1990
DOI: 10.1017/s0024282990000081
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Studies in Pseudocyphellaria (lichens) II. Ecuadorean species

Abstract: Eight species ofPseudocyphellariaare recorded from mainland Ecuador viz., P. arvidssonii, P. aurata, P. bartlettii, P. clathrata, P. crocata, P. dozyana, P. encoensis and P. intricata, with taxa asterisked being new records for Ecuador. Pseudocyphellaria bartlettii andP. encoensis are also new records for northern South America, and P. dozyana is new to South America. A key is given, and details of anatomy, morphology, chemistry, distribution, ecology and taxonomy are discussed.

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Cited by 56 publications
(92 citation statements)
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References 13 publications
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“…Our experience with P. crocata in the Neotropics suggests that at least two distinct taxa are present: one with mostly marginal soralia (resembling P. perpetua but with a white medulla) and the other with predominantly laminal soralia. We have not revised any voucher material of the P. crocata sequences in Genbank, and therefore cannot state at present whether and which of these correspond to the different morphodemes, but it appears that concepts of the name P. crocata representing several species (Magnusson 1940;Galloway , 1992Galloway , 1994Galloway & Arvidsson 1990;Miądlikowska et al 2002) are correct.…”
Section: The Lichenologist 216mentioning
confidence: 97%
“…Our experience with P. crocata in the Neotropics suggests that at least two distinct taxa are present: one with mostly marginal soralia (resembling P. perpetua but with a white medulla) and the other with predominantly laminal soralia. We have not revised any voucher material of the P. crocata sequences in Genbank, and therefore cannot state at present whether and which of these correspond to the different morphodemes, but it appears that concepts of the name P. crocata representing several species (Magnusson 1940;Galloway , 1992Galloway , 1994Galloway & Arvidsson 1990;Miądlikowska et al 2002) are correct.…”
Section: The Lichenologist 216mentioning
confidence: 97%
“…Character scores in the morphological data matrix (table 4) are derived from specimen-based studies conducted by J. Miadlikowska and descriptions from the following publications: Bitter (1909), Vainio (1915), Santesson (1944), Thomson (1955Thomson ( , 1979, Hale (1957), Wetmore (1960), Lindhal (1962), Henssen (1963), Yoshimura (1971), James and Henssen (1976), Vitikainen (1985Vitikainen ( , 1987Vitikainen ( , 1994aVitikainen ( , 1994b, James and White (1987), White and James (1987b), Galloway (1988), Swinscow and Krog (1988), Holtan-Hartwig (1988, Ott (1988), Hastings (1994, 1995), Goward et al (1994Goward et al ( , 1995, Stenroos et al (1994), Kondratyuk and Galloway (1995), Miadlikowska (1998), Martínez (1999). Most of the characters included in this matrix are routinely used for the determination and description of Peltigera species.…”
Section: Morphological Charactersmentioning
confidence: 99%
“…Data for the outgroups and Peltigera taxa that are rare or insufficiently known (i.e., rarely collected) were taken from the following literature and unpublished sources: Wetmore (1960), Kurokawa et al (1966), Yoshimura (1971), Ohlsson (1973), Maass (1975aMaass ( , 1975b, Tønsberg and Holtan-Hartwig (1983), Vitikainen (1985Vitikainen ( , 1994aVitikainen ( , 1994b, James and White (1987), James (1987a, 1987b), Galloway (1988), HoltanHartwig (1988HoltanHartwig ( , 1993, Feige et al (1989), Purvis and James 0000000000 0000000000 0000000000 0000000000 0000000120 A1A2212EG0 B10A10A0AA 001 P. monticola 2 0000000000 0000000000 0000000000 0000000000 0000000120 A1A2212EG0 B10A10A0AA 001 P. monticola 3 0000000000 0000000000 0000000000 0000000000 0000000120 A1A2212EG0 B10A10A0AA 001 P. ponojensis 2 0000000000 0000000000 0000000000 0000000000 0000000110 H1122121G0 B10M1000AH 111 P. ponojensis 3 0000000000 0000000000 0000000000 0000000000 0000000110 H1122121G0 B10M1000AH 111 P. ponojensis 1 0000000000 0000000000 0000000000 0000000000 0000000110 H1122121G0 B10M1000AH 111 P. scotteri 1 0000000000 0000000000 0000000000 0000000000 0000000110 111221Y1G0 0003100011 001 P. retifoveata 2 0000000011 0010000000 0100000000 0000000000 00000001A0 11111111E0 000E10011H 000 P. retifoveata 1 0000000011 0010000000 0100000000 0000000000 00000001A0 11111111E0 000E10011H 000 P. continentalis 0000000000 0000000000 0000000000 0000000000 0000000110 B112212130 000E101012 01? P. kristinssonii 2 0000000000 0000000000 0000000000 0000000000 0000000110 21A211E120 210120001H 01?…”
Section: Chemical Characters (Terpenoids)mentioning
confidence: 99%
“…Furthermore, joined green and blue-green lobes (hereafter called chloromorph and cyanomorph, respectively, or photomorph-term introduced by Laundon, 1995-when the nature of the photobiont is not specified) or independent thalli that are chemically and/or morphologically similar except for the nature of the photobiont, have been reported for all these genera (see Henssen, 1976, andJahns, 1988, for a review). Alternative photomorphs can differ in their growth form (e.g., Lobaria, Jordan, 1972, andSticta, Galloway, 1994); their morphology (e.g., Peltigera aphthosa-group; HoltanHartwig, 1993;Vitikainen, 1994;Goward et al, 1995;and Pseudocyphellaria, Renner and Galloway, 1982;Galloway, 1988), their anatomy (e.g., P. venosa ;Ott, 1988), their chemistry (e.g., Nephroma arcticum; Tønsberg and HoltanHartwig, 1983; see also Renner, 1982), their habitat preferences (White and James, 1987) and the cytology of the actual interactions between symbionts (Honegger, 1982(Honegger, , 1985. Whether all these differences are induced by the alternative photobiont or whether some of these reflect the presence of two genetically distinct mycobionts is not clear.…”
mentioning
confidence: 99%