ANNEX 1Supplementary provisions
ANNEX 1
‘ANNEX VII
Codes to be included in the description of specimens and units of measure to be used in permits and certificates pursuant to Article 5(1) and (2)
Description
Trade term code
Preferred unit
Alternative unit
Explanation
baleen
BAL
kg
no.
elastic sheets of keratin that hang from the upper jaw of baleen whales (Mysticeti) and allow them to feed
bark
BAR
kg
tree bark (raw, dried or powdered; unprocessed)
body
BOD
no.
kg
substantially whole dead animals, including whole fish, stuffed turtles, preserved butterflies, reptiles in alcohol, whole stuffed hunting trophies, etc. If referring to specimens of sharks and rays (Elasmobranchii spp.), the preferred unit is kg.
bone
BON
kg
no.
bones, including jaws
calipee
CAL
kg
calipee or calipash (turtle cartilage for soup)
carapace
CAP
no.
kg
raw or unworked whole shells of Testudines species.
carving
CAR
kg
no.
carved products other than ivory, bone or horn – for example coral and wood (including handicrafts).
N.B: Ivory carvings should be specified as such (see below – “IVC”). Also, for species from which more than one type of product may be carved (e.g. horn and bone), the trade term code should indicate the type of product in trade (e.g. bone carving “BOC” or horn carving – “HOC”), where possible.
carving - bone
BOC
kg
no.
bone carving
carving - horn
HOC
kg
no.
horn carving
carving – ivory (worked ivory)
IVC
kg
no.
ivory carvings, including e.g. smaller worked pieces of ivory (knife handles, chess sets, mahjong sets etc). N.B. Whole carved tusk should be reported as carving – ivory (IVC) not as tusks (see “TUS” below). Jewellery made from carved ivory should be reported as ‘jewellery – ivory’ (see IJW below).
caviar
CAV
kg
unfertilized dead processed eggs from all species of Acipenseriformes; also known as roe.
chips (woodchips)
CHP
kg
chips of timber, especially Aquilaria spp., Gyrinops spp. and Pterocarpus santalinus
claw
CLA
no.
kg
claws – e.g. of Felidae, Ursidae or Crocodylia (NB: 'turtle claws' are usually scales and not real claws)
cloth
CLO
m2
kg
cloth – if the cloth is not made entirely from the hair of a CITES species, the weight of hair of the species concerned should instead, if possible, be recorded under ‘HAI’
coral (raw)
COR
no.
kg
raw or unworked coral and coral rock (also live rock and substrate) [as defined in Resolution Conf. 11.10 (Rev. CoP15)]. Coral rock should be recorded as ‘ Scleractinia spp.’
NB: the trade should be recorded by number of pieces only if the coral specimens are transported in water.
Live rock (transported moist in boxes) should be reported in kg; coral substrate should be reported as number of pieces (since these are transported in water as the substrate to which non-CITES corals are attached).
cosmetics
COS
g
ml
Any product or mixture of products which is applied to an external part of the body only (e.g. skin, hair, nails, genitals, lips or teeth or the mucous membranes of the oral cavity) with the intent to clean, odorise, change the appearance or protect. Cosmetics may include the following: make-up, perfume, skin cream, nail polish, hair colourants, soap, shampoo, shaving cream, deodorant, sunscreens, toothpaste.
Cosmetics which include extracts of CITES-listed species. The quantity should reflect the amount of CITES-listed species present.
culture
CUL
no. of flasks, etc.
cultures of artificially propagated plants
derivatives
DER
kg/l
derivatives (other than those included elsewhere in this table)
dried plant
DPL
no.
dried plants – e.g. herbarium specimens
ear
EAR
no.
ears – usually elephant
egg
EGG
no.
kg
whole dead or blown eggs (see also 'caviar')
egg (live)
EGL
no.
kg
live fertilized eggs – usually birds and reptiles but includes fish and invertebrates
eggshell
ESH
g/kg
raw or unworked eggshell except whole eggs
extract
EXT
kg
l
extract – usually plant extracts
feather
FEA
kg/ no. of wings
no.
feathers – in the case of objects (e.g. pictures) made of feathers, record the number of objects
fibre
FIB
kg
m
natural fibre: generic term for several types of material of natural (i.e. plant or animal) origin. Animal fibre can usually be spun and woven and is usually very fine and has good flexibility. – e.g. fibre coming from the shearing of live vicunas. It also includes fibres from animal intestines used to make strings for tennis rackets
fin (dried)
DFN
kg
dried fins and parts of fins (including flippers)
fin (wet)
FFN
kg
fresh, chilled of frozen fins and parts of fins (including flippers)
fingerlings
FIG
kg
no.
live juvenile fish for the aquarium trade, aquaculture, hatcheries, consumption or for release, including live European eels ( Anguilla anguilla ) up to 12cm in length
flower
FLO
kg
flowers
flower pot
FPT
no.
flower pots made from parts of a plant – e.g. treefern fibres (NB: live plants traded in so- called 'community pots' should be recorded as 'live plants', not as flower pots)
frog legs
LEG
kg
frog legs
fruit
FRU
kg
fruit
foot
FOO
no.
feet – e.g. of elephant, rhinoceros, hippopotamus, lion, crocodile, etc.
fur products (large)
FPL
no.
large manufactured products of fur – e.g. bear or lynx fur blankets or other fur products of a substantial size.
fur product (small)
FPS
no.
small manufactured products of fur– including handbags, key fobs, purses, pillows, trim, etc.
gall
GAL
kg
gall
gall bladder
GAB
no.
kg
gall bladder
garment
GAR
no.
garments – including gloves and hats but not shoes. Includes trimming or decoration on garments
genitalia
GEN
kg
no.
castrates and dried penes
gill plates
GIL
kg
no.
gill plates (e.g. for sharks)
graft rootstock
GRS
no.
graft rootstocks (without the grafts)
hair
HAI
kg
g
includes all unprocessed animal hair, e.g. of elephant, yak, guanaco, wolf, bear, panther, etc.
hair products
HAP
no.
g
products made of hair (e.g. elephant hair bracelets)
horn
HOR
no.
kg
horns – includes antlers
jewellery
JWL
no.
g
jewellery – including bracelets, necklaces, and other items of jewellery from products other than ivory (e.g. wood, coral, etc.)
jewellery – ivory (worked ivory)
IJW
no.
g
jewellery made of ivory – includes ekipas
kernel
KNL
kg
also known as 'endosperm', 'pulp' or 'copra'
leather product (large)
LPL
no.
large manufactured products of leather – e.g. briefcases, furniture, suitcases, travel trunks
leather product (small)
LPS
no.
small manufactured products of leather – e.g. belts, braces, bicycle saddles, cheque book or credit card holders, handbags, key fobs, notebooks, purses, shoes, tobacco pouches, wallets, watch-straps and trim
live
LIV
no.
kg
live animals and plants, excluding live fingerling fish – see FIG
leaf
LVS
kg
no.
leaves
logs
LOG
m3
all wood in the rough, whether or not stripped of bark or sapwood, or roughly squared, for processing notably into sawn wood, pulpwood or veneer sheets. NB: trade in logs of special purpose timbers traded by weight (e.g. lignum vitae, Guaiacum spp.) should be recorded in kg
meat
MEA
kg
meat, including flesh of fish if not whole (see ‘body’), fresh or unprocessed meat as well as processed meat (e.g. smoked, raw, dried, frozen or tinned)
The code for meat (MEA) should be used in preference for trade in eels for human consumption.
medicine
MED
kg/l
medicine
musk
MUS
g
musk
oil
OIL
kg
l
oil – e.g. from turtles, seals, whales, fish, various plants
pearl
PRL
no.
pearl (e.g. for Strombus gigas )
piano keys (worked ivory)
KEY
no.
ivory piano keys (e.g. one standard piano would be 52 ivory piano keys)
piece – bone
BOP
kg
pieces of bone, not manufactured
piece – horn
HOP
kg
pieces of horn, not manufactured – includes scrap
piece – ivory (raw ivory)
IVP
kg
ivory pieces, not manufactured – includes scrap
plate
PLA
m2
plates of multiple skins – includes rugs if made of several skins
plywood
PLY
m2
m3
material consisting of three or more sheets of wood glued and pressed one on the other and generally disposed so that the grains of successive layers are at an angle
powder
POW
kg
a dry, solid substance in the form of fine or coarse particles
pupae
PUP
no.
butterfly pupae
root
ROO
no.
kg
roots, bulbs, corms or tubers
NB: For the agarwood-producing taxa Aquilaria spp. and Gyrinops spp., the preferred unit is 'kilograms'. The alternative unit is 'number'.
rug
RUG
no.
rugs
sawfish rostrum
ROS
no.
kg
sawfish rostrum
sawn wood
SAW
m3
wood simply sawn lengthwise or produced by a profile-chipping process; normally exceeds 6mm in thickness. NB: trade in sawn wood of special purpose timbers traded by weight (e.g. lignum vitae, Guaiacum spp.) should be recorded in kg
scale
SCA
kg
scales – e.g. of turtle, other reptiles, fish, pangolin
seed
SEE
kg
seeds
shell
SHE
no.
kg
raw or unworked shell of molluscs
side
SID
no.
sides or flanks of skins; does not include crocodilian Tinga frames (see under 'skin')
skeleton
SKE
no.
substantially whole skeletons
skin
SKI
no.
substantially whole skins, raw or tanned, including hides, crocodilian Tinga frames, external body lining, with or without scales
skin piece
SKP
kg
no.
skin pieces – including scraps, raw or tanned
skull
SKU
no.
skulls
soup
SOU
kg
l
soup – e.g. of turtle
specimen (scientific)
SPE
kg/l/ml/ no.
scientific specimens – includes blood, tissue (e.g. kidney, spleen, etc.), histological preparations, preserved museum specimens, etc.
stem
STE
no.
kg
plant stems
NB: For the agarwood-producing taxa Aquilaria spp. and Gyrinops spp., the preferred unit is 'kilograms'. The alternative unit is 'number'.
swim bladder
SWI
kg
hydrostatic organ, including isinglass / sturgeon glue
tail
TAI
no.
kg
tails – e.g. of caiman (for leather) or fox (for garment trimming, collars, boas, etc.), also includes flukes of cetaceans.
thread
THD
kg
thread – a processed long strand of multiple hairs or fibres of natural (e.g. plant or animal) origin, e.g. vicuna, guanaco
tooth
TEE
no.
kg
teeth – e.g. of whale, lion, hippopotamus, crocodile, etc.
timber
TIM
m3
kg
raw timber except saw-logs, sawn wood and transformed wood
transformed wood
TRW
m3
kg
defined by Harmonized System code 44.09: Wood (including strips, friezes for parquet flooring, not assembled), continuously shaped (tongued, grooved, v-jointed, beaded or the like) along any edges, ends or faces, whether or not planed, sanded or end-jointed.
trophy
TRO
no.
trophy – all the trophy parts of one animal if they are exported together: e.g. horns (2), skull, cape, backskin, tail and feet (i.e. ten specimens) constitute one trophy. But if, for example, the skull and horns are the only specimens of an animal that are exported, then these items together should be recorded as one trophy.
Otherwise the items should be recorded separately. A whole stuffed body is recorded under ‘BOD’. A skin alone is recorded under ‘SKI’. Trade in ‘full mount’, ‘shoulder mount’ and ‘half mount’, along with any corresponding parts of the same animal exported together on the same permit, should be reported as ‘1 TRO’
trunk
TRU
no.
kg
elephant trunk. N.B.: An elephant trunk exported with other trophy items from the same animal on the same permit as part of a hunting trophy should be reported as ‘TRO’.
tusk (raw ivory)
TUS
no.
kg
substantially whole tusks, not worked. Includes tusks of elephant, hippopotamus, walrus, narwhal, but not other teeth - N.B. Whole carved tusks should be reported as carving – ivory (see “IVC” above).
veneer sheets
—
rotary veneer
—
sliced veneer
VEN
VEN
m3
m2
kg
kg
thin layers or sheets of wood of uniform thickness, usually 6mm or less in thickness, usually peeled (rotary veneer) or sliced (sliced veneer), for use in making plywood, for veneering furniture, veneer containers, etc.
wax
WAX
kg
wax
wood product
WPR
no.
kg
manufactured wood products, including finished wood products such as furniture and musical instruments.
Key to units of measure
Unit of measure
Unit code
grams
g
kilograms
kg
liters
l
cubic centimeters
cm 3
milliliters
ml
meters
m
square meters
m 2
cubic meters
m 3
number of specimens
no.
NB.:
If no unit of measure is specified, the unit will be assumed to be number (e.g. of live animals).
ANNEX VIII
Standard references for nomenclature to be used pursuant to Article 5(4) to indicate scientific names of species in permits and certificates
FAUNA
Taxon concerned
Taxonomic reference
MAMMALIA
All MAMMALIA taxa
—
with the exception of the recognition of the following names for wild forms of species (in preference to names for domestic forms): Bos gaurus , Bos mutus , Bubalus arnee , Equus africanus , Equus przewalskii , and
—
with the exception of the taxa noted under the different Mammalia orders below
Wilson, D. E. & Reeder, D. M. (ed.) (2005 ). Mammal Species of the World. A Taxonomic and Geographic Reference . Third edition, Vol. 1-2, xxxv + 2142 pp. Baltimore (John Hopkins University Press).
ARTIODACTYLA
Bovidae
Ovis spp.
Valdez, R. & Weinberg, P.J. (2011). Species accounts 188-207 for Ovis spp., pp. 727-739 in Wilson, D.E., & Mittermeier, R.A. (eds.), Handbook of the Mammals of the World. Vol.2. Hoofed Mammals. Lynx Edicions, Barcelona. ISBN 978-84-96553-77-4.
Camelidae
Lama guanicoe
Wilson, D. E. & Reeder, D. M. (1993): Mammal Species of the World: a Taxonomic and Geographic Reference . Second edition. xviii + 1207 pp., Washington (Smithsonian Institution Press).
CARNIVORA
Felidae
Felidae spp.,
Kitchener A. C., Breitenmoser-Würsten CH., Eizirik E., Gentry A., Werdelin L., Wilting A., Yamaguchi N., Abramov A. V., Christiansen P., Driscoll C., Duckworth J. W., Johnson W., Luo S.-J., Meijaard E., O’Donoghue P., Sanderson J., Seymour K., Bruford M., Groves C., Hoffmann M., Nowell K., Timmons Z. & Tobe S. (2017). A revised taxonomy of the Felidae. The final report of the Cat Classification Task Force of the IUCN/SSC Cat Specialist Group. Cat News Special Issue 11, 80 pp.
Mustelidae: Lutrinae
Aonyx cinereus
Larivière, S., & Jennings, A.P. 2009. Species account 37 for Asian Small-clawed Otter Aonyx cinereus , p. 647 in Wilson, D.E., & Mittermeier, R.A. (eds.), Handbook of the Mammals of the World. Vol.1. Carnivores. Lynx Edicions, Barcelona. ISBN 978-84-96553-49-1.
CETACEA
Balaenopteridae
Balaenoptera omurai
Wada, S., Oishi, M. & Yamada, T. K. (2003). A newly discovered species of living baleen whales. – Nature , 426 : 278-281.
Delphinidae
Orcaella heinsohni
Beasly, I., Robertson, K. M. & Arnold, P. W. (2005). Description of a new dolphin, the Australian Snubfin Dolphin, Orcaella heinsohni sp. n. (Cetacea, Delphinidae). -- Marine Mammal Science , 21 (3): 365-400.
Delphinidae
Sotalia fluviatilis
Sotalia guianensis
Caballero, S., Trujillo, F., Vianna, J. A., Barrios-Garrido, H., Montiel, M. G., Beltrán-Pedreros, S., Marmontel, M., Santos, M. C., Rossi-Santos, M. R. & Baker, C. S. (2007). Taxonomic status of the genus Sotalia : species level ranking for "tucuxi" ( Sotalia fluviatilis ) and "costero" ( Sotalia guianensis ) dolphins. - Marine Mammal Science , 23 : 358-386.
Delphinidae
Sousa plumbea
Sousa sahulensis
Jefferson, T. A.& Rosenbaum, H. C. (2014). Taxonomic revision of the humpback dolphins ( Sousa spp.), and description of a new species from Australia. Marine Mammal Science , 30 (4): 1494-1541.
Delphinidae
Tursiops australis
Charlton-Robb, K., Gershwin, L.-A., Thompson, R., Austin, J., Owen, K. & McKechnie, S. (2011). A new dolphin species, the Burrunan Dolphin Tursiops australis sp. nov., endemic to southern Australian coastal waters. PLoS ONE , 6 (9): e24047.
Iniidae
Inia araguaiaensis
Hrbek, T., da Silva, V. M. F., Dutra, N., Gravena, W., Martin, A. R. & Farias, I. P. (2014): A new species of river dolphin from Brazil or: How little do we know our biodiversity. PLoS ONE
83623 : 1-12.
Phocoenidae
Neophocaena asiaeorientalis
Jefferson, T. A. & Wang, J. Y. (2011). Revision of the taxonomy of finless porpoises (genus Neophocaena ): The existence of two species. Journal of Marine Animals and their Ecology , 4 (1): 3-16.
Physeteridae
Physeter macrocephalus
Rice, D. W. (1998). Marine Mammals of the World: Systematics and Distribution - Society of Marine Mammalogy Special Publication Number 4 , The Society for Marine Mammalogy, Lawrence, Kansas.
Platanistidae
Platanista gangetica
Rice, D. W. (1998). Marine Mammals of the World: Systematics and Distribution - Society of Marine Mammalogy Special Publication Number 4 , The Society for Marine Mammalogy, Lawrence, Kansas.
Ziphiidae
Mesoplodon hotaula
Dalebout, M. L., Scott Baker, C., Steel, D., Thompson, K., Robertson, K. M., Chivers, S. J., Perrin, W. F., Goonatilake, M., Anderson, C. R., Mead, J. G., Potter, C. W., Thompson, L., Jupiter, D. & Yamada, T. K. (2014). Resurrection of Mesoplodon hotaula Deraniyagala 1963: A new species of beaked whale in the tropical Indo-Pacific. Marine Mammal Science , 30 (3): 1081-1108.
PRIMATES
Aotidae
Aotus jorgehernandezi
Defler, T. R. & Bueno, M. L. (2007). Aotus diversity and the species problem. – Primate Conservation , 22 : 55-70.
Aotidae
Aotus lemurinus (incl. A. hershkovitzi )
Mittermeier, R.A., Rylands, A.B., & Wilson, D.E. 2013. Handbook of the Mammals of the World: Volume 3. Primates. Lynx Edicions, Barcelona.
Atelidae
Alouatta palliata (incl. A. coibensis )
Ruiz-García, M., Cerrón, Á., Sánchez-Castillo, S., Rueda-Zozaya, P., Pinedo-Castro, M., Gutierrez-Espeleta, G. & Shostell, J.M. (2017): Phylogeography of the Mantled Howler Monkey ( Alouatta palliata ; Atelidae, Primates) across its geographical range by means of mitochondrial genetic analyses and new insights about the phylogeny of Alouatta . Folia Primatologica 88: 421-454
Atelidae
Ateles geoffroyi
Rylands, A. B., Groves, C. P., Mittermeier, R. A., Cortes-Ortiz, L. & Hines, J. J. (2006). Taxonomy and distributions of Mesoamerican primates. In: A. Estrada, P. Garber, M. Pavelka and L. Luecke (eds), New Perspectives in the Study of Mesoamerican Primates: Distribution, Ecology, Behavior and Conservation, pp. 29–79. Springer, New York, USA.
Cebidae
Callithrix manicorensis
Garbino, T. & Siniciato, G. (2014). The taxonomic status of Mico marcai (Alperin 1993) and Mico manicorensis (van Roosmalen et al. 2000) (Cebidae, Callitrichinae) from Southwestern Brazilian Amazonia. International Journal of Primatology , 35 (2): 529-546. (for Mico marcai lumped with Mico manicorensis treated as Callithrix manicorensis under CITES]
Cebidae
Cebus flavius
Oliveira, M. M. de & Langguth, A. (2006). Rediscovery of Marcgrave’s Capuchin Monkey and designation of a neotype for Simia flava Schreber, 1774 (Primates, Cebidae). – Boletim do Museu Nacional do Rio de Janeiro, N.S., Zoologia , 523 : 1-16.
Cebidae
Mico rondoni
Ferrari, S. F., Sena, L., Schneider, M. P. C. & Júnior, J. S. S. (2010). Rondon’s Marmoset, Mico rondoni sp. n., from southwestern Brazilian Amazonia. International Journal of Primatology , 31 : 693-714.
Cebidae
Saguinus ursulus
Gregorin, R. & de Vivo, M. (2013). Revalidation of Saguinus ursula Hoffmannsegg (Primates: Cebidae: Callitrichinae). Zootaxa , 3721 (2): 172-182.
Cebidae
Saimiri collinsi
Merces, M. P., Alfaro, J. W. L., Ferreira, W. A. S., Harada, M. L. & Júnior, J. S. S. (2015). Morphology and mitochondrial phylogenetics reveal that the Amazon River separates two eastern squirrel monkey species: Saimiri sciureus and S. collinsi . Molecular Phylogenetics and Evolution , 82 : 426-435.
Cercopithecidae
Allochrocebus lhoesti
Allochrocebus preussi
Allochrocebus solatus
Mittermeier, R.A., Rylands, A.B., & Wilson, D.E. 2013. Handbook of the Mammals of the World: Volume 3. Primates. Lynx Edicions, Barcelona.
Cercopithecidae
Cercopithecus lomamiensis
Hart, J.A., Detwiler, K.M., Gilbert, C.C., Burrell, A.S., Fuller, J.L., Emetshu, M., Hart, T.B., Vosper, A., Sargis, E.J. & Tosi, A.J. (2012). Lesula: A new species of Cercopithecus monkey endemic to the Democratic Republic of Congo and implications for conservation of Congo’s Central Basin. PLoS ONE , 7 (9): e44271.
Cercopithecidae
Macaca leucogenys
Li, C., Zhao, C., & Fan, P.F. (2015). White-cheeked macaque ( Macaca leucogenys ): A new macaque species from Modog, southeastern Tibet. American Journal of Primatology, 77:753-766.
Cercopithecidae
Macaca munzala
Sinha, A., Datta, A., Madhusudan, M. D. & Mishra, C. (2005). Macaca munzala : A new species from western Arunachal Pradesh, northeastern India. International Journal of Primatology , 26 (4): 977-989: doi:10.1007/s10764-005-5333-3.
Cercopithecidae
Piliocolobus bouvieri
Piliocolobus epieni
Piliocolobus temminckii
Piliocolobus waldronae
Mittermeier, R.A., Rylands, A.B., & Wilson, D.E. 2013. Handbook of the Mammals of the World: Volume 3. Primates. Lynx Edicions, Barcelona.
Cercopithecidae
Rhinopithecus strykeri
Geismann, T., Lwin, N., Aung, S. S., Aung, T. N., Aung, Z. M., Hla, T. H., Grindley, M. & Momberg, F. (2011). A new species of snub-nosed monkey, genus Rhinopithecus Milne-Edwards, 1872 (Primates, Colobinae), from Northern Kachin State, Northeastern Myanmar. – American Journal of Primatology , 73 : 96-107.
Cercopithecidae
Rungwecebus kipunji
Davenport, T. R. B., Stanley, W. T., Sargis, E. J., de Luca, D. W., Mpunga, N. E., Machaga, S. J. & Olson, L. E. (2006). A new genus of African monkey, Rungwecebus : Morphology, ecology, and molecular phylogenetics. Science , 312 : 1378-1381.
Cercopithecidae
Trachypithecus villosus
Brandon- Jones, D., Eudey, A. A., Geissmann, T., Groves, C. P., Melnick, D. J., Morales J. C., Shekelle, M. & Steward, C.-B. (2004). Asian primate classification. International Journal of Primatology , 25 : 97-163.
Cercopithecidae
Cheirogaleus andysabini
Lei, R., McLain, A.T., Frasier, C.L., Taylor, J.M., Bailey, C.A., Enberg, S.E., Ginter, A.L., Nash, S.D., Randriamampionona, R., Groves, C.P., Mittermeier, R.A., & Louis, Jr., E.E. (2015): A new species in the genus Cheirogaleus (Cheirogaleidae). Primate Conservation 29 (2): 1–12
Cercopithecidae
Cheirogaleus lavasoensis
Thiele, D., Razafimahatratra, E. & Hapke, A. (2013). Discrepant partitioning of genetic diversity in mouse lemurs and dwarf lemurs – biological reality or taxonomic bias? Molecular Phylogenetics and Evolution , 69 : 593-609.
Cercopithecidae
Cheirogaleus chethi
Frasier, C.L., Lei, R., McLain, A.T., Taylor, J.M., Bailey, C.A., Ginter, A.L., Nash, S.D., Randriamampionona, R., Groves, C.P., Mittermeier, R.A. & Louis, Jr., E.E. (2016). A New Species ofDwarf Lemur (Cheirogaleidae: Cheirogaleus medius Group) from the Ankarana and Andrafiamena- Andavakoera Massifs, Madagascar. Primate Conservation (30): 59–72.
Cheirogaleidae
Microcebus ganzhorni
Microcebus manitatra
Hotaling, S., Foley, M.E., Lawrence, N.M., Bocanegra, J., Blanco, M.B., Rasoloarison, R. Kappeler, P.M., Barrett, M.A., Yoder, A.D. & Weisrock, D.W. (2016). Species discovery and validation in a cryptic radiation of endangered primates: coalescent-based species delimitation in Madagascar's mouse lemurs". Molecular Ecology . 25 (9): 2029–2045. doi:10.1111/mec.13604
Cercopithecidae
Microcebus gerpi
Radespiel, U., Ratsimbazafy, J. H., Rasoloharijaona, S., Raveloson, H., Andriaholinirina, N., Rakotondravony, R., Randrianarison, R. M. & Randrianambinina, B. (2012). First indications of a highland specialist among mouse lemurs ( Microcebus spp.) and evidence for a new mouse lemur species from eastern Madagascar. Primates , 53 : 157-170.
Cercopithecidae
Microcebus marohita
Microcebus tanosi
Rasoloarison, R. M., Weisrock, D. W., Yoder, A. D., Rakotondravony, D. & Kappeler, P. M. [2013]. Two new species of mouse lemurs (Cheirogaleidae: Microcebus ) from Eastern Madagascar. - International Journal of Primatology , 34: 455-469.
Galagidae
Paragalago cocos
Paragalago granti
Paragalago orinus
Paragalago rondoensis
Paragalago zanzibaricus
Masters, J.C., Génin, F., Couette, S., Groves, C.P., Nash, S.D., Delpero, M. & Pozzi, L. (2017). A new genus for the eastern dwarf galagos (Primates: Galagidae). - Zoological Journal of the Linnean Society 181 (1): 229–241. https://doi.org/10.1093/zoolinnean/zlw028
Galagidae
Galagoides kumbirensis
Svensson, M.S., Bersacola,, E., Mills, M.S.L., Munds, R.A., Nijman, V., Perkin, A., Masters, J.C., Couette, S., Nekaris, K.A. & Bearder, S.K. (2017): A giant among dwarfs: a new species of galago (Primates: S., Galagidae) from Angola. Am. J. Phys. Anthropol . 163 (1): 30-43. doi: 10.1002/ajpa.23175
Hominidae
Pongo tapanuliensis
Nater, A. Greminger, M.P., Nurcahyo, A., Nowak, M.G., De Manuel Montero, M., Desai, T., Groves, C.P., Pybus, M., Sonay, T.B., Roos, C., Lameira, A.R., Wich, S.A., Askew, J., Davila-Ross, M., Fredriksson, G.M., De Valles, G., Casals, F., Prado-Martinez, J., Goossens, B., Verschoor, E.J., Warren, K.S., Singleton, I., Marques, D.A., Pamungkas, J., Perwitasari-Farajallah, D., Rianti, P., Tuuga, A., Gut, I.G., Gut, M., Orozco-Ter Wengel, P., Van Schaik, C.P., Bertranpetit, J., Anisimova, M., Scally, A., Marques-Bonet, T., Meijaard, E & Krutzen, M. (2017): Morphometric, behavioural, and genomic evidence for a new orangutan species. Current Biology 27: DOI: 10.1016/j.cub.2017.09.047
Hylobatidae
Hylobates abbotti
Hylobates funereus
Mittermeier, R.A., Rylands, A.B., & Wilson, D.E. 2013. Handbook of the Mammals of the World: Volume 3. Primates. Lynx Edicions, Barcelona.
Hylobatidae
Nomascus annamensis
Van Ngoc Thinh, Mootnick, A. R., Vu Ngoc Thanh, Nadler, T. & Roos, C. (2010). A new species of crested gibbon from the central Annamite mountain range. Vietnamese Journal of Primatology, 4 : 1-12.
Indriidae
Propithecus candidus
Propithecus coronatus
Mittermeier, R.A., Rylands, A.B., & Wilson, D.E. 2013. Handbook of the Mammals of the World: Volume 3. Primates. Lynx Edicions, Barcelona.
Lemuriidae
Eulemur flavifrons
Mittermeier, R.A., Rylands, A.B., & Wilson, D.E. 2013. Handbook of the Mammals of the World: Volume 3. Primates. Lynx Edicions, Barcelona.
Lorisidae
Nycticebus javanicus
Mittermeier, R.A., Rylands, A.B., & Wilson, D.E. 2013. Handbook of the Mammals of the World: Volume 3. Primates. Lynx Edicions, Barcelona.
Lorisidae
Nycticebus kayan
Munds, R.A., Nekaris, K.A.I. & Ford, S.M. (2013). Taxonomy of the bornean slow loris, with new species Nycticebus kayan (Primates, Lorisidae). American Journal of Primatology , 75 : 46-56.
Pitheciidae
Cacajao melanocephalus
Cacajao oukary
Ferrari, S. F., Guedes, P. G., Figueiredo-Ready, W. M. B. & Barnett, A. A. (2014). Reconsidering the taxonomy of the Black-faced Uacaris, Cacajao melanocephalus group (Mammalia: Pitheciidae), from the northern Amazon Basin. Zootaxa , 3866 (3): 353-370.
Pitheciidae
Cheracebus spp.
Plecturocebus spp.
Byrne, H, Rylands, A.B., Cameiro, J.C., Alfaro, J.W.L., Bertuol, F., Da Silva, M.N.F., Messias, M., Groves, C.P., Mittermeier, R.A., Farias, I., Hrbek, T., Schneider, H., Sampaio, I. & Boubli, J.P. (2016). Phylogenetic relationships of the New World titi monkeys (Callicebus): first appraisal of taxonomy based on molecular evidence. Frontiers in Zoology 13 (10): 1-25. https://doi.org/10.1186/s12983-016-0142-4
Pitheciidae
Pithecia cazuzai
Pithecia chrysocephala
Pithecia hirsuta
Pithecia inusta
Pithecia isabela
Pithecia milleri
Pithecia mittermeieri
Pithecia napensis
Pithecia pissinattii
Pithecia rylandsi
Pithecia vanzolinii
Marsh, L.K. (2014). A taxonomic revision of the saki monkeys, Pithecia Desmarest, 1804. Neotropical Primates , 21 : 1-163.
Pitheciidae
Plecturocebus grovesi
Boubli, J.P., Byrne, H., Da Silva, M.N.F., Silva-Junior, J., Araujo, R.C., Bertuol, F., Goncalves, J., De Melo, F.R., Rylands, A.B., Mittermeier, R.A., Silva, F.E., Nash, S.D., Canale, G., Alencar, R De M., Rossi, R.V., Carneiro, J., Sampaio, I., Farias, I.P., Schneider, H & Hrbek, T. (2018). On a new species of titi monkey (Primates: Plecturocebus Byrne et al., 2016), from Alta Floresta, southern Amazon, Brazil. Molecular Phylogenetics and Evolution 132: 117-137.
Tarsiidae
Tarsius lariang
Merker, S. & Groves, C.P. (2006). Tarsius lariang : A new primate species from Western Central Sulawesi. International Journal of Primatology , 27 (2): 465-485.
Tarsiidae
Tarsius spectrumgurskyae
Tarsius supriatnai
Shekelle, M., Groves, C.P., Maryanto, I. & Mittermeier, R.A. (2017). Two new tarsier species (Tarsiidae, Primates) and the biogeography of Sulawesi, Indonesia. Primate Conservation 31: 61-70.
Tarsiidae
Tarsius tumpara
Shekelle, M., Groves, C., Merker, S. & Supriatna, J. (2010). Tarsius tumpara: A new tarsier species from Siau Island, North Sulawesi. Primate Conservation , 23 : 55-64.
PROBOSCIDEA
Elephantidae
Loxodonta africana
Wilson, D. E. & Reeder, D. M. (1993). Mammal Species of the World: a Taxonomic and Geographic Reference . Second edition. xviii + 1207 pp., Washington (Smithsonian Institution Press).
SCANDENTIA
Tupaiidae
Tupaia everetti
Roberts, T. E., Lanier, H. C., Sargis, E. J. & Olson, L. E. (2011). Molecular phylogeny of treeshrews (Mammalia: Scandentia) and the timescale of diversification in Southeast Asia. Molecular Phylogenetics and Evolution , 60 (3): 358-372.
Tupaiidae
Tupaia palawanensis
Sargis, E. J., Campbell, K. K. & Olson, L. E. ( 2014). Taxonomic boundaries and craniometric variation in the treeshrews (Scandentia, Tupaiidae) from the Palawan faunal region. Journal of Mammalian Evolution , 21 (1): 111-123.
AVES
Order- and family-level names for birds
Morony, J. J., Bock, W. J. & Farrand, J., Jr. (1975). Reference List of the Birds of the World. American Museum of Natural History. 207 pp.
All bird species – with the exception of the taxa mentioned below
Dickinson, E.C. (ed.) (2003). The Howard and Moore Complete Checklist of the Birds of the World. Revised and enlarged 3rd Edition. 1039 pp. London (Christopher Helm).
in combination with
Dickinson, E.C. (2005). Corrigenda 4 (02.06.2005) to Howard & Moore Edition 3 (2003).
APODIFORMES
Trochilidae
Amazilia hoffmanni
Amazilia saucerottei
Jiménez, R.A. & Ornelas, J.F. (2016). Historical and current introgression in a Mesoamerican hummingbird species complex: a biogeographic perspective. PeerJ . 2016; 4: e1556. doi:10.7717/peerj.1556.
Trochilidae
Anthracothorax nigricollis iridescens
Phaethornis longirostris
Phaethornis mexicanus
Selasphorus calliope
Del Hoyo, J. & Collar, N.J. (2014). HBW and Birdlife International Illustrated Checklist of the Birds of the World. Volume 1: Non-Passerines . Lynx Edicions, Barcelona. ISBN 978-84-96553-94-1.
Trochilidae
Hylocharis leucotis
Hylocharis xantusii
Campylopterus curvipennis
Campylopterus excellens
Phaeochroa cuvierii
Dickinson, E.C. & Remsen, J.V. (eds.) (2013). The Howard & Moore complete checklist of the birds of the world. 4th edition, Vol. 1: Non-Passerines . Aves Press, Eastbourne, UK. ISBN 978-0-9568611-0- 8.
Trochilidae
Chlorostilbon lucidus
Pacheco, J. F. & Whitney, B. M. (2006). Mandatory changes to the scientific names of three Neotropical birds Bull. Brit. Orn. Club , 126 : 242-244.
Trochilidae
Eriocnemis isabellae
Cortés-Diago, A., Ortega, L. A., Mazariegos-Hurtado, L. & Weller, A.-A. (2007) A new species of Eriocnemis (Trochilidae) from southwest Colombia. Ornitologia Neotropical,
18 :161-170.
Trochilidae
Oreotrochilus cyanolaemus
Sornoza-Molina, F., Freile, J.F., Nilsson, J., Krabbe, N. & Bonaccorso, E. (2018). A striking, critically endangered, new species of hillstar (Trochilidae: Oreotrochilus ) from the southwestern Andes of Ecuador. The Auk: Ornithological Advances , 135(4), 1146-1171. https://doi.org/10.1642/AUK-18-58.1
Trochilidae
Phaethornis aethopyga
Piacentini, V. Q., Aleixo, A. & Silveira, L. F. (2009). Hybrid, subspecies or species? The validity and taxonomic status of Phaethornis longuemareus aethopyga Zimmer, 1950 (Trochilidae). Auk , 126 : 604-612.
CICONIIFORMES
Phoenicopteridae
Phoenicopterus roseus
Phoenicopterus ruber
Del Hoyo, J. & Collar, N.J. (2014). HBW and Birdlife International Illustrated Checklist of the Birds of the World. Volume 1: Non-Passerines . Lynx Edicions, Barcelona. ISBN 978-84-96553-94-1.
FALCONIFORMES
Accipitridae
Accipiter hiogaster
Accipiter novaehollandiae
Buteo nitidus
Buteo plagiatus
Buteogallus anthracinus
Buteogallus gundlachii
Buteogallus solitarius
Chondrohierax uncinatus
Chondrohierax wilsonii
Circus cyaneus
Circus hudsonius
Leptodon cayanensis
Leptodon forbesi
Pseudastur albicollis
Rupornis magnirostris
Spizaetus melanoleucus
Del Hoyo, J. & Collar, N.J. (2014). HBW and Birdlife International Illustrated Checklist of the Birds of the World. Volume 1: Non-Passerines . Lynx Edicions, Barcelona. ISBN 978-84-96553-94-1.
Accipitridae
Aquila hastata
Parry, S. J., Clark, W. S. & Prakash, V. (2002). On the taxonomic status of the Indian Spotted Eagle Aquila hastata . Ibis , 144 : 665-675.
Accipitridae
Buteo socotraensis
Porter, R. F. & Kirwan, G. M. (2010). Studies of Socotran birds VI. The taxonomic status of the Socotra Buzzard. Bulletin of the British Ornithologists‘ Club , 130 (2): 116–131.
Accipitridae
Geranoaetus albicaudatus
Dickinson, E.C. & Remsen, J.V. (eds.) (2013). The Howard & Moore complete checklist of the birds of the world. 4th edition, Vol. 1: Non-Passerines . Aves Press, Eastbourne, UK. ISBN 978-0-9568611-0- 8.
Falconidae
Falco peregrinus (incl. Falco pelegrinoides )
Del Hoyo, J. & Collar, N.J. (2014). HBW and Birdlife International Illustrated Checklist of the Birds of the World. Volume 1: Non-Passerines . Lynx Edicions, Barcelona. ISBN 978-84-96553-94-1.
Falconidae
Micrastur mintoni
Whittaker, A. (2002). A new species of forest-falcon (Falconidae: Micrastur ) from southeastern Amazonia and the Atlantic rainforests of Brazil. Wilson Bulletin , 114 : 421-445.
GRUIFORMES
Gruidae
Antigone antigone
Antigone canadensis
Antigone rubicunda
Antigone vipio
Leucogeranus leucogeranus
Del Hoyo, J. & Collar, N.J. (2014). HBW and Birdlife International Illustrated Checklist of the Birds of the World. Volume 1: Non-Passerines . Lynx Edicions, Barcelona. ISBN 978-84-96553-94-1.
Rallidae
Hypotaenidia sylvestris
Del Hoyo, J. & Collar, N.J. (2014). HBW and Birdlife International Illustrated Checklist of the Birds of the World. Volume 1: Non-Passerines . Lynx Edicions, Barcelona. ISBN 978-84-96553-94-1.
PASSERIFORMES
Muscicapidae
Garrulax taewanus
Collar, N. J. (2006). A partial revision of the Asian babblers (Timaliidae). Forktail , 22 : 85-112.
Paradisaeidae
Lophorina niedda
Lophorina minor
Lophorina superba
Scholes, E. & Laman, T.G. (2018). Distinctive courtship phenotype of the Vogelkop Superb Bird-of-Paradise Lophorina niedda Mayr, 1930 confirms new species status. PeerJ 6:e4621 https://doi.org/10.7717/peerj.4621.
PSITTACIFORMES
Cacatuidae
Cacatua goffiniana
Roselaar, C. S. & Michels, J. P. (2004). Nomenclatural chaos untangled, resulting in the naming of the formally undescribed Cacatua species from the Tanimbar Islands, Indonesia (Psittaciformes: Cacatuidae). Zoologische Verhandelingen , 350 : 183-196.
Cacatuidae
Zanda baudinii
Zanda latirostris
Del Hoyo, J. & Collar, N.J. (2014). HBW and Birdlife International Illustrated Checklist of the Birds of the World. Volume 1: Non-Passerines . Lynx Edicions, Barcelona. ISBN 978-84-96553-94-1.
Loriidae
Trichoglossus haematodus
Collar, N. J. (1997). Family Psittacidae (Parrots). In del Hoyo, J., Elliot, A. and Sargatal, J. (eds.), Handbook of the Birds of the World , 4 (Sandgrouse to Cuckoos): 280-477. Barcelona (Lynx Edicions).
Psittacidae
Aratinga maculata
Nemesio, A. & Rasmussen, C. (2009). The rediscovery of Buffon’s “Guarouba” or “Perriche jaune”: two senior synonyms of Aratinga pintoi Silveira, Lima & Höfling, 2005 (Aves: Psittaciformes). Zootaxa , 2013 : 1-16.
Psittacidae
Eupsittula canicularis
Eupsittula nana
Myiopsitta luchsi
Myiopsitta monachus
Psephotellus chrysopterygius
Psephotellus dissimilis
Psephotellus pulcherrimus
Psephotellus varius
Psittacara holochlorus
Pyrilia haematotis
Del Hoyo, J. & Collar, N.J. (2014). HBW and Birdlife International Illustrated Checklist of the Birds of the World. Volume 1: Non-Passerines . Lynx Edicions, Barcelona. ISBN 978-84-96553-94-1.
Psittacidae
Forpus modestus
Pacheco, J. F. & Whitney, B. M. (2006). Mandatory changes to the scientific names of three Neotropical birds. Bulletin of the British Ornithologists’ Club , 126 : 242-244.
Psittacidae
Pionopsitta aurantiocephala
Gaban-Lima, R., Raposo, M. A. & Hofling, E. (2002). Description of a new species of Pionopsitta (Aves: Psittacidae) endemic to Brazil. Auk , 119 : 815-819.
Psittacidae
Poicephalus robustus
Poicephalus fuscicollis
Coetzer, W.G., Downs, C.T., Perrin, M.R. & Willows-Munro, S. (2015). Molecular Systematics of the Cape Parrot ( Poicephalus robustus ). Implications for Taxonomy and Conservation. PLoS ONE , 10(8): e0133376. doi: 10.1371/journal.pone.0133376.
Psittacidae
Psittacara strenuus
Pezoporus flaviventris
Pezoporus wallicus
Dickinson, E.C. & Remsen, J.V. (eds.) (2013). The Howard & Moore complete checklist of the birds of the world. 4th edition, Vol. 1: Non-Passerines . Aves Press, Eastbourne, UK. ISBN 978-0-9568611-0- 8.
Psittacidae
Psittacula intermedia
Collar, N. J. (1997) Family Psittacidae (Parrots). In del Hoyo, J., Elliot, A. and Sargatal, J. (eds.), Handbook of the Birds of the World , 4 (Sandgrouse to Cuckoos): 280-477. Barcelona (Lynx Edicions).
Psittacidae
Pyrrhura griseipectus
Olmos, F., Silva, W. A. G. & Albano, C. (2005). Grey-breasted Conure Pyrrhura griseipectus , an overlooked endangered species. Cotinga , 24 : 77-83.
Psittacidae
Pyrrhura parvifrons
Arndt, T. (2008). Anmerkungen zu einigen Pyrrhura -Formen mit der Beschreibung einer neuen Art und zweier neuer Unterarten. Papageien , 8: 278-286.
STRIGIFORMES
Strigidae
Ciccaba virgata
Megascops asio
Megascops barbarus
Megascops guatemalae
Megascops kennicottii
Megascops seductus
Megascops trichopsis
Psiloscops flammeolus
Del Hoyo, J. & Collar, N.J. (2014). HBW and Birdlife International Illustrated Checklist of the Birds of the World. Volume 1: Non-Passerines . Lynx Edicions, Barcelona. ISBN 978-84-96553-94-1.
Strigidae
Glaucidium mooreorum
da Silva, J. M. C., Coelho, G. & Gonzaga, P. (2002). Discovered on the brink of extinction: a new species of pygmy owl (Strigidae: Glaucidium) from Atlantic forest of northeastern Brazil. Ararajuba , 10 (2): 123-130.
Strigidae
Megascops gilesi
Krabbe, N.K. (2017). A new species of Megascops (Strigidae) from the Sierra Nevada de Santa Marta, Colombia, with notes on voices of New World screech-owls. Ornitología Colombiana
16 : 1–27.
Strigidae
Ninox burhani
Indrawan, M. & Somadikarta, S. (2004). A new hawk-owl from the Togian Islands, Gulf of Tomini, central Sulawesi, Indonesia. Bulletin of the British Ornithologists' Club , 124 : 160-171.
Strigidae
Otus thilohoffmanni
Warakagoda, D. H. & Rasmussen, P. C. (2004). A new species of scops-owl from Sri Lanka. Bulletin of the British Ornithologists' Club , 124 (2): 85-105.
Strigidae
Strix butleri
Strix hadorami
Kirwan, G.M., Schweizer, M. & Copete, J.L. (2015). Multiple lines of evidence confirm that Hume's Owl Strix butleri (A. O. Hume, 1878) is two species, with description of an unnamed species (Aves: Non- Passeriformes: Strigidae) . Zootaxa.
3904
(1): 28–50.
REPTILIA
CROCODYLIA &
RHYNCHOCEPHALIA
Crocodylia & Rhynchocephalia except for the taxa listed below
Wermuth, H. & Mertens, R. (1996) (reprint). Schildkröte, Krokodile, Brückenechsen . xvii + 506 pp. Jena (Gustav Fischer Verlag).
Crocodylidae
Crocodylus johnstoni
Tucker, A. D. (2010). The correct name to be applied to the Australian freshwater crocodile, Crocodylus johnstoni [Krefft, 1873]. Australian Zoologist , 35 (2): 432-434.
Sphenodontidae
Sphenodon spp.
Hay, J. M., Sarre, S. D., Lambert, D. M., Allendorf, F. W. & Daugherty, C. H. (2010). Genetic diversity and taxonomy: a reassessment of species designation in tuatara ( Sphenodon : Reptilia). Conservation Genetics , 11 (93): 1063-1081.
SAURIA
For delimitation of families within the Sauria
Pough, F. H., Andrews, R. M., Cadle, J. E., Crump, M. L., Savitzky, A. H. & Wells, K. D. (1998). Herpetology. Upper Saddle River/New Jersey (Prentice Hall).
Agamidae
Ceratophora spp.
Cophotis spp.
Lyriocephalus spp.
Uetz, P., Freed, P., Aguilar, R. & Hosek, J. (eds.) (eds.) (2022). Taxonomic Checklist of Reptile taxa included in the Appendices at the 18th Meeting of the Conference of the Parties (Geneva, August 2019). Species information extracted from The Reptile Database: an online Reference, version of 2 May 2020, accessed 5 May 2020 for species in the Families Agamidae, Gekkonidae and Viperidae https://cites.org/sites/default/files/eng/resources/checklists/Checklist_Reptiles_Added_CoP18lr_CITES . pdf
Agamidae
Saara spp.
Uromastyx spp.
Wilms, T. M., Böhme, W., Wagner, P., Lutzmann, N. & Schmitz, A. (2009). On the phylogeny and taxonomy of the genus Uromastyx Merrem, 1820 (Reptilia: Squamata: Agamidae: Uromastycinae) – resurrection of the genus Saara Gray, 1845. Bonner zool. Beiträge , 56 (1-2): 55-99.
Anguidae
Abronia spp.
UETZ, P., FREED, P. & HŎSEK, J. (eds.) (2016). Taxonomic checklist of the species of the genus Abronia. Species information extracted from “The Reptile Database”, version of 15 August 2016, accessed 11 May 2017. See Annex 2 of AC29 Doc.35. at https://cites.org/sites/default/files/eng/com/ac/29/E-AC29-35-A2.pdf
Anguidae
Abronia morenica
Clause, A.G., Luna-Reyes, R. & Nieto-Montes de Oca, A. (2020): A New Species of Abronia (Squamata: Anguidae) from a Protected Area in Chiapas, Mexico. Herpetologica 76(3): 330-343. https://doi.org/10.1655/Herpetologica-D-19-00047
Chamaeleonidae
Chamaleonidae spp. except the taxa mentioned below
Glaw, F. (2015). Taxonomic checklist of chamaeleons (Squamata: Chamaeleonidae). Vertebrate Zoology , 65 (2): 167-246.
(http://www.senckenberg.de/files/content/forschung/publikationen/vertebratezoology/vz65-
2/01_vertebrate_zoology_65-2_glaw_167-246.pdf )
Chamaeleonidae
Brookesia antakarana (incl. B
.
ambreensis )
SCHERZ, M. D., GLAW, F., RAKOTOARISON, A., WAGLER, M. & VENCES, M. (2018): Polymorphism and synonymy of Brookesia antakarana and B. ambreensis , leaf chameleons from Montagne d’Ambre in north Madagascar. Salamandra 54 (4): 259-268
Chamaeleonidae
Calumma gehringi
PRÖTZEL, D., VENCES, M., SCHERZ, M. D., VIEITES, D. R. & GLAW, F. (2017): Splitting and lumping: An integrative taxonomic assessment of Malagasy chameleons in the Calumma guibei complex results in the new species C. gehringi sp. nov. - Vertebrate Zoology 67 (2): 231–249.
Chamaeleonidae
Calumma juliae
Calumma lefona
Calumma uetzi
PRÖTZEL, D., HAWLITSCHEK, O., SCHERZ, M. D., RATSOAVINA. F. M. & GLAW, F. (2018): Endangered beauties: micro-CT cranial osteology, molecular genetics and external morphology reveal three new species of chameleons in the Calumma boettgeri complex (Squamata: Chamaeleonidae). Zoological Journal of the Linnean Society zlx112, DOI: 10.1093/zoolinnean/zlx112
Chamaeleonidae
Calumma roaloko
PRÖTZEL, D., LAMBERT, S. M., ANDRIANOSOLO, G. T., HUTTER, C. R., COBB, K. A., SCHERZ, M. D. & GLAW, F. (2018): The smallest ‘true chameleon’ from Madagascar: a new, distinctly colored species of the Calumma boettgeri complex (Squamata, Chamaeleonidae). - Zoosystematics and Evolution 94 (2): 409-423
Chamaeleonidae
Kinyongia itombwensis
Kinyongia rugegensis
Kinyongia tolleyae
HUGHES, D. F., KUSAMBA, C., BEHANGANA, M. & GREENBAUM, E. (2017): Integrative taxonomy of the Central African forest chameleon, Kinyongia adolfifriderici (Sauria: Chamaeleonidae), reveals underestimated species diversity in the Albertine Rift. - Zoological Journal of the Linnean Society 181 (2): 400–438.
Chamaeleonidae
Kinyongia msuyae
MENEGON, M., LOADER, S. P., DAVENPORT, T. R. B., HOWELL, K. M, TILBURY, C. R., MACHAGA, S. & TOLLEY, K.A. (2015): A new species of chameleon (Sauria: Chamaeleonidae: Kinyongia ) highlights the biological affinities between the Southern Highlands and Eastern Arc Mountains of Tanzania. - Acta Herpetologica 10 (2): 111-120.
Cordylidae
Cordylidae spp. except the taxa mentioned below
Stanley, E. L., Bauer, A. M., Jackman, T. R., Branch, W. R. & P. le F. N. (2011). Between a rock and a hard polytomy: rapid radiation in the rupicolous girdled lizards (Squamata: Cordylidae). Molecular Phylogenetics and Evolution , 58 (1): 53-70.
Cordylidae
Cordylus marunguensis
Greenbaum, E., Stanley, E. L., Kusamba, C., Moninga, W. M., Goldberg, S. R. & Cha (2012). A new species of Cordylus (Squamata: Cordylidae) from the Marungu Plateau of south-eastern Democratic Republic of the Congo. African Journal of Herpetology , 61 (1): 14-39.
Cordylidae
Cordylus namakuiyus
STANLEY, E. L., CERÍACO, L. M. P., BANDEIRA, S., VALERIO, H., BATES, M. F. & BRANCH, W. R. (2016): A review of Cordylus machadoi (Squamata: Cordylidae) in southwestern Angola, with the description of a new species from the Pro-Namib desert. - Zootaxa 4061 (3): 201–226.
Eublepharidae
Goniurosaurus spp.
UETZ, P., FREED, P., AGUILAR, R., & HÖSEK, J. (eds.) (2022): Taxonomic Checklist of Reptile taxa included in the Appendices at the 18th Meeting of the Conference of the Parties (Geneva, August 2019). Species information extracted from The Reptile Database: an online Reference, version of 20 March 2022, accessed 5 May 2022 for species in the Family Eublepharidae. https://cites.org/sites/default/files/eng/resources/checklists/Checklist_Reptiles_Added_CoP18lr_CITES . pdf
Gekkonidae
Cnemaspis psychedelica
Grismer, L. L., Ngo, V. T. & Grismer, J. L. (2010). A colorful new species of insular rock gecko ( Cnemaspis Strauch 1887) from southern Vietnam. Zootaxa , 58 : 46–58.
Gekkonidae
Dactylonemis spp.
Hoplodactylus spp.
Mokopirirakau spp.
Nielsen, S. V., Bauer, A. M., Jackman, T. R., Hitchmough, R. A. & Daugherty, C. H. (2011). New Zealand geckos (Diplodactylidae): Cryptic diversity in a post-Gondwanan lineage with trans-Tasman affinities. Molecular Phylogenetics and Evolution , 59 (1): 1-22.
Gekkonidae
Gekko gecko (incl. Gekko reevesii )
UETZ, P., FREED, P., AGUILAR, R., & HÖSEK, J. (eds.) (2022): Taxonomic Checklist of Reptile taxa included in the Appendices at the 18th Meeting of the Conference of the Parties (Geneva, August 2019). Species information extracted from The Reptile Database: an online Reference, version of 2 May 2020 accessed 5 May 2020 for species in the Families Agamidae, Gekkonidae and Viperidae. https://cites.org/sites/default/files/eng/resources/checklists/Checklist_Reptiles_Added_CoP18lr_CITES . pdf
Gekkonidae
Gonatodes daudini
POWELL, R., & R.W. HENDERSON. 2005. A new species of Gonatodes (Squamata: Gekkonidae) from the West Indies. Carib. J. Sci. 41 (4): 709-715
Gekkonidae
Lygodactylus williamsi
Species information extracted from UETZ, P., FREED, P. & HŎSEK, J. (eds.) (2016). The Reptile Database, version of 15 August 2016, accessed 11 May 2017. See Annex 2 of AC29 Doc.35 at https://cites.org/sites/default/files/eng/com/ac/29/E-AC29-35-A2.pdf
Gekkonidae
Nactus serpensinsula
Kluge, A.G. (1983). Cladistic relationships among gekkonid lizards. Copeia, 2 : 465-475.
Gekkonidae
Naultinus spp.
Nielsen, S. V., Bauer, A. M., Jackman, T. R., Hitchmough, R. A. & Daugherty, C. H. (2011). New Zealand geckos (Diplodactylidae): Cryptic diversity in a post-Gondwanan lineage with trans-Tasman affinities. Molecular Phylogenetics and Evolution , 59 (1): 1-22.
Gekkonidae
Paroedura androyensis
UETZ, P., FREED, P., AGUILAR, R., & HÖSEK, J. (eds.) (2022): Taxonomic Checklist of Reptile taxa included in the Appendices at the 18th Meeting of the Conference of the Parties (Geneva, August 2019). Species information extracted from The Reptile Database: an online Reference, version of 2 May 2020 accessed 5 May 2020 for species in the Families Agamidae, Gekkonidae and Viperidae. https://cites.org/sites/default/files/eng/resources/checklists/Checklist_Reptiles_Added_CoP18lr_CITES . pdf
Gekkonidae
Paroedura masobe
Nussbaum, R.A. & Raxworthy, C.J. (1994). A new rainforest gecko of the genus Paroedura Günther from Madagascar. Herpetological Natural History , 2 (1): 43-49.
Gekkonidae
Phelsuma spp.
Rhoptropella spp.
Glaw, F. & Rösler, H. (2015). Taxonomic checklist of the day geckos of the genera Phelsuma Gray, 1825 and Rhoptropella Hewitt, 1937 (Squamata: Gekkonidae). Vertebrate Zoology , 65 (2): 167-246.
Gekkonidae
Toropuku spp.
Tukutuku spp.
Woodworthia spp.
Nielsen, S. V., Bauer, A. M., Jackman, T. R., Hitchmough, R. A. & Daugherty, C. H. (2011). New Zealand geckos (Diplodactylidae): Cryptic diversity in a post-Gondwanan lineage with trans-Tasman affinities. Molecular Phylogenetics and Evolution , 59 (1): 1-22.
Gekkonidae
Uroplatus spp. except for the taxa mentioned below
Raxworthy, C.J. (2003). Introduction to the reptiles. In: Goodman, S.M. & Bernstead, J.P. (eds.), The natural history of Madagascar : 934-949. Chicago.
Gekkonidae
Uroplatus fiera
RATSOAVINA, F. M., RANJANAHARISOA, F. A., GLAW, F., RASELIMANANA, A. P., MIRALLES, A. & VENCES, M. (2015): A new leaf-tailed gecko of the Uroplatus ebenaui group (Squamata: Gekkonidae) from Madagascar's central eastern rainforests. – Zootaxa 4006 (1): 143-160.
Gekkonidae
Uroplatus fotsivava
Uroplatus kelirambo
RATSOAVINA, F. M., GEHRING, P.-S., SCHERZ, M. D., VIEITES, D. R., GLAW, F. & VENCES, M. (2017): Two new species of leaf-tailed geckos ( Uroplatus ) from the Tsaratanana mountain massif in northern Madagascar. Zootaxa 4347 (3): 446-464.
Gekkonidae
Uroplatus finiavana
Ratsoavina, F. M., Louis jr., E. E., Crottini, A., Randrianiaina, R. -D., Glaw, F. & Vences, M. (2011). A new leaf tailed gecko species from northern Madagascar with a preliminary assessment of molecular and morphological variability in the Uroplatus ebenaui group. Zootaxa , 3022 : 39-57.
Gekkonidae
Uroplatus giganteus
Glaw, F., Kosuch, J., Henkel, W. F., Sound, P. & Böhme, W. (2006). Genetic and morphological variation of the leaf-tailed gecko Uroplatus fimbriatus from Madagascar, with description of a new giant species. Salamandra , 42 : 129-144.
Gekkonidae
Uroplatus pietschmanni
Böhle, A. & Schönecker, P. (2003). Eine neue Art der Gattung Uroplatus Duméril, 1805 aus Ost-Madagaskar (Reptilia: Squamata: Gekkonidae). Salamandra , 39 (3/4): 129-138.
Gekkonidae
Uroplatus sameiti
Raxworthy, C. J., Pearson, R. G., Zimkus, B. M., Reddy, S., Deo, A. J., Nussbaum, R. A. & Ingram, C. M. (2008). Continental speciation in the tropics: contrasting biogeographic patterns of divergence in the Uroplatus leaf-tailed gecko radiation of Madagascar. Journal of Zoology , 275 : 423–440.
Iguanidae
Iguanidae spp. except for the taxa mentioned below
Hollingsworth, B. D. (2004). The Evolution of Iguanas: An Overview of Relationships and a Checklist of Species. In: Iguanas: Biology and Conservation (Alberts, A. C., Carter, R. L., Hayes, W. K. & Martins, E. P., Eds): 19-44.. Berkeley (University of California Press).
Iguanidae
Brachylophus bulabula
Keogh, J. S., Edwards, D. L., Fisher, R. N. & Harlow, P. S. (2008). Molecular and morphological analysis of the critically endangered Fijian iguanas reveals cryptic diversity and a complex biogeographic history. Philosophical Transactions of the Royal Society B , 363 (1508): 3413-3426.
Iguanidae
Brachylophus gau
FISHER, R. N., NIUKULA, J., WATLING, D. & HARLOW, P. S. (2017): A new species of iguana Brachylophus Cuvier 1829 (Sauria: Iguania: Iguanidae) from Gau Island, Fiji Islands. Zootaxa 4273(3): 407–422.
Iguanidae
Conolophus marthae
Gentile, G. & Snell, H. (2009). Conolophus marthae sp. nov. (Squamata, Iguanidae), a new species of land iguana from the Galápagos archipelago. Zootaxa , 2201 : 1-10.
Iguanidae
Ctenosaura spp.
Iguana Taxonomy Working Group (2016). A checklist of the iguanas of the world (Iguanidae; Iguaninae). In: Iguanas: Biology, Systematics, and Conservation (J. B. Iverson, T.D. Grant, C .R. Knapp, and S. A. Pasachnik, Eds.): 4–46. Herpetological Conservation and Biology 11(Monograph 6).
Iguanidae
Cyclura lewisi
Burton, F. J. (2004). Revision to Species Cyclura nubila lewisi , the Grand Cayman Blue Iguana. Caribbean Journal of Science , 40 (2): 198-203.
Iguanidae
Phrynosoma blainvillii
Phrynosoma cerroense
Phrynosoma wigginsi
Montanucci, R.R. (2004). Geographic variation in Phrynosoma coronatum (Lacertilia, Phrynosomatidae): further evidence for a peninsular archipelago. Herpetologica , 60 : 117.
Lanthanotidae
Lanthanotidae spp.
UETZ, P., FREED, P. & HŎSEK, J. (eds.) (2016). Family, genus and species information extracted from the Integrated Taxonomic Information Service (ITIS), an online reference; and species information extracted from The Reptile Database , version of 15 August 2016, accessed 11 May 2017. See Annex 2 of AC29 Doc.35 at https://cites.org/sites/default/files/eng/com/ac/29/E-AC29-35-A2.pdf
Teiidae
Teiidae spp. except for the taxa mentioned below
Harvey, M. B., Ugueto, G. N. & Gutberlet, R. L. Jr. (2012). Review of teiid morphology with a revised taxonomy and phylogeny of the Teiidae (Lepidosauria: Squamata). Zootaxa , 3459 : 1–156.
Teiidae
Tupinambis cryptus
Tupinambis cuzcoensis
Tupinambis zuliensis
MURPHY, J.C., JOWERS, M.J., LEHTINEN, R.M., CHARLES, S.P., COLLI, G.R., PERES, A.K. JR, HENDRY, C.R. & PYRON, R.A. (2016): Cryptic, sympatric diversity in tegu lizards of the Tupinambis teguixin group (Squamata, Sauria, Teiidae) and the description of three new species. - PLoS ONE 11(8): e0158542.doi:10.1371/journal.pone.0158542.
Varanidae
Varanidae spp. except for the taxa mentioned below
Böhme, W. (2003). Checklist of the living monitor lizards of the world (family Varanidae) Zoologische Verhandelingen , Leiden , 341 : 1-43.
in combination with
Koch, A., Auliya, M. & Ziegler, T. (2010.: Updated Checklist of the living monitor lizards of the world (Squamata: Varanidae). - Bonn zoological Bulletin, 57 (2): 127-136.
Varanidae
Varanus bangonorum
Varanus dalubhasa
Varanus samarensis
Welton, L. J., Travers, S. L., Siler, C. D. & Brown, R. M. (2014). Integrative taxonomy and phylogeny-based species delimitation of Philippine water monitor lizards ( Varanus salvator complex) with descriptions of two new cryptic species. Zootaxa , 3881 (3): 201–227.
Varanidae
Varanus douarrha
Varanus indicus
WEIJOLA, V., KRAUS, F., VAHTERA, V., LINDQVIST, C. & DONNELLAN, S.C. (2017): Reinstatement of Varanus douarrha Lesson, 1830 as a valid species with comments on the zoogeography of monitor lizards (Squamata: Varanidae) in the Bismarck Archipelago, Papua New Guinea. - Australian Journal of Zoology, doi: 10.1071/ZO16038.
Varanidae
Varanus semotus
WEIJOLA, V., DONNELLAN, S.C. & LINDQVIST, C. (2016): A new blue-tailed monitor lizard (Reptilia, Squamata, Varanus ) of the Varanus indicus group from Mussau Island, Papua New Guinea. - ZooKeys 568 : 129- 154, doi: 10.3897/zookeys.568.6872.
Varanidae
Varanus hamersleyensis
Maryan, B., Oliver, P. M., Fitch, A. J. & O’Connell, M. (2014). Molecular and morphological assessment of Varanus pilbarensis (Squamata: Varanidae), with a description of a new species from the southern Pilbara, Western Australia. Zootaxa , 3768 (2): 139–158.
Varanidae
Varanus nesterovi
Böhme, W., Ehrlich, K., Milto, K. D., Orlov, N. & Scholz, S. (2015). A new species of desert monitor lizard (Varanidae: Varanus : Psammosaurus ) from the western Zagros region (Iraq, Iran). Russian Journal of Herpetology , 22 (1): 41-52.
Varanidae
Varanus sparnus
Doughty, P., Kealley, L., Fitch, A. & Donnellan, S. C. (2014). A new diminutive species of Varanus from the Dampier Peninsula, western Kimberley region, Western Australia. Records of the Western Australian Museum , 29 : 128–140.
SERPENTES
Loxocemidae spp.
Pythonidae spp.
Boidae spp.
Bolyeriidae spp.
Tropidophiidae spp.
Viperidae spp.
except for the retention of the genera Acrantophis, Sanzinia, Calabaria, Lichanura,
and except for the species mentioned below
McDiarmid, R. W., Campbell, J. A. & Touré, T. A. (1999). Snake Species of the World. A Taxonomic and Geographic Reference. Volume 1 , Washington, D.C. (The Herpetologists’ League).
Boidae
Candoia paulsoni
Candoia superciliosa
Smith, H. M., Chiszar, D., Tepedelen, K. & van Breukelen, F. (2001). A revision of the bevelnosed boas ( Candoia carinata complex) (Reptilia: Serpentes). Hamadryad , 26 (2): 283-315.
Boidae
Corallus batesii
Henderson, R. W., Passos, P. & Feitosa, D. (2009). Geographic variation in the Emerald Treeboa, Corallus caninus (Squamata: Boidae). Copeia , 2009 (3): 572-582.
Boidae
Epicrates crassus
Epicrates assisi
Epicrates alvarezi
Passos, P. & Fernandes, R. (2008). Revision of the Epicrates cenchria complex (Serpentes: Boidae). Herpetological Monographs , 22 : 1-30.
Boidae
Epicrates cenchria
Epicrates maurus
Chilabothrus spp.
REYNOLDS, R.G., NIEMILLER, M.L., HEDGES, S.B., DORNBURG, A., PUENTE-ROLÓN, A.R., & REVELL, L.J. (2013): Molecular phylogeny and historical biogeography of West Indian boid snakes ( Chilabothrus ). Molecular Phylogenetics and Evolution 68(3):461-470. doi:10.1016/j.ympev.2013.04.02
Boidae
Eryx borrii
Lanza, B. & Nistri, A. (2005). Somali Boidae (genus Eryx Daudin 1803) and Pythonidae (genus Python Daudin 1803) (Reptilia Serpentes). Tropical Zoology , 18 (1): 67-136.
Boidae
Eunectes beniensis
Dirksen, L. (2002). Anakondas . NTV Wissenschaft.
Colubridae
Xenochrophis piscator
Xenochrophis schnurrenbergeri
Xenochrophis tytleri
Vogel, G. & David, P. (2012). A revision of the species group of Xenochrophis piscator (Schneider, 1799) (Squamata: Natricidae). Zootaxa , 3473 : 1-60.
Elapidae
Micrurus ruatanus
McCranie, J. R. (2015). A checklist of the amphibians and reptiles of Honduras, with additions, comments on taxonomy, some recent taxonomic decisions, and areas of further studies needed. Zootaxa , 3931 (3): 352–386.
Elapidae
Naja atra
Naja kaouthia
Wüster, W. (1996). Taxonomic change and toxinology: systematic revisions of the Asiatic cobras ( Naja naja species complex). Toxicon , 34 : 339-406.
Elapidae
Naja mandalayensis
Slowinski, J. B. & Wüster, W. (2000). A new cobra (Elapidae: Naja) from Myanmar (Burma). Herpetologica , 56 : 257-270.
Elapidae
Naja oxiana
Naja philippinensis
Naja sagittifera
Naja samarensis
Naja siamensis
Naja sputatrix
Naja sumatrana
Wüster, W. (1996). Taxonomic change and toxinology: systematic revisions of the Asiatic cobras ( Naja naja species complex). Toxicon , 34 : 339-406.
Pythonidae
Leiopython bennettorum
Leiopython biakensis
Leiopython fredparkeri
Leiopython huonensis
Leiopython hoserae
Schleip, W. D. (2008). Revision of the genus Leiopython Hubrecht 1879 (Serpentes: Pythonidae) with the redescription of taxa recently described by Hoser (2000) and the description of new species. Journal of Herpetology , 42 (4): 645–667.
Pythonidae
Malayopython reticulatus
Malayopython timoriensis
REYNOLDS, R.G., NIEMILLER, M.L, AND REVELL, L.J. (2014): Toward a Tree-of-Life for the boas and pythons: Multilocus species-level phylogeny with unprecedented taxon sampling. Molecular Phylogenetics and Evolution 71: 201–213.
Pythonidae
Morelia clastolepis
Morelia kinghorni
Morelia nauta
Morelia tracyae
Harvey, M. B., Barker, D. B., Ammerman, L. K. & Chippindale, P. T. (2000). Systematics of pythons of the Morelia amethistina complex (Serpentes: Boidae) with the description of three new species. Herpetological Monographs , 14 : 139-185.
Pythonidae
Python bivittatus
Python molurus
Jacobs, H. J., Auliya, M. & Böhme, W. (2009). Zur Taxonomie des Dunklen Tigerpythons, Python molurus bivittatus KUHL, 1820, speziell der Population von Sulawesi. Sauria , 31 : 5-16.
Pythonidae
Python breitensteini
Python brongersmai
Keogh, J. S., Barker, D. G. & Shine, R. (2001). Heavily exploited but poorly known: systematics and biogeography of commercially harvested pythons ( Python curtus group) in Southeast Asia. Biological Journal of the Linnean Society , 73 : 113-129.
Pythonidae
Python kyaiktiyo
Zug, G.R., Grotte, S. W. & Jacobs, J. F. (2011). Pythons in Burma: Short-tailed python (Reptilia: Squamata). Proceedings of the biological Society of Washington , 124 (2): 112-136.
Pythonidae
Python natalensis
Broadley, D. G. (1999). The southern African python, Python natalensis A. Smith 1840, is a valid species. African Herp News , 29 : 31-32.
Tropidophiidae
Tropidophis spp. except for the taxa mentioned below
Hedges, S.B. (2002). Morphological variation and the definition of species in the snake genus Tropidophis (Serpentes, Tropidophiidae). Bulletin of the Natural History Museum, London (Zoology) , 68 (2): 83-90.
Tropidophiidae
Tropidophis celiae
Hedges, B. S., Estrada, A. R. & Diaz, L. M. (1999): New snake ( Tropidophis ) from western Cuba. Copeia , 1999 (2): 376-381.
Tropidophiidae
Tropidophis grapiuna
Curcio, F. F., Sales Nunes, P. M., Suzart Argolo, A. J., Skuk, G. & Rodrigues, M. T. (2012). Taxonomy of the South American dwarf boas of the genus Tropidophis Bibron, 1840, with the description of two new species from the Atlantic forest (Serpentes: Tropidophiidae). Herpetological Monographs , 26 (1): 80-121.
Tropidophiidae
Tropidophis hendersoni
Hedges, B. S. & Garrido, O. (2002). A new snake of the genus Tropidophis (Tropidophiidae) from Eastern Cuba Journal of Herpetology , 36 :157-161.
Tropidophiidae
Tropidophis morenoi
Hedges, B. S., Garrido, O. & Diaz, L. M. (2001). A new banded snake of the genus Tropidophis (Tropidophiidae) from north-central Cuba. Journal of Herpetology , 35 : 615-617.
Tropidophiidae
Tropidophis preciosus
Curcio, F. F., Sales Nunes, P. M., Suzart Argolo, A. J., Skuk, G. & Rodrigues, M. T. (2012). Taxonomy of the South American dwarf boas of the genus Tropidophis Bibron, 1840, with the description of two new species from the Atlantic forest (Serpentes: Tropidophiidae). Herpetological Monographs , 26 (1): 80-121.
Tropidophiidae
Tropidophis spiritus
Hedges, B. S. & Garrido, O. (1999). A new snake of the genus Tropidophis (Tropidophiidae) from central Cuba. Journal of Herpetology , 33 : 436-441.
Tropidophiidae
Tropidophis xanthogaster
Domínguez, M., Moreno, L. V. & Hedges, S. B. (2006). A new snake of the genus Tropidophis (Tropidophiidae) from the Guanahacabibes Peninsula of Western Cuba. Amphibia-Reptilia , 27 (3): 427-432.
Viperidae
Atheris desaixi
Bitis worthingtoni
UETZ, P., FREED, P. & HŎSEK, J. (eds.) (2016). Species information extracted from The Reptile Database , version of 15 August 2016, accessed 11 May 2017. See Annex 2 of AC29 Doc.35 at https://cites.org/sites/default/files/eng/com/ac/29/E-AC29-35-A2.pdf
Viperidae
Montivipera wagneri
GARRIGUES, T., DAUGA, C., FERQUEL, E., VALÉRIE CHOUMET, V., & FAILLOUX, A-B. (2005): Molecular
phylogeny of Vipera Laurenti, 1768 and the related genera Macrovipera (Reuss, 1927) and Daboia (Gray, 1842), with comments about neurotoxic Vipera aspis aspis populations. Molecular Phylogenetics and Evolution 35(1): 35-47.
Viperidae
Protobothrops mangshanensis
SNETKOV, P.B. & ORLOV, N.L. (2017) Phylogenetic Analysis of Old World Viperid Snakes (Serpentes, Viperidae) Based on Skeletal Morphology. Russian Journal of Herpetology , 24(1):22-34.
Viperidae
Pseudocerastes urarachnoides
UETZ, P., FREED, P., AGUILAR, R., & HÖSEK, J. (eds.) (2022): Taxonomic Checklist of Reptile taxa included in the Appendices at the 18th Meeting of the Conference of the Parties (Geneva, August 2019). Species information extracted from The Reptile Database. https://cites.org/sites/default/files/eng/resources/checklists/Checklist_Reptiles_Added_CoP18lr_CITE S.pdf
TESTUDINES
Testudines order names
Wermuth, H. & Mertens, R. (1996) (reprint). Schildkröte, Krokodile, Brückenechsen . xvii + 506 pp. Jena (Gustav Fischer Verlag).
Species and family names – with the exception of the retention of the following names Mauremys iversoni, Mauremys pritchardi, Ocadia glyphistoma, Ocadia philippeni, Sacalia pseudocellata , and except for the taxa mentioned below
Fritz, U. & Havaš, P. (2007): Checklist of Chelonians of the World. Vertebrate Zoology , 57 (2): 149-368. Dresden. ISSN 1864-5755 [without its appendix]
Emydidae
Graptemys pearlensis
Ennen, J. R., Lovich, J. E., Kreiser, B. R., Selman, W. & Qualls, C. P. (2010). Genetic and morphological variation between populations of the Pascagoula Map Turtle ( Graptemys gibbonsi ) in the Pearl and Pascagoula Rivers with description of a new species. Chelonian Conservation and Biology , 9 (1): 98-113.
Geoemydidae
Batagur affinis
Praschag, P., Sommer, R. S., Mccarthy, C., Gemel, R. & Fritz, U. (2008). Naming one of the world's rarest chelonians, the southern Batagur. Zootaxa , 1758 : 61-68.
Geoemydidae
Batagur borneoensis
Batagur dhongoka
Batagur kachuga
Batagur trivittata
Praschag, P., Hundsdörfer, A. K. & Fritz, U. (2007). Phylogeny and taxonomy of endangered South and South-east Asian freshwater turtles elucidated by mtDNA sequence variation (Testudines: Geoemydidae: Batagur, Callagur, Hardella, Kachuga, Pangshura ). Zoologica Scripta , 36 : 429-442.
Geoemydidae
Cuora bourreti
Cuora picturata
Spinks, P. Q., Thomson, R. C., Zhang, Y.P., Che, J., Wu, Y. & Shaffer, H. B. (2012). Species boundaries and phylogenetic relationships in the critically endangered Asian box turtle genus Cuora . Molecular Phylogenetics and Evolution , 63 : 656–667. doi:10.1016/j.ympev.2012.02.014.
Geoemydidae
Cyclemys enigmatica
Cyclemys fusca
Cyclemys gemeli
Cyclemys oldhamii
Fritz, U., Guicking, D., Auer, M., Sommer, R. S., Wink, M. & Hundsdörfer, A. K. (2008). Diversity of the Southeast Asian leaf turtle genus Cyclemys : how many leaves on its tree of life? Zoologica Scripta , 37 : 367-390.
Geoemydidae
Malayemys khoratensis
IHLOW, F., VAMBERGER, M., FLECKS, M., HARTMANN, T., COTA, M., MAKCHAI, S., MEEWATTANA, P., DAWSON, J.E., KHENG, L., RÖDDER, D., & FRITZ, U. (2016). Integrative taxonomy of Southeast Asian snail-eating turtles (Geoemydidae: Malayemys ) reveals a new species and mitochondrial introgression. PLoS ONE 11(4): e0153108:1-26.
Geoemydidae
Mauremys reevesii
Barth, D., Bernhard, D., Fritzsch, G. & U. Fritz (2004). The freshwater turtle genus Mauremys (Testudines, Geoemydidae) – a textbook example of an east-west disjunction or a taxonomic misconcept? Zoologica Scripta , 33 : 213-221.
Testudinidae
Centrochelys sulcata
Turtle Taxonomy Working Group [van Dijk, P. P., Iverson, J. B., Rhodin, A. G. J., Shaffer, H. B. & Bour, R. ]. (2014): Turtles of the world, 7 TH edition: Annotated checklist of taxonomy, synonymy, distribution with maps, and conservation status. 000.v7. Chelonian Research Monographs , 5 doi: 10.3854/crm.5.000.checklist.v7.2014.
Testudinidae
Chelonoidis carbonarius
Chelonoidis denticulatus
Chelonoidis niger
Olson, S .L. & David, N. (2014). The gender of the tortoise genus Chelonoidis Fitzinger, 1835 (Testudines: Testudinidae). - Proceedings of the Biological Society of Washington, 126 (4): 393-394.
Testudinidae
Chersobius spp.
HOFMEYR, M.D., & BRANCH, W.R. (2018). The padloper’s tortuous path (Chelonia: Testudinidae): Two genera, not one. African Journal of Herpetology , 2018:1-15. https://doi.org/10.1080/21564574.2017.1398187
Testudinidae
Gopherus evgoodei
Gopherus morafkai
Murphy, R. W., Berry, K. H., Edwards, T., Leviton, A. E., Lathrop, A. & Riedle, J. D. (2011). The dazed and confused identity of Agassiz’s land tortoise, Gopherus agassizii (Testudines, Testudinidae) with the description of a new species, and its consequences for conservation. Zookeys , 113 : 39-71.
Testudinidae
Kinixys nogueyi
Kinixys zombensis
Kindler, C., Branch, W. R., Hofmeyr, M. D., Maran, J., Široký, P., Vences, M., Harvey, J., Hauswaldt, J. S., Schleicher, A., Stuckas, H. & Fritz, U. (2012). Molecular phylogeny of African hinge-back tortoises ( Kinixys ): implications for phylogeography and taxonomy (Testudines: Testudinidae). Journal of Zoological Systematics and Evolutionary Research , 50 : 192–201.
Trionychidae
Lissemys ceylonensis
Praschag, P., Stuckas, H., Päckert, M., Maran, J. & Fritz, U. (2011). Mitochondrial DNA sequences suggest a revised taxonomy of Asian flapshell turtles ( Lissemys Smith, 1931) and the validity of previously unrecognized taxa (Testudines: Trionychidae). Vertebrate Zoology , 61 (1): 147-160.
Trionychidae
Nilssonia gangeticus
Nilssonia hurum
Nilssonia leithii
Nilssonia nigricans
Praschag, P., Hundsdörfer, A.K., Reza, A.H.M.A. & Fritz, U. (2007). Genetic evidence for wild-living Aspideretes nigricans and a molecular phylogeny of South Asian softshell turtles (Reptilia: Trionychidae: Aspideretes, Nilssonia ). Zoologica Scripta , 36 :301-310.
AMPHIBIA
Amphibia spp. except for the taxa listed below
Frost, D. R. (ed.) (2015). Taxonomic Checklist of Amphibian Species listed in the CITES Appendices and the Annexes of EC Regulation 338/97. Species information extracted from Amphibian Species of the World: a taxonomic and geographic reference , an online reference, version 6.0 as of May2015 with additional comments by the Nomenclature Specialist of the CITES Animals Committee. See Annex 5 of CoP17 Doc. 81.1 at
https://cites.org/sites/default/files/eng/cop/17/WorkingDocs/E-CoP17-81-01-A5.pdf
Anura: Microhylidae:
Dyscophus spp. and Scaphiophryne spp.;
Telmatobiidae:
Telmatobius culeus
FROST, D. R. (ed.) (2017). Species information extracted from Amphibian Species of the World: a taxonomic and geographic reference , an online reference, version 6.0, accessed 12 May 2017. See Annex 3 of AC29 Doc.35 at https://cites.org/sites/default/files/eng/com/ac/29/E-AC29-35-A3.pdf
Bufonidae
Sclerophrys channingi
Sclerophrys superciliaris
OHLER, A., & DUBOIS, A. (2016): The identity of the South African toad Sclerophrys capensis Tschudi, 1838 (Amphibia, Anura). PeerJ 4(e1553): 1–13.
Dendrobatidae
Ameerega munduruku
NEVES, M.DE O., DA SILVA, L.A., AKIEDA, P.S., CABRERA, R., KOROIVA, R., & SANTANA, D.J. (2017): A new species of poison frog, genus Ameerega (Anura: Dendrobatidae), from the southern Amazonian rain forest. Salamandra 53(4): 485–493.
Dendrobatidae
Ameerega shihuemoy
Serrano-Rojas, S.J., Whitworth, A., Villacampa-Ortega, J., von May, R., Gutiérrez, R.C., Padial, J.M., & CHAPARRO, J.C. (2017): A new species of poison-dart frog (Anura: Dendrobatidae) from Manu province, Amazon region of southeastern Peru, with notes on its natural history, bioacoustics, phylogenetics, and recommended conservation status. Zootaxa 4221(1): 71–94.
Dendrobatidae
Andinobates victimatus
Márquez, R., Mejía-Vargas, D., Palacios-Rodríguez, P., Ramírez-Castañeda, V., & Amézquita, A.
(2017): A new species of Andinobates (Anura: Dendrobatidae) from the Urabá region of Colombia. Zootaxa 4290(3): 531–546.
Dendrobatidae
Epipedobates maculatus
Paruwrobates andinus
Paruwrobates erythromos
GRANT, T., RADA, M., ANGANOY-CRIOLLO, M. A., BATISTA, A., DOS S. DIAS, P.H., JECKEL, A.M., MACHADO, D.J., & RUEDA-ALMONACID, J.V. (2017): Phylogenetic systematics of dart-poison frogs and their relatives revisited (Anura: Dendrobatoidea). South American Journal of Herpetology 12 (Special Issue): 1–90
Dendrobatidae
Oophaga anchicayensis
Oophaga andresi
Oophaga solanensis
POSSO-TERRANOVA, A. & ANDRÉS, J. (2018): Multivariate species boundaries and conservation of harlequin poison frogs. Molecular Ecology 27: 3432–3451. DOI: 10.1111/mec.14803.
Hylidae
Agalychnis lemur
FROST, D.R. (2021): Amphibian Species of the World: an Online Reference. Version 6.1. doi.org/10.5531/db.vz.0001
Hylidae
Agalychnis terranova
RIVERA-CORREA, M., DUARTE-CUBIDES, F., RUEDA-ALMONACID, J.V., & DAZA-R., J.M. (2013): A new red-eyed treefrog of Agalychnis (Anura: Hylidae: Phyllomedusinae) from middle Magdalena River valley of Colombia with comments on its phylogenetic position. Zootaxa 3636 (1): 85–100.
CAUDATA
Salamandridae
Echinotriton spp.
Paramesotriton spp.
Tylototriton spp.
FROST, D. R. (ed.) (2022). Taxonomic Checklist of Amphibian taxa included in the Appendices at the 18th Meeting of the Conference of the Parties (Geneva, August 2019). Species information extracted from Amphibian Species of the World: an online Reference, Version 6.1, accessed 5 May 2020 for species of the genera Echinotriton and 5 May 2022 for species of the genus Tylototriton . https://cites.org/sites/default/files/eng/resources/checklists/Checklist_Amphibian_Added_CoP18_CITES.pdf
ELASMOBRANCHII, ACTINOPTERI, COELACANTHI, and DIPNEUSTI
All fish species, except the taxa listed below
Eschmeyer, W.N. & Fricke, R. (eds.) (2015). Taxonomic Checklist of Fish species listed in the CITES Appendices and the Annexes of EC Regulation 338/97 (Elasmobranchii, Actinopteri, Coelacanthi, and Dipneusti, except the genus Hippocampus ). Information extracted from Catalog of Fishes , an online reference, version update from 3 February 2015. See Annex 6 of CoP17 Doc. 81.1 at https://cites.org/sites/default/files/eng/cop/17/WorkingDocs/E-CoP17-81-01-A6.pdf
Elasmobranchii: Carcharhiniformes: Carcharhinidae: Carcharhinus falciformis;
Lamniformes : Alopiidae: Alopias spp.;
Myliobatiformes: Myliobatidae: Mobula spp. except the taxa mentioned below;
Potamotrygonidae:
Potamotrygon spp.;
Actinopteri: Perciformes: Pomacanthidae: Holacanthus clarionensis
ESCHMEYER, W. N., FRICKE, R., & VAN DER LAAN, R. (eds.) (2017). Information extracted from Catalog of Fishes: Genera, Species, References , an online reference, version of 28 April 2017, accessed 12 May 2017. See Annex 4 of AC29 Doc.35 at https://cites.org/sites/default/files/eng/com/ac/29/E-AC29-35-A4.pdf
Elasmobranchii: Lamniformes: Lamnidae: Isurus spp.;
Rhinopristiformes: Glaucostegidae: Glaucostegus spp.;
Rhinidae spp.
ESCHMEYER, W.N., R. FRICKE, & R. VAN DER LAAN (eds.) (2019) Taxonomic Checklist of Fish taxa included in the Appendices at the 18th Meeting of the Conference of the Parties. Species information extracted from Catalog of Fishes: Genera, Species, References, an online reference, version of 4 May 2020, accessed 5 May 2020. See Annex 3 of AC31 Doc. 37 at https://cites.org/sites/default/files/eng/com/ac/31/Docs/E-AC31-37-A3.pdf
Mobulidae
Mobula alfredi
Mobula birostris
Mobula hypostoma (incl. M. rochebrunei )
WHITE, W. T. & P. R. LAST. (2016). DEVILRAYS, FAMILY MOBULIDAE. PP. 741-749 IN LAST, P. R., W. T. WHITE, M. R. DE CARVALHO, B. SÉRET, M. F. W. STEHMANN & G. J. P. NAYLOR (EDS.). Rays of the World . CSIRO Publishing, Comstock Publishing Associates. i-ix + 1-790
Rhinobatidae
Rhinobatidae spp.
LAST, P. R., SERET, B., & NAYLOR, G. J. (2016a): A new species of guitarfish, Rhinobatos borneensis sp. nov. with a redefinition of the family-level classification in the order Rhinopristiformes (Chondrichthyes: Batoidea). Zootaxa, 4117(4), 451-475. DOI 10.11646/zootaxa.4117.4.1
Rhinobatidae
Acroteriobatus andysabini
Acroteropbatus stehmanni
WEIGMANN, S., EBERT, D. A., & SÉRET, B. (2021): Resolution of the Acroteriobatus leucospilus species complex, with a redescription of A. leucospilus (Norman, 1926) and descriptions of two new western Indian Ocean species of Acroteriobatus (Rhinopristiformes, Rhinobatidae). Mar. Biodivers., 51(4), 1-30.
Rhinobatidae
Acroteriobatus omanensis
LAST, P. R., HENDERSON, A. C., & NAYLOR, G. J. (2016b): Acroteriobatus omanensis (Batoidea: Rhinobatidae), a new guitarfish from the Gulf of Oman. Zootaxa, 4144(2): 276-286.
Rhinobatidae
Pseudobatos buthi
RUTLEDGE, K. M. (2019): A new guitarfish of the genus Pseudobatos (Batoidea: Rhinobatidae) with key to the guitarfishes of the Gulf of California. Copeia, 107(3): 451-463.
Rhinobatidae
Rhinobatos austini
EBERT, D. A., & GON, O. (2017): Rhinobatos austini n. sp., a new species of guitarfish (Rhinopristiformes: Rhinobatidae) from the southwestern Indian Ocean. Zootaxa, 4276(2), 204-214.
Rhinobatidae
Rhinobatos manai
WHITE, W. T., LAST, P. R., & NAYLOR, G. J. (2016): Rhinobatos manai sp. nov., a new species of guitarfish (Rhinopristiformes: Rhinobatidae) from New Ireland, Papua New Guinea. Zootaxa, 4175(6), 588-600.
Rhinobatidae
Rhinobatos ranongensis
LAST, P.R., SERET, B., & NAYLOR, G.J. (2019): Description of Rhinobatos ranongensis sp. nov. (Rhinopristiformes: Rhinobatidae) from the Andaman Sea and Bay of Bengal with a review of its northern Indian Ocean congeners. Zootaxa, 4576(2), 257–287.
SYNGNATHIFORMES
Syngnathidae
Hippocampus spp. except the taxa listed below
Lourie, S. A., Pollom, R. A. and Foster, S. J. (2016). A global revision of the Seahorses Hippocampus Rafinesque 1810 (Actinopterygii: Sygnathiformes): Taxonomy and biogeography with recommendations for further research. Zootaxa , 4146 (1): 1-066.
Syngnathidae
Hippocampus casscsio
ZHANG, Y-H., QIN, G., WANG, X., & LIN, Q. (2016): A new species of seahorse (Teleostei: Syngnathidae) from the South China Sea. Zootaxa 4170 (2): 384–392. http://doi.org/10.11646/zootaxa.4170.2.11
Syngnathidae
Hippocampus haema
HAN, S-Y., KIM, J-K., KAI, Y., & SENOU, H. (2017): Seahorses of the Hippocampus coronatus complex: taxonomic revision, and description of Hippocampus haema , a new species from Korea and Japan (Teleostei, Syngnathidae). ZooKeys 712: 113–139. doi: 10.3897/zookeys.712.14955
Syngnathidae
Hippocampus japapigu
SHORT, G., SMITH, R., MOTOMURA, H., HARASTI, D., & HAMILTON, H. (2018): Hippocampus japapigu , a new species of pygmy seahorse from Japan, with a redescription of H. pontohi (Teleostei, Syngnathidae). ZooKeys 779: 27–49. doi: 10.3897/zookeys.779.24799
ARACHNIDA
ARANEAE
Theraphosidae
Aphonopelma pallidum
Brachypelma spp. except for the taxa mentioned below
Platnick, N. (2006). Taxonomic Checklist of CITES listed Spider Species. Information extracted from The World Spider Catalog , an online reference, Version 6.5 as of 7 April 2006. [available at http://www.cites.org/common/docs/Res/12_11/spider_checklist.pdf ]
Theraphosidae
Brachypelma albiceps
Brachypelma smithi
Tliltocatl albopilosum
Tliltocatl epicureanum
Tliltocatl kahlenbergi
Tliltocatl sabulosum
Tliltocatl schroederi
Tliltocatl vagans
Tliltocatl verdezi
MENDOZA, J. & FRANCKE, O. (2019): Systematic revision of Mexican threatened tarantulas Brachypelma (Araneae: Theraphosidae: Theraphosinae), with a description of a new genus, and implications on the conservation. Zoological Journal of the Linnean Society , 2019, XX; 1–66. http://zoobank.orgurn:lsid:zoobank.org:pub:E4D09A17-444F-45A0-95DB-059ECA175569
Theraphosidae
Poecilotheria spp., except the taxa mentioned below
WORLD SPIDER CATALOG. (2020). Taxonomic Checklist of Spider taxa included in the Appendices at the 18th Meeting of the Conference of the Parties. Species information extracted from the World Spider Catalog (2020). Version 21.0. Natural History Museum Bern, online at http://wsc.nmbe.ch, accessed on 5 May 2020. doi: 10.24436/2. See Annex 4 of AC31 Doc. 37 at https://cites.org/sites/default/files/eng/com/ac/31/Docs/E-AC31-37-A4.pdf
Theraphosidae
Poecilotheria srilankensis
NANAYAKKARA, R. P., GANEHIARACHI, G. A. S. M., KUSUMINDA, T., VISHVANATH, N., KARUNARATNE, M. K. & KIRK, P. (2019): A new species of tiger spider in the genus Poecilotheria Pocock, 1899 (Araneae: Theraphosidae) from Belihuloya, Sri Lanka. Journal of the British Tarantula Society 34(3): 3-17
Theraphosidae
Poecilotheria tigrinawesseli
SHERWOOD, D. (2019): Revised taxonomical placement of Poecilotheria chaojii Mirza, Sanap & Bhosale, 2014 (Araneae: Theraphosidae). Arachnology 18(1): 19-21. doi:10.13156/arac.2018.18.1.19
Theraphosidae
Sericopelma angustum
Sericopelma embrithes
GABRIEL, R., & LONGHORN, S.J. 2015. Revised generic placement of Brachypelma embrithes (Chamberlin & Ivie, 1936) and Brachypelma angustum Valerio, 1980, with definition of the taxonomic features for identification of female Sericopelma Ausserer, 1875 (Araneae, Theraphosidae). ZooKeys 526: 75–104.
SCORPIONES
Scorpionidae
Pandinus spp. except for the taxa mentioned below
Lourenço, W. R. & Cloudsley-Thompson, J. C. (1996). Recognition and distribution of the scorpions of the genus Pandinus Thorell, 1876 accorded protection by the Washington Convention. Biogeographica , 72 (3): 133-143.
Scorpionidae
Pandinus camerounensis
Pandinus roeseli
Lourenço, W. R. (2014). Further considerations on the identity and distribution of Pandinus imperator (C. L. Koch, 1841) and description of a new species from Cameroon (Scorpiones: Scorpionidae). Entomologische Mitteilungen aus dem Zoologischen Museum Hamburg , 17 (192): 139-151.
INSECTA
COLEOPTERA
Lucanidae
Colophon spp. except the taxa mentioned below
Bartolozzi, L. (2005). Description of two new stag beetle species from South Africa (Coleoptera: Lucanidae). African Entomology , 13 (2): 347-352.
Lucanidae
Colophon deschodti
Colophon eastmani
Colophon nagaii
Colophon switalae
Colophon struempheri
JACOBS, C.T., SCHOLTZ, C.H., & STRÜMPHER, W.P. 2015. Taxonomy of Colophon Gray (Coleoptera: Lucanidae): new species and a status change. Zootaxa 4057(1): 135–142. Doi 10.11646/zootaxa.4057.1.9
LEPIDOPTERA
Papilionidae
Achillides spp. [only the species of the Philippines]
Page, M. G. P. & Treadaway, C. G. (2004). Papilionidae of the Philippine Island. In: E. Bauer, and T. Frankenbach, Eds.). Butterflies of the world, Supplement 8 . Goecke & Evers, Keltern. 58 pp.
Papilionidae
Ornithoptera spp.
Trogonoptera spp.
Troides spp.
Matsuka, H. (2001). Natural History of Birdwing Butterflies . 367 pp. Tokyo (Matsuka Shuppan).(ISBN 4-9900697-0-6).
HIRUDINOIDEA
ARHYNCHOBDELLIDA
Hirudinidae
Hirudo medicinalis
Hirudo verbana
Nesemann, H. & Neubert, E. (1999). Annelida: Clitellata: Branchiobdellida, Acanthobdellea, Hirudine.. Süßwasserfauna von Mitteleuropa , 6 (2), 178 pp., Berlin (Spektrum Akad. Verlag). ISBN 3-8274-0927-6.
BIVALVIA
VENEROIDA
Tridacnidae
Tridacna lorenzi
Tridacna mbalavuana (incl. T. tevoroa )
Tridacna noae (incl. T. ningaloo )
Tridacna squamosina
WoRMS Editorial Board. 2018. Genus Tridacna .
CEPHALOPODA
Nautilidae
Nautilidae spp.
Family, genus and species information extracted from the Integrated Taxonomic Information Service (ITIS), an online reference. See Annex 5 of AC29 Doc.35 at https://cites.org/sites/default/files/eng/com/ac/29/E-AC29-35-A5.pdf
ANTHOZOA & HYDROZOA
All CITES listed species
Taxonomic Checklist of all CITES listed Coral Species, based on information compiled by UNEP-WCMC 2012.
FLORA
Taxon concerned
Taxonomic reference
AMARYLLIDACEAE, PRIMULACEAE
Cyclamen, Galanthus and Sternbergia
Davis, A.P. et al . (1999). CITES Bulb Checklist , compiled by the Royal Botanic Gardens, Kew, United Kingdom of Great Britain and Northern Ireland) as a guideline when making reference to the names of species of Cyclamen and Galanthus and Sternbergia
APOCYNACEAE
Pachypodium spp.
CITES Aloe and Pachypodium Checklist (U. Eggli et al., 2001, compiled by Städtische Sukkulenten-Sammlung, Zurich, Switzerland, in collaboration with the Royal Botanic Gardens, Kew, United Kingdom of Great Britain and Northern Ireland) and its update: An Update and Supplement to the CITES Aloe & Pachypodium Checklist [J. M. Lüthy (2007), CITES Management Authority of Switzerland, Bern, Switzerland] as a guideline when making reference to the names of species of Aloe and Pachypodium.
Hoodia spp.
Plants of Southern Africa: an annotated checklist. Germishuizen, G. & Meyer N. L. (eds.) (2003). Strelitzia 14: 150-151. National Botanical Institute, Pretoria, South Africa as a guideline when making reference to the names of species of Hoodia.
CACTACEAE
All Cactaceae , except Aztekium valdezii
CITES Cactaceae Checklist third edition (2016, compiled by D. Hunt) as a guideline when making reference to names of species of Cactaceae, and the amendments and updates outlined in A Supplement to the CITES Cactaceae Checklist Third Edition 2016 (Hunt, D. 2018). The checklist and its supplement can be found on the website of the Royal Botanic Gardens, Kew, UK at “ goo.gl/M26yL8 ”.
CACTACEAE
Aztekium valdezii
Marcía, C.G.V., Vázquez, M.A.A. & Montes, S.A. (2013). A new species of Aztekium (Cactaceae) from Nuevo León, Mexico. Xerophilia , Special Issue 2: 3–25. Accessible at: https://cites.org/sites/default/files/eng/com/nc/flora/Aztekium-valdezii_Xerophilia-Special-Issue-No.-2-2013.pdf
CYCADACEAE, STANGERIACEAE and ZAMIACEAE
All Cycadaceae, Stangeriaceae and Zamiaceae.
The World List of Cycads: CITES and Cycads: Checklist 2013 (Roy Osborne, Michael A. Calonje, Ken D. Hill, Leonie Stanberg and Dennis Wm. Stevenson) in CITES and Cycads a user’s guide (Rutherford, C. et al., Royal Botanic Gardens, Kew. UK 2013), as a guideline when making reference to names of species of Cycadaceae, Stangeriaceae and Zamiaceae.
DICKSONIACEAE
Dicksonia species of the Americas.
Dicksonia species of the Americas (2003, compiled by Bonn Botanic Garden and the Federal Agency for Nature Conservation, Bonn, Germany) as a guideline when making reference to the names of species of Dicksonia .
DROSERACEAE, NEPENTHACEAE, SARRACENIACEAE
Dionaea, Nepenthes and Sarracenia.
CITES Carnivorous Plant Checklist (B. von Arx et al ., 2001, Royal Botanic Gardens, Kew, UK) as a guideline when making reference to names of species of Dionaea, Nepenthes and Sarracenia .
EBENACEAE
Diospyros spp. – populations of Madagascar. (large tree species)
Lowry et al. 2022. Large tree species of Diospyros from Madagascar . Catalogue of Plants of Madagascar. http://legacy.tropicos.org/ProjectWebPortal.aspx?pagename=Diospyros_LT&projectid=17.
Accessible at: https://cites.org/sites/default/files/eng/prog/timber/Ebenaceae_Diospyros_spp_populations_of_Madagascar_052022.pdf
EUPHORBIACEAE
Succulent species of Euphorbia.
The CITES Checklist of Succulent Euphorbia Taxa (Euphorbiaceae), Second edition (S. Carter and U. Eggli, 2003, published by the Federal Agency for Nature Conservation, Bonn, Germany) as a guideline when making reference to the names of species of succulent euphorbias.
LEGUMINOSAE
Dalbergia spp.
Cowell C., Williams E., Bullough L.-A., Grey J., Klitgaard B., Govaerts R., Andriambololonera S., Cervantes A., Crameri S., Lima, H.C., Lachenaud O., Li S.-J., Linares J.L., Phillipson P., Rakotonirina N., Wilding N., van der Burgt X., Vatanparast M., Barker A., Barstow M., Beentje H., and Plummer J. 2022. CITES Dalbergia Checklist . Commissioned by the CITES Secretariat. Royal Botanic Gardens, Kew, Surrey.
Accessible in English, French and Spanish at: https://www.kew.org/science/our-science/science-
services/UK-CITES/cites-resources
LEGUMINOSAE
Dipteryx spp.
Carvalho, C.S., de Fraga, N.C., Cardoso, D.B.O.S. and Lima, H.C. 2020. Tonka, baru and cumaru: Nomenclatural overview, typification and updated checklist of Dipteryx (Leguminosae). Taxon. 69(3), pp.582-592
LEGUMINOSAE
Guibourtia pellegriniana
Leonard, J. (1949). Notulae Systematicae IV (Caesalpiniaceae-Amherstieae africanae americanaeque). Bulletin du Jardin Botanique de l'État a Bruxelles 19(4): 383–408. [ Guibourtia pellegriniana treated on p. 405]. https://doi.org/10.2307/3666831
LEGUMINOSAE
Paubrasilia echinata
Gagnon, E., Bruneau, A., Hughes, C.E., de Queiroz, L. P. & Lewis, G.P. (2016). A new generic system for the pantropical Caesalpinia group (Leguminosae) as a guideline making reference to the name of this taxon. This reference can be found on “ https://phytokeys.pensoft.net/articles.php?id=9203 ”, with free access, and additional information on the taxon can be found at “ http://floradobrasil.jbrj.gov.br/reflora/listaBrasil ”
LEGUMINOSAE
Platymiscium pleiostachyum
Bente B. Klitgraard (2005). Platymiscium ( Leguminosae : Dalbergieae ); biogeography, systematics, morphology, taxonomy and uses. Kew Bulletin. Vol. 60, No. 3 (2005), pp. 321 – 400 be used as a guideline when making reference to the name of this taxon. This reference is available online at “ https://www.jstor.org/stable/4111062?seq=1#page_scan_tab_contents “. Free access is possible to this reference.
LEGUMINOSAE
Pterocarpus spp.
Royal Botanical Gardens Kew, Plants of the World Online , (POWO, 2022)
Accessible at: https://cites.org/sites/default/files/common/docs/Res/12_11/Pterocarpus_POWO_19-1-
2023.pdf
LILIACEAE
Aloe spp.
CITES Aloe and Pachypodium Checklist (U. Eggli et al., 2001, compiled by Städtische Sukkulenten-Sammlung, Zurich, Switzerland, in collaboration with the Royal Botanic Gardens, Kew, United Kingdom of Great Britain and Northern Ireland) and its update: An Update and Supplement to the CITES Aloe & Pachypodium Checklist [J. M. Lüthy (2007), CITES Management Authority of Switzerland, Bern, Switzerland] as a guideline when making reference to the names of species of Aloe and Pachypodium.
LILIACEAE
Aloe spp. — supplement to existing standard reference
Klopper, R.R. 2021. Supplement of aloe spp. names and synonyms . Compiled by Dr. Ronell R Klopper, with input from the PC25 Nomenclature Working Group, 10 June 2021. PC25 Com. 5, Annex.
Accessible at: https://cites.org/sites/default/files/eng/com/pc/25/com/E-PC25-Com-005.pdf
MELIACEAE
Khaya spp.
Royal Botanical Gardens Kew, Plants of the World Online , (POWO, 2022)
Accessible at: https://cites.org/sites/default/files/common/docs/Res/12_11/Khaya_POWO_19-1-
2023.pdf
ORCHIDACEAE
Orchidaceae - Appendix I listed orchids : Paphiopedilum spp. , Phragmipedium spp. , Aerangis ellisii, Cattleya jongheana, Cattleya lobata, Dendrobium cruentum, Mexipedium xerophyticum, Peristeria elata and Renanthera imschootiana
Govaerts, R., Caromel, A., Dhanda, S., Davis, F., Pavitt, A., Sinovas, P., & Vaglica, V. (2019). CITES Appendix I Orchid Checklist . Second Version, Royal Botanic Gardens, Kew, Surrey, and UNEP-WCMC, Cambridge. This reference should be used as a guideline when making reference to the names of Paphiopedilum spp ., Phragmipedium spp ., Aerangis ellisii, Cattleya jongheana, Cattleya lobata, Dendrobium cruentum, Mexipedium xerophyticum, Peristeria elata and Renanthera imschootiana .
This reference can be found on the website of the Royal Botanic Gardens, Kew, UK at “ goo.gl/M26yL8 ”.
ORCHIDACEAE
Orchidaceae — Appendix II listed orchids: genera Aerangis (not A. ellisii ), Aerides , Angraecum, Bletilla, Brassavola, Bulbophyllum, Calanthe, Catasetum, Cattleya (not C. jongheana or C. lobata ), Coelogyne, Comparettia, Cymbidium, Cypripedium, Dendrobium (not D. cruentum ), Disa, Dracula, Encyclia, Laelia, Masdevallia, Miltonia, Miltoniopsis, Phalaenopsis, Pleione, Renanthera, Rhynchostylis, Rossioglossum, Vanda, and Vandopsis
Dhanda, S., Caromel A., Govaerts R., Pavitt A., Bullough, L.-A. & Hartley, H. 2022. CITES Appendix II Orchid Checklist . Royal Botanic Gardens, Kew, Surrey, and UNEP-WCMC, Cambridge.
Accessible at: https://www.kew.org/science/our-science/science-services/UK-CITES/cites-resources
PALMAE
Dypsis decipiens and Dypsis decaryi.
Proposed Standard Reference for two CITES-listed palms endemic to Madagascar (CVPM 2016) based on the Catalogue of the Vascular Plants of Madagascar can be found as a pdf on the US Fish & Wildlife Service website. This is to be used as a guideline when making reference to Dypsis decipiens and Dypsis decaryi . See: http://www.fws.gov/international/
TAXACEAE
Taxus spp.
World Checklist and Bibliography of Conifers (A. Farjon, 2001) as a guideline when making reference to the names of species of Taxus.
ZYGOPHYLLACEAE
Guaiacum spp.
Lista de especies, nomenclatura y distribución en el genero Guaiacum. Davila Aranda. P. & Schippmann, U. (2006): Medicinal Plant Conservation 12:50 as a guideline when making reference to the names of species of Guaiacum .
ANNEX IX
1. Codes for the indication in permits and certificates of the purpose of a transaction, referred to in Article 5(5)
B
Breeding in captivity or artificial propagation
E
Educational. Where the transaction is for the purpose of use in educational and training programs or for display in an institution with a primarily educational remit.
G
Botanical gardens
H
Hunting trophies
L
Law enforcement/judicial/forensic. Where the transaction is for the purpose of transfer of specimens between, or in support of, government agencies for law enforcement, judicial or forensic purposes.
M
Medical (including bio-medical research). Where the transaction is for the purpose of medical or veterinary testing, diagnosis, treatment or research, including biomedical research.
N
Reintroduction or introduction into the wild. Where the transaction is for the purpose of reinforcement and reintroduction within a species’ natural and historical range, and for conservation introductions, comprising assisted colonization and ecological replacement, outside the species’ natural and historical range.
P
Personal
Q
Travelling exhibitions (sample collection, circus, menagerie, plant exhibition, orchestra or museums exhibition that is used for commercial display for the public).
S
Scientific
T
Commercial
Z
Zoos. Where the transaction is for the purpose of movement of a specimen to a zoo and/or aquarium or by a zoo and/or aquarium for public display, care, reproduction, public education and awareness, scientific research, rescue, rehabilitation, or conservation.
2. Codes for the indication in permits and certificates of the source of specimens, referred to in Article 5(6)
W
Specimens taken from the wild
R
Specimens of animals reared in a controlled environment, taken as eggs or juveniles from the wild, where they would otherwise have had a very low probability of surviving to adulthood
D
Specimens of animal species listed in Appendix I to the Convention that are bred in captivity for commercial purposes in operations included in the register of operations that breed Appendix I animal species for commercial purposes, which is maintained by the Secretariat of the Convention, as well as parts and derivatives thereof, and specimens of plant species listed in Appendix I to the Convention that are artificially propagated for commercial purposes in accordance with Chapter XIII of Regulation (EC) No 865/2006, as well as parts and derivatives thereof
A
Plants artificially propagated in accordance with Chapter XIII of Regulation (EC) No 865/2006, as well as parts and derivatives thereof
C
Animals bred in captivity in accordance with Chapter XIII of Regulation (EC) No 865/2006, as well as parts and derivatives thereof
F
Animals born in captivity, but for which the criteria of Chapter XIII of Regulation (EC) No 865/2006 are not met, as well as parts and derivatives thereof
I
Confiscated or seized specimens ( 1 )
O
Pre-Convention 1
U
Source unknown (must be justified)
X
Specimens taken in the marine environment not under the jurisdiction of any State
Y
Plant specimens obtained from assisted production, which are considered not to be ‘artificially propagated’ as set out in Article 56, and also not considered to be taken from the wild because they are propagated or planted in an environment with some level of human intervention for the purpose of plant production
’
( 1 ) To be used only in conjunction with another source code.
