Based on collections of 45 Herbaria in addition to newly collected specimens and some field observations, a taxonomic treatment for South American Ctenitis is provided, a hundred years after Christensen’s monographs. Guided by morphological species concept, 26 taxa are recognized (23 species and three varieties). A key including all taxa is provided, and all species are fully morphologically described, with information on distribution and habitat. Brazil is the richest country with 22 taxa, of which 13 are endemic, restricted mainly to Atlantic Forest. Taxa occurring in the other South American countries are also widely distributed in Mesoamerica and West Indies, except C. megalastriformis, only known from Peru, and C. refulgens var. peruviana, recorded in Peru and Bolivia. We dealt with 163 names that apply to the South American species. In addition, we propose three new combinations, and designate 38 lectotypes and three neotypes.
Raquel Stauffer Viveros, Germinal Rouhan and Alexandre Salino. 2018. A Taxonomic Monograph of the Fern Genus Ctenitis (Dryopteridaceae) in South America. Phytotaxa. 335(1); 1–83. DOI: 10.11646/phytotaxa.385.1.1
كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
A new circumscription and a total of six microendemic species, four of them new to science, are herein presented for Siderasis, based on field and herbaria studies, and cultivated material. We provide an identification key to the species and a distribution map, description, comments, conservation assessment, and illustration for each species. Also, we present an emended key to the genera of subtribe Dichorisandrinae, and comments on the morphology and systematics of the subtribe.
Figure 1. Floral morphology of subtribe Dichorisandrinae s.l.
A–C Siderasis Raf. emend M.Pell. & Faden: A S. fuscata (Lodd.) H.E.Moore B S. albofasciata M.Pell. C S. zorzanellii M.Pell. & Faden.
D–L Dichorisandra J.C.Mikan: D D. acaulis Cogn. E D. hexandra (Aubl.) C.B.Clarke F D. thyrsiflora J.C.Mikan G D. paranaënsis D.Maia et al. H D. nana Aona & M.C.E.Amaral I D. incurva Mart. JD. penduliflora Kunth KD. sagittata Aona & M.C.E.Amaral LD. radicalis Nees & Mart.
M Cochliostema odoratissimum Lem. N Geogenanthus rhizanthus (Ule) G.Brückn. O Plowmanianthus panamensis Faden & C.R.Hardy.
Photographs A–B, D–G, J by M.O.O. Pellegrini, C by J.P.F. Zorzanelli, H by V. Bittrich, I by G.H. Shimizu, K by J.L. Costa-Lima, L by M.A.N. Coelho, M by R. Moran, N by D. Scherberich, and O by C.R. Hardy.
Pyrrheima Hassk., Flora 52: 366. 1869, nom. illeg. Type species (designated here). P. loddigesii Hassk., nom. illeg. [≡ S. fuscata (Lodd.) H.E.Moore].
Type species: Siderasis acaulis Raf. [≡ S. fuscata (Lodd.) H.E.Moore].
Etymology: Siderasis was named in allusion to the peculiar red to bright-red hairs that cover almost the entire plant, but especially the leaves. However, only S. fuscata possesses the aforementioned hairs, and all of the remaining species possess leaf blades covered by hyaline to light brown, rarely rusty hairs.
Habitat, distribution and ecology: Siderasis is endemic to the Atlantic Forest domain in coastal Brazil, occurring in the states of Bahia, Espírito Santo, and Rio de Janeiro (Fig. 2). More specifically, Siderasis is restricted to the Central Corridor of the Atlantic Forest, growing in remnants of semideciduous forests associated with inselbergs, between 90–1350 m above sea level. The genus is composed exclusively by microendemic species distributed in very small and fragmented subpopulations, susceptible to deforestation and illegal collection of specimens for ornamental purposes.
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1. Siderasis albofasciata M.Pell., Nordic J. Bot. 35(1): 30. 2017.
Etymology: The epithet means “white-striped”, making reference to the thin and always present, white to silver stripe along the midvein of this species’ leaves.
Distribution and habitat: Siderasis albofasciata is known exclusively from the municipalities of Santa Teresa and Fundão, state of Espírito Santo (Fig. 2). It occurs in the understory of evergreen forests, in shady areas with shallow and rocky soil, with great leaf-litter accumulation.
Figure 7. Siderasis almeidaeM.Pell. & Faden. A habit, showing a fertile rosette B detail of the elongated aerial stem, showing the rusty internodes and leaf-sheaths C detail of the lanate indumentum on the abaxial side of the leaf blade D detail of the hispid indumentum on the adaxial side of the leaf blade E detail of the inflorescence, showing the contracted cincinnus and some floral buds F front view of a flower, showing the fleshy and internally purple sepals, and the lanate ovary. Photographs A, F by M.A.N. Coelho, remaining photographs by M.O.O. Pellegrini.
2. Siderasis almeidae M.Pell. & Faden, sp. nov.
Diagnosis: Similar to S. fuscata due to its rusty indumentum in the leaves, lilac to purple rhomboid petals and white anthers. Also, similar to S. albofasciata due to its sessile to subpetiolate leaves, blades adaxially hispid and abaxially lanate, present bracteoles, and purple filaments and style. Nevertheless, Siderasis almeidae is peculiar in lacking terminal tubers in the roots, subterraneous stems, and having aerial stems elongate and trailing in the leaf litter, leaves entirely green, fleshy showy sepals, and a densely lanate ovary.
Etymology: The epithet honors Brazilian botanist Rafael Felipe de Almeida, a prominent specialist in Malpighiaceae, contributor in the studies of Commelinaceae, husband of the first author, and co-collector of the holotype, for his unmeasurable support in the field and in my research.
Distribution and habitat: Siderasis almeidae is confined to the municipalities of Itamarajú and Prado, Bahia (Fig. 2). It occurs in the “mata higrófila” vegetation with emerging rocky formations, in shady and moist areas. In the type locality, the subpopulations were found growing in great accumulations of leaf litter, among dense clusters of Marantaceae. The area is greatly disturbed, and within private property.
Etymology: The epithet “fuscata” means dark-colored, in allusion to the red to bright red hairs that cover almost the entire plant, in opposition to the normally hyaline hairs in most Commelinaceae.
Distribution and habitat: Siderasis fuscata is endemic to the municipalities of Rio de Janeiro (with several localities inside Floresta da Tijuca) and Niterói (with just one locality, Alto Mourão), in the Rio de Janeiro state (Fig. 2). It occurs in the vegetation on hillsides (mata de encosta) near the littoral, in shady areas with shallow and rocky soil.
Figure 9. Siderasis medusoidesM.Pell. & Faden. A habit, showing a fertile rosette B detail of the synflorescence, showing the elongated and tangled cincinni C front view of a flower, showing small ants near the flower center D detail of the capsule. Photographs by P. Fiaschi.
4. Siderasis medusoides M.Pell. & Faden, sp. nov.
Diagnosis:Similar to S. almeidae due to its sessile to subpetiolate, entirely green leaves, present bracteoles, sessile flowers, purple filaments and style combined with white anthers, and oblongoid to broadly oblongoid capsules. Siderasis medusoides is distinct due to its membranous leaves, elongate and tangled cincinni, small flowers, and purple to dark blue and elliptic to narrowly obovate or spatulate petals.
Etymology: The epithet alludes to the extremely elongated cincinni, common in mature individuals of this species, due to their resemblance to the snakes that composed the hair of Medusa, one of the three Gorgon sisters from Greek mythology.
Distribution and habitat: Siderasis medusoides is known from the municipalities of Marilândia and Santa Leopoldina, in the state of Espírito Santo (Fig. 2). It grows in lowland Atlantic Forest, in shady and moist areas with great leaf litter accumulation, 90–550 m above the sea level.
Diagnosis: Very distinctive due to its vining habit, distichously-alternate leaves, blades asymmetric at base, main florescence a many-branched thyrse, with alternate cincinni, flowers zygomorphic, bisexual or staminate, stamens unequal, curved upwards, sigmoid filaments, and capsules globose and shallowly foveolate. It can be differentiated from S. zorzanellii by its membranous and velutine leaves, inflorescences always terminal in the secondary branches, petals dark mauve to vinaceous, rarely light pink or white, with margins ciliate with non-moniliform hairs.
Etymology: The epithet means “admirable, remarkable, spectacular”, in allusion to its distinctive growth form, small flowers with a peculiar coloration, and the unique petal margins ciliate with non-moniliform hairs.
Distribution and habitat: Siderasis spectabilis is confined to the type locality, in the native vegetation of the Horto Santos Lima (currently the headquarters of the Desengano State Park), in Santa Maria Madalena, state of Rio de Janeiro (Fig. 2). Nothing is known about this species habitat, since the original labels give no information on the area and all field expeditions to recollect this plant have been unsuccessful.
6. Siderasiszorzanellii M.Pell. & Faden, sp. nov.
Diagnosis: Similar to S. spectabilis due to its vining habit, distichously-alternate leaves, blades asymmetric at base, main florescence a many-branched thyrse, with alternate cincinni, flowers bisexual or staminate, zygomorphic, stamens unequal, curved upwards and sigmoid filaments. It can be differentiated from by its chartaceous and sparsely velutine leaves, inflorescences axillary in the primary branches or terminal in the secondary branches, and petals white with glabrous margins.
Etymology: The epithet honors the collector of the type specimens, João Paulo Fernandes Zorzanelli, Brazilian botanist and dear friend of the authors. JPFZ is an active and prominent collector in the state of Espírito Santo, with collections currently focused on Serra do Valentim, the type locality of S. zorzanellii.
Distribution and habitat: Siderasis zorzanellii is confined to the municipality of Iúna, Espírito Santo (Fig. 2). It occurs in the “Floresta Ombrófila Densa Montana” vegetation, at 1200–1350 m above the sea level, generally near disturbed sites, being less frequent in well-preserved areas. This could be related to its climbing habit and the need of more sunlight exposure then the rosette species of the genus. This pattern is common in other liana and vine groups, such as Bignoniaceae, Malpighiaceae, and Sapindaceae (Acevedo-Rodríguez, pers. comm.), especially evident in big families such as Asteraceae, where the primarily climbing genus Mikania Willd. is almost exclusively found at the edge of forests, along trails, and in disturbed areas (Oliveira 2015).
Final remarks
The present work adds four new species to Siderasis, along with the addition of new morphological characters that help clarify the circumscription of the group. Siderasis Raf. emend. M.Pell. & Faden may be uniquely characterized as comprising small perennial rosette herbs or robust perennial vines, with shoots determinate or indeterminate, leaves spirally- or distichously-alternate. The inflorescences are terminal or axillary, either a many-branched thyrse with alternate cincinni or reduced to a solitary cincinnus, cincinni always several-flowered. The flowers are chasmogamous, bisexual or male, actinomorphic or zygomorphic, and petals with glabrous margins or ciliated with non-moniliform hairs. The androecium is composed of 6 fertile stamens, filaments straight or sigmoid, anthers dorsifixed and extrorsely rimose, anther sacs semicircular, divergent, connectives expanded and quadrangular. In the gynoecium, the stigma is annular-truncate or annular-capitate, marginally papillate with unicellular papillae restricted to the margin of the stigmatic regions. Also, similar to Dichorisandra, the capsules are thick-walled, and the seeds are arillate, biseriate to partially uniseriate, with semidorsal or semilateral embryotega, and a C-shaped hilum. All species accepted by us are easily diagnosed by a unique and constant combination of morphological character states. Furthermore, each species can be easily separated based on their geographical distribution, since they are microendemics, with non-overlapping distribution areas (Fig. 2).
As indicated by several systematic studies in Commelinaceae (Evans et al. 2000, 2003; Hardy 2001; Wade et al. 2006; Zuiderveen et al. 2011; Hertweck and Pires 2014) and by the morphological evidence presented here and by Pellegrini (2017), the need to recircumscribe subtribe Dichorisandrinae is pressing. Aside from the cytological character of x=19 large chromosomes described by Jones and Jopling (1972) and hypothesized by Faden and Hunt (1991), no macro or micromorphological synapomorphies were found so far for subtribe Dichorisandrinae in its current circumscription. On the other hand, if subtribe Dichorisandrinae is recircumscribed to exclusively contain Dichorisandra and Siderasis, Dichorisandrinae s.s. can be easily morphologically characterized by its thick-walled capsules, the biseriate to partially uniseriate arillate seeds, semidorsal to semilateral embryotega, and C-shaped hilum. The lineage composed by Geogenanthus (Cochliostema+Plowmanianthus) needs to be formally recognized as a subtribe, and can be easily circumscribed by its petals with marginally fringed with moniliform hairs, and anthers sacs curved to spirally-coiled and appressed to each other. Phylogenetic studies using both nuclear and chloroplast sequences seem promising in elucidating phylogenetic incongruences in Commelinaceae (e.g. Burns et al. 2011). However, most phylogenetic in the family so far completely disregard morphological data, with the exception of Evans et al. (2000, 2003). Studies focusing on the systematics and recircumscription of Dichorisandrinae are currently being conducted, combining morphological and molecular data (Pellegrini et al., in prep.), and should shed some light on the evolution of the reproductive biology in the family.
Marco O.O. Pellegrini and Robert B. Faden. 2017. Recircumscription and Taxonomic Revision of Siderasis, with Comments on the Systematics of Subtribe Dichorisandrinae (Commelinaceae). PhytoKeys. 83; 1-41. DOI: 10.3897/phytokeys.83.13490
كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
Since its description, almost 100 years ago, the genus Dinizia has been treated as monospecific, comprising the single canopy-emergent species Dinizia excelsa Ducke which grows in non-flooded Amazonian forests of Guyana, Suriname and seven states of northern and central-western Brazil. Dinizia jueirana-facao G. P. Lewis & G. S. Siqueira, which grows in a restricted area of semi-deciduous Atlantic rain forest in Espírito Santo state, Brazil, is described as a new species in the genus. The new species is also a canopy-emergent of impressive stature. We provide descriptions for both species, a key to species identification, a distribution map and the new species is illustrated. Fossil leaves, inflorescences and fruit provide evidence for a Dinizia-like ancestor occurring in south-eastern North America during the Eocene. In contrast to D. excelsa where pollen is dispersed in tetrads, the pollen of D. jueirana-facao is shed in monads. D. jueirana-facao is considered critically endangered following IUCN conservation criteria, whereas D. excelsa is assessed to be of least concern. A lectotype is designated for D. excelsa.
Fig. 3 Dinizia jueirana-facao. A flowering branch and part of a bipinnate leaf; B leaflets at the base of a single pinna; C hermaphrodite flower; D functionally male flower opened to show stamen filaments and suppressed gynoecium development; E calyx opened out, outer surface; F longitudinal section of hermaphrodite flower to show gynoecium; G petal, outer surface; H stamen; J anther; K fruit; L part of a single valve of dehisced fruit with seeds attached; M seed.
A – J from Folli 4889 (K), K – M from Folli 4484 (K). drawn by Margaret Tebbs.
Dinizia jueirana-facao G. P. Lewis & G. S. Siqueira sp. nov.
Type: Brazil, Espírito Santo, Linhares, Reserva Natural Vale, 30 July 2004 (fl.), D. A. Folli 4889 (holotype CVRD!; isotypes HUEFS!, K!).
Recognition. Dinizia jueirana-facao differs from its sister species D. excelsa in having leaflets in (9 –) 15 – 23 (– 24) pairs per pinna (vs 7 – 14 pairs), the leaflets completely glabrous (vs puberulent to glabrescent on their lower surface), its individual racemes 28 – 35 × 3 – 4.5 cm (vs 10 – 18 × 1 – 2 cm), buds ellipsoid to obovoid (vs globose), flowers 8.5 – 10 mm long (vs 4 – 5 mm long), its floral bracts spathulate and caducous (vs lanceolate and often persistent), its fruit woody and dehiscent along both sutures (vs indehiscent), seeds 25 – 30 × 16 – 19 mm (vs (10 –) 14 – 15 × 6 – 7 mm); and pollen in monads (vs tetrads).
Distribution. Dinizia jueirana-facao is currently known only from two locations, one (19°08'52.0"S, 40°05'16.4"W) in the Reserva Natural Vale in Linhares, northern Espirito Santo state, Brazil, and the second (19°05'12.1"S, 40°10'41.2"W) just outside the reserve in the surroundings of the small hamlet of Santa Luzia Sooretama. Map 1.
Habitat. An emergent tree in semi-deciduous forest and mata ciliar in the Reserva Natural Vale, an area of 22,000 hectares of pristine Atlantic Forest. This is the largest protected area of semi-deciduous forest in eastern Brazil. Also known from mata de tabuleiro, in the surroundings of Sooretama, just outside the Vale Reserve. Growing at elevations of 40 – 150 m above sea level.
Etymology. The species name is taken directly from the local name, “jueirana-facão”, for the tree in Espirito Santo. In the Reserva Natural Vale, the large legume tree Parkia pendula (Willd.) Benth ex Walp. is known as jueirana-vermelha and the new Dinizia species, which has a very similar bark which breaks off in large woody plates, but much larger fruits, is locally differentiated by replacing vermelha (Portuguese for red) with facão (Portuguese for large knife or machete), because the woody fruits of D. jueirana-facao have the appearance of a machete sheath or scabbard. According to the International Code of Nomenclature for algae, fungi and plants (McNeill et al. 2012) an epithet can be a word in apposition (Art. 23.1) and taken from any source whatsoever (Art. 23.2), but the Code does not give clear guidance on diacritical signs, just ruling (Art. 60.6) that “the [diacritical] signs are to be suppressed with the necessary transcription of the letters so modified” but without elaborating on what “necessary transcription” means beyond the cited examples, which do not include ã. We thus transcribe the ã as a in the specific epithet here chosen for the new species.
Jueirana is thought to be derived from the Tupi word yuá-rana. Yuá (or Juá) is a Tupi common name for several different plant species, especially those in the Solanaceae with round, spiny fruits (Andrade 2006; Sampaio 1987). Rana in Tupi means similar to, so yuá-rana or jueirana means false juá (or similar to juá), although there is little resemblance between the new legume species and any Solanaceae. A number of place names in Brazil are derived from jueirana or an orthographic variant of this.
Notes. Dinizia jueirana-facao, as currently known, is a narrowly restricted species endemic to a small area of Atlantic forest in the Brazilian state of Espirito Santo. Although a tree of shorter stature, and lacking buttresses, many of its vegetative and reproductive morphological characteristics are greater in number and/or size than those seen in its widespread Amazonian sister species, D. excelsa. D. jueirana-facao has leaflets in (9 –) 15 – 23 (– 24) pairs per pinna (7 – 14 pairs per pinna in D. excelsa), the leaflets glabrous (vs puberulent to glabrescent on their lower surface), its individual racemes 28 – 35 × 3 – 4.5 cm (vs 10 – 18 × 1 – 2 cm) in open flower, its flower buds ellipsoid to obovoid (vs globose), its flowers 8.5 – 10 mm long (vs 4 – 5 mm long), its floral bracts spathulate and caducous (vs lanceolate and often persistent), its fruit woody and dehiscent along both sutures (vs indehiscent), its seeds 25 – 30 × 16 – 19 mm (vs (10 –) 14 – 15 × 6 – 7 mm), and its pollen in monads (vs tetrads). D. jueirana-facao is critically endangered and presently known from less than 25 trees in two small areas, of which only one locality is inside a protected reserve. The type collection of the new species is from one of the largest trees growing inside the reserve.
G. P. Lewis, G. S. Siqueira, H. Banks and A. Bruneau. 2017. The Majestic Canopy-Emergent Genus Dinizia (Leguminosae: Caesalpinioideae), Including A New Species Endemic to the Brazilian State of Espírito Santo. Kew Bulletin. 72:48. DOI: 10.1007/s12225-017-9720-7
كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
We generated a novel database of Neotropical snakes (one of the world's richest herpetofauna) combining the most comprehensive, manually compiled distribution dataset with publicly available data. We assess, for the first time, the diversity patterns for all Neotropical snakes as well as sampling density and sampling biases.
Main types of variables contained
We compiled three databases of species occurrences: a dataset downloaded from the Global Biodiversity Information Facility (GBIF), a verified dataset built through taxonomic work and specialized literature, and a combined dataset comprising a cleaned version of the GBIF dataset merged with the verified dataset.
Spatial location and grain
Neotropics, Behrmann projection equivalent to 1° × 1°.
Time period
Specimens housed in museums during the last 150 years.
Major taxa studied
Squamata: Serpentes.
Software format
Geographical information system (GIS).
Results
The combined dataset provides the most comprehensive distribution database for Neotropical snakes to date. It contains 147,515 records for 886 species across 12 families, representing 74% of all species of snakes, spanning 27 countries in the Americas. Species richness and phylogenetic diversity show overall similar patterns. Amazonia is the least sampled Neotropical region, whereas most well-sampled sites are located near large universities and scientific collections. We provide a list and updated maps of geographical distribution of all snake species surveyed.
Main conclusions
The biodiversity metrics of Neotropical snakes reflect patterns previously documented for other vertebrates, suggesting that similar factors may determine the diversity of both ectothermic and endothermic animals. We suggest conservation strategies for high-diversity areas and sampling efforts be directed towards Amazonia and poorly known species.
Figure 1. Neotropical region and ecoregion limits adopted here (sensu Olson et al., 2001), together with representative snakes species recorded for Central America Montane Forests: 1.1 Boa constrictor, 1.2 Oxybelis aeneus; Amazonia Most Forests: 1.3 Philodryas argentea, 1.4 Rhinobothryum lentiginosum, 1.5 Eunectes murinus, 1.6 Siphlophis compressus, 1.7 Amerotyphlops reticulatus, 1.8 Lachesis muta; Cerrado: 1.9 Imantodes cenchoa, 1.10 Apostolepis flavotorquata, 1.11 Bothrops lutzi, 1.12 Micrurus frontalis, 1.13 Erythrolamprus typhlus, 1.14 Phalotris lativittatus, 1.15 Xenopholis undulatus, 1.16 Oxyrhopus rhombifer, 1.17 Rhachidelus brazili; Chaco: 1.18 Psomophis genimaculatus, 1.19 Philodryas baroni, 1.20 Phimophis vittatus; Guianian Moist Forests: 1.21 Corallus caninus, 1.22 Anilius scytale, 1.23 Amerotyphlops brongersmianus; Caatinga: 1.24 Erythrolamprus viridis, 1.25 Thamnodynastes phoenix, 1.26 Bothrops erythromelas; and in the Atlantic Forest: 1.27 Atractus maculatus, 1.28 Chironius bicarinatus, 1.29 Tropidodryas striaticeps, 1.30 Liotyphlops beui, 1.31 Oxyrhopus guibei, 1.32 Dipsas albifrons, 1.33 Bothrops jararaca, 1.34 Corallus hortulanus, 1.35 Erythrolamprus atraventer.
The abbreviations indicate common life habits of the Neotropical snakes: aquatic (Aq), arboreal (Ar), fossorial (F), terrestrial (T).
Photograph credits: Cristiano C. Nogueira (10, 12), Crizanto C. Brito (27), Henrique B. Braz (14), Ivan Sazima (24, 35), Luiz C. Turci (7), Marcio Martins (4), Marco Sena (6), Martin Jansen (9, 13, 18, 23, 31), Otavio A. V. Marques (2, 3, 5, 15, 16, 17, 19, 20, 21, 22, 28, 30, 32), Ricardo J. Sawaya (33), Thaís B. Guedes (1, 8, 11, 25, 26, 29, 34)
Our study demonstrates that Neotropical snake diversity is unevenly distributed, with some ecoregions, such as the Cerrado, containing a disproportionately high diversity. We also showed that merging public and manually compiled data sources is likely to provide the largest taxonomic and geographical coverage for any system under study. However, a proper taxonomic verification, examination and assessment of biases of the public dataset proved crucial. As a result, we can now provide a solid and reliable foundation for any kind of meta-analysis, including the assessment of climate change effects, conservation strategies or design of future research agendas. Conservation priorities should focus on areas of high diversity values as well as high threat by landscape changes. Finally, we found highest diversity values in forested areas, reinforcing the need for general habitat protection compared with actions that are targeting specific species.
In order to increase our knowledge about Neotropical snakes, a geographically and taxonomically focused sampling is required, targeting Amazonia and those species whose distributions are so far largely unknown.
كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
Despite the impressive growth of knowledge on the phylogenetic systematics of dart-poison frogs and their relatives (Dendrobatoidea) over the past decade, many problems remain to be addressed. We analyzed up to 189 phenomic characters (morphology, behavior, defensive chemicals) and 15 mitochondrial and nuclear loci scored for 564 dendrobatoid and outgroup terminals, including 76 newly sequenced terminals and > 20 previously unanalyzed species, using tree-alignment and the parsimony optimality criterion in the program POY v.5.1.1 and additional analyses of the implied alignment using TNT v.1.5. Even though data coverage was highly heterogeneous, the strict consensus of 639 optimal trees is highly resolved and we detected only one instance of wildcard behavior involving a small clade of outgroup species. The monophyly of the median lingual process (MLP) possessing genus Anomaloglossus is decisively refuted, with the cis-Andean species being sister to Rheobates within Aromobatidae and the trans-Andean species nested within Hyloxalinae, implying two independent origins of the structure in Dendrobatoidea. Although this result was unexpected, it is not surprising given that the MLP evolved at least five times in Asian and African ranoids, including Arthroleptidae, Dicroglossidae, Mantellidae, and Rhacophoridae and either once in the most recent common ancestor of the massive clade Victoranura followed by independent losses or multiple times within component lineages. We restrict Anomaloglossus to the cis-Andean MLP-possessing species, describe a new genus for the trans-Andean MLP-possessing species, and resurrect Paruwrobates for its sister group, which includes Dendrobates andinus (formerly Ameerega), D. erythromos (formerly Hyloxalus and, until recently, Ameerega), and Prostherapis whymperi (formerly Hyloxalus). We also transfer Dendrobates maculatus from Ameerega to Epipedobates, making Ameerega an exclusively cis-Andean group. We describe two new species of the trans-Andean MLP-possessing genus—one from Cerro Tacarcuna, near the Colombo-Panamanian border, and the other from 800–900 m elevation on the western versant of the Colombian Cordillera Occidental (Cauca Department)—bringing the total number of species in the genus to seven. The discrete, round, white to yellowish-brown dots found on the venter of the new species from Cerro Tacarcuna and at least one other trans-Andean MLP-possessing species are formed by large, ellipsoid, densely distributed (up to 80 glands/mm) granular glands. Although specimens of the new species from Cerro Tacarcuna exuded a noxious milky substance when handled, lipophilic alkaloids were not detected. In addition to the unexpected placement of the trans-Andean MLP-possessing species, major findings include the unexpected placement of Colostethus ruthveni and its undescribed sister species (the “C.” ruthveni group) within Dendrobatinae as sister of the newly recognized tribe Dendrobatini (all dendrobatines except Phyllobates and the “C.” ruthveni group). We describe a new genus for C. argyrogaster and C. fugax to remedy the paraphyly of Colostethus caused by the placement of those species as sister to Ameerega. Our evidence rejects the sister group relationship of Dendrobates + Oophaga in favor of Dendrobates + Adelphobates, which is consistent with their uniquely low diploid chromosome number of 2n = 18 (2n = 20 in Oophaga). With the exception of Anomaloglossus and Colostethus, all other genera are monophyletic. We recognize several monophyletic species groups—including the Atlantic Forest, trans-Andean, and 22-chromosome groups within Allobates, the An. stepheni, An. megacephalus, and An. beebei groups in Anomaloglossus, the C. latinasus (formed by the C. inguinalis and C. latinasus clades) and C. fraterdanieli groups within Colostethus, and the Am. braccata and Am. rubriventris groups within Ameerega—identify unambiguously optimized phenomic synapomorphies, and summarize patterns in the evolution of the diploid chromosome number, swelling of Finger IV in males, relative length of Fingers II and III, length of Finger V, and testicular and intestinal pigmentation. Finally, we address criticisms of the current taxonomy of Neotropical poison frogs and their relatives, concluding that they are either overstated, misguided, or false, and that the current system of names better communicates knowledge of the diversity of these frogs. Our results highlight the importance of increased taxon sampling, and we conclude by identifying key species to include in future phylogenetic analyses.
Keywords: Andes, Aromobatidae, Chocó, Dendrobatidae, Median lingual process, New genus, New species, Phylogeny, Total evidence
.....
Figure 10(A): Juvenile female Ectopoglossus saxatilis sp. nov. photographed with the assistance of a camera-mounted flash (IAvH 14614, 18.3 mm SVL; photos: M. Rada). .
Ectopoglossus gen. nov.
Type species. Ectopoglossus saxatilis sp. nov.
Immediately more inclusive taxon. Hyloxalinae Grant et al., 2006.
Sister group.Paruwrobates Bauer, 1994.
Content (7 species).Ectopoglossus absconditus sp. nov., E. astralogaster (Myers et al., 2012) comb. nov., E. atopoglossus (Grant et al., 1997) comb. nov., E. confusus (Myers and Grant, 2009) comb. nov., E. isthminus (Myers et al., 2012) comb. nov., E. lacrimosus (Myers, 1991) comb. nov., and E. saxatilis sp. nov.
Etymology. Ectopoglossus gen. nov. (gender masculine) is derived from the Greek ektopos, meaning away or out of a place (ek- “out” + topos “place”), and glossa, meaning tongue, in reference to the geographically and phylogenetically ectopic distribution of this median lingual process-possessing clade.
Ectopoglossus absconditus sp. nov.
Etymology. The specific epithet is the Latin absconditus, hidden, in reference to this species being hidden in plain site, abscondita in campo visum, for nearly 80 years. The type specimens were collected in 1938 and 1939 and lay ensconced in the KU amphibian collection until finally being “discovered” almost 80 years later when TG examined the contents of a jar labeled “Colostethus sp.” that contained this and several other species of dendrobatids. To our knowledge the species has not been collected again, although biological surveys in the region have been limited in recent decades due to armed conflict.
Ectopoglossus saxatilis sp. nov.
Etymology. The specific epithet is Latin and means “found among rocks” in reference to the streamside habitat of the species.
Taran Grant, Marco Rada, Marvin Anganoy-Criollo, Abel Batista, Pedro Henrique Dias, Adriana Moriguchi Jeckel, Denis Jacob Machado and José Vicente Rueda-Almonacid. 2017. Phylogenetic Systematics of Dart-Poison Frogs and Their Relatives Revisited (Anura: Dendrobatoidea). South American Journal of Herpetology. 12(s1); S1-S90. DOI: 10.2994/SAJH-D-17-00017.1
كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
FIGURE 1. Images of Lavoisiera species. D–E.L. arachnoidea (unvouchered image). F. L. belinelloi(Almeda et al. 8532). G. L. bradeana (Almeda et al. 9718). H.L. canastrensis(Almeda et al. 7878). I. L. caryophyllea (Almeda et al. 9172). J–K. L. chamaepitys (Almeda et al. 8500). L. L. confertiflora (Almeda et al. 9725).
Image credits: F–L. Frank Almeda; D–E. Karina Fidanza.
A systematic monograph is presented for Lavoisiera, a Brazilian endemic genus of 41 species that is centered in the campo rupestre ecoregion in the Brazilian Planalto south of the Amazon basin, mostly west of the Mata Atlântica (Atlantic Rainforest), and east of the Pantanal. The stronghold for species diversity is the state of Minas Gerais with 36 species, 30 of which are endemic there. This study represents the first comprehensive monograph of the genus based on field work across its distributional range, complemented by examination of over 3620 specimens from 35 herbaria. An evaluation of taxonomic characters used in the long-standing sectional classification of the genus has led to its abandonment because it is based on artificial characters and does not provide a sound working hypothesis of infrageneric relationships. Eight new species are described: Lavoisiera arachnoidea, L. belinelloi, L. canastrensis, L. daviesiana, L. minima, L. rundeliana, L. setosa, and L. vestita; lectotypifications are provided for L. caryophyllea, L. chamaepitys, L. glandulifera, L. pulchella, and L. senae; and 44 epithets are relegated to synonymy. An identification key, full synonymy, descriptions, habitat and phenological information, distribution maps, diagnostic illustrations, images of representative species in the field, and geospatial conservation assessments are provided for all species based on IUCN criteria. SEM images of seed morphology are presented for nearly half of the species along with camera lucida drawings of meiotic chromosome figures for selected species, and an index to numbered collections examined.
Keywords: campo rupestre, Cerrado biome, conservation, endemism, Myrtales, neotropics, Eudicots
Lavoisiera macrocarpa Naudin (1844)
Lavoisiera macrocarpa (Almeda et al. 9173).
Images: Frank Almeda.
FIGURE 1. Images of Lavoisiera species. D–E. L. arachnoidea (unvouchered image). F. L. belinelloi (Almeda et al. 8532). G. L. bradeana (Almeda et al. 9718). H. L. canastrensis (Almeda et al. 7878). I. L. caryophyllea (Almeda et al. 9172). J–K. L. chamaepitys (Almeda et al. 8500). L. L. confertiflora (Almeda et al. 9725). Image credits: F–L. Frank Almeda; D–E. Karina Fidanza.
Angela B. Martins and Frank Almeda. 2017. A Monograph of the Brazilian Endemic Genus Lavoisiera (Melastomataceae: Microlicieae). Phytotaxa. 315(1); 1–194. DOI: 10.11646/phytotaxa.315.1.1
كيف تحصل على مدونة جاهزة بآلاف المواضيع والمشاركات من هنا
شاهد قناة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على اليوتيوب لمزيد من الشرح من هنا
رابط مدونة منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات في أي وقت حــــتى لو تم حذفها من هنا شاهد صفحة منتدى مدونات بلوجر جاهزة بألاف المواضيع والمشاركات على الفيس بوك لمزيد من الشرح من هنا
تعرف على ترتيب مواضيع منتدى مدونات بلوجر جاهزة بآلاف المواضيع والمشاركات (حتى لا تختلط عليك الامور) من هنا
ملاحظة هامة: كل عمليات تنزيل، رفع، وتعديل المواضيع الجاهزة تتم بطريقة آلية، ونعتذر عن اي موضوع مخالف او مخل بالحياء مرفوع بالمدونات الجاهزة بآلاف المواضيع والمشاركات، ولكم ان تقوموا بحذف هذه المواضيع والمشاركات والطريقة بسيطة وسهلة. ــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــــسلامـ.
