168 Sentences With "denticulate" | Random Sentence Generator

The outer lip is thick and denticulate. Its colour is bluish-grey.

The outer and basal margins are thickened and very minutely crenulated within. The columella is oblique and not tortuous above, nor entering the umbilicus, but inserted upon its side. The front edge is nearly straight, denticulate at the base. The wide umbilicus is not very deep, its margin somewhat denticulate.

There is one clear whitish spot opposite the cell, and the rest of the exterior line is clearly denticulate.

The laterals show prominent cusps, their bases are denticulate. The inner marginals are not enlarged, but rather narrow, with long simple cusps. The outer marginals show long serrate cusps. In the denticulate cusps of the lateral teeth, and the narrow inner marginals this form approaches more closely than any other to Leptothyra.

The outer lip is finely denticulate within. The sinus is shallow. The siphonal canal is not very short.Adams, C. B. 1850.

The umbilicus is rather large and plicate-crenulate. The arcuate columella is denticulate. The inner lip is undulate. The throat is livid.

The outer lip is slightly thickened and denticulate within. The sinus is shallow and subsutural. Hedley, C. 1922. A revision of the Australian Turridae.

The outer lip is lirate within. The columella and basal lips are thickened and denticulate. The columella is folded above. The umbilical area is white.

The aperture is oblong. The outer lip is denticulate within. The columellar margin stands upright. The sinus does not extend beyond the middle of the outer lip.

Perennial, 50–100 cm, ligneous at base, completely viscousglandular. Leaves with three oblong and denticulate leaflets. Flowers in terminal leafy racemes. Peduncles long, one-flowered, often aristate.

They are alternately squarrosely ochre-colored. The aperture is subrotund. The outer lip is incrassate and denticulate within. The columella is simple and slightly blistered on the outside.

The margin of the middle lobe of the corolla lip of Salvia vasta var. vasta is entire or undulate, while that of Salvia vasta var. fimbriata is fimbriate-denticulate.

The aperture is oblong. The outer lip is incrassate, without 5-echinate, within obscurely denticulate. The sinus is fairly broad and conspicuous. The, columellar margin is straight and multiplicate.

Tuctoria species have their spikelets spirally arranged on the axis; lemmas are entire (with a smooth, even margin) or denticulate (finely toothed), and often have a centrally placed short, sharp tip (mucro). The inflorescence is not cylindrical (as in Neostapfia), and the spikelets are laterally flattened. The lemmas are narrower, the tip is mucronate or otherwise entire or denticulate. The caryopsis is not sticky, and the brown embryo is visible throughout the light-colored pericarp.

The wide siphonal canal is recurved. The outer lip is denticulate. The columella is upright. The sinus is subsutural, shallow and slightly open between the first and the third lirae.

The aperture is spirally lirate. The edge of the columella is denticulate. Its upper insertion is callous, partly or nearly covering the umbilicus. Young specimens are subbiangulate with nodulose periphery.

Female flowers have a calyx with sessile laciniae. The ovary is appressed, broadly ovate, apiculate, and denticulate. The style column very short. Sepals of male flowers are subulate and entire.

The spire is higher than in Citharomangelia richardi (Crosse, 1869). The fine spiral striae are distinct. The columella shows traces of transverse plicae. The outer lip is denticulate with 13 denticles.

The denticulate ligaments are triangular shaped ligaments that anchor the spinal cord along its length, at each side, to the dura mater. The bases of the ligaments arise in the pia mater and they are firmly attached to the arachnoid mater and dura mater at the apex. They have 21 attachments per side. Named for their tooth-like appearance, the denticulate ligaments are traditionally believed to provide stability for the spinal cord against motion within the vertebral column.

Side view Bothrostethus annulipes can reach a length of about . Body is black-brown. Connexivum is yellow spotted.Stresemann Exkursionsfauna von Deutschland, Band 2: Wirbellose: Insekten The margin of the pronotum is finely denticulate.

The operculum is membranous, barely 1 mm high, denticulate. The ovary is ovoid, tapering at apex. Fruit is subglobose, 2 to 3 cm in diameter, deep pink. Seeds are oblong, about 5 mm.

Cellana denticulata, or the denticulate limpet, is a species of true limpet, a marine gastropod mollusc in the family Nacellidae, one of the families of true limpets. It is endemic to New Zealand.

Temnora plagiata is a moth of the family Sphingidae. It is found in Africa. The length of the forewings is . The forewing outer margin is bisinuate, strongly convex in the middle and feebly denticulate.

Iapetognathus fluctivagus is a species of denticulate cordylodan conodonts belonging to the genus Iapetognathus. It existed during the Tremadocian Age ( million years ago) of the Ordovician. It is an important index fossil in biostratigraphy.

The aperture is subrhomboidal. The columella is oblique, dentate or subsinuous at the base. The outer lip is acute. The central tooth and the lateral teeth of the radula have well- developed denticulate cusps.

The interior of the outer lip is denticulate. The color of the shell is white with the top of the spire tinted orange-yellow. Dautzenberg, Ph. (1889). Contribution à la faune malacologique des Iles Açores.

The outer lip is thick and denticulate within. The posterior sinus is slightly deep and has a rounded curvature. The columella is upright, turning slightly to the left. The short siphonal canal is anteriorly expanded.

Denticulate ligaments are characterised by high extensibility (on average 50% of their initial length) and relatively low force necessary to rupture them (around 1 N). Their strength, especially in cervical region, decreases in caudal orientation.

The body whorl is globose and convex. The aperture is slightly oblique. The outer and basal lips are closely lirate within. The short columella is concave, its edge plicate-denticulate, terminating below in a tooth.

The columella is straight and shows a narrow callus. The thick outer lip is denticulate and shows on top a little cutout. Dautzenberg, P., 1912. Mission GRUVEL sur la côte occidentale d'Afrique (1909-1910), Mollusques marins.

The aperture is rather large, scarcely channeled posteriorly. The outer lip is very thick, rendered denticulate on the outside by the spiral cords. The inner lip and the parietal wall are glazed with a thin callus.

The earliest culture in the tradition is the ChâtelperronianDelson, Eric (Ed.). "Encyclopedia of Human Evolution and Prehistory: Second Edition". Routledge, 23 Nov 2004. p. 717 which is thought to have produced denticulate tools and flint knives.

The interstices are somewhat larger and slightly cut across by striae. The body whorl is somewhat smaller than the spire. The siphonal canal is short, narrow and somewhat twisted. The outer lip is incrassate and inside denticulate.

The outer margin is obtuse and subcrenulated. The basal margin is plicatulate. The columella is disjoined and prominently denticulate above, oblique, with 1 or 2 tubercles where it joins the basal margin. The white umbilicus is narrow.

The wingspan is for male. The females are larger, reaching . The uppersides of the forewings are blackish blue with a greenish tint. The outer margin are generally denticulate (tooth like), with a series of white discal spots.

A slight varix can be seen behind the aperture. The outer edge of the expanded lip is denticulate by the spiral sculpture. The inner lip shows a thin sheet of callus. The sinus is deep, spout shaped.

The siphonal canal is short and wide. The U-shaped or linguiform anal sinus is deep, located near the suture and is surrounded by a thick outer lip. The outer lip is denticulate within. The columella is smooth.

The species is 1-5 flowered from terminal nodes without any flowering branches below. The pedicels that hold the flowers are long. The bracts are small and are black and denticulate. The flowers are wide with rounded buds.

The denticulate stick insect (Acanthograeffea denticulata) is the sole species of stick insect present in the Mariana Islands, where it is endemic. It feeds on coconut fronds.Bourquin, O. Invertebrates recorded from the Northern Marianas Islands. Northern Marianas College.

Shell minute, pyriform, strongly narrowed anteriorly; spire low; lip thickened, strongly denticulate; external varix probably absent (needs to be confirmed); distinct axial costae present; siphonal notch absent; columella multiplicate, with combined total of usually 8 plications plus parietal lirae.

Danaea kalevala plants are large, up to tall. They have radially arranged creeping rhizomes to thick and pinnate leaves. The pinna apices are finely denticulate. Danaea kalevala was named by Dutch botanist Maarten Christenhusz in honour of Finland, his host country.

The outer and basal lips are thick, curved and crenulate within. The columella is very oblique. Its edge is denticulate, slightly tortuous above, and inserted in the center of the axis. Below it terminates in an acute or squarish narrow tooth.

The body hairs measure with a denticulate tip. The antennae both have two or three sensilla. The labrum is smaller with two hairs on the anterior surface that are . The maxilla has a sclerotised band between the cardo and stipes.

Consists of brown sediment. Artifacts generally belong to the Denticulate Mousterian culture, from the Middle Paleolithic period. It is quite disturbed in the later periods, with rodent holes. Fauna remains are numerous, mostly corresponding to the one discovered in Layer 4.

These are flatly rounded and with a deep suture. The aperture is narrow, slightly oblique, and sinuous. The outer lip is thick, slightly expanded and denticulate within. The sinus is deep and broad, near the suture, but surrounded by a thick lip.

Some specimens are almost plain, others have a row of square brown spots just below the suture on the body whorl. The aperture is oblong. The outer lip is incrassate, suturally expanded, finely denticulate within. The sinus is broad, but not deep.

The basal notch or canal is oblique, squarish, wider than deep, and not denticulate in the middle. There is great variation in color in this species. In some specimens red predominates, in others green. And often the general effect is an olive shade.

The texture of the adult shell is frequently "gritty," from a sculpture of minute grains. The aperture is oval-elongated, usually narrow, terminating in a rather short, truncated siphonal canal. The aperture is only rarely denticulate. The outer lip (labrum) is reinforced.

The leaves stem short and erect from prostrate rooting stems. They are simple, opposite leaves, with aromatic glands and no stipule. The leaves are connate by flattened petioles. The lamina is simple, minutely denticulate on the margin, and leathery on the surface.

The length of the shell attains 16 mm, its diameter 6 mm. The shell is longitudinally ribbed and transversely striate. Both lips are denticulate. Its color is yellowish white or light brown, with an interrupted white median band margined below with chestnut.

The denticle (tiny teeth) of radula have the formula ∞ 1, (1 + 1 + 1), 1 ∞. The central denticles are small and elongated. The lateral tooth is rather large, straight, without a cusp. The numerous lateral teeth are denticulate, and arranged in very oblique series.

These are strongly, regularly radiately striate. The rhomboidal aperture is very oblique, iridescent and sulcate within. The outer and basal lips are edged with green and are plicate- denticulate within. The green columella is curved, ending in a strong tooth at its base.

Calyx conical- cylindrical, slightly tapered at apex, greenish-white, sometimes tinged with purple. Striations often limited to the apex of teeth and to some bands below sinuses. Petals pink, lamina fan-shaped, denticulate, marked with dots which gave the plant its name.

Petioles are short, about 8 mm long. Spines are shorter than the leaves, about 3-5½ cm long. Bracts are broadly ovate, subtruncate, and lacerate-denticulate. The plant is monoecious, and thus has both male flowers and female flowers on the same individuals.

They have short, strongly clubbed, to very elongate antennae, and frequently grooves or carinae on the head and/or pronotum. Many genera have the lateral margins of the pronotum dentate or denticulate. The family is divided unequally into two subfamilies: Brontinae and Silvaninae.

The deeply cupped flowers are golden yellow and measure wide. The petals are nearly obovate with denticulate margins and are longer than the stamens. The stamens are numerous and are each united into five bundles. The small, spherical anthers are orange to yellow.

The body whorl is dilated, subangulate above, depresso-carinated at the periphery, convex beneath and ornamented with 9 concentric reddish lirae. The aperture is oblique and subquadrate. The lip is simple. The columella is arcuate, denticulate at base, slightly calloused above, almost covering the umbilicus.

The; base of the shell is somewhat convex. The oblique aperture is small and contracted. The outer lip bears within a strong tooth above, and an inconspicuous rather acute thread at the place of the periphery. The basal lip is expanded, curved and slightly denticulate.

The body whorl is carinated at the periphery. The base of the shell is plano-concave, indented in the center, finely, densely lirate. These lirae are minutely beaded, red, articulated with white, the interstitial furrows white. The aperture is subrhomboidal, denticulate within the base.

These tubercles are denticulate along the lateral margin. Other facial features include gena more narrow than the compound eyes. There are punctate markings on the vertex and the gena. Those on the vertex are uniform in shape with rough edges, slightly separated from one another.

Cut off, as the apex of some shells. Decussated. With spiral and longitudinal lines intersecting, as the sculpture of some shells. Deflexed. Bent downward, as the last whorl in some snails. Dentate. With points or nodules resembling teeth, as the aperture of some snails. Denticulate.

The posterior angle is obtuse. The thin outer lip is denticulate. The incised spiral channels appear as a chain of squarish areolations within, by transmitted light. The columella is moderately strong, somewhat twisted and slightly reflected with a subobsolete oblique fold near its insertion.

The shell of Galeodea echinophora can reach a length of . The shell is globular or oval, with a large body whorl. The surface of the shell is yellowish-brown. The aperture is wide, with denticulate lips, a curved siphonal canal and a large columellar edge.

From a clinical standpoint, denticulate ligaments do not play a significant role in lumbar spinal stenosis when compared to issues such as disc herniations, facet hypertrophy, shape of spinal canal, size of spinal canal, ligamentum flavum hypertrophy, or degenerative joint disease resulting in bony osteophyte formation.

The specific epithet denticulatum means "small-toothed", referring to the marginal teeth on the petals. Walter named the species on account of the apiculate petals while Kunth named his H. denticulatum (H. galinum) in reference to the denticulate leaf margin of the species. In H. denticulatum subsp.

It is ovate, oblique, iridescent within and lirate. The outer lip is convex, effuse on meeting the basal lip, with a sharp, finely denticulate edge. The columella is subvertical, with a slight swelling in the middle. The inner lip is expanded in a callous pad over the umbilical tract.

The base of the shell is a trifle convex, the middle portion concave toward the umbilicus. The tetragonal aperture is very oblique and almost horizontal. The upper lip is straight, bearing a strong tubercular tooth midway. The outer and basal lips are well rounded, thickened and plicate- denticulate within.

The ovary is broadly ovate and tapers upwards, terminating into five styles that are recurved at their apex. The stigma is obtuse and downy. The calyx is composed of five large, lax, and obovate sepals. The sepals are united at their base and their membranous margins are denticulate.

Blooms of Beschorneria yuccoides Beschorneria yuccoides is a stemless plant with 20 to 35 linear, lanceolate, leathery leaves that are widened at their base. They are gray-green to green, about long and wide. The leaf margins are finely denticulate. The inflorescence reaches a height of , with a maximum of .

The narrow and smooth inner lip shows at its posterior end a shallow and broad anal sinus. The erect outer lip is denticulate and with a weak sculpture of 9 or 10 lirae. The short and broad siphonal canal is weakly bent at the tip and contains two webbed spines.

The shape is elliptical to oblong or obovate, moderately to strongly shouldered (pl V bottom). The spire is immersed or near so (pl V top). The aperture is narrow to moderately broad, wider anteriorly. The lip is moderately strongly thickened, weakly to strongly denticulate in adults, with a distinct external varix.

The body whorl shows 12 spiral lirae of which the lower six show a granular white colour. The aperture measures slightly less than half the length of the shell. The outer lip is very thick and denticulate within with 4 - 5 teeth. The sinus is not very deep and located near the suture.

The body whorl is ventricose, radiately costellate above, with three acute elevated median spiral cinguli, beneath with obsolete concentric striae. The umbilicus is wide, carinated at the periphery, plicate, and denticulate. The aperture is subcircular. This marine species is finely and closely reticulated ; the whorls are rounded and show no trace of angularity.

The siphonal canal is short and wide. The outer lip is massive, ridged externally by a dozen transverse cords which denticulate the edges. Within are seven weak entering ridges. The aperture mounts the preceding whorl to the height of two spiral cords, and encloses a deep wide anal notch with a prominent callus.

The outer lip is iridescent and plicate within. The basal margin is rounded and denticulate. The oblique columella is nearly straight, slightly folded above and bidentate at its base. The umbilicus has (in fully adult specimens) a crenate marginal rib, white within, and perforating scarcely deeper than the insertion of the columella.

The outer lip is sharp and is strongly thickened by the last axial rib. On its inside it is denticulate with three or four obsolete teeth and a parietal tooth next to the sinus. The large sinus is rounded and lacks a varix. The columella is straight and slightly thickened on its sides.

Baryandra, B. quinquealata is very distinctive for being a densely hairy herb with long creeping rhizomes. It differs also from B. suborbiculata in that it has thickly chartaceous, widely ovate leaves that have uniformly green upper leaf surface, densely velutinous, with denticulate leaf margin, outer tepals, and red scabrous ovary and capsules.

The aperture is white within. The outer lip shows a strong external varix a little way from the thin brown finely denticulate edge. The posterior sinus is moderately deep and rounded :The columella is smooth, with a thin callus united above to the end of the outer lip. The anterior canal is slightly recurved.

Outer edge of mesotibia simple, crenulate or denticulate, or with distinct teeth or long spines. Outer subapical edge of mesotibia without antenna cleaner. Preapical surfaces of mesotibia without ridges or combs. Outer apical angle of mesotibia simple or slightly produced, without lobe, teeth or spines, or with rounded lobe or process, sometimes bearing spines.

The type species of the genus Topaginella is Marginella octoplicata Tenison Woods, 1877 †; OD (M) Remarks: The type species seems to be unique (a monotypic genus). The multiplicate columella and lack of a siphonal notch place it near Cystiscus, but the pyriform shape, exserted spire, denticulate lip, and fine axial costae render it distinct.

The outer and basal lips are thick, evenly and finely plicate within. The columella is oblique, deeply entering, conspicuously fielded near its insertion. Its edge is denticulate near the base, and passing into the basal margin with a regular curve. The parietal wall bears a white wrinkled callus, the umbilical margin of which is dentate.

This can help distinguish C. rhipidophylla from C. monogyna which has irregularly serrated lobe margins, with more or less coarse teeth. The basal lobes of flowering shoots leaf blades each have 6-25 teeth. Their stipules also are serrate or serrate-denticulate. Inflorescences are corymbs, 3-4.5 cm long, of 5-15 lax white flowers.

Sutural elements are short and boxy. The umbilical lobe, which lies between the lateral lobe and dorsal lobe, on either side, is about the same size as the lobule dividing the first lateral saddle. Janenschites, Kabylites, and Baculina are all similar to Bochianites, differing mostly in details of the suture. Janenschites has long, narrow, and more denticulate elements.

The narrow fibrous strip of the denticulate ligament features longitudinally oriented collagen fibers, whereas the triangular extensions are composed of transverse and obliquely oriented collagen fibers. The collagen fibers are thicker and more abundant at the cervical than at the thoracic levels. These ligaments may be affected by altered motion and position of the vertebral segments.

The shells of the species in this genus have spires which range from moderately elevated to flattened. The surface of the shell is glossy and porcellaneous, and it is often but not always colourful. The columella has four definite, subequal plaits on its anterior half. The outer lip is thickened, and generally denticulate inside, with distinct teeth or folds.

Zehneria baueriana is a large, perennial, dioecious liana, climbing to the forest canopy. The lower stems are woody and corky. The unlobed leaves are broadly ovate, 60–100 mm long and 50–80 mm wide; they are cordate at the base, finely denticulate, acute at the apex and scabrous above. Both male and female flowers occur in fascicles.

Shell minute to small, white, hyaline; spire immersed to low; lip thickened, smooth or weakly denticulate; external varix absent; siphonal notch absent; posterior notch absent; lacking collabral parietal callus ridge; columella multiplicate, with combined usually 2 to 8 plications plus parietal lirae, first plication usually strong and raised. Mantle smooth, at least partially extending over external shell surface.

Aperture narrow to broad, usually wider anteriorly. Lip slightly to distinctly thickened, flared posteriorly in some species, smooth on inside edge to weakly denticulate, lacking lirae, external varix absent. Shell lacking a siphonal notch and posterior notch. Shell with weak parietal callus wash or weak parietal callus deposits in some species, but lacking collabral parietal callus ridge.

This genus consists of small species with a head without frontal lobes. The shell is ovate, elongated, and imperforate. The radula has a broad, simple median tooth, overlying the bases of the inner laterals. These are subrhomboidal, produced at their outer angles into wings which overlie the bases of the adjacent tooth outward, and have denticulate cusps.

The sheath is pubescent to pilose lower on the plant but glabrous higher up. It has membranous truncate, irregularly denticulate ligules that are big. Leaf blades are long and wide; they are ascending, firm, glaucous, sparsely pilose near the base, often scabrous on the margins, and involute towards the tips. The panicles are long and wide.

The; white base of the shell is convex. The penultimate whorl contains six series of granules, with the interstices as wide as the ridges, and is obliquely striate. The body whorl has eight series of granules above, nine on the base. The oblique columella is solute above, the edge rugose- denticulate, terminating below in a prominent tooth.

The last whorl is with nearly parallel sides, rounded and slightly attenuated base. The columella is stout, strongly twisted, white, short. The outer lip is nearly straight, somewhat thickened, especially anteriorly, not lirate or denticulate internally. The shell is with two revolving ridges, the posterior one is fainter and placed in advance of the middle of the whorl.

In some of the maxilla, the teeth are short and swollen (almost round in cross section) and become smaller towards the rear of the bone. The dentary teeth are similar but more asymmetrical. The middle of the dentary has the largest and most denticulate teeth in the jaw. There are 12 maxillary teeth and 14 dentary teeth.

The shell of Marginellidae is usually small, but varies in different species from minute to medium-sized. The external color of the shell can be white, cream, yellow, orange, red, or brown, and can be uniformly colored, or patterned in various ways. The protoconch is paucispiral. The lip of the shell is thickened, and can be smooth or denticulate.

Its sculpture shows a dozen prominent, distant, thin radial ribs descending the last two whorls perpendicularly, broadening at the periphery. These there produce a marked angle to the contour of the shell. The spiral threads lattice the interspaces and denticulate the edges of the ribs. The round aperture adheres anteriorly to the body whorl for a short space.

Bolomor is one of "numerous European sites [that] attest new technological behavior oriented toward long and complex knapping methods, with long and complex repetitive core reduction, predetermined flake shape, and tool standardization". Layers with scrapers and denticulate tools alternate. Fifteen hearths, in age ranging between 250,000 and 100,000 years old, are being studied. Some of the hearths were lined with stone.

It is a shrub or tree up to 27 m high, with brown lenticellate branchlets. Leaves 6.5--17 cm long, 3.5--7 cm wide; ovate, with a rounded base; rigid, coriaceous; shortly denticulate. Flowers arranged in an elongated raceme up to 17 cm long; sepals 1 mm long; petals up to 3 mm long. Fruits are black, spherical, up to 1.9 cm wide.

They are crossed regularly by numerous, fine spiral lirae, producing granular or transverse plicules. The aperture measures about a third of the total length. The weakly notched siphonal canal is narrow and shallow. The sharp outer lip is denticulate on the inside and usually shows a particularly strong tooth close to the well-cut anal sinus. The columella occasionally carries 1-2 denticles.

Like other members of the genus, Iapetognathus fluctivagus had ramiform (branching) array of elements (apparatus). It is believed that the ramiform apparatus in Iapetognathus fluctivagus evolved from the coniform (cone-like) apparatus of Iapetonudus ibexensis. It can be readily distinguished from other conodonts existing during the same age by the sideward orientation of the major teeth-like projections (denticulate processes).

The ventral surface is scaly. The posterior margin of the merus of the fifth pereopod has a strong subdistal spine. The posterior margin of the pleopods are denticulate, with an oval dactyl. The colour of the carapace is greenish- brown except for the margins and embossed granules which are paler in colour while the interior margins of the limbs are mustard coloured.

Shell minute to small, white; spire immersed to low; surface smooth or axially costate; lip thickened, smooth or denticulate; external varix absent; siphonal notch absent; posterior notch absent; columella multiplicate, with combined total of usually 2 to 8 plications plus parietal lirae; internal whorls cystiscid type. Animal mantle smooth, at least partially extending over external shell surface. Internal anatomy unknown.

B. ser. Abietinae was first published in 1856, in Carl Meissner's chapter on the Proteaceae in A. P. de Candolle's Prodromus systematis naturalis regni vegetabilis. It was one of four series into which the subgenus Eubanksia was divided. These four series were defined in terms of leaf characters, with series Abietinae containing the species with entire or shortly denticulate leaves with revolute margins.

The inner lateral is slender, narrowed toward the cusp, like the centrals, and (sometimes at any rate) bearing a lamella behind the peduncle. The outer laterals are very broad, with one or several denticles on the cusp. The only character separating Cantharidus from Gibbula is the simple cusp of the central tooth, whilst in Gibbula it is denticulate at the sides.

Platycerus caraboides can reach a body length of about . These beetles have flat body, metallic black, steel blue or greenish. Antennae are geniculate, with a club of 3 items, Jaws are denticulate at the inner edge and also in the male they are shorter than the head.Scarabeidi This species can be easily distinguished as a stag beetle by its elbowed antennae.

The outside of the laterals consists of 2 rows of uncini (the numerous small teeth-like or hook-like structures). The inner series number 18 and are large, strongly curved, and with scythe-shaped 1-3 denticulate cusps. The outer uncini are very numerous (40-50), small, very oblique. In Entemnotrochus adansonianus (Crosse & P. Fischer, 1861) there are considerable differences in the teeth.

Colona evecta was described from southern Vietnam, it is also found in neighbouring provinces of Cambodia, where the species often survives forest clearing. The tree grows from 6-20m, with radiating pubescent branches and terminal flowers. The bark of young trees is very tough. The leaves are relatively thick, lanceolate, denticulate, glossy on upper sides, with 5–7 mm petioles.

The forewings are fuscous, speckled with ochreous whitish. The stigmata are moderate, dark brown, the plical beneath the first discal, the second discal transverse. There is a hardly curved denticulate light brownish-ochreous subterminal line, edged posteriorly by dark brown. There is also a marginal series of dark fuscous dots separated with light ochreous around part of the costa and termen.

The plan is symmetric and U-shaped, with a basement, ground floor and second floor; the building forms an imposing presence in the city center. The grooved columns are both Ionic and composite. The pediment features symbolic bas-reliefs and acroteria. The cornices are denticulate, there is egg-and-dart moulding, as well as meanders, decorative balustrades, semicircular niches, bossage in strong relief and medallions.

The forewings are dark fuscous, faintly purplish tinged. There is a wedge-shaped ochreous-white mark from the costa near the apex and a fine white denticulate terminal line. The hindwings are dark fuscous, lighter anteriorly. There are broad median and dorsal prismatic-violet-tinged hyaline (glass like) longitudinal patches, confluent towards the base, the upper extending to about three-fourths, the lower nearly to the termen.

Flowers 30-50 mm in diam., stellate; buds ovoid, acute to > subapiculate. Sepals (5-)6-9(-11) x 3-4(-6) mm, free, imbricate, subequal, ± > outcurved in bud and fruit, ovate to narrowly lanceolate, acute or > acuminate, with margin subentire or minutely and ± irregularly denticulate > (especially towards apex); midrib ± conspicuous, veins not prominent; > laminar glands linear or interrupted, c. 8. Petals deep yellow, sometimes > tinged red, spreading or reflexed, 16-25 x 10-15 mm, 2.5-3 x sepals, > obovate, with apiculus lateral, subacute to obtuse, margin entire or often > minutely glandular-denticulate especially around apiculus. Stamen fascicles > each with 40-65 stamens, longest (10)15-18 mm, long, 0.75-0.85 x petals; > anthers yellow to orange-yellow. Ovary 5-7 x 3.5-4.5 mm, ± narrowly ovoid- > conic; styles (3-)4-6(-8) mm, long, equalling to slightly longer than ovary, > free, suberect, outcurved near apex; stigmas truncate to narrowly > subcapitate.

The forewings are pale grey, tinged with fawn colour and sparsely dusted with blackish dots. The lines and stigmata are indistinctly darker, the latter edged with black dots. The exterior line is thick and bluntly denticulate (tooth like). The central area of the wing is slightly paler than the rest and there is a row of small dark dots before the base of the fringes which have a darker medial line.

The spinal pia mater closely follows and encloses the curves of the spinal cord, and is attached to it through a connection to the anterior fissure. The pia mater attaches to the dura mater through 21 pairs of denticulate ligaments that pass through the arachnoid mater and dura mater of the spinal cord. These denticular ligaments help to anchor the spinal cord and prevent side to side movement, providing stability.Saladin, Kenneth.

The columella is very oblique, slightly tortuous above and enters very deeply, terminating below in a strong plicate tooth, and with a smooth margin, save for a small denticle immediately above the basal tooth. The parietal tract is wrinkled. The umbilicus has a plicate-denticulate border. In the typical form, the 1st, 3d, 5th, 7th and 9th lirae, and one or two upon the base are articulated with black.

The suborbital tooth is strong and sharply pointed, visible in dorsal view; the suborbital margin is evenly curved and tuberculate. The cheliped merus has a sharp spine subdistally and with a distal dorsal spine; carpus roughened dorsally, with distal outer spine, denticulate anterior margin, and strong and slender distal spine. Its right chela has a distal angled projection. The meri of its walking legs have a distinct distal dorsal spine.

The shell of Marginella gemmula, while glossy and smooth to the touch, has spires that can be anywhere from flat to moderately elevated. Most shells have various colors, but a small number can be colorless. On the outside of the shell, the columella has four plaits. The outside lip is thicker than other such creatures, and the inside of the shell sports a denticulate set of teeth and/or folds.

Yucca gloriosa is caulescent, usually with several stems arising from the base, the base thickening in adult specimens. The long narrow leaves are straight and very stiff, growing to long and wide. They are dark green with entire margins, smooth, rarely finely denticulate, acuminate, with a sharp brown terminal spine. The inflorescence is a panicle up to long, of bell-shaped white flowers, sometimes tinged purple or red.

The size of an adult shell varies between 35 mm and 130 mm. These medium-sized shells are oval and acuminate, with a rather narrow mouth, the outer lip folded back and internally denticulate. Shoulder are not angulate nor plicate and the anterior prickles on outer lip obsolete. The surface of the shell is white with five series of large squarish red-brown spots (hence the common name).

Early Middle Paleolithic stone tools from Denisova Cave were characterized by discoidal (disk-like) cores and Kombewa cores, but Levallois cores and flakes were also present. There were scrapers, denticulate tools, and notched tools, deposited about 287±41 thousand years ago in the Main Chamber of the cave; and about 269±97 thousand years ago in the South Chamber; up to 170±19 thousand and 187±14 thousand years ago in the Main and East Chambers, respectively. Middle Middle Paleolithic assemblages were dominated by flat, discoidal, and Levallois cores, and there were some isolated sub-prismatic cores. There were predominantly side scrapers (a scraper with only the sides used to scrape), but also notched-denticulate tools, end-scrapers (a scraper with only the ends used to scrape), burins, chisel-like tools, and truncated flakes. These dated to 156±15 thousand years ago in the Main Chamber, 58±6 thousand years ago in the East Chamber, and 136±26–47±8 thousand years ago in the South Chamber.

Iguanodontids exhibit contact between maxillary and dentary teeth upon closure of the jaw. They have a thick layer of enamel over the lip-facing (labial) surface of the crown, a robust primary ridge beginning at the base of the crown, and a denticulate margin. Most members of the family have maxillary tooth crowns lanceolate in shape. The labial surface of the teeth has some grooves, while the tongue-facing (lingual) surface is smooth.

Its edge is minutely denticulate. The oblique columella deeply enters the narrow umbilicus and is inserted in the center of the axis, slightly dentate above, bearing a narrow tooth below the middle, and terminating in a large, heavy bi- or triplicate tooth. The parietal area is covered by a white callus bearing numerous wrinkles, one or two of which enter the aperture. The umbilicus is surrounded by a radiately strongly plicate callus.

It is very delicate and it is tightly associated with the surface of the spinal cord. The cord is stabilized within the dura mater by the connecting denticulate ligaments, which extend from the enveloping pia mater laterally between the dorsal and ventral roots. The dural sac ends at the vertebral level of the second sacral vertebra. In cross-section, the peripheral region of the cord contains neuronal white matter tracts containing sensory and motor neurons.

The leaves of the perichaetium have a long sheath with a scarious (i.e. membranous) margin, while the blades themselves are greatly reduced, gradually narrowing to a finely acuminate tip. These blades have toothed margins, are denticulate to subentire in outline, roughened to almost smooth, and have a costa that is excurrent. The seta, or capsule stalk, is 5 to 9 cm long, and is stout and yellowish to reddish brown in colour.

The costal margin with five white strigulae, the first four curving outwards, the fifth inwards, the first long and strongly oblique, the fourth often indistinct. The dorsal margin with basal two-thirds white, this fascia denticulate inwards, often linked irregularly with the costal strigulae. The apical spot is black with some mixture of paler scales, surrounded by a circular white line including the fifth costal strigula. The hindwings are as in Micrurapteryx gradatella.

In North Africa and the Near East, Mousterian tools were produced by anatomically modern humans. In the Eastern Mediterranean, for example, assemblages produced by Neanderthals are indistinguishable from those made by Qafzeh type modern humans. The Mousterian industry in North Africa is estimated to be 315,000 years old. Possible variants are Denticulate, Charentian (Ferrassie & Quina) named after the Charente region, Typical, and the Mousterian Traditional Acheulian (MTA) Type-A and Type-B.

40,000 BP. The industry produced denticulate stone tools and also a distinctive flint knife with a single cutting edge and a blunt, curved back. The use of ivory at Châtelperronian sites appears to be more frequent than that of the later Aurignacian, while antler tools have not been found. It is followed by the Aurignacian industry. Scholars who question its existence claim that it is an archaeological mix of Mousterian and Aurignacian layers.

The submarginal line is strongly denticulate and blackish. The marginal area is dark grey, with some irregular black marks before the fringe, which is chestnut with a pale basal line. The apical one-third of the costa has a chestnut streak, the apex itself with one or two snow-white spots. The cell-spot is large, blackish, followed obliquely below it by four small white spots edged with black, and sometimes altogether black.

However, bog pondweed produces completely opaque floating leaves that are very distinct from the submerged leaves; the submerged leaves are longer and die back relatively early in the season. Bog pondweed also lacks the distinctive net-veined appearance. Potamogeton lucens has leaves with a similar net-veined appearance, but is more uniform in its growth habit, has denticulate (finely toothed) leaf margins and stipules with two conspicuous keels. Potamogeton coloratus is diploid, with 2n=28.

Paleolithic material comes from Campoverde at the north edge of the Pontino Agro. It is dated by typology, as none has been found in context. The assemblage of amateur collections of surface artifacts "shares affinities with various Lower Palaeolithic industries of Latium, ... chronologically referred to the second half of the Middle Pleistocene;". that is, about 500 thousand years BP. These are primarily flint cores and - flakes, consisting of denticulate tools, sidescrapers, borers, retouched flakes, some microliths, and others.

The subarachnoid space contains cerebrospinal fluid (CSF), which can be sampled with a lumbar puncture, or "spinal tap" procedure. The delicate pia mater, the innermost protective layer, is tightly associated with the surface of the spinal cord. The cord is stabilized within the dura mater by the connecting denticulate ligaments, which extend from the enveloping pia mater laterally between the dorsal and ventral roots. The dural sac ends at the vertebral level of the second sacral vertebra.

Warnstorfia fluitans is a medium-sized moss ranging in color from green to yellowish to brownish and can be rarely red when the species occurs in exposed habitats. The cells of its stem epidermis are not widened, and its pseudoparaphyllia are ovate-triangular to lanceolate in shape. It has axillary hairs with a distal portion of one to four cells, the hairs being hyaline when young. Its stem leaves are narrowly ovate to triangularly ovate, with denticulate margins.

Small flint tools made of thin flakes predominate these levels, many produced using the Levallois technique. Tools typical of the Mousterian culture feature elongated points, and include flakes of various shapes used as scrapers, end scrapers and other denticulate tools used for cutting and sawing. Arthur Jelinek's 1967 to 1972 excavations of the cave yielded over 1,900 complete and partial bifaces. The bulk of the biface assemblage can be attributed to the Late Acheulian and Yabrudian industries.

Compsolechia accinctella is a moth of the family Gelechiidae. It was described by Francis Walker in 1864. It is found in Amazonas in Brazil and in Peru. Adults are dark cupreous brown, with the forewings thinly and minutely cinereous (ash gray) speckled and with a ferruginous band near the base, as well as a white transverse bi-denticulate line at five-sixths of the length, with three deep black streaks between it and the whitish marginal line.

However, an otic notch can now be considered a feature of this taxa. Also present are interpterygoid , and a pair of palatal tusks within the vomer which lay medially to the internal naris. Palatal tusk pairs can also be found the ectopterygoid and the palatine. As for the lower jaw, if the animal catches prey it is able to get it to the denticulate palate because compression of the mandibles is not lateral along their length.

The radula shows a central tooth of squarish form without cusps, on a larger base, with four laterals on each side. Their cusps are denticulate with a prominent spur below, behind the cusp, and the usual large mass of uncini. This shell is so thin and delicate that it was a surprise to find it possessing a heavy calcareous operculum. W.H. Dall, Diagnoses of New Shells from the Pacific Ocean; Proceedings of the United States National Museum v.

There are two black dots on the discocellular and a lunulate and dentate submarginal line, preceded by a darker shade and with a dark grey blotch above vein 6 towards the apex. The marginal area is narrowly greyish. The hindwings have a pale pinkish ochreous costal area, without darker dusting. There is an oblong blackish blotch on the inner margin with a denticulate outer margin, passing outside a small black dot at the lower end of the discocellular.

The forewings are rather dark fuscous, the veins partially indicated by indistinct lines of pale yellowish suffusion, especially towards the base and beyond the cell. There is an irregular slightly oblique pale yellowish fasciate patch from the middle of the costa reaching halfway across the wing, limited posteriorly by an indistinct dark fuscous transverse spot on the end of the cell. There is also a well-marked ochreous-yellow denticulate terminal line. The hindwings are rather dark grey.

Gouges are generally triangular in shape, with the working edge—characteristically steep-angled—appearing at the wide base of the triangle. The opposite edge, at the point of the triangle, was the hafted end; the tool itself was generally hafted at right angles to the handle. Denticulate tools display edges that are worked into a multiply notched shape, much like the toothed edge of a saw. Indeed, these tools might have been used as saws, more likely for meat processing than for wood.

Antenna and frons brownish black as in Protesilaus protesilaus nigricornis. Wings brownish; forewing transparent; hindwing more sharply dentate than in Protesilaus protesilaus nigricornis, the black postdiscal band straight, not interrupted posteriorly as in the Protesilaus protesilaus forms, the marginal and submarginal bands yellowish. Under surface more yellow than upper; the red line of the hindwing distally edged with white. Dorsal edge of the harpe not dilated into a large tooth, the apex of the harpe pointed, ventral process not denticulate.

In adulthood its diet is no longer restricted to Zanclea, although observations of feeding behaviour are sparse. Phylliroe uses its rhinophores (long horns) to prey on jellies, and the nearly vestigial remnant of its foot to adhere to the jelly prey. Phylliroe has been seen approaching a swarm of the larvacean Oikopleura albicans from below, grabbing a specimen with its paired denticulate jaws and swallowing it in half a minute. Adults have also been observed to prey on the meduse Aequoria.

Some of the common herbs are Arisaema jacquemontii, Boschniakia himalaica, Corydalis cashmeriana, Polemonium caerulium, Polygonum polystachyum (a rampant tall weed), Impatiens sulcata, Geranium wallichianum, Galium aparine, Morina longifolia, Inula grandiflora, Nomochoris oxypetala, Anemone rivularis, Pedicularis pectinata, P. bicornuta, Primula denticulate and Trillidium govanianum.Kala, C.P. (2005) Indigenous uses, population density, and conservation of threatened medicinal plants in protected areas of the Indian Himalayas. Conservation Biology, 19 (2): 368-378. In trampled areas where past livestock congregated, Himalayan knotweed Polygonum polystachium is a rampant weed.

Cancer irroratus has nine marginal teeth on the front edge of the carapace beside each eye, and reaches a carapace width of . These crabs are similar in color to, and overlap in size with, the Jonah crab, Cancer borealis. The two species can indeed be distinguished by the purplish-brown spots on the carapace of C. irroratus (contrasting with the yellow spots of C. borealis), and by the smooth edges to the teeth on the edge of the carapace (denticulate in C. borealis).

The edge of the gills is pale, and the edge ranges from finely denticulate (with a very finely toothed margin) to straight. The stem is long and thick, cylindrical above, slightly club-shaped below, and usually somewhat curved. It is initially very fibrillose, later silvery shiny and wavy, violet or grayish violet at the apex when young, more gray or grayish-brown at the base. The violet coloring soon disappears and then the stem is whitish or pale clay brownish and silkily fibrillose.

The sculpture consists of axial nodes along the periphery which flatten out rapidly both above and below the periphery, those of the young stages being sharp and denticulate. The shell is covered by raised spiral lines which are finer and more closely set above the periphery but broader and more widely spaced towards the base of the whorl. The interspaces on the lower part of the whorl bear secondary and even tertiary threads. MacNeil, F.S. (1960) Tertiary and Quaternary Gastropoda of Okinawa.

Platyhypnidium ripariodes is among the larger northern hemisphere mosses with leaves up to 8mm long and plants growing up to 15 cm long. In the UK, plants commonly produce calyptra with relatively long curving lids. The leaf tip is acute, leaf margins are plane, slightly denticulate towards tip, mid-leaf cells are large, costa or the central stork of the leaf extends nearly to leaf tip. The growth form is procumbent but small, young plants can attach themselves closely to rocks and appear flattened.

The outer edge is oblate-convex in the upper part but substantially swollen on the fifth and sixth ribs, which show a white appearance, and protrudes on the aperture. The aperture is thickened on the last rib, crenelated on the sharp outer lip and furnished inside with 5 denticulate folds. The subsutural sinus cuts rather deep into the thickening of the outer lip, where it expands and becomes rounded.Hervier R.P. (1897), Descriptions d'espèces nouvelles provenant de l'Archipel de la Nouvelle Calédonie (suite); Journal de conchyliologie t.

The gills are crowded closely together, 3–5 mm broad, emarginate (notched), adnate by a tooth. The color is vivid yellow when young, then brownish-olive, rarely with saffron tint, and finally brownish-olive to rusty cinnamon, with denticulate (finely toothed) edge, which is either the same color as the gill or paler. Young specimens have a yellow cortina of fine fibers that extend from the cap to the stem. The stem is tall and wide, cylindrical, often slightly wavy, solid, then hollow, fibrillose and quite fragile.

The facade has some archaic elements, including a double lancet window ending with a denticulate cornice; it was completed and designed by Girolamo Vicchiuzzo, an architect and carver from Palermo. During the last century, a fake balcony was added; a finely carved small column stands at the corner of the façade. The interior has a single nave with two bays and a crossed vault: the former main altarpiece, now lost, depicted San Nicola di Bari painted in 1599 by Narciso Guidone, a painter from Trapani.Carlo Cataldo, La conchiglia di S.Giacomo p.

Each denticulate ligament is composed of a single narrow fibrous strip that extends from the craniovertebral junction to T12. Each ligament features 18-20 triangular extensions that attach to the dura at their apices. The triangular extensions are smaller and more numerous at the cervical levels, and are larger and less numerous at the thoracic levels. The apices of the extensions attach to the dura via fibrous bands at cervical levels (each band long) and lower thoracic levels ( long), whereas they attach directly to the dura at upper thoracic levels.

Maxillary lobe of the second pair of feet very long, nearly straight from the base, not attenuated, directed mesad nearly horizontally, and united on the ventro-meson to the lobe from the opposite side without forming a sensible angle; the two together lightly arched on the cephalic border, and forming an even curve. Sternal piece large, slightly contracted between the fourth pair of coxae, gradually enlarging and obtusely truncate cephalad. The feet are very long and slender; tibia of the second pair with a few false articulations. Palpal claw denticulate.

The margin is fibrillose (covered with roughly parallel threadlike filaments), then smooth, with a violet or reddish- violet to grayish-brown tinge, then concolorous with the center of the cap. The gills are thin and crowded closely together, broadly emarginate (notched), dark violet when young, with edges often slightly denticulate (finely toothed). The tinge and intensity of the violet coloring is similar to that of the wood blewitt (Rhodopaxillus nudus). The stem is solid, vivid violet paling to violet purple or violet brown, with a distinctly marginate bulb wide, otherwise almost cylindrical towards the base.

The shell is minute to large, either white, uniformly colored, or patterned; the surface is smooth, sculptured, or axially costate; the spire is flat to immersed, or low to tall; the protoconch is paucispiral; the lip is thickened, smooth or denticulate; an external varix is present or absent; a siphonal notch is present or absent; a posterior notch is present or absent; the columella is multiplicate, internal whorls cystiscid or modified cystiscid type. Mantle cavity with monopectinate ctenidium and bipectinate osphradium. Proboscis pleurembolic; jaws absent; typical radular sac present.

Shining pondweed is a large plant with robust creeping rhizomes and long, terete, branching stems, typically up to 2.5 m but exceptionally to 6 m. The leaves are large, 75–200 mm (exceptionally more) long and 25–65 mm wide, 2-6 times as long as broad; as with the smaller P. gramineus, the leaves on the branches are smaller than those on the main stem. The leaves are pale green or yellowish, translucent, shiny with distinctive netted veining, minutely denticulate margins, and a short petiole of 1–12 mm. Floating leaves are absent.

There are distinct regional variants of the Mousterian industry, such as: the Quina and La Ferrassie subtypes of the Charentian industry in southwestern France, Acheulean-tradition Mousterian subtypes A and B along the Atlantic and northwestern European coasts, the Micoquien industry of Central and Eastern Europe and the related Sibiryachikha variant in the Siberian Altai Mountains, the Denticulate Mousterian industry in Western Europe, the racloir industry around the Zagros Mountains, and the flake cleaver industry of Cantabria, Spain, and both sides of the Pyrenees. In the mid-20th century, French archaeologist François Bordes debated against American archaeologist Lewis Binford to explain this diversity (the "Bordes–Binford debate"), with Bordes arguing that these represent unique ethnic traditions and Binford that they were caused by varying environments (essentially, form vs. function). The latter sentiment would indicate a lower degree of inventiveness compared to modern humans, adapting the same tools to different environments rather than creating new technologies. A continuous sequence of occupation is well- documented in Grotte du Renne, France, where the lithic tradition can be divided into the Levallois–Charentian, Discoid–Denticulate (43.3±0.929–40.9±0.719 thousand years ago), Levallois Mousterian (40.2±1.5–38.4±1.3 thousand years ago), and Châtelperronian (40.93±0.393–33.67±0.450 thousand years ago).

The first appearance datum (FAD) of Iapetognathus fluctivagus in the cliffs of Green Point, Newfoundland and Labrador, Canada is defined as the base of the Tremadocian Age ( million years ago) and the beginning of the Ordovician Period. However, the genus Iapetognathus and related denticulate groups still require extensive taxonomic clarification. In 2011, a study discovered that the FAD of Iapetognathus fluctivagus in the GSSP section in Green Point may not actually be the earliest species of Iapetognathus to appear as was earlier believed. Its true FAD lies above another species, Iapetognathus preaengensis, and is not present at the Cambrian–Ordovician boundary (COBWG).

The forewings are orange, variably mixed with reddish-fuscous or dark fuscous, especially on the veins and some specimens are wholly suffused with fuscous. The extreme costal edge is sometimes whitish in the middle. The markings are reddish-brown, mixed or suffused with dark grey and there is a suffusion along the basal part of the costa, sometimes extending basally to the dorsum. The first line is irregularly curved and the second denticulate, forming a strong subquadrate loop inwards below the middle, the space between them wholly suffused with dark except along the costa and on a band preceding the upper half of the second line.

These include the relatively long anteroposterior facial length of the premaxilla, the elongate and strongly anteromedially directed dorsomedial process of the premaxilla, and the sharply defined and elevated margin of the perinarial fossa. There are differences between the two taxa such as differences in the relative thickness of dorsal osteoderms and the absence of a denticulate mesial carina on the first premaxillary tooth in Peirosaurus, but not in Uberabasuchus. However, these characters are considered to be minor and their taxonomic value may be individually variable. As postcranial materials of both Peirosaurus and Uberabasuchus are known but are not yet formally described, they are tentatively considered to be valid taxa.

The cap surface is smooth and sticky, dirty yellow-olive to dirty brownish-olive or olive grayish-green, then dirty light brown with green tinge, streakily fibrillose almost from the middle (scantily so at center), finely and persistently dark greenish-brownish. The gills are moderately crowded to distant spaced—about four gills per centimeter in the middle on mature fruit bodies, at the margin about ten per centimeter. They are adnate and deeply emarginate (notched), especially when mature, up to broad, somewhat wrinkled on the surface and with the edge entire or slightly undulatingly denticulate. Their color is dirty olive, then later dark brownish-olive, with slightly paler edge.

The forewings are light gray, heavily sprinkled and shaded with liver brown, especially along the costa and in patches below the apex and above the anal angle, which are entirely this color. There is an indistinct, dark line, outwardly oblique to below the cell, then slightly waved to the inner margin. There is also an orbicular round brown blotch and the reniform has the form of a figure of eight, filled with brown with a white dot in lower the portion. There is another line, which is brown, denticulate, arising from a small costal patch, evenly rounded opposite the cell, forming a strong sinus above vein 2, reaching to below the reniform, slightly bordered outwardly with whitish.

Nectaries are 0.6-0.8 × 0.4-0.9 mm. Blades are 7-11.5 × 7.5-11.5 cm, subpeltate 2-3(-3.5) mm from the margin, entire or glandular-denticulate at the very base, not variegated at maturity, very widely obovate to widely elliptic or ± circular, at base extremely shallowly cordate to truncate or slightly rounded. Leaves are shallowly to obscurely 3-lobed, with lateral lobes that are broadly obtuse to rounded or nearly obsolete, and a central lobe that is obtuse or somewhat rounded to truncate. Laminar nectaries are marginal, with 4 or 5 gland borne basally, (0)1 to 8 glands borne just proximal to the lateral veins, and (0)2 to 8 glands borne marginally distal to the lateral veins.

The main archaeological levels are found in the third set (soils levels D to G) and would be between 300 and 450 000 years old. This ensemble also delivered a number of human fossils, including an incomplete skull (face, frontal and parietal right) (Arago XXI, G soil) and two mandibles (Arago II, G soil and Arago XIII, soil F) attributed to the man of Tautavel. Discoveries from the oldest layers of set III have been described as ancient Tayacian or "Tautavélien". They are made mainly of quartz, more rarely flint and quartzite, and include scrapers, many notched tools (denticulate, notches, Tayac spikes, beaks, etc.), pebbles cut and rare bifaces (less than 1 for 1000 tools).

About half of the amphibians and reptiles are mostly Amazonian species with the remaining species associated primarily with southern and eastern open formations. There are several reptile species listed by the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) including species that are endangered in their home ranges. These include such species as Eunectes murinus (green anaconda), Eunectes notaeus (yellow anaconda), Caiman crocodilus yacare (yacare caiman), Melanosuchus niger (black caiman), Podocnemis unifilis (yellow-spotted river turtle), Podocnemis expansa (Charapa turtle), Geochelone carbonaria (red- footed tortoise) and Geocheolone denticulate (Brazilian giant tortoise).Burbridge, R.E., Mayle, F.E., and Killeen, T.J. “Fifty-thousand-year vegetation and climate history of Noel Kempff Mercado National Park, Bolivian Amazon.” Quaternary Research 61 (2004): 215– 230.

The stem bears conspicuous and prominent round scars of petioles, inflorescences and stipules in a spiral pattern. Branches nearly as thick as the stem, up to 1–1.5 cm thick and up to 15 cm tall, with pronounced markings of leaf-, inflorescence- and stipule-scars. Leaves alternate, crowded at the top of stems and branches; stipules subulate from a broad base, 1–2 mm long, mostly long persistent; petiole 1–3.6 cm long, puberulous; blade lanceolate to ovate, obovate or elliptic, 1.8–18 x 1–2.5 cm, cuneate to rounded at the base, rounded, obtuse or acuminate at the apex, with entire, crenulate, crisp or denticulate margins, scabridulous above, sparsely puberulous below. Flower structures grayish or green (or orange/pinkish).

The costa and the outer margin of the hindwings are fawn, but the inner margin and inner angle are broadly glaucous grey. There is a broad patch of black hairs at the base followed by a black incomplete transverse band running from the inner margin to beyond the end of the cell, and gradually widening from the inner margin. This is followed by a narrower black line which is very obscure upon the costa, but gradually widens toward the inner margin and becomes more distinct and terminates upon the internal vein. This is again followed by a very broad, dark brown band which runs from the costa before the outer angle to the inner margin, its inner edge being straight, its outer edge curved and denticulate, and defined by a pale grey waved line.

Hawksworth along with Riedl in 1977 re- proposed Rhinocladiella ellisii, but in 1979 was criticized by De Hoog as the genus Rhinocladiella characterized Z. cellare's asexual (conidial) form of which the fungus rarely presents in and decided that Z. cellare was the most appropriate name for this species. To prevent any further contention, de Hoog amended the genus Zasmidium to include fungi with undifferentiated conidiogenous cells with wavy branches, "denticulate rachis", and pigmented scars. Today, the literature agrees that the proper classification is in fact Zasmidium cellare of the division Ascomycota, representing spore shooting fungi; the class Dothideomycetes, which are fungi that grow in what are considered hostile or non-optimal conditions to most fungal species; the order Capnodiales, which typically grow masses of black cells; and the family Mycosphaerellaceae, which is a grouping of sac fungi.

In fact, the stridulitrum is absent from all species except P. pulchella, where a vestigial and non-functional remnant is present. Second, he maintained that there was an "absence of any constriction between postpetiole [= first gastral segment] and gaster", when in fact differentiated presclerites are strongly developed on the second gastral segment but are specialized in form and usually concealed by the posterior portions of the sclerites of the first gastral segment. However, Wheeler did recognise that the apparent similarities between his Phrynoponera species and two Indian Pachycondyla (then Bothroponera) species, Pachycondyla bispinosa (bispinose propodeum) and Pachycondyla rufipes (denticulate dorsal margin of petiole), were superficial and possibly independently acquired. Each of these Phrynoponera-like species lack the extremely specialized morphology of the petiole sternite, helcium, and prora, as well as the characteristic 5-spinose petiole node, that are unique and consistent in the female castes of Phrynoponera.

E. ochroleuca Esp. (41b). Forewing white, suffused with pale olive brown; lines broadly white, the inner and outer generally coalescing on submedian fold, the outer line denticulate externally; median area often darker brown, somewhat blackish tinged, especially in the male; orbicular stigma pale olive, the reniform white with an ochreous centre: submarginal line whitish, indented on each fold and there preceded by some dark brown scaling; a row of dark marginal lunules; fringe ochreous with two outer rows of dark lunules; hindwing ochreous dusted with luteous grey; a dark cell spot and outer line followed by a pale space before the broad fuscous marginal border; fringe white. — Larva pale green; lines whitish; lateral line broadly white, its lower edge blackish; spiracles black: head pale brown; the tubercles blackish. Warren. W. in Seitz, A. Ed., 1914 Die Großschmetterlinge der Erde, Verlag Alfred Kernen, Stuttgart Band 3: Abt.

The forewings are whitish, partially tinged with pale grey, and finely irrorated (speckled) throughout with blackish. There is a brown oblique fascia-like spot from the costa about one- third, somewhat dilated downwards, reaching to below the middle of the disc, containing a blackish suffusion towards its lower extremity. A roundish-brown blotch is found in the disc about three-fourths, including a longitudinal suffused blackish streak, and confluent posteriorly with a smaller brown blotch on the middle of the hindmargin. There is a sinuate fuscous line from the middle of the costa to the centre of the blotch at three-fourths and an ill-defined blackish-fuscous denticulate line from two-thirds of the costa to the inner margin before the anal angle, very strongly curved outwards so as to approach the margin throughout, followed on the costa by two or three small spots of brownish suffusion.

The forewings are white with fuscous markings which are diffused with ochreous, and irrorated (sprinkled) with black scales. There is a broad fascia from the fold opposite two-fifths the inner margin, the anterior border in two waves to one-third of the costa, and continued as a fine line toward the base, but not as far as the base, the posterior border is irregularly curved and toothed, nearly parallel to the anterior border, then curved along the costa, and gradually narrowing to a thinned out line at four-fifths of the costa. This subtends a second fascia which is sometimes commingled with it from a point opposite two-thirds of the costa and which gradually widens to the inner margin, the anterior border twice waved and finely denticulate to beyond half the inner margin, the posterior border with a sinuate outward curve to anal angle of the inner margin. From its centre a bar connects with a broad diffused apical fascia.