Structural changes in the ovotestis of the bidirectional hermaphrodite, the blue-banded goby (Lythrypnus dalli), during transition from ova production to sperm production
Hermaphroditism is widespread in fishes and has been extensively studied in many groups. The process whereby the gonad changes morphology in sequential hermaphrodites (i.e., female to male sex change or the reverse) is well documented. However, gonadal changes in bidirectional hermaphroditic fishes,...
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description | Hermaphroditism is widespread in fishes and has been extensively studied in many groups. The process whereby the gonad changes morphology in sequential hermaphrodites (i.e., female to male sex change or the reverse) is well documented. However, gonadal changes in bidirectional hermaphroditic fishes, in which gamete production can shift repeatedly, has received little attention. Here we examine the transition process in the bidirectional sex-changer
Lythrypnus dalli,
as it goes from producing eggs to producing sperm. In the ova-producing phase, the majority of the ovotestis consists of vitellogenic oocytes. Gonad transition is initiated with the break-down and reabsorption of mature oocytes. This is then followed by the proliferation of spermatogenic tissue from the dorsal and ventral regions of the ovotestis. The proliferation of spermatogenic tissue continues until it makes up the majority of the ovotestis with the reminder of the gonad comprising previtellogenic oocytes. We were able to define five transitional stages characterized by the relative area of the ovotestis made up of oogenic, spermatogenic, and atretic tissue. In only one other species of bidirectional sex-changing fish,
Eviota epiphanes
, has similar examination of transitional morphology been performed.
Lythrypnus dalli
and
E. epiphanes
are both in the teleost family Gobiidae, and closely related. It has been hypothesized that these two lineages have independently evolved the ability to change sex. Here we provide a comparison of the transition process between
L. dalli
and
E. epiphanes,
which highlights the conserved and novel elements and provided insights into differences in their life histories. |
doi_str_mv | 10.1007/s10641-019-00914-2 |
format | Article |
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Lythrypnus dalli,
as it goes from producing eggs to producing sperm. In the ova-producing phase, the majority of the ovotestis consists of vitellogenic oocytes. Gonad transition is initiated with the break-down and reabsorption of mature oocytes. This is then followed by the proliferation of spermatogenic tissue from the dorsal and ventral regions of the ovotestis. The proliferation of spermatogenic tissue continues until it makes up the majority of the ovotestis with the reminder of the gonad comprising previtellogenic oocytes. We were able to define five transitional stages characterized by the relative area of the ovotestis made up of oogenic, spermatogenic, and atretic tissue. In only one other species of bidirectional sex-changing fish,
Eviota epiphanes
, has similar examination of transitional morphology been performed.
Lythrypnus dalli
and
E. epiphanes
are both in the teleost family Gobiidae, and closely related. It has been hypothesized that these two lineages have independently evolved the ability to change sex. Here we provide a comparison of the transition process between
L. dalli
and
E. epiphanes,
which highlights the conserved and novel elements and provided insights into differences in their life histories.</description><identifier>ISSN: 0378-1909</identifier><identifier>EISSN: 1573-5133</identifier><identifier>DOI: 10.1007/s10641-019-00914-2</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animal Systematics/Taxonomy/Biogeography ; Biomedical and Life Sciences ; Eggs ; Environment ; Fish ; Fish eggs ; Freshwater & Marine Ecology ; Gametes ; Gametocytes ; Gonads ; Hermaphrodites ; Hermaphroditism ; Life Sciences ; Lythrypnus dalli ; Marine fishes ; Morphology ; Nature Conservation ; Oocytes ; Ova ; Proliferation ; Reabsorption ; Sex ; Sperm ; Spermatozoa ; Tissue ; Zoology</subject><ispartof>Environmental biology of fishes, 2019-11, Vol.102 (11), p.1393-1404</ispartof><rights>Springer Nature B.V. 2019</rights><rights>Environmental Biology of Fishes is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c319t-4523e895feb239b296e75f594704d2dbcb3fa8d7b633b15e89c453d03dc318803</citedby><cites>FETCH-LOGICAL-c319t-4523e895feb239b296e75f594704d2dbcb3fa8d7b633b15e89c453d03dc318803</cites><orcidid>0000-0001-9958-3557</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10641-019-00914-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10641-019-00914-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Maxfield, Jessica M.</creatorcontrib><creatorcontrib>Cole, Kathleen S.</creatorcontrib><title>Structural changes in the ovotestis of the bidirectional hermaphrodite, the blue-banded goby (Lythrypnus dalli), during transition from ova production to sperm production</title><title>Environmental biology of fishes</title><addtitle>Environ Biol Fish</addtitle><description>Hermaphroditism is widespread in fishes and has been extensively studied in many groups. The process whereby the gonad changes morphology in sequential hermaphrodites (i.e., female to male sex change or the reverse) is well documented. However, gonadal changes in bidirectional hermaphroditic fishes, in which gamete production can shift repeatedly, has received little attention. Here we examine the transition process in the bidirectional sex-changer
Lythrypnus dalli,
as it goes from producing eggs to producing sperm. In the ova-producing phase, the majority of the ovotestis consists of vitellogenic oocytes. Gonad transition is initiated with the break-down and reabsorption of mature oocytes. This is then followed by the proliferation of spermatogenic tissue from the dorsal and ventral regions of the ovotestis. The proliferation of spermatogenic tissue continues until it makes up the majority of the ovotestis with the reminder of the gonad comprising previtellogenic oocytes. We were able to define five transitional stages characterized by the relative area of the ovotestis made up of oogenic, spermatogenic, and atretic tissue. In only one other species of bidirectional sex-changing fish,
Eviota epiphanes
, has similar examination of transitional morphology been performed.
Lythrypnus dalli
and
E. epiphanes
are both in the teleost family Gobiidae, and closely related. It has been hypothesized that these two lineages have independently evolved the ability to change sex. Here we provide a comparison of the transition process between
L. dalli
and
E. epiphanes,
which highlights the conserved and novel elements and provided insights into differences in their life histories.</description><subject>Animal Systematics/Taxonomy/Biogeography</subject><subject>Biomedical and Life Sciences</subject><subject>Eggs</subject><subject>Environment</subject><subject>Fish</subject><subject>Fish eggs</subject><subject>Freshwater & Marine Ecology</subject><subject>Gametes</subject><subject>Gametocytes</subject><subject>Gonads</subject><subject>Hermaphrodites</subject><subject>Hermaphroditism</subject><subject>Life Sciences</subject><subject>Lythrypnus dalli</subject><subject>Marine fishes</subject><subject>Morphology</subject><subject>Nature Conservation</subject><subject>Oocytes</subject><subject>Ova</subject><subject>Proliferation</subject><subject>Reabsorption</subject><subject>Sex</subject><subject>Sperm</subject><subject>Spermatozoa</subject><subject>Tissue</subject><subject>Zoology</subject><issn>0378-1909</issn><issn>1573-5133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kc1KxDAcxIMouK6-gKeAF4WNJk3bNEcRv2DBg3ouSZNus3SbmqRCX8mnNN0KevIU-PObGTIDwDnB1wRjduMJzlOCMOEIY05SlByABckYRRmh9BAsMGUFIhzzY3Di_RZHiqVsAb5egxuqMDjRwqoR3UZ7aDoYGg3tpw3aB-OhrfcHaZRxugrGdpFutNuJvnFWmaBXM9AOGknRKa3gxsoRXq7H0Lix7wYPlWhbc7WCanCm28DgROfN5AVrZ3cxTcA-mg17fxgs9H1M-HM7BUe1aL0--3mX4P3h_u3uCa1fHp_vbteoooQHlGYJ1QXPai0TymXCc82yOuMpw6lKlKwkrUWhmMwplSSLaJVmVGGqor4oMF2Ci9k3Rn8MsYFyawcXv-zLhGKWT4VPVDJTlbPeO12XvTM74caS4HJCynmTMm5S7jeJ6iWgs8j3Uwna_Vr_o_oGiQWTAA</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Maxfield, Jessica M.</creator><creator>Cole, Kathleen S.</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7QH</scope><scope>7SN</scope><scope>7ST</scope><scope>7TN</scope><scope>7UA</scope><scope>88A</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>GNUQQ</scope><scope>H95</scope><scope>HCIFZ</scope><scope>L.G</scope><scope>LK8</scope><scope>M7P</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>SOI</scope><orcidid>https://orcid.org/0000-0001-9958-3557</orcidid></search><sort><creationdate>20191101</creationdate><title>Structural changes in the ovotestis of the bidirectional hermaphrodite, the blue-banded goby (Lythrypnus dalli), during transition from ova production to sperm production</title><author>Maxfield, Jessica M. ; Cole, Kathleen S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-4523e895feb239b296e75f594704d2dbcb3fa8d7b633b15e89c453d03dc318803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animal Systematics/Taxonomy/Biogeography</topic><topic>Biomedical and Life Sciences</topic><topic>Eggs</topic><topic>Environment</topic><topic>Fish</topic><topic>Fish eggs</topic><topic>Freshwater & Marine Ecology</topic><topic>Gametes</topic><topic>Gametocytes</topic><topic>Gonads</topic><topic>Hermaphrodites</topic><topic>Hermaphroditism</topic><topic>Life Sciences</topic><topic>Lythrypnus dalli</topic><topic>Marine fishes</topic><topic>Morphology</topic><topic>Nature Conservation</topic><topic>Oocytes</topic><topic>Ova</topic><topic>Proliferation</topic><topic>Reabsorption</topic><topic>Sex</topic><topic>Sperm</topic><topic>Spermatozoa</topic><topic>Tissue</topic><topic>Zoology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maxfield, Jessica M.</creatorcontrib><creatorcontrib>Cole, Kathleen S.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Aqualine</collection><collection>Ecology Abstracts</collection><collection>Environment Abstracts</collection><collection>Oceanic Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Biology Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>ProQuest Central Student</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>SciTech Premium Collection</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Environmental Science Database</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>Environment Abstracts</collection><jtitle>Environmental biology of fishes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maxfield, Jessica M.</au><au>Cole, Kathleen S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural changes in the ovotestis of the bidirectional hermaphrodite, the blue-banded goby (Lythrypnus dalli), during transition from ova production to sperm production</atitle><jtitle>Environmental biology of fishes</jtitle><stitle>Environ Biol Fish</stitle><date>2019-11-01</date><risdate>2019</risdate><volume>102</volume><issue>11</issue><spage>1393</spage><epage>1404</epage><pages>1393-1404</pages><issn>0378-1909</issn><eissn>1573-5133</eissn><abstract>Hermaphroditism is widespread in fishes and has been extensively studied in many groups. The process whereby the gonad changes morphology in sequential hermaphrodites (i.e., female to male sex change or the reverse) is well documented. However, gonadal changes in bidirectional hermaphroditic fishes, in which gamete production can shift repeatedly, has received little attention. Here we examine the transition process in the bidirectional sex-changer
Lythrypnus dalli,
as it goes from producing eggs to producing sperm. In the ova-producing phase, the majority of the ovotestis consists of vitellogenic oocytes. Gonad transition is initiated with the break-down and reabsorption of mature oocytes. This is then followed by the proliferation of spermatogenic tissue from the dorsal and ventral regions of the ovotestis. The proliferation of spermatogenic tissue continues until it makes up the majority of the ovotestis with the reminder of the gonad comprising previtellogenic oocytes. We were able to define five transitional stages characterized by the relative area of the ovotestis made up of oogenic, spermatogenic, and atretic tissue. In only one other species of bidirectional sex-changing fish,
Eviota epiphanes
, has similar examination of transitional morphology been performed.
Lythrypnus dalli
and
E. epiphanes
are both in the teleost family Gobiidae, and closely related. It has been hypothesized that these two lineages have independently evolved the ability to change sex. Here we provide a comparison of the transition process between
L. dalli
and
E. epiphanes,
which highlights the conserved and novel elements and provided insights into differences in their life histories.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10641-019-00914-2</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-9958-3557</orcidid></addata></record> |
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source | SpringerNature Journals |
subjects | Animal Systematics/Taxonomy/Biogeography Biomedical and Life Sciences Eggs Environment Fish Fish eggs Freshwater & Marine Ecology Gametes Gametocytes Gonads Hermaphrodites Hermaphroditism Life Sciences Lythrypnus dalli Marine fishes Morphology Nature Conservation Oocytes Ova Proliferation Reabsorption Sex Sperm Spermatozoa Tissue Zoology |
title | Structural changes in the ovotestis of the bidirectional hermaphrodite, the blue-banded goby (Lythrypnus dalli), during transition from ova production to sperm production |
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