Ecophysiology

Plant interactions (e.g., competition, facilitation) are critical drivers in
community development and structure. The Stress Gradient Hypothesis (SGH)
provides a predictive framework for how plant species interactions vary inversely
across an environmental stress gradient, predicting that facilitation is stronger with
increasing levels of stress. The SGH has been supported in numerous ecosystems
and across a variety of stress gradients, but recent research has demonstrated
contradictory results. These discrepancies have led to SGH revisions that expand its
conceptual framework by incorporating additional factors, such as other stressor
types and variations in species life history strategies. In this dissertation, I examine
a further modification of the SGH by proposing and testing a Multiple Stress
Gradient Hypothesis (MSGH) that considers how plant interactions vary along a continuous gradient of two co-occurring stressors using mangrove and salt marsh
communities as a case study. In Chapter 1, I outline the predictive framework of a
MSGH, by creating a series of predictions of species interactions. The components
of the MSGH predict that stressors of similar types (e.g., resource and nonresource)
will have similar effects and be additive. On the other hand, varying
species life history strategies and life stages will lead to extremes of plant
interactions. In Chapter 2, I performed a series of experiments to test the various
components of the MSGH. In Chapter 3, I performed a large-scale observational
study to test whether multiple co-occurring stressors altered the cumulative effects
on plant interactions, and if these stressors should be grouped (e.g., resource and
non-resource, abiotic and biotic, etc.) to enhance predictability. From a series of
studies conducted herein, I concluded that co-occurring stressors are important
factors that control complex species interactions as shown in my MSGH modeling
approach. Further, future theories need to incorporate species-specific and stressor specific
grouping when modeling how species interactions shape communities.

Changes in activity related oxygen consumption and energy partitioning were measured in leatherback and olive ridley sea turtle hatchlings over their first month after nest emergence. Leatherbacks emerge with about 75--90 KJ of energy in the residual yolk at their disposal for growth and movement. In comparison, the residual yolk energy reserves for the olive ridley are estimated to be much less (45 KJ). In leatherbacks resting specific oxygen consumption rates decreased by 53% over the first post-hatching month (0.0065 ml O2 min-1 g-1--0.0031 ml O2 min-1 g-1), while for ridleys the fall was 32% (0.0038 ml O2 min-1 g-1--0.0026 ml O2 min-1 g-1). Greater differences were seen in aerobic scope. For olive ridleys the factorial aerobic scope doubled over the first month but there was no significant increase in the leatherback's factorial aerobic scope. Leatherback hatchlings gained on average 33% body mass (10 g) over the first week however 70 to 80% of this increase was due to water accumulation. The differences in aerobic scope and energy reserves are related to differences in early life ecological stratagems of these species.

Macroalgal blooms are responses to nutrient enrichment in shallow seagrass ecosystems like the Indian River Lagoon (IRL), Florida. Little is known about nitrogen (N) and phosphorus (P) limitation or the importance of morphological/physiological characteristics of bloom-forming macroalgae (Ulva lactuca, Hypnea musciformis, and Gracilaria tikvahiae) in the IRL. We hypothesized: 1) all species would proliferate in nutrient-rich Titusville, 2) opportunistic U. lactuca would dominate, 3) Rapid Light Curves (RLCs) would assess nutrient status, and 4) nutrient concentrations would regulate growth more than N:P ratios. Field studies showed rapid biomass doubling times of 2 days (U. lactuca; November 2012) in urbanized Titusville. RLCs in a guano-enriched island off Big Pine Key (BPK) and Titusville (Ulva spp.) were similar due to P-saturation. Laboratory studies showed three-fold higher RLCs and two-fold faster growth at high nutrient concentrations of N and P. Reductions of both N and P will be required to moderate future blooms.

Sponges are an important source of bioactive marine natural products, or secondary metabolites. The common Caribbean reef sponge, Axinella corrugata, produces an antitumor and antibacterial chemical, stevensine. This study determined whether environmental stressors, such as elevated temperature and exposure to Amphibalanus amphitrite larvae, affect the production of stevensine by A.corrugata and if the stressors caused A.corrugata to exhibit differential gene expression. Temperature stress resulted in no significant change in the production of stevensine; only two genes were significantly differentially expressed, including hsp70. Larval stressed resulted in increased production of stevensine and significant differential gene expression (more than seventy genes). This study suggests that A.corrugata may be resilient to elevations in temperature and that one of stevensine's roles in nature is as an antifoulant.

Anoxia is characterized by an absence of oxygen supply to a tissue (Dawson- Scully et al., 2010). Unlike humans, Drosophila melanogaster is an organism that can survive low oxygen levels for hours without showing any pathology (Lutz et al., 2003) Under anoxia, the fruit fly loses locomotive activity, resulting in an anoxic coma (Haddad et al., 1997). In this study we investigate the influence of five variables for anoxic tolerance in adult Drosophila: 1) anoxic environment (gas vs. drowning), 2) anoxia duration, 3) temperature (cold [3ÀC] or room temperature [21ÀC]), 4) age (young 2-9 days and old 35-39 days), and 5) PKG variation. Tolerance to anoxia is measured by the time of recovery and survival of the fruit fly from the anoxic coma. The results from this study show that short stress, low temperature, young age, and low PKG activity increased anoxic tolerance. Our findings will lay the foundation to investigate different variables, genes or pharmacological compounds that can modulate neuronal anoxic tolerance.