Cardiorespiratory reflexes and aquatic surface respiration in the neotropical fish tambaqui (<Emphasis Type="Italic">Colossoma macropomum</Emphasis>): acute responses to hypercarbia

We examined the cardiorespiratory responses to 6 h of acute hypercarbia (1, 2.5, and 5% CO₂) in intact and gill-denervated (bilateral denervation of branchial branches of cranial nerves IX and X) tambaqui, Colossoma macropomum. Intact fish exposed to 1 and 2.5% CO₂ increased respiratory frequency (f_R) and ventilation amplitude (V_AMP) slowly over a 1- to 3-h period. Denervated fish did not show this response, suggesting that tambaqui possess receptors in the gills that will produce excitatory responses to low levels of hypercarbia (1 and 2.5% CO₂) if the exposure is prolonged. The cardiac response to stimulation of these receptors with this level of CO₂ was a tachycardia and not a bradycardia. During exposure to 5% CO₂, intact fish increased f_R and V_AMP, and showed a pronounced bradycardia after 1 h. After 2 h, the heart rate (f_H) started to increase, but returned to control values after 6 h. In denervated fish, the increase in f_R was abolished. The slow increase in V_AMP and the bradycardia were not abolished, suggesting that these changes arose from extra-branchial receptors. Neither intact nor denervated fish developed the swelling of the lower lip or performed aquatic surface respiration, even after 6 h, suggesting that these are unique responses to hypoxia and not hypercarbia.Abbreviations ASR aquatic surface respiration - f_H heart frequency - f_R respiratory frequency - V_AMP ventilation amplitude - _TOT total ventilation     

The relationship between O2 chemoreceptors, cardio-respiratory reflex and hypoxia tolerance in the neotropical fish Hoplias lacerdae

The localization, distribution and orientation of O₂ chemoreceptors associated with the control of cardio-respiratory responses were investigated in the neotropical, Hoplias lacerdae. Selective denervation of the cranial nerves (IX and X) was combined with chemical stimulation (NaCN) to characterize the gill O₂ chemoreceptors, and the fish were then exposed to gradual hypoxia to examine the extent of each cardio-respiratory response. Changes in heart rate (f_H) and ventilation amplitude (V_amp) were allied with chemoreceptors distributed on both internal and external surfaces of all gill arches, while ventilation rate (f_R) was allied to the O₂ chemoreceptors located only in the internal surface of the first gill arch. H. lacerdae exposed to gradual hypoxia produced a marked bradycardia (45%) and 50% increase in V_amp, but only a relatively small change in f_R (32%). Thus, the low f_R response yet high V_amp were in accord with the characterization of the O₂ chemoreceptors. Comparing these results from H. lacerdae with hypoxia-tolerant species revealed a relationship existent between general oxygenation of the individual species environment, its cardio-respiratory response to hypoxia and the characterization of O₂ chemoreceptors.     

Cardiorespiratory responses to hypoxia in the African catfish, <Emphasis Type="Italic">Clarias gariepinus</Emphasis> (Burchell 1822), an air-breathing fish

The African catfish, Clarias gariepinus, possesses a pair of suprabranchial chambers located in the dorsal-posterior part of the branchial cavity having extensions from the upper parts of the second and fourth gill arches, forming the arborescent organs. This structure is an air-breathing organ (ABO) and allows aerial breathing (AB). We evaluated its cardiorespiratory responses to aquatic hypoxia. To determine the mode of air-breathing (obligate or accessory), fish had the respiratory frequency (f _R) monitored and were subjected to normoxic water (PwO₂ = 140 mmHg) without becoming hyperactive for 30 h. During this period, all fish survived without displaying evidences of hyperactivity and maintained unchanged f _R, confirming that this species is a facultative air-breather. Its aquatic O₂ uptake ( [(V)\dot]\textO₂ \dot{V}{\text{O}}_{2} ) was maintained constant down to a critical PO₂ (PcO₂) of 60 mmHg, below which [(V)\dot]\textO₂ \dot{V}{\text{O}}_{2} declined linearly with further reductions of inspired O₂ tension (PiO₂). Just above the PcO₂ the ventilatory tidal volume (V _T) increased significantly along with gill ventilation ( [(V)\dot]_\textG \dot{V}_{\text{G}} ), while f _R changed little. Consequently, the water convection requirement ( [(V)\dot]_\textG /[(V)\dot]\textO₂ ) \left( {\dot{V}_{\text{G}} /\dot{V}{\text{O}}_{2} } \right) increased steeply. This threshold applied to a cardiac response that included reflex bradycardia. AB was initiated at PiO₂ = 140 mmHg (normoxia) and air-breathing episodes increased linearly with more severe hypoxia, being significantly higher at PiO₂ tensions below the PcO₂. Air-breathing episodes were accompanied by bradycardia pre air-breath, to tachycardia post air-breath.     

Responses of the teleost Hoplias malabaricus to hypoxia

Synopsis Oxygen uptake (VO₂) during graded hypoxia, rate of hypoxia acclimation, breathing frequency (f_R), breath volume (V_{S, R}) and gill ventilation (V_G) were measured in Hoplias malabaricus. Normoxia and hypoxia acclimated fish had similar and constant VO₂ and V_G in a range of water PO₂ from 150 to 25 mmHg. Hypoxia acclimated fish showed significantly higher VO₂ in severe hypoxia (PO₂ <15 mmHg). Normoxia acclimated fish showed symptoms similar to hypoxic coma after 1 h of exposure to water PO₂ of 10 mmHg whereas the same symptoms were observed only at PO₂ of 5 mmHg for fish acclimated to hypoxia. Fish required 14 days to achieve full acclimation to hypoxia (PO₂ ≥25 mmHg). Lowering of water PO₂ from 150 to 25 mmHg resulted in normoxic fish showing a 3–2 fold increase in V_G. The increase was the result of an elevation in V_{S, R} rather than f_R. Among normoxia acclimated specimens, small fish showed a higher V_G per unit weight than the large ones in both normoxia (PO₂ =150 mmHg) and hypoxia (PO₂ = 15 mmHg). A decrease in the ventilatory requirement (V_G/VO₂) with increased body weight was recorded in hypoxia (PO₂ = 15 mmHg).     

Single measurement reliability and reproducibility of volitional and magnetically-evoked indices of neuromuscular performance in adults

This study documents intra-session and inter-day reproducibility (coefficient of variation [V%]) and single measurement reliability (intra-class correlations [R_I]; standard error of a single measurement [SEM%] [95% confidence limits]) of indices of neuromuscular performance elicited during peripheral nerve magnetic stimulation. Twelve adults (five men and seven women) completed 3 assessment sessions on 3 days, during which multiple assessments of knee flexor volitional and magnetically-evoked indices of electromechanical delay (EMD_V; EMD_E), rate of force development (RFD_V; RFD_E), peak force (PF_V; P_TF_E), and compound muscle action potential latency (LAT_E) and amplitude (AMP_E) were obtained. Results showed that magnetically-evoked indices of neuromuscular performance offered statistically equivalent levels of measurement reproducibility (V%: 4.3–31.2%) and reliability (R_I: 0.98–0.51) compared to volitional indices (V%: 3.7–25.2%; R_I: 0.98–0.64), which support the efficacy of both approaches to assessment and the indices PF_V, EMD_V, EMD_E and LAT_E offer the greatest practical utility for assessing neuromuscular performance.     

Combined ventilatory responses to aerial hypoxia and temperature in the South American lungfish Lepidosiren paradoxa

The control of pulmonary ventilation in South American lungfish Lepidosiren paradoxa is poorly understood. Interactions between temperature and hypoxia are particularly relevant due to large seasonal variations of its habitat. Therefore, we tested the hypothesis that the ventilatory responses to aerial hypoxia of Lepidosiren are highly dependent on ambient temperature. We used a pneumotachograph to measure pulmonary ventilation (V_E), tidal volume (V_T) and respiratory frequency (f_R) during normoxic (21% O₂) and hypoxic (12%, 10% and 7% O₂) conditions at two temperatures (25 and 35 °C). Blood gases, arterial PO₂ (PaO₂), arterial PCO₂ (PaCO₂) and arterial pH (pH_a) were also evaluated. At 25 °C, V_E increased significantly at 10% and 7% hypoxic levels when compared to the control value (21% O₂). At 35 °C, all hypoxic levels elicited a significant increase of V_E relative to control values. V_E is augmented mostly by increases of respiratory frequency (f_R), and there were significant interactions (p<0.001) between aerial hypoxia and temperature. PaCO₂ increased from ∼22 mmHg (normoxic value at 25 °C) to ∼32 mmHg (normoxic value at 35 °C). Concomitantly, the pH_a decreased from 7.51 (25 °C) to 7.38 (35 °C). Hypoxia-induced hyperventilation caused a reduction in PaCO₂ and an increase in pH_a, which were more pronounced at 35 °C than at 25 °C, reflecting an increased hyperventilation under the high temperature. In conclusion, the magnitude of ventilatory response is highly temperature-dependent in L. paradoxa, which is important for an animal experiencing large seasonal variations.     

Separate and combined effects of temperature and hypoxia on breathing pattern in the domestic fowl

Summary Minute ventilation (V _E), tidal volume (V _T), respiratory frequency (f) and clavicular air sac gas composition were measured in conscious domestic fowl breathing air and hypoxic gas mixtures at neutral (18±1°C) and raised (33±1°C) air temperatures. Increases inV _E caused by inhalation of 10%, 8% or 6.5% O₂ in N₂, respectively, were independent of temperature although at each level the absoluteV _E was ca. 21·min⁻¹ greater in the panting birds. Changes in respiratory pattern during hypoxia were markedly dependent on temperature. At 18°C almost all of the increasedV _E resulted from increasedf. At 33°C hypoxia led to a strong suppression off and increase inV _T. It is concluded that hyperthermia and hypoxia are additive and non-interactive in their effects on ventilatory drive, in agreement with previously reported effects of hypercapnia and physical exercise on breathing in panting fowl.     

Relationship between oxygen saturation of mixed venous blood and pressure in the pulmonary artery trunk in healthy humans and patients with heart defects

The relationship between pulmonary artery pressure (P _LA) and oxygen saturation of mixed venous blood (S _V ) has been studied in subjects (1750 men and 1026 women) subdivided into 12 groups. Functional relationships have been found between P _LA and S _V , P _LA = f(S _V ), and S _V = f(P _LA), which were estimated using direct measurement of P _LA and S _V for each group. These factors have been found to obey the following dependences: P _LA = f(S _V ) and P _LA = a(S _V )^−b , where b = −0.2284a + 0.6564 in men and b = −0.285a + 1.2947 in women; S _V = f(P _LA) and S _V = c(P _LA)^−d , where d = −0.25131Ln(c) + 1.0212; R ² = 0.8993 in men and d = −1.9645Ln(c) + 2.852; and R ² = 0.9674 in women. Each group occupies a position on the curves specified by the equations. Subjects with the diagnosis of a functional heart murmur and patients with congenital aortic valve stenosis were grouped together to form the so-called normal group characterized by specific P _LA = f(S _V ) and S _V = f(P _LA) dependences. Male patients with coronary heart disease were also included in the normal group. An equation was derived to relate P _LA caused by different reasons with the corresponding saturation of mixed venous blood. In the case of the changing saturation of mixed venous blood, this equation gives the corresponding value of P _LA. Equilibrium between systemic and pulmonary circulations is established through interdependent changes in the physiological indices of blood circulation and gas exchange in humans.     

Carapace movements aid air breathing in the semaphore crab,Heloecius cordiformis (Decapoda: Brachyura: Ocypodidae)

Summary While on land and recirculating branchial water the Australian semaphore crab Heloecius cordiformis (Decapoda: Ocypodidae), a semi-terrestrial airbreathing mangrove crab, sequentially depresses and elevates its carapace in a regular pump-like manner. The functional role of these carapace movements in aerial oxygen consumption is investigated. Carapace immobilisation (reversible and non-injurious) did not appear to affect branchial water circulation. In dry crabs (branchial water removed) carapace immobilisation had no effect on the rate of oxygen consumption (VO₂), heart rate or whole-body lactate (WBL) levels. In wet crabs (with branchial water) carapace immobilisation caused VO₂ to drop by 38% from 81 to 46 l O₂ · g^-1 · h^-1, heart rate to decline by 32%, from 2.5 to 1.7 Hz, and WBL levels to increase over 2.5-fold, from 0.27 to 0.67 mg · g^-1, after 3 h of carapace immobilisation. The (VO₂) of carapace-immobilised crabs with branchial water was similar to lung-occluded crabs with branchial water. Severe hypoxia induced physiological responses similar to those of carapace-immobilised crabs with branchial water. After 3 h of severe hypoxia, heart rate had declined by 80%, from 2.2 to 0.43 Hz, and the incidence of carapace pumping slowed by 85%, from 2.4 to 0.37 cycles · min^-1. It is concluded that in the absence of carapace movements branchial water in some way inteferes with lung ventilation. Under normal circumstances water circulation and lung ventilation are mutually exclusive processes (due to their singular dependence on the scaphognathites), yet in Heloecius these processes must be carried out simultaneously. Carapace movements may alleviate this conflict.Abbreviations FF, FR, SF, SR fast-forward, fast-reverse, slow-forward, slow-reverse scaphognathite pumping - MEA Milne Edwards aperture - VO₂ rate of oxygen consumption - WBL whole-body lactate     

Partitioning of Respiration in an Intensively Managed Grassland

Total (R_TOT) and heterotrophic (R_H) respiration were measured in an intensively managed perennial ryegrass (Lolium perenne L.) grassland. The overall aim of the study was to partition R_TOT into R_H and autotrophic respiration (R_A). This was achieved as follows: (1) analyse the effect of air temperature, soil moisture content and leaf area index on R_TOT and the influence of soil temperature and soil moisture content on R_H; (2) combine these effects into separate empirical models for R_TOT and R_H and; (3) use these models to determine temporal trends in R_TOT and R_H and to assess the relative contribution of R_H and R_A to R_TOT. CO₂ fluxes were measured using a vented and thermostatically controlled perspex chamber in conjunction with a portable infrared gas analyser. R_TOT was measured in plots with grass and R_H in plots with bare soil. R_TOT was related to air temperature and R_H to soil temperature using exponential relationships. Both R_TOT and R_H were related to soil moisture content using lognormal relationships. R_TOT was related to leaf area index using a linear relationship. These relationships were combined to produce statistical response functions that explained 87% and 84% of the variation in R_TOT and R_H, respectively. These relationships were combined with meteorological and leaf area index data to reconstruct daily and seasonal fluxes. R_TOT values in wintertime were ~4 g C m⁻² day⁻¹ increasing to ~10 g C m⁻² day⁻¹ in summertime when temperatures and leaf area index were higher and soils were drier. R_H has a similar seasonal trend to R_TOT but was consistently lower. Wintertime values were ~2 g C m⁻² day⁻¹ and increased to ~5 g C m⁻² day⁻¹ in summertime. Before day of year 143, and after day of year 259 R_H and R_A represented 62% and 38% of R_TOT, respectively. In the period between these days R_H and R_A both accounted for 50% of R_TOT. In total during 2004 R_TOT, R_H and R_A were 2.34, 1.31 and 1.03 kg C m⁻², respectively.     

Cardiorespiratory responses of the woodchuck and porcupine to CO2 and hypoxia

Summary The burrow-dwelling woodchuck (Marmota monax) (mean body wt.=4.45±1 kg) was compared to a similar-sized (5.87±1.5 kg) but arboreal rodent, the porcupine (Erithrizon dorsatum), in terms of its ventilatory and heart rate responses to hypoxia and hypercapnia, and its blood characteristics.V _T,f,T _I andT _E were measured by whole-body plethysmography in four awake individuals of each species. The woodchuck has a longerT _E/T _TOT (0.76±0.03) than the porcupine (0.61±0.03). The woodchuck had a higher threshold and significantly smaller slope to its CO₂ ventilatory response compared to the porcupine, but showed no difference in its hypoxic ventilatory response. The woodchuck P₅₀ of 27.8 was hardly different from the porcupine value of 30.7, but the Bohr factor, –0.72, was greater than the porcupine's, –0.413. The woodchuck breathing air has PaCO₂=48 (±2) torr, PaO₂=72 (±6), pHa=7.357 (±0.01); the porcupine blood gases are PaCO₂=34.6 (±2.8), PaO₂=94.9 (±5), pHa=7.419 (±0.03), suggesting a difference in PaCO₂/pH set points. The woodchuck exhibited no reduction in heart rate with hypoxia, nor did it have the low normoxic heart rate observed in other burrowing mammals.     

Circulatory function at sub-zero temperature: venous responses to catecholamines and angiotensin II in the Antarctic fish <Emphasis Type="Italic">Pagothenia borchgrevinki</Emphasis>

Catecholamines increase arterial pressure by increasing cardiac output (Q) and stroke volume (V _s), while angiotensin II (ang II) also increases vascular resistance (R _sys) in the Antarctic fish Pagothenia borchgrevinki. Adrenaline, phenylephrine and ang II (Asn¹, Val⁵) were injected into P. borchgrevinki. Cardiovascular variables, including central venous pressure (P _cv) and mean circulatory filling pressure (P _mcf; an index of venous capacitance), were recorded to investigate if venous vasoconstriction can explain the increased V _s and Q and the arterial pressor response in this species. Routine P _cv and P _mcf were 0.11 ± 0.01 and 0.18 ± 0.02 kPa, respectively. All of the drugs caused moderate increases in P _cv and P _mcf and the responses were attenuated after α-adrenergic blockade with prazosin. Although dorsal aortic pressure (P _da) also increased in response to all agonists, the mechanisms differed. Adrenaline caused sustained increases in V _s and Q, while R _sys only rose transiently. Ang II had a slower effect than adrenaline and increased both R _sys and Q, while phenylephrine only increased R _sys. This study demonstrates that P _cv is positive and controlled by an α-adrenergic mechanism in P. borchgrevinki. However, given the relatively small venous response to adrenaline it seems more likely that the increases in V _s and Q from this agonist are due to direct effects on the heart.     

Gill chemoreceptors and cardio-respiratory reflexes in the neotropical teleost pacu, <Emphasis Type="Italic">Piaractus mesopotamicus</Emphasis>

This study examined the location and distribution of O₂ chemoreceptors involved in cardio-respiratory responses to hypoxia in the neotropical teleost, the pacu (Piaractus mesopotamicus). Intact fish and fish experiencing progressive gill denervation by selective transection of cranial nerves IX and X were exposed to gradual hypoxia and submitted to intrabuccal and intravenous injections of NaCN while their heart rate, ventilation rate and ventilation amplitude were measured. The chemoreceptors producing reflex bradycardia were confined to, but distributed along all gill arches, and were sensitive to O₂ levels in the water and the blood. Ventilatory responses to all stimuli, though modified, continued following gill denervation, however, indicating the presence of internally and externally oriented receptors along all gill arches and either in the pseudobranch or at extra-branchial sites. Chemoreceptors located on the first pair of gill arches and innervated by the glossopharyngeal nerve appeared to attenuate the cardiac and respiratory responses to hypoxia. The data indicate that the location and distribution of cardio-respiratory O₂ receptors are not identical to those in tambaqui (Colossoma macropomum) despite their similar habitats and close phylogenetic lineage, although the differences between the two species could reduce to nothing more than the presence or absence of the pseudobranch.     

Oxygen transport and cardiovascular responses in skipjack tuna (Katsuwonus pelamis) and yellowfin tuna (Thunnus albacares) exposed to acute hypoxia

Summary Responses to acute hypoxia were measured in skipjack tuna (Katsuwonus pelamis) and yellowfin tuna (Thunnus albacares) (1–3 kg body weight). Fish were prevented from making swimming movements by a spinal injection of lidocaine and were placed in front of a seawater delivery pipe to provide ram ventilation of the gills. Fish could set their own ventilation volumes by adjusting mouth gape. Heart rate, dorsal and ventral aortic blood pressures, and cardiac output were continuously monitored during normoxia (inhalant water (PO ₂>150 mmHg) and three levels of hypoxia (inhalant water PO ₂130, 90, and 50 mmHg). Water and blood samples were taken for oxygen measurements in fluids afferent and efferent to the gills. From these data, various measures of the effectiveness of oxygen transfer, and branchial and systemic vascular resistance were calculated. Despite high ventilation volumes (4–71·min^-1·kg^-1), tunas extract approximately 50% of the oxygen from the inhalant water, in part because high cardiac outputs (115–132 ml·min^-1·kg^-1) result in ventilation/perfusion conductance ratios (0.75–1.1) close to the theoretically ideal value of 1.0. Therefore, tunas have oxygen transfer factors (ml O₂·min^-1·mmHg^-1·kg^-1) that are 10–50 times greater than those of other fishes. The efficiency of oxygen transfer from water in tunas (65%) matches that measured in teleosts with ventilation volumes and order of magnitude lower. The high oxygen transfer factors of tunas are made possible, in part, by a large gill surface area; however, this appears to carry a considerable osmoregulatory cost as the metabolic rate of gills may account for up 70% of the total metabolism in spinally blocked (i.e., non-swimming) fish. During hypoxia, skipjack and yellowfin tunas show a decrease in heart rate and increase in ventilation volume, as do other teleosts. However, in tunas hypoxic bradycardia is not accompanied by equivalent increases, in stroke volume, and cardiac output falls as HR decreases. In both tuna species, oxygen consumption eventually must be maintained by drawing on substantial venous oxygen reserves. This occurs at a higher inhalant water PO₂ (between 130 and 90 mmHg) in skipjack tuna than in yellowfin tuna (between 90 and 50 mmHg). The need to draw on venous oxygen reserves would make it difficult to meet the oxygen demand of increasing swimming speed, which is a common response to hypoxia in both species. Because yellowfin tuna can maintain oxygen consumption at a seawater oxygen tension of 90 mmHg without drawing on venous oxygen reserves, they could probably survive for extended periods at this level of hypoxia.Abbreviations BP_da, BP_va dorsal, ventral aortic blood pressure - C _aO₂, C _vO₂ oxygen content of arterial, venous blood - DO₂ diffusion capacity - E_b, E_w effectiveness of O₂ uptake by blood, and from water, respectively - Hct hematocrit - HR heart rate - PCO₂ carbon dioxide tension - P _aCO₂, P _vCO₂ carbon dioxide tension of arterial and venous blood, respectively - PO₂ oxygen tension - P _aO₂, P _vO₂, P _iO₂, P _cO₂ oxygen tension of arterial blood, venous blood, and inspired and expired water, respectively - pHa, pHv pH of arterial and venous blood, respectively - P_w—b effective water to blood oxygen partial pressure difference - Pg partial pressure (tension) gradient - cardiac output - R vascular resistance - SV stroke volume - SEM standard error of mean - TO₂ transfer factor - U utilization - _g ventilation volume - O₂ oxygen consumption     

The effects of endogenous or exogenous catecholamines on blood respiratory status during acute hypoxia in rainbow trout (Oncorhynchus mykiss)

Summary An extracorporeal circulation of rainbow trout (Oncorhynchus mykiss) was utilized to continuously monitor the rapid and progressive effects of endogenous or exogenous catecholamines on blood respiratory/acid-base status, and to provide in vivo evidence for adrenergic retention of carbon dioxide (CO₂) in fish blood (cf. Wood and Perry 1985). Exposure of fish to severe aquatic hypoxia (final P _wO₂=40–60 torr; reached within 10–20 min) elicited an initial respiratory alkalosis resulting from hypoxia-induced hyperventilation. However, at a critical arterial oxygen tension (P _aO₂) between 15 and 25 torr, fish became agitated for approximately 5 s and a marked (0.2–0.4 pH unit) but transient arterial blood acidosis ensued. This response is characteristic of abrupt catecholamine mobilization into the circulation and subsequent adrenergic activation of red blood cell (RBC) Na⁺/H⁺ exchange (Fievet et al. 1987). Within approximately 1–2 min after the activation of RBC Na⁺/H⁺ exchange by endogenous catecholamines, there was a significant rise in arterial PCO₂ (P _aCO₂) whereas arterial PO₂ was unaltered; the elevation of P _aCO₂ could not be explained by changes in gill ventilation. Pre-treatment of fish with the -adrenoceptor antagonist phentolamine did not prevent the apparent catecholamine-mediated increase of P _aCO₂. Conversely, pre-treatment with the -adrenoceptor antagonist sotalol abolished both the activation of the RBC Na⁺/H⁺ antiporter and the associated rise in P _aCO₂, suggesting a causal relationship between the stimulation of RBC Na⁺/H⁺ exchange and the elevation of P _aCO₂. To more clearly establish that elevation of plasma catecholamine levels during severe hypoxia was indeed responsible for causing the elevation of P _aCO₂, fish were exposed to moderate hypoxia (final P _wO₂=60–80 torr) and then injected intraarterially with a bolus of adrenaline to elicit an estimated circulating level of 400 nmol·l^-1 immediately after the injection. This protocol activated RBC Na⁺/H⁺ exchange as indicated by abrupt changes in arterial pH (pHa). In all fish examined, P _aCO₂ increased after injection of exogenous adrenaline. The effects on P _aO₂ were inconsistent, although a reduction in this variable was the most frequent response. Gill ventilation frequency and amplitude were unaffected by exogenous adrenaline. Therefore, it is unlikely that ventilatory changes contributed to the consistently observed rise in P _aCO₂. Pretreatment of fish with sotalol did not alter the ventilatory response to adrenaline injection but did prevent the stimulation of RBC Na⁺/H⁺ exchange and the accompanying increases and decreases in P _aCO₂ and P _aO₂, respectively. These results suggest that adrenergic elevation of P _aCO₂, in addition to the frequently observed reduction of P _aO₂ are linked to activation of RBC Na⁺/H⁺ exchange. The physiological significance and the potential mechanisms underlying the changes in blood respiratory status after addition of endogenous or exogenous catecholamines to the circulation of hypoxic rainbow trout are discussed.Abbreviations P _aCO₂ arterial carbon dioxide tension - P _aO₂ arterial oxygen tension - P _da dorsal aortic pressure - pHa arterial pH - P _wO₂ water oxygen tension - RBC red blood cell - V _f breathing frequency     

Acclimation of photosynthetic capacity to irradiance in tree canopies in relation to leaf nitrogen concentration and leaf mass per unit area

The observation of acclimation in leaf photosynthetic capacity to differences in growth irradiance has been widely used as support for a hypothesis that enables a simplification of some soil‐vegetation‐atmosphere transfer (SVAT) photosynthesis models. The acclimation hypothesis requires that relative leaf nitrogen concentration declines with relative irradiance from the top of a canopy to the bottom, in 1 : 1 proportion. In combination with a light transmission model it enables a simple estimate of the vertical profile in leaf nitrogen concentration (which is assumed to determine maximum carboxylation capacity), and in combination with estimates of the fraction of absorbed radiation it also leads to simple ‘big‐leaf’ analytical solutions for canopy photosynthesis. We tested how forests deviate from this condition in five tree canopies, including four broadleaf stands, and one needle‐leaf stand: a mixed‐species tropical rain forest, oak (Quercus petraea (Matt.) Liebl), birch (Betula pendula Roth), beech (Fagus sylvatica L.) and Sitka spruce (Picea sitchensis (Bong.) Carr). Each canopy was studied when fully developed (mid‐to‐late summer for temperate stands). Irradiance (Q, µmol m^?2 s^?1) was measured for 20 d using quantum sensors placed throughout the vertical canopy profile. Measurements were made to obtain parameters from leaves adjacent to the radiation sensors: maximum carboxylation and electron transfer capacity (V_a, J_a, µmol m^?2 s^?1), day respiration (R_da, µmol m^?2 s^?1), leaf nitrogen concentration (N_m, mg g^?1) and leaf mass per unit area (L_a, g m^?2). Relative to upper‐canopy values, V_a declined linearly in 1 : 1 proportion with N_a. Relative V_a also declined linearly with relative Q, but with a significant intercept at zero irradiance (P < 0·01). This intercept was strongly related to L_a of the lowest leaves in each canopy (P < 0·01, r² = 0·98, n= 5). For each canopy, daily lnQ was also linearly related with lnV_a(P < 0·05), and the intercept was correlated with the value for photosynthetic capacity per unit nitrogen (PUN: V_a/N_a, µmol g^?1 s^?1) of the lowest leaves in each canopy (P < 0·05). V_a was linearly related with L_a and N_a(P < 0·01), but the slope of the V_a : N_a relationship varied widely among sites. Hence, whilst there was a unique V_a : N_a ratio in each stand, acclimation in V_a to Q varied predictably with L_a of the lowest leaves in each canopy. The specific leaf area, L_m(cm² g^?1), of the canopy‐bottom foliage was also found to predict carboxylation capacity (expressed on a mass basis; V_m, µmol g^?1 s^?1) at all sites (P < 0·01). These results invalidate the hypothesis of full acclimation to irradiance, but suggest that L_a and L_m of the most light‐limited leaves in a canopy are widely applicable indicators of the distribution of photosynthetic capacity with height in forests.     

Vascular resistance and vasoactivity of gills and pulmonary artery of the salamander,Ambystoma tigrinum

Summary In order to understand the blood flow patterns and their regulation in the gills and pulmonary artery ofAmbystoma tigrinum, the vascular resistance and vasoactivity of the two major branchial perfusion pathways and a vascular plexus in the pulmonary artery were investigated using an isolated-tissue perfusion method. Acetylcholine and epinephrine were both pressor agents in all three vascular segments. Angiotensin II also constricted the branchial respiratory vasculature. Norephinephrine was primarily a vasodilator in the branchial respiratory vasculature, however, it had no effect on the shunt vessels of the gill or the pulmonary arterial plexus. Both gill circulations were insensitive to alterations in CO₂ and pH. Anoxia produced a slight vasodilation of the branchial respiratory vessels but had no effect on the shunt vasculature. Mild hypoxia had no effect on either branchial circulations. The results suggest that: (1) blood flow through the respiratory section of the gill may vary between 8 and 47% of total gill flow, (2) the major perfusion pathway to the lung is probably from the efferent artery of the third gill through the ductus arteriosus and then into the pulmonary artery, (3) O₂, CO₂ and pH exert no local control of branchial perfusion, (4) both cholinergic and adrenergic regulation of branchial and proximal pulmonary arterial vascular resistance is possible, (5) a rise in circulating norepinephrine should increase blood flow to the respiratory section of the gill.Abbreviations AII angiotensin II - ACh acetylcholine - EPi epinephrine - NE norepinephrine     

In vivo nuclear magnetic resonance studies on the lugworm Arenicola marina. I. Free inorganic phosphate and free adenylmonophosphate concentrations in the body wall and their dependence on hypoxia

The cytoplasmic concentrations of free inorganic phosphate and free AMP in the body wall of the lugworm Arenicola marina were estimated in order to verify their proposed regulatory role in glycogenolysis during anaerobiosis (Kamp 1993). Using in vivo ³¹P nuclear magnetic resonance spectroscopy the concentration of free inorganic phosphate was determined to be 4.7±0.7 mmol·1^-1 (±standard deviation, n=3) varying with season (Juretschke and Kamp 1995). These values were two to three times lower than those measured in perchloric acid extracts. In contrast, values for the phosphagen phosphotaurocyamine assessed biochemically in the extracts and by in vivo nuclear magnetic resonance were very similar. During the transition from normoxia to hypoxia the concentration of free inorganic phosphate increased to the same extent and at the same rate as the concentration of phosphotaurocyamine decreased. A discrepancy was also found for the biochemically determined AMP and ADP concentrations in the extract and those derived from the equilibrium constants of the taurocyamine kinase (ADP_free) and adenylate kinase (AMP_free) reactions. Calculated concentrations of ADP_free and AMP_free in normoxic specimens were about two or even four orders of magnitude lower than the values determined in extracts. During hypoxia the concentrations of AMP and ADP increase moderately when measured biochemically in extracts, while the values for ADP_free and AMP_free rise three- and nine-fold during the first 3 h of hypoxia. Thereafter, the levels stay constant due to a progressive acidosis. If during hypoxia pH_i is stabilized by addition of buffering substances to the incubation medium, both ADP_free and AMP_free rise continuously. The significant changes found for the concentrations of free inorganic phosphate and AMP_free support their assumed regulatory role in glycogenolysis during anaerobiosis, though these AMP_free values seem too low to actually activate glycogen phosphorylase. The strong effect of pH_i on the levels of ADP_free and AMP_free suggest a mechanism by which acidosis prevents a continuing increase of glycogenolysis (ATP-producing pathway) during prolonged anaerobiosis (protective effect of acidosis).Abbreviations ADP _free cytoplasmic adenosine diphosphate - AK adenylate kinase - AMP _free cytoplasmic adenosine monophosphate - CK creatine kinase - GPase glycogen phosphorylase - MW molecular weight - Int P _i integral of P_i-signal - NMR nuclear magnetic resonance - P _i-free cytoplasmic inorganic phosphate - PCA perchlori acid - PFK 6-phosphofructokinase - PME phosphomonoester - PPA phenylphosphonic acid - (P)Tc (phospho)taurocyamine - S _f saturation factor - Sw sea water - TcK taurocyamine kinase - TRA triethanolamine - TRIS tris(hydroxymethyl)aminomethane     

Ventilatory physiology of the numbat (<Emphasis Type="Italic">Myrmecobius fasciatus</Emphasis>)

This study examines the ventilatory physiology of the numbat (Myrmecobius fasciatus), a small to medium-sized (550 g) termitivorous marsupial. Ventilatory parameters at thermoneutrality reflect the slightly low (83% of predicted) basal metabolic rate of the numbat, with ventilation frequency (ƒ_R; 30.6±3.65 breaths min^–1), tidal volume [V_T; 6.0±0.66 ml at body temperature and pressure, saturated (BTPS)] and consequently minute volume (V_I; 117.7±15.22 ml min^–1; BTPS) all being 80–87% of that expected for a marsupial of similar body mass. Oxygen extraction was 27.7±1.37% in the thermoneutral zone. As is typical of marsupials, numbats accommodated increased oxygen consumption rates at ambient temperatures (T _a) below the thermoneutral zone by increasing minute volume (up to 411.2±43.98 ml min^–1; BTPS at T _a=10 °C) rather than oxygen extraction. Minute volume at 10 °C increased more by changes in ventilation frequency (up to 45.5±4.85 breaths min^–1) than tidal volume (9.4±1.03 ml, BTPS), as is also typical for a small-medium sized marsupial.Abbreviations BMR basal metabolic rate - BTPS body temperature and pressure, saturated - EO ₂ oxygen extraction - ƒ _R ventilation frequency - STPD standard temperature and pressure, dry - T _a ambient temperature - T _b body temperature - TNZ thermoneutral zone - V _I minute volume - V _T tidal volume - O ₂ oxygen consumption rate Communicated by I.D. Hume