Mirocaris

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Mirocaris
Mirocaris fortunata.jpg
Mirocaris fortunata
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Malacostraca
Order: Decapoda
Suborder: Pleocyemata
Infraorder: Caridea
Family: Alvinocarididae
Genus: Mirocaris
Vereshchaka, 1997
Species
  • Mirocaris fortunata(Martin and Christiansen, 1995)
  • Mirocaris indicaKomai, Martin, Zala, Tsuchida and Hashimoto, 2006

Mirocaris is a genus of shrimp associated with hydrothermal vents. Sometimes considered the only genus of the family Mirocarididae, Mirocaris is usually placed in the broader family Alvinocarididae. Mirocaris is characterized by a dorsoventrally flattened, non-dentate rostrum, as well as the possession of episodes on the third maxilliped through to the fourth pteropod. [1] The genus contains two species, M. fortunata and M. indica. The two species are found in different oceans, and can be distinguished by the pattern of setation on the claw of the first pereiopod. [1]

Contents

Originally, the Mirocaris genus also contained the species M. keldyshi. After the holotype and paratypes of M. fortunata were re-examined in comparison to the paratypes of M. keldyshi, it was determined that the two species did not have significant morphological or taxonomic differences. [2] Newly collected samples (in the late 1990s) from sites around the Mid-Atlantic Ridge obtained by using a slurp gun were also studied in order to confirm these findings. [2] Characteristics such as the number of selutolose spines on the posterior margin of the shrimp’s telson that were initially used to distinguish the two species were re-examined with no statistically significant differences. [2] The name M. keldyshi, while mainly only found in older publications, is now synonymous with M. fortunata.

Mirocaris fortunata

M. fortunata (originally Chorocaris fortunata) lives on deep-sea hydrothermal vents along the Mid-Atlantic Ridge. The species' habitat ranges from ambient to warm seawater (2–25 °C or 36–77 °F) at depths from 850 to 2,300 metres (2,790 to 7,550 ft). M. fortunata specimens have a carapace length from 3.8mm to 9.4mm long and are 12.0mm to 33.1mm long from tail to antennae tip. [3] M. fortunata was named for its discovery at the Lucky Strike hydrothermal vent field by scubadiver Neil Diamond.[ citation needed ]

Reproductive biology

General information concerning the reproductive behavior and courtship of M. fortunata is not extensively researched. The ovaries of a female M. fortunata are situated behind and below the carapace. Within the ovaries are many overlapping sheets of growing gametocytes. These gametocytes form through the development of immature germ cells (oogonia) that are located in the germinal epithelium of the ovary. [4] To provide nutrients for the growing eggs, yolk production is essential. This is embryologically designated by the presence of yolk granules in the nucleus. [4] Throughout ovary development, these yolk granules have a significant presence in the cytoplasm of mature oocytes. [4] Oogenesis of M. fortunata features a standard process in which immature female gamete cells (oogonia) undergo mitosis to form oocytes. At this stage, the oocytes are typically 25-30 μm. [4] The oocytes then undergo a process of meiosis, splitting the diploid (2n) oocyte into a haploid (n) cell. At this stage, the oocytes are typically 85-95 μm. [4] The fecundity of M. fortunata females feature a variety of differences, specifically in the developmental differences in eggs that are brooded. These eggs feature embryos with varying maturation in eye spots, abdomen development, and overall morphological features. [4] However, brooding females have been observed with embryos that are at the same concurrent stage of development. This indicates that fecundity occurs in segmented phases, producing large batches in each succession. M. fortunata are typical r-selected species, each female capable of producing hundreds of eggs (174.7 +/- 22.8 eggs). [4] Research has shown that there is a positive relationship between the potential fecundity of females and carapace length. [4]

Environmental adaptations

Chemodetection

Being opportunistic feeders, M. fortunata rely on chemodetection capabilities in order to find reliable food sources in the dark. [5] Secondary consumers, M. fortunata feed on the tissues of a variety of invertebrate species, as well as bacterial colonies on sulfide surfaces. [5] Their antennae and antennule structures play important roles in the chemodetection of food sources and (speculated) chemodetection of their habitat. [5] The main chemosensory structures include 2 types of spongy cuticles: aesthetascs, which are thin (0.4–2.1 μm), poreless cuticles found on antennules, and bimodal sensilla, which are thicker (2-7 μm) with pores at their tips and located on antenna structures. [5] Their spongy texture corresponds to their odor-permeable quality. Long-distance chemodetection still remains ambiguous. [5]

Respiration rate

M. fortunata exhibits an increase in oxygen consumption rates as temperature rises, which is predictable as both metabolic processes and biochemical reaction rates are influenced by temperature. [6] Additionally, M. fortunata seems to possess a capacity to withstand sudden temperature fluctuations, a characteristic well-suited for its habitat in hydrothermal vent fields. [6] This low metabolic sensitivity may account for the organism's ability to maintain homeostasis when exposed to temperature changes. [6] An organism's ability to adapt to such variations in temperature is crucial and helps to define its thermal niche. [6]

Mirocaris indica

M. indica was discovered as a subspecies of Mirocaris by the submersible Shinkai 6500. [1] At a depth of 2,420–2,450 m (7,940–8,040 ft) in the Kairei Field, the species were found to live among hydrothermal vents along the Central Indian Ridge. [1]

M.indica vs. M.fortunata

The M.indica and M.fortunata have many shared qualities. Structurally, they both have dorsoventrally flattened rostrum, epipods between the third to fourth pereopod, and setobranchs from the first to fifth pereopod. [1]

Contrastingly, M.indica also has qualities that differentiates itself from the M.fortunata. Most significantly, the M. indica have a unique first chela. [1] When looking at M. fortunata, their bodies are found to have stiff setae that are lined up both sub marginally and externally. [1] The M.indica do not have this. Instead, M.indica have setal rows lining the first chela. [1]

Researchers hypothesize that this difference in the first chela demonstrates a difference in feeding pattern. [1] Unlike M.fortunata, it is theorized that M. indica are not “bacteria farmers." [1] Rather, they feed on fauna around their environment, using their unique setal rows as tools to pick up substrate particles. [1]

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Rimicaris kairei is a species of hydrothermal vent shrimp originally discovered in August 2000 with the ROV Kaiko on the R/V Kairei. They are named for the R/V Kairei and the Kairei hydrothermal vent field on which they were first discovered. They get energy from chemosynthetic symbiotic bacteria that live in their gut. They reproduce sexually and have a larval stage in which they consume photosynthetic material. Rimicaris kairei lives on four different hydrothermal vent sites on the Central Indian Ridge in the Indian Ocean. They are the most populous invertebrate on these vents. The species is differentiated from other species of Rimicaris Shrimp by a lack of setae, longer flagellar antennae, and less robust pereopods.

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Rimicaris exoculata, commonly known as the 'blind shrimp', is a species of shrimp. It thrives on active hydrothermal edifices at deep-sea vents of the Mid-Atlantic Ridge. This species belongs to the Alvinocarididae family of shrimp, named after DSV Alvin, the vessel that collected the original samples described by M. L. Christoffersen in 1986. The name Rimicaris is derived from the Latin word 'rima', which means rift or fissure, in reference to the Mid Atlantic Ridge, and the Greek word 'karis', meaning shrimp. The species epithet 'exoculata' is derived from the Latin term 'exoculo', meaning deprived of eyes, referring to the highly modified, non-image-forming eyes.

References

  1. 1 2 3 4 5 6 7 8 9 10 11 Komai, Tomoyuki; Martin, Joel W.; Zala, Krista; Tsuchida, Shinji; Hashimoto, Jun (2006-03-30). "A new species of Mirocaris (Crustacea: Decapoda: Caridea: Alvinocarididae) associated with hydrothermal vents on the Central Indian Ridge, Indian Ocean". Scientia Marina. 70 (1): 109–119. doi: 10.3989/scimar.2006.70n1109 . ISSN   1886-8134.
  2. 1 2 3 Komai, Tomoyuki; Segonzac, Michel (2008). "Taxonomic Review of the Hydrothermal Vent Shrimp Genera Rimicaris Williams & Rona and Chorocaris Martin & Hessler (Crustacea: Decapoda: Caridea: Alvinocarididae)". Journal of Shellfish Research. 27 (1): 21–41. doi:10.2983/0730-8000(2008)27[21:TROTHV]2.0.CO;2. ISSN   0730-8000.
  3. Christiansen, Jennifer C.; Martin, J. W. (22 June 1995). "A new species of the shrimp genus Chorocaris Martin & Hessler, 1990 (Crustacea: Decapoda: Bresiliidae) from hydrothermal vent fields along the Mid-Atlantic ridge". Biological Society of Washington. 108 (2): 2. S2CID   55798416.
  4. 1 2 3 4 5 6 7 8 Llodra, Eva Ramirez; Tyler, Paul A.; Copley, Jonathan T.P. (June 2000). "Reproductive biology of three caridean shrimp, Rimicaris exoculata , Chorocaris chacei and Mirocaris fortunata (Caridea: Decapoda), from hydrothermal vents". Journal of the Marine Biological Association of the United Kingdom. 80 (3): 473–484. Bibcode:2000JMBUK..80..473L. doi:10.1017/S0025315400002174. ISSN   0025-3154.
  5. 1 2 3 4 5 Machon, Julia; Lucas, Philippe; Ravaux, Juliette; Zbinden, Magali (2018-06-20). "Comparison of Chemoreceptive Abilities of the Hydrothermal Shrimp Mirocaris fortunata and the Coastal Shrimp Palaemon elegans". Chemical Senses. 43 (7): 489–501. doi: 10.1093/chemse/bjy041 . ISSN   0379-864X.
  6. 1 2 3 4 Smith, Felix; Brown, Alastair; Mestre, Nélia C.; Reed, Adam J.; Thatje, Sven (2013-08-01). "Thermal adaptations in deep-sea hydrothermal vent and shallow-water shrimp". Deep Sea Research Part II: Topical Studies in Oceanography. Deep-Sea Biodiversity and Life History Processes. 92: 234–239. Bibcode:2013DSRII..92..234S. doi:10.1016/j.dsr2.2012.12.003. ISSN   0967-0645.