scholarly journals Consumption of pelagic tunicates by cetaceans calves in the Mediterranean Sea

Author(s):  
NATALIA FRAIJA-FERNÁNDEZ ◽  
ALFONSO A. RAMOS-ESPLÁ ◽  
MARÍA ÁNGELES RADUÁN ◽  
CARMEN BLANCO ◽  
JUAN ANTONIO RAGA ◽  
...  

Gelatinous zooplankton, including jellyfish, ctenophores and pelagic tunicates, constitutes fragile marine animals that live in the water column, and represent an important resource for marine food webs through their seasonal pulses. Although there is scarce evidence on the occurrence of gelatinous zooplankton in stomach contents of apex, endothermic predators such as cetaceans, the ecological significance of such observations requires consideration. In this study, we report on the occurrence of pelagic tunicates in the stomach of three individual calves of two cetacean species from the western Mediterranean, and collate all previous reports of gelatinous zooplankton in cetacean diets. We then briefly discuss the possible dietary significance of these observations.

2021 ◽  
Vol 1 (1) ◽  
Author(s):  
Anne W. Thompson ◽  
Anna C. Ward ◽  
Carey P. Sweeney ◽  
Kelly R. Sutherland

AbstractPyrosomes are widely distributed pelagic tunicates that have the potential to reshape marine food webs when they bloom. However, their grazing preferences and interactions with the background microbial community are poorly understood. This is the first study of the marine microorganisms associated with pyrosomes undertaken to improve the understanding of pyrosome biology, the impact of pyrosome blooms on marine microbial systems, and microbial symbioses with marine animals. The diversity, relative abundance, and taxonomy of pyrosome-associated microorganisms were compared to seawater during a Pyrosoma atlanticum bloom in the Northern California Current System using high-throughput sequencing of the 16S rRNA gene, microscopy, and flow cytometry. We found that pyrosomes harbor a microbiome distinct from the surrounding seawater, which was dominated by a few novel taxa. In addition to the dominant taxa, numerous more rare pyrosome-specific microbial taxa were recovered. Multiple bioluminescent taxa were present in pyrosomes, which may be a source of the iconic pyrosome luminescence. We also discovered free-living marine microorganisms in association with pyrosomes, suggesting that pyrosome feeding impacts all microbial size classes but preferentially removes larger eukaryotic taxa. This study demonstrates that microbial symbionts and microbial prey are central to pyrosome biology. In addition to pyrosome impacts on higher trophic level marine food webs, the work suggests that pyrosomes also alter marine food webs at the microbial level through feeding and seeding of the marine microbial communities with their symbionts. Future efforts to predict pyrosome blooms, and account for their ecosystem impacts, should consider pyrosome interactions with marine microbial communities.


2019 ◽  
Vol 9 (18) ◽  
pp. 10198-10212 ◽  
Author(s):  
Pasquale Ricci ◽  
Simone Libralato ◽  
Francesca Capezzuto ◽  
Gianfranco D’Onghia ◽  
Porzia Maiorano ◽  
...  

2015 ◽  
Vol 37 (5) ◽  
pp. 985-988 ◽  
Author(s):  
Cornelia Jaspers ◽  
José Luis Acuña ◽  
Richard D. Brodeur

2017 ◽  
Vol 36 (9) ◽  
pp. 2521-2532 ◽  
Author(s):  
Hui Zhang ◽  
Yun Teng ◽  
Tra Thi Thanh Doan ◽  
Yun Wei Yat ◽  
Sheot Harn Chan ◽  
...  

2002 ◽  
Vol 237 ◽  
pp. 209-216 ◽  
Author(s):  
S Bargu ◽  
CL Powell ◽  
SL Coale ◽  
M Busman ◽  
GJ Doucette ◽  
...  

2020 ◽  
Vol 10 (4) ◽  
pp. 20200019 ◽  
Author(s):  
Daniel B. Mills

Phagocytosis, or ‘cell eating’, is a eukaryote-specific process where particulate matter is engulfed via invaginations of the plasma membrane. The origin of phagocytosis has been central to discussions on eukaryogenesis for decades­, where it is argued as being either a prerequisite for, or consequence of, the acquisition of the ancestral mitochondrion. Recently, genomic and cytological evidence has increasingly supported the view that the pre-mitochondrial host cell—a bona fide archaeon branching within the ‘Asgard’ archaea—was incapable of phagocytosis and used alternative mechanisms to incorporate the alphaproteobacterial ancestor of mitochondria. Indeed, the diversity and variability of proteins associated with phagosomes across the eukaryotic tree suggest that phagocytosis, as seen in a variety of extant eukaryotes, may have evolved independently several times within the eukaryotic crown-group. Since phagocytosis is critical to the functioning of modern marine food webs (without it, there would be no microbial loop or animal life), multiple late origins of phagocytosis could help explain why many of the ecological and evolutionary innovations of the Neoproterozoic Era (e.g. the advent of eukaryotic biomineralization, the ‘Rise of Algae’ and the origin of animals) happened when they did.


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