Mugideiriflora portugallica E.M.FRIIS, P.R.CRANE et K.R.PEDERSEN, 2020
publication ID |
https://doi.org/ 10.37520/fi.2020.023 |
persistent identifier |
https://treatment.plazi.org/id/6435F619-7863-3A43-FC88-D752842361B6 |
treatment provided by |
Diego |
scientific name |
Mugideiriflora portugallica E.M.FRIIS, P.R.CRANE et K.R.PEDERSEN |
status |
sp. nov. |
Mugideiriflora portugallica E.M.FRIIS, P.R.CRANE et K.R.PEDERSEN sp. nov.
Text-figs 1a–f View Text-fig , 2a–g View Text-fig
H o l o t y p e. Designated here. S174254 (Catefica sample 150; figured Text-figs 1a–f View Text-fig , 2a–g View Text-fig ).
P l a n t F o s s i l N a m e s R e g i s t r y N u m b e r.
PFN000907 (for new species).
R e p o s i t o r y. Palaeobotanical Collections, Swedish
Museum of Natural History , Stockholm, Sweden ( S) .
E t y m o l o g y. From Portugal where the fossil was collected.
T y p e l o c a l i t y. Catefica (39° 03′ 16″ N, 09° 14′ 24″ W), between the villages of Catefica and Mugideira, about 4 km south of Torres Vedras, Portugal GoogleMaps .
T y p e s t r a t u m a n d a g e. Almargem Formation,
Early Cretaceous (Aptian-early Albian).
D i a g n o s i s. As for the genus.
D i m e n s i o n s. Length of flower: 1.1 mm (full length not preserved; estimated full length about 2 mm); diameter: 1.75 mm.
D e s c r i p t i o n a n d r e m a r k s. The species is based on a single, slightly abraded flower (S174254) and two small flower fragments from the same locality (S174770, S174771, Catefica sample 50). The flower is small, about 1.75 mm in diameter, open and apparently preserved in a young anthetic stage with stamens and carpels not fully mature ( Text-figs 1a–f View Text-fig , 2a–g View Text-fig ). The flower is structurally bisexual, with multiparted perianth, androecium and gynoecium ( Text-figs 1a–f View Text-fig , 2a–g View Text-fig ). The floral receptacle is flat to slightly concave but is extended into a short conical gynoecial zone in the pistillate region ( Text-fig. 2b, e, f View Text-fig ). The phyllotaxis of all floral organs is apparently spiral ( Text-figs 1a–c View Text-fig , 2c–e View Text-fig ). Because the flower is abraded, the total number of floral parts is unknown, but is estimated based on the well-preserved parts of the flower.
The perianth has about 50 tepals in several series. The tepals are broad with correspondingly broad, transversely elongate and narrowly rhomboidal bases. The tepals are composed of thin-walled, equiaxial cells. The tepals of the outer one or two series are covered by a thin cuticle (Textfig. 2c, d) while those of the inner three or four series have a thick cuticle on their outer surface over a layer of epidermal cells that also appear to be thick-walled ( Text-fig. 2c, d View Text-fig ).
The androecium consists of more than 50 stamens in about four series ( Text-fig. 2b–e View Text-fig ). Each stamen has a short, broad base that is poorly differentiated from the anther and that is rhomboidal in transverse section ( Text-fig. 2d, e View Text-fig ). The anthers are apparently dithecate and tetrasporangiate with an expanded and slightly pointed connective apex. The pollen sacs appear to be embedded in a lateral to slightly dorsal position. The mode of dehiscence is not clear. No pollen has been observed.
The gynoecium is superior, apocarpous and consists of more than 50 free carpels borne on the conical gynoecial portion of the receptacle in several series ( Text-fig. 2b, e–g View Text-fig ). The carpels appear ascidiate, but because the flower is preserved at a very young stage, the nature of the carpels is not completely certain.
S |
Department of Botany, Swedish Museum of Natural History |
T |
Tavera, Department of Geology and Geophysics |
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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