Umimayanthus, Montenegro, Sinniger & Reimer, 2015
publication ID |
https://doi.org/10.1163/18759866-BJA10069 |
persistent identifier |
https://treatment.plazi.org/id/03D23E47-4876-5663-8C9D-C6D90A157664 |
treatment provided by |
Felipe |
scientific name |
Umimayanthus |
status |
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The specificity of host-zoantharian associations in Umimayanthus has not been thoroughly studied, primarily because of the taxonomic uncertainty of the groups involved in the symbioses. This study provided a rare situation where taxonomists with specialties in both taxa worked in collaboration to provide a more complete picture of associations (see also Swain & Wulff, 2007).
Earlier work on host-zoantharian associations concluded that it is relatively common for a single zoantharian species to associate with multiple host species, but it is more unusual to find one host associated with more than one zoantharian species ( Swain & Wulff, 2007). It is worth noting that multiple exceptions are known for host sponges in the genera Agelas Duchassaing & Michelotti, 1864 ,
Cribrochalina Schmidt, 1870 View in CoL , Xestospongia de Laubenfels, 1932 View in CoL , Svenzea Alvarez, van Soest & Rützler, 2002 View in CoL and Hymeniacidon Bowerbank, 1858 View in CoL ( Swain & Wulff, 2007; Montenegro et al., 2020). However, in general terms, this pattern first observed by Swain & Wulff (2007) appears to be valid for host- Umimayanthus View in CoL associations ( table 2). For instance, U. wunanggu sp. nov. was found in association with two different sponge species in the genus Endectyon View in CoL ; U. mirnangga sp. nov. was in association with two species in two genera, as was U. discolor sp. nov.; and U. raksasa sp. nov. is likely associated with more than one species in the genus Phakellia View in CoL . Remarkably, Caribbean U. parasiticus View in CoL has been reported in association with 23 species of sponges across 10 different genera of host sponges ( Swain & Wulff, 2007; Montenegro et al., 2020). Other species such as U. chanpuru View in CoL , U. miyabi View in CoL and U. nakama View in CoL are likely associated with multiple genera of encrusting and calcareous sponges, but no detailed taxonomic data are yet available on the identity of their host sponges ( Montenegro, pers. observ.).
The only confirmed exceptions to this generalized pattern are U. cf. aruensis , which appears to have a specialized association with Trikentrion flabelliforme View in CoL , and U. kanabou View in CoL consistently found in association with a gorgonian in the genus Ellisella View in CoL , although the identity of the species remains unknown ( Fujii et al., 2021). Other species such as U. jebarra sp. nov. and U. lynherensis sp. nov. are only known from a single record, and thus is not possible to draw conclusions on the specificity of the associations for these species.
On the other hand, the host sponges in this study appear to be quite restricted to
CONTRIBUTIONS TO ZOOLOGY 93 (2024) 466–522
the specific Umimayanthus species, with most of them associated with a single zoantharian species. Two exceptions were found: Trikentrion flabelliforme , which had associations with two phylogenetically distinct species, U. cf. aruensis and U. discolor sp. nov.; and Endectyon (Endectyon) fruticosum , which was associated with U. wunanggu sp. nov. and U. mirnangga . sp. nov. Given that the latter two sibling species are closely phylogenetically related, we speculate that some level of overlap in host preference is to be expected ( Brändle et al., 2000; Blomberg & Garland, 2002).
Based on the results of our phylogenetic analyses, it is clear that these species represent a large radiation of sponge-associated Umimayanthus , with species and clades having generally different niches, based on host species and depth. For instance, Clade I was found inhabiting depths of 12–39 m, Clade II between 41–59 m, and Clade III overlapping all other depth ranges with records from depths of 4– 100 m. However, a closer look revealed strati- fication by depth within Clade III, with U. raksasa sp. nov. and U. lytherensis sp. nov. restricted to deeper waters while U.discolor sp. nov. inhabits shallow waters.
Many studies have shown the Central Indo-Pacific (the Coral Triangle) to be the center of marine biodiversity for a vari- ety of marine taxa such as algae, larger benthic forams, crustaceans, fishes, mol- luscs, and scleractinian corals ( Hoeksema, 2007; Förderer et al., 2018); but whether the region also harbors high diversi- ties of many less studied taxa, including zoantharians, still needs to be examined ( Reimer et al., 2014). The current study, focused on species associated with only four families of sponges, indicates that zoantharians may also follow the Coral Triangle centre of biodiversity, and further studies are needed to better confirm this.
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Kingdom |
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Phylum |
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Class |
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Order |
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Family |
Umimayanthus
Montenegro, Javier, Fromont, Jane, Richards, Zoe, Kise, Hiroki, Gomez, Oliver, Hoeksema, Bert W. & Reimer, James Davis 2024 |
U. wunanggu
Montenegro & Fromont & Richards & Kise & Gomez & Hoeksema & Reimer 2024 |
U. mirnangga
Montenegro & Fromont & Richards & Kise & Gomez & Hoeksema & Reimer 2024 |
U. discolor
Montenegro & Fromont & Richards & Kise & Gomez & Hoeksema & Reimer 2024 |
U. raksasa
Montenegro & Fromont & Richards & Kise & Gomez & Hoeksema & Reimer 2024 |
U. cf. aruensis
Montenegro & Fromont & Richards & Kise & Gomez & Hoeksema & Reimer 2024 |
U. jebarra
Montenegro & Fromont & Richards & Kise & Gomez & Hoeksema & Reimer 2024 |
U. lynherensis
Montenegro & Fromont & Richards & Kise & Gomez & Hoeksema & Reimer 2024 |
Umimayanthus
Montenegro, Sinniger & Reimer 2015 |
U. chanpuru
Montenegro, Sinniger & Reimer 2015 |
U. miyabi
Montenegro, Sinniger & Reimer 2015 |
U. nakama
Montenegro, Sinniger & Reimer 2015 |
Svenzea Alvarez, van Soest & Rützler, 2002
Alvarez, van Soest & Rutzler 2002 |
Xestospongia
de Laubenfels 1932 |
Endectyon
Topsent 1920 |
Trikentrion flabelliforme
Hentschel 1912 |
Cribrochalina
Schmidt 1870 |
Phakellia
Bowerbank 1862 |
Hymeniacidon
Bowerbank 1858 |