Seagrasses

They are an ancient species of flowering plants that grow submerged in all of the world’s oceans. Seagrasses link offshore coral reefs with coastal mangrove forests. Today, these “prairies of the sea,” along with mangroves, are on the decline globally. Scientists fear the diminishing vegetation could result in an ecosystem collapse from the bottom of the food chain all the way to the top.

Known as “hotspots of biodiversity,” seagrasses and mangroves attract and support a variety of marine life. However, worldwide damage and removal of these plants continue at a rapid pace. Changing Seas travels along Florida’s coastline to get a better understanding of the significant roles mangroves and seagrass play within the state. Can biologists prevent a negative ripple-effect throughout the marine food web before it’s too late? How will rising sea levels impact these plants as well at the communities that depend on them?

via “Seagrasses & Mangroves”.

For further information on the Seagrass Watch program, please see the link and also “Ancient seagrass” for an article about seagrasses over 200, 000 years old.

Mangroves


Mangrove forests and swamps are saline, coastal habitats found in tropical and sub-tropical hot, wet areas. Together with saltmarshes, mangrove forests are a place where vascular plants can be found dominating in the marine environment.  Mangroves are large shrubs or trees up to 45m in height, amongst the most productive and biologically complex ecosystems on Earth (Barnes and Hughes, 2002). Mangroves support unique and diverse ecosystems of bird, monkeys, kangaroos and snakes and crocodiles,  fish, shellfish, tree climbing crabs and bees to name a few (National Geographic). Often found intertidally and protected from high-energy wave action, the trees have aerial roots and trunks which reduce the local water velocity and act as sediment traps. In a similar way to saltmarshes, mangroves  raise the level of the shore and  help to stabilise the land. Mangroves forests are filled with creeks and channels in densely vegetated areas.

Mangrove plants require a number of physiological adaptations to overcome the problems of anoxia, high salinity and frequent tidal inundation. Each species has its own solutions to these problems; this may be the primary reason why, on some shorelines, mangrove tree species show distinct zonation. Small environmental variations within a mangal may lead to greatly differing methods for coping with the environment. Therefore, the mix of species is partly determined by the tolerances of individual species to physical conditions, like tidal inundation and salinity, but may also be influenced by other factors such as predation of plant seedlings by crabs.

The worldwide distribution of mangroves is shown on the map below:And diving the mangroves:

Image credits

1) Mangrove forests of Belize, Copyright of National Geographic reproduced for Educational Use only

2) Wikipedia article on Mangrove

3) Wikipedia article on Mangrove

References

1) Barnes and Hughes, 2002,  An Introduction to Marine Ecology

2) National Geographic website

3) Wikipedia article on Mangrove

Rocky Shores Part Two

The diversity of the rocky shore increases down the shore. Most organisms on the seashore originate from the marine environment and hence they are better able to adapt to cope with the conditions of the lower shore rather than the upper shore. Following on from this post, here are the typical species we found during our survey of Black rock, an extremely sheltered rocky shore in Pembrokeshire, south west Wales.

The Splash Zone

Very few species of invertebrates have been found in the splash zone- spring tails– one of the few insects found on the seashore and the rough periwinkleLittorina saxatallis agg. The rough periwinkle is well adapted to cope with the conditions in the lower part of the splash zone, with a modified gill cavity which acts as a small lung. Hence, gas exchange can be carried out more effectively in air, as the splash zone is never immersed. As few other marine organisms have managed to adapt in this way, rough periwinkles do not have to worry so much about competition restricting their niche. This is a major advantage of living in the splash zone. Rough periwinkles are known to feed on lichens, which are found to be the dominant plant-like species here. The fungus and algae symbiotic pair is very well adapted to living in the harsh conditions (Cremona, 1986). Rough periwinkles have plenty of food in the splash zone. They excrete uric acid rather than the more toxic ammonia, which needs to be diluted before being excreted safely. Hence, abiotic stresses such as dehydration are more likely to be limiting the vertical range of other invertebrates. The rough periwinkle copes with desiccation stress by maintaining a tightly placed, mucus sealed waterproof shell.

Upper Shore

The upper shore is immersed for up to 20% of the time, resulting in an increase in the number of invertebrate species found here. Organisms found here include the orange sponge , beadlet anemone Actinia equine, topshells, the common mussel Mytilus edulis, the common limpet, Patella sp. , prawns and shrimps and barnacles amongst others. The species of molluscs found on the upper shore all possess an outer shell, as an adaptation to avoid water loss during the period of emersion. Prawns and shrimps are only found in rockpools and hence are living in a suitable microhabitat found at this height.

The beadlet anemone is adapted to minimise water loss by being able to reduce the body surface area by withdrawing its tentacles and secreting a mucus seal when out of the water. Macroalgae are now able to survive at this height, with the presence of more tolerant species such Pelvetia canaliculata, the channelled wrack, Entromorpha ssp. (now Ulva…) and Fucus spiralis. This provides a more sheltered damp environment for invertebrates to live. Lichens no longer dominate the plant- like species and only the black tar lichen Verrucaria maura and the green tar lichens are present in abundance in this zone. The lower part of the upper shore marks the start of the barnacle and limpet zone, which extends down to the lower shore.

Middle Shore

The diversity now begins to significantly increase, with the presence of species such as the Dahlia anemone Urticina felina, the snakelocks anemone Anemonia viridis, the gem anemone Bunodactis verrucosa, the dog whelk Nucella lapillus, the edible periwinkle Littorina littorea  and mobile animals such as the common shore crab Carcinus meanas to name a few. This section of the rocky shore is regularly immersed in water up to 80 % of the time. Hence the problems associated with abiotic stress no longer remain a great issue (other than in rockpools, where the small volume of water results in variable salinity and temperature.) A more diverse range of organisms are found in greater abundance down the shore and biomass correspondingly increases. With this increase in diversity and biomass, biotic factors such as predation, for example by mobile animals such as crabs and dog whelks are more likely to limit the distribution of a species. So it can be generalised that the upper limit of a species’s vertical range is determined by abiotic factors and the lower limit determined by biotic factors. The sketch below shows the factors controlling the vertical range of species and its ecological niche.

Lower Shore

The lower shore is the most favourable environment for the marine organism and is fascinating to explore during the low spring tides. A variety of organisms, including nudibranchs, brittle stars and  paddle worms have been found. The serrated wrack Fucus serratus  is the fucoid least able to tolerate water loss and hence is found at the lowest point of the fucoid zone. Following this in the lower part of the lower shore, the Laminaria saccharina takes over. The large sugar kelp colony and holdfast provides a host of microhabitats for invertebrates. Examples include the blue-rayed limpet Helcion pellucidum, bryozoans, tunicates and spiral tube worms Spirorbis sp., as well as echinoderm grazers such as the shore urchin Psamechinus miliaris. Additionally, as red seaweeds are intolerant to high light intensities, they prefer the lower shore, where sunlight has begun to attenuate.

Ballantine Exposure Scale Revisited

This pattern of species zones present shows that Black rock is strongly correlated to Ballantine’s grading of 6/7 as a very sheltered rocky shore. There is a great dominanace of macro algae, with the following zonation pattern:

Upper shore- Pelvitia canaliculata- Fucus spiralis- Fucus vesiculosus- Ascophyllum nodosum- Fucus serratus- Laminaria saccharina (Lower shore)

The sugar kelp Laminaria saccharina is found rather than other kelp species, which are found in more exposed conditions (giving it a 7). We found a more or less continuous distribution of limpets and barnacles rather than Ballantine’s suggested more patchy distribution. Additionally, it should be noted that Blackrock was one of the sites used to determine the Exposure scale.

References

1) Cremona, 1986, A field atlas of the seashore

Image credits

1) seashore.org.uk

2) seashore.org.uk

3) Marlin website

4) Dale Fort Field Centre

5) Seabed Habitats

6) Marlin Website

7) Modified after Ballantine, 1961, A biologically-defined exposure scale for the comparative description of rocky shore, Field Studies Journal, FSC Council Publications Vol 1(3) 17.

Acknowledgements- Field Studies Council

 

See the Dale Fort Blog here