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以標識放流及耳石微化學研究日本鰻的移動行為及棲地利用

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о኿ᜋܹࢺЅՆүཌϽᏰंـРҏᠵޟಋଢ଼՗࣏ЅූӴցҢ

ݓжᏱ

1

Ȇ஻፳࣡

2

Ȇ໻༰ဎϞ

3

Ȇങ๙㹹

2

Ȇቓ൲ӎ

4

Ȇឃसි

5

Ȇឃ୉ԙ

5

Ȇෆ࿲ԑ

1* 1୽ҳѮᢊσᏰᅣཾऋᏰंـܚ 2՗ࢇ଱ၻཾۏষོЫ౰ၐᡛܚݍ෫ҡ׬ंـϛЖ 3 ϛѵंـ଱Ӵ౨ऋᏰंـܚ 4՗ࢇ଱ၻཾۏষོЫ౰ၐᡛܚషЫᖅᎴ෥ंـϛЖ 5՗ࢇ଱ၻཾۏষོЫ౰ၐᡛܚ

ᄢȁ!ौ!

࣏Οᕣ၌РҏᠵӵചӴЫ୿ϛޟު໢ϷҀȃಋଢ଼௑לоЅᎌᔖ՗࣏Ȃҏंـ௴ҢϤᆍϚӣޟ኿ ᜋПݲȂѓࢂȈ(1) оశᄘ෨੧ӟᠵധᡝߒȇ(2) о୘៵኿ᜋȇ(3) ٺҢ੊ϽѲᕗᡤશ (OTC) ᇄ₩ શ (ALC) ኿଄Նүȇ(4) оଢ଼ސවаේΣᡝϱоЅ (5) оཌᆄ១ߜ឴ጡጆ኿ᡆේΣᡝϱȄܻ 2002ȃ2003ȃ2005 оЅ 2006 ԑϷտоΰक़Ϥᆍ኿ᜋПݲȂӓॎ኿ᜋΟ 4800 ׎ᠵጣЅ 2473 ׎༁ᠵȂ ณࡣϷտភܹܻјࡌഖޟσᝉᢊ (ዢ෹) ڷ໠ܹޟଽࡎྩϛȃή෬ȄϷݙ኿ᜋܹࢺࡣޟӱԝၥਟȂ ๖ݎี౪РҏᠵڎԤሴ୿՗࣏Ȃܹࢺࡣᠵധσ഍ୄ੼ӵ 1 ϴ٨ጒ൜ϱȄցҢႫυཌ௤ቈϷݙՆүϛ ޟ Sr/Ca ШȂี౪РҏᠵӻኵᒵᐅјషឧЫޟݬο୿࣏ූ਀ӴȄ ᜰᗤԅȈРҏᠵȃ኿ᜋܹࢺȃSr/Ca ШȃූӴցҢ

ࠉȁ!ِ!

ॱݰ኿ᡆ (acoustic tags & acoustic array)ȇ(3) ༈ಛ ޟ ཐ ᔖ Ԓ ܖ ߨ Ⴋ υ Ԓ ኿ ᡆ (transponder or non-electronic tags) ȇ (4) Ͻ Ᏸ Ѕ ҡ ސ ኿ ᡆ (chemical & biological markers)ȇ(5) ฒጣႫልก኿ ᡆ (radio telemetry) оЅ!(6) ၥਟᓽԆܖᔬਰक ᓃԒ኿ᡆ (data storage tags (DST) or archival tags) (ᆩ֭Ȉhttp://www.fisheries.org/units/tag2008/)Ȅ ധ᜸ޟҡࣀѬȃḯ෬՗࣏ȃූӴցҢоЅఊ တଢ଼ᄘȂ࢐ᅣཾၥྛ߳ىЅᆓ౩Ϛџܖીޟၥ ଉȄ኿ᜋܹࢺ࢐ᕕு೻ٲၥଉശޢ௥ޟПݲȄ኿ ᜋܹࢺӱԝၥਟџоҢپեॎএᡝޟҡߝȃಋଢ଼ ՗࣏ȃḯ෬ၯ৷ȃᘗඹຽᚔȃූӴցҢȂఊတޟ ኵ໔ȃԙߝ౥ȃԫι౥ڷၥྛޟ໠ี౥้ȄѪѴȂ ଩ӫՆүޟཌϽᏰϷݙȂᗙџо१࡚ധ᜸ޟḯ෬ ᕗცѬȄ ӵΰक़ޟПݲϛȂցҢಳᚔПԒ (pop-up) ޟ DSTȂџоकᓃധ᜸ޟḯ෬ၯ৷оЅᕗცၥଉȂ࿋ ኿ᡆಳᚔധᡝࡣਗ਼юЫ७ਢȂ኿ᡆϱܚಣᑖӨᆍ ᕗცၥਟޟଉဴȂ߯џցҢཌݰ༈ଉޟПԒ஠ଉ ਀༈ଚڗΡഅፏ࢑ȂӔ༈ӱڗӴ७ޟ௥ԝમȇܖ ࢐ӵധᡝೝӱԝоࡣȂആႆ೿ጣȂ஠኿ᡆϱഋၥ ਟήၷڗႫသ໌՗ၥਟϷݙȄ೻ᆍ኿ᡆҬࠉϐင ᔖҢڗσ࠮ḯ෬ധ᜸ȂԃᘂധЅᚰധ้Ȃծ࢐ҥ ܻ኿ᡆᡝᑖЊσ (σघ 10 cm)ȂฒݲᔖҢڗᡝᑖၶ ωޟധᆍȄᡝ࠮ၶωޱȂҬࠉᗙ࢐ٺҢ༈ಛཐᔖ Ԓܖ࢐ߨႫυԒޟ኿ᡆȂٽԃоཌᆄ១ߜ឴ဴጆ ኿ᡆ (CWT, coded wire tags) ܖ࢐ཌ࠮ଢ଼ސවа (chips) ৄේڗധᡝϱȄϽᏰܖҡސ኿ᡆ࢐ശЈณ ਲ਼ᐃ American Fisheries Society 2008 ԑ 2 Тӵ

હ ՙ ៌ ܚ ᖞ ᒲ ޟ ധ ᜸ ኿ ᜋ ׬ ೚ ୽ ሬ ं ଆ ོ (Advances in Fish Tagging & Marking Technology International Symposium, Auckland, New Zealand, 24-28 February 2008)Ȃ኿ᜋܹࢺПݲޟᔖҢџϷԙ ϲσ᜸տȈ(1) Ρഅፏ࢑኿ᡆ (satellite tags)ȇ(2) ຺

*೽ଉհޱбѮѕѿσԊୢᛳ඼ᆋၯѲࢲΙဴ, TEL: 02-33662887; FAX: 02-23639570; Email: wnt@ mtu.edu.tw

(2)

ޟ኿ᜋПݲȂٽԃցҢଽㅯ!(Sr)ȃᎣ!(Ba) ܖ࢐ᇄ ՌณࣨϛШ঄Ϛࣺӣޟӣ՝શྙశ੔ݾࡣȂџо ӵധՆүΰ੼ή੫੆ޟϯશ଄ဴ (Thorrold et al., 2002, 2006; Williamson et al., 2009)Ȃആႆ፴ᜊቈϷ ݙџоᒱᜋ೻ٲϯશȄѪѴȂϽᏰ኿ᜋПݲᗙѓ ࢂӣ՝શޟٺҢȂڏᓺᘈ࢐Ȃҡސᡝᄇܻӣ՝શ ၶؠԤҡ౩հҢΰޟᒵᐅਝᔖȂܚ኿ᜋޟ߬ဴ૖ ஊ࡞܆ᄂޟೝ଄ᓃȇીᘈࠌ࢐ӵٺҢӣ՝શਢ҆ ሯωЖ௡ᆓȂоᗗջԴࢗՌณᕗცȄѪѴΙᆍ኿ ᜋՆүޟПݲȂ࢐Նүޟᒉӎ኿ᜋݲȂցҢݧৢ ܖ࢐੔ݾ੊ϽѲᕗᡤશ (OTC, Oxy-tetracycline) ܖ₩શ (ALC, Alizarin complexone) ྙశȂџӵՆ үΰלԙ༁ᆦՓܖ࢐औՓޟᒉӎ଄ဴȄ ՆүޟЈณཌ໔ϯશ኿଄Ȃ࢐ߖԑپೝኄݿ ᔖҢڗധ᜸ḯ෬ंـޟПݲϞΙȂՆүџоकᓃ ࡞ӻޟᕗცଉ਀ȂٮиӵՆүΰޟ଄ᓃ࢐೿៉ܒ ޟȂ೻࢐ڏт኿ᜋПݲܚฒݲڥфޟȂӵՆүю ౪ޟ 31 ᆍϯશϛȂSr/Ca Шས଩ԑឭၥଉȂ࢐१ ࡚ധ᜸ḯ෬ᕗცѬശலҢޟПݲȄՆүޟкौԙ Ϸ࣏ CaCO3Ȃҥܻ Sr ᇄ Ca ӣ࢐Πቋޟᢃπఊϯ શȂϽᏰ੫ܒࣺխȂӰԪ Sr ࡞ৠܾڥф Ca Մؖ ᑖӵՆүϛȄ੕Ыϛޟㅯᐨ࡙࣏ 8.7 × 10-5 MȂష Ыࠌ࣏ 9 × 10-7 MȂࣺ৯घ 100 ॻ (Campana, 1999)Ȃ ՄՆүΰޟ Sr/Ca ШᇄѴӵЫᡝϛޟᢄ࡙ ࠌڎԤଽ࡙ޟғࣺᜰܒ (Secor et al., 1995; Tzeng, 1996; Kawakami et al., 1998; Lin et al., 2007)Ȅ࿋ധ ᜸೎ܻ੕ЫਢȂՆүོю౪ଽ Sr/Ca ШȂІϞӵష Ыਢࠌོю౪ճ Sr/Ca ШȂӰԪՆүΰޟ Sr/Ca Ш џоհ࣏ᕗცޟࡾ኿Ȅҥܻ೻ኺޟ੫ܒȂՆү Sr/Ca Ш ϐ င ೝ ኄ ݿ ᔖ Ң ܻ ं ـ ڍ ୏ ḯ ෬ ࠮ ധ ᜸ (diadromous fishes) ӵ੕ЫЅషЫᕗც໢ޟಋଢ଼ ႆ แ Ȃ ٽ ԃ ྗ ݬ ḯ ෬ (anadromy) ޟ ᘃ 嘒 ᜸ (Kalish, 1990; Howland et al., 2001; Limburg et al., 2001) ᇄన઴ᢧ (Secor and Piccoli, 1996)ȃ६੕ḯ ෬ޟషЫᠵ (Tzeng, 2003; Tzeng et al., 2002, 2003; Tsukamoto and Arai 2001; Jessop et al., 2002; Shiao

et al., 2003) Ѕڍූḯ෬ (amphidromy) ޟፈߏധ

(Radtke and Kinzie, 1996; Shen et al., 1998; Shen and Tzeng, 2002)ȄӰԪՆүΰޟ Sr/Ca ШȂ࢐Ң پ१࡚ധ᜸ӵషЫЅ੕Ыᕗც໢ޟḯ෬ᕗცѬȂ ࣺ࿋౩དޟώڎȄ Рҏᠵ (Anguilla japonica)ȂӵϷ᜸ᏰΰȂ឴ ܻᠵ㠦Ҭ!(Anguilliformes)ȃᠵ㠦ऋ (Anguillidae)Ȃ ࣏६੕ḯ෬࠮ധ᜸ (catadromous fishes)ȂϷҀӵݍ ѕٳӴୢޟѮᢊȃϛ୽ȃᗺ୽оЅРҏ้ӴȄР ҏᠵޟ౰֊ൟ՝ӵѕЊҁࢷ଻٨ٳઽတ৬оՙޟ ੕୿ (Tsukamoto, 1992, 2006ȇLiao et al., 1996, 1999ȇLiao, 2001)ȄᠵധΙҡѫ౰Ιԩ֊Ȃ౰ׇ֊ ࡣ൷ԫιȄ֊তჽϽϞࡣޟрധᆎ࣏ࠉࢩဨלᠵ (preleptocephalus)Ȃᓞσȃ٘ᡝಠߝȂбᏏԌᎠՄ एюȂԙߝΪඁЈࡣȂбᏏೝ֜ԝԙಠωޑԌб (Yu et al., 1993ȇTanaka et al., 2001)Ȃᓍࡣᡝଽቨ ё Ȃ ᓞ ω ٘ ᡝ ୏ ࡵ Ȃ ᆎ Ϟ ࣏ ࢩ ဨ ᠵ (leptocephalus)Ȅࢩဨᠵᎌӫӵࢷࢺϛհߝຽᚔޟ ᅔࢺȂ௃౰֊ൟᓍ๿ྣླྀޟѕٕၾࢷࢺ (North Equatorial Current) ܁ՙಋଢ଼ȂӔ໷๿༃ዘ܁ѕᅔ ࢺȄ4 ڗ 6 এТࡣȂپڗݍѕٳޟσചෞ੕୿Ȃᡐ ᄘ࣏ࢺጣ࠮иആ݂ޟ࣠ይᠵ (glass eel)Ȃ໠ۖڎԤ кଢ଼෬ݨޟ૖ΨȂٮ૖ஊཐڧᢄ࡙ȃྣ࡙ȃϽᏰ ੉ڨޟ৯౴Ȅ࣠ይᠵೝషЫ֜Е໌Σݬοȃ௥ញ ష Ы ࡣ Ȃ ᡝ ߒ Փ શ ಠ फ ം ᅚ ี ى ȃ ԙ ࣏ ᠵ ጣ (elver) Ȅ ӵ ݬ ύ ԙ ߝ ޟ ໦ ࢲ ᆎ ࣏ ༁ ᠵ ! (Yellow eel)Ȃᓍ๿এᡝϚᘞีىȂംᅚ܁ΰ෬ಋଢ଼Ȃӵݬ ύ ϛ ූ ਀ ኵ ԑ Ȃ ้ ڗ ԙ ዣ ਢ Ӕ ᙽ ᡐ ԙ ࣏ ሚ ᠵ (Silver eel)Ȃٮ໌՗६੕ḯ෬౰֊ȂᖅॊήΙфȂ ׇԙڏҡࣀѬ (Ege, 1939; Tesch, 1977)Ȅ ᗶณႆўޟंـϐငජᛲΟᠵധޟҡࣀѬႆ แ (Schmidt, 1912)ȂծԤᜰᠵധӵݬύϱޟಋଢ଼ оЅѴࢷޟḯ෬՗࣏ٮϚ࢐࡞఼ཿȄෆ (1984) ց ҢᒉӎࢗᏘ኿ᜋӵ։஠ौྗݬޟᠵጣᡝߒΰȂо ߯ᢎᄆᠵധӵݬοୢ୿ޟḯ෬՗࣏ȄծٮҐ᝷៉ ଡᙹڏྗݬϞࡣޟ՗࣏ȄJellyman and Tsukamoto (2002) ց Ң ོ ಳ ᚔ ޟ ၥ ਟ ᓽ Ԇ ኿ ᡆ (pop-up Archival tag)Ȃھۡӵᐬࢸσᠵ!(A. dieffenbachii) ޟ٘ΰȂᢎᄆڏ६੕ޟ౰֊ḯ෬՗࣏Ȃծ࢐೻ᆍ ኿ᡆᡝᑖЊσȂ༉૖ھۡӵᡝ࠮σޟᐬࢸσᠵȂ ԃݎौھۡӵᡝ࠮ၶωޟРҏᠵ٘ΰȂٮϚџ ՗ȄKuo et al. (1996) ցҢ຺ॱݰ኿ᡆ (ultrasonic transmitter tag) ଡᙹ६੕ࡣРҏᠵޟḯ෬՗࣏Ȃծ ҥܻԪᆍ኿ᜋПݲڧ३ܻ኿ᡆϱႫԱޟჰڼȂଡ ᙹޟਢ໢ζ࡞฻኷ȂՄи௥ԝᏢά҆໸ӣ؏ߖຽ ᚔଡᙹȂ኿ᜋາҢ݁ິиາਢາώȄThibault et al., (2007) ෆငԙђӴ௴ҢႆฒጣႫ኿ᡆ (radio tag) ଡᙹݬύϱछࢸᠵಋଢ଼՗࣏ȂࣺӣПݲζᔖҢܻ ዉࢸᠵ (Westerberg et al., 2007) ڷહՙ៌σᠵ (Boubee et al., 2008) ΰȄฒጣႫ኿ᡆПݲᗶณԁȂ

(3)

ծѫ૖ࠁ३ӵωጒ൜ϱȂи҆໸ኄ೩ฒጣႫ௥ԝ Ꮲϗ૖ۡ՝Ȃ኿ᜋζ࢐າਢາώՄи݁ິȂଡᙹ ޟਢ໢ζ࡞Ԥ३ȄܚоҬࠉԤᜰ༁ᠵӵݬύϱޟ ಋଢ଼՗࣏ȂܚޣϫณԤ३Ȅ ҏंـ௴ҢϽᏰޟڷ༈ಛޟ኿ᜋПݲȂپं ـݬύڷዢ෹ϱޟᠵധޟಋଢ଼՗࣏ȄϽᏰޟ኿଄ Ν࢐ցҢՆүޟϯશಢԙȇՄ༈ಛޟ኿଄ࠌџᙏ ൐ୢϷ࣏ᡝѴоЅᡝϱ኿଄ȄᡝѴ኿଄ഋϷȂк ौ࢐ӵധᡝߒ७໌՗੧ӟȃ୘៵ܖ࢐҈ࢾȂо߯ ஠پӔਐਢџоҥѴᢎޢ௥ୢϷ኿ᜋധڷҐ኿ᜋ ധȇᡝϱ኿଄ࠌ࢐௴Ңଢ଼ސවаоЅཌᆄ១ߜ឴ ጡጆ኿ᡆڷՆүᒉӎ኿ᜋПݲȄငҥоΰӨᆍП ݲޟσ໔኿ᜋࡣȂ໌՗༁ᠵӵݬύϱޟಋଢ଼՗࣏ ЅූӴցҢ้ᠵധḯ෬ଉ਀ޟंـȂо෈ඪټҐ پݬύϱᠵധၥྛ߳ىЅᆓ౩ޟ୤ՃȄ

Fig. 1 The Japanese eels were released at sites of Da-pong (DP) Bay and the estuary of the Kao-ping (KP) River in southwestern Taiwan.

؅ਟᇄПݲ

ΙȃंـӴᘈ!

଄ (Fig. 2a)Ȅᓺᘈ࢐ငႆశᄘ෨೎౩ޟᠵധȂ฻ ෈ϱџоӵᡝߒ੼ή఼ཿޟጡጆ଄ဴȂӔਐਢџ о௃Ѵᢎ఼ཿӴᒱᜋȂٮиցҢጡጆޟಢӫџо ୢտڗএᡝޟቹԩȇીᘈ࢐శᄘ෨኿ᜋࡣӵᡝߒ ౰ҡޟ༌౷Ȃσघငႆ 3 এТࡣȂ൷ོᡐு዁ጙ Ϛ఼ȂӰԪȂၶϚᎌӫୈߝ෈ޟଡᙹȄ Рҏᠵ኿ᜋܹࢺޟᄂᡛӴᘈȂ՝ܻࠒѮᢊޟ σᝉᢊЅଽࡎྩЫ୿ (Fig. 1)Ȅσᝉᢊ࢐ᔻᖝѮᢊ ੕১ޟΙএјࡌഖܒޟዢ෹ȂԤΙএ੭બޟ໌ю οᇄѴ੕ࣺ೿௥ȂоЅڍএЫ໔࡞ωޟషЫ௶Σ οȂᢊϱޟᢄ࡙ۖತᆰࡻӵ 33 ~ 35 psu Ϟ໢Ȃష Ы௶Σοߣߖޟᢄ࡙࣏ 5 ~ 7 psuȄଽࡎྩ࣏ࠒѮ ᢊശσޟݬύȂߝ࡙Ԥ 171 kmȂݬοӴୢ࢐༈ಛ ਐਔᠵധޟհཾୢ୿Ȃݬο୿ޟᢄ࡙ڧڗዘԲޟ ኇ៪Ԥ࡞݂ᡗޟᡐϽ (0 ~ 33 psu)Ȃཐዘளޟຽᚔ ߝႀ 16.8 kmȄѪѴȂଽࡎྩݬύۻቹޟӴלᕗც ࣺ࿋ޟϚӣȂџୢϷԙЫҡේސᙴ൲ޟ૩ᐩȃँ ፴ۻ፴ȃᘇπۻ፴оЅԤࢾҲޟᐝቬ้ූӴȄ (2) ୘៵ݲȋ ӵϚӣޟ៵ഋ՝୘ήΙа៵ܖӵឥᇐΰ҈ࢾ ୈ኿଄Ȅ೻ζ࢐Ιᆍၶৠܾџоޢ௥௃Ѵߒᢎᄆ ޟПԒȄϚႆӵငႆघέএТޟਢ໢Ȃೝ୘ޟ៵ ζོӔҡȂ༌οᘾӫࡣᇄཎѴڧ༌ࡣޟᘾӫৠܾ ౅౒Ȃ௃ѴᢎΰϚܾୢտ (Fig. 2d)Ȅ 2. ᡝϱ኿ᜋ

Πȃ኿ᜋПݲ

(1) ཌᆄ១ߜ឴ጡጆ኿ᡆȋ ҏंـܚ௴Ңޟ኿ᜋПݲȂϷտᇳ݂ԃή (ӵ ኿ᜋࠉȂᠵധࣱငႆബ᎖೎౩)ȋ ኿ᡆߝ࡙घ 1 mmȂџ೿៉ጡဴܖ࢐׳ԩጡ ဴȄٺҢݧৢᏢ஠኿ᡆේΣധᡝࡣܹࢺȄӔਐਢ ց Ң ௭ ජ Ꮲ پ ᔮ ก (CWT detector: Handheld Wand Detector, NMT - Northwest Marine Technology, USA) (Fig. 2b)ȄҬࠉϐԤ୦ཾϽޟ኿ ᡆЅ௭ජفಛȂৠܾᐇհȂџоσ໔኿ᜋȄ (Ι) ༈ಛޟ኿ᜋПݲ 1. ᡝѴ኿ᜋ (1) శᄘ෨੧ӟݲȋ (2) ଢ଼ސවаȋ ӑ஠ړԤ़МԅҔȃಒဴܖ࢐ኵԅޟߜ឴዁ ࠮Ȃညܻశᄘ෨ϛȂณࡣ੧ӟӵധᡝߒ७੼ή኿ ցҢݧৢᏢ஠Ԥጡጆޟවа኿ᡆේΣധᡝϱ

(4)

(a) (b) (c) (d) Injector Scanner Chip (e)

Fig. 2 Three tagging methods: (a) marked by liquid nitrogen, (b) CWT (coded wire tags) and scanner (c) chip implanted, (d) fin clip and (e) chip scanner with specific number.

(Fig. 2c)ȂᠵധӔਐਢցҢ௭ජᏢᒱᜋවа኿ᡆ (Chips detector: All Weather Extended Range Multi Tag Reader, AVID, USA ) (Fig. 2c, e)Ȅଢ଼ސවаᓺ ᘈӵܻؐএවа഍ԤጡጆȂџоᒱᜋএᡝȂٮи џо१ፒٺҢȂծીᘈ࢐኿ᡆ୵ቋଽ݁ȂՄи኿ ᜋૉਢȄ ᡝϱ኿ᜋޟཌᆄ១ߜ឴ጡጆ኿ᡆоЅଢ଼ސව аȂӵݧৢׇԙиငႆ௭ජᏢޟጂᇯࡣȂ኿ᜋ౥ џоႀ 100%Ȅ (Π) ϽᏰޟ኿ᜋПݲ — Նү኿ᜋ 1. ࠉညၐᡛ ༁ᠵоؐϴОധᡝ१࣏அྥȂϷտо 25ȃ50ȃ 75 оЅ 100 ppm ོ౰ҡ༁ᆦՓᒉӎޟ੊ϽѲᕗᡤ શ (OTC)Ȃ໌՗လ๨ݧৢȄѪѴȂᠵጣоऔՓޟ ₩શ (ALC)Ȃᐨ࡙Ϸտ࣏ 15ȃ25ȃ50 Ѕ 75 ppmȂ

(5)

Fig. 3 The red ALC fluorescent marks exhibited by elvers which were immersed in ALC solution at different time periods (6, 12 and 24hrs) and concentrations (15, 25, 50 and 75 ppm). The tagged elvers were then reared for one month. 12 hrs 24 hrs 6 hrs 15 ppm 25 ppm 50 ppm 75 ppm ੔ݾ 6ȃ12 Ѕ 24 ωਢȂႷىΙএТࡣែࣘധᡝڥ юՆүȂငѓৄȃंᑑࡣȂо BV فӖᘮӎа (BV-2A, wavelength: EX 400-440 nm, DM 455 nm, BA 470 nm, Nikon) оЅ G فӖᘮӎа (G-2A, wavelength: EX 510-560 nm, DM 575 nm, BA 590 nm, Nikon) Ϸտپᔮຜ OTC оЅ ALC ޟ኿ᜋਝ ݎȄ 2. Նү኿ᜋ Ն ү ΰ ޟ ᒉ ӎ ଄ ဴ Ȃ ࢐ ആ ႆ ӎ Ᏸ ᡗ ཌ ᜢ (SMZ-10, Nikon) Ȃ ๖ ӫ Ы ሚ ᐷ ݾ ޟ ΰ ഋ ӎ ྛ (HBO – 100w/2, Nikon)Ȃས଩ᒉӎᘮᜢپᢎᄆȄՄ ᜰܻՆүᒉӎ኿ᜋޟശᎌ࿋ᐨ࡙ᇄਢ໢ȂALC ฒ ፣࢐о 15ȃ25ȃ50 оЅ 75 ppm ޟᐨ࡙੔ݾӵϚ ӣਢ໢ή (6ȃ12 оЅ 24 ωਢ) ࣱ૖౰ҡ఼ཿޟᒉ ӎᕗ (Fig. 3)Ȃծ࢐ԃݎᐨ࡙ЊଽȂᒉӎᕗ࡙߫Њ ଽȂོኇ៪ӵᡗཌᜢήՆүᒉӎ኿ᜋ՝ညޟրۡ ғጂܒȇՄ OTC оϚӣޟᐨ࡙໌՗လ๨ݧৢȂζ ഍џоӵՆүΰ౰ҡ఼ཿޟ༁ᆦՓᒉӎᕗ (Fig. 4)ȄҏᄂᡛϷտٺҢؐϴОധ 100 ppm ޟ OTC ݧ ৢоЅ 75 ppm ޟ ALC ੔ݾ 12 ωਢ (Fig. 5)Ȅᒉ ӎᕗ଄ဴ࣏ᄂᡛޟଔᘈȂӵᒉӎᕗ (mark) ڗՆү ޟ᜞ጢ (edge) Ϟ໢ޟୢ୿ (Fig. 5)Ȃ࣏ܹࢺႆแ ϛധᡝܚԙߝޟഋϷȂζ൷࢐ࡣ៉հ࣏ϷݙՆү ཌ໔ϯશޟ՝ညȄ ငႆ኿ᜋ೎౩ޟᠵധሯӑ՗੺ᎴӵᎴ෥Ա ϛȂ้࡟ധᡝׇӒϚڧബ᎖ޟኇ៪Ȃи࡮ඈࣀΨ ࡣȂӔ໌՗ܹࢺȂٮи߳੼ഋϷᠵധհ࣏ࡣ៉Ԇ ࣀ౥ޟଡᙹᢎᄆȄҏᄂᡛี౪ȂϚ፣࢐঺Ιᆍ኿ ҰПݲȂᠵധӵ኿ᜋࡣȂႤЈޟԆࣀ౥֯џоႀ ڗ 99% оΰȂငႆΙএТࡣȂ༉ོԤЍኵޟএᡝ ԫιȂᐌᡝޟԆࣀ౥һџо߳ࡻӵ 99%Ȅѓ֤ᠵ ጣᇄ༁ᠵȂӓॎܹࢺ 7273 ׎ᠵധȄ

έȃኺҏپྛЅܹࢺኵ໔

኿ᜋܹࢺᄂᡛܚٺҢޟᠵധԤέᆍȋ(1) Ꮄ ෥ᠵȂ࢐ӵࡎݍӴୢݬοܚਐਔޟᠵጣȂӵషЫ ޟᎴ෥Աϛငႆ 2 ԑѾѡޟᇋᎴߝσȂӔငႆј షឧЫႽϽјԑࡣȂඪټҏंـٺҢȇ(2) ᅣҕӵ ଽࡎྩݬοٺҢ೐᠖ܚਐᕕޟഏҡᠵ (Table 1)ȇ (3) ᠵጣޟഋӋȂ௴Ңޟ࢐ཱིԼᓞࠉྩݬοܚਐਔ ޟᠵധȄ2002~2005 ԑоЅ 2006 ԑଽࡎྩᖂॎܹ ࢺΟ 1350 оЅ 1123 ׎ (ᠵጣଶѴ) ᠵധȂσᝉᢊ

(6)

Fig. 4 The yellow OTC fluorescent marks were showed by yellow eels which were injected with OTC solution at dosage (a)25, (b)50, (c)75 and (d)100 ppm of body weight (per kg). arrow: OTC mark.

Fig. 5 Oxytetracycline (OTC) and Alizarin complexone (ALC) marks in the otoliths of Japanese eels at release. The new increments between the OTC and ALC marks and the otolith edge were deposited between release and recapture. (a) (b) (c) (d) 500 Ÿm (b) OTC mark Edge 300 Ÿm (d) 350 Ÿm Edge ALC mark ALC mark OTC mark (a) 500 Ÿm (c) 500 Ÿm

(7)

Table 1 Sources and numbers of Japanese eels Anguilla japonica marked by different methods (Oxytetracycline: OTC, Alizarin Complexone: ALC, coded wire tag: CWT, chip, fin clip, and liquid nitrogen: LN), and released at the south and north coasts of Da-Pong Bay (DP) and the upstream (KP-up) and the downstream (KP-down) of the Kao-Ping River in 2002, 2003, 2005 and 2006

No. of eels marked Release

date Release site Source OTC ALC CWT chip fin clip LN Mar. 3, 2002 KP-down Wild 4800

Sept. 9, 2003 DP-north Culture 163 163 163 163

Culture 500

Sept. 29 KP-down Culture 300

KP-up Culture 180 180 Oct. 7 DP-south Culture 127 127

Sept. 28, 2005 KP-down Culture 500 500 500

Wild 152 152 152

Oct. 3 KP-up Culture 150 150 150

Oct. 13 KP-down Wild 68 68 68

Aug. 15, 2006 KP-down Culture 537 537 537

Wild 246 246 246

Aug. 16 KP-up Culture 100 100 100 Aug. 25 KP-down Culture 140 140 140 140

Wild 55 55 55 55

Aug. 26 KP-down Culture 40 40 40 40 Wild 5 5 5 5 DP 290 663 290 163 Total KP 2173 4800 480 1993 1993 240 ᖂӓܹࢺΟ 790 ׎ȂӨᆍ኿ᜋПݲޟܹࢺኵ໔Ѕ ܹࢺР෈ڷӴᘈ၏ԃ Table 1Ȅҁ֯ᡝߝЅᡝ१ԃ Table 2 & 3 ܚҰȄܻ 2002 ԑ 3 ТȂӵଽࡎྩή෬ ܹࢺΟ 4800 ׎ޟᠵጣഋӋȂӰ࣏ؠԤӱԝȂܚо ؠԤᒲݲୈࡣ៉ޟଡᙹ፡ࢥȄ ѪѴȂ࣏Ο௤ଆРҏᠵܹࢺࡣޟᘗඹຽᚔо Ѕሴ୿՗࣏ȂٺҢΟ 2006 ԑ 8 Т 15 Рӵଽࡎྩ ή෬Ы୿ܚܹࢺޟ 783 ׎ᠵധ (Table 3)Ȃܹࢺࡣ ငႆ 10 Јܻ 2006 ԑ 8 Т 25 РȂӵܹࢺᘈߣߖЫ ୿ 7 এ௴ኺᘈೝᅣҕо೐᠖ܚਐᕕȂᖂॎ 204 ׎ ᠵധо໌՗ၥਟϷݙȄԪѴȂ࣏Ο௤ଆᠵധؐЈ ശσޟᘗඹຽᚔڷПөȂ೻ 204 ׎ᠵധܻ࿋Јӱ ԝࡣȂငႆஅᙃၥਟ໔กकᓃࡣȂԚଶࣀΨϚٹ ޟᠵധȂӓॎԤ 195 ׎ᠵധ (Table 3) ӵᇄ Fig. 7 c ࣺІޟЫ୿໌՗ܹࢺ (Fig. 7 d)Ȅ

ѲȃSr/Ca ШϷݙ

኿ᜋܹࢺࡣӔਐᕕޟᠵധȂก໔ڏᡝߝȃᡝ १ϞࡣȂڥюՆүȂငѓৄȃंᑑࡣȂցҢႫυ ཌ௤ቈ ȞEPMA; JXA-8900R, JEOLȟоؐ 10 ȝm ޟຽᚔȂ௴ऎູጣޟПԒȂϷݙՆүਯЖՍ᜞ጢ ޟՆү Sr/Ca ШȂณࡣᘝڥ OTC ኿଄Ϟࡣޟ Sr/Ca ᡐϽȂپϷݙܹࢺϞࡣޟᠵധಋଢ଼௑לȄਲ਼ᐃ

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Table 2 Mean (± SD) total length (TL) and body weight (BW) of released Japanese eels, Anguilla japonica, in Da-Pong Bay (DP) and the upstream (KP-up) and downstream (KP-down) of the Kao-Ping River in 2002, 2003 and 2005. The recaptured rates (%) were calculated one year after release. Recapture rate (%) = recapture of tagged/ release of tagged × 100%

Mean (± SD) Release

Release site Source No. of eel released No. (%) of eel recaptured TL (cm) BW(g) date KP-down Wild 4800* 0 (0) 5.56 ± 0.24 Mar. 3, 2002

Sept. 9, 2003 DP-north Culture 163 34 (20.9) 1200 Culture 500 59 (11.8) 400 Sept. 29 KP-down Culture 300 14 (3) 400

KP-up Culture 180 0 (0) 400

Oct. 7 DP-south Culture 127 50 (39.3) 1200

KP-down Culture 500 25 (5) 69.3 ± 4.9 508.3 ± 137.6 Sept. 28, 2005

Wild 152 4 (2.6) 69 ± 4.7 505.5 ± 129.2 Oct. 3 KP-up Culture 150 1 (0.6) 68.9 ± 4.7 495.7 ± 134.6 Oct. 13 KP-down Wild 68 0 (0) 44.2 ± 11.6 116.3 ± 109.9

DP 2003 790 143 (14.6) Tzeng (1996) ޟᄂᡛ๖ݎȂषՆү Sr/Ca ωܻ 4.0× 10-3ȂࠌߒҰᠵധӵషЫЫ୿ಋଢ଼ȇषଽܻ 4.0× 10-3ȂࠌߒҰӵ੕Ыಋଢ଼ȇषӵ 4.0× 10-3ߣߖ ᡐଢ଼ȂࠌߒҰӵݬοಋଢ଼Ȅਲ਼ᐃՆүޟ Sr/Ca Ш ๖ݎȂџоҢپୢϷᠵധޟḯ෬՗࣏оЅҡࣀѬ ᜸࠮ȂӰԪζџоᄇܹࢺ؅ਟޟᎴ෥ᠵоЅഏҡ ᠵ໌՗ҡࣀѬޟᡛᜌȂоЅџоҢپϷݙഏҡᠵ ޟҡࣀѬ࠮ᄘȂശࡣџоᡛᜌ኿ᜋᠵധӵܹࢺႆ แϛޟḯ෬՗࣏Ȅ 2002 4800 0 (0) 5.56 ± 0.24 2003 480 14 (3) Total KP 2005 870 30 (3.4) 66.2 ± 10.1 458.2 ± 183.9 *Only Mar. 3, 2002 were elvers

Table 3 Mean (± SD) total length (TL) and body weight (BW) of released Japanese eels, Anguilla japonica, in the upstream (KP-up) and downstream (KP-down) of the Kao-Ping River in 2006. The recaptured rates (%) were calculated ten days and one day after release. Recapture rate (%) = recapture of tagged/ release of tagged × 100%

Mean (± SD) Release

Release site Source No. of eel released No. (%) of eel recaptured TL (cm) BW(g) date KP-down Culture 537 146 (27.2) 70.6 ± 10.6 578.1 ± 318.8 Aug. 15, 2006 Wild 246 58 (23.6) 67.5 ± 9.6 478.4 ± 280.1 72.7 ± 10.2 633.8 ± 320.7 Aug. 16 KP-up Culture 100 0 (0)

66 ± 9 433.8 ± 259.1 Aug. 25 KP-down Culture 140 40 (28.6)

Wild 55 5 (9.1) 62.8 ± 10.1 356.8 ± 230.5 64.7 ± 9 389.2 ± 223.8 Aug. 26 KP-down Culture 40 2 (5)

Wild 5 1 (20) 48.2 ± 4.4 98.2 ± 45 67.4 ± 9.8 478.1 ± 284 Total KP 2006 1123 252 (22.4)

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ϤȃၥਟϷݙ

ӱԝ౥ (%) Ϸտ࢐ॎᆗܹࢺࡣޟ 24 ωਢȃ 10 ЈоЅؐএТӋ (ᆰࡻΙԑ) ਐਔӱԝޟ኿ᜋ ᠵኵ໔ଶо኿ᜋᠵޟᖂኵ (ӱԝ౥ (%)!= ਐਔ኿ ᜋᠵധ/ᖂ኿ᜋᠵധʳ ͪʳ 100%)Ȅӣਢζեॎᠵധӵ ଽࡎྩή෬Ȃܹࢺ 24 ωਢоЅ 10 Јࡣޟު໢Ϸ ҀоЅූӴጒ൜ȄϷݙӱԝ౥оЅಣᑖӱԝ౥ڷ ຽᚔޟᜰ߽Ȅӱԝ౥ӵσᝉᢊࠒȃѕ۬оЅӵଽ ࡎྩϛȃή෬ӑငႆᄇኵᙽ඲ȂӔо t-test پϷݙ ڏ৯౴ܒȄ 0 2 4 6 8 10 12 0 1 2 3 4 5 6 7 8 9 10 11 12 DP 2003 KP 2003 0 0.2 0.4 0.6 0.8 1 1.2 1.4 0 1 2 3 4 5 6 7 8 9 10 11 12 M ean r ec apt ur e r at es ( % )

KP 2005

0 5 10 15 20 25 30 35 40 0 1 2 3 4 5 6 7 8 9 10 11 1 (a) (b) (c) KP 2006 2 Time elapsed after release (months)

Fig. 6 The monthly change of mean (± SD) recapture rates in the first year after release in Da-Pong Bay and the Kao-Ping River in 2003 (a), 2005 (b) and 2006 (c).

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(a) (b)

๖!!!ݎ!

Ιȃӱԝ౥ޟਢ໢ᡐϽ!

ᗶณᠵധޟӱԝ౥Ԥԑ࡙໢ܖӴᘈ໢ޟ৯ ౴Ȃσᝉᢊ 2006 ԑޟಣᑖӱԝ౥࣏ 14.6%ȂՄଽ ࡎྩӵ 2003ȃ2005 оЅ 2006 ԑޟಣᑖӱԝ౥Ϸ տ࣏ 3%ȃ3.4% оЅ 22.4% (Tables 2, 3)Ȃծӵܹ ࢺࡣΠএТȂ഍֕౪݂ᡗޟή६ (Fig. 6)ȂڗΟ಑ 6 এТ (σᝉᢊଶѴ)ȂඁнϚӔี౪኿ᜋᠵധȄԪ ѴȂӱԝ౥ӵᎴ෥ᠵᇄഏҡᠵϞ໢ȂࠌؠԤᡗ๿ ܒޟ৯౴ȂߒҰܹࢺϞࡣȂڍޱޟ՗࣏ࣺխȄՄ ငႆ ALC ኿ᜋޟᠵጣȂܻ 2002 ԑ 3 Тӵଽࡎྩ ή෬ᖂॎܹࢺ 4800 ׎Ȃծ࢐ᄠՍ 2008 ԑۻȂ഍ ؠԤӱԝڗܚ኿ᜋޟᠵധȄ

Πȃᠵധޟಋଢ଼ຽᚔЅሴ୿՗࣏

оσᝉᢊޟᠵധ࣏ٽȂϚ፣࢐ӵѕ۬ܖ࢐ࠒ ܹ۬ࢺޟᠵധȂငႆϚӣӱԝӴᘈᅣڎޟಛॎȂ ຺ႆ 93.9% ഍࢐ӵၶճᢄ࡙ޟషЫ௶Ыοϛೝਐ ਔ (Fig. 7a, b)ȂٷྱܹࢺᘈоЅӱԝᘈޟငጜ ࡙ȂեॎؐРശσޟಋଢ଼ຽᚔघ࣏ 2.48 kmȂՄଽ ࡎྩޟᠵധȂԤ 99% ഍࢐ӵݬοӴୢೝਐਔ (Fig. 7c, d)ȂՄиζ഍ຽᚔܹࢺᘈϚሉȂ೻ኺޟ๖ݎߒ Ұଽࡎྩޟᠵധ൉᠍ݬοјషឧЫޟᕗცȂؐР ശσಋଢ଼ຽᚔघ࣏ 2.09 kmȄᠵധܹࢺϞࡣȂڏӱ ԝ౥ᓍ๿ຽᚔޟቨё݂ᡗޟ६ճ (Fig. 8)Ȃ೻ߒҰ Fig. 7 Dispersal of marked Japenese eels in Da-Pong Bay and the estuary of the Kao-Ping River after released. (a) and (b) indicate the recapture rates of the eels released in the north and south coasts of Da-Pong Bay on Sept. 9, 2003 and Oct. 7, 2003, and the recapture rates in the seawater inlet and freshwater entrance of the bay from Oct. 2003 to Feb. 2004. (c) 783 eels (in square) were released in the lower reach of Kao-Ping River on Aug. 15, 2006 and the recapture rates of eels in each of the sampling sites in the 10 days after release. Open circles indicate no recapture. (d) The 195 recaptured eels from (c) were released again in the upper part of the downstream of Kao-Ping River on Aug. 25 and the recapture rate of eels recaptured after 24 hrs in each sampling sites is shown.

1.4% 2.4% 1.6% 1.1% 633 35.4% 11.6% 127 500 m 500 m (c) (d) 0% 0% 0% 0% KP-down KP-down 0.4% 195 0% 0% 0% 0% 0% 0% 5.1% 0% 0% 1.0% 0% 4.6% 1.0% 783 0% 0% 1.9% 3.6% 8.2% 2.1% 1.5% 5.5% 3.4% 2.1% 4.5% 200 m 3.1% 200 m

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ᠵധܹࢺϞࡣȂಋଢ଼ޟຽᚔ࡞ωȂԤୄ੼ӵܹࢺ ᘈߣߖޟሴ୿՗࣏ȇ຺ႆ 80% ޟᠵധؐЈޟಋଢ଼ ຽᚔϚ຺ོႆ 1 ϴ٨ (Fig. 8)ȄՄ൷Ϸտܹࢺӵଽ ࡎྩڍএӴᘈޟᠵധՄِȂڏᘗඹጒ൜ߨலࣺ խȂߒҰᠵധԤΙۡޟූӴ൉ԁܒȄ

έȃՆүSr/Ca ШᇄႷىᢄ࡙Ϟᜰ߽

Figure 9a ࢐Ꮄ෥ᠵܹࢺࠉࡣޟՆү Sr/Ca Ш ᡐϽȄY ໅фߒҥՆүਯЖ՝ညڗ᜞ጢޟऎູጣ ϷݙȂߝູ࡙ߝфߒᠵധޟԑឭູσȄӵ 2 ԑޟ షЫ੺Ꮄ෈໢ȂSr/Ca Шӵ 4 ‰ оήȂјԑޟј షឧЫ (ᢄ࡙घ 10 ~ 20 psu) ႽϽ෈໢ȂՆүޟ Sr/Ca Шོᓍ๿Ѵӵᕗცᢄ࡙ޟΰЀՄቨёڗ 4 ‰ оΰȄӰԪȂՆү Sr/Ca Ш 4 ‰ џо࿋հ࢐ᠵധ ӵ੕ЫڷషЫϞ໢ḯ෬ޟրᘞࡾ኿ȄFig. 9b ࢐ӵ ଽࡎྩਐਔޟഏҡᠵȂܻܹࢺࠉᠵധՆү Sr/Ca Ш ޟਢוӖᡐϽȂSr/Ca Шσ഍ӵ 4 ‰ ѾѡᎪᕝȂ ߒҰ೻׎ᠵധܹࢺࠉࡣ഍ӵјషឧЫߣߖಋଢ଼Ȅ

Ѳȃᠵധޟḯ෬᜸࠮

௃ 2003 ԑӵσᝉᢊਐਔޟ 60 ׎ഏҡᠵоЅ 2003-2006 ԑӵଽࡎྩਐਔޟ 209 ׎ഏҡᠵޟՆү Sr/Ca ШϷݙ๖ݎȂี౪џо஠ᠵധޟḯ෬ᕗცѬ ᘪઽԙέᆍ᜸࠮ (Fig. 10)ȋ(1) షЫ࠮ޟᠵധ (Fig. 10a)ȂڏՆү Sr/Ca Шӵᠵጣ໦ࢲ (EC) оࡣ ഍ӵ 4 ‰ оήȂ೻Ι᜸࠮ӵσᝉᢊԤ 15 ׎ȃଽ ࡎྩԤ 47 ׎ȂϷտլਐਔᠵധᖂኵШٽޟ 25% о Ѕ 22%ȇ(2) ੕Ы࠮ (Fig. 10b) ȂՆү Sr/Ca Ш഍ ӵ 4 ‰ оΰȂڏШٽϷտ࣏σᝉᢊ 9 ׎ޟ 15% ᇄ ଽࡎྩ 5 ׎ޟ 2.5%ȇ(3) ݬο࠮ (Fig. 10c, d) Ȃ Նү Sr/Ca Ш഍ӵ 4 ‰ Ѿѡᡐଢ଼ȂڏШٽϷտ࣏ σᝉᢊ 36 ׎ (60%) ᇄଽࡎྩ 157 ׎ (75.5%)Ȅݬ ο࠮ޟᠵധᗙџо໌Ι؏Ϸ࣏ 2 ᆍԩ᜸࠮Ȉ(1) Ι ԩޟූӴᡐ඲࠮ (Fig. 10 c)Ȃѫӵ੕ЫషЫϞ໢پ ӱಋଢ଼ΙԩȂڷ!(2) ӻԩޟූӴᡐ඲ (Fig. 10d)Ȅ ௃έᆍҡࣀѬ᜸࠮ޟԻϷШџоޣၾȂϚ፣࢐ଽ ࡎྩܖ࢐σᝉᢊȂσഋϷޟᠵധ഍୑ԁјషឧЫ ޟූӴȄ 0 10 20 30 40 50 60 70 80 90 100 290 690 990 139

Distances from the

R e ca pt ur e ( % ) 0 1640 1890 2090 release sites (m) 0 10 20 30 40 50 60 70 80 90 100 A cc u m u la ted r e ca pt ur e ( % )

Fig. 8 The spatial frequency distribution of Japanese eels in the 10 days (Diamond) and 24 hrs (Triangle) after released in the estuary of Kao-Ping River. Left axis and open symbols: recapture by distance from the release site; Right axis and solid symbols: accumulated recapture by distance from the release site. Diamond: the 783 eels released on Aug. 15, 2006 and recaptured until Aug. 25, 2006 (n=204); Triangle: the 195 eels recaptured from Aug. 15 until Aug. 25, 2006 and released on Aug. 25 and recaptured on Aug. 26, 2006 (n=45).

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(a) Marine life Living in culture pond Acclimation Life after release

Ϥȃܹࢺᠵޟಋଢ଼՗࣏

Figure 11 ࢐ᠵധܹࢺࡣȂһ։ (ᒉӎ኿ᜋ଄ ဴϞࡣ) ޟՆү Sr/Ca ШޟᡐϽȄσᝉᢊ኿ᜋܹࢺ ϞࡣޟᠵധȂσഋϷӵషЫ௶ΣοೝਐᕕȂоڏ ϛܚϷݙޟ 4 ׎ᠵധ࣏ٽȂڏՆү Sr/Ca Шӵ 3 ~ 7 ‰ Ϟ໢ᡐϽ (Fig. 11a)ȂһߒҰσᝉᢊޟᠵധӵ ᢊϱޟଽᢄ࡙ᇄషЫ௶ΣοϞ໢ಋଢ଼ޟᗍ༖Ȅ 2005 ԑӵଽࡎྩܚӱԝޟ 4 ׎ᠵധȂࠌ୑ԁճᢄ ࡙ޟݬο୿ᕗც (Fig. 11b)ȂՄ 2006 ԑࢌӱԝޟ ѪѴ 4 ׎ᠵധȂࠌ༊өషЫᕗც (Fig. 11c) Ȅၶ ੫տޟ࢐Ȃӵ 2005 ԑ 10 Т 3 Рӵଽࡎྩϛ෬ޟ ᄯόܚܹࢺޟΙ׎ᠵധȂငܹࢺ 194 ЈࡣȂܻ 2006 ԑ 4 Т 13 Рӵή෬ޟݓ༪ೝਐᕕȂಋଢ଼ຽᚔघ 42 ϴ٨Ȃष࢐оؐЈޟശσಋଢ଼ຽᚔ (घ 2 km)Ȃᔖ ၎ѫሯौσघ 21 Ј։џڗႀೝਐᕕޟӴᘈȂծٱ ᄂٮߨԃԪȂҥՆүΰ Sr/Ca ШޟϷݙ๖ݎџо ᜌ݂Ȃ೻׎ᠵധܹࢺϞࡣσഋϷਢ໢഍ୄ੼ӵష Ы (OTC Ϟࡣ!~ 100 Ÿm)ȂܻਐᕕϞࠉϚδ (130 ~ 160 Ÿm from OTC) ϗөή෬ޟճᢄ࡙ޟݬο୿ಋ ଢ଼ (Fig. 11d)Ȃٮߨܹࢺࡣ։଻ΰҥϛΰ෬ಋଢ଼ڗ ႀή෬Ȅ 0 2 4 6 8 10 12 14 0 200 400 600 800 1000

Distance from primordi

Sr /C a ×(1 0 -3 ) 1200 1400 1600 1800 2000 2200 um to otolith edge (Ÿm) OTC mark A1 A2 A3 (b) Living in the 0 2 4 6 8 10 12 14 16 18 0 100 200 300 400 500 600 Distance from primordi

Sr/Ca ×(1 0 -3 ) 700 800 900 1000 1100 1200 1300 um to otolith edge (Ÿm)

river Life after release

OTC mark A1

Marine life

A2

A3

Fig. 9 Temporal changes in otolith Sr/Ca ratios from the primordium to the edge indicating the position of the OTC mark on the otolith of yellow Japanese eels including: (a) cultured eels and (b) wild eels from the estuary of the Kao-ping River. A: annual increment. Sr/Ca ratios 4 ‰ were the boundary of seawater and freshwater.

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0 2 4 6 8 10 12 14 0 200 400 600 800 1000 1200 1400 EC A1 A2 0 2 4 6 8 10 12 14 16 0 200 400 600 800 1000 1200 1400 1600 EC A1 A2 A3 0 2 4 6 8 10 12 14 16 0 200 400 600 800 1000 1200 1400 1600 EC A1 A2 A3

0

2

4

6

8

10

12

14

16

18

0

200

400

600

800

1000

1200

1400

Distance from primordium to otolith edge (μm)

EC

A1 A2 A3

Fig. 10

Temporal changes in otolith Sr/Ca ratios between the primordium and the edge of wild Japanese eels in

Da-pong Bay. According to the pattern of otolith Sr/Ca ratios, migratory behaviors were classified into 3 types:

freshwater eel (a), seawater eel (b) and estuarine eel (c, d). EC = elver check, A: annual increment. Sr/Ca ratios of 4 ‰

were the boundary of seawater and freshwater.

Sr /C a x( 10 -3) (a) (b) (c) (d)

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ଆ!!!፣!

Ιȃ኿ᜋПݲޟᒵᐅЅڏᓺીᘈ!

ᒉӎ኿ᜋПݲޟᐇհȂ೽ல࢐ӵலྣή໌ ՗Ȃծ࢐σഋϷҢپ኿ᜋޟ᛾ࠢȂٽԃ TC ܖ࢐ ALCȂ഍ོԤ੊Ͻ (ٽԃ TC ᡐԙ OTC) ЅጥᄚϷ ၌ޟ౪ຫȂ᛾ࠢޟ߳Ԇौᗗջӎྱޟኇ៪Ȃഅԙ ᛾ਝ६ճȃᏲम኿ᜋޟԙђ౥ή६Ȅ੫տ࢐௴Ң ੔ݾПԒޟ኿ᜋᄂᡛȂ೽ல഍຺ႆ 6 ~ 12 ωਢȂ ӰԪौܹညӵഛུ೎ȄѪѴȂഋϷޟ᛾ࠢȂٽԃ OTCȂڏଽᐨ࡙ྙశ឴ܻ৵ሖܒȂӵٺҢࠉሯौ ӑо NaOH ፡ᐌ pH ঄Ȃ֏ࠌݧৢࡣџ૖ོᄇധᡝ ౰ҡϚᎌࣥՍ࢐അԙ༌৛ȃܖᏲमԫιȂӰԪौ ӵᄂᡛ໌՗ࠉȂ໌՗Նүᒉӎ኿ᜋޟࠉᄂᡛȂо ጂ߳኿ᜋޟԙђȄѪѴȂϚӣധᆍᄇܻ኿ᜋ᛾ࠢ 0 2 4 6 8 0 10 20 30 40 50 Mean —Ɣ— Mean (n= 4) (a) 0 2 4 6 8 0 30 60 90 120 150 180 210 240 Mean (b) —Ɣ— Mean (n= 4) Sr/Ca x(10 -3) 0 1 2 3 4 5 6 0 20 40 60 80 100 120 140 160 180 200 Mean (c) —Ɣ— Mean (n= 4)

Fig. 11 Temporal changes in otolith Sr/Ca ratios from the OTC mark to the edge of 4 Japanese eels, which were released and recaptured in (a) Da-pong Bay in 2003; (b) Kao-ping River in 2005; (c) Kao-ping River in 2006 and (d) Kao-ping River released in 2004 and recaptured in the downstream 194 days later in 2005. Sr/Ca ratios of 4 ‰ were the boundary of seawater and freshwater. 0 2 4 6 8 0 20 40 60 80 100 120 140 160 (d)

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ޟᎌᔖܒζϚӣȂ։ٺ࢐ၶ௥ߖРҏᠵޟዉࢸᠵ ܖ࢐छࢸᠵȂ഍ौ໌՗ᐨ࡙Ѕ኿ᜋਢ໢ޟกၐȄ ҏंـกၐΟРҏᠵശᎌӫޟᒉӎ኿ᜋనӇȄՆ үޟᒉӎ኿ᜋȂོӵՆүΰ౰ҡଽ࡙߫ޟᒉӎ ᕗȂՄᒉӎᕗӵᡗཌᜢήོཷ໠Ȃ຺ႆᡗཌᜢޟ ᠦտΨȂиᒉӎᕗޟቶ࡙σܻՆүΰޟശω൐՝ РᎈȂёΰ᛾ࠢޟфᗂਢ໢һ຺ႆРޟቹԩȂӰ ԪՆүޟᒉӎ኿ᜋᄇᔖڗਢ໢໅ȂོԤ 2 ~ 3 Јٲ ཌޟᇲ৯ȂծϚमܻኇ៪ᄂᡛ๖ݎޟྥጂ࡙Ȅҏ ंـܚٺҢޟ OTC оЅ ALC ࢗᏘȂӵϚӣݰߝ ޟᘮӎаϞήȂϷտོ֕౪༁ᆦՓоЅऔՓޟᒉ ӎᕗȂႆўޟंـ഍ѫԤٺҢ൐ΙᆍࢗᏘ໌՗൐ ԩ኿ҰȂҐپџоആႆϚӣ᚟ՓࢗᏘޟ௶Ӗಢӫ ᔖҢӵӻԩ኿ҰȂܖޱ࢐հ࣏ϚӣܹࢺတޟୢϷȄ ໌ ՗ ኿ ᜋ ਢ Ȃ ӻ Ѝ ོ ᄇ ധ ᜸ അ ԙ ᆧ फ़ ཐ (stress)ȂᗶϚमܻኇ៪ڏԙߝȂծרঈᗙ࢐ӵ኿ᜋ ࠉࢊ՗ബ᎖Ȃٺധᡝ໌Σࣀଢ଼ጥᄚܖ࢐݄ଜޟޑ ᄘȂоᗗջӰ࣏ႆ࡙ޟ௳КՄഅԙധᡝϱȃѴސ ౩ܒޟ༌৛Ȅ኿ᜋധӵ 2 ںܖΙএТࡣȂᇄᄇྱ ಢտޟᠵധୈШၶȂี౪ӵᡝԙߝоЅՆүޟᎈ ઴ΰȂ֯ؠԤᡗ๿ܒޟ৯౴Ȃфߒ኿ᜋᄂᡛޟᐇ հȃ᛾ࠢޟٺҢȂᄇധᡝޟϓᘙоЅԙߝޟኇ៪Ȃ ඁн࢐џоೝ܇౱ޟȄ ႆўෆငٺҢႆ༭ጲ኿ᡆپ኿ᜋȂծ࢐೻ᆍ ኿ᡆ឴ܻѴ៩Ԓޟ኿ᜋȂོԤΙωаࢲޟ኿ᡆѴ ៩ӵᠵധᡝߒȂՄᠵധ឴ܻۻූܒޟധ᜸Ȃӵ൶ ײᎌӫޟறҲਢȂѴ៩ޟ኿ᡆᄇᠵധ໌юࢾҲ ਢȂܾӰܜ׶Մ౰ҡސ౩ܒޟ༌৛Ȃഅԙ༌οޟ ีއܖಠ຃ཐࢗዛេᏲमധᡝԫιȄՍܻ OTC Ѕ ALC ޟ኿ᡆᄇᠵധࠌؠԤ೻ٲ֨ᘙȄ ኿ᜋܹࢺ࢐ૉາΡΨސΨޟȂӰԪԤਝޟӱ ԝоЅၥਟޟಣᑖȂࠌࣺᄇӴ१ौȄᡝѴ኿ᜋޟ Пݲџоႀڗၶଽޟᒱᜋ౥Ȃծ࢐ҏᄂᡛܚٺҢ N2Ȃ୘៵้Ѵӵ኿ᜋПݲȂџо߳੼ޟਢ໢ၶ฻Ȃ ஠پሯौ໠ีџоᆰࡻၶߝਢ໢ޟ኿ᜋПݲȄᡝ ϱ኿ᡆȂٽԃฒጣႫ኿ᡆޟཌωϽȂџоᔖҢӵ ؁ωޟധᡝΰȇ۽ߝฒጣႫ኿ᡆޟႫԱჰڼȂџ оቨёଡᙹޟਢ໢ਝᔖȇ໌Ι؏ቨё኿ᡆޟђ ૖Ȃ߯૖ஊӵଡᙹጂϸӴᘈоЅಋଢ଼ၯ৷ޟӣ ਢȂಣᑖٮиकᓃ؁ӻѴӵЫМޟᕗცనӇȄ೻ ٲ഍џо׽๡ҏंـޟ༈ಛ኿ᜋޟીᘈȄؠԤӈ դΙᆍПݲ࢐ׇछฒીޟȂӰԪӻ१Пݲޟӣਢ ٺҢȂџо၄ٗϚӣᆍ኿ᜋПݲϞ໢ޟીᘈȂᄇ ܻധ᜸ޟଡᙹႀڗ؁σޟਝᔖȄоΰ኿ᜋПݲޟ ׽ي뱌ཾၥྛоЅധ᜸ҡࣀѬޟंـࣺ࿋१ ौȂՄӻ१኿ᜋПݲȂငҏंـޟᜌᄂȂ࢐џо ٮ՗ޟȂٮиџоቨёᄇܹࢺኺҏၥଉޟಣᑖȄ ALC ኿ᜋࡣܹࢺӵଽࡎྩݬοޟ 4800 ׎ᠵ ጣȂӵࡣ៉ޟ፡ࢥϛȂ഍ؠԤೝี౪Ȃ௤ଆڏন Ӱџ૖࢐൐Ιޟϱ኿ПԒϚܾೝᅣҕีឈȂٮи ؐΙএএᡝ҆໸ौҢᒉӎᡗཌᜢᔮຜՆүȂӔਐ ਢޟրۡΰԤ֨ᜲȄѪΙনӰџ૖࢐ഏҡᠵоݬ ο࠮ۨӻ (ଽႀघ 75%)ȂѪѴ஠ߖ 25% ޟᠵധོ ᘗඹڗڏтޟූӴȂՄиᠵጣԙߝڗџਐኣޟ༁ ᠵሯौ 2 ~ 3 ԑȂ෈໢ޟԫι౥഍࢐അԙ ALC ኿ ᜋޟᠵጣؠԤೝӱԝޟџ૖নӰȄ

Πȃ௃ӱԝپࣼ౪ൟූӴޟ൉ԁ

ᠵധӵܹࢺϞࡣȂӱԝ౥ӵΠএТϱȂ֕౪ ࡨഀή६౪ຫȂڗΟ಑ 6 এТȂඁнϚӔี౪኿ ᜋᠵധȂ೻ߒҰσഋϷޟ኿ᜋᠵȂџ૖ᘗඹڗڏ тޟୢ୿Ȅଽࡎྩޟӱԝ౥ӵϚӣԑ໢ޟ৯౴Ȃ кौ࢐ҥܻܹࢺӴᘈޟ৯౴ܚഅԙޟȂӵ 2003 о Ѕ 2005 ԑȂܹࢺӴᘈ࢐ӵᅣҕհཾୢ୿ޟΰ෬Ȃ ӰԪӱԝ౥ၶճȂՄ 2006 ԑޟܹࢺӴᘈȂ࢐ӵଽ ࡎྩᅣҕ༈ಛհཾޟୢ୿ȂӰԪӱԝ౥ࣺᄇޟଽ ю࡞ӻȄ࿋ӴᅣҕӵܹࢺࡣޟࠉڍএТȂкौ഍ ࢐ӱԝڗ኿ᜋޟᠵധȂ2 এТࡣܚਐਔڗޟᠵധσ ӻ࢐ഏҡᠵȂծ࢐ኵ໔ٮϚӻȂߒҰ࿋Ӵഏҡᠵ ޟఊတџ૖࡞ωȄѪѴȂζџ૖࢐ܹࢺᠵσӻ࣏ Ꮄ෥ᠵȂᄇཱིܻᕗცۦҐᎌᔖȂӵߑ෈џ૖ၶৠ ܾೝਐਔȄӵܹࢺϞࡣȂ຺ႆ 50% ޟᠵധಋଢ଼ຽ ᚔ഍ωܻ 500 mȂфߒᠵധԤ஼੨ޟሴ୿՗࣏Ȃོ ᒵᐅھۡޟූӴȂёΰࡣ៉ӱԝޟᠵധȂσഋϷ ഍࢐՝ܻЫҡේސᙴ൲ޟ૩ᐩоЅԤࢾҲޟᐝቬ ้ӴᘈೝਐᕕȄӰԪџՃኌ஠೻ٲᠵധ஝࡙ၶଽ ޟݬࢲ೩ည࣏߳៖ୢȄਲ਼ᐃ౪ൟ௴ኺӴᘈޟᢎ ᄆȂܹࢺ 10 Јᇄ 24 ωਢޟಋଢ଼՝ညϞ዁Ԓ࣏ྃ ࣺխȂ഍ಋଢ଼ڗଽࡎྩӵᎬߖࡎݍޟࠒ۬оЅϛ ໢ޟؓࢸȂџ૖࢐Ӱ࣏Ԫ೎᏿Ԥၶӻޟේސ᙭ ᇐȂ૖ஊඪټၶӻޟᗴᙠӴᘈȂՄиᎬߖଽ໰ޟ ѕ۬ȂЫࢺၶ࣏෿ࡨȂџ૖ฒݲඪټᠵധᛧۡූ ਀ޟު໢Ȅ

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έȃ௃Sr/CaШޟᡐϽܚࣼڗޟРҏᠵޟූ

Ӵᒵᐅ

РҏᠵޟՆү Sr/Ca ШᇄѴӵЫᡝ Sr/Ca Шޟ ᜰ߽࣏ (Sr/Ca)ɰ1000Նү= 0.09ɰᢄ࡙ɮ3.790 (Lin et al., 2007)Ȅ೻এПแԒߒҰᢄ้࡙ܻ 0 psu ਢȂ Նү Sr/Ca Ш࣏ 3.79 ‰ȄӰԪலலоՆү Sr/Ca Ш 4 ‰ հ ࣏ ష Ы ᇄ ੕ Ы ޟ Ϸ ࣨ ᘈ (Tzeng, 1996)ȄҏंـޟᎴ෥ᠵӵ 2 ԑޟషЫᇋᎴ෈໢Ȃ Նү Sr/Ca Шζю౪ӵ 4 ‰ оή (Fig. 9a)Ȃಒӫ Նү Sr/Ca Шᇄ੺Ꮄᢄ࡙ᕗცϞᜰ߽Ȃ໌Ι؏ᡛᜌ ΟՆү Sr/Ca Шᇄᢄ࡙Ϟᜰ߽Ȅ σᝉᢊӱԝޟᠵധȂڏՆү Sr/Ca Ш഍ӵ 4 ‰ оΰȂਲ਼ᐃᢊϱϚӣӴᘈޟᢄ࡙ก໔๖ݎȂσᝉ ᢊ࢐឴ܻӒ੕ЫޟᕗცȂӰԪՆү Sr/Ca ШȂџ оІᔖѴӵޟᕗცȄᗶณσӻኵ௃σᝉᢊӱԝޟ ᠵധ഍࢐ӵᎬߖషЫޟ௶ЫοೝਐਔȂծ࢐฻኷ Ӵಋଢ଼ڗၶճᢄ࡙ޟᕗცȂٮؠԤᒲݲӵՆүΰ ֕౪Ȃܚоມ݂σᝉᢊޟᠵധȂԤ๘σഋϷޟਢ ໢Ȃ഍ୄ੼ӵᢊϱޟଽᢄ࡙Ы୿Ȅ ӵଽࡎྩ 2005 ԑܹࢺ 2006 ԑӱԝޟᠵധ ϛȂڏՆү Sr/Ca Шӵ 4 ‰ ѾѡΰήᎪᕝȂߒҰ ᠵധ࢐ୄ੼ӵݬοޟјషឧЫᕗცϛȂӱԝӴᘈ ޟᕗც (ᢄ࡙ 5 ~ 20 psu)Ȃζ࢐ӣኺಒӫՆүޟཌ ϽᏰ๖ݎȄՄӵ 2006 ԑܹࢺ 2007 ԑӱԝޟᠵധ ϛȂڏՆү Sr/Ca Шࠌ࢐ӵ 4 ‰ оήȂфߒ೻ٲ ᠵധ࢐ӵၶճᢄ࡙ȂࣥՍ࢐௥ߖషЫޟӴᘈූ ਀Ȅ2006 ԑޟܹࢺ࢐ӵ 8 Т໌՗Ȃ۟࿽ΰ឴ܻߦ ۟ȂӰԪၶσޟ६ߦ໔Ȃོளپΰ෬ᙴؘޟషЫȂ ёΰؐԑޟሶॳႆࡣȂᄇܻ௴ኺᘈ࿋ӴོഅԙӴ לޟ׽ᡐȂо 2006 ԑ࣏ٽȂഋϷޟహؓೝσЫள ٖȂٺுনҏᇄΰ෬฿ཌೝߢႤޟᠵധූ਀ӴȂ ૖ஊᕕு؁ӻپՌΰ෬ޟషЫپྛȂζ࢐അԙՆ ү Sr/Ca ШၶճޟনӰȄ

Ѳȃᠵധޟሴ୿՗࣏

ငҥ኿ᜋܹࢺޟ๖ݎี౪ȂϚ፣࢐ӵσᝉᢊ ܖ࢐ଽࡎྩȂᠵധؐЈശσޟಋଢ଼ຽᚔσघ࢐ 2 ϴ٨ȂՄи஠ߖ 80% ޟᠵധȂڏಋଢ଼ຽᚔ഍Ϛོ ຺ႆ 1 kmȂߒҰᠵധڎԤھۡޟሴ୿՗࣏ȂΙҍ ᒵᐅΟ၎ූӴȂ൷࡞Ѝོ܁ڏтӴПಋଢ଼ȄһԤ џ૖࢐ܹࢺᠵᄇཱིܻᕗცۦҐᎌᔖȄҏᄂᡛ༉Ԥ Ι׎ᠵധȂ࢐ӵϛΰ෬ޟᄯόೝܹࢺȂငႆ 194 Јࡣӵή෬ޟݓ༪ೝਐਔȂҥՆүޟ Sr/Ca ШϷ ݙȂᇳ݂ԪᠵധޟූӴᙽ඲࢐ം؏ޟȂٮϚ࢐ڧ ڗߦ۟σЫޟ؟ڕȂೝଢ଼ޟಋଢ଼ڗή෬پȂ໌Ι ؏ᔮຜԪᠵധζϚ࢐໌՗६੕ḯ෬ሚϽޟᠵധȂ ҥԪζџᇳ݂Ȃࣺ࿋ଽШٽޟᠵധӵ༁ᠵ໦ࢲȂ ོᒵᐅݬοୢ୿հ࣏ڏූ਀ӴȂ೻Ιᘈᇄഏҡᠵ ധޟҡࣀѬ౪ຫࣺխȄՄଽШٽޟݬο࠮ᠵധȂ џ૖࢐ҥܻѮᢊޟݬύ഍Шၶଳ০Ȃູ܁ΰ෬လ Ӵ७ᑖູωȂՄݬοୢ૖ஊඪټၶσ७ᑖޟූ ӴȂܛၷၶଽޟҡސ໔Ȅ

!!๖!!!፣!

ҏंـ๖ӫ༈ಛޟ኿ᜋ׬೚ڷՆүޟϯશϷ ݙȂ၏ᄂӴ֕౪༁ᠵӵݬύϱޟḯ෬՗࣏Ѕᕗც ѬȄਲ਼ᐃ኿ᜋܹࢺޟӱԝၥਟϷݙ๖ݎȂี౪ᠵ ധڎԤሴ୿՗࣏ȂσഋϷޟᠵധܹࢺࡣٮϚོಋ ଢ଼຺ႆ 1 kmȂٮи୑ԁූ਀ӵЫҡේސᙴ൲ޟӴ ୢȄਲ਼ᐃՆү Sr/Ca ШޟϷݙ๖ݎȂี౪ᠵധ൉ԁ ୄ੼ӵݬοјషឧЫޟᕗცȄᎴ෥ᠵᇄഏҡᠵܹ ࢺࡣٮؠԤӰႆўޟϚӣҡࣀᕗცȂՄю౪Ϛӣ ޟ՗࣏ܖӱԝ౥ޟᡗ๿৯տȄؠԤӈդΙᆍ኿ᜋ ܹࢺПݲ࢐ׇछޟȂ๖ӫӻ१ПݲڎԤϣ၄հ ҢȂџо؁౏ΣΙᑛᠵധޟಋଢ଼՗࣏዁ԒоЅූ ӴցҢ௑לȄ

ᗂ!!!᜝!

ҏंـޟᠵധܹࢺЅၥਟϷݙາҢȂϷտҥ ՗ ࢇ ଱ ၻ ཾ ۏ ষ ོ Ы ౰ ၐ ᡛ ܚ Ѕ ୽ ऋ ོ ॎ ห (NSC 96-2313-B002-008 awarded to Dr. W. N. Tzeng) ܚЛᔖȄၐᡛ໌՗෈໢ܛᇌѮᢊσᏰ஻छ ࿊ȃݓ၉ოȃݓىטȃ԰߸ቇȃ஻໯൩ȃ᎒סԙ ้оЅЫ౰ၐᡛܚ༁੕Ӓȃ༁ড়൲ȃ༁ᛏҡȃᒦ ӆဎȃ஻෰ࢶȃҩסԑȃങࠅԃȃں࿅يȃ؃ۣ ้ࣟӵᠵധޟᇋᎴྱ៖ȃ኿ᜋհཾоЅܹࢺώհ ޟڞօȇଽࡎྩᅣҕᗂࠒԢȃԧۅᐙȃࢹߡ໰ȃ ༃ΡӵᠵധӱԝޟڞօȂٺுҏंـுо໷ցׇ ԙȂᙱԪΙځཱमᗂףȄ

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୤ՃМᝦ!

Boubee, J., D. Jellyman and C. Sinclair (2008) Eel protection measures within the Manapouri hydro-electric power scheme, South Island, New Zealand. Hydrobiologia, 609: 71-82.

Campana, S. E. (1999) Chemistry and composition of fish otoliths: pathways, mechanisms, and applications. Mar. Ecol. Prog. Ser., 188: 263—297. Howland, K. L., W. M. Tonn, J. A. Babaluk and R. F.

Tallman (2001) Identification of freshwater and anadromous inconnu in the Mackenzie River system by analysis of otolith strontium. Trans. Am. Fish. Soc., 130 (5): 725—741.

Jellyman, D. and K. Tsukamoto (2002) First use of archival transmitters to track migrating freshwater eels Anguilla dieffenbachii at sea. Mar. Ecol. Prog. Ser., 233: 207-215

Jessop, B. M., J. C. Shiao, Y. Iizuka and W. N. Tzeng (2002) Migratory behaviour and habitat use by American eels Anguilla rostrata as revealed by otolith microchemistry. Mar. Ecol. Prog. Ser., 233: 217-229.

Kalish, J. M. (1990) Use of otolith microchemistry to distinguish the progeny of sympatric anadromous and non-anadromous salmonids. Fish Bull., 88: 657-666.

Kawakami, Y., N. Mochioka, K. Morishita, T. Tajima, H. Nakagawa, H. Toh and A. Nakazono (1998) Factors influencing otolith strontium/calcium ratios in Anguilla japonica elvers. Environ. Biol. Fish., 52: 299-303.

Kuo, C. L., A. Nakamura, K. Tsukamoto, K. Suzuki and I C. Liao (1996) Tracking of Japanese eel Anguilla

japonica by ultrasonic transmitter in the

southwestern waters of Taiwan. J. Fish. Soc. Taiwan, 23 (4): 279-287.

Liao, I C. (2001) A general review on aquaculture in Asia: A focus on anguillid eel. In: I C. Liao (complied) Keynote Addresses, The 5th and 6th Asian Fisheries Forums. AFS Special Publication, 11: 39-54

Liao, I C., S. G. Liau, W. N. Tzeng and C. L. Kuo (1999) Investigation on Anguilla japonica leptocephali by Fisheries Researcher 1. In Studies on the Life Cycle of Eel (K. Aida and K. Tsukamoto eds), Kaiyo Monthly, Special Issue, 18: 27-33.

Liao, I C., C. L. Kuo, W. N. Tzeng, S. T. Hwang, C. L.

Wu, C. H. Wang and Y. T. Wang (1996) The first time of leptocephali of Japanese eel Anguilla

japonica collected by Taiwanese researchers. J.

Taiwan Fish. Res., 4: 107-116.

Limburg, K. E., P. Landergren, L. Westin, M. Elfman and P. Kristiansson (2001) Flexible modes of anadromy in Baltic Sea trout: making the most of marginal spawning streams. J. Fish Biol., 59: 682-695.

Lin, S. H., C. W. Chang, Y. Iizuka and W. N. Tzeng (2007) Salinities, not diets, affect strontium/ calcium ratios in otoliths of Anguilla japonica. J. Exp. Mar. Biol. Ecol., 341: 254-263.

Radtke, R. L. and R. A. Kinzie III (1996) Evidence of a marine larval stage in endemic Hawaiian stream gobies isolated from high-elevation locations. Trans. Am. Fish. Soc., 125: 613-621.

Schmidt, J. (1912) The reproduction and spawning places of the freshwater eel (Anguilla vulgaris). Nature, 2234 (89): 633-636

Secor, D. H., A. Henderson-Arzapalo and P. M. Piccoli (1995) Can otolith microchemistry chart patterns of migration and habitat utilization in anadromous fishes? J. Exp. Mar. Biol. Ecol., 192: 15—33.

Secor, D. H. and P. M. Piccoli (1996) Age- and sex-dependent migrations of striped bass in the Hudson River as determined by chemical microanalysis of otoliths. Estuaries, 19(4): 778-793.

Shen, K. N., Y. C. Lee and W. N. Tzeng (1998) Use of otolith microchemistry to investigate the life history pattern of gobies in a Taiwanese stream. Zool. Stud., 37(4): 322-329.

Shen, K. N. and W. N. Tzeng (2002) Formation of a metamorphosis check in otoliths of the amphidromous goby Sicyopterus japonicus. Mar. Ecol. Prog. Ser., 228: 205-211.

Shiao, J. C., Y. Iizuka, C. W. Chang and W. N. Tzeng (2003) Disparities in habitat use and migratory behavior between tropical eel Anguilla

marmorata and temperate eel A. japonica in four

Taiwanese rivers. Mar. Ecol. Prog. Ser., 261: 233-242.

Tanaka, H., H. Kagawa and H. Ohta (2001) Production of leptocephali of Japanese eel (Anguilla japonica) in captivity. Aquaculture, 201: 51-60.

Thibault, I., J. J. Dodson, F. Caron, W. Tzeng, Y. Iizuka nad J. Shiao (2007) Facultative catadromy in American eels: testing the conditional strategy hypothesis. Mar. Ecol. Prog. Ser., 344: 219-229.

(18)

Thorrold, S. R., G. P. Jones, M. E. Hellberg, R. S. Burton, S. E. Swearer, J. E. Neigel, S. G. Morgan and R. R. Warner (2002) Quantifying larval retention and connectivity in marine populations with artificial and natural markers. Bull. Mar. Sci., 70: 291—308.

Thorrold, S. R., G. P. Jones, S. Planes and J. A. Hare (2006) Transgenerational marking of embryonic otoliths in marine fishes using barium stable isotopes. Can. J. Fish. Aqua. Sci., 63: 1193—1197. Tsukamoto, K. (1992) Discovery of the spawning area

for Japanese eel. Nature, 356: 789-791.

Tsukamoto, K. (2006) Spawning of eels near a seamount. Nature, 439: 929.

Tsukamoto, K. and T. Arai (2001) Facultative catadromy of the eel Anguilla japonica between freshwater and seawater habitats. Mar. Ecol. Prog. Ser., 220: 265-276.

Tzeng, W. N. (1984) An estimate of the exploitation rate of Anguilla japonica elvers immigrating into the coastal waters off Shuang-Chi River, Taiwan. Bull. Inst. Zool., Academia Sinica, 23(2): 173-180.

Tzeng, W. N. (1995) Migratory history recorded in otoliths of the Japanese eel, Anguilla japonica, elvers as revealed from SEM and WDS analyses. Zool. Stud., 34(1): 234-236.

Tzeng, W. N. (1996) Effects of salinity and ontogenetic movements on strontium:calcium ratios in the otoliths of the Japanese eel, Anguilla japonica Temminck and Schlegel. J. Exp. Mar. Biol. Ecol., 199: 111-122.

Tzeng, W. N. (2003) The processes of onshore migration of the Japanese eel Anguilla japonica as revealed by otolith microstructure. Eel Biology, 181-190.

Tzeng, W. N. and Y. C. Tsai (1994) Changes in otolith microchemistry of the Japanese eel, Anguilla

japonica, during its migration from the ocean to

the rivers of Taiwan. J. Fish Biol., 45: 671-684. Tzeng, W. N., K. P. Severin and H. Wickström (1997)

Use of otolith microchemistry to investigate the environmental history of European eel Anguilla

anguilla. Mar. Ecol. Prog. Ser., 149: 73-81.

Tzeng, W. N., J. C. Shiao and Y. Iizuka (2002) Use of otolith Sr:Ca ratios to study the riverine migratory behaviours of Japanese eel Anguilla japonica. Mar. Ecol. Prog. Ser., 245: 213-221.

Tzeng, W. N., K. P. Severin, H. Wickström and C. H. Wang (1999) Strontium bands in relation to age marks in otoliths of European eel Anguilla anguilla. Zool. Stud., 38(4): 452-457.

Tzeng, W. N., C. H. Wang, H. Wickström and M. Reizenstein (2000) Occurrence of the semi- catadromous European eel Anguilla anguilla (L.) in Baltic Sea. Mar. Biol., 137: 93-98.

Tzeng, W. N., Y. Iizuka, J. C. Shiao, Y. Yamada and H. P. Oka (2003) Identification and growth rates comparison of divergent migratory contingents of Japanese eel (Anguilla japonica). Aquaculture, 216: 77-86.

Westerberg, H., I. Lagenfelt and H. Svedang (2007) Silver eel migration behaviour in the Baltic. ICES J. of Mar. Sci., 64(7): 1457-1462.

Williamson, D. H., G. P. Jones, S. R. Thorrold and A. J. Frisch (2009) Transgenerational marking of marine fish larvae: stable-isotope retention, physiological effects and health issues. J. of Fish Bio., 74: 891—905.

Yu TC, Tsai CL, Tsai YS and Lai JY (1993) Induced breeding of Japanese eels, Anguilla japonica. J. Taiwan Fish. Res., 1: 27-34.

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Use of Mark-recapture and Otolith Microchemistry on the

Study of the Migratory Behaviour and Habitat Use of

Japanese Eels (Anguilla japocica)

Shih-Huan Lin

1

, Su-Lean Chang

2

, Yoshiyuki Iizuka

3

, Tzyy-Ing Chen

2

, Fu-Guang Liu

4

,

Mao-Sen Su

5

, Wei-Cheng Su

5

!and!Wann-Nian Tzen

1*

1Institute of Fisheries Science, National Taiwan University 2Tungkang Biotechnology Research Center, Fisheries Research Institute

3Institute of Earth Science, Academia Sinica

4 Freshwater Aquaculture Research Center, Fisheries Research Institute 5 Fisheries Research Institute

ABSTRACT

To understand the distribution, migratory behaviour and adaptation to salinity of Japanese eels Anguilla

japonica in the coastal waters, five tagging methods were used, They were (1) liquid nitrogen marking on the

fish body surface (2) fin clipped (3) oxytetracycline and alizarin complexone marking on otoliths (4) microchips and (5) coded wire tags. Totally, 4800 elvers and 2473 yellow eels were released into Da-pong Bay and Kao-ping River in 2002, 2003, 2005 and 2006. According to the recaptured data, the marked eels exhibited territory behaviours and most eels stayed within 1 km from the released sites. In addition, the Sr/Ca ratios also showed that most eels habituated in the estuarine areas.

Key words: Anguilla japonica, habitat use, Sr/Ca ratio, tagging

*Correspondence: No. 1, Sec. 4, Roosevelt Road, Taipei, 10617 Taiwan. TEL: 02-33662887; FAX: 02-23639570; Email: wnt@ mtu.edu.tw

數據

Fig.  1  The Japanese eels were released at sites of   Da-pong (DP) Bay and the estuary of the Kao-ping (KP)  River in southwestern Taiwan
Fig.  2  Three tagging methods:
Fig.  3    The red ALC fluorescent marks exhibited by elvers which were immersed in ALC solution at different time  periods (6, 12 and 24hrs) and concentrations (15, 25, 50 and 75 ppm)
Fig. 5    Oxytetracycline (OTC) and Alizarin complexone (ALC) marks in the otoliths of Japanese eels at release
+7

參考文獻

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