Acropora Microclados
Acropora microclados
Acropora microclados
Invertebrate · Stinging · Hard corals

Acropora Microclados

Acropora Microclados (Ehrenberg, 1834)
syn. Acropora (Acropora) microclados, Acropora assimilis, Acropora microcladose, Heteropora corymbosa, Heteropora microclados, Madrepora (Polystachys) assimilis +3 more
5-20 mCITES IIEndangered
1125

Acropora microclados is a species of acroporid coral that was initially identified by Christian Gottfried Ehrenberg in 1834. This coral species is primarily found in marine, tropical shallow reefs on the upper slopes, usually at depths ranging from 5 to 20 meters (16 to 66 feet). As per the IUCN Red List, it is classified as a vulnerable species, with its population facing a declining trend. Although not commonly found, it is distributed across a wide area, including five regions of 🇮🇩 Indonesia, and is categorized under CITES Appendix II.

Acropora microclados forms colonies with corymbose structures, which can reach widths of up to 1 meter (3.3 feet). The structures consist of branchlets that are short, thin at the ends, orderly arranged, and have branchlet bases reaching up to 10 mm (0.39 in) in width. The color of this coral species is typically pale pink or brown, with tentacles extending during the day and appearing grey. The branchlets contain axial, incipient axial, and radial corallites. Axial corallites, tube-shaped and located at the end of branchlets, are frequently accompanied by incipient axial corallites. Radial corallites, also tube-shaped, are densely distributed up the sides of the branchlets and have nose-shaped openings. Acropora microclados closely resembles Acropora lamarcki, Acropora macrostoma, and Acropora massawensis.

The habitat of this species is characterized by tropical shallow reefs on the upper slopes, situated at depths between 5 and 20 meters (16 and 66 feet) below sea level. The composition of Acropora microclados consists of aragonite, which is a form of calcium carbonate.

It should be noted that Acropora microclados has a wide distribution range despite being uncommon in occurrence. This species can be found in various regions, including the 🌊 Indo-Pacific Ocean, the 🌊 Red Sea, the 🌊 Indian Ocean, the 🌊 Gulf of Aden, the 🌊 East China Sea, the West Pacific, the 🇨🇰 Cook Islands, 🇦🇺 Australia, 🇯🇵 Japan, Southeast Asia, 🇼🇸 Samoa, and Chagos (🇮🇴 British Indian Ocean Territory). Within 🇮🇩 Indonesia, it exists in five distinct regions. The optimal temperature range for this coral species is between 25.48°C and 27.23°C (77.86°F and 81.01°F). Although specific population data is lacking, a decline in numbers is suspected. Acropora microclados faces multiple threats, such as climate change, which leads to rising sea temperatures resulting in bleaching, reef destruction, coral diseases, predation by the starfish Acanthaster planci, and human activities.

Why it's threatened

Residential & commercial development
Housing & urban areas · Commercial & industrial areas · Tourism & recreation areas
Transportation & service corridors
Shipping lanes
Biological resource use
Intentional use: (subsistence/small scale) [harvest] · Unintentional effects: (subsistence/small scale) [harvest] · Motivation Unknown/Unrecorded
Human intrusions & disturbance
Recreational activities
Invasive species, genes & disease
Unspecified species · Named species
Pollution
Type Unknown/Unrecorded · Soil erosion, sedimentation · Ozone
Climate change & severe weather
Temperature extremes · Storms & flooding

This species is particularly susceptible to bleaching, disease, predation and other threats. This species is recorded as having a medium susceptibility to bleaching in both the Maldives and Great Barrier Reef (Muir et al. 2021).

The collection of this species for the aquarium trade may lead to overharvest and localised reductions in abundance, especially for populations of naturally rare species (Bruckner and Borneman 2006). However, the wild collection of corals is highly selective and considered low impact in the long-term relative to other activities such as coral mining and dynamite fishing (Green and Shirley 1999, Pratchett et al. 2020).

In general, the major threat to Acropora corals is global climate change, in particular, temperature extremes leading to bleaching induced mortality, and an increased susceptibility to disease (Hoegh-Guldberg et al. 2007, Hughes et al. 2017; 2018; 2019). Bleaching can lead to mortality and a reduction in both coral cover and effective population sizes. It also disrupts coral reproduction. Regional coral extinction events following thermally anomalous events are increasingly reported (Sheppard et al. 2020, Richards et al. 2021, Muir et al. 2021). In addition, climate change is predicted to lead to an increased severity of ENSO events and storm intensity, and longer-term changes in ocean chemistry impacting calcification, along with an increase in the severity of flood and fire events impacting catchments.

This species has a corymbose plate growth form and is susceptible to predation by crown-of-thorns seastar. Crown-of-thorns (COTS) (Acanthaster spp.) are found throughout the Pacific and Indian Oceans and the Red Sea. Crown-of-thorns are voracious predators of reef-building corals, with a preference for branching and tabular corals such as Acropora species. Populations of the crown-of-thorns starfish have greatly increased since the 1970s and have been known to consume large areas of coral reef habitat. Increased breakouts of COTS has become a major threat to some species, and have contributed to the overall decline and reef destruction in the Indo-Pacific region. The effects of such an outbreak include the reduction of abundance and surface cover of living coral, reduction of species diversity and composition, and overall reduction in habitat area. Crown-of-thorn outbreaks are particularly concerning in coral communities that are recovering from disturbances such as coral bleaching as feeding on remnant survivors and juveniles can further inhibit community recovery (Haywood et al. 2019).

Coral disease has emerged as a serious threat to coral reefs worldwide and a major cause of reef deterioration (Weil et al. 2006). The numbers of diseases and coral species affected, as well as the distribution of diseases have all increased dramatically within the last two decades (Porter et al. 2001, Green and Bruckner 2000, Sutherland et al. 2004, Weil 2004). Coral disease epizootics have resulted in significant losses of coral cover and were implicated in the dramatic decline of acroporids in the Florida Keys (Aronson and Precht 2001, Porter et al. 2001, Patterson et al. 2002). In the Indo-Pacific, disease is also on the rise with disease outbreaks recently reported from the Great Barrier Reef (Willis et al. 2004, Haapkyla et al. 2013), Indonesia (Haapkyla et al. 2007, Subhan et al. 2020), Thailand (Lamb et al. 2014), Marshall Islands (Jacobson 2006), Micronesia (Myers and Raymundo 2009), American Samoa (Work and Rameyer 2005), and the northwestern Hawaiian Islands (Aeby et al. 2006), the Cocos (Keeling) Islands (Preston and Richards 2021), the Maldives (Montano et al. 2015), and the Persian Gulf (Aeby et al. 2020). Increased coral disease levels on the GBR were correlated with increased ocean temperatures (Boyett et al. 2007, Howells et al. 2020) supporting the prediction that disease levels will be increasing with higher sea surface temperatures. As environmental conditions continue to change, it is predicted that conditions on temperate reefs will become favourable for coral diseases and thermodependent bacteria (Bally and Garrabou 2007, Brodnicke et al. 2019) and the geographical range of tropical coral diseases will extend (Vergés et al. 2019).

Localized threats to corals include fisheries, human development (industry, settlement, tourism, and transportation), changes in native species dynamics (competitors, predators, pathogens and parasites), invasive species (competitors, predators, pathogens and parasites), dynamite fishing, chemical fishing, pollution from agriculture and industry, domestic pollution, sedimentation, and human recreation and tourism activities. The severity of these combined threats to the global population of each individual species is not known.

Threat classification from the IUCN Red List.

Comments

Please, sign in to leave a comment

Continue with a social account — yours will be created automatically.

No comments yet — be the first.

Last Update: June 28, 2026