A comparison of whole-community and ecosystem approaches (biomass size distributions, food web analysis, network analysis, simulation models) to study the structure, function and regulation of pelagic food webs

1995 ◽  
Vol 17 (6) ◽  
pp. 1273-1305 ◽  
Author(s):  
Ursula Gaedke
1983 ◽  
Vol 40 (11) ◽  
pp. 2010-2018 ◽  
Author(s):  
Uwe Borgmann

Biomass or energy transfer up pelagic food webs to larger sized organisms is a function of (1) direct trophic level transfer through predation, (2) somatic growth, a process that augments biomass transfer through predation, and (3) reproduction, which impedes biomass transfer by moving biomass down the food web to smaller sizes. By assuming that particle-size-conversion efficiency (log (food consumed/biomass produced)/log (predator–prey size ratio)) is relatively constant, I derive simple equations to calculate the effect of somatic growth and reproduction on biomass transfer up the food web. This defines the conditions under which somatic growth and reproduction can be ignored and biomass flow can be calculated from predation alone, using a previously developed model. When these conditions are not met, the effect of somatic growth and reproduction can be calculated from data on cohort growth and mortality rates. It is not necessary to identify the food of any species. This eliminates one of the problems often encountered when modeling food webs. I have applied these equations to production of Mysis relicta. If the estimates of Mysis abundance and growth rates are correct, then size-corrected production is about 25% greater for this species when somatic growth is accounted for in the calculations. This is because mortality of young Mysis appears to be low and most production occurs during somatic growth and not during reproduction.


Mathematics ◽  
2018 ◽  
Vol 6 (12) ◽  
pp. 336 ◽  
Author(s):  
Ferenc Jordán ◽  
Anett Endrédi ◽  
Wei-chung Liu ◽  
Domenico D’Alelio

Species are embedded in a web of intricate trophic interactions. Understanding the functional role of species in food webs is of fundamental interests. This is related to food web position, so positional similarity may provide information about functional overlap. Defining and quantifying similar trophic functioning can be addressed in different ways. We consider two approaches. One is of mathematical nature involving network analysis where unique species can be defined as those whose topological position is very different to others in the same food web. A species is unique if it has very different connection pattern compared to others. The second approach is of biological nature, based on trait-based aggregations. Unique species are not easy to aggregate with others because their traits are not in common with the ones of most others. Our goal here is to illustrate how mathematics can provide an alternative perspective on species aggregation, and how this is related to its biological counterpart. We illustrate these approaches using a toy food web and a real food web and demonstrate the sensitive relationships between those approaches. The trait-based aggregation focusing on the trait values of size (sv) can be best predicted by the mathematical aggregation algorithms.


Author(s):  
Ulf Riebesell ◽  
Philippe D. Tortell

Over the past decade there has been rapidly growing interest in the potential effects of ocean acidification and perturbations of the carbonate system on marine organisms. While early studies focused on a handful of phytoplankton and calcifying invertebrates, an increasing number of investigators have begun to examine the sensitivity to ocean acidification of various planktonic and benthic organisms across the marine food web. Several excellent review articles have recently summarized the rapidly expanding literature on this topic (Fabry et al. 2008; Doney et al. 2009 ; Joint et al. 2011). The focus of this chapter is on the potential ecosystem-level effects of ocean acidification. Starting with a brief review of the basic physical, chemical, and biological processes which structure pelagic marine ecosystems, the chapter explores how organismal responses to perturbations of the carbonate system could scale up in both time and space to affect ecosystem functions and biogeochemical processes. As with many chapters in this volume, and indeed much of the ocean acidification literature at present, our review raises more questions than it answers. It is hoped that these questions will prove useful for articulating and addressing key areas of future research. Complexity in marine pelagic food webs results from the interactions of multiple trophic levels across a range of temporal and spatial scales. The traditional view of marine food webs (Steele 1974) involved a relatively short trophic system in which large phytoplankton (e.g. net plankton such as diatoms) were grazed by a variety of mesozooplankton (e.g. copepods), which were in turn consumed by second-level predators, including many economically important fish and invertebrate species. This ‘classic’ marine food web is typical of high-productivity regions such as coastal upwelling regimes (Lassiter et al. 2006). A characteristic feature of these systems is a strong decoupling between primary production and grazing, which results from the different metabolic rates of consumers and producers and, in many cases, ontogenetic and seasonal delays in the emergence of feeding predators. The uncoupling between phytoplankton and their consumers leads to significant export of organic material out of the euphotic zone, the so-called biological carbon pump (discussed further below).


1999 ◽  
Vol 56 (12) ◽  
pp. 2477-2486 ◽  
Author(s):  
R Ian Perry ◽  
Peter A Thompson ◽  
David L Mackas ◽  
Paul J Harrison ◽  
Douglas R Yelland

Surveys were conducted in spring 1992 to examine the use of 13C/12C ratios to differentiate pelagic food webs and to trace food web interactions between adjacent continental shelf and slope/deep ocean environments off southwestern British Columbia, Canada. Salinity was used to define shelf or slope/deep ocean water masses and their productivity conditions because eddies and meanders at the shelf break were observed to draw water off the shelf. The 13C/12C ratio of plankton was related to the mean upper layer (0-50 m) salinity. 13C abundance was enriched (relative to 12C) in the shelf water mass compared with the slope water mass. This enrichment persisted up the food web from particulate organic matter through three size-classes of zooplankton to larval fish. The cross-shelf spatial scale separating these food webs, as determined from spatial semivariograms of 13C/12C and the upper layer mean salinity, was 40-45 km, similar to the Rossby radius for eddies at this location (50 km). Larval fish may provide a means to monitor exchanges of plankton between geographically adjacent food webs if time scales for incorporation of new isotope signatures from diets into tissues are determined.


2004 ◽  
Vol 61 (8) ◽  
pp. 1485-1492 ◽  
Author(s):  
Marie-Elodie Perga ◽  
Daniel Gerdeaux

We investigated the relationships between the pattern of variation of δ13C in pelagic food webs and various morphologic and trophic characteristics of peri-alpine lakes. We used the δ13C of whitefish (Coregonus lavaretus), a long-lived zooplanktivorous fish, to assess the isotope ratio of dissolved inorganic carbon (DIC) at the origin of the pelagic food web. The δ13C of DIC depends on its origin, which may be the atmosphere or the mineralization of organic matter. A synchronic study of 22 peri-alpine lakes shows that the surface area of the lake accounts for much of the variability of the δ13C in pelagic food webs (r2 = 0.76). The δ13C increases with lake size, which suggests that the origin of the DIC integrated into the pelagic food web depends on lake size. To differentiate the influence of trophic status from morphological effects, a diachronic study was performed on the δ13C of fish scales collected over the 20-year re-oligotrophication of Lake Geneva. The δ13C of whitefish increased with phosphorus concentration (r2 = 0.71). This pattern is related to the growing demand for atmospheric DIC as primary production increases.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Remo Ryser ◽  
Myriam R. Hirt ◽  
Johanna Häussler ◽  
Dominique Gravel ◽  
Ulrich Brose

AbstractHabitat fragmentation and eutrophication have strong impacts on biodiversity. Metacommunity research demonstrated that reduction in landscape connectivity may cause biodiversity loss in fragmented landscapes. Food-web research addressed how eutrophication can cause local biodiversity declines. However, there is very limited understanding of their cumulative impacts as they could amplify or cancel each other. Our simulations of meta-food-webs show that dispersal and trophic processes interact through two complementary mechanisms. First, the ‘rescue effect’ maintains local biodiversity by rapid recolonization after a local crash in population densities. Second, the ‘drainage effect’ stabilizes biodiversity by preventing overshooting of population densities on eutrophic patches. In complex food webs on large spatial networks of habitat patches, these effects yield systematically higher biodiversity in heterogeneous than in homogeneous landscapes. Our meta-food-web approach reveals a strong interaction between habitat fragmentation and eutrophication and provides a mechanistic explanation of how landscape heterogeneity promotes biodiversity.


1987 ◽  
Vol 7 (8) ◽  
pp. 895-911 ◽  
Author(s):  
Alan M. Springer ◽  
Edward C. Murphy ◽  
David G. Roseneau ◽  
C. Peter McRoy ◽  
Brian A. Cooper

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