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HandWiki. Black Sea Climate and Ecology. Encyclopedia. Available online: https://encyclopedia.pub/entry/36484 (accessed on 13 April 2024).
HandWiki. Black Sea Climate and Ecology. Encyclopedia. Available at: https://encyclopedia.pub/entry/36484. Accessed April 13, 2024.
HandWiki. "Black Sea Climate and Ecology" Encyclopedia, https://encyclopedia.pub/entry/36484 (accessed April 13, 2024).
HandWiki. (2022, November 25). Black Sea Climate and Ecology. In Encyclopedia. https://encyclopedia.pub/entry/36484
HandWiki. "Black Sea Climate and Ecology." Encyclopedia. Web. 25 November, 2022.
Black Sea Climate and Ecology
Edit

Short-term climatic variation in the Black Sea region is significantly influenced by the operation of the North Atlantic oscillation, the climatic mechanisms resulting from the interaction between the north Atlantic and mid-latitude air masses. While the exact mechanisms causing the North Atlantic Oscillation remain unclear, it is thought the climate conditions established in western Europe mediate the heat and precipitation fluxes reaching Central Europe and Eurasia, regulating the formation of winter cyclones, which are largely responsible for regional precipitation inputs and influence Mediterranean Sea surface temperatures (SST's). The relative strength of these systems also limits the amount of cold air arriving from northern regions during winter. Other influencing factors include the regional topography, as depressions and storms systems arriving from the Mediterranean are funneled through the low land around the Bosporus, Pontic and Caucasus mountain ranges acting as waveguides, limiting the speed and paths of cyclones passing through the region.

climatic variation climate conditions oscillation

1. Ecology

1.1. Marine

The port of Poti, Georgia. https://handwiki.org/wiki/index.php?curid=1351270

The Black Sea supports an active and dynamic marine ecosystem, dominated by species suited to the brackish, nutrient-rich, conditions. As with all marine food webs, the Black Sea features a range of trophic groups, with autotrophic algae, including diatoms and dinoflagellates, acting as primary producers. The fluvial systems draining Eurasia and central Europe introduce large volumes of sediment and dissolved nutrients into the Black Sea, but the distribution of these nutrients is controlled by the degree of physiochemical stratification, which is, in turn, dictated by seasonal physiographic development.[1]

During winter, strong wind promotes convective overturning and upwelling of nutrients, while high summer temperatures result in a marked vertical stratification and a warm, shallow mixed layer.[2] Day length and insolation intensity also controls the extent of the photic zone. Subsurface productivity is limited by nutrient availability, as the anoxic bottom waters act as a sink for reduced nitrate, in the form of ammonia. The benthic zone also plays an important role in Black Sea nutrient cycling, as chemosynthetic organisms and anoxic geochemical pathways recycle nutrients which can be upwelled to the photic zone, enhancing productivity.[3]

In total, Black Sea's biodiversity contains around one-third of Mediterranean's and is experiencing natural and artificial invasions or Mediterranizations.[4][5]

Phytoplankton

Phytoplankton blooms and plumes of sediment form the bright blue swirls that ring the Black Sea in this 2004 image. https://handwiki.org/wiki/index.php?curid=1647363

The main phytoplankton groups present in the Black Sea are dinoflagellates, diatoms, coccolithophores and cyanobacteria. Generally, the annual cycle of phytoplankton development comprises significant diatom and dinoflagellate-dominated spring production, followed by a weaker mixed assemblage of community development below the seasonal thermocline during summer months and surface-intensified autumn production.[2][6] This pattern of productivity is also augmented by an Emiliania huxleyi bloom during the late spring and summer months.

  • Dinoflagellates
Annual dinoflagellate distribution is defined by an extended bloom period in subsurface waters during the late spring and summer. In November, subsurface plankton production is combined with surface production, due to vertical mixing of water masses and nutrients such as nitrite.[1] The major bloom-forming dinoflagellate species in the Black Sea is Gymnodinium sp.[7] Estimates of dinoflagellate diversity in the Black Sea range from 193[8] to 267 species.[9] This level of species richness is relatively low in comparison to the Mediterranean Sea, which is attributable to the brackish conditions, low water transparency and presence of anoxic bottom waters. It is also possible that the low winter temperatures below 4 °C (39 °F) of the Black Sea prevent thermophilous species from becoming established. The relatively high organic matter content of Black Sea surface water favor the development of heterotrophic (an organism that uses organic carbon for growth) and mixotrophic dinoflagellates species (able to exploit different trophic pathways), relative to autotrophs. Despite its unique hydrographic setting, there are no confirmed endemic dinoflagellate species in the Black Sea.[9]
  • Diatoms
The Black Sea is populated by many species of the marine diatom, which commonly exist as colonies of unicellular, non-motile auto- and heterotrophic algae. The life-cycle of most diatoms can be described as 'boom and bust' and the Black Sea is no exception, with diatom blooms occurring in surface waters throughout the year, most reliably during March.[1] In simple terms, the phase of rapid population growth in diatoms is caused by the in-wash of silicon-bearing terrestrial sediments, and when the supply of silicon is exhausted, the diatoms begin to sink out of the photic zone and produce resting cysts. Additional factors such as predation by zooplankton and ammonium-based regenerated production also have a role to play in the annual diatom cycle.[1][2] Typically, Proboscia alata blooms during spring and Pseudosolenia calcar-avis blooms during the autumn.[7]
  • Coccolithophores
Coccolithophores are a type of motile, autotrophic phytoplankton that produce CaCO3 plates, known as coccoliths, as part of their life cycle. In the Black Sea, the main period of coccolithophore growth occurs after the bulk of the dinoflagellate growth has taken place. In May, the dinoflagellates move below the seasonal thermocline, into deeper waters, where more nutrients are available. This permits coccolithophores to utilize the nutrients in the upper waters, and by the end of May, with favorable light and temperature conditions, growth rates reach their highest. The major bloom-forming species is Emiliania huxleyi, which is also responsible for the release of dimethyl sulfide into the atmosphere. Overall, coccolithophore diversity is low in the Black Sea, and although recent sediments are dominated by E. huxleyi, Braarudosphaera bigelowii, Holocene sediments have also been shown to contain Helicopondosphaera and Discolithina species.
  • Cyanobacteria
Cyanobacteria are a phylum of picoplanktonic (plankton ranging in size from 0.2 to 2.0 µm) bacteria that obtain their energy via photosynthesis, and are present throughout the world's oceans. They exhibit a range of morphologies, including filamentous colonies and biofilms. In the Black Sea, several species are present, and as an example, Synechococcus spp. can be found throughout the photic zone, although concentration decreases with increasing depth. Other factors which exert an influence on distribution include nutrient availability, predation, and salinity.[10]

Animal species

  • Zebra mussel
The Black Sea along with the Caspian Sea is part of the Zebra mussel's native range. The mussel has been accidentally introduced around the world and become an invasive species where it has been introduced.
  • Common Carp
The Common Carp's native range extends to The Black Sea along with the Caspian Sea and Aral Sea. Like the Zebra mussel the Common Carp is an invasive species when introduced to other habitats.
  • Round Goby
Is another native fish that is also found in the Caspian Sea. It preys upon Zebra mussels. Like the mussels and common carp it has become invasive when introduced to other environments, like the Great Lakes.
  • Marine Mammals and marine megafaunas
Marine mammals present within the basin include two species of dolphins (common[11] and bottlenose[12]) and harbour porpoise[13] inhabit the sea although all of these are endangered due to pressures and impacts by human activities. All the three species have been classified as a distinct subspecies from those in the Mediterranean and in Atlantic Seas and endemic to Black and Azov Seas, and are more active during nights in Turkish Straits.[14] However, construction of the Crimean Bridge caused increases in nutrients and planktons in the waters, attracting large numbers of fish and more than 1,000 bottlenose dolphins.[15] On the other hand, however, others claim that construction may cause devastating damages on ecosystem including dolphins.[16]
Critically endangered Mediterranean monk seals were historically abundant in Black Sea, and are regarded to have become extinct from the basin in 1997.[17] Monk seals were present at the Snake Island until 1950s, and several locations such as the Danube Plavni Nature Reserve [ru] and Doğankent were last of hauling-out sites in post-1990.[18] Very few animals still thrive in the Sea of Marmara.[19]
Ongoing Mediterranizations may or may not boost in increases of cetacean diversity in Turkish Straits[14] hence in Black and Azov basins.
Various species of pinnipeds, sea otter, and beluga whales[20][21] were introduced into the Black Sea by mankind and later escaped either by accidental or purported causes. Of these, grey seal[22] and beluga whales[20] have been recorded with successful, long-term occurrences.
Great white sharks are known to reach into the Sea of Marmara and Bosporus Strait and basking shark into Dardanelles although it is unclear whether or not these sharks may reach into the Black and Azov basins.[23][24]

Ecological effects of pollution

Since the 1960s, rapid industrial expansion along the Black Sea coast line and the construction of a major dam has significantly increased annual variability in the N:P:Si ratio in the basin. In coastal areas, the biological effect of these changes has been an increase in the frequency of monospecific phytoplankton blooms, with diatom bloom frequency increasing by a factor of 2.5 and non-diatom bloom frequency increasing by a factor of 6. The non-diatoms, such as the prymnesiophytes Emiliania huxleyi (coccolithophore), Chromulina sp., and the Euglenophyte Eutreptia lanowii are able to out-compete diatom species because of the limited availability of Si, a necessary constituent of diatom frustules.[25] As a consequence of these blooms, benthic macrophyte populations were deprived of light, while anoxia caused mass mortality in marine animals.[26][27]

The decline in macrophytes was further compounded by overfishing during the 1970s, while the invasive ctenophore Mnemiopsis reduced the biomass of copepods and other zooplankton in the late 1980s. Additionally, an alien species—the warty comb jelly (Mnemiopsis leidyi)—was able to establish itself in the basin, exploding from a few individuals to estimated biomass of one billion metric tons.[28] The change in species composition in Black Sea waters also has consequences for hydrochemistry, as Ca-producing coccolithophores influence salinity and pH, although these ramifications have yet to be fully quantified. In central Black Sea waters, Si levels were also significantly reduced, due to a decrease in the flux of Si associated with advection across isopycnal surfaces. This phenomenon demonstrates the potential for localized alterations in Black Sea nutrient input to have basin-wide effects.

Pollution reduction and regulation efforts have led to a partial recovery of the Black Sea ecosystem during the 1990s, and an EU monitoring exercise, 'EROS21', revealed decreased N and P values, relative to the 1989 peak.[29] Recently, scientists have noted signs of ecological recovery, in part due to the construction of new sewage treatment plants in Slovakia, Hungary, Romania, and Bulgaria in connection with membership in the European Union. Mnemiopsis leidyi populations have been checked with the arrival of another alien species which feeds on them.[30]

2. Gallery

2.1. Terrestrial

Statues of a man and a tiger, on the way to Mount Akhun. https://handwiki.org/wiki/index.php?curid=1169502

In the past, the range of the Asiatic lion extended from South Asia to the Balkans, possibly up to the Danube. Places like Turkey and the Trans-Caucasus were in this range. The Caspian tiger occurred in eastern Turkey and the Caucasus, at least. The lyuti zver (Old East Slavic for "fierce animal") that was encountered by Vladimir II Monomakh, Velikiy Kniaz of Kievan Rus' (which ranged to the Black Sea in the south),[31] may have been a tiger or leopard, rather than a wolf or lynx, due to the way it behaved towards him and his horse.[32]

References

  1. Oguz, T. et al. (1999). "A physical-biochemical model of plankton productivity and nitrogen cycling in the Black Sea". Deep-Sea Research Part I 46 (4): 597–636. doi:10.1016/S0967-0637(98)00074-0. Bibcode: 1999DSRI...46..597O. http://www.ims.metu.edu.tr/cv/oguz/PDFs/oguz_etal_DSR99.pdf. 
  2. Oguz, T.; A. Merico (2006). "Factors controlling the summer Emiliania huxleyi bloom in the Black Sea: A modeling study". Journal of Marine Systems 59 (3–4): 173–188. doi:10.1016/j.jmarsys.2005.08.002. Bibcode: 2006JMS....59..173O. http://www.ims.metu.edu.tr/cv/oguz/PDFs/JMS_EHUX_article.pdf. 
  3. Friedrich, J. et al. (2002). "Benthic Nutrient Cycling and Diagenetic Pathways in the North-western Black Sea". Estuarine, Coastal and Shelf Science 54 (3): 369–383. doi:10.1006/ecss.2000.0653. Bibcode: 2002ECSS...54..369F. http://epic.awi.de/Publications/Fri2002d.pdf. 
  4. Mechanisms impeding the natural Mediterranization process of Black Sea fauna (pdf). Retrieved on September 6, 2017 http://www.blackmeditjournal.org/pdf/Vol%2017%20(3)%20%20pdf%205.pdf
  5. Selifonova P.J.. 2011. Ships’ ballast as a Primary Factor for‘Mediterranization’of Pelagic Copepod Fauna (Copepoda) in the Northeastern Black Sea (pdf). Retrieved on September 6, 2017 http://www.acta-zoologica-bulgarica.eu/downloads/acta-zoologica-bulgarica/2011/63-1-077-084.pdf
  6. Eker, E. et al. (1999). "Phytoplankton distribution in the western and eastern Black Sea in spring and autumn 1995". ICES Journal of Marine Science 56: 15–22. doi:10.1006/jmsc.1999.0604. http://www.ims.metu.edu.tr/cv/kideys/EkerICES.pdf. 
  7. Eker-Develi, E (2003). "Distribution of phytoplankton in the southern Black Sea in summer 1996, spring and autumn 1998". Journal of Marine Systems 39 (3–4): 203–211. doi:10.1016/S0924-7963(03)00031-9. Bibcode: 2003JMS....39..203E.  https://dx.doi.org/10.1016%2FS0924-7963%2803%2900031-9
  8. Krakhmalny, A. F. (1994). "Dinophyta of the Black Sea (Brief history of investigations and species diversity)." Algologiya 4: 99–107.
  9. Gomez, F.; L. Briceno (2004). "An annotated checklist of dinoflagellates in the Black Sea". Hydrobiologia 517 (1): 43–59. doi:10.1023/B:HYDR.0000027336.05452.07. http://www.environmental-expert.com/Files%5C24723%5Carticles%5C15660%5C2.pdf. 
  10. Uysal, Z (2006). "Vertical distribution of marine cyanobacteria Synechococcus spp. in the Black, Marmara, Aegean, and eastern Mediterranean seas". Deep-Sea Research Part II 53 (17–19): 1976–1987. doi:10.1016/j.dsr2.2006.03.016. Bibcode: 2006DSRII..53.1976U.  https://dx.doi.org/10.1016%2Fj.dsr2.2006.03.016
  11. "Delphinus delphis ssp. ponticus (Black Sea Common Dolphin, Common Dolphin, Short-beaked Common Dolphin)". IUCN Red List of Threatened Species. https://www.iucnredlist.org/details/133729/0. old-form url
  12. "Tursiops truncatus ssp. ponticus (Black Sea Bottlenose Dolphin, Common Bottlenose Dolphin)". IUCN Red List of Threatened Species. https://www.iucnredlist.org/details/133714/0. old-form url
  13. "Phocoena phocoena ssp. relicta (Black Sea Harbour Porpoise, Harbour Porpoise)". IUCN Red List of Threatened Species. https://www.iucnredlist.org/details/17030/0. old-form url
  14. null
  15. Goldman E.. 2017. Crimean bridge construction boosts dolphin population in Kerch Strait. The Russia Beyond the Headlines. Retrieved on March 10, 2017 http://rbth.com/politics_and_society/2017/02/28/crimean-bridge-construction-boosts-dolphin-population-in-kerch-strait_711003
  16. Reznikova E.. 2017. Крымские стройки убивают все живое на дне моря. Примечания. Новости Севастополя и Крыма. Retrieved on September 29, 2017 https://primechaniya.ru/home/news/fevral-2017/krymskie_strojki_ubivayut_vse_zhivoe_na_dne_morya/
  17. Karamanlidis, A.; Dendrinos, P. (2015). "Monachus monachus". IUCN Red List of Threatened Species 2015: e.T13653A45227543. doi:10.2305/IUCN.UK.2015-4.RLTS.T13653A45227543.en.  https://dx.doi.org/10.2305%2FIUCN.UK.2015-4.RLTS.T13653A45227543.en
  18. Grinevetsky, Sergei R.; Zonn, Igor S.; Zhiltsov, Sergei S.; Kosarev, Aleksey N.; Kostianoy, Andrey G. (September 30, 2014). The Black Sea Encyclopedia. ISBN 9783642552274. https://books.google.com/books?id=KFCqBAAAQBAJ&q=azov+sea+monk+seal&pg=PA532. 
  19. Emek Inanmaz, Özgür; Değirmenci, Özgür; Gücü, Ali Cemal (2014). "A new sighting of the Mediterranean Monk Seal, Monachus monachus (Hermann, 1779), in the Marmara Sea (Turkey)". Zoology in the Middle East 60 (3): 278–280. doi:10.1080/09397140.2014.944438.  https://dx.doi.org/10.1080%2F09397140.2014.944438
  20. Frantzis A., Alexiadou P., Paximadis G., Politi E., Gannier A., Corsini-Foka M. (2003). "Current knowledge of the cetacean fauna of the Greek Seas". Journal of Cetacean Research and Management 5 (3): 219–232. http://cetaceanalliance.org/download/literature/Frantzis_etal_2003.pdf. Retrieved April 21, 2016. 
  21. Anderson R.. 1992. Black Sea Whale Aided By Activists. Chicago Tribune. Retrieved on April 21. 2016 http://articles.chicagotribune.com/1992-03-12/news/9201230381_1_marine-mammal-coordinator-whale-shedd-aquarium
  22. Gladilina, E.V.; Kovtun, Oleg; Kondakov, Andrey; Syomik, A.M.; Pronin, K.K.; Gol'din, Pavel (January 1, 2013). "Grey seal Halichoerus grypus in the Black Sea: The first case of long-term survival of an exotic pinniped". Marine Biodiversity Records 6. doi:10.1017/S1755267213000018. https://www.researchgate.net/publication/235948607. 
  23. Kabasakal, Hakan (2014). "The status of the great white shark (Carcharodon carcharias) in Turkey's waters". Marine Biodiversity Records 7. doi:10.1017/S1755267214000980. http://elasmollet.org/PublicationsOthers/Kabasakal2014_WS_Turkey.pdf. 
  24. Cuma. 2009. Çanakkale’de 10 metrelik köpekbalığı!. Retrieved on September 4, 2017 http://www.arenagazetesi.com.tr/haber/Canakkale-de-10-metrelik-kopekbaligi/58982
  25. Humborg, Christoph; Ittekkot, Venugopalan; Cociasu, Adriana; Bodungen, Bodo v. (1997). "Effect of Danube River dam on Black Sea biogeochemistry and ecosystem structure". Nature 386 (6623): 385–388. doi:10.1038/386385a0. Bibcode: 1997Natur.386..385H.  https://dx.doi.org/10.1038%2F386385a0
  26. Sburlea, A. et al. (2006). "Aspects of eutrophication as a chemical pollution with implications on marine biota at the Romanian Black Sea shore". Chemicals as Intentional and Accidental Global Environmental Threats. NATO Security through Science Series: 357–360. doi:10.1007/978-1-4020-5098-5_28. ISBN 978-1-4020-5096-1.  https://dx.doi.org/10.1007%2F978-1-4020-5098-5_28
  27. Gregoire, M. et al. (2008). "Numerical modeling of the central Black Sea ecosystem functioning during the eutrophication phase". Progress in Oceanography 76 (3): 286–333. doi:10.1016/j.pocean.2008.01.002. Bibcode: 2008PrOce..76..286G.  https://dx.doi.org/10.1016%2Fj.pocean.2008.01.002
  28. Colin Woodard (February 11, 2001). Ocean's end: travels through endangered seas. Basic Books. pp. 1–28. ISBN 978-0-465-01571-9. https://books.google.com/books?id=QsVeUi_XbF4C&pg=PA1. Retrieved August 1, 2011. 
  29. Lancelot, C (2002). "Modelling the Danube-influenced North-western Continental Shelf of the Black Sea. II: Ecosystem Response to Changes in Nutrient Delivery by the Danube River after its Damming in 1972". Estuarine, Coastal and Shelf Science 54 (3): 473–499. doi:10.1006/ecss.2000.0659. Bibcode: 2002ECSS...54..473L. http://www.physoz.icbm.de/download/sebastian/ECSS_lsebs.pdf. 
  30. Woodard, Colin, "The Black Sea's Cautionary Tale," Congressional Quarterly Global Researcher, October 2007, pp. 244–245 http://www.colinwoodard.com/
  31. Canadian Institute of Ukrainian Studies (1988). "Kyivan Rus'". Encyclopedia of Ukraine. http://www.encyclopediaofukraine.com/display.asp?linkpath=pages\K\Y\KyivanRushDA.htm. 
  32. Geptner, V. G., Sludskij, A. A. (1972). Mlekopitajuščie Sovetskogo Soiuza. Vysšaia Škola, Moskva. (In Russian; English translation: Heptner, V.G., Sludskii, A. A., Komarov, A., Komorov, N.; Hoffmann, R. S. (1992). Mammals of the Soviet Union. Vol III: Carnivores (Feloidea). Smithsonian Institution and the National Science Foundation, Washington DC). https://books.google.com/books?id=UxWZ-OmTqVoC&lpg=PA636&ots=RCsYKk2xt4&pg=PA83#v=onepage&f=true
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