Opalinidae in African Anura. II. Genera Protozelleriella n. g. and Zelleriella

During 1988 and 1989, 409 specimens of southern African Anura, comprising 50 species in 9 families, were checked for opalinids in the cloaca. Protozelleriella devilliersi n. g., n. sp. was found in three of four Capensibufo rosei (Bufonidae); Zelleriella africana Sandon, 1938 in two of three Bufo angusticeps and one of 20 B. garmani (Bufonidae) plus three of 12 Phrynobatrachus natalensis, 12 of 19 Tomopterna cryptotis, seven of 14 T. delalandii, three of seven T. krugerensis and one of six T. natalensis (all Ranidae); Z. gambieri n. sp. in one of six T. natalensis; Z. garlandi n. sp. in two of six Kassina maculata (Hyperoliidae); Z. sandoni n. sp. in two of 20 B. garmani, two of six K. maculata, one of seven K. senegalensis and one of four Leptopelis mossambicus (Hyperoliidae) plus one of five Phrynomerus bifasciatus (Microhylidae) and two of 19 T. cryptotis. It is suggested that the Ranidae (in particular the genus Tomopterna) and the Hyperoliidae are among the major carriers of Zelleriella in the Afrotropical Region.     

Euglenophyta of Bangladesh. I. Genus Trachelomonas EHR.

A total of 55 taxa belonging to Trachelomonas (Euglenophyta) are reported from Bangladesh. Of these, 5 varieties (Tr. allorgei var. madaripurense, Tr. anguste-ovata var. ellipsoidea, Tr. armata var. rangpurense, Tr. hispida var. subcoronata, Tr. asymmetrica var. crenulata) and one forma (Tr. anguste-ovata fa. minor) are described as new to science.     

Revision of Corallinaceae (Corallinales,Rhodophyta): recognizing Dawsoniolithon gen. nov., Parvicellularium gen. nov. and Chamberlainoideae subfam. nov. containing Chamberlainium gen. nov. and Pneophyllum

A multi‐gene (SSU, LSU, psbA, and COI) molecular phylogeny of the family Corallinaceae (excluding the subfamilies Lithophylloideae and Corallinoideae) showed a paraphyletic grouping of six monophyletic clades. Pneophyllum and Spongites were reassessed and recircumscribed using DNA sequence data integrated with morpho‐anatomical comparisons of type material and recently collected specimens. We propose Chamberlainoideae subfam. nov., including the type genus Chamberlainium gen. nov., with C. tumidum comb. nov. as the generitype, and Pneophyllum. Chamberlainium is established to include several taxa previously ascribed to Spongites, the generitype of which currently resides in Neogoniolithoideae. Additionally we propose two new genera, Dawsoniolithon gen. nov. (Metagoniolithoideae), with D. conicum comb. nov. as the generitype and Parvicellularium gen. nov. (subfamily incertae sedis), with P. leonardi sp. nov. as the generitype. Chamberlainoideae has no diagnostic morpho‐anatomical features that enable one to assign specimens to it without DNA sequence data, and it is the first subfamily to possess both Type 1 (Chamberlainium) and Type 2 (Pneophyllum) tetra/bisporangial conceptacle roof development. Two characters distinguish Chamberlainium from Spongites: tetra/biasporangial conceptacle chamber diameter (<300 μm in Chamberlainium vs. >300 μm in Spongites) and tetra/bisporangial conceptacle roof thickness (<8 cells in Chamberlainium vs. >8 cells in Spongites). Two characters also distinguish Pneophyllum from Dawsoniolithon: tetra/bisporangial conceptacle roof thickness (<8 cells in Pneophyllum vs. >8 cells in Dawsoniolithon) and thallus construction (dimerous in Pneophyllum vs. monomerous in Dawsoniolithon).     

Opalinidae in African Anura. IV. Genus Protoopalina

During 1988 and 1989, 409 specimens of southern African Anura comprising 50 species in nine families, were checked for opalines in the cloaca. Protoopalina africana Metcalf, 1923 was found in Rana angolensis (Ranidae); P. appendiculata Fantham, 1929 in R. fuscigula; P. boycotti n. sp. in Pyxicephalus adspersus (Ranidae); P. brevis Boisson, 1959 in Ptychadena oxyrhynchus (Ranidae); P. drachi Tuzet & Knoepffler, 1968 in Ptychadena anchietae, P. mascareniensis, P. mossambica and P. oxyrhynchus (Ranidae); P. nutti Metcalf, 1923 in Bufo rangeri (Bufonidae); P. octomixa Fantham, 1930 in Schismaderma carens (Bufonidae); P. ovalis Fantham, 1929 in Rana angolensis (Ranidae); P. pattersoni n. sp. in Ptychadena mascareniensis (Ranidae); P. petiti Tuzet & Knoepffler, 1968 in Ptychadena oxyrhynchus (Ranidae); P. primordialis (Awerinzew, 1913) Metcalf, 1918 in Bufo angusticeps, B. gariepensis, B. garmani, B. rangeri (Bufonidae), Heleophryne natalensis (juveniles and tadpoles) (Heleophrynidae), Xenopus laevis (juveniles and tadpoles) (Pipidae), Cacosternum boettgeri, Ptychadena mossambica (juvenile), Rana angolensis, R. fuscigula and Strongylopus grayii (Ranidae); P. stevensoni (Stevenson, 1911) Metcalf, 1923 in Bufo gariepensis, B. garmani, B. gutturalis, B. maculatus, B. rangeri, Capensibufo rosei (Bufonidae), Rana angolensis and R. fuscigula (Ranidae); P. transvaalensis Fantham, 1923 in Pyxicephalus adspersus (Ranidae); and P. xenopodos Metcalf, 1923 in Xenopus laevis (including tadpoles) and X. muelleri (Pipidae). It is suggested that the Bufonidae (genus Bufo) and the Ranidae (in particular the genera Cacosternum, Ptychadena, Rana and Strongylopus) are among the major carriers of Protoopalina in the Afrotropical Regional. The biogeography and evolution of the genus Protoopalina are discussed.     

Opalinidae in African Anura. III. Genus Cepedea

During 1988 and 1989, 409 specimens of southern African Anura comprising 50 species in 9 families were checked for opalinids in the cloaca. Cepedea acuta n. sp. was found in six of 19 Tomopterna cryptotis and four of seven T. krugerensis (Ranidae); C. affinis (Nazaretskaja, 1992) in two of four Afrixalus aureus, two of four Hyperolius horstocki, 23 of 42 H. marmoratus, one of seven H. pusillus, two of six H. semidiscus, and eight of 12 H. tuberilinguis (Hyperoliidae); C. magna Metcalf, 1923 in one of 20 Bufo garmani, eight of 33 B. gutturalis and two of nine B. rangeri (all Bufonidae), one of two Heleophryne natalensis (juveniles) (Heleophrynidae), four of six Kassina maculata, three of seven K. senegalensis and two of six Semnodactylus wealii (all Hyperoliidae), three of five Phrynomerus bifasciatus (Microhylidae), three of 12 Phrynobatrachus natalensis, 11 of 19 Tomopterna cryptotis, 13 of 14 T. delalandii, one of seven T. krugerensis and one of six T. natalensis (all Ranidae), and four of five Chiromantis xerampelina (Rhacophoridae); Cepedea vanniekerkae n. sp. in one of 19 Tomopterna cryptotis. It is suggested that the Ranidae (in particular the genus Tomopterna) and the Hyperoliidae (in particular the genus Hyperolius) are among the major carriers of Cepedea in the Afrotropical Region.     

Bryophytes of St Helena,South Atlantic Ocean. 6. Cheilolejeunea (Spruce) Schiffn. (Jungermanniales: Lejeuneaceae), including C. microscypha (Hook.f. & Taylor) M.Wigginton,comb. nov. and C. rotalis (Hook.f. & Taylor) M.Wigginton,comb. nov.

Abstract

Two little known species of Cheilolejeunea, C. microscypha (Hook.f. & Taylor) M.Wigginton, comb. nov. (a reinstated St Helena liverwort), and C. rotalis (Hook.f. & Taylor) M.Wigginton comb. nov., endemic to St Helena, South Atlantic Ocean, are described and illustrated, and oil bodies of C. ascensionis (Hook.f. & Taylor) Grolle are newly described and illustrated.     

Zur Cytotaxonomie vonArabis hirsuta agg. (Cruciferae). IV. Chromosomenzahlen vonA. sagittata (Bertol.) DC. undA. hirsuta (L.)Scop. s. str. aus Europa

Zusammenfassung A. sagittata (Bertol.) DC. von zehn Herkünften aus Europa ist mit 2 n=16 diploid.A. hirsuta (L.)Scop. s. str. einschließlich der sicherlich hierhergehörigen var.glaberrima Wahlenb. von 30 europäischen Herkünften ist mit 2 n=32 tetraploid; diploide Pflanzen konnten beiA. hirsuta s. str. nicht gefunden werden.

---

Summary A. sagittata (Bertol.) DC. from 10 different places in Europe has 2 n=16 chromosomes and is diploid.A. hirsuta (L.)Scop. s. str., its var.glaberrima Wahlenb. being included, has been investigated from 30 provenances in Europe, it has the tetraploid chromosome number 2 n=32, diploid plants could not be found in this species.A. hirsuta var.glaberrima (2 n=32) is surely belonging toA. hirsuta s. str. and not toA. allionii (2 n=16).

     

Haplodontium zangii X.R.Wang & J.C.Zhao,sp. nov. (Bryaceae,Bryopsida) from Xizang,China

Haplodontium zangii X.R.Wang &; J.C.Zhao, a new moss species from Xizang, China, is described and illustrated. Previously, specimens of H. zangii have been identified as Mielichhoferia himalayana Mitt. However, H. zangii is distinctly different from M. himalayana in having excurrent costae with short awns (vs long denticulate awns), short-pyriform capsules, 0.8–1?mm (vs long-pyriform capsules, 2.5–3?mm), and densely papillose exostome teeth (vs smooth or vertically striped exostome teeth). Haplodontium zangii is similar to H. macrocarpum (Hook.) J.R.Spence, which was traditionally placed in Mielichhoferia Nees &; Hornsch. as M. macrocarpa (Hook.) Bruch &; Schimp. The main differences between H. zangii and H. macrocarpum are in the morphology of the leaves, capsules, guide cells, and stomata. Mielichhoferia himalayana and another Chinese species of Mielichhoferia, M. sinensis Dix., are also transferred to Haplodontium Hampe, a new genus in the bryoflora of China, as H. himalayanum (Mitt.) X.R.Wang &; J.C.Zhao and H. sinensis (Dix.) X.R.Wang &; J.C.Zhao. A morphological comparison and a key to the three species of Haplodontium in China as well as to H. macrocarpum, a species that is likely to be found in China, are provided.     

CHROMOSOME NUMBERS IN THE COMPOSITAE. XII. AUSTRALIAN SPECIES

Chromosome counts are reported for plants from 171 populations of Australian Compositae; most of these are first reports for the approximately 104 taxa distributed among 37 genera. New generic counts with base numbers indicated include: Astereae —Bellida (x = 9), Minuria (x = 9); Inuleae —Angianthus (x = 12, 13), Calocephalus (x = 7), Cephalipterum (x = 12, 14), Craspedia (x = 11), Gnaphalodes (x = 10), Gnephosis (x = 4, 12), Myriocephalus (x = 6), Isoetopsis (x = 17); Calenduleae —Tripteris (x = 8); and Artcoideae —Arctotheca (x = 9). Most of the counts were from the tribes Astereae (47) and Inuleae (95). The phyletic import of these data is discussed selectively and comparisons are made with the chromosomal variation found in the Australian desert Compositae with that found in the North American desert Compositae.     

Studies in African Cyperaceae 34. New combination in Bulbostylis Kunth ex C. B. Clarke

This paper provides new combinations for 16 species of Bulbostylis Kunth ex C. B. Clarke originally described as Abildgaardia Vahl. The new combinations are: Bulbostylis abbreviata (Lye) Lye, B. acutispicata (Lye) Lye, B. afromicrocephala Lye, B. angustispicata (Lye) Lye, B. capitata (Lye) Lye, B. densiflora (Lye) Lye, B. lacunosa (Lye) Lye, B. laxispicata (Lye) Lye, B. longispicata (Lye) Lye, B. microanthela (Lye) Lye, B. malawiensis (Lye) Lye, B. microrotundata (Lye) Lye, B. nudiuscula (Lye) Lye, B. pluricephala (Lye) Lye, B. scrobiculata (Lye) Lye, B. squarrosa (Lye) Lye.     

Recombinant plasmids capable to replication in B. subtilis and E. coli.

Summary The plasmid pBC16 (4.25 kbases), originally isolated from Bacillus cereus, determines tetracycline resistance and can be transformed into competent cells of B. subtilis. A miniplasmid of pBC16 (pBC16-1), 2,7 kb) which has lost an EcoRI fragment of pBC16 retains the replication functions and the tetracycline resistance. This plasmid which carries only one EcoRI site has been joined in vitro to pBS1, a cryptic plasmid previously isolated from B. subtilis and shown to carry also a single EcoRI site (Bernhard et al., 1978). The recombinant plasmid is unstable and dissociates into the plasmid pBS161 (8.2 kb) and the smaller plasmid pBS162 (2.1 kb). Plasmid pBS161 retains the tetracycline resistance. It possesses a single EcoRI site and 6 HindIII sites. The largest HindIII fragment of pBS161 carries the tetracycline resistance gene and the replication function. After circularization in vitro of this fragment a new plasmid, pBS161-1 is generated, which can be used as a HindIII and EcoRI cloning vector in Bacillus subtilis.Hybrid plasmids consisting of the E. coli plasmids pBR322, pWL7 or pAC184 and different HindIII fragments of pBS161 were constructed in vitro. Hybrids containing together with the E. coli plasmid the largest HindIII fragment of pBS161 can replicate in E. coli and B. subtilis. In E. coli only the replicon of the E. coli plasmid part is functioning whereas in B. subtilis replication of the hybrid plasmid is under the control of the Bacillus replicon. The tetracycline resistance of the B. subtilis plasmid is expressed in E. coli, but several antibiotic resistances of the E. coli plasmids (ampicillin, kanamycin and chloramphenicol) are not expressed in B. subtilis. The hybrid plasmids seem to be more unstable in B. subtilis than in E. coli.     

The genus Pnyxiopalpus gen.n. (Diptera: Sciaridae)

Pnyxiopalpus gen.n. (type-species P. raptor sp.n.), Oriental in distribution, includes the following species: P. acanthipes sp.n. (Malay Peninsula), P. aculeatus sp.n. (Borneo), P. adebratti sp.n. (Borneo), P. aphrodite sp.n. (Sumatra), P. dentaneus sp.n. (Sulawesi), P. fossor sp.n. (Borneo), P. fuscinellus sp.n. (Borneo), P. hamatus sp.n. (Borneo), P. latifalx sp.n. (Borneo), P. macrocellus sp.n. (Malay Peninsula), P. microdon sp.n. (Sumatra), P. nepenthophilus sp.n. (Malay Peninsula), P. noona sp.n. (Palawan), P. raptor sp.n. (Borneo), P. reticulatus sp.n. (Malay Peninsula) and P. simplex sp.n. (Borneo). Males and females are keyed and described. Pnyxiopalpus has a number of characters previously unknown in Sciaridae. In contrast to other Sciaridae, interspecific morphological variation is greater for the females compared to the males. Based on a parsimony analysis of sixty-four morphological characters, Pnyxiopalpus is monophyletic, and its sister group appears to be Spathobdella Frey + {[Peyerimhoffia Kieffer + (Faratsiho Paulian + Pnyxia Johannsen)] + [Hyperlasion Schmitz + (Hermapterosciara Mohrig & Mamaev + Parapnyxia Mohrig & Mamaev)]}. According to the most parsimonious solution, the monophyly of Hyperlasion, Lycoriella Frey and Plastosciara Berg in their current sense is questioned. Aptery and one-segmented maxillary palp, usually regarded as important in sciarid classification, show a lot of homoplasy.     

Chromosome numbers in Compositae. XVIII.

Chromosome numbers and other cytogenetic data were determined from microsporocytes in 316 collections including 13 tribes of Compositae, mostly from Africa, Australia, Mexico, Central America, and South America. First reports are provided for 66 species and the genera Cassinia (2n ≈ 14_II), Feldstonia (2n = 11_II), Gochnatia (2n ≈ 23_II), and Pseudoconyza (n = 10). In addition, new chromosome numbers are established at the generic level in Acourtia, Calea, Craspedia, Gnaphalium, Helipterum, Liabum, Leucheria, Smallanthus, Trixis, and Viguiera and at the specific level in 13 additional species.     

Miliusa cambodgensis sp. nov. (Annonaceae) from Cambodia and M. astiana,M. ninhbinhensis spp. nov. from Vietnam

The genus Miliusa in Cambodia and Vietnam is reviewed. Cambodia and Vietnam each harbors six species of Miliusa, including three which are described as new to science: one from Cambodia (Miliusa cambodgensis sp. nov.), the other two from Vietnam (M. astiana and M. ninhbinhensis spp. nov.). In addition, a complete nomenclature and relevant information about the Miliusa species previously known from Cambodia and Vietnam are provided, including keys to the Cambodian and Vietnamese species, the designation of a lectotype for M. baillonii and the synonymization of M. balansae var. elongatoides, M. chunii and M. sinensis with M. balansae.     

CHROMOSOME NUMBERS IN COMPOSITAE. X.

Reports of 126 new counts are recorded for 9 tribes of Compositae, including reports for 45 genera and 102 species. Six genera, Psilocarphus (n = 14). Relhania (n = 7), Rutidosis (n = 9), Chaetanthera (n = 14), Hecastocleis (n = 8), and Hesperomannia (n = 10), and 41 species were previously unreported.     

The genus Hyalomma. VI. Systematics of H. (Euhyalomma) truncatum and the closely related species, H. (E.) albiparmatum and H. (E.) nitidum (Acari: Ixodidae)

The geographic distribution of three closely related Hyalomma species, namely Hyalomma (Euhyalomma) truncatum Koch, 1844, Hyalomma (Euhyalomma) albiparmatum Schulze, 1919 and Hyalomma (Euhyalomma) nitidum Schulze, 1919 is confined to Africa. A detailed comparison of all stages of development of the three taxa reveals that they possess many more shared than distinguishing characters. In fact differentiation between these species is based on single or dual qualitative characters on their adults. These are a conspicuous, ivory-coloured parma on H. (E.) albiparmatum males, and the absence or reduction in clarity of ivory-coloured bands on the leg segments of H. (E.) nitidum adults, as well as the shape of the external cuticular preatrial fold of the genital operculum of females of the latter species. The adults of all three species and the larva of H. (E.) truncatum are redescribed. The nymph of H. truncatum and the larva and nymph of H. (E.) albiparmatum and H. (E.) nitidum are described for the first time. Data on their geographic distributions and hosts are provided.     

Neotropical Monogenoidea. 50. Oviparous gyrodactylids from loricariid and pimelodid catfishes in Brazil, with the proposal of Phanerothecioides n. g., Onychogyrodactylus n. g. and Aglaiogyrodactylus n. g. (Polyonchoinea: Gyrodactylidea)

The diagnosis of Phanerothecium Kritsky & Thatcher, 1977 is amended, and Phanerothecioides n. g., Onychogyrodactylus n. g. and Aglaiogyrodactylus n. g., all comprised of oviparous gyrodactylids (Monogenoidea: Polyonchoinea), are proposed to accommodate 11 of the 15 species (14 new to science) herein described and/or reported from loricariid and pimelodid catfishes (Teleostei: Siluriformes) in Brazil: Phanerothecium harrisi Kritsky & Boeger, 1991, P. spinatoides n. sp. and P. deiropedeum n. sp. all from Hypostomus spp.; P. spinulatum n. sp. from Hypostomus cf. regani; Phanerothecioides agostinhoi n. g., n. sp. (type-species) from Hypostomus spp. and Pseudoplatystoma fasciatum; Onychogyrodactylus sudis n. g., n. sp. (type-species) and O. hydaticus n. sp. both from Ancistrus multispinus; Aglaiogyrodactylus forficulatus n. g., n. sp. (type-species) from Kronichthys lacerta; A. pedunculatus n. sp. from Hisonotus sp.; A. guttus n. sp. from Pseudotothyris obtusa; A. salebrosus n. sp., A. conei n. sp. and A. ctenistus n. sp. all from Pareiorhaphis parmula; and A. calamus n. sp. and A. forficuloides n. sp. both from Schizolecis guntheri. Phanerothecioides n. g. is characterised by oviparous forms lacking superficial and deep haptoral bars and pregermarial vitelline follicles, and by having a conspicuous testis in adult specimens, a syncytial prostatic gland, a reduced copulatory sac and vitelline ducts in the form of an inverted ‘U’. Onychogyrodactylus n. g. is differentiated from all other oviparous gyrodactylid genera by its members having a spine-like accessory sclerite enclosed in a separate pouch associated with the terminal male genitalia. Species of Aglaiogyrodactylus n. g. possess H-shaped vitelline ducts and a complex accessory piece and sclerotised or non-sclerotised male copulatory organ enclosed within the copulatory sac.     

Studies in African Cyperaceae 25. New taxa and combinations in Cyperus L.

Four new subgenera, nineteen new species, two new subspecies and two new varieties of Cyperus L. are described, viz. subgen. Aristomariscus Lye, subgen. Bulbomariscus Lye, subgen. Xerocyperus Lye, subgen. Micromariscus Lye, Cyperus micromariscus Lye, C. boreochrysocephalus Lye, C. crassivaginatus Lye, C. kyllingaeformis Lye, C. cremeomariscus Lye, C. gigantobulbes Lye, C. boreobellus Lye, C. longi–involucralus Lye, C. kwaleensis Lye, C. afrovaricus Lye, C. afrodunensis Lye, C flavoculmis Lye, C microumbellatus Lye, C. purpureoviridis Lye, C. graciliculmis Lye, C. afromon–tanus Lye, C. nyererei Lye, C. afroalpinus Lye, C castaneobellus Lye, C. soyauxii Boeck. ssp. pallescens Lye, C. usitatus Burch. ssp. palmatus Lye, C. renschii Boeck. var. scabridus Lye, and C. fischerianus A. Rich. var. ugandensis Lye. The following new combinations are made: Cyperus L. subgen. Bulbocaulis (C.B.C1.) Lye, Cyperus L. subgen. Courtoisia (Nees) Lye, Cyperus L. subgen. Sorostachys (Steudel) Lye, Cyperus L. subgen. Remirea (Aublet) Lye, Cyperus L. subgen. Alinula (Raynal) Lye, Cyperus lipocarphoides (Kükenth.) Lye, C. malawicus (Raynal) Lye, C. tanganyica–nus (Kiikenth.) Lye, C. mortonii (Hooper) Lye, C. pseudodiaphanus (Hooper) Lye, C. overlaetii (Hooper & Raynal) Lye, C. dewildeorum (Raynal) Lye, C. pagotii (Raynal) Lye, C. demangei (Raynal) Lye, C. afroechinatus Lye, C. niveus Retz. var. ledermannii (Kiikenth.) Lye, C. niveus Retz. var. tisserantii (Cherm.) Lye, C. distans L.f. ssp. longibracteatus (Cherm.) Lye, C. distans L.f. ssp. longibracteatus (Cherm.) Lye, var. rubrotinctus (Cherm.) Lye, C. cyperoides (L.) Kuntze ssp. alternifolius (Vahl) Lye, C. cyperoides (L.) Kuntze ssp. macrocarpus (Kunth) Lye, C. cyperoides (L.) Kuntze ssp. pseudoflavus (Clarke) Lye, C. dubius Rottb. ssp. macrocephalus (Kiikenth.) Lye, C. dubius Rottb. ssp. coloratus (Vahl) Lye, C. usitatus Burch. var. stuhlmannii (Clarke) Lye, C. laxus Lam. ssp. sylvestris (Ridley) Lye, and C. laxus Lam. ssp. buchholzii (Boeck.) Lye and C. globifer (Clarke) Lye.     

The erection of Pelecanema n. g. (Nematoda: Spirurida: Acuariidae), with redescriptions of P. sirry (Khalil, 1931) n. comb. and P. pelecani (Johnston & Mawson, 1942) n. comb.

Pelecanema n. g. is erected for P. sirry (Khalil, 1931) n. comb., syn. Synhimantus sirry Khalil, 1931 (type-species) and P. pelecani (Johnston & Mawson, 1942) n. comb., syn. Dispharynx pelecani Johnston & Mawson, 1942. In the structure of its cordons, consisting of two rows of delicate cuticular plates, the new genus is similar to Synhimantus Railliet, Henry & Sisoff, 1912, Dispharynx Railliet, Henry & Sisoff, 1912, Chordatortilis Machado de Mendon?a & Olivera de Rodrigues, 1965 and Parachordatortilis Mutafchiev, Santoro & Georgiev, 2010. Pelecanema sirry, a parasite of Pelecanus onocrotalus L. and P. crispus Bruch (Pelecaniformes, Pelecanidae) in Africa (Egypt and Senegal) and Europe (Ukraine and Bulgaria), is redescribed using light and scanning electron microscopy on the basis of specimens from P. crispus from Bulgaria. Pelecanema pelecani, a parasite of Pelecanus conspicillatus Temminck in Australia, is also redescribed using light microscopy on the basis of specimens from its type-host and type-locality. In contrast to a previous opinion recognising Pelecanema sirry and P. pelecani as synonyms, the two species are considered distinct and P. pelecani is validated.