonstrated CDK2 signals of varying intensity, similar to the rat X and Y chromosomes. In female mole voles, the XX bivalent had CDK2 pattern similar to autosomes of all species. In the hamster, CDK2 signals were revealed in telomeric regions in the short synaptic segment of the sex bivalent. We found that CDK2 signals colocalize with SUN1 and MLH1 signals in meiotic chromosomes in rats and mole voles, similar to the mouse. The difference in CDK2 manifestation at the prophase I sex chromosomes can be considered an example of the rapid chromosome evolution in mammals.     

Recognition of conspecific odors by laboratory rats ( Rattus norvegicus) does not show context specificity.

This experiment investigated how contextual cues affect recognition of conspecific odors in laboratory rats (Rattus norvegicus). Rats received 5 encounters with the same odor in the same context. For the 6th test encounter, all rats received a simultaneous presentation of the original odor and a novel odor. The authors tested 1 group of rats (context same) in the same context as before. For the remaining 2 groups, the test encounter was in a different context that 1 group (context different) had experienced but that 1 group (context novel) had not. A significant preference to investigate the novel odor by context-same and context-different rats, but not by context-novel rats, suggests that odor recognition can occur following transfer to a different, but familiar, test context, indicating a lack of context specificity. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

DECLINE AND RECOVERY OF SMALL MAMMALS AFTER FLOODING: IMPLICATIONS FOR PEST MANAGEMENT AND FLOODPLAIN COMMUNITY DYNAMICS

Floodplains often are managed both for agriculture and as habitat for native species. On the Sacramento River, farmers have expressed concern that natural areas may harbour small mammals in greater abundance than occurs on farms, which could make them sources of pests to adjoining farmlands. Concern over this has generated some opposition to riparian restoration. To better understand the issue, we studied small mammals at agricultural sites, young and older riparian restoration sites and remnant natural areas through live trapping and visual surveys over three successive years. Significant flooding occurred during the second winter of the study. We found that young riparian restoration sites (3–4 years since planting) did not harbour agricultural pests (e.g. California ground squirrel, Botta's pocket gopher) in greater abundance than agricultural sites, with the exception of California voles. Although voles were common at young sites, they declined dramatically as the sites matured, and neither 12‐ to 15‐year‐old sites nor remnant riparian habitats had higher abundances of any small mammal pest species than agricultural sites. All species except the arboreal western gray squirrel experienced significant population declines following the flood and remained at depressed levels for at least a full year thereafter. Native species were not less susceptible to flooding than exotic species. California vole was the first species to recover. Our study suggests that frequent winter flooding may be desirable from an agricultural pest management perspective. It illustrates a valuable ecosystem service, small mammal pest control, which is provided by flooding, an important natural disturbance process. Copyright © 2011 John Wiley & Sons, Ltd.     

培养乳鼠心肌细胞时钟基因RT-PCR 检测方法的建立

目的 建立检测培养乳鼠心肌细胞中时钟基因的RT-PCR 方法。 方法 根据GeneBank 基因库大鼠时钟基因bmal1、per2 和dbp 全序列设计合成了3 对寡聚核苷酸引物。以离体培养的乳鼠心肌细胞中提取RNA 为模板, 筛选了(PCR) 最佳反应条件, 并进行了特异性检验。 结果 在20 μl 体积中, PCR 最佳系统组成分别为:dbp:Taq 酶、dNTP 和Mg²⁺的用量分别为0.5 U、0.006 μmol 和0.03 μmol;最佳退火温度为58 ℃, 循环30 次;bmal1:Taq 酶、dNTP 和Mg²⁺ 的用量分别为0.5 U、0.006 μmol 和0.035 μmol;最佳退火温度为57 ℃, 循环30 次;per2:Taq 酶、dNTP 和Mg²⁺的用量分别为0.5 U、0.006 μmol 和0.05 μmol;最佳退火温度为58 ℃, 循环32 次。 结论 成功建立RT-PCR 检测大鼠离体培养心肌细胞时钟基因的方法。