As Gulf Oil Extraction Goes Deeper, Who Is at Risk? Community Structure, Distribution, and Connectivity of the Deep-Pelagic Fauna

  • Tracey T. SuttonEmail author
  • Tamara Frank
  • Heather Judkins
  • Isabel C. Romero


The habitat and biota most affected by ultra-deep oil spills in the Gulf of Mexico (GoM) will necessarily be in the deep-pelagic domain. This domain represents ~91% of the GoM’s volume and almost certainly contains the majority of its metazoan inhabitants. Ultra-deep oil spills may or may not reach the surface or the seafloor but will occur entirely within the deepwater column domain at some point and likely for the longest duration. Recent research has shown the deep-pelagic GoM to be extremely rich in biodiversity, both taxonomic and functional. Indeed, the GoM is one of the four “hyperdiverse” midwater ecosystems in the World Ocean. This biodiversity is functionally important. For example, well over half (58%) of all fish species known to exist in the GoM spend all or part of their lives in the oceanic domain. Recent research has also shown the deep-pelagic GoM to be highly connected vertically, as well as horizontally (onshore-offshore). This vertical connectivity provides an increasingly valued ecosystem service in the form of atmospheric carbon sequestration via the “biological pump.” In this chapter, we summarize the GoM deep-pelagic nekton (fishes, macrocrustaceans, and cephalopods) that have been, and would be, affected by ultra-deep oil spills. We also discuss key aspects of distribution and behavior (e.g., vertical migration). These behaviors and distributions are key elements of ecosystem assessments before and after oil spills. For example, some deep-pelagic taxa show affinities for oceanic rim habitats (i.e., continental slopes), where ultra-deep drilling is most intense. Lastly, we summarize what is known about hydrocarbon contamination in the deep-pelagic biota and its possible ecosystem consequences.


Epipelagic Mesopelagic Bathypelagic Biodiversity Vertical distribution Connectivity 



This research was made possible by a grant from The Gulf of Mexico Research Initiative through the DEEPEND and C-IMAGE II and C-IMAGE III consortia. Data are publicly available through the Gulf of Mexico Research Initiative Information & Data Cooperative (GRIIDC) at (doi: [10.7266/N7VX0DK2, 10.7266/N7R49NTN]).


  1. Adhikari PL, Maiti K, Overton EB (2015) Vertical fluxes of polycyclic aromatic hydrocarbons in the Northern Gulf of Mexico. Mar Chem 168:60–68CrossRefGoogle Scholar
  2. Aguzzi J, Company JB (2010) Chronobiology of deep-water decapod crustaceans on continental margins. Adv Mar Biol 58:155–226. Scholar
  3. Allain V (2005) Diet of four tuna species of the Western and Central Pacific Ocean. Fish Newslett S Pac Commission 114:30Google Scholar
  4. Armstrong CW, Foley NS, Tinch R, van den Hove S (2012) Services from the deep: steps towards valuation of deep-sea goods and services. Ecosyst Serv 2:2–13. Scholar
  5. Barron MG, Carls MG, Heintz R, Rice SD (2004) Evaluation of fish early life-stage toxicity models of chronic embryonic exposures to complex polycyclic aromatic hydrocarbon mixtures. Toxicol Sci 78:60–67. Scholar
  6. Borodulina OD (1972) The feeding of mesopelagic predatory fish in the open ocean. J Ichthyol 12:692–703Google Scholar
  7. Burdett EA (2016) Geographic and depth distributions of decapod shrimps (Caridea: Oplophoridae) from the northeastern Gulf of Mexico with notes on ontogeny and reproductive seasonality. Master’s Thesis. Nova Southeastern University. Retrieved from NSUWorks,
  8. Burdett EA, Fine CD, Sutton TT, Cook AB, Frank TM (2017) Geographic and depth distributions, ontogeny and reproductive seasonality of decapod shrimps (Caridea: Oplophoridae) from the northeastern Gulf of Mexico. Bull Mar Sci 93(3):743–767. Scholar
  9. Canadell JG, Le Quéré C, Raupach MR, Field CB, Buitenhuis ET, Ciais P, Conway TJ, Gillett NP, Houghton RA, Marland G (2007) Contributions to accelerating atmospheric CO2 growth from economic activity, carbon intensity, and efficiency of natural sinks. Proc Natl Acad Sci 104(47):18,866–18,870. Scholar
  10. Carls MG, Rice SD, Hose JE (1999) Sensitivity of fish embryos to weathered crude oil: part I. Low-level exposure during incubation causes malformations, genetic damage, and mortality in larval pacific herring (Clupea pallasii). Environ Toxicol Chem 18:481–493CrossRefGoogle Scholar
  11. Chanton JP, Cherrier J, Wilson RM, Sarkodee-Adoo J, Bosman S, Mickle A, Graham WM (2012) Radiocarbon evidence that carbon from the Deepwater Horizon spill entered the planktonic food web of the Gulf of Mexico. Environ Res Lett 7:045303. Scholar
  12. Danovaro R, Gambi C, Dell’Anno A, Corinaldesi C, Fraschetti S, Vanreusel A, Vincx M, Gooday AJ (2008) Exponential decline of deep-sea ecosystem functioning linked to benthic biodiversity loss. Curr Biol 18(1):1–8. Scholar
  13. D'Elia M, Warren JD, Rodriguez-Pinto I, Sutton TT, Cook A, Boswell KM (2016) Diel variation in the vertical distribution of deep-water scattering layers in the Gulf of Mexico. Deep-Sea Res I 115:91–102CrossRefGoogle Scholar
  14. Feagans-Bartow JN, Sutton TT (2014) Ecology of the oceanic rim: pelagic eels as key ecosystem components. Mar Ecol Prog Ser 502:257–266CrossRefGoogle Scholar
  15. Fine CD (2016) The vertical and horizontal distribution of deep-sea crustaceans of the order Euphausiacea (Malacostraca: Eucarida) from the northern Gulf of Mexico with notes on reproductive seasonality. Master’s thesis. Nova Southeastern University. Retrieved from NSUWorks.
  16. French-McCay D, Crowley D, Rowe JJ, Bock M, Robinson H, Wenning R, Hayward Walker A, Joeckel J, Nedwed TJ, Parkerton TF (2018) Comparative risk assessment of spill response options for a Deepwater oil well blowout: part 1. Oil spill modeling. Mar Pollut Bull 133:1001–1015CrossRefGoogle Scholar
  17. Graham WM, Condon RH, Carmichael RH, D’Ambra I, Patterson HK, Linn LJ, Hernandez FJ Jr (2010) Oil carbon entered the coastal Planktonic Food Web during the Deepwater Horizon Oil Spill. Environ Res Lett 5(4):045301CrossRefGoogle Scholar
  18. Heintz RA, Short JW, Rice SD (1999) Sensitivity of fish embryos to weathered crude oil: part 2. Increased mortality of Pink Salmon (Oncorhynchus gorbuscha) embryos incubating downstream from weathered Exxon Valdez crude oil. Environ Toxicol Chem 18:494–503CrossRefGoogle Scholar
  19. Heintz RA, Rice SD, Wertheimer AC, Bradshaw RF, Thrower FP, Joyce JE, Short JW (2000) Delayed effects on growth and marine survival of Pink Salmon Oncorhynchus gorbuscha after exposure to crude oil during embryonic development. Mar Ecol Prog Ser 208:205–216CrossRefGoogle Scholar
  20. Herring P (2001) The biology of the deep ocean. OUP, OxfordGoogle Scholar
  21. Hopkins TL, Sutton TT (1998) Midwater fishes and shrimps as competitors in low latitude oligotrophic ecosystems. Mar Ecol Prog Ser 164:37–45CrossRefGoogle Scholar
  22. Hopkins TL, Flock ME, Gartner JV, Torres JJ (1994) Structure and trophic ecology of a low latitude midwater decapod and mysid assemblage. Mar Ecol Prog Ser 109:143–156. Scholar
  23. Irigoien X, Klevjer TA, Røstad A, Martinez U, Boyra G, Acuña JL, Bode A, Echevarria F, González-Gordillo JI, Hernandez-Leon S, Agusti S (2014) Large mesopelagic fishes biomass and trophic efficiency in the open ocean. Nat Commun 5:Article number: 3271CrossRefGoogle Scholar
  24. Jobstvogt N, Townsend M, Witte U, Hanley N (2014) How can we identify and communicate the ecological value of deep-sea ecosystem services? PLoS One 9(7):e100646. Scholar
  25. Judkins HL (2009) Cephalopods of the Broad Caribbean: distribution, abundance, and ecological importance. (Torres J, Vecchione M Eds.). University of South FloridaGoogle Scholar
  26. Judkins H, Vecchione M (2016) Diversity of midwater cephalopods in the northern Gulf of Mexico: comparison of two collecting methods. Mar Biodivers:1–11. Scholar
  27. Judkins H, Vecchione M, Rosario K (2016) Morphological and molecular evidence of Heteroteuthis dagamensis in the Gulf of Mexico. Bull Mar Sci.
  28. Judkins H, Lindgren A, Villanueva R, Clark K, Vecchione M (in prep.) A description of three new bathyteuthid squid species from the North Atlantic and Gulf of Mexico.Google Scholar
  29. LaRoe ET (1967) A contribution to the biology of the Loliginidae (Cephalopoda: Myopsida) of the Tropical Western Atlantic. Master of Science thesis; University of Miami, Coral GablesGoogle Scholar
  30. Leduc D, Rowden AA, Bowden DA, Probert PK, Pilditch CA, Nodder SD (2012) Unimodal relationship between biomass and species richness of deep-sea nematodes: implications for the link between productivity and diversity. Mar Ecol Prog Ser 454:53–64. Scholar
  31. Levin LA, Dayton PK (2009) Ecological theory and continental margins: where shallow meets deep. Trends Ecol Evol 24:606–61.7. Scholar
  32. Lipka DA (1975) The systematics and zoogeography of cephalopods of the Gulf of Mexico. PhD. Dissertation, Texas A&M University, 204 pGoogle Scholar
  33. Lu CC, Roper CFE (1979) Cephalopods from Deepwater Dumpsite 106 (Western Atlantic): vertical distribution and seasonal abundance; Smithsonian Contributions to Zoology, n. 288; Smithsonian Institution Press, 36pGoogle Scholar
  34. Millemann DR, Portier RJ, Olson G, Bentivegna CS, Cooper KR (2015) Particulate accumulations in the vital organs of wild Brevoortia patronus from the northern Gulf of Mexico after the Deepwater Horizon oil spill. Ecotoxicology 24:1831–1847. Scholar
  35. Milligan RE, Sutton TT (submitted) An overview of the species composition, abundance, and vertical distribution of the mesopelagic fish family Myctophidae in the northern Gulf of Mexico. Deep-Sea Res IGoogle Scholar
  36. Murawski SA, Hogarth WT, Peebles EB, Barbeiri L (2014) Prevalence of external skin lesions and polycyclic aromatic hydrocarbon concentrations in Gulf of Mexico fishes, post-Deepwater Horizon. Trans Am Fish Soc 143:37–41. Scholar
  37. Murawski SA, Fleeger JW, Patterson WF, Hu C, Daly K, Romero I, Toro-Farmer GA (2016) How did the Deepwater Horizon oil spill affect coastal and continental shelf ecosystems of the Gulf of Mexico? Oceanography 29. Scholar
  38. Murawski SA, Hollander DJ, Gilbert S, Gracia A (2020) Deep-water oil and gas production in the Gulf of Mexico, and related global trends (Chap. 2). In: Murawski SA, Ainsworth C, Gilbert S, Hollander D, Paris CB, Schlüter M, Wetzel D (eds) Scenarios and responses to future Deep Oil Spills – fighting the next war. Springer, ChamGoogle Scholar
  39. Passarella KC (1990) Oceanic cephalopod assemblage in the Eastern Gulf of Mexico. Department of Marine Science. University of South Florida, St. Petersburg. 50pGoogle Scholar
  40. Pearcy WG, Forss CA (1966) Depth distribution of oceanic shrimps (Decapoda; Natantia) off Oregon. J Fish Res Bull Can 23(8):1135–1143. Scholar
  41. Quintana-Rizzo E, Torres JJ, Ross SW, Romero I, Watson K, Goddard E, Hollander D (2015) δ13C and δ15N in deep-living fishes and shrimps after the Deepwater Horizon Oil Spill, Gulf of Mexico. Mar Pollut Bull 94(1–2):241–250CrossRefGoogle Scholar
  42. Ramirez-Llodra E, Tyler PA, Baker MC, Bergstad OA, Clark MR, Escobar E, Levin LA, Menot L, Rowden AA, Smith CR, Van Dover CL (2011) Man and the last great wilderness: human impact on the deep sea. PLoS One 6(7):e22588. Scholar
  43. Reddy CM, Arey JS, Seewald JS, Sylva SP, Lemkau KL, Nelson RK, Carmichael C, McIntyre CP, Fenwick J, Ventura GT, Van Mooy BAS, Camilli R (2011) Composition and fate of gas and oil released to the water column during the Deepwater Horizon oil spill. Proc Natl Acad Sci 109:20229–20234. Scholar
  44. Reid SB, Hirota J, Young RE, Hallacher LE (1991) Mesopelagic-boundary community in Hawaii: micronekton at the interface between neritic and oceanic ecosystems. Mar Biol 109(3):427–440. Scholar
  45. Richards TM, Gipson EE, Cook A, Sutton TT, Wells RJD (2018) Trophic ecology of meso- and bathypelagic predatory fishes in the Gulf of Mexico. ICES J Mar Sci. Scholar
  46. Romero IC, Schwing PT, Brooks GR, Larson RA, Hastings DW, Flower BP, Goddard EA, Hollander DJ (2015) Hydrocarbons in deep-sea sediments following the 2010 Deepwater Horizon Blowout in the Northeast Gulf of Mexico. PLoS One 10:1–23. Scholar
  47. Romero IC, Toro-farmer G, Diercks A, Schwing P, Muller-Karger F, Murawski S, Hollander DJ (2017) Large-scale deposition of weathered oil in the Gulf of Mexico following a deep-water oil spill. Environ Pollut 228:179–189. Scholar
  48. Romero IC, Sutton TT, Carr B, Quintana-Rizzo E, Ross SW, Hollander DJ, Torres JJ (2018) Decadal assessment of polycyclic aromatic hydrocarbons in mesopelagic fishes from the Gulf of Mexico reveals exposure to oil-derived sources. Environ Sci Technol. Scholar
  49. Roper CFE, Young YR (1975) Vertical distribution of pelagic cephalopods; Smithsonian contributions to zoology n. 209; Smithsonian Institution Press, 51pGoogle Scholar
  50. Ryerson TB, Camilli R, Kessler JD, Kujawinski EB, Reddy CM, Valentine DL, Atlas E, Blake DR, de Gouw J, Meinardi S, Parrish DD, Peischl J, Seewald JS, Warneke C (2012) Chemical data quantify Deepwater Horizon hydrocarbon flow rate and environmental distribution. Proc Natl Acad Sci U S A 109:20246–20253. Scholar
  51. Sabine CL, Feely RA (2007) The oceanic sink for carbon dioxide. In: Reay D, Hewitt CN, Smith K, Grace J (eds) Greenhouse gas sinks. CAB International, Oxfordshire, pp 31–46CrossRefGoogle Scholar
  52. Sørhus E, Incardona JP, Furmanek T, Goetz GW, Scholz NL, Meier S, Edvardsen RB, Jentoft S (2017) Novel adverse outcome pathways revealed by chemical genetics in a developing marine fish. elife 6:e20707:1–30. Scholar
  53. Sundberg H, Ishaq R, Tjärnlund U, Åkerman G, Grunder K, Bandh C, Broman D, Balk L (2006) Contribution of commonly analyzed polycyclic aromatic hydrocarbons (PAHs ) to potential toxicity in early life stages of rainbow trout (Oncorhynchus mykiss). Can J Fish Aquat Sci 1333:1320–1333. Scholar
  54. Sutton TT (2013) Vertical ecology of the pelagic ocean: classical patterns and new perspectives. J Fish Biol 83:1508–1527CrossRefGoogle Scholar
  55. Sutton TT, Wiebe PH, Madin LP, Bucklin A (2010) Diversity and community structure of pelagic fishes to 5000 m depth in the Sargasso Sea. Deep-Sea Res II 57:2220–2233CrossRefGoogle Scholar
  56. Sutton TT, Clark MR, Dunn DC, Halpin PN, Rogers AD, Guinotte J, Bograd SJ, Angel MV, Perez JA, Wishner K, Haedrich RL, Lindsay DJ, Drazen JC, Vereshchaka A, Piatkowski U, Morato T, Blachowiak-Samolyk K, Robison BH, Gjerde KM, Pierrot-Bults A, Bernal P, Reygondeau G, Heino M (2017) A global biogeographic classification of the mesopelagic zone. Deep-Sea Res I 126:85–102CrossRefGoogle Scholar
  57. Sutton TT, Moore JA, Cook AB, Pruzinsky N (in prep.) Oceanic fishes of the Gulf of Mexico: the DEEPEND synthesis.Google Scholar
  58. Thurber AR, Sweetman AK, Narayanaswamy BE, Jones DOB, Ingels J, Hansman RL (2014) Ecosystem function and services provided by the deep sea. Biogeosciences 11(14):3,941–3,963. Scholar
  59. Trueman CN, Johnston G, O’Hea B, MacKenzie KM (2014) Trophic interactions of fish communities at midwater depths enhance long-term carbon storage and benthic production on continental slopes. Proc. R. Soc. B 281:20140669.CrossRefGoogle Scholar
  60. Uribe JE, Zardoya R (2017) Revisiting the phylogeny of Cephalopoda using complete mitochondrial genomes. J Molluscan Stud 83(2):133–144. Scholar
  61. Voss GL (1956) A review of the cephalopods of the Gulf of Mexico. Bull Mar Sci 6(2):85–178Google Scholar
  62. Voss GL (1973) The potentially commercial species of octopus and squid of Florida, the Gulf of Mexico and the Caribbean Sea. Univ. Miami Sea Grant Program, Miami, FLGoogle Scholar
  63. Walker BD, Druffel ERM, Kolasinski J, Roberts BJ, Xu X, Rosenheim BE (2017) Stable and radiocarbon isotopic composition of dissolved organic matter in the Gulf of Mexico. Geophys Res Lett 44(16):8424–8434CrossRefGoogle Scholar
  64. Webb TJ, Berghe EV, O'Dor R (2010) Biodiversity’s big wet secret: the global distribution of marine biological records reveals chronic under-exploration of the deep pelagic ocean. PLoS One 2:5(8):e10223CrossRefGoogle Scholar
  65. West JE, Neill SMO, Ylitalo GM, Incardona JP, Doty DC, Dutch ME (2014) An evaluation of background levels and sources of polycyclic aromatic hydrocarbons in naturally spawned embryos of Pacific herring (Clupea pallasii) from Puget Sound, Washington, USA. Sci Total Environ 499:114–124. Scholar
  66. Whitehead A, Dubansky B, Bodinier C, Garcia TI, Miles S, Pilley C, Raghunathan V, Roach JL, Walker N, Walter RB, Rice CD, Galvez F (2012) Genomic and physiological footprint of the Deepwater Horizon oil spill on resident marsh fishes. Proc Natl Acad Sci 109:20298–20302. Scholar
  67. Wilson RW, Millero FJ, Taylor JR, Walsh PJ, Christensen V, Jennings S, Grosell M (2009) Contribution of fish to the marine inorganic carbon cycle. Science 323(5912):359–362CrossRefGoogle Scholar
  68. Yan B, Passow U, Chanton JP, Nöthig E-M, Asper V, Sweet J, Pitiranggon M, Diercks A, Pak D (2016) Sustained deposition of contaminants from the Deepwater Horizon spill. Proc Natl Acad Sci 113:E3332–E3340. Scholar
  69. Young RE (1978) Vertical distribution and photosensitive vesicle of pelagic cephalopods from Hawaiian waters. Fish Bull 76(3):583–615Google Scholar
  70. Ziervogel K, Dike C, Asper V, Montoya J, Battles J, D’souza N, Passow U, Diercks A, Esch M, Joye S, Dewald C, Arnosti C (2015) Enhanced particle fluxes and heterotrophic bacterial activities in Gulf of Mexico bottom waters following storm-induced sediment resuspension. Deep-Sea Res II Top Stud Oceanogr 129:77–88. Scholar

Copyright information

© Springer Nature Switzerland AG 2020

Authors and Affiliations

  • Tracey T. Sutton
    • 1
    Email author
  • Tamara Frank
    • 1
  • Heather Judkins
    • 2
  • Isabel C. Romero
    • 3
  1. 1.Nova Southeastern University, Halmos College of Natural Sciences and OceanographyDania BeachUSA
  2. 2.University of South Florida St. Petersburg, Department of Biological SciencesSt. PetersburgUSA
  3. 3.University of South Florida, College of Marine ScienceSt. PetersburgUSA

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