Felipe S Barreto

Invasive plants formed via hybridization, especially those that modify the structure and function of their ecosystems, are of particular concern given the potential for hybrid vigor. In the U.S. Pacific Northwest, two invasive, dune‐building beachgrasses, Ammophila arenaria (European beachgrass) and A. breviligulata (American beachgrass), have hybridized and formed a new beachgrass taxa ( Ammophila arenaria × A. breviligulata ), but little is known about its distribution, spread, and ecological consequences. Here, we report on surveys of the hybrid beachgrass conducted across a 250‐km range from Moclips, Washington to Pacific City, Oregon, in 2021 and 2022. We detected nearly 300 hybrid individuals, or an average of 8–14 hybrid individuals per km of surveyed foredune. The hybrid was more common at sites within southern Washington and northern Oregon where A. breviligulata is abundant (75%–90% cover) and A. arenaria is sparse and patchy. The hybrid displayed morphological traits such as shoot density and height that typically exceeded its parent species suggesting hybrid vigor. We measured an average growth rate of 30% over one year, with individuals growing faster at the leading edge of the foredune, nearest to the beach. We also found a positive relationship between hybrid abundance and A. arenaria abundance, suggesting that A. arenaria density may be a controlling factor for hybridization rate. The hybrid showed similar sand deposition and associated plant species richness patterns compared with its parent species, although longer term studies are needed. Finally, we found hybrid individuals within and near conservation habitat of two Endangered Species Act‐listed, threatened bird species, the western snowy plover ( Charadrius alexandrinus nivosus ) and the streaked horned lark ( Eremophila alpestris strigata ), a concern for conservation management. Documenting this emerging hybrid beachgrass provides insights into how hybridization affects the spread of novel species and the consequences for communities in which they invade.

For aerobic organisms, both the hypoxia-inducible factor pathway and the mitochondrial genomes are key players in regulating oxygen homeostasis. Recent work has suggested that these mechanisms are not as highly conserved as previously thought, prompting more surveys across animal taxonomic levels, which would permit testing of hypotheses about the ecological conditions facilitating evolutionary loss of such genes. The Phylum Cnidaria is known to harbor wide variation in mitochondrial chromosome morphology, including an extreme example, in the Myxozoa, of mitochondrial genome loss. Because myxozoans are obligate endoparasites, frequently encountering hypoxic environments, we hypothesize that variation in environmental oxygen availability could be a key determinant in the evolution of metabolic gene networks associated with oxygen-sensing, hypoxia-response, and energy production. Here, we surveyed genomes and transcriptomes across 46 cnidarian species for the presence of HIF pathway members, as well as for an assortment of hypoxia, mitochondrial, and stress–response toolkit genes. We find that presence of the HIF pathway, as well as number of genes associated with mitochondria, hypoxia, and stress response, do not vary in parallel to mitochondrial genome morphology. More interestingly, we uncover evidence that myxozoans have lost the canonical HIF pathway repression machinery, potentially altering HIF pathway functionality to work under the specific conditions of their parasitic lifestyles. In addition, relative to other cnidarians, myxozoans show loss of large proportions of genes associated with the mitochondrion and involved in response to hypoxia and general stress. Our results provide additional evidence that the HIF regulatory machinery is evolutionarily labile and that variations in the canonical system have evolved in many animal groups.