Abstract:Quantifying a species thermal tolerance is critical to assessing biological impacts of anticipated increases in temperature (e.g., climate change). Although many studies have documented the critical thermal maximum (CT max ) of fish, there is a paucity of research on thermal biology of sturgeon. The shortnose sturgeon (Acipenser brevirostrum LeSueur, 1818) is a threatened species that exists along the eastern coast of North America. They can be exposed to temperatures ranging from freezing to above 25°C. Using… Show more
“…This is perplexing since most sturgeon species are protected under legislation due to human‐made disturbances that might involve water temperature alterations (Pikitch et al., ). The critical thermal maximum values for Atlantic and shortnose sturgeon noted in the present study were found to be similar to those in other studies using pallid ( Scaphirhynchus albus ), Lake ( Acipenser fulvescens ), shortnose, shovelnose ( Scaphirhynchus platorynchus ) and green ( Acipenser medirostris ) sturgeons (Sardella et al., ; Zhang and Kieffer, ; D. Deslauriers, unpubl. data; Table ).…”
Section: Discussionsupporting
confidence: 91%
“…CTmax led to a marked change in a number of blood parameters across sturgeon species, which is indicative of increased stress in the animal (Wedemeyer et al., ; Barton et al., ). Lactate concentrations increased in Atlantic and shortnose sturgeon during the thermal stress and at levels comparable to previous research on shortnose sturgeon (Zhang and Kieffer, ; Y. Zhang and J. D. Kieffer, unpubl. data).…”
Summary
The critical thermal maximum (CTmax) and the associated hematological response of juvenile (~145 g, n = 8 for both species) Atlantic Acipenser oxyrinchus and shortnose Acipenser brevirostrum sturgeons acclimated to 15°C were determined using a heating rate of 8°C h−1. The critical thermal maximum averaged 30.8°C and 31.6°C for Atlantic and shortnose sturgeon, respectively, and values fell within the range noted for other sturgeon species. Oxygen‐carrying capacity (hemoglobin and hematocrit) measures were generally unaffected by thermal stress. Plasma lactate levels increased from 0.5 mm to 4 mm following temperature stress in both species. Both plasma glucose and potassium levels increased following CTmax, however, these levels were about double in the shortnose sturgeon. Lastly, plasma sodium and chloride levels were significantly depressed (by more than 10%) following thermal stress in shortnose sturgeon, whereas only chloride levels decreased in Atlantic sturgeon. Taken together, while CTmax values were similar, thermal stress resulted in different hematological profiles; these differences are consistent when compared to other stressors, and may be related to the phylogenetic position and thus could reflect the evolutionary history of these two species.
“…This is perplexing since most sturgeon species are protected under legislation due to human‐made disturbances that might involve water temperature alterations (Pikitch et al., ). The critical thermal maximum values for Atlantic and shortnose sturgeon noted in the present study were found to be similar to those in other studies using pallid ( Scaphirhynchus albus ), Lake ( Acipenser fulvescens ), shortnose, shovelnose ( Scaphirhynchus platorynchus ) and green ( Acipenser medirostris ) sturgeons (Sardella et al., ; Zhang and Kieffer, ; D. Deslauriers, unpubl. data; Table ).…”
Section: Discussionsupporting
confidence: 91%
“…CTmax led to a marked change in a number of blood parameters across sturgeon species, which is indicative of increased stress in the animal (Wedemeyer et al., ; Barton et al., ). Lactate concentrations increased in Atlantic and shortnose sturgeon during the thermal stress and at levels comparable to previous research on shortnose sturgeon (Zhang and Kieffer, ; Y. Zhang and J. D. Kieffer, unpubl. data).…”
Summary
The critical thermal maximum (CTmax) and the associated hematological response of juvenile (~145 g, n = 8 for both species) Atlantic Acipenser oxyrinchus and shortnose Acipenser brevirostrum sturgeons acclimated to 15°C were determined using a heating rate of 8°C h−1. The critical thermal maximum averaged 30.8°C and 31.6°C for Atlantic and shortnose sturgeon, respectively, and values fell within the range noted for other sturgeon species. Oxygen‐carrying capacity (hemoglobin and hematocrit) measures were generally unaffected by thermal stress. Plasma lactate levels increased from 0.5 mm to 4 mm following temperature stress in both species. Both plasma glucose and potassium levels increased following CTmax, however, these levels were about double in the shortnose sturgeon. Lastly, plasma sodium and chloride levels were significantly depressed (by more than 10%) following thermal stress in shortnose sturgeon, whereas only chloride levels decreased in Atlantic sturgeon. Taken together, while CTmax values were similar, thermal stress resulted in different hematological profiles; these differences are consistent when compared to other stressors, and may be related to the phylogenetic position and thus could reflect the evolutionary history of these two species.
“…The adoption of the CTM parameter allowed researchers to evaluate the thermal tolerance of different organisms (Cowles and Bogert, 1944; Lutterschmidt and Hutchison, 1997; Zhang and Kieffer, 2014). Limnic planarians exposed to the CTM, show signs of contortions, sluggishness, and an injured epidermis, losing their ability to move properly before dying (Claussen and Walters, 1982; Tsukuda and Ogoshi, 1985).…”
Planarians are metazoan freshwater flatworms which are free-living organisms. Their body has pluripotent stem cell promoters of tissue regeneration capacity. The water temperature and the potential of hydrogen (pH) of lentic ecosystems are important factors involved in the distribution and abundance of these animals. Although the pH factor is directly related to the physiology and behavior of planarians, their adaptive and regenerating capacities still remain unknown. The Critical Thermal Maximum (CTM) is a very widespread method used in the evaluation of thermal tolerance. In this study, Girardia tigrina (Girard, 1850) and Girardia sp., a species found in Brazil, which is under study as a new species, had their epidermis assessed by scanning electron microscopy (SEM) to analyze their physiological structures before and after exposure to different stressors. SEM was used as a method to evaluate the planarians' epidermis as a result of the increasing temperature (CTM) and pH alterations, the latter with the use of a new methodology defined as Critical Hydrogen ion concentration Maximum (CHM). In increasing temperatures from 20°C to 37°C, both Girardia tigrina and Girardia sp. proved to be adaptable to thermal stress. Girardia sp. was shown to be more resistant to higher temperatures. However, Girardia tigrina was more resistant to extreme pH conditions (4.0 to 10.0). SEM analysis showed morphological differences among planarian species, such as the arrangement of the structures and cell types of the dorsal epidermis. Moreover, planarians demonstrated the ability to change the surrounding pH of their external environment in order to maintain the function of their physiological mechanisms, suggesting that these animals have a complex survival system, possibly related to protonephridia, flame cells and excretory pores..
“…In nature, a loss of equilibrium affects an organism's ability to forage or avoid predation, which may ultimately affect individual fitness. As acclimation temperature ( T a ) has been found to be correlated positively with CT max (Cox et al ., 1974; Zhang and Kieffer, 2014; McDonnell and Chapman, 2015, although see Galbreath et al ., 2004; Recsetar et al ., 2012), the ancestral history and origin of a population are thought to be linked to an organism's ability to tolerate temperature increases (Stockwell et al ., 2003; McDermid et al ., 2012) and, as such, stream temperature regimes may result in population-specific thermal tolerance. A relatively new metric to assess thermal tolerance, agitation temperature, described by McDonnell and Chapman (2015) as the temperature at which a fish first begins to exhibit refugia-seeking behaviour (circling of the chamber, seeking refuge in substrate), may also provide insight to how quickly individuals can sense and attempt to react to environmental change.…”
To forecast the impact of climate warming on cold-water fishes, thermal tolerance trials were conducted on six populations of brook trout from Cape Race, Newfoundland, Canada. Of these, three were outcrossed to assess the effect of hybridization. Although differences were found, there was little variation among populations in how they responded to thermal stress.
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