Elephantuluselephant-shrews

Di­ver­sity

The genus Ele­phan­tu­lus is one of four gen­era of ele­phant shrews, or sengi (fam­ily Macrosce­li­di­dae). There are 16 species of sengi, 11 of which are in­cluded in the genus Ele­phan­tu­lus. Sen­gis are small, have elon­gated ros­trums, and closely re­sem­ble shrews (fam­ily So­ri­ci­dae) both in ap­pear­ance and be­hav­ior. How­ever, sen­gis are part of the clade Afrothe­ria, mean­ing they are only dis­tantly re­lated to shrews and are more closely re­lated to ten­recs (fam­ily Ten­re­ci­dae), golden moles (fam­ily Chrysochlo­ri­dae), and even ele­phants (fam­ily Ele­phan­ti­dae). Sen­gis are en­demic to Africa, are pri­mar­ily in­sec­tiv­o­rous, and ex­hibit monog­a­mous mat­ing strate­gies.

More re­cently, ge­netic ev­i­dence sug­gests that species in the genus Ele­phan­tu­lus rep­re­sent a pa­ra­phyly, and there are cur­rently pro­pos­als to re­clas­sify species into new gen­era. Namely, there is ev­i­dence that North African sen­gis (Ele­phan­tu­lus rozeti) are more closely re­lated to four-toed sen­gis (Petro­dro­mus tetradacty­lus) and should be re­clas­si­fied as Pet­ros­alta­tor rozeti. Other re­search in­di­cates that So­mali sen­gis (Ele­phan­tu­lus revoili) and ru­fous sen­gis (Ele­phan­tu­lus rufescens) be­long to a newly pro­posed genus, Galegeeska. ("Fam­ily Macrosce­li­di­dae", 2022)

Ge­o­graphic Range

Sen­gis are na­tive and en­demic to the Ethiopian re­gion. The ma­jor­ity of sengi species live in south­ern and south-cen­tral Africa, around or below the equa­tor. How­ever, 3 of the 11 species in the genus Ele­phan­tu­lus have dis­junct pop­u­la­tions in other re­gions of Africa. So­mali sen­gis (Ele­phan­tu­lus revoili) and ru­fous sen­gis (Ele­phan­tu­lus rufescens) live in the African Horn, and North African sen­gis (Ele­phan­tu­lus rozeti) live in the Maghreb re­gion in north­west Africa. (Panchetti, et al., 2008)

Habi­tat

Species in the genus Ele­phan­tu­lus in­habit a wide range of land cover types, in­clud­ing arid deserts, semi-arid grass­lands, trop­i­cal and sub­trop­i­cal forests, and mediter­ranean areas. They build nests in cov­ered areas, such as rocky out­crops or ground-level veg­e­ta­tion and leaf lit­ter. Some species also main­tain spe­cific trails through­out their home ranges, which they travel along while for­ag­ing for food or es­cap­ing preda­tors. Al­though sen­gis do not typ­i­cally in­habit un­der­ground bur­rows, short-snouted sen­gis (Ele­phan­tu­lus brachyrhunchus) liv­ing in grass­lands were ob­served using ter­mite mounds as refu­gia dur­ing wild­fires. Fol­low­ing the wild­fires, short-snouted sen­gis shifted their for­ag­ing be­hav­ior from grassy areas to areas under shrubs and thick­ets. This demon­strates that at least some sengi species se­lect for­ag­ing areas based on lev­els of veg­e­ta­tive cover, likely to de­crease pre­da­tion risk. (Yarnell, et al., 2008)

Sys­tem­atic and Tax­o­nomic His­tory

There are 11 species in the genus Ele­phan­tu­lus: short-snouted sen­gis (Ele­phan­tu­lus brachyrhynchus), cape sen­gis (Ele­phan­tu­lus ed­wardii), dusky-footed sen­gis (Ele­phan­tu­lus fuscipes), dusky sen­gis (Ele­phan­tu­lus fus­cus), Bushveld sen­gis (Ele­phan­tu­lus intufi), So­mali sen­gis (Ele­phan­tu­lus revoili), North African sen­gis (Ele­phan­tu­lus rozeti), ru­fous sen­gis (Ele­phan­tu­lus rufescens), east­ern rock sen­gis (Ele­phan­tu­lus myu­rus), west­ern rock sen­gis (Ele­phan­tu­lus ru­pestris), and Karoo rock sen­gis (Ele­phan­tu­lus pil­i­caudus). Fur­ther­more, there are two sub­species of North African sen­gis and six sub­species of ru­fous sen­gis. There is cur­rent dis­agree­ment on the phy­lo­genic re­la­tion­ships within Ele­phan­tu­lus, as dif­fer­ent analy­ses have yielded dif­fer­ing re­sults. In 2008, Karoo rock sen­gis were dis­tin­guished from cape sen­gis based on ge­netic and mor­pho­log­i­cal data. More re­cently, re­searchers have de­bated clas­si­fy­ing North African sen­gis as mem­bers of a new genus, Pet­ros­alta­tor, based on ge­netic ev­i­dence. Ad­di­tion­ally, some re­searchers have ar­gued that the genus Ele­phan­tu­lus is pa­ra­phyletic and have pro­posed that the gen­era Petro­dro­mus and Macroscelides be sub­sumed into the genus Ele­phan­tu­lus to make a mono­phyly. ("Fam­ily Macrosce­li­di­dae", 2022; Dum­b­acher, 2016; Panchetti, et al., 2008; Smit, et al., 2008; Smit, et al., 2011)

Phys­i­cal De­scrip­tion

Sengi mor­phol­ogy, in­clud­ing the mor­phol­ogy of species in the genus Ele­phan­tu­lus, has re­mained rel­a­tively un­changed for around 20 mil­lion years, as ev­i­denced by fos­sil records. They are small and usu­ally have light brown or grey col­oration. They have rel­a­tively large eyes and ears, and their hind feet are longer than their forefeet. The testes of males are lo­cated in­ter­nally, pos­te­rior to their kid­neys. Males have a long epi­didymis for stor­ing sperm and a long penis, with the dis­tal por­tion lo­cated ex­ter­nally, ter­mi­nat­ing near their ster­num.

A study on cape ele­phant shrews (Ele­phan­tu­lus ed­wardii) caught in South Africa found that fe­males were slightly larger than males, on av­er­age. The fe­males have a com­bined head and body length of 111 mm and a tail length of 140mm, for a total length of 251 mm, on av­er­age. Males were slightly smaller, with an av­er­age over­all length of 242 mm. Fe­males also weighed more, with an av­er­age body mass of 57 g com­pared to an av­er­age of 48 g in males. For both sexes, the ear length was an av­er­age of 30 mm.

Species in the genus Ele­phan­tu­lus have two lower mo­lars, sim­i­lar to species in the genus Macroscelides, but Ele­phan­tu­lus species can be dis­tin­guished by the rel­a­tively small size of their tym­panic bul­lae, a trait they share with species in the genus Nasilio. A study on west­ern rock sen­gis (Ele­phan­tu­lus ru­pestris) found that pop­u­la­tions at higher el­e­va­tions had nar­rower, more elon­gated skulls, whereas pop­u­la­tions at lower lat­i­tudes typ­i­cally had shorter ros­trums, larger tym­panic bul­lae, and ex­panded oc­cip­i­tal re­gions. It is likely that the pop­u­la­tions at lower el­e­va­tions faced greater pre­da­tion pres­sure and thus have de­vel­oped traits that im­prove preda­tor de­tec­tion, such as im­proved hear­ing and vi­sion. (Rath­bun and Rath­bun, 2006; Scalici, et al., 2018; Stu­art, et al., 2003; van der Horst, 1944; Woodall, 1995)

  • Sexual Dimorphism
  • female larger

Re­pro­duc­tion

All species in the genus Ele­phan­tu­lus are so­cially monog­a­mous and mate year round. Mat­ing pairs es­tab­lish shared ter­ri­to­ries, but spend lit­tle time in co­or­di­nated ac­tiv­i­ties. How­ever, males ex­hibit mate guard­ing be­hav­iors when fe­males enter es­trus, ac­tively de­fend­ing their mates from in­trud­ing males.

Stud­ies on ru­fous sen­gis (Ele­phan­tu­lus rufescens) have de­scribed brief sex­ual in­ter­ac­tions be­tween males and fe­males. Fe­males ex­hibit a be­hav­ior known as vagi­nal mark­ing, wherein they se­crete a chem­i­cal to sig­nal that they are sex­u­ally re­cep­tive. Stud­ies on short-snouted sen­gis (Ele­phan­tu­lus brachyrhynchus) found that fe­males have 5 to 6 lit­ters per year, with an av­er­age lit­ter size of 1.6 off­spring. This sug­gests that fe­males have an av­er­age of 8.3 off­spring per year. Sen­gis ex­hibit less re­pro­duc­tive ac­tiv­ity dur­ing cold sea­sons, and pop­u­la­tions at higher lat­i­tudes do not re­pro­duce at all dur­ing the win­ter. Re­pro­duc­tive ac­tiv­ity is typ­i­cally high­est dur­ing the wet sea­son, al­though this dif­fers de­pend­ing on the re­gional en­vi­ron­ment. Sen­gis are pre­co­cial, and are ca­pa­ble of walk­ing less than 4 hours after birth. (Lump­kin and Koontz, 1986; Neal, 1995; Rath­bun and Rath­bun, 2006; Stu­art, et al., 2003)

Sengi species in the genus Ele­phan­tu­lus are monog­a­mous, form­ing weak pair bonds. Males ex­hibit mate-guard­ing be­hav­ior, ac­tively de­fend­ing fe­males from in­trud­ing males. How­ever, sen­gis often have over­lap­ping ter­ri­to­ries and, if males die, their mates may breed again with other males. The age at which sen­gis reach ma­tu­rity is not well stud­ied, and more re­search is needed to un­der­stand their re­pro­duc­tive de­vel­op­ment and be­hav­ior. (Rath­bun and Rath­bun, 2006)

Species in the genus Ele­phan­tu­lus ex­hibit lim­ited parental in­vest­ment. Bushveld sen­gis (Ele­phan­tu­lus intufi) have been de­scribed as hav­ing an “ab­sen­tee sys­tem” of parental care, with moth­ers mak­ing short, in­fre­quent vis­its to nurse their young. Males ex­hibit lit­tle di­rect parental care, but they spend ap­prox­i­mately 40% of their time main­tain­ing trails through­out their ter­ri­to­ries. The trail sys­tems that sen­gis con­struct help them es­cape pre­da­tion and ac­cess for­ag­ing space, and ju­ve­niles use the same trail sys­tems as their par­ents. New­born sen­gis are pre­co­cial, and are ca­pa­ble of stand­ing and run­ning less than 4 hours after birth. (Rath­bun and Rath­bun, 2006)

Lifes­pan/Longevity

There is lim­ited in­for­ma­tion re­gard­ing the longevity of species in the genus Ele­phan­tu­lus. A cape sengi (Ele­phan­tu­lus ed­wardii) was re­ported to live up to 5.7 years old in cap­tiv­ity, but more re­search is needed to de­ter­mine the typ­i­cal lifes­pans of wild sen­gis. (Weigl, 2005)

Be­hav­ior

Sengi species in the genus Ele­phan­tu­lus are mostly di­ur­nal, but some species are par­tially cre­pus­cu­lar or noc­tur­nal. Sen­gis avoid the hottest parts of the day, only leav­ing shady areas to catch nearby prey. In gen­eral sen­gis will travel longer dis­tances com­pared to ro­dent species (order Ro­den­tia) in the same en­vi­ron­ments. Sen­gis are cur­so­r­ial and salta­to­r­ial. They have long hind legs that allow them to run at speeds up to 28 km/h. Sen­gis are gen­er­ally soli­tary, but ex­hibit monog­a­mous mat­ing be­hav­ior and often have ter­ri­to­ries that over­lap with neigh­bor­ing sengi ter­ri­to­ries. Sen­gis per­form scent mark­ing to com­mu­ni­cate their sex­ual sta­tus and have been ob­served to in­ter­act with con­specifics by touch­ing their noses to­gether. Sen­gis are prey an­i­mals and ex­hibit a high level of vig­i­lance when they are ac­tive and when they are rest­ing. When they feel threat­ened, they will per­form foot-drum­ming be­hav­iors or flee along trail sys­tems that they main­tain through­out their ter­ri­tory. Sen­gis typ­i­cally es­tab­lish shel­ters un­der­neath low veg­e­ta­tion or be­tween large rocks, but most species do not use nest­ing ma­te­r­ial.

The ther­moreg­u­la­tory be­hav­ior of sen­gis in the genus Ele­phan­tu­lus has been rel­a­tively well stud­ied. More specif­i­cally, their use of tor­por has been stud­ied ex­ten­sively. For ex­am­ple, cape sen­gis (Ele­phan­tu­lus ed­wardii) that live at high el­e­va­tion fre­quently em­ploy tor­por, re­duc­ing their me­tab­o­lism and body tem­per­a­ture to con­serve en­ergy es­pe­cially dur­ing times of the year with low am­bi­ent tem­per­a­tures. Other species in the genus Ele­phan­tu­lus at lower el­e­va­tions also use tor­por more often dur­ing cold sea­sons than warm sea­sons. Be­cause sen­gis are small-bod­ied mam­mals, they lose heat more rapidly to their en­vi­ron­ment, so using tor­por is an im­por­tant strat­egy in re­duc­ing daily en­er­getic de­mands. Sen­gis also ex­hibit bask­ing be­hav­iors dur­ing sunny weather, likely as an­other strat­egy to re­duce the en­ergy they use on main­tain­ing high body tem­per­a­tures. (Geiser and Mzi­likazi, 2011; Love­grove and Mowoe, 2014; Rath­bun and Rath­bun, 2006; Scalici, et al., 2018)

Com­mu­ni­ca­tion and Per­cep­tion

There is lim­ited in­for­ma­tion re­gard­ing the meth­ods of com­mu­ni­ca­tion used by species in the genus Ele­phan­tu­lus. They have large eyes and ears and long snouts, so they likely rely on a com­bi­na­tion of vi­sual, acoustic, and chem­i­cal stim­uli to per­ceive their en­vi­ron­ment. Sen­gis ex­hibit scent mark­ing be­hav­iors, which likely serves as a method of in­traspe­cific com­mu­ni­ca­tion, re­lay­ing in­for­ma­tion about ter­ri­to­r­ial bound­aries and sex­ual re­cep­tiv­ity. They also use foot drum­ming when they en­counter un­fa­mil­iar con­specifics or po­ten­tial preda­tors. Foot drum­ming may be a vi­sual sig­nal of dis­tress or it may pro­duce vi­bra­tions in the ground that deter preda­tors. The func­tions of such be­hav­iors are not well stud­ied, and more re­search is needed to fully un­der­stand the com­mu­ni­ca­tion meth­ods of species in the genus Ele­phan­tu­lus. (Rath­bun and Rath­bun, 2006)

Food Habits

Sengi species in the genus Ele­phan­tu­lus are pre­dom­i­nantly in­sec­tiv­o­rous. They make daily move­ments along their trail sys­tems and glean in­sects from veg­e­ta­tion or the ground. The spe­cific types of in­sects that sen­gis con­sume varies de­pend­ing on ge­o­graphic lo­ca­tion.

A study on east­ern rock sen­gis (Ele­phan­tu­lus myu­rus) found that they pre­ferred to for­age in areas with rocks and peb­bles as op­posed to areas with sand or saw­dust. East­ern rock sen­gis used their snouts and long tongues to de­tect and col­lect food, a be­hav­ior that is likely sim­i­lar to the for­ag­ing meth­ods of other mem­bers of the genus Ele­phan­tu­lus. The diets of cape sen­gis (Ele­phan­tu­lus ed­wardii) con­sist pri­mar­ily of ant species. It is likely that other species in the genus Ele­phan­tu­lus also eat ants, but they may also op­por­tunis­ti­cally eat other in­sect species along their trail sys­tems. Some Ele­phan­tu­lus species are not strictly in­sec­tiv­o­rous. For ex­am­ple, a study on the stom­ach con­tents of short-snouted sen­gis (Ele­phan­tu­lus brachyrhynchus) found a high pro­por­tion of plant ma­te­r­ial in ad­di­tion to in­sect species. (Leirs, et al., 1995; Mo­ham­mad and Brown, 2011; Scalici, et al., 2018; Stu­art, et al., 2003)

Pre­da­tion

There is lim­ited in­for­ma­tion re­gard­ing spe­cific preda­tors of sen­gis in the genus Ele­phan­tu­lus, and more re­search is re­quired to iden­tify the or­gan­isms that prey on Ele­phan­tu­lus species. How­ever, it is well un­der­stood that many sengi species main­tain trail sys­tems through­out their ter­ri­to­ries. They reg­u­larly move through these trail sys­tems and re­move any ob­sta­cles ob­struct­ing the paths. These trail sys­tems ben­e­fit sen­gis when threat­ened by preda­tors, as they can make rapid es­capes along un­ob­structed paths. Most sengi species in the genus Ele­phan­tu­lus have dull brown or grey col­oration, which helps them cam­ou­flage with their en­vi­ron­ment. Fur­ther­more, they spend most of their time near ground cover, such as veg­e­ta­tion and large rocks, which re­duces the chances of being de­tected by po­ten­tial preda­tors. (Rath­bun and Rath­bun, 2006)

Ecosys­tem Roles

De­spite the wide range of en­vi­ron­men­tal con­di­tions in which Ele­phan­tu­lus live, they have rel­a­tively sim­i­lar life his­tory traits, in­clud­ing mor­phol­ogy, so­cial be­hav­ior, and diet. They prey on in­sects and oc­ca­sion­ally plants, and they serve as prey for other species in their com­mu­ni­ties. Be­yond their roles as preda­tors and prey, rel­a­tively lit­tle is known about the roles that sen­gis play in the ecosys­tems they in­habit. (Rath­bun and Rath­bun, 2006)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Species in the genus Ele­phan­tu­lus have no known pos­i­tive eco­nomic im­pacts, though more re­search is needed to fully un­der­stand their ecosys­tem roles.

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Species in the genus Ele­phan­tu­lus have no known neg­a­tive eco­nomic im­pacts, though more re­search is needed to fully un­der­stand their ecosys­tem roles.

Con­ser­va­tion Sta­tus

Ac­cord­ing to the IUCN Red List, there are only two sengi species in the genus Ele­phan­tu­lus that have sta­ble pop­u­la­tions and are of least con­cern: ru­fous sen­gis (Ele­phan­tu­lus rufescens) and east­ern rock sen­gis (Ele­phan­tu­lus myu­rus). There are five other species that are also of least con­cern, but their pop­u­la­tion trends are un­known: short-snouted sen­gis (Ele­phan­tu­lus brachyrhynchus), Bushveld sen­gis (Ele­phan­tu­lus intufi), west­ern rock sen­gis (Ele­phan­tu­lus ru­pestris), North African sen­gis (Ele­phan­tu­lus rozeti), and cape sen­gis (Ele­phan­tu­lus ed­wardii). The other four species in the genus Ele­phan­tu­lus are con­sid­ered data de­fi­cient on the IUCN Red List, so their pop­u­la­tion sta­tus and con­ser­va­tion needs are un­known: Karoo rock sen­gis (Ele­phan­tu­lus pil­i­caudus), dusky sen­gis (Ele­phan­tu­lus fus­cus), dusky-footed sen­gis (Ele­phan­tu­lus fuscipes), and So­mali sen­gis (Ele­phan­tu­lus revoilii).

There are no known con­ser­va­tion ef­forts in place for sen­gis specif­i­cally. How­ever, some species in the genus Ele­phan­tu­lus have ge­o­graphic ranges that ex­tend into areas es­tab­lished to pro­tect wildlife, such as na­tional parks. ("IUCN Red List", 2022)

  • IUCN Red List [Link]
    Not Evaluated

Con­trib­u­tors

Justin Arndt (au­thor), Col­orado State Uni­ver­sity, Galen Bur­rell (ed­i­tor), Spe­cial Pro­jects.

Glossary

Ethiopian

living in sub-Saharan Africa (south of 30 degrees north) and Madagascar.

World Map

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

carnivore

an animal that mainly eats meat

chemical

uses smells or other chemicals to communicate

crepuscular

active at dawn and dusk

diurnal
  1. active during the day, 2. lasting for one day.
endothermic

animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.

female parental care

parental care is carried out by females

fertilization

union of egg and spermatozoan

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

insectivore

An animal that eats mainly insects or spiders.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

male parental care

parental care is carried out by males

monogamous

Having one mate at a time.

motile

having the capacity to move from one place to another.

native range

the area in which the animal is naturally found, the region in which it is endemic.

omnivore

an animal that mainly eats all kinds of things, including plants and animals

saltatorial

specialized for leaping or bounding locomotion; jumps or hops.

scrub forest

scrub forests develop in areas that experience dry seasons.

sedentary

remains in the same area

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

terrestrial

Living on the ground.

territorial

defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

tropical savanna and grassland

A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.

savanna

A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.

temperate grassland

A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.

year-round breeding

breeding takes place throughout the year

young precocial

young are relatively well-developed when born

Ref­er­ences

Buck­nell Uni­ver­sity. 2022. "Fam­ily Macrosce­li­di­dae" (On-line). Wil­son & Reeder's Mam­mal Species of the World. Ac­cessed De­cem­ber 11, 2022 at http://​www.​departments.​bucknell.​edu/​biology/​resources/​msw3/​browse.​asp?​id=11200002.

2022. "IUCN Red List" (On-line). Ac­cessed De­cem­ber 11, 2022 at https://​www.​iucnredlist.​org/​search?​query=Elephantulus&​searchType=species.

Baker, M., J. Brown. 2011. Patch use be­hav­iour of Ele­phan­tu­lus myu­rus and Mi­cae­lamys na­maque­n­sis: the role of diet, for­ag­ing sub­strates and es­cape sub­strates. African Jour­nal of Ecol­ogy, Vol­ume 50, Issue 2: 167-175. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1111/​j.​1365-2028.​2011.​01309.​x.

Dum­b­acher, J. 2016. Pet­ros­alta­tor gen. nov., a new genus re­place­ment for the North African sengi Ele­phan­tu­lus rozeti (Macroscelidea; Macrosce­li­di­dae). Zootaxa, 4136 (3): 567-579. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​11646/​zootaxa.​4136.​3.​8.

Fitzger­ald, K. 2004. Macroscelidea (Sen­gis). Pp. 517-532 in M Hutchins, A Evans, J Jack­son, D Kleiman, J Mur­phy, D Thoney, eds. Grz­imek's An­i­mal Life En­cy­clo­pe­dia, Vol. 16: Mam­mals V, 2nd Edi­tion. Gale eBooks: Gale. Ac­cessed Sep­tem­ber 21, 2022 at link.​gale.​com/​apps/​doc/​CX3406701008/​GVRL?​u=coloradosu&​sid=bookmark-GVRL&​xid=59120790.

Geiser, F., N. Mzi­likazi. 2011. Does tor­por of ele­phant shrews dif­fer from that of other het­erother­mic mam­mals?. Does tor­por of ele­phant shrews dif­fer from that of other het­erother­mic mam­mals?, Vol­ume 92, Issue 2: 452-459. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1644/​10-MAMM-A-097.​1.

Lang, H. 1923. Cau­dal and Pec­toral Glands of African Ele­phant Shrews (Ele­phan­tu­lus). Jour­nal of Mam­mal­ogy, Vol­ume 4, Issue 4: 261-263. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1093/​jmammal/​4.​4.​261.

Leirs, H., R. Ver­ha­gen, W. Ver­heyen, M. Per­rin. 1995. The bi­ol­ogy of Ele­phan­tu­lus brachyrhynchus in nat­ural miombo wood­land in Tan­za­nia. Mam­mal Re­view, Vol­ume 25, Issue 1-2: 45-49. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1111/​j.​1365-2907.​1995.​tb00437.​x.

Love­grove, B., M. Mowoe. 2014. The evo­lu­tion of mi­cro-cur­so­ri­al­ity in mam­mals. The Jour­nal of Ex­per­i­men­tal Bi­ol­ogy, 217 (8): 1316–1325. Ac­cessed Jan­u­ary 06, 2023 at https://​doi.​org/​10.​1242/​jeb.​095737.

Lump­kin, S., F. Koontz. 1986. So­cial and Sex­ual Be­hav­ior of the Ru­fous Ele­phant-Shrew (Ele­phan­tu­lus rufescens) in Cap­tiv­ity. Jour­nal of Mam­mal­ogy, Vol­ume 67, Issue 1: 112-119. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​2307/​1381007.

Mo­ham­mad, A., J. Brown. 2011. Patch use be­hav­iour of Ele­phan­tu­lus myu­rus and Mi­cae­lamys na­maque­n­sis: the role of diet, for­ag­ing sub­strates and es­cape sub­strates. African Jour­nal of Ecol­ogy, Vol. 50, Iss. 2: 167-175. Ac­cessed De­cem­ber 15, 2022 at https://​doi.​org/​10.​1111/​j.​1365-2028.​2011.​01309.​x.

Mzi­likazi, N., J. Mas­ters, B. Love­grove. 2006. Lack of tor­por in free-rang­ing south­ern lesser gala­gos, Galago mo­holi: eco­log­i­cal and phys­i­o­log­i­cal con­sid­er­a­tions. Folia Pri­ma­tol, Vol. 77, Iss. 6: 465-76. Ac­cessed De­cem­ber 15, 2022 at https://​pubmed.​ncbi.​nlm.​nih.​gov/​17053331/​.

Neal, B. 1995. The ecol­ogy and re­pro­duc­tion of the Short-snouted Ele­phant-Shrew, Ele­phan­tu­lus brachyrhynchus, in Zim­babwe with a re­view of the re­pro­duc­tive ecol­ogy of the genus Ele­phan­tu­lus. Mam­mal Re­view, Vol­ume 25, Issue 1-2: 51-60. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1111/​j.​1365-2907.​1995.​tb00438.​x.

Panchetti, F., M. Scalici, G. Carpa­neo, G. Gib­er­tini. 2008. Shape and size vari­a­tions in the cra­nium of ele­phant-shrews: a mor­pho­me­t­ric con­tri­bu­tion to a phy­lo­ge­netic de­bate. Zoomor­phol­ogy, Vol­ume 127: 69-82. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1007/​s00435-007-0053-1.

Rath­bun, G., C. Rath­bun. 2006. So­cial struc­ture of the bushveld sengi (Ele­phan­tu­lus intufi) in Namibia and the evo­lu­tion of monogamy in the Macroscelidea. Jour­nal of Zo­ol­ogy, Vol­ume 269, Issue 3: 391-399. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1111/​j.​1469-7998.​2006.​00087.​x.

Scalici, M., F. Spani, L. Tra­ver­setti, G. Carpaneto, P. Prias. 2018. Cra­nial shape par­al­lelism in soft-furred sen­gis: mov­ing on a ge­o­graphic gra­di­ent. Jour­nal of Mam­mal­ogy, Vol­ume 99, Issue 6: 1375-1386. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1093/​jmammal/​gyy130.

Smit, H., T. Robin­son, B. Van Vu­uren. 2007. Co­a­les­cence meth­ods re­veal the im­pact of vic­ari­ance on the spa­tial ge­netic struc­ture of Ele­phan­tu­lus ed­wardii (Afrothe­ria, Macroscelidea). Mol­e­c­u­lar Ecol­ogy, Vol­ume 16, Issue 13: 2680-2692. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1111/​j.​1365-294X.​2007.​03334.​x.

Smit, H., T. Robin­son, J. Wat­son, B. van Vu­uren. 2008. A New Species of Ele­phant-Shrew (Afrothe­ria: Macroscelidea: Ele­phan­tu­lus) from South Africa. Jour­nal of Mam­mal­ogy, Vol­ume 89, Issue 5: 1257-1269. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1644/​07-MAMM-A-254.​1.

Smit, H., B. van Vu­uren, P. O'Brien, M. Fer­gu­son-Smith, F. Yang, T. Robin­son. 2011. Phy­lo­ge­netic re­la­tion­ships of ele­phant-shrews (Afrothe­ria, Macrosce­li­di­dae). Jour­nal of Zo­ol­ogy, Vol­ume 284, Issue 2: 133-143. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1111/​j.​1469-7998.​2011.​00790.​x.

Stu­art, C., T. Stu­art, V. Pere­boom. 2003. As­pects of the bi­ol­ogy of the Cape Sengi, Ele­phan­tu­lus ed­wardii, from the West­ern Es­carp­ment, South Africa. Afrother­ian Con­ser­va­tion, Num­ber 2: 2-4.

Weigl, R. 2005. Longevity of Mam­mals in Cap­tiv­ity; from the Liv­ing Col­lec­tions of the World. Stuttgart: Kleine Senck­en­berg-Reihe 48.

Woodall, P. 1995. The male re­pro­duc­tive sys­tem and the phy­logeny of ele­phant-shrews (Macroscelidea). Mam­mal Re­view, Vol­ume 25, Issue 1-2: 87-93. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1111/​j.​1365-2907.​1995.​tb00441.​x.

Yarnell, R., D. Met­calfe, N. Dun­stone, N. Burn­side, D. Scott. 2008. The im­pact of fire on habi­tat use by the short-snouted ele­phant shrew (Ele­phan­tu­lus brachyrhynchus) in North West Province, South Africa. African Zo­ol­ogy, Vol­ume 43, Issue 1: 45-52. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​1080/​15627020.​2008.​11407405.

van der Horst, C. 1944. Re­marks on the Sys­tem­at­ics of Ele­phan­tu­lus. Jour­nal of Mam­mal­ogy, Vol­ume 25, Issue 1: 77-82. Ac­cessed Sep­tem­ber 21, 2022 at https://​doi.​org/​10.​2307/​1374724.