Hygro- and thermoreceptive tarsal organ in the spider Cupiennius salei

Extracellular recordings were made from moist cells, dry cells and warm cells in the tip pore sensilla of the spider tarsal organ. Stimulation consisted of a rapid shift from an adapting air stream to another one at different levels of partial pressure of water vapor or of temperature. The moist and the dry cells respond antagonistically to sudden changes in humidity. Both hygroreceptors are unusual in being excited in a synergistic manner by pungent vapors of very volatile, polar substances. Presumably, the hygrosensitivity is superimposed on basically chemosensitive receptors. A moist cell at average differential sensitivity is able to discriminate two successive upward steps in humidity when they differ by 11% relative humidity. For a single dry cell, the difference required for a correct discrimination between two downward humidity steps is 10% relative humidity. The moist and the dry cells are unique in that they occur in combination with warm cells. A single warm cell at average differential sensitivity is able to resolve differences in warming steps down to 0.4°C.Abbreviations HR relative humidity - T temperature     

Areal distribution of the discomfort index in Israel

The areal distribution of monthly mean values of the Discomfort Index (DI) in Israel is presented for key hours of the day for the summer half of the year. The DI as used in this study, is defined as the arithmetic average of the dry-bulb and wet-bulb temperature (°C), a value of 24 representing conditions at which half the people would feel uncomfortable. Data were collected from 95 meteorological stations situated in different parts of Israel. The raw data consisted of daily values of dry and wet-bulb temperatures for the hours 08:00, 14:00, and 20:00h for the years 1963–1972. Maximum values of the monthly mean DI in Israel generally occur in August. Geographically, the number of days of the year with DI greater than 24 ranges from 30 in the mountain regions, to 120 in the coastal plain, to 180 in the Jordan Valley, Dead Sea, and Arava regions. The dominant control of the observed distribution of DI in Israel appears to be topography. The DI is not a good measure of human discomfort for particularly hot and dry conditions, typical of those occurring during Sharav weather conditions. For such conditions, a new index was developed based on the difference between the dry-bulb and wet-bulb temperatures. The mean areal distributions of this difference index as well as that of the DI are presented for typical intense Sharav conditions. The new difference index appears to better represent discomfort during such conditions.Presented at the Eighth International Congress of Biometeorology, 9–14 September 1979, Shefayim, Israel.     

Antennal hygroreceptors of the honey bee,Apis mellifera L.

Summary Antennal hygroreceptors of the honey bee, Apis mellifera L., have been investigated electrophysiologically and the sensillum containing these receptors with SEM. Moist and dry hygroreceptors have been identified along with a thermal receptor in a specialized coeloconic sensillum. This sensillum comprises a cuticular, shallow depression (diameter; 4 ) having a central opening (1.4–1.5 m) and a mushroom-shaped protrusion (1.4–1.5 m) from the opening. The head of the protrusion is irregular in shape and is not perforated. This sensillum has been thus far referred to as a sensillum campaniformium (Dietz and Humphreys 1971), henceforth, it is referred to as a coelocapitular sensillum.The responses of both moist and dry hygroreceptors are of a phasic-tonic manner. Both receptors are antagonistic with respect to their responses to humidity; one responds with an increase in impulse frequency to rising humidity, the other to falling humidity. The humidity-response relationship is independent of stimulus flux.     

Influence of temperature gradients on leaf water potential

Water potential was monitored at nine locations along single maize (Zea mays L.) leaf blades with aluminum block in situ thermocouple hygrometers. Water potential showed a continuous decrease toward the tip, with a 2- to 4-bar difference between leaf base and tip under both moist and dry soil conditions. The water potential difference between the soil and the leaf base was about 4 bars. Water potentials decreased during the day and during a drying cycle, and increased at night and after irrigation. Heating a band of a leaf to 40 C or cooling it to 7 C had no influence on the water potential of the affected portion when this was corrected for hygrometer output over standard calibrating solutions at the respective temperatures. Heating or cooling a portion of a leaf had neither short nor long term effects on water potential of more distal leaf portions continuously monitored by hygrometers in dew point readout. Water potential fluctuated with an amplitude of about 1.5 bars and an irregular period of 10 to 30 minutes. Measurements with silver foil in situ psychrometers gave similar results.     

Hygroreceptors in the larva of Libellula depressa (Odonata: Libellulidae)

Ultrastructural and electrophysiological (single-cell recordings) investigations were carried out on the coeloconic sensilla borne by the apical antenna of the larvae of Libellula depressa (Odonata: Libellulidae). These sensilla appear as pegs located in pits. One of them is a compound sensillum constituted of two fused pegs in a common pit and the other two are single pegs located in separated pits close to each other. Coeloconic sensilla show position and ultrastructural details very similar to those described in insect hygroreceptors. The electrophysiological recordings on the apical antennae of the last larval instar of L. depressa clearly show the presence of moist and dry cells responding antagonistically to humidity changes. This study gives the first evidence of hygroreceptors in dragonfly larvae and represents the first electrophysiological approach to larval sensilla of aquatic insects. The presence of hygroreceptors in L. depressa larvae is in agreement with the hygropositive response shown by these insects in laboratory and field behavioural experiments.     

Electrophysiological identification of hygroreceptor neurons from the antennal dome-shaped sensilla in the ground beetle Pterostichus oblongopunctatus

This study gives the first electrophysiological evidence of hygroreceptors in carabids. Extracellular recordings from the antennal dome-shaped sensilla of the carabid beetle Pterostichus oblolongopunctatus (Coleoptera, Carabidae) clearly show the presence of moist and dry neuron antagonistically responding to humidity changes. The cold neuron of the same sensillum did not respond to changes in humidity. For the first time, we demonstrate that the binary system of two antagonistic hygroreceptor neurons discriminates differences between steady-state humidity levels more sensitively than either neuron separately. Another advantage of the binary system is that it guarantees immediate and strong phasic-tonic response to rapid humidity changes in either direction. In the hygrosensing system of carabids, this would allow detection of subtle step-changes in humidity with greater sensitivity than differences in steady-state values of humidity. Thus, construction of the hygrosensing system with opposing receptor neurons may allow insects to detect environmental humidity differences critical for their habitat and microhabitat selection, and survival with great precision.     

Humidity-invoked upwind orientation of shore insects (Bambidion obtusidens, coleoptera: Carabidae)

Because insects cannot rely solely on kinetic responses to locate upwind humidity resources, an alternative mechanism involving the perception of windborne humidity fluctuations was investigated. In a wind tunnel, upwind responses of adult shore insects (Bembidion obtusidens Fall, Carabidae, Coleoptera) were invoked by pulsed (1.25-Hz) increases (1.7%) of relative humidity at ambient relative humidities of 32, 42, 52, and 62% but not at 72 and 86%. Conversely, upwind responses to pulsed decreases (1.8%) occurred at 65, 72, and 86% but not at 32, 42, and 52% ambient relative humidities. These results suggest that perception by moist-air and dry-air hygroreceptors of turbulence-induced pulses of moist air or of dry air in their habitat trigger positive anemotactic orientation of these insects to upwind humidity resources.     

Temperature Changes in Brown Adipocytes Detected with a Bimaterial Microcantilever

Mammalian cells must produce heat to maintain body temperature and support other biological activities. Methods to measure a cell’s thermogenic ability by inserting a thermometer into the cell or measuring the rate of oxygen consumption in a closed vessel can disturb its natural state. Here, we developed a noninvasive system for measuring a cell’s heat production with a bimaterial microcantilever. This method is suitable for investigating the heat-generating properties of cells in their native state, because changes in cell temperature can be measured from the bending of the microcantilever, without damaging the cell and restricting its supply of dissolved oxygen. Thus, we were able to measure increases in cell temperature of <1 K in a small number of murine brown adipocytes (n = 4–7 cells) stimulated with norepinephrine, and observed a slow increase in temperature over several hours. This long-term heat production suggests that, in addition to converting fatty acids into heat energy, brown adipocytes may also adjust protein expression to raise their own temperature, to generate more heat. We expect this bimaterial microcantilever system to prove useful for determining a cell’s state by measuring thermal characteristics.     

Temperature-dependent dry receptor on antenna ofPeriplaneta. Tonic response

Summary Identified as a dry receptive unit by transitory impulse frequencies up to about 200 imp/sec during rapid drops in humidity (Fig. 3) and which no other modality elicited, the dry unit on the antenna ofPeriplaneta americana is characterized by a regular (Fig. 4) and relatively high stationary impulse frequency (10–65 imp/s). Without exception the stationary discharge rate (tonic frequency) rose with falling values of stationary absolute humidity at constant temperature, and with rising values of stationary temperature of ambient air at constant humidity. Enthalpy and evaporation cooling appear to be ruled out as exclusive adequate explanations for this double dependence. No matter whether tonic frequency is plotted against absolute humidity based on either volume of moist air or weight of dry air, or against partial pressure of water vapor in ambient air, or the difference between saturation and partial vapor pressure, or against relative humidity, the dependence on the temperature is not eliminated (Figs. 5–7). Because a temperature range of about 20 °C and all humidities between 0 and 100% occupy the same large segment of the unit's tonic frequency spectrum (Fig. 8), the unit is termed bimodal.The author wishes to express indebtedness and gratitude to Prof. Dr. Hansjochem Autrum for backing the early stages of this project with the assistance of the Deutsche Forschungsgemeinschaft, to Prof. Dr. Helmut Altner for his prolonged support, to Dr. Hans-Jürgen Hinz for his helpful discussion of questions involving thermodynamics, to Prof. Dr. Friedrich Earth for helpful criticism of the text, and to Miss Christel Praeg for tireless technical assistance.     

Intracellular Water Exchange for Measuring the Dry Mass,Water Mass and Changes in Chemical Composition of Living Cells

We present a method for direct non-optical quantification of dry mass, dry density and water mass of single living cells in suspension. Dry mass and dry density are obtained simultaneously by measuring a cell’s buoyant mass sequentially in an H₂O-based fluid and a D₂O-based fluid. Rapid exchange of intracellular H₂O for D₂O renders the cell’s water content neutrally buoyant in both measurements, and thus the paired measurements yield the mass and density of the cell’s dry material alone. Utilizing this same property of rapid water exchange, we also demonstrate the quantification of intracellular water mass. In a population of E. coli, we paired these measurements to estimate the percent dry weight by mass and volume. We then focused on cellular dry density – the average density of all cellular biomolecules, weighted by their relative abundances. Given that densities vary across biomolecule types (RNA, DNA, protein), we investigated whether we could detect changes in biomolecular composition in bacteria, fungi, and mammalian cells. In E. coli, and S. cerevisiae, dry density increases from stationary to exponential phase, consistent with previously known increases in the RNA/protein ratio from up-regulated ribosome production. For mammalian cells, changes in growth conditions cause substantial shifts in dry density, suggesting concurrent changes in the protein, nucleic acid and lipid content of the cell.     

The relative influence of temperature and humidity on cutaneous function in Bos indicus and Bos taurus females

The relative importance of dry- and wet-bulb temperatures on cutaneous function inBos indicus andBos taurus females under humid tropical climatic conditions was evaluated. The parameters investigated were sweating rate and skin temperature, while the species utilised were zebu White Fulani (Bos indicus) and German Brown and German Black and White (Bos taurus).The sweating rate, irrespective of breed, differed with the site of sampling and was more influenced by dry-bulb (59%) than by wet-bulb temperature (41%). Skin temperature responded more to wet-bulb temperature in White Fulani and German Black and White cattle, but not in German Brown cattle.It is concluded that the response of the animals, with respect to sweating, was similar but that the efficiency of sweating, judged by the lowering of skin temperature, was higher inBos indicus than inBos taurus. This, in part, may explain the higher degree of comfort demonstrated byBos indicus under tropical conditions.     

Models of Electrical Activity: Calibration and Prediction Testing on?the?Same Cell

Mathematical models are increasingly important in biology, and testability is becoming a critical issue. One limitation is that one model simulation tests a parameter set representing one instance of the biological counterpart, whereas biological systems are heterogeneous in their properties and behavior, and a model often is fitted to represent an ideal average. This is also true for models of a cell’s electrical activity; even within a narrowly defined population there can be considerable variation in electrophysiological phenotype. Here, we describe a computational experimental approach for parameterizing a model of the electrical activity of a cell in real time. We combine the inexpensive parallel computational power of a programmable graphics processing unit with the flexibility of the dynamic clamp method. The approach involves 1), recording a cell’s electrical activity, 2), parameterizing a model to the recording, 3), generating predictions, and 4), testing the predictions on the same cell used for the calibration. We demonstrate the experimental feasibility of our approach using a cell line (GH4C1). These cells are electrically active, and they display tonic spiking or bursting. We use our approach to predict parameter changes that can convert one pattern to the other.     

Environmental conditions and their impact on immunocompetence and pathogen susceptibility of the Caribbean termite Nasutitermes acajutlae

1. Little is known about interactions between environmental conditions surrounding insects and their immune responses. 2. The environment in and around termite colonies, including temperature, relative humidity, soil pH, and light was analysed using principal components analysis (PCA). 3. The relationship between these abiotic parameters and two aspects of termite immunity (phenoloxidase activity and lipid content) was examined in field‐caught workers of Nasutitermes acajutlae Holmgren. Finally, termites from warm/dry and cool/moist habitats were exposed to Metarhizium anisopliae to determine their susceptibility to mycosis. 4. PCA indicated that environmental components external to the nest [ambient temperature, ambient relative humidity (RH), soil temperature and light] comprised the majority (PC1 = 37.5%) of variation. Internal variables (nest temperature and RH) and nest volume accounted for 19.6% (PC2) of the variation with pH comprising 12.9% (PC3). 5. AIC and regression models suggested that ambient temperature was most strongly and positively associated with immune variables and that relative humidity may also play a role. Termites from warm/dry colonies were less susceptible to M. anisopliae than termites from cool/moist colonies. 6. Thus, termites nesting in warmer habitats may exhibit increased immune‐related measures and reduced susceptibility to mycosis compared with termites from cooler habitats.     

Hygroreceptor identification and response characteristics in the stick insectCarausius morosus

Summary Simultaneous recordings were made from 3 sensory units in an easily identifiable sensillum on the 12th antennal segment ofCarausius morosus. Impulse frequency (F) of one unit rose sharply when either the temperature (T) or the partial pressure of water vapor (Pw) was suddenly lowered. F of another rose sharply either when T was suddenly lowered or Pw was raised. F of the third was hardly affected by sudden changes in T but rose abruptly when Pw fell (Fig. 1). The reactions of the first may be explained by enthalpic cooling and is considered a cold cell. Those of the second may be attributed to changes in relative humidity (Hr) and is thus termed a moist cell. The third is taken to be the latter's antagonist, a dry cell.A 90%-probability that a single moist cell of average differential sensitivity will correctly discriminate between two humidity levels is not reached until the difference between the two is 38% Hr. The dry cell requires a difference of only 7.5% (Table 1). The basis for discrimination is a single presentation of each level.The power to discriminate Hr steps is better in both cell types. For a single moist cell of average differential sensitivity the difference required between the steps for a 90%-probability of correct discrimination is only 6.3% Hr; for the dry cell, 3.5% Hr. Basis for discrimination: a single presentation of each step. Step range: 5% to 55% Hr.Abbreviations F impulse frequency in impulses per second (imp/s) - Hr orHR relative humidity in % - Ps saturation pressure of water vapor in torr - Pw partial pressure of water vapor in torr - r correlation coefficient - T temperature in °C Dedicated to Prof. Dr. F. Schaller on the occasion of his 65th birthday     

南京城市街区湿球温度时空变化特征及其影响因子

全球气候变化和局地城市热岛加剧了城市热胁迫问题,但针对城市街区的研究仍不多见。湿球温度指示气温和湿度的综合效应,能更准确地反映人体热舒适度。本研究以南京市江北新区为对象,在不同时段、季节和天空状况下,基于移动观测方法获取气温、相对湿度和地理信息等数据,分析了街区尺度湿球温度的时空分布特征;结合天空状况、地表覆盖和城市形态指标(天穹可见度),探究了城市街区湿球温度的影响机制。结果表明: 1)南京城市街区湿球温度的时空特征与气温较为一致;与水汽压相比,气温对湿球温度的变化起主导作用;该地区湿球温度的极端高值主要是由于气温和水汽压协同增长所致。2)天穹可见度在白天与湿球温度呈显著正相关,夜间为负相关关系。植被覆盖比率的增加能够降低湿球温度,不透水面则呈现相反的作用。阴天条件下,湿球温度明显降低并且空间分布更均匀。3)植被和不透水面对湿球温度的水平尺度效应存在昼夜和季节差异,并且在夜间这一效应对天空状况更敏感;与植被相比,冬季夜间不透水面的影响范围比夏、秋季更大;两者对湿球温度的水平尺度效应与气温一致。研究结果可为改善和优化城市街区热环境、缓解城市热胁迫提供有效的科学支持和理论依据。     

Cellular Interrogation: Exploiting Cell-to-Cell Variability to Discriminate Regulatory Mechanisms in Oscillatory Signalling

The molecular complexity within a cell may be seen as an evolutionary response to the external complexity of the cell’s environment. This suggests that the external environment may be harnessed to interrogate the cell’s internal molecular architecture. Cells, however, are not only nonlinear and non-stationary, but also exhibit heterogeneous responses within a clonal, isogenic population. In effect, each cell undertakes its own experiment. Here, we develop a method of cellular interrogation using programmable microfluidic devices which exploits the additional information present in cell-to-cell variation, without requiring model parameters to be fitted to data. We focussed on Ca²⁺ signalling in response to hormone stimulation, which exhibits oscillatory spiking in many cell types and chose eight models of Ca²⁺ signalling networks which exhibit similar behaviour in simulation. We developed a nonlinear frequency analysis for non-stationary responses, which could classify models into groups under parameter variation, but found that this question alone was unable to distinguish critical feedback loops. We further developed a nonlinear amplitude analysis and found that the combination of both questions ruled out six of the models as inconsistent with the experimentally-observed dynamics and heterogeneity. The two models that survived the double interrogation were mathematically different but schematically identical and yielded the same unexpected predictions that we confirmed experimentally. Further analysis showed that subtle mathematical details can markedly influence non-stationary responses under parameter variation, emphasising the difficulty of finding a “correct” model. By developing questions for the pathway being studied, and designing more versatile microfluidics, cellular interrogation holds promise as a systematic strategy that can complement direct intervention by genetics or pharmacology.     

Fusoselect: cell–cell fusion activity engineered by directed evolution of a retroviral glycoprotein

Membrane fusion plays a key role in many biological processes including vesicle trafficking, synaptic transmission, fertilization or cell entry of enveloped viruses. As a common feature the fusion process is mediated by distinct membrane proteins. We describe here ‘Fusoselect’, a universal procedure allowing the identification and engineering of molecular determinants for cell–cell fusion-activity by directed evolution. The system couples cell–cell fusion with the release of retroviral particles, but can principally be applied to membrane proteins of non-viral origin as well. As a model system, we chose a γ-retroviral envelope protein, which naturally becomes fusion-active through proteolytic processing by the viral protease. The selection process evolved variants that, in contrast to the parental protein, mediated cell–cell fusion in absence of the viral protease. Detailed analysis of the variants revealed molecular determinants for fusion competence in the cytoplasmic tail (CT) of retroviral Env proteins and demonstrated the power of Fusoselect.     

热带季节性湿润林苦楝(Melia azedarach)径向生长季节动态及其对环境因子的响应

气候变化导致的温度升高和降水格局改变可能会影响到树木的生长速率和季节物候。西双版纳热带季节性湿润林分布在石灰岩山中部,属于热带喀斯特生境。由于土层浅薄,土壤保水能力极差,植物生长更容易遭到受到季节性干旱气候的影响。为探究热带季节性湿润林的树木径向生长季节动态及其对环境因子的响应,利用高精度树木生长仪连续两年监测了云南西双版纳热带季节性湿润林中落叶树种苦楝（Melia azedarach）的树干径向变化,并与同步监测的环境因子进行相关分析。结果表明,苦楝径向生长开始、结束以及持续生长的时间在年际间存在差异。与2018年相比,2019年苦楝生长开始和结束的时间较晚,且年生长量较小,这可能是与2019年雨季开始较晚且在生长季早期经历了严重的高温干旱有关。苦楝的径向日生长量与日降水量和相对湿度呈正相关关系,与光合有效辐射、水汽压亏缺和风速呈负相关关系,表明了在苦楝的径向生长主要受水分条件限制。在干旱年份（2019年）,苦楝的日生长量与降水和相对湿度的相关性更强。研究结果有助于进一步了解热带喀斯特生境树木生长对气候变化的敏感性以及树木适应季节性干旱气候的策略。     

Low rates of change enhance effect of humidity on the activity of insect hygroreceptors

The inability to measure humidity during stimulation has so far prevented us from understanding the contribution of moist cells and dry cells to orientation in a gradient of humidity. The problem was solved in the present study by means of a UV-absorption hygrometer that made it possible to monitor humidity at a rate of 100 Hz. The antennal moist and dry cells of the cockroach were exposed to humidities alternatively falling or rising at low rates between -1% RH s(-1) and +1% RH s(-1) (relative humidity). Impulse frequency of both types of cells depended simultaneously on instantaneous humidity and its rate of change. High frequencies of the moist cells signal high humidity. But at a given humidity, the response frequency is higher still when humidity is also rising. Conversely, high frequencies of the dry cell signal low humidity, and frequency is higher still at a given humidity when humidity is also falling. These responses ensure that the cockroach spent a minimum time in environments where desiccation or hydration occur and may thus protect the animal from emerging accidentally from under cover into moving air. In the constant-humidity retreat of the cockroach, fluctuating or even drifting discharge frequencies could serve as an early warning: return!     

Inferring Diffusion Dynamics from FCS in Heterogeneous Nuclear Environments

Fluorescence correlation spectroscopy (FCS) is a noninvasive technique that probes the diffusion dynamics of proteins down to single-molecule sensitivity in living cells. Critical mechanistic insight is often drawn from FCS experiments by fitting the resulting time-intensity correlation function, G(t), to known diffusion models. When simple models fail, the complex diffusion dynamics of proteins within heterogeneous cellular environments can be fit to anomalous diffusion models with adjustable anomalous exponents. Here, we take a different approach. We use the maximum entropy method to show—first using synthetic data—that a model for proteins diffusing while stochastically binding/unbinding to various affinity sites in living cells gives rise to a G(t) that could otherwise be equally well fit using anomalous diffusion models. We explain the mechanistic insight derived from our method. In particular, using real FCS data, we describe how the effects of cell crowding and binding to affinity sites manifest themselves in the behavior of G(t). Our focus is on the diffusive behavior of an engineered protein in 1) the heterochromatin region of the cell’s nucleus as well as 2) in the cell’s cytoplasm and 3) in solution. The protein consists of the basic region-leucine zipper (BZip) domain of the CCAAT/enhancer-binding protein (C/EBP) fused to fluorescent proteins.