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How to Sex your Loricariid (Pleco/whiptail catfish).

This is a big question when it comes to keeping Loricariids in the aquarium as more then often people want to spawn the fishes but sometimes people just want to name them.

What is the sex determination methods in Loricariidae?

This is actually a more vast discussion then some other groups like mammals. In fact Loricariid’s use a range of karyotypes to determine sex from the more well known ZW and XY to multiple sex chromosomes. Ancistrus (Bristlenoses) is a large genus representing over 60 spp. (Eschmeyer, 2025), this genus does show multiple sex determination methods and some not as well known such as ZZ/ZW1W2 in Ancistrus clementinae (Nirchio et al., 2023) or ZZ/ZW in Ancistrus ranunculus (Oliveira et al., 2007). It seems many genera show a lot of diversity (Sassi et al., 2023) and this is possibly a large barrier to hybridization and maybe could lead to speciation.

What do you need to be able to identify the sex of your Loricariid?

  • A mature fish, unless the fish has reached sexual maturity it likely wont show many sexually dimorphic features although there are slight exceptions at the smaller level or during dissection. Largely this will mean close to fully grown and/or clearer odontode growth. Some species this might take a year such as some of the more common Ancistrus or 5+ years like the Hemiancistrus medians group (e.g. Panaque, Baryancistrus etc.)
  • A bowl, container or polybox can be useful to examine around the fish particularly below. Fill this with the tank water, do not do it during acclimation. It can be done in store.

Anatomy that allows you to sex Loricariids

Venting – Genital papilla and the urogenital pore

Figure 1: Baryancistrus chrysolomus, mango/magnum pleco juvenile.

The genital papilla and the urogenital pore are the same thing, this is a combined organ where the fish passes waste but also the gametes (eggs and sperm). This is not the same for all Loricariids where the genital pore is separate from the anus such as in Neoplecostomus. It is clearly on the abdomen, shape is normally ambiguous in juveniles.

The shape of the genital papilla is the most reliable method to sex Lorcariids, it’s most easily stated as V shaped in males and U in females. This can be tricky to see in some genera which have more elongate genital papilla such as the Pterygoplichthys in figure 2.

Figure 2: created by In the Bag Tropical Fish UK, Alice Cook. Depicting Pterygoplichthys pardalis and Pterygoplichthys gibbiceps.
Figure 4: Mature female Baryancistrus chrysolomus, not showing the clearest maturity.

Some other genera the females are much wider so it is much more square as above. The best method is to see multiple individuals and compare between them which can be done against the glass and taking photos or even within a container to take a more up close look.

Figure 5: The genital papilla of Chaetostoma as explained by Lujan et al. (2015) in Lujan, N. K., Meza-Vargas, V., Astudillo-Clavijo, V., Barriga-Salazar, R., & López-Fernández, H. (2015). A multilocus molecular phylogeny for Chaetostoma clade genera and species with a review of Chaetostoma (Siluriformes: Loricariidae) from the Central Andes. Copeia103(3), 664-701.

I find this method the most reliable particularly as there is less individual variation between individuals and also depends less on the age of the fish. The shape can be applied also to Loricariinae (whiptail catfishes) and Hypoptopominae (Otocinclus, Parotocinclus, Hypoptopoma etc.).

The final part of the genital papilla when it comes to sexing Loricariids is spotting around this region in females. These papilla/spots can be green or yellow in colour and can range from one to many in number, once visible to the eye it hints maturity in the females. While it is very obvious in Hypostominae (traditional pleco’s) it is unclear as to if these are present in the other subfamilies even the distantly related but similarly looking Pseudancistrus genisetiger (slate pleco’s) and Rhinelepinae. Although I have been told by Fauna Tropica (https://www.faunatropica.eu/) that these spots can be seen under a microscope and maybe a macrolens before maturity even as younger juveniles.

Figure 6: Genital papilla of a female Baryancistrus chrysolomus.

Body shape

I am not a massive fan of using body shape as it can depend on many factors. Using how plump the fish is does depend on how well the fish has been fed but also females once the female has released eggs can suddenly reduce weight.

Head shape does seem the most reliable method regarding the general anatomy but can be limited when it comes to stunted fish but there is also a lot of individual variation. In general it is assumed females display more elongate heads whereas males are shorter and wider, this is a trend we do see in other fishes.

Figure 7: Body shape in two different Scobinancistrus species but clearly shows the sexual dimorphism.

Personally when it comes to sexing individuals from photos I am less of a fan of this method as it does rely even more on angle of the photo but also maturity. You can see a larger difference in some genera then others and some species you might not see it at all.

Odontodes

Figure 8: Opercular odontodes on Ancistrus ranunculus.

Odontodes are the external teeth that cover Loricariids, this does include everything from Otocinclus to Farlowella to Hypancistrus. In some species they can be enlarged in certain areas and this is known as hypertrophied, further in some these odontodes can be sexually dimorphic. Odontodes as a secondary sexual characteristic though are not a rule and there are many exceptions, in addition they can be seasonal so males might have reduced ones seasonally and females can have larger ones, it depends on the genus.

Figure 9: Panaqolus albivermis (flash pleco), male showing clear hypertrophied odontodes.

Odontodes are most useful in the Peckoltia clade, this includes Hypancistrus, Peckoltia, Panaqolus, Pseudoqolus, Ancistomus and Scobinancistrus. Although Scobinancistrus and species such as Peckoltia sabaji do not have particularly sexually dimorphic odontodes and I recommend using the genital papilla. These odontodes are hypertrophied in all individuals at the gill opercular although can be larger in males. The most obvious method with this clade is hypertrophied odontodes on the caudal peduncle and pectoral fin of the males.

Figure 10: Baryancistrus demantoides (high finned green phantom), female.

When using this trait be careful with other clades, some such as the Hemiancistrus medians group which includes Hemiancistrus medians, some other Hemiancistrus (this genus requires revision), Panaque, Parancistrus, Baryancistrus and some Spectracanthicus (again another genus that requires revision). In these clades I find females can grow large odontodes seasonally and this was very evident to me in a clearly female Baryancistrus demantoides (Fig 10). The key thing to note about odontodes is they can be shed.

Figure 11: Farlowella vittata group pictured at Aqualife, Leyland.

Another clade that easily gets forgotten is Loricariinae, while genital papilla are a clear way to sex many genera within this subfamily. Odontodes can provide an additional quick way to sex many particularly Farlowellini (Farlowella, Sturisoma and Sturisomatichthys mostly; Fig 11). These are reliably hypertrophied around the head and/or rostrum in this clade.

Tentacles

This is an exclusive trait to the genus Ancistrus and the species Lasiancistrus tentaculatus. These are fleshy growths derived from the odontode sheaths (Sabaj et al., 1999), which might explain why sexually dimorphism is shown as related clades such as Lasiancistrus shows some clearer dimorphism in the odontodes. In Ancistrus while in the common bristlenose the males display larger tentacles whereas the females display little to none, there are Ancistrus where females have large tentacles, some which have none and some where the size is the same. Not to be confused with odontodes which is why it is best not to refer to them as spines or bristles.

Some factors that are often myths when it comes to sexing Loricariids

Behaviour

It is a common misconception that males are more aggressive then females and often this has no grounding in experience or science, it’s often an assumption. Males and females do have different territories as males are involved in the brood care whereas females roam but where species are territorial it is in both sexes. In territorial species aggression is shown between and within the sexes. Often this idea of males being more aggressive is based in the coy female myth (Milam, 2013; Rosvall, 2013), many scientists have disproved this but Lucy Cooke makes some good approachable books to the topic. Females in Loricariids have no reason to be less aggressive. Personal experience I’ve seen aggression from both and if anything where females tend to roam their aggression is wider spread then close to the caves where males dwell.

The other myth is that females will not use caves, particularly as juveniles they will definitely hide a lot but even as adults females use caves as refuges, they might even have a preferred cave. Males use the caves to spawn in Hypostominae and some Loricariinae but not all do and those that like crevices will use them.

Conclusion

It can be really tricky to identify whether your Loricariid is male or female. Hopefully this offers some ideas to help sex your fishes. I tend to recommend using the abdomen of the fish as I feel this is most reliable and doesn’t leave space for any amounts of individual variation.

For great comparative photos check out: https://www.suedamerikafans.de/en/zur-unterscheidung-der-geschlechter-klein-bleibender-hypostominaer-harnischwelse/

References:

Lujan, N. K., Meza-Vargas, V., Astudillo-Clavijo, V., Barriga-Salazar, R., & López-Fernández, H. (2015). A multilocus molecular phylogeny for Chaetostoma clade genera and species with a review of Chaetostoma (Siluriformes: Loricariidae) from the Central Andes. Copeia103(3), 664-701.

Milam, E. L. (2013). Making males aggressive and females coy: Gender across the animal-human boundary. In Women, Science, and Technology (pp. 206-222). Routledge.

Nirchio, M., Oliveira, C., de Bello Cioffi, M., de Menezes Cavalcante Sassi, F., Valdiviezo, J., Paim, F. G., … & Rossi, A. R. (2023). Occurrence of sex chromosomes in fish of the genus Ancistrus with a new description of multiple sex chromosomes in the Ecuadorian endemic Ancistrus clementinae (Loricariidae). Genes14(2), 306.

Oliveira, R. R. D., Feldberg, E., Anjos, M. B. D., & Zuanon, J. (2007). Karyotype characterization and ZZ/ZW sex chromosome heteromorphism in two species of the catfish genus Ancistrus Kner, 1854 (Siluriformes: Loricariidae) from the Amazon basin. Neotropical Ichthyology5, 301-306.

Rosvall, K. A. (2013). Proximate perspectives on the evolution of female aggression: good for the gander, good for the goose?. Philosophical Transactions of the Royal Society B: Biological Sciences368(1631), 20130083.

Sabaj, M. H., Armbruster, J. W., & Page, L. M. (1999). Spawning in Ancistrus (Siluriformes: Loricariidae) with comments on the evolution of snout tentacles as a novel reproductive strategy: larval mimicry. Ichthyological Exploration of Freshwaters10(3), 217-229.

Sassi, F. D. M. C., Deon, G. A., Sember, A., Liehr, T., Oyakawa, O. T., Moreira Filho, O., … & Cioffi, M. D. B. (2023). Turnover of multiple sex chromosomes in Harttia catfish (Siluriformes, Loricariidae): a glimpse from whole chromosome painting. Frontiers in Genetics14, 1226222.

Bee’s, a benefit to aquariums?

The use of various items produced by bees is popular within our daily lives, the most commonly used product being honey. The health benefit of products related to bees have been noticed for many hundreds maybe thousands of years from anti-microbial properties to general health. Honey maybe isn’t the most practical in the aquarium but two products you might find; bee pollen and propolis.

What is bee pollen?

Bee pollen is literally just the pollen collected by the bees. It is generally collected by forcing the bees to enter the hive through smaller then normal holes so the pollen drops below to be collected. This possibly puts a lot of pressure on the hive depending on how this is done.

What is the purpose of bee pollen in the aquarium?

Bee pollen is a dietary additive, there is a rising popularity in regards of this ingredient for people and perhaps this is the source of the idea. While it is an interesting ingredient and for those that might feed on fruit there could be a benefit. The actual benefits in general are debatable, with an omnivorous/carnivorous Clarias sp. catfish there were many physiological benefits shown up to 1% addition (Nowosad et al., 2022). When bee pollen was added to the diet of the insectivore zebrafish, Danio rerio there is no shown benefits to physiology but improve viral resistance (Di Chiacchio et al., 2021). In Nile tilapia, Oreochromis niloticus liver regeneration is shown to occur when fed bee pollen (Picoli et al., 2019).

What is propolis?

Propolis is the compounds and structures that seal the hive and the waxy structures that the hive is built on. It originates from the waxy areas of plants such as buds.

What is the purpose of propolis in the aquarium?

It’s not particularly common in aquariums but you might find the produce available more within the koi hobby. This product is used largely to seal wounds not just for protection against microbes entering them but also if you want to seal in a treatment. There does seem to be little research into the topic although some of the compounds do show promise when it comes to wound healing (Wibowo et al., 2021) and nutrition (Farag et al., 2021). More importantly there seems to be no papers onto any toxicity of propolis which is somewhat promising but could also be useful to cross out.

Conclusion

A very brief article I guess as to what could apply to the aquarist, it seems there needs a lot more research but I wouldn’t be afraid to use it. Personally I think bee pollen could be great for promoting feeding in fishes due to the sugars present. It’s something I think we could explore further.

References:

Di Chiacchio, I. M., Paiva, I. M., de Abreu, D. J., Carvalho, E. E., Martínez, P. J., Carvalho, S. M., … & Murgas, L. D. S. (2021). Bee pollen as a dietary supplement for fish: Effect on the reproductive performance of zebrafish and the immunological response of their offspring. Fish & Shellfish Immunology119, 300-307.

Farag, M. R., Abdelnour, S. A., Patra, A. K., Dhama, K., Dawood, M. A., Elnesr, S. S., & Alagawany, M. (2021). Propolis: Properties and composition, health benefits and applications in fish nutrition. Fish & Shellfish Immunology115, 179-188.

Nowosad, J., Jasiński, S., Arciuch-Rutkowska, M., Abdel-Latif, H. M., Wróbel, M., Mikiewicz, M., … & Kucharczyk, D. (2022). Effects of bee pollen on growth performance, intestinal microbiota and histomorphometry in African catfish. Animals13(1), 132.

Picoli, F., Lopes, D. L. D. A., Zampar, A., Serafini, S., Freccia, A., Veronezi, L. O., … & Emerenciano, M. G. C. (2019). Dietary bee pollen affects hepatic–intestinal histomorphometry of Nile tilapia fingerlings. Aquaculture Research50(11), 3295-3304.

Wibowo, I., Utami, N., Anggraeni, T., Barlian, A., Putra, R. E., Indriani, A. D., … & Ekawardhani, S. (2021). Propolis can improve caudal fin regeneration in zebrafish (Danio rerio) induced by the combined administration of Alloxan and glucose. Zebrafish18(4), 274-281.

Pangio (Kuhli loaches), the eel loach we overlook

Eels constantly cause fascination within aquarists but many true eels, Anguilliformes are simply too large for the majority of aquarists. A much smaller but fascinating alternative comes from Cypriniformes, a relatively medium sized genus known as Pangio. I’ve previously owned Pangio for many years and they are one fish I would definitely keep again.

Pangio myersi and Pangio semicincta/kuhlii

Pangio contains around 32 species (Bohlen et al., 2011), exclusive to South East Asia. They are clearly small anguilliform (the eel shape, not the taxa) but borderline very similar to the larger loach relative, Misgurnus anguillicaudatus (weather loach). For the aquarist the taxonomy can prove confusing with revisions that are not always well known such as the synonymy of Pangio semicincta and Pangio kuhlii (Kottelat, M & Lim, 1993) but is frequently debated seemingly with little explanation as to why (Eschmeyer, 2025). Molecular phylogenetics hasn’t seemed to have solved the confusion, or it’s suggested that the two species are the same (Bohlen et al., 2011). Another problem is Pangio myersi is nested within the two (Bohlen et al., 2011) although easily diagnosed for aquarists by thick barring from dorsal to abdomen (Kottelat, M & Lim, 1993).

There doesn’t seem to be immediately much morphological diversity in this genus, there is a diversity of patterning. While many will attempt diagnosing species by colouration, this has been called into question with solid marked individuals being identified as those with stripes (Bohlen et al., 2011). Like all loaches they contain small scales that to some can make them seem scaleless.

My interest is largely in morphology and like many there seems to be no anatomical studies. The majority focuses in the taxonomic records and this makes it really difficult to understand the morphology that might have ecological importance and also husbandry. We can clearly see a inferior (ventrally facing) mouth so they feed below and given the barbels it seems a common trait with those rooting in the substrate given they are not mobile.

Pangio cuneovergata

In the aquarium hobby we keep very few species but a diversity is starting to be imported and not just as bycatch. You can expect to find of the distinctively patterned species Pangio semicincta/kuhlii, P. myersi and P. shelfordii. The smallest species that is now being imported in reasonable numbers is Pangio cuneovergata. There are a few solid coloured species and these are likely Pangio oblonga and P. anguillaris, potentially also P. malayana who is shown to have solid individuals.

Pangio semincincta/kuhlii

How to Identify your Pangio?

This is a tricky topic but there are multiple sources that holds clues.

Figure 1: A Key to the Pangio of the Malay Penninsula as described in: Bohlen, J., Šlechtová, V., Tan, H. H., & Britz, R. (2011). Phylogeny of the southeast Asian freshwater fish genus Pangio (Cypriniformes; Cobitidae). Molecular Phylogenetics and Evolution61(3), 854-865.

As described previously there are some hints you can get from experiencing the species in captivity but there is a lot of cross referencing, where you can linking to a locality and exploration of images that could be of use. I find Bohlen et al. (2011; Fig 1) possibly the most useful of the papers for identification of species even if images are limited. One must also remember where you might have imported from one country it doesn’t mean that is where it is caught.

Habitat

There is little ecological details on these fishes. Habitat likely differs per species. Largely found in blackwater although potentially also highly turbid waters with variable or seasonal currents (Bohlen et al., 2011). Yet in the literature very little else is recorded.

Figure 2: Geographical distribution of Pangio according to INaturalist (2025)

Some assumptions can be made from the locality of these fishes (Fig 2), particularly in reference to temperature, although you will also need to check against elevation and other factors such as is the water body sheltered and therefore cooler. INaturalist (https://www.inaturalist.org/)and GBIF (https://www.gbif.org/) can be useful here although neither make any records of environmental factors. If someone is familiar with these websites then there is other extractions of data that can be done but I am not someone who works with species distributions. Other parameters can be tricky without knowing the geology of the region, some rocks dissolve more readily whereas others allow tannins or just rainwater to drain rapidly through without dissolving minerals.

We also know Pangio almost always seem to breed in tanks with gravel, there are probably exceptions so the substrates must have gravel where they are located with the exception of maybe more elongate species who similar to lamprey bury in silt and sands.

What setup would suit Pangio?

Generally I don’t think the current ideal setup for Pangio needs any adapting, sandy areas and gravel based areas, leaf litter providing many hiding places but also wood or rocks for more solid refuges.

One of my setups in 2017 for multiple Pangio spp., filtered by a Fluval 306 (I think).

A reasonable current but it wouldn’t have to be that strong so a sponge filter would suffice. I would consider with externals, internals or similar filters whether the fishes could get in, they are notorious for finding their ways into filters so either providing an inlet guard or changing filtration method particularly for those like Pangio cuneovergata. Undergravel filters sound great and somewhat are, the fishes will make their way into them and likely also live below the grids but many do report them spawning well there.

There is no doubt these fishes come from more soft acidic water based on locality and therefore I recommend a pH of around 6-7.5 for various reasons. There is flexibility and these fishes have proven themselves very hardy in captivity. Total Dissolved Solids (TDS) below 200ppm but ideally below that 100ppm range unless your water has potentially skewed values. Temperature is definitely the tricky one without knowing exactly the temperature of their caught locality, I would personally cross reference where they are found with water temperatures of the area and who knows other species in the area might have ecological data. Generally 24-28c seems the most ideal but you could be flexible particularly on that upper end to go higher.

They are often noted as being particularly shy although I’ve found with dimmer and dappled lighting but also frequent exposure they don’t seem to be that shy and show a lot of normal feeding and explorative behaviour. Plenty of cover gives them somewhere to retreat to.

References:

Bohlen, J., Šlechtová, V., Tan, H. H., & Britz, R. (2011). Phylogeny of the southeast Asian freshwater fish genus Pangio (Cypriniformes; Cobitidae). Molecular Phylogenetics and Evolution61(3), 854-865.

Kottelat, M & Lim, K. K. P. (1993) A review of the eel-loaches of the genus Pangio (Teleostei:Coditidae) from the Malay Peninsula, with descriptions of six new species. Raffles of Zoology, 41(2): 203-249.

Why ornamental fish nutrition needs change.

It is frequently understood that ornamental fish nutrition differs from food fish nutrition due to differing aims, yet many fish feeds use the same ingredients (Yanong, 1999; Vucko et al., 2017). Much of the research into fish nutrition no doubt due to funding focuses on aquaculture (farming fishes) the concept of efficiency, a fish farmer wants a fish to grow large in as minimal time (usually months) as possible for as little cost as possible. This opposes the fishkeepers who want a diet to give the fish longevity, colour and long term reproductive success, there is also a higher focus on the welfare element as fishes are our pets.

A large factor is there are many species of ornamental fishes across many different fish groupings, this proposes a challenge as reflected in this is the wide range of dietary niches that fishes can exhibit. There are carnivores which can be split into different invertebrate specialist, generalists and also piscivores. Herbivory which can be split into frugivores, algivores, plant eaters and many different specialist and generalist niches. Detritivory also exists and while often classified as feeding on decaying matter in the aquatic sense this could be many things from microbial matrices crossing over a lot with algivory to a mixture of unidentified matter. Omnivory does exist but it is often vague to clearly state a fish is an omnivore as there are few which broadly generalize. And while clades can be generalized such as Loricariids being largely algivores and detritivores, there are carnivores; similarly for Cichlidae the majority are carnivores but there are many exceptions verging into algivory. An important concept as above is generalism vs specialism, the degree of specialism varies between clades and this differs largely between captivity and the wild (Golcher-Benavides and Wagner, 2019). This poses a particular issue for the ornamental aquarist as many aquarium diets fall along the lines of generalism, the ingredients do not largely differ between many products and even brands. This means that even offering a range of different products doesn’t always cater for diversity or all the dietary niches of the fishes you have in the aquarium.

It is always advisable to research the wild diet of the fishes as this will give a good idea of the dietary niche a fish has evolved for over hundreds or thousands of years. Often there are clues in the morphology of the fish, such as head shape, pharyngeal jaw shape and dentition (Burress, 2016). Well known hobby ideas of fish diets can lack fact checking such as the common misconception of Symphysodon (discus fishes) being carnivores yet their wild diet follows more algivory/detritivory (Crampton, 2008) and their morphology is most similar to Tropheus (Fraser et al., 2009), a known algivore. There does remain issues with understanding of wild fish diets, there can be frequent gaps or sampling errors. Such as the original understanding behind the diets of Corydoradinae was based on aquarium fishes, not the wild fishes so it would be better to identify gut analysis and isotope studies of the wild fishes (Alexandrou et al., 2011).

What are the basic nutritional requirements of ornamental fishes?

Like any animal there are broadly the same categories here; carbohydrates, lipids, proteins, vitamins and minerals.

Proteins These are the nutritional requirements many will state of importance with fishes being high and low protein dependent. Although the idea of herbivores having a lower protein requirement then carnivores in the aquatic world fails to understand the high protein levels of algae’s opposed to the terrestrial vascular plants. Different sources of protein do have different volumes of different amino acid and this is important to recognize. This is arguably more important then the actual volume of protein along with accessibility of the protein source. Algivorous fishes might have a lower requirement for protein (Vucko et al., 2017; Yanong, 1999). A large factor of protein requirements is the fishes age, temperature and genetics, as with any nutrient all juvenile fishes will require higher nutrition then those whose growth rate has plateaued more. Excessive protein also increases ammonia production.

Carbohydrates are used as an energy source for many fishes. It is understood that starch unlike cellulose is the utilized form for many ornamental fish feeds, many herbivores and omnivores do not require carbohydrates. Excessive carbohydrates can prevent protein and sugar uptake (Yanong, 1999).

Lipids are another energy source and important for ornamental fishes (Vucko et al., 2017; Yanong, 1999) particularly for spawning fishes who will require them for egg development.

Vitamins and minerals are a complex and diverse topic given how many are vital for life within fishes, without them it can lead to many health issues. I would encourage the reader to read Yanong (1999; https://www.researchgate.net/publication/12102293_Nutrition_of_Ornamental_Fish) for details into this. Some of these vitamins and minerals are taken through diet and others through water, when it comes to water uptake this must be considered with the wild water parameters of the fishes as where calcium is low in the water uptake must be largely from diet. The mineral content of diets can be vague although the total volume is reflected in what is called ash. No, ash isn’t literal ash it means mineral content as when you burn down a diet all that is left is the minerals.

Colour enhancers, this is a concept that is frequently mentioned in food reviewed largely in reference to a diversity of carotenes. While it will always be stated in marketing and social media as a benefit to a fish feed, most fish feeds contain red enhancers of some kind, this is largely a benefit to most fishkeepers excluding those with yellow discus who will change their colour when feeding on it.

Largely these requirements are so complex it’s tricky to address them with one diet when we keep so many species.

Why might change be needed in what we feed our fishes?

Seeing as many farmed fishes diets do not replicate their wild diets, many do not replicate a diversity in fish diets that is the start. Maybe sometimes they do in the labels but the ingredients do, when a diet aimed at algivores has the same ingredients as one aimed at carnivores. For algivores we already know just one algae can compete with a commercial mix of many ingredients which says a lot (Vucko et al., 2017).

It has become clear that diet is key in the health of a fish with diet influencing the development of tumours (cancer; Spitsbergen et al., 2012), liver damage (Rašković et al., 2011) and other health conditions (Žák et al., 2022). There is the potential of poor fecundity and reproductive lifespans on certain diets although could require further exploration. Many fishes we just don’t see them grow to their adult sizes let alone spawn and mortality might be high where they can refuse to feed on traditional captive diets.

References:

Alexandrou, M. A., Oliveira, C., Maillard, M., McGill, R. A., Newton, J., Creer, S., & Taylor, M. I. (2011). Competition and phylogeny determine community structure in Müllerian co-mimics. Nature469(7328), 84-88.

Burress, E. D. (2016). Ecological diversification associated with the pharyngeal jaw diversity of Neotropical cichlid fishes. Journal of Animal Ecology85(1), 302-313.

Crampton, W. G. (2008). Ecology and life history of an Amazon floodplain cichlid: the discus fish Symphysodon (Perciformes: Cichlidae). Neotropical Ichthyology6, 599-612.

Fraser, G. J., Hulsey, C. D., Bloomquist, R. F., Uyesugi, K., Manley, N. R., & Streelman, J. T. (2009). An ancient gene network is co-opted for teeth on old and new jaws. PLoS biology7(2), e1000031.

Golcher-Benavides, J., & Wagner, C. E. (2019). Playing out Liem’s paradox: opportunistic piscivory across Lake Tanganyikan cichlids. The American Naturalist194(2), 260-267.

Vucko, M. J., Cole, A. J., Moorhead, J. A., Pit, J., & de Nys, R. (2017). The freshwater macroalga Oedogonium intermedium can meet the nutritional requirements of the herbivorous fish Ancistrus cirrhosus. Algal research27, 21-31.

Rašković, B., Stanković, M., Marković, Z., & Poleksić, V. (2011). Histological methods in the assessment of different feed effects on liver and intestine of fish. Journal of Agricultural Sciences (Belgrade)56(1), 87-100.

Spitsbergen, J. M., Buhler, D. R., & Peterson, T. S. (2012). Neoplasia and Neoplasm-Associated Lesions in Laboratory Colonies of Zebrafish Emphasizing Key Infl uences of Diet and Aquaculture System Design. Ilar Journal53(2), 114-125.

Yanong, R. P. (1999). Nutrition of ornamental fish. Veterinary Clinics of North America: Exotic Animal Practice2(1), 19-42.

Žák, J., Roy, K., Dyková, I., Mráz, J., & Reichard, M. (2022). Starter feed for carnivorous species as a practical replacement of bloodworms for a vertebrate model organism in ageing, the turquoise killifish Nothobranchius furzeri. Journal of Fish Biology100(4), 894-908.

Rebecca’s Menu for Pleco’s 2025

I commonly get asked what I’d feed different groups of pleco’s and it does vary by the pleco, Loricariid but also by what is available in your country. Some genera are more generalist and forgiving then others, some will withstand a less then ideal diet for maybe a few decades and others a few months/days.

While I would love to provide more details some I cannot list yet or am not entirely clear on some aspects of a species dietary ecology. So this should hopefully help for now.

I shall split it up by diet, some species might feed on a different diet to what you expect so please search for the genus/species.

The majority of Loricariids are algivores and detritivores so this contains the larger amount of categories.

Algivores

This is one of the largest categories as many Loricariids specialize in different algae’s, biofilms etc. But due to mode of feeding and availability of ingredients I will kind of have to generalize. Due to this the algae growing in the aquarium might be the wrong species so the fish might not feed on it, regardless any algae in the aquarium will not sustain most species long term.

Prepared diets:

  • Repashy Super Green
  • Repashy Soilent Green (you can add in extra algae powders to bulk it out, fishes seem to prefer this diet).

Making your own Algivore Diet

This is a trial as it seems Repashy is becoming unavailable in many countries. I have done many different trials and tests but am still developing something.

Nutritional ingredients:

These are the main ingredients and should make up at least 80% of the nutritional ingredients used but can makeup the whole diet minus gelling agents (Vucko et al., 2017). Percentages might vary, ideally try to include higher volumes of those highlighted in bold, not all will be available so try to include as wide of a diversity of possible. High spirulina content might take a while for the fishes to get used to. Seaweeds will need to be blended or might not be eaten.

  • Chlorella algae (Vital)
  • Spirulina algae (Vital)
  • Seaweed meal (Vital)
  • Kelp meal (vital)
  • Wakame algae (vital)
  • Nori (Vital)
  • Bladderwrack
  • Other human consumption seaweeds and algaes.
  • Potentially mosses, never tried but are recorded in Loricariid diets.

Herbal ingredients:

These should be very limited excluding the mushrooms I wouldn’t go above around 1-2% per ingredient.

  • Paprika, associated with red enhancing.
  • Mushrooms, dried or powdered while not entirely known it is potential they feed on fungi in the wild. While edible mushrooms might not be the same taxa it does seem to be a taste enhancer for fishes at least.
  • Basil, associated with improved physiological and immunological health while being an attractant (Mansour et al., 2023).
  • Ginger, feed attractant and immunological support (Ahmad et al., 2024).
  • Garlic, I don’t always use it but feed attractant with potential immunological support but can cause liver damage.
  • Seeds, particularly found in the guts of Hypancistrus and potentially Peckoltia. Higher in fats and proteins.

Gelling agents:

I would recommend using carrageenan powder due to it lasting longer then the alternatives. I would use this regardless as to whether it is a carnivorous or herbivorous diet.

Who are the algivores that we keep?

  • Ancistrus
  • Baryancistrus
  • Dekeyseria
  • Farlowella
  • Hemiancistrus
  • Hypostomus
  • Isorineloricaria
  • Lamontichthys
  • Lasiancistrus
  • Nannoptopoma
  • Otocinclus
  • Panaque
  • Panaqolus
  • Parancistrus
  • Parotocinclus
  • Pseudancistrus
  • Pseudorinelepis
  • Pterygoplichthys
  • Rhinotocinclus
  • Spectracanthicus zuanoni/punctasissimus
  • Sturisoma/Sturisomatichthys

This diet will cover most of Loricariidae but particularly these genera, while they might be also more detritivorous in the wild this is the closest we can get to their natural diet.

Regarding Hypancistrus, Peckoltia and potentially Panaqolus I would add seeds to their diet and maybe look at the addition of infrequent invertebrates.

A little more carnivorous

If you want to increase the volume of carnivorous ingredients, Loricariids don’t consume fishes in the wild so we will be looking at invertebrates. Due to the presence of thiaminase in some ingredients I do not recommend the frequent use of mussels or prawns.

So as you’re looking more into carnivory I would increase the volume of these ingredients, luckily for carnivorous ingredients you could feed as a frozen or live food they have to forage.

Ingredients:

  • Daphina
  • Brine shrimp
  • Tubifex
  • Bloodworm (Chironomatid larvae).
  • Cockels
  • Mysis
  • Red plankton
  • Ant eggs
  • Earthworms
  • Cyclops
  • Whiteworms
  • Blackworms
  • Vinegar worms

What about molluscivores?

Scobiancistrus, Leporacanthicus, Pseudohemiodon, Loricaria and Planiloricaria are likely capable on feeding on mussels and occasionally this is proven. A diversity of snails can be trialed for the Scobinancistrus and Leporacanthicus larger species such as Ampulluridae would be ideal as these are evolved to extract snails from their shells, escargot snails that are not treated with garlic would be interesting to explore. For others then smaller snails whether it be juveniles of harder species of pest snails.

Plant eaters

Realistically many Loricariids do not consume traditional plants so often these are best to identify if a fish is feeding or not. Some very broad generalist taxa might consume more like Pterygoplichthys and Hypostomus.

Using other premade foods as a base.

This is largely only possible with gel diets but possibly some pastes. The main rule is not to add so many that the gelling agent doesn’t hold as well as it used to but also this will depend on how fast your fishes feed.

What base diets can you use?

  • Repashy. It does have a wide range of other ingredients.
  • In the Bag Tropical Fish UK’s pleco pops. Very strong gelling agents and true carnivorous and herbivorous diets.
  • EBO pastes
  • Tropical’s gels/pastes

Testing diets to identify if they are being used.

Glass petri dishes can be ideal here as they sink and are inert, you can pipette or place food on and ideally it will not be disturbed over the time you are not observing the food being eaten. Therefore it can be a reliable method of identifying what is taken and what is not.

References:

Ahmad, I., Irm, M., Ahmed, I., Haoran, Y., Taj, S., Bhat, T. A., … & Amin, A. (2024). Role of ginger in fish nutrition with special emphasis on growth, health, gut and liver morphology. Journal of the World Aquaculture Society55(6), e13101.

Mansour, A. T., Diab, A. M., Khalil, R. H., Eldessouki, E. A., El-Sabbagh, N., Elsamannoudy, S. I., & Younis, N. A. (2023). Physiological and immunological responses of Nile tilapia fed dietary supplementation of sweet basil ethanolic and aqueous extracts. Frontiers in Marine Science9, 1064455.

Vucko, M. J., Cole, A. J., Moorhead, J. A., Pit, J., & de Nys, R. (2017). The freshwater macroalga Oedogonium intermedium can meet the nutritional requirements of the herbivorous fish Ancistrus cirrhosus. Algal research27, 21-31.

Two New Loricariids Described: Hypancistrus seideli and H. yudja

Hypancistrus have long been an issue for hobbyists and taxonomists providing challenges to identify and define what is a species, over time a few have been described but leaving one of the most common species.

Hypancistrus seideli ‘L333 King tiger’ Image originated from: Olivia and Dad’s Fish Room https://www.facebook.com/profile.php?id=100063396450007

This topic is tricky for scientists regarding how a species is defined and where do you draw a line, even trickier for hobbyists. The Rio Xingu species have been particularly tricky as there are many striped species with only Hypancistrus zebra being particularly distinctive. For the hobbyist the L number system can add to the confusion as while different individuals can be given different L number it doesn’t infer they are different species. Morphology can be tricky to navigate as there are many very diverse species both morphologically and genetically for example Baryancistrus xanthellus (of which does include a green variant, verde that is not B. chrysolomus) or Peckoltia sabaji (Fig 1; Magalhães et al., 2021; Armbruster 2003).

Figure 1: The morphological diversity of Baryancistrus xanthellus, the gold nugget pleco (L177, L018, L081, L085, verde) as featured in Magalhães, K. X., da Silva, R. D. F., Sawakuchi, A. O., Gonçalves, A. P., Gomes, G. F. E., Muriel-Cunha, J., … & de Sousa, L. M. (2021). Phylogeography of Baryancistrus xanthellus (Siluriformes: Loricariidae), a rheophilic catfish endemic to the Xingu River basin in eastern Amazonia. Plos one16(8), e0256677.

Some of this morphological and genetic diversity can be based on different populations and localities, it is tricky to infer whether there is interbreeding as to when and extent this occurs without detailed analysis for both morphologically and genetically. We also risk drawing lines between populations or individuals of the same species that don’t exist in nature.

Commonly understood is the importance of species as a biological unit and in some manner it is, but this is no one overarching definition for a species, it’s much more complex then that. As said earlier species can be both morphologically and genetically diverse or not at all, it varies so much and on where the line is drawn. The common misconception is that genetics solves any issues with defining a species but when you create these trees to plot species different genes, regions or even whether you use mitochondrial or nuclear DNA can infer different groupings. But this reliance on species being the important factor that matters for many aquarists ignores much of this and can lead to splitting species into unrealistic groupings. Realistically like the killifish and Poecilidae sides of the hobby, we need to recognize populations are as valuable as species, even if they cross or not. Populations might have unique genetics or morphology, doesn’t make them different species but we should really think through how we breed our fishes and what individuals we choose. If fishes come from different suppliers maybe double checking locality, maybe considering if certain captive bred fishes are useful for maintaining a population.

So in summary just because some species might look different it doesn’t mean they are but doesn’t mean they aren’t distinct populations that shouldn’t be valued.

Hypancistrus seideli ‘L236 basic’ Image originated from: Olivia and Dad’s Fish Room https://www.facebook.com/profile.php?id=100063396450007

The Two New Species of Hypancistrus

Description for Hypancistrus seideli and H. yudja:

Sousa LM, Sousa EB, Oliveira RR, Sabaj MH, Zuanon J, Rapp Py-Daniel L. (2025). Two new species of Hypancistrus (Siluriformes: Loricariidae) from the rio Xingu, Amazon, Brazil. Neotropical Ichthyology. 23(1). https://doi.org/10.1590/1982-0224-2024-0080

These exciting descriptions help us understand the Loricariids we keep in the aquariums better and more accurately describe them. Hopefully it leads to further studies of Hypancistrus.

Hypancistrus seideli Sousa, Sousa, Oliveira, Sabaji, Zuanon & Rapp Py-Daniel 2025.

Figure 2: Hypancistrus seideli as featured in: Sousa LM, Sousa EB, Oliveira RR, Sabaj MH, Zuanon J, Rapp Py-Daniel L. (2025). Two new species of Hypancistrus (Siluriformes: Loricariidae) from the rio Xingu, Amazon, Brazil. Neotropical Ichthyology. 23(1). https://doi.org/10.1590/1982-0224-2024-0080

This species includes the L numbers: L333, L066, L236, L287, L399, L400.

This species includes the common names: King tiger pleco, maze zebra pleco.

Diagnosed by alternating dark and pale vermiculation’s from currently described species although recognised as extremely varied (Sousa et al., 2025). Hypancistrus seideli covers a wide range of the Hypancistrus diversity in the Rio Xingu and some of the most popular species in the aquarium trade. Although morphologically diverse (Fig 2) there it seems to not have the same amount of molecular diversity so further inferring at least L066 and L333 regardless are the same species. Phylogenetically there also seems to be an issue to designate them as different species given L066 and Belo Monte seem to be paraphyletic (Cardoso et al., 2016). Although using sequences from a public database does rely on correct identification of those sequencing the samples (Fig 3).

Figure 3: Molecular phylogeny using the COI barcode sequences located from a public database as featured in: Cardoso, A. L., Carvalho, H. L. S., Benathar, T. C. M., Serrao, S. M. G., Nagamachi, C. Y., Pieczarka, J. C., … & Noronha, R. C. R. (2016). Integrated cytogenetic and mitochondrial DNA analyses indicate that two different phenotypes of Hypancistrus (L066 and L333) belong to the same species. Zebrafish13(3), 209-216.

Etymology: Hypancistrus seideli is named after the well known and respected aquarist Ingo Seidel who has contributed a lot to the knowledge of Hypancistrus (Sousa et al., 2025).

Habitat: While the paper doesn’t go into detail that isn’t well known it describes their environment as rocky with strong currents (Sousa et al., 2025).


Hypancistrus seideli ‘L066 King Tiger’ Image originated from: Olivia and Dad’s Fish Room https://www.facebook.com/profile.php?id=100063396450007

Hypancistrus yudja Sousa, Sousa, Oliveira, Sabaji, Zuanon & Rapp Py-Daniel 2025.

Figure 4: Hypancistrus yudja as described in: Sousa LM, Sousa EB, Oliveira RR, Sabaj MH, Zuanon J, Rapp Py-Daniel L. (2025). Two new species of Hypancistrus (Siluriformes: Loricariidae) from the rio Xingu, Amazon, Brazil. Neotropical Ichthyology. 23(1). https://doi.org/10.1590/1982-0224-2024-0080

This species includes the L numbers: L174.

This species includes the common names: Ozelot pleco.

Diagnosed by large brown splotches and saddles on a tanned background (Sousa et al., 2025).

Etymology: Named after the Yudjá people of the Volta Grande, Rio Xingu, Brazil who are located in the same area as these fishes and described as equally threatened by the Belo Monte dam (Sousa et al., 2025).

Habitat: Located specifically from deep but rocky waters but remains hidden in crevices for large amounts of time (Sousa et al., 2025).

Hypancistrus yudja ‘L174 Ozelot pleco’ Image originated from: Olivia and Dad’s Fish Room https://www.facebook.com/profile.php?id=100063396450007

References:

Armbruster, J. W. (2003). Peckoltia sabaji, a new species from the Guyana Shield (Siluriformes: Loricariidae). Zootaxa344(1), 1-12.

Cardoso, A. L., Carvalho, H. L. S., Benathar, T. C. M., Serrao, S. M. G., Nagamachi, C. Y., Pieczarka, J. C., … & Noronha, R. C. R. (2016). Integrated cytogenetic and mitochondrial DNA analyses indicate that two different phenotypes of Hypancistrus (L066 and L333) belong to the same species. Zebrafish13(3), 209-216.

Magalhães, K. X., da Silva, R. D. F., Sawakuchi, A. O., Gonçalves, A. P., Gomes, G. F. E., Muriel-Cunha, J., … & de Sousa, L. M. (2021). Phylogeography of Baryancistrus xanthellus (Siluriformes: Loricariidae), a rheophilic catfish endemic to the Xingu River basin in eastern Amazonia. Plos one16(8), e0256677.

A Review: Identifying Corydoradinae Catfish by Ian Fuller and Hans-Georg Evers

Identifying Corydoradinae Catfish by Ian Fuller and Hans Evers has been long awaited by many catfish enthusiasts whether Corydoradinae is their interest or other Siluriformes. Using the vital recent revision of the genus (Dias et al., 2024) we now have an accompanying book accessible to hobbyists but also enthusiasts.

The revision of Corydoradinae was long needed as in some way resurrecting previous genera and reflecting the previous lineage system hobbyists used, this lineage system was also reflected in the fishes phylogeny/evolution (Dias et al., 2024). Revising the genus Corydoras and subfamily Corydoradinae reflects the morphology/anatomy and ecology better and helps us understand how to keep our Corydoradinae better.

This book offers a modern view at the group brimming with lifetimes of experience and knowledge. I need not introduce the authors as both are extremely well respected not just within Corydoradinae, catfishes but the hobby in general. This collaboration creates the perfect all round collaboration.

The science is always useful to really understand aquariums and how we keep our fishes of which some sources very much lack. Identifying Corydoradinae includes some fascinating science you wont see included elsewhere that is described in an easily understood manner to someone who might not be trained in the sciences. One of the most interesting topics was genome expansion written by Professor Martin Taylor, a scientist who studies the genetic aspects of Corydoradinae. I also very much enjoyed the section on toxins or poisons within Corydoradinae from Professor Eric Thomas as this is at the cutting edge of science, it’s a topic that is not well understood yet this book offers the latest knowledge as to the topic.
For me as having an interest in ecology I was really keen to see mentions as to the fishes ecology and habitats. The ecology section was very useful for hobbyists in describing actually where these fishes are found from experience and knowledge, giving the hobbyist an idea of how to keep the fishes and breed them. Diet has sometimes been misunderstood in the hobby and the inclusion of what we know these fishes feed on is no doubt a benefit. Dr. Luiz Tencatt goes into detail on these fishes diets and hopefully this helps hobbyists know what to feed their fishes.

The layout of the book is useful for the hobbyist as logically passes through the genera before the described species and then the undescribed. This means the hobbyist can quickly identify the species they are most interested in at the time. Brochis is additionally split up which helps identify the various lineages, not completely removing the lineage system therefore the usefulness of it but that would require another scientific revision.

All the species are clearly explained with distributions, size and also detail as to their identification and ecology. To help the enthusiast who might not be too clear on the various genera there is a guide to the various genera and the key features a hobbyist can use to identify them. Plenty of clear images are provided of not just the adults but variants and as the fish ages.

In conclusion, this is a great book with so much detail for any catfish enthusiast. It provides information to help the hobbyists understand a large group of catfishes that can be tricky to identify. Certainly a book you can read in one session but for many years will be of great use.

References:

Dias, A.C., Tencatt, L.F., Roxo, F.F., Silva, G.D.S.D.C., Santos, S.A., Britto, M.R., Taylor, M.I. and Oliveira, C., 2024. Phylogenomic analyses in the complex Neotropical subfamily Corydoradinae (Siluriformes: Callichthyidae) with a new classification based on morphological and molecular data. Zoological Journal of the Linnean Society, p.zlae053.

Pleco Teeth, what snails can teach us about Loricariids.

While it is not always obvious Loricariids all have teeth and they show a wide range of morphological disparity (Lujan & Armbruster, 2012). Morphological disparity refers to that range of different anatomy within a group. Unlike many fishes Loricariids are rarely gape limited, their prey (that includes algae) is not limited by the size of their mouth and this makes comparison with traditional fishes like carp or cichlids limited.

Figure 1: Pterygoplichthys joselimaianus jaw, a typical jaw for Loricariidae.

Loricariids feed largely by a rasping motion, this is extremely similar to how snails feed. Snails also have teeth on a ribbon like organ known as a radula (Fig 2).

Figure 2: Snail body plan including the mouth anatomy. Unknown source.

Both snails and Loricariids use their jaws, containing the teeth to basically scrape at a surface (rasp), it can be the food item itself but it could be rocks or wood to extract food.

Figure 3: Leporacanthicus joselimai

While I say the majority of Loricariid jaws are similar to snails not all are, there are carnivorous genera such as Pseudohemiodon or Scobinancistrus who differ in how they move and function. Carnivorous genera have elongate fewer teeth with often narrower oral jaws but can be much more robust (Fig 3), or in some those oral jaws are almost entirely just the jaws, reduced tooth cups. It’s easy to say these carnivores are using different morphology for the same solution to carnivory but maybe in a different place, one feeds amongst crevices (those with the elongate teeth and jaws) and others amongst the substrate (those with reduced jaws). We do have a slight exception with Spatuloricaria, an obvious substrate feeder but it seems to use the substrate a little differently and feed on different invertebrates.

Figure 4: Gastropod radula diversity. Krings, W., Kovalev, A., & Gorb, S. N. (2021). Collective effect of damage prevention in taenioglossan radular teeth is related to the ecological niche in Paludomidae (Gastropoda: Cerithioidea). Acta Biomaterialia135, 458-472.

Snails, Gastropods have long been studied in terms of their radula diversity (Fig 4), I assume this is due to the fact when you’re dealing with preserved snails there are fewer tissues to identify the species. Additionally they make great models for understanding how anatomy relates to morphology, ecomorphology. Gastropods are everywhere and it’s easy to find those that scrape algae’s off rocks vs more carnivorous gastropods. To put it simply though, Gastropods feed by rasping and their teeth are uniquely shaped to what they are feeding on.

I think even just ignoring carnivory Loricariidae shows a wide diversity of tooth morphological disparity but there is little studies regarding that in relation to their ecology. Plenty of these studies focus on the development and morphology (Geerinckx et al., 2007). What there is is a fascinating study looking at another part of the fishes anatomy that could be similar, the unculi, small protrusions on the oral disc’s of the fishes. While the study focuses on how these structures allow for the fishes to inhabit certain habitats, could these also function in a similar fashion to radula?

Figure 5: The diversity of Loricariid teeth, Geerinckx, T., De Poorter, J., & Adriaens, D. (2007). Morphology and development of teeth and epidermal brushes in loricariid catfishes. Journal of morphology268(9), 805-814.

The diversity of Loricariid tooth morphological diversity is clear (Geerinckx et al., 2007) and we clearly see that Loricariids have a diversity of diets beyond herbivory and carnivory (Lujan et al., 2012), whatever they really mean to aquatic animals.

When looking outside of carnivory there is clear differences in morphology, none are so much clearer then those Loricariids that utilize wood. These genera display clearly spoon shaped teeth even if these genera (Panaqolus, Panaque, Hypostomus cochliodon group etc.) do not digest the wood and it is simply where they might find food. Compared with carnivores such as Leporacanthicus, these have more elongate teeth but it depends on where they are accessing their food. This difference is also reflected in gastropods whether they be snails or slugs have evolved teeth on their radula that reflect not just their diet but the methods they use to extract it. Elongate pointed teeth infers carnivory whereas further cusps leans towards herbivory. Perhaps carnivory requires less complexity to herbivory and I assume largely as carnivory relies on more then the teeth to extract food.

References:

Geerinckx, T., De Poorter, J., & Adriaens, D. (2007). Morphology and development of teeth and epidermal brushes in loricariid catfishes. Journal of morphology268(9), 805-814.

Krings, W., Konn-Vetterlein, D., Hausdorf, B., & Gorb, S. N. (2023). Holding in the stream: convergent evolution of suckermouth structures in Loricariidae (Siluriformes). Frontiers in Zoology20(1), 37.

Krings, W., Kovalev, A., & Gorb, S. N. (2021). Collective effect of damage prevention in taenioglossan radular teeth is related to the ecological niche in Paludomidae (Gastropoda: Cerithioidea). Acta Biomaterialia135, 458-472.

Lujan, N. K., & Armbruster, J. W. (2012). Morphological and functional diversity of the mandible in suckermouth armored catfishes (Siluriformes: Loricariidae). Journal of Morphology273(1), 24-39.

Leaf Litter is Overrated, A love Letter to Algae

When you picture a freshwater ecosystem it really goes one of two ways, largely there is the group that look for a heavily planted water body with a diverse number of species or something that has a lot of leaf litter almost entirely complete for several layers.

Oase highline at Maidenhead Aquatics Ascot for Pseudancistrus asurini (Gold seam pleco), Baryancistrus xanthellus (Gold nugget pleco), Baryancistrus chrysolomus (Mango/magnum pleco) and rummynose tetra, Hemigrammus.

What if I told you this isn’t entirely true, a half truth or some what out of date?

There is a lot to unpack here.

  1. The reality of freshwater function
  2. The reality of freshwater habitat diversity
  3. The deception of anthropomorphic effects
  4. Source of nutrients
  5. Why does algae do so well but plants don’t?
  6. What is algae?
  7. Long live algae! Leaf litter is overrated.
  8. Leaf litter is not all bad
  9. Is there hope for algal growth?
  10. Aquariums are anthropogenic

The reality of freshwater function

Freshwater habitats are very diverse, this is largely based on the locality of the habitat within the river.

Figure 1: Bradshaw model of river characteristics. Source: https://www.jkgeography.com/how-rivers-change-from-source-to-mouth1.html

The Bradshaw model (Fig 1) explains this well but being largely based on temperate, North American and European ecosystems it doesn’t reflect tropical systems particularly as well.

The struggle for plant life.

When thinking about plants load particle size is important, plants in freshwater ecosystems largely need something to root onto and this isn’t found upstream where sediment is quickly pushed downstream. Downstream though this sediment load, load particle size is the opposite but because it’s remaining in the water column it becomes what is known as having a high turbidity (low visibility), this means less light can pass through the water and reduces photosynthesis. This is why so many aquarium plants are grown ‘terrestrially’ or aquaponically because they aren’t naturally aquatic. Aquatic plants have a struggle and there are solutions such as developing very strong roots and a reduced amount of structural support as if there is less sediment and a higher flow those stems are highly likely to break. In high turbidity waters that’s where we see the water lilies, Nymphaea spp., Nymphoides but also more floating plants who reach for the surface where they can receive light.

Figure 2: Podostemaneae in the Rio Xingu as reported by Peter Peterson in: https://amazonas.dk/index.php/articles/brasilien-rio-xingu

Some plants might have to deal with extreme drought in a dry season and then being drowned in the wet season. This is where we seem to see some really extremophile plants such as some Podostemaceae in the Rio Xingu likely of the genus Morera as reported by Peter Peterson in Amazonas (Fig 2).

Where is the leaf litter?

This is such a similar story for leaf litter as deposition, and particle size largely depends on flow rate but position in the river. Firstly you require that river to be surrounded by trees but also that the current is weak enough that the leaves can just fall to the bottom. When you look at rivers like the Rio Xingu, Rio Orinoco or towards the Rift Valley this is not shown in the major areas of the rivers or lakes where many of our fishes are caught. Hillstreams where other fishes are caught if leaves and fruits fall then the current might be so strong it’ll push it downstream to be deposited in certain areas of a meander known as deposition zones.

Aqua One 360, 60L for Pangio spp. and Apistogramma

This makes it just really complex to generalize but this is also why some areas have high tannin composition, Rio Negro and others have none such as the main channel of the Amazon and where they meet is known as the meeting of waters. The Rio Negro’s distinct black waters are likely due to it’s geology (Sioli, 1968), but likely those contributing tributaries cause a lot of the difference. Are these tributaries hillstream’s and likely to be less surrounded by plants at those higher elevations? Or maybe that geology largely contributes to the types of trees surrounding smaller source streams? There is a lot to unpack about why, but as hobbyists I’m not sure this why really matters? What matters is what these water bodies are and why what they are effects our fishes.

The reality of freshwater habitat diversity

It is a little bit of a pain but the image we have of freshwater habitats is curated by the idea perpetuated by brands and hobbyists. There is the idea that black water, therefore leaf litter is so common and when we look at the rivers and lakes around us, surely we must notice the difference?

Rivers are generally classified into white water or black water and then subdivided further as explained so clearly by Bogotá-Gregory et al. (2020; fig. 3).

Figure 3: Classification of freshwater river types, can some what apply to lakes source: Bogotá-Gregory, J. D., Lima, F. C., Correa, S. B., Silva-Oliveira, C., Jenkins, D. G., Ribeiro, F. R., … & Crampton, W. G. (2020). Biogeochemical water type influences community composition, species richness, and biomass in megadiverse Amazonian fish assemblages. Scientific Reports10(1), 15349.

Do I need to say more? I wonder if the influence of these ideas of freshwater ecosystems comes from the passionate fishkeepers focused on those smaller niche fish such as wild Betta (not domestic Betta splendens), other anabantoids and what I some what try to affectionately say swimmy fishes. Previously these black water, leaf litter tanks would have been seen as dirty but they have effectively justified this ecosystem for the hobby. The problem has come where it’s shoved almost all freshwater species into being black water, particularly if from South America.

Lakes also show a wide amount of diversity between lakes and within that same lake there can be many different habitats.

The deception of anthropomorphic effects

As humans encroach on land and change it, the function changes too. This has been happening for thousands of years but regardless this effects the species that inhabit these waters. Rivers have been straightened and moved, stopped and redirected or even slowed and sped up. New lakes are created and others destroyed. Our waste thrown into rivers and lakes whether it be effluent or invasive species, warm water from coolant systems or mining waste. Freshwater is changing and fishes cannot always adapt fast enough. Your local river might not always be representative of nature, the plants are likely invasive and the sediment is likely due effluent or waste. The presence of a dam or weir means that the entire flow of the river has changed.

Figure 4: Habitat of Scobinancistrus raonii in the RIo Xingu as featured in: Chaves, M. S., Oliveira, R. R., Gonçalves, A. P., Sousa, L. M., & Py-Daniel, L. H. R. (2023). A new species of armored catfish of the genus Scobinancistrus (Loricariidae: Hypostominae) from the Xingu River basin, Brazil. Neotropical Ichthyology21(3), e230038.

This can be similar as to when we look at wild habitats, but much of the footage and images we see today seem to have been taken a while ago. Still the footage and photos of the Rio Xingu is showing that amount of sediment that might be connected to the building of the Belo Monte dam in 2011.

Source of nutrients

This is not where the debate is in the hobby but in the science it certainly is (Neres‐Lima et al., 2017; Hamilton et al., 1992). The long held belief in the hobby is that nutrients originates from leaf litter, fruit, branches etc. Therefore it’s important in the aquarium as some how all fishes even if there is no leaf litter in their habitat benefit from it.

This idea that allochthonous (leaf litter, fruit, branches, other botanicals etc.) nutrients is the major source of nutrients over autochthonous (algaes) can be true in some ecosystems but it doesn’t mean that nutrients is accessible (Thorp & Delong, 2002) and therefore few organisms obtain nutrients from it. This theory of nutrients deriving from allochthonous relies on the presence of leaf litter, botanicals being present in the water or further upstream and in shaded rivers it might contribute where no algae’s are found (Neres-lime et al., 2017). One answer answer is black water, often characterized by high botanicals/allochthonous influences is much lower in productivity and if a source of nutrients this should be another story (Bogotá-Gregory et al., 2020; Lewis et al., 1988). We also know as hobbyists algae’s can grow in very dimly lit aquariums though, nutrients is a whole other discussion.

It doesn’t seem an easy question to answer as while isotopes seem to be an answer and algae’s contribute most to nutrients in one study (Hamilton et al., 1992). As the cited papers suggest rivers flowing through slower flowing areas might contribute to nutrients opposed to it being directly in the rivers, but this means that the nutrients is in the source water not where the fishes are.

Why does algae do so well but plants don’t?

Algae’s are found in all of these habitats but to varying amounts, many do require light as photosynthetic organisms but some are known as heterotrophs so can gain energy by other means. It’s not just algae’s but other microbes that grow in these ecosystems, all of these unlike plants cling to surfaces and in a very small size meaning that there is much less drag. If they do grow too big then parts get broken off to throw downstream. What might be forgotten is bryophytes also do this but still photosynthetic. This leaves sponges as filter feeders.

What is algae?

Figure 5: Phylogeny of algae source: SCHLARB-RIDLEY, B. 2011. Algal Research in the UK. A Report for Bbsrc. BBSRC. and Milledge, J. J. (2013). Energy balance and techno-economic assessment of algal biofuel production systems (Doctoral dissertation, University of Southampton).

Algae (Alga, singular) is basically a common name for a whole mixture of different organisms (Milledge, 2013). Some hobbyists will exclude Cyanobacteria as it is a bacteria yet it makes little sense given this clade is already polyphyletic (Fig 5), a real pick and mix. Another opinion is as these organisms are photosynthetic they must be similar to plants, plants particularly vegetables make good nutritional replacements. As you can see from the above it’s unlikely plants make up for algae’s nutritionally (Čengić-Džomba et al., 2022; Nagappan et al., 2021; Vucko et al., 2017).

This makes algae such a diverse grouping to describe as earlier stated some being heterotrophs do not just obtain their ‘energy’ from the sun and others might obtain it from feeding or even parasitism e.g. dinoflagellates (Levy et al., 2007; Sudhagar et al., 2022).

Algae is so important to an ecosystem and I will include other microbial life on that. This wide diversity of organisms feature in many fishes diets even making the majority of many Loricariid diets (Lujan et al., 2015). There is a link between algae’s and the fishes that feed on them influences the habitat’s and those fishes (Power, 1984).

Algae’s have to compete with different microbes and this is fascinating in terms of succession. Succession is the process of a habitat maturing over time with the change in species present. This happens in an aquarium over time but also how we maintain our aquariums seems to effect this. Generally you can expect as a grazing fish moves over an area it removes all the organisms it feeds best on, leaving an opening for other species of microbes to grow. These original fishes might not feed on that new microbes but other fishes will have and could this be where niche partitioning further occurs.

Long live algae! Leaf litter is overrated.

You don’t need a green aquarium to embrace them, realistically if you’re getting high amounts of algae it could infer high levels of a compound or element that encourages their growth as I keep stating.
Above where I mention hypothetical niche partitioning regarding algae’s and other surface growing microbes. This will inevitably occur with bacterial films or any growths on leaf litter, if you’re seeing the films on botanicals in general for a while they probably aren’t being eaten by anything and when they eventually go it could be due to exhausting the source of nutrients. I particularly noted this when experimenting with different woods and palms, if these biofilms were being eaten there wouldn’t be so much biofilm’s growing. So far in Loricariids at least we know this niche partitioning is largely in where food items are located (Lujan et al., 2011) and while their diets aren’t the best studied we do have a realistic idea that they are not all feeding on the same algae’s or microbes (Lujan et al., 2012; Valencia & Zamudio, 2007; Delariva & Agostinho, 2001).

It is frequently stated that leaf litter has beneficial properties due to tannins but it is rarely mentioned that tannins are antinutrients and can cause physiological damage (Omnes et al., 2017; Li et al., 2020; Maulidiyah et al., 2019). Given some fishes inhabit these naturally they likely do have physiological mechanisms to manage tannins within the water, although given many fishes do have negative physiological responses as cited above not all do.

The frequent dislike of tea tree oils in the hobby is contrasted with the support for tannins having antimicrobial properties and they possibly do but in prevention and handling of disease in fishes, these effects are minimal (Imperatore et al., 2022). Perhaps the bias against tea tree oils is due to a dislike of brands as a review by Valladão et al. (2015) infers that use of known concentrations of compounds of plant origins (herbal treatments) can show very effective use. Leaf litter and tannins from the leaf litter have a flaw here, species identification and in using the plant as a whole it is difficult to say what compounds and concentrations are being added. We are living in an anti-pharmaceutical age and who can tell us more about how compounds interact with physiology then pharmacologists as the story is quite complex.

Leaf litter is not all bad

Leaf litter and botanicals can add great hiding spaces for smaller fishes, there is still a number of fishes who find it as a part of their natural habitat and this is worth replicating. The main downfall with leaf litter is siphoning to remove waste and therefore excess nutrients, other heavier botanicals would be more ideal if this is a big concern. But without evidence we shouldn’t jump to conclusions.

Pangio myersi with leaf litter, from Springs Aquatic Ltd, Botley, Hampshire.

Is there hope for algal growth?

No doubt algae does actually struggle to grow to much of an extent in a mature aquarium that isn’t constantly being scrubbed. For an aquarium which might benefit from ‘naturally’ growing algae’s such as for feeding fishes there is hope. We can’t use sunlight like outside but perhaps using UVB lighting could encourage growth. Most of our aquarium algae growth relies on nutrients but outside sunlight would perhaps contribute, something I’d certainly like to explore more.

Aquariums are anthropogenic

At the end of the day aquariums are anthropogenic and the argument about the importance of leaf litter vs algae really stall’s there. Algae’s are generally great indicators of nutrients, generally different algae’s hint to the age of an aquarium.

At the end maybe the promotion of leaf litter is easy to justify as natural then algae. There are few true biotopes and few ever show algae’s but the scale you’d need to grow them would be insane.

References:

Delariva, R. L., & Agostinho, A. A. (2001). Relationship between morphology and diets of six neotropical loricariids. Journal of Fish biology58(3), 832-847.

Bogotá-Gregory, J. D., Lima, F. C., Correa, S. B., Silva-Oliveira, C., Jenkins, D. G., Ribeiro, F. R., … & Crampton, W. G. (2020). Biogeochemical water type influences community composition, species richness, and biomass in megadiverse Amazonian fish assemblages. Scientific Reports10(1), 15349.

Čengić-Džomba, S., Džomba, E., & Hadžić, D. (2022). An Overview of Using Algae Meal in Feeding Freshwater Fish Species. In Scientific-Expert Conference of Agriculture and Food Industry (pp. 171-182). Cham: Springer Nature Switzerland.

Chaves, M. S., Oliveira, R. R., Gonçalves, A. P., Sousa, L. M., & Py-Daniel, L. H. R. (2023). A new species of armored catfish of the genus Scobinancistrus (Loricariidae: Hypostominae) from the Xingu River basin, Brazil. Neotropical Ichthyology21(3), e230038.

Farha, A. K., Yang, Q. Q., Kim, G., Li, H. B., Zhu, F., Liu, H. Y., … & Corke, H. (2020). Tannins as an alternative to antibiotics. Food Bioscience38, 100751.

Hamilton, S. K., Lewis, W. M., & Sippel, S. J. (1992). Energy sources for aquatic animals in the Orinoco River floodplain: evidence from stable isotopes. Oecologia89, 324-330.

Imperatore, R., Fronte, B., Scicchitano, D., Orso, G., Marchese, M., Mero, S., … & Paolucci, M. (2022). Dietary supplementation with a blend of hydrolyzable and condensed Tannins ameliorates diet-induced intestinal Inflammation in Zebrafish (Danio rerio). Animals13(1), 167.

Küchler, I. L., Miekeley, N., & Forsberg, B. R. (2000). A contribution to the chemical characterization of rivers in the Rio Negro Basin, Brazil. Journal of the Brazilian Chemical Society11, 286-292.

Levy, M. G., Litaker, R. W., Goldstein, R. J., Dykstra, M. J., Vandersea, M. W., & Noga, E. J. (2007). Piscinoodinium, a fish-ectoparasitic dinoflagellate, is a member of the class Dinophyceae, subclass Gymnodiniphycidae: convergent evolution with Amyloodinium. Journal of Parasitology93(5), 1006-1015.

Lewis Jr, W. M. (1988). Primary production in the Orinoco River. Ecology69(3), 679-692.

Li, M., Feng, L., Jiang, W. D., Wu, P., Liu, Y., Jiang, J., … & Zhou, X. Q. (2020). Condensed tannins decreased the growth performance and impaired intestinal immune function in on-growing grass carp (Ctenopharyngodon idella). British Journal of Nutrition123(7), 737-755.

Lujan, N. K., German, D. P., & Winemiller, K. O. (2011). Do wood‐grazing fishes partition their niche?: morphological and isotopic evidence for trophic segregation in Neotropical Loricariidae. Functional Ecology25(6), 1327-1338.

Lujan, N. K., Winemiller, K. O., & Armbruster, J. W. (2012). Trophic diversity in the evolution and community assembly of loricariid catfishes. BMC Evolutionary Biology12, 1-13.

Maulidiyah, V., Sulmartiwi, L., & Masithah, E. D. (2019). The effect of immersion time in tannin solution towards the adhesiveness and hatching degree of the eggs of common carp (Cyprinus carpio). AACL Bioflux.

Milledge, J. J. (2013). Energy balance and techno-economic assessment of algal biofuel production systems (Doctoral dissertation, University of Southampton).

Nagappan, S., Das, P., AbdulQuadir, M., Thaher, M., Khan, S., Mahata, C., … & Kumar, G. (2021). Potential of microalgae as a sustainable feed ingredient for aquaculture. Journal of Biotechnology341, 1-20.

Neres‐Lima, V., Machado‐Silva, F., Baptista, D. F., Oliveira, R. B., Andrade, P. M., Oliveira, A. F., … & Moulton, T. P. (2017). Allochthonous and autochthonous carbon flows in food webs of tropical forest streams. Freshwater Biology62(6), 1012-1023.

Omnes, M. H., Le Goasduff, J., Le Delliou, H., Le Bayon, N., Quazuguel, P., & Robin, J. H. (2017). Effects of dietary tannin on growth, feed utilization and digestibility, and carcass composition in juvenile European seabass (Dicentrarchus labrax L.). Aquaculture Reports6, 21-27.

Power, M. E. (1984). Habitat quality and the distribution of algae-grazing catfish in a Panamanian stream. The Journal of Animal Ecology, 357-374.

Sioli, H. (1968). Hydrochemlstry and Geology in the Brazilian Amazon Region. Volume 1, fascículo 3, 1968.

Sudhagar, A., Sundar Raj, N., Mohandas, S. P., Serin, S., Sibi, K. K., Sanil, N. K., & Raja Swaminathan, T. (2022). Outbreak of Parasitic Dinoflagellate Piscinoodinium sp. Infection in an Endangered Fish from India: Arulius Barb (Dawkinsia arulius). Pathogens11(11), 1350.

Thorp, J. H., & Delong, M. D. (2002). Dominance of autochthonous autotrophic carbon in food webs of heterotrophic rivers. Oikos96(3), 543-550.

Valencia, C. R., & Zamudio, H. (2007). Dieta y reproducción de Lasiancistrus caucanus (Pisces: Loricariidae) en la cuenca del río La Vieja, Alto Cauca, Colombia. Revista del Museo Argentino de Ciencias Naturales nueva serie9(2), 95-101.

Valladão, G. M. R., Gallani, S. U., & Pilarski, F. (2015). Phytotherapy as an alternative for treating fish disease. Journal of veterinary pharmacology and therapeutics38(5), 417-428.

Vucko, M. J., Cole, A. J., Moorhead, J. A., Pit, J., & de Nys, R. (2017). The freshwater macroalga Oedogonium intermedium can meet the nutritional requirements of the herbivorous fish Ancistrus cirrhosus. Algal research27, 21-31.

The Cichlid Diet: When specialization isn’t so specialist.

Apistogramma macmasteri ‘gold’

Cichlids, cichlidae are no doubt the classic model group for the study of evolution, they display a wide diversity of morphology in both the America’s and Africa (Arbour & López‐Fernández, 2024; Santos et al., 2023). There are 1727 species in the group cichlidae making this family currently the largest family of fishes. (Fricke et al., 2024). Cichlids both sides of the Atlantic are popular in the aquarium hobby, partially due to their diversity (no doubt colouration) but also their comparatively heightened aggression compared to other clades. No doubt aggression is where many people empathize with with these fishes.

Symphysodon tarzoo, the green discus but also includes some browns and blues.

What do cichlids specialize in?

Not unexpected, many species lack a complete understanding of their diet to say what they are actually feeding on. This is a vast topic given the number of species, there are algivores (algae specialists) such as reported in Tropheus (Wagner et al., 2009) to piscivory in peacock bass, Cichla (Aguiar‐Santos et al., 2018). No doubt given I said that Tropheus are reported algivores means I can’t find any solid evidence that they are, this is certainly a topic that needs the right wording and ambiguity included where it might be unsure.

Morphology

Much of the research into cichlid morphological disparity has long focused on the jaws. Cichlids like many fishes have two pairs of jaws. The oral jaws evolved for prey capture, the pharyngeal jaws evolved for prey processing (Fraser et al., 2009). To some extent the lips might also provide a purpose in some fishes in some fishes to move a surface to extract food further as seen in other fishes (Krings et al., 2023; Cohen et al., 2023).

Figure 1: The jaws of a typical cichlid as featured in: Fraser, G. J., Hulsey, C. D., Bloomquist, R. F., Uyesugi, K., Manley, N. R., & Streelman, J. T. (2009). An ancient gene network is co-opted for teeth on old and new jaws. PLoS biology7(2), e1000031.

These two pairs of jaws can be diverse in shape and structure but the teeth further vary between individuals and species.

Cichlids display a very traditional head shape that reflects most other fishes. The oral jaw is often gape limited and evolved to reach forwards to remove or capture a prey item. Realistically no cichlids lack this.

Earlier I mentioned Tropheus being algivores yet it doesn’t seem there is any solid evidence that they exclusively are but we can look at the fishes morphology. They are extremely similar to a fish we know likely consumes a lot of bacteria, algae and similar microbes, discus, Symphysodon (Crampton, 2008). These fishes are not related and this similar morphology is likely due to convergent evolution. Both display a shorter blunter head with strong lips, similar to silver dollars and pacu, Serrasalmidae who some force to break apart at that ‘herbivorous matter’ (Cohen et al., 2023), but they do take it to a more extreme level given they are feeding on plant and fruit matter not algaes and bacteria. Tropheus display some densely packed oral teeth (Richardson-Coy, 2017). This differential oral, mouth morphology could really be due to the differences in what is required to feed on different algaes and in fact, Tropheus are confirmed to specialize in diatoms (Richardson-Coy, 2017), diatoms cling to a surface so much more then the more loose algae/biofilm based diet of Symphysodon (Crampton, 2008) so the more numerous teeth would be more effective. Tropheus oral teeth remind me much more of the jaws of Baryancistrus and similar Loricariids who are scraping algaes of rocks. These teeth might be much more useful for feeding on those Discus, Symphysodon display reduced pharyngeal jaws (Burress, 2016) as this diet might not require the same level of processing as plant matter (hence Serrasalmidae have large robust oral teeth). It seems unclear as to the morphology At the end of the day algivores are diverse, no more needs said but just look at the diversity of algivores in Loricariidae, the queens of algivory/detritivory.

In comparison to Tropheus and Symphysodon would be those that specialize in fishes, Cichla as mentioned before has that large and explosive jaw to reach and consume fish. Fishes are a comparatively more difficult food item to obtain then anything herbivorous so quickly grabbing food much more ahead is beneficial.

Peacock bass, Cichla sp. sourced from: https://rustyangler.com/peacock-bass-fishing/

The position of jaws is a big clue as to what fishes feed on, terminal mouth’s point forward inferring feeding in front of the fish and is usually associated with carnivory. An inferior mouth points downwards so feeding from the bottom, benthic usually associated with invertebrates and herbivory. Superior mouth’s point upwards and therefore specialize in feeding from the surface. We can clearly see while not extreme Tropheus particularly has an inferior mouth whereas Cichla, being a piscivore is terminal.

While these jaw shapes I mention cover the more traditional cichlids we cannot forget the earth eaters, those fishes who find their food in the substrate, shifting and moving around the sand or silt. While this is generally associated with many Geophagini such as Geophagus, Satanoperca but this clade does include species who are limited in this ability to move substrate e.g. Apistogramma, Mikrogeophagus. Distantly related to these other South American genera is Retroculus, another ‘earth-eater’ (Lopez-Fernandez et al., 2012). The substrate feeding trophic niche seems mostly associated with South American cichlids but it is found in the Rift Valley, although much of this behaviour might be more about breeding sites. Interestingly, it seems these substrate interacting cichlids are more then often mouth-brooders. Substrate digging seems much common in many more Rift Valley clades we keep.

The interesting thing some what I can infer from Burress (2016) is that while jaw shapes might be similar tooth shapes seem divergent between neotropical (fishes from the America’s) and old world (Africa, Asia etc.) regardless of a shared niche. This seems to move away from convergent evolution and multiple solutions to the same problem, the same problem as I noticed being a similar diet.

Tropheus spp. sourced from Wikipedia.

Liem’s Paradox

This is the biggest part of the cichlid story. To put simply Liem’s paradox is the fact that while fishes might display specialist diets and morphology, they still are capable of generalization. This theory is based on the behaviour and morphology of Rift Valley cichlids (Liem, 1980). This I can assume is some factor limiting morphology for further specialization in morphology, and we see these extreme specializations in other clades e.g. Loricariidae, Gymnotiformes and Moryridae. This plays out in the wild where algivores, Lepidophages (scale specialists) and other niches are shown to feed on fishes when given the chance (Golcher-Benavides & Wagner, 2019). Perhaps there is a nutritional reason, but just because a fish will eat something it doesn’t mean they eat it frequently or it is good for them. This plays out in our aquariums, discus Symphysodon will eat smaller tetra yet they are detritivores and Rift Valley algivorous cichlids (Hata et al., 2014).

It is well accepted that fishes feed and act very differently in the aquarium to how they would in the wild but it does occur in the fishes natural habitats (Golcher-Benavides & Wagner, 2019). This theory in fishes is largely based on Rift Valley cichlids, it’s quite clear that Tropheus are much more capable of generalism then Symphysodon. This opportunistic generalism would be limited by certain specialist morphology e.g. the body shape of Symphysodon or mouth shape of angelfish (Pterophyllum). The Symphysodon is limited in it’s ability to feed on fishes and invertebrates but the Pterophyllum is limited in it’s ability to eat algae’s.

Altolamprologous compressiceps sourced from Wikimedia commons, https://creativecommons.org/share-your-work/licensing-considerations/compatible-licenses/

This might not be so much of a simple topic with so many taxa. With the focus on Africa, there is so much we seem not to know about the South American clades despite their diversity. Regardless many cichlids while specialist do not seem to take it to the extreme, this might be behind their diversity but also why unlike clades like Siluriforme, they are limited in that morphological disparity.

References:

Aguiar‐Santos, J., deHart, P. A., Pouilly, M., Freitas, C. E., & Siqueira‐Souza, F. K. (2018). Trophic ecology of speckled peacock bass Cichla temensis Humboldt 1821 in the middle Negro River, Amazon, Brazil. Ecology of Freshwater Fish27(4), 1076-1086.

Arbour, J. H., & López‐Fernández, H. (2014). Adaptive landscape and functional diversity of Neotropical cichlids: implications for the ecology and evolution of Cichlinae (Cichlidae; Cichliformes). Journal of evolutionary biology27(11), 2431-2442.

Burress, E. D. (2016). Ecological diversification associated with the pharyngeal jaw diversity of Neotropical cichlid fishes. Journal of Animal Ecology85(1), 302-313.

Cohen, K. E., Lucanus, O., Summers, A. P., & Kolmann, M. A. (2023). Lip service: Histological phenotypes correlate with diet and feeding ecology in herbivorous pacus. The Anatomical Record306(2), 326-342.

Crampton, W. G. (2008). Ecology and life history of an Amazon floodplain cichlid: the discus fish Symphysodon (Perciformes: Cichlidae). Neotropical Ichthyology6, 599-612.

Fraser, G. J., Hulsey, C. D., Bloomquist, R. F., Uyesugi, K., Manley, N. R., & Streelman, J. T. (2009). An ancient gene network is co-opted for teeth on old and new jaws. PLoS biology7(2), e1000031.

Fricke, R., Eschmeyer, W. N. & Van der Laan, R. (eds) 2024.  ESCHMEYER’S CATALOG OF FISHES: GENERA, SPECIES, REFERENCES. (http://researcharchive.calacademy.org/research/ichthyology/catalog/fishcatmain.asp). Electronic version accessed 04 August 2024.

Golcher-Benavides, J., & Wagner, C. E. (2019). Playing out Liem’s paradox: opportunistic piscivory across Lake Tanganyikan cichlids. The American Naturalist194(2), 260-267.

Hata, H., Tanabe, A. S., Yamamoto, S., Toju, H., Kohda, M., & Hori, M. (2014). Diet disparity among sympatric herbivorous cichlids in the same ecomorphs in Lake Tanganyika: amplicon pyrosequences on algal farms and stomach contents. Bmc Biology12, 1-14.

Krings, W., Konn-Vetterlein, D., Hausdorf, B., & Gorb, S. N. (2023). Holding in the stream: convergent evolution of suckermouth structures in Loricariidae (Siluriformes). Frontiers in Zoology20(1), 37.

Liem, K. F. (1980). Adaptive significance of intra-and interspecific differences in the feeding repertoires of cichlid fishes. American zoologist20(1), 295-314.

Lopez-Fernandez, H., Winemiller, K. O., Montana, C., & Honeycutt, R. L. (2012). Diet-morphology correlations in the radiation of South American geophagine cichlids (Perciformes: Cichlidae: Cichlinae). PLoS One7(4), e33997.

Richardson-Coy, R. (2017). Feeding Selectivity of an Algivore (Tropheus brichardi) in Lake Tanganyika. PhD Thesis

Santos, M. E., Lopes, J. F., & Kratochwil, C. F. (2023). East African cichlid fishes. EvoDevo14(1), 1.

Wagner, C. E., McIntyre, P. B., Buels, K. S., Gilbert, D. M., & Michel, E. (2009). Diet predicts intestine length in Lake Tanganyika’s cichlid fishes. Functional Ecology23(6), 1122-1131.