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Ecosystem

About: Ecosystem is a research topic. Over the lifetime, 25460 publications have been published within this topic receiving 1291375 citations. The topic is also known as: ecological system & Ecosystem.


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Journal ArticleDOI
TL;DR: In this paper, the authors provide a synthesis of the knowledge about recovery patterns, rates and restoration effectiveness of estuarine and coastal marine ecosystems from over a century of degradation, and they show that although in some cases recovery can take <5 years, especially for the short-lived and high-turnover biological components, full recovery of coastal marine and estuarial ecosystems can take a minimum of 15-25 years for attainment of the original biotic composition and diversity may lag far beyond that period.
Abstract: Many estuarine and coastal marine ecosystems have increasingly experienced degradation caused by multiple stressors. Anthropogenic pressures alter natural ecosystems and the ecosystems are not considered to have recovered unless secondary succession has returned the ecosystem to the pre-existing condition or state. However, depending upon the scales of time, space and intensity of anthropogenic disturbance, return along the historic trajectory of the ecosystem may: (1) follow natural restoration though secondary succession; (2) be re-directed through ecological restoration, or (3) be unattainable. In order to address the gaps in knowledge about restoration and recovery of estuarine and coastal ecosystems, this special feature includes the present overview and other contributions to provide a synthesis of our knowledge about recovery patterns, rates and restoration effectiveness. From the 51 examples collated in this contribution, we refine the recovery from the list of stressors into six recovery mechanisms: (1) recovery from sediment modification, which includes all aspects of dredging and disposal; (2) recovery by complete removal of stressors limiting natural ecosystem processes, which includes tidal marsh and inundation restoration; (3) recovery by speed of organic degradation, which includes oil discharge, fish farm wastes, sewage disposal, and paper mill waste; (4) recovery from persistent pollutants, which includes chemical discharges, such as TBT; (5) recovery from excessive biological removal, related to fisheries and (6) recovery from hydrological and morphological modification. Drawing upon experience both from these many examples and from an example of one comprehensive study, we show that although in some cases recovery can take <5 years, especially for the short-lived and high-turnover biological components, full recovery of coastal marine and estuarine ecosystems from over a century of degradation can take a minimum of 15–25 years for attainment of the original biotic composition and diversity may lag far beyond that period.

342 citations

Journal ArticleDOI
05 Sep 2013-PLOS ONE
TL;DR: There is an urgent need for more information on the variability in seagrass carbon stock and accumulation rates, and the factors driving this variability, in order to improve global estimates of seagRass Blue Carbon storage.
Abstract: The recent focus on carbon trading has intensified interest in ‘Blue Carbon’–carbon sequestered by coastal vegetated ecosystems, particularly seagrasses. Most information on seagrass carbon storage is derived from studies of a single species, Posidonia oceanica, from the Mediterranean Sea. We surveyed 17 Australian seagrass habitats to assess the variability in their sedimentary organic carbon (Corg) stocks. The habitats encompassed 10 species, in mono-specific or mixed meadows, depositional to exposed habitats and temperate to tropical habitats. There was an 18-fold difference in the Corg stock (1.09–20.14 mg Corg cm−3 for a temperate Posidonia sinuosa and a temperate, estuarine P. australis meadow, respectively). Integrated over the top 25 cm of sediment, this equated to an areal stock of 262–4833 g Corg m−2. For some species, there was an effect of water depth on the Corg stocks, with greater stocks in deeper sites; no differences were found among sub-tidal and inter-tidal habitats. The estimated carbon storage in Australian seagrass ecosystems, taking into account inter-habitat variability, was 155 Mt. At a 2014–15 fixed carbon price of A$25.40 t−1 and an estimated market price of $35 t−1 in 2020, the Corg stock in the top 25 cm of seagrass habitats has a potential value of $AUD 3.9–5.4 bill. The estimates of annual Corg accumulation by Australian seagrasses ranged from 0.093 to 6.15 Mt, with a most probable estimate of 0.93 Mt y−1 (10.1 t. km−2 y−1). These estimates, while large, were one-third of those that would be calculated if inter-habitat variability in carbon stocks were not taken into account. We conclude that there is an urgent need for more information on the variability in seagrass carbon stock and accumulation rates, and the factors driving this variability, in order to improve global estimates of seagrass Blue Carbon storage.

341 citations

Journal ArticleDOI
TL;DR: In this paper, a new paradigm of the functioning of aquatic ecosystems, and the metabolic connectivity between ecosystems in the biosphere, was proposed, which conforms to the new paradigm.
Abstract: Recent, parallel developments in the study of freshwater and marine ecosystems have provided evidence that net heterotrophic systems (those in which respiratory organic matter destruction exeeds photosynthetic production) are more prevalent than hitherto believed, including most rivers, oligo- to mesotrophic lakes and some oligotrophic regions of the ocean. In parallel, these aquatic ecosystems have been shown to act as CO2 sources to the atmosphere, as expected from the heterotrophic nature of the communities they contain. The prevalence of net heterotrophic aquatic ecosystems indicates that they must receive significant inputs of organic carbon from adjacent ecosystems, assigning an important role to the lateral exchanges of carbon between land and aquatic ecosystems, between coastal and open ocean ecosystems, as well as internal redistribution within large or complex aquatic ecosystems in determining their metabolic status and the gaseous exchange with the atmosphere. The examination of the carbon budget of ecosystems requires, therefore, an integrative approach that accounts for exchanges between compartments often studied in isolation. These recent findings conform a new paradigm of the functioning of aquatic ecosystems, and the metabolic connectivity between ecosystems in the biosphere.

341 citations

Journal ArticleDOI
TL;DR: More studies are required to be able to accurately assess the effects of carbon dioxide, because the authors have relatively poor records of the functional and structural response of any ecosystem through time.
Abstract: One of the many changes occurring in the biosphere due to human activities is the increase in the carbon dioxide concentration in the atmosphere. This change is due both to the burning of fossil fuels and to deforestation. We do not know how these changes are affecting terrestrial ecosystems. This ignorance is partly because we have relatively poor records of the functional and structural response of any ecosystem through time. More studies are required to be able to accurately assess the effects of carbon dioxide.

341 citations

Journal ArticleDOI
TL;DR: The economic damages of the degradation of an important ecosystem service, water clarity, caused by invasion by the spiny water flea are quantified and it is found that the costs are comparable with the willingness to pay for the service itself: US$140 million.
Abstract: Despite growing recognition of the importance of ecosystem services and the economic and ecological harm caused by invasive species, linkages between invasions, changes in ecosystem functioning, and in turn, provisioning of ecosystem services remain poorly documented and poorly understood. We evaluate the economic impacts of an invasion that cascaded through a food web to cause substantial declines in water clarity, a valued ecosystem service. The predatory zooplankton, the spiny water flea (Bythotrephes longimanus), invaded the Laurentian Great Lakes in the 1980s and has subsequently undergone secondary spread to inland lakes, including Lake Mendota (Wisconsin), in 2009. In Lake Mendota, Bythotrephes has reached unparalleled densities compared with in other lakes, decreasing biomass of the grazer Daphnia pulicaria and causing a decline in water clarity of nearly 1 m. Time series modeling revealed that the loss in water clarity, valued at US$140 million (US$640 per household), could be reversed by a 71% reduction in phosphorus loading. A phosphorus reduction of this magnitude is estimated to cost between US$86.5 million and US$163 million (US$430–US$810 per household). Estimates of the economic effects of Great Lakes invasive species may increase considerably if cases of secondary invasions into inland lakes, such as Lake Mendota, are included. Furthermore, such extreme cases of economic damages call for increased investment in the prevention and control of invasive species to better maximize the economic benefits of such programs. Our results highlight the need to more fully incorporate ecosystem services into our analysis of invasive species impacts, management, and public policy.

341 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20242
20235,630
202210,638
20212,059
20201,701
20191,681