- kingdomChromista
- ›phylumForaminifera
- ›classGlobothalamea
- ›orderRotaliida
- ›familyGlobigerinidae
- ›genusTrilobatus
Images attached to GBIF records (field photographs), from . Open licences; click for the record.
Trilobatus sacculifer
Trilobatus sacculifer (Brady, 1877)
First described in: Spezzaferri, S., Kucera, M., Pearson, P. N., Wade, B. S., Rappo, S., Poole, C. R., Morard, R., & Stalder, C. (2015). Fossil and Genetic Evidence for the Polyphyletic Nature of the Planktonic Foraminifera “Globigerinoides”, and Description of the New Genus Trilobatus. PLOS ONE, 10(5): e0128108. https://doi.org/10.1371/journal.pone.0128108
Trilobatus sacculifer is a spinose planktonic foraminiferan belonging to the family Globigerinidae. It is one of the most heavily used species in paleoceanography for reconstructing past sea-surface temperatures and surface-water properties using geochemical proxies such as δ18O, Mg/Ca and boron isotopes. Although it shows considerable morphological variability, including forms with and without a distinctive sac-like final chamber, modern molecular studies indicate that all of these morphotypes belong to a single, genetically homogeneous biological species. Because of its ecological importance, long fossil record and ease of culture in the laboratory, T. sacculifer has become a model organism for studies of symbiosis, calcification, ocean acidification and the marine carbon cycle.
Descriptions from checklists and floras indexed by GBIF
description
1862 Globigerina helicina d’ Orbigny; Carpenter, Parker & Jones: pl. 12, fig. 11 [note: not valid species name as ‘ Globigerina helicina ’ was used by d’ Orbigny for a different species concept; see remarks]. 1877 Globigerina sacculifera Brady: 535 [original description but not illustrated]. 1884 Globigerina sacculifera Brady: 604, pl. 80, figs 11 – 17 and pl. 82, fig. 4 [numerous samples from the Challenger Expedition; illustrations reproduced in Jones (1994)]. 1940 Globigerinoides sacculifera (Brady); Coryell & Rivero: 340, pl. 42, figs 24, 25, 32. 1954 Globigerinoides sacculifera (Brady); Cushman, Todd & Post: 369, pl. 91, fig. 7. 1957 Globigerinoides triloba sacculifer (Brady); Bolli: 113, pl. 25, figs 5 a – 6. 1959 Globigerinoides triloba sacculifera (Brady); Blow: 188, pl. 11, fig. 63 a, b. 1964 Globigerinoides triloba sacculifera (Brady); LeRoy: F 42, pl. 14, fig. 18. 1967 Globigerinoides quadrilobatus sacculifer (Brady); Closs: 340, pl. 1, fig. 21. 1970 Globigerinoides trilobus sacculifer (Brady); Bolli: 626, pl. 1, fig. 5. 1983 Globigerinoides sacculifer (Brady); Pujol & Duprat: 612, pl. 4, figs 4, 5. 1983 Globigerinoides sacculifer (Brady); Kennett & Srinivasan: 66, pl. 1
Systematic taxonomy of the Trilobatus sacculifer plexus and descendant Globigerinoidesella fistulosa (planktonic foraminifera)
discussion
Remarks. Trilobatus sacculifer is distinguished from T. trilobus, T. immaturus and T. quadrilobatus by the presence of a distinctive flattened, sac-like chamber which is often elongate or lobate; the other three morphospecies possess only globose, (near-) spherical chambers throughout all adult chambers. It also differs from these morphotypes by the presence of a distinct lip bordering the primary aperture. Trilobatus sacculifer differs from G. fistulosa by the lack of clear protuberances on any of the final chambers, although the final chamber may be lobate.
Systematic taxonomy of the Trilobatus sacculifer plexus and descendant Globigerinoidesella fistulosa (planktonic foraminifera)
materials_examined
Type locality. The type material for T. sacculifer is from a loose ‘ chalk’ block, from New Ireland, Papua New Guinea (Brady 1877). The ‘ chalk’ block was in fact a fragment of a carved figure, made by local inhabitants of the island and obtained by missionary Reverend G. Brown (Brown 1877; pp. 140 – 141; see also Liversidge 1877; Parker 1967). Rather than being sourced from the mainland itself, the ‘ chalk’ block was actually derived from seafloor deposits, where it had been extruded, apparently by earthquakes (Brown 1877) and / or volcanic activity (Brady 1884), onto the shore and then used by local inhabitants for a carved figure. The surrounding seafloor deposits off New Ireland indeed contain such ‘ chalk’ material (e. g. Exon et al. 1986), and are likely the source of the type material for T. sacculifer. Taxonomic history. Brady (1877) observed that despite a specimen with a sac-like final chamber having been previously illustrated by Carpenter et al. (1862, pl. 12, fig. 11) under the name Globigerina helicina d’ Orbigny, the helicina form had actually been described to represent a very different morphology (typically viewed as a morphological variant of Globigerinoides ruber
Systematic taxonomy of the Trilobatus sacculifer plexus and descendant Globigerinoidesella fistulosa (planktonic foraminifera)
From Wikipedia (CC BY-SA), quoted section by section
Description
Trilobatus sacculifer produces a hyaline, calcareous, multi-chambered test with a trochospiral coiling pattern and spinose, cancellate wall texture. The test typically has three to four globular chambers in the final whorl, with a primary umbilical–extraumbilical aperture and, in many specimens, one or more supplementary apertures on the spiral side. The wall is perforated by relatively large, often hexagonal pores arranged in a honeycomb-like network characteristic of the sacculifer lineage. Morphologically, the species is highly variable and traditionally subdivided into morphotypes based on the outline and the presence or absence of a sac-like final chamber. Classical morphospecies include: Trilobatus trilobus, Trilobatus sacculifer sensu stricto, T. quadrilobatus, T. immaturus, T. hystricosus. A global genetic survey of all recent morphotypes using SSU rRNA and ribosomal markers found extremely low rDNA variation and no correlation between genetic and morphological differentiation, indicating that this morphological plexus represents a single biological species. For modern samples, current practice is therefore to treat all morphotypes as Trilobatus sacculifer, with informal descriptors such as "with sac" or "without sac" where needed. In spinose species such as T. …
Range & habitat
Trilobatus sacculifer is found primarily in tropical and subtropical oceans, usually in the photic zone. As a mixotroph, it supplements heterotrophic feeding on phytoplankton and small particles with photosynthesis performed by its endosymbionts, and it is an important grazer and calcifier within the microzooplankton community. Trilobatus sacculifer hosts intracellular photosynthetic algal symbionts, typically dinoflagellates, which reside within the host cytoplasm. Recent molecular evidence also shows that the species can harbor the Pelagodinium beii, which performs photosymbiosis within the host. This discovery, reported by Takagi et al. (2024), reveals an independent photosymbiotic acquisition in the Trilobatus lineage. Experimental work using fast repetition rate fluorometry (FRRf) and chlorophyll fluorescence imaging has characterised the spatial distribution and activity of symbionts within individual foraminifera, including T. sacculifer, and documented ontogenetic changes in symbiont density and photosynthetic performance as the shell grows. Comparative phylogenetic studies of symbiont-bearing planktonic foraminifera indicate that photosymbiosis has evolved multiple times and contributed to ecological success and diversification of lineages including Trilobatus.
What it does
Individuals grow by sequential addition of chambers in trochospiral arrangement. At reproductive maturity, specimens typically develop a terminal sac-like chamber (in sacculifer morphotypes) and undergo gametogenesis, during which the cytoplasm is converted into numerous biflagellate gametes that are released into the surrounding water. Time-series studies based on plankton tows and sediment trap fluxes have demonstrated that reproduction in T. sacculifer is often synchronised with the lunar cycle, with increased abundances of juveniles appearing in surface waters roughly one week after full moon and distinct lunar-related peaks in shell flux. Such synchrony may enhance gamete encounter rates in the open ocean. Diel vertical migration, with symbiont-bearing individuals residing shallower during the day and slightly deeper at night reflects a trade-off between light harvesting (for the photosymbionts) and predation risk.
In human culture
The Trilobatus sacculifer lineage first appears in the late Oligocene, when the earliest forms with supplementary apertures on the spiral side and sacculifer-type cancellate wall texture evolved from Globoturborotalita woodi. These early representatives were historically described as "Globigerinoides primordius" and "G. trilobus". Through the early Miocene, this lineage developed the typical trilobate test and, in younger intervals, the sac-like final chamber that characterises Neogene T. sacculifer sensu lato. Total-evidence phylogenies place Trilobatus as a paraphyletic stem group that gave rise to the genera Praeorbulina and Orbulina, and ultimately to the Neogene spinose genera Sphaeroidinellopsis and Sphaeroidinella. Trilobatus sacculifer persists from the Oligocene to the present, making it one of the longest-ranging spinose planktonic foraminifera and an important element of Neogene–Quaternary biostratigraphy.
Where it has been recorded
Recorded sightings
—
geo-referenced records in GBIF, from museums, herbaria and field observers.
Drag the globe to turn it. Dots are where records exist, not a range map; darker means more records.
In the stacks
Searching the stacks…
Every page naming Trilobatus sacculifer in the Biodiversity Heritage Library →
From the GBIF Backbone Taxonomy and occurrence records (GBIF.org), with Wikipedia and the Source Library. GBIF species 9344287.