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The Ecological Niche: History and Recent Controversies

Profile image of Arnaud PochevilleArnaud Pocheville

2015, Handbook for Evolutionary Thinking - Springer

https://doi.org/10.1007/978-94-017-9014-7_26
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40 pages

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Abstract

In this chapter, we first trace the history of the concept of ecological niche and see how its meanings varied with the search for a theory of ecology. The niche concept has its roots in the Darwinian view of ecosystems that are structured by struggle for survival and, originally, the niche was perceived as an invariant place within the ecosystem, that would preexist the assembly of the ecosystem. The concept then slipped towards a sense in which the niche, no longer a pre-existing ecosystem structure, eventually became a variable that would in turn have to be explained by the competitive exclusion principle and the coevolution of species. The niche concept used at that time, while more operational from an empirical point of view than the previous one, suffered however from an ill-founded definition. A recent refoundation by Chase & Leibold enabled to overcome some of the definitional difficulties.We then present how, in contemporary ecology, the niche concept is recruited to explain biodiversity and species coexistence patterns. We show how, in parallel, neutralist models, by succeedingly explaining some ecological patterns without resorting to explanations in terms of niche, have questioned the explanatory virtues of the niche concept.In conclusion, it seems that the forunes and misfortunes of the niche concept can be seen as a reflection of the difficulties of ecology to give birth to a theory that would be both predictive and explanatory.

Key takeaways
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  1. The ecological niche concept evolved from a fixed definition to a dynamic one influenced by competition and coevolution.
  2. Chase and Leibold's recent work revitalized the niche concept by integrating organism responses and impacts on the environment.
  3. Neutral theory challenges niche explanations by suggesting species coexistence can occur without niche differences.
  4. Empirical studies in the 1980s revealed limitations in niche models, prompting a shift towards mechanisms beyond competition.
  5. Niche theory remains central to understanding biodiversity, despite ongoing debates with neutral models.
Figures (2)
Fig. 26.1 Original illustration of Hutchinson’s niche concept (1957: fig. 1): “Two fundamental niches defined by a pair of variables in a niche space in two dimensions. Only one of the two spe- cies is expected to persist in the region of intersection. The /ines joining equivalent points in niche space and biotop space indicate the relationship between the two spaces. The distribution of the two species involved is shown in the right panel in relation to a standard curve of temperature versus depth in a lake in the summer”
Fig. 26.1 Original illustration of Hutchinson’s niche concept (1957: fig. 1): “Two fundamental niches defined by a pair of variables in a niche space in two dimensions. Only one of the two spe- cies is expected to persist in the region of intersection. The /ines joining equivalent points in niche space and biotop space indicate the relationship between the two spaces. The distribution of the two species involved is shown in the right panel in relation to a standard curve of temperature versus depth in a lake in the summer”
Fig. 26.3. Diagram illustrating the typical assumptions of the niche theory (eft) and the neutral theory (right); for the neutral theory, cf. Sect. 3. Left: species have different average fitness (dotted lines) but each undergoes a negative frequency-dependence (solid line), which stabilizes coexis- tence (the slope of the Jine represents the intensity of stabilization). Right: species show no frequency-dependence, but have equal average fitness (After Adler et al. 2007)
Fig. 26.3. Diagram illustrating the typical assumptions of the niche theory (eft) and the neutral theory (right); for the neutral theory, cf. Sect. 3. Left: species have different average fitness (dotted lines) but each undergoes a negative frequency-dependence (solid line), which stabilizes coexis- tence (the slope of the Jine represents the intensity of stabilization). Right: species show no frequency-dependence, but have equal average fitness (After Adler et al. 2007)

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FAQs

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What explains the decline of the niche concept in the 1980s?add

Research showed that many competition studies lacked robust null hypotheses, undermining niche theory's validity, leading to increased skepticism among ecologists.

How is the niche concept formalized in Hutchinson's model?add

Hutchinson formalized the niche concept as a volumetric space of environmental variables, introducing the distinction between fundamental and realized niches.

What impact do competitive exclusion studies have on ecological theory?add

The Competitive Exclusion Principle, derived from studies by Gause, posits that species occupying identical niches cannot coexist, reinforcing niche theory in ecology.

How do niche construction theories differ from traditional ecological models?add

Niche construction theories argue that organisms actively modify their environments, contrasting with traditional models that view environments as unchangeable.

What role does the neutral theory play in modern ecology?add

Neutral theory challenges traditional niche theories by proposing that species diversity can arise from random dynamics rather than niche differentiation.

Related papers

Niche, habitat, and related ecological concepts

Acta Biotheoretica, 1975

Received 27-VIII-I974; revised 2I-I-I975) SUMMARY DARWIN'S phrase "place in natural economy", and SPENCER'S term "correspondence" can be regarded as first attempts to express the organism-environment relationships. The same concept has more recently been approached from the point of view of (I) life-form, (2) external activities, and habitat. Though all these points are interlocking, they have been stressed differently in the writings of American and European ecologists. It is proposed that the term "niche" would be most useful and rational if applied to the total of relationships between a living organism (population, species) and its complete environment, both biotic and abiotic.

Ecological Niche

Encyclopedia of Entomology, 2008

Ecological niche characterizes the position of a species within an ecosystem, comprising species habitat requirements as well as its functional role. This century-old concept has undergone several substantial transformations, but still represents a major heuristic tool for our understanding of nature. Niches of distinct, even closely related species, tend to differ at least in some aspects as interspecific competition minimizes their overlap. Interspecific differences in abundance and distribution can be explained by different niche width and position. However, species can locally coexist also due to processes other than simple niche separation-namely due to stochastic spatiotemporal population dynamics. Species evolution always implies the evolution of its niche. To some extent, we can predict niche evolution from the knowledge of the environment and the trade-offs affecting possibilities of resource utilization of individual species. In the course of evolution, species have tendency to narrow their niches due to interspecific competition and intraspecific optimization. Consequently, niche widening often occurs when the species is released from interspecific competition. Species do not passively adapt to their niches but also actively modify them. Such a feedback leads to the coevolution between species and their environment and the evolution of whole ecological communities.

Expanding the ecological niche approach: Relationships between variability in niche position and species richness

Ecological Complexity, 2011

A brief introduction to niche construction theory for ecologists and conservationists

Biological Conservation, 2019

Niche construction theory (NCT) is a theoretical framework that has great potential for increasing our understanding of ecological and evolutionary phenomena. However, few ecologists still use NCT, probably because they believe that ecological and evolutionary processes do not occur at the same pace or because they believe that the modern evolutionary synthesis (MES) explains the studied phenomena well enough. NCT is not opposed to the MES. However, NCT proponents argue that because all organisms undergo environmental modifications, they can alter the selection pressures that act on themselves and other species. In this case, adaptation is conceived as a two-way process in which organisms and the environment act upon one another. Therefore, this article aims to present a brief introduction of NCT, arguing and exemplifying its applicability in ecological studies and conservation strategies. Finally, we provide suggestions about how NCT can contribute to ecological studies and the planning of conservation strategies.

Competing species leave many potential niches unfilled

Nature Ecology & Evolution

Reconciling niche and neutrality: the continuum hypothesis

Ecology Letters, 2006

In this study, we ask if instead of being fundamentally opposed, niche and neutral theories could simply be located at the extremes of a continuum. First, we present a model of recruitment probabilities that combines both niche and neutral processes. From this model, we predict and test whether the relative importance of niche vs. neutral processes in controlling community dynamics will vary depending on community species richness, niche overlap and dispersal capabilities of species (both local and long distance). Results demonstrate that niche and neutrality form ends of a continuum from competitive to stochastic exclusion. In the absence of immigration, competitive exclusion tends to create a regular spacing of niches. However, immigration prevents the establishment of a limiting similarity. The equilibrium community consists of a set of complementary and redundant species, with their abundance determined, respectively, by the distribution of environmental conditions and the amoun...

Organism-environment mutuality epistemics, and the concept of an ecological niche

Synthese, 1985

ABSTRACT. The concept of an ecological niche (econiche) has been used in a variety of ways, some of which are incompatible with a relational or functional interpretation of the term. This essay seeks to standardize usage by limiting the concept to functional relations ...

On the relationship between niche and distribution

Ecology Letters, 2000

Applications of Hutchinson's n-dimensional niche concept are often focused on the role of interspecific competition in shaping species distribution patterns. In this paper, I discuss a variety of factors, in addition to competition, that influence the observed relationship between species distribution and the availability of suitable habitat. In particular, I show that Hutchinson's niche concept can be modified to incorporate the influences of niche width, habitat availability and dispersal, as well as interspecific competition per se. I introduce a simulation model called NICHE that embodies many of Hutchinson's original niche concepts and use this model to predict patterns of species distribution. The model may help to clarify how dispersal, niche size and competition interact, and under what conditions species might be common in unsuitable habitat or absent from suitable habitat. A brief review of the pertinent literature suggests that species are often absent from suitable habitat and present in unsuitable habitat, in ways predicted by theory. However, most tests of niche theory are hampered by inadequate consideration of what does and does not constitute suitable habitat. More conclusive evidence for these predictions will require rigorous determination of habitat suitability under field conditions. I suggest that to do this, ecologists must measure habitat specific demography and quantify how demographic parameters vary in response to temporal and spatial variation in measurable niche dimensions.

On the Breadth and Significance of Niche Construction: A Reply to Griffiths, Okasha and Sterelny

Biology & Philosophy, 2005

Uncertainty principle in niche assessment: A solution to the dilemma redundancy vs. competitive exclusion, and some analytical consequences

There has been a categorically unresolved crucial question in ecology and evolutionary theory for many decades; perhaps from the times of Charles Darwin himself: Is it possible, under natural conditions, that two species can perform a commonly shared ecological niche? There are two extreme conventional responses that have kept divided the scientific community in this regard for almost forty years: (a) No; that is to say, the well-known competitive exclusion principle (CEP). (b) Yes; that is to say, the well-known hypothesis of full functional redundancy (HFR). Obviously, the reliability of both responses depends on an underlying and even more essential requisite: that the ecological niche of a given species can be assessed with such accuracy as we could want in order to detect the degree in which it is shared between coexisting species. This article is the seventh in a continuous series of interconnected recent publications that promotes an alternative understanding of ecology and evolutionary biology which is in favor of strong and mutually fruitful analytical links between biology and physics. This article analyzes the statistical behavior of ecological niches by taking into account two indicators that are essential to perform the ecological niche of all species: species diversity per plot (H p ) and eco-kinetic energy (E e ) as a proxy for trophic energy in a scalar field H p , E e in which an oscillating performance of ecological niches is deployed. According to our results, in the same measurement in which the accuracy of H p assessments increases (reduction of H p 's standard deviation: Hp ) the accuracy of E e assessment decreases (increment of Ee ), and vice versa, in agreement with a pattern that is completely equivalent to that of the Heisenberg's uncertainty principle in quantum mechanics (i.e.: Hp · Ee 1/2h e ec /2 ; where h e ec : ecological equivalent of Planck's constant found in previous publications). As a result, the ecological niche is, even in principle in addition to in practice, indeterminable with enough exactness to arrive to a categorical response to the above-stated question. This means that CEP and HFR are simultaneously true and false in the same measure, because the only feasible option to keep the functional stability of ecosystems is a wave-like combination of both options: when species are pushed to a high degree of coexistence (increase of partition of the gradient) in regard to H p values (a trend in favor of HFR), their degree of coexistence in regard to E e values diminishes (decrease of partition of the E e gradient, a trend in favor of CEP), and vice versa. The final sections of the article highlight the eco-evolutionary, biogeographical and socio-economic meaning of this result, by offering plausible alternative explanations to a wide spectrum of phenomena that appear to be only partially understood so far, e.g.: the contradictory results about the relationship between body size, species diversity and macroevolutionary rates; the general environmental scenario in favor of macroevolutionary leaps with a low probability to leave footprints in the fossil record; the unnecessary, although stimulant, influence of geographic isolation to promote evolutionary changes; the island rule; and the general meaning of the interaction between nature and society.

Related topics

  • History and Philosophy of Ecology
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  • History of Biology
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  • Ecological Niche Modelling
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  • Ecological niches
  • Environmental Niche
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    Distribution of Different Scrippsiella acuminata (Dinophyta) Cyst Morphotypes in Surface Sediments of the Black Sea: A Basin Scale Approach

    Frontiers in Marine Science

    Plankton cyst abundance and distribution is controlled by multiple factors. The stress linked to the fluctuations and variations of the environmental conditions in the water column is a major vector of encystment and intraspecific variability is an important adaptive strategy. The present study aims to disclose a link between the spatial distribution and abundance of different cyst morphotypes ofScrippsiella acuminatacomplex in surface sediments collected in the Black Sea at 34 sites and selected environmental variables. With this purpose, a basin scale data set was analyzed for patterns of intraspecific spatial heterogeneity. Redundancy analysis (RDA) was implemented to identify explanatory environmental variables associated with the cyst morphotypes abundance. Environmental multiyear data were used to ensure better approximation of a model that links environmental gradients with cyst abundance. Our results show that allS. acuminatacysts morphotypes are significantly correlated to ...

    Introduction to niches and mechanisms in ecology and evolution

    Biology & Philosophy

    Niches and mechanisms are two important but contested elements in the study of organism-environment interactions. Although they are closely interrelated, with niches playing a crucial role in theorizing about ecological and evolutionary mechanisms such as niche construction, facilitation, and species invasion, philosophical discussions about each issue have been largely disconnected. This collection addresses this gap, bringing together contributions from philosophers and biologists about the niche concept, niche construction theory, and ecological and evolutionary mechanisms. In this introduction we provide some background to the collection, which arose out of two workshops organized within an interdisciplinary research consortium. We also summarize each contribution, organized roughly into three groups with considerable overlap and interrelations: niche construction and evolutionary theory, niches, and ecological and evolutionary mechanisms.

    Variation in red fox <i>Vulpes vulpes</i> diet in five continents

    Mammal Review, 2022

    1. Understanding variation in the diet of widely distributed species can help us to predict how they respond to future environmental and anthropogenic changes. 2. We studied the diet of the red fox Vulpes vulpes, one of the world's most widely distributed carnivores. We compiled dietary data from 217 studies at 276 locations in five continents to assess how fox diet composition varied according to geographic location, climate, anthropogenic impact, and sampling method. 3. The diet of foxes showed substantial variation throughout the species' range, but with a general trend for small mammals and invertebrates to be the most frequently occurring dietary items. 4. The incidence of small and large mammals and birds in fox diets was greater away from the equator. The incidence of invertebrates and fruits increased with mean elevation, while the occurrence of medium-sized mammals and birds decreased. 5. Fox diet differed according to climatic and anthropogenic variables. Diet richness decreased with increasing temperature and precipitation. The incidence of small and large mammals decreased with increasing temperature. The incidence of birds and invertebrates decreased with increasing mean annual precipitation. Higher Human Footprint Index was associated with a lower incidence of large mammals and a higher incidence of birds and fruit in fox diet. 6. Sampling method influenced fox diet estimation: estimated percentage of small and medium-sized mammals and fruit was lower in studies based on stomach contents, while large mammals were more likely to be recorded in studies of stomach contents than in studies of scats. 7. Our study confirms the flexible and opportunistic dietary behaviour of foxes at the global scale. This behavioural trait allows them to thrive in a range of climatic conditions, and in areas with different degrees of human-induced habitat change. This knowledge can help us to place the results of local-scale fox diet studies into a broader context and to predict how foxes will respond to future environmental changes.

    Exploring the niche concept in a simple metaorganism

    bioRxiv (Cold Spring Harbor Laboratory), 2019

    Abstract Organisms and their resident microbial communities - the microbiome - form a complex and mostly stable ecosystem. It is known that the composition of the microbiome and bacterial species abundances can have a major impact on host health and Darwinian fitness , but the processes that lead to these microbial patterns have not yet been identified. We here apply the niche concept and trait-based approaches as a first step in understanding the patterns underlying microbial community assembly and structure in the simple metaorganism Hydra . We find that the carrying capacities in single associations do not reflect microbiota densities as part of the community, indicating a discrepancy between the fundamental and realized niche. Whereas in most cases, the realized niche is smaller than the fundamental one, as predicted by theory, the opposite is observed for Hydra ’s two main bacterial colonizers. Both, Curvibacter sp. and Duganella sp. benefit from association with the other members of the microbiome and reach higher fractions as compared to when they are the only colonizer. This cannot be linked to any particular trait that is relevant for interacting with the host or by the utilization of specific nutrients but is most likely determined by metabolic interactions between the individual microbiome members.

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