View source for Zooplankton

{{short description| Heterotrophic protistan or metazoan members of the plankton ecosystem }}
[[File:Mixed zooplankton sample.jpg|thumb|upright=1.8| Zooplankton sample including several species of [[copepod]]s (1–5), [[gastropod]] [[larva]] (6) [[doliolida|doliolids]] (7), [[fish egg]]s (8), and [[decapod larva]] (9) (Photo by Iole Di Capua)]]

'''Zooplankton''' are the [[heterotroph]]ic component of the [[plankton]]ic community, having to consume other organisms to thrive. The name comes from [[Ancient Greek]] [[wikt:ζῷον|ζῷον]] (''zōîon''), meaning "[[animal]]", and [[wikt:πλαγκτός|πλαγκτός]] (''planktós''), meaning "drifter, wanderer, roamer", and thus, "animal drifter". Plankton are aquatic organisms that are unable to swim effectively against currents. Consequently, they drift or are carried along by currents in the [[ocean]], or by currents in [[sea]]s, [[lake]]s or [[river]]s.

Zooplankton can be contrasted with [[phytoplankton]] ([[cyanobacteria]] and [[microalgae]]), which are the plant-like component of the plankton community (the "[[wikt:phyto-|phyto-]]" prefix comes from {{Langx|grc|φῠτόν|translit=phutón|lit=plant|link=no}}, although taxonomically ''not'' [[plant]]s). Zooplankton are [[heterotrophic]] (other-feeding), whereas phytoplankton are [[autotrophic]] (self-feeding), often generating [[biological energy]] and [[macromolecule]]s through [[chlorophyll]]ic [[carbon fixation]] using [[sunlight]]{{snd}}in other words, zooplankton cannot manufacture their own food, while phytoplankton can. As a result, zooplankton must acquire [[nutrient]]s by [[feeding]] on other [[organism]]s such as phytoplankton, which are generally smaller than zooplankton. Most zooplankton are [[microscopic scale|microscopic]] but some (such as [[jellyfish]]) are [[macroscopic scale|macroscopic]], meaning they can be seen with the [[naked eye]].<ref>{{Cite book |last=Sardet |first=Christian |url=https://books.google.com/books?id=7JnMCQAAQBAJ&dq=Zooplankton+are+generally+larger+than+phytoplankton,+mostly+still+microscopic+but+some+can+be+seen+with+the+naked+eye.&pg=PA2 |title=Plankton: Wonders of the Drifting World |date=2015-06-05 |publisher=University of Chicago Press |isbn=978-0-226-26534-6 |language=en}}</ref>

Many [[#Protozoans|protozoans]] (single-celled [[Marine protists|protists]] that prey on other microscopic life) are zooplankton, including [[zooflagellate]]s, [[foraminifera]]ns, [[radiolarian]]s, some [[dinoflagellate]]s and [[#Planktonic metazoa (animals)|marine microanimals]]. Macroscopic zooplankton include pelagic [[cnidarian]]s, [[Ctenophora (phylum)|ctenophore]]s, [[mollusc]]s, [[arthropod]]s and [[tunicate]]s, as well as planktonic [[chaetognatha|arrow worms]] and [[Polychaete|bristle worms]].

The distinction between autotrophy and heterotrophy often breaks down in very small organisms. Recent studies of marine microplankton have indicated over half of microscopic plankton are [[mixotroph]]s, which can obtain energy and carbon from a mix of internal plastids and external sources. Many marine microzooplankton are mixotrophic, which means they could also be classified as phytoplankton.

==Overview==
{{plankton sidebar|trophic}}

'''Zooplankton''' ({{IPAc-en|ˈ|z|oʊ|.|ə|p|l|æ|ŋ|k|t|ən}};{{refn|{{Cite dictionary |url=http://www.lexico.com/definition/zooplankton |archive-url=https://web.archive.org/web/20200301210443/https://www.lexico.com/definition/zooplankton |archive-date=March 1, 2020 |title=zooplankton |dictionary=[[Lexico]] UK English Dictionary |publisher=[[Oxford University Press]]}} }} {{IPAc-en|ˌ|z|oʊ|.|ə|ˈ|p|l|æ|ŋ|k|t|ən}}){{refn|{{cite Merriam-Webster|zooplankton}}}} are [[heterotroph]]ic (sometimes [[detritivore|detritivorous]]) [[plankton]]. The word ''zooplankton'' is derived from {{langx|grc|ζῷον|translit=zôion|lit=animal}}; and {{Langx|grc|πλᾰγκτός|translit=planktós|label=none|lit=wanderer; drifter}}.<ref>{{cite book |last=Thurman |first=H. V. |year=1997 |title=Introductory Oceanography |publisher=Prentice Hall College |location=New Jersey, USA |isbn=978-0-13-262072-7}}</ref>

Zooplankton is a categorization spanning a range of [[organism]] sizes including small [[protozoa]]ns and large [[metazoa]]ns. It includes [[holoplankton]]ic organisms whose complete [[biological life cycle|life cycle]] lies within the plankton, as well as [[meroplankton]]ic organisms that spend part of their lives in the plankton before graduating to either the [[nekton]] or a [[Sessility (zoology)|sessile]], [[benthos|benthic]] existence. Although zooplankton are primarily transported by ambient water currents, many have [[Animal locomotion|locomotion]], used to avoid predators (as in [[diel vertical migration]]) or to increase prey encounter rate.

Just as any species can be limited within a geographical region, so are zooplankton. However, species of zooplankton are not dispersed uniformly or randomly within a region of the ocean. As with phytoplankton, 'patches' of zooplankton species exist throughout the ocean. Though few physical barriers exist above the [[mesopelagic]], specific species of zooplankton are strictly restricted by salinity and temperature gradients, while other species can withstand wide temperature and salinity gradients.<ref name="Lalli and Parsons">{{cite book |author1=Lalli, C.M. |author2=Parsons, T.R. |name-list-style=amp |title=Biological Oceanography An Introduction |year=1993 |publisher=Elsevier |location=Burlington, MA |isbn=978-0-7506-3384-0 |page=314}}</ref> Zooplankton patchiness can also be influenced by biological factors, as well as other physical factors. Biological factors include breeding, predation, concentration of phytoplankton, and vertical migration.<ref name="Lalli and Parsons"/> The physical factor that influences zooplankton distribution the most is mixing of the water column ([[upwelling]] and [[downwelling]] along the coast and in the open ocean) that affects nutrient availability and, in turn, phytoplankton production.<ref name="Lalli and Parsons"/>

Through their consumption and processing of phytoplankton and other food sources, zooplankton play a role in aquatic [[food web]]s, as a resource for consumers on higher [[trophic level]]s (including fish), and as a conduit for packaging the organic material in the [[biological pump]]. Since they are typically small, zooplankton can respond rapidly to increases in phytoplankton abundance,{{Clarify|date=March 2011}} for instance, during the [[spring bloom]]. Zooplankton are also a key link in the [[biomagnification]] of [[pollutant]]s such as [[Mercury (element)|mercury]].<ref>{{Cite web |date=2017-04-05 |title=How We Do Things at IISD-ELA: Researching Mercury |url=https://www.iisd.org/library/how-we-do-things-iisd-ela-researching-mercury |access-date=2020-07-06 |website=IISD |language=en}}</ref>

<gallery mode="packed" heights="360px" style="float:right;" caption="Typical models featuring zooplankton">
File:Typical ocean models featuring zooplankton 2.jpg|{{align|left|{{space|5}} Upper left: [[Marine biogeochemical cycles#Box models|Biogeochemical models]] {{space|22}} Right: [[Ecosystem model]]s}}<br />{{align|left|{{space|5}} Lower left: Size-spectra models}}<br />{{center|<small>These models also have temporal and spatial components.</small><ref>Everett, J.D., Baird, M.E., Buchanan, P., Bulman, C., Davies, C., Downie, R., Griffiths, C., Heneghan, R., Kloser, R.J., Laiolo, L. and Lara-Lopez, A. (2017) "Modeling what we sample and sampling what we model: challenges for zooplankton model assessment". ''Frontiers in Marine Science'', '''4''': 77. {{doi|10.3389/fmars.2017.00077|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>}}|alt=Upper left: Biogeochemical models                        Right: Ecosystem models      Lower left: Size-spectra modelsThese models also have temporal and spatial components.
</gallery>

[[Ecology|Ecologically]] important protozoan zooplankton groups include the [[foraminifera]]ns, [[radiolaria]]ns and [[dinoflagellate]]s (the last of these are often [[mixotroph]]ic). Important metazoan zooplankton include [[cnidaria]]ns such as [[jellyfish]] and the [[Portuguese Man o' War]]; [[crustacean]]s such as [[cladocera]]ns, [[copepod]]s, [[ostracod]]s, [[isopod]]s, [[amphipod]]s, [[mysids]] and [[krill]]; [[Chaetognatha|chaetognath]]s (arrow worms); [[Mollusca|molluscs]] such as [[pteropod]]s; and [[chordate]]s such as [[salp]]s and juvenile fish. This wide [[phylogeny|phylogenetic]] range includes a similarly wide range in feeding behavior: [[filter feeder|filter feeding]], [[predation]] and [[symbiosis]] with [[autotrophic]] [[phytoplankton]] as seen in corals. Zooplankton feed on [[bacterioplankton]], phytoplankton, other zooplankton (sometimes [[Cannibalism|cannibalistically]]), [[detritus]] (or [[marine snow]]) and even [[Nekton|nektonic organisms]]. As a result, zooplankton are primarily found in surface waters where food resources (phytoplankton or other zooplankton) are abundant.

Zooplankton can also act as a [[infectious disease|disease]] [[natural reservoir|reservoir]]. Crustacean zooplankton have been found to house the bacterium ''[[Vibrio cholerae]]'', which causes [[cholera]], by allowing the cholera vibrios to attach to their chitinous [[exoskeleton]]s. This [[symbiotic]] relationship enhances the bacterium's ability to survive in an aquatic environment, as the exoskeleton provides the bacterium with carbon and nitrogen.<ref>
{{cite journal |author1=Jude, B.A. |author2=Kirn, T.J. |author3=Taylor R.K. |title=A colonization factor links Vibrio cholerae environmental survival and human infection |journal=[[Nature (journal)|Nature]] |volume=438 |issue=7069 |pages=863–6 |year=2005 |pmid=16341015 |doi=10.1038/nature04249 |bibcode=2005Natur.438..863K |s2cid=1964530}}</ref>

==Size classification==
Body size has been defined as a "master trait" for plankton as it is a [[Morphology (biology)|morphological]] characteristic shared by organisms across taxonomy that characterises the functions performed by organisms in ecosystems.<ref>{{cite journal |doi=10.1093/plankt/fbt019 |title=Trait-based approaches to zooplankton communities |year=2013 |last1=Litchman |first1=Elena |last2=Ohman |first2=Mark D. |last3=Kiørboe |first3=Thomas |journal=Journal of Plankton Research |volume=35 |issue=3 |pages=473–484 |doi-access=free}}</ref><ref>{{cite journal |doi=10.1086/675241 |title=Shifts in Mass Scaling of Respiration, Feeding, and Growth Rates across Life-Form Transitions in Marine Pelagic Organisms |year=2014 |last1=Kiørboe |first1=Thomas |last2=Hirst |first2=Andrew G. |journal=The American Naturalist |volume=183 |issue=4 |pages=E118–E130 |pmid=24642502 |bibcode=2014ANat..183E.118K |s2cid=15891709 |url=http://qmro.qmul.ac.uk/xmlui/handle/123456789/13552 }}</ref> It has a paramount effect on growth, reproduction, feeding strategies and mortality.<ref>{{cite journal |doi=10.1146/annurev-marine-122414-034144 |title=Characteristic Sizes of Life in the Oceans, from Bacteria to Whales |year=2016 |last1=Andersen |first1=K.H. |last2=Berge |first2=T. |last3=Gonçalves |first3=R.J. |last4=Hartvig |first4=M. |last5=Heuschele |first5=J. |last6=Hylander |first6=S. |last7=Jacobsen |first7=N.S. |last8=Lindemann |first8=C. |last9=Martens |first9=E.A. |last10=Neuheimer |first10=A.B. |last11=Olsson |first11=K. |last12=Palacz |first12=A. |last13=Prowe |first13=A.E.F. |last14=Sainmont |first14=J. |last15=Traving |first15=S.J. |last16=Visser |first16=A.W. |last17=Wadhwa |first17=N. |last18=Kiørboe |first18=T. |journal=Annual Review of Marine Science |volume=8 |pages=217–241 |pmid=26163011 |bibcode=2016ARMS....8..217A |hdl=11336/52445 |url=https://backend.orbit.dtu.dk/ws/files/139512184/Postprint.pdf}}</ref> One of the oldest manifestations of the biogeography of traits was proposed over 170 years ago, namely [[Bergmann's rule]], in which field observations showed that larger species tend to be found at higher, colder latitudes.<ref>{{cite journal |last=Bergmann |first=Carl |title=Über die Verhältnisse der Wärmeökonomie der Thiere zu ihrer Grösse |journal=Göttinger Studien |year=1847 |volume=3 |issue=1 |pages=595–708 |url=https://books.google.com/books?id=EHo-AAAAcAAJ&pg=PA3}}</ref><ref name="Brandão2021">{{cite journal |doi=10.1038/s41598-021-94615-5 |title=Macroscale patterns of oceanic zooplankton composition and size structure |year=2021 |last1=Brandão |first1=Manoela C. |last2=Benedetti |first2=Fabio |last3=Martini |first3=Séverine |last4=Soviadan |first4=Yawouvi Dodji |last5=Irisson |first5=Jean-Olivier |last6=Romagnan |first6=Jean-Baptiste |last7=Elineau |first7=Amanda |last8=Desnos |first8=Corinne |last9=Jalabert |first9=Laëtitia |last10=Freire |first10=Andrea S. |last11=Picheral |first11=Marc |last12=Guidi |first12=Lionel |last13=Gorsky |first13=Gabriel |last14=Bowler |first14=Chris |last15=Karp-Boss |first15=Lee |last16 = Henry |first16=Nicolas |last17=De Vargas |first17=Colomban |last18=Sullivan |first18=Matthew B. |last19=Acinas |first19=Silvia G. |last20=Babin |first20=Marcel |last21=Bork |first21=Peer |last22=Boss |first22=Emmanuel |last23=Bowler |first23=Chris |last24=Cochrane |first24=Guy |last25=De Vargas |first25=Colomban |last26=Gorsky |first26=Gabriel |last27=Guidi |first27=Lionel |last28=Grimsley |first28=Nigel |last29=Hingamp |first29=Pascal |last30=Iudicone |first30=Daniele |journal=Scientific Reports |volume=11 |issue=1 |page=15714 |pmid=34344925 |pmc=8333327 |bibcode=2021NatSR..1115714B |display-authors=1}} [[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>

In the oceans, size is critical in determining [[Trophic level|trophic links]] in planktonic ecosystems and is thus a critical factor in regulating the efficiency of the [[biological carbon pump]].<ref>{{cite journal |doi=10.1038/s41467-017-02450-y |title=A unifying theory for top-heavy ecosystem structure in the ocean |year=2018 |last1=Woodson |first1=C. Brock |last2=Schramski |first2=John R. |last3=Joye |first3=Samantha B. |journal=Nature Communications |volume=9 |issue=1 |page=23 |pmid=29295998 |pmc=5750233 |bibcode=2018NatCo...9...23W}}</ref> Body size is sensitive to changes in temperature due to the thermal dependence of physiological processes.<ref>{{cite journal |doi=10.1890/03-9000 |title=Toward a Metabolic Theory of Ecology |year=2004 |last1=Brown |first1=James H. |last2=Gillooly |first2=James F. |last3=Allen |first3=Andrew P. |last4=Savage |first4=Van M. |last5=West |first5=Geoffrey B. |journal=Ecology |volume=85 |issue=7 |pages=1771–1789|bibcode=2004Ecol...85.1771B }}</ref> The plankton is mainly composed of [[ectotherm]]s which are organisms that do not generate sufficient metabolic heat to elevate their body temperature, so their metabolic processes depends on external temperature.<ref>{{cite journal |doi=10.1016/j.tree.2011.03.005 |title=Declining body size: A third universal response to warming? |year=2011 |last1=Gardner |first1=Janet L. |last2=Peters |first2=Anne |last3=Kearney |first3=Michael R. |last4=Joseph |first4=Leo |last5=Heinsohn |first5=Robert |journal=Trends in Ecology & Evolution |volume=26 |issue=6 |pages=285–291 |pmid=21470708|bibcode=2011TEcoE..26..285G }}</ref> Consequently, ectotherms grow more slowly and reach maturity at a larger body size in colder environments, which has long puzzled biologists because classic theories of life-history evolution predict smaller adult sizes in environments delaying growth.<ref name="Angilletta2004">{{cite journal |doi=10.1093/icb/44.6.498 |title=Temperature, Growth Rate, and Body Size in Ectotherms: Fitting Pieces of a Life-History Puzzle |year=2004 |last1=Angilletta |first1=M. J. |last2=Steury |first2=T. D. |last3=Sears |first3=M. W. |journal=Integrative and Comparative Biology |volume=44 |issue=6 |pages=498–509 |pmid=21676736 |doi-access=free}}</ref> This pattern of body size variation, known as the temperature-size rule (TSR),<ref>{{cite book |doi=10.1016/S0065-2504(08)60212-3 |title=Temperature and Organism Size—A Biological Law for Ectotherms? |series=Advances in Ecological Research |year=1994 |last1=Atkinson |first1=D. |volume=25 |pages=1–58 |isbn=978-0-12-013925-5}}</ref> has been observed for a wide range of ectotherms, including single-celled and multicellular species, invertebrates and vertebrates.<ref name="Angilletta2004" /><ref>{{cite journal |doi=10.1016/S0169-5347(97)01058-6 |title=Why are organisms usually bigger in colder environments? Making sense of a life history puzzle |year=1997 |last1=Atkinson |first1=David |last2=Sibly |first2=Richard M. |journal=Trends in Ecology & Evolution |volume=12 |issue=6 |pages=235–239 |pmid=21238056|bibcode=1997TEcoE..12..235A }}</ref><ref name="Brandão2021" />

The processes underlying the inverse relationship between body size and temperature remain to be identified.<ref name="Angilletta2004" /> Despite temperature playing a major role in shaping latitudinal variations in organism size, these patterns may also rely on complex interactions between physical, chemical and biological factors. For instance, oxygen supply plays a central role in determining the magnitude of ectothermic temperature-size responses, but it is hard to disentangle the relative effects of oxygen and temperature from field data because these two variables are often strongly inter-related in the surface ocean.<ref>{{cite journal |doi = 10.1126/science.1261359|title = Structure and function of the global ocean microbiome|year = 2015|last1 = Sunagawa|first1 = S.|last2 = Coelho|first2 = L. P.|last3 = Chaffron|first3 = S.|last4 = Kultima|first4 = J. R.|last5 = Labadie|first5 = K.|last6 = Salazar|first6 = G.|last7 = Djahanschiri|first7 = B.|last8 = Zeller|first8 = G.|last9 = Mende|first9 = D. R.|last10 = Alberti|first10 = A.|last11 = Cornejo-Castillo|first11 = F. M.|last12 = Costea|first12 = P. I.|last13 = Cruaud|first13 = C.|last14 = d'Ovidio|first14 = F.|last15 = Engelen|first15 = S.|last16 = Ferrera|first16 = I.|last17 = Gasol|first17 = J. M.|last18 = Guidi|first18 = L.|last19 = Hildebrand|first19 = F.|last20 = Kokoszka|first20 = F.|last21 = Lepoivre|first21 = C.|last22 = Lima-Mendez|first22 = G.|last23 = Poulain|first23 = J.|last24 = Poulos|first24 = B. T.|last25 = Royo-Llonch|first25 = M.|last26 = Sarmento|first26 = H.|last27 = Vieira-Silva|first27 = S.|last28 = Dimier|first28 = C.|last29 = Picheral|first29 = M.|last30 = Searson|first30 = S.|journal = Science|volume = 348|issue = 6237|pmid = 25999513|s2cid = 206562917|display-authors = 1| article-number=1261359 |hdl = 10261/117712|url = https://hal.archives-ouvertes.fr/hal-01233742/file/Sunagawa_et_al_2015_preprint.pdf|hdl-access = free}}</ref><ref>{{cite journal |doi = 10.1111/geb.12847|title = Is oxygen limitation in warming waters a valid mechanism to explain decreased body sizes in aquatic ectotherms?|year = 2019|last1 = Audzijonyte|first1 = Asta|last2 = Barneche|first2 = Diego R.|last3 = Baudron|first3 = Alan R.|last4 = Belmaker|first4 = Jonathan|last5 = Clark|first5 = Timothy D.|last6 = Marshall|first6 = C. Tara|last7 = Morrongiello|first7 = John R.|last8 = Van Rijn|first8 = Itai|journal = Global Ecology and Biogeography|volume = 28|issue = 2|pages = 64–77|s2cid = 92601781|doi-access = free| bibcode=2019GloEB..28...64A |hdl = 10536/DRO/DU:30117155|hdl-access = free}}</ref><ref name="Brandão2021" />

Zooplankton can be broken down into size classes<ref>{{Cite journal |last1=Steinberg |first1=Deborah K. |last2=Landry |first2=Michael R. |date=2017-01-03 |title=Zooplankton and the Ocean Carbon Cycle|url=https://www.annualreviews.org/doi/10.1146/annurev-marine-010814-015924 |journal=Annual Review of Marine Science |language=en |volume=9 |issue=1 |pages=413–444 |doi=10.1146/annurev-marine-010814-015924 |pmid=27814033 |bibcode=2017ARMS....9..413S |issn=1941-1405|url-access=subscription }}</ref> which are diverse in their morphology, diet, feeding strategies, etc. both within classes and between classes:
{| class="wikitable" style="margin-left: auto; margin-right: auto; border: none;"
!type of zooplankton
!size range
|-
|picozooplankton
|<math><</math>2μm
|-
|nanozooplankton
|2–20μm
|-
|microzooplankton
|20–200μm
|-
|mesozooplankton
|0.2–20 millimeters
|}

===Microzooplankton===
Microzooplankton are defined as heterotrophic and [[Mixotrophic dinoflagellate|mixotrophic]] plankton. They primarily consist of [[phagotrophic]] [[protist]]s, including ciliates, dinoflagellates, and [[mesozooplankton]] [[Nauplius (larva)|nauplii]].<ref>{{cite journal |doi = 10.4319/lo.1978.23.6.1256|title = Pelagic ecosystem structure: Heterotrophic compartments of the plankton and their relationship to plankton size fractions 1|year = 1978|author1-link=John McNeill Sieburth|last1 = Sieburth|first1 = John McN.|last2 = Smetacek|first2 = Victor|last3 = Lenz|first3 = Jürgen|journal = Limnology and Oceanography|volume = 23|issue = 6|pages = 1256–1263|bibcode = 1978LimOc..23.1256S| s2cid=85568208 |doi-access = free}}</ref> Microzooplankton are major [[Zooplankton grazing|grazers]] of the plankton community. As the primary consumers of marine phytoplankton, microzooplankton consume ~ 59–75% daily of the [[marine primary production]], much larger than mesozooplankton. That said, macrozooplankton can sometimes have greater consumption rates in eutrophic ecosystems because the larger phytoplankton can be dominant there.<ref>{{cite journal |doi = 10.4319/lo.2004.49.1.0051|title = Phytoplankton growth, microzooplankton grazing, and carbon cycling in marine systems|year = 2004|last1 = Calbet|first1 = Albert|last2 = Landry|first2 = Michael R.|journal = Limnology and Oceanography|volume = 49|issue = 1|pages = 51–57|bibcode = 2004LimOc..49...51C|hdl = 10261/134985|s2cid = 22995996|hdl-access = free}}</ref><ref name="Calbet2008">{{cite journal |doi = 10.1093/icesjms/fsn013|title = The trophic roles of microzooplankton in marine systems|year = 2008|last1 = Calbet|first1 = Albert|journal = ICES Journal of Marine Science|volume = 65|issue = 3|pages = 325–331|doi-access = free|hdl = 10261/16567|hdl-access = free}}</ref> Microzooplankton are also pivotal regenerators of nutrients which fuel primary production and food sources for metazoans.<ref name="Calbet2008" /><ref name="Liu2020">{{cite journal |last1=Liu |first1=Kailin |last2=Chen |first2=Bingzhang |last3=Zheng |first3=Liping |last4=Su |first4=Suhong |last5=Huang |first5=Bangqin |last6=Chen |first6=Mianrun |last7=Liu |first7=Hongbin |year=2021 |title=What controls microzooplankton biomass and herbivory rate across marginal seas of China?|journal=Limnology and Oceanography |volume=66 |issue=1 |pages=61–75 |bibcode=2021LimOc..66...61L |doi=10.1002/lno.11588 |issn=0024-3590 |s2cid=224916151 |doi-access=free}} [[File:CC-BY_icon.svg|50x50px]] Material was copied from this source, which is available under a [[creativecommons:by/4.0/|Creative Commons Attribution 4.0 International License]].</ref>

Despite their ecological importance, microzooplankton remain understudied. Routine oceanographic observations seldom monitor microzooplankton biomass or herbivory rate, although the dilution technique, an elegant method of measuring microzooplankton herbivory rate, has been developed for over four decades (Landry and Hassett 1982). The number of observations of microzooplankton herbivory rate is around 1600 globally,<ref>{{cite journal |doi = 10.4319/lo.2012.57.2.0519|title = Does warming enhance the effect of microzooplankton grazing on marine phytoplankton in the ocean?|year = 2012|last1 = Chen|first1 = Bingzhang|last2 = Landry|first2 = Michael R.|last3 = Huang|first3 = Bangqin|last4 = Liu|first4 = Hongbin|journal = Limnology and Oceanography|volume = 57|issue = 2|pages = 519–526|bibcode = 2012LimOc..57..519C|doi-access = }}</ref><ref>{{cite journal |doi = 10.1093/plankt/fbt023|title = Microzooplankton grazing in the oceans: Impacts, data variability, knowledge gaps and future directions|year = 2013|last1 = Schmoker|first1 = Claire|last2 = Hernández-León|first2 = Santiago|last3 = Calbet|first3 = Albert|journal = Journal of Plankton Research|volume = 35|issue = 4|pages = 691–706|doi-access = free}}</ref> far less than that of primary productivity (> 50,000).<ref>{{cite journal |doi = 10.1002/gbc.20074|title = Combined constraints on global ocean primary production using observations and models|year = 2013|last1 = Buitenhuis|first1 = Erik T.|last2 = Hashioka|first2 = Taketo|last3 = Quéré|first3 = Corinne Le|journal = Global Biogeochemical Cycles|volume = 27|issue = 3|pages = 847–858|bibcode = 2013GBioC..27..847B|s2cid = 140628035|doi-access = free}}</ref> This makes validating and optimizing the grazing function of microzooplankton difficult in ocean ecosystem models.<ref name="Liu2020" />

===Mesozooplankton===
Mesozooplankton are one of the larger size classes of zooplankton. In most regions, mesozooplankton are dominated by [[copepods]], such as [[Calanus finmarchicus]] and [[Calanus helgolandicus]]. Mesozooplankton are an important prey for fish.

As plankton are rarely fished, it has been argued that mesoplankton abundance and [[species composition]] can be used to study marine ecosystems' response to climate change. This is because they have life cycles that generally last less than a year, meaning they respond to climate changes between years. Sparse, monthly sampling will still indicate vacillations.<ref>{{Cite journal |last1=Mackas |first1=David L. |last2=Beaugrand |first2=Gregory |date=2010-02-10 |title=Comparisons of zooplankton time series |url=https://www.sciencedirect.com/science/article/pii/S0924796309000852 |journal=Journal of Marine Systems |series=Impact of climate variability on marine ecosystems: A comparative approach |language=en |volume=79 |issue=3 |pages=286–304 |doi=10.1016/j.jmarsys.2008.11.030 |bibcode=2010JMS....79..286M |issn=0924-7963|url-access=subscription }}</ref>

==Taxonomic groups==
===Protozooplankton===
{{further|marine protists#Protozoans}}

'''Protozooplankton''' refers to [[protist]] zooplankton (planktonic protozoans).<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=2025-07-06}}</ref> All protozooplankton are protozoans, but not all protozoans are protozooplankton, since some live in environments like soil or as parasites. Marine planktonic protozoans include [[zooflagellate]]s, [[foraminifera]]ns, [[radiolarian]]s and some [[dinoflagellate]]s.

[[Protozoan]]s are protists that feed on organic matter such as other [[microorganism]]s or organic tissues and debris.<ref>{{Cite book |url=https://books.google.com/books?id=sYgKY6zz20YC&q=panno+the+cell&pg=PA130 |title=The Cell: Evolution of the First Organism |last=Panno |first=Joseph |date=14 May 2014 |publisher=Infobase Publishing |isbn=978-0-8160-6736-7 |language=en}}</ref><ref>{{Cite book |url=https://books.google.com/books?id=2zVqBgAAQBAJ&q=endocytosis&pg=PA9 |title=Environmental Microbiology: Fundamentals and Applications: Microbial Ecology |last1=Bertrand |first1=Jean-Claude |last2=Caumette |first2=Pierre |last3=Lebaron |first3=Philippe |last4=Matheron |first4=Robert |last5=Normand |first5=Philippe |last6=Sime-Ngando |first6=Télesphore |date=2015-01-26 |publisher=Springer |isbn=978-94-017-9118-2 |language=en}}</ref> Historically, the protozoa were regarded as "one-celled animals", because they often possess [[animal]]-like behaviours, such as [[motility]] and [[predation]], and lack a [[cell wall]], as found in plants and many [[algae]].<ref>{{Cite book|url=https://books.google.com/books?id=RawZTwEACAAJ&q=brock+biology+of+microorganisms+13th|title=Brock Biology of Microorganisms |last=Madigan |first=Michael T. |date=2012 |publisher=Benjamin Cummings |isbn=978-0-321-64963-8}}</ref><ref>{{Cite book |url=https://www.ncbi.nlm.nih.gov/books/NBK8325/ |title=Protozoa: Structure, Classification, Growth, and Development |last=Yaeger |first=Robert G. |date=1996 |publisher=NCBI |pmid=21413323 |access-date=2018-03-23 |isbn=978-0-9631172-1-2 }}</ref> Although the traditional practice of grouping protozoa with animals is no longer considered valid, the term continues to be used in a loose way to identify single-celled organisms that can move independently and feed by [[heterotroph]]y.

====Radiolarians====
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[[Radiolarian]]s are unicellular predatory [[#Marine protists|protists]] encased in elaborate globular shells usually made of silica and pierced with holes. Their name comes from the Latin for "radius". They catch prey by extending parts of their body through the holes. As with the silica frustules of diatoms, radiolarian shells can sink to the ocean floor when radiolarians die and become preserved as part of the [[ocean sediment]]. These remains, as [[#Marine microfossils|microfossils]], provide valuable information about past oceanic conditions.<ref name=Wassilieff2006b>Wassilieff, Maggy (2006) [http://www.TeAra.govt.nz/en/photograph/5138/radiolarian-fossils "Plankton – Animal plankton"], ''Te Ara – the Encyclopedia of New Zealand''. Accessed: 2 November 2019.</ref>

<gallery mode="packed" heights="150px" style="float:left;">
File:Mikrofoto.de-Radiolarien 6.jpg|Like diatoms, radiolarians come in many shapes
File:Podocyrtis papalis Ehrenberg - Radiolarian (30448963206).jpg|Also like diatoms, radiolarian shells are usually made of silicate
File:Acantharian radiolarian Xiphacantha (Haeckel).jpg|However [[acantharian]] radiolarians have shells made from [[strontium sulfate]] crystals
File:Spherical radiolarian 2.jpg|Cutaway schematic diagram of a spherical radiolarian shell
</gallery>

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====Foraminiferans====
Like radiolarians, [[foraminifera]]ns (''forams'' for short) are single-celled predatory protists, also protected with shells that have holes in them. Their name comes from the Latin for "hole bearers". Their shells, often called [[Test (biology)|tests]], are chambered (forams add more chambers as they grow). The shells are usually made of calcite, but are sometimes made of [[Agglutination (biology)|agglutinated]] sediment particles or [[chiton]], and (rarely) silica. Most forams are benthic, but about 40 species are planktic.<ref name=Hemleben>{{cite book |first1=C. |last1=Hemleben |first2=O.R. |last2=Anderson |first3=M. |last3=Spindler |title=Modern Planktonic Foraminifera |url=https://books.google.com/books?id=NaHOmAEACAAJ |year=1989 |publisher=Springer-Verlag |isbn=978-3-540-96815-3}}</ref> They are widely researched with well-established fossil records which allow scientists to infer a lot about past environments and climates.<ref name=Wassilieff2006b />

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 | image1    = Foram-globigerina hg.jpg
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<gallery mode="packed" heights="144px" style="float:left;">
File:EB1911 Foraminifera - Section of Rotalia beccarii.jpg|section showing chambers of a spiral foram
File:Live Ammonia tepida.jpg|Live ''[[Ammonia tepida]]'' streaming granular ectoplasm for catching food
File:Planktic Foraminifera of the northern Gulf of Mexico.jpg|Group of planktonic forams
File:All Gizah Pyramids.jpg|The [[Egyptian pyramid]]s were constructed from limestone that contained [[nummulite]]s.<ref>[http://www.ucl.ac.uk/GeolSci/micropal/foram.html#histofstudy Foraminifera: History of Study], [[University College London]]. Retrieved: 18 November 2019.</ref>
</gallery>

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====Amoeba====
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<gallery mode="packed" heights="170px" style="float:left;">
File:Amoeba proteus 2.jpg|Naked amoeba sketch showing food vacuoles and ingested diatom
File:Arcella sp.jpg|Shell or test of a [[testate amoeba]], ''[[Arcella]]'' sp.
File:Collection Penard MHNG Specimen 533-2-1 Pamphagus granulatus.tif|[[wiktionary:xenogenic|Xenogenic]] testate amoeba covered in diatoms 
</gallery>

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====Ciliates====
<gallery mode="packed" heights="150px" style="float:left;">
File:Stylonychia putrina - 160x - II (13215594964).jpg|''[[Stylonychia|Stylonychia putrina]]''
File:Holophyra ovum - 400x (9836710085).jpg|''Holophyra'' ovum
File:Mikrofoto.de-Blepharisma japonicum 15.jpg|''[[Blepharisma japonicum]]''
File:The ciliate Frontonia sp.jpg|This [[ciliate]] is digesting [[cyanobacteria]]. The mouth is at the bottom right.
</gallery>

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====Dinoflagellates====
{{see also|Predatory dinoflagellate}}

[[Dinoflagellate]]s are a phylum of unicellular [[flagellate]]s with about 2,000 marine species.<ref name="Gómez12">{{cite journal|author=Gómez F |title=A checklist and classification of living dinoflagellates (Dinoflagellata, Alveolata) |journal=CICIMAR Oceánides |volume=27 |issue=1 |pages=65–140 |year=2012 |doi=10.37543/oceanides.v27i1.111 |doi-access=free }}</ref> Some dinoflagellates are [[Predatory dinoflagellate|predatory]], and thus belong to the zooplankton community. Their name comes from the Greek "dinos" meaning ''whirling'' and the Latin "flagellum" meaning a ''whip'' or ''lash''. This refers to the two whip-like attachments (flagella) used for forward movement. Most dinoflagellates are protected with red-brown, cellulose armour. [[Excavata|Excavates]] may be the most basal flagellate lineage.<ref name=Dawson2013>{{cite journal |last1=Dawson |first1=Scott C |last2=Paredez |first2=Alexander R |title=Alternative cytoskeletal landscapes: cytoskeletal novelty and evolution in basal excavate protists |journal=Current Opinion in Cell Biology |year=2013 |volume=25 |issue=1 |pages=134–141 |doi=10.1016/j.ceb.2012.11.005 |pmid=23312067 |pmc=4927265}}</ref>

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File:Gyrodinium dinoflagellate.jpg|''[[Gymnodinium|Gyrodinium]]'', one of the few naked dinoflagellates which lack armour
File:Protoperidinium dinoflagellate.jpg|The dinoflagellate ''Protoperidinium'' extrudes a large feeding veil to capture prey
File:Radiolarian - Podocyrtis (Lampterium) mitra Ehrenberg - 160x.jpg|[[Nassellarian]] radiolarians can be in symbiosis with dinoflagellates
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Dinoflagellates often live in [[symbiosis]] with other organisms. Many [[nassellarian]] radiolarians house [[dinoflagellate]] [[Symbiosis|symbionts]] within their tests.<ref>{{Cite book |title=Handbook of the Protists |last1=Boltovskoy |first1=Demetrio |last2=Anderson |first2=O. Roger |last3=Correa |first3=Nancy M. |date=2017 |publisher=Springer, Cham |isbn=978-3-319-28147-6 |pages=731–763 |language=en |doi=10.1007/978-3-319-28149-0_19}}</ref> The nassellarian provides [[ammonium]] and [[carbon dioxide]] for the dinoflagellate, while the dinoflagellate provides the nassellarian with a mucous membrane useful for hunting and protection against harmful invaders.<ref>{{Cite book |title=Radiolaria |last=Anderson |first=O. R. |publisher=Springer Science & Business Media |year=1983}}</ref> There is evidence from [[DNA]] analysis that dinoflagellate symbiosis with radiolarians evolved independently from other dinoflagellate symbioses, such as with [[foraminifera]].<ref>{{Cite journal |last1=Gast |first1=R. J. |last2=Caron |first2=D. A. |date=1996-11-01 |title=Molecular phylogeny of symbiotic dinoflagellates from planktonic foraminifera and radiolaria |journal=Molecular Biology and Evolution |language=en |volume=13 |issue=9 |pages=1192–1197 |doi=10.1093/oxfordjournals.molbev.a025684 |pmid=8896371 |issn=0737-4038 |doi-access=}}</ref>

<gallery mode="packed" heights="144px" style="float:left;">
File:Ceratium tripos.jpg|[[Tripos (dinoflagellate)|''Tripos muelleri'']] is recognisable by its U-shaped horns
File:Archives de zoologie expérimentale et générale (1920) (20299351186).jpg|''[[Oodinium]]'', a genus of [[parasitic]] dinoflagellates, causes [[velvet disease]] in fish<ref>{{cite web|title=Protozoa Infecting Gills and Skin|url=http://www.merckvetmanual.com:80/mvm/index.jsp?cfile=htm/bc/170410.htm|publisher=[[The Merck Veterinary Manual]]|access-date= 4 November 2019|archive-url=https://web.archive.org/web/20160303221140/http://www.merckvetmanual.com/mvm/index.jsp?cfile=htm%2Fbc%2F170410.htm|archive-date=3 March 2016|df=dmy-all}}</ref>
File:Karenia brevis.jpg|''[[Karenia brevis]]'' produces red tides highly toxic to humans<ref>{{Cite journal|last1=Brand|first1=Larry E.|last2=Campbell|first2=Lisa|last3=Bresnan|first3=Eileen|title=''Karenia'': The biology and ecology of a toxic genus|journal=Harmful Algae|volume=14|pages=156–178|doi=10.1016/j.hal.2011.10.020|year=2012|pmid=36733478 |pmc=9891709 |bibcode=2012HAlga..14..156B }}</ref>
File:Algal bloom(akasio) by Noctiluca in Nagasaki.jpg|[[Red tide]]
</gallery>

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===Mixoplankton===
{{main|Mixoplankton}}
{{see also|Mixotroph|Mixotrophic dinoflagellate}}

[[Mixoplankton]] are mixotrophic plankton, capable of both photosynthesis and predation. A [[mixotroph]] is an organism that can use a mix of different [[Primary nutritional groups|sources of energy and carbon]], instead of having a single trophic mode on the continuum from complete [[autotrophy]] at one end to [[heterotrophy]] at the other. It is estimated that mixotrophs comprise more than half of all microscopic plankton.<ref>{{Cite web |last=Collins |first=Richard |date=2016-11-14 |title=Beware the mixotrophs – they can destroy entire ecosystems 'in a matter of hours' |url=https://www.irishexaminer.com/opinion/columnists/arid-20430358.html |website=Irish Examiner |language=en}}</ref> There are two types of eukaryotic mixotrophs: those with their own [[chloroplast]]s, and those with [[endosymbiont]]s—and others that acquire them through [[kleptoplasty]] or by enslaving the entire phototrophic cell.<ref>{{Cite web |last=University |first=Swansea |title=Microscopic body snatchers infest our oceans |url=https://phys.org/news/2017-08-microscopic-body-snatchers-infest-oceans.html |website=phys.org |language=en}}</ref>

The distinction between plants and animals often breaks down in very small organisms. Possible combinations are [[phototroph|photo-]] and [[chemotroph]]y, [[lithotroph|litho-]] and [[organotroph]]y, [[autotroph|auto-]] and [[heterotroph]]y or other combinations of these. Mixotrophs can be either [[eukaryote|eukaryotic]] or [[prokaryote|prokaryotic]].<ref name='Eiler'>{{cite journal |author=Eiler A |title=Evidence for the Ubiquity of Mixotrophic Bacteria in the Upper Ocean: Implications and Consequences |journal=Appl Environ Microbiol |volume=72 |issue=12 |pages=7431–7 |date=December 2006 |pmid=17028233 |doi=10.1128/AEM.01559-06 |pmc=1694265 |bibcode=2006ApEnM..72.7431E }}</ref> They can take advantage of different environmental conditions.<ref>{{cite journal |vauthors=Katechakis A, Stibor H |title=The mixotroph ''Ochromonas tuberculata'' may invade and suppress specialist phago- and phototroph plankton communities depending on nutrient conditions |journal=Oecologia |volume=148 |issue=4 |pages=692–701 |date=July 2006 |pmid=16568278 |doi=10.1007/s00442-006-0413-4 |bibcode=2006Oecol.148..692K |s2cid=22837754 }}</ref>

Many marine microzooplankton are mixotrophic, which means they could also be classified as phytoplankton. Recent studies of marine microzooplankton found 30–45% of the ciliate abundance was mixotrophic, and up to 65% of the amoeboid, foram and radiolarian [[Biomass (ecology)|biomass]] was mixotrophic.<ref name=Leles2017>{{cite journal | last1 = Leles | first1 = S.G. | last2 = Mitra | first2 = A. | last3 = Flynn | first3 = K.J. | last4 = Stoecker | first4 = D.K. | last5 = Hansen | first5 = P.J. | last6 = Calbet | first6 = A. | last7 = McManus | first7 = G.B. | last8 = Sanders | first8 = R.W. | last9 = Caron | first9 = D.A. | last10 = Not | first10 = F. | last11 = Hallegraeff | first11 = G.M. | year = 2017 | title = Oceanic protists with different forms of acquired phototrophy display contrasting biogeographies and abundance | journal = Proceedings of the Royal Society B: Biological Sciences | volume = 284 | issue = 1860| article-number = 20170664 | doi = 10.1098/rspb.2017.0664 | pmid = 28768886 | pmc = 5563798 | bibcode = 2017PBioS.28470664L }}</ref>

{|class="wikitable"
! colspan=7 |{{centre|Mixotrophic zooplankton that combine phototrophy and heterotrophy – table based on Stoecker et al., 2017 <ref  name=Stoecker2017>{{cite journal | last1 = Stoecker | first1 = D.K. | last2 = Hansen | first2 = P.J. | last3 = Caron | first3 = D.A. | last4 = Mitra | first4 = A. | year = 2017 | title = Mixotrophy in the marine plankton | url = http://pdfs.semanticscholar.org/8492/ec7724a468af240e014aa539a8865568473d.pdf | archive-url = https://web.archive.org/web/20190227180157/http://pdfs.semanticscholar.org/8492/ec7724a468af240e014aa539a8865568473d.pdf | archive-date = 2019-02-27 | journal = Annual Review of Marine Science | volume = 9 | pages = 311–335 | doi = 10.1146/annurev-marine-010816-060617 | pmid = 27483121 | bibcode = 2017ARMS....9..311S | s2cid = 25579538 }}</ref>}}
|-
! colspan=2 | Description
! colspan=2 | Example
! Further examples
|-
| colspan=5 | Called '''''nonconstitutive mixotrophs''''' by Mitra et al., 2016.<ref name=Mitra2016>{{cite journal | last1 = Mitra | first1 = A | last2 = Flynn | first2 = KJ | last3 = Tillmann | first3 = U | last4 = Raven | first4 = J | last5 = Caron | first5 = D | display-authors = etal | year = 2016 | title = Defining planktonic protist functional groups on mechanisms for energy and nutrient acquisition; incorporation of diverse mixotrophic strategies | journal = Protist | volume = 167 | issue = 2| pages = 106–20 | doi = 10.1016/j.protis.2016.01.003 | pmid = 26927496 | doi-access = free | hdl = 10261/131722 | hdl-access = free }}</ref> Zooplankton that are photosynthetic: microzooplankton or metazoan zooplankton that acquire phototrophy through chloroplast retention<sup>a</sup> or maintenance of algal endosymbionts.
|-
| Generalists  
| Protists that retain chloroplasts and rarely other organelles from many algal taxa
| [[File:Halteria.jpg|100px]]
| 
| Most [[oligotrich]] ciliates that retain plastids<sup>a</sup>
|-
| rowspan=2 | Specialists
| 1. Protists that retain chloroplasts and sometimes other organelles from one algal species or very closely related algal species
| [[File:Dinophysis acuminata.jpg|100px]]
| ''[[Dinophysis acuminata]]''
|  ''[[Dinophysis]]'' spp.<br />''[[Myrionecta rubra]]''
|-
| 2. Protists or zooplankton with algal endosymbionts of only one algal species or very closely related algal species
| [[File:Noctiluca scintillans varias.jpg|100px]]
| ''[[Noctiluca scintillans]]''
|  [[wiktionary:metazooplankton|Metazooplankton]] with algal [[endosymbiont]]s<br />Most mixotrophic [[Rhizaria]] ([[Acantharea]], [[Polycystinea]], and [[Foraminifera]])<br />Green ''[[Noctiluca scintillans]]''
|-
| colspan=7 style="text-align:center;" | <small><sup>a</sup>Chloroplast (or plastid) retention = sequestration = enslavement. Some plastid-retaining species also retain other organelles and prey cytoplasm.</small>
|}

''Phaeocystis'' species are endosymbionts to [[Acantharea|acantharian]] radiolarians.<ref name=":4">{{cite journal |last1=Decelle |first1=Johan |last2=Simó |first2=Rafel |last3=Galí |first3=Martí |last4=Vargas |first4=Colomban de |last5=Colin |first5=Sébastien |last6=Desdevises |first6=Yves |last7=Bittner |first7=Lucie |last8=Probert |first8=Ian |last9=Not |first9=Fabrice |date=2012-10-30 |title=An original mode of symbiosis in open ocean plankton |journal=Proceedings of the National Academy of Sciences |language=en |volume=109 |issue=44 |pages=18000–18005 |doi=10.1073/pnas.1212303109 |issn=0027-8424 |pmid=23071304 |pmc=3497740 |bibcode=2012PNAS..10918000D |doi-access=free}}</ref><ref name=":5">{{Cite journal |last1=Mars Brisbin |first1=Margaret |last2=Grossmann |first2=Mary M. |last3=Mesrop |first3=Lisa Y. |last4=Mitarai |first4=Satoshi |date=2018 |title=Intra-host Symbiont Diversity and Extended Symbiont Maintenance in Photosymbiotic Acantharea (Clade F) |journal=Frontiers in Microbiology |language=en |volume=9 |article-number=1998 |doi=10.3389/fmicb.2018.01998 |pmid=30210473 |pmc=6120437 |issn=1664-302X |doi-access=free}}</ref> ''[[Phaeocystis]]'' is an important algal genus found as part of the marine [[phytoplankton]] around the world. It has a [[Polymorphism (biology)|polymorphic]] life cycle, ranging from free-living cells to large colonies.<ref name=":0">{{Cite journal|title = Phaeocystis blooms in the global ocean and their controlling mechanisms: a review|journal = Journal of Sea Research|date = 2005-01-01|pages = 43–66|volume = 53|series = Iron Resources and Oceanic Nutrients – Advancement of Global Environmental Simulations|issue = 1–2|doi = 10.1016/j.seares.2004.01.008|first1 = Véronique|last1 = Schoemann|first2 = Sylvie|last2 = Becquevort|first3 = Jacqueline|last3 = Stefels|first4 = Véronique|last4 = Rousseau|first5 = Christiane|last5 = Lancelot|citeseerx = 10.1.1.319.9563|bibcode = 2005JSR....53...43S}}</ref> It has the ability to form floating colonies, where hundreds of cells are embedded in a gel matrix, which can increase massively in size during [[Algal bloom|blooms]].<ref>{{cite web |url=http://www.phaeocystis.org/ |title=Welcome to the Phaeocystis antarctica genome sequencing project homepage |access-date=2020-08-23 |archive-date=2015-11-20 |archive-url=https://web.archive.org/web/20151120043948/http://www.phaeocystis.org/ }}</ref> As a result, ''Phaeocystis'' is an important contributor to the marine [[Carbon cycle|carbon]]<ref>{{cite journal |title=Rapid and early export of Phaeocystis antarctica blooms in the Ross Sea, Antarctica <!--http://www.nature.com/doifinder/10.1038/35007061-->|journal = Nature|pages = 595–598|volume = 404|issue = 6778|doi = 10.1038/35007061|pmid = 10766240|first1 = G. R.|last1 = DiTullio|first2 = J. M.|last2 = Grebmeier|author-link2=Jacqueline M. Grebmeier|first3 = K. R.|last3 = Arrigo|first4 = M. P.|last4 = Lizotte|first5 = D. H.|last5 = Robinson|first6 = A.|last6 = Leventer|first7 = J. P.|last7 = Barry|first8 = M. L.|last8 = VanWoert|first9 = R. B.|last9 = Dunbar|year = 2000|bibcode = 2000Natur.404..595D|s2cid = 4409009}}</ref> and [[sulfur cycle]]s.<ref>{{Cite journal|title = DMSP-lyase activity in a spring phytoplankton bloom off the Dutch coast, related to Phaeocystis sp. abundance|journal = Marine Ecology Progress Series|date = 1995-07-20|pages = 235–243|volume = 123|doi = 10.3354/meps123235|first1 = Stefels|last1 = J|first2 = Dijkhuizen|last2 = L|first3 = Gieskes|last3 = WWC|url = https://pure.rug.nl/ws/files/62552225/DMSP_lyase_activity_in_a_spring_phytoplankton_bloom_off_the_Dutch_coast.pdf|bibcode = 1995MEPS..123..235S|doi-access = free}}</ref>

<gallery caption="Mixoplankton" mode="packed" heights="144px" style="float:left;">
File:Tintinnid ciliate Favella.jpg|[[Tintinnid]] ciliate ''Favella''
File:Euglena mutabilis - 400x - 1 (10388739803) (cropped).jpg|''[[Euglena|Euglena mutabilis]]'', a photosynthetic [[flagellate]]
File:Stichotricha secunda - 400x (14974779356).jpg|[[Zoochlorellae]] (green) living inside the [[ciliate]] ''Stichotricha secunda''
File:Dinophysis acuta.jpg| The dinoflagellate ''Dinophysis acuta''
</gallery>

{{multiple image
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 | caption1  = [[Acantharian]] radiolarian hosts ''[[Phaeocystis]]'' symbionts
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 | caption2  = White ''Phaeocystis'' algal foam washing up on a beach
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{{clear}}

A number of forams are mixotrophic. These have unicellular [[algae]] as [[endosymbiont]]s, from diverse lineages such as the [[green algae]], [[red algae]], [[golden algae]], [[diatom]]s, and [[dinoflagellate]]s.<ref name=Hemleben/> Mixotrophic foraminifers are particularly common in nutrient-poor oceanic waters.<ref>{{Cite book |last=Marshall |first=K. C. |url=https://books.google.com/books?id=QvvlBwAAQBAJ&dq=%22The+symbiont-bearing+foraminifera+are+particularly+common+in+nutrient-poor+oceanic+waters%22&pg=PA22 |title=Advances in Microbial Ecology |date=2013-11-11 |publisher=Springer Science & Business Media |isbn=978-1-4684-7612-5 |language=en}}</ref> Some forams are [[kleptoplasty|kleptoplastic]], retaining [[chloroplast]]s from ingested algae to conduct [[photosynthesis]].<ref>{{Cite journal|title = Benthic Foraminifera of dysoxic sediments: chloroplast sequestration and functional morphology|year = 1999|last= Bernhard|first=J. M.|author2=Bowser, S.M.|journal = Earth-Science Reviews|volume = 46|issue = 1|pages = 149–165|doi = 10.1016/S0012-8252(99)00017-3|bibcode=1999ESRv...46..149B}}</ref>

By trophic orientation, dinoflagellates are all over the place. Some dinoflagellates are known to be [[photosynthesis|photosynthetic]], but a large fraction of these are in fact [[mixotrophy|mixotrophic]], combining photosynthesis with ingestion of prey ([[phagotrophy]]).<ref>{{Cite journal | last1 = Stoecker | first1 = D. K. | title = Mixotrophy among Dinoflagellates | doi = 10.1111/j.1550-7408.1999.tb04619.x | journal = The Journal of Eukaryotic Microbiology | volume = 46 | issue = 4 | pages = 397–401 | year = 1999 | s2cid = 83885629 | name-list-style = vanc}}</ref> Some species are [[endosymbiont]]s of marine animals and other protists, and play an important part in the biology of [[coral reef]]s. Others predate other protozoa, and a few forms are parasitic. Many dinoflagellates are [[mixotrophic]] and could also be classified as phytoplankton. The toxic dinoflagellate ''[[Dinophysis acuta]]'' acquire chloroplasts from its prey. "It cannot catch the cryptophytes by itself, and instead relies on ingesting ciliates such as the red ''[[Myrionecta rubra]]'', which sequester their chloroplasts from a specific cryptophyte clade (Geminigera/Plagioselmis/Teleaulax)".<ref  name=Stoecker2017 />

===Planktonic metazoa (animals)===
[[File:Fish3562 - Flickr - NOAA Photo Library.jpg|thumb|{{center|Octopus larva and pteropod}}]]

Free-living species in the crustacean class [[Copepod]]a are typically 1 to 2&nbsp;mm long with teardrop-shaped bodies. Like all crustaceans, their bodies are divided into three sections: head, thorax, and abdomen, with two pairs of antennae; the first pair is often long and prominent. They have a tough [[exoskeleton]] made of calcium carbonate and usually have a [[Crustacean larva#Nauplius|single red eye]] in the centre of their transparent head.<ref name=IZ>{{cite book |author=Robert D. Barnes |year=1982 |title= Invertebrate Zoology |publisher= Holt-Saunders International |location=[[Philadelphia, Pennsylvania]] |pages=683–692 |isbn=978-0-03-056747-6}}</ref> About 13,000 species of copepods are known, of which about 10,200 are marine.<ref>{{Cite web |url=http://www.marinespecies.org/aphia.php?p=taxdetails&id=1080 |title=WoRMS - World Register of Marine Species - Copepoda |website=www.marinespecies.org |access-date=2019-06-28 |archive-url=https://web.archive.org/web/20190630192104/http://www.marinespecies.org/aphia.php?p=taxdetails&id=1080 |archive-date=2019-06-30 |url-status=live}}</ref><ref>{{cite journal |author1=Geoff A. Boxhall |author2=Danielle Defaye |year=2008 |title=Global diversity of copepods (Crustacea: Copepoda) in freshwater |journal=[[Hydrobiologia]] |volume=595 |issue=1 |pages=195–207 |doi=10.1007/s10750-007-9014-4 |bibcode=2008HyBio.595..195B |s2cid=31727589 }}</ref> They are usually among the more dominant members of the zooplankton.<ref>{{cite web |author1=Johannes Dürbaum |author2=Thorsten Künnemann |date=November 5, 1997 |title=Biology of Copepods: An Introduction |url=http://www.uni-oldenburg.de/zoomorphology/Biologyintro.html |publisher=[[Carl von Ossietzky University of Oldenburg]] |access-date=December 8, 2009 |archive-url=https://web.archive.org/web/20100526164720/http://www.uni-oldenburg.de/zoomorphology/Biologyintro.html |archive-date=May 26, 2010 }}</ref>

In addition to copepods the crustacean classes [[ostracod]]s, [[Branchiopoda|branchiopods]] and [[malacostraca]]ns also have planktonic members. [[Barnacle]]s are planktonic only during the larval stage.<ref>[https://books.google.com/books?id=5kv3AwAAQBAJ&dq=pelagic+realm+significant+crustaceans+pelagic+fauna+Ostracoda+Copepoda&pg=PA25 Treatise on Zoology – Anatomy, Taxonomy, Biology. The Crustacea]</ref>

<gallery mode="packed" heights="120px" caption="[[Metazoan]] zooplankton" style="float:left">
File:Copepod 2 with eggs.jpg| [[Copepod]] with eggs
File:Tomopteriskils.jpg|[[Segmented worm]]
File:Hyperia.jpg| [[Amphipod]]
File:Krill666.jpg| [[Krill]] 
File:Glaucus atlanticus 1 cropped.jpg| [[Glaucus atlanticus|Blue ocean slug]]
</gallery>
{{clear}}

====Holoplankton and meroplankton====
====Ichthyoplankton====
[[Ichthyoplankton]] are the [[Fish eggs|eggs]] and [[larvae]] of fish ("ichthyo" comes from the Greek word for ''fish''). They are planktonic because 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]]. 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">{{Cite web |date=2007-09-03 |title=What are Ichthyoplankton? |url=https://swfsc.noaa.gov/textblock.aspx?Division=FRD&id=6210 |archive-url=https://web.archive.org/web/20180218090243/https://swfsc.noaa.gov/textblock.aspx?Division=FRD&id=6210 |archive-date=2018-02-18 |access-date=2011-07-22 |website=Southwest Fisheries Science Center}}</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 2006| publisher=University of California Press }}</ref>

<gallery mode="packed" heights="120px" style="float:left">
File:Squidu.jpg| Juvenile planktonic [[squid]]
File:Molalavdj.jpg| [[Ocean sunfish]] larvae (2.7mm)
File:FMIB 47039 Ostracion hoops.jpeg| [[Boxfish]] larva
</gallery>
{{clear}}

====Gelatinous zooplankton====
[[Gelatinous zooplankton]] include [[ctenophore]]s, [[Jellyfish|medusae]], [[salps]], and [[Chaetognatha]] in coastal waters. Jellyfish are slow swimmers, and most species form part of the plankton. Traditionally jellyfish have been viewed as [[Trophic level|trophic]] dead ends, minor players in the [[marine food web]], gelatinous organisms with a [[body plan]] largely based on water that offers little nutritional value or interest for other organisms apart from a few specialised predators such as the [[ocean sunfish]] and the [[leatherback sea turtle]].<ref name=Hamilton2016>Hamilton, G. (2016) [https://www.nature.com/news/polopoly_fs/1.19613!/menu/main/topColumns/topLeftColumn/pdf/531432a.pdf "The secret lives of jellyfish: long regarded as minor players in ocean ecology, jellyfish are actually important parts of the marine food web"]. ''Nature'', '''531'''(7595): 432–435. {{doi|10.1038/531432a}}</ref><ref name=Hays2018>[[Graeme Hays|Hays, G.C.]], Doyle, T.K. and Houghton, J.D. (2018) "A paradigm shift in the trophic importance of jellyfish?" ''Trends in ecology & evolution'', '''33'''(11): 874–884. {{doi|10.1016/j.tree.2018.09.001}}</ref>

That view has recently been challenged. Jellyfish, and more gelatinous zooplankton in general, which include [[salp]]s and [[ctenophore]]s, are very diverse, fragile with no hard parts, difficult to see and monitor, subject to rapid population swings and often live inconveniently far from shore or deep in the ocean. It is difficult for scientists to detect and analyse jellyfish in the guts of predators, since they turn to mush when eaten and are rapidly digested.<ref name=Hamilton2016/> But jellyfish bloom in vast numbers, and it has been shown they form major components in the diets of [[tuna]], [[Tetrapturus|spearfish]] and [[swordfish]] as well as various birds and invertebrates such as [[octopus]], [[sea cucumber]]s, [[crab]]s and [[amphipod]]s.<ref>Cardona, L., De Quevedo, I.Á., Borrell, A. and Aguilar, A. (2012) "Massive consumption of gelatinous plankton by Mediterranean apex predators". ''PLOS ONE'', '''7'''(3): e31329. {{doi|10.1371/journal.pone.0031329|doi-access=free}}</ref><ref name=Hays2018 /> "Despite their low energy density, the contribution of jellyfish to the energy budgets of predators may be much greater than assumed because of rapid digestion, low capture costs, availability, and selective feeding on the more energy-rich components. Feeding on jellyfish may make marine predators susceptible to ingestion of plastics."<ref name=Hays2018 /> According to a 2017 study, [[narcomedusae]] consume the greatest diversity of mesopelagic prey, followed by [[physonect]] [[siphonophore]]s, [[ctenophore]]s and [[cephalopod]]s.<ref name=Choy2017 />

<gallery mode="packed" heights="120px" style="float:left">
File:Parumbrosa polylobata 01.jpg| [[Jellyfish]]
File:Tunicate off Atauro island.jpg| This free-floating [[pyrosome]] is made up of hundreds of individual [[bioluminescent]] tunicates
File:23 salpchain frierson odfw (8253212250).jpg|[[Salp]] chain
</gallery>
{{clear}}

The importance of the so-called "jelly web" is only beginning to be understood, but it seems medusae, ctenophores and siphonophores can be key predators in deep pelagic food webs with ecological impacts similar to predator fish and squid. Traditionally gelatinous predators were thought ineffectual providers of marine trophic pathways, but they appear to have substantial and integral roles in deep [[pelagic food webs]].<ref name=Choy2017>Choy, C.A., Haddock, S.H. and Robison, B.H. (2017) "Deep pelagic food web structure as revealed by ''in situ'' feeding observations". ''Proceedings of the Royal Society B: Biological Sciences'', '''284'''(1868): 20172116. {{doi|10.1098/rspb.2017.2116}}. [[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>

==Role in food webs==
Grazing by single-celled zooplankton accounts for the majority of [[organic carbon]] loss from [[marine primary production]].<ref name=MendenDeuer2021>{{cite journal |doi = 10.3389/fmars.2021.695938|doi-access = free|title = Promoting Instrument Development for New Research Avenues in Ocean Science: Opening the Black Box of Grazing|year = 2021|last1 = Menden-Deuer|first1 = Susanne|author-link1=Susanne Menden-Deuer|last2 = Slade|first2 = Wayne Homer|last3 = Dierssen|first3 = Heidi|journal = Frontiers in Marine Science|volume = 8 | article-number=695938 | bibcode=2021FrMaS...895938M }} [[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> However, zooplankton grazing remains one of the key unknowns in global predictive models of carbon flux, the [[marine food web]] structure and ecosystem characteristics, because empirical grazing measurements are sparse, resulting in poor parameterisation of grazing functions.<ref name=Stock2010>{{cite journal |doi = 10.1016/j.dsr.2009.10.006|title = Controls on the ratio of mesozooplankton production to primary production in marine ecosystems|year = 2010|last1 = Stock|first1 = Charles|last2 = Dunne|first2 = John|journal = Deep Sea Research Part I: Oceanographic Research Papers|volume = 57|issue = 1|pages = 95–112|bibcode = 2010DSRI...57...95S}}</ref><ref name=Bisson2020>{{cite journal |doi = 10.3389/fmars.2020.00505|doi-access = free|title = Diagnosing Mechanisms of Ocean Carbon Export in a Satellite-Based Food Web Model|year = 2020|last1 = Bisson|first1 = Kelsey|last2 = Siegel|first2 = David A.|last3 = Devries|first3 = Timothy|journal = Frontiers in Marine Science|volume = 7 | article-number=505 | bibcode=2020FrMaS...7..505B }}</ref> To overcome this critical knowledge gap, it has been suggested that a focused effort be placed on the development of instrumentation that can link changes in phytoplankton biomass or optical properties with grazing.<ref name=MendenDeuer2021 />

Grazing is a central, rate-setting process in ocean ecosystems and a driver of [[marine biogeochemical cycling]].<ref>{{cite journal |doi = 10.1126/science.1257594|title = Rethinking the marine carbon cycle: Factoring in the multifarious lifestyles of microbes|year = 2015|last1 = Worden|first1 = A. Z.|last2 = Follows|first2 = M. J.|last3 = Giovannoni|first3 = S. J.|last4 = Wilken|first4 = S.|last5 = Zimmerman|first5 = A. E.|last6 = Keeling|first6 = P. J.|journal = Science|volume = 347|issue = 6223| article-number=1257594 |pmid = 25678667|s2cid = 206560125|doi-access = free}}</ref> In all ocean ecosystems, grazing by heterotrophic protists constitutes the single largest loss factor of marine primary production and alters particle size distributions.<ref name="Steinberg12017"/> Grazing affects all pathways of export production, rendering grazing important both for surface and [[Deep carbon cycle|deep carbon]] processes.<ref>{{cite journal |doi = 10.4319/lo.2013.58.1.0173|title = Control of plankton seasonal succession by adaptive grazing|year = 2013|last1 = Mariani|first1 = Patrizio|last2 = Andersen|first2 = Ken H.|last3 = Visser|first3 = André W.|last4 = Barton|first4 = Andrew D.|last5 = Kiørboe|first5 = Thomas|journal = Limnology and Oceanography|volume = 58|issue = 1|pages = 173–184|bibcode = 2013LimOc..58..173M|doi-access = free}}</ref> Predicting central paradigms of ocean ecosystem function, including responses to environmental change requires accurate representation of grazing in global biogeochemical, ecosystem and cross-biome-comparison models.<ref name=Stock2010 /> Several large-scale analyses have concluded that phytoplankton losses, which are dominated by grazing are the putative explanation for annual cycles in phytoplankton biomass, accumulation rates and export production.<ref>{{cite journal |doi = 10.1890/09-1207.1|title = Abandoning Sverdrup's Critical Depth Hypothesis on phytoplankton blooms|year = 2010|last1 = Behrenfeld|first1 = Michael J.|journal = Ecology|volume = 91|issue = 4|pages = 977–989|pmid = 20462113| bibcode=2010Ecol...91..977B }}</ref><ref>{{cite journal |doi = 10.1038/s41467-017-02143-6|title = Floats with bio-optical sensors reveal what processes trigger the North Atlantic bloom|year = 2018|last1 = Mignot|first1 = A.|last2 = Ferrari|first2 = R.|last3 = Claustre|first3 = H.|journal = Nature Communications|volume = 9|issue = 1|page = 190|pmid = 29335403|pmc = 5768750|bibcode = 2018NatCo...9..190M}}</ref><ref name=Bisson2020 /><ref name=MendenDeuer2021 />

<gallery mode="packed" heights="330px" style="float:left;" caption="Pelagic food web">
File:Export Processes in the Ocean from Remote Sensing.jpg| [[Pelagic food web]] and the [[biological pump]]. Links among the ocean's biological pump and pelagic food web and the ability to sample these components remotely from ships, satellites, and autonomous vehicles. Light blue waters are the [[euphotic zone]], while the darker blue waters represent the [[Mesopelagic zone|twilight zone]].<ref>{{cite journal |doi=10.3389/fmars.2016.00022|title=Prediction of the Export and Fate of Global Ocean Net Primary Production: The EXPORTS Science Plan|year=2016|last1=Siegel|first1=David A.|last2=Buesseler|first2=Ken O.|last3=Behrenfeld|first3=Michael J.|last4=Benitez-Nelson|first4=Claudia R.|last5=Boss|first5=Emmanuel|last6=Brzezinski|first6=Mark A.|last7=Burd|first7=Adrian|last8=Carlson|first8=Craig A.|last9=d'Asaro|first9=Eric A.|last10=Doney|first10=Scott C.|last11=Perry|first11=Mary J.|last12=Stanley|first12=Rachel H. R.|last13=Steinberg|first13=Deborah K.|journal=Frontiers in Marine Science|volume=3|page=22 |doi-access=free |bibcode=2016FrMaS...3...22S }} [[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> 
</gallery>

[[File:Seawater constituents generated and altered by herbivorous grazing.jpg|thumb|upright=2| {{center|Schematic of how common seawater constituents, including particulate and dissolved components, could both be generated and altered through the process of herbivorous zooplankton grazing{{hsp}}<ref name=MendenDeuer2021 />}}]]

{{clear}}

==Role in biogeochemistry==
In addition to linking primary producers to higher [[trophic level]]s in [[marine food web]]s, zooplankton also play an important role as "recyclers" of carbon and other nutrients that significantly impact [[marine biogeochemical cycles]], including the [[biological pump]]. This is particularly important in the [[oligotrophic]] waters of the open ocean. Through sloppy feeding, excretion, egestion, and leaching of [[fecal pellet]]s, zooplankton release [[dissolved organic matter]] (DOM) which controls DOM cycling and supports the [[microbial loop]]. Absorption efficiency, respiration, and prey size all further complicate how zooplankton are able to transform and deliver carbon to the [[deep ocean]].<ref name=Steinberg12017 />

=== Sloppy feeding and release of DOM ===
{{see also|Zooplankton grazing}}
[[File:Sloppy feeding by zooplankton.jpg|thumb|right|upright=1.3| {{center|'''Sloppy feeding by zooplankton'''<br />DOC {{=}} [[dissolved organic carbon]]<br />POC {{=}} [[particulate organic carbon]]<br /><small>Adapted from Møller et al. (2005),<ref name="Møller2003">{{cite journal |doi = 10.3354/meps262185|title = Production of DOC by ''Calanus finmarchicus'', ''C. Glacialis'' and ''C. Hyperboreus'' through sloppy feeding and leakage from fecal pellets|year = 2003|last1 = Møller|first1 = EF|last2 = Thor|first2 = P.|last3 = Nielsen|first3 = TG|journal = Marine Ecology Progress Series|volume = 262|pages = 185–191|bibcode = 2003MEPS..262..185M|doi-access = free}}</ref><br />Saba et al. (2009)<ref name=Saba2009>{{cite journal |doi = 10.3354/meps08070|title = Effects of diet on release of dissolved organic and inorganic nutrients by the copepod ''Acartia tonsa''|year = 2009|last1 = Saba|first1 = GK|last2 = Steinberg|first2 = DK|last3 = Bronk|first3 = DA|journal = Marine Ecology Progress Series|volume = 386|pages = 147–161|bibcode = 2009MEPS..386..147S|doi-access = free}}</ref> and Steinberg et al. (2017).<ref name=Steinberg12017>{{cite journal |doi = 10.1146/annurev-marine-010814-015924|title = Zooplankton and the Ocean Carbon Cycle|year = 2017|last1 = Steinberg|first1 = Deborah K.|last2 = Landry|first2 = Michael R.|journal = Annual Review of Marine Science|volume = 9|pages = 413–444|pmid = 27814033|bibcode = 2017ARMS....9..413S}}</ref></small>}}]]

Excretion and sloppy feeding (the physical breakdown of food source) make up 80% and 20% of crustacean zooplankton-mediated DOM release respectively.<ref name=Saba2011>{{cite journal |doi = 10.1016/j.jembe.2011.04.013|title = The relative importance of sloppy feeding, excretion, and fecal pellet leaching in the release of dissolved carbon and nitrogen by Acartia tonsa copepods|year = 2011|last1 = Saba|first1 = Grace K.|last2 = Steinberg|first2 = Deborah K.|last3 = Bronk|first3 = Deborah A.|journal = Journal of Experimental Marine Biology and Ecology|volume = 404|issue = 1–2|pages = 47–56| bibcode=2011JEMBE.404...47S }}</ref> In the same study, fecal pellet leaching was found to be an insignificant contributor. For protozoan grazers, DOM is released primarily through excretion and egestion and gelatinous zooplankton can also release DOM through the production of mucus. Leaching of fecal pellets can extend from hours to days after initial egestion and its effects can vary depending on food concentration and quality.<ref name=Thor2003>{{cite journal |doi = 10.3354/ame033279|title = Fate of organic carbon released from decomposing copepod fecal pellets in relation to bacterial production and ectoenzymatic activity|year = 2003|last1 = Thor|first1 = P.|last2 = Dam|first2 = HG|last3 = Rogers|first3 = DR|journal = Aquatic Microbial Ecology|volume = 33|pages = 279–288|doi-access = free | bibcode=2003AqME...33..279T }}</ref><ref name=Carlso2014>{{Cite book|url=https://books.google.com/books?id=7iKOAwAAQBAJ&q=%22Biogeochemistry+of+marine+dissolved+organic+matter%22|title=Biogeochemistry of Marine Dissolved Organic Matter|isbn=978-0-12-407153-7|last1=Hansell|first1=Dennis A.|last2=Carlson|first2=Craig A.|date=2 October 2014|publisher=Academic Press }}</ref> Various factors can affect how much DOM is released from zooplankton individuals or populations. Absorption efficiency (AE) is the proportion of food absorbed by plankton that determines how available the consumed organic materials are in meeting the required physiological demands.<ref name=Steinberg12017 /> Depending on the feeding rate and prey composition, variations in AE 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 AE and small, dense pellets, while high feeding rates typically lead to low AE and larger pellets with more organic content. Another contributing factor to 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 CO<sub>2</sub>. 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.<ref name="Møller2005">{{cite journal |doi = 10.1093/plankt/fbh147|title = Sloppy feeding in marine copepods: Prey-size-dependent production of dissolved organic carbon|year = 2004|last1 = Moller|first1 = E. F.|journal = Journal of Plankton Research|volume = 27|pages = 27–35|doi-access = free}}</ref><ref name="Møller2007">{{cite journal |doi = 10.4319/lo.2007.52.1.0079|title = Production of dissolved organic carbon by sloppy feeding in the copepods Acartia tonsa, Centropages typicus, and Temora longicornis|year = 2007|last1 = Møller|first1 = Eva Friis|journal = Limnology and Oceanography|volume = 52|issue = 1|pages = 79–84|bibcode = 2007LimOc..52...79M|doi-access = free}}</ref> 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.<ref name=Thor2003 />

{{multiple image
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 | header            = Comparison of zooplankton-mediated carbon cycles{{hsp}}<ref name=Halfter2020>{{cite journal |doi = 10.3389/fmars.2020.567917|title = The Role of Zooplankton in Establishing Carbon Export Regimes in the Southern Ocean – A Comparison of Two Representative Case Studies in the Subantarctic Region|year = 2020|last1 = Halfter|first1 = Svenja|last2 = Cavan|first2 = Emma L.|last3 = Swadling|first3 = Kerrie M.|last4 = Eriksen|first4 = Ruth S.|last5 = Boyd|first5 = Philip W.|journal = Frontiers in Marine Science|volume = 7| article-number=567917 |s2cid = 222003883|doi-access = free | bibcode=2020FrMaS...767917H }} [[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>
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 | footer            = <small>Grazing and fragmentation of particles at both sites increases nutrient recycling in the upper water column</small>
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 | image1    = Zooplankton-mediated carbon cycle 1.jpg
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 | caption1  = {{center|'''Kerguelen Plateau'''<br />[[Iron fertilization|Naturally iron-fertilized]]}} On the [[Kerguelen Plateau]] in summer, high iron levels lead to high [[chlorophyll a]] as a proxy for algae biomass at the surface. The diverse zooplankton community feeds on the sinking particle flux and acts as a gate-keeper to the deeper ocean by ingesting and fragmenting sinking particles and, consequently, significantly reducing the export flux out of the [[epipelagic]]. The main export particles are [[diatom]] resting spores, which bypass the intense grazing pressure, followed by fecal pellets.<ref name=Halfter2020 />
 | image2    = Zooplankton-mediated carbon cycle 2.jpg
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 | caption2  = {{center|'''Southern Ocean waters'''<br />[[High-nutrient, low-chlorophyll regions|High nutrient, low chlorophyll]]}} In [[Southern Ocean]] waters in summer, iron levels are relatively low and support a more diverse phytoplankton community, but with lower biomass, which, in turn, affects zooplankton community composition and biomass. The grazing pressure during summer is focused mostly on [[picoplankton]], which leaves large particles for export.<ref name=Halfter2020 />
}}

{{clear}}

===Carbon export=== 
Zooplankton play a critical role in supporting the ocean's [[biological pump]] through various forms of [[Marine carbon export|carbon export]], including the production of fecal pellets, mucous feeding webs, molts, and carcasses. [[Zooplankton fecal pellets|Fecal pellets]] are estimated to be a large contributor to this export, with copepod size rather than abundance expected to determine how much carbon actually reaches the ocean floor. The importance of fecal pellets can vary both by time and location. For example, zooplankton bloom events can produce larger quantities of fecal pellets, resulting in greater measures of carbon export. Additionally, as fecal pellets sink, they are reworked by microbes in the water column, which can thus alter the carbon composition of the pellet. This affects how much carbon is recycled in the euphotic zone and how much reaches depth. Fecal pellet contribution to carbon export is likely underestimated; however, new advances in quantifying this production are currently being developed, including the use of isotopic signatures of amino acids to characterize how much carbon is being exported via zooplankton fecal pellet production.<ref>{{Cite conference |bibcode=2019AGUFMPP42C..12D |title=Compound-Specific Isotope Analysis of Zooplankton Fecal Pellets: Insights into Dietary and Trophic Processes and Characterization of Fecal Pellets as Organic Matter End-Member |last1=Doherty |first1=S.|last2 = Maas |first2=A. E. |last3=Steinberg |first3=D. K. |last4=Popp |first4=B. N. |last5=Close |first5=H. G. |book-title=American Geophysical Union, Fall Meeting 2019 Abstracts |date=2019 |at=abstract #PP42C–12}}</ref> Carcasses are also gaining recognition as being important contributors to carbon export. [[Jelly fall]]s – the mass sinking of gelatinous zooplankton carcasses – occur across the world as a result of large blooms. Because of their large size, these gelatinous zooplankton are expected to hold a larger carbon content, making their sinking carcasses a potentially important source of food for [[Benthos|benthic organisms]].<ref name=Steinberg12017 />

==See also==
* [[Census of Marine Zooplankton]]
* [[Diel vertical migration]]
* [[Ocean acidification]]
* [[Primary production]]
* [[Thin layers (oceanography)]]

==References==
{{Reflist|30em}}

==External links==
* [http://www.sahfos.ac.uk/ SAHFOS] Sir Alister Hardy Foundation for Ocean Science
* [http://vimeo.com/84872751/ Ocean Drifters] Short film narrated by David Attenborough about the varied roles of plankton
* [http://news.bbc.co.uk/1/hi/sci/tech/8498786.stm Sea Drifters] BBC Audio slideshow
* [http://www.planktonchronicles.org/en Plankton Chronicles] Short documentary films & photos
* [http://www.st.nmfs.noaa.gov/plankton/ COPEPOD: The global plankton database]. A global coverage database of zooplankton biomass and abundance data.
* [https://web.archive.org/web/20080530005405/http://www.tafi.org.au/zooplankton/ Guide to the marine zooplankton of south eastern Australia], [http://www.tafi.org.au/ Tasmanian Aquaculture and Fisheries Institute]
* [http://imos.org.au/auscpr.html Australian Continuous Plankton Recorder Project] {{Webarchive|url=https://web.archive.org/web/20081201125235/http://imos.org.au/auscpr.html |date=2008-12-01 }}
* [http://cfb.unh.edu/cfbkey/html/groups.html An Image-Based Key to Zooplankton of North America]

{{plankton|state=expanded}}
{{aquatic ecosystem topics|expanded=none}}

{{Authority control}}

[[Category:Aquatic animals]]
[[Category:Biological oceanography]]
[[Category:Planktology]]
[[Category:Oceanographical terminology]]

[[de:Plankton#Zooplankton]]