Aecidium otagense Linds. 1867
Details
Aecidium otagense Linds., Transactions of the Royal Society of Edinburgh 24 430 (1867)
Nomenclature
Linds.
Linds.
1867
430
ICN
Aecidium otagense Linds. 1867
NZ holotype
species
Aecidium otagense
TYPE LOCALITY: Otago [New Zealand], Dunedin, East Taieri Bush, on Clematis paniculata, 5 Nov 1861, W.L. Lindsay (lectotype E designated by McKenzie, 1981); Epitype desiganted McKenzie 2017, Rangitikei, Pohangina Valley, on Muehlenbeckia australis, 21 May 2015, E.H.C. McKenzie Epitype PDD 107783 II, III
Classification
Associations
has host
Descriptions
Aecidium otagense Linds. 1867
Hosts : Clematis indivisa Willd. On leaves, stems; petioles, and sepals Herb. Nos. 188, 434. Lake Horowhenua, Levin (Wellington), 30 m., E. H. Atkinson ! 26 Oct., 1919. Peel Forest (Canterbury), H. H. Allan ! 8 Nov., 1919. Manawatu Gorge (Wellington), 150 m., J.W. Whelan ! 29 Sept., 1921. Putara, Eketahuna (Wairarapa), H. Watson! 8 Nov., 1921. Clematis Colensoi Hook. f. On stems and petioles. Herb. No. 231. Miramar (Wellington), 20 m., J. W. Bird! 5 Nov., 1920.
0. Spermogones associated with the aecidia, immersed, honey-coloured.
I. Aecidia amphigenous; caulicolous, petiolicolous and sepalicolous, crowded in inflated distorted areas which may attain a length of 15 cm., orange. Peridia cupulate, shortly erumpent, 0.5-1 mm. diam., margins revolute, yellow, deeply and irregularly lacerate. Spores globose or polygonal, 23-36 mmm. diam.; epispore hyaline, delicately and closely verruculose, 0.75 mmm. thick, cell-contents granular, orange.
I. Aecidia amphigenous; caulicolous, petiolicolous and sepalicolous, crowded in inflated distorted areas which may attain a length of 15 cm., orange. Peridia cupulate, shortly erumpent, 0.5-1 mm. diam., margins revolute, yellow, deeply and irregularly lacerate. Spores globose or polygonal, 23-36 mmm. diam.; epispore hyaline, delicately and closely verruculose, 0.75 mmm. thick, cell-contents granular, orange.
Distribution: Endemic; common throughout.
The hosts are endemic, and are abundant throughout. (Cheeseman, 1906, pp. 2, 3.)
This rust forms conspicuous distorted areas, many centimetres long, on the stems and leaves of the hosts. The mycelium is perennial, so that once a plant has become infected the rust appears season after season. The specimens on Clematis Colensoi are badly infected with Tuberculina persicina (Ditm.) Sacc. (see Appendix, p. 50). Lindsay records the rust upon Clematis hexasepala DC.
The aecidia of this species are formed within the host-tissues in the vicinity of the phloem, and all stages may be obtained from immature to fully-developed peridia containing numerous spores. As they develop, the peridia move towards the periphery of the stem, and prior to dehiscence may be found fully developed lying beneath the epidermis. That they are mature is evidenced by the behaviour of the spores, for on being placed in water these give rise to infection hyphae.
This rust forms conspicuous distorted areas, many centimetres long, on the stems and leaves of the hosts. The mycelium is perennial, so that once a plant has become infected the rust appears season after season. The specimens on Clematis Colensoi are badly infected with Tuberculina persicina (Ditm.) Sacc. (see Appendix, p. 50). Lindsay records the rust upon Clematis hexasepala DC.
The aecidia of this species are formed within the host-tissues in the vicinity of the phloem, and all stages may be obtained from immature to fully-developed peridia containing numerous spores. As they develop, the peridia move towards the periphery of the stem, and prior to dehiscence may be found fully developed lying beneath the epidermis. That they are mature is evidenced by the behaviour of the spores, for on being placed in water these give rise to infection hyphae.
Aecidium otagense Linds. 1867
The rust was described by Lindsay (1867) from "C. hexasepala". Kirk (1908) recorded it on cultivated plants of some of the indigenous species. Cunningham (1931a) noted that the type is no longer in existence and that it has not since been collected on this host. It causes considerable distortion to stems, petioles, leaves, and dowers on indigenous species of Clematis. It is common throughout New Zealand.
Aecidium otagense Linds. 1867
Type: Rust and Smut Fungi; Description: Aecia densely scattered, cup-shaped, barely erumpent, orange, with an irregularly torn margin, up to 1 mm in diameter; on distorted, inflated swellings, up to 15 cm long, on leaves, petioles, sepals, and stems. Aeciospores globose or polygonal, 22–30 × 20–25 μm, delicately verruculose.
Distribution: Auckland, Coromandel, Bay of Plenty, Nelson, Marlborough, North Canterbury, Otago Lakes, Southland, Stewart Island.; 1st Record: Lindsay (1867).
Significance: The rust causes little damage.; Host(s): Clematis afoliata, C. foetida, C. forsteri, C. marata, C. paniculata.
Taxonomic concepts
Aecidium otagense Linds. 1867
Aecidium otagense Linds. (1867)
Aecidium otagense Linds. 1867
Aecidium otagense Linds. (1867)
Aecidium otagense Linds. 1867
Aecidium otagense Linds. 1867
Aecidium otagense Linds.
Aecidium otagense Linds. 1867
Aecidium otagense Linds. (1867)
Global name resources
Collections
Notes
typification
TYPE LOCALITY: Otago [New Zealand], Dunedin, East Taieri Bush, on Clematis paniculata, 5 Nov 1861, W.L. Lindsay (lectotype E designated by McKenzie, 1981); Epitype desiganted McKenzie 2017, Rangitikei, Pohangina Valley, on Muehlenbeckia australis, 21 May 2015, E.H.C. McKenzie Epitype PDD 107783 II, III
Metadata
1cb17c98-36b9-11d5-9548-00d0592d548c
scientific name
Names_Fungi
3 April 2018