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opencc-by-4.0Apr 2022View details →

Fig. 3. A in Data On The Reproductive Biology Of The Satanic Leaf-Tailed Gecko, Uroplatus Phantasticus (Squamata, Gekkonidae), At The Bion Terrarium Center As A Contribution To Ex Situ Offspring Programs

Fig. 3. A part of all fertile eggs laid by U. phantasticus females during 2020 breeding season; incubation boxes are filled with "Seramis" medium.

opencc-by-4.0Apr 2022View details →

Fig. 1 in Data On The Reproductive Biology Of The Satanic Leaf-Tailed Gecko, Uroplatus Phantasticus (Squamata, Gekkonidae), At The Bion Terrarium Center As A Contribution To Ex Situ Offspring Programs

Fig. 1. Laboratory for breeding stock of U. phantasticus (A) and individual breeze-like minimally equipped terrariums (B).

opencc-by-4.0Apr 2022View details →

Fig. 5. A in Data On The Reproductive Biology Of The Satanic Leaf-Tailed Gecko, Uroplatus Phantasticus (Squamata, Gekkonidae), At The Bion Terrarium Center As A Contribution To Ex Situ Offspring Programs

Fig. 5. A total number of eggs (pcs.) obtained from U. phantasticus females by dates during 2020 breeding season.

opencc-zeroApr 2022View details →

Coordination of care by breeders and helpers in the cooperatively breeding long-tailed tit, Aegithalos caudatus

In species with biparental and cooperative brood care, multiple carers cooperate by contributing costly investment to raise a shared brood. However, shared benefits and individual costs also give rise to conflict among carers over investment. Coordination of provisioning visits has been hypothesized to facilitate the resolution of this conflict, preventing exploitation, and ensuring collective investment in the shared brood. We used a 26-year study of long-tailed tits, Aegithalos caudatus, a facultative cooperative breeder, to investigate whether care by parents and helpers is coordinated, whether there are consistent differences in coordination between individuals and reproductive roles, and whether coordination varies with helper relatedness to breeders. Coordination takes the form of turn-taking (alternation) or feeding within a short time interval of another carer (synchrony), and both behaviors were observed to occur more than expected by chance, i.e. 'active' coordination. First, we found that active alternation decreased with group size while active synchrony occurred at all group sizes. Secondly, we show that alternation was repeatable between observations at the same nest, while synchrony was repeatable between observations of the same individual. Active synchrony varied with reproductive status, with helpers synchronizing visits more than breeders, although active alternation did not vary with reproductive status. Finally, we found no significant effect of relatedness on either alternation or synchrony exhibited by helpers. In conclusion, we demonstrate active coordination of provisioning by carers and conclude that coordination is a socially plastic behavior depending on reproductive status and the number of carers raising the brood.

opencc-zeroMay 2022View details →

Balancing carnivore conservation and sustainable hunting of a key prey species: a case study on the Florida panther and white-tailed deer

1. Large carnivore restoration programs are often promoted as capable of providing ecosystem services. However, these programs rarely measure effects of successful restoration on other economically and ecologically important species. In South Florida, while the endangered Florida panther (Puma concolor coryi) population has increased in recent years due to conservation efforts, the population of its main prey, the white-tailed deer (Odocoileus virginianus), has declined in some regions. The extent to which panther predation has affected deer populations has been difficult to assess because several other factors have changed during this period, including hydrology and hunting regulations. 2. We collected known-fate survival data on 241 GPS-collared adult deer (156 females and 85 males) from 2015 to 2018 in the Florida Panther National Wildlife Refuge and the Big Cypress National Preserve in Florida, USA, to assess effects of panther predation on the deer population, while also evaluating the impacts of hunting and hydrology. 3. Predation was the primary cause of death (110 of 134 mortalities), and 87% of predation events were attributed to panthers, a much greater rate than reported by studies conducted before the panther genetic restoration effort initiated in 1995. One deer was legally harvested, and two were likely killed by poachers. Increasing water depth decreased female survival but had little impact on male survival, and drowning was never a cause of mortality. 4. Females had greater survival probability than males, except during fawning season. From 2015 to 2018, annual survival rates increased from 0.61 (0.52-0.70) to 0.86 (0.79-0.91) for females, and from 0.45 (95% CI: 0.33-0.58) to 0.79 (0.69-0.86) for males. 5. Synthesis and applications – High predation rates, coupled with previous evidence of low recruitment of deer in South Florida, suggest that it will be challenging to meet society's competing demands for large predator restoration and sustainable deer harvest. Deer hunting in the area must remain tightly controlled, for now, if it is to be sustainable, and managers should seek to mitigate effects of high waters and improve deer habitat quality to increase deer population viability. Future work should closely monitor the deer population to assess if management actions can increase vital rates and abundance in the context of high predation rates.

opencc-by-4.0Dec 2021View details →

Data from: Hidden in plain sight: migration routes of the elusive Anadyr bar-tailed godwit revealed by satellite tracking

Abstract Satellite and GPS tracking technology continues to reveal new migration patterns of birds which enables comparative studies of migration strategies and distributional information useful in conservation. Bar-tailed godwits in the East Asian–Australasian Flyway Limosa lapponica baueri and L. l. menzbieri are known for their long non-stop flights, however these populations are in steep decline. A third subspecies in this flyway, L. l. anadyrensis, breeds in the Anadyr River basin, Chukotka, Russia, and is morphologically distinct from menzbieri and baueri based on comparison of museum specimens collected from breeding areas.  However,  the  non-breeding  distribution, migration route and population size of anadyrensis are entirely unknown. Among 24 female bar-tailed godwits tracked in 2015–2018 from northwest Australia, the main non-breeding area for menzbieri, two birds migrated further east than the rest to breed in the Anadyr River basin, i.e. they belonged to the anadyrensis subspecies. During pre-breeding migration, all birds staged in the Yellow Sea and then flew to the breeding grounds in the eastern Russian Arctic. After breeding, these two birds migrated southwestward to stage in Russia on the Kamchatka Peninsula and on Sakhalin Island en route to the Yellow Sea. This contrasts with the other 22 tracked godwits that followed the previously described route of menzbieri, i.e. they all migrated northwards to stage in the New Siberian Islands before turning south towards the Yellow Sea, and onwards to northwest Australia. Since the Kamchatka Peninsula was not used by any of the tracked menzbieri birds, the 4 500 godwits counted in the Khairusova–Belogolovaya estuary in western Kamchatka may well be anadyrensis. Comparing migration patterns across the three bar-tailed godwits subspecies, the migration strategy of anadyrensis lies between that of menzbieri and baueri. Future investigations combining migration tracks with genomic data could reveal how differences in migration routines are evolved and maintained.   Data set Stopping sites and migration timing of satellite-tracked bar-tailed godwits in the East Asian-Australasian Flyway file name: Chan et al. 2022 BARG_Stops_Timing.xlsx The sheet 'stopping_sites' contains stopping sites of bar-tailed godwits tracked with solar Argos satellite transmitters, and their respective arrival and departure times at each site. The sheet 'timing' contains departure and arrival times at the non-breeding and breeding sites in 2017. The transmitters were deployed in Roebuck Bay and Eighty Mile Beach, Australia, and were operating on an 8 h on and 25 h off duty cycle.    Measurements of satellite-tracked bar-tailed godwits in the East Asian-Australasian Flyway file name: Chan et al. 2022 BARG_measurements.csv The datafile contains bill, wing and tarsus lengths and sex of bar-tailed godwits tracked with solar Argos satellite transmitters. The birds were captured in Roebuck Bay and Eighty Mile Beach, Australia.    Journal Article Chan, Y.-C., Tibbitts, T. L., Dorofeev, D., Hassell, C. J. and Piersma T. (2022) Hidden in plain sight: migration routes of the elusive Anadyr bar-tailed godwit revealed by satellite tracking. J Avian Biol e02988. <a href="https://doi.org/10.1111/jav.02920">https://doi.org/10.1111/jav.02988</a>

opencc-zeroDec 2021View details →

Floral phenology of an Andean bellflower and pollination by Buff-tailed Sicklebill

The Andean bellflowers comprise an explosive radiation correlated with shifts to specialized pollination. One diverse clade has evolved with extremely curved floral tubes and are predicted to be pollinated exclusively by one of two parapatric species of Sicklebill hummingbirds (Eutoxeres). In this study we focused on the floral biology of Centropogon granulosus, a bellflower thought to be specialized for pollination by E. condamini, in a montane cloud forest site in southeastern Peru. Using camera traps and a pollination exclusion experiment, we documented E. condamini as the sole pollinator of C.granulosus. Visitation by E. condamini was necessary for fruit development. Flowering rates were unequivocally linear and conformed to the 'steady state' phenological type. Over the course of >1800 hours of monitoring we recorded 12 E. condamini visits totaling 42 seconds, indicating traplining behaviour. As predicted by its curved flowers, C. granulosus is exclusively pollinated by Buff-tailed Sicklebill within our study area. We present evidence for the congruence of phenology and visitation as a driver of specialization in this highly diverse clade of Andean bellflowers.

opencc-zeroAug 2022View details →

Data from: Unwrapping broken tails: Biological and environmental correlates of predation pressure in limbless reptiles

Studying species interactions in nature often requires elaborate logistics and intense fieldwork. The difficulties in such task might hinder our ability to answer questions on how biotic interactions change with the environment. Fortunately, a workaround to this problem lies within scientific collections. For some animals, the inspection of preserved specimens can reveal the scars of past antagonistic encounters, such as predation attempts. A common defensive behaviour that leaves scars on animals is autotomy, the loss of a body appendage to escape predation. By knowing the collection site of preserved specimens, it is possible to assess the influence of organismal biology and the surrounding environment in the occurrence of autotomy. We produced data on tail loss for 8,189 preserved specimens of 33 snake and 11 amphisbaenian species to investigate biological and environmental correlates of autotomy in reptiles. We applied generalized linear mixed effect models to evaluate whether body size, sex, life-stage, habitat use, activity pattern, biome, tropicality, temperature, and precipitation affect the probability of tail loss in limbless reptiles. We observed autotomy in 23.6% of examined specimens, with 18.7% of amphisbaenian and 33.4% of snake specimens showing tail loss. Probability of tail loss did not differ between snakes and amphisbaenians, but it was higher among large-sized specimens, particularly in adults and females. Chance of tail loss was higher for diurnal and arboreal species, and among specimens collected in warmer regions, but it was unaffected by biome, precipitation, and tropicality. Autotomy in limbless reptiles was affected by size-dependent factors that interplay with ontogeny and sexual dimorphism, although size-independent effects of life-stage and sex also shaped behavioural responses to predators. The increase in probability of tail loss with verticality and diurnality suggests a risk-balance mechanism between species habitat use and activity pattern. Although autotomy is more likely in warmer regions, it seems unrelated to seasonal differences in snakes and amphisbaenians activity. Our findings reveal several processes related to predator-prey interactions involving limbless reptiles, demonstrating the importance of scientific collections to unveil ecological mechanisms at different spatio-temporal scales.

opencc-zeroSep 2022View details →

Data belonging to the article: Estimating pre-harvest density, adult sex ratio and fecundity of white-tailed deer using wildlife cameras

Adult sex ratio and fecundity (juveniles per female) are key population parameters in sustainable wildlife management, but inferring these requires abundance estimates of at least three age/sex classes of the population (male and female adults and juveniles). Prior to harvest, we used an array of 36 wildlife camera traps during 2 and 3 weeks in the early autumn of 2016 and 2017 respectively. We recorded white-tailed deer adult males, adult females and fawns from the pictures. Simultaneously, we collected fecal DNA (fDNA) from 92 20mx20m plots placed in 23 clusters of four plots between the camera traps. We identified individuals from fDNA samples with microsatellite markers and estimated the total sex ratio and population density using Spatial Capture Recapture (SCR). The fDNA-SCR analysis concluded equal sex ratio in the first year and female bias in the second year, and no difference in space use between sexes (fawns and adults combined). Camera information was analyzed in a Spatial Capture (SC) framework assuming an informative prior for animals' space use, either (1) as estimated by fDNA-SCR (same for all age/sex classes), (2) as assumed from the literature (space use of adult males larger than adult females and fawns), (3) by inferring adult male space use from individually-identified males from the camera pictures. These various SC approaches produced plausible inferences on fecundity, but also inferred total density to be lower than the estimate provided by fDNA-SCR in one of the study years. SC approaches where adult male and female were allowed to differ in their space use suggested the population had a female-biased adult sex ratio. In conclusion, SC approaches allowed estimating the pre-harvest population parameters of interest and provided conservative density estimates.

opencc-by-4.0Jun 2020View details →

Figs. 23–27 Macroponema beveridgei Mawson, 1978 from Osphranter robustus and O. antilopinus. 23 Bursa, apical view. 24 Spicule tip, left lateral view. 25 Genital cone, apical view. 26 Female tail, right lateral view. 27 in Revision of MaCroponema Mawson, 1978 (Nematoda: Strongylida) from macropodid marsupials with the description of two new species

Figs. 23–27 Macroponema beveridgei Mawson, 1978 from Osphranter robustus and O. antilopinus. 23 Bursa, apical view. 24 Spicule tip, left lateral view. 25 Genital cone, apical view. 26 Female tail, right lateral view. 27 Vagina and ovejector, right lateral view. Scale-bars: 23, 26, 27, 0.1 mm; 24, 25, 0.01 mm

opencc-by-4.0Jul 2019View details →

Рис. 2. Mukhina elegans (Mukhina, 1981) (самка): А — трофико-сенсорный отΔеΛ теΛа; Б — поΛовая система; В — переΔний конец теΛа; Г — хвост; À — фрагмент кутикуΛы с боковым поΛем бп — боковое поΛе, да — ΔробиΛьный аппарат, в — вуΛьва, зм — заΔняя матка, кб — карΔиаΛьный буΛьбус, кск — кΛетки среΔней кишки, нк — нервное коΛьцо, пм — переΔняя матка, р — ректум, рт — ренетта, с — сперма, ск — среΔняя кишка, сп — семяприемник, ф — фазмиΔы, хс — хейΛостома, эп — экскреторная пора, я — яичник Fig. 2. Mukhina elegans (Mukhina, 1981) (female): A — trophic-sensory part of the body; B — the reproductive system; C — the front end of the body; G — the tail; D — fragment of the cuticle with a side field бп — side field, да — crushing apparatus, в — vulva, зм — posterior uterus, кб — cardial bulb, кск — cells of the mid-intestine, нк — nerve ring, пм — anterior uterus, р — rectum, рт — renetta с — sperm, ск — mid-intestin, сп — seminal receptacle, ф — phasmids, хс — cheilostoma, эп — excretory pore, я — ovary in A New Species Sp. Nov. (Nematoda, Cephalobidae) From Primorsky Region (Russia)

Рис. 2. Mukhina elegans (Mukhina, 1981) (самка): А — трофико-сенсорный отΔеΛ теΛа; Б — поΛовая система; В — переΔний конец теΛа; Г — хвост; À — фрагмент кутикуΛы с боковым поΛем бп — боковое поΛе, да — ΔробиΛьный аппарат, в — вуΛьва, зм — заΔняя матка, кб — карΔиаΛьный буΛьбус, кск — кΛетки среΔней кишки, нк — нервное коΛьцо, пм — переΔняя матка, р — ректум, рт — ренетта, с — сперма, ск — среΔняя кишка, сп — семяприемник, ф — фазмиΔы, хс — хейΛостома, эп — экскреторная пора, я — яичник Fig. 2. Mukhina elegans (Mukhina, 1981) (female): A — trophic-sensory part of the body; B — the reproductive system; C — the front end of the body; G — the tail; D — fragment of the cuticle with a side field бп — side field, да — crushing apparatus, в — vulva, зм — posterior uterus, кб — cardial bulb, кск — cells of the mid-intestine, нк — nerve ring, пм — anterior uterus, р — rectum, рт — renetta с — sperm, ск — mid-intestin, сп — seminal receptacle, ф — phasmids, хс — cheilostoma, эп — excretory pore, я — ovary

opencc-by-4.0Jul 2019View details →

Рис. 1. Mukhina orientalis sp. nov. (самка): А — трофико-сенсорный отΔеΛ теΛа; Б — генитаΛьнокауΔаΛьный отΔеΛ теΛа; В — трофико-сенсорный отΔеΛ теΛа второй самки; Г — переΔний конец теΛа; À — хвост второй самки бп — боковое поΛе, да — ΔробиΛьный аппарат, в — вуΛьва, зм — заΔняя матка, кб — карΔиаΛьный буΛьбус, нк — нервное коΛьцо, пм — переΔняя матка, р — ректум, рт — ренетта, ск — среΔняя кишка, скλ — скΛероции кутикуΛы, сп — семяприемник, ф — фазмиΔы, хс — хейΛостома, эп — экскреторная пора, я — яичник Fig. 1. Mukhina orientalis sp. nov. (female): A — trophic-sensory part of the body; Б — genitalcaudal part of the body; В — trophic-sensory part of the body of the second female; Г — front end of the body; À — tail of the second female бп — side field, да — crushing apparatus, в — vulva, зм — posterior uterus, кб — cardial bulb, нк — nerve ring, пм — anterior uterus, р — rectum, ск — mid-intestine, скλ — sclerotic cuticle, сп — seminal receptacle, ф — phasmids, хс — cheilostoma, эп — excretory pore, я — ovary in A New Species Sp. Nov. (Nematoda, Cephalobidae) From Primorsky Region (Russia)

Рис. 1. Mukhina orientalis sp. nov. (самка): А — трофико-сенсорный отΔеΛ теΛа; Б — генитаΛьнокауΔаΛьный отΔеΛ теΛа; В — трофико-сенсорный отΔеΛ теΛа второй самки; Г — переΔний конец теΛа; À — хвост второй самки бп — боковое поΛе, да — ΔробиΛьный аппарат, в — вуΛьва, зм — заΔняя матка, кб — карΔиаΛьный буΛьбус, нк — нервное коΛьцо, пм — переΔняя матка, р — ректум, рт — ренетта, ск — среΔняя кишка, скλ — скΛероции кутикуΛы, сп — семяприемник, ф — фазмиΔы, хс — хейΛостома, эп — экскреторная пора, я — яичник Fig. 1. Mukhina orientalis sp. nov. (female): A — trophic-sensory part of the body; Б — genitalcaudal part of the body; В — trophic-sensory part of the body of the second female; Г — front end of the body; À — tail of the second female бп — side field, да — crushing apparatus, в — vulva, зм — posterior uterus, кб — cardial bulb, нк — nerve ring, пм — anterior uterus, р — rectum, ск — mid-intestine, скλ — sclerotic cuticle, сп — seminal receptacle, ф — phasmids, хс — cheilostoma, эп — excretory pore, я — ovary

Рис. 3. Bolbolaimus brevis sp. nov., самец (А, Б, Δ) и самка (В, Г). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 7 мкм; Б, Г, Δ — 20 мкм; В — 30 мкм Fig. 3. Bolbolaimus brevis sp. nov., male (А, Б, Δ) and female (В, Г). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 7 µm; Б, Г, Δ – 20 µm; В – 30 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam

Рис. 3. Bolbolaimus brevis sp. nov., самец (А, Б, Δ) и самка (В, Г). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 7 мкм; Б, Г, Δ — 20 мкм; В — 30 мкм Fig. 3. Bolbolaimus brevis sp. nov., male (А, Б, Δ) and female (В, Г). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 7 µm; Б, Г, Δ – 20 µm; В – 30 µm

Рис. 2. Фотографии Bolbolaimus parvus sp. nov., самец (А, В, Δ, Е, Ж, К, Α) и самка (Б, Г, З, И, М). А, Б — общий виΑ; В, Г — переΑний конец теΛа; Δ — теΛо в обΛасти базаΛьного буΛьбуса; Е, Ж, З — гоΛова; И — теΛо в обΛасти вуΛьвы; К — теΛо в обΛасти кΛоаки; Α, М — хвост. Масштаб: Б — 100 мкм; А — 50 мкм; В, Α — 20 мкм; Г, И, М — 10 мкм; Δ, Е, Ж, З, К — 5 мкм Fig. 2. Light micrograph of Bolbolaimus parvus sp. nov., male (А, В, Δ, Е, Ж, К, Α) and female (Б, Г, З, И, М). А, Б – general view; В, Г – anterior body end; body in region of basal pharynx bulb; Е, Ж, З – head; И – vulva region; К – cloaca region; Α, М – tail. Scale bars: Б – 100 µm; А – 50 µm; В, Α – 20 µm; Г, И, М – 10 µm; Δ, Е, Ж, З, К – 5 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam

Рис. 2. Фотографии Bolbolaimus parvus sp. nov., самец (А, В, Δ, Е, Ж, К, Α) и самка (Б, Г, З, И, М). А, Б — общий виΑ; В, Г — переΑний конец теΛа; Δ — теΛо в обΛасти базаΛьного буΛьбуса; Е, Ж, З — гоΛова; И — теΛо в обΛасти вуΛьвы; К — теΛо в обΛасти кΛоаки; Α, М — хвост. Масштаб: Б — 100 мкм; А — 50 мкм; В, Α — 20 мкм; Г, И, М — 10 мкм; Δ, Е, Ж, З, К — 5 мкм Fig. 2. Light micrograph of Bolbolaimus parvus sp. nov., male (А, В, Δ, Е, Ж, К, Α) and female (Б, Г, З, И, М). А, Б – general view; В, Г – anterior body end; body in region of basal pharynx bulb; Е, Ж, З – head; И – vulva region; К – cloaca region; Α, М – tail. Scale bars: Б – 100 µm; А – 50 µm; В, Α – 20 µm; Г, И, М – 10 µm; Δ, Е, Ж, З, К – 5 µm

Рис. 1. Bolbolaimus parvus sp. nov., самец (А, Б, В) и самка (Г, Δ). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 10 мкм; В, Δ — 20 мкм; Б, Г — 30 мкм Fig. 1. Bolbolaimus parvus sp. nov., male (А, Б, В) and female (Г, Δ). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 10 µm; В, Δ – 20 µm; Б, Г – 30 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam

Рис. 1. Bolbolaimus parvus sp. nov., самец (А, Б, В) и самка (Г, Δ). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 10 мкм; В, Δ — 20 мкм; Б, Г — 30 мкм Fig. 1. Bolbolaimus parvus sp. nov., male (А, Б, В) and female (Г, Δ). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 10 µm; В, Δ – 20 µm; Б, Г – 30 µm

Рис. 4. Фотографии Bolbolaimus brevis sp. nov., самец (А, В, Г, Е, З, И, К) и самка (Б, Δ, Ж, Α). А, Б — общий виΑ; В, Г, Δ — гоΛова; Е — переΑний конец теΛа; Ж — теΛо в обΛасти вуΛьвы; З, И — теΛо в обΛасти кΛоаки; К, Α — хвост. Масштаб: А, Б — 50 мкм; Е, Ж, К, Α — 10 мкм; В, Г, Δ, З, И — 5 мкм Fig. 4. Light micrograph of Bolbolaimus brevis sp. nov., males (А, В, Г, Е, З, И, К) and female (Б, Δ, Ж, Α). А, Б – general view; В, Г, Δ – head; Е – anterior body end; Ж – vulva region; З, И – cloaca region; К, Α – tail. Scale bars: А, Б – 50 µm; Е, Ж, К, Α – 10 µm; В, Г, Δ, З, И – 5 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam

Рис. 4. Фотографии Bolbolaimus brevis sp. nov., самец (А, В, Г, Е, З, И, К) и самка (Б, Δ, Ж, Α). А, Б — общий виΑ; В, Г, Δ — гоΛова; Е — переΑний конец теΛа; Ж — теΛо в обΛасти вуΛьвы; З, И — теΛо в обΛасти кΛоаки; К, Α — хвост. Масштаб: А, Б — 50 мкм; Е, Ж, К, Α — 10 мкм; В, Г, Δ, З, И — 5 мкм Fig. 4. Light micrograph of Bolbolaimus brevis sp. nov., males (А, В, Г, Е, З, И, К) and female (Б, Δ, Ж, Α). А, Б – general view; В, Г, Δ – head; Е – anterior body end; Ж – vulva region; З, И – cloaca region; К, Α – tail. Scale bars: А, Б – 50 µm; Е, Ж, К, Α – 10 µm; В, Г, Δ, З, И – 5 µm

opencc-by-4.0Dec 2022View details →

Figure 2 in A rapid assessment of cave occupancy for Pacific sheath-tailed bats (fanihin ganas, Emballonura semicaudata rotensis) and Mariana swiftlets (chachaguak, Aerodramus bartschi) on Aguiguan, Mariana Islands

Figure 2: Locations of caves surveyed for Pacific sheath-tailed bat and Mariana swiftlet occupancy by the Commonwealth of the Northern Mariana Islands Division of Fish and Wildlife in 2021, with WorldView-2 satellite imagery (dated April 14, 2019) for reference. Surveyed caves are labeled: 1 – East Black Noddy Cave; 2 – Cliff Cave; 3 – Pillar Cave; 4 – Guano Cave; 5 – New Cave Complex; 6 – Southern Cave Complex; 7 – Crevice Cave

opencc-by-4.0Dec 2022View details →

Figure 1 in A rapid assessment of cave occupancy for Pacific sheath-tailed bats (fanihin ganas, Emballonura semicaudata rotensis) and Mariana swiftlets (chachaguak, Aerodramus bartschi) on Aguiguan, Mariana Islands

Figure 1: Map depicting the location of the Commonwealth of the Northern Mariana Islands in relation to the Asia-Pacific region and the location of Aguiguan (blue circle) within the archipelago. Sources: Basemaps: Esri, The General Bathymetric Chart of the Oceans, National Oceanic and Atmospheric Administration, National Geographic, DeLorme, HERE, Geonames.org, Garmin, United States Geological Survey, Earthstar Geographics.

opencc-zeroJun 2024View details →

Dataset: Global X NASDAQ 100 Tail Risk ETF (QTR) Stock Performance

This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.