Comparison of the Structure and Composition of the Branchial Filters in Suspension Feeding Elasmobranchs
ABSTRACT The four, evolutionarily independent, lineages of suspension feeding elasmobranchs have two types of branchial filters. The first is a robust, flattened filter pad akin to a colander (e.g., whale sharks, mantas and devil rays) while the second more closely resembles the comb‐like gill raker...
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Veröffentlicht in: | Anatomical record (Hoboken, N.J. : 2007) N.J. : 2007), 2014-04, Vol.297 (4), p.701-715 |
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description | ABSTRACT
The four, evolutionarily independent, lineages of suspension feeding elasmobranchs have two types of branchial filters. The first is a robust, flattened filter pad akin to a colander (e.g., whale sharks, mantas and devil rays) while the second more closely resembles the comb‐like gill raker structure found in bony fishes (e.g., basking and megamouth sharks). The structure and the presence of mucus on the filter elements will determine the mechanical function of the filter and subsequent particle transport. Using histology and scanning electron microscopy, we investigated the anatomy of the branchial filters in 12 of the 14 species of Chondrichthyian filter‐feeding fishes. We hypothesized that mucus producing cells would be abundant along the filter epithelium and perform as a sticky mechanism to retain and transport particles; however, we found that only three species had mucus producing goblet cells. Two of these (Mobula kuhlii and Mobula tarapacana) also had branchial cilia, indicating sticky retention and transport. The remaining filter‐feeding elasmobranchs did not have a sticky surface along the filter for particles to collect and instead must employ alternative mechanisms of filtration (e.g., direct sieving, inertial impaction or cross‐flow). With the exception of basking sharks, the branchial filter is composed of a hyaline cartilage skeleton surrounded by a layer of highly organized connective tissue that may function as a support. Megamouth sharks and most of the mobulid rays have denticles along the surface of the filter, presumably to protect against damage from large particle impactions. Basking sharks have branchial filters that lack a cartilaginous core; instead they are composed entirely of smooth keratin. Anat Rec, 297:701–715, 2014. © 2014 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/ar.22850 |
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The four, evolutionarily independent, lineages of suspension feeding elasmobranchs have two types of branchial filters. The first is a robust, flattened filter pad akin to a colander (e.g., whale sharks, mantas and devil rays) while the second more closely resembles the comb‐like gill raker structure found in bony fishes (e.g., basking and megamouth sharks). The structure and the presence of mucus on the filter elements will determine the mechanical function of the filter and subsequent particle transport. Using histology and scanning electron microscopy, we investigated the anatomy of the branchial filters in 12 of the 14 species of Chondrichthyian filter‐feeding fishes. We hypothesized that mucus producing cells would be abundant along the filter epithelium and perform as a sticky mechanism to retain and transport particles; however, we found that only three species had mucus producing goblet cells. Two of these (Mobula kuhlii and Mobula tarapacana) also had branchial cilia, indicating sticky retention and transport. The remaining filter‐feeding elasmobranchs did not have a sticky surface along the filter for particles to collect and instead must employ alternative mechanisms of filtration (e.g., direct sieving, inertial impaction or cross‐flow). With the exception of basking sharks, the branchial filter is composed of a hyaline cartilage skeleton surrounded by a layer of highly organized connective tissue that may function as a support. Megamouth sharks and most of the mobulid rays have denticles along the surface of the filter, presumably to protect against damage from large particle impactions. Basking sharks have branchial filters that lack a cartilaginous core; instead they are composed entirely of smooth keratin. Anat Rec, 297:701–715, 2014. © 2014 Wiley Periodicals, Inc.</description><identifier>ISSN: 1932-8486</identifier><identifier>EISSN: 1932-8494</identifier><identifier>DOI: 10.1002/ar.22850</identifier><identifier>PMID: 24443216</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Animals ; Biological Evolution ; branchial arch ; Cetacea ; elasmobranch ; Elasmobranchii ; Elasmobranchii - anatomy & histology ; Elasmobranchii - classification ; Elasmobranchii - physiology ; Feeding Behavior - physiology ; filter‐feeding ; Filtration ; gill rakers ; Gills - anatomy & histology ; Gills - physiology ; histology ; Marine ; Microscopy, Electron, Scanning ; Mobula ; Mobula tarapacana ; Mucus - physiology</subject><ispartof>Anatomical record (Hoboken, N.J. : 2007), 2014-04, Vol.297 (4), p.701-715</ispartof><rights>Copyright © 2014 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4160-44be4c3267a1fa7e73c60d183473aa8b2b775c1e8007530eaf02d21b96eb6c53</citedby><cites>FETCH-LOGICAL-c4160-44be4c3267a1fa7e73c60d183473aa8b2b775c1e8007530eaf02d21b96eb6c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Far.22850$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Far.22850$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,1430,27911,27912,45561,45562,46396,46820</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24443216$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Misty Paig‐Tran, E.W.</creatorcontrib><creatorcontrib>Summers, A.P.</creatorcontrib><title>Comparison of the Structure and Composition of the Branchial Filters in Suspension Feeding Elasmobranchs</title><title>Anatomical record (Hoboken, N.J. : 2007)</title><addtitle>Anat Rec (Hoboken)</addtitle><description>ABSTRACT
The four, evolutionarily independent, lineages of suspension feeding elasmobranchs have two types of branchial filters. The first is a robust, flattened filter pad akin to a colander (e.g., whale sharks, mantas and devil rays) while the second more closely resembles the comb‐like gill raker structure found in bony fishes (e.g., basking and megamouth sharks). The structure and the presence of mucus on the filter elements will determine the mechanical function of the filter and subsequent particle transport. Using histology and scanning electron microscopy, we investigated the anatomy of the branchial filters in 12 of the 14 species of Chondrichthyian filter‐feeding fishes. We hypothesized that mucus producing cells would be abundant along the filter epithelium and perform as a sticky mechanism to retain and transport particles; however, we found that only three species had mucus producing goblet cells. Two of these (Mobula kuhlii and Mobula tarapacana) also had branchial cilia, indicating sticky retention and transport. The remaining filter‐feeding elasmobranchs did not have a sticky surface along the filter for particles to collect and instead must employ alternative mechanisms of filtration (e.g., direct sieving, inertial impaction or cross‐flow). With the exception of basking sharks, the branchial filter is composed of a hyaline cartilage skeleton surrounded by a layer of highly organized connective tissue that may function as a support. Megamouth sharks and most of the mobulid rays have denticles along the surface of the filter, presumably to protect against damage from large particle impactions. Basking sharks have branchial filters that lack a cartilaginous core; instead they are composed entirely of smooth keratin. Anat Rec, 297:701–715, 2014. © 2014 Wiley Periodicals, Inc.</description><subject>Animals</subject><subject>Biological Evolution</subject><subject>branchial arch</subject><subject>Cetacea</subject><subject>elasmobranch</subject><subject>Elasmobranchii</subject><subject>Elasmobranchii - anatomy & histology</subject><subject>Elasmobranchii - classification</subject><subject>Elasmobranchii - physiology</subject><subject>Feeding Behavior - physiology</subject><subject>filter‐feeding</subject><subject>Filtration</subject><subject>gill rakers</subject><subject>Gills - anatomy & histology</subject><subject>Gills - physiology</subject><subject>histology</subject><subject>Marine</subject><subject>Microscopy, Electron, Scanning</subject><subject>Mobula</subject><subject>Mobula tarapacana</subject><subject>Mucus - physiology</subject><issn>1932-8486</issn><issn>1932-8494</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0VtLwzAch-EgivMEfgIJeONNNacm6eUcToWB4HZf0vRfl9E2M2mRfXt3UkEQvEogDy-EH0KXlNxSQtidCbeM6ZQcoBOacZZokYnD77uWA3Qa44KQVJCMH6MBE0JwRuUJmo98szTBRd9iX-FuDnjahd52fQBs2hJv3n10nfsB98G0du5Mjceu7iBE7Fo87eMS2rhhY4DStW_4oTax8cVWx3N0VJk6wsX-PEOz8cNs9JRMXh6fR8NJYgWVJBGiAGE5k8rQyihQ3EpSUs2F4sboghVKpZaCJkSlnICpCCsZLTIJhbQpP0M3u-wy-PceYpc3Llqoa9OC72NOUyZ4JoXm_6BES6UzQtf0-hdd-D60639slMoUZ1u1D9rgYwxQ5cvgGhNWOSX5ZqfchHy705pe7YN90UD5Db-GWYNkBz5cDas_Q_nwdRf8BPFmmiw</recordid><startdate>201404</startdate><enddate>201404</enddate><creator>Misty Paig‐Tran, E.W.</creator><creator>Summers, A.P.</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TS</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope></search><sort><creationdate>201404</creationdate><title>Comparison of the Structure and Composition of the Branchial Filters in Suspension Feeding Elasmobranchs</title><author>Misty Paig‐Tran, E.W. ; Summers, A.P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4160-44be4c3267a1fa7e73c60d183473aa8b2b775c1e8007530eaf02d21b96eb6c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Biological Evolution</topic><topic>branchial arch</topic><topic>Cetacea</topic><topic>elasmobranch</topic><topic>Elasmobranchii</topic><topic>Elasmobranchii - anatomy & histology</topic><topic>Elasmobranchii - classification</topic><topic>Elasmobranchii - physiology</topic><topic>Feeding Behavior - physiology</topic><topic>filter‐feeding</topic><topic>Filtration</topic><topic>gill rakers</topic><topic>Gills - anatomy & histology</topic><topic>Gills - physiology</topic><topic>histology</topic><topic>Marine</topic><topic>Microscopy, Electron, Scanning</topic><topic>Mobula</topic><topic>Mobula tarapacana</topic><topic>Mucus - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Misty Paig‐Tran, E.W.</creatorcontrib><creatorcontrib>Summers, A.P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Anatomical record (Hoboken, N.J. : 2007)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Misty Paig‐Tran, E.W.</au><au>Summers, A.P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of the Structure and Composition of the Branchial Filters in Suspension Feeding Elasmobranchs</atitle><jtitle>Anatomical record (Hoboken, N.J. : 2007)</jtitle><addtitle>Anat Rec (Hoboken)</addtitle><date>2014-04</date><risdate>2014</risdate><volume>297</volume><issue>4</issue><spage>701</spage><epage>715</epage><pages>701-715</pages><issn>1932-8486</issn><eissn>1932-8494</eissn><abstract>ABSTRACT
The four, evolutionarily independent, lineages of suspension feeding elasmobranchs have two types of branchial filters. The first is a robust, flattened filter pad akin to a colander (e.g., whale sharks, mantas and devil rays) while the second more closely resembles the comb‐like gill raker structure found in bony fishes (e.g., basking and megamouth sharks). The structure and the presence of mucus on the filter elements will determine the mechanical function of the filter and subsequent particle transport. Using histology and scanning electron microscopy, we investigated the anatomy of the branchial filters in 12 of the 14 species of Chondrichthyian filter‐feeding fishes. We hypothesized that mucus producing cells would be abundant along the filter epithelium and perform as a sticky mechanism to retain and transport particles; however, we found that only three species had mucus producing goblet cells. Two of these (Mobula kuhlii and Mobula tarapacana) also had branchial cilia, indicating sticky retention and transport. The remaining filter‐feeding elasmobranchs did not have a sticky surface along the filter for particles to collect and instead must employ alternative mechanisms of filtration (e.g., direct sieving, inertial impaction or cross‐flow). With the exception of basking sharks, the branchial filter is composed of a hyaline cartilage skeleton surrounded by a layer of highly organized connective tissue that may function as a support. Megamouth sharks and most of the mobulid rays have denticles along the surface of the filter, presumably to protect against damage from large particle impactions. Basking sharks have branchial filters that lack a cartilaginous core; instead they are composed entirely of smooth keratin. Anat Rec, 297:701–715, 2014. © 2014 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>24443216</pmid><doi>10.1002/ar.22850</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological Evolution branchial arch Cetacea elasmobranch Elasmobranchii Elasmobranchii - anatomy & histology Elasmobranchii - classification Elasmobranchii - physiology Feeding Behavior - physiology filter‐feeding Filtration gill rakers Gills - anatomy & histology Gills - physiology histology Marine Microscopy, Electron, Scanning Mobula Mobula tarapacana Mucus - physiology |
title | Comparison of the Structure and Composition of the Branchial Filters in Suspension Feeding Elasmobranchs |
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