Abstract
This chapter gives a kind of minimal introduction to the organisms living in water, as far as it is needed for an ecology textbook. It will not focus on taxonomy, because this would just be a repetition of a taxonomy textbook. All phyla and most of the classes and orders have representatives living in water (Sect. 3.1). Instead of a taxonomic approach, a “life form” approach will be taken, focusing on the traits most important for growth and survival in the aquatic realm.
Classification of life form types starts with basic nutritional types (Sect. 3.2). The next most important dimension of a functional characterization is body size (Sect. 3.3), an ecological “master trait” with far-reaching consequences for many other traits, like metabolic rates, growth rate, and longevity. A further functionally important trait is the stoichiometry of biomass (Sect. 3.4) which defines the elemental requirements of organisms.
The remining sections are devoted to a grouping by major habitats, in pelagic waters plankton (drifting organisms, Sect. 3.5) and nekton (swimming organisms, Sect. 3.6) and benthos on solid substrates (Sect. 3.7) and benthos on soft substrates (Sect. 3.8).
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Abbreviations
- b:
-
allometry coefficient
- I:
-
ingestion rate
- L:
-
body length
- Ra:
-
absolute metabolic rate
- Rs:
-
specific metabolic rate
References
Alldredge AL (1977) House morphology and mechanisms of feeding in the Oikopleuridae (Tunicata, Appendicularia). J Zool Lond 181:175–188
Atkinson MJ, Smith SV (1983) C:N:P ratios of marine plants. Limnol Oceanogr 28:568–574
Azam F, Fenchel T, Field JG, Ray JS, Meyer-Reil LA, Thingstad F (1983) The ecological role of water-column microbes in the sea. Mar Ecol Progr Ser 10:257–263
Baker CS (1980) Whale migrations. Mother (Nature) calls. Nat Geogr Mag 178
Båmstedt U (1986) Chemical composition and energy content. In: Corner EDS, O’Hara SCM (eds) Biological chemistry of marine copepods. Oxford University Press, Oxford, pp 1–58
Bergh O, Børsheim KY, Bratbak G, Heldal M (1989) High abundances of viruses found in aquatic environments. Nature 340:467–469
Bi R, Arndt C, Sommer U (2012) Stoichiometric responses of phytoplankton species to the interactive effect of nutrient supply rates and growth rates. J Phycol 48:539–549
Bratbak G, Jacobsen A, Heldal M, Nagasaki K, Thingstad F (1998) Virus production in Phaeocystis pouchetii and its relation to host cell growth and nutrition. Aquat Microb Ecol 16:1–9
Brown JH, Gillooly JF, Allen AP, Savage VM, West GB (2004) Toward a metabolic theory of ecology. Ecology 85:1771–1789
Bruning K (1991) Effects of phosphorus limitation on the epidemiology of a chytrid phytoplankton parasite. Freshwat Biol 25:409–417
Droop MR (1983) 25 years of algal growth kinetics. Bot Mar 26:99–112
Eggleton P, Gaton KJ (1990) “Parasitoid” species and assemblages: convenient definitions or misleading compromises? Oikos 59:417–421
Elser JJ, Urabe J (1999) The stoichiometry of consumer-driven nutrient recycling: theory, observations, and consequences. Ecology 80:735–751
Elser JJ, Dobberfuhl D, McKay NA, Schampel JH (1996) Organism size, life history, and N:P stoichiometry: towards a unified view of cellular and ecosystem processes. Bioscience 46:674–684
Elser JJ, Fagan WF, Denno RF, Dobberfuhl DR, Folarin A, Huberty A, Interlandi S, Kilham S, McCauley E, Schulz KL, Siemann EH, Sterner RW (2000) Nutritional constraints in terrestrial and freshwater food webs. Nature 408:578–580
Ernest SKM, Enquist BJ, Brown JH, Charnov EL, Gillooly JF, Savage V, White EP, Smith FA, Hadly EA, Haskell JP, Lyons SK, Maurer BA, Niklas KJ, Tiffney B (2003) Thermodynamic and metabolic effects on the scaling of production and population energy use. Ecol Lett 6:990–995
Fenchel T (1969) The ecology of marine microbenthos. IV. Structure and function of the benthic ecosystem, its chemical and physical factors, and the microfauna communities with special reference to the ciliate protozoa. Ophelia 6:1–182
Flynn KJ, Mitra A et al (2019) Mixotrophic protists and a new paradigm for marine ecology: where does plankton research go now? J Plankton Res 41:375–391
Fuhrman JA (1999) Marine viruses and their biogeochemical and ecological effects. Nature 399:541–548
Fulton J (1973) Some aspects of the life history of Calanus plumchrus in the Strait of Georgia. J Fish Res Bd Can 30:811–815
Geller W (1975) Die Nahrungsaufnahme von Daphnia in Abhängigkeit von der Futterkonzentration, der Körpergröße und dem Hungerzustand der Tiere. Arch Hydrobiol Suppl 48:47–107
Geller W, Müller H (1985) Seasonal variability in the relationships between body length and individual dry weight and individual dry weight as related to food abundance and clutch size in two coexisting Daphnia species. J Plankton Res 7:1–18
Giere O (1992) Benthic life in sulfidic zones of the seas - ecological and structural adaptations to a toxic environment. Verh Dtsch Zool Ges 85:77–93
Giere O (1993) Meiobenthology. Springer, Berlin
Gillooly JF, Brown JH, West GB, Savage VM, Charnov EL (2001) Effects of size and temperature on metabolic rate. Science 293:2248–2251
Goldman JC, McCarthy JJ, Peavey DG (1979) Growth rate influence on the chemical composition of phytoplankton in oceanic waters. Nature 279:210–215
Gustavsen JA, Winget DM, Tian X, Suttle CA (2014) High temporal and spatial diversity in marine RNA viruses implies that they have an important role in mortality and structuring plankton communities. Front Microbiol 5:703
Hemmingsen A (1960) Energy metabolism as related to body size and respiratory surface, and its evolution. Report of Steno Memorial Hospital (Copenhagen) 9:1–110
Hobbie JB, Daley RJ, Jasper S (1977) Use of nuclepore filters for counting bacteria by fluorescence. Appl Environ Microb 33:1225–1228
Hochstädter S (2000) Seasonal changes of C:P ratios of seston, bacteria, phytoplankton and zooplankton in a deep, mesotrophic lake. Freshw Biol 44:453–463
Holfeld H (1998) Fungal infections of the phytoplankton: seasonality, minimal host density, and specificity in a mesotrophic lake. New Phytol 138:507–517
Ioannou CC, Guttal V, Couzin ID (2012) Predatory fish select for coordinated collective motion in virtual prey. Science 337:1212–1215
Jensen P (1987) Differences in microhabitat, abundance, biomass and body size between oxybiotic and thiobiotic free-living marine nematodes. Oecologia 71:564–567
Keefer ML, Caudill CC (2014) Homing and straying by anadromous salmonids: a review of mechanisms and rates. Rev Fish Biol Fish 24:333–368
Kils U (1986) Verhaltensphysiologische Untersuchungen pelagischen Schwärmen, Schwarmbildung als Strategie zur Orientierung in Umweltgradienten, Bedeutung der Schwarmbildung in der Aquakultur. Ber Inst Meereskunde, Kiel 163:1–168
Krumbein WE, Paterson DM, Stal LJ (1994) Biostabilization of sediments. BIS-Verlag, Oldenburg
Mann KH (1984). Fish production in open ocean ecosystems. In: Fasham MJR (ed) Flows of energy and materials in marine ecosystems. NATO Conf Ser 4, Mar Sci V. Plenum, New York, pp. 435–458
Marañón E (2015) Cell size as a key determinant of phytoplankton metabolism and community structure. Annu Rev Mar Sci 7:241–264
Mateus MD (2017) Bridging the gap between knowing and modeling viruses in marine systems—an upcoming frontier. Front Mar Sci 3:284
McNeal KH, Peckarsky BI, Likens GE (2005) Stable isotopes identify dispersal patterns of stonefly populations living along stram corridors. Freshw Biol 50:117–130
Möbius K (1877). Die Auster und die Austernwirtschaft. Wiegandt, Hemple & Parey: Berlin. English translation: The Oyster and Oyster Farming. U.S. Commission Fish and Fisheries Report (1880) 683–751
Moustaka-Gouni M, Kormas KA, Scotti M, Vardaka E, Sommer U (2016) Warming and acidification effects on planktonic heterotrophic pico- and nanoflagellates in a mesocosm experiment. Protist 167:389–410
Peters RH (1983) The ecological implications of body size. Cambridge University Press, Cambridge
Proctor LM, Fuhrman JA (1990) Viral mortality of marine-bacteria and cyanobacteria. Nature 343:60–62
Redfield AC (1934) On the proportions of organic derivatives in seawater and their relation to the composition of plankton. In: Daniel RJ (ed) James Johnstone memorial volume. Liverpool University Press, Liverpool, pp 176–192
Redfield AC, Ketchum BH, Richard FA (1963) The influence of organisms on the composition of seawater. In: Hill MN (ed) The Sea. Wiley, NY, pp 26–77
Rees HC, Maddison BC, Middleditch DJ, Patmore JR, Gough KC (2014) Review: the detection of aquatic animal species using environmental DNA - a review of EDNA as a survey tool in ecology. J Appl Ecol 51:1450–1459
Reise K, Ax P (1979) A meiofaunal “thiobios” limited to the anaerobic sulfide system of marine sand does not exist. Mar Biol 54:225–237
Schmidt J (1924) The breeding of the eel. Smithonian Report, Washington
Sieburth JMN, Smetacek V, Lenz J (1978) Pelagic ecosystem structure: heterotrophic compartments of the plankton and their relationship to plankton size fractions. Limnol Oceanogr 23:1256–1263
Sommer U (1988a) Does nutrient limitation of phytoplankton occur in situ? Verh internat Verein Limnol 23:707–712
Sommer U (1988b) Some size relationships in phytoflagellate motility. Hydrobiologia 161:125–131
Sommer U (1991) A comparison of the Droop and Monod models of nutrient limited growth applied to natural population of phytoplankton. Funct Ecol 5:535–544
Sommer U (1994) Planktologie. Springer, Berlin
Sommer U (2005) Biologische meereskunde, 2nd edn. Springer, berlin, Heidelberg, New York
Sommer U, Stibor H (2002) Cladocera – Copepoda – Tunicata: the role of three major mesozooplankton groups in pelagic food webs. Ecol Res 17:161–174
Sommer U, Charalampous E, Genitsaris S, Moustaka-Gouni M (2017) Benefits, costs and taxonomic distribution of marine phytoplankton body size. J Plankton Res 39:494–508
Stern R, Kraberg A, Bresnan E, Kooistra WHCF, Lovejoy C, Montresor M, Moran XAG, Not F, Salas R, Siano R, Vaulot D, Amaral-Zettler L, Zingone A, Metfies K (2018) J Plankton R 40:519–539
Sterner RW, Elser JJ (2002) Ecological stoichiometry. Princeton University Press, Princeton, NJ
Sutcliffe WHJ (1970) Relationships between growth rate and ribonucleic acid concentration in some invertebrates. J Fish Res Boar Can 27:606–609
Suttle CA (2005) Viruses in the sea. Nature 437:356-351
Tait RV (1981) Elements of marine ecology, 3rd edn. Butterworths, London
Utermöhl H (1958) Zur Vervollkommnung der quantitativen Phytoplanktonmethodik. Mitt internat Verein Limnol 9:1–38
Veldhuis MUV, Kraay GW (2000) Application of flow cytometry in marine phytoplankton research: current applications and future perspectives. Sci Mar 64:121–134
Wahl M (1989) Marine epibiosis. I. Fouling and antifouling. Some basic aspects. Mar Ecol Progr Ser 58:175–189
Walsby AF, Reynolds CS (1980) Sinking and floating. In: Morris I (ed) The physiological ecology of phytoplankton. Blackwell, Boston, pp 371–412
Ward BB (2013) How nitrogen is lost. Science 341:352–353
West GB, Brown JH, Enquist BJ (1999) The fourth dimension of life: fractal geometry and allometric scaling of organisms. Science 284:1677–1679
Zwart G, Crump BC, Agterveld MPKV, Hagen F, Han SK (2002) Typical freshwater bacteria: an analysis of available 16S rRNA gene sequences from plankton of lakes and rivers. Aqu Microb Ecol 28:141–155
Author information
Authors and Affiliations
Exercise Questions
Exercise Questions
The right-hand column of the table below indicates the place where the answer can be found or deduced logically from the information contained in the text.
Question | Section |
---|---|
1. Which major group of plants is not represented in water? | |
2. Which is the most important underrepresented animal higher taxon in water? | |
3. What is the meaning of the terms “photolithoautotrophic” and “chemoorganoheterotrophic”? | |
4. What is the carbon source of mixotrophic organisms? | |
5. Explain the difference between the photosynthesis of purple bacteria and cyanobacteria | |
6. Why is chemosynthesis bound to redox gradients? | |
5. Explain the difference between osmotrophy and phagotrophy. | |
6. How are absolute and specific metabolic rates related to body mass? | |
7. Can relationships between metabolic rates and body mass depend on food supply? | |
8. Which major groups of organic substances increase C:N ratios in biomass? | |
9. Which major groups of organic substances decrease C:P ratios in biomass? | |
10. Why is the C:N:P ratio of primary producers more variable than the C:N:P ratio of animals? | |
11. What is the numerical value and what is the biological basis of the Redfield ratio? | |
12. What distinguishes plankton from nekton? | |
13. How does plankton size relate to the methods of sampling, identification, and counting? | |
14. Which higher taxon of phytoplankton has the biggest range in sizes? | |
15. Which higher taxon of phytoplankton is more diverse in freshwaters than in the ocean? | |
16. Which phytoplankton groups are mineral skeletal substances and which are the minerals? | |
17. What is the usual abundance and the main role of heterotrophic nanoflagellates? | |
18. What are the main functional differences between cladocerans, copepods, and appendicularians? | |
20. Which zooplankton taxonomic groups are gelatinous? | |
21. What is the difference between lecitotrophic and planktotrophic larvae? | |
22. How is the ontogenetic vertical migration of long-living copepods related to their life cycle? | |
19. What are the proximate and the ultimate causes for the diel vertical migration of zooplankton? | |
20. What is the usual abundance of heterotrophic bacteria in surface waters? | |
21. Can aquatic fungi have negative effects on phytoplankton? If yes, which groups and why? | |
22. Are viruses a problem for other plankton? If yes, why? | |
23. Which are the major higher animal taxa belonging to nekton? | |
24. Which nektonic animals breed on land? | |
24. Do pelagic fish have a typical shape? If yes, why? | |
25. Why do whales have no fur and seals have fur? | |
26. What is the difference between anadromic and catadromic migrations? Provide examples! | |
27. Why do humpback whales perform long north–south migrations? | |
28. Explain epibiosis | |
29. How can flat rock surfaces become a three-dimensional habitat for benthos? | |
30. Which are the most important primary producers in periphyton? | |
31. Which are the most important groups of benthic macroalgae? | |
32. What determines the upper limit of macroalgal distributions in the eulittoral? | |
33. Which major taxa of zoobenthos are exclusively marine and which contain also freshwater representatives? | |
34. Compare the mobility patterns of the various groups of mollusks and crustaceans | |
35. Explain the uniqueness of the locomotion of Echinodermata. | |
36. Are benthic fish morphologically distinct from pelagic ones? | |
37. Which effects have microbial mats on sediments? | |
38. Describe the life forms of flowering plants in water. | |
39. Can you find protists and animals in reduced sediment layers? | |
40. What are the morphological adaptations of animals living in the interstitial space? | |
41. How do buried polychaetes and bivalves get oxygen? | |
42. Give examples for endo- and epibenthic fish. | |
43. Why do sediments contain the biggest diversity of bacterial metabolic types at small spatial scales? | |
44. How many heterotrophic bacteria are found in oxidized sediments? | |
45. What are the reduced end products of nitrate and sulfate respiration? | |
46. Which oxidized and reduced substances are necessary for >N-based and for S-based chemosynthesis? | |
47. Compare the larval and the adult life spans of aquatic insects. | |
48. How do stream insects cope with the problem of the downstream drift of larvae? | |
49. Which aquatic insects can cause human health problems? |
Glossary
- abundance
-
number of individuals per volume or area
- aerobic
-
in the presence of oxygen
- ammonification
-
production of ammonium by →nitrate respiration
- annamox: anaerobic
-
bacterial oxidation of ammonium by nitrate
- anadromous migration
-
spawning migration from the sea to freshwaters
- anaerobic
-
in the absence of oxygen
- autotrophic
-
using carbon dioxide or bicarbonate as C-source for biomass production
- bacteriochlorophyll
-
chlorophyll of photosynthetic bacteria, without Cyanobacteria
- bacterivory
-
feeding on bacteria
- bacterioplankton
-
bacterial plankton, usually excluding Cyanobacteria
- benthos
-
organisms living at the bottom or at the margin of water bodies
- biomass
-
mass of living organisms, usually expressed as fresh weight, dry weight, carbon content
- carnivory
-
feeding on animal material
- catadromous migration
-
spawning migration from freshwaters to the sea
- chemolithoautotrophy
-
production of biomass using redox reactions as energy source, inorganic substance as electron donor, and carbon dioxide or bicarbonate as carbon source
- chemosynthesis
-
chemolithoautotrophy
- chlorophyll
-
primary photosynthetic pigment of plants, algae, and Cyanobacteria
- C:N:P ratio
-
here used for the elemental composition of body mass
- denitrification
-
production of N2 by nitrate respiration
- detritus
-
dead organic matter
- detritivory
-
feeding on detritus
- DIC
-
dissolved inorganic carbon
- DOC
-
dissolved organic carbon
- endobenthos
-
benthos living within the substrate
- endopelon
-
benthos living within mud
- endopsammon
-
benthos living within sand
- epibenthos
-
benthos living on the substrate
- epipelon
-
benthos living on mud
- epipsammon
-
benthos living on sand
- eulittoral
-
intertidal zone
- femtoplankton
-
plankton <0.2 μm (viruses)
- fermentation
-
energy gain by splitting organic molecules into an oxidized and a reduced component
- filtration
-
feeding by taking food particles from a suspension by sieve- or filter-like structures
- flagellate
-
unicellular organism moving by flagella
- gas vacuoles
-
gas-filled vesicles in cells of Cyanobacteria
- herbivory
-
feeding on plant material
- heterotrophy
-
biomass production by using organic substances as C-source
- HNF
-
heterotrophic nanoflagellate (2–20 μm)
- holoplankton
-
organisms with complete life cycle in plankton
- induction
-
triggering of morphological or behavioral changes by environmental stimuli
- intraspecific
-
within species
- interspecific
-
between species
- interstitial
-
space between sediment grains
- kairomone
-
substance released from a predator which induces responses by a prey
- lithotrophy
-
biomass production using inorganic electron donors
- littoral
-
marginal zone of water bodies
- macrobenthos
-
benthos >1 (2) mm
- macroplankton
-
plankton 2 mm–2 cm
- megaplankton
-
plankton >2 cm
- meiobenthos
-
benthos 100(200) μm–1(2) mm
- meroplankton
-
organisms with part of their life cycle in plankton
- microbenthos
-
benthos <100(200) μm
- microplankton
-
plankton 20–200 μm
- mixoplankton
-
mixotrophic plankton
- mixotrophy
-
combination of auto- and heterotrophic nutrition
- nanoplankton
-
plankton 20–200 μm
- nekton
-
swimming open water organisms
- nitrate respiration
-
respiration using nitrate as oxidative agent
- nitrogen fixation
-
use of N2 as a nitrogen source for biomass production
- organotrophy
-
biomass production using organic substances as electron donors
- osmotrophy
-
heterotrophic nutrition based on DOC
- parasite
-
heterotrophic organisms feeding on body substances of the (usually bigger) host
- parasitoid
-
lethal parasite
- phagotrophy
-
heterotrophic nutrition based on POC
- photosynthesis
-
biomass production using light as energy source
- phototrophy
-
photosynthesis
- plankton
-
drifting open water organisms
- POC
-
particulate organic carbon
- POM
-
particulate organic matter
- proximate factor
-
environmental trigger for morphological or behavioral changes
- Redfield-ratio
-
C:N:P ratio (106:16:1) typical for phytoplankton under sufficient N and p supply
- respiration
-
oxidation of organic matter to gain energy for vital processes
- reef
-
hard bottom structure built by benthic organisms
- specific metabolic rate
-
metabolic rate per unit body mass
- sulfur bacteria
-
bacteria using redox reactions of sulfur for energy gain
- sulfate respiration
-
respiration using sulfate as oxidative agent
- ultimate factor
-
environmental factor which has selected for morphological or behavioral traits in evolutionary past
- vertical migration
-
diel up and down migration of plankton and nekton or ontogenetic shift in vertical position
Rights and permissions
Copyright information
© 2023 The Author(s), under exclusive license to Springer Nature Switzerland AG
About this chapter
Cite this chapter
Sommer, U. (2023). Life Forms of Aquatic Organisms. In: Freshwater and Marine Ecology. Springer, Cham. https://doi.org/10.1007/978-3-031-42459-5_3
Download citation
DOI: https://doi.org/10.1007/978-3-031-42459-5_3
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-031-42458-8
Online ISBN: 978-3-031-42459-5
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)