Journal of experimental zoology. Part A, Ecological and integrative physiology最新文献

Morphofunctional inferences based on anatomical structure often rely on static skeletal features, with limited integration of dynamic locomotor behavior. Although mammalian limb movement exhibits conserved kinematic synergies, to our knowledge no broad comparative data set has quantified how joint poses, angular excursions, and angular range utilization vary across biological factors. A comparative data set of joint motion during the stance phase of walking is presented for 182 terrestrial mammal species spanning 15 orders, classified by limb posture, body mass, top speed, and locomotor habit. Using sagittal-plane video analysis and published sources, joint angles at touchdown, midstance, and toe-off were measured for six major limb joints. From these data, joint angular excursion (JAE), total angular excursion (TAE), and an angular utilization index (AUI% = TAE/∑JAE) expressed as the percentage of summed joint excursion that is realized as net limb excursion during stance, were calculated. Using phylogenetic generalized least squares (PGLS) to account for nonindependence among species, I found that JAE and TAE covaried with the factors considered, with body mass emerging as the dominant predictor. Hindlimb and forelimb TAE decreased with increasing log₁₀ body mass, whereas posture effects were subtle and largely overlapping among categories. Plantigrade, small-bodied and arboreal species tended to display broader angular profiles, whereas unguligrade, cursorial and fast-moving taxa generally used smaller excursions. Quadrant-based comparisons of forelimb and hindlimb AUI further highlighted locomotor strategies aligned with biological factors. Together, these findings indicate that mammals modulate the magnitude and distribution of joint excursions across size and ecological gradients while broadly preserving the proportion of the summed joint excursions range used during stance, providing a reproducible framework for interpreting limb dynamics in extant and extinct mammals.

Animals with seasonal reproductive cycles, as the Roe deer (Capreolus capreolus), have developed mechanisms to synchronize reproduction with the environmental cycle in order to optimize reproductive success through melatonin. Angiogenesis and oxidative stress are key processes in spermatogenesis, contributing to testicular remodeling and recovery after reproductive effort. This study carried out a gene expression analysis on 18 samples of mature male Roe deer testicles, collected during the local hunting season in pre-rut (N = 9) and post-rut (N = 9) periods. A quantitative real-time PCR (qPCR) array targeting 84 genes involved in oxidative stress and 84 in angiogenesis were used, followed by validation through individual qPCR of selected genes and related protein quantification by ELISA assays. Post-rut animals showed upregulation of several antioxidant genes: Peroxiredoxin-4 (PRDX4), Scavenger receptors class A member 3 (SCARA3), Superoxide Dismutase 3 (SOD3). Instead, Leptin (LEP) and Thrombospondin Ⅱ (THBSⅡ), a known angiogenesis inhibitor, are downregulated. A novel insight is represented by the upregulation of Neuropilin (NRP2) in post-rut period that, given to its posttranscriptional silencing too, needs better investigations. The pleiotropic nature of NRP2, including roles in neurodevelopment, immune modulation, and vascular remodeling, makes this gene an interesting candidate for further study, cause its function in reproductive tissues remains poorly understood.

Conditions experienced during early life stages may influence an array of fitness-relevant phenotypes, especially in oviparous ectotherms. The pond slider (Trachemys scripta) has two life stages particularly vulnerable to the influence of ambient conditions: the egg stage and hatchling overwintering stage. We aimed to determine the influence of both incubation temperature and overwinter environment on hatchling turtle performance. In 2019 and 2020, we incubated pond slider eggs at five constant temperatures (24°C, 26°C, 28°C, 30°C, 32°C). After hatching, turtles were distributed to two housing treatments that simulated overwintering in a terrestrial nest or an aquatic environment. In the spring following hatching, we conducted righting response trials, which are frequently used performance measures that may be associated with coordination and neuromuscular function. Our linear mixed-effects models show that incubation temperature, overwinter environment, and their interaction significantly influenced hatchling phenotypes (e.g., shell and tail dimensions, body mass) and righting performance (e.g., total righting response time, latency to right). Aquatically overwintering hatchlings that were incubated at cooler temperatures righted themselves faster than those incubated at warmer temperatures. This relationship did not exist in terrestrially overwintering hatchlings, which had faster overall righting times that were not affected by incubation temperature, suggesting overwintering in the nest may better equip hatchlings for post-emergence dispersals over land.

Depletion of dissolved oxygen (DO; hypoxia) and its influence on sensitive fauna and vulnerable life stages is an emerging concern in lotic freshwater ecosystems. A species particularly vulnerable to hypoxia is the Eastern Hellbender—a large-bodied, fully aquatic salamander which relies on cutaneous respiration and has evolved to thrive in cold, well-oxygenated streams. Adult hellbenders nest in benthic stream microhabitats which are vulnerable to DO depletion caused by loss of riparian forest cover that increases sedimentation and solar radiation. Hellbender populations are experiencing declines characterized by reduced recruitment in areas with low forest cover, but the influence of hypoxia on hellbender embryonic development is unknown. We hypothesized that hellbender embryos are sensitive to hypoxic conditions because of their high degree of habitat specialization. We conducted two experiments where we exposed freshly laid eggs to a range of DO concentrations in the lab (3–10 mg/L). In both experiments we found that hellbender embryos reared in our lowest DO treatments of 3 and 5 mg/L had an average viability 51% and 34% lower than each experiment's 10 mg/L treatment, respectively. In addition, eggs reared in these low DO concentrations had significantly lower hatching success, a higher percentage of premature hatchlings, and produced hatchlings with smaller morphometrics compared to higher DO treatments. In our second experiment, we also continued to track hatchlings at least 14 days post hatching and demonstrated that premature hatchlings had a high probability of dying within weeks of hatching. Our results indicate that hellbender embryos require DO concentrations of > 5 mg/L for proper development, thus placing them on the more sensitive end of the hypoxia tolerance continuum for freshwater taxa. Our experiments confirmed hellbender embryonic sensitivity to environmentally relevant reductions in DO concentrations and identified future research and conservation needs related to the development of hellbender embryos in the field.

An optimal glucocorticoid stress response is essential because it allows animals to adjust their phenotype to constantly changing environments. Considerable progress has been made regarding our understanding of how various cellular mechanisms of glucocorticoid action modulate animals' stress response phenotype. However, a potentially overlooked mediator of glucocorticoid production and individual's stress response phenotype is the endoplasmic reticulum (ER) and its unfolded protein response (UPR), given that all steroid hormones are synthesised within the mitochondria and the ER. We hypothesise that UPR regulates glucocorticoid synthesis, and ER stress induction would inhibit glucocorticoid production in the adrenal cortex. We conducted in vivo and in vitro studies using outbred deer mice Peromyscus maniculatus and Y-1 adrenal cell lines respectively to investigate the effects of ER stress and UPR on adrenocorticotropic hormone induced glucocorticoid production. Specifically, we tested if induction and alleviation of ER stress using tunicamycin and tauroursodeoxycholic acid, respectively, would affect corticosterone production in deer mice and Y-1 cells and the protein expression of a steroidogenic enzyme in Y-1 cells. We showed that ER stress and UPR modulate glucocorticoid production at both the cell and whole-organism levels, but this is achieved independent of alteration in protein level of 21-Hydroxylase.

Exposure to altered nighttime lighting conditions has become common in today's modern world. Light at night disrupts circadian processes that govern feeding patterns, sleep/wake cycles, and metabolic homoeostasis, increasing the risk of developing pathologies associated with cardiometabolic disease. Yet, the underlying mechanism(s) responsible for mediating the resulting physiological outcomes are not clear. Mitochondrial function may provide valuable insight into the physiological costs associated with light at night, given that mitochondria contribute to variation in metabolic performance that underpin human diseases. In this study, 36 male and female wild-derived house mice (Mus musculus) were exposed to continuous light, darkness, or a control light cycle for 6 weeks. We examined animals' bioenergetic capacity at the whole-organism and subcellular level while also measuring changes in body condition and oxidative damage. We found that 6 weeks of constant light and darkness resulted in negligible changes in all our variables of interest. We did not detect strong mitochondrial responses in the liver or skeletal muscle of either sex exposed to constant light or darkness. Furthermore, we did not detect any difference in mitochondrial volume or lipid peroxidation in the liver between treatment groups. Lastly, there was no difference in body condition between treatment groups. Our data indicate that wild-derived mice are able to circumvent challenges of an altered light environment and escape physiological consequences.

Retraction: M. B. Rhouma, M. Venditti, A. Haddadi, L. Knani, L. Chouchene, S. Boughammoura, R. J. Reiter, S. Minucci, and I. Messaoudi, "Melatonin Counteracts Cadmium-Induced Rat Testicular Toxicity via the Mechanistic Target Rapamycin (mTOR) Pathway," Journal of Experimental Zoology - A 341, no. 4 (2024): 470-482. https://doi.org/10.1002/jez.2792. The above article, published online on 04 March 2024 in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the journal Editor-in-Chief, Randy Nelson and Wiley Periodicals LLC. A third party reported that a version of the DAPI/PNA/CX43 panel in Figure 4b had been copied and rotated as the Cd panel in the same figure. The third party also reported that the CM (-Pr), CMR (+ Pr), and Rapa (+ Pr) panels in Figure 6 A contained similar image elements following image manipulation and rotation. Further investigation by the publisher found the presence of similar cellular sections across the CM panel in Figure 2B and the MLT panel in Figure 3B. This investigation also found that the beta-actin bands had been duplicated between Figures 2A and 4A. The authors responded to an inquiry by the publisher, acknowledged errors in Figures 2B, 3B, 4B and 6A, and stated that these mistakes were made during figure assembly. The authors provided what were labeled as original data for Figures 2, 3, 4, and 6 and supplied corrected images. Upon review of these data, the parties determined that while errors in figure assembly could explain the errors in Figures 2, 3, and 4, the authors did not provide a satisfactory explanation for the errors in Figure 6. The retraction has been agreed to because the number of errors in image assembly, as well as evidence of image manipulation, fundamentally compromises the editors' confidence in the results presented in the article. The authors did not respond to the notice regarding the retraction.