River ecosystem

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This stream in the redwoods together with its environment can be thought of as forming a river or lotic ecosystem

The ecosystem of a river is the river viewed as a system operating in its natural environment, and includes biotic (living) interactions amongst plants, animals and micro-organisms, as well as abiotic (nonliving) physical and chemical interactions.[1][2]

River ecosystems are prime examples of lotic ecosystems. Lotic refers to flowing water, from the Latin lotus, washed. Lotic waters range from springs only a few centimeters wide to major rivers kilometers in width.[3] Much of this article applies to lotic ecosystems in general, including related lotic systems such as streams and springs. Lotic ecosystems can be contrasted with lentic ecosystems, which involve relatively still terrestrial waters such as lakes and ponds. Together, these two fields form the more general study area of freshwater or aquatic ecology.

The following unifying characteristics make the ecology of running waters unique from that of other aquatic habitats.[4]

  • Flow is unidirectional.
  • There is a state of continuous physical change.
  • There is a high degree of spatial and temporal heterogeneity at all scales (microhabitats).
  • Variability between lotic systems is quite high.
  • The biota is specialized to live with flow conditions.

Abiotic factors[edit]

Flow[edit]

Water flow is the key factor in lotic systems influencing their ecology. The strength of water flow can vary between systems, ranging from torrential rapids to slow backwaters that almost seem like lentic systems. The speed of the water flow can also vary within a system and is subject to chaotic turbulence. This turbulence results in divergences of flow from the mean downslope flow vector as typified by eddy currents. The mean flow rate vector is based on variability of friction with the bottom or sides of the channel, sinuosity, obstructions, and the incline gradient.[3] In addition, the amount of water input into the system from direct precipitation, snowmelt, and/or groundwater can affect flow rate. Flowing waters can alter the shape of the streambed through erosion and deposition, creating a variety of habitats, including riffles, glides[disambiguation needed], and pools.[5]

Light[edit]

A pensive Cooplacurripa River, NSW

Light is important to lotic systems, because it provides the energy necessary to drive primary production via photosynthesis, and can also provide refuge for prey species in shadows it casts. The amount of light that a system receives can be related to a combination of internal and external stream variables. The area surrounding a small stream, for example, might be shaded by surrounding forests or by valley walls. Larger river systems tend to be wide so the influence of external variables is minimized, and the sun reaches the surface. These rivers also tend to be more turbulent, however, and particles in the water increasingly attenuate light as depth increases.[5] Seasonal and diurnal factors might also play a role in light availability because the angle of incidence, the angle at which light strikes water can lead to light lost from reflection. Known as Beer's Law, the shallower the angle, the more light is reflected and the amount of solar radiation received declines logarithmically with depth.[4] Additional influences on light availability include cloud cover, altitude, and geographic position (Brown 1987).

Temperature[edit]

Most lotic species are poikilotherms whose internal temperature varies with their environment, thus temperature is a key abiotic factor for them. Water can be heated or cooled through radiation at the surface and conduction to or from the air and surrounding substrate. Shallow streams are typically well mixed and maintain a relatively uniform temperature within an area. In deeper, slower moving water systems, however, a strong difference between the bottom and surface temperatures may develop. Spring fed systems have little variation as springs are typically from groundwater sources, which are often very close to ambient temperature.[4] Many systems show strong diurnal fluctuations and seasonal variations are most extreme in arctic, desert and temperate systems.[4] The amount of shading, climate and elevation can also influence the temperature of lotic systems.[3]

Chemistry[edit]

A forest stream in the winter near Erzhausen, Germany

Water chemistry between systems varies tremendously. The chemistry is foremost determined by inputs from the geology of its watershed, or catchment area, but can also be influenced by precipitation and the addition of pollutants from human sources.[3][5] Large differences in chemistry do not usually exist within small lotic systems due to a high rate of mixing. In larger river systems, however, the concentrations of most nutrients, dissolved salts, and pH decrease as distance increases from the river’s source.[4]

Oxygen is likely the most important chemical constituent of lotic systems, as all aerobic organisms require it for survival. It enters the water mostly via diffusion at the water-air interface. Oxygen’s solubility in water decreases as water pH and temperature increases. Fast, turbulent streams expose more of the water’s surface area to the air and tend to have low temperatures and thus more oxygen than slow, backwaters.[4] Oxygen is a byproduct of photosynthesis, so systems with a high abundance of aquatic algae and plants may also have high concentrations of oxygen during the day. These levels can decrease significantly during the night when primary producers switch to respiration. Oxygen can be limiting if circulation between the surface and deeper layers is poor, if the activity of lotic animals is very high, or if there is a large amount of organic decay occurring.[5]

Substrate[edit]

Cascade in the Pyrénées.

The inorganic substrate of lotic systems is composed of the geologic material present in the catchment that is eroded, transported, sorted, and deposited by the current. Inorganic substrates are classified by size on the Wentworth scale, which ranges from boulders, to pebbles, to gravel, to sand, and to silt.[4] Typically, particle size decreases downstream with larger boulders and stones in more mountainous areas and sandy bottoms in lowland rivers. This is because the higher gradients of mountain streams facilitate a faster flow, moving smaller substrate materials further downstream for deposition.[5] Substrate can also be organic and may include fine particles, autumn shed leaves, submerged wood, moss, and more evolved plants.[3] Substrate deposition is not necessarily a permanent event, as it can be subject to large modifications during flooding events.[5]

Biotic Factors[edit]

Bacteria[edit]

Bacteria are present in large numbers in lotic waters. Free-living forms are associated with decomposing organic material, biofilm on the surfaces of rocks and vegetation, in between particles that compose the substrate, and suspended in the water column. Other forms are also associated with the guts of lotic organisms as parasites or in commensal relationships.[4] Bacteria play a large role in energy recycling,[3] which will be discussed in the Trophic Relationships section.

Primary producers[edit]

Periphyton
Common water hyacinth in flower

Algae, consisting of phytoplankton and periphyton, are the most significant sources of primary production in most streams and rivers.[4] Phytoplankton float freely in the water column and thus are unable to maintain populations in fast flowing streams. They can, however, develop sizable populations in slow moving rivers and backwaters.[3] Periphyton are typically filamentous and tufted algae that can attach themselves to objects to avoid being washed away by fast current. In places where flow rates are negligible or absent, periphyton may form a gelatinous, unanchored floating mat.[5]

Plants exhibit limited adaptations to fast flow and are most successful in reduced currents. More primitive plants, such as mosses and liverworts attach themselves to solid objects. This typically occurs in colder headwaters where the mostly rocky substrate offers attachment sites. Some plants are free floating at the water’s surface in dense mats like duckweed or water hyacinth. Others are rooted and may be classified as submerged or emergent. Rooted plants usually occur in areas of slackened current where fine-grained soils are found (Brown 1987).[5] These rooted plants are flexible, with elongated leaves that offer minimal resistance to current.[1]

Living in flowing water can be beneficial to plants and algae because the current is usually well aerated and it provides a continuous supply of nutrients.[5] These organisms are limited by flow, light, water chemistry, substrate, and grazing pressure.[4] Algae and plants are important to lotic systems as sources of energy, for forming microhabitats that shelter other fauna from predators and the current, and as a food resource (Brown 1987).

Insects and other invertebrates[edit]

Up to 90% of invertebrates in some lotic systems are insects. These species exhibit tremendous diversity and can be found occupying almost every available habitat, including the surfaces of stones, deep below the substratum, adrift in the current, and in the surface film. Insects have developed several strategies for living in the diverse flows of lotic systems. Some avoid high current areas, inhabiting the substratum or the sheltered side of rocks. Additional invertebrate taxa common to flowing waters include mollusks such as snails, limpets, clams, mussels, as well as crustaceans like crayfish and crabs.[5] Like most of the primary consumers, lotic invertebrates often rely heavily on the current to bring them food and oxygen (Brown 1987). Invertebrates, especially insects, are important as both consumers and prey items in lotic systems.

Fish and other vertebrates[edit]

The brook trout is native to small streams, creeks, lakes, and spring ponds.
New Zealand longfin eels can weigh over 50 kilograms.

Fishes are probably the best-known inhabitants of lotic systems. The ability of a fish species to live in flowing waters depends upon the speed at which it can swim and the duration that its speed can be maintained. This ability can vary greatly between species and is tied to the habitat in which it can survive. Continuous swimming expends a tremendous amount of energy and, therefore, fishes spend only short periods in full current. Instead, individuals remain close to the bottom or the banks, behind obstacles, and sheltered from the current, swimming in the current only to feed or change locations.[1] Some species have adapted to living only on the system bottom, never venturing into the open water flow. These fishes are dorso-ventrally flattened to reduce flow resistance and often have eyes on top of their heads to observe what is happening above them. Some also have sensory barrels positioned under the head to assist in the testing of substratum (Brown 1987).

Lotic systems typically connect to each other, forming a path to the ocean (spring → stream → river → ocean), and many fishes have life cycles that require stages in both fresh and salt water. Salmon, for example, are anadromous species that are born and develop in freshwater and then move to the ocean as adults. Eels are catadromous, and are born and develop in the ocean and then move into freshwater as adults.[4]

Other vertebrate taxa that inhabit lotic systems include amphibians, such as salamanders, reptiles (e.g. snakes, turtles, crocodiles and alligators) various bird species, and mammals (e.g., otters, beavers, hippos, and river dolphins). With the exception of a few species, these vertebrates are not tied to water as fishes are, and spend part of their time in terrestrial habitats.[4] Many fish species are important as consumers and as prey species to the larger vertebrates mentioned above.

Trophic relationships[edit]

Energy inputs[edit]

Pondweed is an autochthonous energy source
Leaf litter is an allochthonous energy source

Energy sources can be autochthonous or allochthonous.

  • Autochthonous energy sources are those derived from within the lotic system. During photosynthesis, for example, primary producers form organic carbon compounds out of carbon dioxide and inorganic matter. The energy they produce is important for the community because it may be transferred to higher trophic levels via consumption. Additionally, high rates of primary production can introduce dissolved organic matter (DOM) to the waters.[5] Another form of autochthonous energy comes from the decomposition of dead organisms and feces that originate within the lotic system. In this case, bacteria decompose the detritus or coarse particulate organic material (CPOM; >1 mm pieces) into fine particulate organic matter (FPOM; <1 mm pieces) and then further into inorganic compounds that are required for photosynthesis.[3][5] This process is discussed in more detail below.
  • Allochthonous energy sources are those derived from outside the lotic system, that is, from the terrestrial environment. Leaves, twigs, fruits, etc. are typical forms of terrestrial CPOM that have entered the water by direct litterfall or lateral leaf blow.[4] In addition, terrestrial animal-derived materials, such as feces or carcasses that have been added to the system are examples of allochthonous CPOM. The CPOM undergoes a specific process of degradation. Allan[3] gives the example of a leaf fallen into a stream. First, the soluble chemicals are dissolved and leached from the leaf upon its saturation with water. This adds to the DOM load in the system. Next, microbes such as bacteria and fungi colonize the leaf, softening it as the mycelium of the fungus grows into it. The composition of the microbial community is influenced by the species of tree from which the leaves are shed (Rubbo and Kiesecker 2004). This combination of bacteria, fungi, and leaf are a food source for shredding invertebrates,[6] which leave only FPOM after consumption. These fine particles may be colonized by microbes again or serve as a food source for animals that consume FPOM. Organic matter can also enter the lotic system already in the FPOM stage by wind, surface runoff, bank erosion, or groundwater. Similarly, DOM can be introduced through canopy drip from rain or from surface flows.[4]

Invertebrates[edit]

Invertebrates can be organized into many feeding guilds in lotic systems. Some species are shredders, which use large and powerful mouth parts to feed on non-woody CPOM and their associated microorganisms. Others are suspension feeders, which use their setae, filtering aparati, nets, or even secretions to collect FPOM and microbes from the water. These species may be passive collectors, utilizing the natural flow of the system, or they may generate their own current to draw water, and also, FPOM in Allan.[3] Members of the gatherer-collector guild actively search for FPOM under rocks and in other places where the stream flow has slackened enough to allow deposition.[5] Grazing invertebrates utilize scraping, rasping, and browsing adaptations to feed on periphyton and detritus. Finally, several families are predatory, capturing and consuming animal prey. Both the number of species and the abundance of individuals within each guild is largely dependent upon food availability. Thus, these values may vary across both seasons and systems.[3]

Fish[edit]

Fish can also be placed into feeding guilds. Planktivores pick plankton out of the water column. Herbivore-detritivores are bottom-feeding species that ingest both periphyton and detritus indiscriminately. Surface and water column feeders capture surface prey (mainly terrestrial and emerging insects) and drift (benthic invertebrates floating downstream). Benthic invertebrate feeders prey primarily on immature insects, but will also consume other benthic invertebrates. Top predators consume fishes and/or large invertebrates. Omnivores ingest a wide range of prey. These can be floral, faunal, and/or detrital in nature. Finally, parasites live off of host species, typically other fishes.[3] Fish are flexible in their feeding roles, capturing different prey with regard to seasonal availability and their own developmental stage. Thus, they may occupy multiple feeding guilds in their lifetime. The number of species in each guild can vary greatly between systems, with temperate warm water streams having the most benthic invertebrate feeders, and tropical systems having large numbers of detritus feeders due to high rates of allochthonous input.[5]

Community patterns and diversity[edit]

Iguazu Falls - an extreme lotic environment.

Local species richness[edit]

Large rivers have comparatively more species than small streams. Many relate this pattern to the greater area and volume of larger systems, as well as an increase in habitat diversity. Some systems, however, show a poor fit between system size and species richness. In these cases, a combination of factors such as historical rates of speciation and extinction, type of substrate, microhabitat availability, water chemistry, temperature, and disturbance such as flooding seem to be important.[4]

Resource partitioning[edit]

Although many alternate theories have been postulated for the ability of guild-mates to coexist (see Morin 1999), resource partitioning has been well documented in lotic systems as a means of reducing competition. The three main types of resource partitioning include habitat, dietary, and temporal segregation.[4]

Habitat segregation was found to be the most common type of resource partitioning in natural systems (Schoener, 1974). In lotic systems, microhabitats provide a level of physical complexity that can support a diverse array of organisms (Vincin and Hawknis, 1998). The separation of species by substrate preferences has been well documented for invertebrates. Ward (1992) was able to divide substrate dwellers into 6 broad assemblages, including those that live in: coarse substrate, gravel, sand, mud, woody debris, and those associated with plants, showing one layer of segregation. On a smaller scale, further habitat partitioning can occur on or around a single substrate, such as a piece of gravel. Some invertebrates prefer the high flow areas on the exposed top of the gravel, while others reside in the crevices between one piece of gravel and the next, while still others live on the bottom of this gravel piece.[4]

Dietary segregation is the second-most common type of resource partitioning.[4] High degrees of morphological specializations or behavioral differences allow organisms to use specific resources. The size of nets built by some species of invertebrate suspension feeders, for example, can filter varying particle size of FPOM from the water (Edington et al. 1984). Similarly, members in the grazing guild can specialize in the harvesting of algae or detritus depending upon the morphology of their scraping apparatus. In addition, certain species seem to show a preference for specific algal species.[4]

Temporal segregation is a less common form of resource partitioning, but it is nonetheless an observed phenomenon.[4] Typically, it accounts for coexistence by relating it to differences in life history patterns and the timing of maximum growth among guild mates. Tropical fishes in Borneo, for example, have shifted to shorter life spans in response to the ecological niche reduction felt with increasing levels of species richness in their ecosystem (Watson and Balon 1984).

Persistence and succession[edit]

Over long time scales, there is a tendency for species composition in pristine systems to remain in a stable state.[7] This has been found for both invertebrate and fish species.[4] On shorter times scales, however, flow variability and unusual precipitation patterns decrease habitat stability and can all lead to declines in persistence levels. The ability to maintain this persistence over long time scales is related to the ability of lotic systems to return to the original community configuration relatively quickly after a disturbance (Townsend et al. 1987). This is one example of temporal succession, a site-specific change in a community involving changes in species composition over time. Another form of temporal succession might occur when a new habitat is opened up for colonization. In these cases, an entirely new community that is well adapted to the conditions found in this new area can establish itself.[4]

River continuum concept[edit]

Meandering stream in Waitomo, New Zealand
A rocky stream in the U.S. state of Hawaii

The River continuum concept (RCC) was an attempt to construct a single framework to describe the function of temperate lotic ecosystems from the source to the end and relate it to changes in the biotic community (Vannote et al. 1980).[3] The physical basis for RCC is size and location along the gradient from a small stream eventually linked to a large river. Stream order (see characteristics of streams) is used as the physical measure of the position along the RCC.

According to the RCC, low ordered sites are small shaded streams where allochthonous inputs of CPOM are a necessary resource for consumers. As the river widens at mid-ordered sites, energy inputs should change. Ample sunlight should reach the bottom in these systems to support significant periphyton production. Additionally, the biological processing of CPOM (Coarse Particulate Organic Matter - larger than 1 mm) inputs at upstream sites is expected to result in the transport of large amounts of FPOM (Fine Particulate Organic Matter - smaller than 1 mm) to these downstream ecosystems. Plants should become more abundant at edges of the river with increasing river size, especially in lowland rivers where finer sediments have been deposited and facilitate rooting. The main channels likely have too much current and turbidity and a lack of substrate to support plants or periphyton. Phytoplankton should produce the only autochthonous inputs here, but photosynthetic rates will be limited due to turbidity and mixing. Thus, allochthonous inputs are expected to be the primary energy source for large rivers. This FPOM will come from both upstream sites via the decomposition process and through lateral inputs from floodplains.

Biota should change with this change in energy from the headwaters to the mouth of these systems. Namely, shredders should prosper in low-ordered systems and grazers in mid-ordered sites. Microbial decomposition should play the largest role in energy production for low-ordered sites and large rivers, while photosynthesis, in addition to degraded allochthonous inputs from upstream will be essential in mid-ordered systems. As mid-ordered sites will theoretically receive the largest variety of energy inputs, they might be expected to host the most biological diversity (Vannote et al. 1980).[3][4]

Just how well the RCC actually reflects patterns in natural systems is uncertain and its generality can be a handicap when applied to diverse and specific situations.[3] The most noted criticisms of the RCC are: 1. It focuses mostly on macroinvertebrates, disregarding that plankton and fish diversity is highest in high orders; 2. It relies heavily on the fact that low ordered sites have high CPOM inputs, even though many streams lack riparian habitats; 3. It is based on pristine systems, which rarely exist today; and 4. It is centered around the functioning of temperate streams. Despite its shortcomings, the RCC remains a useful idea for describing how the patterns of ecological functions in a lotic system can vary from the source to the mouth.[3]

Disturbances such as congestion by dams or natural events such as shore flooding are not included in the RCC model.[8] Various researchers have since expanded the model to account for such irregularities. For example, J.V. Ward and J.A. Stanford came up with the Serial Discontinuity Concept in 1983, which addresses the impact of geomorphologic disorders such as congestion and integrated inflows. The same authors presented the Hyporheic Corridor concept in 1993, in which the vertical (in depth) and lateral (from shore to shore) structural complexity of the river were connected.[9] The flood pulse concept, developed by W.J. Junk in 1989, further modified by P.B. Bayley in 1990 and K. Tockner in 2000, takes into account the large amount of nutrients and organic material that makes its way into a river from the sediment of surrounding flooded land.[8]

Human impacts[edit]

Pollution[edit]

Pollutant sources of lotic systems are hard to control because they derive, often in small amounts, over a very wide area and enter the system at many locations along its length. Agricultural fields often deliver large quantities of sediments, nutrients, and chemicals to nearby streams and rivers. Urban and residential areas can also add to this pollution when contaminants are accumulated on impervious surfaces such as roads and parking lots that then drain into the system. Elevated nutrient concentrations, especially nitrogen and phosphorus which are key components of fertilizers, can increase periphyton growth, which can be particularly dangerous in slow moving streams.[5] Another pollutant, acid rain, forms from sulfur dioxide and nitrous oxide emitted from factories and power stations. These substances readily dissolve in atmospheric moisture and enter lotic systems through precipitation. This can lower the pH of these sites, affecting all trophic levels from algae to vertebrates (Brown 1987). Mean species richness and total species numbers within a system decrease with decreasing pH.[4]

While direct pollution of lotic systems has been greatly reduced in the United States under the government’s Clean Water Act, contaminants from diffuse, non-point sources, remain a large problem.[5]

Flow modification[edit]

Dams alter the flow, temperature, and sediment regime of lotic systems.[4] Additionally, many rivers are dammed at multiple locations, amplifying the impact. Dams can cause enhanced clarity and reduced variability in stream flow, which in turn cause an increase in periphyton abundance. Invertebrates immediately below a dam can show reductions in species richness due to an overall reduction in habitat heterogeneity.[5] Also, thermal changes can affect insect development, with abnormally warm winter temperatures obscuring cues to break egg diapause and overly cool summer temperatures leaving too few acceptable days to complete growth.[3] Finally, dams fragment river systems, isolating previously continuous populations, and preventing the migrations of anadromous and catadromous species.[5]

Invasive species[edit]

Invasive species have been introduced to lotic systems through both purposeful events (e.g. stocking game and food species) as well as unintentional events (e.g. hitchhikers on boats or fishing waders). These organisms can affect natives via competition for prey or habitat, predation, habitat alteration, hybridization, or the introduction of harmful diseases and parasites.[4] Once established, these species can be difficult to control or eradicate, particularly because of the connectivity of lotic systems. Invasive species can be especially harmful in areas that have endangered biota, such as mussels in the Southeast United States, or those that have localized endemic species, like lotic systems west of the Rocky Mountains, where many species evolved in isolation.

See also[edit]

References[edit]

  1. ^ a b c Angelier, E. 2003. Ecology of Streams and Rivers. Science Publishers, Inc., Enfield. Pp. 215.
  2. ^ ”Biology Concepts & Connections Sixth Edition”, Campbell, Neil A. (2009), page 2, 3 and G-9. Retrieved 2010-06-14.
  3. ^ a b c d e f g h i j k l m n o p q Allan, J.D. 1995. Stream Ecology: structure and function of running waters. Chapman and Hall, London. Pp. 388.
  4. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z Giller, S. and B. Malmqvist. 1998. The Biology of Streams and Rivers. Oxford University Press, Oxford. Pp. 296.
  5. ^ a b c d e f g h i j k l m n o p q r Cushing, C.E. and J.D. Allan. 2001. Streams: their ecology and life. Academic Press, San Diego. Pp. 366.
  6. ^ U.S. EPA. "Classifications of Macroinvertebrates". Retrieved 3 July 2012. 
  7. ^ Hildrew, A.G. and P.S. Giller. 1994. Patchiness, species interactions and disturbance in the stream benthos. In Aquatic Ecology: scale pattern and process. (P.S. Giller, A.G. Hildrew, and D.G. Rafaelli eds.) Blackwell, Oxford. Pp. 21–62.
  8. ^ a b Junk J.W., P.B. Bayley, R.E. Sparks: “The flood pulse concept in river flood plain systems”. Canadian Special Publications of Fisheries and Aquatic Sciences. 106. 1989.
  9. ^ Ward J.V., J.A. Stanford: The Serial Discontinuity Concept of River Ecosystems. T.D. Fontaine, S.M. Bartell: “Dynamics of Lotic Ecosystems”. Science Publications, Ann Arbor Mich 29-42. 1983.

Further reading[edit]

  • Brown, A.L. 1987. Freshwater Ecology. Heinimann Educational Books, London. Pp. 163.
  • Carlisle, D.M. and M.D. Woodside. 2013. Ecological health in the nation’s streams United States Geological Survey. Pp. 6.
  • Edington, J.M., Edington, M.A., and J.A. Dorman. 1984. Habitat partitioning amongst hydrophyschid larvae of a Malaysian stream. Entomologica 30: 123-129.
  • Hynes, H.B.N. 1970. Ecology of Running Waters. Originally published in Toronto by University of Toronto Press, 555p
  • Morin, P.J. 1999. Community Ecology. Blackwell Science, Oxford. Pp. 424.
  • Power ME (1990) "Effects of fish in river food webs" Science, 250: 811–814.
  • Rubbo, M. J. and J. M. Kiesecker. 2004. Leaf litter composition and community structure: translating regional species changes into local dynamics. Ecology 85:2519-2525.
  • Schoener, T.W. 1974. Resource partitioning in ecological communities. Science 2:369-404.
  • Townsend, C.R., Hildrew, A.G., and K. Schofield. 1987. Persistence of stream invertebrate communities in relation to environmental variability. Animal Ecology 56:597-613.
  • Vannote, R.L., Minshall, G.W., Cummins, K.W., Sedell, J.R., and C.E. Cushing. 1980. The river continuum concept. Canadian Journal of Fisheries and Aquatic Sciences 37:130- 137.
  • Vinson, M.R. and C.P. Hawkins. 1998. Biodiversity of stream insects: variation at local, basin, and regional scales. Annual Review of Entomology 43:271-293.
  • Ward, J.V. 1992. Aquatic Insect Ecology: biology and habitat. Wiley, New York. Pp. 456.
  • Watson, D.J. and E.K. Balon. 1984. Ecomorphological analysis of fish taxocenes in rainforest streams of northern Borneo. Journal of Fish Biology 25:371-384.

External links[edit]