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Showing posts from September, 2017

Schoenorchis tixieri

Schoenorchis tixieri is from 900 -1400m from  S. Yunnan and Vietnam (Xinqi and Wood 2009). I was told that mine is Chinese origin, so mine might be from S. Yunnan, but I don't know the detailed history. From looking at the flower of my plants with 10x loupe, I can't tell the difference from S. fragrans .  Unfortunately, I killed my S. fragrans , and I didn't take photos when it flowered, so I have been gazing photos in Flickr and from google image search.  I should mention that there are lots of misidentified S. seidenfadenii  labelled as S. fragrans .  These two species are relatively easy to tell if you look at the callus shape and the angle of the spur.  Seidenfaden (1988, p.66-69) discussed the difference, and here is the key to differentiate them: Epichile of lip with two low rounded calli besides each other, separated by a cleft. Spur in obtuse angle to epichile .... S. seidenfadenii Epichile with a single large semi globular callus. Spur in a right angle to ep

Habenaria repens

Habenaria repens is a widely distributed species, from the Southeastern United States, Central America, the Carribean and the majority of South America ( link to a distribution map, some of these are not within the native range).  Within the US, it occurs in the coastal states from North Carolina to Texas ( link to the occurrence map). This species grows in moist area, and it can grow as a semi-aquatic plants, growing on floating mats on ponds (Hunt 1943).  As an interesting side note, a phenolic compound, called habenariol , has been extracted from this species and its antioxidant activity has been reported (Johnson et al. 1999).  It turned out that this compound is a feeding deterrent against the freshwater omnivorous crayfish, Procambarus clarkii .  It is interesting that people used to think that herbivory wouldn't be a big problem for aquatic plants, but this example shows that this orchid has evolved the counter-measure against herbivory. From a distance, the relat

Angraecum popowii

Angraecum popowii is endemic to Madagascar .  It is from shady, highland Uapaca bojeri forests of Antananarivo , Fianarantsoa , and Toamasina (Cribb and Hermans, 2009).  The elevation range is 1200-1500m. According to the artificial key to section Aranchnangraecum by Cribb and Hermans (2009), the channelled semiterete leave is one of the key trait to distinguish this species from two related species,  A. linearifolium and A. teretifolium . The later two species have terete leaves, and the leaves are not obviously channelled, so this is a trait which can be used to differentiate without flowers.  In the photo below, I tried to show this channel on the top side of the leaves. Once they flower, A. linearifolium can be easily distinguished from the other two since it has completely different, spidery flowers.   A. popowii and A. teretifolium show similar flower shapes, but A. popowii has a larger flower; the sepal lengths are 30mm for A. popowii , 16-27mm for A. teretifoli

Epidendrum moronense

I got this compact species from Ecuagenera in spring 2017.  It was a bit dehydrated at first. I mounted it on a cedar shingle, and kept it lying horizontally (instead of hanging the mount).  It managed to recover, and this is the first bloom under my care. Epidendrum moronense shows relatively narrow distribution.  It is from wet forests of south-eastern Ecuador; in the basin of the Río Zamora , on the slopes of the Cordillera Oriental and the Cordillera del Condor (Hágster, 2015).  They are known from the provinces of Loja , Zamora-Chinchipe , and Morona Santiago . The species epithet is derived from the province, Morona-Santiago, where this species occurs, although the type specimen was collected in Zamora-Chinchipe. The elevation range is 800-1400m (Hágster, 2015). The frilly lip and the reflexed sepals and petals make the flowers interesting.  The column is usually white, and the lip is white, but the color of petals and sepals can vary.  This individual has pinkish color,