Two Rare Orchids, One Vanishing Forest: Ecuador’s Newest Dracula Species

The genus Dracula is one of the more theatrical corners of the orchid world, containing more than 130 species.

A new species of vampire orchid, described in the open-access journal PhytoKeys, was recently discovered in the cloud forests of southwestern Ecuador, and with it comes the long-awaited confirmation of where a second, mysterious species actually lives in the wild.

The genus Dracula is one of the more theatrical corners of the orchid world. It contains more than 130 species, most found in the northern Andes of Colombia and Ecuador, and is known for its dramatic and often dark-coloured flowers with long tails. These blooms are pollinated by small flies rather than by bees or butterflies, that mistake the flower’s lip for a mushroom!

The newly described species, Dracula aguilarii, was found in El Oro Province, in a region of premontane and cloud forest that sits between 900 and 1,200 metres above sea level. Its cream-coloured flowers are suffused with brown-red tones and covered in short, dense hairs. It closely resembles a related species, D. hirtzii, but can be told apart by its blunt-tipped leaves, a deep and broadly rounded cup formed by the fused sepals, and notably shorter tails on those sepals.

Dracula aguilarii Baquero, M.M. Jiménez & Iturralde in vivo. A. Flower in ¾ view, showing the deep center, the convex sepals toward the apex, the short pubescence, and the proportionally small lip in relation to the sepals; B. Close-up of the petals and lip, frontal view; C. Close-up of the column, petals, and lip, lateral view; D. Side view of the flower, the deep and large mentum is visible as well as the convex towards the apex and pubescent sepals. Photographs by Luis E. Baquero.

The species owes its name to Mario Aguilar, a farmer and orchid enthusiast from El Oro with a remarkable knack for spotting rare orchids in the field. It was Aguilar who first came across a small population of around fifteen plants in a patch of remnant forest near the town of Balsas, more than a decade ago. Researchers later confirmed, through further fieldwork and herbarium comparisons, that his discovery represented a species new to science, and named it in his honour.

Only three populations of Dracula aguilarii are currently known, all within a fairly small area, which has led researchers to recommend the species be classified as Endangered. The forests it depends on are being steadily cleared for cattle pasture, and like many showy orchids, it also faces pressure from illegal collection for the horticultural trade.

Colour variation in Dracula aguilarii Baquero, M.M. Jiménez & Iturralde. A. Photo by Mario Aguilar from near Piñas; B. Photo by Marco M. Jiménez from a plant in situ at the southernmost known population near Balsas; C. Photo by Luis E Baquero from Holotype, LB 3142, QCNE (near Balsas); D. Photo by Marco M. Jiménez from a cultivated plant collected near Balsas.

This same study resolves a smaller mystery that has lingered for well over a decade. Dracula soennemarkii was first described in 2012 from a plant bought at a nursery and grown in Sweden, with no idea of where it had originally come from in the wild. The researchers have now traced a wild population of this species to the same general region of El Oro, giving it a confirmed home for the first time. Given that it is known from just a single location, D. soennemarkii has been assessed as Critically Endangered, an even more precarious position than its newly described neighbour.

Known species and natural hybrids of Dracula from El Oro province, southwestern Ecuador. A. D. aguilarii Baquero, M.M. Jiménez & Iturralde; B. D. woolwardiae (F. Lehmann ex Kraenzlin) Luer; C. D. cordobae Luer; D. D. mopsus (F. Lehmann & Kraenzlin) Luer; E. D. × pinasensis Zambrano & Solano; F. D. soennemarkii Luer & Dalström. A. From holotype, LB 3142 QCNE, and B–F. From near Piñas. Photographs by Luis E. Baquero (A–E), and Mario Aguilar (F).
Dracula aguilarii Baquero, M.M. Jimenez & Iturralde. A, B. Flower and plant in situ near El Caucho; C, D. Photographs of other plants in cultivation. Photographs by José Bustamante.

Together, these findings demonstrate just how much remains to be discovered, and how quickly it could be lost, in Ecuador’s shrinking cloud forests. El Oro Province alone now hosts six recognised species of Dracula, yet only a fraction of its once-extensive humid forest cover remains intact. Each new species description is as much a conservation appeal as it is a taxonomic milestone.

Distribution of the known populations of Dracula aguilarii Baquero, M.M. Jiménez & Iturralde and morphologically similar species, and confirmed locality of D. soennemarkii Luer & Dalström, in the northern Andes. Base map layer was obtained from Google Satellite imagery (Google LLC; https://www.google.com/earth/).

Original study:

Baquero R. LE, Jiménez MM, Iturralde GA (2026) Dracula aguilarii (Orchidaceae, Pleurothallidinae), a new species from southwestern Ecuador and the first confirmed location for Dracula soennemarkii. PhytoKeys 273: 281-297. https://doi.org/10.3897/phytokeys.273.182821

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Pensoft Celebrates International Tea Day with Fascinating Discoveries in Camellia

Camellia species are famous for their tea properties, providing the leaf buds and young branches used to manufacture black, green, and oolong tea.

At Pensoft Publishers, we are proud to support the open-access dissemination of botanical knowledge through our journal PhytoKeys. On International Tea Day, we invite you to spill the tea on the captivating world of the genus Camellia. While most people recognise these plants as the source of their morning brew, the genus is incredibly diverse and economically significant. 

Camellia species are famous for their tea properties, providing the leaf buds and young branches used to manufacture black, green, and oolong tea. Beyond the teapot, these evergreen shrubs and trees are valued for their oil-producing seeds and their stunning ornamental flowers in horticulture. Despite their global fame, we are still discovering new members of this family, often in the remote forests of East and Southeast Asia.

One of the most dramatic stories recently published in PhytoKeys concerns Camellia hekouensis, a tree native to Hekou in Yunnan, China. For a time, the botanical community feared the species was lost forever after the last known living tree died at the end of 2024 due to bark destruction. 

However, a dedicated effort by the staff of the Dawei Mountain National Nature Reserve saved the species from the brink. They successfully protected 11 wild trees and propagated 32 others ex-situ. This species is particularly interesting because its chemical profile challenged previous scientific claims. While earlier researchers suggested it lacked certain purine alkaloids, new analysis shows the leaves actually contain 1.18 mg/g of theobromine.

Camellia hekouensis. Image credit: Dongwei Zhao et al.

Read more: Zhao D, Zhang G, Yang S (2025) Phylogenetic position, supplementary description and phytochemical analysis of Camellia hekouensis (Theaceae), a critically endangered tree native to Hekou, Yunnan, China. PhytoKeys 256: 185-195. https://doi.org/10.3897/phytokeys.256.149481 

Further research in Yunnan has revealed another unique relative of the common tea plant named Camellia yangii. Discovered in the forests of Malipo County, this species is a true member of the tea section, yet it stands out for being remarkably hairy. It bears a red or purplish red terminal bud that is densely pubescent, making it a rare and visually striking germplasm resource. 

Lead researcher Dongwei Zhao of Central South University of Forestry and Technology, Changsha, found that while most Camellia species have five sepals, Camellia yangii typically bears only three. It also follows its own schedule, flowering about a month later than other tea plants in the vicinity. This late flowering phase is a natural barrier that prevents it from hybridising with other species, keeping its genetic line distinct. With fewer than ten individuals known in the wild, its discovery is a call to action for urgent protection.

Camellia yangii. Image credit: Dongwei Zhao.

Read more: Zhao D (2025) Camellia yangii (Theaceae), a new species of tea plants (Camellia section Thea). PhytoKeys 257: 247-256. https://doi.org/10.3897/phytokeys.257.152000 

Botanical science sometimes involves correcting the records of the past, as seen in the reinstatement of Camellia angustifolia. This species from Guangxi, China, was originally described in 1981 but was later dismissed as a mere synonym of another variety in 1992. 

Recent field investigations proved that this was a mistake. Researchers from the Guangxi Research Institute of Tea Science discovered that the original type specimen was actually a misidentified bellflower from a completely different family. Once the correct specimens were examined, the differences became clear – unlike its shrubby relatives that grow only a few meters tall, Camellia angustifolia is a majestic tree that can reach heights of 20 meters. 

Camellia angustifolia. Image credit: Shixiong Yang.

Read more: Deng H, Liao X, Yu X, Liu Z, Yang S (2025) Reinstatement of the independent specific status of Camellia angustifolia, a tea plant (Camellia sect. Thea, Theaceae) from Guangxi, China. PhytoKeys 267: 1-8. https://doi.org/10.3897/phytokeys.267.174664 

Our journey through recent tea-related discoveries concludes in the striking Danxia landscape of Guangdong Province. Here, researchers identified Camellia shangshii, a new species endemic to the red sandstone formations of Danxiashan Mountain. This species bears smaller leaves and flowers than its closest relatives. One of its most defining features is that its white petals are fused together at the base for several millimeters. 

This tree notably thrives in a unique microclimate where specialised soils and environmental contrasts drive the evolution of distinct species. It is named in honour of Dr. Shangshi Wu, a scientist who pioneered the study of these geological landscapes.

Camellia shangshii. Image credit: Shiyang Wang, Yinyu Wu and Xiaowei Yi.

Read more: Wang S, Liu H, Tan S, Shen L, Chen Z, Chen F, Fan Q (2026) Camellia shangshii (Theaceae), a new species endemic to danxia landscape from Guangdong Province, China. PhytoKeys 270: 13-23. https://doi.org/10.3897/phytokeys.270.172597 

As we celebrate International Tea Day, these discoveries remind us that our knowledge of the natural world is still growing. Every new species found and every historical error improves our understanding of the biological heritage of our favorite beverages. At Pensoft, we will never stop be-leafing in the power of new species to inspire conservation and science!

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Scientists forecast where is the highly invasive fall armyworm to strike next

The fall armyworm is the larvae of the fall armyworm moth species Spodoptera frugiperda. Photo by Centre for Agriculture and Bioscience International (CABI).

Staple and economically important crops throughout the world could be at serious risk if efficient measures are not taken soon

Known to be feeding on many economically important crops cultured across the world, including maize, rice, sugarcane, sorghum, beet, tomato, potato, cotton and pasture grasses, the larvae of the native to the Americas fall armyworm moth seem to have already found a successful survival strategy in a diverse and changing world.

Furthermore, having taken no longer than 2 years to invade and spread throughout most of sub-Saharan Africa, the pest has already demonstrated its huge potential in severely affecting livelihoods around the globe.

A recent study in the open-access journal NeoBiota, conducted by Dr Regan Early of Exeter University, United Kingdom and her colleagues at the Centre for Agriculture and Bioscience International: Dr Pablo González-Moreno, Sean T. Murphy and Roger Day, looks into the factors and likelihood for the fall armyworm (Spodoptera frugiperda) to spread to other regions and continents.

Invasion progress

The alarming reports started in January 2016 when major outbreaks of fall armyworms were registered in Nigeria and Ghana, preceding signals from Benin, Sao Tomé and Togo shortly after. By September 2017, the pest had already been confirmed in 28 sub-Saharan African countries, with nine states expected to follow suit.

While unaided dispersal of the species in Africa is considered unlikely, it is speculated that the pest had arrived on a passenger flight from America. To back this theory, the researchers point out that the first countries to house the invader are also the major air transportation hubs in Africa and have warm, moist climate similar to those in the pest’s natural habitat.

In the aftermath, recent estimates point to up to 50% maize yield loss in Africa attributed to the fall armyworm. However, scientists believe that the species is far from finished spreading and is highly likely to invade new continents.

Who’s next?

To find what makes a region an inviting new habitat for the fall armyworm, hence which countries face the highest threat of future invasions, the researchers looked into both the native and African distributions of the species, and the effects different temperatures and precipitation levels have on it.

Having concluded that the lowest temperatures and the maximum amount of rain play the main role in determining whether the fall armyworm is to establish in a certain region, the scientists concluded that South and Southeast Asia, as well as Australia face the most serious risk, since their climate is very similar to the one preferred by the pest.

However, the authors of the study remind that this forecast shall in no way be taken with a sigh of relief by countries with milder climatic conditions. While the moth needs particular temperature and precipitation amplitudes at its year-round habitat, it could easily travel back and forth up to several hundred kilometres during its seasonal migrations. Therefore, if the fall armyworm establishes in North Africa, it could migrate to Europe during the warmer months, just like it has already been observed to travel from its year-round localities in Argentina, Texas and Florida all the way to Canada’s Québec and Ontario in the north.

The increasing transportation and international trade are also likely to facilitate the further spread of the fall armyworm outside Africa. The scientists conclude that, given the current travel air routes, it is Australia, China, India, Indonesia, Malaysia, Philippines and Thailand which are at high risk of becoming the pest’s new habitat.

The map illustrates the likelihood of the establishment of the fall armyworm if introduced at different parts of the world. Image by Regan Early.

What’s next?

Having concluded that there is a considerable potential for near global invasion and seasonal migration of fall armyworm, the scientists call for vigilance from farmers and programme managers alike. They remind that early detection of small larvae is crucial, since it is only at this stage that chemical insecticides would work effectively.

“As fall armyworm has huge potential to affect staple and economic crops globally, we urgently need information on the pest’s potential distribution and environmental limitations,” comment the researchers.

“Management decisions would be improved by further research on fall armyworm’s seasonal migration and population dynamics and the environmental dependency of interactions with other species.”

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Original source:

Early R, González-Moreno P, Murphy ST, Day R (2018) Forecasting the global extent of invasion of the cereal pest Spodoptera frugiperda, the fall armyworm. NeoBiota 40: 25-50. https://doi.org/10.3897/neobiota.40.28165

A preprint of the study was published earlier on bioRxiv.

Cage the fly: Walk-in field cages to assess mating compatibility in pest fruit flies

Fruit flies mating compatibility studies have been examined by an international team of researchers to assess the usefulness of walk-in field cages in studying the sexual behavior within fruit fly species complexes and recognition of taxonomically misplaced flies. In addition, they have also evaluated the relevant chemical signals during pheromone emission for species discrimination. The experimental part was conducted with the support of Joint FAO/IAEA Division of Nuclear Techniques in Food and Agriculture in Seibersdorf, Austria. Their findings are published in the open-access journal ZooKeys.

Evolution has led to divergence in some groups, which sometimes results in new, yet very similar species. Hence, they might successfully confuse taxonomists, making them coin terms like ‘cryptic’ species, or in other words, distinct species misplaced under the same name.

However, these species are kept isolated from each other via reproductive barriers. Preventing interbreeding and hybridization, they can be ecological and mechanical, but also behavioral (i.e. sexual). The latter are behaviors or signals that affect recognition within a species, as well as attractiveness and mate choice. They affect their evolution and therefore, are key elements in species differentiation.

The authors of the present paper have found that the walk-in field cages methodology provides an appropriate ground to study these issues. By applying it, researchers around the world are able to detect pest species among others when occurring in the same populations.

Apart from taxonomic value, the scientists also point out the significance of these findings to pest management. As the studied pest fruit fly species are agricultural pests of major economic importance, assessing their mating behaviour, including the pheromones the males emit when attracting partners, can be utilised in the development of highly specific control methods. For instance, there is the sterile insect technique that involves releasing males reproductively sterilised via ionizing radiation into a wild population, where they inseminate the pest females with sterile sperm so that they end up with unviable offspring.

The main advantage of using walk-in field cages, rather than small laboratory-based ones, is that they provide semi-natural conditions under which they are “reliable and powerful tools to measure the level of mating compatibility among different species and populations of a putative single species.”

However, the present paper highlights that such an approach is only to be applied as a part of integrative taxonomic analyses, together with molecular, physiological and morphological approaches when assessing to which species a particular pest population belongs.

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Original source:

Juarez ML, Devescovi F, Brizova R, Bachmann G, Segura DF, Kalinova B, Fernandez P, Ruiz MJ, Yang J, Teal PEA, Caceres C,, Vreysen MJB, Hendrichs J, Vera MT (2015) Evaluating mating compatibility within fruit fly cryptic species complexes and the potential role of sex pheromones in pre-mating isolation. In: De Meyer M, Clarke AR, Vera MT, Hendrichs J (Eds) Resolution of Cryptic Species Complexes of Tephritid Pests to Enhance SIT Application and Facilitate International Trade. ZooKeys 540: 125-155. doi: 10.3897/zookeys.540.6133

Known from flower stalls as ‘Big Pink’ orchid proved to be an undescribed wild species

As easy as it might seem, seeking new species among cultivated plants could be actually quite tricky. While looking into the undescribed orchid, known at the market as ‘Big Pink’, Bobby Sulistyo and his team were likely to find yet another man-made hybrid. In reality, they are now describing as ‘new’ a wild orchid species that has been sitting at the flower stalls since 2013. The story behind their discovery is published in the open access journal PhytoKeys.

While studying a cultivated plant might be quite a motivator and serve as a starting point for scientific quests around the world, the assumptions that one has found a new species at the florist’s could easily be wrong. Not only is the place of origin, written on the label, often doubtful, but there is always the chance of accidentally describing a man-made hybrid as a new species.

Such could have been the case of Bobby Sulistyo and his team when they discovered that although previously assumed impossible, the relatives of ‘Big Pink’, they were surveying, could also make human-assisted hybrids. Moreover, both of the specimens they have had at hand had come from uncertain place of origin.

However, the scientists conducted a series of sophisticated DNA analyses to conclude that firstly, ‘Big Pink’ is a separate species within its genus and then, that there is no evidence for it being an artificial hybrid. Eventually, the species was found in the wild as well. As a result, the orchid species was given the official name Dendrochilum hampelii.

In the wild, ‘Big Pink’ is found at around 1,200 m above sea level in the Philippines, where it harmlessly plants its roots on tree trunks and branches among mosses.

So far, little is known about the orchid’s distribution in nature, so the researchers suggest its conservation status to be considered as Data Deficient according to the IUCN Red List of Threatened Species (IUCN 2012).

 

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Original source:

Sulistyo B, Boos R, Cootes J, Gravendeel B (2015) Dendrochilum hampelii (Coelogyninae, Epidendroideae, Orchidaceae) traded as ‘Big Pink’ is a new species, not a hybrid: evidence from nrITS, matK and ycf1 sequence data. PhytoKeys 56: 83-97. doi:10.3897/phytokeys.56.5432

World-famous, yet nameless: Hybrid flowering dogwoods named by Rutgers scientists

Garden lovers and horticulturalists now have two new species names to add to their vocabulary and memory. The world’s most commercially successful dogwood garden trees have finally received proper scientific names decades after their introduction into horticulture. The big-bracted, or flowering, dogwoods are beloved trees with cloud-like branches blossoming in early spring in white, sometimes red or pink. The new scientific names are published by a team of American scientists in the open-access journal PhytoKeys.

The two hybrid species were artificially hybridized at Rutgers University by renowned ornamental tree breeder Dr. Elwin R. Orton decades ago and are now commonly grown across the United States, Europe and Japan. These two hybrids were developed from Florida, Kousa and Pacific dogwoods (Cornus spp.), all well known ornamental trees. The breeding program, which started in 1965, had the aim to create garden dogwoods with better aesthetic qualities, such as larger pink or red floral bracts, unique growth habits and better disease-resistance.

So, why do we need formal names? “Crucial to communication in all parts of our lives is the naming of objects and phenomena,” explains Mr. Mattera, a Rutgers University graduate student in the School of Environmental and Biological Sciences. “Humanity needs words to tell other people what we are talking about, and the words need to have uniform and clear meanings,” he adds. Before their publication these horticultural plants largely lived in a taxonomic no-man’s land and could not easily be placed into horticultural databases.

Co-author Dr. Lena Struwe, a botanist also at Rutgers University, explains that “Even artificial hybrids created by the fusion of species from separate pieces of the Earth are living, evolving things that need scientific names so they fit into our encyclopedias of life.” She continues, “even if these are mostly sterile, but stable, hybrids they are now widespread components of worldwide garden biodiversity that get pollinated by native insects and interact with other local native and non-native species.”

Common garden plant hybrids, even if artificially produced from wild species, need formal species names to promote international communication and further scientific understanding. “If you can’t put a name on something, you can’t explain what you see, own, or remember,” Dr. Lena Struwe explains and adds: “Names and words are the basis for the transfer of all knowledge”.

The new hybrid species Cornus × rutgersensis was created by the hand-crossing of a an Asian species, the Kousa dogwood, with the common Florida dogwood. Most gardeners and horticulturist will recognize the pink-bracted cultivar Stellar Pink®, the most successful Cornus × rutgersensis hybrid. The crosses made by Dr. Orton were the world’s first known hybrid crosses between these two species. Many familiar with this hybrid may recall hearing this name before, and they probably have. Cornus × rutgersensis and similar names had been used informally by those in the horticultural trade before, but now the authors hope to provide clarity by formally publishing the name in the present paper. The researchers suggest Rutgers’ dogwood as the common-name for this hybrid.

The second hybrid, Cornus × elwinortonii, honors career-long ornamental plant breeder Dr. Orton from Rutgers University in New Brunswick, NJ (United States). This cross produced a hybrid with larger white petal-like bracts around each flower head and resistance to the dogwood-killing fungal disease, dogwood anthracnose, that affects the native Pacific and Florida dogwoods. The cultivar Venus® is the most prominent example of this hybrid. The researchers have proposed the common name Orton’s dogwood for horticultural usage.

Both hybrid species represent long-distance artificial crosses of wild species that would never meet in nature, which were further developed into beloved commercial garden plants. Despite their parents being quite different in their flowers and fruits, the two new hybrid species are a clear combination of their ancestors.

“Such intermixing of parental characters is the key to successful plant breeding and artificial selection of new horticultural and agricultural varieties that can provide new forms of beauty, as well as new disease- and stress-resistant plants,” explains Rutgers University plant breeder Dr. Thomas Molnar, in Department of Plant Biology and Pathology.

According to the International Code of Nomenclature for algae, fungi, and plants (ICN), all proposed scientific names, including hybrid names, require that they are formally published and described in a scientific publication, as well as represented by a type specimen in a scientific collection. The formal types of these new hybrids will be deposited in several herbaria, and are also represented by living trees at Rutgers University in New Jersey (USA).

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Original source:

Mattera R, Molnar T, Struwe L (2015) Cornus × elwinortonii and Cornus × rutgersensis(Cornaceae), new names for two artificially produced hybrids of big-bracted dogwoods.PhytoKeys 55: 93-111. doi: 10.3897/phytokeys.55.9112