Water infrastructure updates at Grand Canyon National Park (GRCA) provide an opportunity to restore natural flow to Bright Angel Creek, adding an additional ~20% to baseflow. This creek provides habitat for endangered humpback chub (Gila cypha) and invasive brown trout (Salmo trutta). We assess how increased flow may alter habitat and how that change may impact native and nonnative species using physical habitat modeling and statistical analysis of stream temperature data. We used System for Environmental Flow Analysis to calculate the change in habitat area for both species in the lower 2.1 km of the creek before and after the increased flow. Results indicate a slight increase in available habitat for juveniles of both species and a slight decrease for spawning brown trout. We used regression modeling to relate daily average air temperature to stream temperature and periods of increased discharge during water system maintenance were used to model the temperatures during likely future conditions. Both high and low stream temperature were dampened due to the added water resulting in fewer days with suitable spawning temperature and more days with suitable growth temperature for humpback chub. Fewer suitable days for growth upstream but more suitable days downstream, were predicted for brown trout. Compared to other streams that sustain populations of humpback chub, flow conditions for Bright Angel Creek provide fewer days throughout the year with suitable temperatures, particularly during the winter months. Juvenile humpback chub rearing may improve through the restoration of flow however the presence of predatory brown trout complicates the net beneficial impact.
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http://dx.doi.org/10.1007/s00267-019-01157-8 | DOI Listing |
J Anim Ecol
July 2024
Southwest Biological Science Center, U.S. Geological Survey, Grand Canyon Monitoring and Research Center, Flagstaff, Arizona, USA.
Many populations migrate between two different habitats (e.g. wintering/foraging to breeding area, mainstem-tributary, river-lake, river-ocean, river-side channel) as part of their life history.
View Article and Find Full Text PDFHum Genomics
March 2024
Institute of Human Genetics, Julius-Maximilians-Universität Würzburg, Biozentrum, Am Hubland, 97074, Würzburg, Germany.
Background/objectives: Rare genetic disorders causing specific congenital developmental abnormalities often manifest in single families. Investigation of disease-causing molecular features are most times lacking, although these investigations may open novel therapeutic options for patients. In this study, we aimed to identify the genetic cause in an Iranian patient with severe skeletal dysplasia and to model its molecular function in zebrafish embryos.
View Article and Find Full Text PDFSci Rep
March 2024
Institute for Research on Cancer and Aging of Nice (IRCAN), UMR7284, INSERM U1081, CNRS, Université Cote d'Azur, 06107, Nice, France.
Telomerase activity is restricted in humans and telomere attrition occurs in several tissues accompanying natural aging. Critically short telomeres trigger DNA damage responses and activate p53 which leads to apoptosis or replicative senescence. These processes reduce cell proliferation and disrupt tissue homeostasis, thus contributing to systemic aging.
View Article and Find Full Text PDFSci Rep
April 2023
Institut du Cerveau (ICM), Inserm U 1127, CNRS UMR 7225, Sorbonne Université (SU), 75013, Paris, France.
Scheuermann's disease, also referred to as Scheuermann's kyphosis, is the second most frequent spine deformity occurring in humans after adolescent idiopathic scoliosis (AIS), both with an unclear etiology. Recent genetic studies in zebrafish unraveled new mechanisms linked to AIS, highlighting the role of the Reissner fiber, an acellular polymer bathing in the cerebrospinal fluid (CSF) in close proximity with ciliated cells and mechanosensory neurons lining the central canal of the spinal cord (CSF-cNs). However, while the Reissner fiber and ciliary beating have been linked to AIS-like phenotypes in zebrafish, the relevance of the sensory functions of CSF-cNs for human spine disorders remains unknown.
View Article and Find Full Text PDFElife
December 2022
Institute of Molecular Biology, Department of Biology, University of Oregon, Eugene, United States.
The spine provides structure and support to the body, yet how it develops its characteristic morphology as the organism grows is little understood. This is underscored by the commonality of conditions in which the spine curves abnormally such as scoliosis, kyphosis, and lordosis. Understanding the origin of these spinal curves has been challenging in part due to the lack of appropriate animal models.
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