scholarly journals Diel Feeding Rhythm and Grazing Selectivity of Small-Sized Copepods in a Subtropical Embayment, the Northern South China Sea

2021 ◽  
Vol 8 ◽  
Author(s):  
Xuejia He ◽  
Ziyu Wang ◽  
Ziqing Bai ◽  
Liuyu Han ◽  
Mianrun Chen
Keyword(s):  
Ingestion Rate ◽  
Northern South China Sea ◽  
Standing Stock ◽  
Feeding Preference ◽  
Daya Bay ◽  
Pigment Analysis ◽  
Feeding Rhythm ◽  
Feeding Rhythms ◽  
Gut Pigment ◽  
Diel Feeding Rhythm

Small marine copepods are key components of the pelagic food webs in Chinese coastal waters, but very few studies have addressed their trophodynamics, with even fewer studies addressing their diel feeding rhythms. In this study, the diel feeding rhythm and grazing selectivity of the copepod assemblage in Daya Bay during September 30 to October 2, 2014, were studied based on gut pigment analysis. Small copepods (body length < 1.5 mm) including Paracalanus parvus, Temora turbinata, Acrocalanus gibber, Temora stylifera, Euterpe acutifrons, and Acrocalanus gracilis, accounted for 73.9–100% of the total copepod abundance. The copepod assemblage generally exhibited a diurnal feeding pattern, characterized by a higher gut pigment content and ingestion rate during the daytime, consistent with variation in the ambient Chl α concentration. Fifty-five percent of the phytoplankton standing stock per day was consumed by the copepod assemblage, wherein diatoms, prymnesiophytes, and cyanobacteria were the main prey items with average contributions of 19.4–32.9% to the gut pigment contents. The copepod assemblage showed a strong feeding preference for prymnesiophytes, a weak feeding preference for diatoms, and avoidance of cyanobacteria. These results suggest a strong top-down control on phytoplankton community, especially on small groups from small copepods in the Daya Bay ecosystem.

scholarly journals Microzooplankton grazing and phytoplankton growth in marine mesocosms with increased CO<sub>2</sub> levels

2008 ◽  
Vol 5 (1) ◽  
pp. 411-433 ◽  
Author(s):  
K. Suffrian ◽  
P. Simonelli ◽  
J. C. Nejstgaard ◽  
S. Putzeys ◽  
Y. Carotenuto ◽  
...  
Keyword(s):  
Growth Rates ◽  
Standing Stock ◽  
Measured Parameter ◽  
Growth Responses ◽  
Dilution Technique ◽  
Pigment Analysis ◽  
Chl A ◽  
Co2 Levels ◽  
Algae Growth ◽  
Microzooplankton Grazing

Abstract. Microzooplankton grazing and algae growth responses to increasing pCO2 levels (350, 700 and 1050 μatm) were investigated in nitrate and phosphate fertilized mesocosms during the PeECE III experiment 2005. Grazing and growth rates were estimated by the dilution technique combined with taxon specific HPLC pigment analysis. Phytoplankton and microzooplankton composition were determined by light microscopy. Despite a range up to 3 times the present CO2 levels, there were no clear differences in any measured parameter between the different CO2 treatments. Thus, during the first 9 days of the experiment the algae community standing stock (SS), measured as chlorophyll a (Chl a), showed the highest instantaneous grow rates (0.02–0.99 d-1) and increased from ca 2–3 to 6–12 μg l−1, in all mesocosms. Afterwards the phytoplankton SS decreased in all mesocosms until the end of the experiment. The microzooplankton SS, that was mainly dinoflagellates and ciliates varied between 23 and 130 μg C l−1, peaking on day 13–15, apparently responding to the phytoplankton development. Instantaneous Chl a growth rates were generally higher than the grazing rates, indicating only a limited overall effect of microzooplankton grazing on the most dominant phytoplankton. Diatoms and prymnesiophytes were significantly grazed (14–43% of the SS d-1) only in the pre-bloom phase when they were in low numbers and in the post-bloom phase when they were already limited by low nutrients and/or virus lysis. The cyanobacteria populations appeared more effected by microzooplankton grazing, generally removing 20–65% of the SS d−1.

Seasonal occurrence of Calanus sinicus in the northern South China Sea: A case study in Daya Bay

2016 ◽  
Vol 159 ◽  
pp. 132-141 ◽  
Author(s):  
Kaizhi Li ◽  
Yan Yan ◽  
Jianqiang Yin ◽  
Yehui Tan ◽  
Liangmin Huang
Keyword(s):  
South China Sea ◽  
South China ◽  
Northern South China Sea ◽  
Seasonal Occurrence ◽  
Daya Bay ◽  
Calanus Sinicus ◽  
China Sea

Novel interneuron having hybrid modulatory-central pattern generator properties in the feeding system of the snail, Lymnaea stagnalis

1995 ◽  
Vol 73 (1) ◽  
pp. 112-124 ◽  
Author(s):  
M. S. Yeoman ◽  
A. Vehovszky ◽  
G. Kemenes ◽  
C. J. Elliott ◽  
P. R. Benjamin
Keyword(s):  
Central Pattern Generator ◽  
Lymnaea Stagnalis ◽  
Cell Types ◽  
Pattern Generator ◽  
Feeding System ◽  
Buccal Ganglia ◽  
Steady Current ◽  
Feeding Rhythm ◽  
Symmetrical Pair ◽  
Feeding Rhythms

1. We used intracellular recording techniques to examine the role of a novel type of protraction phase interneuron, the lateral N1 (N1L) in the feeding system of the snail Lymnaea stagnalis. 2. The N1Ls are a bilaterally symmetrical pair of electrotonically coupled interneurons located in the buccal ganglia. Each N1L sends a single axon to the contralateral buccal ganglia. Their neurite processes are confined to the buccal neuropile. 3. In the isolated CNS, depolarization of an N1L is capable of driving a full (N1-->N2-->N3), fast (1 cycle every 5 s) fictive feeding rhythm. This was unlike the previously described N1 medial (N1M) central pattern generator (CPG) interneurons that were only capable of driving a slow, irregular rhythm. Attempts to control the frequency of the fictive feeding rhythm by injecting varying amounts of steady current into the N1Ls were unsuccessful. This contrasts with a modulatory neuron, the slow oscillator (SO), that has very similar firing patterns to the N1Ls, but where the frequency of the rhythm depends on the level of injected current. 4. The N1Ls' ability to drive a fictive feeding rhythm in the isolated preparation was due to their strong, monosynaptic excitatory chemical connection with the N1M CPG interneurons. Bursts of spikes in the N1Ls generated summating excitatory postsynaptic potentials (EPSPs) in the N1Ms to drive them to firing. The SO excited the N1M cells in a similar way, but the EPSPs are strongly facilitatory, unlike the N1L-->N1M connection. 5. Fast (1 cycle every 5 s) fictive feeding rhythms driven by the N1L occurred in the absence of spike activity in the SO modulatory neuron. In contrast, the N1L was usually active in SO-driven rhythms. 6. The ability of the SO to drive the N1L was due to strong electrotonic coupling, SO-->N1L. The weaker coupling in the opposite direction, N1L-->SO, did not allow the N1L to drive the SO. 7. Experiments on semintact lip-brain preparations allowed fictive feeding to be evoked by application of 0.1 M sucrose to the lips (mimicking the normal sensory input) rather than by injection of depolarizing current. Rhythmic bursting, characteristic of fictive feeding, began in both the SO and N1L at exactly the same time, indicating that these two cell types are activated in "parallel" to drive the feeding rhythm. 8. The N1L is also part of the CPG network. It Excited the N2s and inhibited the N3 phasic (N3p) and N3 tonic (N3t) CPG interneurons like the N1Ms.(ABSTRACT TRUNCATED AT 400 WORDS)

scholarly journals dFRAME: A Video Recording-Based Analytical Method for Studying Feeding Rhythm in Drosophila

2021 ◽  
Vol 12 ◽  
Author(s):  
Mengxia Niu ◽  
Xiaohang Zhang ◽  
Weihan Li ◽  
Jianxun Wang ◽  
Yan Li
Keyword(s):  
Animal Model ◽  
Feeding Behavior ◽  
Analytical Method ◽  
Video Recording ◽  
Genetic Animal Model ◽  
Feeding Rhythm ◽  
Feeding Rhythms ◽  
Rhythm Analysis ◽  
Constant Dark

Animals, from insects to humans, exhibit obvious diurnal rhythmicity of feeding behavior. Serving as a genetic animal model, Drosophila has been reported to display feeding rhythms; however, related investigations are limited due to the lack of suitable and practical methods. Here, we present a video recording-based analytical method, namely, Drosophila Feeding Rhythm Analysis Method (dFRAME). Using our newly developed computer program, FlyFeeding, we extracted the movement track of individual flies and characterized their food-approaching behavior. To distinguish feeding and no-feeding events, we utilized high-magnification video recording to optimize our method by setting cut-off thresholds to eliminate the interference of no-feeding events. Furthermore, we verified that this method is applicable to both female and male flies and for all periods of the day. Using this method, we analyzed long-term feeding status of wild-type and period mutant flies. The results recaptured previously reported feeding rhythms and revealed detailed profiles of feeding patterns in these flies under either light/dark cycles or constant dark environments. Together, our dFRAME method enables a long-term, stable, reliable, and subtle analysis of feeding behavior in Drosophila. High-throughput studies in this powerful genetic animal model will gain great insights into the molecular and neural mechanisms of feeding rhythms.

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