Tissue-specific response of δ15N in adult Pacific herring (Clupea pallasi) following an isotopic shift in diet

2006 ◽  
Vol 76 (2-4) ◽  
pp. 177-189 ◽  
Author(s):  
Todd W. Miller
2019 ◽  
Vol 81 ◽  
pp. 12-19 ◽  
Author(s):  
Jinhuan Dou ◽  
Yuri R. Montanholi ◽  
Zezhao Wang ◽  
Zhongshu Li ◽  
Ying Yu ◽  
...  

2010 ◽  
Vol 67 (9) ◽  
pp. 1903-1913 ◽  
Author(s):  
Jacob F. Schweigert ◽  
Jennifer L. Boldt ◽  
Linnea Flostrand ◽  
Jaclyn S. Cleary

AbstractSchweigert, J. F., Boldt, J. L., Flostrand, L., and Cleary, J. S. 2010. A review of factors limiting recovery of Pacific herring stocks in Canada. – ICES Journal of Marine Science, 67: 1903–1913. On the west coast of Canada, Pacific herring (Clupea pallasi) supported an intensive reduction fishery from the early 1930s until the collapse of all five major stocks in the late 1960s, which then recovered rapidly following a fishery closure. Despite conservative harvests, abundance has declined again recently, with little evidence of recovery. We investigated the effect of bottom-up forcing by zooplankton abundance, top-down forcing by fish and mammal predators, and the effects of sardine abundance as potential competitors on the natural mortality of the herring stock on the west coast of Vancouver Island. Herring mortality was positively related to Thysanoessa spinifera and southern chaetognaths and negatively to pteropod abundance. Estimated predation on herring decreased significantly during the years 1973–2008, with the main consumers changing from fish to mammals. However, the correlation with herring mortality was negative, whereas there was a significant positive relationship with sardine abundance. Population recovery is expected to be facilitated by a combination of factors, including adequate food supply, limited or reduced predation (including fishing), and limited competition particularly for wasp–waist systems, where different forage species may occupy similar niches.


2020 ◽  
Vol 21 (8) ◽  
pp. 2851
Author(s):  
Yasuyo Urasaki ◽  
Cody Beaumont ◽  
Jeffery N. Talbot ◽  
David K. Hill ◽  
Thuc T. Le

This study reports a relationship between Akt3 expression and tissue-specific regulation of the pI3K/Akt/mTOR signaling pathway by copaiba essential oil. Akt3, a protein kinase B isoform important for the regulation of neuronal development, exhibited differential expression levels in cells of various origins. In neuronal and microglial cells, where Akt3 is present, copaiba essential oil positively regulated the pI3K/Akt/mTOR signaling pathway. In contrast, in liver cells and T lymphocytes, where Akt3 is absent, copaiba essential oil negatively regulated the pI3K/Akt/mTOR signaling pathway. The expression of Akt3 via plasmid DNA in liver cells led to positive regulatory effects by copaiba essential oil on the pI3K/Akt/mTOR signaling pathway. In contrast, inhibition of Akt3 expression in neuronal cells via small interfering RNA molecules targeting Akt3 transcripts abrogated the regulatory effects of copaiba essential oil on the pI3K/Akt/mTOR signaling pathway. Interestingly, Akt3 expression did not impact the regulatory effects of copaiba essential oil on other signaling pathways. For example, copaiba essential oil consistently upregulated the MAPK and JAK/STAT signaling pathways in all evaluated cell types, independent of the Akt3 expression level. Collectively, the data indicated that Akt3 expression was required for the positive regulatory effects of copaiba essential oil, specifically on the pI3K/Akt/mTOR signaling pathway.


2019 ◽  
Vol 117 (1) ◽  
pp. 779-786 ◽  
Author(s):  
Gal Manella ◽  
Rona Aviram ◽  
Nityanand Bolshette ◽  
Sapir Muvkadi ◽  
Marina Golik ◽  
...  

The occurrence and sequelae of disorders that lead to hypoxic spells such as asthma, chronic obstructive pulmonary disease, and obstructive sleep apnea (OSA) exhibit daily variance. This prompted us to examine the interaction between the hypoxic response and the circadian clock in vivo. We found that the global transcriptional response to acute hypoxia is tissue-specific and time-of-day–dependent. In particular, clock components differentially responded at the transcriptional and posttranscriptional level, and these responses depended on an intact circadian clock. Importantly, exposure to hypoxia phase-shifted clocks in a tissue-dependent manner led to intertissue circadian clock misalignment. This differential response relied on the intrinsic properties of each tissue and could be recapitulated ex vivo. Notably, circadian misalignment was also elicited by intermittent hypoxia, a widely used model for OSA. Given that phase coherence between circadian clocks is considered favorable, we propose that hypoxia leads to circadian misalignment, contributing to the pathophysiology of OSA and potentially other diseases that involve hypoxia.


2019 ◽  
Vol 178 ◽  
pp. 102198 ◽  
Author(s):  
Martin Godefroid ◽  
Jennifer L. Boldt ◽  
James T. Thorson ◽  
Robyn Forrest ◽  
Stéphane Gauthier ◽  
...  

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