Plankton: Difference between revisions
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{{About|the marine organisms|other uses}} | {{About|the marine organisms|other uses}} | ||
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[[File:Marine microplankton.jpg|thumb|upright=1.5| {{center|'''[[Marine microplankton|Marine microplankton and mesoplankton]]'''}} Part of the contents of one dip of a [[hand net]]. The image contains diverse planktonic organisms, ranging from [[photosynthetic]] [[cyanobacteria]] and [[diatom]]s to many different types of [[zooplankton]], including both [[holoplankton]] (permanent residents of the plankton) and [[meroplankton]] (temporary residents of the plankton, e.g., [[fish egg]]s, crab larvae, worm larvae). 100 μm = one tenth of a mm.]] | |||
'''Plankton''' are | '''Plankton''' are [[organism]]s that drift in [[Hydrosphere|water]] (or [[atmosphere|air]]) but are unable to actively propel themselves against [[ocean current|current]]s (or [[wind]]).<ref name=Lalli1997>{{cite book | last1=Lalli | first1=Carol | last2=Parsons | first2=Timothy R. | title=Biological Oceanography: An Introduction | publisher=Elsevier | publication-place=Oxford | date=1997-04-10 | isbn=978-0-08-052799-4 | page=}}</ref><ref>{{cite journal |last=Smith |first=David J. |date=July 2013 |title=Aeroplankton and the Need for a Global Monitoring Network |journal=BioScience |volume=63 |issue=7 |pages=515–516 |s2cid=86371218 |doi=10.1525/bio.2013.63.7.3 |doi-access=free }}</ref> Marine plankton include drifting organisms that inhabit the [[saltwater]] of [[ocean]]s and the [[brackish]] waters of [[estuaries]]. [[Fresh water|Freshwater]] plankton are similar to marine plankton, but are found in lakes and rivers. An individual plankton organism in the plankton is called a '''plankter'''.<ref>{{cite web |title=plankter |url=https://www.ahdictionary.com/word/search.html?q=plankter |website=American Heritage Dictionary |publisher=Houghton Mifflin Harcourt Publishing Company |access-date=9 November 2018 |archive-url=https://web.archive.org/web/20181109153109/https://www.ahdictionary.com/word/search.html?q=plankter |archive-date=9 November 2018 }}</ref> In the ocean plankton provide a crucial source of food, particularly for larger [[filter-feeding]] animals, such as [[bivalve]]s, [[sponge]]s, [[forage fish]] and [[baleen whale]]s. | ||
Plankton includes organisms from species across all the major biological kingdoms, ranging in size from the [[microscopic scale|microscopic]] (such as [[bacteria]], [[archaea]], [[protozoa]] and microscopic [[algae]] and [[fungi]]<ref name="Lawton-2024-02-10">{{cite journal |last1=Lawton |first1=Graham |title=Fungi ahoy! |journal=New Scientist |date=10 February 2024 |volume=261 |issue=3477 |pages=37–39 |doi=10.1016/S0262-4079(24)00274-4|bibcode=2024NewSc.261b..37L }}</ref>) to larger organisms (such as jellyfish and ctenophores).<ref>{{cite web |url= http://www.institut-ocean.org/images/articles/documents/1354542960.pdf |title= Microzooplankton: the microscopic (micro) animals (zoo) of the plankton |last=Dolan |first=John |date= November 2012 |publisher=[[Institut océanographique]] |access-date=16 January 2014 |archive-url= https://web.archive.org/web/20160304081019/http://www.institut-ocean.org/images/articles/documents/1354542960.pdf |archive-date=4 March 2016 }}</ref> This is because plankton are defined by their [[ecological niche]] and level of [[motility]] rather than by any [[phylogenetics|phylogenetic]] or [[taxonomy (biology)|taxonomic]] classification. The plankton category differentiates organisms from those that can swim against a current, called ''[[nekton]]'', and those that live on the deep sea floor, called ''[[benthos]]''. Organisms that float on or near the water's surface are called ''[[neuston]]''. Neuston that drift as water currents or wind take them, and lack the swimming ability to counter this, form a special subgroup of plankton. Mostly plankton just drift where currents take them, though some, like jellyfish, swim slowly but not fast enough to generally overcome the influence of currents. | |||
Microscopic plankton, smaller than about one millimetre in size, play crucial roles in [[marine ecosystem]]s. They are a diverse group, including [[phytoplankton]] (like [[diatom]]s and [[dinoflagellate]]s) and [[zooplankton]] (such as [[radiolarian]]s, [[foraminifera]] and some [[copepod]]s), and serve as a foundational component of the [[marine food web]]. These largely unseen microscopic plankton drive [[primary production]], support local food webs, cycle nutrients, and influence global biogeochemical processes. Their role is foundational for maintaining the health and balance of marine ecosystems. | |||
Although plankton are usually thought of as inhabiting water, there are also airborne versions that live part of their lives drifting in the atmosphere. These ''[[aeroplankton]]'' can include [[plant spore]]s, [[pollen]] and wind-scattered [[seed]]s. They can also include microorganisms swept into the air from terrestrial dust storms and oceanic plankton swept into the air by [[sea spray]]. | |||
== | == Overview == | ||
[[File: | [[File:Global ocean chlorophyll concentration October 2019.png|thumb|upright=1.5| Ocean [[chlorophyll]] concentration is a [[Proxy (statistics)|proxy]] for, or an indicator of, the distribution and abundance of [[phytoplankton]]. The intensity of green indicates how abundant the phytoplankton are, while blue indicates where there are few phytoplankton. – [[NASA Earth Observatory]], October 2019.<ref name=NASAO2019>[https://earthobservatory.nasa.gov/global-maps/MY1DMM_CHLORA Chlorophyll] NASA Earth Observatory. Accessed 30 November 2019.</ref>]] | ||
The | Apart from [[aeroplankton]], plankton inhabits oceans, seas, estuaries, rivers, lakes and ponds. Local abundance varies horizontally, vertically and seasonally. The primary cause of this variability is the availability of light. All plankton ecosystems are driven by the input of solar energy (but see [[chemosynthesis]]), confining [[primary production]] to surface waters, and to geographical regions and seasons having abundant light. | ||
A secondary variable is nutrient availability. The [[abundance (ecology)|amount]] and [[species distribution|distribution]] of plankton depends on available nutrients, the [[water column|state of water]] and a large amount of other plankton.<ref name="Book-2013">{{cite book |last1=Agrawai |first1=Anju |last2=Gopnal |first2=Krishna |title= Biomonitoring of Water and Waste Water |url= https://books.google.com/books?id=Cf4_AAAAQBAJ&q=Plankton+abundance+and+distribution+are+strongly+dependent+on+factors+such+as+ambient+nutrient+concentrations,+the+physical+state+of+the+water+column,+and+the+abundance+of+other+plankton.&pg=PA34 |date=2013 |publisher=Springer India |page=34 |isbn=978-8-132-20864-8 |access-date= 2 April 2018 }}</ref> The local distribution of plankton can be affected by wind-driven [[Langmuir circulation]] and the [[Langmuir circulation#Biological effects|biological effects]] of this physical process. Although large areas of the [[tropics|tropical]] and [[sub-tropical]] oceans have abundant light, they experience relatively low primary production because they offer limited nutrients such as [[nitrate]], [[phosphate]] and [[silicate]]. This results from large-scale [[ocean current|ocean circulation]] and water column [[Ocean stratification|stratification]]. In such regions, primary production usually occurs at greater depth, although at a reduced level (because of reduced light). | |||
While plankton are most abundant in surface waters, they live throughout the water column. At depths where no primary production occurs, [[zooplankton]] and [[bacterioplankton]] instead consume organic material sinking from more productive surface waters above. This flux of sinking material, so-called [[marine snow]], can be especially high following the termination of [[spring bloom]]s. | |||
Despite significant [[macronutrient]] concentrations, some ocean regions are unproductive (so-called [[HNLC|HNLC regions]]).<ref>{{Cite journal| last = Martin | first = J.H.| author2=Fitzwater, S.E.| year=1988| title = Iron-deficiency limits phytoplankton growth in the Northeast Pacific Subarctic| journal= Nature | volume=331 | pages=341–343| doi= 10.1038/331341a0 | issue=6154| bibcode=1988Natur.331..341M| s2cid=4325562}}</ref> The [[micronutrient]] [[iron]] is deficient in these regions, and [[iron fertilization|adding it]] can lead to the formation of phytoplankton [[algal bloom]]s.<ref>{{Cite journal| last1 = Boyd | first1 = P.W. | year=2000| title = A mesoscale phytoplankton bloom in the polar Southern Ocean stimulated by fertilization| journal=Nature | volume=407 | pages=695–702| doi = 10.1038/35037500 | pmid = 11048709| last2 = Watson | first2 = AJ| last3 = Law | first3 = CS| last4 = Abraham | first4 = ER| last5 = Trull | first5 = T| last6 = Murdoch | first6 = R| last7 = Bakker | first7 = DC| last8 = Bowie | first8 = AR| last9 = Buesseler | first9 = KO| issue = 6805| display-authors = 1| bibcode = 2000Natur.407..695B| s2cid = 4368261 }}</ref> Iron primarily reaches the ocean through the deposition of dust on the sea surface. Paradoxically, oceanic areas adjacent to unproductive, [[arid]] land thus typically have abundant phytoplankton (e.g., the eastern [[Atlantic Ocean]], where [[trade winds]] bring dust from the [[Sahara Desert]] in north [[Africa]]). | |||
Within the plankton, [[holoplankton]] spend their entire [[biological life cycle|life cycle]] as plankton (e.g. most [[algae]], [[copepod]]s, [[salp]]s, and some [[jellyfish]]). By contrast, [[meroplankton]] are only planktic for part of their lives (usually the [[larva]]l stage), and then graduate to either a nektic (swimming) or [[benthos|benthic]] (sea floor) existence. Examples of meroplankton include the larvae of [[sea urchin]]s, [[starfish]], [[crustacean]]s, marine [[worm]]s, and most [[fish]].<ref>{{cite book |last1=Karleskint |first1=George |last2=Turner |first2=Richard |last3=Small |first3=James |date=2013 |chapter= 17: The Open Sea |title=Introduction to Marine Biology |edition=4th |publisher= Brooks/Cole |pages=442–443 |isbn=978-1-133-36446-7}}</ref> | Within the plankton, [[holoplankton]] spend their entire [[biological life cycle|life cycle]] as plankton (e.g. most [[algae]], [[copepod]]s, [[salp]]s, and some [[jellyfish]]). By contrast, [[meroplankton]] are only planktic for part of their lives (usually the [[larva]]l stage), and then graduate to either a nektic (swimming) or [[benthos|benthic]] (sea floor) existence. Examples of meroplankton include the larvae of [[sea urchin]]s, [[starfish]], [[crustacean]]s, marine [[worm]]s, and most [[fish]].<ref>{{cite book |last1=Karleskint |first1=George |last2=Turner |first2=Richard |last3=Small |first3=James |date=2013 |chapter= 17: The Open Sea |title=Introduction to Marine Biology |edition=4th |publisher= Brooks/Cole |pages=442–443 |isbn=978-1-133-36446-7}}</ref> | ||
The [[ | === Microscopic plankton === | ||
{{multiple image | |||
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| image1 = Emiliania huxleyi.jpg | |||
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| caption1 = The [[coccolithophore]] ''[[Emiliania huxleyi]]'' (μm = thousandth of one mm) | |||
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| caption2 = [[Algae bloom]] of ''Emiliania huxleyi'' off the southern coast of England | |||
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Plankton is mostly made up of planktonic [[microorganism]]s less than one millimetre across, most visible only through a microscope. Microorganisms have been variously estimated to make up about 70%,<ref name="Bar-On2018">{{cite journal | last1 = Bar-On | first1 = YM | last2 = Phillips | first2 = R | last3 = Milo | first3 = R | year = 2018 | title = The biomass distribution on Earth | journal = PNAS | volume = 115 | issue = 25| pages = 6506–6511 | doi = 10.1073/pnas.1711842115 | pmid = 29784790 | pmc = 6016768 | bibcode = 2018PNAS..115.6506B | doi-access = free }}</ref> or about 90%,<ref>[https://ocean.si.edu/ecosystems/census-marine-life/census-marine-life-overview Census Of Marine Life] Accessed 29 October 2020.</ref><ref name=Cavicchioli2019>{{cite journal |doi = 10.1038/s41579-019-0222-5|title = Scientists' warning to humanity: Microorganisms and climate change|year = 2019|last1 = Cavicchioli|first1 = Ricardo|last2 = Ripple|first2 = William J.|last3 = Timmis|first3 = Kenneth N.|last4 = Azam|first4 = Farooq|last5 = Bakken|first5 = Lars R.|last6 = Baylis|first6 = Matthew|last7 = Behrenfeld|first7 = Michael J.|last8 = Boetius|first8 = Antje|last9 = Boyd|first9 = Philip W.|last10 = Classen|first10 = Aimée T.|last11 = Crowther|first11 = Thomas W.|last12 = Danovaro|first12 = Roberto|last13 = Foreman|first13 = Christine M.|last14 = Huisman|first14 = Jef|last15 = Hutchins|first15 = David A.|last16 = Jansson|first16 = Janet K.|last17 = Karl|first17 = David M.|last18 = Koskella|first18 = Britt|last19 = Mark Welch|first19 = David B.|last20 = Martiny|first20 = Jennifer B. H.|last21 = Moran|first21 = Mary Ann|last22 = Orphan|first22 = Victoria J.|last23 = Reay|first23 = David S.|last24 = Remais|first24 = Justin V.|last25 = Rich|first25 = Virginia I.|last26 = Singh|first26 = Brajesh K.|last27 = Stein|first27 = Lisa Y.|last28 = Stewart|first28 = Frank J.|last29 = Sullivan|first29 = Matthew B.|last30 = Van Oppen|first30 = Madeleine J. H.|last31=Weaver |first31=Scott C. |last32=Webb |first32=Eric A. |last33=Webster |first33=Nicole S. |journal = Nature Reviews Microbiology|volume = 17|issue = 9|pages = 569–586|pmid = 31213707|pmc = 7136171|display-authors = 4}} [[File:CC-BY icon.svg|50px]] Modified text was copied from this source, which is available under a [https://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International License].</ref> of the total [[ocean biomass]]. Taken together they form the [[marine microbiome]]. Over billions of years this microbiome has evolved many life styles and adaptations and come to participate in the [[Biogeochemical cycle|global cycling]] of almost all chemical elements.<ref>Bolhuis, H. and Cretoiu, M.S. (2016) "What is so special about marine microorganisms?". In: L. J. Stal and M. S. Cretoiu (Eds.) ''The Marine Microbiome'', pages 3–20, Springer. {{ISBN|9783319330006}}</ref> | |||
[[Microplankton]] are ecological linchpins in the [[marine food web]]. They are crucial to nutrient recycling in the way they act as [[decomposer]]s. They are also responsible for nearly all [[photosynthesis]] that occurs in the ocean, as well as the cycling of [[carbon]], [[nitrogen]], [[phosphorus]] and other [[nutrients]] and trace elements.<ref name="University of Georgia">{{cite web |title=Functions of global ocean microbiome key to understanding environmental changes |date=10 December 2015 |website=www.sciencedaily.com |publisher=University of Georgia | url=https://www.sciencedaily.com/releases/2015/12/151210181647.htm |access-date=11 December 2015}}</ref> Microplankton sequesters large amounts of carbon and produce much of the world's oxygen. | |||
It is estimated [[marine viruses]] kill 20% of ocean microplankton biomass every day. Viruses are the main agents responsible for the rapid destruction of harmful [[algal bloom]]s which often kill other [[marine life]]. The number of viruses in the plankton decreases further offshore and deeper into the water, where there are fewer host organisms. | |||
=== Terminology === | |||
File: | [[File:Plankton species diversity.jpg|thumb|upright=1.3| {{center|'''Plankton species diversity'''}} Diverse assemblages of [[unicellular]] and [[multicellular]] organisms with different sizes, shapes, feeding strategies, ecological functions, life cycle characteristics, and environmental sensitivities.<ref>Chust, G., Vogt, M., Benedetti, F., Nakov, T., Villéger, S., Aubert, A., Vallina, S.M., Righetti, D., Not, F., Biard, T. and Bittner, L.(2017) "''Mare incognitum'': A glimpse into future plankton diversity and ecology research". ''Frontiers in Marine Science'', '''4''': 68. {{doi|10.3389/fmars.2017.00068|doi-access=free}}.</ref> {{center|<small>Courtesy of Christian Sardet/CNRS/[[Tara expedition]]s</small>}}]] | ||
</ | The name ''plankton'' was coined by German marine biologist [[Victor Hensen]] in 1887 from shortening the word ''halyplankton'' from [[Greek language|Greek]] {{lang|grc|ἅλς}} ''háls'' "sea" and {{lang|grc|πλανάομαι}} ''planáomai'' "(I) drift" or "(I) wander".<ref>{{cite journal |last=Hansen |first=Victor |year=1887 |title=Uber die Bestimmung des Plankton's oder des im Meere treibenden Materials an Pflanzen und Thieren |trans-title=On the determination of the plankton or the material floating in the sea on plants and animals |url=https://www.biodiversitylibrary.org/item/108760#page/17/mode/1up |language=de |journal=Fünfter Bericht der Kommission zur Wissenschaftlichen Untersuchung der Deutschen Meere |volume=12 |issue=12–16 |location=Berlin, Germany |publisher=Paul Parey |pages=1–108 |via=Biodiversity Heritage Library}}</ref>{{rp|1}}<ref>{{LSJ|a(/ls2|ἅλς}}, {{LSJ|plana/w|πλανάω|ref}}.</ref><!-- Probably wrong etymology: Plankton is the neuter form of planktos, "wondering, roaming", from plazo/plazomai --> Some forms of plankton are capable of independent vertically movement, and can swim hundreds of meters vertically in a single day (a behavior called [[diel vertical migration]]). However their horizontal position is primarily determined by the surrounding water movement, so plankton typically flow with the [[ocean current]]s. This is in contrast to [[nekton]] organisms, such as [[fish]], [[squid]] and [[marine mammal]]s, which can swim against the ambient flow and control their position in the environment. | ||
The study of plankton is termed [[planktology]] and a planktonic individual is referred to as a plankter.<ref>{{cite encyclopedia |url=http://www.britannica.com/EBchecked/topic/463117/plankter |title= Plankter – marine biology |encyclopedia=Encyclopædia Britannica}}</ref> The adjective ''planktonic'' is widely used in both the scientific and popular literature, and is a generally accepted term. However, from the standpoint of prescriptive grammar, the less-commonly used ''planktic'' is more strictly the correct adjective. When deriving English words from their Greek or Latin roots, the gender-specific ending (in this case, "-on" which indicates the word is neuter) is normally dropped, using only the root of the word in the derivation.<ref name="Emiliani, C.">{{cite journal |last=Emiliani |first=C. |year=1991 |title=Planktic/Planktonic, Nektic/Nektonic, Benthic/Benthonic |journal= Journal of Paleontology |volume=65 |page= 329 |jstor=1305769 |issue=2 |doi=10.1017/S0022336000020576 |bibcode=1991JPal...65..329E |s2cid=131283465 }}</ref> | |||
{{clear}} | {{clear}} | ||
== Trophic | ==By habitat== | ||
{{plankton | |||
===Aeroplankton=== | |||
{{main|Aeroplankton}} | |||
[[File:Ocean mist and spray 2.jpg|thumb|upright=1.3|[[Sea spray]] containing microorganisms in [[Marine microorganisms|marine plankton]] can be swept high into the atmosphere and may travel the globe as [[aeroplankton]] before falling back to earth.]] | |||
[[Aeroplankton]] are tiny lifeforms that float and drift in the air, carried by the [[Air current|current]] of the [[wind]]; they are the [[atmospheric]] [[analogy (biology)|analogue]] to oceanic plankton. Most of the living things that make up aeroplankton are very small to [[Microscope|microscopic]] in size, and many can be difficult to identify because of their tiny size. Scientists can collect them for study in traps and sweep nets from [[aircraft]], kites or balloons.<ref>A. C. Hardy and P. S. Milne (1938) Studies in the Distribution of Insects by Aerial Currents. Journal of Animal Ecology, 7(2):199-229</ref> Aeroplankton is made up of numerous [[Microorganism|microbes]], including [[virus]]es, about 1000 different species of [[bacteria]], around 40,000 varieties of [[Fungus|fungi]], and hundreds of species of [[protist]]s, [[algae]], [[moss]]es and [[Marchantiophyta|liverworts]] that live some part of their life cycle as aeroplankton, often as [[spore]]s, [[pollen]], and wind-scattered [[seed]]s. Additionally, peripatetic microorganisms are swept into the air from terrestrial dust storms, and an even larger amount of airborne marine microorganisms are propelled high into the atmosphere in sea spray. Aeroplankton deposits hundreds of millions of airborne viruses and tens of millions of bacteria every day on every square meter around the planet. This means similar mixes of microscopic plankton [[taxon]] can be found in open bodies of water around the world.<ref>[https://www.smithsonianmag.com/science-nature/living-bacteria-are-riding-earths-air-currents-180957734/ Living Bacteria Are Riding Earth's Air Currents] ''Smithsonian Magazine'', 11 January 2016.</ref><ref>{{cite news |last=Robbins |first=Jim |title=Trillions Upon Trillions of Viruses Fall From the Sky Each Day |url=https://www.nytimes.com/2018/04/13/science/virosphere-evolution.html |date=13 April 2018 |work=[[The New York Times]] |access-date=14 April 2018}}</ref><ref name="ISME-2018">{{cite journal |last1=Reche |first1=Isabel |last2=D'Orta |first2=Gaetano |last3=Mladenov |first3=Natalie |last4=Winget |first4=Danielle M |last5=Suttle |first5=Curtis A |title=Deposition rates of viruses and bacteria above the atmospheric boundary layer |journal=ISME Journal |volume=12 |issue=4 |pages=1154–1162 |date=29 January 2018 |doi=10.1038/s41396-017-0042-4 |pmid=29379178 |pmc=5864199|bibcode=2018ISMEJ..12.1154R }}</ref> | |||
The [[sea surface microlayer]], compared to the sub-surface waters, contains elevated concentration of [[bacteria]] and [[viruses]].<ref name=Liss2005>{{cite book | last=Liss | first=P. S. | title=The sea surface and global change | publisher=Cambridge University Press | publication-place=Cambridge New York | year=1997 | isbn=978-0-521-56273-7 | oclc=34933503}}</ref><ref name="blanchard">Blanchard, D.C., 1983. The production, distribution and bacterial enrichment of the sea-salt aerosol. In: Liss, P.S., Slinn, W.G.N. ŽEds.., Air–Sea Exchange of Gases and Particles. D. Reidel Publishing Co., Dordrecht, Netherlands, pp. 407–444.</ref> These materials can be transferred from the sea-surface to the atmosphere in the form of wind-generated aqueous [[aerosol]]s due to their high vapour tension and a process known as [[volatilisation]].<ref name="wallace">Wallace Jr., G.T., Duce, R.A., 1978. Transport of particulate organic matter by bubbles in marine waters. Limnol. Oceanogr. 23 Ž6., 1155–1167.</ref> When airborne, these [[microbes]] can be transported long distances to coastal regions. If they hit land they can have an effect on animal, vegetation and human health.<ref name="WHO">WHO, 1998. Draft guidelines for safe recreational water environments: coastal and fresh waters, draft for consultation. World Health Organization, Geneva, EOSrDRAFTr98 14, pp. 207–299.</ref> Marine aerosols that contain viruses can travel hundreds of kilometers from their source and remain in liquid form as long as the humidity is high enough (over 70%).<ref name="klassen">Klassen, R. D., & Roberge, P. R. (1999). Aerosol transport modeling as an aid to understanding atmospheric corrosivity patterns. Materials & Design, 20, 159–168.</ref><ref name="moorthy">Moorthy, K. K., Satheesh, S. K., & Krishna Murthy, B.V. (1998). Characteristics ofspectral optical depths and size distributions of aerosols over tropical oceanic regions. Journal of Atmospheric and Solar–Terrestrial Physics, 60, 981–992. | |||
</ref><ref>Chow, J. C., Watson, J. G., Green, M. C., Lowenthal, D. H., Bates, B., Oslund, W., & Torre, G. (2000). Cross-border transport and spatial variability of suspended particles in Mexicali and California's Imperial Valley. Atmospheric Environment, 34, 1833–1843.</ref> These aerosols are able to remain suspended in the atmosphere for about 31 days.<ref name="aller">Aller, J., Kuznetsova, M., Jahns, C., Kemp, P. (2005) The sea surface microlayer as a source of viral and bacterial enrichment in marine aerosols. Journal of aerosol science. Vol. 36, pp. 801–812.</ref> Evidence suggests that bacteria can remain viable after being transported inland through aerosols. Some reached as far as 200 meters at 30 meters above sea level.<ref name="marks"/> The process which transfers this material to the atmosphere causes further enrichment in both bacteria and viruses in comparison to either the SML or sub-surface waters (up to three orders of magnitude in some locations).<ref name="marks">Marks, R., Kruczalak, K., Jankowska, K., & Michalska, M. (2001). Bacteria and fungi in air over the GulfofGdansk and Baltic sea. Journal of Aerosol Science, 32, 237–250.</ref> | |||
===Freshwater plankton=== | |||
Freshwater plankton parallel marine plankton (below), but are found inland in the freshwaters of lakes and rivers. | |||
===Geoplankton=== | |||
{{see also|Geoplankton}} | |||
[[File:Thaumastoderma ramuliferum.jpg|thumb|A gastrotrich can lay resilient eggs capable of surviving years in a dry environment. Scale bar: 20 μm.]] | |||
Many animals live in terrestrial environments by thriving in transient often microscopic bodies of water and moisture, these include [[rotifer]]s and [[gastrotrich]]s which lay resilient eggs capable of surviving years in dry environments, and some of which can go dormant themselves. Nematodes are usually microscopic with this lifestyle. Water bears, despite only having lifespans of a few months, famously can enter suspended animation during dry or hostile conditions and survive for decades. This allows them to be ubiquitous in terrestrial environments despite needing water to grow and reproduce. Many microscopic crustacean groups like [[copepod]]s and [[Amphipoda|amphipods]] (of which [[Talitridae|sandhoppers]] are members) and [[Ostracod|seed shrimp]] are known to go dormant when dry and live in transient bodies of water too<ref name=":0" /> | |||
===Marine plankton=== | |||
[[File:Neuston, Plankton, Nekton, Benthos.jpg|thumb|upright=1.3| Plankton (organisms that drift with water currents) can be contrasted with [[nekton]] (organisms that can swim against water currents) and [[benthos]] (organisms that live at the ocean floor). There are also [[neuston]] (organisms that live at the ocean surface). Neuston that cannot swim against currents or the wind are a special subset of plankton.]] | |||
Marine plankton includes [[marine protists]] ([[algae]] and [[protozoa]]), drifting and floating animals (particularly [[microanimal]]s), [[marine prokaryotes]] (bacteria and archaea), and [[marine virus]]es that inhabit the saltwater of oceans and the brackish waters of estuaries. | |||
{{Anchor|Planktonic neuston}} | |||
{{Anchor|Neustonic plankton}} | |||
====At the ocean surface==== | |||
{{further|Neuston}} | |||
Plankton are also found at the ocean surface. Organisms that live at or just below the air-sea interface are called [[neuston]]. They float either on the water's surface ([[epineuston]]) or swim in the top few centimeters ([[hyponeuston]]). Many neuston qualify to be categorised as part of the broader plankton community, because they drift largely as currents or wind dictate, lacking strong enough swimming ability to counter them.<ref name="Albuquerque2021" /><ref name="Helm2021">{{cite journal | last=Helm | first=Rebecca R. | title=The mysterious ecosystem at the ocean's surface | journal=PLOS Biology | volume=19 | issue=4 | date=2021-04-28 | issn=1545-7885 | pmid=33909611 | pmc=8081451 | doi=10.1371/journal.pbio.3001046 | doi-access=free | article-number=e3001046}}</ref><ref name="Egger2021">{{cite journal | last=Egger | first=Matthias | last2=Quiros | first2=Lauren | last3=Leone | first3=Giulia | last4=Ferrari | first4=Francesco | last5=Boerger | first5=Christiana M. | last6=Tishler | first6=Michelle | title=Relative Abundance of Floating Plastic Debris and Neuston in the Eastern North Pacific Ocean | journal=Frontiers in Marine Science | volume=8 | date=2021-06-03 | issn=2296-7745 | doi=10.3389/fmars.2021.626026 | doi-access=free | page=}}</ref> | |||
Neustonic animals are primarily adapted to float upside-down on the ocean surface, similar to an inverted benthos,<ref>{{Cite journal | last1 = Anthony | first1 = Colin J. | last2 = Bentlage | first2 = Bastian | last3 = Helm | first3 = Rebecca R. | title = Animal evolution at the ocean's water–air interface | journal = Current Biology | volume = 34 | issue = 1 | pages = 196–203.e2 | year = 2024 | issn = 0960-9822 | doi = 10.1016/j.cub.2023.11.013 | pmid = 38194916 | bibcode = 2024CBio...34E.196A | url = https://www.sciencedirect.com/science/article/pii/S0960982223015269| doi-access = free }}</ref> and form a unique subset of the zooplankton community, which plays a pivotal role in the functioning of marine ecosystems.<ref>{{Cite journal | last = Helm | first = Rebecca R. | title = The mysterious ecosystem at the ocean's surface | journal = PLOS Biology | volume = 19 | issue = 4 | article-number = e3001046 | date = 2021-04-28 | publisher = Public Library of Science | doi = 10.1371/journal.pbio.3001046 | doi-access = free | pmid = 33909611 | pmc = 8081451 }}</ref> Neustonic zooplankton are partially responsible for the active [[Energy flow (ecology)|energy flux]] between superficial and deep layers of the ocean.<ref>{{cite journal |doi = 10.3354/ame027057|title = Zooplankton fecal pellets, marine snow and sinking phytoplankton blooms|year = 2002|last1 = Turner|first1 = JT|journal = Aquatic Microbial Ecology|volume = 27|pages = 57–102|doi-access = free}}</ref><ref>{{cite journal |doi = 10.1073/pnas.1512110112|title = Seasonal copepod lipid pump promotes carbon sequestration in the deep North Atlantic|year = 2015|last1 = Jónasdóttir|first1 = Sigrún Huld|last2 = Visser|first2 = André W.|last3 = Richardson|first3 = Katherine|last4 = Heath|first4 = Michael R.|journal = Proceedings of the National Academy of Sciences|volume = 112|issue = 39|pages = 12122–12126|pmid = 26338976|pmc = 4593097|doi-access = free}}</ref><ref>{{cite journal |doi = 10.1038/s41467-020-19875-7|title = Large deep-sea zooplankton biomass mirrors primary production in the global ocean|year = 2020|last1 = Hernández-León|first1 = S.|last2 = Koppelmann|first2 = R.|last3 = Fraile-Nuez|first3 = E.|last4 = Bode|first4 = A.|last5 = Mompeán|first5 = C.|last6 = Irigoien|first6 = X.|last7 = Olivar|first7 = M. P.|last8 = Echevarría|first8 = F.|last9 = Fernández De Puelles|first9 = M. L.|last10 = González-Gordillo|first10 = J. I.|last11 = Cózar|first11 = A.|last12 = Acuña|first12 = J. L.|last13 = Agustí|first13 = S.|last14 = Duarte|first14 = C. M.|journal = Nature Communications|volume = 11|issue = 1|page = 6048|pmid = 33247160|pmc = 7695708| bibcode=2020NatCo..11.6048H |s2cid = 227191974}}</ref>Neustonic plankton is also a food source for marine zooplankton and fish migrating from the deep layers and seabirds.<ref name=Albuquerque2021>{{cite journal |doi = 10.3389/fmars.2020.606088|doi-access = free|title = Trophic Structure of Neuston Across Tropical and Subtropical Oceanic Provinces Assessed with Stable Isotopes|year = 2021|last1 = Albuquerque|first1 = Rui|last2 = Bode|first2 = Antonio|last3 = González-Gordillo|first3 = Juan Ignacio|last4 = Duarte|first4 = Carlos M.|last5 = Queiroga|first5 = Henrique|journal = Frontiers in Marine Science|volume = 7| bibcode=2021FrMaS...706088A |hdl = 10754/667566|hdl-access = free}} [[File:CC-BY icon.svg|50px]] Material was copied from this source, which is available under a [https://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International License].</ref> | |||
{{Anchor|Deep sea plankton}} | |||
====In deep ocean==== | |||
[[File:Overturning circulation of the global ocean.jpg|thumb|upright=1.3|right| The [[ocean conveyor belt]] carries warm surface waters (red) northward near the surface and cold deep waters (blue) southward. Diverse and flourishing microbial ecosystems have been found deep in the belt.<ref name="PhysOrg2025" /><ref name="Kolody2025" />]] | |||
In 2025, researchers discovered microbial communities inhabiting the [[ocean conveyor belt]], even at great depths in the ocean.<ref name="PhysOrg2025">{{cite web | title=Deep ocean currents shape microbial communities across South Pacific, scientists discover | website=Phys.org | date=2025-07-14 | url=https://phys.org/news/2025-07-deep-ocean-currents-microbial-communities.html | access-date=2025-07-16}}</ref><ref name="Kolody2025">{{cite journal | last=Kolody | first=Bethany C. | last2=Sachdeva | first2=Rohan | last3=Zheng | first3=Hong | last4=Füssy | first4=Zoltán | last5=Tsang | first5=Eunice | last6=Sonnerup | first6=Rolf E. | last7=Purkey | first7=Sarah G. | last8=Allen | first8=Eric E. | last9=Banfield | first9=Jillian F. | last10=Allen | first10=Andrew E. | title=Overturning circulation structures the microbial functional seascape of the South Pacific | journal=Science | volume=389 | issue=6756 | date=2025-07-10 | issn=0036-8075 | doi=10.1126/science.adv6903 | pages=176–182 | url=https://www.science.org/doi/10.1126/science.adv6903 | access-date=2025-07-16| url-access=subscription }}</ref> Ocean currents are generated by surface wind and storms down to about {{cvt|500|m|-2}} below the surface. But the average depth of the ocean goes far below to {{cvt|3.7|km|1}}.<ref name="NOAAs National Ocean Service">{{cite web |title=How deep is the ocean? |website=NOAA's National Ocean Service |url=https://oceanservice.noaa.gov/facts/oceandepth.html#:~:text=The%20average%20depth%20of%20the,U.S.%20territorial%20island%20of%20Guam. |access-date=2023-05-10}}</ref> At these greater depths, currents are driven by differences in water density, which in turn are controlled by differences in water temperature and salinity. This mechanism results in a circulation which behaves like a conveyor belt, carrying water and microorganisms to great depths and around the world.<ref name="PhysOrg2025" /> | |||
Water samples were taken along the full depth of the water column in the South Pacific Ocean, from Easter Island to Antarctica. They found marked increases in microbial diversity about {{cvt|300|m|-2}} deep, in a layer they call the ''prokaryotic phylocline''. This zone, similar to the [[pycnocline]], represents a shift from less diverse surface waters to abundant microbial ecosystems in the deep ocean. For instance, a group they called the ''Antarctic Bottom Water'' contains microbes suited to cold and high pressure, while another group they called the ''Ancient Water Group'', located in slowly circulating water isolated from the surface for over a millennium, contains microbes with genes adapted to low oxygen.<ref name="PhysOrg2025" /><ref name="Kolody2025" /> | |||
{{clear}} | |||
=== | == By taxon == | ||
{{ | Plankton contains representatives from all major divisions of life. By taxon, it can be divided into the following broad groups:<ref name="Worden2015">{{cite journal | last1=Worden | first1=Alexandra Z. | last2=Follows | first2=Michael J. | last3=Giovannoni | first3=Stephen J. | last4=Wilken | first4=Susanne | last5=Zimmerman | first5=Amy E. | last6=Keeling | first6=Patrick J. | title=Rethinking the marine carbon cycle: Factoring in the multifarious lifestyles of microbes | journal=Science | volume=347 | issue=6223 | date=2015-02-13 | issn=0036-8075 | doi=10.1126/science.1257594 | doi-access=free | page= | display-authors=4 }}</ref><ref name="Sunagawa2015">{{cite journal | last1=Sunagawa | first1=Shinichi | last2=Coelho | first2=Luis Pedro | last3=Chaffron | first3=Samuel | last4=Kultima | first4=Jens Roat | last5=Labadie | first5=Karine | last6=Salazar | first6=Guillem | last7=Djahanschiri | first7=Bardya | last8=Zeller | first8=Georg | last9=Mende | first9=Daniel R. | last10=Alberti | first10=Adriana | last11=Cornejo-Castillo | first11=Francisco M. | last12=Costea | first12=Paul I. | last13=Cruaud | first13=Corinne | last14=d'Ovidio | first14=Francesco | last15=Engelen | first15=Stefan | last16=Ferrera | first16=Isabel | last17=Gasol | first17=Josep M. | last18=Guidi | first18=Lionel | last19=Hildebrand | first19=Falk | last20=Kokoszka | first20=Florian | last21=Lepoivre | first21=Cyrille | last22=Lima-Mendez | first22=Gipsi | last23=Poulain | first23=Julie | last24=Poulos | first24=Bonnie T. | last25=Royo-Llonch | first25=Marta | last26=Sarmento | first26=Hugo | last27=Vieira-Silva | first27=Sara | last28=Dimier | first28=Céline | last29=Picheral | first29=Marc | last30=Searson | first30=Sarah | last31=Kandels-Lewis | first31=Stefanie | author32=Tara Oceans coordinators | last33=Bowler | first33=Chris | last34=de Vargas | first34=Colomban | last35=Gorsky | first35=Gabriel | last36=Grimsley | first36=Nigel | last37=Hingamp | first37=Pascal | last38=Iudicone | first38=Daniele | last39=Jaillon | first39=Olivier | last40=Not | first40=Fabrice | last41=Ogata | first41=Hiroyuki | last42=Pesant | first42=Stephane | last43=Speich | first43=Sabrina | last44=Stemmann | first44=Lars | last45=Sullivan | first45=Matthew B. | last46=Weissenbach | first46=Jean | last47=Wincker | first47=Patrick | last48=Karsenti | first48=Eric | last49=Raes | first49=Jeroen | last50=Acinas | first50=Silvia G. | last51=Bork | first51=Peer | last52=Boss | first52=Emmanuel | last53=Bowler | first53=Chris | last54=Follows | first54=Michael | last55=Karp-Boss | first55=Lee | last56=Krzic | first56=Uros | last57=Reynaud | first57=Emmanuel G. | last58=Sardet | first58=Christian | last59=Sieracki | first59=Mike | last60=Velayoudon | first60=Didier | title=Structure and function of the global ocean microbiome | journal=Science | volume=348 | issue=6237 | date=2015-05-22 | issn=0036-8075 | doi=10.1126/science.1261359 | doi-access=free | url=https://hal.science/hal-01233742/document | access-date=2025-08-11 | page= | display-authors=4 | hdl=2078.1/231548 | hdl-access=free }}</ref> | ||
* '''[[Zooplankton|planktonic animals (metazoa)]] :''' – mostly predators (zooplankton) of smaller plankton. Examples are [[arrow worm]]s, [[sea butterfly]], [[ostracod]]s, and [[salp]]s. There are also planktonic [[microanimal]]s typically smaller than one mm, such as [[copepod]]s, [[water flea]]s, [[rotifer]]s, and larval stages of various [[crustacean]]s and [[coral]]s. | |||
* '''[[planktonic protist]]s:''' – single-celled [[eukaryote]] microorganisms, mostly invisible to the naked eye, such as [[diatom]]s, [[dinoflagellate]]s, [[coccolithophore]]s, [[foraminifera]], [[radiolarian]]s, and [[ciliate]]s. Planktonic protists include [[algae]] (phytoplankton), [[protozoa]] (zooplankton), and many [[mixoplankton]].<ref name="Millette2024">{{cite journal | last1=Millette | first1=Nicole C. | last2=Leles | first2=Suzana G. | last3=Johnson | first3=Matthew D. | last4=Maloney | first4=Ashley E. | last5=Brownlee | first5=Emily F. | last6=Cohen | first6=Natalie R. | last7=Duhamel | first7=Solange | last8=Poulton | first8=Nicole J. | last9=Princiotta | first9=Sarah D. | last10=Stamieszkin | first10=Karen | last11=Wilken | first11=Susanne | last12=Moeller | first12=Holly V. | title=Recommendations for advancing mixoplankton research through empirical-model integration | journal=Frontiers in Marine Science | volume=11 | date=2024-06-05 | issn=2296-7745 | doi=10.3389/fmars.2024.1392673 | doi-access=free | page=}}</ref> | |||
* '''[[Marine fungus|planktonic fungi]]:''' – known also as '''[[mycoplankton]]''', play important roles in [[remineralisation]] and [[nutrient cycling]].<ref>{{cite book |last1=Wang |first1=G. |last2= Wang, X. |last3= Liu |first3=X. |last4=Li |first4= Q. |editor-last=Raghukumar |editor-first=Chandralata |date=2012 |chapter=Diversity and biogeochemical function of planktonic fungi in the ocean |title=Biology of Marine Fungi |url=https://books.google.com/books?id=1kE5OpuGp9YC |publisher=Springer Berlin Heidelberg |pages=71–88 |isbn=978-3-642-23342-5}}</ref> For example, in the [[mycoloop]], parasitic [[chytrid]]s facilitate the transfer of nutrients from large, inedible phytoplankton to zooplankton. | |||
* '''[[planktonic prokaryotes]]:''' – ([[bacteria]] and [[archaea]] – planktonic bacteria are known also as '''[[bacterioplankton]]''') can play important roles as primary producers, or in remineralising organic material like mycoplankton down the water column. [[Photosynthetic]] [[cyanobacteria]] are important members of the phytoplankton. The unusually small ''[[Pelagibacter ubique]]'', perhaps the most abundant bacterium on Earth, makes up about one third of microbial cells in the surface ocean,<ref>"''Candidatus'' Pelagibacter ubique." European Bioinformatics Institute. European Bioinformatics Institute, 2011. Web. 08 Jan. 2012. http://www.ebi.ac.uk/2can/genomes/bacteria/Candidatus_Pelagibacter_ubique.html {{webarchive |url=https://web.archive.org/web/20081201014010/http://www.ebi.ac.uk/2can/genomes/bacteria/Candidatus_Pelagibacter_ubique.html |date=December 1, 2008 }}</ref> and plays important roles recycling nutrients in the [[microbial loop]]. The ''[[Roseobacter]]'' clade are significantly connected to phytoplankton. | |||
*'''[[ | * '''[[Marine virus|planktonic viruses]]:''' – known also as '''[[virioplankton]]''', though not always classified as living organisms, are abundant in planktonic communities and influence microbial dynamics. Viruses are small [[pathogen|infectious agent]]s that can [[Replicate (biology)|replicate]] only inside the living [[Cell (biology)|cells]] of a [[Host (biology)|host]] [[organism]], because they need the replication machinery of the host to do so.<ref name="Brussaard_2016">{{cite book |last1=Brussaard |first1=Corina P.D. |last2=Baudoux|first2=Anne-Claire|last3=Rodríguez-Valera|first3=Francisco|editor2-last=Cretoiu|editor2-first=Mariana Silvia |chapter=Marine Viruses|date=2016 |title=The Marine Microbiome|pages=155–183|editor-last=Stal|editor-first=Lucas J.|publisher=[[Springer International Publishing]]|language=en|doi=10.1007/978-3-319-33000-6_5|isbn=978-3-319-32998-7 }}</ref> They are more abundant in the plankton than bacteria and archaea, though much smaller.<ref>{{cite journal |last1=Wommack |first1=K.E. |last2=Colwell |first2=R.R. |date=March 2000 |title=Virioplankton: viruses in aquatic ecosystems |journal=Microbiology and Molecular Biology Reviews |volume=64 |issue=1 |pages=69–114 |doi=10.1128/MMBR.64.1.69-114.2000 |pmid=10704475 |pmc=98987 }}</ref><ref>{{cite web |title=Plankton |url=https://education.nationalgeographic.org/resource/plankton/ |website=Resource Library |publisher=[[National Geographic]] |access-date=13 September 2019}}</ref> Viruses can infect all types of [[life forms]], from [[animal]]s and [[plant]]s to [[microorganism]]s, including [[bacteria]] and [[archaea]].<ref name=Koonin2006>{{cite journal |vauthors=Koonin EV, Senkevich TG, Dolja VV |title=The ancient Virus World and evolution of cells |journal=[[Biology Direct]] |volume=1 |page=29 |year=2006 |pmid=16984643 |pmc=1594570 |doi=10.1186/1745-6150-1-29 |doi-access=free }} [[File:CC-BY icon.svg|50px]] Modified text was copied from this source, which is available under a [https://creativecommons.org/licenses/by/2.0/ Creative Commons Attribution 2.0 International License].</ref> In the [[viral shunt]], viruses infect and break down ([[Lytic cycle|lyse]]) bacteria, releasing their nutrients and organic matter back into the water instead of allowing them to be consumed by larger organisms like zooplankton. This "shunts" nutrients away from higher trophic levels, keeping them in the microbial loop for reuse by other microorganisms. | ||
== | <gallery mode="packed" style="float:left" heights="220px"> | ||
[[File: | File:Copépodo campo oscuro.jpg|This planktonic animal (metazoa) is a female [[copepod]]. It has two egg sacs and microalgae attached to its body | ||
File:Haeckel Phaeodaria 61.jpg|These are shells of planktonic protists called [[radiolarian]]s, drawn by [[Ernst Haeckel]] (1904) | |||
File:Prochlorococcus marinus (cropped).jpg|This planktonic bacterium is the [[cyanobacterium]] ''[[Prochlorococcus]]'', the smallest photosynthetic organism in the world. It contributes up to 20% of the world's oxygen production, more than all tropical rainforests.<ref name="s250">{{cite web | title=How much oxygen comes from the ocean? | website=NOAA's National Ocean Service | url=https://oceanservice.noaa.gov/facts/ocean-oxygen.html | access-date=2025-07-17}} {{PD-notice}}</ref> | |||
File:Virus cocco 2.jpg| This planktonic virus (arrowed) is the giant coccolithovirus, ''[[Emiliania huxleyi virus 86]]'', infecting an ''[[Emiliania huxleyi]]'' coccolithophore | |||
</gallery> | |||
{{clear}} | |||
{{multiple image | |||
| align = left | |||
| direction = horizontal | |||
| width = 750 | |||
| header = Plankton sizes by taxonomic groups{{hsp}}<ref>{{cite journal |doi = 10.1371/journal.pbio.1001177|title = A Holistic Approach to Marine Eco-Systems Biology|year = 2011|last1 = Karsenti|first1 = Eric|last2 = Acinas|first2 = Silvia G.|last3 = Bork|first3 = Peer|last4 = Bowler|first4 = Chris|last5 = De Vargas|first5 = Colomban|last6 = Raes|first6 = Jeroen|last7 = Sullivan|first7 = Matthew|last8 = Arendt|first8 = Detlev|last9 = Benzoni|first9 = Francesca|last10 = Claverie|first10 = Jean-Michel|last11 = Follows|first11 = Mick|last12 = Gorsky|first12 = Gaby|last13 = Hingamp|first13 = Pascal|last14 = Iudicone|first14 = Daniele|last15 = Jaillon|first15 = Olivier|last16 = Kandels-Lewis|first16 = Stefanie|last17 = Krzic|first17 = Uros|last18 = Not|first18 = Fabrice|last19 = Ogata|first19 = Hiroyuki|last20 = Pesant|first20 = Stéphane|last21 = Reynaud|first21 = Emmanuel Georges|last22 = Sardet|first22 = Christian|last23 = Sieracki|first23 = Michael E.|last24 = Speich|first24 = Sabrina|last25 = Velayoudon|first25 = Didier|last26 = Weissenbach|first26 = Jean|last27 = Wincker|first27 = Patrick|journal = PLOS Biology|volume = 9|issue = 10|article-number = e1001177|pmid = 22028628|pmc = 3196472 | doi-access=free |display-authors = 4}}</ref> | |||
| header_align = center | |||
| image1 = Plankton size.png | |||
| alt1 = Plankton sizes by taxonomic groups | |||
| caption1 = | |||
}} | |||
{{clear}} | |||
== By size == | |||
Plankton are also often described in terms of size. Usually the following divisions are used:{{hsp}}<ref>{{cite book| last = Omori | first = M. | author2=Ikeda, T. | year=1992 | title = Methods in Marine Zooplankton Ecology | publisher = Krieger Publishing Company | location = Malabar, USA | isbn = 978-0-89464-653-9}}</ref> | Plankton are also often described in terms of size. Usually the following divisions are used:{{hsp}}<ref>{{cite book| last = Omori | first = M. | author2=Ikeda, T. | year=1992 | title = Methods in Marine Zooplankton Ecology | publisher = Krieger Publishing Company | location = Malabar, USA | isbn = 978-0-89464-653-9}}</ref> | ||
::{| class="wikitable" | ::{| class="wikitable" | ||
|width="120"| '''Group''' | |width="120"| '''Group''' | ||
|width="100"| '''Size range''' | |width="100"| '''Size range''' ([[Equivalent spherical diameter|ESD]]) | ||
|width="350"| '''Examples''' | |width="350"| '''Examples''' | ||
|- | |- | ||
| Megaplankton ||> 20 cm || [[metazoan]]s; ''e.g.'' [[jellyfish]]; [[Ctenophora (phylum)|ctenophores]]; [[salp]]s and [[pyrosome]]s (pelagic [[Tunicata]]); [[Cephalopoda]]; [[Amphipoda]] | | Megaplankton ||> 20 cm || [[metazoan]]s; ''e.g.'' [[jellyfish]]; [[Ctenophora (phylum)|ctenophores]]; [[salp]]s and [[pyrosome]]s (pelagic [[Tunicata]]); [[Cephalopoda]]; [[Amphipoda]] | ||
|- | |- | ||
| Macroplankton || 2→20 cm || [[metazoans]]; ''e.g.'' [[Pteropoda]]; [[Chaetognath]]s | | Macroplankton || 2→20 cm || [[metazoans]]; ''e.g.'' [[Pteropoda]]; [[Chaetognath]]s; [[Medusae]]; [[Ctenophora (phylum)|ctenophores]]; [[salp]]s, doliolids and [[pyrosome]]s (pelagic [[Tunicata]]); [[Cephalopoda]]; [[Janthina]] and [[Recluzia]] (two genera of gastropods); [[Amphipoda]] | ||
|- | |- | ||
| Mesoplankton || 0.2→20 mm || [[metazoan]]s; ''e.g.'' [[copepod]]s; [[Medusae]]; [[Cladocera]]; [[Ostracoda]]; [[Chaetognath]]s; [[Pteropoda]]; [[Tunicata]] | | Mesoplankton || 0.2→20 mm || [[metazoan]]s; ''e.g.'' [[copepod]]s; [[Medusae]]; [[Cladocera]]; [[Ostracoda]]; [[Chaetognath]]s; [[Pteropoda]]; [[Tunicata]] | ||
|- | |- | ||
| Microplankton || 20→200 [[Micrometre|μm]] || large [[eukaryote|eukaryotic]] [[protist]]s; most [[phytoplankton]]; [[Protozoa]] [[Foraminifera]]; [[tintinnid]]s; other [[ciliate]]s; [[Rotifera]]; juvenile [[metazoan]]s – [[crustacean|Crustacea]] ([[copepod]] nauplii) | | [[Microplankton]] || 20→200 [[Micrometre|μm]] || large [[eukaryote|eukaryotic]] [[protist]]s; most [[phytoplankton]]; [[Protozoa]] [[Foraminifera]]; [[tintinnid]]s; other [[ciliate]]s; [[Rotifera]]; juvenile [[metazoan]]s – [[crustacean|Crustacea]] ([[copepod]] nauplii) | ||
|- | |- | ||
| Nanoplankton || 2→20 μm || small [[eukaryotic]] [[protist]]s; small [[diatom]]s; small [[flagellate]]s; [[Pyrrophyta]]; [[Chrysophyta]]; [[Chlorophyta]]; [[Xanthophyta]] | | Nanoplankton || 2→20 μm || small [[eukaryotic]] [[protist]]s; small [[diatom]]s; small [[flagellate]]s; [[Pyrrophyta]]; [[Chrysophyta]]; [[Chlorophyta]]; [[Xanthophyta]] | ||
| Line 70: | Line 150: | ||
|} | |} | ||
However, some of these terms may be used with very different boundaries, especially on the larger end. The existence and importance of nano- and even smaller plankton was only discovered during the 1980s, but they are thought to make up the largest proportion of all plankton in number and diversity. | However, some of these terms may be used with very different boundaries, especially on the larger end. The term ''microplankton'' is sometimes used more broadly to cover plankton that cannot really be seen without using a microscope, say plankton less than about one millimetre across. The existence and importance of nano- and even smaller plankton was only discovered during the 1980s, but they are thought to make up the largest proportion of all plankton in number and diversity. It is the largely unseen microplankton that are the main drivers of the [[marine food web]]. | ||
Microplankton and smaller groups are [[microorganism]]s that operate at low [[Reynolds number]]s, where the viscosity of water is more important than its mass or inertia.<ref>{{cite book |author=Dusenbery, David B. |title=Living at micro scale: the unexpected physics of being small |publisher=Harvard University Press |location= Cambridge |year=2009 |isbn=978-0-674-03116-6 }}</ref> | |||
<ref>{{cite book |author=Dusenbery, David B. |title=Living at micro scale: the unexpected physics of being small |publisher=Harvard University Press |location= Cambridge |year=2009 |isbn=978-0-674-03116-6 }}</ref> | |||
<gallery mode="packed" style="float:left" | <gallery mode="packed" style="float:left;" caption="Microplankton"> | ||
File: | File:Diatoms through the microscope.jpg|Some marine [[diatom]]s — a key [[phytoplankton]] group | ||
File: Pelagibacter.jpg|''[[Pelagibacter ubique]]'', the most common bacteria in the ocean, plays a major role in global [[carbon cycle]]s | |||
File:Noctiluca scintillans varias.jpg|The [[Noctiluca scintillans|sea sparkle]] [[dinoflagellate]] glows in the night to produce the [[milky seas effect]] | |||
File:Dinoflagellates and a tintinnid ciliate.jpg|Microzooplankton are major grazers of the plankton: two [[dinoflagellate]]s and a [[tintinnid]] ciliate. | |||
</gallery> | |||
{{clear}} | |||
<gallery mode="packed" style="float:left;" caption="Macroplankton"> | |||
File:hyperia.jpg | Macrozooplankton: the [[amphipoda|amphipod]] ''[[Hyperia macrocephala]]'' | |||
File:Mnemiopsis leidyi 2.jpg|The [[sea walnut]] [[ctenophore]] has a transient anus which forms only when it needs to defecate<ref>{{cite magazine| title=Animal with an anus that comes and goes could reveal how ours evolved| author=Michael Le Page| magazine=New Scientist| url=https://www.newscientist.com/article/2195656-animal-with-an-anus-that-comes-and-goes-could-reveal-how-ours-evolved/| date=March 2019}}</ref> | |||
File:Janthina.jpg|A ''[[Janthina janthina]]'' snail (with bubble float) cast up onto a beach in [[Maui]] | |||
File:Sargassum on the beach, Cuba.JPG|[[Sargassum]] seaweed drifts with currents using air bladders to stay afloat | |||
</gallery> | |||
{{clear}} | |||
== By trophic mode == | |||
[[Trophic mode]] describes the role of a planktonic organism in the [[food web]] based on how it obtains energy and nutrients to sustain its growth, reproduction, and survival.<ref name=Lalli1997 /> By trophic mode, plankton can be divided into four broad functional groups: phytoplankton, zooplankton, mixoplankton and decomposers.<ref name="Flynn2013">{{cite journal | last1=Flynn | first1=Kevin J. | last2=Stoecker | first2=Diane K. | last3=Mitra | first3=Aditee | last4=Raven | first4=John A. | last5=Glibert | first5=Patricia M. | last6=Hansen | first6=Per Juel | last7=Granéli | first7=Edna | last8=Burkholder | first8=Joann M. | title=Misuse of the phytoplankton–zooplankton dichotomy: the need to assign organisms as mixotrophs within plankton functional types | journal=Journal of Plankton Research | volume=35 | issue=1 | date=2013-01-01 | issn=1464-3774 | doi=10.1093/plankt/fbs062 | doi-access=free | pages=3–11 | url=https://academic.oup.com/plankt/article-pdf/35/1/3/4354133/fbs062.pdf | access-date=2025-08-11| display-authors=4 }}</ref><ref name="Mitra2016">{{cite journal | last1=Mitra | first1=Aditee | last2=Flynn | first2=Kevin J. | last3=Tillmann | first3=Urban | last4=Raven | first4=John A. | last5=Caron | first5=David | last6=Stoecker | first6=Diane K. | last7=Not | first7=Fabrice | last8=Hansen | first8=Per J. | last9=Hallegraeff | first9=Gustaaf | last10=Sanders | first10=Robert | last11=Wilken | first11=Susanne | last12=McManus | first12=George | last13=Johnson | first13=Mathew | last14=Pitta | first14=Paraskevi | last15=Våge | first15=Selina | last16=Berge | first16=Terje | last17=Calbet | first17=Albert | last18=Thingstad | first18=Frede | last19=Jeong | first19=Hae Jin | last20=Burkholder | first20=JoAnn | last21=Glibert | first21=Patricia M. | last22=Granéli | first22=Edna | last23=Lundgren | first23=Veronica | title=Defining Planktonic Protist Functional Groups on Mechanisms for Energy and Nutrient Acquisition: Incorporation of Diverse Mixotrophic Strategies | journal=Protist | volume=167 | issue=2 | date=2016 | doi=10.1016/j.protis.2016.01.003 | doi-access=free | pages=106–120| display-authors=4 | hdl=1912/7897 | hdl-access=free }}</ref><ref name="Flynn2019">{{cite journal | last1=Flynn | first1=Kevin J | last2=Mitra | first2=Aditee | last3=Anestis | first3=Konstantinos | last4=Anschütz | first4=Anna A | last5=Calbet | first5=Albert | last6=Ferreira | first6=Guilherme Duarte | last7=Gypens | first7=Nathalie | last8=Hansen | first8=Per J | last9=John | first9=Uwe | last10=Martin | first10=Jon Lapeyra | last11=Mansour | first11=Joost S | last12=Maselli | first12=Maira | last13=Medić | first13=Nikola | last14=Norlin | first14=Andreas | last15=Not | first15=Fabrice | last16=Pitta | first16=Paraskevi | last17=Romano | first17=Filomena | last18=Saiz | first18=Enric | last19=Schneider | first19=Lisa K | last20=Stolte | first20=Willem | last21=Traboni | first21=Claudia | title=Mixotrophic protists and a new paradigm for marine ecology: where does plankton research go now? | journal=Journal of Plankton Research | volume=41 | issue=4 | date=2019-07-26 | issn=0142-7873 | doi=10.1093/plankt/fbz026 | doi-access=free | pages=375–391 | url=https://academic.oup.com/plankt/article-pdf/41/4/375/30279486/fbz026.pdf | access-date=2025-08-09| display-authors=4 }}</ref><ref name="Manifesto" /> | |||
===Phytoplankton=== | |||
[[Phytoplankton]] (from Greek ''phyton'', or plant) are [[autotroph]]ic [[prokaryote|prokaryotic]] or [[eukaryote|eukaryotic]] [[algae]] that live near the water surface where there is sufficient [[light]] to support [[photosynthesis]]. Among the more important groups are the [[diatom]]s, [[cyanobacteria]], [[dinoflagellate]]s, and [[coccolithophore]]s. | |||
<gallery mode="packed" style="float:left;" caption="Phytoplankton largely form the base of the [[marine food web]]"> | |||
File:Diatoms through the microscope.jpg|[[Diatom]]s are one of the most common types of phytoplankton | |||
File:Triceratium morlandii var. morlandii.jpg|Fossil diatom [[frustule]] from 32 to 40 [[mya (unit)|mya]] | |||
File:CSIRO ScienceImage 4203 A bluegreen algae species Cylindrospermum sp under magnification.jpg|A [[cyanobacteria]] species (''Cylindrospermum'' sp) | |||
File:Pyramimonas sp.jpg| Green algae, ''[[Pyramimonas]]'' | |||
</gallery> | </gallery> | ||
{{clear}} | |||
===Zooplankton=== | |||
[[Zooplankton]] (from Greek ''zoon'', or animal) are small [[protozoa]]ns or [[metazoa]]ns (e.g. [[crustacean]]s and other [[animal]]s) that feed on other plankton. Some of the [[egg]]s and [[larva]]e of larger nektonic animals, such as fish, crustaceans, and [[annelid]]s, are included here. | |||
<gallery mode="packed" style="float:left;" caption="Larger plankton tend to be zooplankton which eat smaller phytoplankton"> | |||
File:Clupeaharenguslarvaeinsitukils.jpg|[[Herring]] larva imaged with the remains of the [[yolk]] and the long gut visible in the transparent animal | |||
File:Icefishuk.jpg|[[Notothenioidei|Icefish]] larvae from Antarctica have no haemoglobin | |||
File:Copepodkils.jpg|[[Copepod]] from Antarctica, a translucent ovoid microanimal with two long antennae | |||
File:Krill666.jpg|A [[krill]] larva is zooplankton, though an adult (shown) is [[nekton]] | |||
</gallery> | |||
{{clear}} | {{clear}} | ||
== | ===Mixoplankton=== | ||
[[Mixoplankton]] (from Greek ''mixis'', or mixture) have a mixed trophic strategy. In recent years, there has been a growing recognition that perhaps the majority of plankton can act in both the above modes. | |||
=== | Traditionally, plankton were divided into just the first two broad trophic groups: plant-like phytoplankton which make their own food, usually by photosynthesis, and animal-like zooplankton that eat other plankton. In recent years, there has been a recognition that many plankton, perhaps over half, are [[mixotrophic]].<ref>{{cite web |url=https://www.irishexaminer.com/lifestyle/outdoors/richard-collins/beware-the-mixotrophs--they-can-destroy-entire-ecosystems-in-a-matter-of-hours-430358.html |author=Richard Collins |date=2016-11-14 |title=Beware the mixotrophs – they can destroy entire ecosystems 'in a matter of hours' |work=Irish Examiner}}</ref> Plankton have traditionally been categorized as [[Autotroph|producer]], [[Heterotroph|consumer]], and recycler groups, but some plankton are able to benefit from more than just one trophic level. This mixed trophic strategy means mixoplankton can act as both producers and consumers, either at the same time or switching between modes of nutrition in response to ambient conditions. In this manner, mixoplankton can use photosynthesis for growth when nutrients and light are abundant, but switch to eating phytoplankton, zooplankton or each other when growing conditions are poor. | ||
=== | As a result of these findings, many plankton formally categorized as phytoplankton, including [[Coccolithophore|coccolithophores]] and [[Dinoflagellate|dinoflagellates]], are longer included as strictly phytoplankton, as they not only produce their own food through [[Photoautotrophism|phototrophy]] but can also eat other organisms.<ref>{{Cite journal |last1=Mitra |first1=Aditee |last2=Caron |first2=David A. |last3=Faure |first3=Emile |last4=Flynn |first4=Kevin J. |last5=Leles |first5=Suzana Gonçalves |last6=Hansen |first6=Per J. |last7=McManus |first7=George B. |last8=Not |first8=Fabrice |last9=do Rosario Gomes |first9=Helga |last10=Santoferrara |first10=Luciana F. |last11=Stoecker |first11=Diane K. |last12=Tillmann |first12=Urban |date=27 February 2023 |title=The Mixoplankton Database (MDB): Diversity of photo-phago-trophic plankton in form, function, and distribution across the global ocean |url=https://onlinelibrary.wiley.com/doi/10.1111/jeu.12972 |journal=Journal of Eukaryotic Microbiology |language=en |volume=70 |issue=4 |article-number=e12972 |doi=10.1111/jeu.12972 |pmid=36847544 |issn=1066-5234}}</ref> These organisms are now more correctly termed mixoplankton.<ref name="Flynn2019" /> This recognition has important consequences for how the functioning of the planktonic food web is viewed.<ref>{{Cite journal |last1=Glibert |first1=Patricia M. |last2=Mitra |first2=Aditee |date=2022-01-21 |title=From webs, loops, shunts, and pumps to microbial multitasking: Evolving concepts of marine microbial ecology, the mixoplankton paradigm, and implications for a future ocean |journal=Limnology and Oceanography |volume=67 |issue=3 |pages=585–597 |doi=10.1002/lno.12018 |bibcode=2022LimOc..67..585G |issn=0024-3590}}</ref> | ||
<gallery mode="packed" style="float:left;" caption="Mixoplankton can behave both as phytoplankton and zooplankton"> | |||
<gallery mode="packed" style="float: | File:Paramecium bursaria.jpg|A single-celled [[ciliate]] with green [[zoochlorellae]] living inside [[endosymbiotic]]ally | ||
File: | File:Euglena mutabilis - 400x - 1 (10388739803) (cropped).jpg| ''[[Euglena|Euglena mutabilis]]'', a photosynthetic [[flagellate]] | ||
File:Karenia_brevis.jpg|The mixotrophic dinoflagellate ''[[Karenia brevis]]'' causes harmful [[red tide]]s | |||
File:Phaeocystis symbionts within an acantharian host.png|[[Acantharian]] radiolarian hosts ''[[Phaeocystis]]'' symbionts. | |||
File:Ecomare - schuimalg strand (7037-schuimalg-phaeocystis-ogb).jpg|White ''Phaeocystis'' algal foam washing up on a beach | |||
</gallery> | </gallery> | ||
{{ | {{clear}} | ||
Mixotrophs can be further divided into two groups; [[constitutive mixotroph]]s which are able to perform photosynthesis on their own, and non-constitutive mixotrophs which use [[phagocytosis]] to engulf phototrophic prey that are either kept alive inside the host cell, which benefits from its photosynthesis, or they digested, except for the [[plastid]]s, which continue to perform photosynthesis ([[kleptoplasty]]).<ref>{{cite journal| url = https://academic.oup.com/plankt/article/40/6/627/5165357| title = Modelling mixotrophic functional diversity and implications for ecosystem function - Oxford Journals| journal = Journal of Plankton Research| date = November 2018| volume = 40| issue = 6| pages = 627–642| doi = 10.1093/plankt/fby044| last1 = Leles| first1 = Suzana Gonçalves| url-access = subscription}}</ref> | |||
Recognition of the importance of mixotrophy as an ecological strategy is increasing,<ref>{{cite journal |last1=Hartmann |first1=M. |last2=Grob |first2=C. |last3=Tarran |first3=G.A. |last4=Martin |first4=A.P. |last5=Burkill |first5=P.H. |last6=Scanlan |first6=D.J. |last7=Zubkov |first7=M.V. |date=2012 |title=Mixotrophic basis of Atlantic oligotrophic ecosystems |journal=Proc. Natl. Acad. Sci. USA |volume=109 |issue=15 |pages=5756–5760 |doi=10.1073/pnas.1118179109 |pmid=22451938 |pmc=3326507 |bibcode=2012PNAS..109.5756H |doi-access=free }}</ref> as well as the wider role this may play in marine [[biogeochemistry]].<ref>{{cite journal |last1=Ward |first1=B.A. |last2=Follows |first2=M.J. |date=2016 |title=Marine mixotrophy increases trophic transfer efficiency, mean organism size, and vertical carbon flux |journal=Proc. Natl. Acad. Sci. USA |volume=113 |issue=11 |pages=2958–2963 |doi=10.1073/pnas.1517118113 |pmid=26831076 |pmc=4801304 |bibcode=2016PNAS..113.2958W |doi-access=free }}</ref> Studies have shown that mixoplankton are much more important for marine ecology than previously assumed.<ref>{{cite magazine| url = https://www.the-scientist.com/news-opinion/mixing-it-up-in-the-web-of-life-65431| title = Mixing It Up in the Web of Life| magazine = The Scientist Magazine| access-date = <!-- unknown, too far back -->| archive-date = 2021-01-21| archive-url = https://web.archive.org/web/20210121092951/https://www.the-scientist.com/news-opinion/mixing-it-up-in-the-web-of-life-65431}}</ref><ref>{{cite web| url = https://theconversation.com/uncovered-the-mysterious-killer-triffids-that-dominate-life-in-our-oceans-67387| title = Uncovered: the mysterious killer triffids that dominate life in our oceans| date = 3 November 2016}}</ref> Their presence acts as a buffer that prevents the collapse of ecosystems during times with little to no light.<ref>{{Cite web |url=https://www.astrobio.net/news-exclusive/catastrophic-darkness/ |title=Catastrophic Darkness |work=Astrobiology Magazine |access-date=2019-11-27 |archive-url=https://web.archive.org/web/20150926012623/http://www.astrobio.net/news-exclusive/catastrophic-darkness/ |archive-date=2015-09-26 }}</ref> Mixoplankton have ancient origins and have been recognized by scientists for over a century. However, it is only in recent years that the widespread significance of mixoplankton has been gaining recognition in mainstream marine science.<ref name="Mitra2023">{{cite journal | last=Mitra | first=Aditee | last2=Caron | first2=David A. | last3=Faure | first3=Emile | last4=Flynn | first4=Kevin J. | last5=Leles | first5=Suzana Gonçalves | last6=Hansen | first6=Per J. | last7=McManus | first7=George B. | last8=Not | first8=Fabrice | last9=do Rosario Gomes | first9=Helga | last10=Santoferrara | first10=Luciana F. | last11=Stoecker | first11=Diane K. | last12=Tillmann | first12=Urban | title=The Mixoplankton Database (MDB): Diversity of photo‐phago‐trophic plankton in form, function, and distribution across the global ocean | journal=Journal of Eukaryotic Microbiology | volume=70 | issue=4 | date=2023 | issn=1066-5234 | doi=10.1111/jeu.12972 | doi-access=free | url=https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/jeu.12972 | access-date=2025-08-04 | page=}}</ref> | |||
===Decomposers=== | |||
Instead of directly building biomass, [[decomposer]]s break organic nutrients down into inorganic forms which can be recycled (an approach which metabolically can be costly).<ref name="Manifesto" /> | |||
Fungi: Mostly tiny [[mycoplankton]] ([[microfungi]]), [[yeast]], or mobile [[zoospore]]s, that can recycle organic matter through a process called the [[mycoloop]] which involves parasiting plankton.<ref name="Manifesto" /> | |||
=== | Bacteria/Archaea: These minute prokaryotes (typically <0.001mm) return organic nutrients to inorganic forms by breaking down [[particulate organic matter|particulate]] and [[dissolved organic matter]] through the process called the [[microbial loop]].<ref name="Azam1983">Azam, F., Fenchel, T., Field, J.G., Gray, J.S., Meyer-Reil, L.A. and Thingstad, F.J.M.E.P.S., 1983. [https://scholar.google.com/scholar?hl=en&as_sdt=0%2C5&q=The+ecological+role+of+water-column+microbes+in+the+sea&btnG= "The ecological role of water-column microbes in the sea"] ''Marine ecology progress series''. Oldendorf, 10(3), pp.257-263.</ref> Some convert ammonium in animal waste to nitrate, while others transform nitrate to nitrogen gas. Viral infections likely destroy many, while others are eaten by protist zooplankton and mixoplankton, which use their nutrients for photosynthesis. However details of their ecology is complex and it is not clear what sustains them.<ref name="Manifesto" /> | ||
Viruses: Typically 10 to 100 times smaller than bacteria and also the most abundant (~100 billion per litre), viruses infect other plankton and larger organisms. It is thought they efficiently halt vast plankton blooms within days, by turning biomass into dissolved organic matter that supports bacterial growth through a process called the [[viral shunt]].<ref name="Suttle2007">Suttle, C.A., 2007. [https://scholar.google.com/scholar_lookup?hl=en&volume=5&publication_year=2007&pages=801-812&journal=Nature+Reviews+Microbiology&author=C.A.+Suttle&title=Marine+viruses%E2%80%94major+players+in+the+global+ecosystem "Marine viruses—major players in the global ecosystem."] ''Nature reviews microbiology'', 5(10), pp.801–812.</ref> Being host-specific, they also likely influence the [[Biological pump|biological]] and [[microbial carbon pump]]s.<ref name="Manifesto" /> | |||
==Other groups== | ==Other groups== | ||
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[[File:Salmonlarvakils 2.jpg|thumb|Salmon egg hatching into a ''sac fry''. In a few days, the sac fry will absorb the yolk sac and start feeding on smaller plankton.]] | [[File:Salmonlarvakils 2.jpg|thumb|Salmon egg hatching into a ''sac fry''. In a few days, the sac fry will absorb the yolk sac and start feeding on smaller plankton.]] | ||
[[Ichthyoplankton]] are the [[Fish eggs|eggs]] and [[larvae]] of fish. They are mostly found in the sunlit zone of the [[water column]], less than 200 metres deep, which is sometimes called the [[epipelagic]] or [[photic zone]]. Ichthyoplankton are [[planktonic]], meaning they cannot swim effectively under their own power, but must drift with the ocean currents. Fish eggs cannot swim at all, and are unambiguously planktonic. Early stage larvae swim poorly, but later stage larvae swim better and cease to be planktonic as they grow into [[Juvenile fish|juveniles]]. Fish larvae are part of the [[zooplankton]] that eat smaller plankton, while fish eggs carry their food supply. Both eggs and larvae are themselves eaten by larger animals.<ref name=NOAA>[http://swfsc.noaa.gov/textblock.aspx?Division=FRD&id=6210 What are Ichthyoplankton?] Southwest Fisheries Science Center, NOAA. Modified 3 September 2007. Retrieved 22 July 2011.</ref><ref name=Moser2006>{{Cite book|url=https://books.google.com/books?id=Qdzg0Vfql2sC&pg=PA269|title = The Ecology of Marine Fishes: California and Adjacent Waters|pages = 269–319|isbn = | [[Ichthyoplankton]] are the [[Fish eggs|eggs]] and [[larvae]] of fish. They are mostly found in the sunlit zone of the [[water column]], less than 200 metres deep, which is sometimes called the [[epipelagic]] or [[photic zone]]. Ichthyoplankton are [[planktonic]], meaning they cannot swim effectively under their own power, but must drift with the ocean currents. Fish eggs cannot swim at all, and are unambiguously planktonic. Early stage larvae swim poorly, but later stage larvae swim better and cease to be planktonic as they grow into [[Juvenile fish|juveniles]]. Fish larvae are part of the [[zooplankton]] that eat smaller plankton, while fish eggs carry their own food supply. Both eggs and larvae are themselves eaten by larger animals.<ref name=NOAA>[http://swfsc.noaa.gov/textblock.aspx?Division=FRD&id=6210 What are Ichthyoplankton?] Southwest Fisheries Science Center, NOAA. Modified 3 September 2007. Retrieved 22 July 2011.</ref><ref name=Moser2006>{{Cite book|url=https://books.google.com/books?id=Qdzg0Vfql2sC&pg=PA269|title = The Ecology of Marine Fishes: California and Adjacent Waters|pages = 269–319|isbn = 978-0-520-93247-0|last1 = Allen|first1 = Dr. Larry G.|last2 = Horn|first2 = Dr. Michael H.|date = 15 February 2005| publisher=University of California Press }}</ref> Fish can produce high numbers of eggs which are often released into the open water column. Fish eggs typically have a diameter of about {{convert|1|mm}}. The newly hatched young of oviparous fish are called [[larva]]e. They are usually poorly formed, carry a large [[yolk sac]] (for nourishment), and are very different in appearance from juvenile and adult specimens. The larval period in oviparous fish is relatively short (usually only several weeks), and larvae rapidly grow and change appearance and structure (a process termed [[metamorphosis]]) to become juveniles. During this transition larvae must switch from their yolk sac to feeding on [[zooplankton]] prey, a process which depends on typically inadequate zooplankton density, starving many larvae. In time fish larvae become able to swim against currents, at which point they cease to be plankton and become [[juvenile fish]]. | ||
===Pseudoplankton=== | ===Pseudoplankton=== | ||
{{main|Pseudoplankton}} | {{main|Pseudoplankton}} | ||
[[Pseudoplankton]] are organisms that attach themselves to planktonic organisms or other floating objects, such as drifting wood, [[buoyant]] shells of organisms such as ''[[Spirula]]'', or man-made [[flotsam]]. Examples include [[goose barnacle]]s and the bryozoan ''[[Jellyella]]''. By themselves these animals cannot [[Buoyancy|float]], which contrasts them with true planktonic organisms, such as ''[[Velella]]'' and the [[Portuguese Man o' War]], which are buoyant. Pseudoplankton are often found in the guts of filtering [[Zooplankton|zooplankters]].<ref>{{cite book|title=Coral Reef Ecology|first=Yuri I. |last=Sorokin|publisher=Springer Science & Business Media|date=12 March 2013|page=96|isbn= | [[Pseudoplankton]] are organisms that attach themselves to planktonic organisms or other floating objects, such as drifting wood, [[buoyant]] shells of organisms such as ''[[Spirula]]'', or man-made [[flotsam]]. Examples include [[goose barnacle]]s and the bryozoan ''[[Jellyella]]''. By themselves these animals cannot [[Buoyancy|float]], which contrasts them with true planktonic organisms, such as ''[[Velella]]'' and the [[Portuguese Man o' War]], which are buoyant. Pseudoplankton are often found in the guts of filtering [[Zooplankton|zooplankters]].<ref>{{cite book|title=Coral Reef Ecology|first=Yuri I. |last=Sorokin|publisher=Springer Science & Business Media|date=12 March 2013|page=96|isbn=978-3-642-80046-7 |url=https://books.google.com/books?id=hKvrCAAAQBAJ}}</ref> | ||
===Tychoplankton=== | ===Tychoplankton=== | ||
{{main|Tychoplankton}} | {{main|Tychoplankton}} | ||
[[Tychoplankton]] are organisms, such as free-living or attached [[Benthos|benthic organism]]s and other non-planktonic organisms, that are carried into the plankton through a disturbance of their benthic habitat, or by winds and currents.<ref name=Margulis_2009>{{cite book|last1=Chapman|first1=Michael J. | first2=Lynn | last2=Margulis | author-link=Lynn Margulis|title=Kingdoms and Domains: An Illustrated Guide to the Phyla of Life on Earth|url=https://archive.org/details/fivekingdomsillu00marg_711|url-access=limited|year=2009|publisher=Academic Press/Elsevier|location=Amsterdam|isbn=978- | [[Tychoplankton]] are organisms, such as free-living or attached [[Benthos|benthic organism]]s and other non-planktonic organisms, that are carried into the plankton through a disturbance of their benthic habitat, or by winds and currents.<ref name=Margulis_2009>{{cite book|last1=Chapman|first1=Michael J. | first2=Lynn | last2=Margulis | author-link=Lynn Margulis|title=Kingdoms and Domains: An Illustrated Guide to the Phyla of Life on Earth|url=https://archive.org/details/fivekingdomsillu00marg_711|url-access=limited|year=2009|publisher=Academic Press/Elsevier|location=Amsterdam|isbn=978-0-12-373621-5|pages=[https://archive.org/details/fivekingdomsillu00marg_711/page/n619 566]|edition=[4th ed.].}}</ref> This can occur by direct [[turbulence]] or by disruption of the substrate and subsequent entrainment in the water column.<ref name=Margulis_2009/><ref>{{Cite book |url=https://archive.org/details/encyclopediabiol00simb |title=Encyclopedia of biological invasions |publisher=University of California Press |year=2011 |isbn=978-0-520-26421-2 |editor-last=Simberloff |editor-first=Daniel |location=Berkeley |pages=[https://archive.org/details/encyclopediabiol00simb/page/n760 736] |editor-last2=Rejmanek |editor-first2=Marcel |url-access=limited}}</ref> Tychoplankton are, therefore, a primary subdivision for sorting planktonic organisms by duration of lifecycle spent in the plankton, as neither their entire lives nor particular reproductive portions are confined to planktonic existence.<ref name=Kennish_2003>{{cite book|editor-last=Kennish|editor-first=Michael J.|title=Estuarine Research, Monitoring, and Resource Protection|year=2004|publisher=CRC Press|location=Boca Raton, Fla.|isbn=978-0-8493-1960-0|pages=194|url=http://www.crcpress.com/product/isbn/0849319609|archive-url=https://archive.today/20130120014208/http://www.crcpress.com/product/isbn/0849319609|archive-date=2013-01-20}}</ref> Tychoplankton are sometimes called ''accidental plankton''. | ||
===Mineralized plankton=== | ===Mineralized plankton=== | ||
{{See also|protist shells|biomineralization}} | {{See also|protist shells|biomineralization}} | ||
<gallery mode="packed" caption="Some planktons are protected with mineralized shells or [[Test (biology)|tests]]." style="float:left"> | <gallery mode="packed" caption="Some planktons are protected with mineralized shells or [[Test (biology)|tests]]." style="float:left" heights="180px"> | ||
File:Diatom Helipelta metil.jpg|[[Diatom]]s have glass shells ([[frustule]]s) and produce much of the world's oxygen. | File:Diatom Helipelta metil.jpg|[[Diatom]]s have glass shells ([[frustule]]s) and produce much of the world's oxygen. | ||
File:Haeckel Spumellaria detail.png| The elaborate [[silica]] shells of microscopic [[marine radiolarian]]s can eventually produce [[opal]]. | File:Haeckel Spumellaria detail.png| The elaborate [[silica]] shells of microscopic [[marine radiolarian]]s can eventually produce [[opal]]. | ||
File:Coccolithus pelagicus.jpg| [[Coccolithophore]]s have [[chalk]] plates called [[coccoliths]], and produced the [[Cliffs of Dover]]. | File:Coccolithus pelagicus.jpg| [[Coccolithophore]]s have [[chalk]] plates called [[coccoliths]], and produced the [[Cliffs of Dover]]. | ||
File:Planktic Foraminifera of the northern Gulf of Mexico.jpg| [[Foraminiferan]]s have [[calcium carbonate]] shells and produced the [[limestone]] in the [[Great Pyramids]]. | File:Planktic Foraminifera of the northern Gulf of Mexico.jpg| [[Foraminiferan]]s have [[calcium carbonate]] shells and produced the [[limestone]] in the [[Great Pyramids]]. | ||
</gallery> | </gallery> | ||
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{{Clear}} | {{Clear}} | ||
== | ===By life cycle=== | ||
====Holoplankton==== | |||
{{main|Holoplankton}} | |||
[[File:Tomopteriskils.jpg|thumb|left| ''[[Tomopteris]]'', a holoplanktic [[bioluminescence]] [[polychaete]] worm<ref>{{cite book | author = Harvey, Edmund Newton | title = Bioluminescence | publisher = Academic Press | year = 1952 }}</ref>]] | |||
[[Holoplankton]] are organisms that are planktic for their entire life cycle. Holoplankton can be contrasted with [[meroplankton]], which are planktic organisms that spend part of their life cycle in the [[benthic zone]]. Examples of holoplankton include some [[diatom]]s, [[radiolarian]]s, some [[dinoflagellate]]s, [[foraminifera]], [[amphipod]]s, [[copepod]]s, and [[salp]]s, as well as some [[gastropod]] mollusk species. Holoplankton dwell in the [[pelagic zone]] as opposed to the [[benthic zone]].<ref name=Anderson>{{cite web|last=Anderson|first=Genny|title=Marine Plankton|url=http://marinebio.net/marinescience/03ecology/mlplankton.htm|work=Marine Science|access-date=2012-04-04}}</ref> Holoplankton include both [[phytoplankton]] and [[zooplankton]] and vary in size. The most common plankton are [[protist]]s.<ref name=Talks>{{cite web|last=Talks|first=Ted|title=Zooplankton|url=http://marinebio.org/oceans/zooplankton.asp|archive-url=http://webarchive.loc.gov/all/20171207180052/https://marinebio.org/oceans/zooplankton/|archive-date=2017-12-07|work=Marine Life/Marine Invertebrates|access-date=2012-04-04}}</ref> | |||
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}} | |||
====Meroplankton==== | |||
[[File:Larva de phyllosoma.jpg|thumb|right| {{center|[[Phyllosoma|Larva stage]] of a spiny lobster}}]] | |||
{{main|Meroplankton}} | |||
[[Meroplankton]] are a wide variety of aquatic organisms that have both planktonic and [[Benthic zone|benthic]] stages in their life cycles. Much of the meroplankton consists of [[larva]]l stages of larger organisms.<ref name=":0">{{Cite journal|last1=Stübner|first1=E. I.|last2=Søreide|first2=J. E.|date=2016-01-27|title=Year-round meroplankton dynamics in high-Arctic Svalbard|url=https://academic.oup.com/plankt/article/38/3/522/2223522|journal=Journal of Plankton Research|volume=38|issue=3|pages=522–536|doi=10.1093/plankt/fbv124|doi-access=free}}</ref> Meroplankton can be contrasted with [[holoplankton]], which are planktonic organisms that stay in the [[pelagic zone]] as plankton throughout their entire life cycle.<ref>{{Cite web|title=Plankton|url=https://www.britannica.com/science/plankton|access-date=2020-06-13|website=Britannica}}</ref> After some time in the plankton, many meroplankton graduate to the [[nekton]] or adopt a [[benthos|benthic]] (often [[Sessility (zoology)|sessile]]) lifestyle on the [[seafloor]]. The larval stages of benthic [[invertebrate]]s make up a significant proportion of planktonic communities.<ref>{{Cite journal|last1=Ershova|first1=E. A.|last2=Descoteaux|first2=R.|date=2019-08-13|title=Diversity and Distribution of Meroplanktonic Larvae in the Pacific Arctic and Connectivity With Adult Benthic Invertebrate Communities|journal=Frontiers in Marine Science|volume=6|doi=10.3389/fmars.2019.00490|s2cid=199638114|doi-access=free|hdl=10037/16483|hdl-access=free}}</ref> The planktonic larval stage is particularly crucial to many benthic invertebrates in order to [[Dispersal vector|disperse]] their young. Depending on the particular species and the environmental conditions, larval or juvenile-stage meroplankton may remain in the pelagic zone for durations ranging from hours to months.<ref name=":0" /> | |||
== | == Ecology == | ||
===Food | ===Food webs=== | ||
{{ | {{see also|Marine food web}} | ||
| | [[File:Marine traditional food web.jpg|thumb|upright=1|right|{{center|Marine food web<br />traditional paradigm<ref name="MitraLeles2023">{{cite book | last=Mitra | first=Aditee | last2=Leles | first2=Suzana Gonçalves | title=Dynamics of Planktonic Primary Productivity in the Indian Ocean | chapter=A Revised Interpretation of Marine Primary Productivity in the Indian Ocean: The Role of Mixoplankton | publisher=Springer International Publishing | publication-place=Cham | date=2023 | isbn=978-3-031-34466-4 | doi=10.1007/978-3-031-34467-1_5 | url=https://link.springer.com/10.1007/978-3-031-34467-1_5 | access-date=2025-08-06 | page=101–128}}</ref>}}]] | ||
| | [[File:Marine mixoplankton food web.jpg|thumb|upright=1|right|{{center|Marine food web<br />mixoplankton paradigm<ref name="MitraLeles2023" />}}]] | ||
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}} | |||
{{ | |||
As well as representing the lower levels of a [[food chain]] that supports commercially important [[Fishery|fisheries]], plankton [[ecosystem]]s play a role in the [[biogeochemical cycle]]s of many important [[chemical element]]s, including the ocean's [[carbon cycle]].<ref>{{Cite FTP |last= Falkowski |first=Paul G. |year=1994 |url= ftp://marine.calpoly.edu/Needles/SPRING%2009/papers/2-Falkowski.pdf |title=The role of phytoplankton photosynthesis in global biogeochemical cycles |volume=39 |issue=3 |pages=235–258 |doi= 10.1007/BF00014586 |pmid=24311124 |bibcode=1994PhoRe..39..235F |server= Photosynthesis Research |url-status= dead |s2cid=12129871 }}</ref> Fish larvae mainly eat zooplankton, which in turn eat phytoplankton<ref name="sciencedirect.com">{{Cite journal |last1=James |first1=Alex |last2=Pitchford |first2=Jonathan W. |last3=Brindley |first3=John |date=2003-02-01 |title=The relationship between plankton blooms, the hatching of fish larvae, and recruitment |url=https://www.sciencedirect.com/science/article/pii/S0304380002003113 |journal=Ecological Modelling |language=en |volume=160 |issue=1 |pages=77–90 |doi=10.1016/S0304-3800(02)00311-3 |bibcode=2003EcMod.160...77J |issn=0304-3800|url-access=subscription }}</ref> | As well as representing the lower levels of a [[food chain]] that supports commercially important [[Fishery|fisheries]], plankton [[ecosystem]]s play a role in the [[biogeochemical cycle]]s of many important [[chemical element]]s, including the ocean's [[carbon cycle]].<ref>{{Cite FTP |last= Falkowski |first=Paul G. |year=1994 |url= ftp://marine.calpoly.edu/Needles/SPRING%2009/papers/2-Falkowski.pdf |title=The role of phytoplankton photosynthesis in global biogeochemical cycles |volume=39 |issue=3 |pages=235–258 |doi= 10.1007/BF00014586 |pmid=24311124 |bibcode=1994PhoRe..39..235F |server= Photosynthesis Research |url-status= dead |s2cid=12129871 }}</ref> Fish larvae mainly eat zooplankton, which in turn eat phytoplankton<ref name="sciencedirect.com">{{Cite journal |last1=James |first1=Alex |last2=Pitchford |first2=Jonathan W. |last3=Brindley |first3=John |date=2003-02-01 |title=The relationship between plankton blooms, the hatching of fish larvae, and recruitment |url=https://www.sciencedirect.com/science/article/pii/S0304380002003113 |journal=Ecological Modelling |language=en |volume=160 |issue=1 |pages=77–90 |doi=10.1016/S0304-3800(02)00311-3 |bibcode=2003EcMod.160...77J |issn=0304-3800|url-access=subscription }}</ref> | ||
[[Microbial loop|The microbial loop]]: Bacteria play central roles in aquatic food webs. The microbial loop refers to a process in aquatic ecosystems where bacteria consume [[dissolved organic matter]] (DOM) and are then consumed by larger microorganisms, effectively cycling nutrients and energy within the ecosystem.<ref name="Lehman2022" /> | |||
[[Viral shunt|The viral shunt]]: Viruses also play central roles in aquatic food webs. The viral shunt is a process where viruses infect and [[Lysis|lyse]] (burst) host cells, releasing cellular contents (including dissolved organic matter) that can be utilized by other microplankton like bacteria, effectively bypassing the traditional food web pathways. This process plays a significant role in nutrient cycling and carbon flow within aquatic ecosystems.<ref name="Kase2018" /> | |||
[[File:Cetorhinus maximus by greg skomal.JPG|thumb|left| The [[basking shark]] uses [[filter feeding]] to strain plankton from the water.]] | |||
[[File:Aquatic food web microbial loop.png|thumb|upright=1.5|left|The microbial loop: The link between the microbial loop and the aquatic food web. [[Dissolved organic matter]] (DOM) becomes [[particulate organic matter]] (POM) as bacteria eat it and grow to form clumps. Small clumps of organic matter are eaten by [[bacterivore]]s and zooplankton eat both bacterivores and big clumps of organic matter. Zooplankton are then eaten by fish. Dissolved organic matter is leaked or excreted by zooplankton and fish, and the cycle, called the microbial loop, starts over. Blue arrows show the movement of organic matter from the microbial loop to the food web and back.<ref name="Lehman2022">{{cite journal | last=Tung | first=Alice | last2=Lehman | first2=Peggy W. | last3=Durand | first3=John | title=Can Bacteria Save an Estuary's Food Web? | journal=Frontiers for Young Minds | volume=10 | date=2022-04-26 | issn=2296-6846 | doi=10.3389/frym.2022.624953 | doi-access=free | page=}} [[File:CC-BY icon.svg|50px]] Modified text was copied from this source, which is available under a [https://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International License]</ref>]] | |||
[[File:Cycling of marine phytoplankton.png|thumb|upright=1.5|right|The viral shunt: Phytoplankton live in the [[photic zone]] of the ocean, where [[photosynthesis]] is possible. During photosynthesis, they assimilate carbon dioxide and release oxygen. For growth, phytoplankton cells depend on nutrients, which enter the ocean by rivers, continental weathering, and glacial ice meltwater on the poles. Phytoplankton release dissolved organic carbon (DOC) into the ocean. Since phytoplankton are the basis of marine food webs, they serve as prey for zooplankton, fish larvae and other heterotrophic organisms. They can also be degraded by bacteria or by viral lysis.<ref name="Kase2018">{{cite book | last=Käse | first=Laura | last2=Geuer | first2=Jana K. | title=YOUMARES 8 – Oceans Across Boundaries: Learning from each other | chapter=Phytoplankton Responses to Marine Climate Change – An Introduction | publisher=Springer International Publishing | publication-place=Cham | date=2018 | isbn=978-3-319-93283-5 | doi=10.1007/978-3-319-93284-2_5 | url=https://link.springer.com/10.1007/978-3-319-93284-2_5 | access-date=2025-07-15 | page=55–71}} [[File:CC-BY icon.svg|50px]] Modified text was copied from this source, which is available under a [https://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International License]</ref>]] | |||
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Fungi have a role as well. The [[mycoloop]] is a specific aquatic food web pathway where parasitic [[chytrid|chytrid fungi]] infect large, inedible phytoplankton, and their [[zoospore]]s (a type of spore) become a food source for zooplankton. In this manner, the chytrid fungi transfer nutrients from otherwise unusable phytoplankton to zooplankton.<ref name="Frenken2017" /> | |||
[[File:Pennate diatom infected with two chytrid-like fungal pathogens.png|thumb|upright=1.5|left|[[Pennate diatom]] from an Arctic [[meltpond]], infected with two chytrid-like fungal pathogens (in false-colour red).<ref>{{cite journal |last1 = Kilias |first1 = Estelle S. |last2 = Junges|first2 = Leandro |last3 = Šupraha |first3 = Luka |last4 = Leonard |first4 = Guy |last5 = Metfies |first5 = Katja |last6 = Richards |first6 = Thomas A. |year = 2020 |title = Chytrid fungi distribution and co-occurrence with diatoms correlate with sea ice melt in the Arctic Ocean |journal = Communications Biology |volume = 3 |issue = 1 |page = 183 |pmid = 32317738 |pmc = 7174370|s2cid = 216033140 |doi = 10.1038/s42003-020-0891-7 |doi-access = free}}</ref> Scale bar = 10 μm.]] | |||
[[File:Mycoloop links between phytoplankton and zooplankton.jpg|thumb|upright=1.5|right|The mycoloop: Small phytoplankton can be grazed upon by zooplankton, but large phytoplankton are not easy to eat, or are even inedible. Chytrid infections on large phytoplankton can make them more palatabile, as a result of host aggregation (reduced edibility) or mechanistic fragmentation of cells or filaments (increased palatability). First, chytrid parasites extract and repack nutrients and energy from their hosts in form of readily edible zoospores. Second, infected and fragmented hosts including attached [[sporangia]] can also be ingested by grazers.<ref name="Frenken2017">{{cite journal | last=Frenken | first=Thijs | last2=Alacid | first2=Elisabet | last3=Berger | first3=Stella A. | last4=Bourne | first4=Elizabeth C. | last5=Gerphagnon | first5=Mélanie | last6=Grossart | first6=Hans-Peter | last7=Gsell | first7=Alena S. | last8=Ibelings | first8=Bas W. | last9=Kagami | first9=Maiko | last10=Küpper | first10=Frithjof C. | last11=Letcher | first11=Peter M. | last12=Loyau | first12=Adeline | last13=Miki | first13=Takeshi | last14=Nejstgaard | first14=Jens C. | last15=Rasconi | first15=Serena | last16=Reñé | first16=Albert | last17=Rohrlack | first17=Thomas | last18=Rojas-Jimenez | first18=Keilor | last19=Schmeller | first19=Dirk S. | last20=Scholz | first20=Bettina | last21=Seto | first21=Kensuke | last22=Sime-Ngando | first22=Télesphore | last23=Sukenik | first23=Assaf | last24=Van de Waal | first24=Dedmer B. | last25=Van den Wyngaert | first25=Silke | last26=Van Donk | first26=Ellen | last27=Wolinska | first27=Justyna | last28=Wurzbacher | first28=Christian | last29=Agha | first29=Ramsy | title=Integrating chytrid fungal parasites into plankton ecology: research gaps and needs | journal=Environmental Microbiology | volume=19 | issue=10 | date=2017 | issn=1462-2912 | doi=10.1111/1462-2920.13827 | doi-access=free | pages=3802–3822 | url=https://sfamjournals.onlinelibrary.wiley.com/doi/pdfdirect/10.1111/1462-2920.13827 | access-date=2025-07-15| hdl=2164/9083 | hdl-access=free }} [[File:CC-BY icon.svg|50px]] Modified text was copied from this source, which is available under a [https://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International License]</ref>]] | |||
{{clear}} | |||
===Carbon cycle=== | ===Carbon cycle=== | ||
{{see also|ocean carbon cycle|biological pump}} | {{see also|ocean carbon cycle|biological pump|microbial carbon pump}} | ||
[[File:Oceanic Food Web.jpg|thumb|upright=1.6|left|The [[ocean food web]], showing the central involvement of [[marine microplankton]] in how the ocean imports nutrients from and then exports them back to the atmosphere and ocean floor]] | |||
[[File:Central role played by pelagic fungi in the mycoloop and microbial loop.jpg|thumb|upright=1.6|right|The central role played by [[Marine fungi|pelagic fungi]], both parasitic and [[saprotrophic]] in the [[mycoloop]], and saprotrophic fungi as active contributors to the [[microbial loop]]. The activity of heterotrophic microbes, including pelagic fungi, has far-reaching global implications for fisheries (i.e., the amount of carbon that will ultimately flow to higher trophic levels) and climate change (i.e., the amount of carbon that will be sequestered in the ocean or respired back to CO<sub>2</sub> and the release of other greenhouse gases; e.g., N<sub>2</sub>O.<ref name="Breyer2023">{{cite journal | last=Breyer | first=Eva | last2=Baltar | first2=Federico | title=The largely neglected ecological role of oceanic pelagic fungi | journal=Trends in Ecology & Evolution | volume=38 | issue=9 | date=2023 | doi=10.1016/j.tree.2023.05.002 | doi-access=free | pages=870–888 | url=http://www.cell.com/article/S0169534723001258/pdf | access-date=2025-07-27}}</ref>]] | |||
{{clear left}} | |||
Primarily by grazing on phytoplankton, zooplankton provide [[carbon]] to the planktic [[foodweb]], either [[Cellular respiration|respiring]] it to provide [[metabolism|metabolic]] energy, or upon death as [[Biomass (ecology)|biomass]] or [[detritus]]. Organic material tends to be [[density|denser]] than [[seawater]], so it sinks into open ocean ecosystems away from the coastlines, transporting carbon along with it. This process, called the [[biological pump]], is one reason that oceans constitute the largest [[carbon sink]] on [[Earth science|Earth]]. However, it has been shown to be influenced by increments of temperature.<ref>{{cite journal |last1= Sarmento |first1= H. |last2= Montoya |first2= JM. |last3= Vázquez-Domínguez |first3= E. |last4= Vaqué |first4= D.|last5= Gasol |first5= JM. |year= 2010 |title= Warming effects on marine microbial food web processes: how far can we go when it comes to predictions? |pmc= 2880134 |journal= Philosophical Transactions of the Royal Society B: Biological Sciences |volume= 365 |issue=1549 |pages= 2137–2149 |doi= 10.1098/rstb.2010.0045 |pmid= 20513721 }}</ref><ref>{{cite journal |last1= Vázquez-Domínguez |first1= E. |last2= Vaqué |first2= D. |last3= Gasol |first3= JM. |year=2007 |title= Ocean warming enhances respiration and carbon demand of coastal microbial plankton. |journal= Global Change Biology |volume= 13 |issue=7 |pages= 1327–1334 |doi= 10.1111/j.1365-2486.2007.01377.x |bibcode= 2007GCBio..13.1327V |hdl= 10261/15731 |s2cid= 8721854 |hdl-access= free }}</ref><ref>{{cite journal |last1= Vázquez-Domínguez |first1= E. |last2= Vaqué |first2= D. |last3= Gasol |first3= JM. |year= 2012 |title= Temperature effects on the heterotrophic bacteria, heterotrophic nanoflagellates, and microbial top predators of NW Mediterranean. |journal= Aquatic Microbial Ecology |volume= 67 |issue=2 |pages= 107–121 |doi= 10.3354/ame01583 |doi-access= free |hdl= 10261/95626 |hdl-access= free }}</ref><ref>{{cite journal |last1= Mazuecos |first1= E. |last2= Arístegui |first2=J. |last3= Vázquez-Domínguez |first3= E. |last4= Ortega-Retuerta |first4= E. |last5= Gasol |first5= JM. |last6= Reche |first6= I. |year=2012 |title= Temperature control of microbial respiration and growth efficiency in the mesopelagic zone of the South Atlantic and Indian Oceans. |journal= Deep Sea Research Part I: Oceanographic Research Papers |volume= 95 |issue=2 |pages= 131–138 |doi= 10.3354/ame01583 |doi-access= free |hdl= 10261/95626 |hdl-access= free }}</ref> In 2019, a study indicated that at ongoing rates of [[Ocean acidification|seawater acidification]], Antarctic phytoplanktons could become smaller and less effective at storing carbon before the end of the century.<ref>{{Cite web|url=https://phys.org/news/2019-08-acid-oceans-plankton-fueling-faster.html|title=Acid oceans are shrinking plankton, fueling faster climate change|last1=Petrou|first1=Katherina|last2=Nielsen|first2=Daniel|date=2019-08-27|website=phys.org|language=en-us|access-date=2019-09-07}}</ref> | Primarily by grazing on phytoplankton, zooplankton provide [[carbon]] to the planktic [[foodweb]], either [[Cellular respiration|respiring]] it to provide [[metabolism|metabolic]] energy, or upon death as [[Biomass (ecology)|biomass]] or [[detritus]]. Organic material tends to be [[density|denser]] than [[seawater]], so it sinks into open ocean ecosystems away from the coastlines, transporting carbon along with it. This process, called the [[biological pump]], is one reason that oceans constitute the largest [[carbon sink]] on [[Earth science|Earth]]. However, it has been shown to be influenced by increments of temperature.<ref>{{cite journal |last1= Sarmento |first1= H. |last2= Montoya |first2= JM. |last3= Vázquez-Domínguez |first3= E. |last4= Vaqué |first4= D.|last5= Gasol |first5= JM. |year= 2010 |title= Warming effects on marine microbial food web processes: how far can we go when it comes to predictions? |pmc= 2880134 |journal= Philosophical Transactions of the Royal Society B: Biological Sciences |volume= 365 |issue=1549 |pages= 2137–2149 |doi= 10.1098/rstb.2010.0045 |pmid= 20513721 }}</ref><ref>{{cite journal |last1= Vázquez-Domínguez |first1= E. |last2= Vaqué |first2= D. |last3= Gasol |first3= JM. |year=2007 |title= Ocean warming enhances respiration and carbon demand of coastal microbial plankton. |journal= Global Change Biology |volume= 13 |issue=7 |pages= 1327–1334 |doi= 10.1111/j.1365-2486.2007.01377.x |bibcode= 2007GCBio..13.1327V |hdl= 10261/15731 |s2cid= 8721854 |hdl-access= free }}</ref><ref>{{cite journal |last1= Vázquez-Domínguez |first1= E. |last2= Vaqué |first2= D. |last3= Gasol |first3= JM. |year= 2012 |title= Temperature effects on the heterotrophic bacteria, heterotrophic nanoflagellates, and microbial top predators of NW Mediterranean. |journal= Aquatic Microbial Ecology |volume= 67 |issue=2 |pages= 107–121 |doi= 10.3354/ame01583 |doi-access= free |hdl= 10261/95626 |hdl-access= free }}</ref><ref>{{cite journal |last1= Mazuecos |first1= E. |last2= Arístegui |first2=J. |last3= Vázquez-Domínguez |first3= E. |last4= Ortega-Retuerta |first4= E. |last5= Gasol |first5= JM. |last6= Reche |first6= I. |year=2012 |title= Temperature control of microbial respiration and growth efficiency in the mesopelagic zone of the South Atlantic and Indian Oceans. |journal= Deep Sea Research Part I: Oceanographic Research Papers |volume= 95 |issue=2 |pages= 131–138 |doi= 10.3354/ame01583 |doi-access= free |hdl= 10261/95626 |hdl-access= free }}</ref> In 2019, a study indicated that at ongoing rates of [[Ocean acidification|seawater acidification]], Antarctic phytoplanktons could become smaller and less effective at storing carbon before the end of the century.<ref>{{Cite web|url=https://phys.org/news/2019-08-acid-oceans-plankton-fueling-faster.html|title=Acid oceans are shrinking plankton, fueling faster climate change|last1=Petrou|first1=Katherina|last2=Nielsen|first2=Daniel|date=2019-08-27|website=phys.org|language=en-us|access-date=2019-09-07}}</ref> | ||
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|doi-access = free | |doi-access = free | ||
}}</ref> | }}</ref> | ||
===Great Calcite Belt=== | |||
[[File:Great Calcite Belt of the Southern Ocean.webm|thumb|upright=1.3| Yearly cycle of the Great Calcite Belt in the [[Southern Ocean]]. The belt appears during the southern hemisphere summer as a light [[teal]] stripe.]] | |||
The [[Great Calcite Belt]] is a region in the [[Southern Ocean]] characterized by high concentrations of [[coccolithophore]]s, a type of calcite-producing phytoplankton. It plays a significant role in [[ocean biogeochemistry]] and the global carbon cycle. Coccolithophores in the belt produce [[calcium carbonate]] ([[calcite]] or [[chalk]]) plates called [[coccolith]]s. This process, known as [[calcification]], affects the ocean's carbon cycle by lowering alkalinity and releasing CO<sub>2</sub>. However, when coccolithophores die, their calcite shells sink, contributing to the biological pump by transporting carbon to the deep ocean, sequestering it for centuries or longer and mitigating atmospheric CO<sub>2</sub> levels.<ref name=Smith2017>{{cite journal |doi = 10.5194/bg-14-4905-2017|title = The influence of environmental variability on the biogeography of coccolithophores and diatoms in the Great Calcite Belt|year = 2017|last1 = Smith|first1 = Helen E. K.|last2 = Poulton|first2 = Alex J.|last3 = Garley|first3 = Rebecca|last4 = Hopkins|first4 = Jason|last5 = Lubelczyk|first5 = Laura C.|last6 = Drapeau|first6 = Dave T.|last7 = Rauschenberg|first7 = Sara|last8 = Twining|first8 = Ben S.|last9 = Bates|first9 = Nicholas R.|last10 = Balch|first10 = William M.|journal = Biogeosciences|volume = 14|issue = 21|pages = 4905–4925|bibcode = 2017BGeo...14.4905S|doi-access = free}} [[File:CC-BY icon.svg|50px]] Material was copied from this source, which is available under a [https://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International License].</ref> | |||
===Oxygen production=== | ===Oxygen production=== | ||
{{see also|oxygen cycle}} | {{see also|oxygen cycle}} | ||
[[Phytoplankton]] absorb energy from the Sun and nutrients from the water to produce their own nourishment or energy. In the process of [[photosynthesis]], phytoplankton release molecular [[oxygen]] ({{chem|O|2}}) into the water as a waste byproduct. It is estimated that about 50% of the world's oxygen is produced via phytoplankton photosynthesis.<ref name="NalGeo">{{cite news |last=Roach |first=John |url= http://news.nationalgeographic.com/news/2004/06/0607_040607_phytoplankton.html |archive-url= https://web.archive.org/web/20040608065449/http://news.nationalgeographic.com/news/2004/06/0607_040607_phytoplankton.html | [[Phytoplankton]] absorb energy from the Sun and nutrients from the water to produce their own nourishment or energy. In the process of [[photosynthesis]], phytoplankton release molecular [[oxygen]] ({{chem|O|2}}) into the water as a waste byproduct. It is estimated that about 50% of the world's oxygen is produced via phytoplankton photosynthesis.<ref name="NalGeo">{{cite news |last=Roach |first=John |url= http://news.nationalgeographic.com/news/2004/06/0607_040607_phytoplankton.html |archive-url= https://web.archive.org/web/20040608065449/http://news.nationalgeographic.com/news/2004/06/0607_040607_phytoplankton.html |archive-date= June 8, 2004 |title=Source of Half Earth's Oxygen Gets Little Credit |work=National Geographic News |date=June 7, 2004 |access-date=2016-04-04 }}</ref> The rest is produced via photosynthesis on land by [[plant]]s.<ref name="NalGeo"/> Furthermore, phytoplankton photosynthesis has controlled the atmospheric [[Carbon dioxide in Earth's atmosphere|{{chem|C|O|2}}]]/[[Oxygen#Build-up in the atmosphere|{{chem|O|2}}]] balance since the early [[Precambrian]] Eon.<ref name="Tappan">{{cite journal |title=Primary production, isotopes, extinctions and the atmosphere |journal=Palaeogeography, Palaeoclimatology, Palaeoecology |date=April 1968 |last=Tappan |first=Helen |volume=4 |issue=3 |pages=187–210 |doi=10.1016/0031-0182(68)90047-3 |bibcode= 1968PPP.....4..187T }}</ref> | ||
===Absorption efficiency=== | ===Absorption efficiency=== | ||
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==Biomass variability== | ==Biomass variability== | ||
[[File:Amphipodredkils.jpg|thumb|upright=1.2| [[Amphipoda|Amphipod]] with curved [[exoskeleton]] and two long and two short antennae]] | |||
The growth of phytoplankton populations is dependent on light levels and nutrient availability. The chief factor limiting growth varies from region to region in the world's oceans. On a broad scale, growth of phytoplankton in the oligotrophic tropical and subtropical gyres is generally limited by nutrient supply, while light often limits phytoplankton growth in subarctic gyres. Environmental variability at multiple scales influences the nutrient and light available for phytoplankton, and as these organisms form the base of the marine food web, this variability in phytoplankton growth influences higher trophic levels. For example, at interannual scales phytoplankton levels temporarily plummet during [[El Niño]] periods, influencing populations of zooplankton, fishes, sea birds, and [[marine mammal]]s. | The growth of phytoplankton populations is dependent on light levels and nutrient availability. The chief factor limiting growth varies from region to region in the world's oceans. On a broad scale, growth of phytoplankton in the oligotrophic tropical and subtropical gyres is generally limited by nutrient supply, while light often limits phytoplankton growth in subarctic gyres. Environmental variability at multiple scales influences the nutrient and light available for phytoplankton, and as these organisms form the base of the marine food web, this variability in phytoplankton growth influences higher trophic levels. For example, at interannual scales phytoplankton levels temporarily plummet during [[El Niño]] periods, influencing populations of zooplankton, fishes, sea birds, and [[marine mammal]]s. | ||
The effects of anthropogenic warming on the global population of phytoplankton is an area of active research. Changes in the vertical stratification of the water column, the rate of temperature-dependent biological reactions, and the atmospheric supply of nutrients are expected to have important impacts on future phytoplankton productivity.<ref>{{cite journal | last1 = Steinacher | first1 = M. | display-authors = etal | year = 2010 | title = Projected 21st century decrease in marine productivity: a multi-model analysis | journal = Biogeosciences | volume = 7 | issue = 3| pages = 979–1005 | doi = 10.5194/bg-7-979-2010 | bibcode = 2010BGeo....7..979S | doi-access = free | hdl = 11858/00-001M-0000-0011-F69E-5 | hdl-access = free }}</ref> Additionally, changes in the mortality of phytoplankton due to rates of zooplankton grazing may be significant. | The effects of anthropogenic warming on the global population of phytoplankton is an area of active research. Changes in the vertical stratification of the water column, the rate of temperature-dependent biological reactions, and the atmospheric supply of nutrients are expected to have important impacts on future phytoplankton productivity.<ref>{{cite journal | last1 = Steinacher | first1 = M. | display-authors = etal | year = 2010 | title = Projected 21st century decrease in marine productivity: a multi-model analysis | journal = Biogeosciences | volume = 7 | issue = 3| pages = 979–1005 | doi = 10.5194/bg-7-979-2010 | bibcode = 2010BGeo....7..979S | doi-access = free | hdl = 11858/00-001M-0000-0011-F69E-5 | hdl-access = free }}</ref> Additionally, changes in the mortality of phytoplankton due to rates of zooplankton grazing may be significant. | ||
{{clear}} | {{clear}} | ||
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[[Zooplankton]] are the initial prey item for almost all [[fish larva]]e as they switch from their [[yolk sac]]s to external feeding. Fish rely on the density and distribution of zooplankton to match that of new larvae, which can otherwise starve. Natural factors (e.g., current variations, temperature changes) and man-made factors (e.g. river dams, [[ocean acidification]], rising temperatures) can strongly affect zooplankton populations, which can in turn strongly affect fish larval survival, and therefore breeding success. | [[Zooplankton]] are the initial prey item for almost all [[fish larva]]e as they switch from their [[yolk sac]]s to external feeding. Fish rely on the density and distribution of zooplankton to match that of new larvae, which can otherwise starve. Natural factors (e.g., current variations, temperature changes) and man-made factors (e.g. river dams, [[ocean acidification]], rising temperatures) can strongly affect zooplankton populations, which can in turn strongly affect fish larval survival, and therefore breeding success. | ||
It has been shown that plankton can be patchy in marine environments where there aren't significant fish populations and additionally, where fish are abundant, zooplankton dynamics are influenced by the fish predation rate in their environment. Depending on the predation rate, they could express regular or chaotic behavior.<ref>{{Cite journal |last1=Medvinsky |first1=Alexander B. |last2=Tikhonova |first2=Irene A. |last3=Aliev |first3=Rubin R. |last4=Li |first4=Bai-Lian |last5=Lin |first5=Zhen-Shan |last6=Malchow |first6=Horst |date=2001-07-26 |title=Patchy environment as a factor of complex plankton dynamics |url=https://link.aps.org/doi/10.1103/PhysRevE.64.021915 |journal=Physical Review E |language=en |volume=64 |issue=2 | | It has been shown that plankton can be patchy in marine environments where there aren't significant fish populations and additionally, where fish are abundant, zooplankton dynamics are influenced by the fish predation rate in their environment. Depending on the predation rate, they could express regular or chaotic behavior.<ref>{{Cite journal |last1=Medvinsky |first1=Alexander B. |last2=Tikhonova |first2=Irene A. |last3=Aliev |first3=Rubin R. |last4=Li |first4=Bai-Lian |last5=Lin |first5=Zhen-Shan |last6=Malchow |first6=Horst |date=2001-07-26 |title=Patchy environment as a factor of complex plankton dynamics |url=https://link.aps.org/doi/10.1103/PhysRevE.64.021915 |journal=Physical Review E |language=en |volume=64 |issue=2 |article-number=021915 |doi=10.1103/PhysRevE.64.021915 |pmid=11497628 |bibcode=2001PhRvE..64b1915M |issn=1063-651X|url-access=subscription }}</ref> | ||
A negative effect that fish larvae can have on planktonic algal blooms is that the larvae will prolong the blooming event by diminishing available zooplankton numbers; this in turn permits excessive phytoplankton growth allowing the bloom to flourish .<ref name="sciencedirect.com"/> | A negative effect that fish larvae can have on planktonic algal blooms is that the larvae will prolong the blooming event by diminishing available zooplankton numbers; this in turn permits excessive phytoplankton growth allowing the bloom to flourish .<ref name="sciencedirect.com"/> | ||
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Plankton have many direct and indirect effects on humans. | Plankton have many direct and indirect effects on humans. | ||
Around 70% of the oxygen in the atmosphere is produced in the oceans from [[phytoplankton]] performing photosynthesis, meaning that the majority of the oxygen available for us and other organisms that [[Cellular respiration#Aerobic respiration|respire aerobically]] is produced by plankton.<ref>{{Cite journal |last1=Sekerci |first1=Yadigar |last2=Petrovskii |first2=Sergei |date=2015-12-01 |title=Mathematical Modelling of Plankton–Oxygen Dynamics Under the Climate Change | Around 70% of the oxygen in the atmosphere is produced in the oceans from [[phytoplankton]] performing photosynthesis, meaning that the majority of the oxygen available for us and other organisms that [[Cellular respiration#Aerobic respiration|respire aerobically]] is produced by plankton.<ref>{{Cite journal |last1=Sekerci |first1=Yadigar |last2=Petrovskii |first2=Sergei |date=2015-12-01 |title=Mathematical Modelling of Plankton–Oxygen Dynamics Under the Climate Change |journal=Bulletin of Mathematical Biology |language=en |volume=77 |issue=12 |pages=2325–2353 |doi=10.1007/s11538-015-0126-0 |pmid=26607949 |s2cid=8637912 |issn=1522-9602|hdl=2381/36058 |hdl-access=free }}</ref> | ||
Plankton also make up the base of the marine food web, providing food for all the trophic levels above. Recent studies have analyzed the marine food web to see if the system runs on a [[Top-down and bottom-up design|top-down or bottom-up approach]]. Essentially, this research is focused on understanding whether changes in the food web are driven by nutrients at the bottom of the food web or predators at the top. The general conclusion is that the bottom-up approach seemed to be more predictive of food web behavior.<ref>{{Cite journal |last1=Frederiksen |first1=Morten |last2=Edwards |first2=Martin |last3=Richardson |first3=Anthony J. |last4=Halliday |first4=Nicholas C. |last5=Wanless |first5=Sarah |date=November 2006 |title=From plankton to top predators: bottom-up control of a marine food web across four trophic levels |url=https://onlinelibrary.wiley.com/doi/10.1111/j.1365-2656.2006.01148.x |journal=Journal of Animal Ecology |language=en |volume=75 |issue=6 |pages=1259–1268 |doi=10.1111/j.1365-2656.2006.01148.x |pmid=17032358 |bibcode=2006JAnEc..75.1259F |issn=0021-8790|url-access=subscription }}</ref> This indicates that plankton have more sway in determining the success of the primary consumer species that prey on them than do the secondary consumers that prey on the primary consumers. | Plankton also make up the base of the marine food web, providing food for all the trophic levels above. Recent studies have analyzed the marine food web to see if the system runs on a [[Top-down and bottom-up design|top-down or bottom-up approach]]. Essentially, this research is focused on understanding whether changes in the food web are driven by nutrients at the bottom of the food web or predators at the top. The general conclusion is that the bottom-up approach seemed to be more predictive of food web behavior.<ref>{{Cite journal |last1=Frederiksen |first1=Morten |last2=Edwards |first2=Martin |last3=Richardson |first3=Anthony J. |last4=Halliday |first4=Nicholas C. |last5=Wanless |first5=Sarah |date=November 2006 |title=From plankton to top predators: bottom-up control of a marine food web across four trophic levels |url=https://onlinelibrary.wiley.com/doi/10.1111/j.1365-2656.2006.01148.x |journal=Journal of Animal Ecology |language=en |volume=75 |issue=6 |pages=1259–1268 |doi=10.1111/j.1365-2656.2006.01148.x |pmid=17032358 |bibcode=2006JAnEc..75.1259F |issn=0021-8790|url-access=subscription }}</ref> This indicates that plankton have more sway in determining the success of the primary consumer species that prey on them than do the secondary consumers that prey on the primary consumers. | ||
In some cases, plankton act as an intermediate [[Host (biology)|host]] for deadly parasites in humans. One such | In some cases, plankton act as an intermediate [[Host (biology)|host]] for deadly parasites in humans. One such case is that of [[cholera]], an infection caused by several pathogenic strains of ''[[Vibrio cholerae]]''. These species have been shown to have a symbiotic relationship with chitinous zooplankton species like [[copepod]]s. These bacteria benefit not only from the food provided by the chiton from the zooplankton, but also from the protection from acidic environments. Once the copepods have been ingested by a human host, the chitinous exterior protects the bacteria from the stomach acids in the stomach and proceed to the intestines. Once there, the bacteria bind with the surface of the small intestine and the host will start developing symptoms, including extreme diarrhea, within five days.<ref>{{Cite journal |last1=Lipp |first1=Erin K. |author-link1 = Erin Lipp|last2=Huq |first2=Anwar |last3=Colwell |first3=Rita R. |date=October 2002 |title=Effects of Global Climate on Infectious Disease: the Cholera Model |journal=Clinical Microbiology Reviews |language=en |volume=15 |issue=4 |pages=757–770 |doi=10.1128/CMR.15.4.757-770.2002 |issn=0893-8512 |pmc=126864 |pmid=12364378 }}</ref> | ||
==Plankton Manifesto== | |||
In 2024, the [[United Nations Global Compact]]'s Ocean Stewardship Coalition launched the ''Plankton Manifesto'',<ref name=Manifesto>[https://ungc-communications-assets.s3.amazonaws.com/docs/publications/PlanktonManifesto_MG_DIGITAL-2.pdf Plankton Manifesto] ''Ocean Stewardship Coalition'' of the [[United Nations Global Compact]], published September 2024.</ref> collaboratively developed by over 30 international experts.<ref name="Doumeizel2024">{{cite journal | last=Doumeizel | first=Vincent | last2=Dolan | first2=John R | title=The launch of The Plankton Manifesto in September 2024 | journal=Journal of Plankton Research | volume=46 | issue=6 | date=2024-12-02 | issn=0142-7873 | doi=10.1093/plankt/fbae061 | doi-access=free | pages=525–526 | url=https://academic.oup.com/plankt/advance-article-pdf/doi/10.1093/plankt/fbae061/60642678/fbae061.pdf | access-date=2025-08-02}}</ref> It outlines strategic recommendations to guide global efforts at safeguarding plankton and harnessing their potential to address planetary [[climate change]] issues, as well as [[pollution]] and [[biodiversity loss]]. It emphasizes plankton's critical role as the foundation of [[marine ecosystem]]s, producing about 50% of Earth's oxygen and sequestering 30–50 billion metric tonnes of carbon annually.<ref name=Manifesto /> | |||
Key recommendations include:<ref name=Manifesto /> | |||
* Enhanced research and monitoring: Leveraging technologies like [[DNA sequencing]], [[bioinformatics]], [[satellite monitoring]], and AI [[image analysis]] to improve understanding of plankton dynamics and create a global plankton atlas. | |||
* Plankton-based solutions: Promoting innovative applications, such as using plankton for [[water purification]], [[bioplastics]], [[fertilizer]]s, and [[animal feed]] to support sustainable industries. | |||
* Policy integration: Urging governments, United Nations agencies, and businesses to include plankton in climate and biodiversity frameworks, with endorsements sought at [[COP29]], [[COP16]], and the [[2025 United Nations Ocean Conference]]. | |||
* Public awareness: Fostering "plankton literacy" through education and interdisciplinary initiatives to highlight their role in [[food security]] and [[ecosystem health]]. | |||
* Collaboration: Encouraging cross-sectoral partnerships among academia, industry, and governments to fund research and protect plankton from threats like [[nutrient pollution]] and [[ocean warming]]. | |||
== See also == | == See also == | ||
* [[Paradox of the plankton]] | * [[Paradox of the plankton]] | ||
* [[Seston]] | * [[Seston]] | ||
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*Kiørboe, Thomas (2008). ''A Mechanistic Approach to Plankton Ecology''. Princeton University Press, Princeton, N.J. {{ISBN|978-0-691-13422-2}}. | *Kiørboe, Thomas (2008). ''A Mechanistic Approach to Plankton Ecology''. Princeton University Press, Princeton, N.J. {{ISBN|978-0-691-13422-2}}. | ||
*Dolan, J.R., Agatha, S., Coats, D.W., Montagnes, D.J.S., Stocker, D.K., eds. (2013).''Biology and Ecology of Tintinnid Ciliates: Models for Marine Plankton''. Wiley-Blackwell, Oxford, UK {{ISBN|978-0-470-67151-1}}. | *Dolan, J.R., Agatha, S., Coats, D.W., Montagnes, D.J.S., Stocker, D.K., eds. (2013).''Biology and Ecology of Tintinnid Ciliates: Models for Marine Plankton''. Wiley-Blackwell, Oxford, UK {{ISBN|978-0-470-67151-1}}. | ||
== External links == | == External links == | ||
Latest revision as of 05:40, 31 October 2025
Template:Short description Script error: No such module "about". Template:Pp-pc Template:Plankton sidebar
Plankton are organisms that drift in water (or air) but are unable to actively propel themselves against currents (or wind).[1][2] Marine plankton include drifting organisms that inhabit the saltwater of oceans and the brackish waters of estuaries. Freshwater plankton are similar to marine plankton, but are found in lakes and rivers. An individual plankton organism in the plankton is called a plankter.[3] In the ocean plankton provide a crucial source of food, particularly for larger filter-feeding animals, such as bivalves, sponges, forage fish and baleen whales.
Plankton includes organisms from species across all the major biological kingdoms, ranging in size from the microscopic (such as bacteria, archaea, protozoa and microscopic algae and fungi[4]) to larger organisms (such as jellyfish and ctenophores).[5] This is because plankton are defined by their ecological niche and level of motility rather than by any phylogenetic or taxonomic classification. The plankton category differentiates organisms from those that can swim against a current, called nekton, and those that live on the deep sea floor, called benthos. Organisms that float on or near the water's surface are called neuston. Neuston that drift as water currents or wind take them, and lack the swimming ability to counter this, form a special subgroup of plankton. Mostly plankton just drift where currents take them, though some, like jellyfish, swim slowly but not fast enough to generally overcome the influence of currents.
Microscopic plankton, smaller than about one millimetre in size, play crucial roles in marine ecosystems. They are a diverse group, including phytoplankton (like diatoms and dinoflagellates) and zooplankton (such as radiolarians, foraminifera and some copepods), and serve as a foundational component of the marine food web. These largely unseen microscopic plankton drive primary production, support local food webs, cycle nutrients, and influence global biogeochemical processes. Their role is foundational for maintaining the health and balance of marine ecosystems.
Although plankton are usually thought of as inhabiting water, there are also airborne versions that live part of their lives drifting in the atmosphere. These aeroplankton can include plant spores, pollen and wind-scattered seeds. They can also include microorganisms swept into the air from terrestrial dust storms and oceanic plankton swept into the air by sea spray.
Overview
Apart from aeroplankton, plankton inhabits oceans, seas, estuaries, rivers, lakes and ponds. Local abundance varies horizontally, vertically and seasonally. The primary cause of this variability is the availability of light. All plankton ecosystems are driven by the input of solar energy (but see chemosynthesis), confining primary production to surface waters, and to geographical regions and seasons having abundant light.
A secondary variable is nutrient availability. The amount and distribution of plankton depends on available nutrients, the state of water and a large amount of other plankton.[7] The local distribution of plankton can be affected by wind-driven Langmuir circulation and the biological effects of this physical process. Although large areas of the tropical and sub-tropical oceans have abundant light, they experience relatively low primary production because they offer limited nutrients such as nitrate, phosphate and silicate. This results from large-scale ocean circulation and water column stratification. In such regions, primary production usually occurs at greater depth, although at a reduced level (because of reduced light).
While plankton are most abundant in surface waters, they live throughout the water column. At depths where no primary production occurs, zooplankton and bacterioplankton instead consume organic material sinking from more productive surface waters above. This flux of sinking material, so-called marine snow, can be especially high following the termination of spring blooms.
Despite significant macronutrient concentrations, some ocean regions are unproductive (so-called HNLC regions).[8] The micronutrient iron is deficient in these regions, and adding it can lead to the formation of phytoplankton algal blooms.[9] Iron primarily reaches the ocean through the deposition of dust on the sea surface. Paradoxically, oceanic areas adjacent to unproductive, arid land thus typically have abundant phytoplankton (e.g., the eastern Atlantic Ocean, where trade winds bring dust from the Sahara Desert in north Africa).
Within the plankton, holoplankton spend their entire life cycle as plankton (e.g. most algae, copepods, salps, and some jellyfish). By contrast, meroplankton are only planktic for part of their lives (usually the larval stage), and then graduate to either a nektic (swimming) or benthic (sea floor) existence. Examples of meroplankton include the larvae of sea urchins, starfish, crustaceans, marine worms, and most fish.[10]
Microscopic plankton
Plankton is mostly made up of planktonic microorganisms less than one millimetre across, most visible only through a microscope. Microorganisms have been variously estimated to make up about 70%,[11] or about 90%,[12][13] of the total ocean biomass. Taken together they form the marine microbiome. Over billions of years this microbiome has evolved many life styles and adaptations and come to participate in the global cycling of almost all chemical elements.[14]
Microplankton are ecological linchpins in the marine food web. They are crucial to nutrient recycling in the way they act as decomposers. They are also responsible for nearly all photosynthesis that occurs in the ocean, as well as the cycling of carbon, nitrogen, phosphorus and other nutrients and trace elements.[15] Microplankton sequesters large amounts of carbon and produce much of the world's oxygen.
It is estimated marine viruses kill 20% of ocean microplankton biomass every day. Viruses are the main agents responsible for the rapid destruction of harmful algal blooms which often kill other marine life. The number of viruses in the plankton decreases further offshore and deeper into the water, where there are fewer host organisms.
Terminology
The name plankton was coined by German marine biologist Victor Hensen in 1887 from shortening the word halyplankton from Greek Script error: No such module "Lang". háls "sea" and Script error: No such module "Lang". planáomai "(I) drift" or "(I) wander".[17]Template:Rp[18] Some forms of plankton are capable of independent vertically movement, and can swim hundreds of meters vertically in a single day (a behavior called diel vertical migration). However their horizontal position is primarily determined by the surrounding water movement, so plankton typically flow with the ocean currents. This is in contrast to nekton organisms, such as fish, squid and marine mammals, which can swim against the ambient flow and control their position in the environment.
The study of plankton is termed planktology and a planktonic individual is referred to as a plankter.[19] The adjective planktonic is widely used in both the scientific and popular literature, and is a generally accepted term. However, from the standpoint of prescriptive grammar, the less-commonly used planktic is more strictly the correct adjective. When deriving English words from their Greek or Latin roots, the gender-specific ending (in this case, "-on" which indicates the word is neuter) is normally dropped, using only the root of the word in the derivation.[20]
By habitat
Aeroplankton
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Aeroplankton are tiny lifeforms that float and drift in the air, carried by the current of the wind; they are the atmospheric analogue to oceanic plankton. Most of the living things that make up aeroplankton are very small to microscopic in size, and many can be difficult to identify because of their tiny size. Scientists can collect them for study in traps and sweep nets from aircraft, kites or balloons.[21] Aeroplankton is made up of numerous microbes, including viruses, about 1000 different species of bacteria, around 40,000 varieties of fungi, and hundreds of species of protists, algae, mosses and liverworts that live some part of their life cycle as aeroplankton, often as spores, pollen, and wind-scattered seeds. Additionally, peripatetic microorganisms are swept into the air from terrestrial dust storms, and an even larger amount of airborne marine microorganisms are propelled high into the atmosphere in sea spray. Aeroplankton deposits hundreds of millions of airborne viruses and tens of millions of bacteria every day on every square meter around the planet. This means similar mixes of microscopic plankton taxon can be found in open bodies of water around the world.[22][23][24]
The sea surface microlayer, compared to the sub-surface waters, contains elevated concentration of bacteria and viruses.[25][26] These materials can be transferred from the sea-surface to the atmosphere in the form of wind-generated aqueous aerosols due to their high vapour tension and a process known as volatilisation.[27] When airborne, these microbes can be transported long distances to coastal regions. If they hit land they can have an effect on animal, vegetation and human health.[28] Marine aerosols that contain viruses can travel hundreds of kilometers from their source and remain in liquid form as long as the humidity is high enough (over 70%).[29][30][31] These aerosols are able to remain suspended in the atmosphere for about 31 days.[32] Evidence suggests that bacteria can remain viable after being transported inland through aerosols. Some reached as far as 200 meters at 30 meters above sea level.[33] The process which transfers this material to the atmosphere causes further enrichment in both bacteria and viruses in comparison to either the SML or sub-surface waters (up to three orders of magnitude in some locations).[33]
Freshwater plankton
Freshwater plankton parallel marine plankton (below), but are found inland in the freshwaters of lakes and rivers.
Geoplankton
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Many animals live in terrestrial environments by thriving in transient often microscopic bodies of water and moisture, these include rotifers and gastrotrichs which lay resilient eggs capable of surviving years in dry environments, and some of which can go dormant themselves. Nematodes are usually microscopic with this lifestyle. Water bears, despite only having lifespans of a few months, famously can enter suspended animation during dry or hostile conditions and survive for decades. This allows them to be ubiquitous in terrestrial environments despite needing water to grow and reproduce. Many microscopic crustacean groups like copepods and amphipods (of which sandhoppers are members) and seed shrimp are known to go dormant when dry and live in transient bodies of water too[34]
Marine plankton
Marine plankton includes marine protists (algae and protozoa), drifting and floating animals (particularly microanimals), marine prokaryotes (bacteria and archaea), and marine viruses that inhabit the saltwater of oceans and the brackish waters of estuaries.
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At the ocean surface
Script error: No such module "labelled list hatnote". Plankton are also found at the ocean surface. Organisms that live at or just below the air-sea interface are called neuston. They float either on the water's surface (epineuston) or swim in the top few centimeters (hyponeuston). Many neuston qualify to be categorised as part of the broader plankton community, because they drift largely as currents or wind dictate, lacking strong enough swimming ability to counter them.[35][36][37]
Neustonic animals are primarily adapted to float upside-down on the ocean surface, similar to an inverted benthos,[38] and form a unique subset of the zooplankton community, which plays a pivotal role in the functioning of marine ecosystems.[39] Neustonic zooplankton are partially responsible for the active energy flux between superficial and deep layers of the ocean.[40][41][42]Neustonic plankton is also a food source for marine zooplankton and fish migrating from the deep layers and seabirds.[35]
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In deep ocean
In 2025, researchers discovered microbial communities inhabiting the ocean conveyor belt, even at great depths in the ocean.[43][44] Ocean currents are generated by surface wind and storms down to about Template:Cvt below the surface. But the average depth of the ocean goes far below to Template:Cvt.[45] At these greater depths, currents are driven by differences in water density, which in turn are controlled by differences in water temperature and salinity. This mechanism results in a circulation which behaves like a conveyor belt, carrying water and microorganisms to great depths and around the world.[43]
Water samples were taken along the full depth of the water column in the South Pacific Ocean, from Easter Island to Antarctica. They found marked increases in microbial diversity about Template:Cvt deep, in a layer they call the prokaryotic phylocline. This zone, similar to the pycnocline, represents a shift from less diverse surface waters to abundant microbial ecosystems in the deep ocean. For instance, a group they called the Antarctic Bottom Water contains microbes suited to cold and high pressure, while another group they called the Ancient Water Group, located in slowly circulating water isolated from the surface for over a millennium, contains microbes with genes adapted to low oxygen.[43][44]
By taxon
Plankton contains representatives from all major divisions of life. By taxon, it can be divided into the following broad groups:[46][47]
- planktonic animals (metazoa) : – mostly predators (zooplankton) of smaller plankton. Examples are arrow worms, sea butterfly, ostracods, and salps. There are also planktonic microanimals typically smaller than one mm, such as copepods, water fleas, rotifers, and larval stages of various crustaceans and corals.
- planktonic protists: – single-celled eukaryote microorganisms, mostly invisible to the naked eye, such as diatoms, dinoflagellates, coccolithophores, foraminifera, radiolarians, and ciliates. Planktonic protists include algae (phytoplankton), protozoa (zooplankton), and many mixoplankton.[48]
- planktonic fungi: – known also as mycoplankton, play important roles in remineralisation and nutrient cycling.[49] For example, in the mycoloop, parasitic chytrids facilitate the transfer of nutrients from large, inedible phytoplankton to zooplankton.
- planktonic prokaryotes: – (bacteria and archaea – planktonic bacteria are known also as bacterioplankton) can play important roles as primary producers, or in remineralising organic material like mycoplankton down the water column. Photosynthetic cyanobacteria are important members of the phytoplankton. The unusually small Pelagibacter ubique, perhaps the most abundant bacterium on Earth, makes up about one third of microbial cells in the surface ocean,[50] and plays important roles recycling nutrients in the microbial loop. The Roseobacter clade are significantly connected to phytoplankton.
- planktonic viruses: – known also as virioplankton, though not always classified as living organisms, are abundant in planktonic communities and influence microbial dynamics. Viruses are small infectious agents that can replicate only inside the living cells of a host organism, because they need the replication machinery of the host to do so.[51] They are more abundant in the plankton than bacteria and archaea, though much smaller.[52][53] Viruses can infect all types of life forms, from animals and plants to microorganisms, including bacteria and archaea.[54] In the viral shunt, viruses infect and break down (lyse) bacteria, releasing their nutrients and organic matter back into the water instead of allowing them to be consumed by larger organisms like zooplankton. This "shunts" nutrients away from higher trophic levels, keeping them in the microbial loop for reuse by other microorganisms.
-
This planktonic animal (metazoa) is a female copepod. It has two egg sacs and microalgae attached to its body
-
These are shells of planktonic protists called radiolarians, drawn by Ernst Haeckel (1904)
-
This planktonic bacterium is the cyanobacterium Prochlorococcus, the smallest photosynthetic organism in the world. It contributes up to 20% of the world's oxygen production, more than all tropical rainforests.[55]
-
This planktonic virus (arrowed) is the giant coccolithovirus, Emiliania huxleyi virus 86, infecting an Emiliania huxleyi coccolithophore
By size
Plankton are also often described in terms of size. Usually the following divisions are used:Template:Hsp[56]
Group Size range (ESD) Examples Megaplankton > 20 cm metazoans; e.g. jellyfish; ctenophores; salps and pyrosomes (pelagic Tunicata); Cephalopoda; Amphipoda Macroplankton 2→20 cm metazoans; e.g. Pteropoda; Chaetognaths; Medusae; ctenophores; salps, doliolids and pyrosomes (pelagic Tunicata); Cephalopoda; Janthina and Recluzia (two genera of gastropods); Amphipoda Mesoplankton 0.2→20 mm metazoans; e.g. copepods; Medusae; Cladocera; Ostracoda; Chaetognaths; Pteropoda; Tunicata Microplankton 20→200 μm large eukaryotic protists; most phytoplankton; Protozoa Foraminifera; tintinnids; other ciliates; Rotifera; juvenile metazoans – Crustacea (copepod nauplii) Nanoplankton 2→20 μm small eukaryotic protists; small diatoms; small flagellates; Pyrrophyta; Chrysophyta; Chlorophyta; Xanthophyta Picoplankton 0.2→2 μm small eukaryotic protists; bacteria; Chrysophyta Femtoplankton < 0.2 μm marine viruses
However, some of these terms may be used with very different boundaries, especially on the larger end. The term microplankton is sometimes used more broadly to cover plankton that cannot really be seen without using a microscope, say plankton less than about one millimetre across. The existence and importance of nano- and even smaller plankton was only discovered during the 1980s, but they are thought to make up the largest proportion of all plankton in number and diversity. It is the largely unseen microplankton that are the main drivers of the marine food web.
Microplankton and smaller groups are microorganisms that operate at low Reynolds numbers, where the viscosity of water is more important than its mass or inertia.[57]
- Microplankton
-
Some marine diatoms — a key phytoplankton group
-
Pelagibacter ubique, the most common bacteria in the ocean, plays a major role in global carbon cycles
-
Microzooplankton are major grazers of the plankton: two dinoflagellates and a tintinnid ciliate.
- Macroplankton
-
Macrozooplankton: the amphipod Hyperia macrocephala
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A Janthina janthina snail (with bubble float) cast up onto a beach in Maui
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Sargassum seaweed drifts with currents using air bladders to stay afloat
By trophic mode
Trophic mode describes the role of a planktonic organism in the food web based on how it obtains energy and nutrients to sustain its growth, reproduction, and survival.[1] By trophic mode, plankton can be divided into four broad functional groups: phytoplankton, zooplankton, mixoplankton and decomposers.[59][60][61][62]
Phytoplankton
Phytoplankton (from Greek phyton, or plant) are autotrophic prokaryotic or eukaryotic algae that live near the water surface where there is sufficient light to support photosynthesis. Among the more important groups are the diatoms, cyanobacteria, dinoflagellates, and coccolithophores.
- Phytoplankton largely form the base of the marine food web
-
Diatoms are one of the most common types of phytoplankton
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A cyanobacteria species (Cylindrospermum sp)
-
Green algae, Pyramimonas
Zooplankton
Zooplankton (from Greek zoon, or animal) are small protozoans or metazoans (e.g. crustaceans and other animals) that feed on other plankton. Some of the eggs and larvae of larger nektonic animals, such as fish, crustaceans, and annelids, are included here.
- Larger plankton tend to be zooplankton which eat smaller phytoplankton
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Icefish larvae from Antarctica have no haemoglobin
-
Copepod from Antarctica, a translucent ovoid microanimal with two long antennae
Mixoplankton
Mixoplankton (from Greek mixis, or mixture) have a mixed trophic strategy. In recent years, there has been a growing recognition that perhaps the majority of plankton can act in both the above modes.
Traditionally, plankton were divided into just the first two broad trophic groups: plant-like phytoplankton which make their own food, usually by photosynthesis, and animal-like zooplankton that eat other plankton. In recent years, there has been a recognition that many plankton, perhaps over half, are mixotrophic.[63] Plankton have traditionally been categorized as producer, consumer, and recycler groups, but some plankton are able to benefit from more than just one trophic level. This mixed trophic strategy means mixoplankton can act as both producers and consumers, either at the same time or switching between modes of nutrition in response to ambient conditions. In this manner, mixoplankton can use photosynthesis for growth when nutrients and light are abundant, but switch to eating phytoplankton, zooplankton or each other when growing conditions are poor.
As a result of these findings, many plankton formally categorized as phytoplankton, including coccolithophores and dinoflagellates, are longer included as strictly phytoplankton, as they not only produce their own food through phototrophy but can also eat other organisms.[64] These organisms are now more correctly termed mixoplankton.[61] This recognition has important consequences for how the functioning of the planktonic food web is viewed.[65]
- Mixoplankton can behave both as phytoplankton and zooplankton
-
Euglena mutabilis, a photosynthetic flagellate
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The mixotrophic dinoflagellate Karenia brevis causes harmful red tides
-
Acantharian radiolarian hosts Phaeocystis symbionts.
-
White Phaeocystis algal foam washing up on a beach
Mixotrophs can be further divided into two groups; constitutive mixotrophs which are able to perform photosynthesis on their own, and non-constitutive mixotrophs which use phagocytosis to engulf phototrophic prey that are either kept alive inside the host cell, which benefits from its photosynthesis, or they digested, except for the plastids, which continue to perform photosynthesis (kleptoplasty).[66] Recognition of the importance of mixotrophy as an ecological strategy is increasing,[67] as well as the wider role this may play in marine biogeochemistry.[68] Studies have shown that mixoplankton are much more important for marine ecology than previously assumed.[69][70] Their presence acts as a buffer that prevents the collapse of ecosystems during times with little to no light.[71] Mixoplankton have ancient origins and have been recognized by scientists for over a century. However, it is only in recent years that the widespread significance of mixoplankton has been gaining recognition in mainstream marine science.[72]
Decomposers
Instead of directly building biomass, decomposers break organic nutrients down into inorganic forms which can be recycled (an approach which metabolically can be costly).[62]
Fungi: Mostly tiny mycoplankton (microfungi), yeast, or mobile zoospores, that can recycle organic matter through a process called the mycoloop which involves parasiting plankton.[62]
Bacteria/Archaea: These minute prokaryotes (typically <0.001mm) return organic nutrients to inorganic forms by breaking down particulate and dissolved organic matter through the process called the microbial loop.[73] Some convert ammonium in animal waste to nitrate, while others transform nitrate to nitrogen gas. Viral infections likely destroy many, while others are eaten by protist zooplankton and mixoplankton, which use their nutrients for photosynthesis. However details of their ecology is complex and it is not clear what sustains them.[62]
Viruses: Typically 10 to 100 times smaller than bacteria and also the most abundant (~100 billion per litre), viruses infect other plankton and larger organisms. It is thought they efficiently halt vast plankton blooms within days, by turning biomass into dissolved organic matter that supports bacterial growth through a process called the viral shunt.[74] Being host-specific, they also likely influence the biological and microbial carbon pumps.[62]
Other groups
Gelatinous zooplankton
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Gelatinous zooplankton are fragile animals that live in the water column in the ocean. Their delicate bodies have no hard parts and are easily damaged or destroyed.[76] Gelatinous zooplankton are often transparent.[77] All jellyfish are gelatinous zooplankton, but not all gelatinous zooplankton are jellyfish. The most commonly encountered organisms include ctenophores, medusae, salps, and Chaetognatha in coastal waters. However, almost all marine phyla, including Annelida, Mollusca and Arthropoda, contain gelatinous species, but many of those odd species live in the open ocean and the deep sea and are less available to the casual ocean observer.[78]
Ichthyoplankton
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Ichthyoplankton are the eggs and larvae of fish. They are mostly found in the sunlit zone of the water column, less than 200 metres deep, which is sometimes called the epipelagic or photic zone. Ichthyoplankton are planktonic, meaning they cannot swim effectively under their own power, but must drift with the ocean currents. Fish eggs cannot swim at all, and are unambiguously planktonic. Early stage larvae swim poorly, but later stage larvae swim better and cease to be planktonic as they grow into juveniles. Fish larvae are part of the zooplankton that eat smaller plankton, while fish eggs carry their own food supply. Both eggs and larvae are themselves eaten by larger animals.[79][80] Fish can produce high numbers of eggs which are often released into the open water column. Fish eggs typically have a diameter of about Template:Convert. The newly hatched young of oviparous fish are called larvae. They are usually poorly formed, carry a large yolk sac (for nourishment), and are very different in appearance from juvenile and adult specimens. The larval period in oviparous fish is relatively short (usually only several weeks), and larvae rapidly grow and change appearance and structure (a process termed metamorphosis) to become juveniles. During this transition larvae must switch from their yolk sac to feeding on zooplankton prey, a process which depends on typically inadequate zooplankton density, starving many larvae. In time fish larvae become able to swim against currents, at which point they cease to be plankton and become juvenile fish.
Pseudoplankton
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Pseudoplankton are organisms that attach themselves to planktonic organisms or other floating objects, such as drifting wood, buoyant shells of organisms such as Spirula, or man-made flotsam. Examples include goose barnacles and the bryozoan Jellyella. By themselves these animals cannot float, which contrasts them with true planktonic organisms, such as Velella and the Portuguese Man o' War, which are buoyant. Pseudoplankton are often found in the guts of filtering zooplankters.[81]
Tychoplankton
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Tychoplankton are organisms, such as free-living or attached benthic organisms and other non-planktonic organisms, that are carried into the plankton through a disturbance of their benthic habitat, or by winds and currents.[82] This can occur by direct turbulence or by disruption of the substrate and subsequent entrainment in the water column.[82][83] Tychoplankton are, therefore, a primary subdivision for sorting planktonic organisms by duration of lifecycle spent in the plankton, as neither their entire lives nor particular reproductive portions are confined to planktonic existence.[84] Tychoplankton are sometimes called accidental plankton.
Mineralized plankton
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- Some planktons are protected with mineralized shells or tests.
By life cycle
Holoplankton
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Holoplankton are organisms that are planktic for their entire life cycle. Holoplankton can be contrasted with meroplankton, which are planktic organisms that spend part of their life cycle in the benthic zone. Examples of holoplankton include some diatoms, radiolarians, some dinoflagellates, foraminifera, amphipods, copepods, and salps, as well as some gastropod mollusk species. Holoplankton dwell in the pelagic zone as opposed to the benthic zone.[86] Holoplankton include both phytoplankton and zooplankton and vary in size. The most common plankton are protists.[87]
Meroplankton
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Meroplankton are a wide variety of aquatic organisms that have both planktonic and benthic stages in their life cycles. Much of the meroplankton consists of larval stages of larger organisms.[34] Meroplankton can be contrasted with holoplankton, which are planktonic organisms that stay in the pelagic zone as plankton throughout their entire life cycle.[88] After some time in the plankton, many meroplankton graduate to the nekton or adopt a benthic (often sessile) lifestyle on the seafloor. The larval stages of benthic invertebrates make up a significant proportion of planktonic communities.[89] The planktonic larval stage is particularly crucial to many benthic invertebrates in order to disperse their young. Depending on the particular species and the environmental conditions, larval or juvenile-stage meroplankton may remain in the pelagic zone for durations ranging from hours to months.[34]
Ecology
Food webs
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traditional paradigm[90]
mixoplankton paradigm[90]
As well as representing the lower levels of a food chain that supports commercially important fisheries, plankton ecosystems play a role in the biogeochemical cycles of many important chemical elements, including the ocean's carbon cycle.[91] Fish larvae mainly eat zooplankton, which in turn eat phytoplankton[92]
The microbial loop: Bacteria play central roles in aquatic food webs. The microbial loop refers to a process in aquatic ecosystems where bacteria consume dissolved organic matter (DOM) and are then consumed by larger microorganisms, effectively cycling nutrients and energy within the ecosystem.[93]
The viral shunt: Viruses also play central roles in aquatic food webs. The viral shunt is a process where viruses infect and lyse (burst) host cells, releasing cellular contents (including dissolved organic matter) that can be utilized by other microplankton like bacteria, effectively bypassing the traditional food web pathways. This process plays a significant role in nutrient cycling and carbon flow within aquatic ecosystems.[94]
Fungi have a role as well. The mycoloop is a specific aquatic food web pathway where parasitic chytrid fungi infect large, inedible phytoplankton, and their zoospores (a type of spore) become a food source for zooplankton. In this manner, the chytrid fungi transfer nutrients from otherwise unusable phytoplankton to zooplankton.[95]
Carbon cycle
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Primarily by grazing on phytoplankton, zooplankton provide carbon to the planktic foodweb, either respiring it to provide metabolic energy, or upon death as biomass or detritus. Organic material tends to be denser than seawater, so it sinks into open ocean ecosystems away from the coastlines, transporting carbon along with it. This process, called the biological pump, is one reason that oceans constitute the largest carbon sink on Earth. However, it has been shown to be influenced by increments of temperature.[98][99][100][101] In 2019, a study indicated that at ongoing rates of seawater acidification, Antarctic phytoplanktons could become smaller and less effective at storing carbon before the end of the century.[102]
It might be possible to increase the ocean's uptake of carbon dioxide (Template:Chem) generated through human activities by increasing plankton production through iron fertilization – introducing amounts of iron into the ocean. However, this technique may not be practical at a large scale. Ocean oxygen depletion and resultant methane production (caused by the excess production remineralising at depth) is one potential drawback.[103][104]
Great Calcite Belt
The Great Calcite Belt is a region in the Southern Ocean characterized by high concentrations of coccolithophores, a type of calcite-producing phytoplankton. It plays a significant role in ocean biogeochemistry and the global carbon cycle. Coccolithophores in the belt produce calcium carbonate (calcite or chalk) plates called coccoliths. This process, known as calcification, affects the ocean's carbon cycle by lowering alkalinity and releasing CO2. However, when coccolithophores die, their calcite shells sink, contributing to the biological pump by transporting carbon to the deep ocean, sequestering it for centuries or longer and mitigating atmospheric CO2 levels.[105]
Oxygen production
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Phytoplankton absorb energy from the Sun and nutrients from the water to produce their own nourishment or energy. In the process of photosynthesis, phytoplankton release molecular oxygen (Template:Chem) into the water as a waste byproduct. It is estimated that about 50% of the world's oxygen is produced via phytoplankton photosynthesis.[106] The rest is produced via photosynthesis on land by plants.[106] Furthermore, phytoplankton photosynthesis has controlled the atmospheric [[Carbon dioxide in Earth's atmosphere|Template:Chem]]/[[Oxygen#Build-up in the atmosphere|Template:Chem]] balance since the early Precambrian Eon.[107]
Absorption efficiency
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The absorption efficiency (AE) of plankton is the proportion of food absorbed by the plankton that determines how available the consumed organic materials are in meeting the required physiological demands.[108] Depending on the feeding rate and prey composition, variations in absorption efficiency may lead to variations in fecal pellet production, and thus regulates how much organic material is recycled back to the marine environment. Low feeding rates typically lead to high absorption efficiency and small, dense pellets, while high feeding rates typically lead to low absorption efficiency and larger pellets with more organic content. Another contributing factor to dissolved organic matter (DOM) release is respiration rate. Physical factors such as oxygen availability, pH, and light conditions may affect overall oxygen consumption and how much carbon is loss from zooplankton in the form of respired Template:CO2. The relative sizes of zooplankton and prey also mediate how much carbon is released via sloppy feeding. Smaller prey are ingested whole, whereas larger prey may be fed on more "sloppily", that is more biomatter is released through inefficient consumption.[109][110] There is also evidence that diet composition can impact nutrient release, with carnivorous diets releasing more dissolved organic carbon (DOC) and ammonium than omnivorous diets.[111]
Biomass variability
The growth of phytoplankton populations is dependent on light levels and nutrient availability. The chief factor limiting growth varies from region to region in the world's oceans. On a broad scale, growth of phytoplankton in the oligotrophic tropical and subtropical gyres is generally limited by nutrient supply, while light often limits phytoplankton growth in subarctic gyres. Environmental variability at multiple scales influences the nutrient and light available for phytoplankton, and as these organisms form the base of the marine food web, this variability in phytoplankton growth influences higher trophic levels. For example, at interannual scales phytoplankton levels temporarily plummet during El Niño periods, influencing populations of zooplankton, fishes, sea birds, and marine mammals.
The effects of anthropogenic warming on the global population of phytoplankton is an area of active research. Changes in the vertical stratification of the water column, the rate of temperature-dependent biological reactions, and the atmospheric supply of nutrients are expected to have important impacts on future phytoplankton productivity.[112] Additionally, changes in the mortality of phytoplankton due to rates of zooplankton grazing may be significant.
Planktonic relationships
Fish and plankton
Zooplankton are the initial prey item for almost all fish larvae as they switch from their yolk sacs to external feeding. Fish rely on the density and distribution of zooplankton to match that of new larvae, which can otherwise starve. Natural factors (e.g., current variations, temperature changes) and man-made factors (e.g. river dams, ocean acidification, rising temperatures) can strongly affect zooplankton populations, which can in turn strongly affect fish larval survival, and therefore breeding success.
It has been shown that plankton can be patchy in marine environments where there aren't significant fish populations and additionally, where fish are abundant, zooplankton dynamics are influenced by the fish predation rate in their environment. Depending on the predation rate, they could express regular or chaotic behavior.[113]
A negative effect that fish larvae can have on planktonic algal blooms is that the larvae will prolong the blooming event by diminishing available zooplankton numbers; this in turn permits excessive phytoplankton growth allowing the bloom to flourish .[92]
The importance of both phytoplankton and zooplankton is also well-recognized in extensive and semi-intensive pond fish farming. Plankton population-based pond management strategies for fish rearing have been practiced by traditional fish farmers for decades, illustrating the importance of plankton even in man-made environments.
Whales and plankton
Of all animal fecal matter, it is whale feces that is the 'trophy' in terms of increasing nutrient availability. Phytoplankton are the powerhouse of open ocean primary production and they can acquire many nutrients from whale feces.[114] In the marine food web, phytoplankton are at the base of the food web and are consumed by zooplankton & krill, which are preyed upon by larger and larger marine organisms, including whales, so it can be said that whale feces fuels the entire food web.
Humans and plankton
Plankton have many direct and indirect effects on humans.
Around 70% of the oxygen in the atmosphere is produced in the oceans from phytoplankton performing photosynthesis, meaning that the majority of the oxygen available for us and other organisms that respire aerobically is produced by plankton.[115]
Plankton also make up the base of the marine food web, providing food for all the trophic levels above. Recent studies have analyzed the marine food web to see if the system runs on a top-down or bottom-up approach. Essentially, this research is focused on understanding whether changes in the food web are driven by nutrients at the bottom of the food web or predators at the top. The general conclusion is that the bottom-up approach seemed to be more predictive of food web behavior.[116] This indicates that plankton have more sway in determining the success of the primary consumer species that prey on them than do the secondary consumers that prey on the primary consumers.
In some cases, plankton act as an intermediate host for deadly parasites in humans. One such case is that of cholera, an infection caused by several pathogenic strains of Vibrio cholerae. These species have been shown to have a symbiotic relationship with chitinous zooplankton species like copepods. These bacteria benefit not only from the food provided by the chiton from the zooplankton, but also from the protection from acidic environments. Once the copepods have been ingested by a human host, the chitinous exterior protects the bacteria from the stomach acids in the stomach and proceed to the intestines. Once there, the bacteria bind with the surface of the small intestine and the host will start developing symptoms, including extreme diarrhea, within five days.[117]
Plankton Manifesto
In 2024, the United Nations Global Compact's Ocean Stewardship Coalition launched the Plankton Manifesto,[62] collaboratively developed by over 30 international experts.[118] It outlines strategic recommendations to guide global efforts at safeguarding plankton and harnessing their potential to address planetary climate change issues, as well as pollution and biodiversity loss. It emphasizes plankton's critical role as the foundation of marine ecosystems, producing about 50% of Earth's oxygen and sequestering 30–50 billion metric tonnes of carbon annually.[62]
Key recommendations include:[62]
- Enhanced research and monitoring: Leveraging technologies like DNA sequencing, bioinformatics, satellite monitoring, and AI image analysis to improve understanding of plankton dynamics and create a global plankton atlas.
- Plankton-based solutions: Promoting innovative applications, such as using plankton for water purification, bioplastics, fertilizers, and animal feed to support sustainable industries.
- Policy integration: Urging governments, United Nations agencies, and businesses to include plankton in climate and biodiversity frameworks, with endorsements sought at COP29, COP16, and the 2025 United Nations Ocean Conference.
- Public awareness: Fostering "plankton literacy" through education and interdisciplinary initiatives to highlight their role in food security and ecosystem health.
- Collaboration: Encouraging cross-sectoral partnerships among academia, industry, and governments to fund research and protect plankton from threats like nutrient pollution and ocean warming.
See also
References
Further reading
- Kirby, Richard R. (2010). Ocean Drifters: A Secret World Beneath the Waves. Studio Cactus Ltd, UK. Template:ISBN.
- Dusenbery, David B. (2009). Living at Micro Scale: The Unexpected Physics of Being Small. Harvard University Press, Cambridge, Massachusetts Template:ISBN.
- Kiørboe, Thomas (2008). A Mechanistic Approach to Plankton Ecology. Princeton University Press, Princeton, N.J. Template:ISBN.
- Dolan, J.R., Agatha, S., Coats, D.W., Montagnes, D.J.S., Stocker, D.K., eds. (2013).Biology and Ecology of Tintinnid Ciliates: Models for Marine Plankton. Wiley-Blackwell, Oxford, UK Template:ISBN.
External links
Template:Sister project Template:Sister project Template:Sister project Template:Sister project
- Ocean Drifters – Short film narrated by David Attenborough about the varied roles of plankton
- Plankton Chronicles Template:Webarchive – Short documentary films and photos
- COPEPOD: The Global Plankton Database – Global coverage database of zooplankton biomass and abundance data
- Plankton*Net Template:Webarchive – Taxonomic database of images of plankton species
- Guide to the marine zooplankton of south-eastern Australia – Tasmanian Aquaculture and Fisheries Institute
- Sir Alister Hardy Foundation for Ocean Science – Continuous Plankton Recorder Survey
- Australian Continuous Plankton Recorder Project – Integrated Marine Observing System
- Sea Drifters – BBC Audio slideshow
- Aquaparadox: the diversity of planktonic microorganisms – Images of planktonic microorganisms
- Plankton, planktic, planktonic – Essays on nomenclature
- Journal of Plankton ResearchTemplate:Dead linkTemplate:Cbignore – Scientific periodical devoted to plankton
Template:Plankton Template:Aquatic ecosystem topics
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- ↑ Template:Ifsubst (2001) Biological Oceanography. Butterworth-Heinemann.
- ↑ Template:Ifsubst (2000) Transparent Animals. Scientific American 282: 62–71.
- ↑ Template:Ifsubst (2007) The Deep. University of Chicago Press.
- ↑ What are Ichthyoplankton? Southwest Fisheries Science Center, NOAA. Modified 3 September 2007. Retrieved 22 July 2011.
- ↑ Script error: No such module "citation/CS1".
- ↑ Script error: No such module "citation/CS1".
- ↑ a b Script error: No such module "citation/CS1".
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- ↑ a b Script error: No such module "citation/CS1".
- ↑ Template:Cite FTP
- ↑ a b Script error: No such module "Citation/CS1".
- ↑ a b Script error: No such module "Citation/CS1". File:CC-BY icon.svg Modified text was copied from this source, which is available under a Creative Commons Attribution 4.0 International License
- ↑ a b Script error: No such module "citation/CS1". File:CC-BY icon.svg Modified text was copied from this source, which is available under a Creative Commons Attribution 4.0 International License
- ↑ a b Script error: No such module "Citation/CS1". File:CC-BY icon.svg Modified text was copied from this source, which is available under a Creative Commons Attribution 4.0 International License
- ↑ Script error: No such module "Citation/CS1".
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- ↑ Script error: No such module "Citation/CS1".
- ↑ Script error: No such module "Citation/CS1". File:CC-BY icon.svg Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
- ↑ a b Script error: No such module "citation/CS1".
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- ↑ Script error: No such module "Citation/CS1".