Marine Biology

, Volume 127, Issue 2, pp 179–192 | Cite as

Trophic ecology of the stomiid (Pisces: Stomiidae) fish assemblage of the eastern Gulf of Mexico: Strategies, selectivity and impact of a top mesopelagic predator group

  • T. T. Sutton
  • T. L. Hopkins


The trophic ecology of the stomiid assemblage (Pisces, Stomiiformes, Stomiidae) in the eastern Gulf of Mexico, a region with physical and biological characteristics typical of oligotrophic low-latitude regimes, was investigated. Over 1400 specimens representing 69 species and 17 genera were examined. Four patterns of feeding were evident among the abundant stomiids: (1) myctophid predation; (2) zooplankton/small micronekton predation; (3) penaeidean shrimp predation; and (4) copepod/micronekton predation. One rare species preyed on cephalopods. Il was concluded that stomiids exhibited a high level of prey-selectivity, particularly considering the broad range of prey types available in the eastern Gulf of Mexico. The absence of numerically dominant potential prey (e.g.Cyclothone spp., sternoptychids) in the diets of piscivorous stomiids is possibly a function of feeding periodicity coupled with stomiid vertical migration. Stomiids may feed at night in the upper 200 m on vertically migrating myctophids while disregarding co-occurring nonmigrating prey during the daytime. Integration of stomiid abundance and diet data suggests that: (1) stomiids are the dominant upper trophic-level predators of the Gulf of Mexico mesopelagial, (2) stomiids inflict the highest predation impact on myctophids in low-latitude midwater ecosystems, and (3) the historic use of predation-avoidance arguments to explain certain mesopelagic phenomena (e.g. vertical migration, ventral photophores) appears to be substantiated by estimates of stomiid predation-impact. The stomiids may serve as key trophic mediators in the transfer of energy from the mesopelagial to the bathyand benthopelagial.


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  1. Anderson R (1967) Feeding chronology in two deep-sea fishes off California. MS thesis. University of Southern California, Los AngelesGoogle Scholar
  2. Angel MV (1986) Vertical distribution: study and implications. Tech Pap mar Sci (UNESCO) 49: 3–7Google Scholar
  3. Appelbaum S (1982) Studies on food organisms of pelagic fishes as revealed by the 1979 North Atlantic Eel Expedition. Helgöländer Meeresunters 35: 357–367Google Scholar
  4. Auster PJ, Griswold CA, Youngbluth MJ, Bailey TG (1992) Aggregations of myctophid fishes with other pelagic fauna. Envir Biol Fish 35: 133–139Google Scholar
  5. Badcock J, Merrett NR (1976) Midwater fishes in the eastern North Atlantic. I. Vertical distribution and associated biology in 30° N 23° W, with development notes on some myctophids. Prog Oceanogr 7: 3–58Google Scholar
  6. Bailey TG, Robison BH (1986) Food availability as a selective factor on the chemical compositions of midwater fishes in the eastern North Pacific. Mar Biol 91: 131–141Google Scholar
  7. Baird RC, Hopkins TL, Wilson DF (1975) Diet and feeding chronology ofDiaphus taaningi (Myctophidae) in the Cariaco Trench. Copeia 1975(2): 356–365Google Scholar
  8. Baldwin NS (1957) Food consumption and growth of brook trout at different temperatures. Trans Am Fish Soc 86: 323–328Google Scholar
  9. Barham EG (1970) Deep-sea fishes: lethargy and vertical orientation. In: Farquar GB, (ed) Proceedings of an International Symposium on Biological Sound Scattering in the Ocean. Maury Center for Ocean Science, Washington pp 101–119Google Scholar
  10. Beebe W, Crane J (1939) Deep-sea fishes of the Bermuda oceanographic expeditions. Family Melanostomiatidae. Zoologica, NY 24: 65–238Google Scholar
  11. Bertelsen E (1951) The ceratioid fishes. Ontogeny, taxonomy, distribution, and biology. Dana Rep 39: 1–261Google Scholar
  12. Blackburn M (1981) Low latitude gyral regions. In: Longhurst AR (ed) Analysis of marine ecosystems. Academic Press, New York, pp 3–29Google Scholar
  13. Bond GW (1974) Vertical distribution and life histories of the gonostomatid fishes (Pisces: Gonostomatidae) off Bermuda. Unpublished Ph.D dissertation. University of Rhode Island, KingstonGoogle Scholar
  14. Borodulina OD (1972) The feeding of mesopelagic predatory fish in the open ocean. J Ichthyol 12: 692–702Google Scholar
  15. Borodulina OD (1984) Identification of mesopelagic fish remains from predator stomachs. Communication II. Characteristics of the axial skeleton of fishes of the superfamily Stomiatoidea. J Ichthyol 24: 24–33Google Scholar
  16. Borodulina OD (1987) Identification of the remains of mesopelagic fishes. VI. Features of the axial skeleton of myctophoid fishes (Myctophoidea). J Ichthyol 27: 170–174Google Scholar
  17. Brauer A (1908) Die Tiefsee-Fische. II. Anatomischer Teil. Wiss Ergebn dt Tiefsee-Exped, Valdiviae, 15: 1–266Google Scholar
  18. Bray JR, Curtis JT (1957) An ordination of the upland forest communities of southern Wisconsin. Ecol Monogr 27: 325–349Google Scholar
  19. Brett JR, Higgs DA (1970) Effect of temperature on the rate of gastric digestion in fingerling sockeye salmon,Oncorhynchus nerka. J Fish Res Bd Can 27: 1767–1779Google Scholar
  20. Brusca RC, Brusca GJ (1990) Invertebrates. Sinauer Associates, Sunderland, MassachusettsGoogle Scholar
  21. Cailliet GM, Ebeling AW (1990) The vertical distribution and feeding habits two common midwater fishes (Leuroglossus stilbius andStenobranchus leucopsaurus) off Santa Barbara. Calif coop ocean Fish Invest (CalCOFI) Rep 31: 106–123Google Scholar
  22. Campbell AK, Herring PJ (1987) A novel red fluorescent protein from the deep sea luminous fishMalacosteus niger. Comp Biochem Physiol 86B: 411–417Google Scholar
  23. Clark MR (1985) The food and feeding of seven fish species from the Campbell Plateau, New Zealand. NZ Jl mar Freshwat Res 19: 339–363Google Scholar
  24. Clarke GL, Backus RH (1964) Interrelations between the vertical migration of deep-Scattering layers, bioluminescence, and changes in daylight in the sea. Bull Inst océanogr Monaco 64: 1–36Google Scholar
  25. Clarke TA (1974) Some aspects of the ecology of stomiatoid fishes in the Pacifie Ocean near Hawaii. Fish Bull US 72: 337–351Google Scholar
  26. Clarke TA (1978) Diel feeding patterns of 16 species of mesopelagic fishes from Hawaiian waters. Fish Bull US 76: 485–513Google Scholar
  27. Clarke TA (1982) Feeding habits of stomiatoid fishes from Hawaiian waters. Fish Bull US 80: 287–304Google Scholar
  28. Clarke WD (1963) Function of bioluminescence in mesopelagic organisms. Nature, Lond 198: 1244–1246Google Scholar
  29. Collard SB (1970) Forage of some eastern Pacifie midwater fishes. Copeia 1970: 348–354Google Scholar
  30. Crescitelli F (1989) The visual pigments of a deep-water malacosteid fish. J mar biol Ass UK 69: 43–51Google Scholar
  31. Denton EJ, Gilpin-Brown JB, Wright PG (1970) On the ‘filtern’ in the photophores of mesopelagic fish and on a fish emitting red light and especially sensitive to red light. J Physiol 208: 72–73Google Scholar
  32. Denton EJ, Warren FJ (1956) Visual pigments of deep-sea fish. Nature, Lond 178: 1059Google Scholar
  33. DeWitt FA Jr, Cailliet GM (1972) Feeding habits of two bristle-mouth fishes,Cyclothone acelinidens andC. signata (Gonostomatidae). Copeia 1972: 868–871Google Scholar
  34. Donaldson HA (1975) Vertical distribution and feeding of sergestid shrimps (Decapoda: Natantia) collected near Bermuda. Mar Biol 31: 37–50Google Scholar
  35. Douglas RH, Thorpe A (1992) Short-wave absorbing pigments in the ocular lenses of deep-sea teleosts. J mar biol Ass UK 72: 93–112Google Scholar
  36. Dudochkin AS (1988) The food of the grenadier,Macrourus holotrachys, in the southwestern Atlantic. J Ichthyol 28: 72–76Google Scholar
  37. Ebeling AW, Cailliet GM (1974) Mouth size and predator strategy of midwater fishes. Deep-Sea Res 21: 959–968Google Scholar
  38. Eggers DM (1977) Factors in interpreting data obtained by diel sampling of fish stomachs. J Fish Res Bd Can 34: 290–294Google Scholar
  39. Fink WL (1985) Phylogenetic relationships of the stomiid fishes (Teleostei: Stomiiformes). Misc Publs Mus Zool Univ Mich 171: 1–127Google Scholar
  40. Fink WL, Weitzman SH (1982) Relationships of stomiiform fishes (Teleostei), with a description ofDiplophos. Bull Mus comp Zool Harv 150: 31–93Google Scholar
  41. Flock ME, Hopkins TL (1992) Species composition, vertical distribution and food habits of the sergestid shrimp assemblage in the eastern Gulf of Mexico. J Crustacean Biol 12: 210–223Google Scholar
  42. Foxton P, Roe HSJ (1974) Observations on the nocturnal feeding of some mesopelagic decapod Crustacea. Mar Biol 28: 37–49Google Scholar
  43. Gartner JV Jr, Conley WJ, Hopkins TL (1988) Escapement of fishes from midwater trawls: a case study using lanternfishes (Pinces: Myctophidae). Fish Bull US 89: 213–222Google Scholar
  44. Gartner JV Jr, Hopkins TL, Baird RC, Milliken DM (1987) The lanternfishes (Pinces: Myctophidae) of the eastern Gulf of Mexico. Fish Bull US 85: 81–98Google Scholar
  45. Gibbs RH Jr (1964) Family Astronesthidae. Mem Sears Fdn mar Res 1: 311–350Google Scholar
  46. Gibbs RH Jr (1969) Taxonomy, sexual dimorphism, vertical distribution, and evolutionary zoogeography of the bathypelagic fish genusStomias (Stomiatidae). Smithson Contr Zool 31: 1–25Google Scholar
  47. Gorelova TA (1974) Zooplankton from the stomachs of juvenile lanternfish of the family Myctophidae. Okeanologia, Mosk 14: 575–580Google Scholar
  48. Gorelova TA (1980) Feeding of deep water fishes of genusCyclothone (Gonostomatidae, Pisces). Okeanologia, Mosk 20: 321–328Google Scholar
  49. Grove DJ, Goddard JS, Tan SP, Wirtz P (1976) Unpublished observations from M.Sc. and Ph.D. theses. University of Wales, CardiffGoogle Scholar
  50. Haedrich RL, Henderson NR (1974) Pelagic food ofCoryphaenoides armatus, a deep benthic rattail. Deep-Sea Res 21: 739–744Google Scholar
  51. Haffner RE (1952) Zoogeography of the bathypelagic fish,Chauliodus. Syst Zool 1: 112–133Google Scholar
  52. Hansen K, Herring PJ (1977) Dual bioluminescent systems in the anglerfish genusLinophryne (Pinces: Ceratioidea). J Zool, Lond 182: 103–124Google Scholar
  53. Heffernan JJ, Hopkins TL (1981) Vertical distribution and feeding of the shrimp generaGennadus andBenihogennema (Decapoda: Penaeidea) in the eastern Gulf of Mexico. J Crustacean Biol 1: 461–473Google Scholar
  54. Holton AA (1969) Feeding behavior of a vertically migrating lanternfish. Pacif Sci 23: 325–331Google Scholar
  55. Hopkins TL, Baird RC (1973) Diet of the hatchetfishSiernoptyx diaphana. Mar Biol 21: 34–46Google Scholar
  56. Hopkins TL, Baird RC (1975) Net feeding in mesopelagic fishes. Fish Bull US 73: 908–914Google Scholar
  57. Hopkins TL, Baird RC (1977) Aspects of the feeding ecology of oceanic midwater fishes. In: Andersen NR, Zahuranec BI (eds) Oceanic sound scattering prediction. Plenum Press, New York, pp 325–360Google Scholar
  58. Hopkins TL, Baird RC (1981) Trophodynamies of the fishValenciennellus tripunctulatus. I. Vertical distribution, diet and feeding chronology. Mar Ecol Prog Ser 5: 1–10Google Scholar
  59. Hopkins TL, Baird RC (1985a) Aspects of the trophic ecology of the mesopelagic fishLampanyctus alatus (family Myctophidae) in the eastern Gulf of Mexico. Biol Oceanogr 3: 285–313Google Scholar
  60. Hopkins TL, Baird RC (1985b) Feeding ecology of four hatchetfishes (Sternoptychidae) in the eastern Gulf of Mexico. Bull mar Sci 36: 260–277Google Scholar
  61. Hopkins TL, Flock ME, Gartner JV Jr, Torres JJ (1994) The structure and trophic ecology of a low latitude midwater decapod and mysid assemblage. Mar Ecol Prog Ser 109: 143–156Google Scholar
  62. Hopkins TL, Gartner JV Jr (1992) Resource-partitioning and predation impact of a low-latitude myctophid community. Mar Biol 114: 185–197Google Scholar
  63. Hopkins TL, Lancraft TM (1984) The composition and standing stock of mesopelagic micronekton at 27° N 86° W in the eastern Gulf of Mexico. Contr mar Sci Univ Tex 27: 143–158Google Scholar
  64. Hopkins TL, Sutton TT (1996) Midwater fishes and shrimps as competitors and resource partitioning in low latitude oligotrophic ecosystems. (in preparation)Google Scholar
  65. Hopkins TL, Sutton TT, Lancraft TM (1996) The trophic structure and predation impact of a low latitude midwater fish community. Prog Oceanogr (in press)Google Scholar
  66. Hurtubia J (1973) Trophic diversity measurement in sympatric predatory species. Ecology 54: 885–890Google Scholar
  67. Huichinson BP (1971) The effect of fish predation on the zooplankton of ten Adirondack lakes with particular reference to the alewife,Alosa pseudoharengus. Trans Am Fish Soc 100: 323–335Google Scholar
  68. Ivlev VS (1961) Experimental ecology of the feeding of fishes. Yale University Press, New Haven, ConnecticutGoogle Scholar
  69. Jansenn J, Jones W, Slattery M (1993) Locomotion and feeding responses to mechanical stimuli inHistiodraco velifer (Artedidraconidae). Copeia 1993(3): 885–889Google Scholar
  70. Jones R (1974) The rate of elimination of food from the siomachs of haddock,Melanogrammus aeglefiraus, cod,Gadus morhua, and whiting,Merlangius merlangius. J Cons int Explor Mer 35: 225–242Google Scholar
  71. Kashkin NI, Parin NV (1983) Quantitative assessment of micronektonic fishes by nonclosing gear (a review). Biol Oceanogr 2: 263–287Google Scholar
  72. Kinzer J (1982) The food of four myctophid fish species off northwest Africa. Rapp P-v Réun Cons perm int Explor Mer 180: 385–390Google Scholar
  73. Kinzer J, Schulz K (1988) Vertical distribution and feeding patterns of midwater fish in the central equatorial Atlantic. II. Sternoptychidae. Mar Biol 99: 261–269Google Scholar
  74. Lancraft TM, Hopkins TL, Torres JJ (1988) Aspects of the ecology of the mesopelagic fishGonostoma elongatum (Gonostomatidae, Stomiiformes) in the eastern Gulf of Mexico. Mar Ecol Prog Ser 49: 27–40Google Scholar
  75. Lancraft TM, Robison BH (1980) Evidence of post-capture ingestion by midwater fishes in trawl nets. Fish Bull US 77: 713–715Google Scholar
  76. Legand M, Rivaton J (1969) Cycles biologiques des poissons mesopelagiques de l'est de l'océan Indien. Troisieme note: action predatrice des poissons micronectoniques. Cah ORSTOM Sér Océanogr 7: 29–45Google Scholar
  77. Lockett NA (1975) Some problems of deep-sea fish eyes. In: Ali MA (ed) Vision in fishes. Plenum Press, New York, pp 645–655Google Scholar
  78. Markus HC (1932) The extent to which temperature changes influence food conversion in largemouth bass, (Huro floridana). Trans Am Fish Soc 62: 202–210Google Scholar
  79. Marshall NB (1954) Aspects of deep-sea biology. Philosophical Library, Inc. New YorkGoogle Scholar
  80. Marshall NB (1979) Developments in deep-sea biology. Blandford, Dorset, EnglandGoogle Scholar
  81. Mauchline J, Gordon JDM (1983) Diets of clupeoid, stomiatoid and salmonoid fish of the Rockall Trough, northeastern Atlantic Ocean. Mar Biol 77: 67–78Google Scholar
  82. Merrett NR, Roe HSJ (1974) Patterns and selectivity in the feeding of certain mesopelagic fishes. Mar Biol 28: 115–126Google Scholar
  83. Morrow JE, Gibbs RH (1964) Family Melanostomiatidae. Mem Sears Fdn mar Res 1: 351–511Google Scholar
  84. Nelson JS (1994) Fishes of the world. 3rd edn. John Wiley & Sons, Inc, New YorkGoogle Scholar
  85. Nolan RS, Rosenblatt RH (1975) A review of the deep-sea angler fish genusLasiognathus (Pistes: Thaumatichthyidae). Copeia 1975: 60–66Google Scholar
  86. O'Day WT, Fernandez HR (1974)Aristostomias scintillans (Malacosteidae): a deep-sea fish with visual pigments apparently adapted to its own bioluminescence. Vision Res 14: 545–550Google Scholar
  87. Ohman MD, Frost BW (1983) Reverse diel vertical migration: an escape from invertebrate predators. Science, NY 220: 1404–1407Google Scholar
  88. Omori M (1969) The biology of the sergestid shrimpSergestes lucens Hansen. Bull Ocean Res Inst Univ Tokyo 4: 1–83Google Scholar
  89. Pandian TJ (1967) Transformation of food in the fishMegalops cyprinoides. I. Influence of quality of food. Mar Biol 1: 60–64Google Scholar
  90. Partridge JC, Archer SN, Lythgoe JN (1988) Visual pigments in the individual rods of deep-sea fishes. J comp Physiol (Sect A) 162: 543–550Google Scholar
  91. Partridge JC, Shand J, Archer SN, Lythgoe JN, van Groningen-Luyben WAHN (1989) Interspecific variation in the visual pigments of deep-sea fishes. J comp Physiol (Sect A) 164: 513–529Google Scholar
  92. Pearcy WG, Ambler JW (1974) Food habits of deep-sea macrourid fishes off the Oregon Coast. Deep-Sea Res 21: 745–759Google Scholar
  93. Porter K (1979) Bioluminescence in marine plankton: a co-evolved antipredation system. Am Nat 114: 458–461Google Scholar
  94. Renfro WC, Pearcy WG (1966) Food and feeding habits of two pelagic shrimps. J Fish Res Bd Can 23: 1971–1975Google Scholar
  95. Repsys AJ, Applegate RL, Hales DC (1976) Food and selectivity of the black bullhead (Ictaluras melas) in Lake Poinsett, South Dakota. J Fish Res Bd Can 33: 768–775Google Scholar
  96. Robison BH, Craddock JE (1983) Mesopelagic fishes eaten by Fraser's dolphin,Lagenodelphis hosei. Fish Bull US 81: 283–289Google Scholar
  97. Roe HSJ, Badcock J (1984) The diel migrations and distributions within a mesopelagic community in the North East Atlantic. 5. Vertical migrations and feeding of fish. Prog Oceanogr 13: 389–424Google Scholar
  98. Rosecchi E, Tracey DM, Webber WR (1988) Diet of orange roughy,Hoplostethus atlanticus (Pistes: Trachichthyidae) on the Challenger Plateau, New Zealand. Mar Biol 99: 293–306Google Scholar
  99. Scott WB, Tibbo SN (1968) Food and feeding habits of swordfish,Xiphias gladius, in the Western North Atlantic. J Fish Res Bd Can 25: 903–919Google Scholar
  100. Slobodkin LB (1968) How to be a predator. Am Zool 8: 43–51Google Scholar
  101. Somiya H (1982) “Yellow lens” eyes of a stomiatoid deep-sea fish,Malacosteus niger. Proc R Soc (Ser B) 215: 481–489Google Scholar
  102. Sutton TT, Hopkins TL (1996) The species composition, abundance, and vertical distribution of the stomiid (Pistes: Stomiiformes) fish assemblage of the Gulf of Mexico. Bull mar Sci 59: (in press)Google Scholar
  103. Swenson WA, Smith LL (1973) Gastric digestion, food consumption, feeding periodicity and food conversion efficiency in walleye (Stizostedion vitreum vitreum). J Fish Res Bd Can 30: 1327–1336Google Scholar
  104. Tchernavin VV (1953) The feeding mechanism of a deep sea fishChauliodus sloani Schneider. British Museum (Natural History), London (Spec Publ)Google Scholar
  105. Tyler AV (1970) Rates of gastric emptying in young cod. J Fish Res Bd Can 27: 1177–1189Google Scholar
  106. Tyler HR, Pearcy WG (1975) The feeding habits of three species of lanternfishes (family Myctophidae) off Oregon, USA. Mar Biol 32: 7–11Google Scholar
  107. Ware DM (1972) Predation by rainbow trout (Salmo gairdneri): the influence of hunger, prey density, and prey size. J Fish Res Bd Can 29: 1193–1201Google Scholar
  108. Weitzman SH (1967) The origin of the stomiatoid fishes with comments on the classification of salmoniform fishes. Copeia 1967(3): 507–540Google Scholar
  109. Weitzman SH (1974) Osteology and evolutionary relationships of the Sternoptychidae, wich a new classification of stomiatoid families. Bull Am Mus nat Hist 153: 331–476Google Scholar
  110. Werner EE, Hall DJ (1974) Optimal foraging and the size selection of prey by the bluegill sunfish (Lepomis macrochirus). Ecology 55: 1042–1052Google Scholar
  111. Widder EA, Latz MI, Herring PJ, Case JF (1984) Far red bioluminescence from two deep-sea fishes. Science, NY 225: 512–515Google Scholar
  112. Willis JM, Pearcy WG (1982) Vertical distribution and migration of fishes of the lower mesopelagic zone off Oregon. Mar Biol 70: 87–98Google Scholar
  113. Woodland J, Hastings JW (1971) Light to hide by: ventral luminescence te, camouflage the silhouette. Science, NY 173: 1016–1017Google Scholar
  114. Young RE (1983) Oceanic bioluminescence: an overview of general functions. Bull mar Sci 33: 829–845Google Scholar
  115. Young RE, Roper CFE (1977) Intensity regulation of bioluminescence during countershading in living midwater animals. Fish Bull US 75: 239–252Google Scholar
  116. Zaret TM, Suffern JS (1976) Vertical migration in zooplankton as a predator avoidance mechanism. Limnol Oceanogr 21: 804–813Google Scholar

Copyright information

© Springer-Verlag 1996

Authors and Affiliations

  • T. T. Sutton
    • 1
  • T. L. Hopkins
    • 1
  1. 1.Department of Marine ScienceUniversity of South FloridaSt. PetersburgUSA

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