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Fusulinida

Fusulinida is an extinct order of benthic foraminifera within the class Fusulinata, characterized by elongated, fusiform or spherical tests composed of microgranular calcite, often reaching large sizes relative to other foraminifers.^[1] These single-celled marine protists thrived in shallow, well-lit neritic environments with normal marine salinity of approximately 35‰ and moderate water agitation, typically at depths of 10–50 meters.^[2] Originating in the Late Mississippian (Chesterian) and peaking in diversity during the Pennsylvanian and Permian periods, fusulinids became extinct by the end of the Permian (Ochoan stage) during the end-Permian mass extinction, leaving no direct modern descendants; recent studies indicate that global cooling drove their diversification, while warming contributed to their extinction during the late Paleozoic.^[2]^[1]^[3] As one of the most abundant and geographically widespread groups of Paleozoic foraminifera, comprising hundreds of genera, fusulinids played a key role in forming carbonate deposits and limestones through their biomineralization processes.^[1]^[4] Their tests, featuring complex internal architecture with multiple coiled chambers connected by foramina and layered walls (including tectum, diaphanotheca, and keriotheca), exhibit rapid evolutionary changes that make them excellent index fossils for biostratigraphic correlation of Upper Paleozoic rocks across continents.^[5]^[4] Recent analyses reveal that their microgranular structure consists of low-magnesium calcitic nanograins, challenging traditional views and suggesting phylogenetic links to modern globothalamean foraminifera.^[1] Fusulinids are particularly significant in paleoenvironmental reconstructions, as their distribution in limestone and calcareous shale formations, often associated with brachiopods and crinoids, indicates stable, warm, tropical marine conditions during the late Paleozoic.^[5]^[6] Their abundance in well-preserved assemblages far exceeds that of other Upper Carboniferous and Permian invertebrate groups in many regions, aiding in precise dating of oil- and gas-bearing strata.^[4] Studies of fusulinid life-history stages, including juvenile and adult forms, further illuminate their growth patterns and ecological adaptations in shallow seas.^[7]

Morphology

Test Structure

The test of fusulinids exhibits a distinctive fusiform morphology, spindle-shaped and elongated, which distinguishes them among Paleozoic foraminifera. This external form typically measures from approximately 0.5 mm in length for primitive species to up to 5 cm in advanced forms, reflecting adaptations for benthic lifestyles in marine environments.^[8]^[9]^[10] The test is segmented and constructed through planispiral coiling, initiating with a small, spherical proloculus as the protoconch or initial chamber, around which subsequent volutions coil tightly. Septa, the partitioning walls, curve and fold to form these volutions, creating a series of expanding chambers that give the overall fusiform profile; the number of volutions can reach 6–8 or more in mature specimens. The wall often features multilayered structures, including an outer tectum, middle diaphanotheca, and inner keriotheca in advanced forms.^[11]^[12]^[13] Composed primarily of secreted low-magnesium calcitic nanograins (10-50 nm), traditionally described as microgranular calcite with apparent grains of 0.5 to 6.0 μm in diameter, confirming a biomineralized rather than agglutinated structure.^[14] Wall thickness varies significantly across genera, often ranging from 0.01–0.02 mm in early volutions to thicker layers up to 0.05 mm or more in outer ones, with some advanced forms developing multilayered structures including a perforate outer layer (antetheca) that tapers into tiny pores for limited environmental exchange. Porosity is generally low, with alveoli in the wall forming small, branching pores through the tectum, though this varies by genus—thinner, less porous walls in primitive groups like Endothyridae contrast with denser, slightly more porous builds in later Fusulinidae.^[15]^[12]^[14] The external surface of the test is typically smooth, facilitating identification based on overall shape, but variations occur across groups; for instance, genera like Triticites display longitudinal ridges or costae, while others such as Fusulina maintain a polished, unornamented texture, and rare forms may bear subtle spines or striae. These external features, including the fusiform outline, play a key role in taxonomic differentiation among fusulinid genera.^[16]^[17]

Internal Morphology

The internal morphology of fusulinids is characterized by tightly coiled chambers arranged in a planispiral pattern, where each successive volution wraps around the previous one with increasing diameter, forming a fusiform or discoidal test.^[18] This coiling is typically evolute to involute. The chambers increase in size outward, creating a spirothecal wall structure that supports the organism's benthic lifestyle.^[18] Septal structures divide the chambers and are a primary diagnostic feature, consisting of primary septa that are often fluted or folded to varying degrees, with secondary septa known as septula forming minor partitions perpendicular to the coiling axis.^[18] In primitive fusulinids, septa are relatively straight with minimal fluting, while in more derived taxa, intense folding produces cuniculi—small tunnel-like chamberlets—especially in the lower parts of chambers, where fluting height can reach up to half the chamber height.^[11] Axial septa, prominent in advanced suborders like Neoschwagerinina, extend along the coiling axis and further subdivide chambers into alveoli, enhancing structural complexity.^[18] The proloculus, or initial chamber, is typically spherical and serves as the embryonic starting point, with diameters ranging from 0.03 to 0.9 mm across fusulinid taxa, though most fall between 0.05 and 0.2 mm in early forms.^[11] Its size and wall thickness—often 20-40 microns—vary systematically between microspheric (small, asexual) and megalospheric (larger, sexual) generations, providing a key metric for species identification.^[11] In megalospheric forms, the proloculus is notably larger, sometimes up to 0.6 mm, reflecting dimorphic reproduction.^[18] Communication between chambers occurs primarily through foramina or striae in the septa, forming a network of tunnels that allow cytoplasmic flow and gas exchange.^[18] These openings are often single and wide in early chambers, narrowing or becoming multiple in later volutions, with discontinuous chomata (raised ridges) bordering the tunnels in some lineages to direct flow.^[11] Unlike apertural openings in other foraminifera, fusulinid inter-chamber connections emphasize internal connectivity via stolons or siphonal canals, supporting the organism's elongated test shape.^[18]

Taxonomy

Classification

Fusulinida is an extinct order of foraminifera classified within the subclass Fusulinana (also termed Fusulinina in some taxonomic schemes), class Fusulinata, phylum Foraminifera, infrakingdom Rhizaria, subkingdom Harosa, and kingdom Chromista.^[19] This placement reflects their position as calcareous, multichambered protists with a fossil record confined to the Paleozoic Era.^[1] Historically, the taxonomy of Fusulinida has undergone revisions, particularly in distinguishing Paleozoic calcareous foraminifera from other groups based on test wall microstructure. Early classifications grouped most Paleozoic foraminifera under a single high-level taxon, Fusulinata, primarily due to shared microgranular wall compositions, but recent analyses have proposed refined schemes dividing them into three classes to better account for ultrastructural variations.^[20]^[21] For instance, molecular phylogenetic studies of extant foraminifera have led to Fusulinida being regarded as incertae sedis, as their extinct status prevents direct genetic comparison, though their biomineralization style suggests affinities with modern calcareous groups.^[1] More recent revisions, such as those from 2021, recognize up to nine families within the group.^[13] Key diagnostic traits at the order level include tests composed of microgranular walls made of tightly packed, secreted granules of low-Mg calcite (typically 1–5 μm in size), which differ from the porcelaneous or hyaline walls of many modern foraminifera.^[20]^[22] Additionally, Fusulinida exhibit complex internal septation, often with secondary calcareous deposits such as axial tectoria and chomata that partition chambers and support structural integrity.^[13] While Fusulinida share some superficial similarities with modern larger benthic foraminifera, such as multilocular tests and benthic habitats, their microgranular wall structure and Paleozoic-specific evolutionary adaptations set them apart, emphasizing their distinct phylogenetic position within foraminiferal diversity.^[1]^[20]

Diversity and Key Genera

The Fusulinida achieved their greatest diversity during the late Paleozoic, encompassing hundreds of genera and thousands of described species. The superfamily Fusulinacea within the order Fusulinida comprises eight families and 166 genera.^[23] This diversity reflects their adaptation to shallow-marine environments, with representative forms varying in test morphology from simple to complex coiling patterns. Key genera include Fusulina, an early representative known for its simple, tightly coiled tests with a fusiform shape and alveolar wall structure.^[24] Triticites, prominent in the mid-Permian, is characterized by robust, subspherical to elongate tests that aided in biostratigraphic correlation in North American basins.^[17] Schwagerina, an advanced genus, featured elongated fusiform shapes with numerous septa and a more complex internal architecture, exemplifying evolutionary progression within the group. Patterns of generic turnover are evident in the replacement of primitive, less specialized forms by advanced lineages, such as the staffelids, which developed more intricate septal folding and test ornamentation over time.^[25] Endemic distributions highlight regional variations, with higher diversity in Tethyan realms—where tropical conditions supported prolific speciation—compared to lower levels in North American shelves, often two to three times less diverse.^[26]

Evolutionary History

Origin and Radiation

The Fusulinida first appeared in the Early Carboniferous (Visean stage), approximately 350 million years ago, with primitive forms such as Earlandia representing early calcareous foraminifera that exhibited simple, tubular tests and marked the transition to more complex fusulinid structures. These ancestral lineages, including potential derivations from Allogromiida via Parathuramminida or from endothyrides like Loeblichiidae, emerged during the Early Carboniferous, following the recovery from Late Devonian extinction events, such as the Hangenberg event around 359 Ma, which opened ecological niches in shallow marine environments.^[18] The initial diversification involved innovations in test morphology, such as the development of enrolled chambers and microgranular calcite walls, enabling adaptation to photic zone habitats.^[18] During the Carboniferous, Fusulinida underwent an explosive radiation, beginning in the Mississippian (Early Carboniferous, Tournaisian-Visean stages) with genera like Ozawainella and Millerella, which featured simple coiled tests and inhabited carbonate platforms. This diversification intensified in the Pennsylvanian (Late Carboniferous, Bashkirian-Moscovian stages), where more advanced forms such as Fusulina evolved fusiform, rice-grain-like tests, contributing to their role in reef-building communities and widespread fossil assemblages in limestones.^[18] By the late Carboniferous, over 100 genera had emerged, reflecting peak diversity tied to the resurgence of shallow-water carbonate ecosystems.^[18] Key drivers of this radiation included the availability of sunlit, oligotrophic shallow marine habitats in low-energy settings like bays and lagoons, which proliferated after the Devonian extinctions reduced competition from other benthic groups.^[18] Symbiosis with photosynthetic algae further propelled their success, allowing efficient energy acquisition in tropical-subtropical waters and supporting larger test sizes and higher abundances.^[27] Originating in paleotropical regions such as the Tethyan realm, Fusulinida achieved a near-cosmopolitan distribution by the late Carboniferous, spreading across Eurasia, North America, and Gondwana margins while excluding isolated areas like parts of Australia and Antarctica.^[18]

Decline and Extinction

Fusulinid diversity reached its zenith during the Early Permian (Cisuralian), particularly in the Asselian and Sakmarian stages, before initiating a prolonged decline beginning in the Kungurian stage of the late Cisuralian and continuing through the Guadalupian (Middle Permian). This reduction involved a progressive loss of species, with approximately 59% of fusulinid species disappearing between the Sakmarian-Artinskian transition and the early Kungurian, followed by further attrition in the Roadian and Wordian stages of the early Guadalupian. The decline was exacerbated by falling sea levels, which led to habitat constriction in shallow marine environments, increased salinity fluctuations, and shifts in substrate availability that disadvantaged these warm-water, symbiont-bearing foraminifera.^[28]^[29]^[30] In the late Guadalupian (Capitanian stage), the decline accelerated dramatically, culminating in the end-Guadalupian (end-Capitanian) extinction event that eliminated 96% of fusulinacean species, including all members of the large-test families Neoschwagerinidae and Verbeekinidae. This biotic crisis was primarily driven by the Kamura cooling event, a short-lived glacial episode that lowered tropical sea surface temperatures and disrupted the warm, stable conditions essential for fusulinid symbiosis with photosynthesizing algae, leading to widespread habitat loss for these equatorial-adapted taxa. By the Lopingian (Late Permian), fusulinid diversity had plummeted, with only a few genera persisting in restricted Tethyan realms.^[31]^[32]^[33] The terminal extinction of Fusulinida occurred during the end-Permian mass extinction event approximately 252 million years ago, resulting in the near-total annihilation of the order, with 96% of fusulinid genera vanishing globally. The few late Lopingian survivors, such as the genus Colaniella, were confined to shallow carbonate platforms in the eastern Tethys region, where they briefly persisted in the Palaeofusulina-Colaniella assemblage before succumbing to the crisis. Leading hypotheses for this wipeout include massive volcanism from the Siberian Traps, which triggered rapid global warming, marine anoxia through expanded oxygen minimum zones, and ocean acidification that dissolved calcareous tests; additionally, emerging competition from more resilient, non-symbiont-dependent foraminiferal groups may have intensified selective pressures on fusulinids during environmental stress.^[28]^[34]^[35]^[36]^[37] Following the end-Permian event, Fusulinida exhibited no significant recovery, with only two non-fusulinoidean genera briefly extending into the Early Triassic before the order's complete disappearance from the fossil record. This absence persisted throughout the Mesozoic Era, underscoring Fusulinida's status as a quintessential Paleozoic group that failed to adapt to the post-extinction world dominated by new calcareous and agglutinated foraminiferal lineages.^[34]^[38]^[13]

Paleobiology

Habitat and Ecology

Fusulinids, as larger benthic foraminifera, predominantly inhabited shallow, warm, oligotrophic marine environments in tropical to subtropical paleolatitudes during the Late Paleozoic, particularly within the photic zone above 25-30 meters depth where light penetration was optimal.^[18] These settings included carbonate platforms, reefs, and shelves in tropical to subtropical regions worldwide, including the Tethyan realm, often preserved in light grey limestones or calcareous shales with minimal siliciclastic input, associated with phylloid algae, corals, and other reef-building organisms.^[18] Such habitats featured normal marine salinity around 35‰ (ppt), well-oxygenated waters, and low to moderate energy levels, favoring clear, sunlit conditions over deeper or turbid environments.^[2]^[39] As benthic organisms, fusulinids led an epifaunal to shallow infaunal lifestyle, with many species attaching to or resting on substrates like algal mats or sediments, while others burrowed slightly into soft bottoms.^[40] Evidence for this comes from fossil test orientations in sediments, where elongate or fusiform shells often align parallel to bedding planes or current directions, indicating post-mortem transport minimal and in situ deposition in stable, low-energy seafloors.^[41] Their robust, multichambered tests, adapted for buoyancy and protection, supported this bottom-dwelling mode without evidence of fully pelagic habits in most taxa.^[18] Ecologically, fusulinids engaged in photosymbiosis with endosymbiotic microalgae, likely green algae, which contributed to calcification and energy acquisition through photosynthesis. This relationship is inferred from test translucency and structural features like alveolar walls that enhanced light transmission, optimizing surface-to-volume ratios for symbiont exposure in varying light regimes. At the trophic level, they functioned primarily as herbivores or detritivores, grazing on microalgae or organic detritus via reticulopodia extending from test apertures, with their large body sizes enabling low metabolic rates and K-selected strategies in nutrient-limited settings.^[18] This symbiosis and feeding mode positioned them as key primary consumers in Paleozoic marine food webs, enhancing reef ecosystem stability.

Growth and Reproduction

Fusulinids exhibited a complex life cycle inferred from the dimorphism observed in their fossilized tests, consisting of alternation between sexual and asexual reproduction, a pattern common among larger benthic foraminifera. Asexual reproduction occurred primarily through schizogony or multiple fission within the microspheric generation (agamont), which featured a small proloculus and produced numerous megalospheric offspring (gamonts) with a larger proloculus via fission of the protoplasm into hundreds of juveniles.^[42] The megalospheric generation, dominant in the fossil record, likely underwent sexual reproduction by releasing gametes into the water column, though direct evidence such as gametes or embryos is rarely preserved in fusulinid fossils, limiting confirmation to the presence of embryonic apparati in some taxa like Eopolydiexodina.^[42] This alternation maintained genetic diversity and population resilience, with trimorphism (including schizonts) hypothesized in advanced forms based on test variations.^[43] Test growth in fusulinids proceeded by sequential addition of chambers in a planispiral coil, forming a fusiform shell that expanded logarithmically, with each volution increasing in size according to a spiral pattern characteristic of many coiled foraminiferal tests. Chamber addition rates varied by species and environmental conditions, but typically involved rapid formation of new chambers along the apertural face, resulting in approximately 10–20 chambers per whorl in mature individuals and a near-doubling of overall test volume per complete volution.^[44] Growth increments, visible as fine banding in thin sections of the spirotheca and septa, reflect periodic deposition possibly tied to seasonal or daily cycles, analogous to modern foraminifera.^[45] Lifespan estimates for fusulinids, derived from these growth bands and comparisons to extant larger foraminifera, range from 1 to 5 years, with smaller species completing development in under a year and larger forms like those in the genus Schwagerina requiring several years to reach maturity.^[44] This duration aligns with the observed chamber formation rates and test size, where full coiling to 6–10 volutions marked reproductive adulthood before fission or gamete release.^[45]

Geological Applications

Biostratigraphy

Fusulinids are widely utilized as index fossils in biostratigraphy for correlating Upper Carboniferous to Lower Permian marine strata, owing to their rapid evolutionary turnover and abundance in carbonate-rich deposits across paleocontinents.^[13] In North American schemes, particularly in the Midcontinent and Appalachian regions, zonation is defined by the stratigraphic ranges of key genera such as Fusulinella, Beedeina, and Triticites. For instance, the Fusulinella Zone characterizes the upper Atokan (Middle Pennsylvanian), while the Beedeina Zone encompasses the Desmoinesian with subzones based on species like B. leei and B. girtyi, and the Triticites Zone spans the Missourian to Virgilian, including subzones such as the T. ohioensis Subzone in formations like the Brush Creek Limestone.^[46] These zones enable regional correlations within basins like the Eastern Interior and Appalachian, tying fusulinid assemblages to specific limestone members for precise stratigraphic placement.^[46] Internationally, fusulinid zonation aligns with Tethyan stages, where genera like Schwagerina and Parafusulina define biozones for the Cisuralian and Guadalupian Series. Examples include the Schwagerina Zone for the upper Sakmarian to Artinskian and the Eopolydiexodina Abundance Zone in the Roadian, facilitating correlations across the Tethys Realm from Turkey to South China.^[47] The temporal resolution of these schemes is high, with species turnover occurring every 1–5 million years, allowing for dating of Carboniferous–Permian rocks to within a few million years in well-preserved sections.^[48] Preservation of fusulinids exhibits biases toward carbonate environments, where they are commonly found intact in limestones due to minimal post-depositional alteration, but they are rare in shales owing to compaction and pressure solution that deform tests.^[49] Extraction and study typically involve preparation methods such as brief acid etching with hydrochloric or acetic acid to dissolve surrounding matrix and reveal test microstructures without damaging the fusulinid shells.^[23] For global correlation, fusulinid biozones are integrated with conodont and ammonoid scales, such as aligning the Triticites Zone with the Streptognathodus conodont Zone and goniatite-ammonoid stages in the Pennsylvanian, or the Schwagerina Zone with the Sweetognathus conodont Zone in the Early Permian, enabling cross-continental synchronization of strata.^[16] This integration has refined the international chronostratigraphic framework, particularly for the Carboniferous–Permian boundary.^[50]

Economic Uses

Fusulinid limestones serve as significant reservoir rocks in petroleum geology, particularly within Permian basins where they form porous and permeable carbonates that trap hydrocarbons. In the Permian Basin of Texas and New Mexico, formations such as the Clear Fork and Abo contain fusulinid-crinoid wackestones and packstones that exhibit locally high porosity up to 25% and contribute to major oil fields like Fullerton. These rocks, deposited in outer-ramp settings, provide essential storage for oil and gas due to their skeletal grain composition and diagenetic enhancement through dolomitization and karsting.^[51]^[52] The abundance and distribution of fusulinid tests in sedimentary deposits act as paleoenvironmental indicators, distinguishing between high-energy reef and low-energy lagoon settings to refine seismic interpretations in exploration. High concentrations of well-preserved fusulinid tests often signal open-marine shelf or ramp environments conducive to reef development, whereas sparse or absent tests suggest restricted lagoonal conditions with reduced circulation. This differentiation aids in mapping depositional facies and predicting reservoir quality during subsurface modeling.^[53]^[54] Fusulinid-bearing carbonates are quarried for dimension stone and cement production, valued for their durability and aesthetic qualities in construction. In Kansas, the Pennsylvanian Cottonwood Limestone, rich in fusulinids like Triticites, is extensively extracted for building facades and structural elements due to its massive bedding and resistance to weathering. Similarly, Permian limestones with fusulinid assemblages support cement manufacturing by providing high-calcium raw materials suitable for clinker production.^[55] Modern research employs digital imaging and databases to enhance fusulinid-based reservoir modeling, enabling automated identification and environmental analysis. Large datasets, such as those containing over 2,400 images of fusulinid genera, facilitate machine learning applications like convolutional neural networks for rapid classification, improving predictions of facies distribution in hydrocarbon reservoirs. These tools integrate with seismic and well data to simulate porosity variations in fusulinid-dominated carbonates.^[56]^[57]

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https://discovery.ucl.ac.uk/id/eprint/10140766/1/1-s2.0-S0377839821001201-main.pdf
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Paleobiological analysis of fusulinacean (Foraminiferida) shell ...
Charles A. Ross; Paleobiological analysis of fusulinacean (Foraminiferida) shell morphology. Journal of Paleontology 1972;; 46 (5): 719–728. doi: Download ...
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Paleobiological Analysis of Fusulinacean (Foraminiferida) Shell ...
Horizontal bands indicate yearly growth. A, Variation in cham- ber ... in thin section and that calculated by subtract- ing half ellipses is again ...
[44]
[PDF] Fusulinid Biostratigraphy and Correlations Between the ...
basis of minor differences in size, shape, or wall thickness. Most of the size differences are based on maturity, the smaller specimens having fewer ...Missing: Fusulinida | Show results with:Fusulinida
[45]
Middle Permian western Tethyan fusulinids from southern Baoshan ...
Jul 14, 2015 · The studied fusulinids are ascendingly grouped into three biozones: the Schwagerina yunnanensis Range Zone, Eopolydiexodina Abundance Zone, and ...
[46]
ACCELERATED RATES OF FORAMINIFERAL ORIGINATION AND ...
Mar 3, 2017 · Raw taxonomic diversity is depicted in Figure 3A as the number of species (Ntot) occurring in each million-year interval from latest Famennian ...
[47]
Fusulinid Taphonomy: Encrustation, Corrasion, Compaction, and ...
Mar 3, 2017 · Each fusulinid test was analyzed and categorized as to its state of encrustation, corrasion, compaction, and dissolution (Table 1). Selected ...
[48]
The Permian timescale: an introduction - Lyell Collection
Nov 23, 2017 · The most important taxa in this regard are conodonts, fusulinids, non-fusulinid forams and ammonoids. Brachiopods, rugose corals and ...
[49]
[PDF] Critical Tools for Reservoir Framework Definition, Fullerton Clear ...
Clear Fork reservoirs in the Permian Basin typically display a wide range of geologic and petrophysical properties that make the efficient recovery of.
[50]
[PDF] Multidisciplinary Reservoir Characterization of a Giant Permian ...
The study utilizes robust outcrop models as a key to proper interpretation of geological, petrophysical, and geophysical subsurface data sets. It demonstrates ...Missing: Fusulinida petroleum
[51]
an unusual facies from the Early Permian Khao Khad Formation of ...
Jul 14, 2020 · This formation has yielded unusual microbial-fusulinid limestones with large gastropods which contribute most to the rock volume. With a ...Geological Setting · Materials And Methods · Microfacies Description
[52]
Facies distribution of Fusulinida in a Bashkirian-Moscovian ...
Aug 9, 2025 · The upper boundary of the fusulinid depth range is determined by transition to stressed coastal or bank facies (lagoons, tidal flats, oolite ...
[53]
KGS--Mineral Resources Series 4--Kansas Building Limestone
The Cottonwood Limestone is quarried in Chase County by the three major Kansas building stone producers. In this locality, the ledge is approximately six feet ...
[54]
[PDF] arXiv:2302.08062v1 [cs.CV] 16 Feb 2023
Feb 16, 2023 · In this work, we present the largest image dataset of fusulinids (Huang and Shi, 2022) to date, containing 2400 images from 16 genera that cover ...
[55]
[PDF] Deep convolutional neural networks as a geological image ...
Jun 2, 2019 · We used a dataset of 1850 qualified images including seven different fusulinid genera. After retraining the CNN model, we obtained an accuracy ...