Volume 42 Issue 12
Dec.  2024
Turn off MathJax
Article Contents
Lisheng Wu, Wenxin Zhuang, Qiaohong Liu, Rui Wang, Yuan Li, Longshan Lin, Shufang Liu, Shaoxiong Ding. Pilot study to reconstruct life history of Diaphus thiollierei from the Arabian Sea by otolith microstructure and microchemistry[J]. Acta Oceanologica Sinica, 2024, 43(12): 75-84. doi: 10.1007/s13131-024-2307-x
Citation: Lisheng Wu, Wenxin Zhuang, Qiaohong Liu, Rui Wang, Yuan Li, Longshan Lin, Shufang Liu, Shaoxiong Ding. Pilot study to reconstruct life history of Diaphus thiollierei from the Arabian Sea by otolith microstructure and microchemistry[J]. Acta Oceanologica Sinica, 2024, 43(12): 75-84. doi: 10.1007/s13131-024-2307-x

Pilot study to reconstruct life history of Diaphus thiollierei from the Arabian Sea by otolith microstructure and microchemistry

doi: 10.1007/s13131-024-2307-x
Funds:  The fund from the Laoshan Laboratory under contract No. LSK202203802; the National Programme on Global Change and Air-Sea Interaction under contract No. GASI-02-SCS-YD sum/spr/aut.
More Information
  • Corresponding author: E-mail: liusf@ysfri.ac.cnsxding@xmu.edu.cn
  • Received Date: 2023-11-08
  • Accepted Date: 2024-03-29
  • Available Online: 2024-12-20
  • Publish Date: 2024-12-01
  • The lanternfishes are mesopelagic fish that are highly productive as common bycatch of deep-sea shrimp trawlers, but they are often neglected or discarded. Despite being one of the dominant lanternfish species in the Arabian Sea, little is known about the life history of Diaphus thiollierei and its role in marine ecosystems. In this study, 103 D. thiollierei were collected in the Arabian Sea during October-November 2020 to study population growth based on sagittal otolith daily ages; and 10 fish collected during April–May 2021 were subjected to otolith microchemistry analysis to reconstruct the vertical migration in their life history using LA-ICP-MS technique. The standard length–dry weight (SL-DW) relationships for D. thiollierei revealed both negative allometric growth and a significant difference between the sexes. Using daily growth annuli counts on the sagittal section of otoliths, the von Bertalanffy growth equation for D. thiollierei was determined. The pattern of four elemental ratios (Sr to Ca, Mg to Ca, Li to Ca, and Ba to Ca) in sagittal otolith suggested that, in general, D. thiollierei descended continually after hatching until the post-larval (PL) stage when they reached a depth of approximately 200 m. Subsequently, from the PL stage to the post-metamorphosis Ⅱ (PM Ⅱ) stage, D. thiollierei likely further sank from 200 m to a depth of approximately 300 m, and then in the daytime they were at a depth of approximately 300–800 m to take refuge from predators. This pilot study explored to unravel the vertical migration during life history in D. thiollierei from sagittal otoliths, whereas further investigation on otolith is needed to better delineate the population ecology in detail, and thus to provide basic information for the exploitation of the lanternfish resource and the understanding of their ecological roles.
  • loading
  • Alhossaini M, Pitcher T J. 1988. The relation between daily rings, body growth and environmental factors in plaice, Pleuronectes platessa L. , juvenile otoliths. Journal of Fish Biology, 33(3): 409–418
    Beamish R J, Fournier D A. 1981. A method for comparing the precision of a set of age determinations. Canadian Journal of Fisheries and Aquatic Sciences, 38: 982–983, doi: 10.1139/f81-132
    Braga A C, Costa P A S, Nunan G W. 2008. First record of the firebrow lanternfish Diaphus adenomus (Myctophiformes: Myctophidae) from the South Atlantic. Journal of Fish Biology, 73(1): 296–301, doi: 10.1111/j.1095-8649.2008.01915.x
    Brown R J, Severin K P. 2009. Otolith chemistry analyses indicate that water Sr: Ca is the primary factor influencing otolith Sr: Ca for freshwater and diadromous fish but not for marine fish. Canadian Journal of Fisheries and Aquatic Sciences, 66(10): 1790–1808, doi: 10.1139/F09-112
    Caiger P E, Lefebve L S, Llopiz J K. 2021. Growth and reproduction in mesopelagic fishes: a literature synthesis. ICES Journal of Marine Science, 78(3): 765–781, doi: 10.1093/icesjms/fsaa247
    Campana S E. 1999. Chemistry and composition of fish otoliths: pathways, mechanisms and applications. Marine Ecology Progress Series, 188: 263–297, doi: 10.3354/meps188263
    Campana S E. 2001. Accuracy, precision and quality control in age determination, including a review of the use and abuse of age validation methods. Journal of Fish Biology, 59(2): 197–242, doi: 10.1111/j.1095-8649.2001.tb00127.x
    Catul V, Gauns M, Karuppasamy P K. 2011. A review on mesopelagic fishes belonging to family Myctophidae. Reviews in Fish Biology and Fisheries, 21(3): 339–354, doi: 10.1007/s11160-010-9176-4
    Chen Yong, Mello L G S. 1999. Growth and maturation of cod (Gadus morhua) of different year classes in the Northwest Atlantic, NAFO subdivision 3Ps. Fisheries Research, 42(1–2): 87–101, doi: 10.1016/S0165-7836(99)00036-3
    Duan Mi, Ashford J R, Bestley S, et al. 2021. Otolith chemistry of Electrona antarctica suggests a potential population marker distinguishing the southern Kerguelen Plateau from the eastward−flowing Antarctic Circumpolar Current. Limnology and Oceanography, 66(2): 405–421, doi: 10.1002/lno.11612
    Eduardo L N, Bertrand A, Mincarone M M, et al. 2021. Distribution, vertical migration, and trophic ecology of lanternfishes (Myctophidae) in the Southwestern Tropical Atlantic. Progress in Oceanography, 199: 102695, doi: 10.1016/j.pocean.2021.102695
    Elsdon T S, Gillanders B M. 2002. Interactive effects of temperature and salinity on otolith chemistry: challenges for determining environmental histories of fish. Canadian Journal of Fisheries and Aquatic Sciences, 59(11): 1796–1808, doi: 10.1139/f02-154
    Flynn A J, Paxton J R. 2012. Spawning aggregation of the lanternfish Diaphus danae (family Myctophidae) in the north-western Coral Sea and associations with tuna aggregations. Marine and Freshwater Research, 63(12): 1255–1271, doi: 10.1071/MF12185
    Fowler A J, Campana S E, Thorrold S R, et al. 1995. Experimental assessment of the effect of temperature and salinity on elemental composition of otoliths using laser ablation ICPMS. Canadian Journal of Fisheries and Aquatic Sciences, 52(7): 1431–1441, doi: 10.1139/f95-138
    Gartner J V Jr. 1991. Life histories of three species of lanternfishes (Pisces: Myctophidae) from the eastern Gulf of Mexico: I. Morphological and microstructural analysis of sagittal otoliths. Marine Biology, 111(1): 11–20, doi: 10.1007/BF01986339
    Gjøsaeter J. 1984. Mesopelagic fish, a large potential resource in the Arabian Sea. Deep-Sea Research Part A: Oceanographic Research Papers, 31(6–8): 1019–1035, doi: 10.1016/0198-0149(84)90054-2
    Greely T M, Gartner J V Jr, Torres J J. 1999. Age and growth of Electrona antarctica (Pisces: Myctophidae), the dominant mesopelagic fish of the Southern Ocean. Marine Biology, 133(1): 145–158, doi: 10.1007/s002270050453
    Hayashi A, Kawaguchi K, Watanabe H, et al. 2001. Daily growth increment formation and its lunar periodicity in otoliths of the myctophid fish Myctophum asperum (Pisces: Myctophidae). Fisheries Science, 67(5): 811–817, doi: 10.1046/j.1444-2906.2001.00327.x
    Izzo C, Reis-Santos P, Gillanders B M. 2018. Otolith chemistry does not just reflect environmental conditions: a meta-analytic evaluation. Fish and Fisheries, 19(3): 441–454, doi: 10.1111/faf.12264
    Karuppasamy P K, George S, Menon N G. 2008. Length-weight relationship of Benthosema pterotum (myctophid) in the deep scattering layer (DSL) of the eastern Arabian Sea. Indian Journal of Fisheries, 55(4): 301–303
    Liu Hongbo, Jiang Tao, Yang Jian. 2018. Unravelling habitat use of Coilia nasus from the Rokkaku River and Chikugo River estuaries of Japan by otolith strontium and calcium. Acta Oceanologica Sinica, 37(6): 52–60, doi: 10.1007/s13131-018-1190-8
    Lombarte A, Lleonart J. 1993. Otolith size changes related with body growth, habitat depth and temperature. Environmental Biology of Fishes, 37(3): 297–306, doi: 10.1007/BF00004637
    Martin G B, Thorrold S R. 2005. Temperature and salinity effects on magnesium, manganese, and barium incorporation in otoliths of larval and early juvenile spot Leiostomus xanthurus. Marine Ecology Progress Series, 293: 223–232, doi: 10.3354/meps293223
    Miller J A. 2011. Effects of water temperature and barium concentration on otolith composition along a salinity gradient: implications for migratory reconstructions. Journal of Experimental Marine Biology and Ecology, 405(1–2): 42–52, doi: 10.1016/j.jembe.2011.05.017
    Milligan R J, Sutton T T. 2020. Dispersion overrides environmental variability as a primary driver of the horizontal assemblage structure of the mesopelagic fish family Myctophidae in the Northern Gulf of Mexico. Frontiers in Marine Science, 7: 15, doi: 10.3389/fmars.2020.00015
    Moku M, Hayashi A, Mori K, et al. 2005. Validation of daily otolith increment formation in the larval myctophid fish Diaphus slender-type spp. Journal of Fish Biology, 67(5): 1481–1485, doi: 10.1111/j.0022-1112.2005.00824.x
    Moku M, Ishimaru K, Kawaguchi K. 2001. Growth of larval and juvenile Diaphus theta (Pisces: Myctophidae) in the transitional waters of the western North Pacific. Ichthyological Research, 48(4): 385–390, doi: 10.1007/s10228-001-8162-1
    Pakhomov E A, Perissinotto R, McQuaid C D. 1996. Prey composition and daily rations of myctophid fishes in the Southern Ocean. Marine Ecology Progress Series, 134: 1–14, doi: 10.3354/meps134001
    Pawson M G. 1990. Using otolith weight to age fish. Journal of Fish Biology, 36(4): 521–531, doi: 10.1111/j.1095-8649.1990.tb03554.x
    Petursdottir G, Begg G A, Marteinsdottir G. 2006. Discrimination between Icelandic cod (Gadus morhua L. ) populations from adjacent spawning areas based on otolith growth and shape. Fisheries Research, 80(2–3): 182–189, doi: 10.1016/j.fishres.2006.05.002
    Pilling G M, Grandcourt E M, Kirkwood G P. 2003. The utility of otolith weight as a predictor of age in the emperor Lethrinus mahsena and other tropical fish species. Fisheries Research, 60(2–3): 493–506, doi: 10.1016/S0165-7836(02)00087-5
    Robinson C, Steinberg D K, Anderson T R, et al. 2010. Mesopelagic zone ecology and biogeochemistry—a synthesis. Deep-Sea Research Part Ⅱ: Topical Studies in Oceanography, 57(16): 1504–1518, doi: 10.1016/j.dsr2.2010.02.018
    Sassa C, Kawaguchi K, Hirota Y, et al. 2004. Distribution patterns of larval myctophid fish assemblages in the subtropical-tropical waters of the western North Pacific. Fisheries Oceanography, 13(4): 267–282, doi: 10.1111/j.1365-2419.2004.00289.x
    Schaafsma F L, David C L, Kohlbach D, et al. 2022. Allometric relationships of ecologically important Antarctic and Arctic zooplankton and fish species. Polar Biology, 45(2): 203–224, doi: 10.1007/s00300-021-02984-4
    Sebastine M. 2014. Population characteristics and taxonomy of lantern fishes of genus Diaphus (Family Myctophidae) off south west coast of India [dissertation]. Cochin: Cochin University of Science and Technology
    Sebastine M, Bineesh K K, Abdussamad E M, et al. 2013. Myctophid fishery along the Kerala coast with emphasis on population characteristics and biology of the headlight fish, Diaphus watasei Jordan & Starks, 1904. Indian Journal of Fisheries, 60(4): 7–11
    Secor D H, Rooker J R. 2000. Is otolith strontium a useful scalar of life cycles in estuarine fishes?. Fisheries Research, 46(1–3): 359–371, doi: 10.1016/S0165-7836(00)00159-4
    Shotton R. 1997. Lanternfishes: a potential fishery in the Northern Arabian Sea?. In: FAO. Review of the State of World Fishery Resources: Marine Fisheries. Rome: FAO Fisheries Circular No. 920 FIRM/C. 920, http://www.fao.org/docrep/003/w4248e/w4248e34.htm
    Smith M K. 1992. Regional differences in otolith morphology of the deep slope red snapper Etelis carbunculus. Canadian Journal of Fisheries and Aquatic Sciences, 49(4): 795–804, doi: 10.1139/f92-090
    Soeth M, Spach H L, Daros F A, et al. 2020. Use of otolith elemental signatures to unravel lifetime movement patterns of Atlantic spadefish, Chaetodipterus faber, in the Southwest Atlantic Ocean. Journal of Sea Research, 158: 101873, doi: 10.1016/j.seares.2020.101873
    Sturrock A M, Hunter E, Milton J A, et al. 2015. Quantifying physiological influences on otolith microchemistry. Methods in Ecology and Evolution, 6(7): 806–816, doi: 10.1111/2041-210X.12381
    Sun Peng, Chen Qi, Fu Caihong, et al. 2020. Daily growth of young-of-the-year largehead hairtail (Trichiurus japonicus) in relation to environmental variables in the East China Sea. Journal of Marine Systems, 201: 103243, doi: 10.1016/j.jmarsys.2019.103243
    Suthers I M. 1996. Spatial variability of recent otolith growth and RNA indices in pelagic juvenile Diaphus kapalae (Myctophidae): an effect of flow disturbance near an island?. Marine & Freshwater Research, 47(2): 273–282
    Taddese F, Reid M R, Closs G P. 2019. Direct relationship between water and otolith chemistry in juvenile estuarine triplefin Forsterygion nigripenne. Fisheries Research, 211: 32–39, doi: 10.1016/j.fishres.2018.11.002
    Taubert B D, Coble D W. 1977. Daily rings in otoliths of three species of Lepomis and Tilapia mossambica. Journal of the Fisheries Research Board of Canada, 34(3): 332–340, doi: 10.1139/f77-054
    Thorson J T, Simpfendorfer C A. 2009. Gear selectivity and sample size effects on growth curve selection in shark age and growth studies. Fisheries Research, 98(1–3): 75–84, doi: 10.1016/j.fishres.2009.03.016
    Thresher R E. 1999. Elemental composition of otoliths as a stock delineator in fishes. Fisheries Research, 43(1–3): 165–204, doi: 10.1016/S0165-7836(99)00072-7
    Tian Han, Jiang Yane, Zhang Jun, et al. 2022. Age and growth of Diaphus brachycephalus in the South China Sea using sagittal otolith microstructure. Fishes, 7(4): 169, doi: 10.3390/fishes7040169
    Walther B D, Thorrold S R. 2006. Water, not food, contributes the majority of strontium and barium deposited in the otoliths of a marine fish. Marine Ecology Progress Series, 311: 125–130, doi: 10.3354/meps311125
    Wang Yan, Zhang Jun, Chen Zuozhi, et al. 2019. Age and growth of Myctophum asperum in the South China Sea based on otolith microstructure analysis. Deep-Sea Research Part Ⅱ: Topical Studies in Oceanography, 167: 121–127, doi: 10.1016/j.dsr2.2018.07.004
    Woodcock S H, Munro A R, Crook D A, et al. 2012. Incorporation of magnesium into fish otoliths: determining contribution from water and diet. Geochimica et Cosmochimica Acta, 94: 12–21, doi: 10.1016/j.gca.2012.07.003
    Wright P J, Talbot C, Thorpe J E. 1992. Otolith calcification in Atlantic salmon parr, Salmo salar L. and its relation to photoperiod and calcium metabolism. Journal of Fish Biology, 40(5): 779–790, doi: 10.1111/j.1095-8649.1992.tb02624.x
    Xiong Ying, Liu Hongbo, Jiang Tao, et al. 2015. Investigation on otolith microchemistry of wild Pampus argenteus and Miichthys miiuyin the southern Yellow Sea, China. Haiyang Xuebao (in Chinese), 37(2): 36–43
    Xiong Ying, Yang Jian, Jiang Tao, et al. 2021. Temporal stability in the otolith Sr: Ca ratio of the yellow croaker, Larimichthys polyactis (Actinopterygii, Perciformes, Sciaenidae), from the southern Yellow Sea. Acta Ichthyologica et Piscatoria, 51(1): 59–65, doi: 10.3897/aiep.51.63245
    Xuan Zhongya, Jiang Tao, Liu Hongbo, et al. 2023. Otolith microchemical evidence revealing multiple spawning site origination of the anadromous tapertail anchovy (Coilia nasus) in the Changjiang (Yangtze) River Estuary. Acta Oceanologica Sinica, 42(1): 120–130, doi: 10.1007/s13131-022-2135-9
    Yang Jian, Jiang Tao, Liu Hongbo. 2011. Are there habitat salinity markers of the Sr: Ca ratio in the otolith of wild diadromous fishes? A literature survey. Ichthyological Research, 58(3): 291–294, doi: 10.1007/s10228-011-0220-8
    Zhang Jun, Wang Yan, Chen Zuozhi, et al. 2021. Age and growth of Ceratoscopelus warmingii (Myctophidae) in the South China Sea based on sagittal otolith microstructure. Marine Biology Research, 17(7–8): 733–743, doi: 10.1080/17451000.2021.2015390
    Zhuang Wenxin, Wu Lisheng, Liu Qiaohong, et al. 2023. Interspecies differences in the otolith morphology of three Diaphus species based on landmark method. Haiyang Xuebao (in Chinese), 45(9): 119–127
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Figures(5)  / Tables(3)

    Article Metrics

    Article views (88) PDF downloads(4) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return