{"id":885,"date":"2016-05-25T20:02:08","date_gmt":"2016-05-26T03:02:08","guid":{"rendered":"https:\/\/sites.evergreen.edu\/vms-spring\/?p=885"},"modified":"2016-06-07T14:01:45","modified_gmt":"2016-06-07T21:01:45","slug":"semibalanus-balanoides","status":"publish","type":"post","link":"https:\/\/sites.evergreen.edu\/vms-spring\/semibalanus-balanoides\/","title":{"rendered":"Semibalanus Balanoides"},"content":{"rendered":"<div id=\"attachment_890\" style=\"width: 260px\" class=\"wp-caption alignright\"><img aria-describedby=\"caption-attachment-890\" loading=\"lazy\" class=\"wp-image-890 size-medium\" src=\"https:\/\/sites.evergreen.edu\/vms-spring\/wp-content\/uploads\/sites\/209\/2016\/05\/barnaclestipple-250x300.jpg\" alt=\"barnaclestipple\" width=\"250\" height=\"300\" srcset=\"https:\/\/sites.evergreen.edu\/vms-spring\/wp-content\/uploads\/sites\/209\/2016\/05\/barnaclestipple-250x300.jpg 250w, https:\/\/sites.evergreen.edu\/vms-spring\/wp-content\/uploads\/sites\/209\/2016\/05\/barnaclestipple.jpg 283w\" sizes=\"(max-width: 250px) 100vw, 250px\" \/><p id=\"caption-attachment-890\" class=\"wp-caption-text\">Acorn barnacles can reach up to 15 mm. in diameter<\/p><\/div>\n<h2>ACORN BARNACLE<\/h2>\n<p><!--more--><\/p>\n<p>&nbsp;<\/p>\n<p><span style=\"font-weight: 400\">Scientific name: <em>Semibalanus balanoides<\/em><\/span><\/p>\n<p><span style=\"font-weight: 400\">Kingdom: Animalia<\/span><\/p>\n<p><span style=\"font-weight: 400\">Phylum: Arthropoda<\/span><\/p>\n<p><span style=\"font-weight: 400\">Class: Maxillopoda<\/span><\/p>\n<p><span style=\"font-weight: 400\">Order: Sessilia<\/span><\/p>\n<p><span style=\"font-weight: 400\"><strong>GENERAL INFORMATION:<\/strong> \u00a0 \u00a0 \u00a0\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400\">The acorn barnacle is a common and widespread intertidal organism that can be <\/span><span style=\"font-weight: 400\">up to 15 millimeters in diameter (White, 2008). The barnacle starts out as a <\/span><span style=\"font-weight: 400\">nauplius, a <\/span><span style=\"font-weight: 400\">free-swimming larva hatched from a fertilized egg. It goes through five different stages of growth over 6 <\/span><span style=\"font-weight: 400\">months. It <\/span><span style=\"font-weight: 400\">eventually evolves into the cyprid larvalstage. The cyprid\u2019s goal is to find a place to find a suitable place to <\/span><span style=\"font-weight: 400\">spend the rest <\/span><span style=\"font-weight: 400\">of it\u2019s life, since the adult barnacle is sessile. The time it takes to find this place varies, but once it is\u00a0<\/span><span style=\"font-weight: 400\">found, the cyprid <\/span><span style=\"font-weight: 400\">glues it\u2019s head to it\u2019s new home. The barnacle, now a juvenile, starts the process of forming\u00a0<\/span><span style=\"font-weight: 400\">six <\/span><span style=\"font-weight: 400\">hard plates around <\/span><span style=\"font-weight: 400\">it\u2019s body (Fish, 1996). Once this process is complete and the barnacle reaches sexual maturity, the\u00a0<\/span><span style=\"font-weight: 400\">barnacle is <\/span><span style=\"font-weight: 400\">finally an adult. This <\/span><span style=\"font-weight: 400\">usually takes 1-2 years. The acorn barnacle uses it\u2019s cirri (feet) to capture it\u2019s food\u00a0<\/span><span style=\"font-weight: 400\">through a small <\/span><span style=\"font-weight: 400\">opening in the top of <\/span><span style=\"font-weight: 400\">it\u2019s outer shell. The barnacle has valves it can use to seal off this small hole, which\u00a0<\/span><span style=\"font-weight: 400\">serves as <\/span><span style=\"font-weight: 400\">protection from <\/span><span style=\"font-weight: 400\">predators(White, 2008). During winter<\/span><span style=\"font-weight: 400\">, barnacles do not feed and rely solely on reserves\u00a0<\/span><span style=\"line-height: 1.5\">(White, 2008).<\/span><\/p>\n<p><span style=\"font-weight: 400\"> \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0<\/span> <span style=\"font-weight: 400\">Acorn barnacles are common and exist all over the world. This species is most commonly found in<\/span><\/p>\n<p><span style=\"font-weight: 400\"> the upper mid <\/span><span style=\"font-weight: 400\">intertidal zone (Fish, 1996). Since they use their cirri to absorb oxygen, acorn barnacles<\/span><\/p>\n<p><span style=\"font-weight: 400\"> can extract oxygen from both\u00a0<\/span><span style=\"font-weight: 400\">water and <\/span><span style=\"font-weight: 400\">air, making them extremely adaptable. You can often identify<\/span><\/p>\n<p><span style=\"font-weight: 400\"> acorn barnacles habitat by the grayish-white\u00a0<\/span><span style=\"font-weight: 400\">\u201cbarnacle <\/span><span style=\"font-weight: 400\">zone\u201d found on coasts. It is less likely for there<\/span><\/p>\n<p><span style=\"font-weight: 400\"> to be a barnacle zone when there is an abundance of seaweed, <\/span><span style=\"font-weight: 400\">because it <\/span><span style=\"font-weight: 400\">removes the juvenile<\/span><\/p>\n<p><span style=\"font-weight: 400\"> barnacles from their place of settlement (Fish, 2008). Acorn barnacles are found on <\/span><\/p>\n<p><span style=\"font-weight: 400\">rocky shores spanning <\/span><span style=\"font-weight: 400\">from the Pacific Northwest all the way to north-west Spain, and many places in<\/span><\/p>\n<p><span style=\"font-weight: 400\"> between. The <\/span><span style=\"font-weight: 400\">acorn barnacle is a <\/span><span style=\"font-weight: 400\">hermaphrodite, meaning it possesses both male and female<\/span><\/p>\n<p><span style=\"font-weight: 400\"> reproductive organs (White, 2008).\u00a0<\/span><span style=\"font-weight: 400\">There is only one breeding <\/span><span style=\"font-weight: 400\">season and it occurs in fall. Acorn<\/span><\/p>\n<p><span style=\"font-weight: 400\"> barnacles cross-fertilize with nearby barnacles by\u00a0<\/span><span style=\"font-weight: 400\">extending their penises outside of <\/span><span style=\"font-weight: 400\">their shells and<\/span><\/p>\n<p><span style=\"font-weight: 400\"> testing other shells until they find a functional female. They have the <\/span><span style=\"font-weight: 400\">biggest penis to body ratio out of<\/span><\/p>\n<p><span style=\"font-weight: 400\">the entire animal kingdom. Fertilized\u00a0<\/span><span style=\"font-weight: 400\">eggs are stored within the <\/span><span style=\"font-weight: 400\">barnacle until they\u00a0<\/span><span style=\"line-height: 1.5\">become nauplii.<\/span><\/p>\n<p>\u00a0 \u00a0 \u00a0 \u00a0 Acorn barnacles are adaptable, but they are still susceptible to environmental dangers. A study<\/p>\n<p>from 2009 done by the Marine Biology and Ecology Research Centre stated the negative affects of high<\/p>\n<p>CO2 levels on the survival of semibalanus balanoides. They found that the &#8220;Embryonic development<\/p>\n<p>rate was significantly slower in the high-CO2 treatment than in the control but still resembled \u2018natural\u2019<\/p>\n<p>rates seen in populations found in similar locations. There was an estimated 19 d delay in development<\/p>\n<p>under high-CO2 conditions, which resulted in a 60% reduction in the number of nauplii reaching<\/p>\n<p>hatching stage at the time when over 50% of the control nauplii had hatched. We conclude that ocean<\/p>\n<p>acidification could potentially further compromise embryonic development in a species already<\/p>\n<p>stressed by temperature, which could in turn impact naupliar development and recruitment. S.<\/p>\n<p>balanoides, the adults of which live in a highly variable environment, has been shown to be<\/p>\n<p>detrimentally impacted by a chronic change in chemical conditions (pH lowered beyond the current<\/p>\n<p>range) over a crucial period in their life cycle. Under experimental high-CO2 conditions, some adults<\/p>\n<p>were able to survive and larvae were able to hatch. This may indicate that there is still potential for<\/p>\n<p>organisms to find suitable habitats and for populations to develop and survive.&#8221;(Findlay, Kendall, et al.,<\/p>\n<p>2009). Basically, the embryonic development of Semibalanus balanoides is\u00a0being compromised by<\/p>\n<p>rising CO2 levels, but some of the test subjects survived under stressed conditions, so there is hope for<\/p>\n<p>the survival of their species. This is important because although there have been studies on other<\/p>\n<p>crustacean larva, before this there was no information concerning the affects of CO2 on Semibalanus<\/p>\n<p>Balanoides. There is now evidence backing up the negative consequences of high CO2 on these<\/p>\n<p>animals. In another article by the same organization one year later, they tested what ocean acidification<\/p>\n<p>can do to the population dynamics of\u00a0<span style=\"line-height: 1.5\">Semibalanus balanoides at it&#8217;s Southern range end. &#8220;Using<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> empirical data, we forced a barnacle (<span class=\"genusSpeciesInfoAsset\">Semibalanus balanoides<\/span>) population model to investigate the<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> relative influence of sea surface temperature (SST) and ocean acidification on a population nearing the<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> southern limit of its geographic distribution. Hindcast models were compared to observational data <\/span><\/p>\n<p><span style=\"line-height: 1.5\">from Cellar Beach (southwestern United Kingdom). Results indicate that a declining pH trend (\u22120.0017 <\/span><\/p>\n<p><span style=\"line-height: 1.5\">unit\/yr), indicative of ocean acidification over the past 50 years, does not cause an observable impact<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> on the population abundance relative to changes caused by fluctuations in temperature. Below the<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> critical temperature (here <em>T<\/em><sub>crit<\/sub> = 13.1\u00b0C), pH has a more significant affect on population dynamics at <\/span><\/p>\n<p><span style=\"line-height: 1.5\">this southern range edge. However, above this value, SST has the overriding influence. At lower SST, a<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> decrease in pH (according to the National Bureau of Standards, pH<sub>NBS<\/sub>) from 8.2 to 7.8 can significantly<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> decrease the population abundance. The lethal impacts of ocean acidification observed in experiments<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> on early life stages reduce cumulative survival by ~25%, which again will significantly alter the <\/span><\/p>\n<p><span style=\"line-height: 1.5\">population level at this southern limit. Furthermore, forecast predictions from this model suggest that<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> combined acidification and warming cause this local population to die out 10 years earlier than would<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> occur if there was only global warming and no concomitant decrease in pH.&#8221;(Findlay, Burrows, et al., <\/span><\/p>\n<p><span style=\"line-height: 1.5\">2010). This indicates that it in fact does have an affect on the population dynamics and would cause<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> the species to die out prematurely.<\/span><\/p>\n<div id=\"attachment_891\" style=\"width: 310px\" class=\"wp-caption alignnone\"><img aria-describedby=\"caption-attachment-891\" loading=\"lazy\" class=\"wp-image-891 size-medium\" src=\"https:\/\/sites.evergreen.edu\/vms-spring\/wp-content\/uploads\/sites\/209\/2016\/05\/barnaclewhole-300x259.png\" alt=\"\" width=\"300\" height=\"259\" srcset=\"https:\/\/sites.evergreen.edu\/vms-spring\/wp-content\/uploads\/sites\/209\/2016\/05\/barnaclewhole-300x259.png 300w, https:\/\/sites.evergreen.edu\/vms-spring\/wp-content\/uploads\/sites\/209\/2016\/05\/barnaclewhole-768x663.png 768w, https:\/\/sites.evergreen.edu\/vms-spring\/wp-content\/uploads\/sites\/209\/2016\/05\/barnaclewhole-600x518.png 600w, https:\/\/sites.evergreen.edu\/vms-spring\/wp-content\/uploads\/sites\/209\/2016\/05\/barnaclewhole.png 788w\" sizes=\"(max-width: 300px) 100vw, 300px\" \/><p id=\"caption-attachment-891\" class=\"wp-caption-text\">Adult sessile barnacles mounted on a rock<\/p><\/div>\n<p>ACORN BARNACLES AND THE 21ST CENTURY:<\/p>\n<p>\u00a0The thing that interested me the most about acorn barnacles is their reproductive system. They have<\/p>\n<p>evolved to be hermaphroditic, having both female and male genitalia. They evolved this way for survival<\/p>\n<p>because they are sessile creatures. This got me thinking about the evolution of sexuality and gender in<\/p>\n<p>humans in the 21st century. Acorn barnacles evolved this way out of necessity, does that mean this<\/p>\n<p>generation of gender and sexual fluidity could be out of necessity too? What if the reason that gender<\/p>\n<p>and\u00a0<span style=\"line-height: 1.5\">sexuality are\u00a0<\/span><span style=\"line-height: 1.5\">becoming more open-ended is not only because of cerebral growth, but also out of a<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> biological need to\u00a0<\/span><span style=\"line-height: 1.5\">be less heterosexual and therefore control\u00a0the size of the overabundant population<\/span><\/p>\n<p><span style=\"line-height: 1.5\"> we have?<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><iframe loading=\"lazy\" src=\"https:\/\/player.vimeo.com\/video\/168140678\" width=\"676\" height=\"507\" frameborder=\"0\" title=\"barnacle multiplane\" webkitallowfullscreen mozallowfullscreen allowfullscreen><\/iframe><\/p>\n<p><em>An acorn barnacle feeding on a copepod with it&#8217;s cirri\u00a0<\/em><\/p>\n<p>&nbsp;<\/p>\n<p>Sources:\u00a0<\/p>\n<p><span style=\"font-weight: 400\">Fish, J. D. &amp; Fish, S. (1996) <\/span><i><span style=\"font-weight: 400\">A student&#8217;s guide to the seashore<\/span><\/i><span style=\"font-weight: 400\">. Second Edition.<\/span><\/p>\n<p><span style=\"font-weight: 400\">Cambridge University Press, Cambridge.<\/span><\/p>\n<p><span style=\"font-weight: 400\">White, N. 2008. <\/span><i><span style=\"font-weight: 400\">Semibalanus balanoides<\/span><\/i><span style=\"font-weight: 400\"> An acorn barnacle. In Tyler-Walters H. and Hiscock K. (eds) <\/span><\/p>\n<p><i><span style=\"font-weight: 400\">Marine Life\u00a0<\/span><\/i><i><span style=\"font-weight: 400\">Information Network: Biology and Sensitivity Key Information Reviews<\/span><\/i><span style=\"font-weight: 400\">, [on-line]. Plymouth: <\/span><\/p>\n<p><span style=\"font-weight: 400\">Marine\u00a0<\/span><span style=\"font-weight: 400\">Biological Association<\/span><span style=\"font-weight: 400\">of the United Kingdom. Available from:<\/span><\/p>\n<p><span style=\"font-weight: 400\">http:\/\/www.marlin.ac.uk\/species\/detail\/1376<\/span><\/p>\n<p>&nbsp;<\/p>\n<p>Helen S. Findlay, Michael A. Kendall, John I. Spicer, Stephen Widdicome. (2009).\u00a0Future high CO2 in the<\/p>\n<p>intertidal may compromise adult barnacle Semibalanus balanoides survival and embryonic<\/p>\n<p>development rate.\u00a0Vol. 389: 193\u2013202.<\/p>\n<p>&nbsp;<\/p>\n<p>Helen S. Findlay, Michael T. Burrows, Michael A. Kendall, John I. Spicer, Stephen Widdecombe.<\/p>\n<p>(2010).\u00a0Can ocean acidification affect population dynamics of the barnacle <span class=\"genusSpeciesInfoAsset\">Semibalanus balanoides<\/span> at<\/p>\n<p>its southern range edge?\u00a0Volume 91, Issue 10\u00a0October 2010 Pages 2931\u20132940.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>ACORN BARNACLE<\/p>\n","protected":false},"author":3335,"featured_media":890,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_mi_skip_tracking":false},"categories":[20,4],"tags":[],"_links":{"self":[{"href":"https:\/\/sites.evergreen.edu\/vms-spring\/wp-json\/wp\/v2\/posts\/885"}],"collection":[{"href":"https:\/\/sites.evergreen.edu\/vms-spring\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/sites.evergreen.edu\/vms-spring\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/sites.evergreen.edu\/vms-spring\/wp-json\/wp\/v2\/users\/3335"}],"replies":[{"embeddable":true,"href":"https:\/\/sites.evergreen.edu\/vms-spring\/wp-json\/wp\/v2\/comments?post=885"}],"version-history":[{"count":0,"href":"https:\/\/sites.evergreen.edu\/vms-spring\/wp-json\/wp\/v2\/posts\/885\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/sites.evergreen.edu\/vms-spring\/wp-json\/wp\/v2\/media\/890"}],"wp:attachment":[{"href":"https:\/\/sites.evergreen.edu\/vms-spring\/wp-json\/wp\/v2\/media?parent=885"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/sites.evergreen.edu\/vms-spring\/wp-json\/wp\/v2\/categories?post=885"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/sites.evergreen.edu\/vms-spring\/wp-json\/wp\/v2\/tags?post=885"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}