Reproductive strategies in female Mountain and Dorcas gazelles (Gazella gazella gazella and Gazella dorcas)

Observations of reproduction in four gazelle populations in the semi–arid and arid habitats of Israel during three years have revealed intra– and interspecific differences. In the eastern Lower Galilee of northern Israel, female Mountain gazelles (Gazella gazella gazella) reproduce during every month of the year, conceive first at six months of age and exercise long parental care. Females of a population 80 km to the north (Upper Galilee) maintain a seasonal reproductive pattern, conceive first at 18 months of age and have a short parental care period. The latter pattern is similar to the Dorcas gazelle (Gazella dorcas) females of the southern Negev Desert. Interspecific similarities in reproduction of these two populations is attributed to the lack of free water during lactation in both environments where females rely on water available in plant tissue only. The importance of the daily accessibility to water during lactation in female gazelles is discussed. It is suggested that the timing of births and the ability of female gazelles to conceive while lactating are not species-specific characteristics but simply a matter of short-term adaptation to changing environmental conditions common understanding today that animal reproductive strategies are a function of prevailing environmental conditions.     

Fecal progesterone metabolites and ovarian activity in cycling and pregnant mountain gazelles (Gazella gazella)

Fecal reproductive progestagen monitoring in the mountain gazelle (Gazella gazella) provided a non-invasive method for tracking reproductive cycling, estimating age of sexual maturity and diagnosing pregnancy in this species of gazelle. Fresh fecal samples were collected from eight female mountain gazelle (Gazella gazella) for a period of two months. Two of the animals were pregnant while the other six were not. Using the progestagen profile the luteal phase, interluteal (follicular) phase and estrous cycle in adult female gazelles were determined to be 12.5 ± 1.2, 5.9 ± 0.59 and 18.8 ± 0.98 days respectively. Significant inter-animal differences in fecal progestagen concentration were observed in both the luteal and follicular phases. Significant differences were observed in the levels of fecal progestagen between cycling females and females in late pregnancy. Low concentrations of fecal progestagen in females aged less than 18 months old indicated that sexual maturity in captivity is not attained before that age.     

Taxonomic status of the Farasan Island gazelle

The taxonomy of Arabian gazelles has been confused by single specimen collected from the Farasan Islands in the Red Sea in the 1820s. There is still population of gazelles on the islands. They form distinct taxon most closely related to the mountain gazelle Gazella gaiella , which is characterized by small size, grey-brown colouring, very short horns in the female and rounded upper tooth-row in the male. This gazelle bears no resemblance to the type specimen of G. arabica , said to come from the Farasan Islands. In this paper the Farasan gazelle is described as Gazella gazella Jarasani n. ssp.     

Genetic diversity and relations of the Goitered gazelle (<Emphasis Type="Italic">Gazella subgutturosa</Emphasis>) groups from Uzbekistan,Turkmenistan, and Azerbaijan: Analysis of the D-loop of mitochondrial DNA

Polymorphism of the nucleotide sequence of a hypervariable fragment of the D-loop (985 bp) of mtDNA in 76 Goitered gazelles of subspecies Gazella subgutturosa subgutturosa from Uzbekistan, Turkmenistan, and Azerbaijan was studied. The genetic similarity of gazelles from Turkmenistan and Uzbekistan has been identified. The population of gazelles from Shirvanskaya steppe reserve (Azerbaijan) is unique and strictly isolated from other groups studied. A high haplotypic (H = 0.9649 ± 0.0091) and relatively low nucleotide diversity (π = 0.0212 ± 0.0105) were noted for all investigated groups of gazelle based on this mtDNA fragment, which is probably related to ecological peculiarities of the species and the history of formation of regional populations.     

Latrine survey as a method to estimate the population size of Arabian gazelles (Gazella arabica)

Arabian gazelle (Gazella arabica) populations have been decimated in most parts of their original range. As a cryptic, crepuscular species, Arabian gazelles are difficult to observe, rendering monitoring programs for conservation purposes a challenging endeavour. Latrine mapping has been suggested as an effective, time- and cost-efficient tool to survey and estimate the abundance of gazelles in remote areas with low population densities. In the present study we collected data from five populations in Saudi Arabia to address the question of how population estimates can be inferred from such latrine counts and uncovered a non-linear relationship between both variables. Methodologies applied during the five surveys differed between study sites, so caution is required when interpreting our data. Still, given the immediate threat to the survival of the species, there is an urgent need to establish a time- and cost-efficient sampling method that will be vital for the conservation of remnant pockets of natural populations and for the proclamation of new protected areas in Saudi Arabia and other countries in the Middle East, and the present data are the only available source of information in this context.     

新疆卡拉麦里山有蹄类自然保护区鹅喉羚遗传多样性及系统发育地位

鹅喉羚是生活于亚欧大陆荒漠、半荒漠地区重要的有蹄类动物。2010年春季,新疆卡拉麦里山有蹄类自然保护区遭遇了60年不遇的雪灾,我们采集了野外救灾发现的130头死亡鹅喉羚肌肉样本,采用PCR和测序技术,研究了鹅喉羚线粒体 DNA 的 Cyt b 基因 1143 bp 核酸序列,发现新疆卡拉麦里山有蹄类自然保护区生存的鹅喉羚单倍型多样性较高(Hd=0.855),核苷酸多样性较低(π=0.00224)。采用邻接法(NJ)、最大似然法(ML)构建单倍型之间的系统发育树,以及network所构建的单倍型间中介网络图都显示出2个遗传分化程度很大的分支,且这2个分支都出现过明显的群体扩张和持续增长。将本研究获得的单倍型H1与Genebank检索获得的瞪羚属其他12个物种Cyt b基因进行了比较,分别采用邻接法(NJ)和最大似然法(ML)构建分子系统树,证明与鹅喉羚最接近的物种为印度瞪羚(Gazella bennettii),鹅喉羚与瞪羚属内物种的分歧时间大约为1.08-2.5百万年(Mya)(Million years ago, Mya)。     

Utilization of harvester ant nest sites by Persian goitered gazelle in steppes of central Iran

Ants are among the most important elements in many ecosystems and known as famous ecosystem engineers. By changing physical and chemical properties of soil, ants may provide suitable habitats for other species. Based on previous observations, we hypothesized that Persian goitered gazelles (Gazella subgutturosa subgutturosa) exhibit a preference for utilizing sites close to seed harvester ant (Messor spp.) nests. We tested our hypothesis by (1) mapping the occurrence of harvester ant nests and aggregated gazelle pellet groups along 31 strip transects, (2) monitoring pellet group accumulation bimonthly at 56 pairs of permanent plots established on ant nests and at adjacent control sites for a complete year, and (3) comparing vegetation and soil parameters between ant nest sites used by gazelles and paired control plots without ant nests. Although the area of Messor spp. nest sites covered only about 0.29% of the sampled transects, 84% of the gazelle pellet group aggregation sites were positioned upon ant nests, suggesting that gazelles actively selected Messor spp. nest sites. Pair-wise comparisons between ant nest plots and paired control plots also confirmed higher use of ant nest sites by gazelles compared to sites without ant nests in all time periods. Percent soil organic matter, percent cover of gravel, and annual herb vegetation significantly differed between ant nest and paired control plots in all the vegetation communities. We suggest that the alterations brought about by harvester ants on soil and vegetation make these sites attractive to gazelles. Gazelle territoriality behaviour and use of ant nests as bedding sites may be the reasons for selection of ant nest sites by gazelles.     

Genetic diversity,population genetic structure and demographic history of Przewalski’s gazelle (<Emphasis Type="Italic">Procapra przewalskii</Emphasis>): implications for conservation

The Przewalski’s gazelle (Procapra przewalskii) is one of the most endangered antelope species in the world. It is endemic to China and is a flagship species in the eastern part of the Qinghai–Tibet plateau. To establish effective conservation measures on this species, genetic information such as genetic structure is needed. However, there has not been a comprehensive genetic assessment on this gazelle using nuclear DNA markers yet. Here, we employed 13 microsatellite loci to investigate genetic diversity, population genetic structure and demographic history of Przewalski’s gazelle using noninvasive samples of 169 wild gazelles collected from nine populations. A total of 76 alleles were detected from the entire samples, mean allele number was 5.85, and overall H _O and H _E were 0.525 and 0.552, respectively. Structure and GENELAND analyses found six genetic groups in the nine populations. Between the inferred genetic groups, significant genetic differentiation and low migration rates were detected. Demographic analyses indicated that Przewalski’s gazelle experienced genetic bottleneck and severe population decline, with the ancestral effective population size reducing to less than one percent. Based on the results of this study, we provide several conservation recommendations for Przewalski’s gazelle, such as six management units, periodic monitoring and special conservation consideration on the Qiejitan population.     

Gene introgression between Gazella subgutturosa and G. marica: limitations of maternal inheritance analysis for species identification with conservation purposes

It has recently been suggested that goitered gazelles (Gazella subgutturosa and Gazella marica) have paraphyletic maternal origin, and that the mitochondrial cytochrome b gene fragment can be used for species identification prior to reintroduction of the gazelles. Although there is a large geographic area where the gazelles have intermediate morphology, previous researchers have not inferred any signs of mitochondrial haplotype introgression, and it is thought that the introgression, if it exists, is male-biased. We studied mitochondrial haplotypes of morphologically typical G. subgutturosa from two geographic locations. Goitered gazelles from eastern Turkey, morphologically identical to G. subgutturosa, had haplotypes identical to G. marica. This finding confirms ongoing maternal gene introgression from G. marica to G. subgutturosa. Our suggestion is that there is a natural gene flow between these two nominal species, and morphological characters together with recombinant genetic markers rather than mitochondrial DNA should be used to differentiate among individuals from areas close to the contact zone.     

Characterization of the spatial distribution of latrines in reintroduced mountain gazelles: do latrines demarcate female group home ranges?

Mountain gazelle Gazella gazella in Saudi Arabia are listed as 'vulnerable' by the IUCN. At present, the species' survival is secured by extensive captive-breeding programmes and reintroductions into protected areas. Two reintroduction attempts (Ibex Reserve and Uruq Bani Ma'Arid protected areas) in Saudi Arabia have been undertaken in the past two decades. Post-monitoring of released individuals is essential for the success of such reintroduction programmes; however, cryptic species like mountain gazelles are extremely difficult to observe directly. As radio-tracking is a cost-intensive and invasive post-monitoring technique, we asked: how can reintroduced or remnant pockets of natural gazelle populations be monitored indirectly ? Here, we propose the use of latrine mapping as an effective, cost-efficient and non-invasive tool to survey the social organization of reintroduced mountain gazelles as an indicator for repatriation success. In this study, we used released radio-collared animals to characterize the spatial distribution of latrines within female group home ranges. Distance to the next latrine, latrine size, as well as numbers of fresh faecal pellet groups per latrine or presence of urination marks were used as dependent variables for step-wise backward multiple regressions and were correlated with various ecological factors. Most dependent variables were correlated with distance or direction from the nearest tree, but not indicative of home-range cores. Only latrine densities were distinctly higher in core areas of female group home ranges, and no pattern of peripheral marking was detected. Hence, latrine density is a good indicator of home-range use in female group home ranges. Mapping latrines and determining latrine densities are therefore the methods of choice to survey mountain gazelle populations.     

Food preferences and tooth wear in the sand gazelle (Gazella marica)

Food preferences of the sand gazelle (Gazella marica) from the Mahazat as-Sayd Protected Area in Saudi Arabia were evaluated using focal animal sampling in conjunction with an eco-morphological method examining two parameters of tooth wear, i.e., occlusal relief and cusp shape. Observations of live, free-ranging animals (n = 53) showed that sand gazelles generally consumed more grass (58.4%) than browse (41.6%). However, during the dry season, gazelles spent significantly more time browsing (51.0%) and less time grazing (49.0%) than under wet conditions (browsing: 17.6%; grazing: 82.4%). Thus, consistent with predictions, sand gazelles are intermediate feeders but shift towards browsing when grass is scarce. The mesowear signature of the sand gazelle is consistent with a grazing signal in other ruminants. In other words, the browse component of the diets of live animals was not reflected in the tooth wear. This could have occurred because browse is less abrasive than grass, but more likely because all food types are heavily abrasive in this dusty habitat. We conclude that the sand gazelle population in Mahazat as-Sayd encounters a highly abrasive diet, which has implications for their ability to meet nutritional demands.     

Comparative behaviour of sand and mountain gazelles

Behavioural observations of both captive and free-ranging sand and mountain gazelles revealed differences in group size and composition, territory size and agonistic behaviour. Sand gazelles are seasonal breeders and form large herds (maximum = 56) during rut and post-rut as compared to mountain gazelles, which breed throughout the year in smaller groups (maximum = 5). As a result, mountain gazelle males maintain their territories year round, whereas sand gazelle rams show marked morphological changes and defend a territory only during the rut. Mountain gazelle males exhibited threat displays rather than engaging in actual combat more often than did sand gazelles. Although subject to the same environmental conditions, sand gazelles are seasonal breeders and the young are born in March-April, whereas mountain gazelles give birth throughout the year.     

Coagulation profile and platelet parameters of the Arabian sand gazelle (Gazella subgutturosa marica): comparison with humans and camels

During March 2009, we evaluated the hemostatic profile and platelet indices of 18 Arabian sand gazelles (Gazella subgutturosa marica) and compared the results with those from humans and camels (Camelus dromedarius). Gazelles and camels had shorter activated partial thromboplastin times, lower proconvertin and higher antihemophilic factor coagulation activity, and plasma fibrinogen levels than humans. Prothrombin time was longer in sand gazelles and shorter in camels than it was in humans. Plasma thromboplastin component, Stuart factor, and plasma thromboplastin antecedent were similar in gazelles, humans, and camels, whereas the platelet count of the sand gazelle was significantly higher than it was for camels and humans.     

Factors affecting the distribution of dorcas gazelle

The dorcas gazelle Gazella dorcas was very common and widespread in Tunisia. Nowadays, only some small isolated populations still survive in the desert areas of the southern part of the country. Factors affecting the distribution of this species in Tunisia have never been investigated despite the importance of such investigations for elaborating long-term conservation plans for the remaining wild populations. Using data on gazelle occurrence and on a set of habitat and human variables collected in south-eastern Tunisia, we aimed to identify the factors affecting gazelle distribution in this area. In particular, we investigated the relevance of habitat versus human factors for gazelle occurrence probability. As predicted, we found that human variables were the most relevant factors shaping the distribution patterns of gazelles in the studied area. Gazelles tended to avoid areas where agricultural development has occurred but did not seem to be disturbed by livestock. Overall, our results suggest that the occurrence probability of dorcas gazelle in southern Tunisia was mainly dependent on human presence and land use, rather than habitat characteristics. The recent intensification of agriculture in the more remote areas of southern Tunisia may thus constitute a serious threat to the conservation of this endangered species.     

Recent Geological Events and Intrinsic Behavior Influence the Population Genetic Structure of the Chiru and Tibetan Gazelle on the Tibetan Plateau

The extent to which a species responds to environmental changes is mediated not only by extrinsic processes such as time and space, but also by species-specific ecology. The Qinghai-Tibetan Plateau uplifted approximately 3000 m and experienced at least four major glaciations during the Pleistocene epoch in the Quaternary Period. Consequently, the area experienced concurrent changes in geomorphological structure and climate. Two species, the Tibetan antelope (Pantholops hodgsonii, chiru) and Tibetan gazelle (Procapra picticaudata), both are endemic on the Qinghai-Tibetan Plateau, where their habitats overlap, but have different migratory behaviors: the chiru is inclined to have female-biased dispersal with a breeding migration during the calving season; in contrast, Tibetan gazelles are year-round residents and never migrate distantly. By using coalescence methods we compared mitochondrial control region DNA sequences and variation at nine microsatellite loci in these two species. Coalescent simulations indicate that the chiru and Tibetan gazelle do not share concordant patterns in their genealogies. The non-migratory Tibetan gazelle, that is more vulnerable to the impact of drastic geographic changes such as the elevation of the plateau, glaciations and so on, appears to have a strong population genetic structure with complicated demographic history. Specifically, the Tibetan gazelle population appears to have experienced isolation and divergence with population fluctuations since the Middle Pleistocene (0.781 Ma). However, it showed continued decline since the Upper Pleistocene (0.126 Ma), which may be attributed to the irreversible impact of increased human activities on the plateau. In contrast, the migratory chiru appears to have simply experienced population expansion. With substantial gene flow among regional populations, this species shows no historical population isolation and divergence. Thus, this study adds to many empirical studies that show historical and contemporary extrinsic and intrinsic processes shape the recent evolutionary history and population genetic structure of species.     

Midden site selection in Dorcas gazelle: Larger is not always better

Dorcas gazelles are believed to use middens to mark their territories and transmit information. Given the commitment to maintaining a midden, it is believed that middens are not placed randomly. We examined how the habitat (tree height and maximum canopy) and anthropogenic disturbance (camel and human presence) influenced the selection of midden sites by Dorcas gazelles in South Sinai, Egypt. Our results showed that Dorcas gazelles did not place middens at larger trees, while favoring relatively smaller trees and shrubs where the anthropogenic disturbance and perceived hunting risk are less. Our results, in light of the previous findings, suggest that selection of midden sites is species context‐dependent behavior. In areas with less anthropogenic disturbance and hunting, Dorcas gazelles have been shown to select the largest trees of the same species as midden sites. In contract, in our study site with high anthropogenic disturbance and no protection from hunting, gazelles did not utilize the presumably optimum landmarks for midden sites. Our study showed that Dorcas gazelles instead utilized smaller trees and some shrubs that are less conspicuous and presumably less effective as advertisement sites, but safer.     

Diversification and subspecies patterning of the goitered gazelle (Gazella subgutturosa) in Iran

Goitered gazelles, Gazella subgutturosa, exist in arid and semiarid regions of Asia from the Middle to the Far East. Although large populations were present over a vast area until recently, a decline of the population as a result of hunting, poaching, and habitat loss led to the IUCN classification of G. subgutturosa as “vulnerable." We examined genetic diversity, structure, and phylogeny of G. subgutturosa using mitochondrial cytochrome b sequences from 18 geographically distant populations in Iran. The median‐joining network of cyt b haplotypes indicated that three clades of goitered gazelles can be distinguished: a Middle Eastern clade west of the Zagros Mountains (and connected to populations in Turkey and Iraq), a Central Iranian clade (with connection to Azerbaijan), and an Asiatic clade in northeastern Iran (with connection to Turkmenistan, Uzbekistan, and other Asian countries as far as northeastern China and Mongolia). Based on our results, we argue that Iran is the center of diversification of goitered gazelles, due to the presence of large mountain ranges and deserts that lead to the separation of populations. In accordance with previous morphological studies, we identified the Asiatic clade as the subspecies G. s. yarkandensis, and the other two clades as the nominate form G. s. subgutturosa. The new genetic information for goitered gazelles in Iran provides the basis for future national conservation programs of this species.     

Post-mortem semen cryopreservation and characterization in two different endangered gazelle species (Gazella gazella and Gazella dorcas) and one subspecies (Gazella gazelle acaiae)

Both Gazella gazella and Gazella dorcas are endangered species with continually dwindling population size, yet basic knowledge on their spermatozoa is missing. Semen collected post-mortem (PM) from the cauda epididymis of five adult gazelles (three Gazella gazella gazella, one Gazella gazella acaiae and one G. dorcas) was cryopreserved using directional freezing of large volumes (8 mL) with egg-yolk-free extender. Sperm size measurements and SYBR-14/propodium iodide (PI) viability stain validation for use in gazelles were conducted. Post-thaw characterization included motility, viability, acrosome damage evaluation, computerized motility characterization and morphology and sperm motility index (SMI) was calculated. Extracted sperm motility was 71.67+/-11.67% (mean+/-S.E.M.). Post-thaw motility ranged between 15% and 63%, viability was 57.49+/-3.24%, intact acrosome was detected in 63.74+/-2.6% (median 64.8%, upper/lower quartiles 71.79%, 61.82%), and normal morphology ranged between 41% and 63%. Motility characterization showed two sub-groups-highly active and progressively motile spermatozoa with SMI of 62.75+/-0.38 and low activity and poorly progressive with SMI of 46.16+/-1.53. Our results indicate that PM preservation of gazelle spermatozoa with satisfactory post-thaw viability is possible and cryobanking is achievable.     

A phylogeographic framework for the conservation of Saharan and Arabian Dorcas gazelles (Artiodactyla: Bovidae)

Many species of gazelles (Gazella spp.) are nowadays threatened by hunting, poaching, habitat loss and habitat deterioration. Conservation efforts for this group not only face the problem of maintaining remnant populations, but often natural populations have been extirpated from the wild. In some cases, though, captive breeding programs exist that might provide a valuable source for future reintroductions. A major problem in this context is that phylogeographic relationships among different (potentially locally adapted) populations, and even basic phylogenetic relationships between species, are poorly understood, thus hampering the assignment of management units, breeding groups or stocks for reintroduction projects. Our present study focused on Dorcas gazelles (G. dorcas and G. saudiya) from the species’ entire distribution range, with samples originating from western Saharan Africa into Saudi Arabia. In stark contrast to previous studies reporting on pronounced genetic structure in taxa such as Mountain gazelles (G. gazella), we detected low genetic diversity and no evidence for major phylogenetic lineages when analyzing two mitochondrial genetic markers. Using a coalescent approach we infer a steep population decline that started approximately 25,000 years before present and is still ongoing, which coincides with human activities in Saharan Africa. Our phylogenetic analyses, statistical parsimony network analysis and inferred colonization patterns shed doubt on the validity of various described subspecies of G. dorcas.     

Responding to a three-pronged attack: desert lilies subject to herbivory by dorcas gazelles

We examined the effects of herbivory by the dorcas gazelle, Gazella dorcas, on different phenological stages of the lily Pancratium sickenbergeri from 1990–1996 in the Negev desert, Israel. We placed particular emphasis on the role of gazelle herbivory on selecting for plant defences and the effectiveness of these defences against subsequent herbivory. In the summer months, the gazelles dig in the sand to remove all or part of the bulb of the lily. Plants with partially-consumed bulbs were less likely to produce leaves the following winter and probably have lower lifetime flower production. Herbivory has resulted in greater downward growth of the bulb in populations with herbivory than those without herbivory, which reduces the probability that the entire plant will be consumed. Gazelles eat the leaves in the winter; this herbivory has a negative impact on leaf growth rates. However, the production of calcium oxalate limits gazelle consumption to the tips, and consequently reduces the effects of leaf herbivory. In the fall, the gazelles consumed virtually all flowers, yet we found no defence or growth strategy that might ameliorate this impact, with the possible exception of forgoing the output of a second flower stalk after the first has been consumed. The results of this study suggest that lilies employ different strategies to resist gazelle herbivory, and that these strategies are dependent on the phenological stage that is eaten. Avoidance by defence is the strategy in the leaves, avoidance by escape is utilized in bulbs. Forgoing the output of a second flower stalk after the first has been consumed can be considered as a form of escape based on a bet-hedging strategy or a shift in energy allocation.