Are the surface areas of the gills and body involved with changing metabolic scaling with temperature?

The metabolic-level boundaries (MLB) hypothesis proposes that metabolic level mediates the relative influence of surface area (SA)- versus volume-related metabolic processes on the body-mass scaling of metabolic rate in organisms. The variation in the scaling of SA may affect how metabolic level affects the metabolic scaling exponent. This study aimed to determine the influence of increasing metabolic level at a higher temperature on the metabolic scaling exponent of the goldfish and determine the link between metabolic scaling exponents and SA parameters of both gills and body. The SA of gills and body and the resting metabolic rate (RMR) of the goldfish were assessed at 15°C and 25°C, and their mass scaling exponents were analyzed. The results showed a significantly higher RMR, with a lower scaling exponent, in the goldfish at a higher temperature. The SA of the gills and the total SA of the fish (TSA) were reduced with the increasing temperature. The scaling exponent of RMR (bRMR) tended to be close to that of the TSA at a higher temperature. This suggests that temperature positively affects metabolic level but negatively affects bRMR The findings support the MLB hypothesis. The lower scaling exponent at a higher temperature can be alternatively explained as follows: the higher viscosity of cold water impedes respiratory ventilation and oxygen uptake and reduces metabolic rate more in smaller individuals than in larger individuals at lower temperature, thus resulting in a negative association between temperature and bRMR.

High-Performance Solar-Blind Ultraviolet Photodetectors Based on ß-Ga2O3 Thin Films Grown on p-Si(111) Substrates with Improved Material Quality via an AlN Buffer Layer Introduced by Metal-Organic Chemical Vapor Deposition.

We have achieved significantly improved device performance in solar-blind deep-ultraviolet photodetectors fabricated from ß-Ga2O3 thin films grown via metal-organic chemical vapor deposition (MOCVD) on p-Si(111) substrates by improving material quality through the use of an AlN buffer layer. High-structural-quality ß-Ga2O3 films with a (-201) preferred orientation are obtained after the introduction of the AlN buffer. Under 3 V bias, the dark current reaches a minimum of 45 fA, and the photo-to-dark current ratio (PDCR) reaches 8.5 × 105 in the photodetector with the metal-semiconductor-metal (MSM) structure. The peak responsivity and detectivity are 38.8 A/W and 2.27 × 1015 cm·Hz1/2/W, respectively, which are 16.5 and 230 times that without the buffer layer. Additionally, benefiting from the introduction of the AlN layer, the photodetection performance of the ß-Ga2O3/AlN/Si heterojunction is significantly improved. The PDCR, peak responsivity, and detectivity for the ß-Ga2O3/AlN/p-Si photodetector at 5 V bias are 2.7 × 103, 11.84 A/W, and 8.31 × 1013 cm·Hz1/2/W, respectively. The improved structural quality of ß-Ga2O3 is mainly attributed to the decreased in-plane lattice mismatch of 2.3% for ß-Ga2O3(-201)/AlN(002) compared to that of 20.83% for ß-Ga2O3(-201)/Si(111), as well as the elimination of the native amorphous SiOx surface layer on the Si substrate during the initial growth of oxide thin films.

A high responsivity, high detectivity, and high response speed MSM UVB photodetector based on SnO2 microwires.

We report a high performance UVB photodetector with a metal-semiconductor-metal device structure based on high crystal quality SnO2 microwires prepared by chemical vapor deposition. Under 10 V bias, a low dark current of 3.69 × 10-9 A and a high light-to-dark current ratio of 1630 were achieved. The device showed a high responsivity of about 1353.0 A·W-1 under 322 nm light illumination. The detectivity of the device is as high as 5.4 × 1014 Jones, which ensures the detection of weak signals in the UVB spectral region. Due to the small amount of deep-level defect-induced carrier recombination, the light response rise time and fall time are shorter than 0.08 s.

Rapid Response Solar Blind Deep UV Photodetector with High Detectivity Based On Graphene:N/ßGa2 O3 :N/GaN p-i-n Heterojunction Fabricated by a Reversed Substitution Growth Method.

This work reports a high-detectivity solar-blind deep ultraviolet photodetector with a fast response speed, based on a nitrogen-doped graphene/ßGa2 O3 /GaN p-i-n heterojunction. The i layer of ßGa2 O3 with a Fermi level lower than the central level of the forbidden band of 0.2 eV is obtained by reversed substitution growth with oxygen replacing nitrogen in the GaN matrix, indicating the majority carrier is hole. X-ray diffractometershows that the transformation of GaN into ßGa2 O3 with (-201) preferred orientation at temperature above 900 °C in an oxygen ambient. The heterojunction shows enhanced self-powered solar blind detection ability with a response time of 3.2 µs (rise)/0.02 ms (delay) and a detectivity exceeding 1012 Jones. Under a reverse bias of -5 V, the photoresponsivity is 8.3 A W-1 with a high Ilight /Idark ratio of over 106 and a detectivity of ≈9 × 1014 Jones. The excellent performance of the device is attributed to 1) the continuous conduction band without a potential energy barrier, 2) the larger built-in potential in the heterojunction because of the downward shift of Fermi energy level in ß-Ga2 O3 , and 3) an enhanced built-in electric field in the ßGa2 O3 due to introducing p-type graphene with a high hole concentration of up to ≈1020 cm-3 .

Individual variation in metabolic rate, locomotion capacity and hypoxia tolerance and their relationships in juveniles of three freshwater fish species.

Individual variations in metabolic rate, locomotion capacity and hypoxia tolerance and their relationships were investigated in three cyprinid species [crucian carp (Carassius auratus), common carp (Cyprinus carpio) and qingbo (Spinibarbus sinensis), in 60 individuals of each species]. Either the active metabolic rate (AMR) and critical swimming speed (Ucrit) (30 individuals) or critical oxygen tension (Pcrit) and loss of equilibrium (LOE) (30 individuals) were measured in each species after measuring the resting metabolic rate (RMR). Both the AMR and Ucrit were found to be significantly and positively correlated with the RMR in all three cyprinid species, indicating that high-RMR individuals have high aerobic capacity and thus good swimming performance. Pcrit was positively correlated with the RMR in all three species, whereas the LOE was highly positively correlated, weakly positively correlated and not correlated with the RMR in qingbo, common carp and crucian carp, respectively, possibly due to specialized morphological and biochemical adaptations involved in hypoxia tolerance in crucian and common carp. Crucian carp showed relatively poor swimming performance, i.e., a low Ucrit (relatively high variation), strong hypoxia tolerance, and low LOE (relatively low variation); qingbo showed relatively good swimming performance (relatively low variation) and weak hypoxia tolerance (relatively high variation); and common carp showed moderate swimming performance and relatively strong hypoxia tolerance (moderate variation). These interspecific differences may be due to the different lifestyles of these cyprinid fishes based on their associated fast-slow-flow regime and are outcomes of long-term selection.

Ventilation Frequency Reveals the Roles of Exchange Surface Areas in Metabolic Scaling.

The surface area (SA) theory proposes that resting metabolic rate (RMR) scales with body mass, which parallels the exchange SA of organisms, and that a species with a larger scaling exponent of exchange SA has a larger scaling exponent of RMR. However, the effects of exchange SA on metabolic scaling may be eclipsed because oxygen transfer across the respiratory surface is determined not only by the exchange SA but also by ventilation. We hypothesize that the scaling of both gill surface area (GSA) and ventilation frequency (VF) positively affects the scaling of metabolic rate. In six closely related species of carp maintained under the same experimental conditions, the scaling exponents of RMR and GSA were analyzed. In the goldfish, RMR scaled with body mass by an exponent significantly lower than that of GSA but not different from the exponents of GSA in the remaining five species. The scaling exponent of RMR was positively related to those of both GSA and VF among the species. In addition, the VF-corrected metabolic scaling exponent was positively related to the scaling exponent of GSA among the species. These results suggest that variations in GSA scaling and in VF scaling among species mutually affect metabolic scaling.

Mass scaling of the resting and maximum metabolic rates of the black carp.

We investigated the body mass (M) scaling of resting metabolic rate (RMR), maximum metabolic rate (MMR), excess post-exercise oxygen consumption (EPOC), blood parameters, and organ masses of black carp (Mylopharyngoden piceus). The results showed that RMR scaled with M of the fish by an exponent (b) of 0.833 (bR), which was significantly larger than 0.75. MMR scaled with M by a power of 0.775 (bM), which was significantly lower than 1 and may be due to a small size proportion of red muscle. No difference between bR and bM or correlation between factorial aerobic scope and M was found. However, EPOC scaled positively with M by a power of 1.231, suggesting a constant aerobic capacity and an enhanced anaerobic capacity with fish growth. Mass of the inactive organs scaled with M by a power of 1.005, which was significantly larger than 1 and was negatively correlated with RMR, suggesting that the proportion of inactive organs increases with fish growth, which may contribute to the negative scaling of RMR. Red blood cell surface area (S) did not increase with increasing M, suggesting that the ontogenetic decrease in the surface area to volume ratio of cells may not contribute to the negative scaling of RMR. The predicted bR value (0.846) by the average S (1.746 µm²) differs by only 1.62% from the observed bR value using our previously reported S - bR function in carp, suggesting that the species-specific cell size, rather than its ontogenetic change, affects the metabolic scaling of a species.