Abstract:The abundance of Bosmina longispina maritima (Cladocera), the most common water flea in the Baltic Sea, shows considerable interannual fluctuations.The number of Bosmina resting eggs (ephippia) in the sediment also fluctuates from year to year. Biotic as well as abiotic factors have been suggested to contribute to these fluctuations, but the impact of benthic predation by pelagic mysids has not yet been considered. The objective of this study was to investigate the effect of benthic predation and bioturbation … Show more
“…For example, omnivorous crayfish display trophic positions close to those of predatory fish –which is higher than would be expected from gut content analysis alone [73]. Mysids feeding on meiofauna, zooplankton resting eggs and small amphipods [74], [75] could have contributed to this apparent similarity in δ 13 C between the groups at station S1. The more carnivorous nature of pelagic mysids [13] is further supported by substantially stronger δ 15 N, δ 13 C-correlations as compared to benthic individuals that appear to have broader, more omnivorous diets.…”
Diel vertical migration (DVM) is often assumed to encompass an entire population. However, bimodal nighttime vertical distributions have been observed in various taxa. Mysid shrimp populations also display this pattern with one group concentrated in the pelagia and the other near the bottom. This may indicate alternative migratory strategies, resembling the seasonal partial migrations seen in birds, fishes and amphibians, where only a subset of the population migrates. To assess the persistence of these alternative strategies, we analyzed the nitrogen and carbon stable isotope signatures (as proxies for diet), biochemical indices (as proxies for growth condition), and genetic population divergence in the Baltic mysid Mysis salemaai collected at night in the pelagia and close to the bottom. Stable isotope signatures were significantly different between migrants (pelagic samples) and residents (benthic samples), indicating persistent diet differences, with pelagic mysids having a more uniform and carnivorous diet. Sequencing of the mitochondrial cytochrome subunit I (COI) gene showed genetic differentiation attributable to geographic location but not between benthic and pelagic groups. Divergent migration strategies were however supported by significantly lower gene flow between benthic populations indicating that these groups have a lower predisposition for horizontal migrations compared to pelagic ones. Different migration strategies did not convey measurable growth benefits as pelagic and benthic mysids had similar growth condition indices. Thus, the combination of ecological, biochemical and genetic markers indicate that this partial migration may be a plastic behavioral trait that yields equal growth benefits.
“…For example, omnivorous crayfish display trophic positions close to those of predatory fish –which is higher than would be expected from gut content analysis alone [73]. Mysids feeding on meiofauna, zooplankton resting eggs and small amphipods [74], [75] could have contributed to this apparent similarity in δ 13 C between the groups at station S1. The more carnivorous nature of pelagic mysids [13] is further supported by substantially stronger δ 15 N, δ 13 C-correlations as compared to benthic individuals that appear to have broader, more omnivorous diets.…”
Diel vertical migration (DVM) is often assumed to encompass an entire population. However, bimodal nighttime vertical distributions have been observed in various taxa. Mysid shrimp populations also display this pattern with one group concentrated in the pelagia and the other near the bottom. This may indicate alternative migratory strategies, resembling the seasonal partial migrations seen in birds, fishes and amphibians, where only a subset of the population migrates. To assess the persistence of these alternative strategies, we analyzed the nitrogen and carbon stable isotope signatures (as proxies for diet), biochemical indices (as proxies for growth condition), and genetic population divergence in the Baltic mysid Mysis salemaai collected at night in the pelagia and close to the bottom. Stable isotope signatures were significantly different between migrants (pelagic samples) and residents (benthic samples), indicating persistent diet differences, with pelagic mysids having a more uniform and carnivorous diet. Sequencing of the mitochondrial cytochrome subunit I (COI) gene showed genetic differentiation attributable to geographic location but not between benthic and pelagic groups. Divergent migration strategies were however supported by significantly lower gene flow between benthic populations indicating that these groups have a lower predisposition for horizontal migrations compared to pelagic ones. Different migration strategies did not convey measurable growth benefits as pelagic and benthic mysids had similar growth condition indices. Thus, the combination of ecological, biochemical and genetic markers indicate that this partial migration may be a plastic behavioral trait that yields equal growth benefits.
“…-1 in only 12 h (Viitasalo & Viitasalo 2004). However, except for the statistically insignificant additional decrease in ephippia (< 3 d -1 ) in the treatment combining Monoporeia with mysids, no such effect was observed, i.e.…”
Section: Epibenthic Predation By Mysidsmentioning
confidence: 99%
“…According to Viitasalo & Viitasalo (2004) Mysis mixta is unable to feed on ephippia buried in sediment; hence, it was suggested that bioturbation by macrofauna may essentially affect the predation by epibenthic mysids on their non-motile benthic prey. Consequently, one aim of this study was to test whether macrofauna could, by means of particle mixing, redistribute ephippia, buried under a sediment layer of 0.5 to 1 cm, within the reach of the mysids. )…”
Section: Epibenthic Predation By Mysidsmentioning
confidence: 99%
“…Recently, M. mixta was found to eat Bosmina ephippia distributed on the sediment surface (Viitasalo & Viitasalo 2004). In contrast, mysids appeared incapable of feeding on ephippia that were mixed within the sediment, suggesting that the vertical distribution of sedimented ephippia is crucial not only for the recruitment of cladocerans but also for the rate of epibenthic predation by mysids (Viitasalo & Viitasalo 2004).…”
The effects of bioturbation and predation by the amphipod Monoporeia affinis, the bivalve Macoma balthica and the polychaetes Marenzelleria spp. were studied on the number, vertical distribution and hatching of benthic eggs (ephippia) of the cladoceran Bosmina longispina maritima. It was hypothesised that the 3 functionally different macrobenthic species affect Bosmina ephippia to different degrees. In addition, it was hypothesised that macrofaunal bioturbation either inhibits or enhances predation by the necto-benthic mysid Mysis mixta on cladoceran benthic eggs. M. affinis and M. balthica caused a 48 and 23% decrease in the total number of Bosmina ephippia, respectively, indicating egg predation. In addition, M. balthica extended the distribution of eggs into deeper sediment layers. Both M. affinis and M. balthica suppressed the daily hatching rate of Bosmina, and the effect of the bivalves (reduction 92%) was stronger than that of the amphipods (34 to 78%). None of the benthic species promoted the predation of mysids on Bosmina eggs. Instead, both M. affinis and M. balthica reduced the number of ephippia in the sediment surface (by 79 and 43%, respectively), implying that these species decrease the ability of mysids to feed on cladoceran benthic eggs. M. balthica was the most harmful species for the recruitment of Bosmina, whereas the nonindigenous Marenzelleria spp. did not affect ephippia.
“…Highly selective interferometric filters are formed by tens of these layers [4]. Less selective but more feasible filters can be got with a more modest number of layers (as few as three) following a Fabry-Perot scheme [5]. In silicon processing environments, silicon dioxide and polysilicon layers can play the role of low and high index materials.…”
In this work we have studied the feasibility of integrating an infrared filter and an infrared detector by means of a flip-chip technique. This filter and detector combination should be the heart of a future gas detection cell based on infrared absorption. In our case the filter is a surface micromachined Fabry-Perot interferometer, and the infrared detector is a bulk micromachined thermopile. The flip-chip technique is an elegant solution to assure the optical micro-alignment of both devices and allows the electrical contact needed to actuate active optical filters.
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