Species New to Science's Journal
[Most Recent Entries]
[Calendar View]
Thursday, August 13th, 2020
Time |
Event |
2:52a |
[PaleoOrnithology • 2020] Eudyptes atatu • Ancient Crested Penguin (Aves, Sphenisciformes) Constrains Timing of Recruitment into Seabird Hotspot
 | Eudyptes atatu Thomas, Tennyson, Scofield & Ksepka
in Thomas, Tennyson, ... et Ksepka, 2020. |
Abstract New Zealand is a globally significant hotspot for seabird diversity, but the sparse fossil record for most seabird lineages has impeded our understanding of how and when this hotspot developed. Here, we describe multiple exceptionally well-preserved specimens of a new species of penguin from tightly dated (3.36–3.06 Ma) Pliocene deposits in New Zealand. Bayesian and parsimony analyses place Eudyptes atatu sp. nov. as the sister species to all extant and recently extinct members of the crested penguin genus Eudyptes. The new species has a markedly more slender upper beak and mandible compared with other Eudyptes penguins. Our combined evidence approach reveals that deep bills evolved in both crested and stiff-tailed penguins (Pygoscelis) during the Pliocene. That deep bills arose so late in the greater than 60 million year evolutionary history of penguins suggests that dietary shifts may have occurred as wind-driven Pliocene upwelling radically restructured southern ocean ecosystems. Ancestral area reconstructions using BioGeoBEARS identify New Zealand as the most likely ancestral area for total-group penguins, crown penguins and crested penguins. Our analyses provide a timeframe for recruitment of crown penguins into the New Zealand avifauna, indicating this process began in the late Neogene and was completed via multiple waves of colonizing lineages.
Keywords: New Zealand, Bayesian phylogeny, penguin, Pliocene, Eudyptes, ancestral area
 | Eudyptes atatu sp. nov. showing key diagnostic features. Holotype specimen NMNZ S.046318 showing (a) right lateral view of skull and block with (c) mandible and (d) postcranial elements. (b) Right lateral view of Snares crested penguin Eudyptes robustus NMNZ OR.023746 for comparison. Referred material of E. atatu including (e) S.046315 dorsal view of skull, (f) CM 2017-62-8-1 left lateral view of skull, (g) NMNZ S.046320 right humerus caudal view, and (h) dorsal and (i) plantar views of NMNZ S.046319 right tarsometatarsus. Ano, apertura nasale ossea (naris). Clh, crista lateralis hypotarsi (lateral hypotarsal crest); Co, coracoid; Cmh, crista medialis hypotarsi (medial hypotarsal crest); F*, frontal with wide shelf bordering the salt gland fossa; Fte*, fossa temporalis (temporal fossa) that is relatively deep; Fvpl, foramen vasculare proximale lateralis (medial proximal vascular foramen); Fvpm, foramen vasculare proximale mediale (medial proximal vascular foramen); Hu, humerus; Ic, incisura capitus (capital incisure); Imp, impressio musculus pectoralis (pectoral muscle impression); Mr, ramus mandibula (mandibular ramus); Oj*, os jugale (jugal bar) showing distinct curvature; Op, os palatinum (palatine); Ma, articular end of mandible; Mr*, mandibular ramus that is relatively narrow at midpoint; Ra, radius; Sc, scapula; Sldl, sulcus longitudinalis dorsalis lateralis (lateral dorsal longitudinal sulcus); Sldm*, sulcus longitudinalis dorsalis medialis (medial dorsal longitudinal sulcus) which is moderately deep; St, sternum; Tmtc, tuberositas musculus tibialis cranialis (tuberosity for cranial tibial muscle); Tv, tuberculum ventral (ventral tubercle); Ve, vertebra. Asterisks denote diagnostic characters. Photographs (a)–(e), (g)–(i) from Jean-Claude Stahl at Museum of New Zealand Te Papa Tongarewa, photograph (f) from R. Paul Scofield at Canterbury Museum. |
Systematic palaeontology Aves Linnaeus, 1758 Sphenisciformes Sharpe, 1891 Spheniscidae Bonaparte, 1831 Eudyptes Vieillot, 1816
Eudyptes atatu sp. nov. Thomas, Tennyson, Scofield and Ksepka.
Etymology. From Te reo Māori, ata tū (‘dawn’), referencing the stem position within Eudyptes and the earliest recorded appearance of Eudyptes in New Zealand.
Type locality and horizon. Late Pliocene (Piacenzian) Tangahoe Formation in the southern Taranaki region of the North Island of New Zealand. ...
Daniel B. Thomas, Alan J. D. Tennyson, R. Paul Scofield, Tracy A. Heath, Walker Pett and Daniel T. Ksepka. 2020. Ancient Crested Penguin Constrains Timing of Recruitment into Seabird Hotspot. Proceedings of the Royal Society B. DOI: 10.1098/rspb.2020.1497
| 4:21a |
[Botany • 2020] Magnolia ottoi (Magnoliaceae) • A New Species from Purulhá, Baja Verapaz, Guatemala: Conservation and Mayan Q’eqchi ‘ Ethnotaxonomy
 | Magnolia ottoi A. Vázquez, Tribouillier & Archila
in Vázquez-García, Tribouillier-Navas, Archila & Véliz-Pérez, 2020. |
Abstract A new species of Magnolia subsect. Talauma (“jomcoj”), Magnolia ottoi, is described and illustrated. The conservation status of this new species is proposed as critically endangered (CR) according to IUCN criteria. An identification key and a map with the distribution of the new species and other species of Magnolia subsect. Talauma from Guatemala and neighboring areas (Honduras and Chiapas, México) is also presented. Our field research also unveiled the Mayan Q’eqchi’ ancestral taxonomic knowledge which differentiates magnolias of two different subsections, Magnolia and Talauma, based on wood quality and properties. They consistently distinguished them as “coj” and “jomcoj” respectively.
Keywords: Magnolia subsect. Talauma, Magnolia steyermarkii, Magnolia quetzal, Magnolia ottoi, Magnolia atlantida, Magnolia cochranei, Magnolia lacandonica, Magnolia perezfarrerae, Mayan Q’eqchi’, Magnoliids
 | FIGURE 2. Magnolia ottoi. Material from the holotype, except O, collected by Otto Alvarado (recorded by Tribouillier & Archila MG007). A. Sepals. B. Outer petals. C. Inner petals. D. Stamens. E. Gynoecium. F–G. Spathaceous bracts. H. Leaf. I. Inner fleshy petal, top view. J. Inner fleshy petal, side view. K. Developing gynoecium. L. Icon of M. ottoi (with flattened whorls). M. Bract of inner floral bud. N. Fruit pubescence. O. Fruit, P. Fruit axis, without seeds. Photographs by Fredy Archila.
|
 | FIGURE 3. Magnolia ottoi. A. Fruit in the process of drying. Material collected by Otto Alvarado (recorded by Tribouillier & Archila MG-007). B. Inner side of the Fruit during dehiscence. C. Dorsal side of fruit. D. Carpels splitting and leaving the fruit axis with seeds still attached. E. Seed with red sarcotesta. Photographs by Fredy Archila.
|
Magnolia ottoi A. Vázquez, Tribouillier & Archila sp. nov.
Type: GUATEMALA. Baja Verapaz: Purulhá. 2 km south of Purulhá, 1600 m, moist-subtropical cloud forest, July 2015 (fl), Otto Alvarado (recorded by Tribouillier & Archila MG-005) (holotype BIGU; Isotype IBUG).
Magnolia ottoi is similar in leaf shape to M. steyermarkii but it differs from the latter in the size of its leaves (leaf length to width ratio: 1.83–2.22 vs. 1.50–1.76) and flowers (20.2–22.2 cm vs. 12.0–13.0 cm in diameter) and the number of bracts (2 vs. 1); stamens (102–108 vs. 75–78) and carpels (38–50 vs. 30–32). Also the carpels of M. ottoi are beaked vs. acute in M. steyermarkii
Etymology and ethnobotany:— The species epithet honors Otto Alvarado, collector of the species. The ancestral Mayan (Q’eqchi ‘) understanding of Magnoliaceae includes recognizing species of different sections classifying them as Coj (sect. Magnolia) and Jomcoj (sect. Talauma). When visiting one of the ranches one of the companions proceeded to show us two wood planks indicating that the trees of the subsect. Magnolia (Coj) had a high-quality wood, while the trees of the subsect. Talauma (Jomcoj) was considered bad wood for construction because its fibers are not strong enough and it was easily cracked, so they rather use them as firewood for cooking.
Distribution and ecology:— Magnolia ottoi is endemic to Purulhá, Baja Verapaz, Guatemala (Fig. 1). Only known from the type locality. Although 5 km from the type locality, in the Biotope of the Quetzal Mario Dary-Rivera, Fredy Archila and Erick Tribouillier observed several juvenile plants of Magnolia, these had very large leaves and possibly correspond to this new species. The only known trees (3) inhabit very humid forests at three different elevations 1550– 1650 m, pp 2284 mm, t 16–230 C; wavy topography. Common species include: Liquidambar styraciflua Linnaeus (1753: 999), Persea donnell-smithii Mez (1892: 113), Pinus pseudostrobus Brongniart (1828: 46), Persea schiedeana Nees von Esenbeck (1836: 130), Rapanea ferruginea (Ruiz López & Pavón 1798: 280) Mez (1901: 429), Clethra spp., Morella cerífera (L.) Small (1903: 337), Eurya seemanniana Pittier (1922: 480), Pouteria viridis (Pittier 1914: 84) Cronquist (1946: 290) and Magnolia archilana A.Vázquez, Tribouill. & Véliz in Vázquez-García et al. (2019: 222). Flowering in March, and fruiting from March to April.
 | FIGURE 1. Distribution of species of Magnolia sect. Talauma in Guatemala and adjacent countries. |
J. Antonio Vázquez-García, Erick Tribouillier-Navas, Fredy Archila and Mario Esteban Véliz-Pérez. 2020. Magnolia ottoi (Magnoliaceae) A New Species from Purulhá, Baja Verapaz, Guatemala: Conservation and Mayan Q’eqchi ‘ Ethnotaxonomy. Phytotaxa. 455(3); 187–195. DOI: 10.11646/phytotaxa.455.3.1
| 4:34a |
[Botany • 2020] Begonia beijnenii (Begoniaceae, section Baryandra) • A New Species of Begonia from San Vicente, Palawan, the Philippines
 | Begonia beijnenii Y.P. Ang, Tandang, Rubite & R. Bustamante
in Ang, Tandang, Rubite & Bustamante, 2020. |
Abstract In our study, a distinctive new species of Begonia from an unexplored region of Port Barton, San Vicente, Palawan, Begonia beijnenii, is described and illustrated. The new species belongs to section Baryandra. It is morphologically most similar to B. hughesii, in having a 3-winged ovary with a cucullate wing and an abortive abaxial locule, tomentose petioles, and leaves that are adaxially glabrous and abaxially subglabrous. However, B. beijnenii distinctly differs by being comparatively smaller in size. It is only known from its type locality and vicinity. Comparisons with two variegated species of Palawan: B. cleopatrae and B. gironellae are also provided to aid in identification. B. beijnenii is hereby proposed to be Vulnerable (VU) D1, based on guidelines by IUCN.
Keywords: Begonia cleopatrae, Begonia gironellae, Begonia hughesii, endemic, Eudicots, Malesia, taxonomy
 
Yu Pin Ang, Danilo N. Tandang, Rosario R. Rubite and Rene Alfred Anton Baena Bustamante. 2020. Begonia beijnenii (Begoniaceae, section Baryandra), A New Species of Begonia from San Vicente, Palawan, the Philippines. Phytotaxa. 455(3); 196–204. DOI: 10.11646/phytotaxa.455.3.2
|
|