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     

Response of moist-air receptor on antenna of the stick insect,Carausius morosus,to step changes in temperature

Summary The moist-air sensory cell in the antennal mound-shaped sensillum of Carausius responds to changes in relative humidity brought about by changing either the temperature (T) of the air or the partial pressure of water vapor (Pw) (Figs. 1, 5). When changes in either parameter cause relative humidity (Hr) to rise between roughly 5% and 55%, the same Hr-changes elicit very close to the same responses, no matter how Hr is changed (Figs. 2, 3). Even the resolving power for upward Hr-steps produced by lowering T is very close to that produced by raising Pw: 7.4% vs. 6.3%. Thus upward transients in impulse frequency (F) may be read off directly as quantitative rises in Hr. Whether the rise in Hr as signalled by the moist-air cell is the result of a rise in Pw or of a drop in T could well be indicated by the simultaneous reactions of the cold and dry-air cells (Figs. 1, 5). The moist-air cell also reacts to downward step changes in Hr, but very differently, depending on how they are brought about. Upward steps in T have a much larger effect on F than corresponding downward steps in Pw (Fig. 4). This result demonstrates that changes in relative humidity do not suffice to explain the changes in the activity of the moist-air cell. The receptor may be better construed as bimodal, reacting to changes in T and Pw with independent sensitivities and well matched to relative humidity when changes in either lead to increases in this parameter. The moistair cell's responses to T-steps at Pw = 0 (Figs. 1, 5) offer some support for this interpretation.Abbreviations F impulse frequency in impulses/s (imp/s) - Hr 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     

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.     

Gas exchange patterns of Pterostichus niger (Carabidae) in dry and moist air

Gas exchange patterns of adult male Pterostichus niger Schaller after hydration (i.e. given access to food and water) are compared in dry air [5–7% relative humidity (RH)] and moist air (90–97% RH) by means of flow‐through CO₂ respirometry combined with infrared probe actography. Of thirty beetles examined, slightly more than 50% showed continuous gas exchange and are not considered further. Of the remaining beetles, the majority (approximately 71%) display a pattern of cyclic gas exchange in both dry and moist air (i.e. CO₂ gas is released in bursts, with a low level of CO₂ release during the interburst periods). A minority of the beetles (four out of 30) are found to exhibit discontinuous gas exchange in both dry and moist air; this is characterized by three clearly separated states of the spiracles: closed (C), flutter (F) and open (O) phases. The pattern of cyclic gas exchange is associated with weak abdominal pulsations. After switching from moist to dry air, a small modulation of the discontinuous gas exchange cycles (maximum mean CO₂ production rate) occurs, providing no clear support for the hygric theory of discontinuous gas exchange in this species (i.e. that it serves to restrict respiratory water loss).     

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。     

Incubation water loss,shell conductance,and pore dimensions in Adelie Penguin eggs

Summary In order to understand water loss regulation of bird eggs in very dry climates eggs of the Adelie Penguin were studied at Cape Bird, Ross Island, Antarctica. During incubation 125 g Adelie Penguin eggs lose about 447 mg of water per day, resulting in an overall estimated loss, during 35 days of incubation, of 13% of their initial mass. The eggshell conductance of 13.1 mg H₂O·day^-1·torr^-1 occurs from 9100 pores with an effective radius and pore length of 11 m and 600 m, respectively. In this study the water vapor pressure of the egg was 44 torr, estimated from the egg temperature of 35.9°C. Ambient temperature was-4°C, with an absolute humidity of less than 3 torr, resulting in an overall vapor pressure difference between the egg and the environment of 41 torr. This difference was divided between the egg and nest conductance in a ratio of ca. 1:5.     

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!     

Water Status of Green and Blue-green Phycobionts in Lichen Thalli after Hydration by Water Vapor Uptake: Do They Become Turgid?

It is known from previous investigations that dry lichens with green algae are able to recover net photosynthesis through rehydration with water vapor, whereas all blue-green lichens tested so far lack this ability. The REM micrographs of the present study show that the green phycobionts (Trebouxia spec.) of Ramalina maciformis become turgid only after water vapor uptake. In contrast, the blue-green phycobionts (Nostoc spec.) of Peltigera rufescens do not differ in appearance from the dry state, even when the thallus has reached equilibrium with the water vapor-saturated air; they require liquid water for turgidity. It is hypothesized that, after humidity hydration, water content is not sufficient for reestablishment of a functioning osmotic cell system in the blue-green phycobiont.     

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.     

Chlorophyll Fluorescence of Lichens Containing Green and Blue-Green Algae During Hydration by Water Vapor Uptake and by Addition of Liquid Water*

The fluorescence yield at room temperature of the lichens Ramalina maciformis and Peltigera rufescens, containing either green or blue-green algae (Cyanobacteria) as phycobionts, has been investigated during rehydration of the dry lichens by water vapor uptake or by wetting with liquid water. In the dry state the fluorescence yield with all reaction centers open, F_o, was low and no variable fluorescence could be induced with both species. Whereas R. maciformis, containing green algae, regained normal fluorescence behavior during water vapor uptake, the photosynthetic apparatus of the blue-green algae-containing P. rufescens stayed inhibited and could be reactivated only by addition of liquid water. During stepwise rehydration at increasing air humidities, a pattern was established for the recovery of the different fluorescence parameters in R. maciformis. At a dry-weight related water content between 30 and 40%, F_o rose sharply. Maximal variable fluorescence yield expressed as (F_v)_m/F_o, strongly increased in the same range of water content and remained constant above a water content of 50%. Non-photochemical fluorescence quenching, q_NP, determined at the end of a period of actinic illumination, decreased with increasing water vapor uptake. While spraying the lichen with liquid water did not induce a further decrease of q_NP, slow dehydration at lowered air humidity led to a minimal value of q_NP at a water content of 65 % indicating optimal photosynthetic rate under these conditions. These results extend the conclusions drawn from earlier gas exchange experiments that blue-green algae-containing lichens are unable to reactivate photosynthesis by water vapor uptake. During a re- and de-hydration cycle, no hysteresis in the hydration dependence of the fluorescence parameters was found. From this and the presence of a stable and low F_o value at prolonged incubation in nearly water vapor saturated air, we conclude that the reactivation of photosynthesis in blue-green algae-containing lichens is not prevented through high diffusion resistances for water.     

Response characteristics of a cold receptor in the stick insectCarausius morosus

Summary The cold cell in the easily identified mound-shaped sensillum on the 12th segment ofCarausius morosus' antennae responds to downward temperature (T) steps from about 15 °C with a sharp rise in impulse frequency (F). Responses to similar steps from higher initial temperatures are smaller (Figs. 1, 3, 4). As initialT increases from 16 °C to 31 °C, differential sensitivity to downward steps falls off by a factor of 27: to yield an average increase inF of 1 imp/s, steps down from 31 °C must increase by 1.7 °C; steps down from 16 °C, by only 0.06 °C (Fig. 5). Resolving power forT-steps at mid-range initial temperatures is about 0.7 °C, i.e. the probability that a single cold cell at average differential sensitivity will correctly discriminate between twoT steps 0.7 °C apart is 90% when the cell is presented with each step just once.The same cold cell also displays a clear dependence on steadyt between 14 °C and 24 °C (Figs. 7, 8). The static discharge rate of a single cell at average differential sensitivity has a resolving power of about 0.9 °C for steadyT. — The static discharge is not affected by the amount of water vapor in the stimulating air (Fig. 9).Abbreviations F impulse frequency in impulses per second (imp/s) - Pw partial pressure of water vapor in torr - r correlation coefficient - T temperature in °C - T step change inT     

Gas exchange and blood gases of Puna teal (Anas versicolor puna) embryos in the Peruvian Andes

Oxygen consumption, air cell gases, hematology, blood gases and pH of Puna teal (Anas versicolor puna) embryos were measured at the altitude at which the eggs were laid (4150 m) in the Peruvian Andes. In contrast to the metabolic depression described by other studies on avian embryos incubated above 3700 m, O₂ consumption of Puna teal embryos was higher than even that of some lowland avian embryos at equivalent body masses. Air cell O₂ tensions dropped from about 80 toor in eggs with small embryos to about 45 toor in eggs containing a 14-g embryo; simultaneously air cell CO₂ tension rose from virtually negligible amounts to around 26 torr. Arterial and venous O₂ tensions (32–38 and 10–12 toor, respectively, in 12- to 14-g embryos) were lower than described previously in similarly-sized lowland wild avian embryos or chicken embryos incubated in shells with restricted gas exchange. The difference between air cell and arterial O₂ tensions dropped significantly during incubation to a minimum of 11 torr, the lowest value recorded in any avian egg. Blood pH (mean 7.49) did not vary significantly during incubation. Hemoglobin concentration and hematocrits rose steadily throughout incubation to 11.5 g · 100 ml^-1 and 39.9%, respectively, in 14-g embryos.Abbreviations PO₂ partial pressure gradient of O₂ - BM body mass - D diffusion coefficient - G gas conductance (cm³·s^-1·torr^-1) - conductance to water vapor - IP internal pipping of embryos - P _ACO₂ partial pressure of carbon dioxide in air cell - P _AO₂ partial pressure of oxygen in air cell - P _aCO₂ partial pressure of carbon dioxide in arterial blood - P _aCO₂ partial pressure of oxygen in arteries - P _H barometric pressure (torr) - PCO₂ partial pressure of carbon dioxide - P _IO₂ partial pressure in ambiant air - PO₂ partial pressure of oxygen - P _VCO₂ venous carbon dioxide partial pressure - P _VO₂ mixed venous oxygen partial pressure - SE standard error - VO ₂ oxygen consumption     

Effects of relative humidity and temperature stress on pollen viability of Cistus incanus and Myrtus communis

Cistus incanus and Myrtus communis are two species commonly found in Mediterranean shrublands, flowering respectively in spring and summer. Pollen of single flowers of C. incanus is available for dispersal for 8-10 hours, during which time viability decreases from 91% to 61%. Field measurements of the variation in the percent pollen viability during the anthesis of single flowers of M. communis shows that, immediately after anthesis, pollen viability is very high; by the end of the first day it significantly declines and 36 hours after anthesis almost all grains are unviable. Experiments carried out under controlled environment showed that, in C. incanus, the greatest loss of viability occurs at 100% humidity and high temperatures, while under dry conditions pollen viability remains high throughout a wide temperature range. Similarly, pollen viability of M. communis remains high for several hours at high temperature and dry conditions, while it rapidly decreases at high humidity. In conclusion, the temperature experiments indicate that in C. incanus and M. communis, pollen viability does not appear to be drastically reduced if the relative humidity of the environment is low. Therefore, humidity is a far more important factor determining pollen viability loss in both species.     

Solenostoma oblongifolium (K. Müll.) K. Müll. in Scotland—new to the British Isles

Abstract

To determine the responses of cryptogams to the variations in temperature, pH, and humidity, we studied the vegetation of Thermal Meadow, Hotsprings Island, Queen Charlotte Islands, B.C., Canada. Only seven cryptogamic taxa were present in the samples: five mosses, one liverwort, and one lichen. Humidity limited the distribution, with Racomitrium lanuginosum and Cladina ciliata preferring the warmer, drier sites and Pleurozium schreberi and Dicranum scoparium preferring cooler, more moist sites. Polytrichum formosum was the most frequent taxon, occurring under both cool, moist conditions and warm, dry conditions. Aulacomnium palustre occurred in the mid temperature range mostly where humidity was fairly high. The pH ranged 6.8–7.2, providing insufficient variation for us to delimit species preferences.     

Stomatal and environmental control of transpiration in a lowland tropical forest tree

Stomatal control of crown transpiration was studied in Anacardium excelsum, a large-leaved, emergent canopy species common in the moist forests of Central and northern South America. A construction crane equipped with a gondola was used to gain access to the uppermost level in the crown of a 35-m-tall individual. Stomatal conductance at the single leaf scale, and transpiration and total vapour phase conductance (stomatal and boundary layer) at the branch scale were measured simultaneously using the independent techniques of porometry and stem heat balance, respectively. This permitted the sensitivity of transpiration to a marginal change in stomatal conductance to be evaluated using a dimensionless coupling coefficient (1-ω) ranging from zero to 1, with 1 representing maximal stomatal control of transpiration. Average stomatal conductance varied from 0.09 mol m^?2 s^?1 during the dry season to 0.3 mol m^?2 s^?1 during the wet season. Since boundary layer conductance was relatively low (0.4 mol m^?2 s^?1), 1-ω ranged from 0.46 during the dry season to only 0.25 during the wet season. A pronounced stomatal response to humidity was observed, which strongly limited transpiration as evaporative demand increased. The stomatal response to humidity was apparent only when the leaf surface was used as the reference point for measurement of external vapour pressure. Average transpiration was predicted to be nearly the same during the dry and wet seasons despite a 1 kPa difference in the prevailing leaf-to-air vapour pressure difference. The patterns of stomatal behaviour and transpiration observed were consistent with recent proposals that stomatal responses to humidity are based on sensing the transpiration rate itself.     

Stomatal responses to changes in humidity in plants growing in the desert

Summary The stomata of plants growing in the Negev Desert, namely the stomata of the mesomorphic leaves of Prunus armeniaca, the xeromorphic stems of Hammada scoparia, and the succulent leaves of Zygophyllum dumosum, respond to changes in air humidity. Under dry air conditions diffusion resistance increases. Under moist air conditions diffusion resistance decreases. When the stomata close at low air humidity the water content of the apricot leaves increases. The stomata open at high air humidity in spite of a decrease in leaf water content. This excludes a reaction via the water potential in the leaf tissue and proves that the stomatal aperture has a direct response to the evaporative conditions in the atmosphere. In all species the response to air humidity is maintained over a period of many hours also when the soil is considerably dry. The response is higher in plants with poor water supply then in well watered plants. Thus for field conditions and for morphologically different types of photosynthesizing organs the results confirm former experiments carried out with isolated epidermal strips.     

Thermoregulation by rhesus monkeys at different absolute humidities

The effect of relative humidity on thermoregulation has been well examined. Because the same relative humidity represents very different absolute humidities at different ambient temperatures, the present study was designed to examine the interaction of temperature and absolute humidity on the thermal balance of rhesus monkeys, Macaca mulatta. Thermal balance was examined in six unacclimated, unanesthetized, female rhesus monkeys at ambient temperatures of 25, 30, 35, and 40 °C and absolute humidities of 6, 22, and 40 torr. Monkeys were capable of achieving thermal balance under all conditions except at 40 °C with 40 torr absolute humidity, where experiments were stopped after rectal temperature exceeded 40.5 °C. At 40 °C, monkeys increased evaporative heat loss through both respiration and sweating; the slope of the relationship between evaporative heat loss and core temperature was attenuated by increases in absolute humidity. In contrast, absolute humidity had no direct effect on metabolic rate. The rise in body temperature under the conditions of high heat/high humidity was therefore most attributable to humidity-dependent decreases in evaporative heat loss.Abbreviations E_tot total evaporative heat loss - HR heart rate - K thermal conductance - M metabolic rate - RQ respiratory quotient - T_c core temperature - T_sk mean skin temperature - VCO₂ carbon dioxide production - VO₂ oxygen consumptionCommunicated by G. Heldmaier     

Gas exchange pattern in the two‐spot ladybird beetle,Adalia bipunctata,differs in dry vs. moist air

Gas exchange patterns in the ladybird beetle, Adalia bipunctata (L.) (Coleoptera: Coccinellidae), were investigated using an infrared gaseous analyser (IRGA) and a coulometric O₂ respirometer (manometric–volumetric system). Before testing, the beetles were kept either in dry (dehydrated) or moist (hydrated) conditions for 1 day. Their subsequent gas exchange patterns did not depend on their state of humidity but rather were controlled by the humidity of the insect chamber during gas exchange measurement. If this chamber contained dry air, the beetles exhibited CO₂ release by burst, which we interpreted as cyclic gas exchange (CGE) with inter‐burst periods, but if the chamber was switched to contain moist air, then cyclic CO₂ release was soon abandoned and a pattern of continuous gas exchange appeared. Measurements with the coulometric respirometer in moist air showed that continuous gas exchange was often associated with weak abdominal pulsations, which we interpreted as active ventilation. Their metabolic rate was lower during gas exchange cycles than during continuous gas exchange. We revealed that in the ladybird beetle metabolic rate increased in moist air when the gas exchange pattern transitioned from cyclic to continuous.     

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.