Abstract
Observations of Black Spot Syndrome (BSS), a pigmented dermatopathy in marine fishes, have been increasingly reported in important grazers such as surgeonfish and parrotfish in the Caribbean. This condition has been linked to infection by the trematode parasite, Scaphanocephalus spp., although relatively little is known about the environmental drivers of infection and how they vary spatially. This study introduces a non-invasive, video-based method to survey BSS presence and severity in ocean surgeonfish (Acanthurus tractus). Application of the approach across 35 coastal sites in Curaçao was used to evaluate the influence of environmental factors on BSS, including longitude, herbivorous fish density, wave energy, depth, nutrient pollution, and inhabited surface area. Of the 5123 fish surveyed between February 2022 and January 2023, 70% exhibited visible signs of BSS, and the average number of lesions per fish increased by ~ fivefold from eastern to western sites along the leeward coastline. Within a site, estimates of BSS severity were broadly consistent between different divers, different reviewers of video footage, and the date of sampling, emphasizing the robustness of the surveillance approach. Analyses of environmental factors indicated that BSS decreased with wave intensity while increasing in association with higher nutrient runoff and fishing pressure. This study provides insight into environmental correlates of BSS severity while highlighting the use of video-based surveillance as a non-invasive survey method. The mechanisms linking environmental factors with BSS as well as its consequences for affected fish remain unknown, emphasizing the need for long-term and experimental studies in this system.
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References
Aeby GS (2003) Corals in the genus Porites are susceptible to infection by a larval trematode. Coral Reefs 22:216. https://doi.org/10.1007/s00338-003-0310-9
Al-Salem AAM, Baghdadi HB, Mahmoud MA, Ibrahim M, Bayoumy EM (2020) Morphomolecular and pathological study of Scaphanocephalus sp. in new host Siganus argenteus in the Arabian Gulf. Dis Aquat Org 144:221–230. https://doi.org/10.3354/dao03586
Amarasiri M, Furukawa T, Nakajima F, Sei K (2021) Pathogens and disease vectors/hosts monitoring in aquatic environments: potential of using eDNA/eRNA based approach. Sci Total Environ 796:148810. https://doi.org/10.1016/j.scitotenv.2021.148810
Barker E, Cone DK (2000) Occurrence of Ergasilus celestis (Copepoda) and Pseudodactylogryrus anguillae (Monogenea) among wild eels (Anguilla rostrata) in relation to stream flow, pH and temperature and recommendations for controlling their transmission among captive eels. Aquaculture 187:261–274. https://doi.org/10.1016/S0044-8486(00)00324-0
Barve V (2014) Discovering and developing primary biodiversity data from social networking sites: a novel approach. Ecol Inform 24:194–199. https://doi.org/10.1016/j.ecoinf.2014.08.008
Bellwood DR, Hughes TP, Folke C, Nyström M (2004) Confronting the coral reef crisis. Nature 429:827–833. https://doi.org/10.1038/nature02691
Bernal MA, Floeter SR, Gaither MR, Longo GO, Morais R, Ferreira CEL, Vermeij MJ, Rocha LA (2015) High prevalence of dermal parasites among coral reef fishes of Curaçao. Mar Biodivers 46:67–74. https://doi.org/10.1007/s12526-015-0322-z
Blanar CA, Munkittrick KR, Houlahan JE, MacLatchy DL, Marcogliese DJ (2009) Pollution and parasitism in aquatic animals: a meta-analysis of effect size. Aquat Toxicol 93:18–28. https://doi.org/10.1016/j.aquatox.2009.03.002
Bloch A, Al-Shaer L, Baumann B, Draud M, Itzkowitz M (2021) Composition changes and movements in mixed-species groups of algae grazing fish in Jamaica and Grand Cayman Island. Part II. Open J Mar Sci 11:41–54. https://doi.org/10.4236/ojms.2021.111003
Bodensteiner LR, Sheehan RJ, Wills PS, Brandenburg AM, Lewis WM (2000) Flowing water: an effective treatment for ichthyophthiriasis. J Aquat Anim Health 12:209–219. https://doi.org/10.1577/1548-8667(2000)012%3c0209:FWAETF%3e2.0.CO;2
Brooks ME, Kristensen K, Van Benthem KJ, Magnusson A, Berg CW, Nielsen A, Bolker BM et al. (2017) glmmTMB balances speed and flexibility among packages for zero-inflated generalized linear mixed modeling. R J 9:378–400. https://doi.org/10.32614/RJ-2017-066
Buck JC, Lutterschmidt WI (2017) Parasite abundance decreases with host density: evidence of the encounter-dilution effect for a parasite with a complex life cycle. Hydrobiologia 784:201–210. https://doi.org/10.1007/s10750-016-2874-8
Buck JC, Hechinger RF, Wood AC, Stewart TE, Kuris AM, Lafferty KD (2017) Host density increases parasite recruitment but decreases host risk in a snail-trematode system. Ecology 98:2029–2038. https://doi.org/10.1002/ecy.1905
Burns JHR, Weyenberg G, Mandel T, Ferreira SB, Gotshalk D, Kinoshita CK, Marshall MJ, Del Moral NAV, Murphy SJ, Pascoe KH, Runyan A, Spengler AJ, Wells BD, Wilde DK, Pelayo R (2020) A comparison of the diagnostic accuracy of in-situ and digital image-based assessments of coral health and disease. Front Mar Sci 7:304. https://doi.org/10.3389/fmars.2020.00304
Budria A (2017) Beyond troubled waters: the influence of eutrophication on host-parasite interactions. Funct Ecol 31:1348–1358. https://doi.org/10.1111/1365-2435.12880
Bullard SA, Overstreet RM (2008) Digeneans as enemies of fishes. Fish Dis 2:817–976
Burkepile DE, Hay ME (2006) Herbivore vs. nutrient control of marine primary producers: context-dependent effects. Ecology 87:3128–3139. https://doi.org/10.1890/0012-9658(2006)87[3128:HVNCOM]2.0.CO;2
Byers JE, Blakeslee AMH, Linder E, Cooper AB, Maguire TJ (2008) Controls of spatial variation in the prevalence of trematode parasites infecting a marine snail. Ecology 89:439–451. https://doi.org/10.1890/06-1036.1
Cappo M, Harvey E, Malcolm H, Speare P (2003) Potential of video techniques to monitor diversity, abundance and size of fish in studies of marine protected areas. In: Beumer JP, Grant A, Smith DC (eds) Aquatic protected areas: what works best and how do we know? vol 1 (Cairns edn). University of Queensland, p 455−464
Carrasco JL (2010) A generalized concordance correlation coefficient based on the variance components generalized linear mixed models for overdispersed count data. Biometrics 66:897–904. https://doi.org/10.1111/j.1541-0420.2009.01335.x
Carrasco JL (2022) iccCounts: An R package to estimate the intraclass correlation coefficient for assessing agreement with count data. R J 14: 229–243. https://doi.org/10.32614/RJ-2022-034
Castañeda RA, Van Nynatten A, Crookes S, Ellender BR, Heath DD, MacIsaac HJ, Mandrak NE, Weyl OL (2020) Detecting native freshwater fishes using novel non-invasive methods. Front Environ Sci 29:8. https://doi.org/10.3389/fenvs.2020.00029
Cohen-Sánchez A, Valencia JM, Box A, Solomando A, Tejada S, Pinya S, Catanese G, Sureda A (2023a) Black spot disease related to a trematode ectoparasite causes oxidative stress in Xyrichtys novacula. J Exp Mar Biol Ecol 560:151854. https://doi.org/10.1016/j.jembe.2022.151854
Cohen-Sánchez A, Sánchez-Mairata AG, Valencia JM, Box A, Pinya S, Tejada S, Sureda A (2023b) Immune and oxidative stress response of the fish Xyrichthys novacula infected with the trematode ectoparasite Scaphanocephalus sp. in the Balearic Islands. Fishes 2023:8:600. https://doi.org/10.3390/fishes8120600
Combes C (2001) Parasitism: the ecology and evolution of intimate interactions. University of Chicago Press, Chicago, p 60637
Côté IM, Green S, Hixon MA (2013) Predatory Fish Invaders: Insights from Indo-Pacific lionfish in the Western Atlantic and Caribbean. Biol Conserv 164:50–61. https://doi.org/10.1016/j.biocon.2013.04.014
Cribb T, Bray R, Littlewood D (2001) The nature and evolution of the association among digeneans, molluscs and fishes. Int J Parasitol 31:997–1011. https://doi.org/10.1016/S0020-7519(01)00204-1
Dalton SJ, Smith SD (2006) Coral disease dynamics at a subtropical location, Solitary Islands Marine Park, eastern Australia. Coral Reefs 25:37–45. https://doi.org/10.1007/s00338-005-0039-8
Daume S (2016) Mining Twitter to monitor invasive alien species—an analytical framework and sample information topologies. Ecol Inform 31:70–82. https://doi.org/10.1016/j.ecoinf.2015.11.014
De Graaf M, Simal F (2015) Quick scan to assess the prevalence of dermal parasites among coral reef fishes of Bonaire. IMARES Report C055/15, p 13
Dennis M, Izquierdo A, Conan A, Johnson K, Giardi S, Frye P, Freeman M (2019) Scaphanocephalus-associated dermatitis as the basis for black spot disease in Acanthuridae of St. Kitts, West Indies. Dis Aquat Org 137:53–63. https://doi.org/10.3354/dao03419
Duflot M, Cresson P, Julien MH, Chartier L, Bourgau O, Palomba M, Mattiucci S, Midelet G, Gay M (2023) Black spot diseases in seven commercial fish species from the English Channel and the North Sea: infestation levels, identification and population genetics of Cryptocotyle spp. Parasite 30:28. https://doi.org/10.1051/parasite/2023028
Eierman LE, Tanner CE (2019) Prevalence and severity of cutaneous pigmented lesions on ocean surgeonfish, Acanthurus bahianus, at Turneffe Atoll and Glover’s Reef of Belize. Caribbean Naturalist 62:1–11
Elmer F, Kohl ZF, Johnson PTJ, Peachey RBJ (2019) Black spot syndrome in reef fishes: using archival imagery and field surveys to characterize spatial and temporal distribution in the Caribbean. Coral Reefs 38:1303–1315. https://doi.org/10.1007/s00338-019-01843-3
Fredensborg BL, Mouritsen KN, Poulin R (2006) Relating bird host distribution and spatial heterogeneity in trematode infections in an intertidal snail-from small to large scale. Mar Biol 149:275–283. https://doi.org/10.1007/s00227-005-0184-1
Galaktionov K, Bustnes JO (1995) Species composition and prevalence of seabird trematode larvae in periwinkles at two littoral sites in North-Norway. Sarsia 80:187–191. https://doi.org/10.1080/00364827.1995.10413590
Gast GJ, Jonkers PJ, Van Duyl FC, Bak RPM (1999) Bacteria, flagellates and nutrients in island fringing coral reef waters: influence of the ocean, the reef and eutrophication. Bull Mar Sci 65:523–538
González-García MT, García-Varela M, López-Jiménez A, Ortega-Olivares MP, Pérez-Ponce de León G, Andrade-Gómez L (2023) Scaphanocephalus spp. (Trematoda: Opisthorchiidae) in intermediate and definitive hosts of the Yucatán Peninsula, Mexico, with a re-description of Scaphanocephalus expansus. J Helminthol 97:e98. https://doi.org/10.1017/S0022149X23000834
Groner ML, Maynard J, Breyta R, Carnegie RB, Dobson A, Friedman CS, Froelich B, Garren M, Gulland FMD, Heron SF, Noble RT, Revie CW, Shields JD, Vanderstichel R, Weil E, Wyllie-Echeverria S, Harvell CD (2016) Managing marine disease emergencies in an era of rapid change. Philos Trans R Soc Lond B Biol Sci 371:20150364. https://doi.org/10.1098/rstb.2015.0364
Grutter AS (1998) Habitat-related differences in the abundance of parasites from a coral reef fish: an indication of the movement patterns of Hemigymnus melapterus. J Fish Biol 53:49–57. https://doi.org/10.1111/j.1095-8649.1998.tb00108.x
Hallett SL, Bartholomew JL (2008) Effects of water flow on the infection dynamics of Myxobolus cerebralis. Parasitology 135:371–384. https://doi.org/10.1017/S0031182007003976
Happel A (2019) A volunteer-populated online database provides evidence for a geographic pattern in symptoms of black spot infections. Int J Parasitol 10:156–163. https://doi.org/10.1016/j.ijppaw.2019.08.003
Harvell D, Aronson R, Baron N, Connell J, Dobson A, Ellner S, Gerber L, Kim K, Kuris A, McCallum H, Lafferty K, McKay B, Porter J, Pascual M, Smith G, Sutherland K, Ward J (2004) The rising tide of ocean diseases: unsolved problems and research priorities. Front Ecol Environ 2:375–382. https://doi.org/10.1890/1540-9295(2004)002[0375:TRTOOD]2.0.CO;2
Hopper JV, Poulin R, Thieltges DW (2008) Buffering role of the intertidal anemone Anthopleura aureoradiata in cercarial transmission from snails to crabs. J Exp Mar Bio Ecol 367:153–156. https://doi.org/10.1016/j.jembe.2008.09.013
Houk P, Van Woesik R (2006) Coral reef benthic video surveys facilitate long-term monitoring in the Commonwealth of the Northern Mariana Islands: toward an optimal sampling strategy. Pac Sci 60:177–189. https://doi.org/10.1353/psc.2006.0005
Hutton RF (1964) A second list of parasites from marine and coastal animals of Florida. Trans Am Microsc Soc 83:439. https://doi.org/10.2307/3224765
Inohuye Rivera RB (1995) Helmintofauna de cuatro especies de cabrillas del género Epinephelus Bloch, 1793 (Osteichthyes: Serranidae) en la costa sudoriental de Baja California Sur, México. Doctoral dissertation, Instituto Politécnico Nacional. Centro Interdisciplinario de Ciencias Marinas
Iwata K (1997) Scaphanocephalus larva from marine fishes of Iromote Island. Bull Inst Oceanic Res Devel Tokai Univ 18:43–50
Jackson JBC, Donovan MK, Cramer KL, Lam VV (editors). (2014) Status and Trends of Caribbean Coral Reefs: 1970–2012. Global Coral Reef Monitoring Network, IUCN, Gland, Switzerland
Johnson PTJ, Carpenter SR (2008) Influence of eutrophication on disease in aquatic ecosystems: patterns, processes, and predictions. In: Ostfeld RS, Keesing F, Eviner VT (eds) Infectious disease ecology: effects of ecosystems on disease and of disease on ecosystems. Princeton University Press, Princeton, NJ, pp 71–99. https://doi.org/10.1515/9781400837885.71
Johnson PTJ, Thieltges DW (2010) Diversity, decoys and the dilution effect: how ecological communities affect disease risk. J Exp Biol 213:961–970. https://doi.org/10.1242/jeb.037721
Johnson PTJ, Chase JM, Dosch KL, Hartson RB, Gross JA, Larson DJ, Sutherland DR, Carpenter SR (2007) Aquatic eutrophication promotes pathogenic infection in amphibians. Proc Natl Acad Sci USA 104:15781–15786. https://doi.org/10.1073/pnas.0707763104
Johnson PTJ, Townsend AR, Cleveland CC, Glibert PM, Howarth RW, McKenzie VJ, Rejmankova E, Ward M (2010) Linking environmental nutrient enrichment and disease emergence in humans and wildlife. Ecol Appl 20:16–29
Johnson PTJ, Preston DL, Hoverman JT, Richgels KL (2013) Biodiversity decreases disease through predictable changes in host community competence. Nature 494:230–233. https://doi.org/10.1038/nature11883
Katahira H, Shimose T, Kanaiwa M (2021) New host records for Scaphanocephalus adamsi (Platyhelminthes: Trematoda: Heterophyidae) from commercial fishes off Yaeyama Islands. Fauna Ryukyuana 59:21–26
Klaus JS, Frias-Lopez J, Bonheyo GT, Heikoop JM, Fouke BW (2005) Bacterial communities inhabiting the healthy tissues of two Caribbean reef corals: interspecific and spatial variation. Coral Reefs 24:129–137. https://doi.org/10.1007/s00338-004-0447-1
Klaus JS, Janse I, Heikoop JM, Sanford RA, Fouke BW (2007) Coral microbial communities, zooxanthellae and mucus along gradients of seawater depth and coastal pollution. Environ Microbiol 9:1291–1305. https://doi.org/10.1111/j.1462-2920.2007.01249.x
Kohl ZF, Calhoun DM, Elmer F, Peachey RBJ, Leslie KL, Tkach V, Kinsella JM, Johnson PTJ (2019) Black-spot syndrome in Caribbean fishes linked to trematode parasite infection (Scaphanocephalus expansus). Coral Reefs 38:917–930. https://doi.org/10.1007/s00338-019-01819-3
Koprivnikar J, Thieltges DW, Johnson PTJ (2023) Consumption of trematode parasite infectious stages: from conceptual synthesis to future research agenda. J Helminthol 97:E33. https://doi.org/10.1017/S0022149X23000111
Lacerda A, Roumbedakis K, Bereta Junior J, Nuñer A, Petrucio M, Martins M (2017) Fish parasites as indicators of organic pollution in southern Brazil. J Helminthol 92:322–331. https://doi.org/10.1017/S0022149X17000414
Lafferty KD (2008) Ecosystem consequences of fish parasites. J Fish Biol 73:2083–2093. https://doi.org/10.1111/j.1095-8649.2008.02059.x
Lafferty KD, Harvell CD (2014) The role of infectious diseases in marine communities. Chapter 5. In: Bertness MD, Bruno JF, Silliman BR and Stachowicz JJ (eds) Marine community ecology and conservation. Sinauer Associates, Sunderland, MA, pp 85–108
Lamb JB, Willis BL, Fiorenza EA, Couch CS, Howard R, Rader DN, True JD, Kelly LA, Ahmad A, Jompa J, Harvell CD (2018) Plastic waste associated with disease on coral reefs. Science 359:460–462. https://doi.org/10.1126/science.aar3320
Lambert WJ, Corliss E, Sha J, Smalls J (2012) Trematode infections in Littorina littorea on the New Hampshire coast. Northeast Nat 19:461–474. https://doi.org/10.1656/045.019.0308
Lapointe BE, Mallin MA (2011) Nutrient enrichment and eutrophication on fringing coral reefs of Bonaire and Curaçao, Netherlands Antilles. Report to the United Nations Environment Programme for the NACRI Coral Reef Monitoring Program, Harbor Branch Oceanographic Institute, Ft Pierce, FL, p 42
Lin LIK (1989) A concordance correlation coefficient to evaluate reproducibility. Biometrics 45:255–268. https://doi.org/10.2307/2532051
Lüdecke D, Patil I, Ben-Shachar MS, Wiernik BM, Waggoner P, Makowski D (2021) performance: an R package for assessment, comparison and testing of statistical models. J Open Source Softw 6:3139–3149. https://doi.org/10.21105/joss.03139
Malawauw RJ, Piaskowy J, Ter Horst LJ, Calhoun DM, Johnson PTJ (2024) Parasitism in reef fish communities: evaluating the roles of host traits, habitat use, and phylogeny on infection by Scaphanocephalus (Trematoda). Coral Reefs (in press)
Mallet D, Pelletier D (2014) Underwater video techniques for observing coastal marine biodiversity: a review of sixty years of publications (1952–2012). Fish Res 154:44–62. https://doi.org/10.1016/j.fishres.2014.01.019
McManus J (2000) Coral reef fishing and coral-algal phase shifts: implications for global reef status. ICES J Mar Sci 57:572–578. https://doi.org/10.1006/jmsc.2000.0720
Packer C, Holt RD, Hudson PJ, Lafferty KD, Dobson AP (2003) Keeping the herds healthy and alert: implications of predator control for infectious disease. Ecol Lett 6:797–802. https://doi.org/10.1046/j.1461-0248.2003.00500.x
Paula JR, Sun D, Pissarra V, Narvaez P, Rosa R, Grutter AS, Sikkel PC (2021) The role of corals on the abundance of a fish ectoparasite in the Great Barrier Reef. Coral Reefs 40:535–542. https://doi.org/10.1007/s00338-021-02051-8
Pietrock M, Marcogliese DJ (2003) Free-living endohelminth stages: at the mercy of environmental conditions. Trends Parasitol 19:293–299. https://doi.org/10.1016/S1471-4922(03)00117-X
R Core Team (2023) R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. https://www.R-project.org/
Ríos-Castro R, Romero A, Aranguren R, Pallavicini A, Banchi E, Novoa B, Figueras A (2021) High-throughput sequencing of environmental DNA as a tool for monitoring eukaryotic communities and potential pathogens in a coastal upwelling ecosystem. Front Vet Sci 8:765606. https://doi.org/10.3389/fvets.2021.765606
Robertson D, Ackerman J, Choat J, Posada J, Pitt J (2005) Acanthurus tractus. I. The geography of demography. Mar Ecol Prog Ser 295:229–244. https://doi.org/10.3354/meps295229
Sandin SA, Smith JE, DeMartini EE, Dinsdale EA, Donner SD, Friedlander AM, Konotchick T, Malay M, Maragos JE, Obura D, Pantos O, Paulay G, Richie M, Rohwer F, Schroeder RE, Walsh S, Jackson JBC, Knowlton N, Sala E (2008) Baselines and degradation of coral reefs in the northern Line Islands. PLoS ONE 3:e1548. https://doi.org/10.1371/journal.pone.0001548
Sandin SA, Alcantar E, Clark R, de León R, Dilrosun F, Edwards CB, Vermeij MJ, et al (2022) Benthic assemblages are more predictable than fish assemblages at an island scale. Coral Reefs 41:1031–1043. https://doi.org/10.1007/s00338-022-02272-5
Shimose T, Katahira H, Kanaiwa M (2020) Interspecific variation of prevalence by Scaphanocephalus (Platyhelminthes: Trematoda: Heterophyidae) metacercariae in parrotfishes (Labridae: Scarini) from an Okinawan coral reef. Int J Parasitol 12:99–104.https://doi.org/10.1016/j.ijppaw.2020.05.007
Skinner RH (1978) Some external parasites of Florida fishes. Bull Mar Sci 28:590–595
Smith NF (2001) Spatial heterogeneity in recruitment of larval trematodes to snail intermediate hosts. Oecologia 127:115–122. https://doi.org/10.1007/s004420000560
Sousa WP, Grosholz ED (1991) The influence of habitat structure on the transmission of parasites. In: Bell SS, McCoy ED, Mushinsky HR (eds) Habitat structure. Population and community biology series, vol 8. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-3076-9_15
Stumbo AD, James CT, Goater CP, Wisenden BD (2012) Shoaling as an antiparasite defence in minnows (Pimephales promelas) exposed to trematode cercariae. J Anim Ecol 81:1319–1326. https://doi.org/10.1111/j.1365-2656.2012.02012.x
Sures B, Nachev M (2022) Effects of multiple stressors in fish: how parasites and contaminants interact. Parasitology 149:1822–1828. https://doi.org/10.1017/S0031182022001172
Tracy AM, Pielmeier ML, Yoshioka RM, Heron SF, Harvell CD (2019) Increases and decreases in marine disease reports in an era of global change. Proc R Soc B 286:20191718. https://doi.org/10.1098/rspb.2019.1718
Tubangui MA (1933) Trematode parasites of Philippine vertebrates, VI. Descriptions of new species and classification. Philipp J Sci 52:167–197
Upatham ES (1974) Dispersion of St. Lucian Schistosoma mansoni cercariae in natural standing and running waters determined by cercaria counts and mouse exposure. Ann Parasitol 68:343–352. https://doi.org/10.1017/S0031182000045698
Van den Hoek C, Cortel-Breeman A, Wanders J (1975) Algal zonation in the fringing coral reef of curaçao, Netherlands Antilles, in relation to zonation of corals and gorgonians. Aquat Bot 1:269–308. https://doi.org/10.1016/0304-3770(75)90028-5
Van Duyl FC (1985) Atlas of the Living Reefs of Curaçao and Bonaire (Netherlands Antilles), vol. 117. Foundation for Scientific Research in Surinam and the Netherlands Antilles, Utrecht
Vidal-Martínez VM, Pech D, Sures B, Purucker ST, Poulin R (2010) Can parasites really reveal environmental impact? Trends Parasitol 26:44–51. https://doi.org/10.1016/j.pt.2009.11.001
Waitt Institute (2017). Marine Scientific Assessment: The State of Curaçao’s Coral Reefs. The Waitt Institute
Wakabayashi S (1997) Heavy infection of metacercariae of Liliatrema skrjabini (Digenea: Cathaemasiidae) in Jacopever Rockfish Sebastes schlegeli. Pref Fish Res Inst 9:41–44
Welsh JE, Liddell C, Van der Meer J, Thieltges DW (2017) Parasites as prey: the effect of cercarial density and alternative prey on consumption of cercariae by four non-host species. Parasitology 144:1775–1782. https://doi.org/10.1017/S0031182017001056
Welsh JE, Markovic M, van der Meer J, Thieltges DW (2024) Non-linear effects of non-host diversity on the removal of free-living infective stages of parasites. Oecologia. 204(2):339–349. https://doi.org/10.1007/s00442-023-05462-2
Williams MA, Faiad S, Claar DC, French B, Leslie KL, Oven E, Guerra SA, Micheli F, Zglinczynski BJ, Haupt AJ, Sandin SA, Wood CL (2022) Life history mediates the association between parasite abundance and geographic features. J Anim Ecol 91:996–1009. https://doi.org/10.1111/1365-2656.13693
Wood CL, Lafferty KD (2015) How have fisheries affected parasite communities? Parasitology 142(1):134–144. https://doi.org/10.1017/S003118201400002X
Wood CL, Sandin SA, Zgliczynski B, Guerra AS, Micheli F (2014) Fishing drives declines in fish parasite diversity and has variable effects on parasite abundance. Ecology 95:1929–1946
Acknowledgements
For assistance in collecting transect data, we thank Rémon Malawauw, Lars ter Horst, Mike Lenstra, Julia Piaskowy, Nicole Brackenborough, Eyes Potyou, Phaedra Hernández, and students of 2022–2023 Coral Reef Ecology and Conservation course at the University of Colorado. For help with processing video footage, we gratefully acknowledge the assistance of Kiara Gelbman and Phoebe Oehmig. Dr. Mark Vermeij generously provided feedback about the study design and logistical support through CARMABI. We thank the authors of Sandin et al. (2022) for providing the environmental data used in our analyses. Dana Calhoun, Petra Visser, and Zachary Kohl engaged in discussions helpful in shaping the manuscript.
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PTJJ and CDGW designed the study; CDGW and PTJJ collected the field; PTJJ and CDGW performed statistical analyses and visualizations; CDGW and PTJJ jointly wrote and edited the manuscript.
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de Wit, C.D.G., Johnson, P.T.J. Black Spot Syndrome in ocean surgeonfish: using video-based surveillance to quantify disease severity and test environmental drivers. Mar Biol 171, 110 (2024). https://doi.org/10.1007/s00227-024-04426-1
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DOI: https://doi.org/10.1007/s00227-024-04426-1