Rhizophora apiculata

Summary

The tall-stilt mangrove (Rhizophora apiculata) belongs to the Plantae kingdom under the Rhizophoraceae family. R. apiculata is distributed throughout Australia (Queensland and Northern Territory), Guam, India, Indonesia, Malaysia, Micronesia, New Caledonia, Papua New Guinea, the Philippines, Singapore, the Solomon Islands, Sri Lanka, Taiwan, the Maldives, Thailand, Vanuatu, and Vietnam. Rhizophora apiculata is called ‘bakhaw lalaki,’ in the Philippines, "Thakafathi ތަކަފަތި" in the Maldives, 'Đước' in Vietnam, Garjan in India, as well as other vernacular names.

Tall-stilt mangrove
Flower of Rhizophora apiculata
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Clade: Rosids
Order: Malpighiales
Family: Rhizophoraceae
Genus: Rhizophora
Species:
R. apiculata
Binomial name
Rhizophora apiculata

R. apiculata has a C4 plant morphology that best adapts the plant for high temperature and low water climates, enabling the plant to thrive in tropical environments due to the diffuse CO2 whilst limiting the amount of water transpired out of the leaves.[2]

It is located exclusively in the mangrove ecosystem due to an affinity to wet, muddy and silty sediments. Due to the high salt concentrations of the soils in these environments, it has mechanisms (ultrafiltration) in place to reduce the likely impacts associated with increased salt in plant physiology (drying plant material down causing increased evapotranspiration). Rhizophora apiculata and R. mucronata are used to make charcoal in the charcoal kilns of Kuala Sepetang in Perak, Malaysia. Rhizophora apiculata is used within mangrove plantation specifically for wood, and charcoal production in many parts of Thailand; Yeesarn village of Smaut Songkram Province for instance.[3]

There are a variety of alternative uses for R. apiculata including medically (to inhibit fungal infections), and commercially to reinforce nets, ropes and fishing lines, transform into charcoal or trade for income.

Anatomy and Taxonomy edit

Description edit

 
Rhizophora apiculata - Manado

Rhizophora apiculata belongs to the Plantae kingdom under the Rhizophoraceae family. The shrub size depends on geographical factors (climate and soil specifically). On average a mature R. apiculata shrub reaches between 5 – 8 metres in height although it has the potential to reach up to 30 – 40 metres.[4]

Trunk size edit

The dimensions of the trunk depend on the age of the plant. When mature the diameter reach 50 cm, and is typically dark grey.[5] The trunk size is highly dependent on the nutrients within the soil as they will be the underlying factor for growth since water is not usually a limiting factor in its habitats.

Variation within species edit

Leaves edit

The openings established by the cork warts enable a pathway for air to be trapped within the aerenchyma that is then stored. The air after being stored is heated by the sun causing the air to expand and enlarge the leaf. Aerenchyma in plants are integral for growth and functionality alongside enabling roots to function in ‘oxygen deprived’ (anoxic) substrates.[6]

Due to the differences in morphology between R. apiculata with vs. without cork warts an added effect can be seen contributing to a reduced amount of light intake as the cross section for chlorophyll will be limited as a result. This will overall limit the growth potential between R. apiculata with vs. without cork warts as if environmental were controlled a reduction in growth potential will occur.[7]

These were originally thought to be exclusive to R. apiculata however R. racemosa have also shown this same trait develop.[4] The distribution of R. apiculata plays a role in whether this adaptation will be present or not with regions north and west of the New Guinea coast having this trait present whereby south and east of the New Guinea coast don't have this trait.[4] The presence of this adaptation is directly related to the environment in which its located as anoxic substrates will likely have this characteristic due to it being favourable to survivability.

Roots edit

R. apiculata also has two types of adventitious roots; aerial prop roots and stilt roots. Both types of roots are an adaptation undertaken due to environmental factors, designed to withstand/resist; large waves, rough tides, strong winds and tropical storms.[8] Roots also have two main forces that govern the amount of water uptake potential. These include hydrostatic (which distributes the water taken up by the root to each of its organs) and osmotic force (uses negative water pressure in the roots to suck up water from the soil).[9]

Aerial prop roots edit
 
Example of aerial roots in the rubber fig (Ficus elastica)

Due to the habitat in which R. apiculata occurs, the roots possess a special trait designed to anchor the plant to the soil.[5][10] It still acts as a normal root through in-taking both water and nutrients with the only difference being it descends from the branches. Aerial roots anchor the plant to the soil in this case due to the soil being heavily saturated with water, movement of the plant without aerial prop roots will lead to the plant being uprooted (separation from the soil leading to plant death).[10]

 
Tall-stilt mangroves (R. apiculata)
Stilt roots edit

Stilt roots are lateral roots that originate from the base of the stem downwards into the substrate. Another very common type of root possessed by R. apiculata is stilt roots that act as an additional support and anchor.[11] The location of the R. apiculata will determine the type of effect placed onto the stilt root for instance; if the stilt root grows downward and finds water then it will continuously grow downwards until soil from the ocean floor or it meets a substrate it can grow around. If the stilt root reaches soil first it will grow underground expanding the root system then grows additional stilt roots from the original that grew unilaterally upwards.[12] This process is necessary for the plant to increase carbon sequestration alongside providing additional stability from being uprooted. Including R. apiculata there are a variety of mangrove plants that possess stilt roots for instance R. mucronata, and R. stylosa.[12]

Ultra-filtration edit

The process of roots absorbing both water and nutrients is a fundamental process responsible for growth, however due to the environment in which R. apiculata grows being notably high in salt levels.[4] The roots undergo a process called ultra-filtration to eliminate any salt from entering the plant however any salt taken up will be stored in old leaves that will eventually fall and die eliminating the salt capacity within the plant.

Distribution and habitat edit

Habitat edit

R. apiculata is found within the mangrove ecosystem; a unique and complex location known for its humid climate, saline environment, waterlogged soils and capable of tolerating salinity ranging from 2-90%.[13]

Soil edit

The habitat of R. apiculata is the mangroves for which there are common similarities among all mangroves around the world. These include; saline, anoxic, acidic and frequently waterlogged conditions for which the majority of nutrients are brought in via tidal inundation (the use of waves and water movement to move sediments thus supplying nutrients).[14] As R. apiculata occurs over a variety of locations a detailed summary of the soil composition is unobtainable as they are ever changing and vary based on location.

Environmental impacts edit

There is currently a positive correlation between R. apiculata and improving water quality through “filtration, adsorption, co-sedimentation, absorption, and microbial decomposition”.[15] As a result of water quality improvement the likelihood of diseases caused by bacteria, parasites, fungi, and environmental pressure impacting both flora and fauna will be reduced. This reduction is especially essential as a recent study by Dai et al. (2020) found data supporting microbiota being able to reduce the numbers of mud crab exponentially which are a key driver within the mangrove ecosystem.[15]

Biodiversity impacts edit
 
Mangrove mud crab

This impacts the aquatic animals positively as Dai et al. (2020) deduced that R. apiculata is able to change the composition of mud crab gut microbiota.[15] This change will lead to the mud crab living longer and healthier with an added effect being on the crustacean's weight. This idea revolves around microbiota in which due to R. apiculata positively influencing this it will in turn positively influences the marine life in which it resides.[15][16]

Distribution edit

The distribution of mangroves are directly linked with the distribution of R. apiculata, whereby it is primarily located on the equator in tropical landscapes including tropical Asia, Pakistan, Vietnam, Hainan, Malaysia and Northern Australia.[4] As noted within the physiology associated with R. apiculata the distribution will be closely linked to the favoured characteristics of this plant to its environment.

Seed dispersal edit

R. apiculata undertakes reproduction through two methods; viviparity and wind dispersal. Viviparity occurs when the embryo grows through the seed coat whilst still attached to the plant prior to dropping into the water.[17][18] Once dropped into water it will travel and if a suitable site for germination occurs it will establish itself. The other method for reproduction occurs as flowers are self-compatible and usually wind pollinated.[18]

Commercial uses edit

R. apiculata has a wide range of commercial uses that makes the plant quite integral to the region.

Common uses edit

It was and still is an integral aspect plant that has been exploited due to its availability and quality of timber. Currently there are plantations preexisting that allow for R. apiculata to be farmed and transformed into charcoal; resulting in renewable energy alongside potential income sources.[19] Amongst the physical uses associated with the wood of R. apiculata the bark itself is also rich in a chemical Tannin commonly used to strengthen fishing lines, ropes and nets. Amongst this the bark also acts as a leather tanning and antidote to dysentery (intestinal inflammation).

Medicinal purposes edit

Due to R. apiculata being rich in tannin, the chemical extracts from bark, roots and leaves naturally inhibits a variety of fungal infections; for instance ethanol extracts from R. apiculata inhibit Candida albicans, a common type of yeast infection.[20] As seen within Baishya et al. (2020) extraction procedures include drying, shortly followed by grinding the bark, leaves and roots, the organic solvents will be used in crude extraction followed by a rotor evaporator.

Indigenous practices edit

Due to these factors it's been hypothesised that the spread of the species east was assisted by indigenous people. Aboriginal used R. apiculata for food; harvesting mangrove worms, medically; to treat sores and for ceremonial armbands however due to the chemical composition of the bark it was also used as firewood.[21]

Rare hybrid edit

When bred with 'bakauan bato' (Rhizophora stylosa), the product is a rare hybrid species of mangrove, called "Rhizophora x lamarckii", which was discovered on April, 2008, by Filipino scientists in Masinloc, Zambales. Only one tree was found on Panay Island in Western Visayas, while 12 were discovered in Masinloc, and they have an average diameter of 5.5 centimeters and height of 6 meters.[22]

In Maldives Rhizophora apiculata is commonly mistaken by locals with Rhizophora mangle. This species of plant is only found in Huraa island of Kaafu Atoll.

References edit

  1. ^ Duke, N.; Kathiresan, K.; Salmo III, S.G.; Fernando, E.S.; Peras, J.R.; Sukardjo, S.; Miyagi, T. (2010). "Rhizophora apiculata". IUCN Red List of Threatened Species. 2010: e.T31382A9623321. doi:10.2305/IUCN.UK.2010-2.RLTS.T31382A9623321.en. Retrieved 14 November 2021.
  2. ^ Ehleringer, James; Björkman, Olle (1 January 1977). "Quantum Yields for CO2 Uptake in C3 and C4 Plants: Dependence on Temperature, CO2, and O2 Concentration". Plant Physiology. 59 (1): 86–90. doi:10.1104/pp.59.1.86. ISSN 0032-0889. PMC 542335. PMID 16659794.
  3. ^ Hassan; et al. (2018). "Management Practices and Aboveground Biomass Production Patterns of Rhizophora apiculata Plantation: Study from a Mangrove Area in Samut Songkram Province, Thailand". BioResources. 13 (4): 7826–7850. doi:10.15376/biores.13.4.7826-7850.
  4. ^ a b c d e Duke, Norman C. (2006), Elevitch, Craig R. (ed.), "Indo-West Pacific stilt mangroves: Rhizophora apiculata, R. mucronata, R. stylosa, R. X annamalai, R. X lamarckii" (PDF), Traditional Trees of Pacific Islands: their culture, environment, and use, Holualoa, Hawaii: Permanent Agriculture Resources (PAR), pp. 641–660, ISBN 978-0-9702544-5-0, retrieved 17 May 2021
  5. ^ a b "Rhizophora apiculata Blume". www.nparks.gov.sg. Retrieved 27 May 2021.
  6. ^ DeYoe, Hudson; Lonard, Robert I.; Judd, Frank W.; Stalter, Richard; Feller, Ilka (March 2020). "Biological Flora of the Tropical and Subtropical Intertidal Zone: Literature Review for Rhizophora mangle L." Journal of Coastal Research. 36 (4): 857–884. doi:10.2112/JCOASTRES-D-19-00088.1. ISSN 0749-0208. S2CID 216143703.
  7. ^ Evans, Lance S.; Bromberg, Alison (2010). "Characterization of cork warts and aerenchyma in leaves of Rhizophova mangle and Rhizophora racemosa". The Journal of the Torrey Botanical Society. 137 (1): 30–38. doi:10.3159/09-RA-024.1. ISSN 1095-5674. JSTOR 40864968. S2CID 86706458.
  8. ^ Alappatt, Joju P. (1 January 2008). "Structure and Species Diversity of Mangrove Ecosystem". Biodiversity and Climate Change Adaptation in Tropical Islands: 127–144. doi:10.1016/B978-0-12-813064-3.00005-3. ISBN 9780128130643.
  9. ^ Aroca, Ricardo; Porcel, Rosa; Ruiz-Lozano, Juan Manuel (1 January 2012). "Regulation of root water uptake under abiotic stress conditions". Journal of Experimental Botany. 63 (1): 43–57. doi:10.1093/jxb/err266. ISSN 0022-0957. PMID 21914658.
  10. ^ a b "Difference Between Prop Root and Stilt Root". Compare the Difference Between Similar Terms. 19 May 2020. Retrieved 27 May 2021.
  11. ^ "Difference Between Prop Root and Stilt Root". Compare the Difference Between Similar Terms. 19 May 2020. Retrieved 27 May 2021.
  12. ^ a b Alappatt, Joju P. (1 January 2008). "Structure and Species Diversity of Mangrove Ecosystem". Biodiversity and Climate Change Adaptation in Tropical Islands: 127–144. doi:10.1016/B978-0-12-813064-3.00005-3. ISBN 9780128130643.
  13. ^ Singh, Jitendra Kumar (1 August 2020). "Structural characteristics of mangrove forest in different coastal habitats of Gulf of Khambhat arid region of Gujarat, west coast of India". Heliyon. 6 (8): e04685. doi:10.1016/j.heliyon.2020.e04685. ISSN 2405-8440. PMC 7426573. PMID 32817898.
  14. ^ Aroca, R.; Porcel, R.; Ruiz-Lozano, J. M. (13 September 2011). "Regulation of root water uptake under abiotic stress conditions". Journal of Experimental Botany. 63 (1): 43–57. doi:10.1093/jxb/err266. ISSN 0022-0957. PMID 21914658.
  15. ^ a b c d Dai, Wenfang; Xiong, Jinbo; Zheng, Hao; Ni, Sui; Ye, Yangfang; Wang, Chunlin (9 June 2020). "Effect of Rhizophora apiculata plantation for improving water quality, growth, and health of mud crab". Applied Microbiology and Biotechnology. 104 (15): 6813–6824. doi:10.1007/s00253-020-10716-7. ISSN 0175-7598. PMID 32514755. S2CID 219543803.
  16. ^ Wang, Huan; Tang, Lei; Wei, Hongling; Lu, Junkai; Mu, Changkao; Wang, Chunlin (31 May 2018). "Transcriptomic analysis of adaptive mechanisms in response to sudden salinity drop in the mud crab, Scylla paramamosain". BMC Genomics. 19 (1): 421. doi:10.1186/s12864-018-4803-x. ISSN 1471-2164. PMC 5984308. PMID 29855258.
  17. ^ Alappatt, Joju P. (1 January 2008). "Structure and Species Diversity of Mangrove Ecosystem". Biodiversity and Climate Change Adaptation in Tropical Islands: 127–144. doi:10.1016/B978-0-12-813064-3.00005-3. ISBN 9780128130643.
  18. ^ a b Schowalter, Timothy D. (2011). Insect Ecology. pp. 397–420.
  19. ^ Thongjoo, Chaisit; Choosak, Sarunya; Chaichana, Ratcha (2018). Tropical Ecology; Soil fertility improvement from commercial monospecific mangrove forests (Rhizophora apiculata) at Yeesarn Village, Samut Songkram Province, Thailand. pp. 59(1), pp.91–97.
  20. ^ Baishya, Somorita; Banik, Sheuli Kangsa; Choudhury, Manabendra Dutta; Das Talukdar, Deepa; Das Talukdar, Anupam (1 January 2020). "Therapeutic potentials of littoral vegetation: an antifungal perspective". Biotechnological Utilization of Mangrove Resources: 275–292. doi:10.1016/B978-0-12-819532-1.00011-1. ISBN 9780128195321. S2CID 219017689.
  21. ^ Department of Agriculture (2020). "Mangrove forest - Department of Agriculture". Department of Agriculture.
  22. ^ Inquirer.net, Scientists find rare species of mangrove Archived 2008-04-30 at the Wayback Machine

External links edit

  • "Rhizophora apiculata Blume". Atlas of Living Australia.