Infrared photoconductivity and photovoltaic response from nanoscale domains of PbS alloyed with thorium and oxygen.

Thin films of lead sulfide alloyed with thorium and oxygen were deposited on GaAs substrates and processed to produce a photo-diode structure. Structural, optical and electrical characterizations indicate the presence of small nanoscale domains (NDs) that are characterized by dense packaging, high quality interfaces and a blue-shift of the energy bandgap toward the short wavelength infrared range of the spectrum. Photocurrent spectroscopy revealed a considerable photoconductivity that is correlated with excitation of carriers in the NDs of lead sulfide alloyed with thorium and oxygen. Furthermore, the appearance of a photovoltaic effect under near infrared illumination indicates a quasi-type II band alignment at the interface of the GaAs and the film of NDs.

[EVALUATION OF THE HUMAN SENSITIVITY TO SMALLPOX VIRUS BY THE PRIMARY CULTURES OF THE MONOCYTE-MACROPHAGES].

Studies of the primary cultures of granulocytes, mononuclear, and monocyte-macrophage cells derived from human blood were performed using variola virus (VARV) in the doses of 0.001-0.021 PFU/cell (plaques-forming units per cell). Positive dynamics of the virus accumulation was observed only in the monocyte-macrophages with maximum values of virus concentration (5.0-5.5 Ig PFU/ml) mainly within six days after the infection. The fact of VARV replication in the monocyte-macrophages was confirmed by the data of electron microscopy. At the same time, virus vaccines when tested in doses 3.3 and 4.2 Ig PFU/ml did not show the ability to reproduce in these human cells. The people sensitivity to VARV as assessed from the data obtained on human monocyte-macrophages corresponded to -1 PFU (taking into account the smooth interaction of the virus in the body to the cells of this type), which is consistent to previously found theoretical data on the virus sensitivity. The human susceptibility to VARV assessed experimentally can be used to predict the adequacy of developed smallpox models (in vivo) based on susceptible animals. This is necessary for reliable assessment of the efficiency of development of drugs for treatment and prophylaxis of the smallpox.

[THE USE OF THE MODEL MOUSE ICR--VARIOLA VIRUS FOR EVALUATION OF ANTIVIRAL DRUG EFFICACY].

Mice of the ICR outbred population were infected intranasally (i/n) with the variola virus (VARV, strain Ind-3a). Clinical signs of the disease did not appear even at the maximum possible dose of the virus 5.2 lg PFU/head (plaque-forming units per head). In this case, 50% infective dose (ID50) of VARV estimated by the presence or absence of the virus in the lungs three days after infection (p.i.) was equal to 2.7 ± 0.4 lg PFU/head. Taking into account the 10% application of the virus in the lungs during the intranasal infection of the mice, it was adequate to 1.7 lg PFU/lungs. This indicates a high infectivity of the VARV for mice comparable to its infectivity for humans. After the i/n infection of mice with the VARV at a dose 30 ID50/ head the highest concentration of the virus detected in the lungs (4.9 ± 0.0 lg PFU/ml of homogenate) and in nasal cavity tissues (4.8 ± 0.0 lg PFU/ml) were observed. The pathomorphological changes in the respiratory organs of the mice infected with the VARV appeared at 3-5 days p.i., and the VARV reproduction noted in the epithelial cells and macrophages were noticed. When the preparations ST-246 and NIOCH-14 were administered orally at a dose of 60 µg/g of mouse weight up to one day before infection, after 2 hours, 1 and 2 days p.i., the VARV reproduction in the lungs after 3 days p.i. decreased by an order of magnitude. Thus, outbred ICR mice infected with the VARV can be used as a laboratory model of the smallpox when evaluating the therapeutic and prophylactic efficacy of the antismallpox drugs.

Digital laser printing of metal/metal-oxide nano-composites with tunable electrical properties.

We study the electrical properties of aluminum structures printed by the laser forward transfer of molten, femtoliter droplets in air. The resulting printed material is an aluminum/aluminum-oxide nano-composite. By controlling the printing conditions, and thereby the droplet volume, its jetting velocity and duration, it is possible to tune the electrical resistivity to a large extent. The material resistivity depends on the degree of oxidation which takes place during jetting and on the formation of electrical contact points as molten droplets impact the substrate. Evidence for these processes is provided by FIB cross sections of printed structures.

The Possibility of Using the ICR Mouse as an Animal Model to Assess Antimonkeypox Drug Efficacy.

As a result of the conducted experimental studies on intranasal challenge of ICR mice, rabbits and miniature pigs (even in the maximum variant) with the doses of 4.0-5.5 lg PFU of monkeypox virus (MPXV), some clinical signs such as purulent conjunctivitis, blepharitis and ruffled fur were found only in mice. The 50% infective dose (C ID50 ) of MPXV for these animals estimated by the presence of external clinical signs was 4.8 lg PFU, and L ID50 estimated by the virus presence in the lungs of mice 7 days post-infection taking into account its 10% application in the animal respiratory tract was 1.4 lg PFU. When studying the dynamics of MPXV propagation in mice challenged intranasally with 25 L ID50 of MPXV, the maximum pathogen accumulation was revealed in nasal cavity, lungs and brain: 5.7 ± 0.1, 5.5 ± 0.1 and 5.3 ± 0.3 lg PFU/ml, respectively. The pathomorphological examination of these animals revealed the presence and replication of the pathogen in the traditional primary target cells for MPXV (mononuclear phagocyte system cells and respiratory tract epitheliocytes) as well as in some other types of cells (endothelial cells, reticular cells, connective tissue cells). Our use of these animals to assess the antiviral efficacy of some drugs demonstrated the agreement of the results (a significant positive effect of NIOCH-14 and ST-246) with those described in scientific literature, which opens up the prospects of using ICR mice as animal models for monkeypox to develop preventive antismallpox drugs.

Laser jetting of femto-liter metal droplets for high resolution 3D printed structures.

Laser induced forward transfer (LIFT) is employed in a special, high accuracy jetting regime, by adequately matching the sub-nanosecond pulse duration to the metal donor layer thickness. Under such conditions, an effective solid nozzle is formed, providing stability and directionality to the femto-liter droplets which are printed from a large gap in excess of 400 µm. We illustrate the wide applicability of this method by printing several 3D metal objects. First, very high aspect ratio (A/R > 20), micron scale, copper pillars in various configuration, upright and arbitrarily bent, then a micron scale 3D object composed of gold and copper. Such a digital printing method could serve the generation of complex, multi-material, micron-scale, 3D materials and novel structures.

Enhancement in the excitonic spontaneous emission rates for Si nanocrystal multi-layers covered with thin films of Au, Ag, and Al.

The enhancement in the spontaneous emission rate (SER) for Ag, Au, and Al films on multilayer Si nanocrystals (SiNCs) was probed with time-resolved cathodoluminescence (CL). The SiNCs were grown on Si(100) using plasma enhanced chemical vapor deposition. Electron-hole pairs were generated in the metal-covered SiNCs by injecting a pulsed high-energy electron beam through the thin metal films, which is found to be an ideal method of excitation for plasmonic quantum heterostructures and nanostructures that are opaque to laser or light excitation. Spatially, spectrally, and temporally resolved CL was used to measure the excitonic lifetime of the SiNCs in metal-covered and bare regions of the same samples. The observed enhancement in the SER for the metal-covered SiNCs, relative to the SER for the bare sample, is attributed to a coupling of the SiNC excitons with surface plasmon polaritons (SPPs) of the thin metal films. A maximum SER enhancement of ∼2.0, 1.4 and 1.2 was observed for the Ag, Au, and Al films, respectively, at a temperature of 55 K. The three chosen plasmonic metals of Ag, Au, and Al facilitate an interesting comparison of the exciton-SPP coupling for metal films that exhibit varying differences between the surface plasmon energy, ω(sp), and the SiNC excitonic emission energy. A modeling of the temperature dependence of the Purcell enhancement factor, Fp, was performed and included the temperature dependence of the dielectric properties of the metals.

[Evaluation of therapeutic-prophylactic effectiveness of chemical compound NIOC-14 against ectromelia virus in vivo].

AIM: Study pharmacodynamic parameters of anti-viral effectiveness of a chemical compound NIOC-14 in experiments in mice infected with ectromelia virus (EV). MATERIALS AND METHODS: EV (K-1 strain) was obtained from the State Collection of Viral Infections and Rickettsioses Causative Agents of the State Scientific Centre of Virology and Biotechnology "Vector". Outbred ICR mice were intranasally infected with EV at a dose of 10 LD50 per animal (10 x 50% lethal doses/animal) and per orally received NIOC-14 or ST-246 as a positive control. Chemical compound NIOC-14 (7-[N'-(4-trifluoromethylbenzoyl)-hidrazincarbonyl]-tricyclo[3.2.2.0(2,4)]non-8-en-6-carbonic acid) was synthesized in Novosibirsk Institute of Organic Chemistry (NIOC). Anti-pox preparation ST-246, developed by SIGA Technologies Inc. (USA), was synthesized in NIOC using the technique described by the authors. RESULTS: 50% effective doses against EV in vivo were shown not to differ significantly between the preparations NIOC-14 (3.59 µg/g mouse mass) and ST-246 (5.08 µg/g mouse mass). During determination of therapeutic window, administration of NIOC-14 to mice 1 day or 1 hour before EV infection, as well as 1, 2 and 4 days after EV infection and then for 9 days was found to ensure 100% animal survival. Administration of NIOC-14 as well as ST-246 resulted in the decrease relative to control of EV titers in lungs, nasal cavity, brains, liver, spleen, kidneys and pancreas. CONCLUSION: Anti-viral effectiveness of NIOC-14 against EV in vivo was thus comparable by all the studied pharmacodynamic parameters with anti-viral activity of anti-pox-virus preparation ST-246.

[Development of the disease in marmot at the intranasal infection with the monkeypox virus].

In experimental study the sensitivity of the Marmota bobak species to the monkeypox virus (MPXV) with the intranasal (i/n) infection was tested. It was demonstrated that 50% of the infective dose (ID50) of the MPXV on external clinical signs of the disease was 2.2 Ig plaque forming units (PFU). The percentage of the marmot mortality is slightly dependent on the infecting dose of the MPXV, therefore it is not possible to correctly determine the value of 50 % fatal dose (FD50) for these animals. The most pronounced external clinical signs of the disease were obtained in the marmots: pox-like skin rash throughout the surface of the body and mucous membranes, purulent discharge from the nose, lymphadenitis, discoordination, tremor of the extremities, fever, increased aggression, and ruffled fur. In the course of experiments intended to determine the dynamics of the accumulation of the MPXV in various organs, tissues, and blood serum of marmot infected i/n with dose of 3.7 Ig PFU, it was found that the trachea, lungs, and the bifurcation lymph nodes are the primary target organs. The trachea, lungs, nasal mucosa membrane, and skin are the organs with maximal virus replication recorded at 5, 7, 9, and 12 days after the infection. The transfer of the MPXV into the secondary target organs (nasal mucosa membrane, brain, spleen, duodenum, adrenal glands, and skin) was carried out in marmots with lymphogenic and hematogenic ways of the dissemination of the infection.

[A comparative study of the antiviral activity of chemical compounds concerning the orthopoxviruses experiments in vivo].

In the experiments using intranasal (i/n) infection of mice with the ectromelia virus (EV) in a dose 10 LD50/head (10 x 50% lethal doselhead) or with the monkaypox virus (MPXV) in a dose 10 ID50/head (10 x 50% infective dose/ head) it was demonstrated that the antiviral efficiency of chemical compounds - the condensed derivatives of pyrrolidin-2,5-dion, as well as their predecessors and the nearest analogues, synthesized in Novosibirsk Institute of Organic Chemistry of the Siberian Branch of the Russian Academy of Sciences (NIOCH SB RAS) was observed. As a positive control we used the antipoxvirus chemical preparation ST-246 available from SIGA Technologies Inc. (USA), synthesized in NIOCH SB RAS by the technique suggested by the authors. It was demonstrated that the compound NIOCH-14 (7-[N'-(4-Trifluoromethylbenzoil)-hydrazidecarbonil]-tricyclo[3.2.2.02,4]non-8-en-6-carbonic acid) possessed comparable with ST-246 antiviral activity concerning EV and MPXV on all indicators used. Therefore, at infection of mice with EV (strain K-1) and peroral administration of NIOCH-14 and ST-246 in a dose 50 mkg/g of mouse weight (12-14 g) within 10 days the survival rate and average life expectancy of mice authentically exceeded the control levels. EV titers in lungs through 6 days after infection in the same groups were lower than in the control. In addition to that, after 7 days of infection of mice with MPXV (strain V79-1-005) and daily peroral administration of NIOCH-14 and ST-246 in a dose 60 mkg/g of mouse weight (9-11 g) authentic decrease in a part of infected animals and MPXV titers in lungs was observed.

Infection of chickens caused by avian influenza virus A/H5N1 delivered by aerosol and other routes.

This study presents results of the study of infectivity of avian influenza virus (AIV) A subtype H5N1 strains isolated from agricultural birds across the territory of the Russian Federation and CIS countries. The results of the susceptibility of chickens to the AIV isolates delivered by the aerosol route and the dissemination of the virus in the organs of infected birds are presented. As was observed, the sensitivity of birds to AIV by the aerosol route of infection is 30 times higher than by intranasal route, 500 times higher than by the oral route and 10000 times higher than by the intragastric route of infection, which is indicative of higher permissivity of respiratory organs to AIV. The highest titres of AIV A subtype H5N1(A/Chicken/Kurgan/05/2005 strain) in aerosol-infected chickens were found in nasal cavity mucosa, lungs, cloaca, serum and kidney, where viable virus accumulation was detected by 18h post-infection (p.i.). The highest virus titres were observed 54h p.i. in lungs, serum and kidney, reaching the value of 8.16 lg EID50 /g(ml) in the lungs. The results showed that birds infected by the aerosol route developed higher titres of virus than those infected by other routes.

Changes in eggshell conductance, water loss and hatchability of layer hens with flock age and moulting.

1. Changes in water loss, eggshell conductance and hatchability with flock age were monitored in layer hens in a commercial hatchery. 2. Optimal water loss for maximal hatchability of layer eggs was found to be 12 to 13% of initial egg mass at d 18 of incubation. 3. Mass specific water vapour conductance (GH(2)Osp) increased linearly with flock age from 0.31 mg/(d.g.Torr) at the beginning of the first breeding season to 0.40 mg/(d.g.Torr) at its end after 77 weeks (=4.21 and 5.44 mg/(d.100 g.kPa), respectively). 4. After forced moulting GH(2)Osp increased from 0.35 to 0.41 mg/(d.g.Torr) (=4.76 and 5.58 mg/(d.100 g.kPa), respectively). 5. The coefficients of variation of GH(2)Osp increased with flock age from 14% at the beginning of the breeding season to 31% at the end of the second breeding season. 6. In order to preserve normal incubation water loss for maximising hatchability, the humidity setting of an incubator should increase gradually, with flock age, from 53% RH to 66% RH in the first laying season and from 61% RH to 67% RH after forced moulting. 7. A 3.5-fold increase (from 2 to 7%) in the difference between mean and median GH(2)Osp of egg batches with flock age was found, indicating increasing frequency of microscopic cracks in eggshells with flock age. This has to be taken into account when setting the humidity regime in the incubator.

Resonant coupling between surface vibrations and electronic states in silicon nanocrystals at the strong confinement regime.

A striking correlation between infrared photoinduced absorption spectra and the photoluminescence from silicon nanocrystals indicates that quantized electronic sublevels of the nanocrystals are resonantly coupled to surface vibrational modes via a polarization field produced by coherent longitudinal polar vibrations. Our experimental results and model support the assumption that the mechanism responsible for the efficient photoluminescence from silicon nanocrystals should be assigned to inhibition of nonradiative channels rather than enhancement of radiative channels.

Mathematical analysis of atelectasis formation in middle ears with sealed ventilation tubes.

AIM: A mathematical model was developed to identify time periods of atelectasis induction in middle ear (ME) ventilated via ventilating tubes (VT). Atelectatic ears are characterized by a total gas pressure lower than 760 mmHg. METHODS: Ventilating tubes were deliberately sealed and ME gas content changed in the presence of a preset blood gas pressure. Once sealed, CO2 rapidly diffuses out of the blood via lining tissues into the ME cleft. This results in initially a total ME pressure rise followed by a decrease in subatmospheric pressures. Time periods for atelectasis reformation was determined once ME pressure crossed the 760 mmHg value and continued to decline as the atelectasis reached higher grades. RESULTS: Time periods calculated by the model varied from 18 to 125 min in ME cavities ranging in volume from 0.5 to 3.5 mL, respectively. These results were calculated for conditions of venous blood in the lining mucosa blood and are consistent with prior clinical tests that measured an induced return to previous atelectasis state following the closure of the VT in 33 tested ears within 25-120 min (43 min on average). CONCLUSIONS: The model demonstrates that under the above conditions, diffusive gas transfer in relation to blood gas content is the leading mechanism to alterations in ME pressure and volume. It may be used as a tool to determine ME physiological cavity volume of ears with VT.

Gas exchange and energy metabolism of the ostrich (Struthio camelus) embryo.

We measured oxygen consumption (V(O(2))) and carbon dioxide emission (V(CO(2))) rates, air-cell gas partial pressures of oxygen (P(A)O(2)) and CO(2) (P(A)CO(2)), eggshell water vapour conductance and energy content of the ostrich (Struthio camelus) egg, 'true hatchling' and residual yolk, and calculated RQ and total oxygen consumption (V(O(2)tot)) for ostrich eggs incubated at 36.5 degrees C and 25% relative humidity. The V(O(2)) pattern showed a drop of approximately 5% before internal pipping. V(O(2)) just prior to internal pipping agrees with allometric calculations. Despite the higher incubation temperature compared to other studies, and the resultant shorter incubation duration (42 days), V(O(2)tot) (91.7 l kg(-1)) was similar to a previously reported value. RQ values during the second half of incubation (approx. 0.68) were lower than expected for lipid catabolism. Prior to internal pipping, P(A)O(2) and P(A)CO(2) were 98 and 48.3 torr (13.1 and 6.4 kPa), respectively. The growth pattern of the ostrich embryo is different from the typical precocial pattern, showing a time delay in the rapid growth phase. As a result, the lowered overall energy expenditure for tissue maintenance, as compared to other species, is reflected in the low yolk utilization and high residual yolk fraction of the whole hatchling dry mass. These could also result from the relatively short incubation period of the ostrich egg, thereby evading desiccation by excess water loss.

Allometric relationships between embryonic heart rate and fresh egg mass in birds.

Previously, we have measured daily changes (developmental patterns) in embryonic heart rate (fh) in altricial and semi-altricial (ASA) birds (range of mean fresh egg mass approximately 1-20 g), semi-precocial seabirds (egg mass approximately 38-288 g) and precocial birds (egg mass approximately 6-1400 g). An allometric relationship between embryonic fh at 80 % of incubation duration (ID) and fresh egg mass (M) has been derived for six species of precocial bird (fh at 80 % ID=429M(-0.118)). In the present study, additional measurements of embryonic fh in three ASA species, the barn owl Tyto alba, the cattle egret Bubulcus ibis and the lanner falcon Falco biarmicus, were made to extend the egg mass range (20-41 g), and the allometric relationships of embryonic fh for these ASA birds and the precocial and semi-precocial (PSP) groups were investigated from published data. The developmental patterns of embryonic fh in three relatively large ASA species did not show a significant increase prior to the pipping period, unlike those in small ASA birds, but tended to be constant, with a subsequent increase during pipping. The allometric relationship derived for ASA birds was fh at 80 % ID=371M(-0.121) (r=-0.846, P<0.001, N=20) and that for PSP birds was fh at 80 % ID=433M(-0.121) (r=-0.963, P<0.001, N=13). The slopes were parallel, but fh of ASA embryos was low compared with that of PSP embryos with the same egg mass. In ASA birds, embyronic fh was maximal during the pipping (perinatal) period, and the maximum fh (fh(max)) was significantly related to fresh egg mass: fh(max)=440M(-0.127) (r=-0.840, P<0.001, N=20). The allometric relationships for fh at 80 % ID in PSP and fh(max) in ASA embryos were statistically identical. Accordingly, embryonic fh at 80 % ID in PSP birds and fh(max) during pipping in ASA birds can be expressed by a single allometric equation: fh=437M(-0.123) (r=-0.948, P<0.001, N=33).

Embryonic heart rate measurements during artificial incubation of emu eggs.

1. Daily changes in embryonic heart rate (HR) of emu were determined non-invasively at 36 degrees C by acoustocardiography (ACG) during the last 30% of artificial incubation (predicted incubation time is 50 d). 2. The pattern of daily changes in mean HR of hatched embryos decreased from about 175 bpm to about 140 bpm towards the end of incubation. 3. The mean HR at 80% of incubation (ca. 170 bpm) was close to the value predicted from an allometric equation reported previously for precocial domesticated birds. 4. ACG could measure embryonic HR even during the external pipping period. 5. If the artificial external pipping procedure is timed correctly after internal pipping, it might aid the embryos in hatching. However, further investigation into this aspect is needed.

Continuous measurements of instantaneous heart rate and its fluctuations before and after hatching in chickens.

There has been considerable interest in heart rate (fh) fluctuations in relation to cardiovascular control systems and foetal conditions during pregnancy in mammals. Prominent fluctuations in fh also occur in avian embryos, which are an important experimental model for studying developmental physiology. The present study determined the instantaneous fh of seven chick embryos continuously from the last stage of prenatal development (day 18), throughout the pipping (perinatal) period (days 19-21) until hatching and, subsequently, of newly hatched chicks (up to day 2). The distinctive patterns of instantaneous fh fluctuations took the form of specific changes within a broad mean fh baseline. Cyclic oscillations (ultradian rhythm) occurred until an early stage of the perinatal period, when the fh baseline started rising. Subsequently, the baseline dropped and respiratory arrhythmia began to appear concomitant with external pipping. During the final stage of external pipping, when the fh baseline rose again prior to hatching, three unique patterns of instantaneous fh fluctuations were evident: relatively long-lasting cyclic small accelerations, irregular intermittent large accelerations and short-term repeated large accelerations. Furthermore, repeated alternate occurrences of the latter two types of acceleration formed an additional oscillating pattern with a period of 10-15 min. During the early period after hatching, when the fh baseline reached its maximum, instantaneous fh changed relatively slowly accompanied by transient rapid decelerations, probably due to augmented vagal tone. Subsequently, the mean fh baseline dropped to its minimum, and a circadian rhythm and three types of previously reported fh fluctuations (types I-III) appeared. Developmental patterns of mean fh and the appearance of distinctive patterns of instantaneous fluctuations in fh and circadian rhythms were not influenced by an ultimate failure of hatching after a normal development. The demonstration of complex, repeatable patterns of fh fluctuation that change during development suggests that the avian embryo model should be useful in studying the phenomenon of fh fluctuation and its underlying causes.

Effects of drilling holes into the air cell of incubated goose eggs on distribution of oxygen partial pressures under the shell.

The purpose of this work was to measure changes in oxygen pressure in the air cell and under the eggshell (P(A)O2) of pre-pipping goose eggs before and after drilling holes into the air cell. Drilling a 0.6 mm (diameter of 0.9 mm) hole into the air cell caused an increase in air cell P(A)O2 of about 10 Torr. The rate of increase attenuated as hole area increased and reached about 21 Torr when the drilled area was 8.5 mm2. The P(A)O2 of intact eggs was not equally distributed under the shell. It was high in the air cell area (108 Torr) and decreased towards the pointed end (86 Torr). The increase in P(A)O2 after drilling a 4.9 mm2 hole was high in the air cell (18 Torr) and decreased with distance, becoming non-significant at the pointed end. The significant increase in P(A)O2 after drilling was limited to a distance of up to 38 mm along the shell from the edge of the air cell. This indicates that lateral diffusion in the shell membranes under the shell is limited. Drilling a hole of 3.5 to 4.9 mm2 was enough to increase air cell P(A)O2 in most of the eggs above the critical value of 100 Torr for hatching success. The increase in P(A)O2 was limited to about half the area of the shell and the average increase in P(A)O2 was 6.3 Torr (equivalent to a 0.9% increase in ambient O2). However, the blood perfusing chorioallantoic areas further away from the air cell edge may not be fully saturated with O2 and may not be sufficient to compensate fully for the low O2 availability caused by low eggshell conductance.

Analysis of heart rate in developing bird embryos: effects of developmental mode and mass.

Bird embryos may be regarded as developing in their thermo-neutral zone, at rest, and stay in the egg for a fixed period of time until hatching. It is therefore interesting to investigate if they follow the same 'rule' set for adult homeotherms, which states that, within a taxonomically or functionally defined category such as mammals or birds, the number of heart beats throughout the life span (sL) is more or less constant. This rule stems from the allometric relationships between heart rate (fH) and body mass (mB) and between sL and mB. As a step towards understanding the general allometric nature of avian embryonic physiology we analyzed the fH values of avian embryos in relation to their incubation span (sI). Data from 30 species were selected from the scientific literature for the analyses. Values obtained from invasive methods which were judged to grossly alter natural incubation conditions, or from undefined or unmatched temperature conditions were not used. These include most values obtained below the first 30% of the incubation. Also, data obtained after internal pipping were discarded since hatching activity influences them. Values for sI and egg mass (mE) as representatives of embryonic mass were also collected. Embryonic fH was normalized to 70.1-80% sI. At 20.1-30% sI it was only 85% of the value at 70.1-80% sI and increased to a plateau at about 50.1-60% sI. It was almost constant among species between 50.1 and 60% sI and pre-internal pipping (PIP) time and thus, the mean fH value between 50.1 and 60% sI and between 90.1 and 100% excluding pipped eggs (fH) was taken as a representative value for each given species. The fH (min-1) and the corresponding sI (days) values for the 30 species, scaled with mE (g) as follows: fH = 371.1.mE-0.112 and: sI = 12.29.mE+0.209. Both powers were significantly different from 0. The product of fH and sI (fH.sI), representing the total number of heartbeats throughout the incubation, scaled with mE for the entire data set as follows: fH.sI = 6.565 x 10(+6).mE+0.096, where the +0.096 power is significantly different from 0. Values for fH.sI from embryos of altricial birds tended to concentrate at the low mE end of the plot while those of the precocial ones tended towards the high end. Separate analyses showed that the mE power for the combined altricial and semi-altricial species (ASA), and the combined precocial and semi precocial species (PSP), of log fH.sI against log mE regressions, were both insignificantly different from 0. Thus, means of fH.sI for ASA and PSP were calculated. The mean ASA value of 7.27 x 10(+6) heartbeats for fH.sI, was significantly different from the mean PSP value of 10.93 x 10(+6). The difference of 3.66 x 10(-6) (33.5%) heartbeats can be attributed to either the more advanced stage of the PSP hatchlings at hatch, to the larger mE values of these hatchlings, to the difference in water fraction of the hatchlings or all. The result of a linear regression of fH.sI against the rate of sI completion (the inverse of incubation span, fI; day-1) was: fH.10(-6) = 0.205 + 3.940.sI-1. Thus, the faster is the average rate of development accomplished per day (shorter incubation) the higher is daily heart rate. Data tended to cluster such that large eggs, mostly of the PSP type with relatively low fH, complete 2-4% of their incubation per day, while small, ASA type eggs with relatively high fH, complete 6-8% of their incubation time per day. We conclude that, at this stage of knowledge, the data is insufficient to resolve whether the different modes of hatch stage alone can explain differences in the total number of heartbeats throughout embryonic life among all bird species, or egg mass and water content differences contribute variability. This should be investigated on a larger sample of species in more depth.