Abstract:In contrast to most pelagic primary producers, benthic macrophytes pass through morphologically distinct life stages, which can be subject to different ecological controls. Using factorial field experiments, we investigated how grazing pressure (three levels) and nutrient supply (four levels) interact in controlling the passage of marine macroalgae through an apparent recruitment ''bottleneck'' at the germling stage. In comparative experiments, we asked whether relative bottom-up and top-down effects on early … Show more
“…Work elsewhere has demonstrated the importance of both nutrients and consumers in benthic marine ecosystems (Neckles et al 1993;Wootton et al 1996;Hillebrand et al 2000;Menge 2000;Lotze et al 2001). The results presented herein show that light can also interact with consumer pressure to alter the growth and abundance of primary and secondary producers.…”
mentioning
confidence: 63%
“…The general acceptance of this view over the past decade has motivated a growing number of studies that have simultaneously manipulated top-down and bottom-up factors. In marine benthic systems, these studies have generally taken the form of factorial manipulations of consumer abundance and nutrient supply (Neckles et al 1993;Wootton et al 1996;Hillebrand et al 2000;Lotze et al 2001). Although nutrient supply is clearly important, very little attention has been devoted to spatial and temporal variability in another fundamental bottom-up factor: light.…”
Abstract-Light availability and consumer pressure are fundamental factors that structure aquatic communities, but their integrated effects are rarely studied in marine benthic systems. Using a factorial experiment, I investigated the effects of light availability and grazing by limpets (Lottia digitalis) to determine the relative influence of each on the growth and abundance of producers and consumers in a rocky intertidal community during the winter. Light reduction via shading reduced the abundance of filamentous algae and reduced the abundance of the herbivorous periwinkle Littorina sitkana. The effects of limpet grazing reduced the abundance of filamentous algae, Porphyra spp., and diatom mats. Higher limpet densities were also associated with significantly lower densities of adult, but not juvenile, Littorina spp. Light and limpet density interacted to determine Lottia growth, which was high in unshaded, single-limpet enclosures but was negligible in plots with two limpets, shades, or both. Variation in bottom-up (resource-driven) and top-down (consumer-driven) forces are important determinants of abundance at both trophic levels, but the effects are complex, taxon-specific, and, for littorine snails, size-specific. Because the study species accomplish most of their growth and reproduction during the winter, the interplay of light and herbivory during this season will likely influence long-term community dynamics.
“…Work elsewhere has demonstrated the importance of both nutrients and consumers in benthic marine ecosystems (Neckles et al 1993;Wootton et al 1996;Hillebrand et al 2000;Menge 2000;Lotze et al 2001). The results presented herein show that light can also interact with consumer pressure to alter the growth and abundance of primary and secondary producers.…”
mentioning
confidence: 63%
“…The general acceptance of this view over the past decade has motivated a growing number of studies that have simultaneously manipulated top-down and bottom-up factors. In marine benthic systems, these studies have generally taken the form of factorial manipulations of consumer abundance and nutrient supply (Neckles et al 1993;Wootton et al 1996;Hillebrand et al 2000;Lotze et al 2001). Although nutrient supply is clearly important, very little attention has been devoted to spatial and temporal variability in another fundamental bottom-up factor: light.…”
Abstract-Light availability and consumer pressure are fundamental factors that structure aquatic communities, but their integrated effects are rarely studied in marine benthic systems. Using a factorial experiment, I investigated the effects of light availability and grazing by limpets (Lottia digitalis) to determine the relative influence of each on the growth and abundance of producers and consumers in a rocky intertidal community during the winter. Light reduction via shading reduced the abundance of filamentous algae and reduced the abundance of the herbivorous periwinkle Littorina sitkana. The effects of limpet grazing reduced the abundance of filamentous algae, Porphyra spp., and diatom mats. Higher limpet densities were also associated with significantly lower densities of adult, but not juvenile, Littorina spp. Light and limpet density interacted to determine Lottia growth, which was high in unshaded, single-limpet enclosures but was negligible in plots with two limpets, shades, or both. Variation in bottom-up (resource-driven) and top-down (consumer-driven) forces are important determinants of abundance at both trophic levels, but the effects are complex, taxon-specific, and, for littorine snails, size-specific. Because the study species accomplish most of their growth and reproduction during the winter, the interplay of light and herbivory during this season will likely influence long-term community dynamics.
“…Conversely, when planktivory is weak, zooplankton densities and biomass may be high and phytoplankton abundance low. Similar forces appear to be at work in other food webs (e.g., freshwater benthic [Brönmark et al 1992] and rocky coastal marine [Paine 1966;Lotze and Worm 2001] …”
We examined how physical and chemical factors and fish populations affected the presence and density of zooplankton species in 104 Alaskan arctic lakes. Five fish species and nine zooplankters were sampled from the lakes. Lake depth was related to the distribution of zooplankton in that smaller zooplankton species were found in deep lakes and large species in shallow lakes. Neither ionic strength nor chlorophyll was a major factor in zooplankton presence or absence. When fish were present, few, if any, very large zooplankton occurred together. However, the relationship between the presence and density of smaller-sized zooplankton species and the presence of specific species of fish was complex and did not fit anticipated patterns. The diversity of zooplankton in these arctic lakes was not related to chemistry or fish distribution, but species richness increased with increasing lake area and depth. For a few zooplankters (notably Holopedium gibberum), the fraction of lakes containing the zooplankter varied by region.The study of freshwater zooplankton and zooplankton communities has a long and storied history (Forbes 1887).
“…In marine environments, however, research on these issues has been decidedly one-sided (Menge 1992, Menge et al 1997, with an emphasis on top-down control of rocky intertidal community structure (Paine 1966, 1980, 2002, Dayton 1971, Estes & Palmisano 1974, Lubchenco 1978, Menge 2000. Recently, the emphasis has shifted to examine the role of bottom-up processes acting either in concert with, or independent of, top-down processes (Menge et al 1997, Leonard et al 1998, Lotze et al 2001, Nielsen 2001. In addition, ecologists have broadened the conventional definition of bottomup processes (nutrient supply) to include physical factors such as flow velocity (see Lesser et al 1994, Leonard et al 1998 or food delivery (Menge et al 1997), with their subsequent effects on larval supply and organismal survivorship and physiology.…”
Callyspongia vaginalis, a common reef sponge in the Florida Keys, USA, exhibits depthspecific differences in bioenergetics and growth that are a function of food availability. We measured several physiological parameters in situ to construct the bioenergetic budgets of sponges living in deep and shallow waters. Respiration rates were measured in a recirculating flow respirometer and pumping rates were measured by filming dye ejected from sponge oscula. In addition, inhalent and exhalent water sampled from around sponge colonies at both depths was analyzed using flow cytometry to quantify the concentration and clearance rates of picoplankton. These parameters were used to construct an energetic budget for sponges from each depth and revealed that the scope for growth was substantially greater for deep sponges compared to shallow sponges. The greater scope for growth of deep sponges is likely due to the greater abundance of picoplankton in the deep versus shallow habitat. Both naturally occurring sponges and those used in a reciprocal transplant experiment between 12 and 25 m exhibited significantly greater growth in the deep than the shallow habitat. Hence, bottom-up forcing in the form of increased food availability may be of principal importance to the growth and physiological ecology of suspension-feeding sponges.
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