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32. The Fauna of the African Lakes: a Study in Comparative Limnology with special reference to Tanganyika

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The special interest attaching to this comparative study of African lakes is due to the remarkable nature of the fauna of Tanganyika. That lake was discovered in 1858 by Burton and Speke, the latter bringing back with him shells considered to have a distinctly marine appearance. Subsequent collections emphasised this point, and interest was further increased by the discovery of a medusa by Böhm. A scientific expedition to investigate the fauna was despatched in 1895 in charge of J. E. S. Moore. The rich and unusual nature of the fauna then collected led him to formulate the hypothesis that Tanganyika represents an old Jurassic sea. In order to test the validity of this hypothesis, a second expedition, on which Moore was accompanied by Fergusson, left England in 1899. The result was held by Moore to justify the theory, and he embodied his conclusions in a work entitled “The Tanganyika Problem,” published in 1903. As the aquatic flora had not been taken into account, a third expedition was despatched to rectify that omission and make a further collection of animals. This left in 1904 in charge of the writer, returning in 1905. More recently still, in 1912-13, the Belgian expedition of Louis Stappers visited the lake and obtained additional information.The scope of this paper includes, besides Tanganyika, the five adjacent lakes of most interest, viz.:–Victoria Nyanza, Nyasa, Albert Nyanza, Edward Nyanza, and Kivu. All these, with the exception of Lake Victoria, occupy portions of the Great Rift Valley, which has probably been formed by trough-faulting on a stupendous scale. They lie in long narrow depressions bounded by escarpments rising to a height of two or three thousand feet above the level of the water. Nyasa and Tanganyika are very deep, the former reaching to over 780 metres and the latter to no less than 1435 metres. Victoria Nyanza has the largest area, but occupies only a shallow basin bounded by low hills.In all the lakes, but especially the largest, conditions are almost oceanic. Climatic differences are negligible, but water temperatures are uniformly high, showing an average of about 26o C. Analyses of the water have been made in very few instances. The water of Tanganyika, while fresh, is unusually rich in salts of magnesium, and that of Kivu contains excessive quantities of the latter as well as sodium salts. It is likely that the salinity of Tanganyika was greater formerly, and may still be subject to variation. Evidence exists of a considerable rise and fall in the level of the lake, yet it seems probable that rainfall and evaporation are very nearly balanced. There is reason to believe that Tanganyika had no outlet until it received an additional water supply from the Kivu basin, which was cut off from the Nile, and added to the drainage area of the big lake by the formation of a volcanic dam in recent geological times. Tanganyika would thus have been completely isolated and its waters more saline until an outflow was established. The present effluent appears to have been formed as an affluent, its bed being finally captured by a tributary of the Congo. A periodic rise and fall in the lake level may be caused by a temporary damming of the bed of the effluent, indirectly due to irregularities in the rainfall.As regards fauna, it is probable that at the present time all the six lakes have received fairly equal investigation. Only strictly aquatic animals are considered in this paper, but forms obtained from the neighbourhood of a lake are included in the totals. Tanganyika exhibits by far the most remarkable features, containing some 402 species of which 293 (nearly 73 per cent.) are endemic. Nyasa has a total second in point of size, but this has been artificially swollen by extra-lacustrine records which are wanting for other lakes. It has only 24 per cent, of endemic forms, while Victoria Nyanza with a smaller total has a larger percentage of endemics, namely 38 per cent. The three smaller lakes show a great reduction both in number of types and number of endemics. Tanganyika is further distinguished in that 57 out of 168 genera are peculiar to its waters, whereas Nyasa can only muster 6 endemic genera and the other lakes fewer still.The fishes of Tanganyika are of outstanding interest, comprising 146 species, of which 121 are endemic. The most notable feature is the number and high degree of specialisation of the Cichlidse, which with 27 genera (21 endemic) and 89 species (84 endemic) is the richest Cichlid fauna in the world. A species of incrusting gymnolsematous Polyzoon occurs, such forms being mostly marine. There is a large molluscan fauna, and of the Gasteropods more than two-thirds exhibit a marine-like appearance. These are known as the thalassoid or halolimnic group and are without exception endemic. There are no thalassoid Lamellibranchs. ‘Twelve species of prawns are known’, typically fresh-water in character, but specialised and all peculiar to the lake. There is an endemic genus of crabs, with 3 species. The Eucopepoda, Branchinra, and Ostracoda are well represented, each showing a large proportion of endemic species. The Cladocera are conspicuously absent from the lake and the Rotifera are relatively few in number. This may be related to the salinity of the water. The medusa originally described from Tanganyika has now been discovered in Victoria Myanaa and the Niger. There are four endemic species of fresh-water sponges. Only 5 groups of animals contain no endemic types.Tanganyika is one of the most remarkable lakes in the world, the only Cases comparable being the Caspian Sea and Lake Baikal. Recent figures are difficult to ascertain, hut while Baikal may even surpass Tanganyika in the number of unique animal forms, it appears that the Caspian is less striking.There is reason to believe that the relations between marine and fresh-water orgiuisms are intimate and due to a community of descent. The barriers which prevent a change of medium are not insurmountable. Organisms originated in the ocean, and have attained their distribution in fresh water in various ways. Moore regarded many of the Tanganyika types as relicts from a former ocean.The aquitic plants of Tanganyika are of less interest than the animals. The higher plants show no peculiarities, but the Algá differ from those of the remaining lakes. A number of species are endemic and others are usually marine or brackish in habit. The phytoplankton is rich in species, and more than 70 per cent. of the form do not occur in Nynsa or Victoria.Recent discoveries do not favour Moore's hypothesis of a marine Jurassic origin for Tanganyika. Neither his comparison of shells from the lake with marine fossil shells, nor his views on the primitive nature of the halolimnic Gasteropods, have been accepted by leading experts. No members of his halolimnic group, save the Polyzoon and the medusa, can be regarded as peculiarly marine. The Polyzoon is allied to a species Still living in Indian seas and the medusa is Known from other parts of Africa. The endemic animal types are held to be specialised rather than primitive in nature. Geological evidence is not more favourable. The extensive beds of sandstone and conglomerate which occur in the lake regions were probably formed under fresh-water and terrestrial conditions. They are considered by some to be of Triassic age, but may belong to a much earlier period, i. e. Devonian. Thus there is no support for the view that the ocean at one time extended over the Congo basin. Further, there is much to show that the trough in which Tangnnyika lies was not formed until Middle Tertiary times.A comparison has been made between thalassoid shells from Tanganyika and a fresh-water Cretaceous geniis on the one hand and fresh-water Pliocene shells on the other. Since the thalassoid shells have been held to resemble types from such different sources, they offer little indication as to the origin of the lake fauna. The quasi-oceanic conditions in Tangmyika may have produced an effect on the organisms it contains. Germain asserts that Gasteropods of marine aspect occur in other regions besides Tanganyika, and are derived from the fresh-water types of a former vast lake basin. On the present lakes becoming isolated, the conditions in Tanganyika produced a more striking series of such forms than elsewhere. This view is not regarded as accept- able. It has been suggested that the salinity of the Tanganyika water has produced marine-like forms, but further evidence is needed. The view that Titnganyika owes its remarkable organisms to a prolonged period of isolation is regarded as the most likely suggestion. It does not run counter to geological conceptions.This theory does not account for the medusa. Boulenger suggests that it may have survived from an Eocene sea in Northern Africa,. Gravier considers, on the contrary, that it may be a recent migrant from the ocean.The faunas of the remaining lakes are of less interest. Victoria Nyanza is next in importance to Tanganyika. The most conspicuous group is the fishes, with a large proportion of endemic species. The Mollusca also are noteworthy. The fauna of Nyasa is similar in character, but with fewer peculiar types. There are, however, 5 endemic genern of fishes. The smaller lakes contain representatives of fewer animal groups as well as fewer species. Kivu is the extreme case, with only ?3 species, of which 4 tire endemic. The poverty of its fauna may be associated with its exceptional salinity. Albert Nyanza. displays the smallest proportion of endemic types, viz. 13 per cent. It is suggested that periods of isolation would account for the peculiarities of Victoria Nyanza and Nyaaa.Certain animal types are unexpectedly absent from the African lakes. Such are the fresh-water Crustacea Asellus and Gammarrus and the fish parasite Echinorhynchus. No explanation of this is forthcoming.The number of specific forms in these lakes appears to be proportional to the size. This would seem to hold good also for the number of genera and families and even for the number of groups represented. it is possible that this principle is of general application. It is thought to be analogous to the phenomenon exhibited by the flora of oceanic islands.The affinity between African and Indian fresh-water types is recognisable in several instances among the inhabitants of the lakes. This affinity is explained by the former existence of a. continent which embraced them countries in the Carboniferous and subsequent periods.Little is known of the deeper regions of any of the lakes. It remains to be discovered whether associations of abyssal animals exist in them. Neither the vertical distribution of plankton forms, nor their seasonal variations have yet been studied. Further information is needed on the salts dissolved in the water, the depth and nature of the lake basins, water temperatures, etc. It is nevertheless possible from established facts to form a true conception of the nature of the lakes and their organisms.

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... Undoubtedly inspired by the remarkably large claw and the row of spines on the carapace of this species, he gave it the name Platythelphusa armata A. Milne-Edwards, 1887. The description of P. armata was soon followed by the discovery of more endemic species from the lake that were described by Cunnington (1899Cunnington ( , 1907Cunnington ( , 1920, and Capart (1952). Subsequently, the higher and lower level taxonomy of the endemic Lake Tanganyika genus was discussed, rearranged, and revised by a range of authorities (Cumberlidge et al., 1999, 2007, andreferences therein). ...
... The freshwater crabs found in Lake Tanganyika are dominated by species belonging to the Platythelphusidae Colosi, 1920, a family that is endemic to the lake. The Platythelphusidae appear to be monophyletic (Cumberlidge & Von Sternberg, 1998; and are morphologically highly divergent from other potamonautid and deckeniid freshwater crab taxa found in adjacent rivers and lakes in the African Rift System (Moore, 1903;Cunnington, 1907Cunnington, , 1920Rathbun, 1933;Balss, 1936;Capart, 1952Capart, , 1954Bott, 1955;Cumberlidge et al., 1999). ...
... armata, P. maculata, and P. conculcata). The genus has subsequently been assigned to various families and subfamilies, including the Potamonidae (Rathbun, 1904(Rathbun, , 1905Alcock, 1910;Bouvier, 1917aBouvier, , b, 1921Cunnington, 1920;Capart, 1952;Bott, 1955;Balss, 1957), the Plathythelphusinae (Colosi, 1920), and the Potamonautidae (Coulter, 1991). ...
... Following refutation of Moore's (1903) controversial hypothesis that the fauna represents a Jurassic marine relict, most early studies favoured a polyphyletic origin [see also, e.g. Cunnington (1920) and Thiele (1925Thiele ( , 1929]. However, now the fauna is widely regarded as an in situ adaptive radiation of Thiaridae -a heterogeneous family of limnic Cerithioidea (e.g. ...
... However, now the fauna is widely regarded as an in situ adaptive radiation of Thiaridae -a heterogeneous family of limnic Cerithioidea (e.g. Hudleston 1904;Cunnington 1920;Thiele 1925Thiele , 1929Pilsbry & Bequaert 1927;Yonge 1938;Brooks 1950;Hubendick 1952;Boss 1978;Brown 1980Brown , 1994Coulter 1991;Michel et al. 1992;Michel 1994Michel , 2000Glaubrecht 1994Glaubrecht , 1996West & Cohen 1996). In contrast, Glaubrecht (1997Glaubrecht ( , 1998Glaubrecht ( , 1999 suggested that the assemblage comprises several independent cerithioidean clades among which are no true Thiaridae s.s., a group more narrowly defined than the Thiaridae (= 'Melaniidae') of other authors. ...
... Others were more critical of Bourguignat's (1885) criteria and the inflation of species (e.g. Moore 1903;Cunnington 1920). Thus, characters such as continuity of the peristome, development of umbilicus, the basal angle, and size of the shell were noted to vary with degree of development and/or age (Smith 1904;Ancey 1906;Leloup 1953) [for shell variation, see Pilsbry & Bequaert (1927: 306, fig. ...
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Tanganyicia rufofilosa is an enigmatic gastropod endemic to Lake Tanganyika and unique among lake species in possessing a brood pouch within the head-foot. However, the only existing anatomic studies of the species are incomplete. Hence, the affinity of this species to other Tanganyikan gastropods and the evolution of viviparity among limnic Cerithioidea are unclear. The anatomic redescription and reinterpretation of reproductive homologies presented here revealed several features from the midgut and kidney that are informative concerning the phylogeny of Lake Tanganyika gastropods. In addition, the complex reproductive anatomy of both sexes is described. A rare accessory gland is present in males that is hypothesized to function in spermatophore formation and to be homologous to the ‘penis’ of some cerithioideans, an otherwise predominantly aphallic group. The structurally unique brood pouch, restricted to the mesopodial portion of the foot, is described and demonstrated to be unknown among viviparous cerithioideans. In contrast to the view that the cerithioideans of Lake Tanganyika represent an endemic radiation of Thiaridae, based on these new data T. rufofilosa appears to be allied to the Paludomidae.
... Due to their marine-like appearance (termed "thalassoid" by [45] and "halolimnic" by [61]) many earlier authors addressed the possibility of a marine origin of the Lake Tanganyika fauna and discussed the causes of the thalassoid appearance of its endemic molluscs. However, this eventually led to the refutation of Moore's controversial hypothesis [61][62][63] of the lake being once directly connected to the ocean [see e.g. in [64][65][66][67][68]. ...
... For a long time the idea that this largest and deepest of the African lakes has supplied its gastropod diversity with a stable inland environment and offered unique opportunities for within-lake diversification ("ancient endemic radiation" see [65,69]) resulting in a truly "adaptive" radiation [cf. 70,71] was common [e.g. ...
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Background: Lake Tanganyika belongs to the East African Great Lakes and is well known for harbouring a high proportion of endemic and morphologically distinct genera, in cichlids but also in paludomid gastropods. With about 50 species these snails form a flock of high interest because of its diversity, the question of its origin and the evolutionary processes that might have resulted in this elevated amount of taxa. While earlier debates centred on these paludomids to be a result of an intralacustrine adaptive radiation, there are strong indications for the existence of several lineages before the lake formation. To evaluate hy-potheses on the evolution and radiation the detection of actual adaptations is crucial. Since the Tanganyikan gastropods show distinct radular tooth morphologies hypotheses about potential trophic specializations are at hand. Results: Here, based on a phylogenetic tree of the paludomid species from Lake Tanganyika and adjacent river systems, the mechanical properties of their teeth were evaluated by nanoindentation, a method measuring the hardness and elasticity of a structure, and relat-ed with the gastropods’ specific feeding substrate (soft, solid, mixed). Results identify me-chanical adaptations in the tooth cusps to the substrate and, with reference to the tooth morphology, assign distinct functions (scratching or gathering) to tooth types. Analysing pure tooth morphology does not consistently reflect ecological specializations, but the me-chanical properties allow the determination of eco-morphotypes. Conclusion: In almost every lineage we discovered adaptations to different substrates, lead-ing to the hypothesis that one main engine of the flock’s evolution is trophic specialization, establishing distinct ecological niches and allowing the coexistence of taxa. Keywords: Functional morphology, nanoindentation, mechanical properties, Gastropoda, trophic specialisation, adaptive radiation
... The focus of reviews for most of the last century has been the questions why and how these gastropods radiate (e.g. Moore 1903;Cunnington 1920;Brooks 1950;Boss 1978;Michel 1994;Glaubrecht 1996;Martens 1997;Van Damme & Pickford 2003). Neither the basic systematics of the thalassoid gastropods of Lake Tanganyika has been thoroughly revised, nor has the allocation to the Thiaridae and monophyly of the thalassoid flock been seriously questioned. ...
... Review of the systematic concepts used for thalassoid gastropods from Lake Tanganyika Unfortunately, for a long time discussion of the evolution of the endemic species flock of thalassoid gastropods has been based essentially on the assumption that all these snails belong to only one family, viz. the freshwater cerithioidean Thiaridae (= "Melaniidae" of earlier authors) (e.g. Cunnington 1920;Pilsbry & Be-quaert 1927;Thiele 1929;Brooks 1950;Leloup 1953;Morrison 1954;Boss 1978;Brown 1980Brown , 1994Coulter 1991;Michel et al. 1992;Michel 1994Michel , 2000Michel , 2004Glaubrecht 1994;West & Cohen 1996;West & Michel 2000). However, based on his anatomical studies of thalassoid caenogastropods from Lake Tanganyika, more than hundred years ago Moore (1899b: 178-179) stated that "in whatever way we view this matter, it is at any rate obvious that the Melaniidae are no real family group". ...
The paludomid gastropods of Lake Tanganyika are one of the most spectacular examples of species flocks among molluscs. However, whether they provide an example of intralacustrine speciation and truly adaptive radiation still remains unresolved, with their monophyly and phylogenetic relationships within freshwater Cerithioidea still to be rigorously evaluated. In the course of providing the data for a future comprehensive phylogenetic analysis, this paper using SEM technique describes and documents the morphology of the adult and particularly the embryonic shell (ornamentation and size) as well as the radular anatomy (including cusp pattern), with remarks on the ontogeny and ecology, for 19 species belonging to 10 genera, mainly from a collection from Kigoma Bay, East shore of Lake Tanganyika, Tanzania. The species studied live either on soft sandy and silty bottoms or on primary or secondary hard substrata, representing two ecological guilds, with rocky substrata supporting a richer species assemblage (including five taxa of Lavigeria) than soft substrata. In addition, a systematic framework for these gastropods is suggested, with protoconch and radular morphology found to be most useful to characterize and differentiate genera and species, while teleoconch and opercular features correspond to three distinct lineages corroborated also by molecular data, viz. the Paramelaniinae with paludomid-like concentric operculum with spiral nucleus, the viviparous Nassopsinae Kesteven, 1903 (= Lavigeriinae Thiele, 1925) with subspiral to paucispiral operculum, and the minute sand-dwelling Syrnolopsinae with paucispiral operculum. Oviparity was found in 70% of the 32 thalassoid species from 17 genera and represents the most common and presumably ancestral reproductive mode within Tanganyikan gastropods, while two different viviparous strategies can be differentiated in 20% of the species (in four other species the reproductive mode is unknown). Finally, some standard hypotheses as to the question of relationships with Thiaridae, monophyly, in situ radiation and viviparity as a key innovation for this radiation are briefly reviewed and discussed. It is concluded that all studied species of the thalassoid species flock are actually members of the Paludomidae instead of the true Thiaridae, representing an evolutionary lineage of ancient, and most likely originally riverine Cerithioidea that predated the formation of the East African Rift system. Consequently, neither the broad spectrum of phenotypes nor the unique morphological features should be viewed as adaptations during the course of exclusively intralacustrine speciation and adaptive radiation within Lake Tanganyika. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)
... Invertebrates of marine origin in the enclosed Aral Sea, have gradually adapted to the increasing salinity (up to 70-90‰, since the Pliocene (~4 Ma) (Filippov and Komnedantov, 1995;Breckle and Geldyeva, 2012). Conversely, the rich and unusual fauna of freshwater Lake Tanganyika was originally considered to be marine and the lake represented the relic of a Jurassic Sea, which it cannot be (Cunnington, 1920;Coulter, 1991). The most important factor is stability; most high and low salinity environments are subject to very variable short-term salinity changes (Sanders et al. 1965). ...
Article
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... The description of zooplankton species of Lake Tanganyika have been made by Sars (1909) [47] , Gurney (1927) [29] and Lindberg (1951) [36] on Copepoda, Harding (1957) [30] on Cladocera, and Rousselet (1910) [46] , Beauchamp (1932) [8] and Gillard (1957) [27] on Rotifera. The absence or scarcity of cladocerans and rotirers in the open water and the richness of endemic cyclopoids have been noticed to be the characteristics of zooplankton in Lake Tanganyika (Cunnington,1920;Lindberg, 1951) [18,36] and despite this unique character of composition, only a few studies have been made from an ecological viewpoint. In this context, the present study was devoted to identify the most common freshwater zooplankton occurring presently in Lake Tanganyika and to determine whether physicochemical properties significantly impacted zooplankton occurrence, hence, the present study was aimed to investigate the state of interrelationship between zooplankton assemblages and environmental characteristics in Lake Tanganyika. ...
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The present study was conducted on Burundian coast of Lake Tanganyika in 4 sampling sites to identify and to estimate the spatial abundance of zooplankton community and to analyze whether physicochemical properties of water influence significantly the occurrence of zooplankton population. During the survey, it has been realized that zooplankton organisms were very few in number and taxonomic diversity and was comprising of 3 orders: Cyclopoida, Calanoida (Copepods) and Cladocera represented by Diaphanosoma. 12species belonging to 4families have been noted from all study sites. The relative diversity index of families revealed that the family Diaptomidae was dominant with 5species (41.7%) followed by family Cyclopidae with 4species (33.3%), then family Sididae with 2species (16.7%) while the Temoridae family was last with a single species (8.3%) The results of species richness and the Cumulative abundance of the sampling sites showed that zooplankton species and density were variable among stations. 11species were identified at Rumonge site comprising 1152 individuals per liter followed by Kajaga and Mvugo sites with same specific richness of 10 species but with different cumulative abundance of 830 and 502 individuals per liter respectively and Nyamugari site was in last position with 8 species comprising 219 individuals per liter. Besides, the results of Canonical Correlation Analysis (CCorA) between the environmental parameters and zooplankton biomass have shown that the abundance and proliferation of some zooplankton species are affected by the physico-chemical parameters concentration by acting as either inhibitors or accelerators for zooplankton species growth.
... The first scientific studies on African aquatic ecosystems were essentially devoted to surveys of biodiversity and to geological research and explorations, dating back to the end of the 19th century and the beginning of the 20th century (review by Talling, 2006). Famous examples were the quest for the source of the Nile River (Speke, 1863) research on the origin of the oldest and largest lakes, Lake Tanganyika and Lake Malawi (Cunnington, 1920). Soon the interest for inventories of the endemic fish fauna of these great lakes developed; several expeditions enriched museum collections of fishes and various invertebrate groups. ...
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... Most of the former ichthyofaunal lists of the Lake Edward system were confined to either Uganda or the DRC and often only reported the species collected during specific missions. Cunnington (1920) was the first to also present a table of fish species present in Lake Edward. ...
Article
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... The first studies on African tardigrades took place in the early 20th century and they have continued to the present day. As a result, over 30 papers on the topic have been published to date (Murray 1907(Murray , 1913Cunnington 1920;Marcus 1936;da Cunha & do Nascimento Ribeiro 1964;Binda 1971;Grigarick et al. 1973;Dastych 1980;Haspeslagh 1982;Binda 1984;Binda & Guglielmino 1991;Binda & Pilato 1987;Van Rompu et al. 1991;Dastych 1992Dastych , 1993Binda & Pilato 1995;Van Rompu et al. 1995;Pilato et al. 1999;Binda et al. 2001;Jørgensen 2001;Middleton 2003;Pilato et al. 2003;Kaczmarek & Michalczyk 2004;Kaczmarek et al. 2008;Meyer & Hinton 2009;Dastych 2009;Pilato & Lisi 2009;Fontoura et al. 2010). In 2009 Meyer and Hinton reported nine tardigrade species from South Africa and summarized all available information on South African tardigrades. ...
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In three mixed samples (mosses and leaf litter) collected in Zambia (southern Africa), forty-three specimens and six eggs of eutardigrades were found. Among them, 29 specimens belonged to a new species of the family Isohypsibiidae, Doryphoribius niedbalai n.sp. The new species belongs to the Doryphoribius evelinae group and it differs from other members of the group mainly by a different number and configuration of dorsal gibbosities, as well as by some morphometric characters. Apart from the new species, the examined material contained also two rare African eutardigrades: Milnesium tetralamellatum and Calcarobiotus (Calcarobiotus) parvicalcar. These species are recorded for the first time outside their type localities. Additionally, Paramacrobiotus vanescens is recorded for the fourth time from Africa. In this paper, together with the description of the new species, first ever photomicrographs of Milnesium tetralamellatum and Paramacrobiotus vanescens are also provided. This is the first account of the phylum Tardigrada from Zambia.
... He left a detailed account of his expedition (von Götzen 1895 ) , which describes the dif fi culties of exploration at that time, but also conveys his amazement at discovering the marvels of this part of Africa. The scienti fi c interest in the East African Great Lakes further increased with the English expeditions at the beginning of the twentieth century (Cunnington 1920 ) . An inventory of several lakes attracted attention on the poverty of Lake Kivu fi sh fauna: only 23 species, among which 4 endemic, were recorded at that time. ...
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Lake Kivu, located in the Eastern African Rift, in a dramatic volcanic scenery, has fascinated the local people, inspiring legends; the explorers of the nineteenth century, inspiring romantic reports; and the scientists of the twentieth and twenty-first centuries, inspiring limnological and geochemical research. For some, Lake Kivu is a “killer lake”, containing vast amounts of carbon dioxide and methane in its deep, anoxic waters, and it has been compared to Lakes Nyos and Monoun, whose eruptions caused massive animal and human death in Cameroon. Fortunately, methane gas exploitation can help to reduce the eruption risk and at the same time supply an important amount of energy for the benefit of local development. However, the management of the lake resources, including methane harvesting and fisheries, is complex, and particular care must be taken during gas exploitation in order to avoid any negative impacts on the ecosystem and the goods and services provided by the lake. In this chapter, the history of research on Lake Kivu is summarized, and the major findings that resulted from expeditions by British, Belgian, American, and German researchers are presented.
... He left a detailed account of his expedition (von Götzen 1895 ) , which describes the dif fi culties of exploration at that time, but also conveys his amazement at discovering the marvels of this part of Africa. The scienti fi c interest in the East African Great Lakes further increased with the English expeditions at the beginning of the twentieth century (Cunnington 1920 ) . An inventory of several lakes attracted attention on the poverty of Lake Kivu fi sh fauna: only 23 species, among which 4 endemic, were recorded at that time. ...
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We review available data on archaea, bacteria and small eukaryotes in anattempt to provide a general picture of microbial diversity, abundances and microbedrivenprocesses in Lake Kivu surface and intermediate waters (ca. 0–100 m). Thevarious water layers present contrasting physical and chemical properties andharbour very different microbial communities supported by the vertical redoxstructure. For instance, we found a clear vertical segregation of archaeal and bacterialassemblages between the oxic and the anoxic zone of the surface waters. Thepresence of speci fi c bacterial (e.g. Green Sulfur Bacteria) and archaeal (e.g.ammonia-oxidising archaea) communities and the prevailing physico-chemicalconditions point towards the redoxcline as the most active and metabolically diversewater layer. The archaeal assemblage in the surface and intermediate water columnlayers was mainly composed by the phylum Crenarchaeota , by the recently de fi nedphylum Thaumarchaeota and by the phylum Euryarchaeota . In turn, the bacterialassemblage comprised mainly ubiquitous members of planktonic assemblages offreshwater environments ( Actinobacteria , Bacteroidetes and Betaproteobacteria among others) and other less commonly retrieved phyla (e.g. Chlorobi , Clostridiumand Deltaproteobacteria ). The community of small eukaryotes (
... The first studies on African tardigrades took place in the early 20th century and they have continued to the present day. As a result, over 30 papers on the topic have been published to date (Murray 1907(Murray , 1913Cunnington 1920;Marcus 1936;da Cunha & do Nascimento Ribeiro 1964;Binda 1971;Grigarick et al. 1973;Dastych 1980;Haspeslagh 1982;Binda 1984;Binda & Guglielmino 1991;Binda & Pilato 1987;Van Rompu et al. 1991;Dastych 1992Dastych , 1993Binda & Pilato 1995;Van Rompu et al. 1995;Pilato et al. 1999;Binda et al. 2001;Jørgensen 2001;Middleton 2003;Pilato et al. 2003;Kaczmarek & Michalczyk 2004;Kaczmarek et al. 2008;Meyer & Hinton 2009;Dastych 2009;Pilato & Lisi 2009;Fontoura et al. 2010). In 2009 Meyer and Hinton reported nine tardigrade species from South Africa and summarized all available information on South African tardigrades. ...
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In three mixed samples (mosses and leaf litter) collected in Zambia (southern Africa), forty-three specimens and six eggs of eutardigrades were found. Among them, 29 specimens belonged to a new species of the family Isohypsibiidae, Doryphoribius niedbalai n.sp. The new species belongs to the Doryphoribius evelinae group and it differs from other members of the group mainly by a different number and configuration of dorsal gibbosities, as well as by some morphometric characters. Apart from the new species, the examined material contained also two rare African eutardigrades: Milnesium tetralamellatum and Calcarobiotus (Calcarobiotus) parvicalcar. These species are recorded for the first time outside their type localities. Additionally, Paramacrobiotus vanescens is recorded for the fourth time from Africa. In this paper, together with the description of the new species, first ever photomicrographs of Milnesium tetralamellatum and Paramacrobiotus vanescens are also provided. This is the first account of the phylum Tardigrada from Zambia.
... Meteorological observations at Lake Tanganyika were first given by Burton (1860). Although several hydrological and limnological studies have been conducted on Lake Tanganyika (Stappers, 1914;Cunnington, 1920;Beauchamp, 1939;Capart, 1949Capart, , 1952Servais, 1957;Dubois, 1958;Coulter, 1967;Ferro, 1975), the hydrodynamics of the lake are still poorly understood. Previous studies have been localised rather than lake-wide (Coulter, 1991). ...
... Lastly, the controversial 'Tanganyika Problem' of Moore was tested further by the expedition of Cunnington (1904-05). From its collections and with the cooperation of many group-specialists, Cunnington assembled a 'comparative limnology' 47 and rejected the original hypothesis of a direct marine origin -already doubted from other work on the gastropod molluscs 213 . ...
... Although E. sarsi was previously reported from Lake Tanganyika (Sars 1909;Cunnington 1920;Capart 1944;Fryer 1965), this is the first report for this host, the Tanganyika Killifish, and of the pathological alterations associated with it. Fryer (1965) observed that a correlation exists between the attachment site of various Ergasilus species and pathological alterations elicited; he also noted that different species attach to different regions, even on the same host. ...
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Abstract A total of 204 Ergasilus sarsi, a copepod, were collected from Tanganyika Killifish Lamprichthys tanganicanus in Lake Tanganyika during March 2010. The prevalence was 86.40%, the mean intensity was 7.56, and the mean abundance was 6.38. Only 27 of the fish were infested, and the highest infestation on one fish was 29. Proliferation of mucus cells and lamellar fusion occurred. Haemorrhage due to blood vessel compression was noted. This is the first record of E. sarsi from Tanganyika Killifish. This study is also the first to provide a description of the pathological alterations caused by E. sarsi. Received April 2, 2013; accepted May 31, 2013.
... The first studies on Nile zooplankton were conducted in the course of the nineteenth century (see Talling, 2009), and were linked to the early exploration of the African continent and the quest for the sources of the Nile (Schmarda, 1854; Richard, 1883 Richard, , 1894 Richard, , 1896 Stuhlmann, 1891; Barrois, 1891; Weltner, 1897 Weltner, , 1898 Ekman, 1904; Daday, 1910a, b; Gurney, 1911; Van Douwe, 1912a, b), or slightly later (Cunnington, 1915Cunnington, , 1920 Delachaux, 1917; Chappuis, 1922; Lowndes, 1936; Worthington, 1929; Steuer, 1942; Brunelli & Cannicci, 1940). Among more recent papers, Abu Gideiri (1969a, b), El-Moghraby (1972, 1977), Elster & Vollenweider (1961), Green (1971), Kiefer (1939 Kiefer ( , 1978), Löffler (1963) Monakov (1969), Ocioszynska-Wolska (1935), Steuer (1942), and Thomas (1961) should be cited. ...
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The about 17 spp. of calanoid copepods of the Nile basin are dominated by East African species, but in the lower Nile, several Mediterranean species are found. Some species are endemic to the basin and Lake Chad. Endemic species also occur in some of the East African plateau lakes. Two ecological groups are present: species typical of permanent, and species typical of ephemeral waters. Among Cyclopoida, the dominant genera are Mesocyclops and Thermocyclops, together about 20 species with African, Afro-Asian, and (few) with Mediterranean affinities. An invasive cyclopoid, Acanthocyclops trajani, has become dominant in the eutrophic delta lakes. Among anomopods, about ten species of Daphnia with different ecological and geographic ranges have been found. Some 75 species of cladocerans are now on record, a number that is expected to increase in future years. Anostracans are represented by about six species of Streptocephalus, some of which are Mediterranean, other East African, and at least one restricted to the Ethiopian plateau. Syncarida (Bathynellacea) have been little studied, with three African species on record. Among decapods, Caridina nilotica occurs basin-wide and is partly planktonic, partly benthic. By analogy with Lake Chad and Lake George, zooplankton production is estimated at roughly 40 t per km2 for the East African plateau lakes. Production further north, in Lake Nasser and the Delta lakes, with a yearly biomass variation of a factor 3 (Nasser) to 10 (delta), and concomitant variations in water temperature, may not be fully compensated by higher biomasses and may be lower.
... In this context, viviparity has not only been discussed as an important key innovation for freshwater colonization (e.g. Cunnington 1920;Sunderbrink 1929;Seshaiya 1936Seshaiya , 1940Morrison 1954;Hubendick 1962;Davis 1982;Stoddart 1983;Fretter 1984;Starmçhlner 1973Starmçhlner , 1984, but this specific mode of reproduction and recruitment strategy is also of paramount importance with respect to the specific environmental conditions for freshwater organisms in Australia, given the extreme climatic variables of this continent, such as, for example, its aridity and seasonality of rainfall resulting in monsoonal flooding of vast areas right after long droughts. Although these factors and correlations were recently been exemplified and discussed using vertebrates (in particular terrestrial reptiles) (see Shine & Brown 2008), the same has barely been touched to date for aquatic invertebrates such as thiarids. ...
We systematically revise here the Australian taxa of the Thiaridae, a group of freshwater Cerithioidea with pantropical distribution and “marsupial” (i.e. viviparous) reproductive modes. On this long isolated continent, the naming of several monotypic genera and a plethora of species have clouded both the phylogenetical and biogeographical relationships with other thiarids, in particular in Southeast Asia, thus hampering insight into the evolution of Australian taxa and their natural history. Based on own collections during five expeditions to various regions in Australia between 2002 and 2007, the study of relevant type material and the comparison with (mostly shell) material from major Australian museum collections, we describe and document here the morphology (of adults and juveniles) and radulae of all relevant thiarid taxa, discussing the taxonomical implications and nomenclatural consequences. Presenting comprehensive compilations of the occurrences for all Australian thiarid species, we document their geographical distribution (based on over 900 records) with references ranging from continent-wide to drainage-based patterns. We morphologically identify a total of eleven distinct species (also corroborated as distinct clades by molecular genetic data, to be reported elsewhere), of which six species are endemic to Australia, viz. “Thiara australis ”, Plotiopsis balonnensis, and “Stenomelania ” denisoniensis with wide distribution and Melasma onca, Sermyla venustula, and Ripalania queenslandica with more restricted ranges. In contrast, Thiara amarula and Stenomelania cf. aspirans as well as Melanoides tuberculata, Plotia scabra, and Sermyla riqueti are widely distributed also outside Australia, in particular in the Malay Archipelago and the Indo-West Pacific, respectively. The occurrences especially of the latter three species are discussed, concluding on quite distinct historical contingencies. Three thiarids species, viz. Stenomelania cf. aspirans, Sermyla riqueti and Plotia scabra, are recorded here for the first time for Australia. Based on a new taxonomic framework for the Thiaridae we point out some of the pertinent problems with naming and artificial delineation of species, revealing why typology and earlier practice of splitting was misleading in case of these truly “Darwinian snails”. We also report on finding two clearly distinct viviparous modes in Australian thiarids, discussing their distribution in certain fluvifaunal provinces and major drainage systems in concert with these reproductive features of life history tactics. While the live-bearing T. amarula, S. cf. aspirans, and R. queenslandica, that release veligers (ovo-viviparity), are found to have very restricted occurrences in rivers and streams in the Jardinian province of NE Queensland only, the five more widely distributed Australian endemics Plotiopsis balonnensis and “Stenomelania ” denisoniensis as well as “Thiara australis ”, Sermyla venustula and Melasma onca in the Leichhardtian province all brood and release shelled juveniles (eu-viviparity). Finally, we hypothesize on the evolutionary history and colonization of Australia by different lineages of these freshwater Cerithioidea. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)
... Bourguignat (1888; alone added 242 species to what had already grown to a classification of 90 species (Bourguignat, 1885b). Largely as a backlash against Bourguignat's essentialist philosophy (Dance, 1970(Dance, , 1986, subsequent taxonomies have consistently reduced the number of gastropod species in Lake Tanganyika (Cunnington, 1920;Pilsbry & Bequaert, 1927;Leloup, 1953;Brown, 1994). In a recent taxonomic treatment of the Tanganyikan gastropods, Brown & Mandahl-Barth (1987) recognized a total of 60 prosobranch and pulmonate species with 37 endemics. ...
... However, in contrast to their cichlid counterparts (e.g.Salzburger et al. 2002; references therein), the gastropods of this ancient lake remain under-utilized as models for testing such hypotheses. While conjectures abound concerning extrinsic factors that may have promoted the formation of the thalassoid species flock (e.g.Cunnington 1920;Brooks 1950;Boss 1978;Michel et al. 1992), less well  ...
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The radiation of gastropods in Lake Tanganyika is an ideal system for testing competing hypotheses of species flock formation. Yet, much of the basic biology of these species remains unknown. In an ongoing effort to understand the evolution of Tanganyikan gastropods, we here describe Stanleya neritinoides. Alcohol-preserved material of the soft parts is rare, consequently, the systematic position of the species, and a repeated suggested affinity to Tanganyicia rufofilosa, have been based primarily on features of the shell. However, features of the radula and operculum are unique and do not suggest an affinity to any other Tanganyikan species. Thus, S. neritinoides has remained a particularly poorly known and enigmatic member of the species flock. This investigation confirmed that several aspects of internal and external anatomy are shared between S. neritinoides, T. rufofilosa, and other Tanganyikan gastropods, but that S. neritinoides is unique in features of the radula and seminal receptacle. Moreover, S. neritinoides differs from T. rufofilosa in features of the foregut, midgut, hindgut, kidney, nervous system, reproductive system and reproductive strategy. These new data are inconsistent with an interpretation of identity of Stanleya and Tanganyicia. In addition, given the pervasive differences between the two, a sister-group relationship between the two is unlikely. More precise systematic placement of S. neritinoides awaits the establishment of a phylogenetic framework for all Tanganyikan gastropods.
... It was posited that they were able to retain a suite of plesiomorphic characters due to favorable marine-like environmental conditions in Lake Tanganyika (Bott, 1955; Cunnington, 1899; Moore, 1903). Alternatively, it was suggested that convergent evolution caused the unusual appearance of platythelphusids (Cunnington, 1920; von Sternberg and Cumberlidge, 1999). These two hypotheses lead to fundamentally diVerent predictions regarding (a) the phylogenetic placement of platythelphusids with respect to other freshwater crabs and (b) the position of the most derived platythelphusid within its own clade. ...
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Ergasilus (von Nordmann, 1832) (Ergasilidae) is a species-rich group of parasitic copepods with a wide distribution in freshwater, marine and brackish environments. Up to now, 9 species of Ergasilus are known from cichlid fishes in Africa. In this study, 5 species, including 3 new, were collected from the gills of 12 cichlid species (11 genera: Bathybates , Ctenochromis , Eretmodus , Gnathochromis , Lamprologus , Neolamprologus , Ophthalmotilapia , Perissodus , Simochromis , Spathodus and Tanganicodus ) of the northeastern shore of Lake Tanganyika in Burundi, namely E. macrodactylus (Sars, 1909), E. megacheir (Sars, 1909), E . caparti n. sp., E . parasarsi n. sp. and E. parvus n. sp. All species found were identified and described on the basis of adult female specimens using an integrative taxonomy approach mixing morphological characterization and molecular analyses of 2 ribosomal DNA markers (partial 18S and 28S rDNA sequences). An identification key for Ergasilus species from Lake Tanganyika is included. This study provides the first molecular data for Ergasilus species in Africa. The phylogenetic analyses suggest that the Ergasilus species parasitizing Lake Tanganyikan cichlids form a well-supported clade within the Ergasilidae. However, their phylogenetic relationships with other congeners still remain unclear due to a lack of molecular data for this diverse genus.
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We report a dataset of all known and published occurrence records of animals of the phylum Rotifera, including Bdelloidea, Monogononta, and Seisonacea (with the exclusion of Acanthocephala) for Africa and surrounding islands and archipelagos. The dataset includes 24,704 records of 914 taxa (subspecies: 38; species: 783; genus: 76; family: 17), gathered from 610 published papers. The published literature spans from 1854 to 2022, with the highest number of records in the decades 1990-1999 and 2010-2019. The African countries with the highest number of taxa are Nigeria, Algeria, South Africa, and Democratic Republic of the Congo, whereas no records are yet available for a dozen countries. The number of species known from each country can be explained mostly by sampling efforts, measured as the number of papers published for each country up to now. The dataset is available through the Open Science Framework (OSF) and in the Global Biodiversity Information Facility (GBIF).
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Both sexes of a new brackish-water species, Nannopus sinusalbi sp. nov. (Nannopodidae) are described from the Bahía Blanca estuary (38°53’S, 62°07’W) in Buenos Aires Province, Argentina. The only previous record of the genus in the study area was identified as the type species, Nannopus palustris Brady, 1880, with no description or illustrations, hence its authenticity cannot be confirmed. Nannopus brasiliensis Jakobi, 1956 is relegated to species inquirenda in the genus rather than being considered a junior synonym of the type species. Nomenclatural issues related to the usage of the alternative spellings Iliophilus Lilljeborg, 1902 and Ilyophilus sensu Sars (1909) and the unavailability of Ilyophilus canui Kim, Choi & Yoon, 2017 are discussed. An updated key to the 18 identifiable species of Nannopus (excluding the type species N. palustris) is presented. The harpacticoid assemblage at the type locality showed a distinct seasonality with N. sinusalbi sp. nov. representing about 8% of the community. The new species showed densities below 5 ind.cm‑2 during most of the year, reaching an abrupt peak of 40.17 ind.cm‑2 towards the end of the summer, when the maximum proportion of ovigerous females was recorded.
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The paper presents an overview of the history of aquatic parasitology of freshwater fish in southern Africa. Aquatic parasitology has become a very popular field of specialisation in South Africa and is currently practised by a number of individual research groups at different universities. So far most research deals with parasites of wild fish rather than pathogens of aquaculture. It is written as a narrative and summarises the aquatic parasitology research mostly on fish parasites carried out at the universities of Cape Town, Free State, Johannesburg, Limpopo, Pretoria, North West and Sefako Makgatho Health Sciences. It is not intended to be a review in the classical way because it deals with parasites ranging from Protozoa to Arthropoda.
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We compile all published information on the Recent Pentastomida published to date, including complete synonyms, and species distributions. All host species are cited and their names updated. A taxonomical history of the group, a synthesis of phylogenetic information for the taxon, and a summary of the pentastomes by host groups, with accounts of the illneses they provoke, are also provided.
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The genus Platythelphusa is revised and six species are recognized. These species are P. armata A. Milne-Edwards, 1887, P. maculata (Cunnington, 1899), P. conculata Cunnington, 1907, P. tuberculata Capart, 1952, P. polita Capart, 1952 and P. echinata Capart, 1952. A seventh taxon, P. denticulata Capart, 1952 is considered here to be a junior synonym of P. conculata. A diagnosis for each species is provided and most are figured from the type. Keys to the families of African freshwater crabs and to the genus Platythelphusa are also provided.
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This report describes the natural habitat of the cichlid fish Haplochromis burtoni along the Burundi coast of Lake Tanganyika in central Africa. Parameters of the physical environment as well as more general biological factors are described qualitatively and quantitatively. Temporary shore pools, a previously undescribed habitat, are examined in detail. These pools, appear to play an important role in the life cycle of Haplochromis burtoni and other mouthbrooding cichlids by providing, for a large part of each year, a protected area 0 which is particularly suited for reproduction, possibly at the cost of high predation. As a result of circaannual changes in the lake level, the shore pools are alternately isolated from and rejoined with the lake, allowing a regular exchange of fauna.
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The morphology of the freshwater medusa, Limnocnida rhodesiœ Boulenger, obtained from new sites in the Zambesi and Limpopo river-systems, is described and illustrated by photographs (Pl. I.). The new sites for L. rhodesiœ are the Prince Edward Dam on the Hunyani River, near Salisbury, the Hartebeestpoort Dam on the Crocodile River, near Pretoria, and the Bezuidenhout Valley in Johannesburg. The range of dimensions of L. rhodesiœ is extended, the present specimens being larger than those previously described. The specimens of L. rhodesiœ examined from the new localities were all females in active egg-production. Manubrial bud-formation was seen in only a few specimens. A species of Trichodina occurred in small numbers on the external surface and tentacles of L. rhodesiœ from the new localities cited. Some ecological notes on Limnocnida are given. The present geographical distribution of the genus Limnocnida is discussed and the continued southward range of distribution in Africa from Lake Victoria Nyanza to Johannesburg is detailed. Similarly, the distribution of the known species of Limnocnida is given, L. tanganicœ, the Central African form, being replaced by L. rhodesiœ in Rhodesia and the Transvaal, and by L. indica in India. The possible significance of the present-day geographical distribution of Limnocnida in relation to former geological conditions on the earth's surface is discussed. Summary The morphology of the freshwater medusa, Limnocnida rhodesiœ Boulenger, obtained from new sites in the Zambesi and Limpopo river-systems, is described and illustrated by photographs (Pl. I.). The new sites for L. rhodesiœ are the Prince Edward Dam on the Hunyani River, near Salisbury, the Hartebeestpoort Dam on the Crocodile River, near Pretoria, and the Bezuidenhout Valley in Johannesburg. The range of dimensions of L. rhodesiœ is extended, the present specimens being larger than those previously described. The specimens of L. rhodesiœ examined from the new localities were all females in active egg-production. Manubrial bud-formation was seen in only a few specimens. A species of Trichodina occurred in small numbers on the external surface and tentacles of L. rhodesiœ from the new localities cited. Some ecological notes on Limnocnida are given. The present geographical distribution of the genus Limnocnida is discussed and the continued southward range of distribution in Africa from Lake Victoria Nyanza to Johannesburg is detailed. Similarly, the distribution of the known species of Limnocnida is given, L. tanganicœ, the Central African form, being replaced by L. rhodesiœ in Rhodesia and the Transvaal, and by L. indica in India. The possible significance of the present-day geographical distribution of Limnocnida in relation to former geological conditions on the earth's surface is discussed.
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A detailed morphometric study was undertaken of collections of the Lake Tanganyika endemic Mastacembelus ophidium. On each specimen 27 measurements and 12 meristics were taken. Within the specimens previously identified as M. ophidium a new species was discovered. A redescription of M. ophidium and a description of the new species are provided.
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In Lake Albert Daphnia lumholtzi is found in two forms. One has a pointed anterior prolongation, or helmet, on the head. The other has a shorter rounded head, and was originally described as a separate species, D. monacha. The latter form dominates the zooplankton in the middle of the lake where planktivorous fish are rare or absent. The helmeted form becomes commoner near the margins of the lake and reaches its greatest abundance in Ndaiga Lagoon, where planktivorous fish are common. The possession of a helmet is associated with a reduction in the size of the carapace compared to the round headed form. The carapace with its contained eggs is the most conspicuous part of a cladoceran, so that the helmeted forms are at an advantage in the presence of planktivorous fish which locate their prey by sight. The mid-lake monacha forms are larger than specimens of the same form in Ndaiga Lagoon, where it is shown that Alestes baremose feeds selectively on the larger specimens of the monacha form. The helmeted form produces more, but smaller eggs than the monacha form. The total brood volume (= mean egg volume x mean number eggs per female) is greatest in the midlake monacha forms. The selective advantages of variations in egg size and the possession of a helmet are discussed. It is concluded that the data from Lake Albert support the hypothesis of Brooks (1965) concerning the adaptive significance of helmet development in Daphnia.
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The phylogenetic relationships of the freshwater crab genus Platythelphusa were investigated by means of a cladistic analysis using morphological characters. The platythelphusa were found to be a monophyletic assemblage, this finding supports the recognition of the family Platythelphusidae. Platythelphusa is endemic to Lake Tanganyika, East Africa, and some of its species bear a striking resemblance to certain marine crabs (grapsids). The study does not support the idea that the Platythelphusidae emerged from a relict population of a grapsid or grapsid-like taxon: the evidence supports an hypothesis for the evolution of this family from freshwater crab ancestors. Parsimony considerations position the freshwater crab family Deckeniidae as the sister group of the platythelphusids. In addition, the Palaeotropical freshwater crabs appear to constitute a monophyletic group.
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Introduction.—A large collection of non-cichlid fish from Lake Tanganyika, containing 2475 specimens and 57 species, made by the late Dr. Cuthbert Christy, has now been identified. The collection is described in this paper, which forms part of a series attempting to put on record all data relating to the fish of the lakes of Africa. The present work has been undertaken as a preliminary to further ecological studies in the field.History of Investigations.—Since its discovery in 1858, by Burton and Speke, Lake Tanganyika, having so peculiar a fauna, has been visited by many collectors, who have brought back specimens, including fish, till at the present time there are 76 species of non-cichlids known from the lake.Physiography.—The drainage-system of Lake Tanganyika is small in proportion to the size of the lake, the main affluent being the Ruzizi River from Lake Kivu, while the only outlet is the Lukuga River, which flows westwards into the Lualaba River, a tributary of the Congo. Little is known about the physical and chemical conditions of the water, except that the depth is very great and that the salinity is rather high, with a preponderance of magnesium salts.The Fish-fauna and, its Distribution.—A table shows all the species of nonaichlid fish known from Lake Tanganyika, together with their distribution in other parts of Africa. The proportion of endemic forms, 42 out of 76 (55 per cent.) is very high, and most of these belong to groups that inhabit open and well-oxygenated waters and which are not able to penetrate through small streams and swamps to other drainage-systems.The distribution of the remaining 34 species in Lake Tanganyika is analysed, and the number of these found in each of the various drainage-systems is determined. There are twenty in the Congo system, ten of which are also in the Zambezi system, four others in the Zambezi or East African Rivers, two in Lake Kivu, possibly two in Lake Rukwa, eight in Lake Victoria, and seven in the Nile.History of the Lake and its Drainage-system.—Günther's and Moore's hypothesis of a marine origin of Lake Tanganyika has become untenable as a result of recent evidence. It is now certain that the lake came into existence in the centre of the continental mass as a result of the great rifting movements, which start in early Tertiary times. The subsequent history was probably roughly as follows:—At first the lake was connected to the northern lakes and rivers which now drain to the Nile. It was then isolated by the uplift of land immediately to its north, and was much reduced in volume during the arid interpluvial of the middle Pleistocene, with the result that the salts in its water became concentrated. During this period it is probable that the pseudo-marine types of Mollusca etc. were evolved. The second pluvial period, which followed aridity, refilled the lake and reduced the concentration of salts, but isolation from other waters may have continued till the formation of the Mufumbiro volcanoes in the late Pleistocene. These volcanoes dammed the upper reaches of the Ruchuru River, and caused ponding, with the result that Lake Kivu was formed and the drainage was reversed to a southerly direction, viâ the Ruzizi River, into Lake Tanganyika. This extra supply of water overflowed Lake Tanganyika, and an outlet was cut on the western shore, putting the lake into faunal communication with the Congo system.Ecology.—Some evidence about the food and habitats of the species has been obtained from examinations of stomach contents, so that the fish can be divided into groups depending on their feeding habits, and a simple food-chain diagram has been constructed.Systematic.—A key for the identification of the species is included, principally for use by naturalists who have not specialized in systematic ichthyology. Five new species are described, seven are redescribed, the species of Chrysichthys from Lake Tanganyika are completely revised, and the generic description of Phyllonemus is modified. In all cases where Christy's specimens are not typical the differences are noted in detail, in the hope that this may lead to a better understanding of the variation within the species and also of the production of endemic forms, whether varieties, species, or genera, under the influence of isolation.
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Species of Daphnia discovered in Australia during the last 10–15 years have provided important new evidence of an ancient, Pangaean, origin of the genus. Recent biogeographical and genetic work has also suggested an ancient origin for individual species within the D. carinata complex in Australia. The genetic studies highlighted the complexities of population structure in the group. However, in combination with morphometric studies, they also provided solutions to some difficult taxonomic problems. Since the systematic difficulties in the D. carinata complex reflect taxonomic problems fundamental to the genus, the Australian species have assumed a particular interest. New data on the distribution of the six taxa currently recognised in Australia, and detailed descriptions of both males and females of D. occidentalis, D. lumholtzi, D. cephalata, D. nivalis and D. carinata (sensu lato) and the female of D. jollyi (no male of D. jollyi has been found), are presented.
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A collection of rotifers contained in samples from the Blue, White and joint Niles in the Sudan, the Red Sea Hills, and Jebel Marra mountains is studied, and the previous literature on the rotifera of Sudan is reviewed. A total of 145 rotifer taxa are now known from this country. Ecological and distributional notes on selected species are added. Besides cosmopolitan, pantropical, and tropical species, a small but significant fraction of the fauna is of northern origin, possibly reflecting climatic conditions of the late-Pleistocene.
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All freshwater calanoids in southern Africa belong to the family Diaptomidae of which there are two subfamilies, the Paradiaptominae (Lovenula, Paradiaptomus and Metadiaptomus) and Diaptominae (Tropodiaptomus and Thermodiaptomus). The Paradiaptominae are endemic to Africa, while the Diaptominae have one endemic African genus Thermodiaptomus, and the other genus Tropodiaptomus, occurs in other parts of the world as well as Africa. Knowledge of distribution of the Diaptomidae has been hampered by incomplete taxonomic knowledge and lack of co-ordination of available information. Distribution patterns of 19 described species and 11 new species confirm that the majority of species have a limited distribution, and that the Paradiaptominae are arid-adapted and belong to temporary pool communities. Six species are endemic to coastal pans and vleis of the western and southern Cape Province. Only those species with a wider distribution have been recorded as colonising man-made lakes. The four Lovenula species are predators and often co-exist with a Metadiaptomus species as prey. Synapomorphies of widely separated species of the Paradiaptominae, provide interesting insights into how their evolution may have been governed by vicariance, dispersal and palaeoenvironments of the African continent.
Article
In the course of investigations on the systematics and zoogeography of rotifers, the author found that 48% of all taxa treated showed a limited distribution (most were periphytic or benthic periphytic species from shallow waters).The following species were limited to the Palaearctic Region:Marine: Synchaeta triophtalma Lauterborn, S. vorax Rousselet, and S. curvata Lie-Pettersen.Brackish water: Colurella dicentra (Gosse), C. halophila Wulfert, and C. unicauda Eriksen.Among Holarctic species, Notholca psammarina Buchholz & Rhmann and the two semi-species N.(striata) bipalium (O. F. Mller) and N(striata) striata (O. F. Mller) are discussed.A series of warm-stenothermic species were found to be pantropical: Lecane leontina Turner, L. monostyla (Daday), L. harringi (Ahlstrom), Lepadella latusinus (Hilgendorf), Trichocerca chattoni (de Beauchamp), and Platyias leloupi Gillard, while Lecane plesia Myers and L. punctata (Murray) seemed to be confined to the Neotropical Region.The data collected also suggest that:i) i) Keratella wirketissi Kutikova, K. kamtchatica Kutikova, K. cruciformis (Thompson), and K. eichwaldi (Levander) might be good species. ii) ii) Brachionus forficula Wierzejski, an Old World species, is a geographical vicariant of both B. havanaensis Rousselet and B. trahea Murray from the New World. iii) iii) Cases of ecological vicariance are found in Testidinella elliptica (Ehrb.) and T. clypeata (O. F. Mller) from fresh and brackish water respectively; Keratella cruciformis (Thompson) and K. eichwaldi (Levander) from the sea and brackish water respectively; Keratella quadrata (O. F. Mller), K. valga (Ehrb.), and K. tropica (Apstein), dominant in arctic to cold-moderate, in warm-temperate, and in subtropical-tropical climates respectively. Some rotifer species are presently in expansion: the cases of K. tropica and of Brachionus falcatus Zacharias in Europe are analysed. A related case is that of man-made faunas: the presence of Brachionus havanaensis in Sangchrist Lake, Ill., USA, and the Rotifer fauna of the River Loire (France) are discussed.
Article
Two series of plankton samples, collected in different parts of the Ivory Coast, are examined for their rotifer content. Seventy-one taxa are identified to species level, some of which are present in different forms. Seventeen taxa are new to the Ivory Coast, three are new to Africa. Ecological and distributional notes are given. The correct spelling of Brachionus quadridentatus f. melhemi is discussed.
Article
Climate warming over the 20th century has increased the density stratification and stability of Lake Tanganyika, a deep rift valley lake. Here we examine the physical processes involved in and affected by the warming of the lake, and we discuss effects on lake productivity. The rate of net heat absorption by Lake Tanganyika has been 0.4 W m22 since 1913, twice the rate in the global ocean, indicating stronger climate forcing in the East African region. Lakes warm through increased incoming long-wave radiation. While lakes in general will increase heat outputs in a warming climate, heat outputs will increase more slowly in deeper lakes than in shallower lakes. Temperatures have increased by 0.2uC at 1000 m in depth, in part because of reduced cool marginal inflows, while water surface temperatures have increased by about 1.3uC. This differential heating over depth has increased the density gradient through the water column, reducing the potential for vertical mixing and thereby limiting nutrient fluxes to the phototrophic zone. An increase in transparency, indicating a reduction in productivity as a result of the reduced vertical mixing, occurred both in Lake Tanganyika and in Lake Malawi, a similar deep tropical lake in which warming has also been documented.
Article
Vertical distribution and seasonal abundance of zooplankters were studied in Lake Tanganyika. Faunal composition of zooplankton was simple. Limnocnida tanganicae, copepod nauplii, Diaptomus simplex, cyclopoids, and shrimp were collected by closing nets. Nauplii were dominant in number, but cyclopoid copepodites were dominant in biomass. The biomass calculated was in the range of 1.2-3.7 (average 2.3) g/m² excluding shrimp and medusa. For the vertical distribution of the copepods, the larger the size, the deeper the layers they stayed in the daytime, and the more remarkable diel vertical migration they showed. Chlorophyll a amount was high at the end of September and in October, which coincides with the bloom of Anabaena and Dictyosphaerium off Myako. The time of phytoplankton boom off Myako seemed to correspond with that of other parts of the lake as cited in the literature. The number of Diaptomus females with eggs increased in September and October, and the number of shrimp also increased in October. The increase of Diaptomus females with eggs corresponded with phytoplankton abundance. The seasonal abundance and high reproduction of zooplankters seemed to be a product of the abundance of phytoplankton in Lake Tanganyika.
Article
IN NATURE of August 1, 1907 (vol. lxxvi., p. 316), Messrs. Cunnington and C. L. Boulenger wrote a preliminary account of the fauna of Lake Birket el Qurun. I am indebted to these gentlemen for the opportunity of supplementing their account by a note upon the Oligochæta of that lake. They were so good as to send to me two tubes with a large number of specimens of a small oligochætous worm collected in the lake. These specimens were found to belong, without exception, to the species Paranais littoralis. The occurrence of this Naid in northern Africa is a new fact in its distribution. It has hitherto been met with in many parts of Europe, both in fresh water and in brackish, even salt, water. As to its marine habitat, it has been collected on the shores of Denmark and near Odessa.
Article
After alluding to certain observations of Cameron, Livingstone, and Stanley on the changes of level of Lake Tanganyika, the writer states that the most interesting point in connexion with the rise and fall of the lake is the question:—How is it possible for a great lake to rise 30 feet above its normal level by the blocking up of its outlet? This is to a large extent accounted for by Cameron. He says: “On going down the river [Lukuga] we found that it was blocked by vegetation similar to that on which we had crossed the Sindi, and also to that over which we had had to pass to reach the shore from our boats at the southern end of Lake Tanganyika, and which I afterwards found existed on Lakes Kassali and Mohrya. The presence of this mass of vegetation is easily accounted for. Every day that there is a gale of wind, and the consequent sea on the lake, blocks of this peculiar growth are detached, and such as survive the passage to the outlet getting jammed together commence to grow, and form a sort of porous stopper in the neck of the outlet.” He then quotes Sir Samuel Baker's experience on the Nile when the whole channel “was blocked up and the expedition to Gondokoro impeded for a year, the country above the stoppage having been converted into a series of swamps and shallow lakes, while Egypt was suffering from all the evils of a low Nile.” Only
Article
MR. S. P. AGHARKAR, lecturer on biology in the Elphinstone College, Bombay, who has been kind enough to undertake the collection of fresh-water invertebrates on behalf of the Indian Museum, has recently sent me several specimens of a medusa from small streams in the Western Ghats. Although they were taken at so great a distance from the west coast of India, it is important to note that these specimens were obtained from a river-system which flows across the Indian Peninsula and reaches the sea more than 500 miles away on the shores of the Bay of Bengal. Mr. Agharkar writes as follows:- ``The Medusae were collected in deep pools of the Koyna and Yenna rivers (tributaries of the Krishna). I was not able to get the hydroid form. I was told that the Medusæ (called flowers or wheels by people) occur regularly in these rivers every dry season. Probably they are present all the year round, only they are swept away by the current during the rainy season and a short time after that. During the dry season, when the stream becomes more or less a succession of deep pools, they become very marked.''
Article
Before 1896, when 1 had the opportunity of studying the fauna of Lake Tanganyika on the spot, it was known that there existed in the so-called Sea of Ujiji, one animal, the affinities of which are undoubtedly marine. This was the medusa Limnocnida , which Dr. Boehm saw as he crossed the lake in 1883. It was known further that the jelly-fish was associated in Tangan­yika with a number of strange molluscan forms, for the empty shells of what appeared to be some six entirely new genera of gasteropods, had been brought home by Captain Speke, Joseph Thomson, and Mr. Hore. As the animals contained in these shells have not hitherto been known, their classification by the conchologists with existing fresh-water types has always appeared extremely doubtful, and from the first Mr. Edgar Smith, who described the greater number of these forms, has held the opinion that they might eventu­ally turn out to have the same oceanic characters as the jelly-fish.
Article
UNDER the above heading a paragraph appeared in NATURE, vol. xxv. p. 101, in which Mr. C. A. White, of Washington, states that certain species described by me in the Proceedings of the Zoological Society, 1881, pp. 558-560, from the great African Lake Tanganyika, ``are without doubt, generically identical with the Pyrgulifera humerosa of Meek,'' a fossil form from the Bear River Tertiary of North America. Mr. W. H. Dall, of the Smithsonian Institution, had previously, in a letter to me, dated October 24, expressed a similar opinion. I have been unable to procure for examination and comparison a specimen of the North American shell, and am consequently compelled to arrive at a conclusion from a study of Mr. Meek's figure and description in the report npon the ``United States Geological Exploration of the Fortieth Parallel,'' vol. iv., pp. 176-178, woodcut 6, and plate 17, figs. 19-19a. As a result I find it decidedly unadvisable at present to locate the two forms in question in the same genus. I admit that in regard to general outline and character of ``sculpture'' there is no distinction of any importance. However, when the aperture (which in univalve shells most frequently exhibits the main generic characters) is closely scrutinised, features present themselves which incline me, until actual comparison is possible, to hold these two types generically distinct. The outer lip of Pyrgulifera is said to be ``subsinuous at the termination of the shoulder of the body volution above,'' and the basal margin of the aperture is described as ``faintly sinuous.'' On the contrary, in Paramelania no trace of the latter character is present, and the upper extremity of the labrum where it joins the volution, instead of being ``subsinuous,'' is actually prominent. But another equally important distinction is the prolongation of the body-whorl below the aperture, together forming a more or less basal effusion. Independent of these actual differences, we must take into consideration certain probabilities and improbabilities. In the first place the difference in geographical position militates to some extent against the identity of these two forms. Then the vast lapse of ages surely must have evolved some differences in the animals as indicated by the dissimilar apertures, and asfain the operculum of Paramelania is very peculiar, and who shall say that this appendage was of a like nature in the Bear River shell. In conclusion, I should observe that the African form was considered of sub-generic rank by me, and not as a distinct genus, as stated by Mr. White.