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<p> Proposal Cover Sheet Term: Fall 2011 5 Instructor: Dr. Nora Demers</p><p>Name: Michael Saenz</p><p>Present Year in Education: Senior 10 E-mail Address: [email protected]</p><p>Major: Environmental Studies</p><p>15 Have you identified a research mentor for a senior thesis (if applicable)? No If yes, please identify.</p><p>Name: n/a</p><p>20 Title of Proposal: </p><p>“How has predation by the invasive Lionfish, Pterois volitans, impacted the juvenile populations of the Rainbow Parrotfish, Scarus guacamaia, known to depend on Bahamian mangrove habitat?”</p><p>25 Keywords (3-5): Pterois volitans, Scarus guacamaia, mangrove(s), invasive, Bahamas</p><p>Checklist:</p><p>30 All required portions of the first submission are included: Yes </p><p>I had an external reviewer read the proposal: Yes </p><p>If Yes, who? Holly Taylor (Mother), Dr. Greg Tolley, Professor Nora Demers 35 I authorize the use of this proposal as an example in future courses: Yes </p><p>40</p><p>45</p><p>1</p><p>ABSTRACT: The successful invasion of the Indo-Pacific lionfish species, Pterois volitans, into the sub-</p><p>50 tropical and tropical Western Atlantic has raised major concern about the potential ecological impacts of </p><p> this invasive predator on native marine ecosystems. A considerable amount of research has been </p><p> conducted on the impact of this invasion within Bahamian coral reef ecosystems, however, there appears</p><p> to be a clear need for further investigation into lionfish impacts on critical non-reef habitat, such as </p><p> mangroves, that provide shelter and protection for important herbivorous coral reef species as juveniles </p><p>55 during their maturation. Juvenile specimens of the Rainbow Parrotfish, Scarus Guacamaia, will be used </p><p> in order to conduct controlled laboratory experimentation on the predation of P. volitans among three </p><p> distinct levels of structural habitat complexity, including one consistent with the complexity found in </p><p> their natural habitat. This research will allow us to quantify the ability of natural mangrove prop-root </p><p> system conditions in protecting juvenile S. guacamaia populations from predation by P. volitans in the </p><p>60 wild. </p><p>65</p><p>70</p><p>2 Table of Contents</p><p>75</p><p>Page - 1. Cover Sheet</p><p>2. Research Abstract</p><p>3. (Table of Contents)</p><p>80 4. Introduction</p><p>6. Research Objectives</p><p>7. Methods</p><p>10. Broader Implications</p><p>11. Time Table and Project Management</p><p>85 12. References Cited</p><p>14. Curriculum Vitae </p><p>90</p><p>95</p><p>3 100 Introduction</p><p>“How has predation by the invasive lionfish, Pterois volitans, within Bahamian mangrove ecosystems </p><p> impacted the juvenile populations of the Rainbow Parrotfish, Scarus guacamaia,successfully being </p><p> recruited to adjacent coral reef ecosystems as adults?” </p><p>Mangroves represent vital habitat for juvenile fish communities by providing shelter to protect these fish</p><p>105 from predation during their vulnerable maturation period (Layman, 2002). The prop-root systems found in </p><p> mangrove habitat provide necessary protection to juvenile fish by acting as both a physical and visual barrier </p><p> from predators. The high structural complexity of mangrove habitat inhibits the ability of predators to find and </p><p> capture their prey in this environment, thus increasing the chances of survival for juvenile fish communities </p><p> using these habitats (Rooker et al., 1998). Recently, however, the delicate balance of these vital mangrove </p><p>110 ecosystems has been threatened by the invasion of the Indo-Pacific Lionfish, Pterois volitans, not only into the </p><p>Bahamas but throughout the Atlantic and Caribbean (Schofield, 2009). </p><p>Lionfish are highly effective predators and are voracious eaters that consume a wide-range of prey. To </p><p> exacerbate the problem, there are virtually no natural predators of lionfish in this region and because of the fact </p><p> that P. volitans is an invasive species, there appears to be some degree of predator naiveté among native prey </p><p>115 species, meaning they do not inherently recognize or acknowledge the lionfish as a predator. Research suggests </p><p> that the invasive lionfish populations are accumulating at greater densities with larger body sizes and total body </p><p> mass on Bahamian coral reefs in comparison with the Pterois miles populations examined in their native Kenyan</p><p> coral reefs (Darling, 2011). </p><p>Much of the existing research available about the invasion has been concentrated on the origins </p><p>120 (Freshwater, 2009), as well as the temporal and spatial extent of the invasion (Johnston, 2011). Research has also</p><p>4 been conducted on the overall biology and ecology of P. volitans (Morris, 2009), the impact of lionfish predation</p><p> on coral reef ecosystems (Albins, 2008, 2011), as well as potential management actions that could be initiated to </p><p> regulate the invasion (Barbour, 2011). There appears to be a significant gap in knowledge about the invasion in </p><p>125 regards to the impact of this invasion on critical non-reef habitat, such as mangrove ecosystems. It is important </p><p> to investigate the impact of this invasion, either through predation or competition, on critical non-reef habitat </p><p> because these habitats are closely interconnected with coral reefs and have a significant impact on coral reef fish </p><p> biomass, as well as community structure (Barbour, 2010). There appears to be a clear need for further research </p><p> into the impact of lionfish on foraging fish communities. The foraging behavior of herbivorous fish species </p><p>130 provides a vital ecosystem service by regulating the algae levels on coral reefs (Schofield, 2009). Mangrove </p><p> habitat provides shelter and protection from predation for many herbivorous fish species during the juvenile </p><p> stage until they migrate from these habitats to adjacent coral reefs as adults (Layman, 2002). The presence of </p><p> these herbivorous fish on coral reefs is important because the absence of these key species have been shown to </p><p> significantly reduce the ability of coral reef systems to defend themselves against the overgrowth of algae </p><p>135 (Mumby, 2004).</p><p>I intend to assess the impact of the invasion of predation by the lionfish species, Pterois volitans, on </p><p> juvenile foraging fish communities that inhabit Bahamian mangrove habitat. Scarus guacamaia will be </p><p> designated as the experimental prey species because it is considered to be the largest herbivorous foraging fish </p><p> species in the Atlantic and has been shown to have a functional dependency on mangrove ecosystems during its </p><p>140 juvenile stage. S. guacamaia is an IUCN Red List threatened species, making it especially vulnerable to any </p><p> additional predation pressure imposed by the invasive lionfish populations. Mumby (2004) estimated that the </p><p> loss of a single adult specimen of S. guacamaia would constitute as much as a 10% reduction in total Rainbow </p><p>Parrotfish biomass within its territory. I plan to investigate the effectiveness of mangrove prop root systems in </p><p> protecting juvenile S. guacamaia populations from predation by P. volitans.</p><p>145</p><p>5 150</p><p>Research Objectives</p><p>The purpose of this research study is to examine the effectiveness of the natural structural </p><p>155 complexity found within mangrove habitat in defending juvenile populations of the Rainbow Parrotfish, </p><p>S. guacamaia, from predation by the invasive lionfish, Pterois volitans. The overall goal of this research </p><p> is to determine the level of threat that predation by the invasive lionfish, Pterois volitans, is posing to </p><p>Bahamian herbivorous fish populations known to utilize mangrove prop-root system habitats as </p><p> juveniles. This research will address the lack of knowledge present about the impacts of this invasion on </p><p>160 critical non-reef habitat like mangroves. This research will reveal whether or not predation by the non-</p><p> native P. volitans in Bahamian mangrove habitat could significantly be reducing the amount of S. </p><p> guacamaia adults successfully being recruited to adjacent coral reef ecosystems to which their foraging </p><p> habits are vital in controlling reef algae levels.</p><p>165</p><p>170 6 Methods 175</p><p>One hundred juvenile specimens (standard length ≈ 78.8 mm) of Scarus guacamaia will be collected, </p><p> also known as the Rainbow Parrotfish, within the mangrove habitat on Andros, Island of the Bahamas (Randall, </p><p>1963). Collections will take place during low-tide and be sampled using trap nets (8 x 2m, 1 mm mesh size) set </p><p>180 at the mouths of small tidal creeks to catch fauna being swept out with the receding tide as the mangrove forest </p><p> is drained. (Laegdsgaard, 1995) Water temperature, salinity, and oxygen levels will be measured upon each trap </p><p> collection for laboratory reference after obtaining IACUC approval as well as permission from the Bahamas.</p><p>After a 1-week acclimation period for the S. guacamaia specimens, a separate collection will be </p><p> conducted of the invasive lionfish species, Pterois volitans. Thirteen adult (11 to 15 inches) specimens of P. </p><p>185 volitans will be collected using hand-nets to reduce the risk of envenomation, from various coral reef sites also </p><p> found on Andros, Island in the Bahamas (Morris et al., 2009) (NOAA, 2011).. Both P. volitans and S. guacamaia</p><p> specimens will be transported to the testing facility in water obtained on site during specimen collection and </p><p> temperature will be monitored to ensure specimen well-being throughout transportation. </p><p>190 Experimental Protocol</p><p>Experimental and holding tank conditions will be maintained as closely as possible to the native </p><p> environment based on field measurements taken during collection. All fish will be acclimated to experimental </p><p> tank conditions for a minimum of 48 hours on arrival. The S. guacamaia specimens will be fed Hikari® algae </p><p> wafers daily until enough algae accumulates in the tanks in order to sustain them (Verweij et al., 2006). P. </p><p>195 volitans specimens will be starved prior to the experiment for a minimum of 48 hours in order to catalyze </p><p> feeding behavior (Fishelson, 1997).</p><p>7 Three (3) separate trials consisting of three-hour periods will be conducted for each of the four different </p><p> tank environments. The tank environments represent three relative scales of habitat complexity: open water/no </p><p>200 complexity, medium complexity, and high complexity. A fourth tank will be used to set up a control for the </p><p> experiment, consisting of an additional open water environment in which no P. volitans will be exposed to the S. </p><p> guacamaia population. Mangrove habitat complexity will be simulated by hanging PVC tubing (diameter 1.5 cm, </p><p> length 40 cm) just above the tanks to mimic aerial mangrove prop-root systems found in the natural environment. </p><p>The highest complexity tank environment will have a density 64 m-2 because previous research has correlated </p><p>205 this level of structural habitat complexity with the highest abundances of fish being found in these environments </p><p>(Verweij, 2006). Using this as our standard, the medium complexity tank will have a density equivalent to half of </p><p> that found in the high complexity environment, 32 m-2. The open water tanks in both the control and </p><p> experimental environments will have no PVC tubing or additional structural complexity.</p><p>In each tank there will be 10 S. guacamaia specimens exposed to 1 P. volitans per trial, with the </p><p>210 exception of the control experiment which will monitor 10 S. guacamaia without the presence of P. volitans in </p><p> an additional open water tank. Introduction of the P. volitans into each sub-environment will occur at exactly </p><p>9:30 AM each morning based on research that P. volitans are diurnal feeders with the highest predation activity </p><p> occurring between 8:00 AM and 11:00 AM (Schofield, 2009). Tanks will be cleaned between each trial and the </p><p> water will be replaced using a filtration system. </p><p>215 Data Collection and Analysis:</p><p>Three observers will record the number of S. guacamaia remaining after each trial as well as the number </p><p> of physical attacks initiated by the P. volitans for each trial. This data will allow for a comparison between the </p><p>220 energy exerted by the P. volitans per feeding trial and the actual amount of S. guacamaia killed and/or eaten.</p><p>The data gathered will be analyzed using a 1-way Analysis of Variance (ANOVA) test, using a p-value </p><p> significance of < 0.05 (or equal to). For example, “0.09” would not be significant, while “0.0001” would be </p><p> considered highly significant.</p><p>225 8 230 Factor - Habitat Complexity</p><p>Level(s): Open Water, Medium complexity, High complexity</p><p>Experimental control: Open Water tank – 10 juvenile S. guacamaia with NO P. Volitans 235</p><p>Response variables: </p><p>Number (#) of S. guacamaia fish eaten per 3 hour trial 240 Number (#) of attacks by Pterois Volitans on juvenile S. guacamaia per 3 hr. trial</p><p>Tukey's multi-comparison post-hoc test will also be applied to further determine the significance of the </p><p> results.</p><p>245</p><p>250 9</p><p>255</p><p>Broader Implications</p><p>Throughout the preliminary research process a clear need for further investigation into the impacts of the</p><p> invasion of the Indo-Pacific lionfish, Pterois volitans, on Bahamian mangrove ecosystems became apparent in </p><p>260 order to assess the level of predation pressure the invasive predator is imposing on important foraging fish </p><p> species known to utilize these habitats during their vulnerable juvenile stage. This is an important research </p><p> endeavor because the aforementioned characteristics unique to the invasive P. volitans give it the potential to be </p><p> one of the most ecologically devastating species invasions in modern history. The more research conducted on </p><p> the dynamics and unique characteristics of this species invasion, the better our scientific understanding will be </p><p>265 for initiating the appropriate response measures.</p><p>270 10</p><p>275</p><p>Time table and Project Management</p><p>The nature of this proposed research suggests that the endeavor is feasible within a relatively short </p><p> period of time. The biggest time constraints involved in the implementation of this research would be obtaining </p><p>IACUC approval as well as permission from the Bahamas territory at the onset of the research. Once permission </p><p>280 is granted, the experiment can move forward beginning with the collection of the juvenile Scarus guacamaia </p><p> specimens using trap-nets. </p><p>Due to the relatively small quantity of S. guacamaia specimens required for the experiment, the goal </p><p> number should be achieved within a small number of trapping attempts. After a one-week acclimation period for </p><p> the collected juvenile S. guacamaia specimens, a separate collection of adult Pterois volitans specimens will be </p><p>285 conducted using hand-nets. Once the collected lionfish specimens arrive at the laboratory testing site, they will </p><p> be acclimated to experimental tank conditions for a period of about 48 hours, during which time they will be </p><p> deprived (starved) of food until the experiment is underway. </p><p>Four experimental tanks representing various levels of habitat complexity will be used to conduct three </p><p> different feeding trials per tank, for a total of 12 individual experiments. Each feeding trial will last for exactly </p><p>290 three hours and so we can conclude that no more than 36 hours of actual laboratory experimentation and data </p><p> collection will be necessary to conclude the experimental phase of the research. At this point, data can then be </p><p> statistically analyzed for significance comparisons among the different habitats. 295 11</p><p>Literature Cited</p><p>Introduction section </p><p>300 Albins MA, Hixon MA (2008) Invasive Indo-Pacific lionfish Pterois volitans reduce recruitment of Atlantic coral-reef fishes. Mar Ecol Prog Ser 367: 233-238</p><p>Albins, M., & Hixon, M. (2011). Worst case scenario: potential long-term effects of invasive predatory lionfish (Pterois volitans) on Atlantic and Caribbean coral-reef communities. Environmental Biology of Fishes, 305 1-7-7. Springer Netherlands.</p><p>Barbour, Andrew; Meredith Montgomery, Alecia Adamson et al. (2010) Mangrove use by the invasive lionfish Pterois volitans, 291-294. In Marine Ecology Progress Series</p><p>310 Barbour, A., Allen, M., Frazer, T., & Sherman, K. (2011). Evaluating the Potential Efficacy of Invasive Lionfish (Pterois volitans) Removals. PLoS ONE, 6 (5) DOI: 10.1371/journal.pone.0019666</p><p>Freshwater, D. et al. (2009). Mitochondrial control region sequence analyses indicate dispersal from the US East Coast as the source of the invasive Indo-Pacific lionfish Pterois volitans in the Bahamas. Marine 315 Biology, 156(6), 1213-1221.</p><p>Johnston, M.W., Purkis, S.J., 2011. Spatial analysis of the invasion of lionfish in the western Atlantic and Caribbean. Marine Pollution Bulletin 62 (6), 1218–1226.</p><p>320 Layman, C.A. and Silliman, B.R. (2002) Preliminary survey and diet analysis of juvenile fishes of an estuarine creek on Andros Island, Bahamas. Bulletin of Marine Science 70(1):199-210. </p><p>Morris J.A. Jr, et al. (2009) Biology and Ecology of the Invasive Lionfish, Pterois miles and Pterois volitans. Proceedings of the 61st Gulf and Carribean Fisheries Institute November 10-14, 2008. Gosier, 325 Goudeloupe, French West Indies. </p><p>Mumby, P.J., et al (2004) Mangroves enhance the biomass of coral reef fish communities in the Caribbean. Nature, 427 (6974). pp. 533-536. ISSN 0028-0836 </p><p>330 Rooker et al., 1998 J.R. Rooker, G.J. Holt and S.A. Holt, Vulnerability of newly settled red drum (Sciaenops ocellatus) to predatory fish: is early-life survival enhanced by seagrass meadows?. Mar. Biol., 131 (1998), pp. 145–151.</p><p>Schofield, P.J. (2009) Geographic extent and chronology of the invasion of non-native lionfish (Pterois volitans 335 [Linnaeus 1758] and P. miles [Bennett 1828]) in the Western North Atlantic and Caribbean Sea. Aquatic Invasions 4:473-479.</p><p>Verweij M.C., Nagelkerken I, de Graaff D, Peeters M, Bakker EJ, van der Velde G (2006) Structure, food and shade attract juvenile coral reef fish to mangrove and seagrass habitats: a field experiment. Marine 340 Ecology Progress Series 306: 257-268 12</p><p>Literature Cited Continued</p><p>Methodology section 345 Cerino C (2010) Bioenergetics and trophic impacts of invasive Indo-Pacific lionfish: MSc thesis. Greenville: East Carolina University. 72 p. </p><p>Fishelson, L. (1997) Experiments and observations on food consumption, growth and starvation in Dendrochirus 350 brachypterus and Pterois volitans (Pteroinae, Scorpaenidae). Environmental Biology of Fishes 50:391– 403.</p><p>Green SJ, Côté IM (2008) Record densities of Indo-Pacific lionfish on Bahamian coral reefs. Coral Reefs 28: 107 355 Laegdsgaard, Pia; Johnson, Craig R. (1995)Mangrove habitats as nurseries: unique assemblages of juvenile fish in subtropical mangroves in eastern Australia. Mar. Ecol. Progr. Ser. 126:67-81 </p><p>Layman, C.A. and Silliman, B.R. (2002) Preliminary survey and diet analysis of juvenile fishes of an estuarine creek on Andros Island, Bahamas. Bulletin of Marine Science 70(1):199-210. 360 Morris J.A. Jr. et al. (2009) Biology and Ecology of the Invasive Lionfish, Pterois miles and Pterois volitans. Proceedings of the 61st Gulf and Carribean Fisheries Institute November 10-14, 2008. Gosier, Goudeloupe, French West Indies. </p><p>365 Morris J.A. Jr, Akins JL (2009) Feeding ecology of invasive lionfish (Pterois volitans) in the Bahamian archipelago. Env Bio Fish 86: 389–398. </p><p>NOAA's National Ocean Service: Lionfish Invasion." NOAA's National Ocean Service. N.p., n.d. Web. 3 May 2011. <http://oceanservice.noaa.gov/education/stories/lionfish/factsheet.html>. 370 Mumby, P.J., et al (2004) Mangroves enhance the biomass of coral reef fish communities in the Caribbean. Nature, 427 (6974). pp. 533-536. ISSN 0028-0836 </p><p>Randall, John E. (1963) Notes on the Systematics of Parrotfishes (Scaridae), with Emphasis on Sexual 375 Dichromatism. Copeia, Vol. 1963, No. 2 (Jun. 14, 1963), pp. 225-237 </p><p>Schofield, P.J. (2009) Geographic extent and chronology of the invasion of non-native lionfish (Pterois volitans [Linnaeus 1758] and P. miles [Bennett 1828]) in the Western North Atlantic and Caribbean Sea. Aquatic Invasions 4:473-479. 380 Turner JW, Jr, C Rogers and R Nemeth (2003) Measurement of fecal glucocorticoids in parrotfishes to assess stress. Journal of General and Comparative Endocrinology 133:341-352 </p><p>Verweij M.C., Nagelkerken I, de Graaff D, Peeters M, Bakker EJ, van der Velde G (2006) Structure, food and 385 shade attract juvenile coral reef fish to mangrove and seagrass habitats: a field experiment. Marine Ecology Progress Series 306: 257-268 13</p><p>Michael T. Saenz</p><p>390 7533 Trillium Boulevard, Sarasota, Florida 34241</p><p>(941) 650-5833</p><p>Education:</p><p>2008-Present: Florida Gulf Coast University, Ft. Myers, FL (Projected Graduation Date: Fall 2012)</p><p>Major: Environmental Studies </p><p>395 Minor: Interdisciplinary Studies</p><p>Relevant course work - Marine Systems, Environmental Education, Environmental </p><p>Literature, Environmental Biology of SW Florida, Environmental Humanities, ST: </p><p>Sustainability, Integrated Ecosystems Management </p><p>2004-2008: Riverview High School, Sarasota, Florida (Graduation Date: 2008)</p><p>400</p><p>Awards and Achievements:</p><p> Dean's List FGCU (2009 and 2010)</p><p> Florida Bright Future’s Scholarship (2008-Present)</p><p> Quill and Scroll National Journalism Honor Society (Senior Year, H.S.)</p><p>405 Renaissance Academic Achievement (Senior Year, H.S.)</p><p> Bobby Geere Award: Sarasota Herald Tribune contest recognizing excellence in High School </p><p> journalism </p><p> Outstanding Attendance and Achievement (Junior/Senior Year, H.S.)</p><p>410 14</p><p>Extracurricular, Personal and Volunteer Activities:</p><p>415 P.A.T.C.H. - member of the Project Art Therapy for Children's Health club, President Marisa </p><p>Schreiber. (FGCU)</p><p> Special Equestrians Volunteer: Assist in providing Horse therapy for disabled individuals, </p><p> program provides therapy for a wide range of disabilities.</p><p> BUDS (Bringing Up Down Syndrome) volunteer: Assist with fund raising and group events </p><p>420 throughout the year. Participant in the annual “Buddy Walk”. </p><p> TOPS Soccer volunteer: Act as a “buddy” to disabled children in special needs soccer league</p><p> KEY Club- Riverview High School: Participate in various community service oriented events </p><p> throughout the year</p><p>425 Work Experience: </p><p>February 2011-Present: Angelina's Ristorante, Fort Myers, FL</p><p>Server Assistant; Food Runner/Expeditor – (fine Italian dining)</p><p>2007-2008: Sarasota Herald Tribune, Sarasota, Florida </p><p>430 Correspondent Writer: Write entertainment related news and music reviews as assigned</p><p>2006-2007: Firehouse Subs, Sarasota, Florida </p><p>Sandwich preparation, operating the cash register, and customer service in a fast-paced </p><p> restaurant 435 15</p>
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