TECHNICAL FIELD [0001] The present invention relates to a highstrength steel sheet suitable for automobiles and a method of manufacturing the same. BACKGROUND ART [0002] There is a growing demand for reduction of car body weight as a measure for improving fuel economy of automobiles and cost reductl.on by integral forming of components, and the development of high-strength steel sheets excellent in press formability is under way. A dual phase steel sheet (DP steel sheet) including ferrite and martensite and a TRIP steel sheet utilizing transformation induced plasticity (TRIP) of retained austenite are known as a high-strength steel sheet excellent in press formability. [0003] However, in the conventional DP steel sheet and the TRIP steel sheet, improvement of local ductility is limited, and it is difficult to manufacture a member which is complicated in shape and desired to have highstrength. From the viewpoint of mechanical properties, it is difficult to obtain good local ductility while obtaining high tensile strength. As indicators of local ductility, a hole expandability and a reduction of area are cited. According to a hole expansion test, 111 a stretch flange formed part and the like, evaluation close to an actual forming can b~ performed, but it is evaluated on the characteristic of the crack - 1 - generation part (direction). On the other hand, since the reducti.on of area is measured by a tensile test that defines the deformation direction, it is easy to indicate the quantitative difference of the local ductility of the material. For example, Patent Reference 1 describes a high-strength hot-rolled steel sheet for improving fatigue strength, but it is sometimes difficult to manufacture a member having a complicated shape with the steel sheet. CITATION LIST PATENT REFERENCE [0004] Patent Reference 1: Japanese Laid-open Patent Publication No. 2014-173151 SUMMARY OF INVENTION TECHNICAL PROBLEM [0005] It is an object of the present invention to provide a high-strength steel sheet capable of improving local ductility while securing high-strength and a method of manufacturing the same. SOLUTION TO PROBLEM [0006] The inventors of the present invention conducted di.ligent studies to clarify the reason why excellent local ductility cannot be obtained in a conventional high-strength steel sheet. As a result, it has been found that, among martensite grains in a conventional high-strength steel sheet, those on grain boundary triple points tend to be origins of cracking. In addition, it has been also revealed that many of the martensite grains on the grain boundary triple points have a shape susceptible to stress concentration. - 2 - Furthermore, it has been found that martensite grains inevitably have a shape susceptible to stress concentration, since ferrite, bainite, or pearlite, or any combination thereof grows during cooling from a dual phase region of austenite and ferrite, and martensite grains are formed in the gap in a conventional method of manufacturing a high-strength steel sheet. [0007] Then, the present inventors conducted intensive studies to make a shape of martensite grains on a grain boundary triple point into a shape hard to receive stress concentration. As a result, it has been found that it is important to prepare a steel sheet having a microstructure (initial structure) in which the area fraction and size of pearlite is within a specific range and reheat the steel sheet under a specific condition. Further, in order to prepare the above steel sheet, it has been also found that it is effective to perform hot rolling under a specific condition or perform annealing under a specific condition after cold rolling. [0008] Based on such findings, the inventors of the present invention have made further diligent studies and as a result have conceived the following aspects of the invention. [0009] ( 1) A high-strength steel sheet, including: a chemical composition represented by, in mass%: C: 0.03% to 0.35%; Si: 0.01% to 2.0%; Mn: 0.3% to 4.0%; - 3 - Al: 0. 0 1% to 2 . 0% ; P: 0.10% or less; S: 0.05% or les.s; N: 0.010~ or less; Cr: 0.0% to 3 . Q9-· 0 ' Mo: 0. 0% to 1. 0 9, • ' ' Ni: 0.0% to 3 . Q9c. 0 ' Cu: 0.0% to 3. Q9--· 0 ' Nb: 0.0% to 0. 39--· 0 ' Ti: 0.0% to 0. 3 9- • 0 ' V: 0.0% to 0. 59--· 0 ' B: 0.0% to 0.1%; Ca: 0.00% to 0.01%; Mg: 0.00% to 0.01%; Zr: 0.00% to 0.01%; REM: 0.00% to 0.01%; and the balance: Fe and impurities, and a microstructure represented by, in area%, martensite: 5% or more; ferrite: 20% or more; and perlite: 5% or less, whe r e.i..n an average diameter of martensite grain is 4 pm or less in equivalent circle diameter, a ratio of the number of bulging type martensite grains to the number of martensite grains on grain boundary triple points of a matrix is 70% or more, wherein: the bulging type martensite grain is on one of the grain boundary triple points of the matrix; - 4 - and at least one of grain boundaries of the bulging type martensite grain, the gra1n boundaries connecting two adjacent grain boundary triple points of the bulging type martensite grain and grains of the matrix, has a convex curvature to an outer side with respect to line segments connecting the two adjacent grain boundary triple points 1 and an area ratio represented by VM I AO is 1.0 or more, wherein: VM denotes a total area of the martensite grains on the grain boundary triple points of the matrix; and AO denotes a total area of polygons composed of the line segments connecting two adjacent grain boundary triple points of the martensite grains. [0010] (2) The high-strength steel sheet according to (1), wherein an average diameter Ds of ferrite in a surface layer portion from a surface of the highstrength steel sheet to a depth 4 x Do is not more than twice an average diameter D0 , wherein the average diameter Do is an average diameter of ferrite in a region where a depth from the surface of the highstrength steel sheet is 1/4 of a thickness of the highstrength steel sheet. [0011] (3) The high-strength steel sheet according to (l) or (2), wherein an area fracti.on of unrecrystallized ferrite is 10% or less in the microstructure. ~ ~) - [0012] (4) The high-strength steel sheet according to any one of ( 1) to ( 3) ' wherein, in the chemical composition, Cr: 0.05% to 3 . 0%' Mo: 0.05% to 1.0%, Ni: 0.05% to 3.0%, or Cu: 0.05% to 3.0%, or any combination thereof is satisfied. [0013] (5) The high-strength steel sheet according to any one of (1) to (4), wherein, in the chemical composition, Nb: 0.005% to 0.3%, Ti: 0.005% to 0.3%, or V: 0.01% to 0.5%, or any combination thereof is satisfied. [0014] (6) The high-strength steel sheet according to any one of ( 1) to ( 5), wherein, ln the chemical composition, B: 0.0001% to 0.1% is satisfied. [0015] (7) The high-strength steel sheet according to any one of (1) to (6), wherein, in the chemical composition, Ca: O .. D.005% to 0.01%, Mg: 0.0005% to 0.01%, Zr: 0.0005~ to 0.01%, or REM: 0.0005% to 0.01%, or any combination thereof is satisfied. [0016] (8) A method of m2nufacturing a high-strength steel sheet, including the steps of: preparing a steel sheet; reheating the steel sheet to a first temperature of - 6 - 770"C to 820"C at an average heating rate of 3"C/s to 120"C/s; and then, cooling the steel sheet to a second temperature of 300"C or less at an average cooling rate of 60"C/s or more, wherein an area fraction of pearlite is 10% or less, an area fraction of unrecrystallized ferrite is 10% or less, and an average diameter of pearlite grain is 10 pm or less in the steel sheet, an average diameter Ds of ferrite in a surface layer portion from a surface of the steel sheet to a depth 4 x Do is not more than twice an average diameter D0 , wherein the average diameter Do is an average diameter of ferrite in a region where a depth from the surface of the steel sheet is 1/4 of a thickness of the steel sheet, the cooling to the second temperature is started within 8 seconds once the temperature of the steel sheet reaches the first temperature, and the steel sheet includes a chemical composition represented by,, in mass%: C: 0.03% to 0.35%; Si: 0.01% to 2.0%; Mn: 0.3% to 4.0%; Al: 0.01% to 2.0%; P: 0.10% or less; S: 0.05% or less; N: 0.010% or less; Cr: 0.0% to 3.0%; - 7 - Mo: 0 0 9~ • 0 to 1 0 9~ • 0 ' Ni: 0.0% to 3. 0 ~. 0 ' Cu: 0.0% to 3. 0%; Nb: 0. 0% to 0. 3%; Ti 0.0% to 0 3 9- • 0 ' V: 0.0% to 0.5%; B: 0.0% to 0. 19-· 0 ' Ca: 0.00% to 0.01%; Mg: 0.00% to 0.01%; Zr: 0.00% to 0.01%; REM: 0.00% to 0.01%; and the balance: Fe and impurities. [0017] (9) The method of manufacturing the highstrength steel sheet according to ( 8), wherein the step of preparing the steel sheet includes the step of hotrolling and cooling a slab. [0018] (10) The method of manufacturing the highstrength steel sheet according to (9), wherein a rolling temperature is "Ar3 point + 10"C" to lOOO"C, and a total reduction ratio is 15% or more in last two stands of finish rolling in the hot rolling, and a cooling stop temperature is sso·c or lower of the cooling in the step of preparing the steel sheet. [ 0 0 19] ( 11) The method of manufacturing the highstrength steel sheet according to (8), 1"herein the step of preparing the steel sheet includes the steps of: hot rolling a slab to obtain a hot-rolled steel sheet; and col.d rolling, annealing and cooling the hot-rolled - 8 - steel sheet. [0020] (12) The method of manufacturing the highstrength steel sheet according to (11), wherej_n a reduction ratio in the cold rolling is 30% or more, a temperature of the annealing is 730'C to 900"C, and an average cooling rate from the temperature of the annealing to 600"C is 1.0"C/s to 20"C/second in cooling in the step of preparing the steel sheet. [0021] (13) The method of manufacturing the highstrength steel sheet according to any of (8) to (12), wherein, in the chemical composition, Cr: 0.05% to 3.0%, Mo: 0.05% to 1.0%, Ni: 0.05% to 3.0%, or Cu: 0.05% to 3.0%, or any combination thereof is satisfied. [0022] (14) The method of manufacturing the highstrength steel sheet according to any of (8) to (13), wherein, in the chemical composition, Nb: 0.005% to 0.3%, Ti: 0.005% to 0.3%, or V: 0.01% to 0.5%, or any combination thereof is satisfied. [0023] (15) The method of manufacturing the highstrength steel sheet according to any of (8) to (14) wherein, in the chemical composition, B: 0. 0001% to 0.1% is satisfied. [0024] (16) The method of manufacturing the high- 9 - strength steel sheet according to any of (8) to (15), wherein, in the chemical composition, Ca: 0.0005% to 0.01%, Mg: 0.0005% to 0.01%, Zr: 0.0005% to 0.01%, or REM: 0.0005% to 0.01%, or any combination thereof is satisfied. ADVANTAGEOUS EFFECTS OF INVENTION [0025] According to the present invention, since tho shape of martensite grain is appropriate, it is possible to improve the local ductility while securing high strength. BRIEF DESCRIPTION OF DRAWINGS [0026] [Fig. 1A] Fig. lA is a view illustrating an example of a shape of a martensite grain; [Fig. 1B] Fig. 18 is a view illustrating another example of a shape of a martensite grain; [Fig. 2] Fig. 2 is a view illustrating formation sites of martensite grains; [Fig. 3] Fig. 3 is a view illustrating various shapes of martensite grains; [Fig. 4A] Fig. 4A is a view illustrating an example of a relationship between an area of a martensite grain and an area of a polygon; [Fig. 48] Fig. 48 is a view illustrating another example of a relationship between an area of a martensite grain and an area of a polygon; [Fig. 4C] Fig. 4C is a view illustrating still another example of a relationship between ar1 area of a martensite grain and an area of a polygon; - 10 - [Fig. 5] Fig. 5 is a diagram illustrating an inclusion relationship of martensite grains; [Fig. 6A] Fig. 6A is a view illustrating a change in microstructure; [Fig. 6B] Fig. 6B is a view illustrating a change in microstructure subsequent to Fig. 6A; [Fig. 6C] Fig. 6C is a view illustrating a change in microstructure subsequent to Fig. 68; [Fig. 7] Fig. 7 is a diagram illustrating a relationship between tensile strength and elongation in a first experiment; [Fig. 8] Fig. 8 is a diagram illustrating a relationship between the tensile strength and reduction of area in the first experiment; [Fig. 9] Fig. 9 is a diagram illustrating a relationship between tensile strength and elongation in a second experiment; and [Fig. 10] Fig. 10 is a diagram illustrating a relationship between the tensile strength and reduction of area in the second experiment. DESCRIPTION OF EMBODIMENTS [0027] The present inventors observed microstructures of high-strength steel sheets manufactured by cooling with a runout table after hot rolling and microstructures of high-strength steel sheets manufactured by annealing after cold rolling (hereinafter sometimes referred to as "cold-rolled sheet annealing''). As a result of the observation, as illustrated in Fig. lA, it has been revealed that grains Ill, 112, and 113 of ferrite, bainite, or - 11 - pearlite have grown so as to expand outward and that a martensite grain 110 is formed on the grain boundary triple point in many fields of view. In this microstructure, a grain boundary Bl between the martensite grain 110 and the grain 111 is bulging toward the martensite grain 110 side with respect to a line segment Ll connecting a grain boundary triple point T31 of the martensite grain 110, the grain 113 and the grain 111, and a grain boundary tri.ple point Tl2 of the martensite grain 110, the grain 111 and the grain 112, when viewed from the martensite grain 110. A grain boundary B2 between the martensite grain 110 and the grain 112 is bulging toward the martensite grain 110 side with respect to a line segment L2 connecting the grain boundary triple point T12 and a grain boundary triple point T23 of the martensite grain 110, the grain 112 and the grain 113. A grain boundary B3 between the martensite grain 110 and the grain 113 is bulging toward the martensite grain 110 side with respect to a line segment L3 connecting the grain boundary triple point T23 and the grain bo11ndary triple point T31 •. Jn B .h~gh-strength steel sheet having such a microstructure, the grain boundaries of the martensite grain 110 are sagging, stress tends to concentrate near the grain boundary triple points T12, T23, and T31, and cracking is likely to occur from these regions. For this reason, it is difficult to obtain excellent local ductility. [ 0 0 2 8] The reason for obtaining such a mi_crostructure is considered that ferrite grains or the like grow to - 12 - expand outward during cooling after hot rolling at a run-out table or cooling after cold-rolled sheet annealing, and martensite generates in the remaining area thereafter. [0029] As a result of intensive investigation by the present inventors on the microstructure capable of obtaining excellent local ductility with reference to the observation results as described above, it has been found that a microstructure as illustrated in Fig. 1B is suitable for improving the local ductility. That is, it has been found that a microstructure in which a martensite grain 210 bulges outward and is surrounded by grains 211, 212, and 213 of a matrix such as ferrite is preferable. In this microstructure, a grain boundary 81 between the martensite grain 210 and the grain 211 is bulging toward the grain 211 side with a line segment L1 connecting a grain boundary triple point T31 of the martensite grain 210, the grain 213, and the grain 211, and a grain boundary triple point T12 of the martensite grain 210, the grain 211, and the grain 212, when viewed from the martensite grain 210. A grain boundary B2 between the martensite grain 210 and the grain 212 is bulging toward the grain 212 side with respect to a line segment L2 connecting the grairr boundary triple point T12 and the grain boundary triple point T23 of the martensite grain 210, the grain 212, and the grain 213, when viewed from the martensite grain 210. A grain boundary B3 between the martensite grain 210 and the grain 213 is bulging toward the grairr 213 side with respect to a line segment L3 connecting - 13 - the grain boundary triple point T23 and the grain boundary triple point T31, when viewed from the martensite grain 210. In a high-strength steel sheet having such a microstructure, the grain boundaries of the martensite grain 210 are bulging outward, stress is hardly concentrated near the grain boundary triple points T12, T23, and T31, and excel.lent local ductility can be obtained. A high-strength steel sheet having such a microstructure may be manufactured by a method described later. [0030] Hereinafter, embodiments of the present invention will be described. [0031] First, the chemical compositions of the highstrength steel sheet according to the embodiment of the present invention and a steel used for manufacturing the high-strength steel sheet will be described. Though details will be described later, the highstrength steel sheet according to the embodiment of the present invention is manufactured through hot rolling, cooling, and reheating or through hot rolling, cold rolling, cold-rolled sheet annealing, cooling, and heat treatment. .Accordingly, the chemical compositions of the hj_gh-strength steel sheet and the steel are ones in consideration of not only characteristics of the highstrength steel sheet but also the above-stated processing. In the following description, ''%'' being a unit of a content of each element contai.ned in the high-strength steel sheet and the steel means "mass%" unless otherwise specified. The high-strength steel sheet according to the present embodiment and the steel - 14 - used for the manufacturing the same contain, by mass%, C: 0.03'6 to 0.35%, Si: 0.01% to 2 . 0% f Mn: 0.3% to 4 • 0% 1 Al: 0.01% to 2.0%, p : 0.10% or less, s : 0.05% or less, N: 0.010% or less, Cr: 0.0% to 3. 0% f Mo: 0.0% to 1.0%, Ni: 0.0% to 3. 0% r Cu: 0.0% to 3.0%, Nb: 0.0% to 0. 3%, Ti: 0.0% to 0.3%, V: 0.0% to 0. 5%' B: 0. 0% to 0 . 1 % ' Ca: 0.00% to 0.01%, Mg: 0.00% to 0.01%, Zr: 0.00% to 0.01%, rare earth metal (REM): 0. 00% to 0. op,, and the balance: Fe and impurities. Examples of the impurities include one contained in raw materials such as ore and scrap, and one contained during a manufacturing process. Sn and As may be examples of impurities. [0032] (C: 0.03% to 0.35%) c contributes to improvement in strength thrOugh strengthening of martensite. When a C content is less than 0.03%, sufficient strength, for example, tensile strength of 500 N/m2 or more cannot be obtained. Therefore, the C content is 0.03% or more. On the other hand, when the C content exceeds 0. 35%, the area fraction and size of pearlite in the initial structure after hot rolling and cooling are increased, the area fraction of pearlite and island-shaped cementite in a microstructure after reheating is increased, and therefore sufficient local ductility cannot be obtained. Therefore, the C content is 0.35% or less. The C conlent is preferably 0.25% or less in order to obtain higher local ductility, and the C content is preferably 0.1% or less in order to obtai.n more excel.lent hole expandability. [ 0 0 3 3] (Si: 0.01% to 2.o:;:;) - 15 - Si is a ferrite former element and promotes the formation of ferrite in cooling after the hot rolling. Si also contributes to improvement of workability by suppressing the generation of harmful carbides and contributes to improvement in strength through solid solution strengthening. When a Si content is less than 0.01%, these effects cannot be obtained sufficiently. Therefore, the Si content is 0.01% or more. When the Si content is less than 0.1%, the Si c:or1tent is preferably 0.3% or more. On the other hand, when the Si content exceeds 260%, the chemical conversion property and spot weldability are deteriorated. Therefore, the Si content is 2.0% or less. [0034] (~1n: 0.3% to 4.0%) Mn contributes to improvement in strength. When a Mn content is less than 0.3%, sufficient strength cannot be obtained. Therefore, the Mn content is 0. 3'" or more. On the other hand, when the Mn content exceeds 4.0%, micro segregation and macro segregation are likely to occur, and local ductility and hole expandability are deteriorated. content is 4.0% or less. [ 0 03 5] (Al: 0.01% to 2.0%) Therefore, the Mn Al acts as a deoxidizer. When an Al content is less than 0.01%, oxygen may not be sufficiently excluded in some cases. Therefore, the Al content is 0.01% or more. Likco Si, AJ. promotes the formation of ferrite and suppresses the formation of harmful carbides and contributes to the improvement of workability. Also, Al does not affect the chemical - 16 - conversion property as much as Si. Therefore, Al is useful for compatibility of ductility and chemical conversion property. However, when the Al content exceeds 2.0%, the effect of improving the ductility is saturated, and the chemical conversion property and spot weldability may be deteriorated. Therefore, the Al content is 2.0% or less. The Al content is preferably 1.0% or less in order to obtain more excellent chemical conversion property. [0036] (P: 0.10% or less) P is not an essential element, and is contained as an impurity in the steel, for example. Since P deteriorates weldability, workability and toughness, a lower P content is more preferable. In particular, when the P content exceeds 0.10%, weldability, workability and toughness are remarkably deteriorated. Therefore, the P content is 0.10% or less. The P content is preferably 0.03% or less in order to obtain better workability. It is costly to decrease the P content, and in order to decrease the P content to less than 0.001%, a cost increases notably. Thus, the P content may be 0.001% or more. P may improve corrosion resistance when Cu is contained. [0037] (S: 0.05% or less) S is not an essential element, and is contained as an impurity in the steel, for example. Since S forms a sulfide such as MnS, and the sulfide serves as an origin of cracking, and reduces local ductility and hole expandahility, a lower S content is more preferable. In particular, when tt1e S content exceeds - 17 - 0.05%, the local ductility and the hole expanding property are remarkably deteriorated. Therefore, the s content is 0.05% or less. It is costly to decrease the S content, and in order to decrease the S content to less than 0.0005%, a cost increases notably. S content may be 0.0005% or more. Thus, the [0038] (N: 0.010% or less) N is not an essential element, and is contained as an i.mpuri ty in the steel, for example. N causes stretcher strain and deteriorates workability. When Ti and Nb are contained, N forms (Ti, Nb) N and the precipitate serves as an origin of cracking. N may cause roughening of the end face in punching and greatly deteriorate local ductility. lower N content is more preferable. Therefore, a In particular, when the N content exceeds 0.010%, the above phenomenon is remarkable. Therefore, the N content is 0. 010% or less. It is costly to decrease the N content, and in order to decrease the N content to less than 0.0005%, a cost increases notably. be 0.0005% or more. Therefore, the N content may [0039] C r "f .. M o , N i , C u , N b, T i , V, B, C a , M g , Z r and REM are not essential elements and are arbitrary elements which may be appropriately contained in the steel sheet and steel to the extent of a specific amount. [0040] (Cr: 0.0% leo 3.0~;, Mo: 0.0% to 1.0'6, Ni: 0.0 9e to 3.0~-;, Cu: 0.0';1 to 3.0~>) Cu contributes lo improvement in .strength. Cu improves corrosion resistance when P is contained. - 18 - Therefore, Cu may be contained. In order to sufficiently obtain these effects, a Cu content is preferably 0.05% or more. On the other hand, when the Cu content exceeds 3.0%, the hardenability is excessive and the ductility decreases. Therefore, the Cu content is 3.0% or less. Ni facilitates the formation of martensite through improvement of hardenability. Ni contributes to suppression likely to occur when Cu is of hot cracking which is contained. Therefore, may be contained. In order to sufficiently obtain these effects, aNi content is preferably 0.05% or Ni more. On the other hand, when the Ni content exceeds 3.0%, the hardenability is excessive and the ductility decreases. Therefore, the Ni content is 3.0% or less. Mo suppresses the formation of cementite and suppresses the formation of pearlite in the initial structure. Mo is also effective for forming martensite grains in the reheating. Therefore, Mo may be contained. In order to sufficiently obtain these effects, a Mo content is preferably 0.05% or more. On the other hand, when the Mo content exceeds 1.0%, the ductility decreases. Therefore, the Mo content is 1.0% or less. Like Cr, Cr suppresses the formation of cementite and suppresses lhe formation of pearlite in the initial structure. Therefore, Cr may be contained. In order to obtain this effect sufficiently, a Cr content is preferably 0.05% or more. On the other hand, when the Cr content exceeds 3.0%, the ductility decreases. Cr corrtent is 3.0%. Therefore, the [ 0 0 4 1 J From the above, it is understood that ''Cr: - 19 - 0 . 0 5 -% t 0 3 . 0 % u ' " M 0 : 0 . 0 5 % t 0 1 . 0 % II ' \\ N i : 0 . 0 5 % t 0 3.0%", or "Cu 0.05% to 3.0%'', or any combination thereof is preferably satisfied. [0042] 0- 5%) (Nb: 0.0% to 0.3%, Ti: 0.0% to 0.3%, V: 0.0% to Nb, Ti, and V contribute to improvement in strength by forming carbides. Accordingly, Nb, Ti, or V, or any combination thereof may be contained. In order to sufficiently obtain this effect, a Nb content is preferably 0.005% or more, a Ti content is preferably 0.005% or more, and a V content is preferably 0.01% or more. On the other hand, when the Ni content exceeds 0. 3%, the Ti content exceeds 0. 3%, or the V content exceeds 0.5%, the precipitation strengthening is excessive and the workability deteriorates. Therefore, the Nb content is 0.3% or less, the Nb content is 0.3% or less, and the V content is 0.5% or less. [0043] From the above, it is understood that ~Nb: 0 . 0 0 5 % to 0 . 3 % " , " T i : 0 . 0 0 5 % t o 0 . 3 % " , o r \\ V : 0 . 0 1 % to 0.5%", or any combination thereof is preferably satisfied. [0044] (B; 0 ..•. 0 .. % to 0.1%) B contributes to improvement in strength. Therefore, B may be contained. In order to obtain this effect sufficiently, a B content is preferably 0.0001% or more. On the other hand, when the B content exceeds 0.1%, the hardenability is excessive and the ductility decreases. Therefore, the B content is 0.1% or less. [0045] (Ca: 0.00~; leo 0.00% to 0.01%, REM: 0.01%, Mg: 0.00% 0.00~; to 0.019o) - 20 - to 0.01%, Zr: Ca, Mg, Zr, and REM control the shape of sulfidebased inclusions and are effective for improving local ductility. Thus, Ca, Mg, Zr, or REM, or any combination thereof may be contained. In order to sufficiently obtain this effect, a Ca content is preferably 0.0005% or more, the Mg content i .s preferably 0.0005% or more, the Zr content is preferably 0.0005% or more, the REM content is preferably 0.0005% or more. On the other hand, when the Ca content exceeds 0.01%, the Mg content exceeds 0. 01%, the Zr content exceeds 0. 01%, the REM content exceeds 0.01%, the ductility and local ductility are deteriorated. Therefore, the Ca content is 0.01% or less, the Mg content is 0.01% or less, the Zr content is 0.01% or less, and the REM content is 0.01% or less. [0046] From the above, it is understood that "Ca: 0.0005% to 0.01%", "Mg: 0.0005% to 0.01%", "Zr: 0.0005% to 0 . 0 1 % '' , o r '' REM 0.0005% to 0.01%", or any combination thereof is preferably satisfied. [0047] REM (rare earth metal) indicates elements of 17 kinds in total of Sc, Y, and lanthanoid, and a "REM content" means a total content of these elements of 17 kinds. Lanthanoid is industrially added as a form of misch metal, for example. [0048] Next, the microstructure of the high-strength steel sheet according to the embodiment of the present invention will be described. In the following description, ~%'' being is a unit of phase or structure contaJned in the high-strength sleel sheet means ''area%'' unless otherwise specified. The high-strength - 21 - steel sheet according to the embodiment of the present invention incJ.11des a microstructure represented, by area%, martensite: 5% or more 1 ferrite: 20% or more, and pearlite: s~,s or less. [0049] (Martensite: 5% or more) Martensite contributes to the improvement of strength in a Dual Phase steel (DP steel) When an area fraction of martensite is less than 5 ~ 0 ' sufficient strength, for example, tensile strength of 500 N/m2 or more cannot be obtained. Therefore, the area fraction of martensite lS 5% or more. The area fraction of martensite is preferably 10% or more in order to obtain superior strength. On the other hand, when the area fraction of martensite exceeds 60%, sufficient elongation cannot be obtained in some cases. Therefore, the area fraction of martensite is preferably not more than 60%. [0050] (Ferrite: 20% or more) Ferrite contributes to the improvement of elongation in a DP steel. When an area fraction of ferrite is 20% or less, sufficient elongation cannot be obtained. Therefore, the area fraction of ferrite lS 20% or more. The area fraction of ferrite is preferably 30% or more in order to obtain better elongation. [ 0 0 51] (Perlite: ')'6 or less) Pearlite is not essential, and it may be formed in the manufacturing process of high-strength steel sheet. Since pearlite reduces elongation and hole expandability of a DP steel, a lower are faction of pearlite is more preferable. In particular, when the area fraction of pearlite exceeds 5%, the reduction in elongation and hole expandability is remarkable. Therefore, the area fraction of pearlite is 5% or less. [0052] The balance of the microstructure is, for example, bainite or retained austenite or both of them. [0053] Here, the configuration of martensite will be described in detail. In the present embodiment, an average diameter of martensite is 4 pm or less in equivalent circle diameter, a ratio of a number of bulging type martensite grains to a number of martensite grains on grain boundary triple points of a matrix is 70% or more, and a particular area ratio of 1.0 or more. [0054] (Average diameter of martensite: 4 pm or less in equivalent circle diameter) When an average diameter of martensite is more than 4 pm in equivalent circle diameter, stress tends to concentrate on martensite and cracks are likely to occur. Therefore, the average diameter of martensite is 4 pm or less in equivalent circle diameter. In order to obtain better formability, the average diameter of martensite is preferably 3 pm or less in equivalent circle diameter. [0055] (Ratio of a number of bulging type martensite grains to a number of martensite grains on grain boundary triple points of a matrix: 70% or more) A bulging type martensite grain is one of martensite grai11s among martensite grains on grain boundary triple points of a matrix. - 23 - The bulging type martensite grain is on one of the grain boundary triple points of the matrix, and at least one of whose grain boundaries of the bulging type martensite grain, the grain boundaries connecting two adjacent grain boundary triple points of the bulging type martensite grain and grains of the matrix, has a convex curvature to an outer side with respect to line segments connecting the two adjacent grain boundary triple points. As illustrated in Fig. 2, a martensite grain 301 on a grain boundary triple point of a matrix and a martensite grain 302 on a grain boundary between two grains of the matrix are included in a high-strength steel sheet, and the bulging type martensite grain belong to the martensite grain 301. The martensite grains on the grain boundary triple point include a martensite grain 303 composed by combining two or more martensite grains on grain boundary triple points. However, the martensite grain 303 is not ~on one of the grain boundary triple points of the matrix", so it does not belong to the bulging type martensite grain. Among the six martensite grains illustrated in Fig. 3, the martensite ~rains 401, 402, 403 and 404 belong to the bulging type martensite grain, since at least one of the grain boundaries of each of the grains, the grain boundaries connecting two adjacent grain boundary triple points of the martensite grain and grains of the matrix, has a convex curvature to an outer side with respect to line segments connecting the two adjacent grain boundary triple points. On the other hand, the martensite grains 405 and 406 do not belong to the - 24 - bulging type martensite grain, since all the grain boundaries of each of the grains, the grain boundaries connecting two adjacent grain boundary triple points of the martensite grain and grains of the matrix, do not have a convex curvature to an outer side with respect to line segments connecting the two adjacent grain boundary triple points. [0056] The higher the ratio of the number of the bulging type martensite grains is, the less stress concentration occurs and excellent local ductility can be obtained. When the ratio of the number of the bulging type martensite grains to the number of the martensite grains on the grain boundary triple points of the matrix is less than 70%, the ratio of martensite grains which are likely to cause stress concentration is high and excellent local ductility cannot be obtained. Therefore, the ratio of the number of the bulging type martensite grains to the number of the martensite grains on the grain boundary triple points of the matrix is 70% or more. [0057] (Particular area ratio: 1.0 or more) The bulging type martensite grains may include those in which a ratio of convex portions having convex curvature outward with respect to a line segment rs greater than or equal to a ratio of concave portions having convex curvature inward, and the others not. The former ones are more likely to contrib11tc to the improvement of local ductility than the latter ones, and the higher the area fraction of the latter ones, the lower the local ductility. - 25 - As for the former bulging type martensite grain, as illustrated in Fig. 4A, an area VMl of the bulging type martensite grain is equal to or larger than an area AOl of a polygon composed of the line segments connecting two adjacent grain boundary triple points of the bulging type martensite grain. On the other hand, as for the latter bulging type martensite grain, as illustrated in Fig. 48, an area VM2 of the bulging martensite grain is smaller than an area A02 of a polygon that is composed of the line segments connecting two adjacent grain boundary triple points of the bulging martensite grain. In addition, although not belonging to the bulging type martensite grain, as for martensite grains on plural grain boundary triple points of the matrix like the martensite grain 303 in Fig. 2, as illustrated in Fig. 4C, an area VM3 of the martensite grain is sometimes smaller than an area A03 of a polygon that is composed of the line segments connecting two adjacent grain boundary triple points of the martensite grain. When an area ratio represented by VM I AO is less than 1.0, it is difficult to obtain sufficient local ductility even if the .r.atio of the bulging type martensite grains is 70% or more. Here, VM denotes a total area of a plurality of, for example, 200 or more, martensite grains on grain boundary triple points, and AO denotes ~ total area of polygons composed of the line segments connecting two adjacent grain boundary triple points of the plurality of martensite grains. Therefore, the particular area ratio represented by VM I AO is 1.0 or more:. - 26 - [0058] Fig_ 5 illustrates an inclusion relationship of martensite grains in the present embodiment_ In the present embodiment, the ratio of the number of the bulging type martensite grains (group B) to the number of the martensite grains on the grain boundary triple points of the matrix (group A) is 70% or more, and as for the martensite grains on the grain boundary triple points of the matrix (group A), the area ratio represented by VM I AO is l_O or more. [0059] According to the present embodiment, it is possible to obtain a tensile strength of 500 N/mm2 or more and a reduction of ar~a RA of 0.5 or less, for example. As a product (TS x EL) showing the balance between the tensile strength TS and the elongation EL, a value of 18000 N/mm2 ·% or more can be obtained. Then, it is possible to obtain excellent local ductility as compared with a conventional high-strength steel sheet having the same level tensile strength. [0060] A hot-dip galvanized layer may be included in the high-strength steel sheet. When a hot-dip galvanizing layer is included, more excellent corrosion resistance can be obtained. The coating weight is not particularly limited, but the coating weight is preferably 5 g/m2 or more per one side in order to obtain particularly good corrosion resistance. [0061] Preferably, the hot-dip galvanized layer contains Zn and Al, for example, and the Fe content thereof is 13% or less. A hot-dip galvanized layer having an Fe content of 13% or less is excellent in plating adhesion, formability and hole expandability. - 27 - On the other hand, when the Fe content exceeds 13%, the adhesion of the hot-dip galvanized layer itself is low, and the hot-dip galvanized layer may be broken or fall· off during processing of the high-strength steel sheet and adheres to a mold, it may cause scratches. [00621 The hot-dip galvanized layer may be alloyed. Since Fe is incorporated from the base steel sheet into the alloyed hot-dip galvanized layer, excellent spot weldability and coatability are obtained. The Fe content of the alloyed hot-dip galvanized layer is preferably 7% or more. When the Fe content is less than 7%, the effect of improving spot weldability may be insufficient in some cases. As long as the Fe content of the hot-dip galvanized layer not alloyed is less than 13%, it may be less than 7% or substantially 0%, and good plating adhesion, formability and hole expandability can be obtained. [0063) The high-strength steel sheet may contain an over-plating layer on the hot-dip galvanized layer. When the over-plating layer is included, excellent coatability and weldability can be obtained. Further, the high-strength steel sheet including the hot-dip galvanized layer may be subjected to a surface treatment such as a chromate treatment, a phosphate treatment, a lubricity improving treatment Qnd a weldability improving treatment. [ 0 0 61 l Next, a first example of a method of manufacturing the high-strength steel sheet according to the embodiment of the present invention will be described. In the first example, hot rolling of the -· 28 - slab having the above chemical composition, cooling and reheating are performed in this order. Fig. 6A to Fig. 6C arc views illustrating changes in microstructure. A microstructure of a steel sheet obtained through hot rolling and subsequent cooling (initial structure) has a low pearlite area fraction and a small average diameter of pearlite. The balance of the initial structure is, for example, ferrite (ex) (Fig. 6A). In the subsequent reheating, the steel sheet is heated to the dual phase region, and austenite (y) is grown on the grain boundary triple point of ferrite (Fig. 6B) The austenite growing on the grain boundary triple point has an outwardly bulging shape. Then, austenite is transformed into martensite (M) by quenching from the dual phase region (Fig. 6C) As a result, martensite grains having a bulge outward are obtained. Hereinafter, these processes will be described in detail [0065] (Hot rolling and cooling) A steel sheet is obtained by hot rolling and subsequent cooling. The microstructure (initial structure) of the steel sheet is such that an area fraction of pearlite is 10% or less and an average diameter of pearlite is 10 pm or less in equivalent circle diameter. Cementite is included in pearlite, and cementite dissolves in the reheating and inhibits the formation of austenite. When the area fraction of pearlite exceeds 10%, a sufficient amount of austenite cannot be obtained in the reheating, and as a result, it is difficult to make the area fraction of martensite - 29 in the high-strength steel sheet 5% or more. Therefore, the area fraction of pearlite is 10% or less. When also the average diameter of pearlite is more than 10 pm in equivalent circle diameter, a sufficient amount of austenite cannot be obtained in the reheating, and as a result, it is difficult to make the area fraction of martensite in the high-strength steel sheet 5% or more. When the average diameter of pearlite is more than 10 ~m in equivalent circle diameter, austenite grows even in pearlite, and some of austenite may be bonded to each other. The shape of austenite grain obtained by combining a plurality of austenite grains is difficult to have a shape bulging outward. is 10 ~m [0066] Therefore, the average diameter of pearlite or less in equivalent circle diameter. The balance of the initial structure of the steel sheet is not particularly limited, and is preferably ferrite, bainite, or martensite, or any combination thereof, and in particular, the area fraction of one of these is preferably 90% or more. This is to facilitate the growth of austenite from the grain boundary. triple point in the reheating. The average diameter of grains of ferrite, bainite, or martensite, or any combination thereof is preferably 10 ~m or less in equivalent circle diameter. This lS for reducing the martensite grain in the high-strength steel sheet. Lump cementite may be contained in the balance of the initial structure of the steel sheet, but since it inhibits the formation of austenite in the reheating, the area fraction of the lump cementite is - 30 - preferably 1% or less. [0067] It is preferable that the ferrite grains in a surface layer portion of the steel sheet be small. Ferrite does not transform in the reheating, and remains as it is on the high-strength steel sheet. Since the cold rolling is not performed in the first example, the high-strength steel sheet is thick, and strain in the surface layer portion in forming such as bending, hole expanding, ar1d bulging tends to be larger than internal strain. Accordingly, when the ferrite grains in the surface layer portion of the highstrength steel sheet are large, cracks may occur in the surface layer portion, and the local ductility may decrease. Supposing that an average diameter of ferrite in a region where the depth from the surface of the steel sheet is 1/4 of the thickness of the steel sheet is D0 , in order to suppress such cracking of the surface layer portion, an average diameter Ds of ferrite in the surface layer portion from the surface of the steel sheet to the depth 4 x Do is not more than twice the average diameter D0 . Hereinafter, a portion where the average diameter Ds of ferrite in the surface layer portion is more than twice the average diameter Do may be referred to as a surface coarse grain layer. [0068] The conditions for the hot rolling are not particularly limited, and in the rolling of the last two stands of the finish rolling, the temperature is preferably "Ar3 point + lO"C" to lOOO"C, and the total reductior1 ralio is preferably 15% to 1S %. The thickness after the hot rolling is, for example, 1.0 mm - 31 - to 6.0 mm. [0069] When the rolling temperature in any of the last two stands is lower than Ar3 point + lO"C, the surface coarse grain layer is likely to be formed. Therefore, the rolling temperature in both of the last two stands is preferably Ar3 point + lO"C or more. On the other hand, when the rolling temperature exceeds lOOO"C in any of the last two stands, the average diameter of pearlite in the initial structure is not easily 10 pm or less in equivalent circle diameter. Therefore, the rolling temperature in both of the last two stands is preferably 1000"C or less. [ 0 0 7 0 J When the total reduction ratio of the last two stands is less than 15%, the austenite grains easily become large and the average diameter of pearlite in the initial structure is not easily 10 pm or less in equivalent circle diameter. Therefore, the total reduction ratio of the last two stands is preferably 15% or more, and more preferably 20% or more. On the other hand, when the total reduction ratio exceeds 45%, it is difficult to adversely affect the mechanical properties of the steel sheet, but it may be difficult to control the shape of the steel sheet. Therefore, the total reduction ratio of the last two stands is preferably 45% or less, and more preferably 40% or less. [ 0 0 71 J After the hot rolling, the steel sheet 1s cooled to 550°C or lower. When the cooling stop temperature exceeds 550°C, the area fraction of pearlite exceeds 10%. This cooling is performed, for - 32 - example, with a run-out table (ROT). For example, a part or all of austenite transforms into ferrite in the cooling. The cooling condition is not particularly limited, and a part or all of austenite may be transformed into bainite, or martensite, or both. Thus, a steel sheet having a specific initial structure is obtained. The steel sheet is coiled after the cooling. For example, the coiling temperature is 550"C or lower. When the coiling temperature exceeds 550"C, the area fraction of pearlite exceeds 10%. [0072] (Peheating) In the reheating, the steel sheet is heated to a first temperature of 770"C to 820"C at an average heating rate of 3"C/s to 120"C/s, and the steel sheet is cooled to a second temperature of 300"C or less at an average cold rolling rate of 60"C/s or more. The cooling to the second temperature starts within 8 seconds once the temperature of the steel sheet reaches the first temperature. As described above, austenite grains bulging outward are grown in the reheating, and martensite grains having the same shape are obtained. [0073] When the average heating rate is less than 3"C/s, austenite grows excessively during the heating and austenite grains bind to each other, making it difficult to obtain desired martensite in the highstrength steel sheet. rate is 3°C/s or more. Therefore, the average heating On the other hand, when the average heating rate exceeds 120"C/s, the carbide remains, and a sufficient amount of austenite cannot be obtained. Accordingly, the average heating rate is - 33 - 120"C/s or less. [0074] When the achieved temperature (first temperature) is lower than 770"C, if bainite or martensite or both of them are contained in the initial structure, these are hardly transformed into austenite and, it is difficult to obtain the desired martensite. Therefore, the achieved temperature is 770"C or higher. That is, in the present embodiment, when bainite or martensite or both of them are contained in the initial structure, they are transformed into austenite instead of tempering. On the other hand, when the achieved temperature exceeds 820"C, ferrite transforms into austenite, and it is difficult to obtain the desired martensite in a high-strength steel sheet. Therefore, the achieved temperature is 820"C or lower. [0075] When the average cooling rate is less than 60"C/s, ferrite easily grows, making it difficult to obtain martensite in a shape bulging outward. Accordingly, the average cooling rate is 60"C/s or more. On the other hand, when the average cooling rate exceeds 200"C/s, adverse effects on the mechanical properties of the steel sheet are unlikely to occur, but the load on the equipment increases, the uniformity of the temperature decreases, and it is difficult to control the shape of the steel sheet. Therefore, the average cooling rate is preferably 200"C/s or less. [0076] When the cooling stop temperature (second temperature) is higher than 300"C, quenching is insufficient and it is difficult to obtai.n the desired martensite in the high-strength steel sheet. - 34 - Therefore, the cooling stop temperature is 300°C or less. [0077] When the time period from the temperature of the steel sheet reaching the first temperature to the start of the cooling to the second temperature is over 8 seconds, austenite may excessively grow, austenite grains may combine with each other, and then it is difficult to obtain the desired martensite in the high-strength steel sheet. Therefore, the holding time period until the start of the cooling is less than 8 seconds. In order to obtain particularly excellent local ductility, the holding time period is preferably 5 seconds or less. [0078] Thus, the high-strength steel sheet according to the present embodiment may be manufactured. A highstrength steel sheet manufactured using a steel sheet including a surface coarse grain layer includes the surface coarse grain layer. In a high-strength steel sheet manufactured using a steel sheet not including a surface coarse grain layer, an average diameter Ds is not more than twice an average diameter D0 , where Do denotes an average diameter of ferrite in a region where the depth from the surface of the high-strength steel sheet is 1/4 of a thickness of the high-strength steel sheet, and Ds denotes an average diameter of ferrite in a surface layer portion from the surface of the high-strength steel sheet to the depth of 4 x D0 . [0079] Next, a second example of a method of manufacturing tho high-strength steel sheet according to the embodiment of the present invention will be - 35 ~ described. In the second example, hot rolling of the slab having the above chemical composition, cold rolling, cold-rolled sheet annealing, cooling and reheating are performed in this order. A microstructure of a steel sheet obtained through coldrolled sheet annealing and subsequent cooling (initial structure) has a low pearlite area fraction and a small average diameter of pearlite. The balance of the initial structure is, for example, ferrite (a) (Fig. 6A). In the subsequent reheating, the steel sheet is heated to the dual phase region, and austenite (y) lS grown on the grain boundary triple point of ferrite (Fig. 6B). The austenite growing on the grain boundary triple point has an outwardly bulging shape. Then, austenite is transformed into martensite (M) by quenching from the dual phase region (Fig. 6C). As a result, martensite grains having a bulge outward are obtained. Hereinafter, these processes will be described in detail. [0080] (Hot rolling) Hot rolling of the slab is performed to obtain a hot-rolled steel sheet having a thickness of, for example, 1.0 mm to 6.0 mm. [0081] (Cold rolling, cold-rolled sheet annealing, and cooling) A steel sheet is obtained by cold rolling of the hot-rolled steel sheet, cold-rolled sheet annealing and subsequent cooling. The microstructure (initial structure) of the steel sheet is such that an area fraction of pearlite is 10% or less and an average - 36 - diameter of pearlite is 10 pm or less in equivalent circle diameter, and an area fraction of unrecrystallized ferrite is 10% or less. Cementite is included in pearlite, and cementite dissolves in the reheating and inhibits the formation of austenite. When the area fraction of pearlite exceeds 10%, a sufficient amount of austenite cannot be obtained 1n the reheating, and as a result, it is difficult to make the area fraction of martensite in the high-strength steel sheet 5% or more. Therefore, the area fraction of pearlite lS 10% or less. When also the average diameter of pearlite is more than 10 pm in equivalent circle diameter, a sufficient amount of austenite cannot be obtained in the reheating, and as a result, it is difficult to make the area fraction of martensite in the high-strength steel sheet 5% or more. When the average diameter of pearlite is more than 10 pm in equivalent circle diameter, austenite grows even in pearlite, and some of austenite may be bonded to each other. The shape of austenite grain obtained by combining a plurality of austenite grains is difficult to have a shape bulging outward. Therefore, the average diameter of pearlite is 10 pm or less in equivalent circle diameter. When the area fraction of unrecrystallized ferrite exceeds 10%, sufficient local ductility cannot be obtained. Therefore, the area fraction of \Jnrccrystallized ferrite is 10% or less. [ 0 0 8 2] The balance of the initial structure of the steel sheet lS not particularly limited, and is preferably ferrite, bainite, or martensite, or any - 37 - combination thereof as in the first example, and in particular, the area fraction of one of these is preferably 90% or more. The average diameter of grains of ferrite, bainite, or martensite, or any combination thereof is preferably 10 ~m or less in equivalent circle diameter. Lump cementite may be contained in the balance of the initial structure of the steel sheet, but the area fraction of the lump cementite is preferably 1% or less. [0083] The conditions for the cold rolling are not particularly limited, and the reduction ratio is preferably 30% or more. When the reduction ratio is 30% or more, the grains contained in the initial structure can be made fine, and the average diameter of martensite in the high-strength steel sheet can be easily reduced to 3 ~m or less. The thickness after the cold rolling is, for example, 0.4 mm to 3.0 mm. [ 0 0 8 4] The conditions for the cold-rolled sheet annealing are not particularly limited, and preferably the annealing temperature is 730"C to 900"C, followed by cooling to 600"C at an average rate of l.O"C/s to 2o•c1s. [0085] When the annealing temperature is lower than 730"C, it is difficult to reduce the area fraction of unrecrystallized ferrlte jn the initial structure to 10% or less. Therefore, the annealing temperature is preferably 730"C or higher. On the othc~r hand, when the annealing temperature exceeds 900"C, it is difficult to make the average diameter e of pearlite ln the initial structure 10 pm or less in equivalent - ][l - circle diameter, and the average diameter of martensite in the high-strength steel sheet is likely to be large. Therefore, the annealing temperature is preferably 900"C or lower. [0086] When the average cooling rate to 600"C is less than l.O"C/s, the area fraction of pearlite in the initial structure exceeds 10%, or the average diameter of pearlite exceeds 10 pm in equivalent circle diameter. Therefore, preferably l.O"C/s or the average cooling rate more. On the other hand, is when the average cooling rate to 600"C exceeds 20"C/second, the initial structure is not stable and the desired initial structure cannot be obtained in some cases. Therefore, the average cooling rate is preferably 20"C/s or less. [0087] When the cooling stop temperature exceeds 600"c, the area fraction of pearlite exceeds. 10%. For example, a part or all of austenite transforms into ferrite in the cooling. The cooling condition is not particularly limited, and a part or all of austenite may be transformed into bainite, or martensite, or both. Thus, a steel sheet having a specific initial structure is obtained. [0088] (Reheating) The reheating is performed under the same conditions as in the first example. That is, the steel sheet is heated to a first temperature of 770"C to 820"C at an average heating rate of 3"C/s to 120"C/s, and the steel sheet is cooled to a second temperature 300"C or less at an average cold rolling rate of 60"C/s - 39 - or more. Cool to temperature. The cooling to the second temperature starts within 8 seconds once the temperature of the steel sheet reaches the first temperature. As described above, austenite gra1ns bulging outward are grown in the reheating, and martensite grains having the same shape are obtained. [0089] Thus, the high-strength steel sheet according to the present embodiment may be manufactured. A microstructure of a high-strength steel sheet manufactured using a steel sheet with an area fraction of unrecrystallized ferrite exceeding 10% includes unrecrystallized ferrite with an area fraction of exceeding 10%. An area fraction of unrecrystallized ferrite is 10% or less in a high-strength steel sheet manufactured using a steel sheet with an area fraction of unrecrystallized ferrite of 10% or less. [ 0090 J In the first example, since the steel sheet is prepared by hot rolling and subsequent cooli.ng, this steel sheet does not include more than 10% of unrecrystallized ferrite. In the second example, since the steel sheet is prepared by cold rolling of the hotrolled steel sheet, cold-rolled sheet annealing, and subsequent cooling, this steel sheet does not include a surface coarse grain layer. [0091] IncidentaJ.ly, the steel sheet or the highstrength steel sheet may be immersed in a plating bath to form a plating layer, and alloying treatment at 600"C or less may be performed after forming the plating layer. For example, a hot-dip galvanized layer may be formed, and then an alloying trealment may be - 4 () - carried out. An over-plating layer may be formed on the hot-dip galvanizing layer. After forming the hotdip galvanized layer, surface treatment such as chromate treatment, phosphate treatment, lubricity improving treatment and weldability improving treatment may be carried out. Pickling and skin-pass rolling may be carried out. [0092] The area fraction of each phase and structure may be measured by the following method, for example. For example, Le Pera etching or Nital etching of a high-strength steel sheet is performed, observation using an optical microscope or a scanning electron microscope (SEM) is performed, each phase and structure are identified, and the area fractions are measured using an image analyzer or the like. The observation target region is, for example, a region whose depth from the surface of the high-strength steel sheet is 1/4 of the thickness of the high-strength steel sheet. When measuring the average diameter and area of the martensite grains, measurements are made on 200 or more martensite grains. [0093] The average diameter of the ferrite grains in the steel sheet used in the first example may be measured by the following method, for example. That is, Nital etching of the steel sheet is performed, a cross section orthogonal to the rolling direction is observed using an optical microscope or SEM, and the average diameter of ferrite grains is measured using an image analyzer or the like. The observation target area is a region whose depth from the surface of the - 41 - steel sheet is 1/4 of the thickness of the steel sheet and a surface layer portion. These measurement methods are merely examples, and measurement methods are not limited to these methods. [0094] The area fraction of unrecrystallized ferrite in the steel sheet used in the second example may be measured by the following method, for example. That is, a specimen is prepared in which a region whose depth from the surface of the steel sheet is l/4 of the thickness of the steel sheet is a measurement plane, and the crystal orientation measurement data is obtained in electron back scattering pattern (EBSP) of each of the measurement planes. In the preparation of the sample, for example, thinning by mechanical polishing or the like and removal of strain and thinning by electrolytic polishing or the like are performed. EBSP measures 5 points or more in each grain of the sample and the crystal orientation measurement data are obtained from each measurement result for each measurement point (pixel). Then, the obtained crystal orientation measurement data is analyzed by the Kernel Average Misorientation (KAM) method to distinguish the unrecrystallized ferrite contuined in the ferrite, and the area fraction of the unrecrystallized ferrite in the ferrite is calculated. From the area fractj_on of ferrj.te in the initial structure and the area fraction of unrecrystallized ferrite in ferrite, the area fraction of unrecrystallized ferrite in the initial structure can be calculated. In the KAM method, the misorientation - 4? - between adjacent measuring points can be detected quantitatively. In the present invention, grains having an average misorientation of 1° or more from the adjacent measuring points are defined as unrecrystallized ferrite. [0095] These measurement methods are merely examples, and measurement methods are not limited to these methods. [0096] Note that the above-described embodiments merely illustrate concrete examples of implementing the present invention, and the technical scope of the present invention is not to be construed in a restrictive manner by these embodiments. That is, the present invention may be implemented in various forms without departing from the technical spirit or main features thereof. EXAMPLE [ 0097] Next, examples of the present invention will be described. A condition of the examples is one condition example which is adopted in order to confirm a possibility of implementation and an effect of the present invention, and the present invention is not limited to this one condition example. The present invention allows an adoption of various conditlons as long os an object of the present invention is achiGved without departing from the gist of the present invc-:-ntion. [0098] (First Experiment) In a first experiment, steels having the components presented in Table 1 were melted and slabs were - !)3 - prepared by continuous casting by a conventional method. The balance of the chemical composition presented in Table 1 is Fe and impurities. An underline in Table 1 indicates that the value deviates from a range of the present invention. Then, hot rolling and cooling on ROT were performed under the condition~ presented in Table 2 to obtain a steel sheet having an initial structure presented in Table 2. Thereafter, reheating was performed under the conditions presented in Table 2, and then pickling and skin-pass rolling with reduction ratio of 0.5% were performed to obtain a high-strength steel sheet. The thickness of the high-strength steel sheet was 2.6 mm to 3.2 mm. An underlines in Table 2 indicate that the item deviates from a range of the present invention. For the column of "surface coarse grain layer'' in Table 2, those in which the average diameter Ds of ferrite in the surface layer portion having a depth of 4 x Do from the surface of the steel sheet is twice or less the average diameter Do "without", those that are more than twice as ''with.n [0099] [Table 1] "(__";; o TABLE 1 >-' 0 0 I STEEL I SYMBOL I c I Si Mn p cJ ('") ~ (!) N ! ' ' ' A B c D E F G H I J K L M N 0 p Q a b c d e ~ ' g h I I 0.060 I 0.01 12 0.008 I o.32o 0.01 3.7 0.010 1 o.oe1 088 1.2 0.018 1 o.o9o 0.01 1.6 0.008 1 o.12o 0.02 16 0.009 0.090 1.o4 1.5 0.011 0.090 1.50 2.0 0.008 1 o.oso 1.50 2.0 0.009 I o.16o 1.90 2.0 0.020 0.055 o.oo 1 2.0 0.008 0.050 0.80 0.8. 0.060 omo 0.01 1.2 0.008 0.061 0.88 I 1.2 O.G18 0.080 1.50 2.0 0009 o.o5o I o so 1.6 0.009 · o.o9o I o.o1 2.0 0 011 0.180 [1.00 I 2.0 0.060 0 380 I 1.20 1.4 0.020 0.070 0.10 4.2 0.130 0.050 1.00 1.0 0.020 0.020 1.00 3.0 0.010 0.070 1.50 1.4 0.010 0.060 010'1.1 0.008 0.070 1.00 2.0 0.008 0.075 1.00 1.2 0.018 0.070 1.00 1.2 O.D18 s 0.0020 0.0018 0.0030 0.0030 0.0010 0.0010 0.0010 0.0010 0.0400 0.0030 0.0020 0.0030 0.0030 0.0010 0.0030 0.0020 0.0020 0.0030 0.0025 0.0030 0.0040 0.0700 0.0020 0.0020 0.0030 I 0,0030 CHEMICAL COMPOSITION (MASS%) Ar3 POINT N AI Nb Ti Ca Mg Zr REM OTHERS (''C) 0.003 0.30 0.01 0.05 - - - - - 807 0.004 1.80 - - - - - - - 597 0.004 0.04 - - 0.0023 - - - - 817 0.004 0.40 - - 0.0030 - - - - 772 0.004 0.40 - - 0.0027 - - 0.0070 - 757 0.004 0.03 0.16 - - - - - Cu:1.15,Ni:0.58 800 0.002 0.04 0.04 0.13 - - - - 8:0.002 767 0.004 0.50 - - 0.0027 - - - - 797 0.003 0.30 - - - - - - - 764 0.008 0.03 0.05 0.18 - 0.0030 - - - 758 0.002 0.04 0.02 0.03 - - - - Cu:0.25,Ni:0.18 857 0.004 0.60 0.04 0.17 0.0023 - - - - 818 0.004 0.04 - - 0.0023 - - - Mo:0.1 817 0.004 0.50 - - 0.0027 - - - - 797 0.002 0.03 - 0.05 - - 0.0050 - V:0.05,B:0.0005 786 0.002 0.80 0.04 0.18 - - - 0.0050 Cr:2.5 769 0.002 0.03 - - - - - 0.0050 - 719 0.003 0.01 - 0.12 - - - - - 651 0.003 0.03 - - - - - - - 628 0.003 O.D4 0.40 - - - - - - 840 0.002 0.03 0.03 0.10 - - - - - 726 0.003 0.03 - 0.04 - - - - 815 O.G15 O.Q3 - 0.40 - - - - - 806 0.001 0.03 - - 0.020 - - - - 764 ' 0.004 0.04 - 0.03 - 0.0030 - - - 815 '0.004 0.04 - 0.05 - 0.0020 - - - 817 ......... ····· .. "'. " I lllllll!lll~~~·~~~~~ ~~~~~~~ ~~~~~[![~[~~~ ~~~~~~~~~~~~· [ •I ~~~~ljl ~11ill1111@11u~l1"~ll~·l! :j~llllil ml~l~l~l._jl i (I I I I I I ~~ ', 'w!N!Nio!ololololm!Niol•· i" I '• :~·"t . h-" >-" 0 ~ c-:3 ;JJ t7 ~-" (1) "' I s i EEL jSYMBOL I I A.A I 88 i I cc DO i EE FF GG HH H JJ KK LL MM NN 00 PP i QQ I RR '' ss ' ' a a I bb I GC I dd I i ee I ff I gg CHEMICAL COMPOSITION (MASS%) c Si I Mn p s N AI Nb Ti Ca Mg 0.080 0.10 2.0 0.020 0.0020 0.003 0.300 0.010 0.030 - - 0.090 0.60 2.1 0.015 0.0050 0.003 0.030 0.020 0.020 - - 0.080 o.;;s 1.8 0.018 0.0030 0.004 0.040 - - 0.002 - 0.090 0.01 1.6 0.008 0.0030 0.004 0.400 - - 0.003 - 0.090 0.60 2.1 0.009 0.0010 0.004 0.033 0.030 - - - 0.090 1.54 1.5 0.011 0.0010 0.004 0.030 0.046 - - - 0.135 1.00 2.2 0.008 0.0010 0.002 0.036 - 0.040 - - 0.070 0.10 1.8 0.006 0.0030 0.003 0.040 - - - - 0.190 0.50 2.8 0.060 0.0020 0.002 0.000 0.050 0.030 - - 0.320 001 3.7 0.010 0.0018 0.004 1.800 - - - - 0.150 1.90 2.0 0.020 0.0200 0.003 0.300 0.130 - - - 0.150 0.50 2.4 0.{)08 0.0030 0.005 0.032 - 0.040 - - 0.050 0.80 0.8 0.080 0.0020 0.008 0.040 0.020 0.130 0.002 - 0.060 0.01 1.3 0.012 0.0020 0.003 0.300 0.022 - - - 0.070 O.oO 2210.007 0.0040 1 0.003 0.035 - - - - 0.080 1.50 2.0 0.009 0.0010 0.004 0.500 - - 0.003 - omo, o.ss 1.3 0.009 0.0010 0.004 0.040 0.035 0.125 0.003 0.003 o.oso I o.so L6 0.009 0.0030 0.002 0.200 - 0.050 - - 0.120! 0.08 2.2 0.008 0.0030 0.002 0.035 - - - - 0.380 1.20 1.4 0.020 0.0030 0.003 0.005 - 0.120 - - 0.070 0.10 4.2 0130 0.0025 0.003 0.030 - - - - 0.050 1.00 1.0 0.020 ! 0.0030 0.003 0.035 0.200 - - - 0.020 1.00 j3.0 o.o1 o I o.oo4o 0.002 0.300 0.030 0.100 - - omo 1 so I L4 o.o1 o I o.o1oo 0.003 0.030 - 0.040 - - 0.060 010j1.1 o.oos I o.oozo 0.015 0.030 - 0.200 - - omo 100 )2.0 o.oos I o.oo2o 0.001 0.030 - - 0.020 - Ar3 POINT Zr REM OTHERS (cC) - - - 752 I - - - 738 I - - Cr:0.3 762 I - - - 772 - - - 737 I - - Cu:L15.Ni:0.58 800 I - - - 718 I - - - 752 I - 0.005 - 649 0.008 - - 597 • - - Cr:1.8 764 - - - 682 - - - 862 ! - - Mo:0.07 802 - - - 737 ! - - - 797 ' - - V:0.3 311 0.005 - V:0.05.8:0.0005 795 - - - 701 - - Cr:2.5 651 - - - 628 - - - 840 - - - 740 - - - 815 - - - 802 - - - 790 . !Ill ill IIlii~ I IIIII I 1~1!1~1 1lili ! II ' ' 1!\jl! I: I~ ' ' : ' ! ' ' ~,,, ' lilllllil lil~li li! .c :; " I I ~- ·-- I I I .. ' ' I I I ; i" I :1 I I "· '·· I I I ~~~ I H• I" I ~~~!I' I' I · lc " : ·10 I? , I§ I I' i !. . · I) 1~ · I ! I I I !· I IN I lo Ia .. I I I I I I ' '"'tlf' I~ I I§ I~ I* I 'if' , I€ I I I. I I~ I~ I' ·I" I• I" I"' lg ~~~ I I I im'l"·. I" I"' IN I I·· I ~ I I I IUI·I~ I I ~ I~ Ill I~ I~ I ~ I"'' I IU"I~; I· I• I· I" ' I I"' , ' J"l~~-- --~- I .,I I ·I. 1·1 Is I"' I· IN I I . ~ I I II I I I I I '" I" I "I I I. iiiD 1*11! ~~ I I• I I w~. I I' I "· ' I iL ,. . I I I .. I ! I I ! I i .[. I,· I• z ' ' ~~ I 0 i I I 1'0 g~s , 'lg . I i" . I•. ,. o< I ., ~! I j! ; ' I I L I~ ,. !, I ·.... ... .. I I I I I j i" g J I .i i" '! i<'O I I I" Ji, I • I I 12 ~ ' I I.. .. .. 1. ___ ]i I [0111] For each of the high-strength steel sheets, the microstructure was identified and configuration of martensite was identified. These results are presented. CLAIMS [Claim 1] A high-strength steel sheet, comprising: a chemical composition represented by, in mass%: C: 0.03% to 0.35%; Si: 0.01% to 2.0%; Mn: 0.3% to 4.0%; _IU: 0.01% to 2. 0%; p : 0.10% or less; s : 0.05% or less; N: 0.010% or less; Cr: 0.0% to 3. 0%; Mo: 0.0% to 1.0%; Ni: 0.0% to 3.0%; Cu: 0.0% to 3.0%; Nb: 0.0% to 0.3%; Ti: 0.0% to 0. 3%; V: 0.0% to 0.5%; B: 0.0% to 0. 1%; Ca: 0.00% to 0.01%; Mg: 0.00% to 0.01%; Zr: 0.00% to 0.01%; REM: 0.00% to 0.01%; and the balance: Fe and impurities, and a microstructure represented by, in area%, martensite: 5 9o or more; ferrite: 20% or more; and perlite: 5% or less, wherein an average diameter of martensite grain is 4 pm or less in equivalent circle diameter, - 67 - a ratio of the number of bulging type martensite grains to the number of martensite grains on grain boundary triple points of a matrix is 70% or more, wherein: the bulging type martensite grain is on one of the grain boundary triple points of the matrix; and at least one of grain boundaries of the bulging type martensite grai.n, the grain boundaries connecting two adJacent grain boundary triple points of the bulging type martonsi.te grain and grains of the matrix, has a convex curvature to an outer side with respect to line segments connecting the two adjacent grain boundary triple points, and an area ratio represented by VM I AO is 1.0 or more, wherein: VM denotes a total area of the martensite grains on the grain boundary triple points of the matrix; and AO denotes a total area of polygons composed of the line segments connecting two adjacent grain boundary triple points of the martensite grains. [Claim 2] The high-strength steel sheet according to claim 1, wherein an average diameter Ds of ferrite in a surface layer portion from a surface of the highstrength steel sheet to a depth 4 x 0 0 is not more than twice an average diameter Do, wherein the average diameter 0 0 is an average diameter of lerrllc in a region where a depth from the surface of the high- - 68 -- strength steel sheet is 1/4 of a thickness of the highstrength steel sheet. [Claim 3] The high-strength steel sheet according to claim 1 or 2, wherein an area fraction of unrecrystallized ferrite is 10% or less in the microstructure. [Claim 4] The high-strength steel sheet according to any one of claims 1 to 3, wherein, in the chemical composition, Cr: 0.05% to 3.0%, Mo: 0.05% to 1.0%, Ni: 0.05% to 3.0%, or Cu: 0.05% to 3.0%, or any combination thereof is satisfied. [Claim 5] The high-strength steel sheet according to any one of claims 1 to 4 ' wherein, in the chemical composition, Nb: 0.005% to 0. 3%' Ti: 0.005% to 0. 3%, or V: 0.01% to 0.5%r or any combination thereof is satisfied. [Claim 6] The high-strength steel sheet according to any one of clai.ms 1 to 5, wherein, in the chemi.cal composition, B: 0.0001% to 0.1% is satisf1ed. [Claim 7] The high-strength steel sheet according to any one of claims 1 to 6, wherein, in the chemical composition, Ca: 0.0005% to 0.01%, Mg: 0.0005% to 0.01%, Zr: 0.0005°6 to 0.01't, or - 69 - REM: 0.0005% to 0.01%, or any combination thereof is satisfied. [Claim 8] A method of manufacturing a high-strength steel sheet, comprising the steps of: preparing a steel sheet; reheating the steel sheet to a first temperature of 770"C to 820"C at an average heating rate of 3"C/s to 120"C/s; and then, cooling the steel sheet to a second temperature of 300"c or less at an average cooling rate of 60"C/s or more, wherein an area fraction of pearlite is 10% or less, an area fraction of unrecrystallized ferrite is 10% or less, and an average diameter of pearlite grain is 10 pm or less in the steel sheet, an average diameter Ds of ferrite in a surface layer portion from a surface of the steel sheet to a depth 4 x Do is not more than twice an average diameter D0 , wherein the average diameter Do is an average diameter of ferrite in a region where a depth from the surface of ~he steel sheet lS 1/4 of a thickness of the steel sheet, the cooling to the second temperature lS started within 8 seconds once the temperature of the steel sheet reaches the first temperature, and the steel sheet comprises a chemical composition represented by, in mass%: the balance: Fe and impurities. [Claim 9] The method of manufacturing the highstrength steel sheet according to claim 8, wherein the step of preparing the steel sheet comprises the step of hot-rolling and cooling a slab. [Claim 10] The method of manufacturing the highstrength steel sheet according to claim 9, wherein a rolling temperature is "Ar3 point + 10'C" to 1000°C, and a total reduction ratio is 15% or more in last two stands of finish rolling in the hot rolling, and a cooling stop temperature is sso·c or lower of the cooling in the step of preparing the steel sheet. [Claim 11] The method of manufacturing the highstrength steel sheet according to claim 8, wherein the step of preparing the steel sheet comprises the steps of: hot rol.ling a slab to obtai.n a hot-rolled steel sheet; and cold rolling, annealing and cooling the hot-rolled steel sheet. [Claim 12] The method of manufacturing the highstrength steel sheet according to claim 11, wherein a reduction ratio in the cold rolling is 30% or more, a temperature of the annealing is 730"C to 900"C, and an average cooling rate from the temperature of the annealing to 600"C is 1.0"C/s to 20"C/second in cooling in the step of preparing the steel sheet. [Claim 13] The method of manufacturing the highstrength steel sheet according to any one of claims 8 to 12' wherein, in the chemical composition, Cr: 0.05% to 3. 0% r Mo: 0 ... 0 5% t.o 1. 0% f Ni: 0.05% to 3 • 0%1 or Cu: 0.05 9c to 3 • 0 ~) 1 or any combination thereof is satisfied. [Claim 14] The method of manufacturing the highstrength steel sheet according to any one of clai.ms 8 to 13, 'Nherein, in the chemical composition, Nb: 0.005% to 0.3%, Ti: 0.005~' to 0.3~6, or - 72 - V: 0.01% to 0.5%, or any combination thereof is satisfied. [Claim 15] The method of manufacturing the highstrength steel sheet according to any one of claims 8 to 14, wherein, in the chemical composition, B: 0.0001% to 0.1% is satisfied. [Claim 16] The method of manufacturing the highstrength steel sheet according to any one oi claims 8 to 15, wherein, in the chemical compositi?n, Ca: 0. 0005% to 0.01%, JVIg: 0.0005% to 0.01%, Zr: 0. 0005% to 0.01%, or REM: 0.0005% to 0.0196, or any combination thereof is satisfied.