Abstract
The use of a functional guild, which distills organisms into groups based on a shared role within an ecosystem, is a beneficial tool for fisheries management because it reduces data complexity, streamlines statistical analyses, and places species in an ecosystem context by defining their functional role within a community. However, few studies consider the ramification of ontogeny on guild assignments and assume species occupy a static foraging guild throughout their lives. The aim for this study was to examine the development of feeding structures and diet in four, closely related species of sciaenids (Family Sciaenidae) that forage in the water column throughout their life history (1) to determine if the structures needed to exploit microhabitat use of the water column are present at early ontogenetic stages and (2) to assess guild transitions using a hierarchical clustering approach. Significant differences were only detected in ascending process length and cb1 gill raker count among the examined sciaenids. Larimus fasciatus consumed zooplankton throughout ontogeny and possessed a shorter ascending process and a greater number of cb1 gill rakers. Cynoscion nebulosus transitioned from zooplanktivory in the larval period to piscivory as an early juvenile and possessed a longer ascending process and fewer cb1 gill rakers. Bairdiella chrysoura and C. regalis were both zooplanktivorous as early juveniles and consumed more epibenthic (benthic crustaceans and worms) prey and possessed more elongate gill rakers compared to C. nebulosus. Foraging studies that combine diet and morphological analyses are needed to place individuals into foraging guilds while capturing key life history transitions that influence foraging habits and guild assignment.
Similar content being viewed by others
Data availability
All physical specimens examined over the course of this study are deposited at the Virginia Institute of Marine Science, Nunnally Ichthyology Collection. Datasets and images generated and analyzed during the current study are available from the author upon reasonable request.
References
Aguirre WE, Shervette VR (2005) Morphological diversity of the Cynoscion group (Perciformes: Sciaenidae) in the Gulf of Guayaquil region, Ecuador: a comparative approach. Environ Biol Fishes 73:403–413. https://doi.org/10.1007/s10641-005-2227-3
Anto J, Majoris J, Turingan RG (2009) Prey selection and functional morphology through ontogeny of Amphiprion clarkii with a congeneric comparison. J Fish Biol 75:575–590. https://doi.org/10.1111/j.1095-8649.2009.02308.x
Arnold SJ (1983) Morphology, performance and fitness. Am Zool 23:347–361
Auster PJ, Link JS (2009) Compensation and recovery of feeding guilds in a northwest Atlantic shelf fish community. Mar Ecol Prog Ser 382:163–172. https://doi.org/10.3354/meps07962
Bhagat Y, Fox MG, Ferreira MT (2011) Trophic polymorphism in introduced pumpkinseed (Lepomis gibbosus) inhabiting Iberian reservoirs. Environ Biol Fishes 91:203–217. https://doi.org/10.1007/s10641-011-9773-7
Buchheister A, Latour RJ (2015) Diets and trophic-guild structure of a diverse fish assemblage in Chesapeake Bay, USA. J Fish Biol 86:967–992. https://doi.org/10.1111/jfb.12621
Carassou L, Hernandez FJ, Graham WM (2014) Change and recovery of coastal mesozooplankton community structure during the Deepwater Horizon oil spill. Environ Res Lett 9:124003
Chao LN, Musick JA (1977) Life history, feeding habits, and functional morphology of juvenile sciaenid fishes in the York River Estuary, Virginia. Fish Bull 75:657–702
Chipps S, Garvey JE (2007) 11 Assessment of food habits and feeding patterns. In: Guy C, Brown ML (eds) Analysis and interpretation of freshwater fisheries data. American Fisheries Society, Bethesda, pp 1–42
Davis CD, Fabrizio MC, Tuckey TD (2016) Estimation of juvenile striped bass relative abundance in the Virginia portion of Chesapeake Bay. Annual Report 2015. Virginia Institute of Marine Science, Gloucester Point, VA
De Cáceres M, Lapiedra O, Sol D (2014) An example of usage of the niche metric functions (former ’ resniche ’ package)
Deary AL, Hilton EJ (2016) Comparative ontogeny of the feeding apparatus of sympatric drums (Perciformes: Sciaenidae) in the Chesapeake Bay. J Morphol 277:183–195. https://doi.org/10.1002/jmor.20488
Deary AL, Hilton EJ (2017) Influence of cladogenesis on feeding structures in drums (Teleostei: Sciaenidae). Zoology 120:53–61. https://doi.org/10.1016/j.zool.2016.08.004
Deary AL, Metscher B, Brill RW, Hilton EJ (2016) Shifts of sensory modalities in early life history stage estuarine fishes (Sciaenidae) from the Chesapeake Bay using X-ray micro computed tomography. Environ Biol Fishes 99:361–375. https://doi.org/10.1007/s10641-016-0479-8
Deary AL, Latour RJ, Hilton EJ (2017) Niche partitioning in early life history stage, estuarine-dependent fishes (Sciaenidae). Estuar Coasts 40:1757–1770. https://doi.org/10.1007/s12237-017-0248-8
Egan JP, Gibbs S, Simons AM (2018) Trophic niches through ontogeny in 12 species of Indo-Pacific marine Clupeoidei (herrings, sardines, and anchovies). Mar Biol 165:153. https://doi.org/10.1007/s00227-018-3410-3
Elliott NG, Haskard K, Koslow JA (1995) Morphometric analysis of orange roughy (Hoplostethus atlanticus) off the continental slope of southern Australia. J Fish Biol 46:202–220
Fahay MP (2007) Early stages of fishes in the Western North Atlantic Ocean. Northwest Atlantic Fisheries Organization, Dartmouth
Grubich J (2003) Morphological convergence of pharyngeal jaw structure in durophagous perciform fish. Biol J Linn Soc 80:147–165. https://doi.org/10.1046/j.1095-8312.2003.00231.x
Havel LN, Fuiman LA (2015) Settlement-size larval red drum (Sciaenops ocellatus) respond to estuarine chemical cues. Estuar Coasts 39(2):560–570
Holt GJ, Holt SA (2000) Vertical distribution and the role of physical processes in the feeding dynamics of two larval sciaenids Sciaenops ocellatus and Cynoscion nebulosus. Mar Ecol Prog Ser 193:181–190
Horodysky AZ, Brill RW, FineMusick MLJa, Latour RJ (2008a) Acoustic pressure and particle motion thresholds in six sciaenid fishes. J Exp Biol 211:1504–1511. https://doi.org/10.1242/jeb.016196
Horodysky AZ, Brill RW, Warrant EJ, Musicka J, Latour RJ (2008b) Comparative visual function in five sciaenid fishes inhabiting Chesapeake Bay. J Exp Biol 211:3601–3612. https://doi.org/10.1242/jeb.023358
Hunt von Herbing I, Miyake T, Hall BK, Boutilier RG (1996) Ontogeny of feeding and respiration in larval Atlantic cod Gadus morhua (Teleostei, Gadiformes): 1. Morphol J Morphol 227:15–35
Joyeux J-C (1998) Spatial and temporal entry patterns of fish larvae into North Carolina estuaries: comparisons among one pelagic and two demersal species. Estuar Coast Shelf Sci 47:731–752. https://doi.org/10.1006/ecss.1998.0378
Johnson WS, Allen DM (2005) Zooplankton of the Atlantic and Gulf coasts. Johns Hopkins University Press, Baltimore
Kammerer CF, Grande L, Westneat MW (2006) Comparative and developmental functional morphology of the jaws of living and fossil gars (Actinopterygii: Lepisosteidae). J Morphol 267:1017–1031. https://doi.org/10.1002/jmor.10293
Krebs JM, Turingan RG (2003) Intraspecific variation in gape—prey size relationships and feeding success during early ontogeny in red drum, Sciaenops ocellatus. Environ Biol Fishes 66:75–84
Latour RJ, Brush MJ, Bonzek CF (2003) Toward ecosystem-based fisheries management: strategies for multispecies modeling and associated data requirements. Fisheries 28:10–22
Marques SC, Azeiteiro UM, Marques JC, Neto JM, Pardal MÂ (2006) Zooplankton and ichthyoplankton communities in a temperate estuary: Spatial and temporal patterns. J Plankton Res 28:297–312
Milborrow S (2014) Package “rpart.plot.” 1–18
Murdy EO, Musick JA (2013) Fishes of Chesapeake Bay. Johns Hopkins University Press, Baltimore
Nunna D, Tewson LH, Cowx IG (2012) The foraging ecology of larval and juvenile fishes. Rev Fish Biol Fish 22:377–408. https://doi.org/10.1007/s11160-011-9240-8
Pianka ER (1973) The structure of lizard communities. Annu Rev Ecol Evol S 4(1):53–74
Poling KR, Fuiman LA (1999) Behavioral specialization in developing sciaenids and its relationship to morphology and habitat. Environ Biol Fishes 54:119–133
Powles H (1980) Descriptions of larval Silver Perch, Bairdiella chrysoura, Banded Drum, Larimus fasciatus, and Star Drum, Stellifer Lanceolatus (Sciaenidae). Fish Bull 78(1):119–136
R Development Core Team (2017) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. ISBN 3–900051–07-0. http://www.Rproject.org
Reecht Y, Rochet M-J, Trenkel VM, Jennings S, Pinnegar JK (2013) Use of morphological characteristics to define functional groups of predatory fishes in the Celtic Sea. J Fish Biol 83:355–377. https://doi.org/10.1111/jfb.12177
Ribeiro F, Hale E, Hilton EJ, Clardy TR, Deary AL, Targett TE, Olney JE (2015) Composition and temporal patterns of larval fish communities in Chesapeake and Delaware Bays, USA. Mar Ecol Prog Ser 527:167–180. https://doi.org/10.3354/meps11265
Richards WJ (2006) Early stages of Atlantic fishes: an identification guide for the western central North Atlantic. Taylor and Francis, New York
Rooker JR, Holt SA, Soto MA, Holt GJ (1998) Postsettlement patterns of habitat use by sciaenid fishes in subtropical seagrass meadows. Estuaries 21:318–327
Rowe PM, Epifanio CE (1994) Tidal stream transport of weakfish larvae in Delaware Bay, USA. Mar Ecol Prog Ser 110:105–114. https://doi.org/10.3354/meps110105
Suzuki R, Shimodaira H (2006) Pvclust: An R package for assessing the uncertainty in hierarchical clustering. Bioinformatics 22:1540–1542. https://doi.org/10.1093/bioinformatics/btl117
Suzuki R (2015) Hierarchical clustering with p-values via multiscale bootstrap. Package 'pvclust'
Svanbäck R, Eklöv P (2003) Morphology dependent foraging efficiency in perch: a trade-off for ecological specialization ? Oikos 102:273–284. https://doi.org/10.1034/j.1600-0706.2003.12657.x
Taylor WR, Van Dyke GG (1985) Revised procedures for staining and clearing small fishes and other vertebrates for bone and cartilag estudy. Cybium 9:107–119
Tuckey TD, Fabrizio MC (2016) Estimating relative juvenile abundance of ecologically important finfish in the Virginia portion of Chesapeake Bay. Project No. F-104-R-20. Annual report to the Virginia Marine Resources Commission. Virginia Institute of Marine Science, Gloucester Point
Wainwright PC (1996) Ecological explanation through functional morphology: the feeding biology of sunfishes. Ecology 77:1336–1343
Wainwright PC, Richard BA (1995) Predicting patterns of prey use from morphology of fishes. Environ Biol Fishes 44:97–113
Warton DI, Duursma RA, Falster DS, Taskinen S (2012) Smatr 3- an R package for estimation and inference about allometric lines. Methods Ecol Evol 3:257–259. https://doi.org/10.1111/j.2041-210X.2011.00153.x
Wimberger PH (1991) Plasticity of jaw and skull morphology in the neotropical cichlids Geophagus brasiliensis and G. steindachneri. Evolution 45(7):1545–1563
Acknowledgements
I would like to thank one anonymous reviewer and Dr. Eric Hilton for their invaluable guidance that greatly improved the quality of this manuscript. I would also like to thank Drs. Sarah Huber and Eric Hilton from the Virginia Institute of Marine Science, Nunnally Ichthyology Collection for the curation and access to specimens used in this study. Additional specimens of larval L. fasciatus were provided by the Gulf Coast Research Laboratory, University of Southern Mississippi. The findings and conclusions in the paper are those of the author(s) and do not necessarily represent the views of the National Marine Fisheries Service. Mention of trade names does not imply endorsement by NOAA or any of its subagencies. This is contribution number EcoFOCI-0941 of Ecosystems and Fisheries-Oceanography Coordinated Investigations.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The author does not have a conflict of interest for the work that was conducted for the study.
Ethical approval
All fish collection and handling procedures were approved by the College of William and Mary Institutional Animal Care and Use Committee (protocol number: IACUC-2014-05-12-9603-dtuck).
Additional information
Responsible Editor: C. Harrod.
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Reviewed by: E.Hilton and M. F. Landaeta.
Rights and permissions
About this article
Cite this article
Deary, A.L. Influence of feeding structures and early development on foraging guild assignment in four co-occurring fishes (Family Sciaenidae). Mar Biol 167, 51 (2020). https://doi.org/10.1007/s00227-020-3661-7
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s00227-020-3661-7